23MW17.xx Revolution CT Revolution CT ES User Manual - UM - 5951015-1EN - 1

Revolution™ CT, Revolution™ CT ES
User Manual
5951015-1EN
Revision 1
© 2023 GE HealthCare.
GE is a trademark of General Electric Company used under trademark license.
Contents
1 User Information . . . . . . . . . . . . . . . . . . . . . . . . . . 1
1.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . 1
1.2 User Documentation . . . . . . . . . . . . . . . . . . . . . . . 1
1.3 GE Approved Accessories, Components and Compatible 3rd Party Medical Devices . . . . 2
2 Regulatory Information. . . . . . . . . . . . . . . . . . . . . . . . 5
2.1 Applicable Regulations and Standards . . . . . . . . . . . . . . . . . . 5
2.2 Product Description. . . . . . . . . . . . . . . . . . . . . . . . 8
2.3 Product Manufacturer . . . . . . . . . . . . . . . . . . . . . . . 9
3 Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
3.1 General Safety Guidelines . . . . . . . . . . . . . . . . . . . . . .11
3.2 Safety Conventions . . . . . . . . . . . . . . . . . . . . . . . .12
3.3 Symbols and Warning Labels . . . . . . . . . . . . . . . . . . . . .13
3.3.1 Symbols . . . . . . . . . . . . . . . . . . . . . . . . .13
3.3.2 Equipment Warning Labels . . . . . . . . . . . . . . . . . . .18
3.4 Radiation Safety . . . . . . . . . . . . . . . . . . . . . . . . .27
3.5 Implantable Device Safety. . . . . . . . . . . . . . . . . . . . . .32
3.6 Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . .33
3.7 Electromagnetic Compatibility Safety . . . . . . . . . . . . . . . . . .37
3.8 Fire Safety . . . . . . . . . . . . . . . . . . . . . . . . . . .37
3.9 Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . .37
3.9.1 General Mechanical Safety . . . . . . . . . . . . . . . . . . .37
3.9.2 Patient Positioning . . . . . . . . . . . . . . . . . . . . . .38
3.9.3 Gantry Air Inlets . . . . . . . . . . . . . . . . . . . . . . .45
3.10 Use of Defibrillator. . . . . . . . . . . . . . . . . . . . . . . .47
3.11 Emergency Devices and Emergency Egress . . . . . . . . . . . . . . . .47
3.12 Laser Safety . . . . . . . . . . . . . . . . . . . . . . . . . .51
3.13 Reconstructed Image Orientation . . . . . . . . . . . . . . . . . . .54
3.14 Data Safety . . . . . . . . . . . . . . . . . . . . . . . . . .56
3.15 Application Specific Safety Topics . . . . . . . . . . . . . . . . . . .58
3.15.1 Axial and Helical Scanning . . . . . . . . . . . . . . . . . . .58
3.15.2 Cardiac Imaging . . . . . . . . . . . . . . . . . . . . . .59
3.15.3 CT Integrated Cardiac Module . . . . . . . . . . . . . . . . . .61
3.15.4 Advanced Application Safety . . . . . . . . . . . . . . . . . .61
3.15.5 Measurements . . . . . . . . . . . . . . . . . . . . . . .61
5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES i

3.15.6 Segment Tools . . . . . . . . . . . . . . . . . . . . . . .62
3.15.7 Filming and Saving Images . . . . . . . . . . . . . . . . . . .63
3.15.8 Head Imaging . . . . . . . . . . . . . . . . . . . . . . .63
3.15.9 Interventional Scanning . . . . . . . . . . . . . . . . . . . .64
3.15.10 GSI Scanning . . . . . . . . . . . . . . . . . . . . . . .66
3.15.11 Deep Learning Image Reconstruction (DLIR) . . . . . . . . . . . . .71
3.15.12 Max Field of View (MaxFOV 2) Reconstruction DFOV Greater than 50.0 cm . . . .71
3.15.13 Auto Positioning . . . . . . . . . . . . . . . . . . . . . .73
3.16 Application Software Safety . . . . . . . . . . . . . . . . . . . . .74
3.17 Accuracy of Measurements . . . . . . . . . . . . . . . . . . . . .74
3.17.1 Measure Distance for Axial, Helical, and Cine Images . . . . . . . . . . .74
3.17.2 Measure Distance for Scout Images . . . . . . . . . . . . . . . .74
3.17.3 Measure Angle . . . . . . . . . . . . . . . . . . . . . . .76
3.17.4 Voxel Dimensions . . . . . . . . . . . . . . . . . . . . . .76
3.17.5 ROI . . . . . . . . . . . . . . . . . . . . . . . . . .76
3.17.6 CT Number . . . . . . . . . . . . . . . . . . . . . . . .77
3.17.7 Range, Precision and Accuracy of Displayed Values . . . . . . . . . . .78
3.18 Accessory Safety . . . . . . . . . . . . . . . . . . . . . . . .79
3.19 Maintenance and Cleaning and Disinfection . . . . . . . . . . . . . . . .83
3.19.1 General Cleaning and Disinfection . . . . . . . . . . . . . . . . .83
3.19.2 Cleaning and Disinfection Agents . . . . . . . . . . . . . . . . .84
3.20 Hazardous Substances . . . . . . . . . . . . . . . . . . . . . .85
3.21 System Performance . . . . . . . . . . . . . . . . . . . . . . .86
4 Read Me First . . . . . . . . . . . . . . . . . . . . . . . . . . 89
4.1 About This Manual . . . . . . . . . . . . . . . . . . . . . . . .89
4.2 Scan Monitor . . . . . . . . . . . . . . . . . . . . . . . . . .90
4.2.1 Home and Health Dashboards . . . . . . . . . . . . . . . . . .91
4.2.2 New Patient . . . . . . . . . . . . . . . . . . . . . . . .95
4.2.3 Patient Schedule. . . . . . . . . . . . . . . . . . . . . . .96
4.2.4 Using Remote Control Panel Patient Positioning Controls with AVIMOS. . . . . .98
4.2.5 Scan Setup . . . . . . . . . . . . . . . . . . . . . . . 104
4.3 Image Monitor . . . . . . . . . . . . . . . . . . . . . . . . 111
4.4 User Interface Conventions . . . . . . . . . . . . . . . . . . . . 120
4.5 System Troubleshooting Tips . . . . . . . . . . . . . . . . . . . . 124
5 Pediatrics and Small Patients . . . . . . . . . . . . . . . . . . . . 125

5.1 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . 125
5.2 Radiation Exposure . . . . . . . . . . . . . . . . . . . . . . . 125
5.2.1 Radiation exposure sensitivity . . . . . . . . . . . . . . . . . 125
5.2.2 Dose reporting considerations . . . . . . . . . . . . . . . . . 125
ii Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

5.2.3 Minimize pediatric and small patient doses . . . . . . . . . . . . . 127
5.3 Pediatric and small patient scans . . . . . . . . . . . . . . . . . . 128
5.3.1 Optimize pediatric protocols for your facility . . . . . . . . . . . . . 128
5.3.2 Pediatric protocols . . . . . . . . . . . . . . . . . . . . . 129
5.3.3 Color Coding for Kids Protocol Selection . . . . . . . . . . . . . . 129
5.3.4 Set up a pediatric or small patient exam . . . . . . . . . . . . . . 131
5.3.5 Adjust pediatric and small patient scan parameters . . . . . . . . . . . 131
6 Large Patient . . . . . . . . . . . . . . . . . . . . . . . . . . 135

6.1 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . 135
6.2 Large Patients . . . . . . . . . . . . . . . . . . . . . . . . 135
6.2.1 Scanning large patients . . . . . . . . . . . . . . . . . . . 135
6.2.2 Guidelines for adjusting individual exposure parameters by patient. . . . . . 136
6.2.3 Radiation exposure and dose reporting . . . . . . . . . . . . . . 137
7 Dose Check . . . . . . . . . . . . . . . . . . . . . . . . . . . 139

7.1 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . 139
7.1.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . 139
7.1.2 Protocol Considerations . . . . . . . . . . . . . . . . . . . 140
7.1.3 Terminology . . . . . . . . . . . . . . . . . . . . . . . 140
7.2 Set the Dose Check Administrator Role . . . . . . . . . . . . . . . . . 141
7.3 Set the Dose Check AV Exceeding User Role . . . . . . . . . . . . . . . 142
7.4 Configure the System for Dose Check . . . . . . . . . . . . . . . . . 143
7.5 Configure the AV by Age Threshold . . . . . . . . . . . . . . . . . . 145
7.6 Build Protocols With Access Controls . . . . . . . . . . . . . . . . . 147
7.7 Build Protocols with Notification Values . . . . . . . . . . . . . . . . 148
7.8 Build Protocols with Notification Values by Factor . . . . . . . . . . . . . 149
7.9 Scan Using Alert Value Checking . . . . . . . . . . . . . . . . . . . 150
7.10 Scan Using Notification Value Checking . . . . . . . . . . . . . . . . 152
7.11 Dose Check during Interventional (SmartStep) Scans . . . . . . . . . . . . 154
7.12 Use the Dose Audit Tool . . . . . . . . . . . . . . . . . . . . . 154
8 Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . 159
8.1 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . 159
8.2 UDI Marking . . . . . . . . . . . . . . . . . . . . . . . . . 159
8.3 Scanner Desktop. . . . . . . . . . . . . . . . . . . . . . . . 159
8.4 Auto Positioning Depth Xtream Camera . . . . . . . . . . . . . . . . 178
8.5 Xtream Tablet Gantry Display . . . . . . . . . . . . . . . . . . . . 178
8.5.1 Overview . . . . . . . . . . . . . . . . . . . . . . . . 178
8.5.2 Tool bar and Cradle/Tilt Information . . . . . . . . . . . . . . . 180
5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES iii

8.5.3 Collision or Emergency Stop Status Indicator . . . . . . . . . . . . . 184
8.6 Gantry . . . . . . . . . . . . . . . . . . . . . . . . . . . 186
8.6.1 Gantry display . . . . . . . . . . . . . . . . . . . . . . 186
8.6.2 Gantry and console interfaces . . . . . . . . . . . . . . . . . 191
8.6.3 Operate the gantry controls . . . . . . . . . . . . . . . . . . 197
8.6.4 Cardiac trigger monitor . . . . . . . . . . . . . . . . . . . 201
8.7 Table . . . . . . . . . . . . . . . . . . . . . . . . . . . 204
8.7.1 System operation and limitations that reduce the risk of collision with the patient . 205
8.7.2 Use the Load/Unload foot pedals . . . . . . . . . . . . . . . . 207
8.7.3 Patient comfort and accessories . . . . . . . . . . . . . . . . . 207
8.7.4 Table X-Y Accuracy for the Flat Table Top Workflow . . . . . . . . . . . 209
8.8 Hand-Held Controller . . . . . . . . . . . . . . . . . . . . . . 219
8.9 Hardware Components . . . . . . . . . . . . . . . . . . . . . 221
8.9.1 Components . . . . . . . . . . . . . . . . . . . . . . . 222
8.9.2 Coverage . . . . . . . . . . . . . . . . . . . . . . . . 222
8.9.3 Axial interval . . . . . . . . . . . . . . . . . . . . . . . 223
8.9.4 Helical pitch, scan mode, and collimation . . . . . . . . . . . . . . 223
8.9.5 Detector configuration . . . . . . . . . . . . . . . . . . . . 223
8.10 Power Distribution Unit . . . . . . . . . . . . . . . . . . . . . 224
8.11 System Cabinet. . . . . . . . . . . . . . . . . . . . . . . . 225
8.12 X-ray Tube and Generator . . . . . . . . . . . . . . . . . . . . 227
8.13 Purchasable Options . . . . . . . . . . . . . . . . . . . . . . 227
9 Startup and Shutdown . . . . . . . . . . . . . . . . . . . . . . . 233

9.1 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . 233
9.2 System Startup and Shutdown . . . . . . . . . . . . . . . . . . . 233
9.2.1 Prepare the system . . . . . . . . . . . . . . . . . . . . . 233
9.2.2 Sign On/Sign Off . . . . . . . . . . . . . . . . . . . . . . 233
9.2.3 System Start Up . . . . . . . . . . . . . . . . . . . . . . 236
9.2.4 Power Management. . . . . . . . . . . . . . . . . . . . . 238
9.3 Daily Quality Assurance . . . . . . . . . . . . . . . . . . . . . 239
9.3.1 Tube Warmup . . . . . . . . . . . . . . . . . . . . . . 239
9.3.2 Calibration . . . . . . . . . . . . . . . . . . . . . . . 240
9.3.3 Daily QA workflow . . . . . . . . . . . . . . . . . . . . . 243
9.3.4 Tube Conditioning . . . . . . . . . . . . . . . . . . . . . 244
9.3.5 Run Fast Calibrations . . . . . . . . . . . . . . . . . . . . 245
9.4 Software Update. . . . . . . . . . . . . . . . . . . . . . . . 246
9.5 Power Loss with SmartPower (Partial UPS) . . . . . . . . . . . . . . . 253
10 Patient Schedule . . . . . . . . . . . . . . . . . . . . . . . . 255

10.1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . 255
iv Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

10.2 Patient Schedule . . . . . . . . . . . . . . . . . . . . . . . 255
10.2.1 Schedule features . . . . . . . . . . . . . . . . . . . . . 255
10.2.2 New and completed records . . . . . . . . . . . . . . . . . 259
10.2.3 Add a patient to the Schedule . . . . . . . . . . . . . . . . . 259
10.2.4 Edit a patient in the schedule . . . . . . . . . . . . . . . . . 260
10.2.5 Delete a patient from the schedule . . . . . . . . . . . . . . . 263
10.2.6 View more patient information on the schedule . . . . . . . . . . . 264
10.2.7 Select a patient from the schedule . . . . . . . . . . . . . . . 264
10.2.8 Check a patient's status . . . . . . . . . . . . . . . . . . . 264
10.2.9 Search for a Patient on the Schedule . . . . . . . . . . . . . . . 265
10.2.10 HIS/RIS Search . . . . . . . . . . . . . . . . . . . . . 265
10.2.11 Setting up the HIS/RIS Refresh . . . . . . . . . . . . . . . . 267
10.2.12 Update the patient schedule . . . . . . . . . . . . . . . . . 269
10.2.13 SCP Configuration . . . . . . . . . . . . . . . . . . . . 270
10.2.14 Return Tag Configuration . . . . . . . . . . . . . . . . . . 272
11 Scan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 275
11.1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . 275
11.2 Scan Theory. . . . . . . . . . . . . . . . . . . . . . . . . 276
11.2.1 Dose Deterministic Effects . . . . . . . . . . . . . . . . . . 276
11.2.2 CT Perfusion. . . . . . . . . . . . . . . . . . . . . . . 279
11.2.3 Total Scan Time . . . . . . . . . . . . . . . . . . . . . 284
11.2.4 Automatic Exposure Control. . . . . . . . . . . . . . . . . . 284
11.2.5 Slice Thickness Reference Noise Index and Noise Index Values . . . . . . . 288
11.2.6 SmartmA/ODM . . . . . . . . . . . . . . . . . . . . . . 290
11.2.7 Auto Prescription . . . . . . . . . . . . . . . . . . . . . 299
11.3 Exam Workflow . . . . . . . . . . . . . . . . . . . . . . . . 310
11.3.1 Exam Workflow Concepts . . . . . . . . . . . . . . . . . . 311
11.3.2 Exam Workflow Windows. . . . . . . . . . . . . . . . . . . 311
11.3.3 Exam Workflow Procedures . . . . . . . . . . . . . . . . . . 318
11.4 Scan Parameters . . . . . . . . . . . . . . . . . . . . . . . 378
11.4.1 Scan Type . . . . . . . . . . . . . . . . . . . . . . . 378
11.4.2 Coverage Speed collection . . . . . . . . . . . . . . . . . . 380
11.4.3 kV and mA Control . . . . . . . . . . . . . . . . . . . . . 384
11.4.4 Anatomy Selection. . . . . . . . . . . . . . . . . . . . . 400
11.4.5 Scan parameters workflow . . . . . . . . . . . . . . . . . . 401
11.5 Timing Parameters . . . . . . . . . . . . . . . . . . . . . . 424
11.5.1 Timing Parameters collection . . . . . . . . . . . . . . . . . 424
11.5.2 Timing parameters workflow . . . . . . . . . . . . . . . . . 425
11.6 Recon Parameters . . . . . . . . . . . . . . . . . . . . . . . 427
11.6.1 Recon Parameter descriptions . . . . . . . . . . . . . . . . . 427
11.6.2 Primary Recon collection. . . . . . . . . . . . . . . . . . . 444
11.6.3 Primary Recon parameters workflow . . . . . . . . . . . . . . . 447
5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES v

11.6.4 Secondary Recon Parameters . . . . . . . . . . . . . . . . . 453
11.6.5 Graphic Rx Recon from Axial Reference Image . . . . . . . . . . . . 460
11.7 Auto Voice . . . . . . . . . . . . . . . . . . . . . . . . . 463
11.8 Additional Scan Features. . . . . . . . . . . . . . . . . . . . . 466
11.8.1 Add, duplicate or delete a group or series . . . . . . . . . . . . . 466
11.8.2 Optimize technical parameters . . . . . . . . . . . . . . . . . 469
11.8.3 Optimize GSI technical parameters . . . . . . . . . . . . . . . 470
11.8.4 Optimize patient dose . . . . . . . . . . . . . . . . . . . 471
11.8.5 View the Dose Report . . . . . . . . . . . . . . . . . . . . 473
11.8.6 Dose Information . . . . . . . . . . . . . . . . . . . . . 474
12 Scan Applications . . . . . . . . . . . . . . . . . . . . . . . . 475

12.1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . 475
12.2 ASiR-V. . . . . . . . . . . . . . . . . . . . . . . . . . . 475
12.3 SmartPrep . . . . . . . . . . . . . . . . . . . . . . . . . 479
12.3.1 SmartPrep Workflow . . . . . . . . . . . . . . . . . . . . 480
12.3.2 SmartPrep Windows/Elements . . . . . . . . . . . . . . . . . 480
12.3.3 Set up a SmartPrep series . . . . . . . . . . . . . . . . . . 489
12.3.4 Acquire a scan without Dynamic Transition . . . . . . . . . . . . . 492
12.3.5 Acquire a scan with Dynamic Transition . . . . . . . . . . . . . . 494
12.3.6 Retake Monitor . . . . . . . . . . . . . . . . . . . . . . 496
12.3.7 Scan Phase — Diagnostic Scan . . . . . . . . . . . . . . . . . 496
12.4 Smart Prep with Auto ROI (Option). . . . . . . . . . . . . . . . . . 496
12.4.1 Auto ROI Workflow Overview . . . . . . . . . . . . . . . . . 497
12.5 Enhanced Xtream Injector . . . . . . . . . . . . . . . . . . . . 500
12.5.1 About Enhanced Xtream Injector . . . . . . . . . . . . . . . . 501
12.5.2 Enhanced Xtream Injector window. . . . . . . . . . . . . . . . 502
12.5.3 Contrast report . . . . . . . . . . . . . . . . . . . . . . 505
12.5.4 Set up the Enhanced Xtream Injector . . . . . . . . . . . . . . . 506
12.6 SmartStep . . . . . . . . . . . . . . . . . . . . . . . . . 507
12.6.1 Workflow overview . . . . . . . . . . . . . . . . . . . . 508
12.6.2 Prepare for an exam . . . . . . . . . . . . . . . . . . . . 509
12.6.3 Set up the scan . . . . . . . . . . . . . . . . . . . . . . 511
12.6.4 GraphicRx with Axial System Preference . . . . . . . . . . . . . . 513
12.6.5 Acquire a scan . . . . . . . . . . . . . . . . . . . . . . 513
12.6.6 SmartStep Display screen . . . . . . . . . . . . . . . . . . 515
12.6.7 Display images . . . . . . . . . . . . . . . . . . . . . . 518
12.7 GSI . . . . . . . . . . . . . . . . . . . . . . . . . . . 519
12.7.1 GSI Overview . . . . . . . . . . . . . . . . . . . . . . 519
12.7.2 Material Density and Monochromatic images . . . . . . . . . . . . 519
12.7.3 Quality Check images . . . . . . . . . . . . . . . . . . . . 520
12.7.4 KVP-Like images . . . . . . . . . . . . . . . . . . . . . 520
vi Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

12.7.5 High kVp images . . . . . . . . . . . . . . . . . . . . . 520
12.7.6 GSI MAR images . . . . . . . . . . . . . . . . . . . . . 520
12.7.7 Kidney stone evaluation with GSI . . . . . . . . . . . . . . . . 521
12.7.8 GSI Profile Editor . . . . . . . . . . . . . . . . . . . . . 521
12.7.9 GSI Assist mA Mode . . . . . . . . . . . . . . . . . . . . 531
12.7.10 GSI Profiles. . . . . . . . . . . . . . . . . . . . . . . 531
12.7.11 GSI Manual . . . . . . . . . . . . . . . . . . . . . . . 552
12.7.12 ASiR-V in conjunction with GSI data . . . . . . . . . . . . . . . 553
12.7.13 GSI Annotation . . . . . . . . . . . . . . . . . . . . . 553
12.7.14 GSI Recon . . . . . . . . . . . . . . . . . . . . . . . 553
12.8 Volume Shuttle (Axial) . . . . . . . . . . . . . . . . . . . . . 556
12.8.1 Overview. . . . . . . . . . . . . . . . . . . . . . . . 556
12.8.2 Volume Shuttle Theory . . . . . . . . . . . . . . . . . . . 556
12.8.3 Considerations . . . . . . . . . . . . . . . . . . . . . . 558
12.8.4 Reconstruction . . . . . . . . . . . . . . . . . . . . . . 560
12.8.5 Working with an Injector and Axial Shuttle . . . . . . . . . . . . . 560
12.8.6 Acquire a scan . . . . . . . . . . . . . . . . . . . . . . 560
13 Lung Cancer Screening . . . . . . . . . . . . . . . . . . . . . . 563

13.1 Indications for Use. . . . . . . . . . . . . . . . . . . . . . . 563
13.2 Lung Cancer Screening Overview . . . . . . . . . . . . . . . . . . 563
13.2.1 I-ELCAP (International Early Lung Cancer Action Program) . . . . . . . . 563
13.2.2 NLST (National Lung Screening Trial) . . . . . . . . . . . . . . . 564
13.2.3 USPSTF (U.S. Preventative Services Task Force). . . . . . . . . . . . 565
13.2.4 Centers for Medicare and Medicaid Services (CMS) . . . . . . . . . . . 565
13.3 Appropriateness and Inclusion Criteria . . . . . . . . . . . . . . . . 566
13.3.1 Patient Eligibility . . . . . . . . . . . . . . . . . . . . . 566
13.4 GE Lung Cancer Screening Protocol Considerations . . . . . . . . . . . . 567
13.4.1 Acquisition and Reconstruction Guidelines . . . . . . . . . . . . . 568
13.4.2 Dose Guidelines . . . . . . . . . . . . . . . . . . . . . 568
13.4.3 Automatic Exposure Control. . . . . . . . . . . . . . . . . . 569
13.4.4 Noise Reduction Features . . . . . . . . . . . . . . . . . . 569
13.4.5 Enabling Dose Check Notification . . . . . . . . . . . . . . . . 569
13.4.6 Considerations for Acquisition and Post-Processing Patient Scanning . . . . . 569
13.4.7 Image Analysis Technical Considerations. . . . . . . . . . . . . . 570
14 Cardiac . . . . . . . . . . . . . . . . . . . . . . . . . . . . 573
14.1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . 573
14.2 Patient preparation and set up before Scanning . . . . . . . . . . . . . 573
14.2.1 Consent Forms . . . . . . . . . . . . . . . . . . . . . . 573
14.2.2 Exam Prep Instructions . . . . . . . . . . . . . . . . . . . 573
14.2.3 Breathing instructions . . . . . . . . . . . . . . . . . . . 573
14.2.4 IV setup and contrast . . . . . . . . . . . . . . . . . . . . 576
5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES vii

14.2.5 Attach ECG electrodes to the patient . . . . . . . . . . . . . . . 576
14.2.6 Check Electrode Impedance . . . . . . . . . . . . . . . . . . 581
14.2.7 Cardiac Phase Background . . . . . . . . . . . . . . . . . . 584
14.2.8 Display an ECG Trace on the operator console . . . . . . . . . . . . 586
14.3 Cardiac Scan Parameters. . . . . . . . . . . . . . . . . . . . . 586
14.3.1 Scan Type . . . . . . . . . . . . . . . . . . . . . . . 586
14.3.2 Primary Recon . . . . . . . . . . . . . . . . . . . . . . 587
14.3.3 Secondary Recon . . . . . . . . . . . . . . . . . . . . . 587
14.3.4 One Heart Cycle recon . . . . . . . . . . . . . . . . . . . 588
14.3.5 Cardiac Scan Modes . . . . . . . . . . . . . . . . . . . . 590
14.3.6 Cardiac scan modes (for helical 40mm only). . . . . . . . . . . . . 590
14.3.7 Anatomy Selection. . . . . . . . . . . . . . . . . . . . . 594
14.3.8 Cardiac Modulated mA . . . . . . . . . . . . . . . . . . . 595
14.3.9 Auto Gating . . . . . . . . . . . . . . . . . . . . . . . 595
14.3.10 Graphic Prescription (Graphic Rx) Detailed View . . . . . . . . . . . 601
14.3.11 Scan Overlap . . . . . . . . . . . . . . . . . . . . . . 603
14.3.12 Single Table Position . . . . . . . . . . . . . . . . . . . 604
14.3.13 Set the ECG and Gating settings . . . . . . . . . . . . . . . . 604
14.4 Cardiac Study Workflow . . . . . . . . . . . . . . . . . . . . . 609
14.4.1 Acquire a scout scan . . . . . . . . . . . . . . . . . . . . 609
14.4.2 Acquire a heart localizer or calcium score scan (optional, but recommended) . . 610
14.4.3 SmartPrep Workflow . . . . . . . . . . . . . . . . . . . . 611
14.4.4 Acquire a Timing Bolus (optional) . . . . . . . . . . . . . . . . 611
14.4.5 Acquire a contrast enhanced cardiac scan . . . . . . . . . . . . . 614
14.5 Cardiac Recon . . . . . . . . . . . . . . . . . . . . . . . . 616
14.5.1 Cardiac QC Recon . . . . . . . . . . . . . . . . . . . . . 616
14.5.2 Primary Recon . . . . . . . . . . . . . . . . . . . . . . 616
14.5.3 Recon Link to Auto Gating . . . . . . . . . . . . . . . . . . 617
14.5.4 Prescribing Basic Cardiac Secondary Recons . . . . . . . . . . . . 617
14.5.5 Smart Phase. . . . . . . . . . . . . . . . . . . . . . . 619
14.5.6 Interactive ECG Editor . . . . . . . . . . . . . . . . . . . . 622
14.5.7 Graphically adjust reconstruction timing . . . . . . . . . . . . . . 623
14.5.8 Insert, delete, or move an R-peak trigger . . . . . . . . . . . . . . 623
14.5.9 Switching between Smart Arrhythmia Management Exposures . . . . . . . 624
14.5.10 Display secondary recon images . . . . . . . . . . . . . . . . 624
14.6 SnapShot Freeze . . . . . . . . . . . . . . . . . . . . . . . 624
15 View Images . . . . . . . . . . . . . . . . . . . . . . . . . . 627

15.1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . 627
15.2 Image Display . . . . . . . . . . . . . . . . . . . . . . . . 630
15.2.1 Access images in File Manager . . . . . . . . . . . . . . . . . 630
15.2.2 Access images from the Reconstruction and Image Processing window . . . . 635
viii Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

15.2.3 Selecting viewports for images in the Reconstruction and Image Processing Task List.
638
15.2.4 View images in a cine loop . . . . . . . . . . . . . . . . . . 638
15.2.5 View a reference image . . . . . . . . . . . . . . . . . . . 641
15.3 Image Tools . . . . . . . . . . . . . . . . . . . . . . . . . 641
15.3.1 Display normal . . . . . . . . . . . . . . . . . . . . . . 641
15.3.2 Edge, smoothing and lung enhancement filters . . . . . . . . . . . 641
15.3.3 Gray Scale Enhancement . . . . . . . . . . . . . . . . . . 643
15.3.4 Flip/rotate images . . . . . . . . . . . . . . . . . . . . . 645
15.3.5 DICOM Gray Scale Presentation State (GSPS) objects . . . . . . . . . . 646
15.3.6 Magnify or minify an image . . . . . . . . . . . . . . . . . . 647
15.3.7 Apply a matte . . . . . . . . . . . . . . . . . . . . . . 647
15.3.8 Move images within a viewport . . . . . . . . . . . . . . . . 647
15.3.9 Inverse the video display . . . . . . . . . . . . . . . . . . 648
15.3.10 Adjust the W/L . . . . . . . . . . . . . . . . . . . . . 648
15.4 Measurements . . . . . . . . . . . . . . . . . . . . . . . . 649
15.5 Additional Image Tools . . . . . . . . . . . . . . . . . . . . . 652
15.6 User Preferences . . . . . . . . . . . . . . . . . . . . . . . 662
16 Display Applications . . . . . . . . . . . . . . . . . . . . . . . 669

16.1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . 669
16.2 Add/Subtract . . . . . . . . . . . . . . . . . . . . . . . . 669
16.3 Direct Multi Planar Reformat (DMPR) . . . . . . . . . . . . . . . . . 676
16.3.1 Reformat Tools panel . . . . . . . . . . . . . . . . . . . . 678
16.3.2 Reformat planning. . . . . . . . . . . . . . . . . . . . . 688
16.4 Exam Split . . . . . . . . . . . . . . . . . . . . . . . . . 693
16.4.1 Selecting exams to be split . . . . . . . . . . . . . . . . . . 694
16.4.2 Configure hosts for exam split . . . . . . . . . . . . . . . . . 695
16.4.3 Split exams when the scan is completed . . . . . . . . . . . . . . 696
16.5 Prospective Exam Split . . . . . . . . . . . . . . . . . . . . . 699
16.6 Advanced Processing . . . . . . . . . . . . . . . . . . . . . . 703
17 Filming . . . . . . . . . . . . . . . . . . . . . . . . . . . . 705
17.1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . 705
17.2 Film Composer . . . . . . . . . . . . . . . . . . . . . . . . 705
17.2.1 Tools on the Film Composer . . . . . . . . . . . . . . . . . . 705
17.3 Filming . . . . . . . . . . . . . . . . . . . . . . . . . . 712
17.3.1 Filming from Navigation Viewport in Scan/Review Session . . . . . . . . 712
17.3.2 Filming from File Manager . . . . . . . . . . . . . . . . . . 713
17.3.3 Filming from Navigation Viewport in Scan/Review Session and File Manager . . 714
17.3.4 Scout Image with Cross Reference Line . . . . . . . . . . . . . . 714
5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES ix

17.4 Tools in Maximized Film Composer . . . . . . . . . . . . . . . . . 714
17.4.1 Display Tools . . . . . . . . . . . . . . . . . . . . . . 714
17.4.2 Measure . . . . . . . . . . . . . . . . . . . . . . . . 721
17.4.3 Annotate . . . . . . . . . . . . . . . . . . . . . . . . 722
17.4.4 Analyze . . . . . . . . . . . . . . . . . . . . . . . . 725
17.5 Filming Status . . . . . . . . . . . . . . . . . . . . . . . . 726
17.6 Exam Mix Case Support with Warning Attention . . . . . . . . . . . . . 727
18 Reformat . . . . . . . . . . . . . . . . . . . . . . . . . . . 729
18.1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . 729
18.2 Reformat . . . . . . . . . . . . . . . . . . . . . . . . . . 730
18.2.1 Open Reformat . . . . . . . . . . . . . . . . . . . . . . 730
18.2.2 Use the Reformat Image Controls for Volume Share 5 Applications. . . . . . 731
18.2.3 Use the Reformat Image Controls for Volume Share 7 Applications. . . . . . 733
18.2.4 Use the keyboard shortcuts . . . . . . . . . . . . . . . . . . 737
18.2.5 Use the right-click functions . . . . . . . . . . . . . . . . . 738
18.3 Display . . . . . . . . . . . . . . . . . . . . . . . . . . 739
18.3.1 Annotation . . . . . . . . . . . . . . . . . . . . . . . 740
18.3.2 ROI . . . . . . . . . . . . . . . . . . . . . . . . . 740
18.3.3 Modify active (red) annotation . . . . . . . . . . . . . . . . . 741
18.3.4 Review Controller screen . . . . . . . . . . . . . . . . . . 743
18.3.5 Toolbar . . . . . . . . . . . . . . . . . . . . . . . . 745
18.3.6 Export Summary Table screen . . . . . . . . . . . . . . . . . 748
18.3.7 ROI Preferences screen . . . . . . . . . . . . . . . . . . . 752
18.3.8 Annotate an image . . . . . . . . . . . . . . . . . . . . 753
18.3.9 Save preset annotation . . . . . . . . . . . . . . . . . . . 753
18.3.10 Measure . . . . . . . . . . . . . . . . . . . . . . . 754
18.3.11 Manage Colormaps . . . . . . . . . . . . . . . . . . . . 755
18.3.12 Add an ROI . . . . . . . . . . . . . . . . . . . . . . . 756
18.4 View Types . . . . . . . . . . . . . . . . . . . . . . . . . 756
18.5 Volume Render . . . . . . . . . . . . . . . . . . . . . . . . 759
18.5.1 Up ramp VR adjustments . . . . . . . . . . . . . . . . . . 761
18.5.2 Surface rendering . . . . . . . . . . . . . . . . . . . . . 762
18.5.3 Render modes . . . . . . . . . . . . . . . . . . . . . . 762
18.5.4 VR Controls screen . . . . . . . . . . . . . . . . . . . . 763
18.5.5 Create a multi-VR object . . . . . . . . . . . . . . . . . . . 766
18.6 Segmentation . . . . . . . . . . . . . . . . . . . . . . . . 767
18.7 Batch . . . . . . . . . . . . . . . . . . . . . . . . . . . 778
18.7.1 Batch types . . . . . . . . . . . . . . . . . . . . . . . 778
18.7.2 Batch protocol . . . . . . . . . . . . . . . . . . . . . . 778
18.7.3 Preview, film, or save a batch . . . . . . . . . . . . . . . . . 779
18.7.4 Export Docking Station . . . . . . . . . . . . . . . . . . . 779
x Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

18.7.5 Batch screen . . . . . . . . . . . . . . . . . . . . . . 780
18.7.6 Export Images screen . . . . . . . . . . . . . . . . . . . . 784
18.7.7 Film/Save Options screen . . . . . . . . . . . . . . . . . . 785
18.7.8 Set up a batch oblique . . . . . . . . . . . . . . . . . . . 787
18.7.9 Batch film images . . . . . . . . . . . . . . . . . . . . . 788
18.7.10 Save a curved parallel plane or rotating curve batch . . . . . . . . . . 790
19 Data Management . . . . . . . . . . . . . . . . . . . . . . . . 791

19.1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . 791
19.2 File Manager . . . . . . . . . . . . . . . . . . . . . . . . 791
19.2.1 Controls area . . . . . . . . . . . . . . . . . . . . . . 792
19.2.2 Exam list . . . . . . . . . . . . . . . . . . . . . . . . 796
19.2.3 Series list. . . . . . . . . . . . . . . . . . . . . . . . 804
19.3 Job Management Screen . . . . . . . . . . . . . . . . . . . . . 806
19.4 Archive/Network . . . . . . . . . . . . . . . . . . . . . . . 809
19.4.1 Configure Network Hosts window . . . . . . . . . . . . . . . . 810
19.4.2 Working with archive nodes and network hosts. . . . . . . . . . . . 814
19.4.3 Certificate Management for DICOM over TLS. . . . . . . . . . . . . 815
19.4.4 Malware Protection . . . . . . . . . . . . . . . . . . . . 821
19.4.5 Local DB Retrieve Exams, Series, or Images . . . . . . . . . . . . . 827
19.4.6 Manually Send Exam, Series or Images . . . . . . . . . . . . . . 828
19.4.7 View the Backlog/Queue . . . . . . . . . . . . . . . . . . . 828
19.4.8 Eject (Detach) Media . . . . . . . . . . . . . . . . . . . . 829
19.4.9 Check the Network History . . . . . . . . . . . . . . . . . . 830
19.4.10 Workarounds . . . . . . . . . . . . . . . . . . . . . . 830
19.5 CD, DVD and USB Interchange . . . . . . . . . . . . . . . . . . . 830
19.6 Data Export . . . . . . . . . . . . . . . . . . . . . . . . . 842
19.7 Patient Data . . . . . . . . . . . . . . . . . . . . . . . . . 852
19.8 Scan Data Manager . . . . . . . . . . . . . . . . . . . . . . 858
19.9 Recon Management . . . . . . . . . . . . . . . . . . . . . . 866
19.9.1 Recon Management concepts . . . . . . . . . . . . . . . . . 866
19.9.2 General Recon Management Window . . . . . . . . . . . . . . . 867
19.9.3 Completed Recon Management Window . . . . . . . . . . . . . . 867
19.10 Reconstruction and Image Processing Task List . . . . . . . . . . . . . 868
19.10.1 Reconstruction and Image Processing Task List window . . . . . . . . 868
19.10.2 Reconstruction in the Reconstruction and Image Processing Task List . . . . 870
19.10.3 Reformatting in the Reconstruction and Image Processing Task List . . . . . 872
19.10.4 Series Numbering . . . . . . . . . . . . . . . . . . . . 872
19.10.5 Selecting viewports for images in the Reconstruction and Image Processing Task List
873
19.10.6 Image Tools Column . . . . . . . . . . . . . . . . . . . . 874
19.10.7 Output Options . . . . . . . . . . . . . . . . . . . . . 876
5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES xi

19.10.8 Data Transfer . . . . . . . . . . . . . . . . . . . . . . 876
20 Protocols . . . . . . . . . . . . . . . . . . . . . . . . . . . 879
20.1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . 879
20.2 Manage Protocols . . . . . . . . . . . . . . . . . . . . . . . 880
20.3 Protocol Management with kV Assist/Auto Prescription . . . . . . . . . . . 887
20.3.1 Considerations when enabling Auto Prescription in a Protocol . . . . . . . 887
20.3.2 Build a protocol with Auto Prescription . . . . . . . . . . . . . . 891
20.3.3 Auto Prescription Profile Editor . . . . . . . . . . . . . . . . . 893
20.3.4 Create Auto Prescription User Profile . . . . . . . . . . . . . . . 894
20.3.5 Considerations when enabling kV Assist . . . . . . . . . . . . . . 897
20.3.6 Build a protocol with kV Assist . . . . . . . . . . . . . . . . . 898
20.4 SmartPlan Settings in Protocol Management . . . . . . . . . . . . . . 899
20.4.1 SmartPlan Overview . . . . . . . . . . . . . . . . . . . . 899
20.4.2 SmartPlan Theory . . . . . . . . . . . . . . . . . . . . . 899
20.4.3 Enabling SmartPlan . . . . . . . . . . . . . . . . . . . . 899
20.4.4 SmartPlan Management . . . . . . . . . . . . . . . . . . . 904
20.5 Auto ROI (Option) Settings in Protocol Management . . . . . . . . . . . . 906
20.6 Auto ROI (Option) Management. . . . . . . . . . . . . . . . . . . 907
20.7 Auto Voice Management . . . . . . . . . . . . . . . . . . . . . 909
20.8 Auto Gating Configuration . . . . . . . . . . . . . . . . . . . . 913
20.9 Protocol Exchange . . . . . . . . . . . . . . . . . . . . . . . 918
20.10 IPM Service . . . . . . . . . . . . . . . . . . . . . . . . 925
20.11 GSI Profile Editor . . . . . . . . . . . . . . . . . . . . . . . 927
21 Access Controls . . . . . . . . . . . . . . . . . . . . . . . . . 929

21.1 Security Overview . . . . . . . . . . . . . . . . . . . . . . . 929
21.2 Application Access Controls . . . . . . . . . . . . . . . . . . . . 931
21.2.1 Introduction. . . . . . . . . . . . . . . . . . . . . . . 931
21.2.2 Users and groups . . . . . . . . . . . . . . . . . . . . . 932
21.2.3 Groups and privileges . . . . . . . . . . . . . . . . . . . . 932
21.2.4 Open EA3 . . . . . . . . . . . . . . . . . . . . . . . 932
21.2.5 Configure local users . . . . . . . . . . . . . . . . . . . . 933
21.2.6 Add a local user. . . . . . . . . . . . . . . . . . . . . . 936
21.2.7 Add a local group . . . . . . . . . . . . . . . . . . . . . 937
21.2.8 Add an enterprise group . . . . . . . . . . . . . . . . . . . 938
21.2.9 Add or remove a user from a group . . . . . . . . . . . . . . . 939
21.2.10 Change a user's full name . . . . . . . . . . . . . . . . . . 941
21.2.11 Change Application Password . . . . . . . . . . . . . . . . . 941
21.2.12 Change password from Login . . . . . . . . . . . . . . . . . 943
21.2.13 Prompt a user to change password . . . . . . . . . . . . . . . 943
xii Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

21.2.14 Lock or unlock a user . . . . . . . . . . . . . . . . . . . 943
21.2.15 Remove a user, group, or membership . . . . . . . . . . . . . . 943
21.2.16 Configure EA3 properties . . . . . . . . . . . . . . . . . . 945
21.2.17 Configure the Enterprise tab . . . . . . . . . . . . . . . . . 948
21.2.18 Auto configuration . . . . . . . . . . . . . . . . . . . . 950
21.2.19 Manual configuration . . . . . . . . . . . . . . . . . . . 952
21.3 Operating System (OS) Access Controls . . . . . . . . . . . . . . . . 953
22 System Management . . . . . . . . . . . . . . . . . . . . . . . 957

22.1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . 957
22.2 System Tools . . . . . . . . . . . . . . . . . . . . . . . . 957
22.2.1 Using Message Viewer. . . . . . . . . . . . . . . . . . . . 957
22.2.2 Save Cyber Security Audit Logs . . . . . . . . . . . . . . . . . 957
22.2.3 Apply Product Network Filters . . . . . . . . . . . . . . . . . 959
22.2.4 Find system software version information and third party software license . . . 959
22.3 System Preferences . . . . . . . . . . . . . . . . . . . . . . 960
22.3.1 Introduction. . . . . . . . . . . . . . . . . . . . . . . 960
22.3.2 Set General Preferences . . . . . . . . . . . . . . . . . . . 960
22.3.3 Set Access Control Preferences . . . . . . . . . . . . . . . . . 963
22.3.4 Set Viewport Preferences. . . . . . . . . . . . . . . . . . . 964
22.3.5 Set Patient Data Entry Preferences . . . . . . . . . . . . . . . . 969
22.3.6 Set Image Database Preferences . . . . . . . . . . . . . . . . 970
22.3.7 Set Networking Preferences . . . . . . . . . . . . . . . . . . 971
22.3.8 Set Exam Split Preferences . . . . . . . . . . . . . . . . . . 973
22.3.9 Set Protocol Selection Preferences. . . . . . . . . . . . . . . . 974
22.3.10 Set Contrast Management Preferences . . . . . . . . . . . . . . 975
22.3.11 Set Patient Handling Preferences . . . . . . . . . . . . . . . . 977
22.3.12 Set ECG Preferences . . . . . . . . . . . . . . . . . . . . 978
22.3.13 Set Interventional Preferences . . . . . . . . . . . . . . . . 980
22.3.14 Set Scan Room Display Preferences . . . . . . . . . . . . . . . 981
22.3.15 Set Lighting Preferences . . . . . . . . . . . . . . . . . . 983
22.3.16 Set PPS Preferences . . . . . . . . . . . . . . . . . . . . 984
22.3.17 Set Patient Schedule. . . . . . . . . . . . . . . . . . . . 985
22.3.18 Set the Patient Information Display . . . . . . . . . . . . . . . 986
22.3.19 Set Intelligent Protocoling Preferences . . . . . . . . . . . . . . 987
22.3.20 Set Cloud Connectivity . . . . . . . . . . . . . . . . . . . 988
22.3.21 Set Related Protocol . . . . . . . . . . . . . . . . . . . . 989
22.4 System Troubleshooting . . . . . . . . . . . . . . . . . . . . . 993
22.4.1 Open a Unix shell . . . . . . . . . . . . . . . . . . . . . 993
22.4.2 Collect Data with SPR Snap . . . . . . . . . . . . . . . . . . 994
22.4.3 System Time Adjustment Tool . . . . . . . . . . . . . . . . . 995
22.4.4 Restart an Application . . . . . . . . . . . . . . . . . . . 997
22.4.5 Close Volume Viewer / Reformat . . . . . . . . . . . . . . . . 997
5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES xiii

22.4.6 Fast Cal with GSI Refresh . . . . . . . . . . . . . . . . . . . 997
22.4.7 Xtream Camera Reset . . . . . . . . . . . . . . . . . . . . 998
22.4.8 Use iLinq . . . . . . . . . . . . . . . . . . . . . . . . 998
22.4.9 Enabling Tip Virtual Assist (TVA) . . . . . . . . . . . . . . . . 999
23 General Information . . . . . . . . . . . . . . . . . . . . . . .1003

23.1 Introduction. . . . . . . . . . . . . . . . . . . . . . . . . 1003
23.2 CT Operation Theory . . . . . . . . . . . . . . . . . . . . . . 1003
23.3 General Information . . . . . . . . . . . . . . . . . . . . . . 1006
23.4 Network . . . . . . . . . . . . . . . . . . . . . . . . . . 1008
23.4.1 Purpose of Revolution™ CT, Revolution™ CT ES Scanner Connection to Network . 1008
23.4.2 Network Interface Technical Specifications . . . . . . . . . . . . . 1009
23.4.3 Network Information Flows Specifications . . . . . . . . . . . . . 1009
23.4.4 Required characteristics and configuration for network support of Revolution™ CT,
Revolution™ CT ES Scanner specifications . . . . . . . . . . . . . . 1012
23.4.5 Network Compatibility . . . . . . . . . . . . . . . . . . . 1013
23.4.6 Hazardous Situations Due to Failure of IT—network . . . . . . . . . . 1017
23.5 System Operational Modes . . . . . . . . . . . . . . . . . . . . 1018
23.5.1 Overview. . . . . . . . . . . . . . . . . . . . . . . . 1018
23.5.2 Scout . . . . . . . . . . . . . . . . . . . . . . . . . 1018
23.5.3 Axial . . . . . . . . . . . . . . . . . . . . . . . . . 1018
23.5.4 Cine . . . . . . . . . . . . . . . . . . . . . . . . . 1019
23.5.5 VolumeShuttle™ (Axial) . . . . . . . . . . . . . . . . . . . 1019
23.5.6 Helical . . . . . . . . . . . . . . . . . . . . . . . . 1019
23.5.7 Cardiac Axial . . . . . . . . . . . . . . . . . . . . . . 1020
23.5.8 ECG-Modulated mA . . . . . . . . . . . . . . . . . . . . 1020
23.5.9 SmartTrack . . . . . . . . . . . . . . . . . . . . . . . 1022
23.5.10 Gemstone Spectral Imaging . . . . . . . . . . . . . . . . . 1022
23.5.11 SmartStep . . . . . . . . . . . . . . . . . . . . . . . 1024
23.6 Image Display . . . . . . . . . . . . . . . . . . . . . . . . 1025
23.7 Scout Based Attenuation Characterization . . . . . . . . . . . . . . . 1031
Appendix A Operator Messages. . . . . . . . . . . . . . . . . . . . .1037

A.1 Operator Messages . . . . . . . . . . . . . . . . . . . . . . . 1037
Appendix B Abbreviations . . . . . . . . . . . . . . . . . . . . . .1061

B.1 Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . 1061
Appendix C Units of Measure . . . . . . . . . . . . . . . . . . . . .1065

C.1 Units of Measure. . . . . . . . . . . . . . . . . . . . . . . . 1065
Appendix D Lexicon. . . . . . . . . . . . . . . . . . . . . . . . .1069

D.1 Lexicon . . . . . . . . . . . . . . . . . . . . . . . . . . 1069
xiv Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

Appendix E Dose Information Reference . . . . . . . . . . . . . . . . .1077
E.1 Dose Information Reference . . . . . . . . . . . . . . . . . . . . 1077
Appendix F Changes Impacting Dose or Dose Display/Reporting . . . . . . . . .1079

F.1 Changes Impacting Dose or Dose Display/Reporting . . . . . . . . . . . . 1079
F.1.1 Display of Z-Location with Highest Max Z-Location CTDIvol . . . . . . . . . 1079
F.1.2 Optimizing ODM on Revolution Apex . . . . . . . . . . . . . . . 1080
F.1.3 Update to Auto Prescription Size Adjusted Noise Index Strength Settings . . . . 1081
F.1.4 Dose Impact of Auto Prescription GE Reference Profile Changes . . . . . . . 1082
5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES xv

Page intentionally left blank
Revision History
Table 1
Revision Date Reason for Change
1 August 2023 Initial release
The original language of this document is English, Direction Number 5951015-1EN, Revision 1, and is applica-
ble to Revolution™ CT, Revolution™ CT ES 1.0 software, version 23MW17.xx.
5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES xvii

User Information
1 User Information
1.1 Introduction
Anyone who operates this system should have received prior training before they attempt to
scan patients. This training should include medical and X-ray education, If necessary, additional
training is available from a GE Applications Specialist. Contact your institution’s GE Healthcare sales
representative for additional information about further safety and operational training. This manual
does not provide medical explanations, but it does suggest potential applications for some of the
software features. It describes potential safety problems and how to avoid them.
Everyone who uses this equipment must read and understand all instructions, precautions and
warnings. Procedures and safety precautions described in the Safety chapter should be read
periodically.
Only designated persons (service personnel) are to install this system. They are to refer to the proper
pre-installation and installation manuals when installing the system.
Only designated persons are to perform service on this system. They are to refer to the proper service
manuals when servicing this system.
Do not use the equipment if a known safety problem exists. Call your local service provider and
have the system repaired.
1.2 User Documentation

Description
The user documentation is designed for safe and effective use of the system, and is divided into the
following parts:
1. User Manual: This manual contains all the user information required to operate the scanner in a
safe and proper manner.
2. Technical Reference Manual: This manual contains safety information and specifications related
to dose and image quality performance of the system. The manual is intended to assist with
quality assurance testing and planned maintenance to ensure system performance.
3. Application Tips and Workarounds: This manual details workaround information for software
and system information.
4. eUser Leaflet: This manual contains the safe and foreseeable medical emergency information
that is provided in paper form.
5. Private & Security Manual: This manual contains privacy and security features/capabilities
information for the scanner securely.
Accessing User Documentation

The system user information is designed to provide you with safety and operation information for you
to safely and effectively use the system.
5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES 1

User Information
To start the user information:

1. CT User Manual
• Insert the USB flash drive you wish to view into the USB port of the computer.
• Click the icon, and select Learning Solutions from the drop-down menu.
• Select the language in which you want to view the documentation.
2. AWS User Manual
NOTE
For desktop host computer systems that use:
-Z800
-Z420
A PMT tower (along with a USB interface) will be utilized. Figure 79 on page 161
showing the PMT now too please.
• Click the icon, and select Learning Solutions from the drop-down menu.
• Select AWS from the drop-down menu.
• Select the language in which you want to view the documentation.
To exit the user information:

• Click X to close user manual.
1.3 GE Approved Accessories, Components and

Compatible 3rd Party Medical Devices
With each use, check all accessories for damage and remove them from service if damaged or cracked.
Use only GE approved equipment together with this system.
Table 1 GE Approved Accessories
Type Model
SmartStep Kit (includes hand controller and foot- GE 5149705-4

switch)
Axial Head Holder 2115996-4
Coronal Head Holder 2115990-3
Cradle Extender 2115993-4
2 Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

User Information
Table 2 GE Approved Components
Type Manufacturer/Model
Partial UPS* Eaton Powerware 9355-15-14GE
External Hard Drive Seagate 2 TB USB 2.0/3.0
Bar Code Reader Honeywell 1300G
GE CT Flat Tabletop AAPM TG-66 Kit GE 5924000
Patient grounding strap Wrist band GE 5788434

Ground cord GE 5788435
SmartStep Monitor Boom (includes LCD monitor and GE 5115174-30, GE 5115174-33

mountings)
Water Phantom 5432878
QA Phantom 5477995
Metalless Compatible Phantom Holder 2331933-2
Carrying case for Phantom 5537763
Cradle Pad for Revolution 5433273 46-278986P2 (part of 46-229452G1)
Extender Pad 5122945-5
Knee Head Support Pad 46-278968P2 (part of 46-229452G1)
Shoulder Ankle Support Pad 46-278986P2 (part of 46-229452G1)
P9150SN Body Strap A 2152502
P9150SP Body Strap B 2152503
P9150SQ Body Strap C 2152504
P9150TS Body Strap A 2169679
P9150TT Body Strap B 2169680
P9150TU Body Strap C 2169681
Head strap 5835369 (part of 5835306 kit)
Chin strap 5835370 (part of 5835306 kit)
Head Strap (Qty 3) 46-237412P1
Strap Security 46-229450P1(part of 46-229452G1)
Strap 46-297629P1
Cardiac ECG wrist strap and cable 5812787

User Information
GE Approved Components continued

Table tray 2329064-2
IV holder 2309994-2
Table 3 GE Approved Compatible 3rd Party Medical Devices
Cardiac trigger monitor IVY 7800

IVY CTM-400
Patient contrast injector: Nemoto Dual Shot Alpha 7 (GE CiA425 Class IV)
For Enhanced Xtream Injector Option Nemoto Dual Shot Alpha (GE CiA425 Class IV)
Nemoto Dual Shot GX (GE CiA425 Class IV)
Medrad Stellant D (GE CiA425 Class IV)
Medrad Stellant Flex (GE CiA425 Class IV)
Medrad Centargo (GE CiA425 Class IV)
RTP Flat Tabletop (CT Cradle Overlay) Diacor OGS-4 (GE E6315JE)
CIVCO MTIL3311 (GE E8505MJ)
Respiratory Monitor Varian RGSC 1.1
Table Slicker for Revolution™ CT, Revolution™ CT ES GE 5538512
Foot Slicker for Revolution™ CT, Revolution™ CT ES GE 5603918
*See Revolution™ CT, Revolution™ CT ES User Manual Section 9.4 Power Loss with Partial UPS for
functional description
NOTE
Not all accessories are available in all markets.

Regulatory Information
2 Regulatory Information
2.1 Applicable Regulations and Standards

The CT system is classified as an electrical protection Class I (IEC 61140), ingress protection IPX0 (IEC
60529) equipment, not suitable for use in the presence of a flammable anesthetic mixture with oxygen
or nitrous oxide. No sterilization is applied. The patient table cradle and patient support accessories
are considered Type B applied parts. The integrated cardiac module is considered a Type CF applied
part. The SmartStep foot switch is classified as ingress protection IP68 (IEC 60529).
This product complies with the requirements of the following regulations and standards:
Code of Federal Regulations, Title 21, Part 820 — Quality System Regulation
Code of Federal Regulations, Title 21, Subchapter J — Radiological Health
Federal U.S. law restricts this device for sale by or on the order of a physician.
Revolution™ CT, Revolution™ CT ES systems comply with the following IEC standards including
applicable related amendments (not listed) and national deviations (not all listed).
• The system should be used only with GE approved equipment
• Detailed information concerning electromagnetic compatibility can be found in the
electromagnetic compatibility chapter of the Technical Reference Manual.
IEC 60601-1:2005 Medical electrical equipment - Part 1: General requirements for basic safety and
essential performance
ES 60601-1:2005
EN 60601-1:2006
CAN/CSA-C22.2 No. 60601-1:14
IEC 60601-1-2:2007 Medical electrical equipment - Part 1-2: General requirements for basic safety
and essential performance - Collateral standard: Electromagnetic compatibility -
Requirements and tests
IEC 60601-1-2:2014 Medical electrical equipment - Part 1-2: General requirements for basic safety
and essential performance - Collateral standard: Electromagnetic disturbances -
Requirements and tests
IEC 60601-1-3:2008 Medical electrical equipment – Part 1-3: General requirements for basic safety and
essential performance – Collateral standard: Radiation protection in diagnostic
X-ray equipment
(CT SCANNER with radiation protection in accordance with IEC 60601-1-3:2008)
IEC 60601-2-28:2010 Medical electrical equipment - Part 2-28: Particular requirements for the basic
safety and essential performance of X-ray tube assemblies for medical diagnosis
(X-RAY TUBE ASSEMBLY Tube Unit Assembly IEC 60601-2-28:2010)

safety and essential performance of X-ray tube assemblies for medical diagnosis
(X-RAY TUBE ASSEMBLY Tube Unit Assembly IEC 60601-2-28:2017)
safety and essential performance of X-ray equipment for computed tomography
(CT SCANNER products stated above IEC 60601-2-44:2009)
The products comply with the requirements of the following regulations and standards:
Regulation (EU) 2017/745 of the European Parliament and of the Council concerning medical devices
when it bears the following CE marking of conformity:
Authorized representative for Europe/European registered place of business:

GE Medical Systems SCS
283 rue de la Minière
78530 BUC France
Tel +33 130704040
This product passed all conformity assessment (approval) procedures that correspond to the
requirements of applicable technical regulations of the Customs Union.
Mark of conformity with the This product meets the requirements of the Technical
Technical Regulations. Regulations on medical devices, approved by Resolution
No. 753 of the Cabinet of Ministers of Ukraine of 2 October
2013.
NOTE
Only after Ukrainian regulatory registration is
complete, this label will be located on the Gan-
try
Authorized Representative in Ukraine

GE HEALTHCARE UKRAINE, LLC.
02000, Ukraine, Kyiv, 1V Pavla Tychyny
Avenue, office No. 408
+38 (044) 390 06 08
Уповноважений представник в Україні:

ТОВ «ДЖИІ ХЕЛСКЕР УКРАЇНА.»

02000, Україна, місто Київ, проспект Павла Тичини, будинок 1В, офіс 408
Тeл.: +38 (044) 390 06 08
Authorized Representative in Kazakhstan
General Electric Kazakhstan LLP
26/41, Zenkova Street, Medeu District, Almaty, 050010,
Kazakhstan
T +7 727 3560020
«Дженерал Электрик Қазақстан» ЖШС
Қазақстан, Алматы қаласы, Медеу ауданы, көшесі
ЗЕНКОВ, үй 26/41, пошталық индексі 050010
T +7 727 3560020
ТОО «Дженерал Электрик Казахстан»
Казахстан, город Алматы, Медеуский район, улица
Зенкова, дом 26/41, почтовый индекс 050010
T +7 727 3560020
Authorized representative of the manufacturer for claims in the Republic of Belarus:
GE Healthcare LLC
Room 30, 14 floor, premises I, 10, Presnenskaya Naberezhnaya, inner city territory Presnensky
municipal district,
Moscow, 123112
Tel Office: +7 495 739 6931, Fax: +7 495 739 6932, Tel Customer Service: 8 800 333 6967
88003336967@ge.com
http://www3.gehealthcare.ru/
Authorized Representative in Russia
GE Healthcare LLC, Room 30, 14 floor, premises I, 10, Presnenskaya Naberezhnaya, inner city territory
Presnensky municipal district, Moscow, 123112,
phone:+7 495 739 69 31, fax: +7 495 739 69 32.
Table 4 Regulatory Information applicable for Brazil
Product and Registration Information
Product Name Computed Tomography System
Model Revolution CT / Revolution CT ES

Content 01 Revolution CT, Instructions for Use, Accessories

and Parts / 01 Revolution CT ES, Instructions for Use,
Accessories and Parts
ANVISA Registration Number 80071260343
Importer and Distributer Information
Name GE HEALTHCARE DO BRASIL COMÉRCIO E SERVIÇOS

PARA EQUIPAMENTOS MEDICOS-HOSPITALARES LTDA.
Address Av. Magalhães de Castro, 4800 - Andar 10 Conj. 101 e

102, Torre 3 - Cidade Jardim -
CEP: 05676-120 - São Paulo/SP - Brasil
CNPJ Number 00.029.372/0001-40
Phone Number 3004 2525 (Capital)

08000 165 799 (Other Locations)
2.2 Product Description

2.2.1 Intended Use of the System
The system is intended for head, whole body, cardiac, and vascular X-ray Computed Tomography
applications.
2.2.2 Indications for Use of the System

The system is intended to produce cross-sectional images of the body by computer reconstruction of
xray transmission projection data from the same axial plane taken at different angles. The systems
with 160 mm detector coverage have the capability to image whole organs in a single rotation. Whole
organs include but are not limited to brain, heart, liver, kidney, pancreas, etc.. The system may acquire
data using Axial, Cine, Helical, Cardiac, and Gated CT scan techniques from patients of all ages. These
images may be obtained either with or without contrast. This device may include signal analysis and
display equipment, patient and equipment supports, components and accessories.
This device may include data and image processing to produce images in a variety of trans-axial and
reformatted planes. Further, the images can be post processed to produce additional imaging planes
or analysis results.
The system is indicated for head, whole body, cardiac, and vascular X-ray Computed Tomography
applications.
The device output is a valuable medical tool for the diagnosis of disease, trauma, or abnormality and
for planning, guiding, and monitoring therapy.
If the spectral imaging option is included on the system, the system can acquire CT images using
different kV levels of the same anatomical region of a patient in a single rotation from a single source.
The differences in the energy dependence of the attenuation coefficient of the different materials
provide information about the chemical composition of body materials. This approach enables images

to be generated at energies selected from the available spectrum to visualize and analyze information
about anatomical and pathological structures.
Gemstone Spectral Imaging (GSI) provides information of the chemical composition of renal calculi
by calculation and graphical display of the spectrum of effective atomic number. GSI Kidney stone
characterization provides additional information to aid in the characterization of uric acid versus non-
uric acid stones. It is intended to be used as an adjunct to current standard methods for evaluating
stone etiology and composition.
2.2.3 Contraindications
None known.
2.2.4 Clinical Benefit

Computed Tomography (CT) provides a non-invasive, non-surgical method to visualize anatomy. CT
is a valuable tool for physicians in the diagnosis of disease or anatomical abnormalities, planning
of medical or surgical treatments, and evaluation and management in a variety of diseases and
conditions.
Furthermore, CT may be used as guidance during minimally invasive procedures such as biopsies or
ablations to locate targeted lesions and avoid critical structures.
2.3 Product Manufacturer

This section lists the manufacturer of the Revolution™ CT, Revolution™ CT ES product.
Table 5 Revolution™ CT, Revolution™ CT ES Product Manufacturer
Model Name Legal Manufacturer* Manufacturer Address

Manufacturing Site
Revolution™ CT GE Medical Systems, LLC* 3000 North Grandview Blvd.

Revolution™ CT ES Waukesha, WI 53188 USA
Revolution™ CT GE Hangwei Medical Systems Co. West Area of Building No.3, No.1
Revolution™ CT ES Ltd Yongchang North Road,
Beijing Economic and Technologi-
cal Development Area,
BEIJING 100176 CHINA
Revolution™ CT GE Healthcare Japan Corporation 7-127, Asahigaoka 4-Chome

Hino-Shi, Tokyo 191-8503, Japan


Safety
3 Safety
3.1 General Safety Guidelines

This chapter provides information about safety precautions and procedures. It is important for you
to read and understand the contents of this chapter so the correct precautions and procedures are
followed. This manual should be kept near the scanner desktop for easy access.
United States Federal Regulation 21CFR 801.109
CAUTION
FEDERAL LAW RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF

A PHYSICIAN.
Any serious incident related to the use of this GE Healthcare device should be reported to both the
manufacturer and the health authority/competent authority where the device is installed.
To report to GE Healthcare: either contact your local service representative or report to: In-
box.complaints@ge.com.
Please provide the following information:
• The catalog number or the model designation of the device as stated on its identification plate
affixed on the device
• The System ID/serial number/lot number of the device
• Date of incident
• Description of incident, including any patient or user impact/injury
• Your contact information (facility, address, contact name, title, and telephone number).
• Although this equipment incorporates a high degree of protection against X-ray and laser
radiation outside the useful beam, and also makes the X-ray radiation dose to patient and laser
output power low enough to be proportionate to its intended use, it is impossible to eliminate the
X-ray radiation risks inherent with the use of X-ray technology and the laser radiation risk with the
use of the laser light marker completely without impacting the benefit of the product. See X-ray
radiation safety and laser safety section to reduce the unintended/excessive radiation risks as far
as possible.
• This product was designed and manufactured to ensure maximum safety of operation. It should
be operated and maintained in strict compliance with the safety precautions, warnings and
operating instructions contained herein, and in any other documentation specific to the product.
• The system has been designed to meet all the safety requirements applicable to medical
equipment. However, anyone attempting to operate the system must be fully aware of potential
safety hazards.

Safety
• The manufacturer or vendor of the equipment makes no representation, however, that the act of
reading this manual renders the reader qualified to operate, test or calibrate the system.
• The owner should make certain that only properly trained, fully qualified personnel are
authorized to operate the equipment. A list of authorized operators should be maintained.
• This manual should be kept at hand, studied carefully and reviewed periodically by the
authorized operators.
• Unauthorized personnel should not be allowed access to the system.
• Do not leave the patient unobserved at any time.
• Become familiar with the functional hardware so that you can recognize serious problems. Do not
use the system if it appears damaged or fails. Wait for qualified personnel to correct the problem.
• Abbreviations used in the operator manuals can be found in this manual.
• If the product does not operate properly or if it fails to respond to the controls as described in this
manual, the operator should:
• First ensure the safety of the patient.
• Next ensure the protection of the equipment.
• Evacuate the area as quickly as possible in any potentially unsafe situation.
• Follow the safety precautions and procedures as specified in this manual.
• Immediately contact the local service office, report the incident and await further
instructions.
• The images and calculations provided by this system are intended as tools for the competent
user. They are explicitly not to be regarded as a sole incontrovertible basis for clinical diagnosis.
Users are encouraged to study the literature and reach their own professional conclusions
regarding the clinical utility of the system.
• Understand the product specifications, system accuracy, and stability limitations. These
limitations must be considered before making any decision based on quantitative values. In case
of doubt, please consult your sales representative.
• Do not block the ventilation ports of the electronic equipment. Always maintain at least 6
inches (15 cm) clearance around the ventilation ports to prevent overheating and damage to the
electronic hardware.
• The supplier will make available on request circuit diagrams, component parts lists, descriptions,
calibration instructions which will assist the user's appropriately qualified technical personnel to
repair those parts designated to be repairable.
3.2 Safety Conventions

This manual addresses three safety classifications:

Safety
DANGER
THE MOST SEVERE LABEL DESCRIBES CONDITIONS OR ACTIONS WHICH

RESULT IN A SPECIFIC HAZARD. YOU WILL CAUSE SEVERE OR FATAL
PERSONAL INJURY, OR SUBSTANTIAL PROPERTY DAMAGE IF YOU IGNORE
THESE INSTRUCTIONS.
WARNING
THIS LABEL IDENTIFIES CONDITIONS OR ACTIONS WHICH RESULT IN

A SPECIFIC HAZARD. YOU WILL CAUSE SEVERE PERSONAL INJURY, OR
SUBSTANTIAL PROPERTY DAMAGE IF YOU IGNORE THESE INSTRUCTIONS.
CAUTION
THIS LABEL APPLIES TO CONDITIONS OR ACTIONS THAT HAVE POTENTIAL

HAZARD. YOU MAY CAUSE MINOR INJURY OR PROPERTY DAMAGE IF YOU
IGNORE THESE INSTRUCTIONS.
This manual uses pictures, or icons, to reinforce the printed message. It uses the corresponding
international symbol or icon next to the danger, warning or caution message. For example, the upright
hand with the lightning bolt across it warns of electrical hazards.
3.3 Symbols and Warning Labels
3.3.1 Symbols
This chapter uses the international symbol or icon along with the danger, warning or caution message.
Table 6 Symbols Used in Labeling
Symbol Description
Alternating current
3 Phase alternating current
Protective earthing point

Safety
Symbols Used in Labeling continued

Symbol Description
ON / Power ON
OFF / Power OFF
Input power
Output Power
Type B applied part
Functional earth ground
Electrical shock hazard
Caution or warning
Hand Pinch
Radiation

Safety

Symbol Description
Maximum Weight Capacity
Emergency Stop
ETL Mark: Proof of product compliance (electrical, gas and other

safety standards) to North American safety standards. Authorities
Having Jurisdiction (AHJs) in 50 states and Canada and retailers
accept the ETL classified/and recognized as proof of product safe-
ty..
The system shall conform to applicable requirements of 21CFR

Subchapter J
WEEE: This symbol indicates that when the end-user wants to dis-
card this product, it must be sent to separate collection facilities
for recovery and recycling.
CE Mark: Manufacturer's declaration that the product complies

with the essential requirements of the relevant European health,
safety and environmental protection legislation.
The Common Mark of Products Circulation certifies that the prod-

ucts bearing this mark passed all conformity assessment (appro-
val) procedures established by technical regulations of the Cus-
toms Union and correspond to the requirements of all technical
regulations of the Customs Union applied to these products.
Authorized representative for Europe/European registered place

of business.

Safety
Table 7 Symbols Used in Labeling
Symbol Description
Made for Indicates the manufacturer (responsible design owner)
Made by or by Indicates the manufacturing Location
Refer to instruction manual/booklet

Attention, consult accompanying documents
Pushing prohibited
Do not stand on table foot cover
Do not stack on power box
Do not sit on power box

Safety

Symbol Description
Do not stand on power box
Legal Manufacturer
Date of manufacture
Prescription Use Only
Dust-tight
Protected against the effects of continuous immersion in water
Serial number
Catalog number
Medical Device
X-Ray filtration (Al Equivalent Filtration)

Safety

Symbol Description
Minimum filtration
Laser symbol
Focal Spot XL
Focal Spot L
Focal Spot S
3.3.2 Equipment Warning Labels

The following Warning Labels are used on the equipment:
3.3.2.1 Laser Warning Labels
Figure 1 Warning labels located at the bottom of the gantry cover (Reference 21CFR 1040.10
(g)(4))

Safety
CAUTION
LASER RADIATION
DO NOT STARE INTO BEAM
CLASS 2 LASER PRODUCT
CAUTION
LASER RADIATION
Do Not Stare into Beam
635, 670nm Laser Diode
1 Milliwatt Maximum Output
Class II Laser Product
Figure 2 Labels on the front of the gantry (Reference 21CFR 1040.10 (h))
CAUTION
LASER APERTURE
Do not stare into beam
Figure 3 Labels on the front of gantry, rear of table, back of PDU, back of Scanner Desktop, and
side of System Cabinet.

Safety
CAUTION
AVOID INJURY. READ AND UNDERSTAND INFORMATION IN MANUALS

BEFORE OPERATING PRODUCT.
3.3.2.2 X-ray Warning Labels
Figure 4 Label located on Scan Control Interface (Reference 21CFR 1020.30 (j))
WARNING
THIS X-RAY UNIT MAY BE DANGEROUS TO PATIENT AND OPERATOR

UNLESS SAFE EXPOSURE FACTORS, OPERATING INSTRUCTIONS AND
MAINTENANCE SCHEDULES ARE OBSERVED.
To be used by authorized personnel only.
3.3.2.3 Table Warning Labels
Figure 5 Pinch warning label located on the table

Safety
WARNING
AVOID INJURY. FINGER PINCHING CAN CAUSE PHYSICAL INJURY. KEEP

FINGERS AWAY FROM THIS AREA BEFORE MOVING THE CRADLE.
Standard Weight Capacity Table

Table could include either of the following two labels:
Figure 6 Weight limit warning label located on the standard weight capacity table
WARNING
AVOID INJURY. DO NOT EXCEED TABLE MAXIMUM CAPACITY OF 227 KG (500

LB).
Figure 7 Weight limit label located on the standard weight capacity table
Heavy Weight Capacity Table
Figure 8 Weight limit label located on the heavy weight capacity table

Safety
3.3.2.4 Power Distribution Unit (PDU) Warning Labels
Figure 9 PDU move warning on back of PDU
WARNING
PDU CAN MOVE AND DAMAGE CABLES. DO NOT LEAN ON OR MOVE WHEN
CONNECTED TO POWER.
Figure 10 PDU move caution on back of PDU
CAUTION
PDU CAN MOVE AND DAMAGE CABLES. DO NOT LEAN ON OR MOVE WHEN
CONNECTED TO POWER.
Figure 11 WEEE Label

Safety
3.3.2.5 Scanner Desktop Labels
Figure 12 Label on reading manuals before operating
CAUTION
AVOID INJURY. READ AND UNDERSTAND INFORMATION IN MANUALS

BEFORE OPERATING PRODUCT.
Figure 13 WEEE Label
3.3.2.6 External Accessory Labels
Figure 14 IV pole caution label on leg of IV pole
CAUTION
DO NOT LOAD MORE THAN 4,5 KG OR 10 POUNDS. VERIFY THAT

EXTENSION COLLAR IS SECURELY TIGHTENED BEFORE USE.
You may also see this statement as a warning.

Safety
Figure 15 IV pole warning label on leg of IV pole
WARNING
DO NOT LOAD MORE THAN 4.5 KG OR 10 POUNDS. VERIFY THAT

EXTENSION COLLAR IS SECURELY TIGHTENED BEFORE USE.
Figure 16 Table tray caution label on leg of table tray
CAUTION
DO NOT LOAD MORE THAN 9KG OR 20 LBS.
Figure 17 Table tray warning label on leg of table tray
WARNING
DO NOT LOAD MORE THAN 9 KG OR 20 POUNDS.

Safety
Figure 18 Axial head holder caution
CAUTION
ACCESSORY MAY FALL AND CAUSE INJURY IF NOT LATCHED TO CRADLE.

MAKE SURE THAT ACCESSORY IS LATCHED TO UNDERSIDE OF CRADLE.
EXCESSIVE WEIGHT CAN BREAK ACCESSORY AND CAUSE INJURY. DO NOT
LOAD MORE THAN 34 KG OR 75 POUNDS.
Figure 19 Axial head holder warning
WARNING
FALL HAZARDS. ACCESSORY MAY FALL AND CAUSE INJURY IF NOT

LATCHED TO CRADLE. MAKE SURE THAT ACCESSORY IS LATCHED TO
UNDERSIDE OF CRADLE. EXCESSIVE WEIGHT CAN BREAK ACCESSORY AND
CAUSE INJURY. DO NOT LOAD MORE THAN 34 KG (75 LBS).

Safety
Figure 20 Coronal head holder caution
CAUTION
DO NOT HIT THE ACCESSORY AGAINST THE GANTRY. PATIENT INJURY OR

EQUIPMENT DAMAGE COULD RESULT.
Figure 21 Coronal head holder warning
WARNING
FALL AND IMPACT HAZARDS. DO NOT HIT ACCESSORY AGAINST GANTRY.

PATIENT INJURY OR EQUIPMENT DAMAGE COULD RESULT. ACCESSORY
MAY FALL AND CAUSE INJURY IF NOT LATCHED TO CRADLE. MAKE SURE
THAT ACCESSORY IS LATCHED TO UNDERSIDE OF CRADLE. EXCESSIVE
WEIGHT CAN BREAK ACCESSORY AND CAUSE INJURY. DO NOT LOAD MORE
THAN 34 KG (75 LBS).
Figure 22 Bumperless extender warning

Safety
WARNING
FALL HAZARDS. ACCESSORY MAY FALL AND CAUSE INJURY IF NOT

LATCHED TO CRADLE. MAKE SURE THAT ACCESSORY IS LATCHED TO
UNDERSIDE OF CRADLE. EXCESSIVE WEIGHT CAN BREAK ACCESSORY AND
CAUSE INJURY. DO NOT LOAD MORE THAN 34 KG (75 LBS).
3.4 Radiation Safety

(Reference 21CFR 1020.30 (h)(1)(i))
3.4.1 X-Ray Protection

WARNING
IMPROPERLY USED X-RAY EQUIPMENT MAY CAUSE INJURY. READ AND

UNDERSTAND THE INSTRUCTIONS IN THIS BOOK BEFORE YOU ATTEMPT
TO OPERATE THIS EQUIPMENT. IF YOU FAIL TO FOLLOW SAFE X-RAY
PRACTICES OR IGNORE THE ADVICE PRESENTED IN THE MANUAL, YOU
AND YOUR PATIENT RISK EXPOSURE TO HAZARDOUS RADIATION.
Authorized Users
This equipment incorporates a high degree of protection against X-ray radiation outside the useful
beam. But this equipment cannot substitute the essential requirement that every user must take
adequate precautions to prevent the possibility of any person carelessly, unwisely, or unknowingly
exposing themselves or others to radiation.
Everyone having anything to do with X-ray equipment must receive proper training and become
fully acquainted with the recommendations of the National Council on Radiation Protection and
Measurements and the International Commission on Radiation Protection.
NCRP reports are available from:
NCRP Publications
7910 Woodmont Avenue
Room 1016
Bethesda, Maryland 20814

Safety
WARNING
EVERYONE HAVING ANYTHING TO DO WITH X-RAY EQUIPMENT MUST TAKE

ADEQUATE STEPS TO ENSURE PROTECTION AGAINST INJURY.
All persons authorized to use the equipment must understand the dangers posed by X-ray exposure so
that they can prevent any injury or damage that may result from such exposure. GE Healthcare urges
you to use protective materials and devices to prevent any injury or damage from X-ray exposure.
3.4.2 General Radiation Safety

WARNING
NEVER SCAN A PATIENT WITH UNAUTHORIZED PERSONNEL IN THE SCAN

ROOM. WARN VISITORS AND PATIENTS ABOUT POTENTIAL FOR HARM IF
THEY FAIL TO FOLLOW INSTRUCTIONS.
WARNING
NEVER CALIBRATE, TEST THE SYSTEM, OR WARM THE TUBE WITH

PATIENTS OR PERSONNEL PRESENT IN THE SCAN ROOM WITHOUT
ADEQUATE RADIATION SAFETY PRECAUTIONS BEING UTILIZED.
• Stay behind a lead screen or lead glass shield during each X-ray exposure.
• Use technique factors prescribed by the radiologist or diagnostician. Use a dose that produces the
best diagnostic results with the least X-ray exposure.
• The x-ray exposure indicator is an amber light located on the secondary gantry display on the
front and rear of the gantry directly below the primary gantry display.

Safety
Figure 23 Secondary gantry display location
CAUTION
REDUCTION OF DOSE WITHOUT REGARD TO PATIENT BODY HABITUS

CAN LEAD TO PHOTON STARVATION WHICH IN TURN CAN CAUSE
IMAGE ARTIFACTS.
1 Secondary gantry display

Safety
WARNING
USE OF CONTROLS OR ADJUSTMENTS, OR PERFORMANCE OF

PROCEDURES OTHER THAN THOSE SPECIFIED HEREIN, MAY RESULT
IN HAZARDOUS RADIATION EXPOSURE.
3.4.3 Scans Acquired at the Same Tomographic Plane

IEC standard 60601-2-44, clause 203.107 states that you must be warned when scans are acquired at
the same tomographic plane, i.e. same scan location. The need for the warning is to make users aware
of the potential dose that can be given to the patient when acquiring scans at the same table location.
When acquiring scans in this mode:
• Utilize the dose information displayed on the Scan Settings screen. The dose information
displayed is covered in the next section, CTDIvol.
• An optional DICOM Structured Report (SR) Dose Report is saved in Series 997.
• Use proper techniques for the application and anatomy you are scanning.
A warning message is posted when Confirm Settings is selected for the following scan types:
SmartPrep, Cine, Axial or SmartStep scans with zero table increment (scan interval)
WARNING
THIS SERIES CONTAINS ONE OR MORE GROUPS WITH MULTIPLE SCANS AT

THE SAME TOMOGRAPHIC PLANE, I.E. SAME LOCATION.
Do you want to continue?
After reading the message, if you wish to continue with the scan, click Continue, otherwise click
Cancel.
WARNING
PROLONGED EXPOSURE TO X-RAY IN ONE SPOT MAY CAUSE REDDENING

OR RADIATION BURNS. USERS MUST BE AWARE OF THE TECHNIQUES
USED AND EXPOSURE TIME TO ENSURE SAFE OPERATION.
3.4.4 Geometric Dose Efficiency

A warning message is posted when the Geometric Dose Efficiency in the Z-direction is less than 70%.
Geometric Dose Efficiency is a measure of how much of the X-ray beam in the Z-direction is used by the
system.

Safety
WARNING
THE FOLLOWING GROUPS IN THE SERIES CONTAINS GEOMETRIC

EFFICIENCY IN THE Z DIRECTION OF LESS THAN 70%: IMAGES 1-12,13-28.
NOTE
Images 1-12, 13-28 is an example of a location where Geometric Efficiency in Z is less
than 70%.
3.4.5 Backup Timer Indicator

The system has backup timers that terminate the X-ray if it remains on longer than the prescribed scan
time.
A warning message is posted when a scan is stopped by the backup timer.
WARNING
X-RAY EXPOSURE TERMINATED BY BACKUP TIMER INSTEAD OF NORMAL

CONTROL.
3.4.6 Starting Scans from the Scan Room

WARNING
PRESSING THE START SCAN BUTTON ON GANTRY STARTS X-RAY

EXPOSURE IMMEDIATELY OR AFTER PREP DELAY TIMER EXPIRES.
X-ray exposure to the operator may occur.

Follow the guidelines in General Radiation Safety to reduce exposure.
3.4.7 CTDIvol
As you setup the scan parameters from the Scan Settings screen, the Dose Information area at the
bottom center of the scan monitor contains updated dose information. This dose information is based
on a measurement of the CTDI or CT Dose Index, which is the current standard for CT dosimetry
and performance. By using a measurement called CTDIvol, a single value is provided to estimate the
relative dose for an exam.
The CTDIvol is a weighted average measurement in a reference phantom. This dose is expressed in
milliGrays. For additional information on specific CTDIvol doses and their calculations, refer to your
Technical Reference manual.

Safety
The DLP or Dose Length Product is the product of the CTDIvol and the scan length for a group of scans.
This number can be summed over the entire exam to give an estimate of the total dose. The value is
expressed in milliGray centimeters.
The Projected DLP shows the DLP that would result from scanning the current group or groups.
The Accumulated DLP displays the total exam DLP up to the current point in time. Scout dose is
included in the DLP totals but is generally a very small part of the exam.
The dose information updates when technique values such as kV, mA, scan time, slice thickness, and
scan field of view are changed.
Dose information is saved as a screen save image in Series 999 upon selecting End Exam. Series 997
contains the DICOM Dose Structured Report.
3.5 Implantable Device Safety

WARNING
CT SCANS MAY CAUSE INTERFERENCE WITH IMPLANTED OR EXTERNALLY

WORN ELECTRONIC MEDICAL DEVICES SUCH AS PACEMAKERS,
DEFIBRILLATORS, NEUROSTIMULATORS AND DRUG INFUSION PUMPS. THE
INTERFERENCE COULD CAUSE OPERATIONAL CHANGES OR MALFUNCTION
OF THE ELECTRONIC MEDICAL DEVICE.
3.5.1 Recommendations prior to scanning

• If practical, try to move external devices out of the scan range.
• Ask patients with neurostimulators to shut off the device temporarily while the scan is performed.
• Minimize the X-ray exposure to the electronic medical device.
• Use the lowest possible X-ray tube current consistent with obtaining the required image quality.
• Do not scan directly over the electronic device for more than a few seconds.
NOTE
For procedures such as CT Perfusion or CT Interventional scans that require
scanning over the electronic medical device for more than a few seconds, attending
staff should be ready to take emergency measures to treat adverse reactions if they
occur.
3.5.2 Recommendations after scanning

• Have the patient turn the device back on if it had been turned off prior to scanning.
• Have the patient check the device for proper functioning, even if the device was turned off.
• Advise the patient to contact his or her healthcare provider as soon as possible if the patient
suspects their device is not functioning properly after a CT scan.

Safety
NOTE
Recommendations from FDA Preliminary Public Health Notification: Possible
Malfunction of Electronic Medical Devices Caused by Computed Tomography (CT)
Scanning date July 14, 2008.
WARNING
THIS SYSTEM IS INTENDED FOR USE BY HEALTHCARE PROFESSIONALS

ONLY. THIS SYSTEM MAY CAUSE RADIO INTERFERENCE OR MAY DISRUPT
THE OPERATION OF NEARBY EQUIPMENT. IT MAY BE NECESSARY TO TAKE
MITIGATION MEASURES, SUCH AS REORIENTING OR RELOCATING THE
SYSTEM OR SHIELDING THE LOCATION.
3.6 Electrical Safety
DANGER
ELECTRICAL SHOCK HAZARD. AVOID ALL CONTACT WITH ANY ELECTRICAL

CONDUCTOR. DO NOT REMOVE OR OPEN SYSTEM COVERS OR PLUGS.
INTERNAL CIRCUITS USE HIGH VOLTAGE CAPABLE OF CAUSING SERIOUS
INJURY.
An electrical hazard may exist if any light, monitor, or visual indicator
stays on after the system is shut down. To prevent possible injury, turn
off the main power supply wall switch, and contact your service office
immediately.

Safety
DANGER
NO USER SERVICEABLE PARTS. REFER SERVICE TO QUALIFIED

SERVICE PERSONNEL. ONLY ALLOW PEOPLE WHO KNOW THE PROPER
PROCEDURES, AND USE OF THE PROPER TOOLS, TO INSTALL, ADJUST,
REPAIR, OR MODIFY THE EQUIPMENT.
To guarantee safe, reliable equipment performance, prepare the site
according to GE Healthcare requirements. This includes making sure the
equipment is connected to a supply mains with a protective earth. If you
have any questions about these requirements, contact GE Healthcare.
Fuses blown within 36 hours of being replaced may indicate
malfunctioning electrical circuits within the system. Have the system
checked by qualified service personnel, and do not attempt to replace
any fuse.
DANGER
INFORMATION ON INTERNAL GANTRY COMPONENTS IS PROVIDED FOR

USER EDUCATION. THE GANTRY CONTAINS DANGEROUS VOLTAGES AND
MOVING PARTS.
TO PREVENT ELECTRICAL SHOCK OR CRUSHING INJURIES, DO NOT
REMOVE COVERS OR ENTER THE GANTRY. ONLY TRAINED, QUALIFIED
SERVICE PERSONNEL MAY REMOVE GANTRY OR OTHER EQUIPMENT
COVERS.
DANGER
ELECTRICAL FIRE. CONDUCTIVE FLUIDS THAT SEEP INTO THE ACTIVE

CIRCUIT COMPONENTS OF THE SYSTEM MAY CAUSE SHORT CIRCUITS
THAT CAN RESULT IN ELECTRICAL FIRES. THEREFORE, DO NOT PLACE ANY
LIQUID OR FOOD ON ANY PART OF THE SYSTEM.
To avoid electrical shocks or burns caused by the use of the wrong type of fire extinguisher, make sure
that only fire extinguishers approved for use on electrical fires are used.
Surplus lengths of power cords or other cables from mobile accessory units that may be used during
patient scanning should be stored in safe and isolated areas. For example: Excess cable may be wound
in a figure eight and stored at the base of the stationary equipment. This minimizes signal interference
and protects cables from damage due to traffic.

Safety
CAUTION
THE ACCESSORY RECEPTACLES LOCATED ON THE GANTRY ARE NOT FOR

GENERAL USE. VERIFY THAT ACCESSORY REQUIREMENTS DO NOT EXCEED
THE LABELED RATINGS. WHEN ONE RATING VALUE IS PROVIDED FOR A
GROUP OF RECEPTACLES, THE COMBINED POWER CONSUMPTION FOR
THAT GROUP SHOULD NOT EXCEED THE LABELED RATING.
CAUTION
THE ACCESSORY RECEPTACLES LOCATED ON THE SCANNER DESKTOP ARE

NOT FOR GENERAL USE. VERIFY THE ACCESSORY POWER REQUIREMENTS
DO NOT EXCEED THE LABELED RATINGS OF THE RECEPTACLES. WHEN
ONE RATING VALUE IS PROVIDED FOR A GROUP OF RECEPTACLES,
THE COMBINED POWER CONSUMPTION FOR THAT GROUP SHOULD NOT
EXCEED THE LABELED RATING.
CAUTION
THE ACCESSORY RECEPTACLES LOCATED ON THE SCANNER DESKTOP ARE

NOT FOR GENERAL USE. THE COMBINED POWER CONSUMPTION OF THE
ACCESSORIES SHOULD NOT EXCEED 960 WATTS.
CAUTION
INCLUDED POWER CORD IS ONLY TO BE USED WHEN CONNECTING GE

APPROVED ACCESSORIES TO THE GANTRY OR SCANNER DESKTOP.
A CT System combined with GE approved accessories complies with the IEC 60601-1 standards related
to safety and performance of medical electrical systems. Refer to the standard for more information.
• Do not connect electric devices to the CT System that are not approved by GE. Do not connect
additional extension cords or outlet strips. It may create increased electrical leakage current and
there is possibility of electric shock.
• The manufacturer is not responsible for any interference caused by using other than
recommended interconnect cables or by unauthorized changes or modifications to this
equipment. Unauthorized changes or modifications could void the users' authority to operate
the equipment.
• The GE console monitors, video amp and media tower are intended to be powered by the CT
System using cables provided. Do not connect these devices to power sources other than the
CT system (for example, wall outlets, or other electrical equipment). It may create increased
electrical leakage current and there is possibility of electric shock.

Safety
• Note that some external powered equipment may only be connected by a signal cable to GE
equipment (for example, a network hub). A separation device is required for equipment that is
powered by a different power source.
The design of the CT scanner uses an equal potential grounding system. All components within the
system are provided power on a common ground, so all the components are suitable for use in the
patient environment. Three primary grounding points exist, they include:
• A system power ground point located in the NGPDU.
• A reference ground point located between the gantry and the table base.
• A protective earth ground points located at the rear of the gantry for accessory use.
ALL patient-accessible metal surfaces are grounded to the same potential as the A1 Disconnect.
Power Indicator Light Locations
Component Indicator Light Location
Gantry Indicator Locations: Gantry control buttons backlight, Gantry primary and secondary
display and service panel 120VAC LED.
System ON: gantry control panel backlighting, service panel 120VAC LED will be lit and
primary gantry display will display the table vertical position.
Sleep: On the secondary gantry display the crescent moon will be statically lit (no flash-
ing).
Power Down: The secondary gantry display will be off.
Power Distribu- Indicator Location: PDU light at the front.

tion Unit
System ON: The light indicator will be ON.
Sleep or Power Down: The light indicator will be ON.
Scanner Desktop Indicator Locations: Monitors Power ON/OFF buttons lights, Scanner Desktop/NIO Cabinet
power on/off light located at the front.
System ON: The light indicators will be ON.
Sleep or Power Down: The light indicators will be ON.
Scan Control In- Indicator: Standby Button Light.

terface
System ON: The button light will be ON.
Sleep or Power Down: The button light will be flashing.
System Cabinet Indicators: System Cabinet provides a green light to the service personal to indicate is
(Image Genera- energized. SDA computer and disks and Image Generation computer front panel Power
tion) ON/OFF lights.
System ON: The light indicators will be ON.
Sleep or Power Down: The light indicators will be ON.

Safety
(continued)
Component Indicator Light Location
System On light Indicator: Optional light, customer provided, it indicates that the PDU is energized (A1
breaker is ON).
System ON: System On light On.
Sleep or Power Down: System On light On.
3.7 Electromagnetic Compatibility Safety

The system needs special precautions regarding EMC and needs to be installed and put into service
according to the EMC information provided in the Technical Reference Manual.
Use of RF (Radio Frequency) sources that intentionally transmit, such as cellular telephones,
transceivers, radio-controlled products, or other RF emitting equipment may cause performance
outside the system's published specifications or other adverse operation.
3.8 Fire Safety

DANGER
THIS DEVICE IS NOT SUITABLE FOR USE IN THE PRESENCE OF A

FLAMMABLE ANESTHETIC MIXTURE WITH AIR, OR IN THE PRESENCE OF
A FLAMMABLE ANESTHETIC MIXTURE WITH OXYGEN OR NITROUS OXIDE.
3.9 Mechanical Safety
3.9.1 General Mechanical Safety

WARNING
DO NOT USE THE TABLE BASE AS A FOOT REST. YOU COULD ENTRAP AND
INJURE YOUR FOOT WHILE LOWERING THE TABLE. DO NOT PLACE YOUR
HANDS BETWEEN THE TABLE BASE AND THE TABLE SIDE PANELS.

Safety
CAUTION
IN THE EVENT OF CRADLE RELEASE DUE TO POWER LOSS OR OTHER

CAUSE, THE MAXIMUM COASTING DISTANCE OF THE TABLE CRADLE IS 220
MM.
WARNING
WHEN EITHER THE OPERATOR’S SHOES OR THE FOOT PEDAL COVER

SURFACE IS WET, THE FOOT PEDAL COVER IS SLIPPERY. THIS COULD
CAUSE A SLIP AND/OR FALL WHEN STANDING ON THE COVER. USE
CAUTION WHEN STANDING ON THE FOOT PEDAL COVER TO POSITION THE
PATIENT.
WARNING
WHEN THE OPERATOR IS STANDING ON THE FOOT PEDAL COVER

BETWEEN TABLE AND GANTRY, THE OPERATOR COULD BE TRAPPED IF
THE TABLE ADVANCES INTO THE GANTRY. DO NOT USE TABLE MOTION
CONTROLS WHILE AN OPERATOR IS STANDING ON THE FOOT PEDAL
COVER.
3.9.2 Patient Positioning

Standard Weight Capacity Table
DANGER
DO NOT EXCEED TABLE MAXIMUM CAPACITY OF 227 KG (500 LB). THIS

COULD CAUSE THE TABLE TO FAIL AND THE PATIENT COULD FALL.
Table could include either of the following two labels:
Figure 24 Warning label located on standard weight capacity table

Safety
WARNING
AVOID INJURY. DO NOT EXCEED TABLE MAXIMUM CAPACITY OF 227 KG (500

LB).
Figure 25 Weight limit label located on the standard weight capacity table
Heavy Weight Capacity Table
Figure 26 Weight limit label located on heavy weight capacity table
CAUTION
TEMPORAL SAMPLING MAY BE DEGRADED DUE TO CHANGES IN TIMING

FOR THE TABLE TO MOVE FROM LOCATION TO LOCATION IF PROPER
POSITIONING METHODS ARE NOT FOLLOWED. MAKE SURE THAT THE
PATIENT IS SECURELY POSITIONED ON THE TABLE AND THEIR ARMS ARE
NOT ALLOWED TO DRAG ON THE TABLE OR ALLOW CLOTHING, SHEETS OR
BLANKETS TO GET CAUGHT CAUSING A TABLE MOVE PROBLEM.

Safety
CAUTION
WHEN USING THE EXTERNAL LASER ALIGNMENT LIGHT FOR PATIENT

POSITIONING PURPOSES, BE AWARE THAT THE PATIENT'S ELEVATION
MAY BE SLIGHTLY LOWER WITH THE CRADLE EXTENDED THAN WITH
THE CRADLE FULLY RETRACTED. THIS IS BECAUSE THE CRADLE MAY
BEND SLIGHTLY UNDER A PATIENT'S WEIGHT. THIS DIFFERENCE SHOULD
BE TAKEN INTO CONSIDERATION FOR APPLICATIONS WHERE PATIENT
POSITION INFORMATION IS CRITICAL, SUCH AS TREATMENT PLANNING.
TO MINIMIZE THESE EFFECTS, AFTER USING THE EXTERNAL LASER
ALIGNMENT SYSTEM TO POSITION THE PATIENT, ADVANCE THE PATIENT
TO THE CT SCAN PLANE. TURN ON THE CT ALIGNMENT LIGHTS TO
DETERMINE IF THEY LINE UP WITH THE MARKERS ON THE PATIENT. IF
NECESSARY, COMPENSATE FOR THE BEND IN THE CRADLE BY ELEVATING
THE TABLE. WHEN THE CT ALIGNMENT LIGHTS LINE UP WITH THE
MARKERS, SET THE LANDMARK FOR THE SCAN USING THE INTERNAL
LASER ALIGNMENT LIGHT.
WARNING
WHEN USING PATIENT POSITIONING ACCESSORIES AND STRAPS, MAKE

SURE THERE ARE NO AREAS WHICH MIGHT CAUSE A PINCH POINT OR
INTERFERE WITH PATIENT TUBING OR IV.
WARNING
CHECK TO MAKE SURE THE POWER INJECTOR HAS ENOUGH IV TUBING TO

ALLOW FREE MOVEMENT OF THE CRADLE. MAKE SURE THE UNIT ITSELF
DOES NOT INTERFERE WITH TABLE TRAVEL. ENSURE EXCESS TUBING
LENGTH IS SECURED TO THE TABLE TOP. DO NOT LOOP ADDITIONAL IV
TUBING IN THE PATIENT'S FINGERS.
Check the length of all patient health lines (IV tubing, oxygen line, etc.) and make sure they
accommodate cradle travel. Position these lines so they cannot catch on anything within the patient
vicinity or between the table and gantry during cradle travel.
WARNING
THE PATIENT POSITIONING STRAPS PROVIDED WITH THE SYSTEM DO NOT

SUPPORT THE FULL WEIGHT OF THE PATIENT. PATIENT POSITIONING
STRAPS SHOULD BE USED TO AID IN PATIENT POSITIONING AND ARE NOT
MEANT TO FULLY RESTRAIN THE PATIENT.

Safety
CAUTION
GANTRY STRAPS ARE DESIGNED TO HOLD ACCESSORY CABLES THAT

CONNECT TO THE GANTRY REAR PANEL. DO NOT USE FOR LIFTING OR
SUPPORT.
CAUTION
GANTRY STRAPS SHOULD ONLY BE USED FOR HOLDING ACCESSORY

CABLES THAT CONNECT TO THE GANTRY REAR PANEL. PLACING INJECTOR
LINES THROUGH THE GANTRY STRAPS COULD CAUSE INTERFERENCE
ISSUES AND PATIENT HARM.
Figure 27 NG2000 Table

Safety
Figure 28 NG2000V Table
CAUTION
IF THE TABLE IS LOWERED WITH ANYTHING IN THE DESIGNATED AREA

BELOW THE TABLE, THE TABLE COULD BE DAMAGED ALONG WITH THE
EQUIPMENT OR OBJECT UNDER THE TABLE.
WARNING
TO PREVENT PINCHING OR CRUSHING OF THE PATIENT'S EXTREMITIES,

KEEP THE PATIENT'S HANDS AND FEET AWAY FROM THE EDGE OF THE
MOVING TABLE TOP/CRADLE AND ITS SURROUNDING EQUIPMENT, OR
BETWEEN TABLE BASE AND SIDE PANELS OF THE TABLE. TAKE SPECIAL
CARE WHEN POSITIONING PHYSICALLY LARGE PATIENTS.
WARNING
TO PREVENT PINCHING OR CRUSHING OF THE PATIENT, WATCH THE

PATIENT AND EQUIPMENT CAREFULLY AT ALL TIMES DURING TABLE
MOVEMENT. IF UNWANTED MOTION OCCURS OR MOTION DOES NOT STOP,
PRESS THE EMERGENCY STOP SWITCHES ON THE CONSOLE OR GANTRY.

Safety
WARNING
THE HEAD HOLDER MAY CRACK, POSSIBLY INJURING THE PATIENT'S HEAD
OR NECK, IF THE PATIENT TRIES TO BRACE HIMSELF OR HERSELF ON THE
HEAD HOLDER DURING POSITIONING. THE HEAD HOLDER AND CRADLE
EXTENDER ARE ONLY DESIGNED TO SUPPORT 75 POUNDS (34 KG). ASK
THE PATIENT TO MOVE UP INTO THE HEAD HOLDER OR MANUALLY HELP
THE PATIENT INTO POSITION.
CAUTION
USE OF ANY CRADLE EXTENSION ACCESSORIES SUCH AS THE TABLE

EXTENSION, HEAD HOLDER, CORONAL HEAD HOLDER, AND PHANTOM
HOLDER ARE NOT ACCOUNTED FOR IN THE TABLE GANTRY INTERFERENCE
MATRIX. THEREFORE, ADDITIONAL CARE NEEDS TO BE TAKEN TO CLOSELY
MONITOR ANY TABLE UP/DOWN, IN/OUT MOVEMENT TO AVOID CONTACT
OF THE EXTENDED ACCESSORY WITH THE GANTRY.
CAUTION
CARE SHOULD BE TAKEN TO ENSURE THE PATIENT POSITIONING STRAPS,

PATIENT CLOTHING, OR OTHER MATERIAL WILL NOT BE CAUGHT DURING
TABLE MOTION.
CAUTION
THE PATIENT HEAD HOLDER OR TABLE EXTENDER SHOULD BE

ADEQUATELY SECURED TO ENSURE STABILITY. IF THEY ARE NOT SECURED
PROPERLY, DEGRADATION OF IMAGE QUALITY MAY RESULT DUE TO
INTRODUCED MOTION OF THE HEAD HOLDER OR TABLE EXTENDER.
CAUTION
IF THE HEAD IS POORLY POSITIONED SUCH THAT THE ANATOMY IS OVER

THE JUNCTION OF THE ATTACHMENT OF THE HEAD HOLDER OR FOOT
EXTENDER TO THE CRADLE, IMAGES WITH DIFFERENT CT NUMBERS AND
INTENSITIES MAY BE SEEN IN THE VOLUME. REVIEW THE SCOUT IMAGE
PRIOR TO SCANNING TO MAKE SURE THE PATIENT IS NOT POSITIONED
OVER THIS JUNCTION. IF A REPEAT SCAN IS NEEDED, RE-POSITION THE
PATIENT PRIOR TO RE-SCANNING. DO NOT REPEAT USING EXACTLY THE
SAME PATIENT POSITION.

Safety
3.9.2.1 Remote Controlled Patient Positioning RCP AVIMOS Safety
WARNING
DURING REMOTE TABLE/GANTRY MOVEMENT, TO PREVENT PINCHING

OR CRUSHING OF THE PATIENT, WATCH THE PATIENT, EQUIPMENT,
ACCESSORIES, AND HEALTH LINES CAREFULLY AT ALL TIMES.
WARNING
REMOTE CONTROL PANEL AVIMOS MONITOR MUST BE FUNCTIONAL

AND VISIBLE WHEN USING REMOTE CONTROL BUTTONS FOR REMOTE
MOVEMENT OR POSITIONING.
CAUTION
USE AVIMOS MONITOR TO ENSURE ALIGNMENT OF LASER LIGHTS WITH

PATIENT REFERENCE POINT PRIOR TO SETTING EXTERNAL LANDMARK
REMOTELY. IF YOU CANNOT SEE ALIGNMENT LIGHT OR PATIENT
REFERENCE POINT, DO NOT SET LANDMARK REMOTELY.
CAUTION
CONFIRM THAT THE CORRECT LANDMARK (INTERNAL OR EXTERNAL) HAS

BEEN PRESSED BASED ON THE VISIBLE ALIGNMENT LIGHT POSITION ON
THE PATIENT.
CAUTION
ESTABLISH COMMUNICATION WITH THE PATIENT BEFORE USING THE

REMOTE CONTROL PANEL.
CAUTION
PLEASE ENSURE THAT THE ASSISTED VIDEO MONITORING SYSTEM

WORKS NORMALLY WHEN USING REMOTE CONTROL PANEL. THE REMOTE
CONTROL PANEL SHOULD NOT BE USED IF THE ASSISTED VIDEO
MONITORING SYSTEM IS NOT OPERATIONAL. DO NOT ATTEMPT TO CLEAN
OR ALIGN. CONTACT YOUR GE SERVICE REPRESENTATIVE IN CASE ANY
SERVICING IS NEEDED.

Safety
CAUTION
THE ALIGNMENT LIGHTS MAY BE DIFFICULT TO SEE ON THE AVIMOS

MONITOR IF THE PATIENT WEARS DARK CLOTHING. REQUEST PATIENT
TO CHANGE INTO LIGHT COLORED GARMENT OR ENTER SCAN ROOM TO
ALIGN THE PATIENT AND SET THE LANDMARK.
3.9.3 Gantry Air Inlets

WARNING
BLOCKED GANTRY AIR INLETS CAN CAUSE SYSTEM OVERHEATING THAT

REDUCES IMAGE QUALITY.
Diagnostic errors may occur when reading images.

Remove any objects blocking the gantry air inlets located on each side of the gantry.

Safety
Figure 29 Gantry Air Inlet Location examples (only left side shown)

Safety
3.10 Use of Defibrillator

WARNING
THE CT SYSTEM IS NOT CLASSIFIED AS DEFIBRILLATION-

PROOF NOR AS DEFIBRILLATION-PROTECTED ELECTRONIC MEDICAL
EQUIPMENT. EMERGENCY DEFIBRILLATION SHOULD BE PERFORMED
BY APPROPRIATELY TRAINED, SKILLED PERSONNEL FAMILIAR WITH
THE LIMITATIONS AND OPERATION OF DEFIBRILLATION EQUIPMENT
AND FAMILIAR WITH HOW TO HANDLE EQUIPMENT THAT IS NOT
DEFIBRILLATION-PROTECTED IN THE PATIENT ENVIRONMENT.
3.11 Emergency Devices and Emergency Egress

(Reference 21CFR 1020.33 (f)(2)(ii))
3.11.1 Emergency Devices

The system has two types of Emergency buttons:
1. Emergency Stop — When pressed, all table and gantry motions are halted, generation of X-rays is
stopped, laser alignment lights are turned off. The system aborts any data acquisition in progress,
and attempts to save all data acquired prior to the abort. Use the Emergency Stop button for
patient related emergencies.
2. System Emergency Off Button — When pressed, the power to all system components is removed,
stopping all table and gantry motion and generation of X-rays. The system aborts any acquisitions

Safety
in progress, and data obtained prior to the abort can become corrupt or lost. Use the System
Emergency OFF button for catastrophic emergencies, such as fire or earthquake.
CAUTION
IF YOU PRESS THE EMERGENCY STOP OR EMERGENCY OFF BUTTONS

DURING A SCAN, THE SYSTEM WILL ABORT THE DATA ACQUISITION.
3.11.2 Emergency Stop

NOTE
Every operator should take a few minutes to locate the Emergency Stops on their system
before scanning the first patient.
The system has five Emergency Stop buttons:
• Two on the front cover of the gantry.
Figure 30 Front cover of gantry
• Two on the rear cover of the gantry.

Safety
Figure 31 Rear cover of the gantry
• One on the Scan Control Interface.
Figure 32 Scan Control Interface
Number Description
1 Emergency Stop Button
Press an Emergency Stop button in the event of a patient related emergency or if the cradle, table
or gantry starts to move unexpectedly.

Safety
• Once an Emergency Stop button is pressed, the Reset gantry control button, on the gantry
control panel, flashes about once every two seconds.
• Press the Reset gantry control button to restore power to the gantry and table.
When Emergency Stop is applied, the maximum stopping distance of the moving cradle is 10 mm.
Emergency Stop Button Symbols
Emergency Stop buttons may be accompanied by one of the symbols below.
3.11.3 System Emergency OFF Buttons using Main Disconnect

Control
In the event of a fire, flood, earthquake, or any other catastrophic emergency, all power to the system
should be turned off. Pressing the System Emergency OFF button (red, circular button located on the
wall) immediately removes all power to the system by removing power to the Main Disconnect Control
(MDC). Because the system has no time to save data, or shutdown in an orderly fashion, pressing the
System Emergency OFF button can corrupt system files or result in loss of patient data.
The facility designer determines the quantity and locations of the Emergency OFF buttons. GE
recommends placing an Emergency OFF button near the doorway of every room in the system scan
suite. Ask your supervisor to show you the location of all the Emergency OFF buttons in the system
suite. Follow facility guidelines to report an emergency.
Reset the Emergency OFF Button
1. Press the Start button on the Main Disconnect Control.
Power to the Power Distribution Unit (PDU), scanner desktop and system electronics will be
restored.
2. Press the Reset gantry control button on the gantry panel.
Power to the gantry drives, X-ray system, and table drive will be restored.
CAUTION
THE X-RAY AND DRIVE POWER IS DISABLED. PLEASE WALK INTO THE SCAN
ROOM AND PRESS THE RESET BUTTON ON THE GANTRY CONTROL PANEL.
3.11.4 Emergency Patient Care During X-ray ON

• Press STOP SCAN to abort X-ray and stop gantry/table movement.

Safety
• Press PAUSE SCAN to pause scanning after the current scan completes.
• During an exam, the system pauses between scans if you Press any button on the control panel
other than the alignment lights. It stops X-ray if you Press the same button(s) during a scan.
• Select Resume on the screen to continue the exam.
3.11.5 Emergency Egress

System operation may be stopped due to power failure or a safety event (something coming into
contact with the collision sensors), or the system may be halted by the operator in response to
emergency conditions.
The cradle unlatch button should only be used in emergency egress situations.
To safely remove the patient:
1. Grab and squeeze the Cradle Handle release switch. Continue to squeeze the Cradle Handle
release switch while pulling the cradle to its out position.
2. Alternatively, forcefully pull the cradle to its out position, using the cradle lip or cradle handle.
3. Assist the patient off the table.
3.12 Laser Safety

(Reference 21CFR 1040.10 (h) 21CFR1020.33 (g)(4))
A laser alignment light system is available in order to accurately define the patient scan region.
The sagittal, coronal, and transverse alignment lights are within ±1 mm of the gantry coordinate
system (x, y and z-axis) centered at gantry isocenter.
Pressing the Alignment Light button, on the gantry control panel or remote control panel, toggles
the laser alignment lights on/off. When turning alignment lights on, the system automatically moves
the gantry components from the park or idle position to the alignment lights position. Alignment
lights are used to establish landmark locations. Three alignment lights are displayed: axial, sagittal
and coronal. There are internal and external alignment lights, but the internal alignment lights are not
displayed when Remote Control Panel is displayed on the operator console. Align the appropriate set
of alignment lights with the desired anatomical reference. A poorly positioned and centered patient
can impact the mA values calculated for AEC exposures.
The laser alignment light switch is provided as an alternative to beam attenuators.
Press the Internal and External Landmark buttons to establish the table’s reference point when
positioning the patient. This reference point is normally the anatomic reference point used when
positioning the patient. For example, if the patient’s anatomic reference point is the sternal notch,
then the sternal notch would be centered to the laser alignment light.
• For Internal Landmark, the gantry displays a table location of 0 mm. This sets the zero point for
which S and I scan locations are centered around.
• For External Landmark , the gantry displays a table location approximately 240 mm from the
internal landmark, depending on table characterization.

Safety
A landmark must be set before you click Confirm Settings. At Done Scanning, the landmark is cleared.
For scan setup details, see the Set up and position the patient procedure.
WARNING
THE LASER BEAM CAN CAUSE EYE INJURY.
• Tell all patients to close their eyes before you switch ON the
alignment lights.
• Instruct your patients to keep their eyes closed until you turn OFF the
alignment lights.
NOTE
Closely monitor infants and infirm patients, and prevent them from accidentally staring
into the beam.
WARNING
THE DETECTOR AND DAS ROTATE TO POSITION THE ALIGNMENT LIGHTS

OVER THE LASER PORTS.
• Keep your hands away from the gantry opening.

• Make sure the gantry covers are in place.
• The alignment light indicator is an amber light located on the secondary gantry display on the
front and rear of the gantry directly below the primary gantry display.

Safety
Figure 33 Secondary gantry display location
1 Secondary gantry display
• Warning labels regarding laser safety are provided on the gantry, as described in the Warning
Labels and Symbols section.
Maintenance
• Laser alignment lights do not require user maintenance.
• Qualified service personnel must inspect the lights periodically to assure proper alignment.

Safety
CAUTION
LASER RADIATION — DO NOT VIEW DIRECTLY WITH OPTICAL

INSTRUMENTS. DO NOT EXPOSE USERS OF TELESCOPIC OPTICS. CLASS
1M LASER PRODUCT MAX POWER: 0.39MW WAVELENGTH: 635NM IEC
60825–1:2007–03
3.13 Reconstructed Image Orientation

CAUTION
GE CT IMAGE RECONSTRUCTION IS IN AN ORIENTATION VIEWING

FROM THE PATIENT'S FEET. THE RECONSTRUCTED ORIENTATION IS THE
ORIENTATION THE IMAGE IS INSTALLED IN THE IMAGE DATA BASE AND IS
THE ORIENTATION IMAGES ARE NETWORKED WITH TO A REMOTE VIEWING
STATION.

Safety
Figure 34 Patient Orientation
The patient position information stored in the image header correctly reflects the orientation (RAS)
information for the patient. Viewing applications will correctly reflect Right (R), Left (L), Anterior (A)
and Posterior (P) of the patient.
The reconstructed image orientation may differ from preferred anatomical viewing presentation in
which the patient's Right is on the viewers Left and patient's Left is on the viewers Right. For example,
when the patient is scanned Head First and Prone the patients’s Left is on the viewer’s Left and the
patient’s Right is on the viewer’s Right. The image presentation will need to be modified to display
preferred anatomical viewing. Some viewing stations may not have the capability to flip the image
presentation, but if the capability exists, you must use display tools such as Flip to change the
presentation of the image.
Some remote viewing stations may have the capability to set default viewing protocols. This is another
tool that can be used to set an anatomical viewing presentation.
Post processing applications automatically orient images in anatomical viewing orientation. These
applications create axial images in anatomical viewing presentation. Please see Display Applications
for more information. The system also provides the capability to create Gray Scale Presentation State
Objects (GSPS) to flip the image orientation.
WARNING
THE SYSTEM POSTS A WARNING MESSAGE IF PATIENT ORIENTATION HAS

BEEN CHANGED OR DOES NOT MATCH AFTER START OF EXAM.

Safety
3.14 Data Safety

CAUTION
INCORRECT DATA ENTRIES OR PROCEDURES COULD RESULT IN

MISINTERPRETATION OR MISDIAGNOSIS.
WARNING
SYSTEM DISK SPACE IS LOW. PLEASE PERFORM A SYSTEM RESTART

FROM THE MODE MENU. IF PROBLEM PERSISTS, CONTACT YOUR SERVICE
REPRESENTATIVE.
WARNING
SCAN DATA STORAGE SPACE IS GETTING LOW. PLEASE FINISH ACTIVE

RECONSTRUCTIONS AND UNRESERVE OBSOLETE SCAN DATA .
WARNING
DO NOT LOAD ANY NON-GE APPROVED SOFTWARE ONTO THE COMPUTER.
WARNING
THE SYSTEM POSTS A WARNING MESSAGE IF THERE IS A FAILURE DURING

THE ARCHIVE OF PATIENT DATA.
WARNING
THE SYSTEM POSTS A WARNING MESSAGE IF THERE IS A FAILURE DURING

THE NETWORK TRANSFER OF PATIENT IMAGE DATA.
WARNING
LOW IMAGE SPACE. PLEASE REMOVE IMAGES AND EMPTY THE RECYCLE
BIN.

Safety
WARNING
MISSING SLICES HAVE BEEN INTERPOLATED TO MAKE REFORMATTED

IMAGES.
CAUTION
WHEN ENTERING PATIENT ID INFORMATION THE SYSTEM MAY CONTAIN

MULTIPLE INSTANCES OF THE SAME PATIENT ID. MULTIPLE SCHEDULE
RECORDS CAN BE DUE TO MULTIPLE PROCEDURES BEING ORDERED
UNDER SEPARATE ACCESSION NUMBERS OR NEW AND COMPLETED
RECORDS IN THE PATIENT SCHEDULE FOR THE SAME PATIENT ID. WHEN
ENTERING THE PATIENT ID VERIFY THAT THE CORRECT ACCESSION
NUMBER AND EXAM DESCRIPTION SELECTED IS WHAT IS DESIRED.
SCANNING WITH AN INCORRECT ACCESSION NUMBER MAY CAUSE
PROBLEMS RECONCILING EXAMS ON A PACS SYSTEM. PLEASE SEE THE
SCHEDULING PATIENTS CHAPTER FOR MORE INFORMATION.
NOTE
The Patient Schedule chapter is in the User Manual.
CAUTION
WHEN COMPARING GE CT IMAGES WITH OTHER IMAGES, CONSULT THE

DICOM CONFORMANCE STATEMENT FOR THE DETAILS ON THE DICOM
IMAGE POSITION, FRAME OF REFERENCE UID AND SLICE LOCATION
VALUES STORED.
CAUTION
SOME ANNOTATION VALUES ARE STORED IN PRIVATE DICOM ELEMENTS.

WHEN VIEWING IMAGES ON A REMOTE STATION THESE ANNOTATIONS
VALUES MAY NOT BE VISIBLE ON THE IMAGE. CONSULT THE DICOM
CONFORMANCE STATEMENT FOR INFORMATION ON PRIVATE DICOM DATA
FIELDS.
CAUTION
THE TABLE LANDMARK HAS CHANGED. THIS CHANGES THE LOCATION OF

ALL SCANS YOU HAVE PRESCRIBED. DOUBLE CHECK ALL SCAN LOCATIONS
BEFORE YOU START SCANNING.

Safety
WARNING
THE SYSTEM POSTS A WARNING MESSAGE PRIOR TO THE MODIFICATION

OF ANY EXISTING PATIENT DATA BY THE USER.
3.15 Application Specific Safety Topics
3.15.1 Axial and Helical Scanning

WARNING
HELICAL SCANNING HAS THE INHERENT ABILITY TO PRODUCE ARTIFACTS

WHEN SCANNING HIGHLY SLOPED ANATOMY (E.G. PEDIATRIC OR ADULT
HEADS). FACTORS WHICH WORSEN THIS EFFECT ARE: FASTER TABLE
SPEEDS AND THICKER IMAGE THICKNESS. IN SOME CASES THESE
ARTIFACTS COULD BE MISTAKEN FOR A HEMORRHAGE NEAR THE
CRANIUM, OR A THICKENING OF THE SKULL.
To reduce the occurrence of these artifacts, you may prescribe slower
table speeds and/or thinner slices (such as 2.5 mm) during helical scans
near the vertex of a pediatric or adult head.
WARNING
IT HAS BEEN DOCUMENTED IN RADIOLOGY LITERATURE THAT AN

ARTIFACT MAY OCCUR IN THE CHEST THAT BEARS THE DOUBLE MARGIN
OF THE GREAT VESSELS, WHICH EMULATES A DISSECTION OF THE VESSEL
DURING 0.28 - 1.0 SECOND SCANS. THIS CAN OCCUR IN AXIAL OR HELICAL
SCANS. IF YOU HAVE SCANNED AXIALLY WITH A 0.28 - 1.0 SECOND
ROTATION TIME AND OBSERVE THIS PHENOMENON, RE-SCAN THE AREA
WITH A GATED SCAN, IF AVAILABLE ON YOUR SYSTEM, OR USE ANOTHER
DIAGNOSTIC MEANS TO DISTINGUISH BETWEEN POTENTIAL ARTIFACT OR
PATIENT PATHOLOGY.

Safety
3.15.2 Cardiac Imaging

CAUTION
A PATIENT WITH ANY OF THE CONDITIONS LIST BELOW MAY REQUIRE

ADDITIONAL ATTENTION. IF PATIENTS ARE SCANNED WITH THESE
CONDITIONS, THE SOFTWARE MAY NOT BE ABLE TO DETECT THE R-
PEAKS AND THE IMAGES THEREFORE MAY BE PRODUCED AS UNGATED
SEGMENT IMAGES: - PATIENT WITH MULTIPLE PRE-CONTRACTIONS OR
EXTRA SYSTOLE (E.G. PVC,PAC) - PATIENTS WITH PERSISTENT OR EXTREME
ARRHYTHMIA - PATIENTS WITH BI-VENTRICULAR LEAD (DUAL CHAMBER)
PACEMAKERS
CAUTION
ECG SIGNAL CLARITY AND INTEGRITY MUST BE CONFIRMED PRIOR TO

PERFORMING ECG-GATED ACQUISITIONS. ITEMS WHICH MAY REQUIRE
ADJUSTMENTS OF EQUIPMENT SETTINGS OR POSITIONING, OR PATIENT
SET-UP INCLUDE: -EXTERNAL INTERFERENCE - ATYPICAL PATIENT ECG
(E.G. ELEVATED T-WAVES, LOW ECG AMPLITUDE OR SIGNAL STRENGTH)
- SUBOPTIMAL PATIENT CONNECTION ECG LEAD PLACEMENT SHOULD
FOLLOW RECOMMENDED GUIDELINES TO OPTIMIZE RESULTS. IF THE ECG
LEAD BECOMES DISCONNECTED DURING THE SCAN, OR THE HEART RATE
DROPS BELOW 30 BPM, THE IMAGES WILL BE RECONSTRUCTED AS NON-
GATED SEGMENT IMAGES. THIS IS DONE TO AVOID INACCURACY OF THE
Z-LOCATION OF IMAGES WHERE NECESSARY.
CAUTION
PATIENT MOTION, RESPIRATION, BEAT-TO-BEAT VARIABILITY OF HEART

RATE, HEART MOTION, OR SIGNIFICANT CHANGE IN HEART RATE OVER
THE SCAN DURATION COULD CAUSE AN ECG GATED ACQUISITION TO
HAVE DEGRADED IMAGE QUALITY. IT IS IMPORTANT TO EXPLAIN TO THE
PATIENT THE PATTERN OF BREATHING INSTRUCTIONS TO EXPECT, THE
WARM FEELING THAT CAN BE FELT FROM THE CONTRAST INJECTION AND
TO POSITION THE PATIENT COMFORTABLY SUCH THAT THE ARMS WILL
NOT MOVE WITH RESPECT TO THE BODY DURING THE SCAN. HEART RATE
INFORMATION AND PHASE LOCATION WILL BE UPDATED TO INDICATE
ANY MOVEMENT OF TRIGGER LOCATIONS SINCE HEART RATE AND PHASE
VALUES ARE CALCULATED BASED ON TIME BETWEEN CONSECUTIVE
TRIGGERS AND ARE NOT DIAGNOSTIC VALUES.

Safety
CAUTION
ENSURE THE ECG PATCHES ARE NOT PAST EXPIRATION DATE AND THAT
THE GEL ON THE PADS IS STILL MOIST FOR PROPER CONDUCTION OF THE
ECG SIGNAL FOR SUCCESSFUL GATING.
CAUTION
THERE IS A POSSIBILITY THAT THE ECG SIGNAL MAY NOT BE DETECTED

BY THE SCANNER DUE TO IMPROPER LEAD PLACEMENTS, OR A LEAD
FALLING OFF DURING THE SCAN. IT IS IMPORTANT TO PLACE NEW
LEADS ON THE PATIENT BEFORE THE SCAN. MAKE SURE THE LEADS ARE
ATTACHED PROPERLY, AND USE ONLY GE RECOMMENDED ECG LEADS. IT IS
IMPORTANT TO CONFIRM ECG TRACE CLARITY BEFORE THE SCAN.
CAUTION
IF DURING THE SCAN THE HEART RATE DROPS SIGNIFICANTLY LOWER

THAN THE PRESCRIBED HEART RATE, THERE IS A POTENTIAL FOR GAPS
IN THE GATED IMAGE LOCATION. TO AVOID IMAGE LOCATION GAPS, A
NON-GATED IMAGE IS RECONSTRUCTED FOR THE PERIOD WHERE THE
PATIENT HEART RATE DROPPED BELOW THE EXPECTED OR CONFIRMED
HEART RATE AT THE START OF THE EXAM. A NON-GATED IMAGE MAY HAVE
MORE MOTION AND MAY NOT BE RECONSTRUCTED AT THE PRESCRIBED
PHASE.
CAUTION
MANUAL EDITS OF THE ECG GATING WAVEFORM MAY BE PERFORMED

RETROSPECTIVELY IN SOME ECG GATED EXAMS AS LONG AS SCAN DATA
EXISTS ON THE CONSOLE. IMAGES CAN BE RECONSTRUCTED WITH USER
MODIFIED GATING TRIGGERS AND THE ORIGINAL GATING INFORMATION
CAN BE RETRIEVED AFTER EDITS HAVE BEEN MADE.
WARNING
CURVED AND LUMEN REFORMATION CAN INTRODUCE DISTORTIONS IN

THE SHAPE OF OBJECTS.

Safety
3.15.3 CT Integrated Cardiac Module

WARNING
THE CT INTEGRATED CARDIAC MODULE IS FOR USE SOLELY IN

ACQUIRING CT IMAGES USING CARDIAC GATING/TRIGGERING, NOT FOR
PHYSIOLOGICAL MONITORING. THE PATIENT’S CURRENT CONDITION MAY
NOT BE REFLECTED, RESULTING IN IMPROPER EMERGENCY TREATMENT.
3.15.4 Advanced Application Safety

CAUTION
3D OR SLAB RECONSTRUCTIONS PROVIDE ADDITIONAL SUPPLEMENTAL

INFORMATION, COMPLEMENTING DIAGNOSIS THAT SHOULD BE BASED ON
CLASSICAL TECHNIQUES.
WARNING
NON-GE ACQUIRED IMAGES CAN BE LOADED IN VOLUME VIEWER BUT

GE DOES NOT GUARANTEE THE QUALITY OR RELIABILITY OF ANY
RECONSTRUCTION, SEGMENTATION OR MEASUREMENTS PERFORMED ON
THESE IMAGES. NON-GE IMAGES CAN EASILY BE IDENTIFIED BY THE
CORRESPONDING IMAGE ANNOTATION. FOLLOW THE DICOM ACQUISITION
PARAMETER GUIDELINES LISTED IN EACH APPLICATION USER GUIDE.
CONSULT GE-PUBLISHED DICOM CONFORMANCE STATEMENT OF VOLUME
VIEWER. (NOTE: THIS IS AVAILABLE VIA THE INTERNET ON THE
GE HEALTHCARE HOME PAGE, PRODUCTS/INTEROPERABILITY/DICOM
CONFORMANCE.)
3.15.5 Measurements
CAUTION
THE REPORT CURSOR SHOWS THE VOXEL VALUE NEAREST TO THE

CENTER LOCATION OF THE REPORT CURSOR IN THE ORIGINAL LOADED
SLICES.

Safety
WARNING
DO NOT USE 3D OR SLAB VIEWS ONLY TO PERFORM ANY MEASUREMENTS

(DISTANCE, ANGLE, REGION OF INTEREST, REPORT CURSOR, AREA,
VOLUME…). ALWAYS CHECK MEASUREMENT POINTS’ POSITION AND
REFER TO 2D BASELINE VIEWS (ACQUISITION IMAGES OR REFORMATTED
IMAGES OF MINIMAL THICKNESS) TO CONFIRM MEASUREMENTS.
CAUTION
THE SOFTWARE CALCULATES AND DISPLAYS MEASUREMENTS WITH A

RESOLUTION OF ONE DECIMAL (SUCH AS 0.1 MM, 0.1 DEGREE, ETC.).
YOU SHOULD BE AWARE THAT THE REAL MEASUREMENT ACCURACY
IS GENERALLY LESS FOR A NUMBER OF DIFFERENT REASONS (IMAGE
RESOLUTION, ACQUISITION CONDITIONS…). DISTANCE, ANGLE AND AREA
MEASUREMENTS ARE VALID ONLY IF ALL TRACE SEGMENTS ARE LONGER
THAN THE INTER-SLICE DISTANCE.
WARNING
DEPENDING ON WW/WL SETTINGS, OBJECTS MAY DISPLAY DIFFERENTLY.

CHECK WW/WL BEFORE DEPOSITING MEASUREMENT POINTS.
WARNING
CHECK WITH ORIGINAL DATASETS THE RELIABILITY OF SEGMENTATIONS

AND MEASUREMENTS PERFORMED IN SAVED OBJECTS AFTER POST
PROCESSING AND RELOADING.
3.15.6 Segment Tools

WARNING
BEFORE USING ANY SEGMENTATION TOOL (THRESHOLD, SCALPEL,

REMOVE & KEEP OBJECT, AUTOSELECT, “FLOATER” FILTERS…), ALWAYS
MAKE SURE THAT IT WILL NOT REMOVE PATHOLOGIES OR OTHER
ESSENTIAL ANATOMICAL STRUCTURES.

Safety
WARNING
WHEN USING ANY SEGMENTATION TOOLS (AUTOSELECT, THRESHOLD,

PAINT ON SLICE, QUICK PAINT…), CHECK CONTOURS TO CHECK THE
RELIABILITY OF THE SEGMENTATION. MAKE SURE THE CONTOURS
MATCH THE CORRECT SEGMENTATION AND VOLUMES. CHECK THAT THE
SEGMENTED VOLUMES MATCH CONTOURS.
3.15.7 Filming and Saving Images

CAUTION
THE FORMATS AND IMAGE QUALITY OF EXPORTED ELECTRONIC FILMS

ARE NOT SUITABLE FOR DIAGNOSTIC PURPOSES. IMAGE QUALITY MAY
BE DEGRADED BY DATA COMPRESSION TECHNIQUES USED TO EXPORT
ELECTRONIC FILMS.
CAUTION
WHEN FILMING OR SAVING IMAGES FOR DIAGNOSTIC PURPOSES, ALWAYS

MAKE SURE THE PATIENT NAME AND GEOMETRY INFORMATION IS
DISPLAYED ON ALL VIEWS, AND THAT THEY MATCH THE INFORMATION
ON THE REFERENCE VIEW.
CAUTION
WHEN SAVING IMAGES WITH A NEW SERIES DESCRIPTION, MAKE SURE

THIS DESCRIPTION MATCHES THE SAVED IMAGES.
3.15.8 Head Imaging

WARNING
POSSIBLE ARTIFACTS MAY EMULATE PATHOLOGY BETWEEN THE BRAIN

TISSUE AND BONE IN THE HEAD IMAGES. TO MINIMIZE THE POSSIBILITY
OF ARTIFACTS, IT IS RECOMMENDED THAT THE PATIENT’S HEAD IS
POSITIONED SO THE ORBITAL-MEATAL LINE IS PARALLEL TO THE SCAN
PLANE. ALSO FOLLOW USER MANUAL INSTRUCTIONS FOR SELECTION
OF SCAN FIELD OF VIEW FOR HEAD SCANS TO ENSURE OPTIMUM
RECONSTRUCTION ALGORITHMS ARE USED.

Safety
3.15.9 Interventional Scanning

Interventional scanning allows multiple scans at one location for interventional procedures. The
system allows up to 90 seconds of scanning in one place. After 90 seconds, the operator must prescribe
a new scan to continue. The accumulated scan time from a procedure is displayed on the In-Room
Monitor.
CAUTION
CARE MUST ALWAYS BE TAKEN WHEN A BIOPSY IS PERFORMED THAT IS IN

PROXIMITY TO TISSUES THAT NORMALLY MOVE (E.G. HEART, BOWEL) OR IN
TISSUES THAT MAY UNEXPECTEDLY MOVE DURING THE PROCEDURE. IT IS
IMPORTANT TO REMEMBER THAT INTERVENTIONAL SCANNING PROVIDES
IMAGES AND DATA BASED ON WHERE THE ANATOMY/TISSUES/NEEDLE
ARE LOCATED AT THE TIME OF THE CT ACQUISITION. WITH MOTION, THE
RELATIVE POSITIONS AND ORIENTATIONS WILL CHANGE.
NOTE
Users should be familiar with the guideline for interventional studies provided
by American College of Radiology (http://www.acr.org): ACR–SIR–SPR PRACTICE
PARAMETER FOR THE PERFORMANCE OF IMAGE-GUIDED PERCUTANEOUS NEEDLE
BIOPSY (PNB).
CAUTION
EXPOSURE TIME TO THE PATIENT CAN BE UP TO 90 S PER CONFIRM

COMPARED TO 60 S FOR ALL OTHER SCAN MODES.
CAUTION
THE FOOT PEDAL IS ACTIVE IF THE SYSTEM IS IN THE “PREPPED” STATE.

CARE SHOULD BE TAKEN NOT TO STEP ON THE FOOT PEDAL AND MAKE AN
UNWANTED EXPOSURE.
CAUTION
THE FOOT PEDAL SHOULD NOT BE DETACHED OR ATTACHED TO THE

GANTRY WHEN THE SYSTEM IS IN THE READY TO SCAN STATE. ALWAYS
MAKE SURE THE SYSTEM IS NOT IN THE PREPPED OR READY STATE WHEN
MANIPULATING THE FOOT PEDAL CONNECTION TO THE GANTRY.

Safety
WARNING
INTERVENTIONAL SCANNING WHEN THE FLUORO PAN HAS ENTERED THE

SCAN FIELD OF VIEW CAN RESULT IN IMAGE ARTIFACTS. EXERCISE CARE
TO PLACE THE FLUORO PAN ON THE CRADLE IN SUCH A WAY THAT
IT WILL NOT INTERFERE WITH IMAGING DURING THE INTERVENTIONAL
PROCEDURE.
Clinicians working in the scan room should wear appropriate protective clothing. Lead aprons, groin
and thyroid protection, as well as protective eye wear are available through the GE Accessories
Catalog.
3.15.9.1 Interventional Options

The interventional options add several components to the scan room. These are the In-Room Monitor,
Hand-held Control for table movement as well as image review, and the X-ray Control Foot pedal.
Each of the interventional option components is connected to the system by a cable. When using the
system, ensure that the cables cannot catch on anything when the gantry or table is moved.
CAUTION
THE CABLING PROVIDED FOR THE INTERVENTIONAL HAND-HELD

CONTROLLER (HHC) AND FOOT PEDAL WITH THE INTERVENTIONAL
OPTIONS MAY PRESENT A TRIP HAZARD. ENSURE THAT THE CABLING
CANNOT CATCH ON ANYTHING WHEN THE GANTRY OR TABLE IS MOVED
AND THAT THE CABLES ARE OUT OF THE WAY WHILE LOADING AND
UNLOADING THE PATIENT.
3.15.9.2 Table Float

During the scan, the clinician has the option to float the table between scans. When the Table Float
mode is selected, the table is unlatched and can be moved freely by anyone at the bedside.
WARNING
UNINTENDED TABLE MOTION MAY CAUSE A SERIOUS INJURY. TABLE MAY

BE BUMPED OR JARRED DURING AN INTERVENTIONAL PROCEDURE. CARE
MUST BE TAKEN WHEN PERFORMING INTERVENTIONAL PROCEDURES IN
THE FLOAT MODE. IT IS THE CLINICIAN'S RESPONSIBILITY TO ENSURE
THAT THEY HAVE CONTROL OF THE TABLE WHEN IN THIS MODE OF
OPERATION. TABLE MUST NOT BE LEFT UNATTENDED WHEN IN THE FLOAT
MODE. ENSURE THAT THE TABLE IS LATCHED BEFORE LEAVING THE TABLE
SIDE.

Safety
CAUTION
UNINTENDED CRADLE MOTION DURING SCANNING, CAUSED BY THE

CRADLE BEING UNLATCHED, CAN LEAD TO UNEXPECTED SCAN RESULTS.
IT IS THE CLINICIAN'S RESPONSIBILITY TO MAINTAIN CONTROL OF THE
TABLE WHEN IN THIS MODE OF OPERATION.
CAUTION
COLLISION WITH THE SUSPENDED INTERVENTIONAL MONITOR CAN

RESULT IN INJURY. TAKE CARE WHEN MOVING THE MONITOR.
TECHNOLOGISTS AND CLINICIANS IN THE SCAN ROOM SHOULD BE
AWARE OF THE LOCATION OF THE MONITOR TO AVOID INADVERTENTLY
COLLIDING WITH IT.
CAUTION
THE SUPPORT ARM FOR THE INTERVENTIONAL MONITOR IS DESIGNED

ONLY FOR THE LOAD OF THE MONITOR ITSELF. HANGING ADDITIONAL
EQUIPMENT FROM THE ARM OR THE MONITOR COULD CAUSE THE ARM TO
FAIL, RESULTING IN DAMAGE OR INJURY.
3.15.10 GSI Scanning
3.15.10.1 Image Quality
CAUTION
THE GENERAL ASSUMPTION FOR MATERIAL SEPARATION AND

MONOCHROMATIC IMAGE GENERATION IS THAT THE MATERIALS DO NOT
HAVE A K-EDGE IN BETWEEN 40 AND 140 KEV.
WARNING
WHEN RECONSTRUCTING DATA TO EVALUATE FOR GOUT PLEASE MAKE

SURE TO USE THE GE REFERENCE PROTOCOL FOR GOUT OR A USER
PROTOCOL WITH THE CLINICAL CATEGORY “EXTREMITY” AND CLINICAL
IDENTIFIER “GOUT” ALONG WITH THE GE GSI GOUT PROFILE. FAILURE
TO USE THIS METHOD COULD RESULT IN THE MIS-CATEGORIZATION OF
MATERIAL IN MD IMAGES FOR THE EVALUATION OF GOUT.

Safety
CAUTION
MATERIAL DENSITY (MD) IMAGES AND VUE IMAGES ARE SUPPLEMENTAL

IMAGES THAT SHOULD BE REVIEWED WITH MONOCHROMATIC 70 KEV
IMAGES.
The ability to separate materials into the corresponding material basis pair is a function of both
the material itself and the attenuation characteristics of the basis pairs. If the basis pairs chosen
have attenuation characteristics that are similar or close to each other, the resulting material density
images will not produce adequate separation and may result in images that have less than optimal
image quality.
CAUTION
AXIAL GSI SCANS AT THE 0.625 AND 1.25 MM SLICE THICKNESSES MAY
HAVE A CENTER SMUDGE ARTIFACT. YOU MAY REDUCE THE CENTER
SMUDGE ARTIFACT BY RECONSTRUCTING IN A WIDER SLICE THICKNESS.
CAUTION
WHEN GENERATING A WATER(IODINE) MATERIAL DENSITY PAIR ON THE

GSI VIEWER OR GSI VOLUME VIEWER, FAINT RINGS MAY BE SEEN IN THE
WATER(IODINE) IMAGES. IF THERE IS AN AREA OF CONCERN, COMPARE
THE IMAGE TO MONOCHROMATIC IMAGES.
CAUTION
BODY SCAN FIELD OF VIEW DOES NOT HAVE HEAD SPECIFIC CORRECTIONS
FOR BEAM HARDENING. SUB-OPTIMAL IMAGE QUALITY MAY BE SEEN IN
THE HEAD ANATOMY.

Safety
3.15.10.2 Measurements
WARNING
MATERIAL DENSITY IMAGES, UNLIKE CONVENTIONAL CT IMAGES AND

MONOCHROMATIC IMAGES, USE UNITS OF MILLIGRAMS PER CC (MG/CM3)
OR MICROGRAMS PER CC (UG/CM3) FOR PIXEL DATA INSTEAD OF HU
(HOUNSFIELD UNITS). THEREFORE DENSITY IMAGE SERIES SHOULD NOT
BE USED UNDER ANY CIRCUMSTANCE WITH SOFTWARE APPLICATIONS
THAT USE HU VALUES. ALWAYS CHECK UNITS OF STATISTICAL MEASURE
WITHIN THE APPLICATION TO CONFIRM EXPECTED UNITS.
3.15.10.3 Window Width and Window Level
CAUTION
THE WINDOW WIDTH AND WINDOW LEVEL FOR GSI IMAGES WILL VARY
DEPENDING ON THE KEV SELECTED COMPARED TO NON-GSI IMAGES.
PLACE AN ROI ON AN ANATOMICAL AREA AND NOTE THE MEAN VALUE. SET
THE WINDOW LEVEL TO MEAN VALUE AND ADJUST THE WINDOW WIDTH
TO THE DESIRED VIEWING LEVEL.
CAUTION
THE MD DATA VALUES HAVE BEEN APPROPRIATELY SCALED TO

PROVIDE BETTER DYNAMIC RANGE FOR VISUALIZATION ON DIFFERENT
VIEWING PLATFORMS. THIS SCALING IS REFLECTED IN THE UNITS
THAT ARE REPORTED NEXT TO THE W/L. RESCALING THE VALUES FOR
VISUALIZATION ALSO CHANGES THE VALUES REPORTED OR DISPLAYED BY
QUANTITATIVE TOOLS, E.G., ROIS, REPORT CURSOR, ETC. TO CONVERT TO
OTHER UNITS, YOU NEED TO PERFORM A MULTIPLICATION. FOR EXAMPLE,
IF THE SCALING IS 200 UG/CM3 THEN A REPORTED VALUE OF 20 IS
ACTUALLY 200 × 20 UG/CM3 = 4000 UG/CM3 OR 4 MG/CM3.

Safety
3.15.10.4 Imaging Reliability
WARNING
MONOCHROMATIC, MATERIAL DENSITY TRANSFORMATIONS ARE BASED

ON DATA WITHIN THE GSI DATA FILE. ALTHOUGH THE APPLICATION
CHECKS THAT EXAM ID AND OTHER DICOM PARAMETERS ARE THE SAME
TO ENSURE THE PAIRS ARE MATCHING, GOOD CLINICAL PRACTICES
SHOULD BE PUT IN PLACE TO AVOID MIXING PATIENT DATA.
WARNING
THE SAVED MD SERIES SHOULD NOT BE USED IN OTHER SOFTWARE

APPLICATIONS THAT RELY ON HOUNSFIELD VALUES.
WARNING
CURVED AND LUMEN REFORMATION CAN INTRODUCE DISTORTIONS IN

THE SHAPE OF OBJECTS. TO AVOID MISINTERPRETATION, YOU SHOULD
ALWAYS CORRELATE THE CURSOR POSITION IN CURVED REFORMATION
VIEWS WITH THE ORIGINAL AND REFORMATTED IMAGES.
3.15.10.5 Metal Artifact Reduction (MAR)
WARNING
MAR IMAGES SHOULD BE REVIEWED WITH BOTH MAR APPLIED AND

NOT APPLIED TO HAVE A COMPARISON BETWEEN THE NATIVE IMAGE
AND THE IMAGE WITH METAL REMOVED. THIS IS IMPORTANT IN CASES
WHERE METAL SCREWS ARE PRESENT AND APPLICATION OF MAR COULD
EMULATE LOOSE OR BROKEN METAL.
WARNING
THE USE OF MAR WHEN USED WITH METAL OUTSIDE THE BODY IN
THE SCANNED VOLUME MAY EMULATE PATHOLOGY SUCH AS SUBDURAL
HEMATOMA. IF AN AREA OF CONCERN IS SEEN, RECONSTRUCTION
WITH AND WITHOUT MAR SHOULD BE DONE FOR COMPARATIVE IMAGE
REVIEW OR USE ANOTHER DIAGNOSTIC MEANS TO DISTINGUISH BETWEEN
POTENTIAL ARTIFACT OR PATIENT PATHOLOGY.

Safety
3.15.10.6 Image Filters
WARNING
THE USE OF IMAGE ENHANCE FILTERS WHEN USED IN THE HEAD

MAY EMULATE PATHOLOGY IN THE BONE BRAIN INTERFACE. IT IS
RECOMMENDED TO USE CLINICAL IDENTIFIER NEURO.ROUTINE HEAD,
NEURO.ROUTINE HEAD WITH CONTRAST, STROKE.ROUTINE HEAD,
STROKE.ROUTINE HEAD WITH CONTRAST, TRAUMA.ROUTINE HEAD, OR
TRAUMA.ROUTINE HEAD WITH CONTRAST TO ENABLE HEAD SPECIFIC
FILTERS THAT REDUCE ARTIFACT NEAR THE BONE BRAIN INTERFACE. IF
AN AREA OF CONCERN IS SEEN, RECONSTRUCTION WITH AND WITHOUT
IMAGE ENHANCE FILTERS SHOULD BE DONE FOR COMPARATIVE IMAGE
REVIEW OR USE ANOTHER DIAGNOSTIC MEANS TO DISTINGUISH BETWEEN
POTENTIAL ARTIFACT OR PATIENT PATHOLOGY.
CAUTION
SERIES RECONSTRUCTED WITH IMAGE ENHANCE FILTERS SHOULD NOT

BE USED IN THE SMARTSCORE APPLICATION. USE OF THESE FILTERS MAY
AFFECT THE MEASURED CALCIUM SCORE.
WARNING
THE USE OF IMAGE ENHANCE FILTERS MAY EMULATE A FILLING DEFECT

IN THE VESSEL. IF AN AREA OF CONCERN IS SEEN, RECONSTRUCTION
WITH AND WITHOUT IMAGE ENHANCE FILTERS SHOULD BE DONE FOR
COMPARATIVE IMAGE REVIEW OR USE ANOTHER DIAGNOSTIC MEANS TO
DISTINGUISH BETWEEN POTENTIAL ARTIFACT OR PATIENT PATHOLOGY.
CAUTION
THE USE OF IMAGE ENHANCE FILTERS MAY CHANGE THE TEXTURE OF THE
IMAGE. IF AN AREA OF CONCERN IS SEEN, RECONSTRUCTION WITH AND
WITHOUT IMAGE ENHANCE FILTERS SHOULD BE DONE FOR COMPARATIVE
IMAGE REVIEW.

Safety
3.15.11 Deep Learning Image Reconstruction (DLIR)

WARNING
THE USE OF DLIR IMAGES HAS NOT BEEN VALIDATED FOR CALCIUM
SCORING AND PERFUSION APPLICATION QUANTITATIVE ANALYSIS. DLIR
IMAGES SHOULD NOT BE USED FOR THIS PURPOSE.
WARNING
DLIR IMAGES HAVE REDUCED PARTIAL VOLUME EFFECTS, WHICH CAN

RESULT IN A CHANGE IN THE APPARENT SHAPE OF METAL IN THESE
IMAGES COMPARED TO NON DLIR IMAGE RECONSTRUCTION. IF THERE
IS AN AREA OF CONCERN, ALWAYS COMPARE TO A NON-DLIR IMAGE
RECONSTRUCTION.
WARNING
REDUCED CONTRAST OF SMALL STRUCTURES MAY BE SEEN WHEN

USING DLIR-HIGH OR DLIR-MEDIUM. IF AREA OF CONCERN IS SEEN,
RECONSTRUCTION USING DLIR-LOW SHOULD BE DONE.
CAUTION
THERE IS A POTENTIAL FOR PATTERNED NOISE TO BE VISIBLE WITH

LOW NOISE DATA. USING THE DLIR-LOW OR DLIR-MEDIUM OR LARGER
WINDOW WIDTH AND WINDOW LEVEL SETTINGS WHEN IMAGING SOFT
TISSUE REGIONS (LIKE THE LIVER) WILL REDUCE THIS EFFECT.
3.15.12 Max Field of View (MaxFOV 2) Reconstruction DFOV Greater

than 50.0 cm
CAUTION
SHADING ARTIFACTS MAY BE SEEN IN OFF CENTERED MAXFOV 2 IMAGES. IF

AN AREA OF CONCERN IS SEEN, COMPARE TO NON MAXFOV 2 IMAGES.

Safety
WARNING
THE USE OF MAXFOV 2 IMAGES HAS NOT BEEN VALIDATED FOR

PERFUSION APPLICATON QUANTITATIVE ANALYSIS. MAXFOV IMAGES
SHOULD NOT BE USED FOR THIS PURPOSE.
CAUTION
THE IMAGE QUALITY IN THE REGION OUTSIDE THE 50 CM SFOV IN MAXFOV

2 PROCESSED IMAGES IS NOT EXPECTED TO BE AS GOOD AS THAT WITHIN
THE SCAN FOV, AND IS NOT INTENDED FOR DIAGNOSTIC IMAGING. IF
DESIRED, TO BETTER VISUALIZE THE AREA OUTSIDE THE SCAN FIELD OF
VIEW, MANUALLY PLACE A CIRCULAR ROI AT ISOCENTER WITH A DIAMETER
EQUAL TO THE SCAN FIELD OF VIEW'S.
CAUTION
MAXFOV 2 PROCESSED IMAGES MAY DIFFER SLIGHTLY INSIDE THE 50

CM SFOV FROM IMAGES NOT PROCESSED WITH MAXFOV 2. IF AN AREA
OF CONCERN IS SEEN, RECONSTRUCTION WITH AND WITHOUT MAXFOV
2 SHOULD BE DONE FOR COMPARATIVE IMAGE REVIEW TO CONFIRM
DIAGNOSTIC UTILITY.
CAUTION
THE RESOLUTION WITHIN THE 50CM DFOV DIFFERS SLIGHTLY BETWEEN

IMAGES WITH AND WITHOUT MAXFOV 2 PROCESSING. IF AN AREA OF
CONCERN IS SEEN, RECONSTRUCTION WITH AND WITHOUT MAXFOV
2 SHOULD BE DONE FOR COMPARATIVE IMAGE REVIEW TO CONFIRM
DIAGNOSTIC UTILITY.
Table 8 Image Quality Accuracy MaxFOV 2
When scanned object extends in- Water CT Number Accuracy Skin Line Accuracy
to DFOV region
50.1- 70.0 cm 0 +/-40 HU 0 +/-2.0mm
70.1- 80.0cm 0/ +/-60 HU 0 +/-3.0mm
WARNING
UNAPPROVED ACCESSORIES MAY CAUSE RECONSTRUCTION ARTIFACTS IN

MAXIMUM FIELD OF VIEW (MAXFOV 2) RECONSTRUCTION IMAGES.

Safety
CAUTION
IF THE SKIN LINE OF THE PATIENT JUST TOUCHES THE EDGE OF THE 50
CM SCAN FIELD OF VIEW, IT IS POSSIBLE FOR THIS TO RESULT IN SHADING
OF MAXFOV 2 RECONSTRUCTED IMAGES. IF THE PATIENT BOUNDARY GOES
OUTSIDE OR STAYS INSIDE OF THIS CENTRAL 50 CM REGION THEN NO
SHADING SHOULD OCCUR. FROM THE SHOW LOCALIZER IMAGE WITH A
HELICAL SCAN PRESCRIBED, USE THE IRRADIATION LINES ON THE AP AND
LATERAL SCOUT TO VERIFY THAT THE SKIN EDGE IS EITHER INSIDE OR
FULLY OUTSIDE THE INDICATED SFOV LINE. IF THE SKIN EDGE IS JUST
TOUCHING THE SFOV LINE, USE BODY STRAPS TO WRAP THE PATIENT OR
MOVE THE TABLE ELEVATION 0.5 TO 1 MM UP OR DOWN. TAKE ANOTHER
AP AND LATERAL SCOUT TO CONFIRM THE SKIN EDGE IS OFF THE SFOV
LINES.
3.15.13 Auto Positioning

CAUTION
During table motion to the scout scan start position, make sure to keep
observing the patient for potential collision of the patient body with the
CT gantry due to patient motion, or damages to devices connected to
the patient like intravenous injectors, anesthesia machines or ECG gating
devices.
Pressing the Pause button on the gantry display or any of the motion
buttons on the control panel can stop the Auto Positioning motion.
In case of emergency, press the emergency button to stop the Auto
Positioning motion immediately.
CAUTION
The accuracy of the scout scan range determined by the Auto Positioning
option is affected by the sheets/blankets/body strap covering the patient
body, blockage of the depth camera view by people/devices around
and /or above the patient table, lighting conditions and existence of highly
reflective surfaces. Make sure to check the validity of the scan range on the
patient video shown on the gantry display, and adjust it manually on the
video when necessary, before starting the automatic table motion.

Safety
3.16 Application Software Safety

CAUTION
DO NOT INITIATE AN SPRSNAP IF THE SYSTEM IS ACTIVELY COLLECTING

DATA WITH X-RAY ON.
3.17 Accuracy of Measurements

This section includes information on accuracy of measurements used when reviewing images.
3.17.1 Measure Distance for Axial, Helical, and Cine Images

CAUTION
MEASURE ERROR USING THE STRAIGHT LINE DISTANCE GRAPHIC IS ± THE

LARGEST VOXEL DIMENSION.
CAUTION
NOTE THAT THE MEASUREMENTS ARE ACCURATE ONLY IF THE TRACE

SEGMENTS ARE LONGER THAN THE SLICE INTERVAL.
3.17.2 Measure Distance for Scout Images

Accuracy of measurements for scout images in the “X” direction varies with object thickness and
distance from isocenter in the “Y” direction. Note the orientations of the “X” and “Y” in Figure 35 on
page 75 below assume a scout scan plane of 0 degrees. If the scout plane is rotated, then the “X” and
“Y” orientation changes accordingly.
• For measurements of anatomy in the “X” direction that are at isocenter (“Y”):
The measure error using the straight line distance graphic is less than 5 % of the measured
distance plus 2 mm.
• For measurements of anatomy in the “X” direction that are NOT at isocenter (“Y”):
The measure error using the straight line distance graphic is less than 5 % of the measured
distance plus 2 mm plus 3 % of measured distance per centimeter from isocenter.
• For measurements of anatomy in the “Z” direction:
Measure error using the straight line distance graphic is less than two times the image pixel size.

Safety
Figure 35 Scout Scan Plane
Number Description
1 isocenter
2 Y-axis
3 X-axis
4 Z-axis
5 x-ray tube focal spot
6 scan plane
7 patient table

Safety
3.17.3 Measure Angle

CAUTION
MEASUREMENT ACCURACY USING THE ANGLE GRAPHIC IS EQUAL TO

THE DISPLAYED ANGLE VALUE ± 10 DEGREES FOR AN ANGLE MEASURED
BETWEEN SEGMENTS WHICH ARE FIVE TIMES LARGER THAN THE IMAGE
PIXEL SIZE. ACCURACY IMPROVES AS THE LENGTH OF THE SEGMENTS
INCREASES.
3.17.4 Voxel Dimensions

CAUTION
THE IMAGE SET RESOLUTION, THAT IS, THE DIMENSIONS OF THE VOXELS
(VOLUME ELEMENTS) THAT CONSTITUTE THE IMAGE SET, IS DETERMINED
BY THE SIZE OF THE FIELD-OF-VIEW, THE MATRIX SIZE, AND THE INTER-
SLICE DISTANCE. IDEALLY, VOXELS SHOULD BE ISOTROPIC (WITH THE
SAME DIMENSIONS ALONG ALL THREE AXES). THAT IS, THE INTER-SLICE
DISTANCE SHOULD BE THE SAME AS THE VOXEL DIMENSION IN THE
ACQUISITION PLANE. IN PRACTICE, HOWEVER, CONSIDERATIONS SUCH
AS PATIENT IRRADIATION DOSE LEVELS WILL USUALLY LEAD TO THE
CHOICE OF A LARGER INTER-SLICE DISTANCE. BE AWARE THAT DETAILS
WITH DIMENSIONS IN THE ORDER OF OR LESS THAN THE INTER-SLICE
DISTANCE CANNOT BE IDENTIFIED OR MEASURED WITH ANY DEGREE OF
RELIABILITY.
3.17.5 ROI
CAUTION
AREA MEASUREMENT ACCURACY USING A REGION OF INTEREST GRAPHIC

(RECTANGLE, SMOOTH CURVE, ELLIPSE OR FREE DRAW) IS EQUAL TO
THE DISPLAYED AREA ± THE PERIMETER OF THE REGION MULTIPLIED BY
(LARGEST VOXEL VALUE)2/2. MEAN AND STANDARD DEVIATION VALUES
FOR THE INTENSITY OF THE PIXELS IN THE REGION ARE ALSO AFFECTED
BY THIS ACCURACY. IF THE ROI IS ROTATED, THE AREA MEASUREMENT CAN
VARY UP TO 5 %. REGION OF INTEREST STATISTICS ARE BASED ON THE
PIXELS INSIDE THE GRAPHIC DEFINING THE REGION.

Safety
CAUTION
CT NUMBERS ARE NOT ABSOLUTE; MISDIAGNOSIS IS POSSIBLE. SYSTEM

AND PATIENT VARIABLES MAY AFFECT CT NUMBER ACCURACY. IF YOU
RELY SOLELY UPON CT NUMBERS WITHOUT TAKING VARIABLES INTO
CONSIDERATION, YOU COULD MISDIAGNOSE AN IMAGE.
3.17.6 CT Number
(Reference 1020.33 (j)(1), 1020.33 (j)(2))
Besides anatomic location and area, each CT pixel also represents a CT number, which in turn
indicates tissue density.
An image pixel represents a three dimensional volume, or voxel. It represents anatomy with a
location, an area, and a pixel (density) value. The system flattens the 0.625, 1.25, 2.5, 3.75, and 5
mm scan thickness into a two dimensional screen image. If a pixel represents a variety of tissues,
the system averages the contents to produce an averaged, rather than accurate, pixel value. Uniform
tissues (within the voxel) produce fairly accurate pixel values.
CT pixel shading shows relative density. Denser materials weaken X-ray and produce whiter pixels.
(Assumes Inverse Video OFF)
Reformat displays non axial planes created from contiguous pixels extracted from multiple images.
3D locates similar pixel values within contiguous images, and generates a mathematical model to
produce images that appear three dimensional. BMD samples pixel values to estimate bone or tissue
density.
Reconstruction assigns one value to every image pixel. CT uses pixel values of -32767 to +32767.
MR uses pixel values of +16,000. The screen pixel translates the assigned value into one of the 256
shades of gray. Vary the gray scale window width and level to select anatomy for display. Window
Width determines the quantity of gray pixel values. Window Level selects the center Window Width
pixel value.
Example: Two windows may contain identical widths of 100 values, but display completely different
anatomy, because one has a level of -100 and the other has a level of 150.
3.17.6.1 CT Number Mean and Standard Deviation

• An ROI averages the values of the enclosed pixels, and displays the resulting Mean value.
• Standard Deviation describes the difference between the minimum and maximum ROI value.
• A large ROI provides a larger, more accurate statistical sample than a small ROI.
The system provides, using the image display software, the capability to draw and edit rectangular and
elliptical regions of interest (ROI), with the ability to calculate and report the mean value and standard
deviation of the image pixel data contained within the ROI and the area of the ROI.

Safety
It also provides the capability to draw and edit a circular region of interest, with the ability to calculate
and report the mean value, standard deviation, minimum, maximum and area (mm2) of the image
pixel data contained within the ROI.
3.17.6.2 CT Number Accuracy

CT Number of water: 0 HU ± 3 HU
CT Number of air: –1000 HU ± 10 HU
WARNING
QUALITATIVE OBSERVATIONS FROM ENHANCED CONTRAST IMAGES

SHOULD BE COMPARED TO THOSE FROM IMAGES WITHOUT ENHANCED
CONTRAST. THE QUANTITATIVE ACCURACY OF CT NUMBERS MAY BE
CHANGED WHEN USING ANY OF THE ENHANCED CONTRAST LEVELS
(I.E. EC1, EC2, EC3, EB1, EB2, EB3). WHEN PERFORMING QUANTITATIVE
ASSESSMENT OR ANALYSIS OF CT NUMBERS, ONLY USE IMAGES
RECONSTRUCTED WITHOUT ENHANCED CONTRAST.
3.17.7 Range, Precision and Accuracy of Displayed Values

Table 9 Range, precision and accuracy of displayed values
Primary Gantry Display Range, Precision, Accuracy
Vertical height indicator Display Range: 0 to 999.9 mm

Display Precision: +/-1.5 mm
Display Accuracy: +/-1.5 mm
Horizontal cradle position Display Range: 0 to 9999.9 mm

Display Precision: +/-.25 mm
Display Accuracy: +/- 0.06 %
Scannable Range Display Range: 0 to 9999.9 mm

Secondary Gantry Display Range, Precision, Accuracy
Prep Delay Timer Display Range: 0 - 999 s

Display Precision: +/- 1 s
Display Accuracy: +/- 1 s
Breath hold timer Display Range: 0 - 99 s


Safety
3.18 Accessory Safety

WARNING
DO NOT CONNECT ACCESSORIES OR OTHER ITEMS THAT ARE NOT

APPROVED AS PART OF THE SYSTEM. DO NOT USE ACCESSORIES FROM
OTHER MODALITIES.
WARNING
NONE OF THE ACCESSORIES SUPPORT THE FULL WEIGHT OF A PATIENT.

IF YOU SIT, STAND, OR OTHERWISE APPLY EXCESSIVE PRESSURE TO THESE
DEVICES, THEY COULD BREAK OR COME OFF THE CRADLE AND MAY CAUSE
INJURY. IF AN ACCESSORY BREAKS, USE CAUTION WHEN PICKING IT UP
AND DO NOT CONTINUE TO USE IT.
CAUTION
USING ACCESSORIES WHICH ARE NOT GE APPROVED MIGHT AFFECT DOSE

AND IMAGE QUALITY.
WARNING
ACCESSORIES THAT ARE NOT SECURED TO TABLE MAY INTERFERE WITH

GANTRY IF NOT POSITIONED PROPERLY.
WARNING
WITH EACH USE, CHECK ALL ACCESSORIES FOR DAMAGE AND REMOVE
THEM FROM SERVICE IF DAMAGED OR CRACKED.
3.18.1 Monitor Safety

CAUTION
FOR A TWO-MONITOR CONFIGURATION IT IS NECESSARY TO CHECK THE

MONITOR CALIBRATION REGULARLY TO ENSURE IMAGES ARE DISPLAYED
IDENTICALLY ON BOTH MONITORS.

Safety
3.18.2 IV Pole Safety

Care should be taken in the amount of weight placed on the pole. Ensure that the pole is tightened
prior to use.
WARNING
THE IV POLE MAY BEND WHEN EXCESSIVE WEIGHT IS PLACED ON THE

POLE. ENSURE NO MORE THAN 4.5 KG OR 10 LB IS PLACED ON THE IV
POLE.
WARNING
ENSURE THAT THE IV POLE EXTENSION COLLAR IS TIGHTENED PRIOR TO

USE TO PREVENT THE POLE HEIGHT FROM COLLAPSING.
3.18.3 Table Tray Safety

Care should be taken in the total weight of objects that are placed on the tray.
WARNING
OBJECTS THAT MAY BE SUSCEPTIBLE TO TIPPING SHOULD BE STRAPPED

DOWN WITH THE VELCRO™ STRAP PROVIDED.
3.18.4 Systems With Metal-Free Cradles and Accessories

CAUTION
PREVENT DAMAGE TO METAL-FREE ACCESSORIES! CAREFULLY EXAMINE

THE METAL-FREE CLASP ASSEMBLY ON THE ACCESSORY AND THE CATCH
ON THE CRADLE BEFORE ATTEMPTING TO ATTACH THE ACCESSORY FOR
THE FIRST TIME.

Safety
3.18.5 Power Injector Safety

CAUTION
THE INJECTOR AND THE SYSTEM ARE OPERATED INDEPENDENTLY AFTER

THE START SCAN BUTTON IS PRESSED. WHEN YOU WANT TO STOP BOTH
THE SYSTEM AND THE INJECTOR, USE THE STOP SCAN BUTTON ON THE
SCAN CONTROL INTERFACE AND THE STOP INJECTOR FUNCTION ON THE
INJECTOR SYSTEM.
3.18.6 Phantom Safety

WARNING
THE PHANTOM HOLDER CAN SAFELY SUPPORT A MAXIMUM WEIGHT OF 22

LBS (10 KG). DO NOT EXCEED THIS WEIGHT.
3.18.7 Varian RPM Respiratory Gating System Safety

WARNING
WHEN USING THE VARIAN RPM RESPIRATORY GATING SYSTEM

CAMERA AS PART OF RADIOTHERAPY TREATMENT PLANNING, FOLLOW
MANUFACTURER’S INSTRUCTIONS FOR INSTALLING MOUNTING POLE AND
CAMERA TO THE TABLE.
WARNING
RPM ACCESSORY MAY FALL AND CAUSE INJURY IF NOT PROPERLY

SECURED TO THE WALL HANGER.
WARNING
MAKE SURE RPM CAMERA ASSEMBLY IS PROPERLY MOUNTED AND SECURE

ON THE TABLE OVERLAY PRIOR TO EACH USE.

Safety
WARNING
CAMERA BRACKET ASSEMBLY IS NOT INTENDED TO RETRACT THE PATIENT

FROM THE GANTRY BORE
WARNING
CAMERA SHALL BE INSTALLED PER MANUFACTURER’S INSTALLATION

INSTRUCTION FOR EACH USE
WARNING
TO PREVENT POTENTIAL INJURY, INSPECT PRIOR TO EACH USE. CONTACT

YOUR SERVICE PROVIDER IN CASE OF ANY LOST HARDWARE.
WARNING
MISMATCH IN PATIENT INFORMATION BETWEEN THE CT SYSTEM AND

THE RESPIRATORY GATING DEVICE WILL PREVENT ADVANTAGE 4D FROM
ASSOCIATING RESPIRATORY DATA WITH THE IMAGE DATA FROM THE CT
EXAM. MAKE SURE THAT THE PATIENT INFORMATION INCLUDING THE
PATIENT ID IS ENTERED THE SAME IN BOTH DEVICES.
When using Advantage 4D make sure that the selected respiratory motion
file is for the currently selected patient.
WARNING
RECOMMENDED GANTRY ROTATION SPEEDS FOR RESPIRATORY GATED

IMAGING ARE 0.5 SEC/ROTATION AND 1.0 SEC/ROTATION. THE
RESPIRATORY GATING SIGNAL MAY NOT BE STABLE AT FASTER GANTRY
ROTATION SPEEDS.
WARNING
PORTABLE AND MOBILE RF COMMUNICATION EQUIPMENT SHOULD NOT

BE USED CLOSE TO THE RESPIRATORY GATING MONITORING CAMERA.
PLEASE REFER TO THE SUPPLIER REFERENCE GUIDE FOR RECOMMENDED
SEPARATION DISTANCES.

Safety
3.19 Maintenance and Cleaning and Disinfection

• To guarantee safe, reliable equipment performance, the site must be prepared according to GE
Healthcare requirements, as specified in the Pre-Installation Manual.
• There are no user serviceable parts in this system. The product should be installed, maintained,
and serviced by qualified service personnel according to procedures laid down in the product
service manuals.
• The system in whole or in part should not be modified in any way without prior written approval
by GE Healthcare.
• Planned maintenance must be carried out regularly to ensure safe operation of the equipment.
• For user maintenance of the system and performance tests, refer to the maintenance and
calibration information in the Technical Reference Manual.
Environmental Concerns
This symbol indicates that the waste of electrical and electronic equipment must not be disposed
of as unsorted municipal waste and must be collected separately. Please contact an authorized
representative of the manufacturer for information concerning the decommissioning of your
equipment.
3.19.1 General Cleaning and Disinfection

General Cleaning Background: cleaning should be done by site personnel (e.g., technologists or
housekeeping personnel) unless otherwise indicated in the following maintenance schedules.
Keep the equipment clean. Remove body fluids and/or contrast spills to prevent health risk and
damage to internal parts. Thorough cleaning, including prompt removal of soil, is essential for
adequate processing and will reduce the risk of infection for patients.
Ensure system components or accessories are not worn out, cracked, or torn to ensure proper cleaning
and disinfection. Replace worn out components or accessories immediately.
When using any open cell foam (sponges without coating), always place a barrier between the
patient's skin and the sponge. If sponges are soiled, discard them as they cannot be cleaned or
disinfected.
Item Required Maintenance Service Interval
General Clean As required
Patient Cradle Clean pads and inside of the cra- Between each patient
dle.

Safety
(continued)
Item Required Maintenance Service Interval
Pads, Straps, Patient Accessories Clean all areas that were touched Between each patient
by the patient. Clean other areas as
needed
Head Holder Insert Inspect for bodily fluids, dispose Between each patient
and replace if saturated
3.19.2 Cleaning and Disinfection Agents

Do not clean connectors on the cables for ECG, respiratory equipment, etc. If you need to clean these
components, contact GE Service.
Use dry use cleaning for electronic components.
The following cleaners and disinfectants have been evaluated based on their chemical compatibility
with the device materials. The cleaners and disinfectants listed here may not be available in all
countries. Follow hospital procedures for infection control in compliance with local regulations.
Keep the equipment clean. Remove body fluids and/or contrast spills to prevent health risk and
damage to internal parts. See 5881700-1xx for detailed Cleaning and Disinfection Instructions for Use.
Follow cleaning/disinfection agent manufacturer instructions for disinfection contact time.
Inspect to ensure visual cleanliness prior to disinfection. Cleaning is the removal of visible soil (for
example, organic and inorganic material) from objects and surfaces and normally is accomplished
manually or mechanically using water with detergents or enzymatic products. Thorough cleaning is
essential before disinfection because inorganic and organic materials that remain on the surfaces of
instruments interfere with the effectiveness of these processes.
Disinfection should follow recommendations for low- to intermediate-level disinfection as defined
in CDC guidance www.cdc.gov/hicpac/pdf/guidelines/disinfection_nov_2008.pdf. The system surfaces
are noncritical surfaces and are disinfected with low- to intermediate-level disinfectants. Ensure the
appropriate contact time as defined by the disinfectant manufacturer.
In situations that arise requiring a sterile field, ie interventional procedures, alternative means/
barriers should be used. The system is rated for Intermediate-Level disinfection, in cases of non-intact
skin, ie open wound, a barrier should be applied. Additionally, upon inspection of the head holder
insert, if saturated in bodily fluids please dispose and replace.
Apply cleaning/disinfection solutions to a lint-free cloth or use a wipe. Spraying directly onto the CT
scanner can damage parts like the tilt centers and control panels.
The following cleaning and disinfection agents in the list below are approved for use on the product by
GE Healthcare and are USA EPA registered disinfectants agents:
• Sani-Cloth® Bleach Wipes*
• Sani-Cloth® Prime*
• Sani-Cloth® HB
• Clorox Healthcare™ Bleach Germicidal Cleaner Spray*
• Clorox Healthcare™ Bleach Germicidal Wipes*

Safety
• Clorox Healthcare™ Hydrogen Peroxide Cleaner Disinfectant Wipes*

• Clorox Multi Surface Cleaner + Bleach*
• Micro-kill Bleach Solution*
• Micro-kill Bleach Germicidal Bleach Wipes*
*denotes effectivity claims made by governing bodies or manufacturers for Covid-19.

The following cleaning and disinfection agents are approved for use on the product by GE Healthcare
but are not on the USA EPA list which may be used for facilities outside of the United States..
• 10% Bleach Solution (Common household bleach, diluted 1:10-mix 1 part bleach with 9 parts tap
water, disinfection wet time of 5 minutes)
• Distel
• Incidin Plus
• Perasafe
Follow the labeled instructions of the cleaning agent manufacturer and observe the dilution/
concentration and contact time instructions. Use tap (utility) water for dilution.
Always clean and disinfect the equipment between each patient.
NOTE
As preferred cleaning and disinfection practices change and new products become
available, GE Healthcare continues to test the material compatibility of these agents
for GE devices. See https://cleaning.gehealthcare.com/?cmpid=covid-quick-links for any
newly qualified agent.
3.20 Hazardous Substances

The X-ray Tube Assembly contains potentially dangerous materials but does not present any danger as
long as it is neither opened nor disassembled.
WARNING
DO NOT DISCARD THE X-RAY TUBE ASSEMBLY AMONG INDUSTRIAL WASTE

OR DOMESTIC GARBAGE.
WARNING
A DAMAGED X-RAY TUBE ASSEMBLY SHOULD NOT BE DISPATCHED

THROUGH THE NATIONAL POSTAL SERVICE.
The X-ray Tube Assembly contains the following potentially hazardous materials:
• Lead: Lead salts are toxic and their ingestion may cause serious problems. The manipulation/
handling of lead is subject to regulations.

Safety
• Oil: Univolt 54 and Crosstrans 206 mineral oil are not toxic, but the prevailing environmental
regulations should be observed for their disposal or recuperation. For example, it is forbidden to
dispose of these oils in the wastewater or sewage system or in the natural environment.
Your local GEMS field service will advise you on the suitable means of disposal of equipment.
The X-ray Tube Assembly to be discarded should be forwarded to the GEMS Service network, and it will
be disposed of in a GEMS recycling center.
Precautions
Take all the necessary precautions for the personnel handling the recovery or destruction of X-ray
Tube Assemblies, and in particular against the risks due to lead.
These personnel must be informed of the danger involved and of the necessity to observe the safety
measures.
Mercury
Revolution™ CT, Revolution™ CT ES systems manufactured before January, 2015 include LCD monitors
that contain mercury.
Dispose according to Local, State, or Federal laws.
3.21 System Performance

CAUTION
UPON SYSTEM STARTUP, WHEN AN UNRECOGNIZED X-RAY TUBE IS

DETECTED, THE SYSTEM DISPLAYS THE FOLLOWING NOTIFICATION
TO THE OPERATOR: ATTENTION AN UNRECOGNIZED X-RAY TUBE
HAS BEEN INSTALLED ON THE SYSTEM. - GE CANNOT ASSURE
THAT SYSTEM PERFORMANCE WILL CONFORM TO SPECIFICATIONS.
ADVISORY MESSAGES WILL BE POSTED TO THE OPERATOR ABOUT
AN UNRECOGNIZED TUBE DURING TUBE WARM-UP, DURING FAST
CALIBRATION, AND IN THE DOSE REPORT.
CAUTION
PRIOR TO THE START OF TUBE WARM-UP, WHEN AN UNRECOGNIZED

X-RAY TUBE IS DETECTED, THE SYSTEM DISPLAYS THE FOLLOWING
NOTIFICATION TO THE OPERATOR: ATTENTION AN UNRECOGNIZED TUBE
HAS BEEN INSTALLED ON THE SYSTEM. TUBE COOLING ALGORITHMS
ARE DESIGNED SPECIFICALLY FOR GE TUBES AND THE PERFORMANCE
OF THE SYSTEM CANNOT BE GUARANTEED. WARNING SCANS MAY HAVE
BEEN TAKEN WITHIN THE LAST TWO HOURS. WARMUP SCANS MAY CAUSE
SUBSEQUENT COOLING DELAYS. NOTE: TUBE WARMUP WILL RUN IN
AUTOSCAN MODE.

Safety
CAUTION
PRIOR TO THE START OF FAST CALIBRATION, WHEN AN UNRECOGNIZED

X-RAY TUBE IS DETECTED, THE SYSTEM DISPLAYS THE FOLLOWING
NOTIFICATION TO THE OPERATOR: ATTENTION AN UNRECOGNIZED TUBE
HAS BEEN INSTALLED ON THE SYSTEM. FAST CALIBRATION TECHNIQUES
ARE DESIGNED SPECIFICALLY FOR GE TUBES AND GE CANNOT GUARANTEE
THAT THE PERFORMANCE OF THE SYSTEM WILL MEET SPECIFICATIONS
WITH AN UNRECOGNIZED TUBE.
CAUTION
PRIOR TO CONFIRMATION OF A SCAN PRESCRIPTION, WHEN AN

UNRECOGNIZED X-RAY TUBE IS DETECTED, THE SYSTEM DISPLAYS
THE FOLLOWING NOTIFICATION AS A PART OF THE PRE-SCAN DOSE
INFORMATION TO THE OPERATOR: UNRECOGNIZED TUBE -- DOSE NOT
VALIDATED BY GE.
CAUTION
WHEN AN UNRECOGNIZED X-RAY TUBE IS DETECTED, THE SYSTEM

DISPLAYS THE FOLLOWING NOTIFICATION AS A PART OF THE POST-SCAN
DOSE REPORT TO THE OPERATOR: ATTENTION UNRECOGNIZED TUBE
IN USE. THE REPORTED DOSE INFORMATION IS CALCULATED BASED ON
EMPIRICAL OBSERVATIONS OF SYSTEMS WITH GE TUBES. GE CANNOT
ASSURE THE ACCURACY OF REPORTED DOSE INFORMATION FOR ANY
CONFIGURATIONS THAT INCLUDE TUBES OTHER THAN GE TUBES.

Safety

Read Me First
4 Read Me First
4.1 About This Manual

This section explains the purpose and design of this user manual. It provides information on the
purpose, prerequisite skills, organization, format, and graphic conventions used throughout the
manual.
The manual does not identify components or features that are standard or purchasable options. If a
feature or component included in the manual is not on your system, it is either not available on your
system or your site has not purchased the option.
4.1.1 Notices
The following notice symbols are used to emphasize information that is considered important,
requires special notice, or includes helpful troubleshooting tips.
NOTICE
NOTICE INDICATES INFORMATION WHERE ADHERENCE TO PROCEDURES

IS CRUCIAL OR WHERE YOUR COMPREHENSION IS NECESSARY TO APPLY A
CONCEPT OR EFFECTIVELY USE THE PRODUCT.
NOTE
Note provides additional information that is helpful to you. It may emphasize certain
information regarding special tools or techniques, items to check before proceeding, or
factors to consider about a concept or task.
Troubleshooting tips provide information that allow you to investigate the resolution of
some type of problem, locate the difficulty, and make adjustments to solve the problem.
4.1.2 Purpose of this guide

This user manual is written for health care professionals and technologists to provide the information
needed to properly operate the system. The manual is intended to allow you to understand the system
components and features and to use the system to its maximum potential. The manual does not teach
imaging or clinical diagnostics.
This user manual should be kept with the equipment. Review the procedures and safety precautions.
It is important for you to read and understand the content in this manual before attempting to use the
system.

Read Me First
4.1.3 Prerequisite skills

The operator profile may be limited to registered CT technologists certified by national registries,
state licenses, or organizational certification; physicians with or without specific training in radiology;
physicists or other personnel trained to operate the equipment.
This manual is not intended to teach imaging. You will need to have sufficient knowledge to perform
the diagnostic imaging procedures within your modality.
4.2 Scan Monitor

The scan monitor is used to prescribe and acquire scan data.
It is divided into the following areas:
Figure 36 Scan Monitor - Home Dashboard displayed
Figure 37 Scan Monitor - System Health Dashboard displayed

Read Me First
Number Description
1 Click the tabs to display either the

Home Dashboard or the System Health
Dashboard
2 Patient Schedule drawer
3 New Patient icon
4 Patient Tab area
Table 10 Scan Function icons
Icon Description
New Patient Opens the New Patient window to create a new patient entry. Once the patient
information is completed and the protocol is selected, the Scan Setup window
opens.
Patient Schedule
Opens the Patient Schedule to preprogram or retrieve patient information from
Digital Imaging and Communications in Medicine (DICOM) or Hospital Information
System/Radiology Information System (HIS/RIS).
4.2.1 Home and Health Dashboards

Click the Home to access the Home Dashboard. Click the System Health tab to access the System
Health Dashboard.
Each dashboard displays a different set of cards:

Read Me First
Table 11 Home Dashboard Cards
- provides information and functions related to the

current state of the scanner x-ray tube.
Image Space- communicates the amount of available

disk space on the system.
Recon Status- provides information on the number of

recon jobs in progress and suspended.

Read Me First
Displayed when connection with Edison server is bro-

ken and/or unavailable.
Displayed before running an antivirus scan

Read Me First
Table 12 System Health Dashboard Cards
System Restart - displays time elapsed from the last

system start
UPS - provides information on the charging status or

battery power of the partial UPS system when Smart-
Power Option is installed.

Read Me First
No software update available
Software update is available

• Contact your service representable
• Click Install Now start software install
Displayed when the system has been running for less

than 24 hours.
4.2.2 New Patient

Click to open the New Patient window.

Read Me First
Figure 38 New Patient window
Number Description
1 Patient Information area
2 Protocol Selection area
4.2.3 Patient Schedule

Click to open the Patient Schedule drawer.
Figure 39 Patient Scheduler drawer - Open

Read Me First
Figure 40 Patient Schedule drawer - Closed
Figure 41 Patient Schedule window

Read Me First
Figure 42 Patient Schedule window
4.2.4 Using Remote Control Panel Patient Positioning Controls

with AVIMOS
Remote Control Panel (RCP) allows a technologist to perform all patient positioning activities remotely
from the operator console, including utilization of alignment lights and movement controls to move
and center the patient to set the external landmark. Patient positioning controls are activated by
button selection on the operator console and by pressing the Move to Scan button on the scan control
interface.
The RCP can be configured only by a GE Service Engineer and requires the installation and use of
the approved Assisted Video Monitoring System (AVIMOS). GE service representative will set up the
AVIMOS components including in room cameras, video processing computer, display monitor and the
connected mouse.
4.2.4.1 Assisted Video Monitor System (AVIMOS)

Use the Assisted Video Monitoring System (AVIMOS) to observe the patient during movement while
using the Remote Control Panel (RCP) and to visualize the external laser lights to assist with proper
positioning and centering of the patient to set the external landmark.

Read Me First
Figure 43 AVIMOS Monitor Display
NOTE
This is a closed circuit system and does not store video images.
Display Description
A (Upper Left Quadrant) Display side camera image - monitor laser light and landmark position
B (Upper Right Quadrant) Display rear camera image- monitor patient
C (Lower Left Quadrant) Display front camera image- monitor patient
D (Lower Right Quadrant) AVIMOS controls

Read Me First
Table 13 AVIMOS Controls Quadrant D
Mouse Click/Button Icon Function
Double click mouse left button Double click display quadrant to enlarge to full-
screen view.
When full screen view, Double Click return to 4-quad-
rant view
Mouse Wheel Rolling Button is for communication only

Instruction to use middle mouse wheel to scroll
through 3 camera displays
Privacy Mode Single click to toggle monitor display off to provide

patient privacy
Display Mode Single click to toggle monitor display on to observe

patient in scan room
System Restart Single click to restart the application and the Opera-
tion System followed with a confirmation message.
System Shutdown Single click to shut down the display application and
the Operation System followed with a confirmation
message.
4.2.4.2 Daily Check for AVIMOS

To ensure patient safety, complete the following daily check of the AVIMOS function prior to
operating RCP (Remote Control Panel). If AVIMOS does not function correctly, contact your GE service
representative and do not use RCP until AVIMOS is functional.
Follow the steps below to perform an AVIMOS daily check before using RCP:

Read Me First
1. Be sure there is no person in the scan room.

2. Ensure that AVIMOS monitor can be seen while using RCP patient positioning controls.
3. Use RCP control to turn on external Laser Alignment Lights.
4. View Display A to ensure that side camera provided unobstructed view and that laser lines are
visible.
5. Use RCP control to move Cradle In to maximum limit.
6. View Display B to ensure that the back camera provided an unobstructed view of gantry bore and
patient table cradle during movement.
7. Use RCP Control to move Cradle Out until patient cradle arrives the max out limitation.
8. View Display C to ensure that front camera provided unobstructed view of gantry bore and patient
table cradle during movement.
4.2.4.3 Remote Control Panel
Figure 44 Remote Control Panel (RCP) Open

Read Me First
Table 14
1 Remote Control Click to open RCP

Tab
2 X or SHIFT +ESC Click or use keystrokes to close RCP at any time
3 Warning Message
WARNING
DURING REMOTE TABLE/GANTRY MOVEMENT, TO PREVENT

PINCHING OR CRUSHING OF THE PATIENT, WATCH THE
PATIENT, EQUIPMENT, ACCESSORIES, AND HEALTH LINES
CAREFULLY AT ALL TIMES.
4 RCP Instruction or Ready for selec- Select any button below, then press Move to Scan on the
Error Message tion Scan Control Interface when prompted.
Movement Control Press and hold Move to Scan on the Scan Control Interface to
Button selected begin table motion. Release to stop table motion. To clear the
selection click anywhere within the panel. Communicate with
the patient any instructions or actions to expect.
Alignment Light or Press Move to Scan on the Scan Control Interface to activate
External Landmark selected control. To clear the selection click anywhere within
Control Button se- the panel. Communicate with the patient any instructions or
lected actions to expect.
Hover Text To Close (Shift+Esc)
RCP Error Inter- Remote Control Panel cannot be activated. Gantry hardware
face unavailable. Perform a Scan Hardware Reset from the Service
Tools menu. If problem persists, contact your service repre-
sentative
RCP Error Hard- Remote Control Panel is deactivated. Press Reload to attempt
ware to re-establish connection. Verify that during use the physical
gantry controls are not being pressed, E-Stop has not been
activated, and the cradle is latched.
RCP Error Soft‐ System software error. If in a active scan session complete
ware the exam using the gantry controls. Or perform a System
Restart from the Mode menu. If problem persists, contact
your service representative.
RCP not available Remote Control Panel is not available. Close if any of the
following application(s) are running: [applicable applications
will be listed]
5 RCP Patient See RCP Patient Positioning Controls table below

Positioning Con-
trols

Read Me First
Table 15 RCP Patient Positioning Controls
Click button for Desired action Click RCP Move to Scan function
button
Move Cradle Out Slow speed Flashing green indicates ready.

Press and hold for movement.
Release to stop movement.
Remains ready until another RCP button is
selected or RCP is closed.
Move Cradle In Slow speed
Selected movement will occur while in ready
state.
Move Cradle Up Slow speed
Move Cradle Down Slow speed
Move Cradle Out Fast speed
Move Cradle In Fast speed
Move Cradle Up Fast speed
Move Cradle Down Fast speed
Load - move table up and cradle in.
NOTE
System Preference for auto position
is On: the cradle moves to pre-de-
termined position of the prescribed
landmark location.

Read Me First
RCP Patient Positioning Controls continued

Click button for Desired action Click RCP Move to Scan function
button
Unload - move cradle out and table down to

home position.
Toggle internal Alignment Light On/ Off Flashing green indicates ready
Button changes to green to indicate when Press and release to perform selected action
ready Move to Scan becomes inactive upon release.
Re-select desired action if necessary
Set External Landmark
Using RCP positioning Controls

1. Click the Remote Control Panel tab to open RCP. At any time, click X or Shift + Esc to close
RCP. When open the RCP covers both monitors and no other actions are allowed at the operator
console when RCP is open.
RCP cannot be used at the same time as other movement control. Pressing the Foot Pedal or any
gantry control button deactivates the RCP, requiring the user at the console to click X to close or
click Reload to continue using RCP.
NOTE
RCP cannot be opened after pressing Confirm in a scan task series or during an
active scan.
NOTE
RCP cannot be used during a SmartStep interventional series.
2. Click desired positioning control button on RCP.
3. Follow on screen instructions for Move to Scan function button when flashing.
4.2.5 Scan Setup

When an exam is in process, the Scan Setup window displays.

Read Me First
Figure 45 Scan Setup window
Number Description
1 Tabs area.
Displays the patient session.
2 State area.
Indicates the scanning state of the system.
• Scanning
• Done Scanning
3 Patient Position area.

• Shows the patient position and orientation that the patient should be positioned
for on the table.
• Indicates the anatomical reference that the landmark should be set at.
• Indicates the Auto Voice language category.
4 Scan Timeline area.

View prep group delays and real-time scan progress information. Use the scroll wheel
to review all scan groups.

Read Me First
(continued)
Number Description
5 Scan Task List area.

The series scanning tasks to complete an exam.
Task Status
• No checkmark — Not confirmed
• Blue background — Confirmed but not scanned
• Gray background and checkmark — Scanned
6 Scan Settings window.

Set and adjust scan parameters.
7 Quick Settings area.

Contains other functional tools related to the scan type selected.
8 Auto View viewport.

Displays scouts and non-clinical QC images. Show Localizer viewport for graphic scan
prescription.
9 Navigation viewport.
Displays scouts and QC images. Show Localizer viewport for graphic scan prescription.
10 Total Accumulated Dose area.

The total accumulated dose for the exam.
11 Dose Display area.

Displays projected dose information based on current scan settings. It also displays
other real-time information when the active application requires it.
Figure 46 Image Quality widget

Read Me First
Figure 47 Acquisition Window and Heart Rate widget
Figure 48 Patient Tab Status
Number Description
1 Patient waiting to be scanned.
2 Patient on the table.
3 Open patient exam sessions.
4 Oldest open patient exam session.
5 List of recently closed patient exam sessions.

Read Me First
Figure 49 Scan Progress window
Number Description
1 Scan Timeline
2 ECG Trace
3 Scan group parameters
4 Real-Time Information

Read Me First
Figure 50 Scan Timeline
Number Description
1 Prep delay
2 Exposure time of group
3 Inter-group delay
4 Total Scan Time of group; calculated by Prep delay + Exposure time of all groups +
Group delay
Figure 51 Real-Time Information
Number Description
1 Messages for moving table
2 Prep-group delay countdown
3 Status of injector
4 Pause / Resume control

Read Me First
Figure 52 Done Scanning window (PPS enabled)
Figure 53 Done Scanning window (PPS disabled)

Read Me First
Figure 54 Reports window
4.3 Image Monitor

The image monitor is used to reconstruct and post-process scan data.

Read Me First
Figure 55 Image Monitor
Number Description
1 Icons and System Status area
2 Reconstruction and Image Processing area
3 Image Viewports
4 File Manager
4.3.1 Icons and System Status Area

This area displays the mode icon, system utilities icon, recon management icon, system messages and
the date and time.

Read Me First
Figure 56 Icons and System Status area

Read Me First
Number Icon Description
1 Mode Icon Opens the Mode menu with the following selections:
• Protocol Management
• Protocol Management
• Auto Gating Configuration
• Auto Voice Management
• Auto ROI Management (Available on Apex Select 40mm sys-
tems)
• SmartPlan Management
• GSI Profile Editor
• Auto Prescription Profile Editor
• Protocol Exchange
• Access Controls
• User Admin Tool
• Dose Check Management
• Audit Tool
• Audit Log Viewer
• System Preferences
• Learning Solutions
• Switch User
• Power Management
• Restart
• Sleep
• Power Down
2 System Utilities Icon A collection of all necessary user maintenance calibration routines and other
utility functions.
Opens the System Utilities menu with the following selections:
• Daily Prep
• Tube Warm Up
• Fast Cal
• System Tools
• Message Viewer
• Save Cybersecurity Audit Logs
• Service
• Service Tools
• Check Security

Read Me First
(continued)
Number Icon Description
• Troubleshooting
• iLinq
• Unix Shell
• SPR Snap
• Close Volume Viewer/Reformat
• Restart Application
• TiP Virtual Assist
3 Recon Management Recon Management lists progress of completed reconstruction jobs
4 System Messages Click on the message for a list of all system messages.
5 Date and Time The current date and time.
4.3.2 Reconstruction and Image Processing Area

This area allows you to define additional image processing tasks during the scan process, including
reconstructions and manual and automatic reformats, in one centralized location. It also allows you to
monitor both the creation and transfer of those image sets.
Figure 57 Reconstruction and Image Processing area

Read Me First
Figure 58 Reconstruction and Image Processing window
Number Description
1 Task List
2 Add Recon
3 Add Reformat/Add Application
4 Study-based transfer options
5 Image Tools
6 Command Line
7 Task Status
8 Image display assignment indicator
4.3.3 Image Viewports

Image Viewports can be found on both the scan monitor and image monitor. The four viewports on the
image monitor are used for image processing.

Read Me First
Figure 59 Image Viewports
Figure 60 Viewport Controls

Read Me First
Number Description
1 Hover over bar
2 Frequently used tools
3 Next / Prior series controls
4 Maximize image icon
5 Series binding icon
6 Image scroll bar
4.3.4 File Manager

Click to open the File Manager browser. Select exam/series/images from the patient list and click
to launch the session tab.
Figure 61 File Manager - Open
File Manager serves three main functions: exam organization and status, accessing files, and opening
an exam.
Figure 62 File Manager - Closed

Read Me First
Figure 63 File Manager
Number Description
1 Controls area
2 Exam list
3 Series list
4 Image display / Image list
Figure 64 File Manager Image Navigation

Read Me First
Number Description
1 Image list icon
2 Maximize image icon
4.4 User Interface Conventions

NOTE
When the system is configured in a language other than English, messages, buttons,
menus or hover-over text on User Interface screens may be in English.
4.4.1 Select items from a list

Single item Click the item.
Multiple contiguous Click a start point in the list, press Shift, click an end point in the list, and all items
items between start and end are selected.
• Press and hold Ctrl and click each item.

Multiple non-contig-
• Close or X also closes a window without executing the actions or implementing
uous items
parameters.
4.4.2 Cancel
Cancel closes a window without executing the actions or implementing parameters described on a
window.
4.4.3 Button and text appearance

Buttons that are gray are inactive.
Figure 65 Active Button and Inactive Button
Table 16 Text Field Notifications
Settings updated by the user display with a white background.

White Background
Underlined Text Text fields that can be changed are underlined.

Read Me First
Click the icon next to the parameter to open.
Anchored Popover
For updated settings that are invalid, the background is highlighted white with a red
outline, and the settings collection is flagged with an alert icon notifying the user.
Confirm Settings is also disabled.
White Background
Red Outline
Changes to highlighted scan parameters are copied to all selected groups.
Multiple Groups High-

lighted Gray
White Background
Settings updated by the system are outlined in blue.
Blue Outline
White Background
Indicates settings copied from the primary recon.
Green Outline
Indicates a Severe Alert. Click on the icon in the Status area for the system message.
Red Alert
Indicates a Notification Alert. Click on the icon in the Status area for the system
message.
Blue Alert

Read Me First
Table 17 Gantry Display Indicators
Not selected, not displayed

Use the gantry controls enter key to turn on the selection.
On, not displayed
On, displayed
Use the gantry controls navigation button to toggle between which selection to
display.
4.4.4 Patient Tabs

Patient tab colors indicate patient/exam status.
Table 18 Patient tabs
Currently selected patient tab
Indicates no background processing and no action is required of the

user.
Indicates that a tab has been created, but patient information entry
and protocol selection have not been completed.
Indicates the patient currently on the table but this session’s patient
tab is not selected by the user.
Indicates image reconstruction in progress
Indicates at least one image reconstruction task needs manual inter-

vention or an error occurred.
4.4.5 Pop-up windows

Pop-up windows may require an acknowledgement by clicking OK, Accept or Apply to close the
window.

Read Me First
4.4.6 Mouse controls

The two-button mouse with a scroll wheel is used to make selections on the scan and image monitors.
Figure 66 Mouse Buttons
Table 19 Mouse Actions
Number Mouse Action Description
1 Left-click Click the left mouse button.
2 Right-click Click the right mouse button.
3 Scroll Wheel Turn the scroll wheel.
Click and drag Click and hold the left mouse button while moving the
mouse.
Right-click and Click and hold the right mouse button while moving the
drag mouse.
Scroll wheel-click Click and hold the scroll wheel while moving the mouse.
and drag
Double-click Click the left mouse button twice in rapid succession.
Triple-click Click the left mouse button three times in rapid succes-
sion.

Read Me First
4.5 System Troubleshooting Tips

• Complete all portions of Fast Cal. This assures that the air calibration and generator calibrations
are up to date on the system.
• Scan aborts may occur during scanning. Always be aware of the scan progress during an exam
and click Resume as soon as it is posted to continue.
• When directed to reset the scan hardware, click System Utilities > Service
Tools > Resets > Scan > Run. The system notifies you if/when reset is complete and successful.
After complete, click Dismiss.
• In general, wait for a screen transition to take place before making another selection. Typing
values before the user interface displays can result in the wrong screen displayed or the wrong
value entered.
• If the scanner desktop becomes unresponsive, but the mouse is still moveable, select Alt + F3.
This will reconnect the system.
• If the scanner desktop becomes unresponsive for several minutes, click and select Shutdown,
then Restart to restart the system. If you cannot select Shutdown, turn off the scanner desktop
power switch, wait 10 seconds, then turn the power switch back on.
• In some cases, the system will notify you of errors and steps to recover from the error. You should
contact your services representative as soon as possible, if notified.

Pediatrics and Small Patients
5 Pediatrics and Small Patients
5.1 Overview
Use special care when imaging patients outside the typical adult size range. GE Healthcare strongly
suggests reducing radiation dose to ALARA (As Low As Reasonably Achievable) in all patients,
especially pediatric and small patients, whenever it is determined that a CT scan is necessary. CT
is an extremely valuable tool for diagnosing injury and disease, but its use is not without risk. This
chapter discusses the importance of minimizing the radiation dose in small patients and children
consistent with ALARA principles.
5.2 Radiation Exposure
5.2.1 Radiation exposure sensitivity

Radiation exposure is a concern in both adults and children. However, children are more sensitive to
radiation than adults and have a longer life expectancy. Radiation risk is higher in young patients, as
they have more rapidly dividing cells than adults. The younger the patient, the more sensitive they are.
Using the same exposure parameters on a child as used on an adult may result in larger doses to the
child. There is no need for these larger doses to children, and CT settings can be adjusted to reduce
dose significantly while maintaining diagnostic image quality.
The National Cancer Institute and The Society for Pediatric Radiology developed a brochure, Radiation
Risks and Pediatric Computed Tomography: A Guide for Health Care Providers, and the FDA issued a
Public Health Notification, Reducing Radiation Risk from Computed Tomography for Pediatric and Small
Adult Patients dated November 2, 2001, that discuss the value of CT and the importance of minimizing
the radiation dose, especially in children. These documents can be accessed at http://www.fda.gov.
5.2.2 Dose reporting considerations

It is widely understood and accepted that adult techniques should never be applied to small patients
or pediatrics since smaller objects have higher dose at the same technique. The chart below illustrates
the sharp increases in relative dose as the part scanned gets smaller in size using the same technique.

Figure 67 Relationship between dose and phantom size for head and body filters at 120 kV.
Similar curves are obtained for the 70, 80, 100, and 140 kVs.
Another consideration about dose is since it is not possible to characterize dose given to individual
patients, the CT dose indices are provided to help make relative comparisons. These dose index
values can be used to compare CT systems and to help select appropriate operating conditions for
scanning. However, it is important to recognize that the dose reported by these indices is inversely
proportional to phantom size (see the above chart). This means that for the same scan technique,
smaller phantoms (patients) will produce a higher absorbed dose than larger phantom (patients).
Therefore, it is critical to remember that the body filter uses the 32 cm CTDI phantom and the head
filter uses the 16 cm CTDI (Computed Tomography Dose Index) phantom for dose reporting purposes
(CTDIvol is displayed in the Dose Information area on the Scan Settings window). The table below
indicates the phantom size used for calculating dose for each SFOV (Scan Field Of View).
In other words, when looking at the actual absorbed dose to the patient, understand that the dose
may be higher than reported if the part scanned is smaller than the phantom tested. Keep this in mind
when adjusting scan parameters to fit patients who are smaller than the phantoms tested.
Table 20 CTDI phantom used dose report based on SFOV type
SFOV type CTDI phantom
Ped Head
Small Head 16 cm phantom
Head
Ped Body
32 cm phantom
Small Body

CTDI phantom used dose report based on SFOV type continued

SFOV type CTDI phantom
Medium Body
Large Body
Cardiac Small
Cardiac Medium
Cardiac Large
5.2.3 Minimize pediatric and small patient doses

There are several steps that can be taken to reduce the amount of radiation that pediatrics and small
patients receive from CT examinations. Everyone shares the responsibility of minimizing CT radiation
dose. Use the following suggestions for minimizing unnecessary doses.
5.2.3.1 Perform only necessary CT examinations

Is CT the most appropriate study? This important communication between the patient's physician and
the radiologist is essential in determining the need for the CT examination. The indications and the
appropriate technique to be used should be reviewed by the radiologist prior to every scan including
the patient’s number of previous scans, reasons for the scan, and consideration of other effective
lower dose modalities. In all circumstances, the expected benefits of the scan must always exceed the
overall risk.
5.2.3.2 Scan only the organ or anatomical region indicated

Limit scan coverage to cover only the organ or anatomical region of the body indicated to avoid
unnecessary exposure.
5.2.3.3 Minimize multi-phase contrast CT examinations

Scan only one series if possible.
• CT studies with and without contrast material are not always needed.
• Multiphase imaging may double or triple the dose and may not add diagnostic information to the
study.
• If multi-phase studies are needed, use a lower dose technique for the non-contrast series
compared to the contrast series and limit the scan only to the organ or anatomical region
indicated.
5.2.3.4 Properly center all patients in the gantry

Center all patients in the gantry to allow the bow tie filters to deliver dose where it is needed and filter
more where it is not.

• This is especially important using automatic exposure control techniques such as SmartmA, and
Organ Dose Modulation to further reduce unnecessary radiation exposure.
• Patients not properly centered may be under or over exposed to radiation if the table height is set
too high or too low.
5.2.3.5 Lower mA settings for chest and bone imaging

Consider using a lower mA setting and higher Noise Indexes if SmartmA is used for chest and bone
imaging. Higher resolution/dose imaging is typically unnecessary for these types of studies where
there is high inherent contrast between the structures being imaged.
5.2.3.6 Scan signal-to-noise

Limit the highest quality images requiring the highest radiation dose to very specific indications such
as angiography or visualizing small subtle lesions. Studies with higher noise may be just as diagnostic
and require lower dose.
5.2.3.7 Use pediatric positioning accessories

Use papoose boards and neonatal immobilizers, as needed, with certain patients.
• These accessories are sometimes helpful to secure the patient and keep the patient still.
• Results in less patient motion and therefore, less repeated exams.
5.2.3.8 Make a kid friendly environment

Help pediatric patients feel less scared.
• Put pictures of animals on the wall or ceiling.
• Use stuffed animals.
• Play games.
• Depending on the patient age, explain the procedure so they know what to expect when they
enter the scan room. This will aid in patient cooperation and potentially less repeat studies and
dose due to patient motion.
5.3 Pediatric and small patient scans
5.3.1 Optimize pediatric protocols for your facility

Work with your team of radiologists, medical physicists, and CT technologists to evaluate techniques
that may reduce radiation dose and still provide adequate diagnostic information. In addition to the
recommended protocols installed on your system and suggestions in this manual, these websites offer
excellent sources of additional information on how to optimize scanning protocols:
• American College of Radiology (ACR): www.acr.org/

• Society of Pediatric Radiology (SPR): http://www.pedrad.org/

• National Cancer Institute (NCI): http://www.nci.nih.gov/aboutnci
• Image Gently: http://www.imagegently.com/
• FDA website: http://www.fda.gov/
5.3.2 Pediatric protocols

The Pediatric Protocol area was designed to help facilitate protocol selection for pediatric patients
by providing age based protocol areas for Head, Orbit and Miscellaneous and color coding system
for Neck, Upper Extremity, Chest, Abdomen, Spine and Pelvis. It is highly recommended to place and
select pediatric protocols from the pediatric selector based on age, height, and weight. By entering
the pediatric patient's weight in the Patient Information screen, the system automatically selects the
appropriate color code area for the anatomical area selected.
The system automatically selects the pediatric selector when the patient’s age is less than or equal
to the age value set in the Maximum Pediatric Age. This value is set from Mode menu, System
Preferences, Protocol Selection.
Figure 68 Protocol Category drop-down menu
5.3.3 Color Coding for Kids Protocol Selection

Based on the Broselow-Luten Pediatric System, the Color Coding for Kids system was developed to
help you select the correct pediatric CT protocol. The system divides the protocols into nine color
zones based on height and weight, and incrementally increases scan technique as the patient’s size
increases. This arrangement of protocols assists you in reducing the variations in pediatric protocol
selection. If the patient weight is unavailable, a Broselow-Luten Tape can also be used to obtain the
weight based on the length.

Once you select the Pediatric selector, the Pediatric Protocol List displays. Next to the name of the
protocol a color icon along with the zone number will be indicated. The notes area of the protocol
selector will display the zone ranges for weight and length, color name and the weight/color zone
number.
NOTE
Weight-specific protocols are enforced for all anatomical areas except Head, Orbit, and
Miscellaneous. Protocols in the Head and Orbit categories are usually defined based on
patient age as opposed to patient weight/height.
Figure 69 Pediatric Protocol Category window
Table 21 Color codes
Zone number Zone color Zone weight (lb) Zone weight (kg) Zone length (cm)
1 Pink 13.2 to 16.5 6.0 to 7.5 59.5 to 66.5
2 Red 16.5 to 20.9 7.5 to 9.5 66.5 to 74.0
3 Purple 20.9 to 25.4 9.5 to 11.5 74.0 to 84.5
4 Yellow 25.4 to 32.0 11.5 to 14.5 84.5 to 97.5
5 White 32.0 to 40.8 14.5 to 18.5 97.5 to 110.0
6 Blue 40.8 to 49.6 18.5 to 22.5 110.0 to 122.0
7 Orange 49.6 to 69.5 22.5 to 31.5 122.0 to 137.0

Color codes continued

Zone number Zone color Zone weight (lb) Zone weight (kg) Zone length (cm)
8 Green 69.5 to 89.3 31.5 to 40.5 137.0 to 150.0
9 Black 89.3 to 121.3 40.5 to 55 --
5.3.4 Set up a pediatric or small patient exam

Use this procedure each time you start a new patient exam for a pediatric patient. It is recommended
that you complete the patient information setup before you get the patient on the table to reduce
patient table time. The data can also be input by using Patient Schedule or a bar code reader.
1. From the scan monitor, click the New Patient icon .
• The Patient Information screen displays the new Exam Number.
• The maximum Exam Number is 49,999, which is reset by your Field Engineer.
2. From the Patient Information area, type data into the appropriate fields.
• Press Tab to advance to the next field. Alternatively, use the mouse to navigate to each field.
3. If you have not entered a value in the Age field, click Pediatric.
4. From the Pediatric Protocol Selection screen, click an anatomical area.
• With the patient's weight entered, the system automatically selects the appropriate pediatric
color code area for the anatomical area selected.
• Use the arrows to scroll through the list.
• Click a protocol from the list to download the scan parameter values.
5. From the Pediatric Protocol Category screen, select the weight/length category based on the size
of your patient or verify the correct Color category has been selected if you entered a weight.
• The protocols in the selected color code are then displayed accordingly.
• The default weight/color selector displays the patient weight entered on the Patient
Information screen, or the last weight/color selection (if no patient information was
entered).
• If you enter a patient weight on the Patient Information screen and select a color/weight
that is not consistent with the entered information, a red alert displays next to the protocol
name. You must acknowledge that you have chosen a protocol that does NOT match the
patient size.
Alert message: Selected color is not suitable for the entered patient weight of 29 Kg (65 lbs).
6. Proceed with the Acquire a Scout scan procedure.
5.3.5 Adjust pediatric and small patient scan parameters

Use the following guidelines for adjusting individual exposure parameters by patient.

5.3.5.1 Adjust the parameters by size, age, weight, height, and indications
Use pediatric protocols based on the age, weight, height, and indications to avoid over exposure.
• Recommended pediatric color coded protocols are installed on the system and are arranged in
colors according to height and weight for easy selection.
• These protocols should be considered as a baseline. It is strongly encouraged that you work with
your radiologist and medical physicist to determine the lowest possible dose at the image quality
desired.
• Consider the diameter of the part being scanned as a final determination before scanning. For
instance, the part may be smaller or larger than what is indicated by the weight of the patient.
5.3.5.2 Consider decreasing the kV

Decrease the kilovoltage to 70, 80 or 100 kV for smaller patients.
• A decrease in kV should not be done without increasing the mA to maintain noise levels and
contrast to noise ratios.
• Lower kV selections increase HU values. Therefore, increase the window width for viewing images
to maintain a similar appearance.
• Since lower kV selections lower X-ray penetration, it is important to not use low kV selections on
too large of a patient, which can potentially result in compromised image quality. Work with your
radiologist and medical physicist to establish low kV protocols and patient size limits.
• Refer to CTDI Dose Values and Adjustment Factors in the Dose and Performance chapter of the
Technical Reference Manual as a guide for making adjustments to mAs for changes in kV in a
protocol.
• For example, consider a protocol with a technique of 120 kV, 70 mA, Medium Body SFOV. As
a starting point, in order to maintain CTDIvol while changing the kV, the technique could be
adjusted as follows for pediatric patients:
• 340 mA at 70 kV
• 215 mA at 80 kV
• 110 mA at 100 kV
• 70 mA at 120 kV
• 50 mA at 140 kV
• To assure sufficient X-ray penetration, the following chart is intended as a relative guide to the
maximum patient diameter that can be scanned based on a kV and mA’s selection. It does not
indicate a recommended technique factor (that is generally higher) since the technique factor
also depends on the image quality needed for the diagnostic task.

Figure 70 Maximum patient diameter guide for low kV selection (1) and Lateral Patient Diameter
in cm (2)
5.3.5.3 Center the patient properly when using SmartmA

Properly center the patient. This is critical with SmartmA.
• Double check and verify the table height is centered to the patient.
• Raise or lower the table as needed before taking the scouts.
• After the scouts are taken and prescription is done, verify the mA table calculations before
confirming the scan.
• Make sure minimum mA and maximum mA values are set appropriately.
• See Set the mA procedure in the Scan chapter.
5.3.5.4 Increase the pitch

Increase the pitch.
• Increasing the pitch decreases the amount of radiation needed to cover the region indicated,
usually without compromising the diagnostic quality of the scan.
• Increasing pitch from 1.0 to 1.375:1 decreases dose by a factor of about 27%.
5.3.5.5 Use Small SFOV Filters

Use the smallest SFOV whenever possible, depending on the exam and size of the patient.
• Matching the appropriate SFOV bowtie filter to the size of the patient ensures the dose is
delivered where it is needed, and filtered where it is not needed.

• Small SFOV supports DFOVs up to 32 cm in diameter.

• Ped Head SFOV supports DFOVs up to 32 cm in diameter and uses IBO processing to correct
for beam hardening effects. It is particularly useful for infants 18 months or less in age.
• Small Head SFOV should be used for patients from 1.5 years old to 10 years old.
• Ped Body SFOV supports DFOV’s up to 32 cm in diameter.
• Both the Ped Body and Ped Head SFOVs are limited to 42 kW. This limits the maximum mA
possible to 350 at 120 kVp.

Large Patient
6 Large Patient
6.1 Overview
CT is an extremely valuable imaging tool for diagnosis of injury and disease. In the radiology
community, it is widely understood that very large patients (> 300 lb / 136 kg) are a challenge for
imaging due to the increase of the X-ray attenuation in this patient population. The degree of X-ray
attenuation in these large patients may degrade image quality as the patient size increases using the
same scan technique as used for normal sized patients (< 300 lb (136 kg)). The system allows patients
with weights up to 500 lb (227 kg).
This section presents the concepts necessary to successfully scan large patients.
6.2 Large Patients
6.2.1 Scanning large patients
6.2.1.1 Perform only necessary CT examinations

Is CT the most appropriate study? This important communication between the patient's physician and
the radiologist is essential in determining the need for the CT examination.
The indications and the appropriate technique to be used should be reviewed by the radiologist
prior to every scan including the patient’s number of previous scans, reasons for the scan, and
consideration of other effective modalities. In all circumstances, the expected benefits of the scan
must always exceed the overall risk.
6.2.1.2 Patient weight and patient size

There are multiple factors that need to be taken into consideration when prescribing a protocol
for large patients besides weight such as height, muscularity, and body habitus. It is essential to
remember that the maximum table loading weight is 500 lb (227 kg).
The patient's transverse dimension of the anatomical area being scanned is another important factor
of a larger patient exam because of system hardware imaging requirements of an air gap and design
limitations of a CT system.
The distance between the edge of gantry bore and the patient's body surface must be more than 5
cm to prevent blockage of the reference channels. If the maximum diameter of the patient is beyond
the imaging capability of the 50 cm SFOV, the image quality can be degraded due to partial reference
channel blockage. CT scanners expect an air gap around the imaged object and when the reference
channel does not see air, this may cause degradation of image quality. If the diameter of the patient in
all directions is beyond the imaging capability of the 50 cm SFOV, the image quality may be severely
degraded and may not be useful for diagnosis if there is full reference channel blockage.

Large Patient
6.2.1.3 Properly position large patients in the gantry

Body straps may be useful with certain patients. These accessories are sometimes helpful in making
the patient more round as opposed to elliptical, and in securing the patient to prevent contact with
the gantry as they move through. Once the patient is positioned on the table, move the patient in and
out of the gantry to make sure they are able to be safely moved through the gantry during the exam.
Properly centering the patient is essential to minimize image quality degradation. The bowtie filter
provides maximum X-ray intensity through the center and 90% less X-ray at the edge of the SFOV. The
Large Body bowtie filter (Large SFOV) should be used since it has the largest field of unattenuated
X-ray. When possible, center the anatomy of interest in the center of the gantry to take advantage of
the increased X-ray intensity.
Additionally, a correctly centered patient is essential when using automatic exposure control
techniques such as SmartmA to reduce unnecessary radiation exposure. If patients are not properly
centered when using automatic exposure control, the mA selected by the system may be inadequate
or may be greater than required compared to when the positioning is correct. Often in order to fit a
large patient safely in the gantry for imaging, a lower table position than desired is necessary. In these
situations where the patient is miscentered, the use of SmartmA is not recommended.
6.2.2 Guidelines for adjusting individual exposure parameters by

patient
6.2.2.1 Adjust parameters

The aim of adjusting imaging parameters is to improve the image quality by increasing the amount of
X-ray quantum energy received by detector. We strongly encourage you to work with your radiologist
and medical physicist to determine the appropriate dose for the image quality desired. Each large
patient should be evaluated individually to determine appropriate imaging parameters.
6.2.2.2 High kV
It is important to use higher kilovoltage selections on the very large patient. Using 140 kV is
recommended for large patients because it provides higher X-ray penetration of anatomical structures
being imaged. On the other hand, higher kV selections can decrease HU (Hounsfield Unit) values so the
window width for viewing the images may need to be decreased to maintain a similar appearance.
6.2.2.3 mA adjustment
The reasonable use of scan technique with SmartmA on a large patient can reduce patient dose
effectively. However, significant differences may exist between the selected noise index and the
image standard deviation when a very large patient provides insufficient detector signal (or prevents
sufficient detector signal). In this case, electronic noise sources can become the dominant image noise
source vs. X-ray noise. Under these conditions, special projection data dependent filters are applied at
various threshold levels to help preserve image quality.
For more information on SmartmA refer to SmartmA in the Scan Parameters section.

Large Patient
NOTE
If the size of the large patient section is beyond 50 cm SFOV, SmartmA technique is not
recommended since noise and mA prediction may not always be reliable. Manual mA is
recommended.
6.2.2.4 Lower pitch / slow rotation time

Decreasing the pitch and rotation time will allow more mA to be delivered over the area of interest
without compromising the diagnostic quality of the anatomical area scanned; however, this will be at
the expense of extending the exposure time for the acquisition.
6.2.2.5 Scan Type

Compared to the Helical scan type, the Axial scan type provides a greater opportunity to increase mAs
to achieve improved image quality for large patients but at the compromise of the total exam scan
time.
NOTE
Using lower pitches, slower rotation times, or axial instead of helical with large patients
to improve image quality, comes at the cost of longer scan times which means longer
breath holds.
NOTE
When utilizing the Hyper Drive option with 80 mm detector coverage and 1.375:1 and
1.531:1 pitch, it is better to use faster rotation times to minimize motion artifacts.
Consider the following to offset increasing acquisition times beyond the patient's capability to hold
their breath:
• If multi-phase studies are needed, use lower dose techniques for the non-contrast series
compared to the contrast series and limit the scan to only the organ or anatomical region
indicated.
• Break the imaging range into multiple groups to match patient's breath-hold capability.
6.2.2.6 Increase slice thickness

Generally speaking, thicker slice images can provide lower noise than thinner slice images for the
same dose. Consider using 1.25 or 2.5 mm slice thickness with 50% overlap as opposed to 0.625 mm
slices for areas with large anatomical structures when reformats may be needed.
6.2.3 Radiation exposure and dose reporting

It is well known that normal weight adult techniques should not always be applied to large patients
since this will likely decrease the image signal-noise ratio for the acquisition due to inadequate
exposure. Generally speaking, higher radiation exposure is usually used for very large patients to
improve image quality to compensate for dose attenuation.

Large Patient
It is critical to remember that the body filter only uses the 32 cm CTDI phantom for dose reporting
purposes (CTDIvol displayed in the Dose Information area on the Scan Settings screen and the Dose
Report). In other words, when looking at the actual absorbed dose for the large patient, understand
that the dose may be lower than reported if the part scanned is larger than the phantom tested. Keep
this in mind when adjusting scan parameters to fit patients who are larger than the phantoms tested.
NOTE
You have to balance between image quality level for diagnosis and responsibility for the
delivery of higher radiation doses for larger patients, especially in abdomen and pelvis
exams.

Dose Check
7 Dose Check
7.1 Overview
NOTE
PLEASE REFER TO THE SAFETY CHAPTER FOR IMPORTANT SAFETY INFORMATION

REGARDING THE USE OF THE EQUIPMENT AND SOFTWARE ON THIS SYSTEM.
Attention: Consult accompanying documents.
For dose measurements and calculations, refer to the Technical Reference Manual, Dose and
Performance chapter.
7.1.1 Introduction
Dose Check alerts you when the estimated dose index is above the limit set by the operating group,
practice, or institution. Dose Check complies with the NEMA XR-25 standard.
Dose Check creates awareness of the dose index of the prescribed scan, and launches a notification if
the dose index is above the limit. The notification is set at a level above routine or normally expected
doses, but not so high as to pose a significant risk to the patient. Depending on patient size or imaging
requirements, it may be appropriate to scan at a value above the Notification Value (NV).
Notification Values are not necessarily the same as the published Diagnostic Reference Levels (DRLs).
However, these may be consulted as a guide to determine the appropriate NV for your site and patient
population. Because routine scanning does involve a range of applicable techniques due to patient
sizes and imaging needs, another consideration on where to set the notification level will be the
frequency in which your practice would want it posted.
Dose Check also issues an alert when the accumulated dose index would exceed the institution’s
established range. GE has pre-populated the system-level Alert Value (AV) at 1000 mGy CTDIvol in
accordance with the FDA November 8, 2010 letter to MITA.
Dose Check should be incorporated into your department’s Quality Assurance (QA) processes to assure
that scan protocols are defined with the “as low as reasonably achievable” (ALARA) parameters, and to
vary examination protocols to take into account patient body habitus. The feature provides for audit
capability and tracking when Notification and Alert Values are exceeded and the capability to output
the protocols on the system and the associated NVs entered for them.
Dose Check provides the following:
• Checks against a Notification Value and issues an alert if the estimated dose for the scan is above
your limit.
• Checks against an Alert Value where the user needs specific authority to continue the scan at the
current estimated dose without changing the scan parameters.
• Defines Alert Values for Adult and Pediatric imaging with an age threshold.
• Audit logging and review.

Dose Check
• Protocol Change Control.
7.1.2 Protocol Considerations

Before using Dose Check, the site physicist, and/or radiation safety officer in collaboration with the
radiologist, should understand the current dose levels of site scanning protocols and the maximum
dose limit at the site’s clinical practice. Using this information, an appropriate starting point for the
Notification Value for each protocol and system Alert Value should be set.
Guidance from such bodies as the American College of Radiology (ACR), US Food and Drug
Administration (FDA), European Union (EU), International Commission on Radiological Protection
(ICRP) and American Association of Physicists in Medicine (AAPM) may be useful in determining
Notification and Alert values. The AAPM Working Group on Standardization of CT Nomenclature and
Protocols has published a list of reference Notification values based on anatomical location. These can
be found at www.aapm.org.
7.1.3 Terminology
7.1.3.1 Notification Value (NV)

The dose value that is the site’s typical dose level for each scan group. NV value can be checked by
CTDIvol, DLP or both. This value should be set to an average value of all patient sizes that will be
imaged using the scan protocol. Notification Values cannot be set for scan groups with Scout scan
type. When setting the NV value, give consideration to an appropriate upper limit to account for the
percentage of exams that you would normally expect the value to be exceeded. Scans that exceed NV
values will be logged.
7.1.3.2 Alert Value (AV)

The dose value in which specific authorization is needed to continue with a scan that exceeds this
value. AV value can be checked by CTDIvol, DLP or both.
7.1.3.3 Dose Check Administrator

A user role with authorization to enable NV and AV checking.
7.1.3.4 Dose Check AV Exceeding User

A user role with authorization to exceed AV values during scanning.
7.1.3.5 Protocol Change Control

Requires user authorization to modify and save protocol parameters.

Dose Check
7.2 Set the Dose Check Administrator Role

NOTE
Refer to the Access Controls chapter for instructions on setting local users, an enterprise
server, and defining local or enterprise groups.
The Dose Check Administrator role is assigned at the group level. Users assigned to a group with this
role can enable Dose Checking, set Alert Values (AV), set Alert Value (AV) Age Threshold and review and
export the Audit Log. We recommend that only one user be assigned to the Dose Check Administrator
group after having discussions with the radiologist, physicist and department managers.
1. From the image monitor, click .
2. From the Mode menu, click Access Controls, then User Admin Tool.
3. From the EA3 Administration window, enter your username and password.
NOTE
The user should be someone with administrative privileges.
4. Click the Local Users tab.
5. From the Local Users tab, click Add Local User.
6. From the Add User window, enter the following:
• User ID
• Full Name
• Password
• Confirm Password
NOTE
The User ID must be unique from others used on the system.
7. Click Add User.
8. Click the Groups tab.
9. From the Groups tab, click Add Local Group.
NOTE
Alternately, the system can be configured for enterprise groups if enterprise
authentication has been enabled. Refer to the Access Controls chapter for
information on configuring enterprise authentication.
10. From the Add Local Group window, type a unique group name.
11. Click Add Group.
• The group is highlighted in the Local Groups list.
• All information and buttons in the center panel refer to the highlighted group.

Dose Check
12. From the Roles area, select Dose Check Administrator and click Apply Roles.
• A green label confirms the applied roles.
• An error message displays if it is unsuccessful.
NOTE
Roles can be assigned at either the User or Group level.
7.3 Set the Dose Check AV Exceeding User Role

NOTE
Refer to the Access Controls chapter for instructions on setting local users, an enterprise
server, and defining local or enterprise groups.
The AV Exceeding User role is assigned at the group level. Users assigned to a group with this role
can approve scanning when an AV value has been exceeded. We recommend that only one user be
assigned to the AV Exceeding User group after having discussions with the radiologist, physicist and
department managers.
3. From the EA3 Administration window, enter your username and password
NOTE
The user should be someone with administrative privileges.
4. Click the Local Users tab.
• User ID
• Full Name
• Password
NOTE
The User ID must be unique from others used on the system.
7. Click Add User.
8. Click the Groups tab.

Dose Check
NOTE
Alternately, the system can be configured for enterprise groups if enterprise
authentication has been enabled. Refer to the Access Controls chapter for
information on configuring enterprise authentication.
10. From the Add Local Group window, type a unique group name.
11. Click Add Group.

• The group is highlighted in the Local Groups list.
• All information and buttons in the center panel refer to the highlighted group.
12. From the Roles area, select Dose Check AV Exceeding User and click Apply Roles.
NOTE
Roles can be assigned at either the User or Group level.
7.4 Configure the System for Dose Check

Use this procedure to configure the system for dose checking by Notification Value (NV) and Alert Value
(AV). You must have one user assigned to a group with the Dose Administrator role to confirm dose
check settings.
2. From the Mode menu, click Access Controls, then Dose Check Management.
3. From the Dose Check Management window, in the NV (Notification Value) Checking area, select
CTDIvol and/or DLP.
NOTE
The system default for Notification Value (NV) Checking is CTDIvolOn and DLP Off.
The GE Reference protocols will not contain any NV values.

Dose Check
Figure 71 Dose Check Enabled
4. From the Dose Check Management window, in the AV (Alert Value) Checking area, select CTDIvol
and/or DLP.
NOTE
The Alert Value (AV) should be determined by the site’s radiologist and physicist.
5. Enter a value for CTDIvol and/or DLP.
• The maximum AV value for CTDIvol is 2,000 mGy.

Dose Check
• The maximum AV value for DLP is 400,000 mGy-cm.

• The system default is AV checking by CTDIvolOn with a value of 1,000 mGy and/or DLPOff
with a value of 0 mGy-cm.
6. Click Save.
7. Enter Logon Name, Password , then click Accept or click Cancel to close with out saving changes.
7.5 Configure the AV by Age Threshold

Use this procedure to configure the system for dose checking by AV (Alert Value) Checking by Age
Threshold. You must have one user assigned to a group with the Dose Administrator role to confirm
dose check settings.
AV (Alert Value) Checking by Age Threshold allows the user to set AV values for adult and pediatric age
ranges.
AV (Alert Value) is based on the following criteria:
• Age value in Patient Information.
• If no age value is present, the system defaults to the higher age range.
NOTE
During protocol management, the AV (Alert Value) under Age Threshold is always used if
prescribed.
2. From the Mode menu, click Access Controls, then Dose Check Management.
3. From the Dose Check Management window, in the AV (Alert Value) Checking area, select Age
Threshold and enter the patient’s age.

Dose Check
Figure 72 AV (Alert Value) Checking by Age Threshold “On”
4. Enter a value for CTDIvol Alert (mGy) and/or DLP (mGy-cm).

• The maximum AV (Alert Value) for CTDIvol is 2,000 mGy.
• The maximum AV (Alert Value) for DLP is 400,000 mGy-cm.
• The system default is AV checking by CTDIvolOn with a value of 1,000 mGy and/or DLPOff
with a value of 0 mGy-cm.
• The value must be lower than the adult AV (Alert Value).
5. Click Save.
6. Enter Logon Name, Password, then click Accept or click Cancel to close with out saving changes.

Dose Check
7.6 Build Protocols With Access Controls

Use this procedure to build protocols with Access Controls. When Access Controls is enabled, the
system requires an authorized user to accept protocol parameter updates. See the Access Control
chapter for details.
An authorized user can be determined by one of two ways.
• Protocol Management will be authorized with no Log On Name and Password required if the user
currently logged in has the Standard User role.
• If Access Controls is not enabled, when Protocol Management is selected, the user will be
presented with an authorization window.

2. From the Mode menu, click Protocol Management, then Protocol Management.
3. From the CT Login authentication window, enter your Log On Name and Password.

Dose Check
Figure 73 CT Login Authentication Window
4. Click OK.
You will then be able to accept protocol parameter updates when building protocols.
7.7 Build Protocols with Notification Values

Use this procedure to set Notification Values (NV) in user protocols.
NV values can only be set in Protocol Management.
The CT Login authentication window will open.

Dose Check
3. Enter your Log On Name and Password and click OK to continue.

4. From the Protocol Selection window, select Adult or Pediatric.
5. From the Anatomical area, select an anatomical region.
6. From the Protocol Selection window, select a protocol and click Edit.
7. Click the series task to go to the first non-scout series in the protocol.
8. From the Dose Display area, enter the CTDIvol or DLP NV value by group.
9. Click Confirm Changes.
10. Click Save or Save As to save the new protocol parameters.
• The system compares all the CTDIvol and DLP values in the scan groups to the entered NV
value.
• Notification Values cannot be set for scan groups with Scout scan type.
• The protocol parameters will not be accepted until the NV value is no longer exceeded or
the user has entered a Diagnostic Reason for continuing to accept the scan parameters
exceeding the NV value.
• Saving a protocol with a dose level exceeding an NV demands a high degree of consideration.
In most cases, you will click Cancel to go back to adjust the parameters. If there is a clinical
reason to save a protocol exceeding an NV, enter the diagnostic reason.
11. In the Diagnostic Reason field, enter the reason for the scan exceeding the NV value.
12. Click Confirm to accept the Diagnostic Reason.
13. Click Confirm Changes to accept the protocol scan parameters.
14. Click Save or Save As to return to the Protocol Selection window.
NOTE
Viewing or exporting a Protocol Summary in the Audit Tool should be done after the
protocols are saved, not while editing.
7.8 Build Protocols with Notification Values by Factor

Use this procedure to set the Notification Values (NV) in user protocols for all scan groups by a factor.
For example, if the CTDIvol in a scan group were 5 and a factor of 1.5 was entered, the new NV value for
the group would be 7.5.
• Values can by entered in increments of 0.1.
• Values must be > 0.
• The maximum value is 10.

3. Enter your Log On Name and Password and click OK to continue.

Dose Check
4. From the Protocol Selection window, select Adult or Pediatric.

5. From the Anatomical area, select an anatomical region.
6. From the Protocol Selection window, select a protocol and click Edit.
7. Click the series task to go to the first non-scout series in the protocol.
8. From the Dose Display area, click NV CTDIvol or DLP.
9. Select Factor from the drop-down menu and type the desired factor for CTDIvol and/or DLP.
10. Click Confirm Changes.
11. Click Save or Save As to return to the Protocol Selection window.
7.9 Scan Using Alert Value Checking

Use this procedure to scan using Alert Value (AV) Checking.
The CTDIvol or DLP value will be highlighted when the estimated dose for the protocol exceeds the AV
value set for the system.

Dose Check
Figure 74 Alert Value (AV) Exceeded Warning
Adjust the scan parameters for the series until the exceeded AV value is below the prescribed AV
value. If the AV value is still exceeded after you click Confirm, a confirmation message will display. The
scan cannot be confirmed until the AV value is no longer exceeded, or a user with a Dose Check AV
Exceeding user role has authorized the scan.
Performing a scan exceeding an AV value demands a high degree of consideration for appropriateness.
In most cases, you will click Cancel to go back to adjust parameters. If there is a true diagnostic need
to perform a scan exceeding an AV value, enter the diagnostic reason.
1. Type the Logon Name.
2. Type the Password.
3. In Diagnostic Reason field, enter the reason for exceeding the AV value.

Dose Check
4. Click Confirm to proceed to scanning.
7.10 Scan Using Notification Value Checking

Use this procedure to scan using Notification Value (NV) Checking.
The CTDIvol or DLP value will be highlighted when the estimated dose for a scan group exceeds the NV
value set for each scan group.
Figure 75 NV Exceeded in Dose Display
Adjust the scan parameters for the scan group until the exceeded NV value is below the prescribed NV
value. If the NV value is still exceeded after you click Confirm, a confirmation message will display. The
scan cannot be confirmed until the NV value is no longer exceeded, or you have entered a diagnostic
reason for continuing the scan with the exceeded NV value.

Dose Check
Figure 76 Notification Value (NV) Exceeded Warning
1. In Diagnostic Reason field, enter the reason for exceeding the NV value.
2. Click Confirm to proceed to scanning.

Dose Check
7.11 Dose Check during Interventional (SmartStep)

Scans
Like non-interventional series, Dose Check for a SmartStep series is based upon the estimated dose
for the series when the user selects Confirm. Thus, if a Dose Check Notification Value or Alert Value is
exceeded for a SmartStep series, the user would see the Dose Check Notification Confirmation or Dose
Check Alert Confirmation screen only once prior to beginning scanning of the SmartStep series. This is
to prevent interruption during interventional scanning by avoiding excessive Dose Check Confirmation
screens.
7.12 Use the Dose Audit Tool

The Dose Audit Tool provides:
• Dose Check Log details exams which exceeded NV or AV values.
• Protocol Summary for protocol NV values.
• Invalid Protocols are listed.
• Export to save Dose Check Log, Audit Log, Protocol Summary and Invalid Protocols data to media.
7.12.1 Display a Dose Check Log

2. From the Mode menu, click Access Controls, then Dose Audit Tool.
3. From the Audit Tool window, click Dose Check Log.
4. From the Log List area, select the desired log and click OK.
NOTE
If the log data is near the maximum size, the system posts a message to export it.
7.12.2 Display the Protocol Summary

3. From the Audit Tool window, click Protocol Summary.
A protocol summary list display.
7.12.3 Display the Invalid Protocols


Dose Check
3. From the Audit Tool window, click Invalid Protocols.

A list of invalid protocols display.
7.12.4 Export Dose Check Log, Audit Log, Protocol Summary,

Invalid Protocols Data, User Protocols and Image Analysis Report
NOTE
The system will prompt to archive the Audit Log every 60 days. If an Export of the Audit
log is not done, the system will prompt again in 60 days. Select Ok if you do not wish to
export the Audit Log.
3. Insert CD-R media in the DVD RW drive or insert USB media in the USB port of the media tower.
4. From the Audit Tool window, click Export.
5. In the Export Media area, select CD/DVD or USB.
6. In the Export Contents area, select one or more data types: Dose Check Log, Audit Log, Protocol
Summary, User Protocols or Image Analysis Report.
NOTE
USB must be conditioned to FAT32 file type before media copying begins.
NOTE
If Protocol Summary is selected, also select either All Protocols or Invalid
Protocols.

Dose Check
7.
8. Click OK.
7.12.5 Use the Audit Log Viewer

Audit Log Viewer provides the following functions for the Administrator.
• Display the audit logs

• Search audit logs with a Free Search (by word or phrase), by Events or by Outcome
1. From the image monitor, click

2. From the Mode menu, click Access Controls, then Audit Log Viewer.
4. On the Audit Log Viewer screen, select your desired search method.
• Free Search provides the ability to search by word or phrase.
• Events provides the ability to search by selecting an event
• Outcome provides the ability to search by selecting an outcome

Dose Check
5. Click Search to apply the search parameters. Click Reset to cancel search if needed.
7.12.6 Print Image Analysis Report

1. From a PC insert the USB to which you exported the Image Analysis Report.
2. Select folder IAReports.
3. Select the folder which contains the date of the report you wish to print. The folder name is
IA_yyyymmddhhmmss.
NOTE
When Export is selected all Image Analysis reports are exported.
4. Double click to open the folder.
5. Click IA_report.html.
6. The report will open in a web browser.
7. Right click and select Print Preview.
8. Change orientation to landscape
9. Select print in preview window.

Dose Check

Equipment
8 Equipment
8.1 Overview
NOTE
PLEASE REFER TO THE SAFETY SECTION FOR IMPORTANT SAFETY INFORMATION

This chapter helps you to become familiar with your specific CT system, including the system
components and hardware.
For more general information about CT system components and hardware, refer to the following
sections:
• X-ray Source
• CT Detector
• Gantry
• Power Distribution Unit
• Table
• System Cabinet
• Scanner Desktop
8.2 UDI Marking

Every medical device has a unique marking for identification. The UDI marking appears on the device
labeling.
Figure 77 UDI marking
8.3 Scanner Desktop

The scanner desktop includes the components described below.

Equipment
Figure 78 Scanner Desktop — Configuration 1
Table 22 Scanner Desktop — Configuration 1
Number Description
1 Media Tower
2 Scan monitor
3 Display monitor
4 Scan Control Interface and Keyboard
5 Mouse
6 Computer
NOTE
Your system may include the Media Tower. This is a DVD-RW drive, which writes to
DVD-RAM bare media, DVD-R, and CD-R.

Equipment
Figure 79 Media Tower— Configuration 1
Number Description
Digital Video Disk Read/Write (DVD-RW) drive

This is a DVD-RW drive, which writes to DVD-RAM bare media, DVD-R, and CD-R.
1 • Use the CD/DVD option and the DVD-RW drive to write and restore from CD-R or DVD-R.
• Use the Data Export option to save information to CD-R.
• Use to Export Protocols.
USB Connection
Located in lower-right corner of the media tower. The CD/DVD/USB recognizes Hard Disk Drive
(USB drive) or USB key (Flash memory) with VFAT format. It does not recognize any hardware
with extension 3 format.
• Supports connecting a USB media storage device to:
• Use Media Creator to write and restore images.
• Use Data Export to export data to non DICOM file type.
2
• Use to export Dose Check Audit log information.
• Use to save scan files, protocols, and service files to USB.
• Only one USB for saving scan data can be connected at a time.
• The storage device should have a minimum size of 32 GB to store/restore system state data.
Scan data typically requires external USB drives with storage capacity of 1 TB and above.

Equipment
Scanner Desktop — Configuration 1 continued

Number Description
Connections for service computer functions

Located on the front of the Scanner Desktop and front of the PMT tower.
• The Service Security Access Key connection to the system uses one of the USB ports on the
front of the PMT tower.
3 • The Service key should always be removed prior to any software reboot if left in by your
local service.
• The service ports on the front of the computer chassis include an Ethernet connection and
USB port. The Ethernet port is for service laptop connection to the system. The USB port
can be used for external storage device connection but suggested location is the PMT tower
USB ports. Intended use is only for trained service personnel.
4 Computer power on/off switch

Located on the back of the computer chassis as Item #2 below (item #1 is the Scanner Desktop
power indicator).
• Use to Turn off/on the computer if system functions are not accessible at the scanner
desktop controls.
• Use to completely Power Off the computer chassis.

Equipment
Figure 80 Scanner Desktop — Configuration 2
Number Description
1 Scan monitor
2 Display monitor
4 Mouse
5 Computer

Equipment
Figure 81 Computer — Configuration 2

Equipment
Number Description
Digital Video Disk Read/Write (DVD-RW) drive

This is a DVD-RW drive, which writes to DVD-RAM bare media, DVD-R, and CD-R.
1 • Use the CD/DVD option and the DVD-RW drive to write and restore from CD-R or DVD-R.
• Use the Data Export option to save information to CD-R.
USB Connection
Located in lower-right corner of the computer. The CD/DVD/USB recognizes Hard Disk Drive (USB
drive) or USB key (Flash memory) with VFAT format. It does not recognize any hardware with
extension 3 format.
2

Equipment
Scanner Desktop — Configuration 2 continued

Number Description
Connections for service computer functions

Located in lower-right corner of the computer.
• The Service Security Access Key connection to the system uses one of the USB ports on the
front of the computer.
3 • The Service key should always be removed prior to any software reboot if left in by your
local service.
• The service ports on the front of the computer chassis include an Ethernet connection and
USB port. The Ethernet port is for service laptop connection to the system. The USB port
can be used for external storage device connection but suggested location is the PMT tower
USB ports. Intended use is only for trained service personnel.

Located on the back of the computer chassis as Item #1 below (Item #2 is the Scanner Desktop
power indicator).
• Use to power on/off the computer if system functions are not accessible at the Scanner
Desktop controls.
• Use to completely power off the computer chassis.
Figure 82 Scanner Desktop - Configuration 3

Equipment
Number Description
1 Scan monitor
2 Display monitor
4 Mouse
5 Computer
Figure 83 Scanner Desktop Console — Configuration 3

Equipment
Table 27 Scanner Desktop Console — Configuration 3
Number Description

Located on the front of the computer as Item #1 in the image above.
Desktop controls.
NOTE
To Power up the system, the user does not need to press the Power button of the
SCIM. Press the power button of the desktop computer only. The system will begin
the boot sequence and start.
USB Connection
extension 3 format.
2

Equipment
Figure 84 Scanner Desktop - Configuration 4
Number Description
1 Scan monitor
2 Display monitor
4 Mouse
5 Computer
6 Power Box

Equipment
Figure 85 Scanner Desktop Console — Configuration 4

Equipment
Table 29 Scanner Desktop Console — Configuration 4
Number Description

Located on the front of the computer as Item #1 in the image above.
Desktop controls.
NOTE
To Power up the system, the user does not need to press the Power button of the
SCIM. Press the power button of the desktop computer only. The system will begin
the boot sequence and start.
USB Connection
extension 3 format.
2
8.3.1 Computer
The system uses a PC computer running Linux operating system. The system includes system, image
and scan data disks and stores up to 700,000 5122 images, with one terabyte for 1500 scan data files.
The computer is usually located under the Scanner Desktop.
8.3.2 Reconstruction hardware

The reconstruction engine provides advanced processing capabilities for reconstructing routine
imaging modes. Reconstruction hardware, including scan data disks, is contained in the system
cabinet, not in the console chassis.
8.3.3 Monitors
The system includes two monitors, a scan monitor and a display monitor.

Equipment
Figure 86 System Monitors
Number Description
1 Scan monitor
2 Display monitor
NOTICE
WHEN POWERING ON, IT TAKES 30 MINUTES FOR THE MONITORS TO

REACH THEIR SET BRIGHTNESS AND CONTRAST LEVELS. DURING THIS
TIME, DO NOT MAKE ANY ADJUSTMENTS TO THE BRIGHTNESS OR
CONTRAST LEVELS.
NOTE
If you leave your system on overnight, you should turn off the monitors to minimize
burn-in.
If a monitor experiences burn-in, turn off the monitor and leave it off for the same
duration as caused the burn-in.
8.3.4 Scan Control Interface and Keyboard

The Scan Control Interface and keyboard consist of an alphanumeric keyboard, 10-key number
keypad, buttons specific to initiating scan and communication with the patient.
All buttons on the Scan Control Interface, except the Exposure Indicator, are backlit (illuminated) when
the system is energized and dark when the system is off. The Exposure Indicator illuminates only when
an exposure is taking place. Some buttons can also flash as an indication to the operator.

Equipment
Figure 87 Scan Control Interface and Keyboard
Table 30 Scan Control Interface Buttons
Number Button Function Description
In the event of an emergency, pressing emergency

1 Emergency Stop stop will stop all table and gantry motions, as well as
any X-ray exposure in progress.
Exposure indica-
2 Illuminates when an exposure is taking place.
tor
The Start Scan indicator flashes green once the tube

has reached exposure speed. Press the button to start
3 Start Scan the scan. Start Scan will flash for 30 seconds before
timing out. Press Start Scan button again to bring the
system back to the ready state.
Pauses scanning, once the current scan is completed.

4 Pause Scan You can resume the scan by clicking Resume from the
Scan Progress screen.
Immediately stops the scan. You can resume the scan

5 Stop Scan
by clicking Resume from the Scan Progress screen.

Equipment
Scan Control Interface Buttons continued

The Move to Scan button has two functions, to ad-

vance the cradle to the start position and to perform
6 Move to Scan action when using the remote control panel.
Press Move to Scan when the indicator flashes green
within three minutes.
Stops cradle motion in/out. Click Resume from the

7 Stop Move
Scan Settings screen to resume the scan.
8 Cradle Home Moves the cradle to the home position.
Press Talk and speak towards the intercom to com-

municate with the scan room.
9 Talk
The green LED (next to button) lights when Talk is
pressed.
This dial controls the Auto Voice volume to the pa-

tient. An upward adjustment of the dial increases the
Volume Control volume while a downward adjustment of the dial de-
10 (Auto Voice to creases the volume. The dial has numbers indicating
gantry) what volume level you have set.
The LED light is solid green when Auto Voice is play-
ing.
This dial controls the volume of the operator’s voice

Volume Control to the patient. An upward adjustment of the dial in-
11 (operator to pa- creases the volume while a downward adjustment of
tient) the dial decreases the volume. The dial has numbers
indicating what volume level you have set.

Equipment
Scan Control Interface Buttons continued

This dial controls the volume of the patient’s voice

to the operator. An upward adjustment of the dial in-
creases the volume while a downward adjustment of
the dial decreases the volume. The dial has numbers
on it indicating what volume level you have set.
Volume Control NOTE
12 (patient to opera-
When the volume is turned on, the intercom
tor)
will auto-mute after 2-3 seconds of inactiv-
ity in the scan room to minimize hissing
sound from higher ambient noise. The mut-
ed intercom will then automatically pick up
and immediately play back the sounds of
anyone talking in the scan room.
Push the Power button to power up the scanner desk-

top.
13 Power
The Power button is lit when the scanner desktop is
on.
8.3.5 Preset W/L keys – F5 through F11

The F5 through F11 function keys are used to apply preset Window Width (WW)and Window Level (WL)
values in the following applications: File Manager Viewer, Patient Session Tab Viewer, and Reformat.
The WW/WL values are defined in System Preferences Viewports.
Table 31 Preset W/L function keys
F key Description Translated text
F1 Film Image
F4 Film Series
F5 Previous
F6 Abdomen
F7 Head
F8 Lung
F9 Mediastinum
F10 Spine
F11 Vertebrae

Equipment
8.3.6 Page Up/Page Down keys

Figure 88 Page up and down keys
Use the Page Up and Page Down to review the next and prior images in a viewport.
8.3.7 W/L control keys

Figure 89 Arrow Keys
Use these keys to change the W/L settings for images in a viewport. The Up/Down keys increase/
decrease the window level and the Left/Right keys decrease/increase the window width.
8.3.8 Operate the mouse controls

The two-button mouse with a scroll wheel is used to make selections on the scan and display
monitors.

Equipment
Figure 90 Mouse Buttons
Table 32 Mouse Actions
Number Mouse Action Description
1 Left-click Click the left mouse button.
2 Right-click Click the right mouse button.
3 Scroll Wheel Turn the scroll wheel.
Click and drag Click and hold the left mouse button while moving the
mouse.
Right-click and Click and hold the right mouse button while moving the
drag mouse.
Scroll wheel-click Click and hold the scroll wheel while moving the mouse.
and drag
Double-click Click the left mouse button twice in rapid succession.
Triple-click Click the left mouse button three times in rapid succes-
sion.

Equipment
8.4 Auto Positioning Depth Xtream Camera

The automated workflow for patient positioning and Scout scanning uses a depth Xtream camera to
detect the patient orientation and position on the table, and to calculate the Scan Range of Scout and
isocenter of the scanning.
Figure 91 Auto Positioning Depth Xtream Camera
8.5 Xtream Tablet Gantry Display
8.5.1 Overview
A touch screen display is mounted above the gantry control panel on the left and right sides of the
gantry front cover. The touch screen display provides the following functions:
• Create New Patient or Unknown Patient exam.
• Set up the Automatic Patient Positioning and Scout scanning with Auto Patient Positioning option
installed.
• Display gantry and table position information.
• Display multiple system status.
• Display patient and exam information.
• Display Patient ECG waveform.
• Play movie.

Equipment
Figure 92 Gantry display and Gantry Control Panel

Equipment
Table 33 Gantry display components
No. Icon Description
1. Gantry Display
2. Gantry Control Panel
8.5.2 Tool bar and Cradle/Tilt Information

Figure 93 Gantry display
Depending on the current state, the Tool bar display the following icons.

Equipment
Table 34 Toolbar Icons
Breath hold Light Pressing this allows you to demonstrate to the patient how to use
the Breath hold Light and Countdown Timer.
1. • A blinking green breathe light (1) indicates get ready to hold

your breath.
• A solid yellow light (2) indicates to hold your breath.
• Count down (3) indicator counts down the seconds to sec-

onds to breathe time.
• A solid green breathe light (1) indicates breathe time.
Table and Gantry Tilt Press this icon to view the current scannable range based on the
Movement Limits table position on the Gantry Display.
2. NOTE
The “Scannable Range” is calculated based on a lim-
it and collision matrix, taking into account the table
height and the reference point position.
Movie Press this icon to access movies that help to explain CT examina-
tion procedures to patients.
3.

Equipment
Toolbar Icons continued

4. Settings Press this icon to set the functions of the Gantry Display.
There are the following three types of setting configurations.
Preference can set the method of protocol narrow down, display

and Patient Schedule privacy setting.
Monitor Setup can set the brightness of Displays, Control Panels,

Light Belt and lighting effect.
5. Clean mode Press this icon to clean the screen surface.
6. Patient Schedule Press this icon to open the Patient Schedule.

Equipment

7. Electrocardiogram, ECG Indicate the status of ECG leads are not connected to
patient.
Indicate the status of ECG connection error to
the console ethernet port.
8. Tools Press this icon to access available tools.
9. Cradle information Press this icon to display or hide the vertical height and horizon-
tal cradle position, and tilt degree of the gantry.
The vertical height indicator displays the height of the cradle in
relation to ISO center.
The horizontal cradle position displayed is the position of the cra-
dle based on the established anatomic reference of the patient.
This reference is established using the internal or external land-
mark. The number is preceded by an S if the position is superior
to the reference point or an I if the position is inferior to the
reference point.
10. Used to check impedance values between ICM leads and patient
body.
Indicates the status of leads are not connected to patient.
The Cradle/Tilt information area displays the following indicator icons. Depending on the system
status, an indicator icon may be highlighted and the corresponding status is activated.

Equipment
Table 35 Status Bar Icons
Collision Indicator The Collision light illuminates and a picture of CT system with
high-lighted collision sensors is posted on the gantry display
(Figure8-13) when there is a possibility that the table, cradle and
gantry could collide.
The light also illuminates when reaching the travel limits of table
and cradle motion. In the case of interference, you may need to
1. raise or lower the table or determine if resistance is being caused
by any patient restraints, accessories, or by the patient.
NOTE
The picture of CT scanner with high-lighted collision
sensors on the gantry display can be hidden by touch-
ing the display.
Cradle Unlocked Indicator The Cradle Released indicator illuminates indicating the cradle is
unlatched. When the cradle is unlatched, it is free floating.
2.
8.5.3 Collision or Emergency Stop Status Indicator

When a collision sensor on the table or gantry detects a collision, the Collision Status Indicator is
displayed on the Gantry Display. The Indicator displays the CT scanner image and highlights the
triggered collision sensor. According to the indicated position, find the location where the collision
occurred, and move the table or clear the colliding object.

Equipment
Figure 94 Collision Indicator
After the user presses the Emergency Stop button, the Gantry Display shows the emergency stop
status and indicates how to reset the system.
Figure 95 Emergency Stop Indicator

Equipment
8.6 Gantry
8.6.1 Gantry display

There are two gantry displays: the primary display and the secondary display. The gantry primary
display shown below provides gantry and table status information as described in the following table.
Figure 96 Gantry Primary Display
Table 36 Gantry Primary Display Components
Number Component Description
1 Table/Cradle Information Area Displays information related to the table elevation and
the cradle location. This information is used in the scan
room while positioning the patient.
The Vertical Height indicator displays the vertical height

Vertical height indicator of the table in relation to ISO center.
Display Range: 0 to 999.9 mm
Display Precision: +/-1.5 mm
Display Accuracy: +/-1.5 mm

Equipment
Gantry Primary Display Components continued

The Horizontal Cradle Position displays the position of

the cradle based on the established anatomic reference
of the patient. This reference is established using the
internal or external landmarks. The number is preceded
Horizontal cradle position
by an S if the position is superior to the reference point
or an I if the position is inferior to the reference point.
Shown when Scannable Range is selected via the Menu

area display button. It clears after 15 seconds, when
another menu area selection is displayed or when you
confirm the scan prescription, hide the scannable range
information with another button press, press a Land-
Scannable Range mark button, or longitudinal motion occurs.
Table Travel Limits displayed are calculated based on a
limit and collision matrix that takes into consideration
the table height and landmark location on the cradle.
2 Status Indicator Area Displays information related to connection of accesso-

ries (ECG, respiratory gating), positioning interference,
and cradle unlatch. This information is used in the scan
room while positioning the patient.
The Collision light illuminates when there is a possibility

that the table, cradle, and gantry could collide. There
are elevation collision sensors on the front and rear ta-
ble covers. The collision sensors are active during table
Collision indicator
elevation.
The light also illuminates if there is ten pounds of resist-
ance during cradle motion in/out or when reaching the
travel limits of the table, cradle, and gantry motion. In
the case of interference, you may need to raise or lower
the table, determine if resistance is being caused by any
patient restraints, accessories, or by the patient.
Cradle unlocked indicator

The Cradle Released indicator illuminates indicating the
cradle is unlatched. When the cradle is unlatched, it is
free floating.

Equipment

Internal ECG indicator

The Internal ECG indicator is lit when an internal ECG
gating signal is seen by the scanner.
External ECG indicator
The External ECG indicator is lit when an external ECG

gating signal is seen by the scanner.
3 Patient Exam Information Area Shown when Patient/Exam Information is selected via
or the Menu area display button (see row at end of table).
ECG Area (Not shown above)
Shown (see example above) when ECG is selected via

the Menu area display button (see row at end of table).
Patient Name Area
NOTE
The orientation of the gantry in this display
is not linked to the orientation configured for
the operator console. The gantry is always
displayed orientated on the right.
4 Menu Area Displays user selectable menu items. Navigate this area
using the Back/Enter/Forward buttons on the Gantry
Controls panel.
The Settings menu item is used to change the following:

• ECG settings
Settings
• Display brightness setting
• Background color selection
• Screen saver selection
See System Preferences section for available settings.

Equipment

Movie
The Movie menu item is used to display explanatory
movies and slideshows.
Scannable Range
The Scannable Range menu item is used to display
scannable range information in the Patient Orienta-
tion/Entry Area.
Patient/Exam Information
Select to display Patient/Exam information in
thePatient/Exam Information – ECG area.
Active Lead Selection
Select to change the Active Lead. Selections are lead I,

lead II, lead III or auto
ECG
Select to display ECG information in the Patient/Exam
Information – ECG area.
Impedance Check
Select to initiate an impedance measurement, if the
internal ECG trigger device is selected and active.
The gantry secondary display shown below provides gantry and table status information as described
in the following table.

Equipment
Figure 97 Gantry Secondary Display
Table 37 Gantry Secondary Display
Number Description Description
Displays the delay time before a scan starts.

Prep delay timer
Display Range: 0 - 999 s
1
Exposure indicator
2 The Exposure Indicator illuminates when an exposure is taking place.
The Laser Light Indicator illuminates when the laser alignment light is
on.
Laser light indicator
CAUTION
3
FOR PATIENT SAFETY, IT IS IMPORTANT TO HAVE
PATIENTS CLOSE THEIR EYES ANYTIME THE LASER
ALIGNMENT LIGHT IS ON.
Gantry energized indi-

cator
Illuminates when gantry and PDU power are energized and the console
4
computer is powered off.

Equipment
Gantry Secondary Display continued

Number Description Description
The face blinks to let the patient know they will need to hold their
Breathing light breath. The total breath hold time is shown to let them know for how
long. This prepares them for the upcoming breath hold.
5
The face turns solid during the breath hold and the numbers start
counting down.
The illuminated face turns off when the timer gets to 0.
Breath hold timer Displays the count down of the breath hold time.
Display Range: 0 - 99 s
6
8.6.2 Gantry and console interfaces

If your system has connections for GE approved accessories, the figures and tables below show where
to connect these accessories (refer to the GE Approved Accessories list found in the Safety chapter).
8.6.2.1 Left rear plug-in panel
Figure 98 Left Rear Plug-in Panel

Equipment
Table 38 Left Rear Plug-in Panel Components
Number Description
1 Respiratory gating power connection
2 Respiratory gating trigger connection (not used)
Respiratory gating Ethernet connection (not

3
used)
4 Cardiac gating power connection
5 Cardiac gating trigger connection
6 Ethernet connection for ECG monitor
7 Ground
8 Power connection (spare)
9 Ethernet connection (spare)
8.6.2.2 Console AC power box
Figure 99 Console AC Power Box — Configuration 1

Equipment
Table 39 Console Rear Plug in Panel Components — Configuration 1
Number Description
1 Power Indicator - Scanner Desktop internal components
2 Circuit Breaker / Switch - Scanner Desktop internal components
Circuit Breaker / Switch - Optional GEHC supplied motorized Scanner

3
Desktop table
4 Power Indicator - Accessories
5 Circuit Breaker / Switch – Accessories
6 AC Power Outlet – Peripheral Media Tower
7 AC Power Outlet – Monitor (Prescription)
8 AC Power Outlet – Monitor (Display)
9 AC Power Outlet – Scan Room Monitor (Optional)
10 Accessory Grounds
11 AC Power Outlet – RPM_1
12 AC Power Outlet – RPM_2
13 AC Power Outlet – Injector_1 (see Note)
17 AC Power Outlet – Spare (intended for RPM connection)
18 AC Power Outlet – Spare (intended for RPM connection)
AC Power Outlet – Optional GEHC supplied motorized Scanner Desktop

19
table
NOTE
Gantry and console outlets should not be used for the MedRad injector
components or ISI900. A separate grounding cable should be attached
between the injector and the CT system.

Equipment
Number Description
3 Accessory Grounds
6 AC Power Outlet – Monitor (Prescription) (J1)
7 AC Power Outlet – Monitor (Display) (J2)
8 AC Power Outlet – Host Computer (J3)
9 AC Power Outlet – Scan Room Monitor (Optional) (J4)
10 AC Power Outlet – Spare System Power (J5)
12 AC Power Outlet (Internal) – Ethernet Network Switch (Not Shown) (J7)
13 AC Power Outlet (Internal) – Video Splitter (Optional) (Not Shown) (J8)
14 AC Power Outlet – RPM_1 (J9)

Equipment
Console Rear Plug in Panel Components — Configuration 2 continued

Number Description
16 AC Power Outlet – Injector_1 (J11) (see Note)
20 AC Power Outlet – Spare for Accessory (J15)
NOTE

Equipment
Number Description
3 Accessory Grounds
6 AC Power Outlet – Monitor (Prescription) (J1)
7 AC Power Outlet – Monitor (Display) (J2)
8 AC Power Outlet – Host Computer (J3)
9 AC Power Outlet – Scan Room Monitor (Optional) (J4)
12 AC Power Outlet (Internal) – Ethernet Network Switch (Not Shown) (J7)
13 AC Power Outlet (Internal) – Video Splitter (Optional) (Not Shown) (J8)
NOTE

Equipment
CAUTION
THESE RECEPTACLES ARE NOT FOR GENERAL USE. THE RPM POWER
CONSUMPTION SHOULD NOT EXCEED 720 WATTS. THE INJECTOR POWER
CONSUMPTION SHOULD NOT EXCEED 780 WATTS.
DANGER
INFORMATION ON INTERNAL GANTRY COMPONENTS IS PROVIDED FOR

USER EDUCATION. THE GANTRY CONTAINS DANGEROUS VOLTAGES
AND MOVING PARTS. TO PREVENT ELECTRICAL SHOCK OR CRUSHING
INJURIES, DO NOT REMOVE COVERS OR ENTER THE GANTRY. ONLY
TRAINED, QUALIFIED SERVICE PERSONNEL MAY REMOVE GANTRY OR
OTHER EQUIPMENT COVERS.
8.6.3 Operate the gantry controls

Gantry controls are described in the table, below.
Figure 102 Gantry Controls

Equipment
Table 42 Gantry Controls
Number Icon Function Description
If you want to stand by the gantry and start the scan,

you can press Start Scan after you have confirmed
the prescription and the table has been moved to
the start location. Once the tube has reached the
1 Start Scan
exposure speed, the button flashes green for 30 sec-
onds and then times out. Press the Start Scan button
again to bring the system back to the ready to scan
state.
• Stops the prep display and X-ray exposure.

2 Stop Scan
• Halts all gantry and table motions.
3 Cradle In Moves the cradle into the gantry.
Moves the table up.
NOTE
4 Table Up When the table elevation is below the mini-
mum scan height, the elevation speed will
be the fast speed when only the slow con-
trol is enabled.
Moves the cradle out of the gantry.

Cradle In or Out can be used to move the patient to
5 Cradle Out the scan location after clicking confirm settings.
Cradle In or Out LED flashes for three minutes before
it times out.
6 Table Down Moves the table down.

Equipment
Gantry Controls continued

When pressed simultaneously with Table Up/Down

7 Fast Speed
or Cradle In/Out, speeds up the movement.
Press to toggle all laser alignment lights on/off and

to move the gantry components from the park or
idle position to the alignment lights position. Align-
ment lights are used to establish landmark locations.
Three alignment lights are displayed:
• Axial, divides anatomy into superior and inferior
sections.
• Sagittal, divides the anatomy into right and left
sections.
• Coronal, divides anatomy into anterior and pos-
terior sections.
8 Laser Alignment Light
CAUTION
FOR PATIENT SAFETY, ALWAYS

HAVE PATIENTS CLOSE THEIR EYES
ANYTIME THE LASER ALIGNMENT
LIGHTS ARE ON.
The sagittal, coronal, and transverse alignment lights

are within ±1 mm of the gantry coordinate system (x,
y and z-axis) centered at gantry iso center.
NOTE
The laser alignment light switch is provided
as an alternative to beam attenuators.

Equipment

Press to establish the table’s reference point when

positioning the patient using the internal alignment
light.
This reference point is normally the anatomic refer-
ence point used when positioning the patient.
For example, if the patient’s anatomic reference
point is the sternal notch, then the sternal notch
would be centered to the internal laser alignment
9 Internal Landmark light.
The gantry displays a table location of 0 mm. This set
the zero point by which S and I scan locations are
centered.
A landmark must be set before you click Confirm
settings.
At Done Scanning, the landmark is cleared.
For scan setup details, see the Set up and position
the patient procedure.
Press to establish the table’s reference point when

positioning the patient using the external alignment
light.
This reference point is normally the anatomic refer-
ence point used when positioning the patient.
For example, if the patient’s anatomic reference
point is the sternal notch, then the sternal notch
would be centered to the external laser alignment
light.
The gantry displays a table location of 240 mm. This
set the zero point by which S and I scan locations are
centered.
10 External Landmark
A landmark must be set before you click Confirm
settings.
At Done Scanning, the landmark is cleared.
For scan setup details, see the Set up and position
the patient procedure.
During installation of Radiation Therapy planning
room laser lights, the CT scanner external alignment
lights may be disabled and the gantry display table
location may be different if the external landmark
button is pressed.
Use the internal landmark for patient scanning dur-
ing radiation therapy planning.

Equipment

Press once to unlock the table cradle, to freely move

the cradle with your hands. Use it to move the pa-
11 Cradle Lock/Release tient out of the gantry in an emergency.
Press a second time returns the cradle to the locked
position and the landmark is maintained.
Press and hold to simultaneously move the cradle

out of the gantry. Once the cradle has been removed
12 Table Home
from the gantry, the table begins to lower to its low-
est limit.
Flashes white about once every two seconds when

13 E-Stop Reset E-stop has been activated. Restores power to the
gantry and table.
Press to demonstrate the breathing light and count-

Breathing Lights
14 down time to the patient. Refer to Table 37 on
Demo
page 190 for breathing lights description.
15 Accent Lights On/Off Toggles accent lights on/off.
Bore Lighting Intensi-

16 Increases the bore lighting intensity.
ty Up
Bore Lighting Intensi-

17 Decreases the bore lighting intensity.
ty Down
Moves to next (left) selectable area on the Gantry

18 Back Primary Display. If more than one row, moves left
and then up and left.
Selects highlighted menu item on the Gantry Primary

19 Enter
Display.
Moves to next (right) selectable area on the Gantry

20 Forward Primary Display. If more than one row, moves right
and then down and right.
8.6.4 Cardiac trigger monitor
8.6.4.1 Integrated cardiac trigger monitor

For cardiac gated exams that require the cardiac trigger monitor, use the Integrated Cardiac Module
that is connected to the cradle.

Equipment
Figure 103 Integrated Cardiac Module
Table 43 Integrated Cardiac Module Components
Number Components Description
Connected to the ground cable that connects to the cable

1 Functional Ground
retractor below the cradle.
Connected to the RS-422 communication cable that con-

2 Network Interface Cable
nects to the cable retractor below the cradle.
6-Pin AAMI ECG Patient Cable Con-

3 Connection used for the 4-lead patient cable.
nector
Connection used for the 4-leads when the simulator mode

4 4-Lead ECG Simulator
is required.
POWER (Green LED) – Indicates that power is applied to

the Cardiac Module.
COMMUNICATION (Yellow LED) – Flashes when the Car-
5 Annunciator LEDs
diac Module is transmitting and receiving data.
STATUS (Yellow LED) – Flashes when is operating normal-
ly.
6 Respiratory connector Unused connector
7 Light Pipe Light for room ambient.

Equipment
8.6.4.2 Patient grounding strap

The addition of a patient grounding strap to the system improves ECG waveform signal quality for
ECG-gated scans. It does not replace the recommended process for patient preparation. Always follow
the proper patient preparation procedure.
Figure 104 Patient Grounding Strap, Cable, and Grounding Connection Behind Integrated Cardiac
Module
1 Cable grounding connection
2 Grounding strap cable
3 Patient grounding strap
4 Grounding cable connection to wrist strap
Connecting Patient Ground Strap

1. Connect the grounding strap cable from the grounding point behind the integrated cardiac
module to the patient grounding wrist strap.
2. Place the patient grounding strap on the patient’s wrist. The strap should have direct contact with
the patient’s skin.
3. Connect the grounding strap cable from the grounding point (Cable Grounding Connection)
behind the integrated cardiac module to the patient grounding wrist strap.
See grounding strap manufacturer’s website, referenced on product packaging, for cleaning
instructions.

Equipment
8.6.4.3 External cardiac trigger monitor

If using the External ECG monitor (IVY 7800) instead of the ICM, follow the steps below:
1. Locate the gantry’s left‐rear plug-in panel.
Figure 105 Left Rear Plug-in Panel
2. Plug the power connection for the cardiac trigger monitor into the electrical connection port (4).
3. Connect the coaxial cable to the connection port above the heart (5).
NOTE
Do not loop the cable. This could introduce noise into the ECG trace.
4. Connect the Ethernet cable from the cardiac trigger monitor to the port labeled Monitor (6).
5. On the Gantry Display Menu Area, select Settings > ECG Settings to select the External ECG as the
primary cardiac device. The External ECG can also be selected from the Console user interface.
8.7 Table
NOTE
All patient tables may not be available in all regions.
The standard table configuration has a weight limit of 500 pounds (227 kg) with an incremental
accuracy of ±0.25 mm. The vertical range of the table is 50 to 103 cm. Refer to Table 163 on page 1008 in
the General Information section for table scannable range.

Equipment
The heavy table configuration has a weight limit of 675 pounds (306 kg) with an incremental accuracy
of ±0.25 mm. The vertical range of the table is 56 to 103 cm. Refer to Table 163 on page 1008 in the
General Information section for table scannable range.
When interruption of Supply Mains occurs, the maximum stopping distance of the moving cradle is 220
mm.
To safely remove the patient in an emergency egress situation, grab and squeeze the Cradle Handle
release switch. Continue to squeeze the Cradle Handle release switch while pulling the cradle to its out
position.
Figure 106 Patient Table Cradle Release Handle Switch
8.7.1 System operation and limitations that reduce the risk of

collision with the patient
• The range of table motion is limited to prevent a collision between the table cradle and the
gantry. The system will maintain a 25 mm clearance between the table cradle and the gantry.
• The system design minimizes gaps between moving covers and structures so that fingers cannot
get into the gap.
• Table motion controls require continuous activation by an operator.
• Emergency stop controls are readily available that stop motion within 10 mm.
• The cradle motion is force limited to 200 N as a protective measure to reduce the risk of
entrapment and pinching.
• The gantry employs covers to protect the patient against rotating parts, and provides cover
interlocks to inhibit gantry rotation when the covers are open.
• Sensors are located beneath the table to detect collision and stop motion.

Equipment
Figure 107 Table Collision Sensor Locations
Sensors are located underneath the front and back of the table. These sensors indicate where there is
potential for collisions with items such as wheel chairs or stretchers. When a sensor is touched, table
and gantry movement stops immediately. In this event, clear the area and continue positioning the
table.
There is a mark on the cradle for maximum scannable range.
CAUTION
IF THE TABLE IS LOWERED WITH ANYTHING IN THE RED X AREA, AS

INDICATED IN THE FIGURE BELOW, THE TABLE COULD BE DAMAGED
ALONG WITH THE EQUIPMENT OR OBJECT UNDER THE TABLE.
Figure 108 Restricted Area Below Table

Equipment
CAUTION
USE OF ANY CRADLE EXTENSION ACCESSORIES SUCH AS THE TABLE

EXTENSION, HEAD HOLDER, CORONAL HEAD HOLDER, AND PHANTOM
HOLDER ARE NOT ACCOUNTED FOR IN THE TABLE GANTRY INTERFERENCE
MATRIX. THEREFORE, ADDITIONAL CARE NEEDS TO BE TAKEN TO CLOSELY
MONITOR ANY TABLE MOVEMENT TO AVOID CONTACT OF THE EXTENDED
ACCESSORY WITH THE GANTRY.
8.7.2 Use the Load/Unload foot pedals

The Load and Unload pedals adjust the table up and down and in and out of gantry. The Load and
Unload pedals are always active.
• The Load pedal moves the patient table up to a height of 99 cm and moves the cradle into the
gantry, if no scan protocol is selected.
• The Load pedal moves the patient to a preset location, based on the anatomical reference in the
selected protocol.
• While the Unload pedal is pressed, it moves the patient table out of the gantry and moves the
cradle to the full out home position, and then lowers the table to a minimum height of 50 cm
(standard table configuration) or 56 cm (heavy table configuration).
To move the patient into the gantry, press and hold the Load pedal.
To move the patient out of the gantry, press and hold the Unload pedal until the table is at a suitable
position to remove the patient from the table.
• The Load and Unload pedals are only to be used when first positioning the patient on the
table for an exam and when removing the patient after the exam is complete.
8.7.3 Patient comfort and accessories
8.7.3.1 Cradle pad

Attach the cradle pad to the velcro on top of the cradle.
To remove the cradle pad, pull the pad loose from the cradle velcro.
8.7.3.2 Cradle extender, Axial and Coronal head holders

To attach these accessories to the table:
1. Align the accessory tongue with the pocket at the end of the cradle.
2. Keep fingers clear of the cradle.
3. Push the tongue all the way into the pocket until it latches into place.

Equipment
4. Rubber shims may have been installed on the head holder or foot extender to give it a tighter fit.
Please take care when latching the accessory to make sure that it is completely latched. Push the
latch forward until you hear a click. Verify that the latch is fully latched.
To remove these accessories from the table:

• Pinch the two L-shaped parts together and pull the accessory out of the cradle.
• An alternate method is to apply a light force to the catch towards the cradle, pinch the L-shaped
catch together, and pull accessory out of the cradle.
8.7.3.3 Cradle extender pad

Attach the cradle extender pad to the velcro on top of the cradle extender.
To remove the cradle extender pad, pull the pad loose from the cradle extender velcro.
8.7.3.4 Table tray

To attach the table tray to the table:
1. Fit the legs of the tray-support form into the holes at the rear of the table.
2. Place the tray on top of the support form.
3. Use the strap to secure objects that might tip.
NOTE
Do not place the cardiac trigger monitor on the tray. The tray’s weight limit is 19.8
pounds (9 kg).
To remove the table tray from the table:
1. Remove any straps used to secure objects.
2. Remove the tray from the top of the support form.
3. Remove the legs of the tray-support form from the holes at the rear of the table.
8.7.3.5 IV pole
To attach the intravenous (IV) pole to the table:
1. Insert the IV pole into the hole at the rear of the table or into the table tray.
The maximum weight that can be attached to the IV Pole is 10 pounds (4.5 kg).
2. Tighten the extension lock to secure the pole.
To remove the intravenous (IV) pole from the table:

1. Loosen the extension lock that secures the pole.
2. Remove the IV pole from the hole at the rear of the table or from the table tray.

Equipment
8.7.3.6 Positioning straps

To attach positioning straps:
1. Slide the bead end into the positioning track on the cradle.
2. Wrap the straps around the patient and fasten the velcro ends together.
To remove positioning straps:

1. Unfasten the velcro ends from around the patient.
2. Slide the bead end out of the positioning track on the cradle.
8.7.4 Table X-Y Accuracy for the Flat Table Top Workflow
8.7.4.1 Recommended Treatment Planning Workflow

Use this workflow to position the patient for Radiotherapy Treatment Planning.
A laser alignment light system is available in order to accurately define the patient scan region.
However, it is not intended for the purpose of patient marking for Radiotherapy Treatment Planning.
Radiotherapy Treatment Planning requires the use of an external laser light system.
1. Position the patient on the table.
2. From the gantry controls, press the Cradle Out button to return to the home position.
3. Press the Internal Landmark button .
4. Press the Cradle In button to position the cradle between 890 mm to 850 mm and then
press the Cradle Out button to the home position.
• This centers the cradle.

• Each in and out motion of the cradle is one cycle.

Equipment
• The cradle must cycle the number of times as determined in the Verify the table lateral
motion procedure.
• Determine the number of extension/retraction cycles needed based on testing.
5. Center a landmark on the flat table top using the sagittal room alignment laser line.
6. Use the external room laser light to position patient elevation as desired and draw temporary
alignment marks on the skin.
7. Fasten radio-opaque fiducial markers on the temporary alignment marks.
8. Press the Laser Alignment Light button .
9. Press the Cradle In button until the axial landmark location for imaging placed in Step 7
(for example, sternal notch) aligns with the axial internal laser light.
10. Adjust the patient elevation until the gantry elevation laser matches the patient alignment marks
placed in Step 7.
11. Press the Internal Landmark button to establish as the scan reference.
12. Acquire the CT exam with the landmark established in Step 7.

13. Turn on the external room lasers.
14. Press the Cradle Out button .
15. Change the table elevation to match the patient alignment marks placed in Step 7.
16. Review the images and confirm that the radio-opaque markers placed in Step 7 align with the
image coordinate isocenter.
17. Determine treatment isocenter with simulation software such as Advantage Sim.
18. Adjust room lasers as defined by simulation software.
19. Tattoo the patient for therapy.
8.7.4.2 Verify the table elevation accuracy

The purpose of this procedure is to allow a clinical end-user to verify that the workflow for CT
simulation with table elevation adjustment between the room and gantry laser system is working.
Proper readjustment of table elevation, independent of weight distribution, is verified by generation of

Equipment
post-elevation adjustment images with less than 1.0 mm distance between image center and the QA
device feature.
Materials
• flat table top
• 100 pounds of standard weights (25-pound plates recommended)
• MedTec CT Simulation Laser QA device phantom or equivalent device (requires 2 IPPS™ Lok-Bars)
Figure 109 MedTec RT Phantom
Figure 110 CT orthogonal reformat image of laser QA device (abdomen window level)
Elevation adjustment
1. Position the weights and attach the QA device to notches near the center of the flat cradle.

Equipment
Figure 111 Side view of weights and placements relative to the QA device
Number Description
1 table
2 weights
3 QA device
4 flat table top
5 notch 1
6 laser line of sight
2. Adjust the table height until the following occur:

• The room sagittal laser light intersects the side horizontal QA device lines. The coronal
laser light produces the line parallel to the flat table top on the side of the device.
Figure 112 Example of laser light on flat table top
• The room sagittal laser light intersects the top QA device lines.
3. Start an exam.
4. Acquire the Scout over the range of the QA device.
5. Use Graphic Rx to define an Axial scan that produces between 10 mm - 20 mm of images at
the thinnest slice width available.

Equipment
6. From the Scan Settings window, click Anatomy Selection.

Set the DFOV so the image produces isotopic pixels.
• For example, with a scanner producing 0.625 mm slices, a 512 x 512 image with a DFOV
of 32.0 cm will produce images with 0.6253 pixels.
• Formula: Pixel size = DFOV in mm divided by 512.
7. Read and record the table elevation reported on the gantry.
Table 44 Table Elevation Record
Label Record (mm)
Table Elevation
(QA aligned to room laser)
Table Elevation
(QA realigned to gantry laser)
Room 1
Image Center to QA pre-adjustment distance
Image Center to QA post- adjustment distance
8. Start the CT scan to image the QA device.

This image set represents the status prior to elevation adjustments.
9. When the scan is done, readjust the elevation of the table so the gantry sagittal laser lights
align with the sagittal lines on the side of the QA device.
10. Read and record the table elevation in the table elevation record.
11. Repeat the same CT scan series to produce the alignment-adjusted images.
8.7.4.3 Analyze the table elevation

Use the verification analysis procedure for the flat table top to analyze the clinical table elevation.
1. Load the non-adjusted Axial CT image series into a viewing tool with zoom and distance
measuring capability.
2. Scroll to the image so the horizontal feature in the QA device is best visualized in the center QA
feature.
3. Magnify the images to the highest possible zoom to show the cross-hairs representing image
center and the horizontal feature.

Equipment
Figure 113 Sample image prior to elevation adjustment using gantry sagittal laser
4. Use the measurement tool to determine the distance from image center to the center of the QA
feature.
Figure 114 Sample image after to elevation adjustment using gantry sagittal laser
NOTE
Green lines represent lines drawn using a measurement tool; numerical report out
is shown in red.
5. Record the number in the results as “pre-adjustment distance”.

Equipment
Label Record (mm)
Table Elevation
Table Elevation
Room 1
Image Center to QA post- adjustment distance
6. Repeat Steps 1 to 4 for the adjusted-elevation image set.

7. Record the measurement under “post-adjustment distance”.
Label Record (mm)
Table Elevation
Table Elevation
Room 1
Image Center to QA post- adjustment

distance
Results
Post-adjustment QA distance represents the accuracy of table vertical position achievable with the
Recommended Workflow for Treatment Planning.
The post-adjustment image center to QA distance should be less than 1.0 mm, verifying that the gantry
lasers (with elevation adjustment) and room lasers both indicate image center, using the QA feature
location in the image as evidence.
8.7.4.4 Verify the table lateral motion

Sample Analysis
The table below is an example of data used in the interpretation of results discussion.

Equipment
Table 47 Sample Table Measurement Record
Label Record
Measurement Location H2
Weight 100 pounds
Room 1 0.0 mm
Scan Plane 1 -1.5 mm
Room 2 -3.5 mm
Room 3 -3.5 mm
Room 4 -4.5 mm
Room 5 -4.5 mm
Room 6 -5.5 mm
Results
Depending upon the desired level of offset, this method can be used to determine the number of
cycles needed.
• From “Room 6”, note that the initial cradle lateral shift was 5.5 mm. Therefore, if the cradle was
not cycled prior to scanning, the offset at the scan plane relative to the room lasers could be this
large.
• One cycle equals a cradle in and out motion. Some systems may only require one cycle; others
may require three cycles.
• In this example, after one cycle (extend between 890 mm to 850 mm, then retract), the offset at
the scan plane improves by 3.5 mm. Therefore, the actual offset is 2.0 mm (5.5 mm to 3.5 mm)
• In this example, after two cycles, the offset at the scan plane improves by 4.5 mm. Therefore, the
actual offset is 1.0 mm (5.5 mm to 4.5 mm).
8.7.4.5 Measure the table lateral motion

Have your site physicist perform this procedure to measure the amount of lateral cradle motion
between the room and gantry laser system. Use the results to determine how to compensate for it in
the Recommended Workflow for Treatment Planning. This procedure need only be executed once.
Materials
• flat table top
• 100 pounds of standard weights (25-pound plates recommended)
• One metric ruler (minimum 1.0 mm resolution)

Equipment
Setup
• Install flat table top on cradle.
• If your system is a PET/CT system, move table base to CT position.
• Set elevation at 150 mm below isocenter.
When reading the metric scale, it is important to read to 0.5 mm.
NOTE
Determine the number of ½ cradle cycles required for cradle to be centered.
1. From the gantry controls, press the Cradle Out button to return to the home position.
2. Manually slide the front of the cradle to the left or right.

3. Set four 25-pound weights on the flat table top without moving the cradle.
4. Place the metric ruler at the H2 location on the flat table top.
Figure 115 Side view of weights and metric ruler placement
Number Description
1 table
2 weights
3 metric ruler
5. Press the Cradle In button until the ruler aligns with the overhead room laser.
6. Center the ruler on a whole number.

Equipment
Figure 116 Example shows ruler center at 15 cm
Number Description
1 gantry sagittal line
2 room laser line
7. Define a ± coordinate system.
Figure 117 Example shows a piece of paper that defines left as positive and right as negative
8. Press the Laser Alignment Light button .
9. Press the Cradle In button until the internal gantry laser aligns with the long edge of the
ruler.

Equipment
10. Record the laser position on the ruler.

This measurement is labeled “Scan Plane 1” in the table below.
11. Press the Cradle Out button until the ruler aligns with the overhead room laser again.
12. Record the laser position on the ruler.

This measurement is labeled “Room 2” in the table below.
13. Press the Cradle Out button to return to the home position.
14. Repeat Steps 5 through 11 two more times.
Results
Use this table to record the results.
Table 48 Table Measurement Record
Label Record
Measurement Location
Weight
Room 1 mm
Scan Plane 1 mm
Room 2 mm
Room 3 mm
Scan Plane 2 mm
Room 4 mm
Room 5 mm
Scan Plane 3 mm
Room 6 mm
8.8 Hand-Held Controller

During interventional procedures, the clinician makes exposures using the foot switch, and uses the
Hand-Held Controller (HHC) to move the cradle in and out, unlatch and latch the cradle, and review
images displayed on an in-room monitor. The HHC also provides a number of system controls that are

Equipment
described in the table below. The cradle may be positioned with the HHC or by unlatching the cradle
to manually position the patient.
Hand-Held Controller Buttons
Figure 118 Hand-Held Controller

Equipment
Table 49 Hand-Held Controller buttons
Number Button Description
1 Prep Prepares the system for X-ray acquisitions.
Positions the cradle to the start location that is pre-

2 Move to start location scribed from the View Edit screen or moves the
cradle to the last scanned location.
3 Cradle move in Moves the cradle towards the gantry.
Moves the cradle a predefined bump distance to-

wards the gantry. The bump distance is defined
4 Bump in
from the parameters screen. The default Bump dis-
tance is half the scan thickness.
Initiates Auto Move mode, which enables the table

to move automatically as the foot pedal is pressed
in the direction of the movement selected.
5 Auto Move
NOTE
Auto Move is not valid for SmartStep.
Pressing the Change focus button will toggle

through the viewports in circular order and return
6 Change focus
to the default layout. The primary focus viewport
will be enlarged.
Displays the prior image in the sequence. Press and

7 Prior image hold the button to review the images in paging
mode.
Scrolls through six different window width and level

8 W/L toggle
settings.
9 Alignment light Enables the laser positioning lights.
10 Cradle move out Moves the cradle away from the gantry.
Moves the cradle a predefined bump distance away

11 Bump out from the gantry. The bump distance is defined on
the parameters screen.
A toggle button that releases the cradle so it can

12 Cradle Release be moved using the cradle handle. Press the button
again to latch the cradle.
Displays the next image in the sequence. Press and

13 Next image hold the button to review the images in a paging
mode.
8.9 Hardware Components

Equipment
8.9.1 Components
Pre-Patient Collimator
The collimator contains two independently controlled blades. The motion of the blades provides
continuously variable beam thickness and Z-axis position. The collimator also has three bow-tie beam
filters that filter and shape the beam to optimize dose and image quality.
Gemstone Clarity Detector
Features a unique 3-dimensional post patient collimator to ensure HU uniformity and to minimize
scatter / beam hardening artifacts associated with wide coverage systems.
• Provides 160 mm coverage, 512 slices from 256 detector rows in the Z direction. The 256 rows are
0.625 mm in the Z direction.
or
• Provides 80mm coverage, 256 slices from 128 detector rows in the Z direction. The 128 rows are
0.625 mm in the Z direction.
Each signal can be collected from an individual detector row.

The Gemstone scintillator material is created from garnet gemstones fused with a rare earth phosphor
composition.
8.9.2 Coverage
The Axial Detector Coverage/Beam Collimation:
• For the 512 slice system are 5, 20, 40, 80, 100, 120, 140, and 160 mm beam collimation/detector
coverage (0.625 mm).
• For the 256 slice system are 5, 20, 40 and 80 mm beam collimation/detector coverage (0.625 mm).
Table 50 Images per Rotation
Detector Coverage (mm)

Slice Thick-
ness (mm) 5 20 40 80 100 120 140 160
5 1i 4i 8i 16i 20i 24i 28i 32i
5z NA NA 15i 31i 39i 47i 55i 63i
2.5 2i 8i 16i 32i 40i 48i 56i 64i
2.5z NA NA 31i 63i 79i 95i 111i 127i
1.25 4i 16i 32i 64i 80i 96i 112i 128i
1.25z NA NA 63i 127i 159i 191i 223i 255i
0.625 NA 32i 64i 128i 160i 192i 224i 256i
0.625z NA 64i 128i 256i 319i 384i 448i 512i

Equipment
8.9.3 Axial interval

The interval is equal to the number of images per rotation times the beam collimation, e.g., in the
256 x 0.625 mode, 256 images are generated, each 0.625 mm thick for a total of 160 mm of coverage
protection. For collimation greater than 40 mm, a slight overlap is applied when the acquisition
contains multiple table locations.
8.9.4 Helical pitch, scan mode, and collimation

Scan modes for helical are expressed in terms of pitch. Helical pitch is defined as the ratio of table
travel per rotation in millimeters divided by the beam collimation. Previous systems expressed scan
modes with names and defined pitch as table travel per rotation in millimeters divided by the detector
row width.
For example: 55/40 mm = 1.375: 1 (Table Speed (55) divided by the Beam Collimation (40 mm) equals a
Pitch of 1.375.
The following pitches are available:
Table 51 Beam Collimation
Detector Configuration Beam Collimation Pitch
32 x 0.625 20.0 mm 0.5:1 interleaved helices
64 × 0.625 40.0 mm 0.5:1, 0.9:1 interleaved helices
64 × 0.625 40.0 mm 1.375:1 interspaced helices
128 × 0.625 80.0 mm 0.5:1 interleaved helices
128 × 0.625 80.0 mm 0.9:1 interleaved helices
Interleaved helices minimize helical artifact and give the best detail. Interspaced helices have
more interpolated data and increased helical artifact when compared to interleaved mode. Using
interspaced helices compared to interleaved helices will provide lower dose.
8.9.5 Detector configuration

Parameter selections in the Coverage Collection determine the detector configuration.
NOTE
For the 256 slice system, 80 mm configuration, collimations greater than 80 mm are not
selectable.

Equipment
8.9.5.1 Axial
The parameters selected to set the detector coverage (detector configuration) determine the slice
thickness and speed.
• Beam Collimation or detector coverage allows selection of 5, 20, 40, 80, 100, 120, 140, and 160
mm.
• Axial slice thickness choices range from 0.625 to 5.0 mm thick.
• Number of images per rotation is equal to the detector coverage divided by the slice thickness,
except for the 1.25i slice thickness.
• Rotation Time can be adjusted to optimize acquisition time. Rotation Times are 0.28, 0.35, 0.5, 0.6,
0.7, 0.8, 0.9 and 1.0 seconds.
8.9.5.2 Helical
There are five main parameter selections for helical.
• Detector Coverage determines the beam collimation, 20 mm, 40 mm or 80 mm, in the Z direction.
• Helical Thickness determines the primary and secondary reconned image slice thickness.
• Slice thickness choices range from 0.625 mm to 5.0 mm.
• Pitch, detector coverage and rotation time used determines the speed of the table per gantry
rotation. There are two pitch selections with associated table speed.
• Rotation Time determines the speed the gantry rotates in 360°.
• Rotation Time can be adjusted to optimize acquisition time. Rotation Times are 0.28, 0.35, 0.5, 0.6,
0.7, 0.8, 0.9 and 1.0 seconds.
8.10 Power Distribution Unit

The Power Distribution Unit (PDU) supplies power to various parts of the system including gantry
components, table and operator console. On the front of the PDU are controls to indicate that power is
on, a push button to turn power on/off to the gantry and table, and an Emergency Stop button.

Equipment
Figure 119 PDU Controls
Table 52 PDU Controls
Number Function Description
1 Power Indicates power is On/Off to the unit
2 Gantry enable Enables/disables power to the gantry and table
Use the Emergency Stop to stop all table and gantry motions. X-ray
is stopped, and laser alignment lights are turned off. The cradle and
3 Emergency Stop base are also unlatched.
The system aborts any data collection acquisition in progress and
attempts to save any data acquired.
8.11 System Cabinet

The System Cabinet contains the acquisition and image generation compute hardware along with
supporting electronics. This cabinet supplies interfaces between the Scanner Desktop and the Gantry,
allowing for acquisition control, raw data storage, and image generation process.
NOTE
Your system cabinet type will depend on your system software configuration.

Equipment
SDAC System Cabinet
CSDAC System Cabinet - generation 2

Equipment
CSDAC System Cabinet - generation 3
System Cabinet VII
8.12 X-ray Tube and Generator

Refer to the Revolution™ CT, Revolution™ CT ES Technical Reference Manual, System Specifications
(Chapter 7), CT System X-ray Tube Ratings (Section 6) for the maximum tube power limits.
8.13 Purchasable Options

The system supports the following configuration options:
NOTE
Not all Purchasable Options are available in all markets or in all configurations.

Equipment
Table 53 Purchasable Options
Option Description
70 kV Scan Mode Enables 70 kV scan mode.
High Definition Enables High Resolution scanning (focal spot deflection).

Only available with GE Tube.
Cardiac Scan Modes Enables Cardiac scan acquisition modes, External ECG gating
and guides the user in selecting the appropriate cardiac imag-
ing mode based on patient profile.
Provides retrospective review of the gating information and
capability to edit the triggering information on the ECG wave-
form.
ECG Gating Enables internal ECG trigger device. Provides capability to dis-
play and view the ECG waveform on the operator console.
Temporal Enhance Enables Temporal Enhance prescription used with Snapshot

Freeze motion correction.
Reconstruction mode to create images to support SnapShot
Freeze cardiac image post processing.
SmartPhase Enables a reconstruction mode that automatically selects the

phase of least motion within the earliest acquisition part.
Smart Arrhythmia Management Enables automatic retry, if needed when an arrhythmia is de-
tected during gated acquisitions.
SmartMar (metal artifact reduction) A reconstruction technique that reduces photon starvation ar-
tifacts caused by metal implantations.
SmartPrep with Dynamic Transition Enables real-time monitoring of IV contrast and a user-se-
lectable mode to dynamically transition to the diagnostic
scan phase when a user entered Enhancement Threshold is
reached in the Transition ROI.
Fast Scout Enables 2x table speed for scout acquisitions
HyperDrive Enables 0.28s and 0.35s rotation time with 1.375 and 1.531
pitch modes for Helical scanning. Check with product data
sheet for more information and details.
Overlapped Recon Overlapped image reconstruction for Axial scan type.
Organ Dose Modulation mA profile as a function of tube angle to reduce organ specific
dose.
Digital Tilt Protocols that allows prospective tilted MPR.
0.28 Sec Rotation Enables 0.28 second scanning.
256 Slice Enables up to 256 slice generation using 160 mm detector

coverage.

Equipment
Purchasable Options continued

Option Description
3D Dose Modulation Rotational and Z-axis dose modulation.
Dynamic Perfusion Enables protocols that use multiple groups to accomplish vari-
able sampling.
CARDIQ Xpress Provides the user with multiple tools to post process images
from cardiac data sets.
CARDIQ Xpress 2.0 Reveal Provides the user with multiple tools to post process images
from cardiac data sets.
CardIQ Xpress Reveal DL (OC) With the CardIQ Xpress Reveal DL Option, users will benefit
from an improved Heart Segmentation with the implementa-
tion of a new DL-based algorithm to generate Heart Volume
Rendering.
AutoBone Xpress Facilitates removal of bone and CT table from CT Angiography

(CTA) studies of the abdomen and lower extremities.
Advanced Vessel Analysis Xpress — AVA Ex- Provides enhanced analysis of vascular features, which in-
press clude stenosis analysis, pre/post stent planning procedures
and directional vessel tortuosity visualization.
VesseIIQ Xpress and AutoBone (OC) VesselIQ Xpress and AutoBone software option facilitates re-
moval of bone and CT table from CT Angiography (CTA) studies
of the abdomen and lower extremities.
It provides enhanced analysis of vascular features, which in-
clude stenosis analysis, pre/post stent planning procedures
and directional vessel tortuosity visualization.
CT Colon (CTC) Pro 3D_EC — CT Colon Pro 3D Provides comprehensive software package for evaluation of
quick, accurate, noninvasive colon exams.
CardEP Post processing image analysis software for the application of

cardiovascular and electrophysiology imaging.
Volume Viewer 5.0 — Volume Viewer Provides protocols for reformat, 3D rendering and volume ren-
dering.

Equipment

Option Description
Volume Viewer 7.0 — Volume Viewer Volume Viewer provides excellent 3D visualization and pro-
cessing capabilities for reading and comparing CT, MR, 3D
X-ray, PET, PET/MR and PET/CT datasets.
Volume Viewer also features a broad portfolio of high perform-
ancea nalysis tools, automating routine tasks and helping to
make 3D image processing a stress-free component of your
routine workflow. Volume Viewer is the pre-requisite to the
following Image analysis tools on-console:
• AutoBone Xpress and Vessel IQ Xpress
• CardIQ Xpress 2.0
• CT Perfusion 4D Neuro
Volume Viewer is standard on the console.
CT Perfusion 4D Multi-Organ — Perfusion 4D Multi-organ package includes protocols for neuro stroke and
tumor perfusion imaging and body tumor including liver per-
fusion imaging.
CT Perfusion 4D Neuro — Perfusion 4D Neuro Package includes protocols for neuro stroke and brain tumor
perfusion.
CT Perfusion 4D Neuro enhanced (OC) Perfusion 4D Neuro software option is a fast, easy-to-use auto-
mated software for analyzing CT Perfusion images related to
stroke. Its simple user interface and automated perfusion post-
processing make it easy to diagnose quickly and accurately.
The protocol-driven design leads the user step-by-step, reduc-
ing keystrokes and improving repeatability so you get the in-
formation you want quickly and reliably.
Revolution Multi-Phase CTA Stroke Protocol Enables Multi-Pass Head and Neck CTA protocols.
GSI Software Option (GSI Xtream) Enables processing of different energy image data sets to char-
acterize materials.
Available only with GE Tube
SmartPower Enables Partial UPS Feature
Enhanced Xtream Injector • Enables Class 4 in CiA425 of a CiA425 compliant injector

allowing ON/OFF and injector parameters to be set from
the CT scanner.
• The Xtream Injector is a start synchronization of CT scan-
ner and injector.
Tube License Enables non-GE tube usage for High Definition and GSI Soft‐
ware Option (GSI Xtream).
Revolution CT Recon Server Xtream Enables additional computational hardware to increase image
reconstruction throughput.

Equipment

Option Description
Xtream Stroke Enables optimization of system workflow for stroke use cases
[CID Stroke category].
Pre-Requisite: Revolution CT Recon Server Xtream
Xtream ER/Trauma Enables optimization of system workflow for ER/Trauma [CID

ER/Trauma category].
Pre-Requisite: Revolution CT Recon Server Xtream
SmartStep A mode of scanning designed to be used by the Radiologist or

Physician during interventional procedures.
Accomplished by using the integrated Hand Held Controller
(HHC) and foot switch.
DLIR Enables deep learning image reconstruction to create TrueFi-

delity™ CT Images.
DLIR for GSI Enables deep learning image reconstruction to create TrueFi-
delity™ CT Images for GSI reconstruction types
Advanced Cybersecurity Controls Enables advanced security features for access control and data
security.
Intelligent Protocoling Enables automatic recommendation of protocols to the user

for a study session.
MaxFOV 2 Allows user to reconstruct up to an 80 cm FOV image
Lung Cancer Screening Enables Lung Cancer Screening protocols
SmartScore 4.0 (OC) SmartScore 4.0 software option is designed to identify the
presence of regional and global coronary artery calcification
from a CT scan, then measure and score the results.
Scores can be calculated using a standard Agatston/Janowitz
(AJ) method. When correlated with a patient’s personal infor-
mation, the score can yield an estimation of a patient’s risk for
coronary artery disease.
McAfee Standalone Antivirus Enables user management of antivirus scanning on console.
AntiMalware McAfee ePO McAfee ePolicy Orchestrator (McAfee ePO) provides a central-
ized management console that simplifies and accelerates your
security effectiveness with visibility and control from device to
cloud.
Requires connecting to EPO server for Virus Definition updates
and license verification.
Smart Subscription Connection Connection devices to digital processing applications. These

options are offered for commercial sale and distribution via a
alternate Product Configuration Matrix (PCM)

Equipment

Option Description
Smart Subscription AW Server Connection devices to digital processing applications. These

options are offered for commercial sale and distribution via a
alternate Product Configuration Matrix (PCM)
1024 Reconstruction Matrix 1024 Reconstruction Matrix is an additional image reconstruc-

tion matrix selection, to the normal 512 matrix. 1024 matrix
is for improved local detail resolution in lung exams acquired
with a large DFOV and IAC's in the axial plane and better
resolution for cardiac stents. 1024 matrix can be used with
40 mm Axial, Helical, Cine and Cardiac scan modes. It is also
compatible with ASiR-V, Smart MAR, IQ Enhance and Enhance
Filters.

Startup and Shutdown
9 Startup and Shutdown
9.1 Overview
This section describes how to power the system on and off and how to log on and off of the system. It
includes quality control information to verify that your system is operating properly.
For optimal performance, you should restart your system at least once every 24 hours. It is
recommended to shut down and start up the system at least once per week.
9.2 System Startup and Shutdown
9.2.1 Prepare the system

• Clean the accessories and check for damage.
• Check and remove dried contrast agent:
• Scan window (around the gantry opening)
• Table extension and cradle surfaces — especially the patient restraint plastic channels on the
table
• Accessories (head holders, pads and cushions, et cetera)
• Check supplies.
9.2.2 Sign On/Sign Off

When Access Controls is enabled, the sign on/sign off feature becomes active. It requires signing on to
the system by the operator of record for system access. Use of sign on/sign off depends on whether
your site is connected to a central, user repository. Sites with networks are referred to as enterprise
systems; other sites are referred to as standalone systems. The sign on/sign off feature can be used
with either system.
Signing off does not prohibit other users from signing on. Sign off is designed to protect patient
privacy. It is not intended to stop approved users from signing on. When you sign back on after a sign
off, the system returns the last state of the system.
9.2.2.1 Sign on window

The Sign on window displays when you restart the system or when someone has signed off.

Figure 120 Sign on window
Element Description
Sign on Name Enter your sign on name. Your system administrator can setup a unique
sign on name through your hospital enterprise system.
Password Enter your password. The password is assigned by the system administra-
tor.

(continued)
Element Description
EmergencySign on Launches the Emergency Sign on window when Access Controls (EA3) is
enabled. It does not require an ID or password on your enterprise system.
You must enter your name in the field before Emergency Sign on will be
allowed.
Figure 121 Emergency Sign on window
Sign on Click to sign on.
Cancel Quit the sign on procedure.
9.2.2.2 Sign On
If Access Controls is enabled, use the following procedure to sign on to the system.
1. From the Sign on window, enter your sign on name.
2. Enter your password.

NOTE
If you do not have a valid account, click Emergency Sign on. The Emergency Sign
on window displays. Signing on does not require an ID or password. You must enter
your name in the field before sign on will be allowed.
3. Click Sign on.
9.2.2.3 Sign Off

If Access Controls is enabled, use the following procedure to sign off from the system.
2. From the Mode menu, click Switch User.
NOTE
Signing off does not prohibit other users from signing on. Sign off is designed to protect
patient privacy. It is not intended to stop approved users from signing on. When you sign
back on after a sign off, the system returns to your last known state.
NOTE
When signed on as Emergency User, only 5 exams can be scanned. The user is then
prompted to sign back on to the system to be able to scan additional exams.
NOTE
Switch User is not active when the system is in the scanning state, that is, if scan
confirmed and scan monitor is on the scan progress screen.
9.2.3 System Start Up

NOTICE
AFTER A POWER INTERRUPTION, WAIT TWO MINUTES BEFORE TURNING

ON POWER TO THE MAIN DISCONNECT CONTROL.
NOTICE
USB MEDIA IS ATTACHED. REMOVE THE USB AND SELECT RESTART /

SLEEP / POWER DOWN TO PROCEED.

NOTE
It May take up to 30 minutes for the detector to reach an optimal thermal state after
startup.
SmartID verifies the tube ID at start up. If the tube ID verification fails, attention messages display
indicating that the X-ray tube is not recognized. You can continue scanning; however, you will need
to contact your service representative. Hi Res and GSI scanning are disabled when a non-GE tube is
installed.
1. Make sure the power switch on the back of the computer cabinet, in the upper right corner is
turned ON.
2. Make sure no USB device is connected.
3. Determine power state of system.
• The power button on the scan control interface will be lit when the system is in an
operational state.
• If the system is in a power down or sleep state, the power button on the scan control
interface flashes slowly. When the operator console is powered off, the moon icon on the
gantry display is lit.
• Power was off to the entire system (Main disconnect Control A1 Power Panel breaker is
turned off)
4. If power is turned off to the entire system:

• Turn on power to the Main Disconnect Control.
• Press < E-Stop Reset> on the gantry controls to allow x-ray, table and gantry motions.
5. Once power is on and the system is in power down or sleep state:

Press the power on button on the scan control interface to start the system.
The power on button will flash for a few seconds indicating that the system has received the
command.

Follow any instructions on the console display as the system starts up.
NOTE
Systems with Configuration 3 or 4 scanner desktop do not require pressing the
power on button on the scan control interface to that the system.
Figure 122 Scan Control Interface Power On button
6. If system or in-room monitors fail to start up:

If the system fails to start up completely, toggle the power switch on the back of the computer
cabinet, in the upper right corner, to ON.
If the in-room monitor remains black after a startup, recover by pressing the power button or
input select button on the affected monitor. The log on screen appears.
9.2.4 Power Management

NOTICE
DO NOT RESTART THE SYSTEM WITH A USB DEVICE CONNECTED.
NOTICE
MOVING THE SYSTEM INTO POWER DOWN STATE WILL LOSE THE THERMAL
STATE OF THE DETECTOR.
For Optimal system performance:

• If your site turns off main power, use Power Down.
• If your site does not turn off main power, use Sleep. Sleep powers off the host computer, but
leaves power to the gantry. There is no wait time needed for the rotor to stop as power remains
to the gantry. To start the system from Sleep, press the flashing power button on the Scan Control
Interface.
System Restart should be done daily. Restart shuts down applications and operating system software
as well as resetting the scan hardware. There is no wait time needed for the rotor to stop during the
Restart processes. The system returns to operational state without user intervention.

1. Close any open study.

2. Remove any USB devices before restarting or shutting down.
NOTE
If a save or restore of scan data is in progress, wait for the process to complete,
exit Scan Data Manager, and remove the USB device. If the system shuts down
unexpectedly while a USB drive is connected, remove the USB drive prior to
restarting the system.
4. From the Mode menu, click Power Management, then select Power Down, Sleep or Restart.
5. Check the console display for messages that require your attention. Follow any instructions.
6. From the dialog box , click Power Down or Restart.
7. The system indicates when it is entering the power down/sleep state or when restart is complete.
If power down or sleep was selected, the monitors will turn off when process is complete. If
restart was selected, the system indicates when the restart is complete.
9.3 Daily Quality Assurance

To ensure consistent image quality, establish and maintain a regular quality assurance program.
9.3.1 Tube Warmup

The system operates most efficiently within certain parameters. These parameters are established by
warming the tube using a preset group of exposures. When you perform a tube warmup at least once
every 24 hours and at any system prompt, it reduces the possibility of image artifacts, and may aid in
prolonging the life of the tube.
When you start the scan, a series of air scans are performed as part of the tube warmup scans.

9.3.2 Calibration
9.3.2.1 Daily calibration

The system requires that all kV and mA settings be within specific ranges. These ranges are established
and maintained by performing air calibrations. These calibrations are performed as part of the daily
system preparation following a tube warmup procedure.
Daily calibration (Fast Cal) must be performed every 24 hours to maintain image quality.
Table 54 Single kV Fast Cal notifications
Fast Cal State State User Information
Single kV Fast Cal was completed When a single kV Fast Cal was done
and current. within last 24 hours, calibration is
fresh and in good condition. Users
can use the system normally.
NOTE
Hover the mouse over the
Fast Cal card and a mes-
sage will be displayed,
showing the timestamp
of the last single kV Fast
Cal run.
Single kV Fast Cal has not been A Fast Cal needs to occur once ev-
completed within 24 hours. ery 24 hours, in order to ensure
good image quality.
Run single kV Fast Cal.
Single kV Fast Cal is unknown. If the single kV Fast Cal completion

timestamp file is missing or Cal his-
tory cannot be determined, user
must run Fast Cal to ensure good
image quality.
A new timestamp will be created to
record the completion of the new
Fast Cal just ran.
Messages will vary depending on if GSI software option has been installed.

Table 55 Single kV Fast Cal & GSI notifications
Both single kV and GSI Fast Cal are When a Fast Cal was done with-
good. in last 24 hours and, a GSI Fast
Cal was done within 168 hours (7
days).
GSI Fast Cal is good however, sin- The last single kV Fast Cal was
gle kV Fast Cal has not been com- done more than 24 hours ago how-
pleted within 24 hours. ever, a GSI Fast Cal was done with-
in 168 hours (7 days).
GSI Fast Cal has not been complet- GSI FastCal was not done within
ed within 168 hours (7 days). last 168 hours.
Run Fast Cal with GSI.
The last single kV Fast Cal run is If the single kV Fast Cal completion
unknown however, GSI Fast Cal is timestamp file is missing or Cal his-
good. tory cannot be determined, user
must run Fast Cal to ensure good
image quality.
Fast Cal just ran.

Single kV Fast Cal & GSI notifications continued

The last single kV Fast Cal run is If the GSI Fast Cal completion time-
known however, GSI Fast Cal is un- stamp file is missing or Cal history
known. cannot be determined, user must
run Fast Cal with GSI to ensure
good image quality.
Fast Cal just ran.
When both the last single kV and If the Fast Cal completion time-
GSI Fast Cal were run however, stamp files for both single kV and
both are unknown. GSI are missing, Cal history cannot
be determined, user must run Fast
Cal with GSI to ensure good image
quality.
Fast Cal just ran.
Daily calibration performs several automatic checks:

• Tube Warmup, if needed.
• The system confirms the gantry is in balance with a gantry balance check.
• The system confirms the scan window is clean with a scan window check. If the scan window is
dirty or obstructed, it could lead to image degradation.
The system prompts you to clean it and remove any obstructions. Click Retry to repeat a scan
window check, or click Continue to proceed to Fast Cal without repeating the check.
The number of tube warmup scans depends on the current temperature of the tube.
The system finishes the Fast Cal procedure by performing a set of 3 scans.
1. Bad Channel
2. BasisAir
3. GSIRefreshAir (only if GSI Software Option (GSI Xtream) option installed)

Figure 123 Fast Cal Progress Window
9.3.2.2 Full system calibration

Full system calibrations are normally performed by a qualified Service Engineer following a tube
change or as part of preventive maintenance.
9.3.2.3 Non-GE X-ray tube

When the system is configured to use a non-GE X-ray tube or if the tube is unrecognized by the system,
an alert is posted during system startup, tube warmup, and fast calibrations that a non-GE X-ray tube
is detected in the system configuration. System configurations with non-GE X-ray tubes will be noted in
the Dose Report. A notification about using a non-GE X-ray tube will also display in protocol selection
and management.
NOTE
If the system has an unrecognized X-ray tube:
• The performance of the system cannot be guaranteed.
• Tube warmup scans may cause subsequent tube cooling delays. The tube warmup
will run in Auto scan mode.
• Fast calibration techniques are designed specifically for GE tubes. GE cannot
guarantee that the performance of the system will meet specifications with an
unrecognized tube.
9.3.3 Daily QA workflow

1. From the image monitor, click the Utilities icon .
2. From the Utilities menu, click Daily Prep, then Fast Cal.
The Service-Calibration Tools window opens.
3. When the fast calibration is complete, perform a quality assurance scan.
4. Restart the system, if not restarted in the last 24 hours.

9.3.4 Tube Conditioning

NOTICE
Please refer to the Safety chapter for important safety information

regarding the use of the equipment and software on this system.
The system operates most efficiently within an optimal thermal operating state. Operating within this
state reduces the possibility of image artifacts and may aid in prolonging the life of the tube. The
System dashboard Conditiontion card displays the Tube state and allows tube conditioning to be
performed.
• SmarTube warmup optimizes system scanning performance by including an indication of the
temperature state of the tube. Operating the system in the green zone will maximize tube life.
• The tube state is indicated by the Tube Conditioning cards. The time indicated on the card
represents approximately how long before the tube is cold. If the tube temperature is not in the
optimal range, a message will display when your cursor is hovered over the card to indicate the
tube condition.
Table 56 Tube Conditioning Cards
Conditioning Card Tube Message User Action
Tube is optimal. Normal scanning temperature. Proceed

with scanning.
Time indicates how long the tube can re-
main idle before tube warmup is required.
Tube is cold. Run tube Click the tube icon, or Condition Now.
warmup. Time indicates how long the tube can re-
Tube warmup recom- Wait for the warmup to complete before

mended. scanning.
Time indicates how long the tube can re-
• Perform conditioning when the status is tube warm up is recommended or when the tube is cold.

• For the best care of your tube, never skip the tube conditioning.
• To avoid delays in scanning, check the tube state before moving patients into the scan room.
• If a patient exam is started when the system is below the optimal thermal state, the system
displays a message to the user describing scanning limitations; mA is limited and GSI scanning is
prohibited in this state. You must accept scanning limitation or you can end the exam, ensure the
patient is out of the room and perform Condition Now or Choose Conditioning.
Table 57 Cold mA Limits by Focal Spot and kV Standard Resolution Performix™ HDw
Focal Spot 70 kV 80 kV 100 kV 120 kV 140 kV
S 165 mA 165 mA 165 mA 165 mA 165 mA
L 330 mA 330 mA 330 mA 330 mA 330 mA
XL 330 mA 330 mA 370 mA 370 mA 370 mA
Table 58 Cold mA Limits by Focal Spot and kV High Resolution Performix™ HDw
Focal Spot 70 kV 80 kV 100 kV 120 kV 140 kV
S 165 mA 165 mA 165 mA 165 mA 165 mA
L 330 mA 330 mA 330 mA 330 mA 330 mA
Acceptable mAs (mAs = mA × Rotation Time) can be achieved by changing rotation times as
needed.
• If the detectors are cold due to an A1 Power Panel (breaker) being off, turn the system on and
wait two hours before performing a tube warmup. This allows the detectors to return to operating
temperature.
Condition Now
1. Ensure no one is present in the scan room.
2. Click System Dashboard Tab.
3. Click Condition Now. The Tube Conditioning status bar displays.
4. Press Start Scan button on the keyboard. The Tube Conditioning status bar displays progress and
closes upon completion. The tube conditioning scans can be paused and resumed or cancelled by
clicking the applicable button.
9.3.5 Run Fast Calibrations

NOTE
PLEASE REFER TO THE SAFETY CHAPTER FOR IMPORTANT SAFETY INFORMATION

• If the detector is not at operating temperature, a message will indicate when the detector is at the
appropriate temperature.

• If there is a large shift in room temperature (±10 degrees), perform a Fast Cal to maintain optimum
IQ. Once the room temperature has stabilized, perform another Fast Cal.
For the permissible environmental operating conditions for the CT scanner, see Technical
Reference Manual Chapter 7 Systems Specifications, Environmental Specifications.
• The system will indicate if more than 24 hours have elapsed since the last Fast Cal.
• If a scan abort occurs during Fast Cal, notify your Service Engineer.
• The system will indicate if an unrecognized tube has been installed on the system. Fast
Calibration techniques are designed specifically for GE tubes and GE cannot guarantee that the
performance of the system will meet specifications with an unrecognized tube. Fast Cal will run in
AutoScan mode.
• When the GSI option is installed, GSI calibrations will be performed during Fast Cal.
1. Clear the gantry of any objects or personnel. Any obstruction in the gantry may lead to artifacts in
scanned images.
2. From the Utilities menu, click Daily Prep, then Fast Cal.
The Service-Calibration Tools window opens.
3. Click Run.
4. Press Start Scan. Respond to all messages that display during the calibration (approximately 15
to 20 minutes). Execute any necessary actions indicated in the messages.
• If the system detects a dirty scan window (which may be caused by a beam obstruction,
something in the gantry, contrast, dirt, or other matter on the scan window), a message
displays. Clean the scan window and click Retry or click Continue to skip the check.
• The following automated calibration check procedures occur: tube warmup (if needed),
balance check, scan window check, bad channel, collimator screening, focal spot air, focal
spot size monitor and basis air scans. If the GSI option is installed GSI refresh air scans will be
taken every 7 days. Read the screen messages for calibration status.
5. The system returns to the Service-Calibration Tools window when the checks are complete. Click
Dismiss to exit the window.
9.4 Software Update

Software Update facilitates software updates to the CT Scanner. Software download must be enabled
by your Field Service Engineer.
When Software Update is enabled, and the system is connected to the GEHC Service Platform, the
system automatically receives any available software updates.
The user is notified of available updates on the System Status Dashboard Health Menu.

Table 59
SW Update
No software update available.
SW Update
• Software Update Available and being download-
ed
• Showing percentage completed
SW Update
• Software Update Available.
• Installation time: xx min
• Restart and Install Updates(s)
SW Update
Update Available, call GE service to install.
Use this procedure to download software updates.

1. Click System State Tab > > System Health to view the SW Update Card.
2. When time is available, Click Update Now.
3. If the current signed-in user in not authorized to install the SW Update, the system opens a dialog
box with the message Please login as an authorized user to install this SW update.
4. Once the authentication (if required) is successful, the Software Delivery Manager displays listing
the SW updates available to install.

5. On the IRIS Software Delivery Manager, the user can perform one of the following actions:
a. Click Details to see more details about the SW Update.
b. Click Decline to open a form to document the reason to decline the update. The information
provided is logged on the system and sent to InSite back office. A Decline System Update
confirmation displays. Type First Name, Last Name, Role, Reason for Declining. Click box
I acknowledge that I am declining download of recommended update(s). Click Decline
Update.
c. Click the X button to dismiss this window.

d. Click Install Now which opens another message request to confirm and to Proceed.
6. If the SW update is a Service Pack, then the following alert displays, prompting the user to
confirm the system is going to be restarted.

7. If the SW update is a full load (LFC) that will delete all data on the system disk, then the following
alert displays for the user to confirm:
a. The user is aware of the potential loss of data that was not backed up.
b. The system is going to be restarted.
NOTE
Before powering down, restarting the system or going into sleep mode, please close
any open Exam tab sessions and complete pending recon jobs. Failure to do so will
result in the loss of data currently in progress.
8. At this point the system will reboot and the SW update will be installed.
9. In case of a Service Pack, once the SP installation has completed successfully, the following
message displays:

10. If the SP installation has failed, the following message displays:
11. In case of an LFC, multiple boots might follow. During the installation process, the following
progress bar displays:
12. Once the LFC process has completed successfully, the following message displays.

13. If the LFC process has completed with warnings, the following message displays,
14. If the LFC process has failures, the following message displays.

9.5 Power Loss with SmartPower (Partial UPS)

In a power loss event, the Partial Uninterrupted Power Supply (Partial UPS) with the SmartPower
Option allows system components, scanner desktop, system cabinet and table to remain operational
for the duration of the battery life. Scanning will be disabled while on battery power.
When the SmartPower option is installed, the system will report the status on the UPS Card, and will
monitor battery status to ensure a controlled power down occurs when the battery is depleted.
System is on wall power and UPS battery charge is

full.
System is on wall power and UPS battery is charging

System is operating on battery backup.

Scanning is disabled.
Table functions to remove patient.
Complete any reconstructions, DMPR and image
transfer tasks.
System is operating on battery backup and battery

power is low.
When the battery is low the system will prompt the
user that a shutdown will occur within 60 seconds.
The user may cancel the shutdown. This should be
done only if there is an urgent task that can be com-
pleted within 3 minutes.
When battery level is critically low , the system will in-
itiate controlled power down sequence automatically.
System cannot communicate with UPS or UPS is in

fault condition.

Patient Schedule
10 Patient Schedule
10.1 Overview
Use Patient Schedule to enter patient information and protocols in advance of the patient's arrival.
Patient Schedule can also display patient information from the HIS/RIS.
At scan time, select a patient from the list, enter the patient ID number, enter the accession number or
use the optional bar code reader to open the patient's information.
You can edit patient information from the Schedule. If this patient record was entered at the scanner,
you can proceed with the exam or save the updated information back to the schedule. If the patient
record came from the HIS/RIS you can update patient information only if you proceed with the exam.
10.2 Patient Schedule
10.2.1 Schedule features
10.2.1.1 Schedule window

Click the Patient Schedule drawer on the left side of the left monitor to display the Schedule window.
Figure 124 Schedule window

Patient Schedule
10.2.1.2 Schedule columns

Show Completed WL' in preferences -> scheduler configuration UI -> Configuration UI
The default columns displayed on the Schedule include:
• Patient name – the name displayed “Last name, First name”.
• Patient ID
• Accession Number
• Exam Description
• Scheduled date – in the date/time format configured on this system.
• Scheduled time
• Exam status – only 2 states are supported – new and completed. This column will not be displayed
if completed exams are configured to not be displayed.
Additional columns are available. These include:

• Referring physician
• Protocol name
• Patient name in ideographic form (for Chinese or Japanese language configuration only)
You can select the columns to display or hide on the Schedule by right clicking on the table header and
using the Column Chooser drop-down as shown below. The changes you make display each time the
drawer is opened, even after restarting the system.
NOTE
Take care to add only the columns you need. Too many columns on a table can make it
more difficult to find the information you need, and may slow you down when using the
table.
Figure 125 Schedule Column Chooser
Changing Column Order

Patient Schedule
You can change the order in which columns display by clicking and holding the cursor
1. Position the cursor over the heading of the column you want to move.
2. Press and hold the left mouse button.
3. Drag the column to the location you want it to appear.
4. Release the left mouse button.
10.2.1.3 Schedule buttons and icons
Table 60 Schedule buttons and icons
You can select a patient from the Schedule by double

clicking on the patient’s row or by highlighting the
patient and clicking Select Patient in the bottom right
of the Schedule.
Click the Info icon to open the Patient Information

window and show all patient information including
age, weight and history, as well as allergies, pregnan-
cy status and medical alerts. The Info icon displays
both on patient records pulled from the HIS/RIS, and
from patients entered locally.
Caution Info Icon — Indicates some important infor-

mation about the patient that will affect the exam. For
example, the patient has an allergy to the standard
contrast agent, so a different contrast agent is needed
for this patient’s exam.
Remove patient from the Schedule. The button dis-

plays only for entries that were not received from the
HIS/RIS. Patients received from the HIS/RIS can be
deleted only on the HIS/RIS.
10.2.1.4 Schedule drop-down menu

Access additional Schedule related functions from the drop-down menu at the top right of the
Schedule.

Patient Schedule
Figure 126 Schedule Drop-down menu
Table 61 Schedule Drop-down menu
Element Description
Add Patient Open the Patient Schedule information window,

where you can enter the patient's information and
add the number of a specific protocol. You can add
the patient, then start an exam or add a patient to the
schedule for a future exam. Add Patient is enabled
only if no other tab is in the “Not Yet Scanned” state.
Add Patient performs the same function as the New
Patient icon, in the upper left of the monitor.
Edit Patient Open the Patient Schedule information window,

where you can edit the selected patient's information.
Refresh List Update the Schedule from HIS/RIS. This menu item is
visible only if a HIS/RIS is configured on this system.
The drop-down selection also displays the time since
the last update.
HIS/RIS Search Open the search window. This menu item is visible
only if a HIS/RIS is configured on this system.
Refresh Setup Allows you to setup automatic refreshes from the

HIS/RIS at specific intervals, and to specify what data
you query from the HIS/RIS.
Preferences Allows you to set up a connection to a HIS/RIS.
Delete All Completed Delete all completed exams from the Schedule.

Patient Schedule
10.2.2 New and completed records

Patient Schedule incudes a column labeled Status. In the Status column, an N or a C is listed next to
each patient entry.
• N indicates the record is incomplete or is a new record. These are records for patient studies that
are scheduled in Patient Schedule, but are not yet completed.
• C indicates the record is completed.
NOTE
When accessing patient information from the HIS/RIS you should have only new records
in your schedule list. Having completed records may cause scanning a patient with
the wrong accession number. To clear completed records; select Preferences from the
Schedule drop-down menu. Then select Scheduler Configuration UI and Configuation
UI. Uncheck the Show Completed WL box . This setting assures that completed records
are not added to the schedule list.
Figure 127 Show Completed WL
10.2.3 Add a patient to the Schedule

To manually add a patient to the Patient Schedule, follow these steps:
1. Click the New Patient icon .
From the scan monitor, click the Patient Schedule drawer. Then select Add Patient from the
Schedule drop-down menu in the top right corner of the window.
2. Complete all relevant fields on the Patient Information window. Refer to Setup the patient
information in the Scan chapter for more information.
If you are using Exam Split with Hard Exam Split mode to add a patient, you must enter an exam
description.

Patient Schedule
3. From the pull down, click Save to Schedule to add the patient to the schedule or Cancel to close
the window without adding the patient.
NOTE
If a protocol is selected, clicking Accept at this point will begin the exam.
NOTE
If there is already a Patient on the table session active, Save to Schedule or Cancel
will be the only choices presented.
10.2.4 Edit a patient in the schedule

You can edit the information of patients added on the scanner then save the information back to the
schedule. You can edit information of patients that were added to the schedule from the HIS/RIS only
if you will proceed with the exam for that patient. Saving the edits of patients from the HIS/RIS is
prohibited because the edits would be lost the next time the schedule is refreshed from the HIS/RIS.
NOTE
You cannot edit patient records from HIS/RIS if Enable RIS Worklist Edit is not selected
in Patient Schedule Preferences.
1. From the scan monitor, click the Patient Schedule drawer.
2. From the Schedule window, select a patient.
3. Click on the Information icon on the left of the patient record or:
Select the patient you wish to edit, right click and select Edit Patient.
4. Edit the patient information.
5. Click Save.

Patient Schedule
Figure 128 Patient information card open with MORE tab displayed

Patient Schedule
Figure 129 Patient information card open with Less tab displayed

Patient Schedule
NOTE
The above pictures are showing how the user can obtain additional information from
the order entry. The "More" expanded view will automatically display, if there is
additional DICOM information embedded into the RIS order pertaining to:
• (0x0010,0x21C0) PregnancyStatus
• (0x0010,0x2000) MedicalAlerts
• (0x0010, 0x2110) ContrastAllergies
• (0x0038, 0x0500) PatientState
• (0x0038, 0x0050) SpecialNeeds
If the user does not want to see this information set during a one-time patient exam;
simply click the "Less" button at the bottom.
If the user no longer wants to see information automatically populate the Pregnancy
Status, Medical Alerts, Contrast Allergies, Patient State, Special Needs fields; the user
must finish all patient exams before any steps are followed:
1. Open patient scheduler tray
2. On the top right, click the 3-bar icon
3. Select the WF Preferences option
4. Navigate to the Return Tag Configuration UI and open the folder
5. Remove all the DICOM tags you are no longer interested in displaying
*If you choose to unselect boxes for certain associated DICOM tags, those DICOM tags
will not be available in the scanned image, since it is not returning during a RIS query.
NOTE
Return tag configuration needs application restart to apply the changes.
10.2.5 Delete a patient from the schedule

2. From the Schedule window, select patients to be removed.
3. Click the Delete icon at the right of the patient row . This applies only for locally created
patients. Alternatively, click Delete All Completed from the schedule drop-down menu to remove
all the completed patients, those marked with C.
4. Click OK to confirm.

Patient Schedule
10.2.6 View more patient information on the schedule

Use this feature to view all patient information. This information is pulled from the HIS/RIS using a
DICOM Modality Worklist (MWL). Patient information can also be entered locally.
2. From the Schedule window, click the Information icon for the patient. The screen is
populated from your HIS/RIS. It also displays information entered locally.

If there is a caution for the patient, you will see the Caution Info icon .
3. Click Close to close the Patient Information window.
10.2.7 Select a patient from the schedule

Use this procedure to select a patient from the Patient Schedule to begin an exam.
1. Click anywhere on the Patient Schedule drawer.
2. From the Patient schedule list, select the desired patient and click Select Patient.
The Patient Information screen fields are populated.
• Multiple records for the same patient can be selected.
• Multiple records must be selected in order to use Exam Split.
3. Select desired protocol and then click Accept. The system displays the scan series tasks in the
protocol.
10.2.8 Check a patient's status

To check the patient’s status, follow these steps:
2. View the Status column.
• N – New Record or Not Completed
• C – Completed
3. Click and drag the scroll bar to browse through the list.

Patient Schedule
10.2.9 Search for a Patient on the Schedule

Figure 130 Schedule Search
Type a character in the search box at the top right of the Schedule. All patient names, patient IDs and
exam descriptions that contain that character display both on the Schedule and on the drop-down list
below the search box.
The drop-down list indicates the field containing the characters. The schedule title bar highlights
orange when the list is filtered. For each additional character typed, the list of patients is filtered. The
search/filter is case sensitive.
10.2.10 HIS/RIS Search

Use this feature to search the HIS/RIS for a patient. This functionality is available only if a HIS/RIS is
configured on this system.
2. Select HIS/RIS Search from the Schedule drop-down menu.
3. Enter all or a portion of the:
• Patient Name — first or last
• Patient ID
• Accession Number
• Procedure ID
4. Define the search parameters using the Date Range check boxes. For example, find all patients
scheduled for exams on the current day by clicking Today.
5. Define the search parameters using the Search RIS for check boxes.

Patient Schedule
• This system — searches for patients scheduled only on the scanner on which you are
working.
• This modality — searches for patients scheduled on all CT systems on the HIS/RIS
connection
• All Modalities — searches for patients scheduled on all devices, such as CT and MR scanners.
Figure 131 HIS/RIS Search
Figure 132 HIS/RIS search results

Patient Schedule
All patient names, patient IDs and exam descriptions that contain that character display both on the
Schedule and on the drop-down list below the search box.
The drop-down list indicates the field containing the characters, up to 5 entries for each field. If there
are more than 5, a link at the bottom of the category indicates how many more matches were found,
such as: “35 more”. If the user clicks on that link, it searches only that field for those entries and shows
the matches in the schedule. For each additional character typed, the list of patients is filtered. The
search/filter ignores the case of any characters entered.
10.2.11 Setting up the HIS/RIS Refresh

You set how the schedule refreshes on the Refresh Setup window. Once set, the list is refreshed
the same way each time you select Refresh from HIS/RIS. You can also set the schedule to update
automatically.
2. Select Refresh Setup from the Schedule drop-down menu.
• Select This System to pull the patient schedule for the scanner on which you are working.
AE Title: The calling AE title for the CT system is used by the Patient Schedule application
when a Modality Worklist C-FIND request is performed. If the local system's calling AE title
does not match the expected AE in the remote HIS/RIS configuration (or the local system
is not configured on the remote HIS/RIS), the remote HIS/RIS may fail to return worklist
entries to the local system. The calling AE title defined in System Preferences is used when
opening the association to the HISRIS. This AE will also be used in the Scheduled Station AE
Title (0040,0001) tag in the C-FIND request if This System option is selected in the Schedule
Refresh Setup menu.
Figure 133 Schedule Refresh Setup window showing This System selected

Patient Schedule
The local system's calling AE title is generally the same as the hostname but it can be a
different value depending on the site-specific operation of the hospital HIS/RIS server. Check
with Modality Worklist’s site IT administration to identify what Calling AE title should be
configured for this system.
• Select This Modality to pull the patient schedule for all of the CT systems on the HIS/RIS
connection.
• Define the search parameters using the Date Range check boxes. For example, pull all exams
scheduled for the current day by clicking Today.
• Select All Modalities to pull the patient schedule for all of the systems on any modality
(for example CT, MR, etc.) on the HIS/RIS connection. This is the default setting. Not
recommended. Depending on your site, this may be a very long list.
3. Enter values for the Date Range.

4. Indicate how and when the refresh occurs.
• Check the Refresh Worklist on Startup button to refresh the Patient Schedule from the
HIS/RIS each time the system is restarted. This box is selected by default.
• Check the Refresh worklist only when button is clicked button to prevent automatic
updates and refresh the Patient Schedule from the HIS/RIS only when the user selects
Refresh List from the Schedule drop-down menu.
• Check the Auto-Refresh Timing button to activate automatic updates to the Patient
Schedule. This box is selected by default.
• Select the frequency of the automatic refresh using the drop-down list of time increments.
You can choose increments of time from 2 minutes to 1 hour.
5. Click Save to update Refresh Setup with your changes or Close to quit Refresh Setup without
changing the settings.

Patient Schedule
Figure 134 Refresh Setup
10.2.12 Update the patient schedule

Follow these steps to manually launch a refresh of the Patient Schedule. You can also have the system
refresh the Schedule automatically. Refer to Setting up the HIS/RIS Refresh on page 267 refresh for
more information.
To update the patient schedule from the HIS/RIS and Modality Work List, follow these steps:
2. Select Refresh List from the Schedule drop-down menu.

Patient Schedule
NOTE
Patient records may fail to display if the record has data contained in DICOM fields that
does not follow the DICOM standard. A message will be posted to the system error log
noting the faulty DICOM field.
Patient records will also fail to display in Patient Schedule if DICOM tag 0008, 0005 or
Specific Character Set is not filled with the correct character set designation.
Character sets supported are:
• ISO_IR 100 Latin 1 (example Swedish and Latin alphabet)
• ISO_IR 87 Japanese/Kanji
• ISO_IR 6 US-ASCII
10.2.13 SCP Configuration

Use SCP Configuration to connect the system to your site’s HIS/RIS system.
2. Select Preferences from the Schedule drop-down menu.
3. Select MWL SCP Configurations, then SCP Configuration from the menu tree on the left of the
window.

Patient Schedule
Figure 135 SCP Configuration
4. To add a new host, click the New button. To edit an existing host, double click the host from the
list at the top of the window.
5. Your service engineer can provide you with the specific values for these fields.
• Host/IP: This is the name given to the network node of the currently selected node. The
IP represents the location of the node within the network. You must enter the IP (Internet
Protocol) address correctly or the connection cannot be made.
• Port Number: This is a predetermined number specific to the type of host and the protocol
used.
• AE Title: The AE Title of HIS RIS Server.
• Default Selected: Check this box to indicate that the connection you are configuring is to be
considered the default.
6. Once you have entered or updated the information about the host, click Ping to make certain the
connection has been made correctly.
7. Click Save to add the configuration.
Deleting an SCP Configuration
1. Navigate to the SCP Configuration window, following steps 1 through 3 above.

2. Highlight the configuration you want to delete from the list at the top of the window.
3. Click Remove. Click Yes on the confirmation window.

Patient Schedule
Figure 136 Delete SCP configuration confirmation
10.2.14 Return Tag Configuration

Some of the DICOM tags in MWL queries may not be supported by all SCPs.
Return Tag Configuration allows users to include or exclude configurable tags in MWL queries.
2. Select Preferences from the Schedule dropdown menu.
3. Select Return Tag Configuration UI, then Return Tag Configuration from the menu tree on the
left of the window.

Patient Schedule
Figure 137 Refresh Query Tag Selection
4. Select a tag from the checkbox.

5. Click Save to save the settings.
6. A tag that is checked will be returned when a query is performed.

Patient Schedule

Scan
11 Scan
11.1 Overview
NOTICE
PLEASE REFER TO THE SAFETY SECTION FOR IMPORTANT SAFETY

INFORMATION REGARDING THE USE OF THE EQUIPMENT AND SOFTWARE
ON THIS SYSTEM.
11.1.1 Considerations
• If you encounter a message that you need to remove images to be able to scan the current series,
first remove images to create space for scanning.
• In general, if a scan fails and a request to Resume is posted, click Resume to continue. Click
Resume again if the first action fails. If the scan still fails to restart, shutdown and restart the
system.
11.1.2 GSI—specific Considerations

High and low kV and mA are fixed and cannot be changed.
GSI MAR for GSI imaging should only be selected when the entire metal object is fully contained in the
volume that is being scanned. Reconstruction with and without GSI MAR should always be prescribed
for comparative image review.
GSI is not available for interventional scan modes (SmartPrep baseline or monitoring images or
SmartStep).
GSI preset families set the SFOV, rotation time, pitch, focal spot size and detector coverage for a scan.
Selecting a different GSI preset family is the only way to change these parameters.
Quality Check images are created from high kVp data that do not have all standard corrections applied
and are identified accordingly. The Quality Check images are not stored in the image database and are
intended only to allow the user to check basic scanning coverage and anatomy coverage.
High KVP images are created with the full single energy reconstruction algorithm using the high kVp
data.
Monochromatic images with a keV of 40 to 140.
Virtual Unenhanced (VUE) images can be reconstructed prospectively or prescribed post scan. VUE is
not available for Head SFOV.
Material Density images can be reconstructed prospectively, prescribed post scan or created in the GSI
Viewer on the Advantage Windows when the GSI Data File has been prescribed for the reconstruction.
Monochromatic images with GSI MAR cannot be prescribed for the primary recon.

Scan
If a Tube Optimization message displays, one of the following responses is required:

• Wait for the up-front delay.
• Decrease the total scan range.
• Split the group.
• Increase ISD or IGD.
• Increase Prep Delay.
• Select a scan parameter setting from the GSI Image Quality widget Calculate list.
• Change mA mode to GSI Manual and select a different GSI profile and then select a different GSI
Preset Family.
11.2 Scan Theory
11.2.1 Dose Deterministic Effects

There is the possibility that in normal use, the patient could be exposed to radiation dose levels of
1Gy CTDI100 (peripheral) or above, at which deterministic effects may become apparent. Management of
the high radiation dose is critical to maintain radiation safety. The available scan settings concerning
radiation dose, air kerma, air kerma rate, radiation quality, and image quality include: mA, kV, scan
time, detector coverage, and SFOV.
The table below provides the scan duration in seconds required to meet 1Gy CTDI100 (peripheral) at
200 mA exposure at the same scan location. This table assumes 200 mA and provides scan time as a
practical example for an average patient. The product of the scan time shown and 200 mA yields the
mAs required to result in 1Gy CTDI100 (peripheral). Note that for each kV / Aperture / SFOV combination in
the table, any mA and scan time combination that meets or exceeds the equivalent mAs of this table
can also result in deterministic effects of radiation. For obese patients, the mA may be larger than the
practical example shown in the table, and the resulting mAs should be used to determine the exposure
to the patient.
Table 62 Dose Deterministic Effects
Cine scan duration (sec.) at 200mA required to meet 1Gy CTDI100 Peripheral
Ped Body
Ped Head Medium Body Large Body
SFOV Head Small Body
Small Head Cardiac Medium Cardiac Large
Cardiac Small
CTDI
16cm 16cm 32cm 32cm 32cm
Phantom
Focal Spot XL L S XL L S XL L S XL L S XL L S
160 N/A 167 167 N/A 137 137 N/A 301 301 N/A 254 254 N/A 311 311
70
140 N/A 165 165 N/A 136 136 N/A 301 301 N/A 254 254 N/A 307 307

Scan
Dose Deterministic Effects continued

Ped Body
Cardiac Small
CTDI
Phantom
120 N/A 161 163 N/A 133 133 N/A 295 295 N/A 249 249 N/A 301 304
100 N/A 161 161 N/A 133 133 N/A 219 234 N/A 246 246 N/A 301 301
80 N/A 156 156 N/A 129 129 N/A 283 283 N/A 239 239 N/A 292 292
40 N/A 155 155 N/A 128 128 N/A 280 280 N/A 237 237 N/A 289 289
20 N/A 142 148 N/A 117 122 N/A 257 267 N/A 217 225 N/A 265 275
10 N/A 121 129 N/A 100 106 N/A 219 234 N/A 185 197 N/A 226 241
5 N/A 94 103 N/A 78 85 N/A 172 188 N/A 145 159 N/A 177 194
160 N/A 111 111 N/A 93 93 N/A 207 207 N/A 170 170 N/A 198 198
140 N/A 110 110 N/A 92 92 N/A 207 207 N/A 170 170 N/A 196 196
120 N/A 108 109 N/A 90 90 N/A 202 202 N/A 166 166 N/A 192 194
100 N/A 108 108 N/A 90 90 N/A 150 160 N/A 164 164 N/A 192 192
80 80 N/A 104 104 N/A 87 87 N/A 194 194 N/A 159 159 N/A 186 186
40 N/A 103 103 N/A 86 86 N/A 192 192 N/A 158 158 N/A 184 184
20 N/A 95 98 N/A 79 82 N/A 176 183 N/A 145 150 N/A 169 175
10 N/A 81 86 N/A 67 72 N/A 150 160 N/A 123 131 N/A 144 153
5 N/A 63 69 N/A 53 58 N/A 118 129 N/A 97 106 N/A 113 123
160 N/A 62 62 N/A 52 52 N/A 113 113 N/A 94 94 N/A 104 104
140 N/A 61 61 N/A 51 51 N/A 113 113 N/A 94 94 N/A 102 102
120 N/A 60 60 N/A 50 50 N/A 111 111 N/A 92 92 N/A 100 101
100 100 N/A 60 60 N/A 50 50 N/A 82 88 N/A 91 91 N/A 100 100
80 N/A 58 58 N/A 49 49 N/A 106 106 N/A 88 88 N/A 97 97
40 N/A 57 57 N/A 48 48 N/A 105 105 N/A 87 87 N/A 96 96
20 N/A 52 54 N/A 44 46 N/A 96 100 N/A 80 83 N/A 88 92

Scan
Dose Deterministic Effects continued

Ped Body
Cardiac Small
CTDI
Phantom
10 N/A 45 48 N/A 38 40 N/A 82 88 N/A 68 73 N/A 75 80
5 N/A 35 38 N/A 29 32 N/A 65 71 N/A 54 59 N/A 59 65
160 40 40 40 34 34 34 72 72 72 61 61 61 65 65 65
140 40 40 40 34 34 34 72 72 72 60 61 61 65 65 65
120 39 39 39 33 33 33 71 71 71 60 60 60 63 63 64
100 39 39 39 33 33 33 53 53 56 59 59 59 63 63 63
120 80 38 38 38 32 32 32 68 68 68 57 57 57 61 61 61
40 37 37 37 32 32 32 67 67 67 57 57 57 61 61 61
20 N/A 34 35 29 29 30 62 62 64 52 52 54 56 56 58
10 N/A 29 31 25 25 27 53 53 56 44 44 47 47 47 51
5 23 23 25 19 19 21 41 41 45 35 35 38 37 37 41
160 29 29 29 25 25 25 51 51 51 43 43 43 45 45 45
140 28 28 28 24 24 24 50 51 51 43 43 43 45 45 45
120 28 28 28 24 24 24 50 50 50 42 42 42 44 44 44
100 28 28 28 24 24 24 37 37 39 42 42 42 44 44 44
140 80 27 27 27 23 23 23 48 48 48 41 41 41 43 43 43
40 27 27 27 23 23 23 47 47 47 40 40 40 42 42 42
20 N/A 24 25 21 21 22 43 43 45 37 37 38 39 39 40
10 N/A 21 22 18 18 19 37 37 39 31 31 34 33 33 35
5 16 16 18 14 14 15 29 29 32 25 25 27 26 26 28

Scan
11.2.2 CT Perfusion
NOTICE

ON THIS SYSTEM.
NOTE
Refer to the accompanying documents.
See the system Technical Reference Manual, Dose and Performance chapter for
information on dose measurements and calculations.
11.2.2.1 Purpose of CT Perfusion

CT perfusion studies are used to assess delivery and perfusion of blood in an organ and/or its
tissues. Such studies are valuable for evaluating blood supply to neoplastic and non-neoplastic tissue
(including normal and ischemic tissue). In particular, CT perfusion imaging allows the evaluation
of cerebral ischemia or of the extent of angiogenesis associated with a tumor. CT perfusion should
be performed only for a valid medical reason and with the minimum radiation dose necessary to
achieve an adequate exam. Use of perfusion scans in children should be particularly reviewed for
clinical impact and justified. Pediatric patients are more radiosensitive than adults and have a longer
post-exam life expectancy, so particular attention should be paid to displayed CTDIvol when modifying
protocols.
CT perfusion imaging relies on the linear relationship between CT attenuation, expressed in
Hounsfield Unit (HU) and represented in a particular pixel of an image, versus the amount of iodinated
contrast material perfusing the corresponding region of tissue attenuating the X-rays. Dynamic CT
scanning enables the calculation of perfusion parameter maps, e.g., anatomic images where the pixel
value represents mean transit time, blood flow, blood volume, and permeability maps depending
upon the post-processing model used.
Scan technique parameters (e.g., kV, mAs) for CT perfusion studies should be set at values lower
than those used for routine diagnostic scanning of the same anatomical area. Perfusion imaging
involves visualization of temporal changes in iodine enhancement, rather than resolution of small
or subtle anatomical detail. The post-scan software processing of the data is relatively insensitive to
the increased noise levels; hence perfusion scans do not require use of the same radiation levels.
In general, lower kV improves visualization of iodine contrast and consequently allows use of lower
radiation doses. Lower kV settings are therefore recommended to be used as long as sufficient image
quality for perfusion post-processing can be obtained. Body perfusion imaging of obese patients,
for example, may be an application that requires use of higher kV values. Users should carefully
review the manufacturer’s reference perfusion protocols, which reflect the recommended kV, mA, and
scan time for a typical perfusion acquisition. Additional guidance may be obtained from professional
societies, regulatory agencies, educational textbooks, or peer-reviewed literature. The AAPM provides
a set of reasonable scan protocols for CT brain perfusion imaging that is freely available via its public
webpage. See the recommended readings.

Scan
Because CT perfusion requires specialized post-processing software, a CT perfusion acquisition should

not be performed unless this software is readily available to the institution. All users should be
trained in both CT perfusion acquisitions and post-processing and should follow professional society
perfusion practice guidelines. Before any changes are made to the manufacturer’s reference protocols,
both a radiologist and medical physicist familiar with CT perfusion should be consulted. Changes
in protocol and the reason for the changes should be communicated to the radiologic technologist.
Any changes to the protocols should be evaluated with respect to the image quality (less than
diagnostic level), temporal sampling and radiation dose of the manufacturer’s original reference
perfusion protocols. It is essential that all users understand that CT perfusion images will be much
noisier than images of the same body region acquired for most other diagnostic purposes, and that
this level of image quality is sufficient for the calculation of perfusion parameters.
11.2.2.2 Components of a CT Perfusion Study

Assessment of tissue perfusion for stroke includes a diagnostic quality non-contrast brain exam, an
optional CT angiogram of the circle of Willis that may include the carotid arteries, and a CT perfusion
exam. It may also include a post-contrast CT scan of the brain for assessment of residual lesion
enhancement. In the assessment of tumors, a noncontrast scan for localization of the area of interest
is often done prior to the CT perfusion exam.
In all cases, the CT perfusion exam should have technique factors that are lower than those used
for the other components of the study (e.g., the non-contrast, post-contrast, and angiogram scans).
Specific acquisition times for the perfusion exam depend on the post-processing algorithm used, but
in all cases the exam must be performed over a relatively long period of time (typically 40 to 50
seconds and potentially up to 3 minutes; consult model-specific user manual and radiologist) in order
to measure the time dependent physiologic process of blood flow through the brain. Since the scan
location is fixed, the same anatomy is irradiated repeatedly during this scan time. Scan times are also
affected by the concentration, volume, and rate of delivery of the contrast agent.
The lenses of the eyes are more radiosensitive than the skin. Scanning through the orbits should
be avoided, if possible, by the use of patient positioning. Consult the medical physicist to ascertain
appropriate deterministic thresholds across the body.
11.2.2.2.1 Body perfusion considerations

Perfusion scanning of the torso, typically referred to as body perfusion CT, is not currently performed
as frequently as head perfusion scans. It is essential to refer to manufacturers’ reference protocols
(if provided) and to involve a radiologist and medical physicist familiar with the principles and
techniques for body CT perfusion imaging, as well as communicate with the radiologic technologist.
Because of the higher attenuation of the torso, body perfusion scans may require a higher kV than
head perfusion scanning. Again, the image quality obtained should be noisier than most conventional
body CT scans, as the post-processing algorithm is able to extract the needed time attenuation
information from the noisy data set. Respiratory motion is an important consideration in body
perfusion CT, and methods to limit diaphragmatic motion during the scan, or realign anatomic regions
after the scan using registration algorithms should be used to minimize errors introduced from the
movement of the tissue of interest during the course of the perfusion scan. In the rare event that a
body perfusion scan would be performed in a pediatric patient, sedation in small children may be
required.

Scan
11.2.2.2.2 Perfusion acquisition types

Some perfusion scans are performed in a continuous exposure mode, in which the table does not
move and the X-rays are turned on over the entire scan period. This provides the highest degree of
temporal sampling; however, such temporal sampling may not be required for a particular application.
This acquisition mode delivers the highest dose to the patient, since the X-ray beam is always on.
Other techniques and recommended protocols may include a mode where the table does not move
but the X-rays are alternately turned on intermittently during the scan (such as Axial with a specified
time between passes). This method can be used to reduce the dose if the temporal sampling rate
remains adequate for the post processing software which requires a minimum temporal sampling of
3.2 seconds.
The temporal sampling rate varies based on the scan type selected for the acquisition and can affect
the total dose for the acquisition. Table 63 on page 281 lists the scan types that can be used for
acquisition of perfusion data.
Table 63 Perfusion data acquisition scan types
Scan Type Coverage Temporal Sampling Rate Acquisition/Dose Consid-

(Time Between Passes) erations
Axial/Cine 40, 80, 100, 120, 140, 160 adjustable Intermittent scanning
mm lowers dose
Cardiac Axial 40, 80, 100, 120, 140, 160 adjustable Intermittent scanning
mm lowers dose
Communication of Table 63 on page 281 should be conveyed by the facility to the radiologist, qualified
medical physicist and radiologic technologist.
The exam duration for tumor perfusion, whether in the head or body, needs to extend over a longer
time interval than a general perfusion scan, starting prior to the arrival of the contrast bolus and
include a period of approximately 3 to 3.5 minutes to adequately support the collection of data for
the computation of permeability maps. Initially, the temporal sampling rate must be the same as that
used for stroke protocols in order to adequately measure the first passage of contrast material through
the region. Subsequently, sparser sampling can occur, with temporal intervals ranging from 5 to 20
seconds. This reduces dose by decreasing the number of exposures.
11.2.2.2.3 Scan parameter effects on dose
11.2.2.2.3.1 kV effects on dose

The effect on dose from changing kV is non-linear. Holding all other parameters constant, changing
from 80 kV to 120 kV will result in approximately a two- to four-fold increase in dose.
NOTE
ATTENTION: CONSULT ACCOMPANYING DOCUMENTS.

See the system Technical Reference Manual for more details.

Scan
11.2.2.2.3.2 mA effects on dose

Changing the mA or mAs has a linear effect on dose. Holding all other parameters constant, doubling
the mA or mAs will double the dose.
NOTE
The effects of kV and mA or mAs on dose are multiplicative. For example, a three-fold
increase in dose that occurs from increasing kV combined with a two-fold increase in
dose from doubling the mA will result in a six-fold increase in overall dose.
11.2.2.2.4 Considerations for peak skin dose

The highest radiation dose accruing acutely at a single site on a patient’s skin, referred to as the “peak
skin dose,” is an important parameter in assessing risk of erythema (skin reddening) and epilation
(hair loss). The necessity for repeated scanning of the same location over extended times results
in skin doses that can be higher than those associated with routine CT applications. Factors that
influence these doses include kV, mA, scan time, perfusion acquisition type, and table movement,
if any, during the perfusion acquisitions. As with patient dose, lower kV settings are recommended
and should be used as appropriate to achieve appropriate image quality for perfusion evaluation with
respect to image noise based on body size, region scanned, and scanner type. In all cases, you should
refer to the manufacturers’ reference perfusion protocols as they reflect the appropriate kV, mA, and
scan times for typical perfusion acquisitions. Additional guidance may be found at professional society
and/or regulatory websites. See the recommended readings.
11.2.2.2.5 Required image attributes for perfusion imaging

The purpose of a CT perfusion series is to assess tissue perfusion and delivery of blood to the organ
and/or tissues of the organ; the acquisition parameters are different from those needed for routine
low contrast CT imaging applications. The acceptable noise level in CT perfusion is typically higher
than that for acquisitions routinely used in diagnostic imaging. Automatic exposure control should
not be used unless the manufacturer’s reference perfusion protocol employs it. Protocols should be
adjusted accordingly for patient age, injection rate, injection volume, and exam type (stroke versus
tumor evaluation and head versus body).
CT perfusion scans need to acquire data over a sufficiently long duration to accommodate the transit
time associated with the physiological process of the contrast bolus moving through the vascular
system. The acquisition duration for a stroke study must cover the time from prior to the arrival of the
contrast material bolus through the approach of the venous signal to baseline. This duration is directly
dependent on the volume of contrast material injected, the rate of injection, and the patient’s cardiac
output. If contrast material volumes or injection rates change from exam to exam, the scan duration
will need to be adjusted accordingly. Consult the perfusion post-processing software manual for more
detailed imaging and CT perfusion information.
11.2.2.2.6 Contrast injection considerations

As the iodine concentration of contrast material decreases, contrast material volume or flow rate
may need to be adjusted to deliver the required enhancement. You should pay close attention to the

Scan
shape of the bolus, follow the bolus with saline, and use an injector capable of delivering the required
injection rates.
The contrast injection rate should be determined by referring to the applicable section of this user
manual, contrast agent labeling, and in consultation with a physician. Special consideration should be
given for children due to their smaller size.
11.2.2.2.7 Other considerations and references

Due to the necessity to obtain data over an extended time period in order to calculate relevant
perfusion parameters, repeated scanning of the same location is required. As a result, CT perfusion
acquisitions produce peak skin doses higher than those associated with routine diagnostic CT
imaging. Deterministic effects (e.g., tissue reactions such as skin reddening and hair loss) are a
dose-threshold phenomena that can appear with peak skin doses > 2 Gy. As with all CT scanning, the
CTDIvol value displayed on the operator console should always be confirmed prior to the scan. For
CT perfusion without table motion, the value of CTDIvol tends to over estimate the actual peak skin
dose by approximately a factor of two (see reference to Bauhs below). User manuals may contain an
informative section that describes means for conversion of the displayed CTDIvol or dose profile to an
estimated phantom peripheral dose, which may serve as an estimate for peak skin dose. A typical CT
perfusion study should not result in a console-displayed CTDIvol of more than 1,000 mGy. Care should
be taken and consideration given prior to rescanning a patient within a short time with a perfusion
acquisition for the same anatomy due to concerns about reaching a cumulative peak skin dose value
greater than the deterministic threshold for skin injury.
Sites should have a Quality Assurance (QA) program for oversight and review of any protocol changes.
As with other scan types, the CTDIvol for a CT perfusion acquisition is recorded in both the DICOM
screen capture and the DICOM CT dose structured report and should be used for QA follow up for all
scanning.
Additional information on CT perfusion may be obtained in the user manuals for the CT perfusion
post-processing software, from the ACR practice guide for CT perfusion, and from the AAPM website
that contains reference perfusion protocols as well as other perfusion related information (please visit
FDA website for documents related to radiation dose quality assurance).
All the reference protocols provided within the software of this system, including those for CT
perfusion, are included in the Applications Protocol document supplied with the system. This
document provides a concise description of each scanning series within the protocol, technique
factors, and dose information for each.
11.2.2.2.8 Recommended reading

1. Ting Lee, “Functional CT: physiological models”, Trends in Biotechnology Vol. 20 No. 8 (Suppl.),
2002.
2. Jessica C. Tan, MD,1 William P. Dillon, MD,1 Songling Liu, MD,1 Felix Adler, MD,1 Wade S. Smith,
MD,2 and Max Wintermark, MD, “Systematic Comparison of Perfusion-CT and CT-Angiography in
Acute Stroke Patients”, Annals of Neurology Vol 61 No 6 June 2007.
3. Brix, G, ML Bahner, U Hoffman, A Horvath, and W Schreiber. 1999. “Regional blood flow, capillary
permeability, and compartmental volumes: Measurements with dynamic CT-Initial Experience”,
Radiology 210 : 269-276.

Scan
4. Cenic, A, DG Nabavi, RA Craen, AW Gelb, and TY Lee. 1999. “Dynamic CT measurement of cerebral
blood flow: A validation study”, American Journal of Neuroradiology 20 : 63-73.
5. Dillon, WP, and D Gress. 1999. “Intraarterial thrombolysis for cerebral infarction: To treat or not to
treat, and how?”, AJNR 20 : 1194-96.
6. Hunter GJ, Hamburg LM, Ponzo JA, Huang-Hellinger FR, Morris PP, Rabinov J, Farkas J, Lev MH,
Schaefer PW, Ogilvy CS, Schwamm L, Buonanno FS, Koroshetz WJ, Wolf GL, Gonzalez RG. “Rapid
assessment of cerebral perfusion and arterial anatomy in hyperacute stroke with 3D functional
computed tomography: early clinical results”, AJNR 19 (1):29-39, 1998.
7. Nabavi, DG, A Cenic, RA Craen, AW Gelb, JD Bennet, R Kozak, and T Lee. 1999. “CT assessment
of cerebral perfusion: Experimental validation and initial clinical experience”, Radiology 213 :
141-149.
8. J. A. Bauhs, T. J. Vrieze, A. N. Primak, M. R. Bruesewitz, and C. H. McCollough, 2008, "CT dosimetry:
comparison of measurement techniques and devices," Radiographics Vol. 28, pp. 245-253.
9. ACR-ASNR-SPR Practice Guideline for the Performance of Computed Tomography (CT) Perfusion
in Neuroradiologic Imaging at American College of Radiology website
10. AAPM CT Scan Protocols website
11. FDA website on "Radiation Dose Quality Assurance: Questions and Answers"
11.2.3 Total Scan Time

The Total Scan Time is automatically set by the system and is determined by the type of scan and scan
range. This setting can only be changed by resetting one of the other factors. The Total Scan Time is
useful for determining breath hold times and contrast injection timing.
11.2.4 Automatic Exposure Control

Patients come in all shapes and sizes. For the purpose of achieving a desirable image quality with a
scan technique that reflects the patient’s size and shape, there are several approaches to employing
automatic and manual mA setting modes of CT operation. These approaches are designed to adjust
the X-ray output of the system according to the X-ray attenuation presented by a patient’s anatomy.
For example, the patient’s weight or Body Mass Index (BMI) may be used as a guide to set a fixed
mAs for the acquisition. Alternatively, some measure of patient thickness or girth, such as anterior-
posterior (AP) thickness, lateral width, or patient circumference can be used as a basis to choose an
appropriate fixed mAs value, i.e., a value that yields an image adequate for diagnosis with a patient
dose as low as reasonably achievable. However, these methods have at least two inherent limitations.
First, as they produce a fixed mAs value, they do not adjust for differences in body-region thickness
and associated variation in X-ray attenuation along the patient length and/or around the patient
circumference. Second, the use of weight, thickness or circumference is an incomplete surrogate for
X-ray attenuation, which is one of the most relevant physical parameters affecting image quality and
which depends on the elemental composition and density of human tissue as well as on its shape and
thickness.
Automatic Exposure Control (AEC), on the other hand, is designed to adjust the scanner radiation
output to meet a desired, pre-set level of image quality/noise criterion by empirically assessing the
patient’s attenuation and automatically modulating the mA accordingly. AEC can provide a desired

Scan
level of image quality/noise at a lower patient dose than would be possible with a fixed scanner
radiation output. In general, CT systems may accomplish AEC in two ways:
1. Modulating the mA dynamically during scanning in the X-Y and/or Z dimensions to adapt to
variations in the patient’s attenuation.
2. Adjusting the mAs to a fixed value based on measurement and calculation of the patient’s
overall attenuation: the mAs is constant during scanning, but its value has been quantitatively
determined so as to yield an average pre-set level of image noise.
Most AEC systems operate as described in list item #1 above. Discussion of AEC, hereafter, applies to
these types of systems unless otherwise indicated.
11.2.4.1 How AEC works

On the basis of a patient’s attenuation, AEC sets mA values as the X-ray tube rotates around the
patient. The technology uses knowledge about the scanner’s imaging chain and the measured
attenuation of the patient to appropriately adjust mA values in order to achieve the desired, constant
image noise/quality criterion.
Larger patients typically require scanning at a higher mAs than the mAs used for smaller patients.
Similarly, thicker projections (e.g., laterally through the shoulders versus AP through the shoulders)
typically require more mAs to achieve the same resultant image noise/quality criterion. Finally,
anatomy with greater attenuation (e.g., abdomen or pelvis compared to the lungs) requires more
mAs to achieve the same image noise/quality criterion.
11.2.4.2 Adaptation to anatomy

As patient attenuation changes throughout the course of the scan, either rotationally around the
patient or along the length of the patient, AEC is designed to adjust dynamically the mA for each
body part and projection. If the attenuation does not change, AEC sets the mA at a constant value
that is appropriate for the overall patient thickness and that achieves the desired image noise/quality
criterion.
11.2.4.3 When to use AEC

AEC technology has the greatest impact when the portion of the patient being scanned has non-
uniform size, shape, or density. In these cases, AEC adjusts scanner radiation output to the changing
anatomy and modulates the mA in the Z-direction (along the patient) and/or in the XY-direction
(around the patient). Even though AEC is used, before scanning the operator must still select scan
parameters, including AEC parameters, which provide a desired image noise/quality criterion. Scan
parameters including AEC parameters must be chosen to carefully balance patient radiation dose and
image performance.
Even when the patient’s anatomy has consistent size, shape, and density throughout the planned scan
range, AEC technology chooses the appropriate exposure settings to achieve the image noise/quality
criterion requested by the user.
When bismuth or other shields are considered for use in the planned scanned range, consult the
system user manual for specific information. If used with SmartmA, they should be put in place after
the scout scans are acquired to reduce technique overcompensation. Use of shields with SmartmA
after the scout scan could result in not meeting the prescribed NI in the reconstructed images.

Scan
11.2.4.4 When not to use AEC

AEC might not be available for all scanning modes or on all scanners. When AEC is available, if users
do not understand the relationship between AEC parameters, image noise, and dose, AEC should not
be used. Also, if the patient cannot be centered in the scanner, AEC is not recommended because the
attenuation calculations used for AEC are designed with the assumption that the patient is centered
in the gantry. Finally, if there is any question, radiologic technologists should always consult their
medical physicist and radiologist to ensure that proper exposure techniques are used.
11.2.4.5 AEC does not guarantee reduction of radiation doses in all patients
The use of AEC does not always result in dose reduction, especially when compared to a fixed mA/mAs
protocol. For example, when providing the desired image noise/quality criterion setting for a large
patient, AEC might appropriately increase the scanner radiation output as compared to that for an
average-sized patient. For most examinations of average-sized or small patients, and for the same
image noise/quality criterion settings, AEC use will result in the same or lower CTDIvol as that of a fixed
mA/mAs protocol. (However, a larger patient would appropriately require more fixed mA than for a
smaller patient.)
NOTE
Radiologic technologists must be fully aware that proper patient centering is critical
for accurate AEC function. Improper patient centering can result in an exposure that is
either too high or too low to achieve the desired image noise/quality criterion. Note that
proper patient centering can be more challenging for smaller pediatric patients, and so
special care should be taken. Use the output from the patient centering feature to aid in
properly centering the patient.
11.2.4.6 System recommended patient centering

To optimize dose and image quality when using AEC, the patient should be centered within the
scan field of view. When the patient is closer to the tube, the patient appears larger in a scout.
Correspondingly, when the patient is further from the tube, the patient appears smaller in a scout. As
result, radiation doses may exceed optimal values when the patient size is magnified, and be lower
than optimal when the patient size is minified.
For example:
• Radiation doses may be higher than optimal when using AEC with the following conditions.
• Anterior-posterior (AP) scout and the patient is positioned more than 2 cm above isocenter.
• Posterior-anterior (PA) scout and the patient is positioned more than 2 cm below isocenter.
• Radiation doses may be lower than optimal when using AEC with the following conditions.
• AP scout and the patient is positioned more than 2 cm below isocenter.
• PA scout and the patient is positioned more than 2 cm above isocenter.

Scan
The lateral scout is not impacted by the magnification/minification effect of vertical positioning and
will provide more consistent dose levels with AEC. However, patient centering remains critical for
optimal image quality in this case.
The patient centering feature helps to detect suboptimal centering prior to the diagnostic scan. For
each z-position on the scout, the system estimates center of mass of the projection. Based on this
information, the system displays a line at the weighted average of projection centered over the entire
scout.
11.2.4.7 Effect of AEC control setting

For a given patient, changing the image noise/quality criterion setting in AEC will affect the patient
dose: asking for lower image noise/higher image quality criterion will result in more dose to the
patient as the Noise Index value is decreased (made smaller). In contrast, asking for higher image
noise/lower image quality criterion by increasing (make larger) the Noise Index value will result in less
dose to the patient.
11.2.4.8 AEC considerations of patient size, shape, composition, and age

For a given AEC image noise/quality criterion setting, larger patients and more attenuating body
regions may result in a higher scanner radiation output. Smaller patients and less attenuating body
regions may result in a lower scanner radiation output.
While AEC can be an effective dose-reduction tool for pediatric patients, special care should be taken
with this patient group. The GE Healthcare online education module available on the Image Gently
website describes issues to consider when using our AEC features with pediatric patients.
11.2.4.9 Dynamic AEC scanning

When a scanning protocol contains multiple X-ray tube rotations at the same table location, the
effect on patient dose of incorrect selection of protocol settings will be multiplied by the number
of rotations. For such protocols, operators must take extra care when setting manual mAs or AEC
parameters to achieve the desired level of image noise/quality criterion. For example, in perfusion
scanning, the image noise can often be much higher (yielding a lower dose) than for routine diagnostic
scanning of the same region because the primary application of perfusion scan data is for quantitative
analysis and characterization of perfusion parameters rather than for diagnostic visualization. The
manufacturer’s reference protocol provides an indication as to whether use of AEC is or is not
recommended with these scan modes.
11.2.4.10 How to tell if the dose has changed

For every patient, and any time AEC settings are changed, in order to confirm a correct level of scanner
radiation output for that patient’s size and exam protocol, users should examine the projected CTDIvol
and DLP displayed prior to performing the scan, as a step in operator confirmation of system settings.
When a large patient is scanned at a particular setting of image noise/quality criterion, the CTDIvol
and DLP will be higher than for a smaller patient at the same AEC settings. Projected CTDIvol and
DLP values are displayed on the scanner’s dose display on the user interface prior to confirmation
of settings for scanning. After scanning, the values are updated to reflect the average of the actual
mAs values used in the scan and are displayed on the user interface as well as recorded in the DICOM
secondary screen capture and DICOM radiation dose structured reports.

Scan
11.2.4.11 Summary
AEC is a versatile and powerful tool designed to tailor the scanner’s radiation output to each patient
based on the patient’s size, age, shape and attenuation and the user’s requested level of image
noise/quality criterion. AEC technology uses estimated patient attenuation values to adjust the mA
dynamically in order to achieve the requested level of image noise/quality criterion. However, AEC
settings must be chosen with the same care used to choose all other parameters that affect radiation
dose to the patient. Before the scan parameters are confirmed, careful attention must be paid
to CTDIvol and DLP displayed on the user interface; scanner radiation output associated with the
prescribed protocol must be checked and confirmed prior to scanning. Used properly, AEC is a key
technology to help ensure that the appropriate radiation dose is used for every patient.
11.2.4.12 AEC Messaging

Blue or Red alert messages will be seen in Scan Settings and in Protocol management when the kV or
mA control mode is changed from or to and Automatic Exposure Control Mode. Messages will be seen
for the following changes:
• From Manual mA to SmartmA mode
• From SmartmA to Manual mA mode
• From Manual kV or kV Assist Δ to kV Assist mode
• From kV Assist to Manual kV or kV Assist Δ mode
• From Manual kV or User Override to Auto Prescription mode
• From Auto Prescription to User Override mode
• From ODM to Manual mA mode
• From ODM to SmartmA mode
11.2.5 Slice Thickness Reference Noise Index and Noise Index

Values
The Noise Index (NI) is the primary SmartmA input parameter that controls the X-ray output and
ultimately provides the tradeoff between the desired image quality and patient dose. Any user-defined
value between 1 and the maximum Noise Index value can be entered for the Noise Index when
building a protocol.
The Noise Index value will approximately equal the standard deviation in the central region of
the image when a uniform phantom (with the patient's attenuation characteristics) is scanned and
reconstructed using the standard reconstruction algorithm.
The Noise Index corresponds to the relative level, or index, of noise in the reconstructed image: a
higher Noise Index means the images will contain relatively more noise and will be obtained with
lower mA, therefore lowering relative patient dose, while a lower Noise Index means the images will
contain relatively less noise and will be obtained with higher mA, leading to relatively higher patient
dose. The Noise Index should always be reviewed and modified by the user to meet the clinical need,
taking into consideration the user preference for image quality and the tradeoff with patient dose.

Scan
A guide for how to adjust for Noise Index at another slice thickness is given in the equation in
SmartmA/ODM.
When SmartmA is enabled, if the user changes the slice thickness, the Noise Index will change
according to the following equation to maintain approximate equivalent dose.
Where factors for each slice thickness are given in Table 64 on page 289.
Table 64 Slice Thickness Factors
Slice Thickness Factor

(mm)
5 0.71
3.75 0.82
2.5 1
1.25 1.41
0.625 1.8
For example, if a prescription for the primary recon has a prescribed Noise Index of 10 for a slice
thickness of 5 mm, and the user changes the slice thickness to 2.5 mm, then the prescribed Noise
Index will change according to the following:
Table 65 Noise Index Values
Anatomy 5.0 mm 2.5 mm 1.25 mm 0.625 mm
Head/Orbit 2.7 3.3 4 4.4
Neck 4.2 5.1 6.2 6.9
Abdomen 9.7 12.3 15.6 18
Pelvis/Spine 11.7 14.6 18.4 21
Chest 12.3 15.4 19.3 22
Upper Extremity 7.8 9.6 11.8 13.3
Lower Extremity 4.1 5 6.1 6.7

Scan
NOTE
The Noise Index values in this table do not adjust based on Slice Thickness Factors.
These values are recommended values for each anatomical area.
11.2.6 SmartmA/ODM
11.2.6.1 SmartmA
11.2.6.1.1 SmartmA background

A significant factor in the quality of a CT image is the amount of X-ray quantum noise contained
in the scan data used to reconstruct the image. Technologists understand how the choice of X-ray
scan technique factors affect noise contained in the reconstructed image. In theory, noise decreases
approximately inversely with kV and with the inverse square root of the mAs and slice thickness.
For example, increasing the mA from 50 to 200 (a factor of 4) theoretically decreases quantum noise
by a factor of 2 (the square root of 4). The final noise in the image is further influenced by the
specific mathematical algorithm employed in the image reconstruction process, which may alter the
theoretical relationships described above. In helical imaging, quantum noise increases with increasing
helical pitch; however, the exact relationship is likewise dependent on the details of the helical image
reconstruction process.
The most significant factor that influences the quantum noise in scan data is the X-ray attenuation,
related to the size and tissue composition of the scanned anatomy.
Figure 138 Example small patient (120 kVp, 1.25 mm, 0.5 s axial) with factor of 5 noise increase
(simulated): 1 = SD 8 @ 640 mA, 2 = SD 40 @ 25 mA
As an example, for a given fixed exposure scan technique, the quantum noise can vary by at least a
factor of 5 from the smallest to the largest patient. Figure 138 on page 290 shows an example of a
five times noise increase simulated for a small patient. With a fixed mA scan protocol, the technologist
must select the mA using a qualitative estimate of the patient attenuation. This may be accomplished
using the patient's weight and/or waist diameter measurements, body mass index, or with qualitative
visual classification. Because these methods provide rough X-ray attenuation estimates and do not

Scan
account for attenuation changes within the patient region being scanned, the technologist must
use a high enough technique margin to avoid compromising the diagnostic quality of the images.
Theoretically, radiation dose is inversely related to the square of the noise, so many patients are likely
receiving more dose than necessary for the required diagnostic quality using such manual methods.
GE's suite of Automatic Exposure Control (AEC) features enable substantial patient dose reduction,
while maintaining diagnostically acceptable image quality. Specifically, SmartmA is an automatic tube
current modulation feature that makes the necessary mA adjustments much more accurately than
those manually estimated for the patient, and can thereby achieve a more consistent image noise
in spite of the wide range of patient size. Since image noise variability is substantially reduced, a
significant overall patient dose reduction is possible with proper scan parameter selection.
11.2.6.1.2 SmartmA theory

SmartmA, available on all GE multi-slice CT scanners and first introduced on GE single slice scanners
in 19941,2, is the CT equivalent of the auto exposure control systems employed for many years in
conventional X-ray systems. The goal of SmartmA is to make reconstructed images contain X-ray
quantum noise at a level desired by the user, independent of patient size and/or anatomy. In addition
to adjusting for patient attenuation along the z-axis, SmartmA modulates patient exposure as a
function of X-ray tube angle as the tube rotates around the patient anatomy, leading to concurrent mA
modulation in the x, y and z-axes.
SmartmA tube current modulation is determined from several sources of information. The primary
source of information is the overall attenuation and shape of the patient anatomy. Using the
information contained in a single scout scan of the patient scout, the CT system computes the required
mA to be used based on the selected Noise Index setting, the calculated attenuation of the patient
anatomy being scanned, and ASiR-V selection.
SmartmA enables substantial dose reduction by adjusting tube current to minimize X-rays over
angles that have less importance in determining the overall image noise content. In anatomy that
is highly asymmetric, such as the shoulders, X-rays are significantly less attenuated in the anterior-
posterior direction than in the lateral direction. Thus, the overwhelming abundance of X-rays can be
substantially reduced closer to the anterior-posterior direction, without a significant effect on overall
image noise. For each scanned section in the z-axis direction, the system calculates an mA for the
lateral and anterior-posterior patient axes from an estimation of the patient attenuation through the
long and short axes, respectively.
The system determines the tube current using the patient's scout projection data and a set of
empirically determined noise prediction coefficients. The scout projections contain density, size,
and shape information as a function of the patient habitus in the z-direction. The total projection
attenuation (projection area) contains the patient density and size information, while patient shape
information, i.e. oval ratio, an estimate of the eccentricity of the patient habitus as a function of z,
is contained within amplitude and width information derived from the scout projection data. These
patient characteristics determine how much X-ray will reach the detector for a specified technique
and hence predict the image standard deviation due to X-ray noise for the standard reconstruction
algorithm.
To predict the image noise at a given z-position, the projection area and oval ratio are obtained from
the patient's scout. The expected X-ray noise for the reference technique (reference noise) is then
derived as a function of the projection area and oval ratio from the scout using coefficients determined

Scan
by a least squares fit of the noise measurements from a set of phantoms representing a clinical range
of patient sizes and shapes.
Knowing the reference noise and the difference between the reference technique and the user
selected prescribed technique, the mA required to obtain the prescribed Noise Index is calculated
using well known X-ray physics relationships. It is known that the noise is inversely related to the
number of photons and the number of photons is related to the slice thickness, image acquisition
time, and mA. In the GE SmartmA design, adjustment factors for helical pitch are also incorporated
in the calculation to account for noise differences that scale between helical selections and the axial
reference technique.
Practical SmartmA Example
Patient exposure for a SmartmA scan is reduced when compared to a similar scan employing fixed mA.
This is demonstrated in Figure 139 on page 292 which shows the mA as a function of rotation angle for
fixed mA and SmartmA scan of a uniform oval polyethylene phantom. The image on the left overlays
the fixed mA and SmartmA mA profiles as a function of X-ray tube angle, with the accompanying
reduction in overall patient exposure using SmartmA clearly indicated by a reduction in relative mAs
as a function of tube rotation angle. The exact mA reduction range when using SmartmA, and the
consequent reduction in patient dose, depends on the prescribed Noise Index, and the size and shape
of the patient, with a greater reduction expected for a relatively larger and more asymmetric patient
when a relatively low Noise Index is prescribed.
Figure 139 Sample comparison of SmartmA modulation with a fixed mA scan.
NOTE
Note that values are illustrative, with exact values dependent on the specific
implementation of SmartmA.
While the SmartmA mA table specifies different mA values per rotation, corresponding to the mA
in the anterior-posterior direction and in the lateral direction, i.e. at 0 and 180° and 90° and 270°,
respectively, the actual mA is continually varying in a smooth fashion between the specified mA values
as a function of X-ray tube angle to the patient, as shown in Figure 139 on page 292.

Scan
11.2.6.1.3 References
1 L. Kopka and M. Funke, "Automatically adapted CT tube current: Dose reduction and image quality in
phantom and patient studies," Radiology 197 (P), 292 (1995)
2 D. R. Jacobson, W. D. Foley, S. Metz, and A. L. Peterswen, "Variable milliampere CT: Effect on noise
and low contrast detectability," Radiology 210 (P), 326 (1996)
11.2.6.1.4 SmartmA FAQs

What suggestions do you have for a new SmartmA user?
• If you are not familiar with the concept of Noise Index, you can use the GE reference protocols
that have AEC enabled. As a general starting point, use the standard deviation from an acceptable
image for approximation of a Noise Index, or consult the literature until you find the highest Noise
Index value that provides acceptable diagnostic quality. Experiment by scanning some phantoms
with different Noise Index values to gain some confidence. A 30 cm diameter water phantom or
a 35 cm diameter low density polyethylene phantom have an attenuation similar to the average
adult abdominal patient.
• It is important to review the image quality that is obtained with the prescribed Noise Index to
optimize the user's maximum and minimum mA range and Noise Index values accordingly. The
maximum mA value set by the user sets the maximum allowed mA, or clipping mA value.
• You should also check the mA table on the scan set up screen to see what mA is actually being
used. If you see that it is frequently at the maximum mA range, and you have determined that
you require lower noise in your images than you are currently obtaining, consider increasing the
Noise Index if more noise can be tolerated in your reconstructed images without compromising
the diagnostic value, or increase the maximum mA limit if it is not at the maximum limit of the
X-ray generator.
• If you normally reconstruct images with thin sections for 3D reformatting and thicker slices for
axial viewing it is important to understand that the first prospective reconstructed slice thickness
is used for calculating SmartmA. Generally you would want to set the Noise Index for the thicker
slice images. For example, you might want a Noise Index of 10.0 for 5 mm thick images for
viewing but you may also want 0.625 mm slices for 3D reformatting. If you prescribe the 0.625 mm
slice recon first, followed by the 5 mm recon, SmartmA will calculate the mA needed to obtain
an image noise of 10 for the 0.625 mm slices since it is prescribed first. In this case, to avoid
excessively high mA and high dose, the user needs to readjust the Noise Index using the following
approximation. Please note that the following equation is to be used as a starting point, with the
actual Noise Index for thin slices possibly varying from the exact solution given by this equation:
Example:

Scan
Why is the standard deviation I measure in the image different than the Noise Index I selected for
the scan?
• There are many factors that can account for this. But, first consider that the prescribed Noise
Index causes the tube current to be adjusted so that the system projects a similar X-ray intensity
through the patient to the detector. Hence it regulates the X-ray noise or quantum noise in the
scan projection data. The noise in the image depends on additional factors within the image
reconstruction chain, including, but not limited to, the selection of reconstruction algorithms,
reconstructed slice thickness selection (if different than your prospective selection), and the use
of image space filters. In addition, it is very difficult to make standard deviation measurements
on patient data since the standard deviation is affected by small CT number variations of the
heterogeneous anatomy and by patient motion or beam hardening artifacts. Even with uniform
phantoms, standard deviation measurements will produce some variability in measured results
because of the inherent nature of quantum statistics.
• Another situation that can cause significant differences between the selected Noise Index and the
image standard deviation is when very large patients provide insufficient detector signal. In these
cases, electronic noise sources can become the dominant image noise source instead of X-ray
noise. In these cases at various threshold levels, special projection data dependent filters begin
to be applied to help preserve image quality. These filters on the projection data affect the noise
properties of the reconstructed image. The highest kV is recommended when excessively large
patients need to be scanned.
• Another factor is how well the patient is centered in the SFOV. Image noise can increase
significantly if the patient is mis-centered. This occurs because the bowtie filter projects
maximum X-rays intensity at isocenter since this is the region of maximum attenuation if the
patient is centered. If the patient is mis-centered, there are fewer X-rays projected to the thickest
part of the patient, and hence image noise will increase. The optimum strategy is to find the
highest Noise Index sufficient for the clinical task and let SmartmA select the mA without using
significant constraints.
Will I get a dose reduction when I use AEC?

SmartmA will use a patient exposure that depends on the Noise Index you select and the size of the
patient you are scanning. If, you do not obtain a dose reduction over a population of patients, you may
have selected a lower Noise Index than you really need, resulting in, on average, higher mA values than
fixed mA protocols. One strategy to avoid using more exposure is to set the maximum mA parameter
to the same level as your fixed mA protocols, capping the maximum patient exposure to the same
level as your fixed mA protocol. Hence, SmartmA will never be allowed to use more exposure then
previously employed. However, image noise will increase in regions where the mA is limited by the
maximum mA selection and the IQ will degrade with increasing patient size. The optimum strategy is
to find the highest Noise Index sufficient for the clinical task and let SmartmA select the mA without
using significant mA limits.
Why do my images seem noiser with SmartmA?

• SmartmA estimates the attenuation (size and shape) of the patient from a single scout image
and produces an X-ray intensity to maintain the prescribed Noise Index. The estimation of patient

Scan
attenuation may not match the actual attenuation of the heterogeneous anatomy being imaged.
Thus, if images appear noisier when SmartmA is employed, the user may need to use a lower
Noise Index. This may be the case if the user finds that the average mA employed for the
population of patients in question using SmartmA is generally lower than using previous fixed
mA protocols. This situation indicates that the user is now employing lower dose compared to
previous protocols and hence higher noise levels would be expected.
• Certain patient images may also be noisier than the experience of the user suggests. For example,
experience leads the user to expect significantly lower noise in thin patients than obese patients,
while SmartmA attempts to make the image noise approximately similar for all patient sizes. Most
importantly, the user needs to find the highest Noise Index to enable a confident diagnosis of the
clinical indication since this results in the lowest patient dose.
• If the user desires somewhat lower noise in small patients, the user may want to create Small,
Nominal, and Large patient protocols. The user can then use a slightly lower Noise Index for the
smaller patients and a slightly higher Noise Index for larger patients.
• A noise limiting strategy that can be employed is to increase the minimum mA setting in the
SmartmA protocol. If the user determines that image quality is generally not acceptable below
some minimum mA value, then the user may set this value as the low mA range limit. This will
prevent the SmartmA feature from using mA values that are lower than desired. Note that this
strategy can sometimes defeat the overall purpose of SmartmA, causing image noise to fall below
the prescribed Noise Index, and furthermore increase dose to the patient.
• Another possibility for higher noise than is expected is if the user looks at multiple reconstructed
images that have thinner slices than the prospective scan prescribed slice thickness. SmartmA
uses prospective slice thickness as a factor when the mA table is generated. The user must ensure
that the Noise Index is set for the first prospective image based on image thickness used for axial
image viewing (see the first FAQ). This caveat applies equally for fixed mA and SmartmA scanning.
• Higher noise images can occur when patients are not well centered in the scan field of view. The
bowtie filter attenuation increases with distance from isocenter, hence the thickest part of the
patient should be approximately centered in the scan field of view, in line with the minimum filter
attenuation, otherwise image noise will increase since the patient thickness adds to the bowtie
filter thickness. This is especially important for highly asymmetric anatomy such as shoulder
anatomy. Again, this effect applies equally for fixed mA and SmartmA scanning.
• Recognize also that there are some obese patients that exceed the capabilities of the tube and
generator to satisfy the selected Noise Index. This is also no different than fixed mA scanning. For
such obese patients, one strategy is to select a higher kV setting when possible.
Why is the mA annotated on the image sometimes slightly different than the mA I see in the mA
table?
The mA displayed on the image is determined by measuring the generator mA during the scan and
averaging the measured result over the total number of views used to reconstruct the image. The
number of views used to produce the image may be more than one gantry rotation for a helical scan.
Hence the annotated value is a combination of the mA table values that depends on how many views
from each rotation were used for the image. In addition, the generator is automatically adjusting the
filament current to account for changing conditions during the scan to keep the mA within the desired
tolerance of the commanded mA table. For example, this is why you may see an mA value of 41 in the
image where the mA table indicated 40.

Scan
I understand that noise in the image changes with reconstruction parameter selections, but
why is the noise sometimes different when I retro reconstruct the same scan data at a different
display field of view?
When you select a parameter within a reconstruction algorithm, the system may sometimes readjust
the actual filter kernel. This readjustment will change the image standard deviation. This will happen
if the display field of view (DFOV) selection exceeds a certain dimension for each reconstruction
algorithm and is especially apparent with higher resolution algorithms such as bone and edge. The
change in kernel is required when the DFOV selection makes the pixel size too large to support the
intended spatial resolution. This characteristic is independent of SmartmA.
Does SmartmA require two scout images in order to function correctly?

No, all AEC features (SmartmA, ODM, kV Assist and Auto Prescription) are designed to require only one
scout acquisition.
What are the appropriate kV and mA to use for a scout scan to ensure accuracy of AEC?
The AEC algorithm calculates the patient’s size and shape from the most recently scanned scout and
uses this information to help determine the optimal mA profile (when SmartmA is enabled) and kV
(when kV Assist or Auto Prescription is enabled).
If too low a kV and/or mA are used to scout the patient, the scout image may have relatively low
signal, causing AEC to calculate an inaccurate patient size and shape. This could ultimately lead to an
inaccurate SmartmA profile or kV selection, resulting in suboptimal dose and/or IQ.
Therefore, it is important to use a kV and mA for the scout scan that is appropriate to the patient size
to assure accuracy of AEC.
In general, it is recommended that the user scan at the kV and mA prescribed in the GE Reference
Protocols. For convenience, the recommended kV and mA for scout scans are summarized in the table
below.
It is recommended to avoid scanning adults and larger pediatric scouts at 70 kV.
Adult / Pediatric Patient Size Patient Diameter Recommended Scout

(cm) kV / mA
Pediatric Very Small ≤ 12 70 kV / 10 mA
Pediatric Small – Medium ≤ 35 80 kV / 10 mA - 100 kV / 10 mA
Adult Small – Medium ≤ 35 80 kV / 10 mA - 100 kV / 10 mA
120 kV / 10-20 mA for normal

scout speed. For Fast Scout
Adult Large > 35 speed preference 20 - 40 mA.
How is the SmartmA mA determined when NI and ASiR-V interact?

To determine the SmartmA mA value required to achieve the prescribed NI, the effect of the prescribed
ASiR-V percentage on the level of noise in the primary reconstructed image is considered. The effect of
increasing ASiR-V percentage in SmartmA is to lower the mA value required to achieve the prescribed
NI. What this means is: as the ASiR-V percentage increases, the SmartmA will decrease the mA value

Scan
to achieve NI prescribed. Image noise will increase, however, ASiR-V percentage will offset the noise
increase.
What affects the SmartmA mA value?

SmartmA mA values are dependent on three categories of inputs: patient-dependent, scan technique
and primary image reconstruction parameters.
Patient-dependent: Attenuation size and shape of the anatomy being scanned determined from the
scout.
Scan Technique:
• Scan type (Axial, Cine, Helical, Cardiac)
• kV
• SFOV
• Rotation time
• Pitch
• Detector Coverage (Helical only)
• Standard or High-Definition mode
Primary Reconstruction Parameters:

• Noise index
• Slice thickness
• ASiR-V percentage
• Reconstruction Type (HD or non-HD kernel)
• Helical Recon Mode (Plus/Full)
What is the recommended range of NI for different anatomical regions?

The recommended range of NI for different anatomical regions is contained in the Noise Index Values
table, in the Slice Thickness Reference Noise Index and Noise Index Values section of this manual.
11.2.6.2 SmartmA
In addition to adjusting for patient attenuation in the z-axis, SmartmA adjusts patient exposure as a
function of X-ray tube angle as the tube rotates around the patient, thus leading to mA modulation in
the x, y and z-axes. For each scanned section in the z-axis direction, the system calculates an mA for
the lateral and anterior-posterior patient axes from an estimation of the patient attenuation through
the long and short axes, respectively.
Patient exposure for a SmartmA scan is reduced when compared to a similar scan employing manual
mA. This is shown in Figure 139 on page 292 which illustrates the mA as a function of rotation angle for
manual mA and SmartmA of a uniform oval shaped phantom. The image on the left shows the fixed
mA and SmartmA mA profiles as a function of X-ray tube angle, with an accompanying reduction in
overall patient exposure. In this case a manual mA technique can be thought of as the equivalent of an
AutomA based modulation, as employed in the AutomA feature on previous products.

Scan
While the SmartmA mA table specifies different mA values per rotation, corresponding to the mA in the
anterior-posterior direction and in the lateral direction, i.e. at 0, 180° and 90° and 270°, respectively,
the actual mA is continually varying in a smooth fashion between the specified mA values as a function
of X-ray tube angle to the patient, as shown in Figure 139 on page 292.
Figure 139 on page 292 shows a sample SmartmA mA profile as a function of gantry rotation for a
uniform oval polyethylene phantom with the same prescribed Noise Index using (blue) Manual mA and
(orange) the SmartmA mode of Automatic Exposure Control (AEC). The reduction in patient exposure
enabled by SmartmA is clearly illustrated as a function of X-ray tube angle compared to the patient
exposure illustrated by the manual mA profile. The expected mA reduction range when using SmartmA
depends on the size and shape of the patient, and on the prescribed Noise Index, with a greater
reduction expected for a relatively larger and more asymmetric patient, when a relatively low Noise
Index is prescribed.
11.2.6.3 Organ Dose Modulation (ODM)

Organ Dose Modulation (ODM) is a mode to reduce the tube current (mA) when the X-ray tube is in the
anterior position relative to the patient. This technique builds on the SmartmA AEC feature to further
reduce the dose to radiosensitive anterior organs.
When ODM is enabled, the mA is reduced during an angular range of 100 degrees for head protocols
and 150 degrees for body protocols. The mA in the posterior views is not changed.
The effectiveness of ODM to reduce dose to radiosensitive organs requires the correct centering of the
patient in the A/P direction relative to the isocenter of the SFOV.
Figure 140
Number Description
1 Tube current reduction area
2 Head first
3 Feet first

Scan
The mA reduction rate on front side of the patient and the mA reduction tube angle are below.
Table 66 mA Reduction Rate for ODM
SFOV mA Reduction Rate mA Reduction Range FWHM

(front side) (tube angle)
Head, Small Head, Ped Head Up to 30% 100
Large Body, Medium Body, Small Up to 40% 150

Body, Ped Body
Image noise may increase up to 10 percent while maintaining diagnostic quality within the prescribed
ODM range (axial) or within the prescribed ODM range plus half the detector coverage on each side
(helical).
11.2.7 Auto Prescription
11.2.7.1 Overview
Auto Prescription is a profile driven feature that selects scan parameters defined for a patient by
patient size and works with SmartmA to optimize dose and image quality. The benefits of Auto
Prescription include providing a consistent desired image quality across a wide range of patient sizes,
eliminating multiple size- based protocols and reducing the amount of patient size dependent scan
parameter adjustments at scan time. A Auto Prescription Profile specifies the patient size ranges and
specifies which settings are changed by patient size. kV and mA limits are required settings for each
patient size range and optional settings may be selected including, SFOV, ASIR-V%, Rotation Time,
Pitch and Noise Index (NI). If NI is set in the profile, then a reference slice thickness will also be set in
the Profile.
Auto Prescription determines the patient size from the attenuation information of the patient’s scout
over the prescribed scan range and then applies the scan settings specified for that patient size range
within the Auto Prescription Profile. In addition, If NI is not set in the profile’s patient size range,
Prescribed NI defined in the protocol will be adjusted based on the Size Adjusted Noise Index (SANI)
and Clinical Task settings within the Auto Prescription Profile. SmartmA utilizes the selected kV and NI
parameters to determine mA.
NOTE
NI is not adjusted from the value in the protocol if the patient size falls in the Reference
Patient Size Range.
11.2.7.2 Background: Impact of kV changes on CT Imaging

kV is a required setting for each patient size range because careful optimization of tube voltage (kV) in
combination with tube current (mA) is important to achieving the goal of setting technique parameters
that provide the desired image quality at the lowest radiation dose for each patient. The behavior
of Image quality and radiation output are impacted by the selection of both kV and mA parameters.
Two significant factors that impact the quality of a CT image are the amount of X-ray quantum noise
and of X-ray contrast (either from the contrast agent administered to the patient or from the tissues

Scan
in the patient) in the scan data used to reconstruct the image. These factors impact the CT image
quality indicator Contrast-to-Noise Ratio (CNR). CNR gives an indication of how well structures can be
seen through the image noise. CNR can be improved by increasing the contrast between structures,
lowering the noise level, or both.
Image quality is impacted by what X-rays the system generates (how many [tube current] and at
what energies [tube voltage]), and how much they are attenuated (patient size and composition). The
patient attenuation is impacted by the size and composition of the anatomical region being scanned.
While mA has a large impact on image noise, kV has a large impact on both image noise and image
contrast. Tube current selection is related to the desired image noise, but it must be noted that it is
also greatly impacted by the tube voltage selection. Tube voltage is related to desired image contrast
because individual materials have different levels of x-ray attenuation at different X-ray energies. For
example, Iodine has a relatively large change in attenuation at different energies providing more
image contrast, and water has relatively little change in attenuation at different energies proving very
little change in image contrast.
Table 67 Impact of lower kV with fixed parameter
Fixed parame- Image Contrast mA Noise CTDIvol CNR

ter (Iodine)
mA ( Manual ↑ Fixed ↑ ↓ Small ↓

mA )
Noise ( Smart- ↑ ↑ Fixed ↑ ↑

mA )
CTDIvol ↑ ↑ Small ↑ Fixed ↑
CNR ↑ ↑ ↑ ↓ Fixed
Because of these IQ impacts resulting from kV selection, lowering kV can be used to optimize patient
exams in the following ways:
• improving image quality in terms of image contrast
• decreasing the amount of contrast agent delivered to the patient
• lowering the amount of radiation dose associated with a CT scan
CT image contrast increases as kV decreases. This effect is relatively small for non-enhanced soft
tissue and relatively large for bone and iodine. Relative to a Reference kV, an increase in image
contrast (C) from a lower kV scan can be offset by an equal increase in image noise (N) to maintain
contrast-to-noise ratio (CNR).
For many cases, maintaining the CNR of a particular material may not be clinically acceptable. Instead,
both CNR and overall image noise should be taken into account. Auto Prescription balances the
consideration of CNR and image noise based on your selection of Clinical Task.

Scan
Contrast-to-Noise Ratio (CNR) example
Soft Tissue Low Contrast 120 kV Angiography High Contrast 80 kV
Changing kV also impacts CT number (Hounsfield unit) measurement, therefore there are some
clinical cases where changing kV may not be clinically acceptable.
Changing kV and mA will also change the overall appearance of the images, therefore it is advised to
adjust ww/ wl accordingly.
11.2.7.3 Auto Prescription Key Concepts and Theory

At scan time, Auto Prescription utilizes attenuation information from the patient scout over the
scan range to determine the patient size. Utilizing the kV Profile to apply each setting from the
corresponding Patient Size Range. If NI is set within the kV Profile, then no additional NI adjustments
are done. When NI is set in the protocol and the Patient Size is above or below Reference Patient Size,
then Auto PrescriptionAuto Prescription will adjust the NI for the selected technique based on the Size
Adjusted NI strength and the Clinical Task within the kV Profile.
See Protocol Management with Auto Prescription and Auto Prescription Profile Editor. in the
Revolution™ CT, Revolution™ CT ES User Manual.
11.2.7.4 Reference Size Patient

For Auto Prescription to work effectively to compensate for variation in patient size and tissue
composition, the parameters within the protocol must be set for desired image quality and dose
for a Reference Size Patient.
Auto Prescription profiles contain one or more size ranges. Size ranges consist of minimum and
maximum limits that are specified in units of Dw, water equivalent diameter in cm, AP (Anterior
Posterior measurement in cm), LAT (lateral measurement in cm), and AP +LAT (Anterior Posterior plus
Lateral measurement in cm). In addition, the patient range limits may be viewed and set in Weight ( lbs
or kg) or BMI, however the kV Profile cannot be saved in these units. The system will automatically

Scan
convert the values to the selected size units. The profile must contain a size range that includes the
Reference Size Patient. The patient range inclusive of the Reference Size Patient will be designated
with the icon
The Reference Size Patient used by Auto Prescription is 28.9 cm Dw.
NOTE
The Reference Patient Size of 28.9 cm Dw converts to different AP, LAT, or AP + LAT
depending on the scan field of view type that is used at scan time, as illustrated in the
table below. For Head and Body SFOVs, the Reference Patient size of 28.9 cm Dw is
converted to AP, LAT, and AP + LAT using a Chest/Abdomen/Pelvis conversion factor. For
Cardiac SFOVs, the Reference Patient size of 28.9 cm Dw is converted to AP, LAT, and AP
+ LAT using a Thorax conversion factor, which is more appropriate for Cardiac scanning.
However, note that the Reference Patient Size that is shown in the Auto Prescription
Profile Editor always corresponds to the Reference Patient Size for a Body SFOV.
Table 68 Reference Size Patient Value conversion by Size Unit
Reference Patient Size (Head and Reference Patient Size (Cardiac Size Units
Body SFOV) SFOV)
28.9 28.9 Dw (water equivalent diameter)

(cm)
58.0 65.3 AP + LAT (Anterior Posterior plus

Lateral) (cm)
23.8 26.6 AP (Anterior Posterior) (cm)
34.2 39.4 LAT (Lateral) (cm)
25.2 25.2 BMI
~160 ~160 Weight (lbs)
~73 ~73 Weight (kg)
11.2.7.5 Estimating Patient Size and Patient Size Units

Auto Prescription profiles contain one or more size ranges that may be specified in one of several
Patient Size Metrics, such as AP + Lat, AP, Lat, and Water Equivalent Diameter (Dw).
At scan time, an estimate of the patient size over the scan range is calculated from the patient
attenuation data of the scout. The attenuation information used is Dw, which is then converted to the
Patient Size Metric defined in the selected Auto Prescription profile to determine which size range from
the profile the patient falls within.

Scan
Dw Dw is the term used for Water Equivalent Diameter, which is the diameter (in
cm) of a cylinder of water that would give the same x-ray attenuation of the
object or patient being scanned. More details can be found in AAPM Reports
204 and 220.
The conversion from Dw to other Patient Size Metrics is based on work from previous studies1, 2, 3 that
analyzed phantom and clinical datasets and derived formulas to convert between Dw and AP + Lat, AP,
Lat, Weight, and BMI. In general, AP + Lat has a strong correlation to Dw, and so AP + Lat is the default
Patient Size Metric used in the GE Reference Profiles. While not as strongly correlated to Dw, Lat may
be appropriate for chest or cardiac scans.
BMI and Weight, on the other hand, are generally poor correlates for patient attenuation. Therefore,
while the user can set up a profile in Weight or BMI, they must switch to another Patient Size Metric
before being able to save a profile. When switching from one Patient Size Metric to another, all size
values in the profile will automatically convert to the newly selected Patient Size Metric.
Note: See Scout Based Attenuation Characterization for more information on Dw.
[ 1 ] Menke J. Comparison of Different Body Size Parameters for Individual Dose Adaptation in Body CT
of Adults. Radiology 2005; 236:565–571.

Scan
[ 2 ] Burton CS., Szczykutowicz TP. Evaluation of AAPM Reports 204 and 220: Estimation of effective
diameter, water-equivalent diameter, and ellipticity ratios for chest, abdomen, pelvis, and head CT
scans. J Appl Clin Med Phys 2018; 19:1: 228–238.
[ 3 ] Boone JM, Strauss KJ, Cody DD, et al. Size-specific Dose Estimates (SSDE) in Pediatric and Adult
Body CT Examinations. AAPM Report 204, 2011.
11.2.7.6 Clinical Task

NOTE
If NI is set within the profile, the Clinical Task setting is disabled.
When NI is set within a protocol, the goal of Auto Prescription is to maintain the same contrast-to-
noise ratio (CNR) in the image that would be achieved for the kV used for the Reference Size Patient
even if the kV is lower or higher than the kV for the Reference Size Patient (Reference kV).
The Clinical Task selection determines the level of NI adjustment required to balance the change in
image contrast with the maximum tolerated noise change for the intended clinical intent of the exam.
For example, Clinical Tasks containing bone or iodine produce relatively larger increases in image
contrast at lower kVs, so they can sustain relatively higher increases in noise, thereby offering more
potential for radiation dose savings than a clinical task without iodine enhancement.
Table 69 Clinical Task Settings
Clinical Task Description
NOTE
NI adjustment will be a relative increase when the kV is lower than the reference kV and will be
a relative decrease when the kV is higher than the reference kV.
Soft Tissue Non-Contrast Small adjustment of Noise Index across kV, optimized
for scan situations where contrast agents are not
used. The regions of primary importance are non-en-
hanced tissue regions.
Soft Tissue +C Low Contrast Moderate adjustment of Noise Index across kV, opti-
mized for scan situations where iodinated contrast
agents are used. The regions of primary importance
are both enhanced and non-enhanced tissue regions
with lower noise compared to Soft Tissue +C High
Contrast.
Soft Tissue +C High Contrast Moderate adjustment of Noise Index across kV, opti-
mized for scan situations where iodinated contrast
agents are used. The regions of primary importance
are both enhanced and non-enhanced tissue regions
with higher noise compared to Soft Tissue +C Low
Contrast.

Scan
Clinical Task Settings continued

Clinical Task Description
Bone Non-Contrast Large adjustment of Noise Index across kV, optimized

for scan situations where iodinated contrast agents
are not used. The regions of primary importance are
bony regions.
Angiography Large adjustment of Noise Index across kV, optimized

are used. The regions of primary importance are
both enhanced and non-enhanced tissue regions with
higher noise compared to Cardiac.
Cardiac Large adjustment of Noise Index across kV, optimized

are used. The regions of primary importance are both
enhanced and non-enhanced tissue regions.
Gated High Contrast Large adjustment of Noise Index across kV, optimized
are used. The regions of primary importance are en-
hanced tissue regions.
11.2.7.7 Size Adjusted Noise Index (SANI)

NOTE
If Noise Index is selected as a Auto Prescription Profile parameter, then Size Adjusted
Noise Index is disabled.
For patients larger than the Reference patient size, Noise Index is increased to reduce radiation dose.
For patients smaller than the Reference patient size, Noise Index is decreased to improve image
quality.
This size-dependent Noise Index adjustment is made to the Noise Index set in the protocol prior to any
additional adjustments that may be made based on Profile kV and Clinical Task.
Table 70 Size-adjusted Noise Index Strength Settings
Smaller than Reference Patient Size Larger than Reference Patient Size
No Change No Change
Very Small Decrease Very Small Increase
Small Decrease Small Increase
Moderate Decrease Moderate Increase
Large Decrease Large Increase
Very Large Decrease Very Large Increase

Scan
NOTE
For any given Size Adjusted Noise Index strength, the percent increase or decrease in the
Noise Index (relative to the Noise Index set in the protocol) gets larger as the patient size
gets further away from the Reference Patient Size. For example, the increase in Noise
Index for a patient that is much larger than the Reference Patient Size will be greater
than that for a patient that is only slightly larger than the Reference Patient Size.
Figure 141 on page 307 shows the estimated relative decrease or increase in NI across patient size for
each SANI strength setting relative to using a constant NI. For patient sizes smaller than the Reference
Patient Size, the noise will never decrease by more than 45% relative to the Reference NI. For patient
sizes larger than the Reference Patient Size, the noise will never increase by more than 60% relative to
the Reference NI.
At scan time, Size Adjusted Noise Index adjusts the Noise Index set in the protocol based on the patient
size calculated from the scout.
Table 71 on page 308, Table 72 on page 309 and Table 73 on page 310 show the estimated relative
decrease or increase in CTDIvol across patient size for each SANI strength for the specific scan settings
shown. Example 1, figure 1, Example 2, figure 1 and Example 3, figure 1 show CTDIvol relative to the
Reference Patient Size, whereas Example 1, figure 2, Example 2, figure 2 and Example 3, figure 2 show
CTDIvol relative to if the same patient size were scanned at a constant NI. Note that these figures show
estimated relative CTDIvol for the fixed scan settings described in the figure headings (e.g., 120 kV, 9
NI, 5mm slice thickness, and specific pitch and rotation time values commonly used for small, average,
and large sized patients). The actual relative increase or decrease in CTDIvol for a given patient size and
SANI strength may vary based on the maximum achievable tube output at each kV, pitch, and rotation
time setting for the prescribed Noise Index and scan range.
The following table summarizes Figures Example 1, Figure 1 through Example 3, Figure 2.
Figure What does it show Patient Size Range kV / NI / Slice Detector Cover-
Thickness age / Pitch / Rota-
tion Time
Example 1, figure 1 CTDIvol relative to 20 – 60 AP + Lat 120 kV / 9 NI / 5mm 80mm / p1.531 /

Reference Patient 0.28s
Size

if same patient size 0.28s
were scanned at
constant NI

Size

were scanned at
constant NI

Scan
(continued)
Figure What does it show Patient Size Range kV / NI / Slice Detector Cover-
Thickness age / Pitch / Rota-
tion Time
Example 3, figure 1 CTDIvol relative to 60 – 100 AP + LAT 120 kV / 9 NI / 5mm 80mm / p0.508 /
Size
Example 3, figure 2 CTDIvol relative to 60 – 100 AP + LAT 120 kV / 9 NI / 5mm 80mm / p0.508 /
were scanned at
constant NI
Figure 141 SANI Strength estimated NI change by Patient Size

Scan
Table 71 Relative CTDIvol versus Patient Size using Constant Noise Index - Example 1
Detector Coverage 80 mm, Pitch 1.531, Rotation Time 0.28 seconds

Patient Size Range: 20 – 60 AP + Lat
120 kV, 9 NI, 5 mm slice thickness
CTDIvol Relative to
Reference patient
size
CTDIvol relative
to same patient
size using constant
noise index

Scan
Detector Coverage 80 mm, Pitch 0.992, Rotation Time 0.5s

CTDIvol Relative to
Reference patient
size
CTDIvol relative
to same patient
size using constant
noise index
The decrease in rel-
ative CTDIvol begin-
ning around patient
sizes less than 25
AP + Lat is due to
the system reaching
the minimum mA
limit for all SANI
strength settings.

Scan
Detector Coverage 80 mm, Pitch 0.508, Rotation Time 1.0 second

CTDIvol Relative to
Reference patient
size
The flattening of the
relative CTDIvol be-
ginning around pa-
tient sizes greater
than 80 AP + Lat
is due to the sys-
tem reaching the
maximum mA lim-
it across each SANI
strength setting.
CTDIvol relative
to same patient
size using constant
noise index
The increase in rel-
ative CTDIvol begin-
ning around patient
sizes greater than
80 AP + Lat is due to
the system reaching
the maximum mA
limit across each
SANI strength set-
ting.
11.3 Exam Workflow

Scan
11.3.1 Exam Workflow Concepts
11.3.1.1 Positioning a patient

Before placing patients in the system each day, the accessories that may be used during the day while
scanning should be inspected such as the head holder, table extension, patient positioning pads and
straps to make sure they are in good working condition.
Positioning pads and straps should be inspected and cleaned to prevent the possibility of artifacts
being introduced due to foreign matter such as contrast on the surfaces of these items. Do not use
accessories that maybe broken or torn.
Make sure patients are comfortable as possible on the table or in the head holder. Use positioning
sponges and pads along with positioning straps to aid in the positioning of the patient to help
them hold the position needed to complete the exam. If patients are comfortable, they will be able
cooperate and hold still during the exam.
Make sure any sheets, blankets and patient clothing or gowns don’t get caught as the table is moving.
Use the positioning straps to help contain these items so they are not loose or hanging off the cradle.
Make sure to explain the procedure to the patient so they understand what is going to happen and
what to expect. This will reduce incidences of the patient moving because they are surprised by the
position they are put in the gantry or the movement of the table.
11.3.1.2 Using protocols

All parameters for scanning a patient can be set up in a protocol. This saves you time when prescribing
scan parameters for each patient. When a new patient is scanned, type in the patient information and
choose a protocol. The protocol may be adjusted based on a patient without permanently altering the
original set of parameters. Once the parameters are set and the prescription is confirmed, scanning
can begin.
See the Protocols chapter for more information.
11.3.1.3 Using contrast

When intravenous (IV) contrast is to be used, make sure the injector or syringes of contrast are setup
before performing the localizer (scout) scan. The Contrast settings collection on the Scan Settings
window must be selected. When selected, a +C annotation is displayed on the image next to the image
number, indicating that IV contrast was used for that exam.
See Enter Contrast Settings for more information.
11.3.2 Exam Workflow Windows
11.3.2.1 Patient Information window

From the scan monitor, open the Patient Schedule drawer and click a patient entry.
Alternatively, click from the scan monitor to open a new patient window.

Scan
Figure 142 Patient Information window
See Set up the patient's information for character limits in each field.

Scan
11.3.2.2 Patient Position area

The Patient Position area is on the Scan Setup window.
Figure 143 Patient Position area
If user clicks anywhere within the yellow box area (as shown in Figure 143 on page 313), the user can
change: Landmark, Orientation, Position, Copy Forward & Auto Voice.

Scan
Element Description
Anatomical Landmark Reference Choose a preset center point, or designate a center point with a two
Point letter abbreviation or 0. This should be set the same as your scout
images.
Preset Center Points
• OM: (orbital-meatal line)
• SN: (sternal notch)
• XY: (xyphoid process
• IC: (illiac crest)
• AJ: (ankle joint)
• KN: (knee)
• SP: (symphysis pubis)
Patient Orientation Set the proper patient orientation and position.

Patient Position Place the cursor on the head or feet of the patient and click to change
the head-first or feet-first patient orientation.
Place the cursor over the abdominal area or table base and click to
rotate the patient in 90° increments to change the patient position.
Copy Forward Select to copy Patient Orientation and Patient Position settings from
the previously scanned series.
Auto Voice Language Click to set the Auto Voice language for the exam.
11.3.2.3 Scan Settings window

The Scan Settings window is an area on the Scan Setup window. Parameter fields that can be
modified are underlined. Additionally, parameter fields with small boxes next to them indicate that a
pop-up window can be opened to define more values. Each exam or protocol can contain on the scan
monitor task list: 15 series, 15 groups per series and 5120 images per series.
NOTE
The Scan Settings window will change based on the scan type selected.

Scan
Figure 144 Scan Settings window
Figure 145 Scan Setup window — Context Menu
Table 74 Scan Setup window — Context Menu Selections
Element Description
Create New Scout Series Set up a new scout series for the exam.
Create New Axial Series Set up a new Axial series for the exam.
Revisit Protocol Go back and change the protocol selected.

Scan
Table 75 Scan Setup window — Buttons
Element Description
Done Scanning Ends data acquisition for the exam.
Confirm Settings Ends prescription preview mode.
NOTE
This is not available if the patient has not been landmarked or if
invalid parameters exist in the Scan Settings window.
Close Exam Closes the patient exam session.
Table 76 Scan Setup window — Right-click Selections
Element Description
Duplicate Series Right-click on a series task to duplicate it.
Rename Series Rename the selected task.
Delete Series Right-click on a series task to delete it.
Copy Right-click on a series task to copy it.
Paste Right-click on the series where you want the copied series to be pasted below it.
Add Group Right-click on a group task to add an additional contiguous group.
Duplicate Group Right-click on a group to duplicate it.
Add Smart Prep Group Right-click on a group task to add a Smart Prep scan task.
Delete Group Right-click on a group task to delete it.
Undo Removes the last recorded right menu action.

Scan
Scan Setup window — Right-click Selections continued

Element Description
Link All Links all groups within a series. This allows you to adjust the start location of the
first group and the end location of the last group, and to adjust the location of
scan rotation boundaries between the groups while keeping the groups contigu-
ous. The link icon appears on the scan series task when Link All is enabled.
Link All enabled assures a full field of view contiguous data set between groups,
when at least one group of axial or cardiac scan type contains a detector coverage
of 80 mm or greater.
DFOV, Image Thickness and Interval must be the same when Link All is enabled.
Primary recon of linked groups will not start until the scan is complete and
Continue is selected.
An Invalid DMPR task message displays when All Anatomy Recon, which contain
at least one group of axial or cardiac scan type, contains a detector coverage of 80
mm or greater and are not Linked. If DMPR is desired, select Link All.
Scanned groups cannot be unlinked.
Duplicate Groups is not valid for scanned linked groups.
Unlink All Unlinks all scan groups in the series, allowing them to be moved independently.
Split Splits any One or More table position prescription within a single physical scan
group and separates them into individual physical scan groups.
Split and Link Splits any One or More table position prescription within a single physical scan
group and separates them into individual physical scan groups; then the start and
end between groups are linked and contiguous.

Scan
Table 77 Scan Set up window – Task Color Indication
Element Description
Task color in- Indicates the Show Localizer Group Color on the task when enabled in System Preferences
dication
NOTE
After 6 groups have been added, subsequent groups will be added with the
group 1 color. If groups 2-6 are deleted, when adding or duplicating a group, the
color added will be the same as the last group deleted.
Tab color in- Underlines the group name on the group tab.
dication
11.3.3 Exam Workflow Procedures

This is an overview of the steps necessary for a patient scan, from patient set up to image
management.
1. Set up and position the patient.
2. Set up the patient’s information.
3. Select a protocol.
4. Acquire a Scout scan.
5. Acquire the scan data.
a. Set the Scan Parameters.

Scan
b. Center the patient.

c. Adjust the Graphic Rx.
d. Set the Timing Parameters.
e. Set the Recon Parameters.
Set any DMPR tasks, if required.
f. Set the transfer options.
If using Dose Watch, dose reports should be set to Transfer by Exam.
g. Apply any additional scan features.
h. Enter contrast descriptions.
i. Start the scan.
Check the following before you confirm:
i. Start/End locations for each recon
ii. Direction of scans
iii. mA table for SmartmA
iv. Duplicate a series, if necessary.
6. Close the exam.
7. View the images.
8. Archive the images.
9. Network the images.
11.3.3.1 Set up and position the patient

Prepare the scan room before bringing in the patient. Make sure that you have all the necessary
supplies and accessories. If you will be using IV contrast, set up the injector or syringes before running
the scout scan.
Patient Positioning Controls can be accessed on Gantry Controls (GCP) or Remote Control Panel (RCP).
Review Gantry Control and Using Remote Control Panels prior to completing these steps. If using RCP,
ensure that AVIMOS monitor is visible and displays unobstructed views of the table and gantry bore
from Front, Back and Side of the gantry.
1. Attach the head holder or foot extender to the end of the cradle toward the gantry, if needed.
2. Press and hold the Unload button on the table foot pedal, GCP or RCP to adjust the table height
for transferring the patient onto the table.
The cradle moves to home and to a minimum height of 49 cm.
3. Transfer the patient onto the table.
• Make sure to follow the manufacturer’s directions for use of a protective table slicker when
scanning, otherwise artifacts may appear in images.

Scan
• Blocked reference channels can cause image artifacts. Make sure that there are no blankets,
clothing, tubing, or straps hanging down below the table when scanning. Keep items
wrapped close to the table by using the patient restraint straps.
4. Press and hold the Load button on the table foot pedal, GCP or RCP.
• The table moves up to a height of 210 mm and advances the table and cradle into the gantry.
If a protocol has been selected, the table will move to a preset height and location based on
the anatomical reference in the protocol.
• Release the foot pedal when the patient is properly positioned. Use the gantry controls to
further adjust the position.
5. Make the patient comfortable and immobilize as needed. Connect body straps to the cradle and
wrap them around the patient.
• Use the head holder straps to immobilize the patient's head.
• Make sure items such as blankets and straps are not hanging off the table or allowed to touch
or be dragged through the gantry during the scan, otherwise artifacts may appear in the
images.
6. If needed, attach the IV pole.

7. Press the Laser Alignment Light button on gantry control or press Move to Scan with RCP
Alignment Light to turn on the laser alignment lights. The Gantry rotates to the laser light
position and illuminates internal and external alignment lights if RCP is closed. It illuminates only
the external alignment light if RCP is open. Do not position the patient with the laser lights shining
into his or her eyes.
8. Use the following patient positioning control GCP or RCP controls to refine the patient's position
and align the appropriate laser lights with the target anatomical reference.
Table Up Table Down
Cradle In Cradle Out
NOTE
If it is not possible to move the table down:
• Check to make sure there is nothing blocking the table or gantry path.
• Check the gantry display or the message log for collision sensor errors, which
prevent downward movement.
• Resolve any issues and press the table up/down buttons.
• If the problem persists, contact your service representative.
9. Press the Internal Landmark button if using internal alignment lights or press External
Landmark if using external alignment lights to align patient. You cannot click Confirm Settings
until after you have pressed a landmark button.
• The landmark sets a known anatomical reference for the radiologist to correlate anatomy.

Scan
• The landmark sets the zero location. When scanning towards the patient’s head, you are
scanning superior to the zero location. When scanning towards the patient’s feet, you are
scanning inferior to the zero location. You should set the zero location to known anatomy.
For example, when scanning a head, the landmark or zero location is typically the orbital
meatal (OM) line.
• A landmark or zero reference point is required before you scan a patient. It can be set before
or after you start a new patient exam.
• When using the external laser alignment light to position the patient, be aware that the
patient’s elevation may be slightly lower with the cradle extended than with the cradle fully
retracted. The cradle may bend slightly under the patient’s weight. Take this difference into
consideration for applications where patient position is critical, such as treatment planning.
To minimize these effects, after positioning the patient using the external laser alignment,
advance the patient to the CT scan plane. Turn on the CT alignment lights to determine
if they line up with the markers on the patient. Compensate for the bend in the cradle
by elevating the table. When the CT alignment lights line up with the markers, reset the
landmark for the scan using the Internal laser alignment light.
Figure 146 External Alignment Light Only with RCP Open
10. From the Scan Control Interface, set volumes with the Patient-to-Operator and Operator-to-
Patient , or Auto Voice communication controls. Press the Talk control to test the Operator-to-
Patient volume level.

Scan
Patient-to-Operator Operator-to-Patient Auto Voice communica- Talk control

communication volume communication volume tion volume control
control control
11.3.3.2 Set up the patient's information

Use this procedure from the CT operator console, each time you start a new patient exam. Set up
the patient information before you get the patient on the table. This reduces the amount of time
the patient has to be in a potentially difficult position. When entering patient information, the only
required field for scanning is the Patient ID. This procedure describes how to manually input the data.
The data can also be input by using Patient Scheduler or a bar code reader.
1. From the scan monitor, click .
• The Patient Information window displays the new Exam Number after a protocol is selected
and transitions to the Scan Settings window.
• The maximum Exam Number is 49,999, which will be reset by your Field Engineer.
• If patient information is entered from a HIS/RIS system, these data fields support up to 64
characters. If patient information is edited or manually entered, character limits are those
noted in the table below.
Table 78 Patient Information fields
Field Parameters
Accession Number Up to 16 characters
Patient ID* Up to 64 characters
Patient Name* Up to 64 characters
Sex Male, Female or Other
Month/Day/Year (MM/DD/YYYY)
Birthdate Day/Month/Year (DD/MM/YYYY)
Year/Month/Day (YYYY/MM/DD)
Years, Months, Weeks, Days
Age NOTE
Maximum age that can be entered is 150
years.
Weight Kilograms or Pounds

Scan
Patient Information fields continued

Field Parameters
Height Feet and Inches or Centimeters
Referring Physician* Up to 64 characters
Radiologist Up to 64 characters
Operator Up to 64 characters
History Up to 60 characters
Exam Description Up to 64 characters
Protocol Number Up to 5 characters
Req. Proc. ID Up to 16 characters
Date Exam Date Month, Day, Year
Time Exam Time Hour, Minute
2. From the Patient Information window, enter data into the appropriate fields.
• Press Tab to advance to the next text field, or use the mouse to navigate to each field.
• The cursor must be within the Patient Information window for the input to be accepted.
• Patient ID is a required field. If the patient does not have an identification number, enter text
in the field or if information is unknown use the Unknown Patient feature Enter Patient ID
and Patient Name using Unknown Patient.
• Once an identification number has been assigned, you can edit exam information using Edit
Patient after Close Exam.
• Select Delete All Completed exams when patient information is updated from the HIS/
RIS. This ensures that completed accession numbers are not inadvertently selected for a
second scanning. This could cause patient reconciliation issues on the Picture Archiving
Communications System (PACS).
• Birth dates can only be entered for the past 150 years. The format for date entry depends on
your system settings: MM/DD/YYYY, YYYY/MM/DD, DD/MM/YYYY.
• Patients in Japan may know their birth date only by emperor reign year. Configure the birth
date fields to YYYY/MM/DD date format and enter the reign year in the year field. For example,
enter S26, if your patient was born in the 26th year of Showa's reign, which corresponds
to 1951. The Era codes are Heisel (H), Showa (S), Taisho (T), Meiji (M). The system stores
the converted birth year in the birth date field on the New Patient and Patient Schedule
windows and in the image header.
• If needed, select items from any of the stored Preset Selection values: Referring Physician,
Radiologist, Operator, Exam Description. The selections are displayed as you type a
character and the list is filtered.

Scan
• The patient session will not be created if the following characters are used in the patient
information fields:
Language Characters
Dutch Ĳ, ĳ
Finnish Š, š, Ž, ž
French €, Œ, œ, Ÿ
German €
NOTE
Patient information selected from Patient Schedule in which the patient name is
blank or needs to be updated with non-English characters will not be able to be
edited if DICOM tag 0008, 0005, or Specific Character Set is not filled with the correct
character set designation.
For example, if Swedish characters are desired for patient name, DICOM tag 0008,
0005 must reference ISO_IR 100.
Character sets supported are:
• ISO_IR 100 Latin 1 (example Swedish and Latin alphabet)
• ISO_IR 87 Japanese/Kanji
• ISO_IR 6 US-ASCII
11.3.3.2.1 Enter Patient ID and Patient Name using Unknown Patient

Use this procedure to assign Patient ID and Patient Name when information about the patient is
unknown.
1. From the scan monitor, click
2. To populate the field on the Patient Information window, click . The Patient
ID will be listed as Trauma_yyyy_mm_dd_hh_mm_ss and Patient Last Name will

Scan
be Patient_yyyy_mm_dd_hh_mm_ss, the Unknown Patient icon will be highlighted.
3. Enter any remaining patient information.

4. Select desired protocol(s) and begin the exam.
NOTE
The Patient ID and Last Name field cannot be edited if the Unknown Patient icon has
been selected. To enter Patient ID or Last Name, deselect the Unknown Patient icon.
11.3.3.2.2 Enter patient ID or accession number with the bar code reader
1. From the scan monitor, click .
2. To populate the field on the Patient Information window, aim the bar code reader at either the
Patient ID or Accession Number bar codes on the patient requisition.
3. Enter any remaining patient information.
4. Select desired protocol(s) and begin the exam.
11.3.3.2.3 Modify the Patient Information presets

Use these procedures to modify the Preset fields on the Patient Information window. The presets are
saved across software loads from the saved System State.
2. Click System Preferences.
3. From the System Preferences window, click the Patient Data Entry tab.
4. Click any of the preset fields or click Add New and type in the desired text field.
• Referring Physician
• Radiologist
• Operator

Scan
• Contrast Oral
• Contrast IV
NOTE
For Referring Physician, Radiologist or Operator, enter the first name, last name or
both.
NOTE
Selecting another Preferences tab will save the data entered.
Change an item on the list
1. From the Preset fields window, select the item you want to change.
2. Enter the new information in the text field.
3. Press Enter.
Add an item to the list

1. From the Preset fields window, click Add New.
2. Enter the new information in the text field.
3. Click Save.
Delete an item from the list

1. From the Preset fields window, select the item you want to delete.
The item is displayed in the text field
2. Click X to delete the item.
11.3.3.3 Select a protocol

Use this procedure to select a protocol for scanning.

Scan
Figure 147 Protocol Selection window
NOTE
Suggested Protocols box displays only when Intelligent Protocoling Option is installed.
NOTE
The value in the Worklist Key dropdown box on the Intelligent Protocol System
Preference screen determines which Worklist Key is used. Refer to Intelligent
Protocoling System Preferences.
1. If the Intelligent Protocoling Option is installed, the system tracks the most commonly selected
protocols for the Worklist Key from the patient worklist and displays up to 6 protocols in the
Suggested Protocol area. The suggested protocols display only if a protocol has been selected at
least 5 times for a given Worklist Key.

Scan
NOTE
Only recommended protocols from adult protocols display when the adult selector
is displayed and only recommended protocols from pediatric protocols display
when the pediatric selector is displayed.
If the AutoSelect protocol preference is set to On, and a protocol has been selected
at least 20 times for a given modality worklist entry and the confidence is 30 percent
higher than the next highest protocol, the system selects a protocol and displays it
in the Selected Protocols area. The user can click Accept to use this protocol(s) for a
patient scan. Prior to selecting Accept, read and verify the protocol name(s) selected
are the protocols desired for the exam. If not, use the X icon next to the protocol
name to delete a protocol that is not desired and select the desired protocol(s) from
any protocol per select a protocol.
2. Select the desired protocol category, then search for a specific protocol using one of the following
methods.
NOTE
Multiple protocols can be selected
• Select a protocol from the Favorites list area.
• Select an anatomical region and then select a protocol.
• Search for a protocol in the Protocol Search field and then select a protocol.
• Select a protocol from the Suggested Protocol area.
The suggested protocol(s) will display in the Suggested Protocols area.

3. Click Accept.
NOTE
Prior to selecting Accept, read and verify the protocol name(s) selected are the
protocols desired for the exam. If not, use the X icon next to the protocol name to
delete a protocol that is not desired and select the desired protocol(s)
NOTE
When multiple protocols are selected the protocol name shown on the right
monitor is the protocol name of the last protocol selected. Tasks listed start with the
tasks from the first protocol selected, then 2nd protocol and so on.
NOTE
If you click Accept when a scan data save or restore is in progress, a message
displays indicating that the scan resource cannot be acquired.
11.3.3.4 Acquire a scout

Use this procedure to acquire a scout from which you can prescribe the scan locations.

Scan
Figure 148 Scout collection
1. Confirm that the patient orientation matches the patient orientation in the Patient Position area
of the Scan Settings window.
• Click on the patient image to change to a head-first or feet-first orientation.
• Click on the table or above the patient body to rotate the body in 90° increments.
2. From the Scout collection on the Scan Settings window, confirm the Start and End locations, kV,
mA, and Auto Voice settings (if applicable).
• To change a parameter, open the desired settings collection and click in the field to enter a
new value. Plus (+) can be used for S values and Minus (-) for I values when using the ten-digit
key pad.
• A user message dialog displays when the system updates the Start and End Location to be
S-I. The Start and End Locations have been updated to set scan range from S to I. Verify Start
and End Locations are as desired
• A blue alert message displays when the Start or End location is outside the table range.
Start or End Location has been updated to be within the table range. Verify Start and End
Locations are as desired.
• Technique factors are set low (120 kV and a low mA are common), since these scans are
normally used only for planning purposes.
• When Fast Scout is used on larger patients, use a higher mA value than you would use for a
normal speed scout.
• Dose calculation for the scout scan uses the effective mA value. This value can be found in
DICOM tag 0045, 1066 SmartScout effective mA.
3. Set the Scout Plane to designate the type of scout to acquire.

• 0° = 12 o'clock

Scan
• 90° = 3 o'clock
• 180° = 6 o'clock
• 270° = 9 o'clock
4. In the Window Width and Window Length fields, type the desired values.
5. When performing a gated exam, set up the patient monitor and check that a trace is displayed to
verify that the system is receiving the ECG monitor signal.
• Click On to enable gating.
• If the ECG signal has not been detected, the system displays a message to check the
connection. Check that all ECG leads are connected to the patient and that the monitor
power is on. See the Cardiac chapter for more details.
6. Click Confirm Settings.

7. Press Move to Scan.
NOTE
Move to Scan flashes green on the scan control interface indicating you need to
press it.
Press Stop Move if you need to stop table movement.
8. Press Start Scan.

Scan
NOTE
When a 90° or 270° azimuth scout is acquired, the system will assess patient
centering. If the patient is centered, a single green line with a check mark will
display on the image. If the patient is off‐centered greater than 2 cm, the system will
display the table height location and an up or down arrow to indicate the elevation
needed to reach that height. Use the gantry control to press and hold the indicated
button along with the fast button to move the table to the recommended height.
Figure 149 Patient centering image
Figure 150 Patient off-centered
• Press Stop Scan if you need to stop the scan.

• Press Pause Scan if you need to pause the current scan.
• This finishes the current scan, then pauses the next scan. Click Resume when you are
ready to scan again.
• In Axial scans, the scan stops after the next scan.

Scan
• In Helical scans, the entire scan is completed. Use Stop Scan; not Pause Scan.
9. Repeat the previous two steps to acquire the second scout scan.
10. Click Continue to move to the next scan task.
11.3.3.5 Center the patient

Following the acquisition of a lateral scout, the system will display a patient centering line and
recommended table elevation height for the diagnostic CT scan. The recommended table height
will be displayed on the lateral scout image and will include an arrow to indicate the table motion
direction and target elevation height (also on the gantry display).
Figure 151 Patient Centering Line and Recommended Table Elevation Height on Lateral Scout
Image
Manually adjust the table elevation height to the recommended value with the gantry controls, so the
patient is centered properly in the gantry, thereby optimizing technique for the prescribed scan. Do
not use the Load or Unload pedals while doing this adjustment. The patient centering line and
recommended table elevation height will be cleared from the scout image when the user proceeds to
the next scan or scan prescription edit.
Considerations

Scan
• The recommended table elevation height for a specific scout image can also be found in the
System Messages area.
• If a patient centering line is displayed but not the recommended table elevation height, the
patient is already centered for the diagnostic scan.
• Always make sure that the patient centering line is appropriate for your clinical need. The user
is ultimately in control of table elevation adjustments and patient positioning for the scan. The
patient centering notification should be used to estimate center line for simple cases.
• Zoom operations in the viewport may hide the patient centering line and recommended table
elevation. Reset the viewport option with right-click menu options.
• This feature is always enabled and cannot be turned on or off.
NOTE
If a patient centering line cannot be estimated or truncated data was detected, the
following notification will be displayed:
“System is not able to calculate optimal patient centering position. Verify that table
elevation is centered to the body part of interest and the resultant CTDIvol and DLP meet
the clinical goal for the acquisition and follow the radiation exposure guidelines for your
department.”
NOTE
Patient positioning accessories may affect dose and image quality. AEC will compensate
for changes in attenuation due to the accessories by adjusting mAs to achieve
the prescribed image noise/quality criterion. Consult the accessory manufacturer’s
instructions for use for recommended adjustments, if needed, for manual scan modes.
11.3.3.6 Exam Workflow on Gantry Display
11.3.3.6.1 Initial Screen

On the initial screen, the user can create a new exam by selecting a patient from Patient Schedule or
by creating an anonymous emergency patient directly.

Scan
Figure 152 Gantry Display initial screen
Table 79 Icons
Patient Schedule Displays Patient Schedule window.
1.
Emergency Patient
2. Displays Emergency Patient window.
11.3.3.6.2 Patient Selection

Patient list information is obtained from the RIS server. If you need to refresh the listed information,
you can
press the Refresh icon on the Toolbar.
To select a patient, touch on the patient's line. the screen changes to New Patient screen.

Scan
Figure 153 Patient Schedule
Table 80 Toolbar Icons
Patient List Patient List with Patient's Name, ID, Date of Birth or Age, Exam
Date and Time, Exam Description, Exam Session Number.
1. The list can be sorted by Name, ID or Exam Date and Time.

Press the header of the corresponding column to sort the column
ascending or descending. The user can select which content dis-
played in the patient list at the gantry display preference.
Refresh
2. Refreshs the listed information.

Scan

Hide Patient Information

Hides a patient's private information (Name, ID, Date of Birth, or
3.
Age). Press the icon again to redisplay the patient information.
Search Box
Finds the patient with the Patient Name or ID, then select the
4.
patient to create new exam.
Figure 154 Patient Schedule with Patient Information Hidden
The user can drag the scroll bar on the right of the Patient List to look through patients.
If you want to exit Patient Schedule without selecting any patients, you can press the Patient Schedule
icon in the top left corner to exit Patient Schedule.
11.3.3.6.3 Emergency Patient

From the Emergency Patient screen, an exam can be started without entering any Patient information.
The patient ID and last name is automatically assigned by the system.
Patient ID is assigned as Trauma_yyyy_mm_dd_hh_mm_ss and the patient's last name as
Patient_yyyy_mm_dd_hh_mm_ss.

Scan
Figure 155 Emergency Patient screen
If the user selects Emergency Patient on the Gantry Display initial screen, the tag area displays only
Trauma tags.
The protocol list includes only protocols with trauma tags.

Scan
11.3.3.6.4 New Patient

In the New Patient, the user needs to confirm patient information, select desired anatomical area and
protocol.
Figure 156 New Patient Interface

Scan
Table 81 New Patient Interface Components
Patient Information
Exam Description
Operator Name
To be confirmed before scan start. Exam description and Opera-
1. tor name can select from list. To register the data in the list, use
Patient Data Entry in System Preference.
Anatomy Selector and Icons
2. To select anatomical area to display desired scan protocols
3. Anatomical area can be selected from this pull-down menu. Also

Related / Favorite /Suggested/ this menu includes Related and Favorite for the corresponding
Protocol Anatomy Selection protocols in the list below. The Favorite Protocol is specified
Box by the user. A Favorite protocol can be specified for each ex-
amination site (see Chapter 20 for more information). The Re-
lated Protocol automatically matches and applies a filter to pro-
tocols based on the exam description.Suggested Protocols are
displayed when Intelligent Protocoling Option is installed.
Protocol Category Selection

Box Selection in this box are ; GE Adult, GE Pediatric, User Adult and
4.
User Pediatric.
5. Contrast / Tags Box

When Related is select above, the contrast type that most related
to the exam description will be shown. When Favorite is selected,
this is for Tag selection area.

Scan
New Patient Interface Components continued

6. Key Words Search Field Desired protocols can be searched from this. By touching the
field, a key board is displayed and you can type the keywords.
7. Protocol List
Protocols narrowed down by the categories above are listed.
8. Exit
Touch this button when this exam needs to end.
9. Confirm
Touch this button whenever the desired protocols are selected.
The screen moves to the Scout Progress screen. (if the selected
protocol does not have a scout scanning, it directly goes to the
Scan progress screen.)
When desired scan protocol is high-lighted, then touch Confirm button to proceed to scout scan.

Scan
11.3.3.6.5 Bar Code Reader on Gantry
Figure 157 Bar code reader on gantry
To use bar code reader on the gantry:

1. The Gantry display is idle, with Patient Schedule List opened or closed.
2. Use the bar code reader to scan either the Accession number or the Patient ID bar code on the
request form.
3. Select desired protocol and begin the exam.
11.3.3.6.6 Related Protocols

Related protocols is a feature that recommends the most relevant protocols according to the Exam
Description of the selected exam. It is only available on the gantry display user interface.
When Related is selected in Related / Favorite / Protocol Anatomy Selection Box, a Key Word Selection
Box displays. Once this is selected, then protocols which include the Key Word in Exam Description are
displayed in the protocol list.

Scan
Figure 158 Related protocols Interface (1: Related / Favorite / Protocol Anatomy Selection Box, 2:
Key Word Selection Box)
In case the automatically identified information is not accurate, user can change these keywords to
refine the resultant protocol list.
Related protocols work within the selected GE/User and Adult/Pediatric combination, so when user
switches between GE/User or between Adult/Pediatric, the resultant protocol list is updated.
In order to exit Related Protocols, any of the following can be used:
• Close the Related protocols list by pressing the “X” icon of the search field
• Select any other categories from Related/Favorite/Protocol Anatomy Selection Box
• Select anatomy from the Related/Favorite/Protocol Anatomy Selection Box
• Select anatomy on the Anatomy Selector
• Select anatomy from the nine icons around the Anatomy Selector
When desired scan protocol is high-lighted, then touch Confirm button to proceed to scout scan.
11.3.3.6.7 Scout Setting

When the Auto Positioning option is installed, video of patient is displayed on the screen and the
system automatically selects anatomical reference and projects recommended Scout Range in the
video according to the protocol selected. User can adjust start and end location of the Scout Range.
The system also sets the optimal table height based on the Scout Range.

Scan
NOTE
A mismatch bay be seen between Auto Positioning and Patient Centering
recommendations after lateral scout is acquired. Always make sure that the patient
centering line is appropriate for your clinical need. If the mismatch is seen consistently,
verify the Adjustment Factor set in System Preferences for Auto Table Elevation.
Figure 159 Scout Image Interface with Auto Positioning Option
NOTE
Auto Positioning sets the scan range based on the Anatomical Reference set in the scan
protocol.
Anatomical References supported by Auto Positioning include:
• OM – Orbital Meatal line
• SN – Sternal Notch
• XY – Xyphoid
• IC – Iliac Crest
• SP-Symphysis pubis
• KN – Knee
• AJ – Ankle Joint

Scan
If the anatomical reference set in the scan protocol is not in the above list, the Scout Image Range
Indicator will not show up automatically. If this occurs, use Internal Landmark or External Landmark
button to position patient manually.
Table 82 Scout Image Interface components
1. Patient Information Displays Patient Name, Patient ID, Accession Number, Birth Date,
Age, Gender, Exam Description , Operator and selected protocol
number and title.
2. Patient Position area Displays Patient Orientation and Anatomical Reference in the
selected protocol. The system recognizes the patient orientation,
if it is different from the protocol setting, this area turns to red
like below.
CAUTION
Patient orientation detected by camera does

not match the orientation defined in the scan
protocol. Please check and adjust patient or
orientation setting.
To change the patient orientation, press the
arrow icons to change head/feet first and/or
supine, prone or right/left decubitus.

Scan
Scout Image Interface components continued

3. Scout Parameter Displays start/end locations, kV and mA, and scout plane.
Changes according to the setting of Scout Range Indicator.
4. Patient Video Shows video of the patient on the cradle.

this icon tells that the screen shows real-time patient vid-
eo. Touching this icon turns off real-time anatomical reference se-
lection and scout range recommendations, and the icon changes
to
5. Scout Range Indicator The blue lines with handles indicate scan range, and the solid
box represents start location and the open box represents end lo-
cation. Those handles can be touched and moved to the desired
location.
NOTE
The accuracy of scout scant range determined by
the system is affected by the sheets/blankets/body
strap covering the patient body, blockage of the depth
camera view by people/devices around and/or above
the patient table, lighting conditions and existence of
highly reflective surfaces. Make sure to check validity
of the scan range shown on the gantry display and
adjust it manually on the video when necessary before
starting the automatic table motion.

Scan
Scout Image Interface components continued

Confirm and table move in When all the setting is confirmed for scan, touch this button. The
table moves into the gantry and stops at the scan start location.
6. After the system gets ready for scanning, then Scan Start button
on Gantry Panel and Scan Control Interface start to blink.
Exit Use this to End Exam
7.
During the movement of the table, the user can pause and resume the movement on the Touch
Screen.
Once the table has arrived at the position and stopped, the system is ready for the scout scan.
Figure 160 Collision detected
Patient may collide with gantry. Adjust patient.

Scan
NOTE
For patient safety, Xtream camera will predict potential collision area (such as patient
body or accessories) with gantry and highlighted in orange on the video. User needs to
clear the collision area to enable table automatic movement or user can confirm scout
scan under collision condition but press foot LOAD pedal continuously to move table to
the target position.
Figure 161 Collision detected
Keep watching during auto motion for patient movement and collisions.

Scan
Figure 162 Table moved to the target position
Position reached. Ready to scan.
11.3.3.6.8 Scan Progress

After Scan Start button is pressed (either on the Gantry Panel or Scan Control Interface at Operator
Console), the Prep Delay (counting down) is displayed on the Gantry Display.
Figure 163 Scan Progress screen for Prep Delay

Scan
Figure 164 Scan Progress screen during scanning
During scanning, the Exposure Indicator on the Gantry Panel and Scan Control Interface is illuminated.
11.3.3.6.9 Play a Movie

Play a movie by pressing the Movie icon on the Toolbar.
Figure 165 Play a Movie
When you touch the screen, the movie's control icons are displayed.
Touch the icon to play the movie. Touch the screen during play the movie to pause and touch the X in
the upper right to end play the movie.
11.3.3.7 Adjust the Graphic Rx

Use this procedure to adjust the graphic prescription and set up a scan series. If your protocol is set up
correctly or if SmartPlan is enabled, you may not need to make many changes. You can just adjust the
graphic lines representing the series and confirm.

Scan
Figure 166 Graphic Rx — Right-click Menu Selections
Table 83 Graphic Rx — Right-click Menu Selections
Selection Description
Cut Lines Toggles between individual cut lines and scan volume graphic over-
lays. Not valid for an Axial scan type with detector coverage 80 mm or
greater.
Dimensions Displays text boxes for Start Location, End Location, and DFOV.
SFOV Displays SFOV indication lines based on the selected bowtie filter.
IEC Displays X-ray irradiation lines for Helical scan types only.
Display Normal Resets image operations on the selected viewport.
Report Cursor Displays cursor statistics.
Grid Displays ISO center grid to assist with patient centering.
Reset All Resets all display settings to normal.
Screen Save Creates 8–bit secondary capture or SSAVE.
Table 84 Graphic Rx — Buttons
Localizer Displays localizer graphic objects over the top of scout images. Click
the button to turn Off and ON the Localizer display.
All Groups / Selected Groups Displays all groups when highlighted and only selected groups when
Off. Click the button to turn Off and ON the All Groups / Selected
Groups display.

Scan
Projected NI (Noise Index) Displays orange lines showing areas where the prescribed noise index
is exceeded. Click the button to turn Off and ON the Projected NI
(Noise Index) display.
Detailed View OFF / ON Displays detailed view for Cardiac Axial scan types only. Click the
button to turn Off and ON the Detailed View display.
/
Enlarge Viewport Enlarges the Show Localizer viewport to 768 x 768 image size.
Click the button to toggle between 512 x 512 and 768 x 768 image size.
ODM Displays ODM modulated range in pink. Click the button to turn Off
and ON the ODM display.
NOTE
For Axial scans, ODM is constrained to the detector cover-
age range. For Helical scans, ODM is constrained to the
detector coverage x pitch.

Scan
Figure 167 Graphic Rx — Handles

Scan
Table 85 Graphic Rx — Handles
Number Selection Description
Represented as a solid box.

• Left‐click on the solid box adjusts the Start Location
1 Start Location of the prescription.
• Shift and left‐click on the solid box adjusts the Start
Location and End Location at the same time.
Represented as an open box.

• Left‐click on the open box adjusts the End Location
2 End Location of the prescription.
• Shift and left‐click on the open box adjusts the Start
Location and End Location at the same time.
Represented as an X.
• Left‐click on X moves the slices in the slice direction
only. If all groups are selected, then X moves all
groups simultaneously.
3 Move/Adjust Scan Range / RAS • Shift and left‐click on X moves the lines to adjust
the Start Location and End Location, and the Right
Anterior Superior (RAS) coordinates simultaneously.
For RAS coordinates, shift and left‐click on X moves
the lines up and down on a lateral scout, and side-
to-side on an Anterior/Posterior (A/P) scout.
Represented as a diamond.
• Left‐click on ◊ to adjust the DFOV and keep the RAS
coordinates fixed.
4 DFOV • Shift and left‐click on ◊ to adjust the DFOV and
RAS coordinates at the same time. Adjusts the DFOV
center by keeping the opposite DFOV handle from
the selected side anchored.
Represented as dashed lines.

5 SFOV • These are representative of the max allowable
DFOV.
Represented as cross-hatch line.

• The desired DFOV for the image reconstruction
should be inside of the SFOV.
6 Outside of SFOV • When the DFOV is outside of SFOV, the image recon-
structed will display incomplete anatomy.
• The Cross-hatch line will alert the user that the
DFOV falls outside of the SFOV.

Scan
Table 86 Graphic Rx — Mouse Controls
Left‐click and release Select viewport
Middle-click and drag Window Width and Window Level
Middle scroll wheel Page through images.
Right-click and release Opens right-click menu options.
SFOV Represented as dashed lines. These are representative of the max

allowable DFOV.
Outside of SFOV Represented as cross-hatch line. The desired DFOV for the image re-
construction should be inside of the SFOV. When the DFOV is outside
of SFOV, the image reconstructed will display incomplete anatomy.
The Cross-hatch line will alert the user that the DFOV falls outside of
the SFOV.
Right-click and drag Zooming. Use this control to minimize the scout image display to see
the entire extent of the scout image and the scan range prescribed.
Right-click and drag + Ctrl Panning
1. Press and hold Shift and click and drag the center X to position the graphic lines over the
anatomy you want to cover.
NOTE
There is no default indication of the SFOV on the scout image during Graphic Rx.
When move the DFOV outside of the SFOV, there will show up the SFOV line and
cross-hatched line outside of the SFOV. And blue alert message also shows to
remind the user.
• The slices are represented as a solid overlay group of lines on the scout image.
• Adjust the position of the scan range and RAS coordinates to the desired location.
• If you change the landmark after the scout has been completed, Graphic Rx will not let you
to change A/P centers on a lateral scout. Since the landmark changed, a new scout should be
acquired so Graphic Rx can be used.
2. Click and drag the solid box to the start location.
NOTE
The start Location is not the same when row edit is On and it is adjusted graphically.
This may occur when making small adjustments in Graphic Rx quickly. Always
verify that the Start and End locations for each scan group are as desired prior to
confirming the scan.
NOTE
For Axial or Cardiac scan types, the position set is the full FOV location.

Scan
3. Click and drag the empty box to the end location.
NOTE
Press Shift and simultaneously click and drag either the solid or empty box to adjust
both the start and end locations at the same time.
4. Click and drag the diamond key to set the Display Field of View (DFOV) equally around the center
of the DFOV.
Alternatively, press Shift and simultaneously click and drag the diamond key to adjust the DFOV
and the R/L center or A/P center on the selected side.
5. From the Graphic Rx viewport, right-click and choose an option to show or hide the slices.
• Select Cut Lines to show a line for each image reconstructed.
• Deselect Cut Lines to show a transparent area of coverage with no slice lines displayed.
6. From the Graphic Rx viewport, right-click and deselect IEC to remove the indicators of the helical
scan irradiated area.
• For helical acquisitions, the full X-ray irradiated area is shown for all groups using a pair of
magenta lines that are the length of the SFOV.
• For multiple groups, solid magenta lines are shown for the primary scan group selected.
Dashed magenta lines are shown for secondary scan groups.

Scan
Figure 168 Show Irradiation Lines
7. Review the Graphic Rx values in the Anatomy Selection collection to make sure they are correct.
11.3.3.8 Enter Contrast Settings

Use this procedure to enter contrast settings for the scan if you are using Intravenous (IV) or Gastro-
Intestinal (GI) contrast.

Scan
Figure 169 Contrast settings collection

Scan
Figure 170 IV Constrast/Oral Contrast Pop-Over with IV Contrast Settings

Scan
Table 87 Contrast settings collection
IV Contrast On or Off. When On, images are labeled +C. Contrast Agent settings
are optional.
IV Contrast Settings Displays Agent and Concentration.

Clicking on this setting will open the IV Contrast/ Oral Contrast pop-
over window to IV Contrast settings. To populate contrast presets, see
Set Contrast Management Preferences.
NOTE
When IV contrast is Off and a SmartPrep task is added,
IV contrast is turned On automatically and the Contrast
Volume is set to 0. DICOM tag 0018, 1041 will not be added
to the image header unless the Volume setting is greater
that 0.
Enhanced Xtream Injector On - Communication enabled between the CT Scanner and the In-
jector. Injection Settings are shared between the scanner and the
injector and injection starts with the Start Scan button on the CT
System.
Off- No communication between CT Scanner and Injector. Injection
Settings on the scanner are informational and will need to be adjust-
ed manually to reflect the actual settings on the Injector. Injection
will need to be started with controls on the injector and manually
coordinated with the start of scanning.

Scan
Contrast settings collection continued

Injector Settings Displays Phase, Volume, Flow Rate, Pressure Limit and Duration when
IV Contrast is ON. Clicking on this settings opens the IV Contrast/Oral
Contrast pop-over window to IV Contrast settings.
The default values of these settings are as follows:
• Phase 1
• Volume 100 ml
• Flow Rate 2.0 ml/s
• Duration 50 s
• Pressure Limit 150 psi
Enhanced Xtream Injector ON requires these values be updated to

actual settings needed for the exam.
While it is not required to update these values if you are not using an
integrated injector (Enhanced Xtream Injector is OFF) , the Contrast
Volume DICOM tag will store the 100 ml default setting.
NOTE
Be sure to enter the correct Volume to be injected, even
if Enhanced Xtream Injector is OFF, to have the correct
value stored in the Contrast Volume DICOM tag. When IV
contrast is Off and a SmartPrep task is added, IV contrast
is turned On and the Contrast Volume is set to 0. DICOM
tag 0018, 1041 will not be added to the image header
unless the Volume setting is greater that 0.
Oral Contrast On or Off On allows entry of the oral contrast settings.

Scan
Contrast settings collection continued

Oral Contrast Settings Displays the concentration and volume. Clicking this setting will open
the IV Contrast/Oral Contrast pop-over window to Oral Contrast
Settings.
NOTE
The Oral Contrast Volume field does not accept a value
greater than three digits. If volume amount is greater than
three digits, enter the volume in the Contrast Agent
Name field.
IV Contrast/ Oral Contrast Pop Over Click the IV Contrast Tab or the Oral Contrast Tab to switch the
Window display to the applicable settings screen.
IV Contrast settings:
Select an Agent and Concentration preset or enter Agent and Concen-
tration and click Add.
Enter the Pressure Limit.
Click Add Phase for the # of phases needed.
For each phase, enter Injection Delay, Type, Flow Rate, Volume and
Duration. See Table 72 for setting details.
Oral Contrast settings:
Enter Agent, Concentration and Volume.
NOTICE
WHEN USING IV CONTRAST, MAKE SURE THE INJECTOR OR SYRINGES

WITH CONTRAST ARE SETUP BEFORE SCANNING THE LOCALIZER (SCOUT)
SCAN. IV CONTRAST MUST BE SELECTED FROM THE CONTRAST SETTINGS
COLLECTION.
Follow these steps to enter contrast settings for an exam.

1. From the Scan Settings window, click the Contrast settings collection to open it.
2. Click IV Contrast and/or Oral Contrast and set to On if that type of contrast is being used.
3. Click IV Contrast Settings and/or Oral Contrast Settings to open the appropriate settings.
NOTE
+C annotation is displayed when IV contrast is On and indicates that IV contrast was
used for the series.
NOTE
Once the IV Contrast Setting or Oral Contrast Setting has been selected, they
cannot be changed after a scan has been acquired.

Scan
4. Select a contrast preset from the list to enter agent and concentration. Enter volume, flow rate,
duration for each contrast phase.
NOTE
If the agent and concentration are not listed in the preset list, enter the Agent Name,
enter Concentration and click Add.
5. If you are using an integrated injector with the scanner, click On for Enhanced Xtream Injector to
enable communication with a compatible injector to share Injector Settings and synchronize start
of injection with start of scan. Refer to Enhanced Xtream Injector.
6. Click Apply.
11.3.3.9 Start a scan

Use this procedure to start a scan.
1. Review the following parameters for each acquisition before confirming the scan:
a. Start/End locations
b. Direction of scan
c. Projected Noise Index and mA table for SmartmA and SmartmA/ODM
4. Deliver breathing and table move instructions, as needed.
Considerations
• Press Stop Scan to stop scans between multiple helical groups and do not press Stop Move.
• Scan aborts may occur during Scout, Axial or Helical scanning. Always be aware of the scan
progress during an exam and select Resume to continue.
• The scan may fail to confirm, posting a message that not enough image space exists, even though
the disk image space icon indicates there is enough space or File Manager may not have
exams listed.
This occurs because images are stored on the system disk in more than one partition. Remove
consecutive exams to free up image space to confirm and proceed with the scan.
Disk Status

Scan
Icon Image Space Card States Status Operator Message
Image space is Greater than 5% free image space

normal range
Image space ap- Available image space is between

proaching full 5% and 2% free
Image space full Available image space is less than

2%
NOTE
If you encounter the message that you need to delete images to be able to scan
the current series, first check the recycle bin and remove images to create space for
scanning, next if scouts have not been acquired, end the exam and start a new exam.
However, if scouts have been acquired, use Revisit Settings and prescribe the series
again.
NOTE
Hovering the cursor over the status icon displays an estimate of the number of images
remaining based on an average image file size.
Recycle Bin Status
Icon Status Images
Between 0% and 12% full 0–1200

Scan
Between 89% and 100% 8801–10,000

full
11.3.3.10 Duplicate a series

Use this procedure to duplicate a series that has already been scanned.
On the Scan Settings window, right-click on the series to be duplicated in the task list and select
Duplicate Series.
NOTE
The Prep Delay for group 1 is set to zero.
NOTE
The Smart Prep group will be remembered if the series contained Smart Prep. Delete the
Smart Prep group if it is not needed.
11.3.3.11 Stop a scan
11.3.3.11.1 Abort a scan in progress

Use this procedure to abort the X-ray and stop gantry and table movement.
1. On the scan control interface, press Stop Scan.
2. Click Resume from the Scan Progress window to resume the scan.
11.3.3.11.2 Pause a scan in progress

Use this procedure to pause the current scan. This finishes the current scan, then pauses the next scan.
1. On the scan control interface, press Pause Scan.
2. Click Resume from the Scan Progress window to resume the scan.
11.3.3.11.3 Emergency stop scan, electronics, and x-radiation

Use this procedure in the event of a patient related emergency or if the cradle, table, or gantry starts to
move unexpectedly.
1. On the scan control interface or gantry, press Emergency Stop.
All table and gantry motions and X-ray exposures are stopped.
2. On the gantry, press Reset to clear the Emergency Stop.

Scan
NOTE
For helical scans, you need to evaluate each situation. Pause Scan will not stop a helical
scan in progress. The scan will complete and the system will stop and not scan any
additional groups. Stop Scan will stop a helical scan. Resume will resume a helical scan
from the location it was stopped.
11.3.3.12 Close the exam

When an exam is completed, click Done Scanning, then Close Exam.
• Done Scanning transitions the exam from a scanning session (on the scan monitor) to image
processing done scanning session (on the image monitor).
• Close Exam removes the scanning session completely from the user interface.
11.3.3.13 Acquire a GSI scan

Use this procedure to acquire a GSI data set of interleaved high- and low-energy views in any
anatomical area. The data can be used to reconstruct the following GSI image types: Monochromatic,
Material Density, High kVp, kVp-like, Virtual UnEnhanced with and without Metal Artifact Reduction,
and also Quality Check Images.
NOTE
Prior to scanning make sure that GSI profiles and scan protocols have been created in
Protocol Management that will support the clinical indication being scanned.
1. Select the GSI protocol in the desired anatomical area from the GE Reference or Adult selector.
2. Acquire a scout. A scout series is required for GSI Assist mA mode to be available.
3. Define the Start/End locations manually or graphically.
4. Confirm that the Clinical Category and Clinical Identifier match the clinical task. If not, update.
5. If the GSI prescription is a Helical scan type, set the desired Interval.
6. Verify your selections if using a predefined protocol or select your desired options
a. For GSI kV Mode, confirm if GSI Assist or GSI Manual mA mode is on.
b. Check if CID Link is On. If it is set to On, the system links to the GSI Profile that is mapped to
the Clinical Category/Clinical Identifier pair. If CID Link is Off, the GSI profile can be directly
selected.

Scan
Figure 171 mA Mode selection

Scan
Figure 172 GSI mA mode

Scan
Figure 173 GSI Assist mA mode settings
i. Verify the Noise Index meets the need of the clinical intent
ii. Review the Dose and Scan settings chosen by GSI Assist
iii. If changes are desired, click the Adjust button on the GSI Image Quality Widget.

Scan
Figure 174 GSI Assist Widget
Figure 175 GSI Adjust Widget
1. Review options given for different scan settings.

2. Choose the option that best fits your needs from a scan time, pitch, rotation time
and CTDIvol.
iv. If other settings are still desired, change mA mode to GSI Manual.
c. If GSI Manual mA Mode

Scan

Scan
Figure 177 GSI Profile selection

Scan
Figure 178 GSI Manual Settings
i. Verify Dose and Scan Settings for desired Clinical ID meet Clinical Intent.
ii. If other settings are desired change the GSI Family via the Adjust button widget.
iii. If other settings not shown in the widget, the GSI Profile may be changed.
7. Review/Set the timing parameters in the Timing Collection.

Scan
8. Set the Recon parameters.

Recons can be set up three ways: Linked to GSI Assist with a Recon Clinical Category and Clinical
Identifier, linked to GSI Assist with direct selection of a GSI profile when CID Link is Off, not linked
to GSI Assist, that is, set up in the protocol. GSI Assist Link can be used for secondary recon
regardless of the GSI mA mode selected for scanning.
a. Recons setup Linked to GSI Assist — The primary recon is set up on the left monitor as
with non-GSI, and the parameters selected are limited. MAR is not permitted for the primary
recon. Monochromatic images, High kVp, kVp-like images and Data File are supported.
i. Open Primary Recon collection
ii. Set up recon parameters
iii. Choose between Monochromatic 40-140 keV High kVp or kVp-Like 100 or 120
iv. Add a secondary recon
v. Select GSI-Assist Link On
vi. Select Clinical Category and Clinical Identifier
NOTE
Use of appropriate CID is critical to image quality for the following specific
recon tasks:
• Gout analysis images must use Extremity.Gout.
• Non-contrast head image must use Neuro.Routinehead.
vii. Recon settings will populate from the GSI Profile mapped to the Clinical Category and
Clinical Identifier.
viii. Or alternatively turn off CID Link to directly select a GSI profile.

Scan
Figure 179 Recon with GSI Assist and CID Link On

Scan
b. Recons setup not Linked to GSI Assist — The primary recon is setup on the left monitor as
with non-GSI and the parameters selected are limited. MAR is not permitted for the primary
recon. Monochromatic images, High kVp, kVp-like images and Data File are supported.
i. Open Primary Recon collection.
ii. Set recon parameters.
iii. Set GSI Image Type. Choose between Monochromatic, High kVp, kVp-Like or if needed
Data File.

Scan
iv. Add a secondary recon.

v. Set up Parameters in the GSI common Recon settings – parameters across all GSI recons.
vi. Add Recon creates a GSI common settings task. Add GSI Recon under the main GSI recon
is used to create additional GSI recons with common parameters such as slice thickness,
kernel, DFOV, etc.
vii. Create GSI-specific recon tasks as appropriate (Different Monochromatic Levels, Material
Density, Virtual UnEnhanced Images, High kVp or kVP-like images), MAR On or Off, Data
File On or Off
viii. Add other GSI common setting tasks as needed for additional Kernels, DFOV, etc.

Scan
Figure 180 Recon without GSI Assist

Scan
11.4 Scan Parameters

See the Scan Parameters workflow for procedures on how to set the following scan parameters.
11.4.1 Scan Type

The Scan Type and related scan parameters are set in the Scan Type collection.
From the Scan Settings window, click Scan Type to display the Scan Type collection.
Figure 181 Scan Type collection
Element Description
Scan Type Enables one of the following scan types: Axial, Helical, Cardiac, or Cine.
Hi Res Mode Enables and disables Hi Res Mode. Hi Res Mode is compatible with Axial,
Helical, and Cardiac scan types.
Rotation Time The available rotation times depend on the scan type selected. See Rotation
Time.

Scan
11.4.1.1 Axial
Axial scanning is the traditional “step and shoot” method of acquiring data. The X-ray tube and Data
Acquisition System (DAS) expose and rotate one 360° loop. The table and patient move a preset
distance (interval) and the process is repeated.
11.4.1.2 Helical
Helical or spiral scanning is a method of acquiring images in a continuous data set. The X-ray tube
and DAS expose and rotate continuously through 360° while the patient is passed through the area of
exposure at a set rate of movement depending on the rotation time and helical pitch. The information
gathered is then reconstructed into images of the prescribed slice thickness and interval.
11.4.1.3 Cardiac Axial

See the Cardiac chapter for more details.
11.4.1.4 Cine
Cine is a method of scanning that rotates the gantry 360° continuously with no delay in between
passes while gathering input from one location over time. You may set the acquisition in groups
expanding the time to be scanned. This is especially beneficial when determining the function of
anatomy and physiology (example: hemangioma).
11.4.1.5 Hi Res Mode

Hi Res Mode provides the capability to acquire 2.5 more views using deflection of the X-ray beam
in both non-cardiac and cardiac acquisitions. The additional views can be used to improve image
quality to reduce aliasing, improve off‐center imaging, or improve resolution. Normal algorithms can
be used; however, they will not improve resolution in the image. The HD reconstruction algorithms
can enhance the inherent resolution in Hi Res Mode acquisitions for DFOV less than 25 cm. The Hi-Res
Mode algorithms have a two appended or HD prefixes added to the algorithm name. Hi Res Mode may
be useful when a large DFOV is used and targeting to a smaller DFOV is desired.
NOTE
Hi Res Mode is available for the following scan types and detector coverages.
• Axial – 20, 40, 80, 100, 120, 140, 160 mm detector coverage
NOTE
For the 256 slice system, 80 mm configuration, collimations greater than 80 mm are
not selectable.
• Helical
• 0.531:1 pitch 20mm detector coverage
• 0.516:1 pitch 40 mm detector coverage

Scan

• Cardiac Axial – 40, 80, 100, 120, 140, 160 mm detector coverage
NOTE
not selectable.
Hi Res images are annotated with HR in the lower‐left annotation area of the image.
11.4.1.6 Rotation Time

Rotation time is a parameter that can be adjusted for patient size and applications.
For scanning an average sized patient for an abdominal study, the 0.5 second rotation time may
provide adequate mAs for image quality. For scanning a larger patient, you may need to use the 1.0
second rotation time. Both studies would be completed using sub-second rotation times because of
the flexibility in having various rotation times.
• Axial – 0.28 s, 0.35 s, 0.5 s, 0.6 s, 0.7 s, 0.8 s, 0.9 s, 1.0 s
• Cine – 0.28 s, 0.35 s, 0.5 s, 1.0 s
• Helical – 0.28 s, 0.35 s, 0.5 s, 0.6 s, 0.7 s, 0.8 s, 0.9 s, 1.0 s
NOTE
For Advantage 4D scans, rotation times less than 0.5 s should not be used.
• Cardiac Axial – 0.28 s, 0.35 s
11.4.2 Coverage Speed collection

From the Scan Settings window, click Coverage Speed to open the Coverage Speed collection.
Figure 182 Coverage Speed collection — Axial

Scan
Table 88 Coverage Speed — Axial
Element Description
Table Positions • One (Single)

• One or More (Multiple)
Use when the scan range is greater than 160 mm if using Smart Cover-
age or when the fixed coverage scan range is greater than the detector
coverage.
• Two or More (Multiple)
Use to ensure that each axial scan with 80 mm or greater detector
coverage contains 2 axial slabs. Two or more is not available for cardiac
scan type.
Detector Coverage • Smart Coverage (system adjusts to best coverage based on the start
and end location prescribed)
• 5.0 mm
• 40 mm
• 80 mm
• 100 mm
• 120 mm
• 140 mm
• 160 mm
Also see the Equipment chapter; Detector Configuration section for more
information.
NOTE
For the 256 slice system, 80 mm configuration, collimations
greater than 80 mm are not selectable.
Number of Passes The number of rotations for the data acquisition. Only available if the inter-
val is 0.
Minimum Time Between The time between rotations for the data acquisition when the interval is 0.
Passes The minimum time is dependent on the rotation time.
• 0.28 s rotation – 0.88 s minimum

Scan
Coverage Speed — Axial continued

Element Description
Scan Interval 0, detector coverage or greater than detector coverage
Rotation Time 0.28 s, 0.35 s, 0.5 s, 0.6 s, 0.7 s, 0.8 s, 0.9 s, 1.0 s
Total Exposure Time The coverage time determines the total X-ray On duration of the scan.
Table 89 Coverage Speed — Helical
Element Description
Detector Coverage • 40 mm
• 80 mm
information.
Pitch • 0.516:1 pitch (40 mm detector coverage)

• 0.984:1 pitch (40 mm detector coverage)
• 1.375:1 pitch (40 mm and 80 mm detector coverage)
NOTE
0.508:1, 0.992:1, 1.375:1 and 1.531:1 pitch (80 mm detector cov-
erage) are not valid with Ped Head, Small Head or Head SFOV.
Coverage Speed Determined by the detector configuration and rotation time used.
Rotation Time 0.28 s, 0.35 s, 0.5 s, 0.6 s, 0.7 s, 0.8 s, 0.9 s, 1.0 s
Total Exposure Time Determined by the coverage speed and the scan range prescribed.

Scan
Figure 183 Coverage Speed collection — Cardiac Axial
Table 90 Coverage Speed — Cardiac Axial
Element Description
Table Positions • One (Single)

• One or More (Multiple)
Use when the scan range is greater than 160 mm if using Smart Cover-
age or when the fixed coverage scan range is greater than the detector
coverage.
Detector Coverage • Smart Coverage (system adjusts to best coverage based on the start
and end location prescribed)
• 40 mm
• 80 mm
• 100 mm
• 120 mm
• 140 mm
• 160 mm
information.
NOTE
Minimum Time Between The time between rotations for the data acquisition when the interval is 0.
Passes The minimum time is 1.5 seconds.
Number of Passes The number of rotations for the data acquisition at the same table position.

Scan
Coverage Speed — Cardiac Axial continued

Element Description
Scan Interval Determined by the system.
Rotation Time 0.28 s, 0.35 s
Total Exposure Time Determined by the table positions, number of passes and phase ranges for
each acquisition part.
Overlap Amount • Minimum: Lowest dose

• More: Better image quality
Table 91 Coverage Speed — Cine
Element Description
Table Positions One (Single)

One or More (Multiple) 40mm only
Detector Coverage • 40 mm
• 80 mm
• 100 mm
• 120 mm
• 140 mm
• 160 mm
information.
NOTE
Number of Passes The number of rotations for the data acquisition.
Duration 1–60 s
Scan Interval 0
Rotation Time 0.28 s, 0.35 s, 0.5 s, 1.0 s
Total Exposure Time Determined by the duration.
11.4.3 kV and mA Control

From the Scan Settings window, click kV and mA Control to open the kV and mA Control collection.
Settings include: kV Mode, kV, mA Mode and Noise Index.

Scan
Figure 184 kV and mA Control collection
11.4.3.1 kV Mode
From the kV and mA Control collection, select the applicable mode from the dropdown menu.
Additional settings will be required based on the initial kV mode selected.
In this software release, to help compensate for patient size and tissue composition without impacting
workflow, two options for assisted kV selection have been integrated into the scanner, kV Assist and
Auto Prescription.
Auto Prescription offers greater control in setting kV and other scan parameters for different patient
sizes and will completely replace kV Assist in a future software release. Your protocols with kV Assist
will continue to work. However, GE recommends that you begin to modify the protocols to utilize Auto
Prescription.
To encourage the use of Auto Prescription, the kV Mode dropdown menu will show kV Assist only
under certain circumstances. In Protocol Management, kV Assist will be an available selection only if
the protocol being edited previously had kV Assist. At scan time, kV Assist will appear in the menu
only if the selected protocol already has a group with kV Assist prescribed. If the selected protocol has
manual kV or kV Assist, then kV Assist will be available as a selection.
11.4.3.1.1 Manual kV Mode

When Manual kV Mode is selected, you can enter a kVp value for each prescribed scan group.
When building protocols with kV Assist or Auto Prescription enabled, you must still select a reasonable
and appropriate manual kVp value to ensure that the diagnostic scan utilizes an appropriate kVp in the
event that these features are disabled.
11.4.3.1.2 kV Assist kV Mode

When kV Assist Mode is selected, the system determines the patient size based on the acquired scout
scan and the scan range settings. It re-calculates patient size with any change to collimation, scan
range or AP, RL locations.
kV Assist takes into account the patient size information from the Scout, the initial/baseline kV and the
initial/baseline Noise Index/mA as the starting point, along with the user preference parameters for
the selection of kV. The recommendation from kV Assist will be a consistent set of parameters affecting
scanning of the images.
• kV

Scan
• mA/Noise Index – to meet Contrast-To-Noise Ratio (CNR) for clinical task

• WW/WL adjustment based on the selected kV can be enabled by the user to optimize contrast to
noise and image quality for image viewing. WW/WL should be optimized for image viewing based
on the kV and mA.
kV Assist determines the recommended technique based on the baseline protocol, the scan
conditions.
kV Assist will optimize the scan parameters based on the selected clinical task.
In each clinical task, the system determines the patient size from the scout projection data. This is
used in conjunction with a reference protocol (i.e., the X-ray scan technique factors that would be used
without kV Assist) to determine the expected amount of image contrast for the relevant materials. The
system then determines the Noise Index/tube current needed to provide the proper balance between
CNR and image noise at each of the tube voltages. The combination of tube voltage and Noise Index/
tube current that results in the lowest CTDIvol at the desired image quality is then selected. Note that
the tube voltage with the lowest CTDIvol may not be selected for some patient sizes and applications
in order to maintain the desired image quality (e.g., in order to avoid situations where potential image
artifacts could occur).
For cardiac scans with kV Assist, the system determines a size adjustment of the Noise Index (for
SmartmA scans), SFOV and mA based on the patient size from the scout projection data. The NI/mA for
a reference size patient is given in the protocol, and this is adjusted by kV Assist prior to (and used in)
the kV selection. This allows for the inclusion of size-specific image quality needs in cardiac scanning
without having multiple size-based protocols
kV Assist works with manual mA, SmartmA or SmartmA ODM.
• SmartmA will utilize the prescribed NI and kV settings after kV Assist runs to set the mA values.
• SmartmA will propose adjusted solutions if the prescribed NI cannot be achieved.
kV Assist requires a scout scan at the same patient position and orientation of the diagnostic series in
order to determine the Patient Size.
See the Protocol chapter for additional details on setting up kV Assist in protocols.
11.4.3.1.2.1 Window Width, Window Level Considerations when using kV Assist

Images of the same anatomy scanned with different tube voltages display differently. This is expected,
due to Contrast-to-Noise Ratio changes. For example, images obtained with X-ray scan technique
factors set by kV Assist could be brighter in areas (due to increased contrast) and noisier (due to
increased noise). Even though similar information is present in the image, the change to the image
appearance could be distracting.
WW/WL adjustment based on the kV solution will be enabled by Auto WW/WL ON in primary recon to
optimize contrast to noise and image quality for image viewing. The user can disable this by setting
the Auto WW/WL OFF.
11.4.3.2 Auto Prescription kV Mode

When Auto Prescription Mode is selected, the system determines the patient size based on the
acquired scout scan and the scan range settings. It re-calculates patient size with any change to

Scan
collimation, scan range or AP, RL locations. Based on the estimated patient attenuation from the scout,
Auto Prescription then matches the re-calculated patient size to a kV Profile Patient Size Range and all
settings within that size range are applied to the scanning protocol.
patient size and works with SmartmA to optimize dose and image quality. A Auto Prescription Profile
specifies the patient size ranges and specifies which settings are changed by patient size. kV and mA
limits are required settings for each patient size range and optional settings may be selected including,
SFOV, ASIR-V%, Rotation Time, Pitch and Noise Index (NI). If NI is set in the profile, then a reference
slice thickness will also be set in the Profile.
Auto Prescription determines the patient size from the attenuation information of the patient’s scout
over the prescribed scan range and then applies the scan settings specified for that patient size range
within the Auto Prescription Profile. In addition, If NI is not set in the profile’s patient size range,
Prescribed NI defined in the protocol will be adjusted based on the Size Adjusted Noise Index (SANI)
and Clinical Task settings within the Auto Prescription Profile. SmartmA utilizes the selected kV and NI
parameters to determine mA.
NOTE
NI is not adjusted from the value in the protocol if the patient size falls in the Reference
Patient Size Range.
Auto Prescription works only in conjunction with SmartmA or SmartmA ODM.
• SmartmA will utilize the prescribed NI and kV settings after Auto Prescription runs to set the mA
values.
• SmartmA will propose adjusted solutions if the prescribed NI cannot be achieved
Auto Prescription requires a scout scan at the same patient position and orientation of the diagnostic
series in order to determine the patient size.
If the patient size is outside of a patient size range, a blue alert displays and Auto Prescription provides
a solution for the closest size range in the profile.
When using Auto Prescription, the selected kV Profile is critical to the success of the exam. Before
changing a Auto Prescription profile, ensure that you have reviewed the profile and understand how
the profile uses NI. When the profile sets NI in the protocol, it is important that the protocol NI is set for
the Reference kV of the selected profile.
At scan time, changing any parameter set in the Auto Prescription profile, except the minimum and
maximum mA range, will override the Auto Prescription solution. The kV mode changes to User
Override. The Auto Prescription widget displays the values that are different and provide ability to
re-apply the Auto Prescription settings if desired.
When a scan is prescribed using SmartmA, scan setup uses limits for the min/max mA to allow you to
limit the range over which the system can modulate the mA. The maximum mA limit allows the user
to restrict the maximum amount of radiation emitted from the system during the scan. When kV is
changed manually, ensure that the min/max mA values are sufficient to achieve the desired patient
scan.

Scan
11.4.3.2.1 WW/WL Considerations when using Auto Prescription

Images of the same anatomy scanned with different tube voltages display differently. This is expected,
due to Contrast-to-Noise Ratio changes.
For example, images obtained with X-ray scan technique factors set by kV Assist could be brighter in
areas (due to increased contrast) and noisier (due to increased noise). Even though similar information
is present in the image, the change to the image appearance could be distracting.
WW/WL adjustment based on the kV solution will be enabled by Auto WW/WL ON in primary recon to
optimize contrast to noise and image quality for image viewing. The user can disable this by setting
the Auto WW/WL OFF. If Auto Prescription or User Override are enabled, Auto WW/WL can also be
enabled for secondary reconstructions.
See Protocol Management kV Assist /Auto Prescription in the Protocols chapter for additional details
on setting up Auto Prescription in protocols.
11.4.3.3 mA Mode
From the kV and mA Control collection, select mA Mode. The X-ray system provides focal spots S, L
and XL that are automatically selected by the system based on kV, mA and exposure time.
The focal spot that will be used is shown in the kV and mA Control collection.
Refer to the Revolution™ CT, Revolution™ CT ES Technical Reference Manual, System Specifications
(Chapter 7), CT System X-ray Tube Ratings (Section 6) for the maximum tube power limits. The mA
value may be adjusted based on the tube power limits to indirectly select the focal spot.
Figure 185 kV and mA Control collection — Focal Spot
11.4.3.3.1 Manual mA Mode

When building protocols, make sure the Manual mA value field is populated with a reasonable mA
value, even if the protocol will use SmartmA or SmartmA ODM, in case SmartmA or SmartmA ODM is
turned off when in Manual mA Mode.
11.4.3.3.2 SmartmA Mode

When SmartmA Mode is selected, the mA on the Scan Settings window is annotated with the
minimum and maximum mA range to be considered for the scan group. SmartmA or SmartmA ODM
will determine the actual mA range based on the patient size and attenuation.

Scan
Images reconstructed from a SmartmA enabled scan are annotated with a tilde symbol (~) next to the
Noise Index, as shown in Image Annotation.
Figure 186 Image Annotation
NOTE
SmartmA is disabled if the patient orientation does not match the scout orientation.
The system will inform and instruct you that Patient Orientation or Patient Position has
changed from the previous series, and that AEC features have been disabled. You can
choose to reacquire a new scout image to reorient the patient to be consistent with the
orientation of the previous scout or change to Manual mA Mode.
The following message will be displayed if SmartmA is unavailable due to patient orientation or
position mismatch:
NOTICE
SMARTMA, ODM AND KV ASSIST UNAVAILABLE DUE TO PATIENT

ORIENTATION/POSITION MISMATCH. SCAN A SCOUT WITH THE SAME
PATIENT ORIENTATION/POSITION OR MANUAL MA AND KV MUST BE SET.
The system uses the patient attenuation data collected from the most recent scout scanned for the
exam, the patient habitus, the prescribed, and other settings in the mA table to determine the mA to
be used for the acquisition. You can view the predicted mA values for each rotation of the acquisition
by accessing the mA table. The Patient Orientation and Patient Position for the series must match the
scout. If there is no scout or the patient orientations do not match, SmartmA will be disabled, and the
following message will be displayed:
NOTE
SCOUT IMAGE NOT FOUND. RECHECK OR CONTINUE WITHOUT SCOUT:

Recheck Image Browser Continue without Scout Scout image not found in Image
Browser. Please check again. SmartmA, ODM and kV Assist unavailable due to lack of
valid scout. Scan a scout or Manual mA and kV must be set.
The mA table will indicate when one or more scan rotations are at the maximum or minimum mA
value specified for the prescribed scan. This is to notify you to check the parameters to ensure the
acquisition will provide the expected results.

Scan
NOTE
Even if you are using SmartmA, the Manual mA field should be filled in with a reasonable
value in case SmartmA should be inadvertently disabled.
11.4.3.3.3 mA Max and mA Min

mA Max and mA Min values allow the user to specify a minimum and maximum mA range for
SmartmA. The mA Max value sets the maximum mA allowed, or the high mA clipping value. The mA
Min value sets the minimum mA allowed.
11.4.3.3.4 ODM Mode

From the kV and mA Control collection, click the mA Mode menu and select Smart mA & ODM.
Table 92 ODM Selections
Element Description
mA Mode menu Enables or disables the ODM feature.

When enabled, up to three locations within the group can have ODM applied, with
the locations specified either graphically on the scout image or by the start and
end locations of the respective applied ODM regions.
Start Location / End Displays the start and end location of the ODM region.
Location When the ODM feature is enabled, the first start and end location are set by
default at the starting edge of the scan range.

Scan
ODM Selections continued

Element Description
ODM region By default, one set of start and end location entry fields are created.
The maximum number of ODM regions within a group is one.
When enabled the entire scan range for the group is included.
When the scan range is changed, and is less than the previous scan range, ODM
range will adjust to stay within the valid scan range.
mA Table Information When ODM is applied, the mA Table shows the maximum mA within each rotation
for each of the following regions: (A) anterior, (P) posterior, (L) left of the patient,
(R) right of the patient.
Scan rotations where ODM is applied have an accompanying drop in the applied
mA in the (A) anterior direction when compared to the (P) posterior direction,
and will be indicated with an asterisk (*) next to the rotation. If the Patient
Orientation changes from, Head First to Feet First, then the positions of (L) and (R)
are reversed.
ODM can be set in Protocol Management.
NOTE
The mA Table shows a decimated version of the full mA profile that
will be scanned. Because the mA Table displays the maximum mA
for each rotation for each direction, there may be cases in which the
displayed anterior mA in the mA Table is the same as the displayed
posterior mA, even though ODM is applied for that rotation.
For example, this may occur when a helical rotation contains both
a region with ODM applied and a region without ODM applied. In
this case, the maximum mA displayed for both the anterior and pos-
terior directions is likely to come from the region within the rotation
where ODM is not applied, since it is likely to be higher mA than
the region where ODM is applied. It is important to understand that
this is a caveat of how mA is displayed in the mA Table and that
the actual scanned mA profile is appropriately reducing the mA in
regions where ODM is applied.
On the scout localizer image, the prescribed ODM region will be displayed in purple if ODM is selected
in the Graphic Rx toolbar.

Scan
Figure 187 ODM region enabled
NOTE
The ODM region can be moved only in the z-direction, not for A/P or R/L direction.
When ODM is enabled for a scan, it will be indicated in the kV and mA Control collection. ODM will be
set in one or more locations in the scan group. It does not mean all the rotations in the scan group
have ODM applied.
NOTE
SmartmA is ON when ODM is enabled.
ODM is available with standard Axial, Helical or Cine scanning modes.
ODM is not available for Cardiac scan types.
ODM is not available for scan groups which are not compatible with AEC scan modes.
If ODM is enabled and the scan type is modified to a state which is not valid for ODM, the system will
notify the user.
The following message will be posted when ODM is not available:

Scan
NOTICE
ODM HAS BEEN DISABLED. VERIFY , MIN MA / MAX MA, RESULTANT CTDIVOL
AND DLP MEET THE CLINICAL GOAL OF THE ACQUISITION AND FOLLOW
THE RADIATION EXPOSURE GUIDELINES FOR YOUR DEPARTMENT.
Image Annotation
To indicate that an image was generated within a scan region where ODM is enabled, an asterisk is
added after the Noise Index value.
11.4.3.3.5 GSI Assist mA Mode

When GSI Assist mA Mode is selected, the system will use the first GSI preset and associated mA
listed in the GSI Profile based on the patient attenuation from the scout, noise index value based on a
non-GSI protocol, and Clinical task category and Clinical Identifier if CID link is On. CID Link On/Off is
also applicable to GSI Manual.
GSI Assist mA Mode is designed to provide assistance in the selection of a GSI acquisition mode
with similar dose to a non-GSI scan using a noise index value based on a non-GSI scan. The optimal
acquisition mode and mA is selected based on the patient’s size, Clinical Identifier and Noise Index.
GSI Assist mA Mode is available only for head and body scanning (not recommended for pediatrics).

Scan

Scan
Figure 189 GSI Profile selection

Scan
Figure 190 GSI Manual Settings
11.4.3.4 Noise Index

Noise Index is an indication or index of the level of reconstructed image noise requested for the
diagnostic imaging task being performed. As the Noise Index increases, the required exposure (mA
and/or kV level) decreases and image noise increases; conversely overall image noise levels decrease

Scan
and the required patient exposure increases with a decrease in the prescribed Noise Index. You can
specify the Noise Index in the Noise Index field. The Noise Index field is enabled only when one of the
following mA modes is enabled:
• SmartmA
• SmartmA & ODM
• GSI Assist
A change in prescribed Noise Index necessarily adjusts dose to the patient, which is viewable at the
bottom center of the Dose Display area. Patient dose will be decreased or increased as the Noise Index
is accordingly increased or decreased.
The Projected Noise Index can be viewed from the Image Quality widget on the Scan Settings
window. Projected noise index calculation shows the mA modes for which the Projected Noise Index is
displayed. For helical scans with more than one rotation or cardiac or axial scans containing multiple
exposures at different locations, an estimate of the noise can be calculated for each z-location along
the scan range. The Projected Noise Index value displayed in the Image Quality Widget is calculated
from the estimated noise values at each z-location along the prescribed scan range according to
Projected noise index calculation.
Table 93 Projected noise index calculation
mA Mode Projected Noise Index on the Image Quality Widget

is calculated as:
SmartmA the maximum of the estimated noise values at each

z-location along the prescribed scan range
SmartmA & ODM the maximum of the estimated noise values at each
GSI Manual the average of the estimated noise values at each

GSI Assist the average of the estimated noise values at each

When using GSI Manual mode, the Image Quality widget displays only the Projected Noise Index.
When using the other three mA modes shown in the table above, the Image Quality widget will
also display the Prescribed Noise Index and indicate whether the Prescribed Noise Index will be
met. When the Projected Noise Index is higher than the Prescribed Noise Index, the Projected Noise
Index will be highlighted orange. When selected, Adjust will display recommended solutions to
change scan parameters to help meet the Prescribed Noise Index. The Solutions window displays
the recommended parameters, the change in noise and the change in DLP associated with the change.
NOTE
The Max mA recommended will take into account tube cooling.
11.4.3.5 GSI Noise Index

Scan
11.4.3.5.1 GSI Prescribed Noise Index

With GSI Assist mA Mode enabled, you must prescribe a Noise Index in the kV mA collection. The value
would be the Noise Index value that is desired for an equivalent non-GSI SmartmA scan. GSI Assist mA
Mode is not automatic exposure control like SmartmA. It will not attempt to maintain the noise index
across the volume. The prescribed Noise Index value is used by GSI Assist mA Mode to calculate the mA
and projected Noise Index based on the selected GSI profile, preset family and GSI acquisition mode.
11.4.3.5.2 GSI Projected Noise Index

As indicated in Projected noise index calculation and discussed in Section 4.3.3, the Projected Noise
Index shown in the Image Quality Widget for a GSI scan is the average of the estimated noise values
along the prescribed scan range.
The appearance of orange bars in specific regions along the scout indicates that the Prescribed Noise
Index is not being met at these specific locations. This may be the case, for example, through areas of
relatively higher attenuation, such as the shoulder region (see Graphic Rx shows orange bars through
shoulder region, indicating that the prescribed Noise Index cannot be met in this region.). When
scanning in single kV Mode (that is, non-GSI), the Projected Noise Index displayed in the Image Quality
Widget is equal to the maximum estimated noise along the scan range, and thus would appear orange
for the case shown in Graphic Rx shows orange bars through shoulder region, indicating that the
prescribed Noise Index cannot be met in this region..
However, in GSI Assist Mode, the Projected Noise Index is the average of the estimated noise along
the prescribed scan range. Thus, even though orange bars appear along the scout in Graphic Rx shows
orange bars through shoulder region, indicating that the prescribed Noise Index cannot be met in this
region., the Projected Noise Index may still meet (or be below) the Prescribed Noise Index due to its
calculation being an average rather than a maximum as in the case of single kV (see Projected Noise
Index indication).
In cases where orange bars appear on the scout image, the Projected Noise Index for individual
regions can be confirmed by hovering over the orange bar.

Scan
Figure 191 Graphic Rx shows orange bars through shoulder region, indicating that the prescribed
Noise Index cannot be met in this region.
Figure 192 Projected Noise Index indication
Projected noise index calculation shows the Projected Noise Index indication vs. Prescribed Noise
Index for the scout scan shown in Graphic Rx shows orange bars through shoulder region, indicating

Scan
that the prescribed Noise Index cannot be met in this region. The Projected Noise Index shown in the
Image Quality Widget for a GSI scan is the average of the estimated noise values along the prescribed
scan range. Because it is an average, the Projected Noise Index may be lower than or equal to the
Prescribed Noise Index, even in cases where orange bars appear in some region or regions along the
scout
11.4.3.5.3 GSI Assist - Optimal Preset Family and Settings

When GSI Assist is enabled, the optimal GSI family and settings chosen are those with the closest
CTDIvol to the non-GSI CTDIvol, based on the prescribed Non-GSI Noise Index, scan parameters
(especially the slice thickness and pitch), patient size and scan range.
11.4.3.6 Cardiac Modulated mA

See the Cardiac chapter for detailed information on Cardiac AEC.
11.4.4 Anatomy Selection

The user can set the start and end location for the scan, either graphically or using a numerical
entry. The system determines the minimum number of exposures and the smallest collimation or
collimations that will cover the prescribed region to minimize both scan time and dose.
Figure 193 Anatomy Selection collection
Element Description
Start Location The start location for the scan.
End Location The end location for the scan.

Scan
(continued)
Element Description
Range Range of images.
Number of Image Number of image acquisitions.
SFOV Define how much anatomy is scanned.
DFOV Allows you to target a particular piece of anatomy for display and determines
how much of the SFOV is reconstructed into an image.
A/P center Allows you to define the DFOV center of the image in the Anterior/Posterior
directions relative to the SFOV.
R/L center Allows you to define the DFOV center of the image in the Right/Left directions
relative to isocenter of the SFOV.
Auto Scan Shows whether Auto Scan is on or off.
Category Click to select a Clinical Identifier Category.
Clinical Identifier Allows you to define clinical categories and specific procedure identifiers
to enable specific behavior for image reconstruction and/or to automate
associated post processing tasks. CID can be used to optimize work flow for
specific clinical use cases.
11.4.5 Scan parameters workflow

Use this procedure to set scan parameters according to your patient's size and anatomy. These
parameters will determine the image quality you achieve. Always make sure to remove any objects
that may cause artifacts. Review the scout image for objects that may cause artifacts.
Considerations
• If the patient orientation is different from the previous scan, the following message is seen:
Patient orientation/position has changed from the previous series. Please verify the
orientation/position of this series is as intended or change the orientation/position, if needed.
• If the landmark has changed, the following message is seen:
The table landmark has changed. This changes the location of all scans you have prescribed.
Double check all scan location before you start scanning.
1. From the Scan Settings window, select a scan task from the protocol.
NOTE
You must execute each scan task in order. Click Confirm Settings for each scan task,
and then scan that scan series. You may then click Continue to move to the next
scan task. Scan tasks can be deleted if you want to skip them. Scan tasks can also be
reviewed when completed.
2. Make sure the patient orientation is the same as it was for the scout.

Scan
If necessary, click the patient image in the Patient Position area to change the patient orientation
and position.
NOTE
There may be times when you change the patient’s position from the way it was
built in the protocol. In this case, you will have to change the patient’s orientation
each time you advance to the next series unless you use the Copy Forward feature.
3. Choose the Scan Type.
4. Set the Coverage Speed options.
5. Set the Primary Recon options.
See Recon Parameters for details.
6. Set kV and mA Control.
• Set the mA.
• Set the kV.
7. Set the Anatomy Selection.

a. Set the Start and End locations.
• To graphically set the locations, see Adjust the Graphic Rx.
• To explicitly set the locations, see Set the Start and End locations.
• A user message dialog displays when the Start or End Location is 250 mm greater
than the Start or End location of the last valid Scout scanned. Start or End Location is
outside of the Scout range. Verify Start and End Locations are as desired.
• A blue alert message displays when the Start or End location is outside the table range.
Start or End Location has been updated to be within the table range. Verify Start and
End Locations are as desired.
b. Set the SFOV.

c. Set the DFOV.
d. Set the A/P center and R/L center.
e. Set the Clinical Category/Clinical Identifier.
8. Set the Contrast options.
a. Select a contrast mode.
b. Select contrast presets.
9. Set the Timing parameters.
See Timing Parameters for details.
10. Set the Gating and Trace options.
11. Set the Secondary Recon options.
See Recon Parameters for details.

Scan
11.4.5.1 Choose the Scan Type

Use this procedure to choose a scan type to specify how the scan data is acquired.
1. From the Scan Settings window, click Scan Type.
2. From the Scan Type collection, choose the desired scan type.
• Click Axial for a step and shoot method.
• Routine head studies typically use Axial scans acquired with a 1 second rotation time.
• Hi Res chest studies may use Axial scans acquired with a sub-millimeter (0.625 mm)
slice.
• Click Helical for a continuous table movement method.

• A wide range of exam types use Helical scans.
• To stop a scan between multiple Helical groups, press Stop Scan not Stop Move.
• Click Cine when one location needs to be scanned over a period of time, such as for
hemangioma studies.
Full is continuous exposure that supports table movement equal to the beam collimation or
no table movement, where the scan is taken at one table position.
• Click Cardiac to help freeze motion of the heart and vascular structures with a Helical-gated
or Cine-gated scan.
If the Scan Type is changed from another scan type, the mA value automatically updates. Review
it to be sure it is acceptable.
3. For Hi Res Mode, click On in combination with the Axial, Helical, or Cardiac scan type to produce
images with improved resolution in the x and y directions.
• Hi Res Mode is supported to enable collection of more views in the x and y directions to
support increased resolution using HD algorithms or improvement in IQ as a result of having
more views, such as for off‐center DFOV imaging.
• The standard set of reconstruction algorithms are compatible with Hi Res acquisitions,
however, the inherent resolution will be reduced to match non Hi Res acquisitions.
• The Hi Res Modes supported include the following:
• Axial – 40, 80, 100, 120, 140, 160 mm detector coverage
NOTE
For the 256 slice system, 80 mm configuration, collimations greater than 80
mm are not selectable.
• Helical
0.516:1 pitch 40 mm detector coverage

Scan

• Cardiac Axial – 40, 80, 100, 120, 140, 160 mm detector coverage
NOTE
For the 256 slice system, 80 mm configuration, collimations greater than 80
mm are not selectable.
4. Click a Rotation Time.

• Axial – 0.28 s, 0.35 s, 0.5 s, 0.6 s, 0.7 s, 0.8 s, 0.9 s, 1.0 s
• Cine – 0.28 s, 0.35 s, 0.5 s, 1.0 s
• Helical – 0.28 s, 0.35 s, 0.5 s, 0.6 s, 0.7 s, 0.8 s, 0.9 s, 1.0 s
• Cardiac Axial – 0.28 s, 0.35 s
5. Click Save.
11.4.5.2 Set the Coverage Speed options

Use this procedure to set the coverage speed options for detector coverage, image slice thickness,
pitch, table speed, and rotation time.
1. From the Scan Settings window, click Coverage Speed.
2. Choose the Detector Coverage.
3. For a Helical scan type, choose the Pitch.
NOTE
Total Exposure Time is updated automatically when a pitch is selected.
• The pitch is the table travel in millimeters per rotation divided by the detector coverage.
• 4 Row Interleaved provides a 40% mAs reduction, is 1.5 to 3 times faster than single slice
helical and has minimal helical artifacts, but interleaved pitch 0.5:1 provides only one
third of the coverage compared to interspaced mode.
• 4 Row Interspaced provides data acquisition 2 to 6 times faster than single slice
helical, but requires more interpolation, has more helical artifacts, and only a 20% mAs
reduction.
• Helical pitches include: 0.508:1, 0.516:1, 0.984:1, 0.992:1, 1.375:1 and 1.531:1.
4. For Axial, Cine and Cardiac scan types, the detector coverage and slice thickness determine the
images per rotation.

Scan
Table 94 Images per Rotation
Detector Coverage (mm)

Slice Thick-
ness (mm) 2
5 40 80 100 120 140 160
0
4
5 1i 8i 16i 20i 24i 28i 32i
i
N
5z NA 15i 31i 39i 47i 55i 63i
A
8
2.5 2i 16i 32i 40i 48i 56i 64i
i
N
2.5z NA 31i 63i 79i 95i 111i 127i
A
1
1.25 4i 632i 64i 80i 96i 112i 128i
i
N
1.25i 1i NA NA NA NA NA NA
A
N
1.25z NA 63i 127i 159i 191i 223i 255i
A
3
0.625 NA 264i 128i 160i 192i 224i 256i
i
6
0.625z NA 4128i 256i 319i 384i 448i 512i
i
• The choice for one determines the choices for the other. Some combinations are not allowed.
• The choice of detector coverage and slice thickness determines the images per rotation.
Some combinations are not allowed.
NOTE
not selectable.
5. For an Axial or Cine scan type, the interval is set equal to the detector coverage. The interval value
can be increased or decreased. If the interval is greater than the detector coverage, the gap is
between each rotation of data, not between the slices.
For an Axial scan type, the interval or spacing defaults to the equal number of images per
rotations multiplied by the slice thickness.
• The interval for Axial scanning can be zero, equal to, or greater than the width of the detector
configuration.

Scan
• Axial interval with skip refers to a gap between scan groups. This can be useful, for example,
when performing a survey exam, such as a high resolution chest exam.
6. Note the Total Exposure Time.

7. Click Apply.
NOTE
The Total Exposure Time shown in the Coverage Speed collection does not account for
the interscan delay prescribed in the protocol.
11.4.5.3 Set the kV and mA Control

Use one of the following procedures to set the kV for the imaging study.
11.4.5.3.1 Set the mA

Use this procedure to set the mA for the scan prescription.
1. From the Scan Settings window, click kV and mA Control.
2. Choose an mA Mode.
• Set to Manual mA and enter an mA value.
• Set to SmartmA or SmartmA and ODM to enable mA modulation in the x-y and z-directions.
• Select a Noise Index value that provides acceptable diagnostic quality. As the Noise
Index increases the required mA decreases and image noise increases. The optimum
strategy is to find the highest Noise Index sufficient for the clinical task and let SmartmA
select the mA without using significant constraints. Use a slightly lower Noise Index for
small patients and a slightly higher Noise Index for large patients.
• Enter Min mA and Max mA values, which constrain the mA range used during the scan.
• For cardiac scans, see guidelines for AEC with Cardiac Modes.
3. Click Apply.
4. Review: For SmartmA and ODM scans, review if the scan is meeting the prescribed Noise Index
from the Image Quality widget to view the calculated X and Y, or A, P, R and L values.
If not, click Adjust to be presented with a list of solutions with dose changes to realize the noise
versus dose in the prescribed Noise Index.
• This can only be done during scan set up and not in Protocol Management.
• The system will display an indication when one or more rotations are at the Min mA or
Max mA value specified for SmartmA. If the system indicates this condition, check the scan
parameters in the mA Table to ensure the acquisition will provide the expected results.
11.4.5.3.2 Set the kV Mode and applicable settings

Manual kV

Scan
Use this procedure to manually prescribe the kV.

1. From the Scan Settings window, click kV and mA Control > kV Mode.
2. Option 1: Select Manual kV. The kV setting becomes editable. Enter the desired value
Typical applications are listed below for the available kVP values.
• Click 70 kV for pediatric imaging.
• Click 80 kV for Bone Mineral Densitometry and Perfusion imaging in the brain and pediatric
imaging.
• Click 100 kV for pediatric and small patient imaging.
• Click 120 kV for routine imaging of the chest, abdomen, and pelvis areas.
• Click 140 kV for imaging the posterior fossa, thick areas, and heavy patient
NOTE
Prior to enabling either kV Assist or Auto Prescription at scan time ensure that you
review kV Assist Theory, Auto Prescription Editor, and Building Auto Prescription in
a Protocol.
Option 2: Auto Prescription, kV Profile setting is displayed, select an appropriate kV Assist Profile
from the dropdown menu.
Option 3: kV Assist, click on the kV Assist popover.
Select the Clinical Task, select the clinical task appropriate for the exam.
Select the kV Min, enter a kV
Select the kV Max, enter a kV
Ensure that the kV Baseline was set appropriately for the average size patient.
Scanning with Auto Prescription

1. Select a protocol with Auto Prescription enabled, or from the kV and mA Control collection,
set the kV Mode to Auto Prescription and select a Auto Prescription Profile appropriate for the
clinical task.
NOTE
Auto WW/WL On when Auto Prescription in enabled, allows the system to adjust
WW/ WL based on the change in image contrast and noise when kV changes at scan
time. Auto WW/WL may be turned On or Off at scan time in both the Primary Recon
and Secondary Recons.
Any secondary recons added will have Auto WW/WL On by default if Auto WW/WL is
On in the primary recon. Auto WW/WL can be enabled in Secondary recons only if
Auto WW/WL is On for the Primary Recon group. To manually change the WW and
WL values for a group, kV Mode must be set to User Override, Auto WW/WL must be
turned Off.
2. Acquire the Scout acquisition. Auto Prescription will not run with an invalid scout.
3. For each group within the series, set the scan range.

Scan
Auto Prescription does the following:

• determines the patient size over the scan range
• determines the corresponding patient size range from the selected profile
• applies all profile settings in the applicable settings collection identified by white dot
• displays all profile settings on the Auto Prescription Widget
NOTE
If the patient’s size does not match a size range within the Auto Prescription
profile, the system displays the Auto Prescription solution of the closest size
range.
The maximum mA will update based on the tube heat and exposure time limits.
4. Review all settings and the image quality widget. Make any necessary adjustments to meet dose
and IQ for the exam.
NOTE
Changing any profile setting value, except minimum or maximum mA, will override
the Auto Prescription Solution. kV mode will change to User Override and the
Widget will highlight the values that differ. Click Revert to kV Assist Solution to
change the values back to the Auto Prescription solution.
Auto Prescription Widget Solution User Override
kV values that are lower or higher than the reference size patient kV may impact the WW/WL
and the contrast brightness. Make necessary adjustments to these settings. See WW/WL
Considerations when using Auto Prescription.
5. Click Confirm.
At scan time, if the user overrides the kV selected by Auto Prescription, the system automatically
adjusts the prescribed NI to maintain a similar Contrast-to-Noise ratio, based on the clinical task from
the profile, as the kV and NI that was chosen by Auto Prescription. The system displays a yellow

Scan
notification banner, and the user has the option to keep the recommended adjusted NI or to revert to
the previous NI.
Scanning with kV Assist
Use this procedure to prescribe a scan with kV Assist. See the Protocols chapter for information about
kV Assist.
1. Select a protocol and verify the Manual kV, mA or applicable SmartmA (Noise Index minimum/
maximum mA), Slice Thickness, Rotation Time, Pitch, SFOV, and WW/WL values that are
acceptable.
2. From the kV and mA Control collection, set the kV Mode to kV Assist.
NOTE
Auto WW/WL will be On in the Primary Recon collection by default for the primary
recon to optimize the protocol’s reference WW and WL based on the expected
change in image contrast and noise when kV Assist is enabled. Select On to use the
WW and WL values set in the Primary Recon. To change the WW and WL values, kV
mode must be set to Manual kV or kV Assist Delta.
3. Specify the Clinical Task for the study.
4. Review the resulting kV, Noise Index or Manual mA and WW/WL values to ensure they are
acceptable.
NOTE
Manual mA or Smart mA parameters cannot be changed when kV Assist is on. Be
sure to set these settings prior to turning on kV Assist. Secondary recons will not
automatically adjust WW and WL.
Once kV Assist has been enabled, kV Assist Delta mode can be selected.
Changing kV, Manual mA or SmartmA parameters when kV Assist is on will reset the kV Mode to
kV Assist Delta mode.
For Cardiac scans, changing SFOV will also reset the kV Mode to kV Assist Delta mode. When
kV Mode is switched to kV Assist Delta, the kV Assist Delta values will be reset to the currently
selected values.
Re-select kV Assist mode to run kV Assist with the modified baseline parameters.
11.4.5.4 Scanning with SmartPlan Enabled

1. Select a protocol with SmartPlan enabled. See Enabling SmartPlan.
2. Scan the scout series.
3. Click Continue. SmartPlan adjusts Start and End Location based on the assigned CID.
Additionally, A/P and R/L will be adjusted when Center Adjust is On, and DFOV if DFOV Adjust
is On. Adjusted values will have a white background with a blue border. These parameter updates
will also be reflected in the graphic Rx localizer.

Scan
In the following conditions, SmartPlan may not optimally identify the scan start and end
locations, A/P centering, R/L centering or DFOV. Please adjust the anatomy selection settings
manually in these conditions.
• Scout image does not contain the anatomy prescribed by the CID in the protocol. For
example, if the CID is Thoracic.Chest Abd Pelvis but the scout image contains only the
abdomen and pelvis.
• Scout image does not include entire anatomy of interest that SmartPlan algorithm utilizes to
determine the localizer positions. This could happen if the scan range is insufficient or if the
patient clinical condition does not contain all the necessary anatomical landmarks.
• Scout is not valid for the prescribed CID. This could occur if patient position is changed, or if
the required scout plane is not acquired prior to the SmartPlan series.
• Scan range is reduced by 50% or more as a result of the user adjusted SmartPlan offsets. The
system displays the following message: SmartPlan Offsets applied, intended anatomy may
not be included. Adjust scan range manually. Notify your protocol manager to adjust Offsets in
SmartPlan Management
• Scan range is 0 or scan direction changes as a result of the applied user adjusted SmartPlan
offsets. The system displays the following message: SmartPlan Offsets not applied, intended
anatomy was not found. Adjust scan range manually. Notify your protocol manager to adjust
Offsets in SmartPlan Management.
4. Review scan primary recon and secondary recon settings, make any necessary adjustments.
5. Click Confirm.
11.4.5.5 Set the Anatomy Selection
11.4.5.5.1 Set the Start and End Locations

The start and end locations are set in millimeters superior to and inferior from the anatomical
reference point. The locations designate the points of anatomy to be scanned. The easiest way to
set the start and end locations is to turn on Show Localizer and adjust the scan range graphically.
If specific locations are known, use this procedure to designate the beginning and end points of the
anatomy to be scanned.
2. For a Helical scan type, click Start.
For Axial, Cine or Cardiac scan types, click Full FOV Start
3. Type a beginning point.
• The numbers must be preceded by the correct designation of S for superior (toward the
head) from the centering point, or I for inferior (toward the feet).
• Plus + can be used for superior and minus - for inferior.
4. For a Helical scan type, click End.

For Axial, Cine or Cardiac scan types, click Full FOV End

Scan
5. Type an end point.

• The numbers must be preceded by the correct designation of S for superior (toward the
head) from the centering point, or I for inferior (toward the feet).
• Plus + can be used for superior and minus - for inferior.
11.4.5.5.2 Set the Scan Field of View

Scan Field of View (SFOV) limits how much anatomy is scanned. Use this procedure to select a SFOV
that covers the anatomy of interest. The SFOV should always be larger than the diameter of the
patient, regardless of what anatomy is being imaged.
2. Choose an SFOV.
• Click Ped Head to image infants 18 months or less in age. It allows you to enter up to a 32
cm DFOV and is limited to 42 kW. It has a special processing to correct for beam hardening
effects.
• Click Ped Body to image to image infants 18 months or less in age. It allows you to enter up
to a 32 cm DFOV and is limited to 42 kW.
• Click Small Head to image small heads up to 32 cm. It has a special processing to correct for
beam hardening effects.
• Click Head to image adult heads up to 32 cm. It has a special processing to correct for beam
hardening effects.
• Click Small Body to image small bodies, extremities that are centered in the middle of the
gantry, and the QA phantom. It allows you to enter up to a 32 cm DFOV.
• Click Medium Body to image most medium body work. If you measure the anatomy that you
are scanning and it measures over 30 cm, you need to use Medium Body. It allows you to
enter up to a 50 cm DFOV.
• Click Large Body to image most adult body work. If you measure the anatomy that you are
scanning and it measures over 30 cm, you need to use Large Body. It allows you to enter up
to a 50 cm DFOV.
• Click Cardiac Small, Cardiac Medium or Cardiac Large for cardiac studies.
NOTE
Cardiac Medium is limited to 36 cm DFOV.
NOTE
Image reconstruction includes native reconstruction to reduce artifacts from beam
hardening.

Scan
11.4.5.5.3 Set the Display Field of View (DFOV) for the primary recon
Follow these steps to enter a DFOV that covers the anatomy of interest. This allows you to target a
particular piece of anatomy for display and determines how much of the SFOV is reconstructed into an
image. Within the DFOV, an image center must be set with R/L Center and A/P Center.
1. From the Scan Settings window, click the Anatomy Selection collection.
2. Click DFOV.
3. Enter the value of the patient's measurements.
• Measure the patient at the widest point and add 2 cm. This will show all the anatomy and the
soft tissue around it.
• If an R/L value or A/P value is more than half of the DFOV, then the R/L, A/P image annotation
does not display on the images. For example, if the DFOV is 10 cm and the R value is 56 mm,
the image annotation displays R. Use an R/L value or A/P value that is less than half of the
DFOV in mm to avoid this.
• The minimum DFOV is 5.0 cm.
• The maximum DFOV depends on the selected SFOV.
NOTE
Alternatively, set the DFOV graphically. On the Show Localizer image, click and drag the
diamond handles to increase or decrease the DFOV. The system automatically updates
the value in the feature area.
11.4.5.5.4 Set the R/L Center coordinates for the primary recon
Use this procedure to set the R/L Center parameter, which allows you to define the DFOV center of the
image in the Right/Left directions relative to isocenter of the SFOV. This is useful for minor adjustments
to imperfections in centering the patient on the table or if an offset structure, such as the spine or
kidney, is what you want centered. If large adjustments are needed, consider repositioning the patient
on the table.
1. From the Scan Settings screen, click the Anatomy Selection collection.
2. Click R/L Center.
3. To find the coordinates, place the mouse over the Show Localizer Anterior/Posterior (AP) scout
image and look at the Right (R) and Left (L) readout at the bottom of the image.
4. Type an R or L prefix and the R/L center coordinates, in millimeters.
• The range of values can be from 0 to one-half the SFOV (example: Head SFOV is 32 cm so the
maximum offset R/L is 16 cm or 160 mm). Typically, you would not want the offset to exceed
one-half the DFOV or the resulting image does not show a right or left marker; it does show
markers as R-R or L-L.
• Entering a value other than zero off centers the image in the right and left axes of the patient.

Scan
• Plus + can be used for R values and Minus - for L values for faster data entry using the ten key
pad.
NOTE
Alternatively, the R/L Center may be set graphically using the X annotation on the A/P
scout image reference lines. Press and hold Shift, and then click and drag the X to center
over the area of interest.
11.4.5.5.5 Set the A/P Center coordinates for the primary recon
Use this procedure to set the A/P Center parameter, which allows you to define the DFOV center of the
image in the Anterior/Posterior directions relative to the SFOV. This is useful for minor adjustments to
imperfections in centering the patient on the table or if an offset structure, such as the spine or kidney,
is what you want centered. If large adjustments are needed, consider repositioning the patient on the
table.
1. From the Scan Settings screen, click the Anatomy Selection collection.
2. Click A/P Center.
3. To find the coordinates, place the mouse over the Show Localizer lateral scout image and look at
the Anterior (A) or Posterior (P) readout at the bottom of the image.
4. Type an A or P prefix and the A/P Center coordinates, in millimeters.
• The maximum offset for A/P Center is one half the SFOV from isocenter selected (example:
Head SFOV is 32 cm so the maximum offset A/P is 16 cm or 160 mm).
• Entering a value other than zero off centers the image in the anterior and posterior axes of
the patient.
• Plus + can be used for Anterior (A) values and Minus - for Posterior (P) values for faster data
entry using the ten key pad.
NOTE
Alternatively, the A/P Center may be set graphically using the X annotation on the lateral
scout image reference lines. Press and hold Shift, and then click and drag the X to center
over the area of interest.
11.4.5.5.6 Set the Clinical Identifier for the primary recon

Use this procedure to set the Clinical Identifier parameter, which allows you to define clinical
categories and specific procedure identifiers to enable specific behavior for image reconstruction
and/or to automate associated post processing tasks. CID can be used to optimize work flow for
specific clinical use cases.
1. From the Scan Settings screen, click on the Anatomy Selection collection.
2. Click Clinical Identifier.
3. Click the Category drop-down and select: Neuro, Stroke, Cardiac, Trauma, Thoracic, Abdominal,
Pelvis or Extremity.

Scan
NOTE
You must select a Category before selecting a Clinical Identifier.
4. Click the Clinical Identifier drop-down and select the appropriate clinical identifier:
Table 95 Clinical Identifiers
Clinical Clinical Body Part GSI Special Processing

Category Identifier Examined Profile
DICOM
0018,
0015
Neuro General HEAD
Routine Head BRAIN GE GSI recon processing optimized for non contrast
Head head scans
NC • DLIR optimized reconstruction for thick
slice, 2.5 or 5mm soft tissue imaging with
manual kV mode, Recon type Standard
and Enhanced Contrast is: {Off, EB1, EB2,
or EB3 non contrast (C-) or delay contrast
(+C). Not applied when kV is 100. When
the soft tissue reconstruction is enabled
the images will be annotated with an
additional /ST after the DL setting, e.g.
DL-H/ST
• Head specific Image Enhancement Fil-
ters are enabled
Routine Head BRAIN GE • DLIR optimized reconstruction for thick

w Contrast Head slice, 2.5 or 5mm soft tissue imaging with
Con- manual kV mode, Recon type Standard
trast and Enhanced Contrast is: {Off, EB1, EB2,
DL-H/ST
ters are enabled
Orbits ORBIT
Soft Tissue NECK GE Soft

Neck Tissue
Neck

Scan
Clinical Identifiers continued

DICOM
0018,
0015
CTA HEAD- GE
NECK Head
Neck
CTA
COW CIRCLEOF- GE
WILLIS Head
CTA
Carotids CAROTID GE Neck

CTA
Perfusion BRAIN Fast Reconstruction Flow
Dynamic CTA BRAIN
Multiphase HEAD-
CTA NECK
Facial Bones FACIAL-

BONES
Sinus PARANA-
SALSINUS
IAC_Tempo- IAC
ral Bone
Tumor Perfu- NECK

sion
Stroke General BRAIN
Routine Head BRAIN • DLIR optimized reconstruction for thick

DL-H/ST
ters are enabled

Scan

DICOM
0018,
0015
Routine Head BRAIN • DLIR optimized reconstruction for thick

w Contrast slice, 2.5 or 5mm soft tissue imaging with
DL-H/ST
ters are enabled
CTA CIRCLEOF-
WILLIS
Perfusion BRAIN 1. Fast reconstruction flow 2. No QC images dis-

played, full IQ images displayed on left monitor 3.
Sets the highest reconstruction priority. Recontruc-
tions will be moved to top of the image reconstruc-
tion priority after any pending scout or Smart Prep
reconstructions are completed.
Dynamic CTA BRAIN
Multiphase HEAD-
CTA NECK
Cardiac General HEART
CCTA CORONAR-
YARTERY
LV Function PULMO-
NARYA
Left Atrium HEART
CACS HEART
TAVI THORACI-
CAORTA
Mitral Valve HEART

Scan

DICOM
0018,
0015
Gated Chest THORACI-

CAORTA
Triple Rule- THORACI-

out CAORTA
PE PULMO-
NARYA
Static Stress HEART

Perfusion
Static Rest HEART

Perfusion
Dyn Stress HEART

Perfusion
Dyn Rest Per- HEART

fusion
Myocardial HEART
Viability
Morphology HEART
Trauma General Protocol Sets the highest reconstruction priority. Recontruc-

(implies Category tions will be moved to top of the image reconstruc-
Emergent) tion priority after any pending scout or Smart Prep
reconstructions are completed.

Scan

DICOM
0018,
0015
Trauma Routine Head BRAIN Sets the highest reconstruction priority.

Recontructions will be moved to top of the image
reconstruction priority after any pending scout or
SmartPrep reconstructions are completed.
• DLIR optimized reconstruction for thick
DL-H/ST
ters are enabled
Trauma Routine Head BRAIN Sets the highest reconstruction priority.

with Contrast Recontructions will be moved to top of the image
reconstruction priority after any pending scout or
SmartPrep reconstructions are completed.
• DLIR optimized reconstruction for thick
DL-H/ST
ters are enabled
Thoracic General CHEST GE Body

80 All
Routine CHEST GE Ab-

Chest domen
Con-
trast
HiRes Chest CHEST

Scan

DICOM
0018,
0015
Lung Nodule CHEST
Chest Abd CHESTAB- GE Ab-

DOMEN domen
Con-
trast
Aorta THORACI- GE
CAORTA Chest
CTA
PE PULMO- GE
NARYA Chest
CTA
Chest Abd CHES- GE Rou-

Pelvis TABDPEL- tine Ab-
VIS domen
Con-
trast
Lung Airway BRON-

CHUS
Lung Paren- CHEST

chyma
Respiratory CHEST
Gated
CTA THORACI- GE
CAORTA Chest
CTA
Tumor Perfu- CHEST

sion
Spine General SPINE GE MSK

NC Arti-
factRed
Cervical CSPINE GE MSK

NC Arti-
factRed

Scan

DICOM
0018,
0015
Thoracic TSPINE GE MSK

NC
Artifac-
tRed
Lumbar LSPINE GE MSK

NC Arti-
factRed
Thoracic and TLSPINE GE MSK

Lumbar NC Arti-
factRed
Complete SPINE GE MSK

NC Arti-
factRed
Abdominal General ABDOMEN GE Body

80 All
Abdomen ABDOMEN GE Ab-

domen
Con-
trast
Abdomen w ABDOMEN GE Ab-

Contrast domen
Con-
trast
Renal Stone KIDNEY GE Ab-

domen
NC
Colonogra- COLON GE Ab-

phy domen
NC
Abd Pelvis ABDOMEN- GE Rou-

PELVIS tine Ab-
domen
Con-
trast

Scan

DICOM
0018,
0015
Pelvis PELVIS GE Rou-

tine Ab-
domen
Con-
trast
Bony Pelvis HIP GE MSK

NC Arti-
factRed
CTA ABDOMI- GE Ab-

NALAORTA domen
CTA
Runoff ABDOMI- GE Run-

NALAORTA off CTA
Renal RENALA GE Ab-

domen
Con-
trast
Pancreas PANCREAS GE Ab-

domen
Con-
trast
Multiphase LIVER GE Ab-

Liver domen
Con-
trast
Tumor Perfu- LIVER GE Ab-

sion domen
Con-
trast
Abd Pelvis w ABDOMEN- GE Rou-

Contrast PELVIS tine Ab-
domen
Con-
trast

Scan

DICOM
0018,
0015
Urogram URETER GE Rou-

tine Ab-
domen
Contras
t
Pelvis General PELVIS GE MSK

NC Arti-
factRed
Pelvis PELVIS GE Rou-

tine Ab-
domen
Con-
trast
Bony Pelvis PELVIS GE MSK

NC Arti-
factRed
Hip HIP GE MSK

NC Arti-
factRed
Sacroiliac SIJOINT GE MSK

NC Arti-
factRed
Cystogram BLADDER GE Rou-

tine Ab-
domen
Con-
trast
Pelvis w Con- PELVIS GE Rou-

trast tine Ab-
domen
Con-
trast
Extremity General EXTREMI- GE MSK

TY NC Arti-
factRed

Scan

DICOM
0018,
0015
Upper Ex- ARM GE MSK

tremity NC
Artifac-
tRed
Lower Ex- LEG GE MSK

tremity NC Arti-
factRed
Upper Ex- ARM GE

tremity CTA Chest
CTA
Lower Ex- ILIACA GE Run-

tremity CTA off CTA
Shoulder SHOULD- GE MSK

ER NC Arti-
factRed
Scapula SCAPULA GE MSK

NC Arti-
factRed
Elbow ELBOW GE MSK

NC Arti-
factRed
Wrist WRIST GE MSK

NC Arti-
factRed
Knee KNEE GE MSK

NC Arti-
factRed
Ankle FOOT GE MSK

NC Arti-
factRed
Gout EXTREMI- GE Gout GSI recon processing optimized for Gout

TY

Scan
11.4.5.5.7 Set the Clinical Identifier for the secondary recon

Use this procedure to set the Clinical Identifier parameter, which allows you to define clinical
categories and specific procedure identifiers to enable specific behavior for image reconstruction
and/or to automate associated post processing tasks.
NOTE
Primary recon does not have to be enabled to prescribe a secondary recon.
1. From the Scan Settings screen, click on the Anatomy Selection collection.
2. Click Clinical Identifier.
NOTE
Use of appropriate CID is critical to image quality for the following specific recon
tasks:
• Gout analysis images must use CID Extremity.Gout
• Non-contrast head images must use CID Neuro.RoutineHead
3. Click the Category drop-down and select: Neuro, Stroke, Cardiac, Trauma, Thoracic, Abdominal,
Pelvis or Extremity.
NOTE
You must select a Category before selecting a Clinical Identifier.
4. Click the Clinical Identifier drop-down and select the appropriate clinical identifier. See table
above.
11.5 Timing Parameters
11.5.1 Timing Parameters collection

From the Scan Settings window, click Timing to display the Timing Parameters collection.
Figure 194 Timing Parameters collection

Scan
11.5.2 Timing parameters workflow

Use this procedure to set up the timing parameters for the scan prescription. The patient’s condition
has a significant effect on timing. Make sure that you know how long the patient can hold her breath.
This helps when working with Auto Voice.
It is important to use scan delays for contrast injections. You can only inject once and you must get it
right the first time. Different anatomy enhances at different rates. Check with your radiologist for the
right scan delays for injectors.
1. From the Scan Settings window, click Timing.
2. If you need a scan delay before the exposure starts, set a Prep Delay time.
• The range is 0 to 600 seconds for the first group and any additional groups.
• Auto Voice automatically sets Minimum Prep Delay time based on message length and the
Preset Delay time set for the Voice, Lights, Timer selection.
• Breathing Lights / Timer sets a Minimum Prep Delay time.
3. For an Axial scan type, set an Inter Scan Delay time.

4. Set the Voice, Lights, Timer options. See 11.7 Auto Voice on page 463 for details.
• 26 languages are available for preset Auto Voice message types Suspension, Inspiration, and
Expiration. The user can define additional languages and record additional message types.
• Preset Delay Time sets a delay from the time the pre-message ends until the X-ray turns on.
This is helpful for patients who need a longer time to follow breathing instructions.
• One of three play back options can be set for each scan group
• Pre and Post
• Pre only
• Post only
If Lock Group Delay was set to On, the system will display an alert if the group delay changes
by 5 seconds or more from the delay prescribed in the protocol. If the Increased Group Delay
message is displayed, either change the settings to reduce the group delay, or click Disable
Lock Group Delay.
NOTE
Lights/Timer is not valid with Cardiac, not valid with Pre Only, and Post Only.
5. To start the scan, click Confirm Settings.

Scan
11.5.2.1 Set Prep Delay time

Prep Delay time establishes how long the system waits before turning the X-ray on for a given group of
scans. Use this procedure to set a Prep Delay time for giving contrast with a timed delay.
NOTE
The minimum Prep Delay may be affected by parameter choices: SFOV, Rotation Time,
Pitch, and Start Location prescribed relative to the prior group. The system updates the
group delay in the Scan Settings window to meet system requirements. Please check
the system message bar on the right monitor before scanning.
2. From the Timing collection, click Prep/Group Delay.
3. Type a scan delay time (in seconds).
NOTE
The system starts to acquire the scan after you press Start Scan and the Prep Delay time
counts down to zero.
Start the injection at the same time as starting the scan to ensure accuracy when the
intravenous (IV) bolus arrives in the appropriate anatomy.
The Prep Delay will be set to zero when resuming a scan after Stop Scan or Pause Scan
is selected during the Prep Delay countdown.
11.5.2.2 Set Inter Scan Delay time

Inter Scan Delay (ISD) allows time for the table to move the correct amount of millimeters set for the
Image Interval. It can also be used for tube cooling by extending the time between exposures and
allowing time for heat to dissipate.
Follow these steps to set an Inter Scan Delay time for an Axial scan prescription.
NOTE
ISD is available for Axial scans only.
2. From the Timing collection, click Inter Scan Delay.
3. Type a scan delay time (in seconds) between each Axial scan.
• The value is dependant on the detector coverage selected when One or More is selected.
• When the scan interval is zero, the value is set by the system based on the selected Rotation
Time and Minimum Time Between Passes.
• The valid range is 1 to 300 seconds.
• Typically, the ISD is set at 1 to 1.7 seconds so the exam is done as quickly as possible.

Scan
11.5.2.3 Enable Lock Group Delay

1. From Protocol Management, click Timing.
2. From the Timing Collection, click Lock Group Delay, Select On for any group other than group 1 in
a series.
When enabled, any parameter change at scan time that increases the delay between the groups
by 5 seconds or more from the value set in Prep/Group delay will display an alert to the user.
11.6 Recon Parameters

Primary Recon parameters can be reviewed and set from the Scan Settings window on the scan
monitor. Secondary Recon parameters can be reviewed and set from the Reconstruction and Image
Processing area on the image monitor.
11.6.1 Recon Parameter descriptions
11.6.1.1 Recon Type

Available Recon Types include: Soft, Soft #, Stnd, Stnd #, Detail, Lung, Bone, Bone Plus, Chest, Edge,
Ultra, HD Stnd, HD Detail, HD Lung, HD Edge, HD Ultra, HD Bone and HD Bone Plus.
11.6.1.2 Lung Algorithm

The Lung algorithm setting provides edge enhancement between structures with large density
differences, such as calcium and air, resulting in a sharper lung field when compared to Standard
algorithm.
For best image quality, prescribe a 5 mm scan thickness when you plan to use the Lung algorithm.
If you plan to prescribe a High Resolution Lung study with 3.75, 2.5, 1.25 or 0.625 mm, use the Bone
algorithm.
The Lung setting enhances the contrast of small objects. For best viewing and film quality, select a
window width of 1,000 to 1,500 and a window level of -500 to -600.
The Lung algorithm setting increases the CT number values at the edge of high contrast objects. If you
plan to take CT number measurements of vessels or nodules in the lung, please check and compare
your results with Standard algorithm images. ROI and Histogram functions use CT numbers.
NOTE
The edge enhancement provided by the Lung setting may not be appropriate in
some clinical cases and image characteristics may vary with larger DFOVs. Please take
individual viewing preferences into account when you choose the Lung setting.
11.6.1.3 Hi Res
Hi Res reconstruction algorithms provide the capability to select reconstruction algorithms that
enhance the inherent resolution in Hi Res mode acquisitions or use the additional views to reduce

Scan
aliasing artifacts, improve off‐center DFOV imaging, and decrease streaking from dense structures. The
algorithms that have a HD prefix added to the algorithm name provide increased resolution for DFOV
of 25 cm or less. The normal algorithms can be used, which will not provide improved resolution but
may be useful when large DFOV is used followed by a targeted reconstruction smaller DFOV, reducing
aliasing and view spacing artifact.
11.6.1.4 Axial Plus Recon Mode

The system provides a Plus recon mode for an Axial scan type. This mode improves reconstructed
image quality at the rotation boundries of the scan.
This mode is available only on Secondary Recons, can be optionally combined with ASiR-V, and is
available only for collimations greater than or equal to 40 mm. Recon Plus is not available with an All
Recon that contains multiple groups.
11.6.1.5 GSI Recon Type and Material Density Pairs

Reconstruction algorithms supported for GSI imaging are Soft, Standard, Detail, Bone, and Bone Plus.
MD with the reconstruction algorithm indicates a Material Density image type.

Scan
Figure 195 GSI Secondary Recon Settings

Scan
• Water (Iodine): Wa (I)

• Water (Calcium): Wa (Ca)
• Iodine (Water): I (Wa)
• Iodine (Calcium): I (Ca)
• Calcium (Water): Ca (Wa)
• Calcium (Iodine): Ca (I)
• Uric Acid (HAP): UA (HAP)
• HAP(Uric Acid): HAP (UA)
• Uric Acid (Calcium): UA (Ca)
• Calcium(Uric Acid): Ca (UA)
• HAP (Iodine): HAP (I)
• Iodine(HAP): I (HAP)
• HAP (Water): HAP (Wa)
• Water(HAP): Wa (HAP)
• Fat (HAP): Fat (HAP)
• HAP(Fat): HAP(Fat)
• Fat (Iodine): Fat (I)
• Iodine(Fat): I (Fat)
• Fat (Water): Fat (Wa)
• Water (Fat): Water (Fat)
GSI annotation information will not be displayed in AW applications on the operator console or on AW
4.3 or below.
11.6.1.6 Cardiac Axial Plus Recon Mode

See the Cardiac chapter for detailed information.
11.6.1.7 Full and Plus Recon Modes for Helical scan types
The system provides the ability to manage dose, slice profile, and helical artifact through the Full and
Plus recon modes.
• Full mode provides a thinner slice profile but requires 10–15% more mA than Plus mode with
equal image noise.
• Plus mode has up to a 20% wider slice profile than Full, but requires 15–20% less mA with equal
noise. At the same mA, Plus mode provides reduced image noise.
• Reduction of helical artifacts can be seen with Plus mode.
• Plus mode uses additional views of data to reconstruct an image.

Scan
• When acquiring images in Plus mode, exposure time increases slightly to assure that enough
views are collected to reconstruct all image locations prescribed.
11.6.1.8 Smart Metal Artifact Reduction (MAR)

Smart MAR is an option intended to reduce photon starvation artifacts, beam hardening artifacts, and
streak artifacts caused by metal implants in the head, spine, hips, extremities, and shoulders. The
metal shape and its position in the body may influence the performance of MAR results.
When using MAR, reconstruct the data with and without MAR for comparative image review.
Effective MAR imaging requires that patient anatomy not extend beyond the 50 cm SFOV.
MAR can be enabled in secondary reconstructions only.
Comparative images with and without MAR should always be reconstructed.
An "M" displays on the image next to annotation for recon algorithm to indicate MAR was enabled for
the reconstruction.
MAR is compatible with Axial 40 mm and Helical scan type.
MAR is compatible with Hi-Res Mode
In Hi-Res mode, MAR is not compatible with Lung, Edge, HD Lung, HD Detail and HD Edge recon
algorithm.
MAR is compatible with secondary recon only
MAR is compatible with all pitches
The interval can be greater than or equal to 0.3125 mm.
MAR annotation is added to the left side of the image.
11.6.1.9 IQ Enhance for Helical scan types

IQ Enhance is a special reconstruction process that can be prescribed to minimize artifacts commonly
occurring in thin slice helical acquisitions. If you select the Helical scan type, IQ Enhance is available in
the Primary Recon and Secondary Recon parameter collections, if the slice thickness is 0.625 mm or
1.25 mm. The interval for these slice thicknesses must be equal to the slice thickness (0.625 or 1.25) or
one half the slice thickness (0.312 or 0.625).

Scan
Figure 196 Image Enhance images
An "E" displays on the image next to the annotation for to indicate IQ Enhance is enabled for the
acquisition.
NOTE
IQ Enhance is not compatible with Axial, Cine or Cardiac scan types.
11.6.1.10 Enhanced Contrast for Axial and Helical scan types with Head
SFOV
Enhanced Contrast is a special reconstruction option to boost the differentiation between the gray
and white matter regions in the brain. The Enhanced Contrast reconstruction option enables improved
visual contrast between gray and white matter regions without the noise amplification present when
using a narrow window width display setting.
Six levels of Enhanced Contrast are selectable: EC1, EC2, EC3, EB1, EB2 and EB3 where the higher
number corresponds to additional differentiation between gray and white matter. EC selections focus
on CT number separation of gray and white matter for better differentiation, EB selections focus on
improving the gray and white edge boundary resolution for better differentiation. As the reconstructed
CT number is modified by the Enhanced Contrast option, it is recommended that it not be used for
quantitative soft tissue imaging.
If you select Axial or Helical scan type with Head, Small Head or Ped Head SFOV, 100, 120 or 140
kV, HiRes Off, Soft, Soft #, Stnd or Stnd # algorithm and Number of Passes: 1, Enhanced Contrast is
available in the Primary Recon and Secondary Recon parameter collections.

Scan
Figure 197 Enhanced Contrast selections
Figure 198 Enhanced Contrast – Off (Left); Enhanced Contrast – EC2 (Middle); Enhanced Contrast
– EB3 (Right)
11.6.1.11 Fine Z for Axial scan type with Head SFOV

The Fine Z reconstruction option (annotated as: #Z) has been designed for high resolution Neuro
Axial acquisitions. This reconstruction method is designed for high resolution imaging tasks such as
assessing detail in the inner ear.
The method utilizes both projection space resolution enhancement and adaptive image space
processing to achieve the improvement in z resolution.
The Fine Z mode is recommended most for clinical tasks which require significant use of oblique
reformats or sagittal or coronal views.
The Fine Z reconstruction option may be applied either prospectively in primary reconstruction, as
well as in any secondary reconstruction requests. As this is designed for increased z resolution, it is
available only for high resolution kernels and only when the highest z direction sampling is selected,
for example, 0.625Z. The other additional constraints for the Fine Z reconstruction option are given in
the following table.

Scan
Parameter Available selection
Scan Type Axial or Axial Hi Res
Scan Field of View (SFOV) HEAD, Small Head, Ped Head
kV Mode Manual, kV Assist, kV Assist Δ, Auto Prescription, User

Override
Reconstruction Type (for example, Kernel) Bone, Bone Plus, Edge, Ultra, HD Bone, HD Bone Plus,
HD Ultra, HD Edge
Slice Thickness 0.625Z
NOTE
Fine Z is not available when Clinical Category is Stroke and Clinical Identifier is
Perfusion.
Figure 199 Fine Z selections

Scan
Figure 200 Fine Z – Off (Left); Fine Z – On (Right)
11.6.1.12 Image Enhance Filters, edge smoothing and lung enhancement

filters
The edge and smoothing filters enhance anatomical structure. Edge Enhancement filters sharpen the
image and are useful for bone windows. There are three levels of Edge Enhancement: E1, E2,and E3,
where E1 applies the least amount of enhancement and E3 applies the most. When these filters are
used, the image is annotated with E1, E2 or E3.
The smoothing filters decrease the appearance of noisy images or enhance low-contrast areas on soft
tissue. There are three levels of Smoothing filters : S1, S2, and S3, where S1 applies the least amount of
smoothing and S3 applies the most. When these filters are used, the image is annotated with S1, S2 or
S3.
The Lung Enhancement filter is designed specifically to use for lung windows. When the Lung
Enhancement filter is applied, the image is annotated with the word LU.
11.6.1.12.1 Image Enhance Filters optimized for Neuro Imaging

Image Enhance Filters provide the user additional freedom to select the desired spatial resolution and
noise. An adverse effect of traditional enhancement filters is that undershoot (i.e. a dark rim) can occur
around high contrast areas such as the skull. Image Enhance Filters optimized for neuro imaging can
avoid this undershoot.

Scan
Figure 201 Skull image with Image Enhance Filters
No Image Enhancement Filter E3 EH3
In this figure, the middle and right images have an edge Image Enhancement Filter applied. The right
image does not have the dark undershoot at the boundary present on the middle image. The strength
of the head-specific filters (EH1, EH2, EH3) is also lower than the traditional filters (E1, E2, E3) as the
highest strength of the traditional filters is not applicable to soft tissue imaging.
The head-optimized Image Enhance Filters are used when the scan field of view is Small Head,
Ped Head or Head AND the Clinical Identifier is the one of the following: {Neuro. Routine Head,
Neuro.Routine Head w Contrast, Trauma.Routine Head, or Trauma.Routine Head w Contrast,
Stroke.Routine Head, or Stroke.Routine Head w Contrast} and the Recon Type is: {Stnd, Stnd#,
Soft, or Soft#}. The images will be annotated with an "H" in the filter description to indicate a
head-specific filter, e.g. E3 vs. EH3.
11.6.1.13 Quality Check (QC) Images

QC images are non-diagnostic, preview images generated by the system to check if the scan
acquisition was successful, prior to full IQ images. QC images are displayed in the two viewports
on the scan monitor. QC images have an annotation at the bottom to indicate that they are not for
diagnostic use. QC images are only generated once during a scan series, and are not saved or available
after the scan series is acquired.
The QC image reconstruction queue includes only 1 active entry and 1 pending entry. The newest scan
will preempt any pending QC entry. Depending on the number of scans or groups of scans taken you
will not see QC images from every scan. If the Xtream Stroke option is installed and Stroke Perfusion
Clinical Identifier is enabled, QC images will not display for the primary recon. Do not use QC images
to make decisions if rescanning is needed, the primary reconstruction images should be used for this
determination.
QC Images will be auto-generated with the Primary Recon for the following scan types: Axial , Cardiac
Axial, Helical and Cine.
11.6.1.14 Deep Learning Image Reconstruction (DLIR)

Scan
11.6.1.14.1 DLIR (Single Energy)

Intended Use
The Deep Learning Image Reconstruction option is intended for head, whole body, cardiac, and
vascular CT scans.
Indications for Use
The Deep Learning Image Reconstruction option is a deep learning based reconstruction method
intended to produce cross-sectional images of the head and whole body by computer reconstruction
of X-ray transmission data taken at different angles and planes, including Axial, Helical (Volumetric),
and Cardiac acquisitions, for all ages. Deep Learning Image Reconstruction can be used for head,
whole body, cardiac, and vascular CT applications.
11.6.1.14.2 DLIR for GSI

Intended Use
The Deep Learning Image Reconstruction for Gemstone Spectral Imaging option is intended for whole
body, vascular, and contrast enhanced head CT applications.
Indications for Use
The Deep Learning Image Reconstruction for Gemstone Spectral Imaging option is a deep
learning based CT reconstruction method intended to produce cross-sectional images by computer
reconstruction of dual energy X-ray transmission data acquired with Gemstone Spectral Imaging, for
all ages. Deep Learning Image Reconstruction for Gemstone Spectral Imaging can be used for whole
body, vascular, and contrast enhanced head CT applications.
NOTE
DLIR for GSI has not been tested for compatibility with Low Dose CT Lung Cancer
Screening.
11.6.1.14.3 DLIR Reconstruction Overview

The Deep Learning Image Reconstruction (DLIR) option is intended for image reconstructions to
remove noise from the image but with a desire for a texture that is more consistent with Filter Back
Projection image reconstruction.
Before using DLIR, the site physicist, in collaboration with the radiologist, should conduct image
quality evaluations with varying DLIR strengths. Medium is recommended as an appropriate starting
point for DLIR strength on your existing clinical protocols.
DLIR is available for secondary reconstruction prescription only. Any exam can have multiple
secondary reconstruction series.
DLIR cannot be prescribed in the same reconstruction series as ASIR-V. However, additional
reconstruction series can be prescribed with ASIR-V if desired.
DLIR is compatible with the following scan types with Hi-Res mode ON or OFF:
DLIR is not compatible with the following Scan Types:

Scan
• Axial, Cine, Detector Collimation less than 10 mm

• Volume Helical Shuttle
• SmartStep, SmartView and 3D Guidance
• SmartPrep
• Smart Score Pro
• HiRes Axial and Helical scan types (non Cardiac)
DLIR is not compatible with the following Features:

• IQ Enhance Plus
• Axial overlapped recon
• Cardiac Filter
• Helical Segment recon
• Scan range less than 10 mm
• Full mode with 0.625 mm slice thickness at 0.516:1 and 0.531:1 pitch
When DLIR is applied to a Helical scan, the following settings must be applied
• Interval must be equal to the slice thickness or a half of the slice thickness for 1.25 mm to 5 mm
slice thickness.
• Interval must be equal to the slice thickness for 0.625 mm slice thickness.
DLIR is compatible with the following Reconstruction Types:

• Stnd for Axial, Cine or Helical scan mode with Hi-Res ON or OFF.
• Stnd and Detail for Cardiac Cine and Cardiac Helical scan modes
• HD Stnd for HiRes Cardiac Cine and HiRes Cardiac Helical scan modes (when HiRes scan mode is
offered on the CT system)
If the GSI for DLIR option is installed, Head SFOV DLIR will be not compatible with GSI Reconstructions.
For GSI reconstruction tasks, DLIR can be prescribed only if the Recon Type is Standard and if the
interval is equal to or one half the slice thickness. DLIR for GSI may not be prescribed under the
following conditions:
• SFOV is Head and Cardiac
• GSI Image Type is High kVP
• Scan Range is less than 40 mm.
DLIR can be set in a reconstruction task at scan time or within a GSI Profile.
11.6.1.14.3.1 DLIR for routine Neuro imaging

A reconstruction optimized for deep learning reconstruction of thick-slice soft tissue neuro imaging is
available.

Scan
This reconstruction is used when the scan field of view is Small Head, Ped Head or Head, AND the
Clinical Identifier is one of the following: {Neuro.Routine Head, Neuro.Routine Head w Contrast,
Trauma.Routine Head, or Trauma.Routine Head w Contrast, Stroke.Routine Head, or Stroke.Routine
Head w Contrast} AND Recon Type is Stnd and Enhanced Contrast is: {Off, EB1, EB2, or EB3}. Image
annotation will display /SH after the DLIR setting.
This soft tissue reconstruction is designed for non-contrast and delay contrast scanning (C-) and (C+),
wherein the images are typically viewed in thicker slices (e.g. 2.5 mm or 5 mm).
Figure 202 DLIR Neuro Soft Tissue
AR50 DL-H DL-H/ST
11.6.1.14.4 Creating a DLIR Reconstruction

The system allows additional secondary reconstruction of your scan groups, prescribed pre-scan or
post scan.
From the image monitor, in the Reconstruction and Image Processing area, select Duplicate Recon or
Add Recon for a particular series.
1. Prescribe the Start and End location for the reconstruction task.
2. Under Recon Settings, click DLIR and select strength Low, Medium or High.
NOTE
ASIR-V will be set to OFF automatically and cannot be re-enabled unless DLIR is set
to OFF.
3. Set all parameters for the reconstruction task.
NOTE
Helical recon interval setting must be equal to the slice thickness or one half the
slice thickness. DLIR will be set to OFF if any other interval is set.
Recon Type is Stnd or HD Stnd depending on the scan type. If any other recon type
is set, the system will notify the user that the recon type is incompatible with DLIR.

Scan
Figure 203 Secondary Recon Setting Collection with DLIR settings
4. Select Run.
NOTE
DLIR annotation is not not displayed in Reformat, Volume Viewer or any of the other
Volume Viewer post processing applications. This occurs when SmartMAR is On in
conjunction with DLIR. View images in the File Manager or Review Session to view
the DLIR annotation.
11.6.1.15 Max Field-of-view (MaxFOV 2)

Intended Use:
The MaxFOV 2 reconstruction software is intended for head and whole body CT scans.
Indications for Use:
The deep learning based Max Field-of-view (MaxFOV 2) is a CT image reconstruction method intended
to produce images of the head and whole-body using Axial, Helical, and Cine acquisitions. MaxFOV
2 is designed to extend the nominal display field of view (DFOV) for cases where patient size and
positioning requirements result in a portion of the patient’s body to be outside of the nominal DFOV.
These extended FOV images are intended for use in radiation therapy planning and are clinically useful
for the simulation and planning of radiation therapy for the treatment of cancer for patients. They can
also be used for visualization of patient anatomy for cases not involving therapy planning. MaxFOV 2 is
intended for patients of all ages, especially bariatric patients.

Scan
11.6.1.15.1 MaxFOV 2 Theory

The diameter of a CT scanner’s bore is typically larger than the diameter of the imaging area or Display
Field of View (DFOV). As a result, a patient’s anatomy occasionally extends outside the imaging area.
This may occur with large patients or if the patient is displaced to one side.
In radiation therapy planning, the patient’s arms or other anatomy sometimes extend outside the
imaging area in order to accommodate the treatment position. Anatomy that extends outside the
imaging area cannot be reconstructed with a conventional reconstruction algorithm. In addition, the
truncated data results in a peripheral shading artifact which obscures anatomy inside the imaging
region. For some applications, it may be desirable to view the anatomy that extends beyond the
conventional imaging region and/or to remove the shading artifact.
In radiation therapy, it is increasingly important that the patient’s entire anatomy be included in the
CT image in order to calculate the treatment dose distribution. When fusing CT images with images
from other modalities, which may have larger imaging regions, it is also useful to be able to extend the
CT imaging region.
11.6.1.15.2 MaxFOV 2 Overview

Max Field-of-view (MaxFOV 2) is a deep learning reconstruction method that allows the user to
increase the max display field of view (DFOV) beyond the conventional scanner limit.
The increase in the max DFOV from 50 cm to 80 cm is a significant increase in viewing area that allows
clinicians to visualize more anatomical information and helps them locate the complete skin surface
for optimal radiation therapy simulation and planning.
The goal of Max Field of view reconstruction is to help the radiation therapy planner accurately (within
a few millimeters) locate the air/skin boundary.
The image quality in the region beyond the scan FOV is not expected to be as good as that within the
Scan FOV, CT Number accuracy differs and is not intended for diagnostic imaging.
The MaxFOV 2 is validated with the GE certified flat table top, use of the other flat table tops may not
produce the same image quality.
Image quality can also degrade if there is a large air gap between the body and arm, if the arm extends
outside of the scan FOV (50 cm).
Do not change the table height after confirmation of the MaxFOV 2 acquisition.
Image quality can degrade if the object being scanned extends outside of the scan FOV (50 cm) over
more than 90 degrees (over more than one quarter of the 360 degrees) and the density of the object is
significantly different from water.

Scan
Figure 204 Object being scanned extends outside of the SFOV over more than 90 degrees
11.6.1.15.3 Creating a Max Field-of-view (MaxFOV 2)
NOTICE
PLEASE REFER TO THE MAXFOV 2 SECTION OF SAFETY CHAPTER

FOR IMPORTANT SAFETY INFORMATION REGARDING THE USE OF THE
EQUIPMENT AND SOFTWARE ON THIS SYSTEM.
When MaxFOV 2 option is installed, the user is able to prescribe a DFOV between 50.1 cm and 80 cm.
MaxFOV 2 is available only in secondary recon prescriptions when SFOV is Large Body, and Collimation
less than or equal to 40 mm.
MaxFOV 2 is not compatible with GSI, SmartPrep, SmartStep, Cardiac and Hi-Res scan types.
MaxFOV 2 is not compatible with the following reconstruction settings:
• DLIR
• IQ Enhance
• SmartMAR
• Ultra
• Edge
To enable MaxFOV 2 reconstruction

1. Click Anatomy Collection > DFOV
2. Enter a value between 50.1 and 80 cm or graphically adjust DFOV on the Show Localizer image.

Scan
11.6.1.16 Flip / Rotate

The reconstructed orientation of an image can be changed from the default mode by selecting one of
the following flip/rotate options in the Primary Recon and Secondary Recon collections.
• None
• FLR (Flip Left Right)
• FTB (Flip Top Bottom)
• FLR / FTB (Flip Left Right / Flip Top Bottom)
NOTE
Flip / Rotate options cannot be selected for images being acquired in the decubitus
patient positions.
NOTE
Flip/Rotate options are only available after service checks that the viewing stations will
display the data correctly.
11.6.1.17 Enhanced Contrast for GSI Neuro

Enhanced Contrast is a special reconstruction option to boost the differentiation between the gray
and white matter regions in the brain. The Enhanced Contrast reconstruction option enables improved
visual contrast between gray and white matter regions without the noise amplification present when
using a narrow window width display setting. Three levels of Enhanced Contrast are selectable for GSI:
EB1, EB2 and EB3 where the higher number corresponds to additional differentiation between gray
and white matter. EB selections focus on improving the gray and white edge boundary resolution in
combination with CT number separation of gray and white matter for better differentiation. As the
reconstructed CT number is modified by the Enhanced Contrast option, it is recommended that it not
be used for quantitative soft tissue imaging.
If GSI scan type with:
• Small Head, Head, or Ped Head SFOV;
• 70 keV, 65 keV, or 60 keV Monochromatic GSI Image Type;
• Stnd or Soft Recon Type;
• and DataFile is OFF is selected,
Enhanced Contrast is available in Primary or Secondary reconstructions. In the GSI Profile Editor,
Enhanced Contrast is selectable for Head profiles that satisfy the conditions above.

Scan
Figure 205 GSI Enhanced Contrast selections
Figure 206 GSI Enhanced Contrast – Off (Left); Enhanced Contrast – EB2 ( Middle); Enhanced
Contrast – EB3 (Right)
11.6.2 Primary Recon collection

From the Scan Settings window, click the Primary Recon collection.

Scan
Figure 207 Primary Recon collection - Axial
Table 96 Primary Recon collection - Axial
Element Description
Thickness Image thickness with each Axial rotation.
Recon Type Reconstruction algorithm.
Enhanced Contrast Enables Enhanced Contrast recon option. See Enhanced Contrast for Axial and Helical
scan types with Head SFOV for detailed information.
Fine Z Only available for Axial Hi Res Head SFOV with slice thickness of 0.625Z. See Fine Z
selections
Image Enhance E1, E2, E3 or S1, S2, S3, lu See Image Enhance Filters
Filter
ASiR-V See ASiR-V for detailed information.
SnapShot Freeze Only available for Cardiac. See the Cardiac chapter for detailed information.
Window Width Can be set for different groups.
Window Level Can be set for different groups.
Flip / Rotate See Flip / Rotate for detailed information.
Phase Only available for Cardiac. See the Cardiac chapter for detailed information.

Scan
Figure 208 Primary Recon collection – Helical
Table 97 Primary Recon collection – Helical
Element Description
Thickness Image thickness.
Recon Mode • Full

• Plus
IQ Enhance See IQ Enhance for Helical scan types for detailed information.
Interval Image interval.
Filter

Scan
Flip / Rotate See Flip / Rotate for detailed information.
11.6.3 Primary Recon parameters workflow

Most recon parameters are set from the protocol and from adjustments made with graphic lines on the
scout image. When setting recon parameters, it is important to know specifically what you are looking
for. If you are looking for fractures, you would want to use a different set of parameters than if you
were looking for a mass.
11.6.3.1 Copy Forward

Copy Forward Patient Orientation, Patient Position and Anatomical Reference is a feature that adjusts
these three bundled parameters in a scanning protocol based on the values in the previous series. This
feature is located in Protocol Management.
NOTE
Auto Voice Language category is not copied forward across each series when changed in
a single series. Update the language category in each series prior to confirm and scan of
the first series. Auto Voice language category can only be changed if no scans have been
taken in the series.
NOTE
Copy Forward is set at the destination or recipient series.
For example, if Copy Forward was turned “On” in Series 2 of a protocol, and during
scan Patient Orientation, Patient Position and Anatomical Reference were changed from
Head First, Supine, SN to Feet First, Prone, OM for Series 1, these three settings will be
automatically copied for scanning Series 2.
Similar to Copy Patient Orientation / Position, Copy Forward works within the same
patient exam.
The Copy Series feature can be used to duplicate (reuse) the following parameters from the primary
reconstruction in the previous scanned series.
• Start Location
• End Location
• Time Between Passes (Cine scan type only)
• Interval (Helical scan type only)
• DFOV
• R/L Center
• A/P Center
The Copy Forward feature can also be used to duplicate (reuse) the following parameters within series
from primary reconstruction to secondary reconstructions:

Scan
• Start Location
• End Location
• Time Between Images (Cine scan type only)
• DFOV
• R/L Center
• A/P Center
To activate Copy Forward, type d or D (duplicate) in the Parameter text field in the receiving
reconstruction or subsequent scan series.
11.6.3.2 Set the Slice Thickness

1. From the Scan Settings window, click Primary Recon.
2. Choose the Thickness.
• The smaller the slice thickness, the more technique you need to use. The thinner the slice
thickness, the higher the noise will be in the slice. Adjust protocol factors to provide desired
image quality and noise level for the acquisition.
• A thinner slice provides better detail. However, contrast resolution will be decreased.
11.6.3.3 Set the Image Interval

The Image Interval is for Helical scans only and is automatically set to match the slice thickness by the
system. This is known as contiguous (back to back) scans. Use this procedure to set an Image Interval
if you want a contiguous, overlapped, or spacing (skip) in the scan prescription.
1. Click Interval.
2. Type an interval value in mm.
For a Helical scan type, the table moves in mm per rotation, while exposing the patient.
• The image interval defaults to equal the slice thickness (for primary reconstructions only).
• The maximum interval is twice the slice thickness.
• The interval can be less than or greater than the slice thickness.
• IQ Enhance is compatible with 0.625 mm and 1.25 mm slice thicknesses. Interval for
acquisitions with IQ Enhance must be equal to the slice thickness (0.625 mm or 1.25 mm) or
an overlap of 50% (0.312 mm or 0.625 mm).
11.6.3.4 Set the Recon Type

Use this procedure to set the Recon Type, which designates the algorithm used for image
reconstructions.
1. From the Scan Settings window, click the Primary Recon collection.

Scan
2. Click Recon Type.

3. Select the appropriate algorithm for the primary or first reconstruction.
The algorithms from top to bottom increase spatial resolution and decrease low contrast
detectability.
NOTE
There is a potential for artifacts, such as basket weave or aliasing, to be visible when
higher noise recon types are viewed in a standard window width and window level.
It is important to utilize the appropriate window width and window level for the
selected recon type to avoid these potential artifacts. If reconstruction is limited
to a single series, it is recommended to use Standard recon type and apply Image
Enhance Filters or CT visualization post filters in Volume Viewer ( E1, E2, E3 or Lung)
and view with Bone window width/ window level.
•
Figure 209 Example of Basketweave Artifact
Click Soft for tissues with similar densities, but not useful for non-enhanced scans.
• Click Soft # for head anatomy with similar densities. Results in finer texture and similar noise
compared to Soft.
NOTE
Soft # is only available when Head, Small Head or Ped Head is selected, scan
type is Axial or Helical and Hi Res mode is Off.

Scan
• Click Stnd for routine exams, e.g., chest, abdomens, and pelvis scans.
• Click Stnd # for head anatomy with similar densities. Results in finer texture and similar noise
compared to Stnd.
NOTE
Stnd # is only available when Head, Small Head or Ped Head is selected, scan
type is Axial or Helical and Hi Res mode is Off.
• Click Detail for post myelograms, where hybrid tissue detail and bone edges are important.
• Click Lung for interstitial lung pathology.
• Click Bone for high resolution exams and sharp bone detail.
• Click Bone Plus for sub mm detailed head work. It can be used for any study that normally
used the bone algorithm, but is very useful in cases where the Edge algorithm was used.
This is because the Bone Plus algorithm has no reconstruction penalty and is very close in
standard deviation to Edge.
• Click Edge for small bone work in the head, as well as high resolution scans.
• Click Chest for mediastinum and lung detail studies. It provides soft tissue resolution and
contrast when viewing the images in a soft tissue/mediastinal W/L and high resolution of the
lung tissue when viewing the images in a lung W/L.
• Click Ultra for improved detail in the inner ear.
NOTE
Cardiac scan mode choices are: Soft, Stnd, Detail, Lung and Bone.
4. If Hi Res mode is enabled, select a higher resolution algorithm that has similar characteristics to
the non-Hi Res algorithms.
• HD Stnd
• HD Lung
• HD Detail
• HD Bone
• HD Bone Plus
• HD Edge
• HD Ultra
5. If Cardiac Hi Res mode is enabled, select a higher resolution cardiac algorithm that has the same
characteristics as the non-Hi Res cardiac algorithms.
• HD Soft
• HD Stnd
• HD Stnd Plus
• HD Detail
• HD Detail Plus

Scan
• HD Lung
• HD Edge
11.6.3.5 Set Recon Options for Helical scan types
11.6.3.5.1 Recon Mode

To adjust the Recon Mode, select Full or Plus.
NOTE
Plus Recon mode is not annotated on the Series Text Page.
Full mode is not allowed with 0.625 mm slice thickness at either 0.508:1 pitch, 0.969:1, 0.984:1 pitch,
1.375:1 pitch or 1.531:1 pitch.
11.6.3.5.2 IQ Enhance
To adjust IQ Enhance, click IQ Enhance to select either On or Off.
IQ Enhance is used to minimize artifacts seen in helical thin slice images.
IQ Enhance is allowed with both 0.625 mm and 1.25 mm slice thickness, and the image interval can
either be 50% or 100% of the slice thickness.
IQ Enhance annotation is added to the left side of the image.
11.6.3.6 ASiR-V for all scan types

Follow these steps to enable ASiR-V and select an ASiR-V percentage level.
1. From the Primary Recon collection, click ASiR-V.
2. ASIR-V can be adjusted by clicking on the Primary or Secondary recon settings ASiR-V % menu.
11.6.3.7 Enhanced Contrast for Axial and Helical Head SFOV types
Follow these steps to enable Enhanced Contrast.
1. From the Primary Recon or Secondary Recon parameter collection, click Enhanced Contrast.
2. Click on the Enhanced Contrast menu to select the desired value: EC1, EC2, EC3. EB1, EB2 or EB3.
• Enhanced Contrast is used to boost the differentiation between the gray and white matter regions
in the brain.
• Enhanced Contrast is allowed with Axial and Helical scan types, Head, Small Head and Ped Head
protocols, 100, 120 and 140 kV, Hi Res Off, Number of Passes: 1, and Soft, Soft #, Stnd or Stnd #
kernels.
• Enhanced Contrast annotation is added to the left side of the image.

Scan
11.6.3.8 Adjust Window Width and Window Level for all scan types
Follow these steps to adjust Window Width and Window Level.
1. Open the Primary Recon collection.
2. Click Window Width and type the desired value.
3. Click Window Level and type the desired value.
11.6.3.9 Image Flip Orientation

1. Open the Primary Recon collection.
2. Click on Image Flip Orientation and choose the desired selection.
To flip or rotate the image so the image will be reconstructed in the orientation desired for
viewing, select one of the following options:
• FLR (Flip Left Right)
• FTB (Flip Top Bottom)
• FLR / FTB (Flip Left Right / Flip Top Bottom)
The Image Flip Orientation option is turned off when software is delivered. A service representative
can enable it once you are sure that remote viewing stations display the flipped and rotated images
correctly.
Images are annotated with:
• FI: LR
• FI: TB
• FI: Rotate 180
All Image Flip Orientation annotations display on the left side of the image when prescribed in recon.
NOTE
Flip and Rotate is valid only for Supine and Prone patient position. Filp and Rotate
selection is not shown and is not valid when the scan type is Cardiac.
NOTE
Image Flip Orientation and non-Image Flip Orientation images can not be mixed in the
same series.
NOTE
If Image Flip Orientation in Recon and Continuous Cursor are enabled on a system, the
RAS coordinates displayed on the left side of the image have the Image Flip Orientation
annotation intermixed with the RAS information. If Image Flip Orientation was not
applied to the image, there is a blank space in between the RAS information.

Scan
11.6.3.10 Image Enhance Filters

Follow these steps to enable an image enhance filter.
1. From the Primary Recon or Secondary Recon parameter collection, click Image Enhance Filter.
2. Click on the menu to select the desired value: E1, E2, E3 or S1, S2 or S3 or lu.
Image Enhance Filter annotation is added to the left side of the image.
NOTE
lu filter is not valid when SFOV is Head.
11.6.4 Secondary Recon Parameters

The system allows up to 99 additional secondary reconstructions of your scan groups, prescribed pre-
scan, that use all or any portion of a group or across groups to change several of the reconstruction
parameters. You can prescribe more secondary reconstructions post-scan.
Figure 210 Secondary Recon collection — Axial

Scan
Table 98 Secondary Recon collection — Axial
Element Description
Thickness Image thickness with each Axial rotation.
Recon Type Reconstruction algorithms.
Recon Mode Plus • On

• Off
Filter
DLIR See DLIR for detailed information.
Flip and Rotate None
Matrix Size Matrix size of the image. 512 or 1024.

Scan
Figure 211 Secondary Recon collection — Helical
Table 99 Secondary Recon collection — Helical
Element Description
Thickness Image thickness.
Interval Image interval.
scan types with Head SFOV on page 432 for detailed information.

Scan
Secondary Recon collection — Helical continued

Element Description
Recon Options • Full

• Plus
IQ Enhance See IQ Enhance for Helical scan types on page 431 for detailed information.
Filter
DLIR See DLIR for detailed information.
MAR Turn MAR on to remove artifacts caused by metal. See SmartMAR
Matrix Size Matrix size of the image. 512 or 1024.
The following parameters may be automatically copied from the primary reconstruction with the Copy
Forward feature.
• Start Location
• End Location
• Time Between Images (Cine scan type only)
• DFOV
• R/L Center
• A/P Center
NOTE
These parameters will have a green box around them when Copy Forward is active.
Graphic Rx for secondary reconstructions will indicate if Copy Forward is “On” with a salmon colored
handle on the graphic object. If the user adjusts the handle, Copy Forward is disabled, and the handle
goes back to the original group color; the green box is also removed from the text fields. Alternatively,
if the user types in a text field where Copy Forward is enabled, is no longer outlined in green and the
corresponding handle on the graphic object returns to the original group color.
Rather than relying on creating additional reconstructions post scan for additional data sets, you are
able to create these sets prospectively. This frees the operator from sitting at the console, directly
contributes to increased productivity, and reduces the opportunity for error.
Secondary reconstructions are assigned series numbers based on the series they are prescribed in,
e.g., in the scenario where Series 2 has three additional secondary reconstructions, these are listed in

Scan
the task list display indented from the original series. These reconstructions become Series 301, 302,
and 303 in the exam.
To add a secondary reconstruction, from the image monitor, in the Reconstruction and Image
Processing area, select Duplicate Recon or Add Recon for a particular series. You can also select
which viewport a reconstruction will display in. Refer to the View Images chapter for more details.
Follow the primary reconstruction workflow to set the reconstruction parameters.
A reformat step can also be added on secondary reconstructions, as well as output and transfer
options. Refer to the Display Applications chapter for more details.
NOTE
To display Graphic Rx when Recon All contains multiple groups, double click on the
Recon task.
11.6.4.1 Overlapped Axial Recon mode

The system supports the reconstruction of overlapped data from Axial scan type 40, 80, 120, 140, 160
mm detector coverage. The reconstruction of overlapped Axial data can improve reformatted data.
The interval cannot be adjusted.
Images reconstructed with the Z recon mode will be annotated with a Z in the upper‐left area of the
images.
Figure 212 Image Annotation for Overlapped Axial Recon mode
11.6.4.2 Recon by Pass

Recon by Pass allows a secondary recon prescription by pass number for Axial, Cine and Cardiac
acquisitions scanned as multiple passes such as for Perfusion.
Recon by Pass parameters
1 Axial or Cardiac Recon by Pass parameters
2 Cine Recon by Pass parameters

Scan
11.6.4.3 Secondary Recon Slice Thickness

NOTE
For the 256 slice system, 80 mm configuration, collimations greater than 80 mm are not
selectable.
• Axial:
• 5 mm detector coverage — 1.25i, 1.25 mm, 2.5 mm, 5.0 mm
• 40 mm detector coverage — 0.625 mm, 0.625 z mm, 1.25 mm, 1.25 z mm, 2.5 mm, 2.5 z mm,
5.0 mm, 5.0 z mm
5.0 mm, 5.0 z mm
5.0 mm, 5.0 z mm
5.0 mm, 5.0 z mm
5.0 mm, 5.0 z mm
5.0 mm, 5.0 z mm
• Cine:
• 40 mm detector coverage — 0.625 mm, 1.25 mm, 2.5 mm, 5.0 mm
5.0 mm, 5.0 z mm
• Helical:
• 40 mm detector coverage — 0.625 mm, 1.25 mm, 2.5 mm, 3.75 mm, 5.0 mm
• 80 mm detector coverage — 0.625 mm, 1.25 mm, 2.5 mm, 3.75 mm, 5.0 mm
• Cardiac Axial:
• 40 mm detector coverage — 0.625 mm, 1.25 mm, 2.5 mm

Scan

11.6.4.4 1024 Reconstruction Matrix

1024 matrix is an additional matrix size available for image reconstruction in addition to the 512
reconstruction matrix. Image noise for this matrix size will increase compared to image noise for 512
matrix due to a decrease in pixel size depending on DFOV and Recon Type selected. 1024 displays
underneath the exam date on right upper corner of the image.
1024 matrix is compatible with the following:
• Detector Coverage 20mm, 40mm
• Scan type: Axial, Helical, Cine, Cardiac
• Normal Res Mode and Hi Res Mode
• Recon Type: Soft # (Small Head, Head, Ped Head only), Soft, Stnd # (Small Head, Head, Ped Head
only), Stnd, Detail, Lung, Bone, Bone Plus, Edge, Chest, Ultra, HD Stnd, HD Lung, HD Detail, HD
Bone, HD Bone Plus, HD Edge, HD Ultra
• SFOV: Small Head, Head, Small Body, Med Body, Large Body, Ped Head, Ped Body
• all system supporting DFOVs: 5cm – 50cm
• Thickness: 0.625, 1.25, 2.5, 3.75, 5
• Smart MAR
• IQ Enhance
• Image Enhance Filters
1024 matrix is not compatible with the following:

• Detector Coverage 5mm, 80mm or greater
• Scout, SmartPrep, SmartStep, VolumeShuttle, DMPR, SmartScore , Snap Shot Freeze/Freeze2,
DLIR, GSI, MaxFOV2, Fine Z, Enhanced Contrast
• Some functions of Advantage Windows, (LUNG VCAR, STROKE VCAR and THORACIC VCAR)
Considerations:
• 1024 reconstruction matrix size is available only in Secondary Recon, not in Primary Recon.
• The max image number per series for 1024 matrix is 2000.
• Use appropriate clinical parameters to provide the image improvement, such as improved local
detail resolution in Lung exams acquired with large DFOV; IAC on Axial plane; better resolution for
cardiac stent.
• Image size (megabytes) for 1024 matrix is 4 times larger compared to a 512 matrix.
• Recon times and transfer times are longer.
• Due to an increase in image noise for 1024 recons (especially at wider DFOVs), narrow windows
(e.g., Soft Tissue) might not provide acceptable IQ.

Scan
• Potential aliasing artifact as resolution is increased for Edge/Edge Plus reconstruction algorithms.
• High resolution artifacts such as aliasing (For example using Edge/Edge Plus reconstruction
algorithms) can be increased in 1024 matrix. If an area of concern is seen, perform a
reconstruction using 512 matrix.
11.6.5 Graphic Rx Recon from Axial Reference Image

Use this procedure to graphically prescribe the following secondary reconstructions parameters using
an axial image as a reference image:
• Set Start recon location (valid only for single group reconstructions)
• Set End recon location (valid only for single group reconstructions)
• Display field of view (DFOV)
• A/P center
• R/L center
• WW/WL
The graphic object for the scout or axial image will be displayed in the group color when System
Preferences > Viewports > Show Localizer Group Color is enabled.
Figure 213 Image Processing Monitor with single group

Scan
Figure 214 Axial Graphic Rx Viewport Controls
Figure 215 Axial Graphic Rx Viewport Right Click Menu Controls

Scan
Function Definition/Action
Display Normal Reset image to normal display settings
Report Cursor Toggles report cursor on and off
Grid Raises/lowers ISO center grid to assist with Patient Centering
Reset All Reset all images in the series to normal display settings
Screen Save Create 8-bit secondary capture or SSAVE
Figure 216 Axial Graphic Rx Viewport Toolbar
Icon Tool name Description
Maximize Viewport Expands selected Graphic Rx view-

port from 512 x 512 to 768 x 768
Propagate to All Groups Press the button to propagate the

RL/AP center, WW/WL, and DFOV
settings displayed in the active
group viewport to all groups when
the series is an All Recon.
Set Recon Start Location Set recon start location to match

current slice location active in the
viewport
Set Recon End Location Set recon end location to match

current slice location active in the
viewport
Set WW/WL Sets WW/WL settings for the recon-

struction to match current value
displayed in the viewport
Axial images from the primary recon must be complete and available on the system in order to display
in the axial Graphic Rx viewport.
If all the images from the primary recon are not available, the Axial Graphic Rx viewport will remain
blank.
1. From the Reconstruction and Image Processing task list, select the secondary reconstruction task
to prescribe. For multigroup image series, the first group will be active, and all 4 image viewports
will be displayed as in Figure 1. Note: The Axial Graphic Rx Viewport will not be displayed when
multiple group tabs are selected in the recon settings screen.

Scan
2. In the Axial Graphic Rx Viewport, click and drag on any of the blue squares on the circle to change
the size of the circle to set the DFOV for the reconstruction. The circle can be adjusted to any value
between the minimum DFOV and maximum DFOV.
3. Click and drag on the + at the center of the circle to define the RL and AP centers for your
reconstruction.
NOTE
To adjust DFOV and AP/RL centering simultaneously, Shift +Left Click and drag on
any of the blue boxes.
4. Adjust WW/ WL of the image in the viewport and click to set the WW/ WL for the
reconstruction.
5. Scroll through the images to find where you would like the reconstruction to begin. Click on
the Axial Graphic Rx tool bar to set this as the Start location.
6. Scroll through the images to find where you would like the reconstruction to end. Click to set
as the End Location.
7. To apply DFOV, R/L, AP and WW/WL settings to all groups, click the Propagate icon , then
adjust the size of the circle, the centering of the circle and adjust the WW/WL values. To set Start
and End Locations for all groups, use the Scout Graphic Rx Viewports or select multiple groups
and utilize multi-row edit.
8. Make any other adjustments to recon settings.
9. Click Run to generate images.
11.7 Auto Voice

Auto Voice provides recorded breathing instructions for the patient. Consistent breathing instructions
assist with more precise timing during an exam. Auto Voice also provides a pre-message in the Smart
Prep feature. The system also comes equipped with microphones at the console and gantry for
communicating with the patient.
The system has three, pre-recorded messages in 26 selectable languages that cannot be deleted. You
can also record up to 17 additional messages for each language.
The default language for Auto Voice is set in your protocol. Default language options include:
• Arabic (Female)
• Arabic (Male)
• Cantonese
• Chinese
• English (Female)
• English (Male)
• Farsi
• French

Scan
• German (Female)
• German (Male)
• Italian
• Japanese
• Korean
• Mongolian
• Polish
• Portuguese (European)
• Portuguese (Brazil)
• Punjabi
• Russian
• Spanish (European)
• Spanish (Latin America)
• Swedish
• Vietnamese
11.7.1 Auto Voice workflow

Use the Auto Voice feature to provide automated breathing instructions to the patient.
1. Set the Auto Voice language.
2. Add an Auto Voice language, if necessary.
3. Record an Auto Voice message.
4. Change the Auto Voice preset delay.
5. Delete an Auto Voice message, if necessary.
11.7.2 Set the Auto Voice language

Use this procedure to set the language for Auto Voice.
1. From the Scan Settings window, in the Patient Position area, click Auto Voice.
2. Select the desired Auto Voice language from the drop-down menu.
This selection will apply to all Auto Voice selections for the exam.
NOTE
After any scan is taken in the current series, the language cannot be changed.
The language can be changed if a new series is started.

Scan
11.7.3 Set the Voice/Lights/Timer options

Use this procedure to set the Voice/Light/Timer settings so the system will automatically give
breathing instructions to the patient based on the applied settings.
The Light and Timer features are visible on the gantry if selected for use.
1. From the Scan Settings window, click the Timing collection.
2. Click Voice, Lights, Timer.
3. Select the commands you want to use for breathing instructions.
• Three pre-recorded voices are available in 26 languages.
• You can record additional voice instructions. See Record an Auto Voice message.
• You can set an Auto Voice preset delay.
4. Set the playback option for the message set. This can be set for each scan group. There are three
selections available: Pre and Post, Pre Only, or Post Only.
NOTE
Lights/Timer is not valid with Cardiac, not valid with Pre Only, and Post Only.
NOTE
When an abort or pause occurs the post message instruction will always play. On
Resume, only the message instruction will play, if Post was selected, there will be
only the Pre message played. Manually breathe the patient in these cases.
5. Turn on Breathing Lights.
NOTE
Breathing Lights does not require that the voice is selected.
6. Turn on Timer, if desired.
7. Click OK.
11.7.4 Change the Auto Voice preset delay

The Preset Delay adds a delay between the completion of the Pre-scan message and X-ray on. This
delay can be set when creating a protocol. Use this procedure to set the preset delay.
1. From the Scan Settings window, click the Timing collection.
2. Click Voice, Lights, Timer.
3. In the Preset Delay Time field, enter a time.
The valid range is 0 to 7 seconds.
4. Click OK.

Scan
11.8 Additional Scan Features
11.8.1 Add, duplicate or delete a group or series

NOTE
Add, duplicate, delete group or series is not active if only some groups are confirmed.
Click on the group to return to active state to perform these operations.
11.8.1.1 Add a group

Use this procedure to insert another set of images following the prior group with all of the same
factors, except for the Start and End locations within the same series.
1. From the Scan Settings window, right-click on the last task in the series.
2. Click Add Group.
• Each time you click Add Group a new group is added.

• The start location of the new group is automatically set contiguous to the end of the prior group.
• The end location is determined by the number of slices, slice thickness, and scan interval (Axial
scan type) or image interval (Helical scan type).
11.8.1.2 Rename a group

Use this to label the group with a user-defined name in the scan task list. Note that this does not label
the group names in the recon task list.
1. From the Scan Settings window, right-click on the last task in the series.
2. Click Rename Group.
3. Enter the new name for the group.
11.8.1.3 Duplicate a group

Use this procedure to insert another set of images following the prior group with all of the same
factors within the same series.
To duplicate an entire group from a series, follow these steps:
1. Right-click on the group you want to duplicate.
2. Click Duplicate Group.
11.8.1.4 Multi-group edit

Use this procedure to edit scan and recon parameters across multiple groups in the same series.
The Scan Settings window has a set of parameters enabled when a series task is loaded.

Scan
When multiple groups are included in a series, the system enables group edit for the following subset
of parameters:
Table 100 Multi-group edit parameters
Scan Type Collection Name Parameters
Scout kV and mA Con- • kV

trol • mA
Timing • Voice
• Lights
• Timer
Primary Recon • WW
• WL
Axial, Helical, Cine, Anatomy Selec- • SFOV

Cardiac tion • DFOV
• A/P Center
• L/R Center
• Clinical Identifier
kV and mA Con- • kV
trol • mA
• NI
Timing • ISD
• Voice
• Lights
• Timer
Scan Type Rotation Time
Coverage Speed • Scan Interval

• Rotation Time

Scan
Multi-group edit parameters continued

Scan Type Collection Name Parameters
Primary Recon • Thickness

• Recon Type
• Enhanced Contrast
• ASiR-V%
• WW
• WL
Secondary Recon • Thickness

• Recon Type
• ASiR-V%
• WW
• WL
• DFOV
• A/P Center
• L/R Center
Multi-group is enabled when the parameter label and all groups are highlighted dark gray.
Series level parameters cannot be enabled for multi-group edit. kV mode or mA mode in kV mA
Control cannot be enabled for multi-group edit.
To edit a parameter across groups, follow these steps:
1. If not enabled, click on the parameter label you want to edit across groups.
2. Click on the parameter field and enter the desired value.
11.8.1.5 Delete a group

To remove an entire group from a series, follow these steps:
1. Right-click on the group you want to delete.
2. Click Delete Group.
11.8.1.6 Copy a series

Use this procedure to copy a series to paste (insert) at a defined location in the task list.
To copy a series, follow these steps:
1. Right-click on the series you want to copy.
2. Click Copy.

Scan
11.8.1.7 Paste a series

Use this procedure to paste (insert) a copied series at a defined location in the task list.
To paste a copied series, follow these steps:
1. Follow the steps in Copy a series on page 468.
2. Right-click on the series that you want to paste (insert) the copied series below.
3. Click Paste.
11.8.1.8 Duplicate a series

To duplicate a series, follow these steps:
1. Right-click on the series you want to duplicate.
2. Click Duplicate Series.
11.8.2 Optimize technical parameters

If the system cannot complete the entire scan prescription with the technical parameters selected, the
Optimize Message bar displays above the Projected Dose area.
Figure 217 Optimize Message bar with mA
Select the option that is most reasonable for the patient exam.
1. From the Optimize Message bar, select the parameter that is best for your prescription.
• Change one parameter (In the example, mA) to continue the scan.
• Up Front Delay is the time before you can proceed with scanning.
• This parameter can be changed by the amount shown in the Delay button selection.
• The Start Scan button is not active until the Up Front Delay time expires.
• The following message will be posted when no Up Front Delay is possible:
"Up Front Delay not possible, recommended delay is greater than 10 minutes."
• The mA parameter can be changed to what displays in the Change mA button selection.
• If you choose to reduce mA, you may be reducing image quality.
• Make sure that you always use enough mA to get the best image quality.
• Adjust the Prep Delay based on instructions for Voice/Lights/Timer.

Scan
• If multiple groups are prescribed, the Optimize Message bar updates for each group,
allowing you to make choices for each group.
• Once you have made choices that satisfy the system without compromising image quality, a
message displays that tube cooling is no longer needed.
2. Click Confirm Settings to start the scan.
11.8.3 Optimize GSI technical parameters

If the system cannot complete the entire scan prescription with the technical parameters selected, the
Optimize Message bar displays above the Projected Dose area. The calculate list from the GSI Image
Quality Widget displays a list of GSI Presets and mA values. Select the most reasonable option for the
patient exam.
Figure 218 GSI Image Quality Widget View List
1. From the GSI Image Quality widget, select List .
2. Select a GSI Preset family and mA from the list to continue the scan. Values that are indicated with
a yellow border and triangle may require an additional Up Front Delay, the time before you can
proceed with scanning. In some cases there may not be an Up Front Delay possible. The Start
Scan button is not active until the Up Front Delay time expires.
• Make sure you always use enough mA to get the best image quality.

Scan
Figure 219 GSI Image Quality Widget Calculate List
1. From the GSI Image Quality widget, select Calculate .
2. Select a GSI Preset family and mA from the list to continue the scan. Values that are indicated in
yellow may require an additional Up Front Delay, the time before you can proceed with scanning.
In some cases there may not be an Up Front Delay possible. The Start Scan button is not active
until the Up Front Delay time expires.
• Make sure you always use enough mA to get the best image quality.
11.8.4 Optimize patient dose

For years GE has followed the As Low as Reasonably Achievable (ALARA) principle in helping our
customers optimize dose. GE has provided many tools to help the clinician minimize dose while
achieving clinically diagnostic image quality.
GE CT is a proven leader in delivering dose efficiency in every scanner category. GE has achieved this
position through a "total system" approach. The following features are some that contribute to our
"total system" approach and affect patient dose. Not all features are available on each system.

Scan
11.8.4.1 Pediatric Protocols

Pediatric protocols are based upon a child's size, age, and weight and tailor the dose or treatment to
the size of the patient.
The Head and Orbit categories are age-based. The rest of the categories, except Miscellaneous, are
height and weight-based.
11.8.4.2 SmartmA
SmartmA modulates X-ray tube mA to account for specific patient anatomy based on data gathered
from the scout image. You input the desired image quality (Noise Index) and the system adjusts the mA
to achieve this within the bounds of the inputted minimum and maximum mA.
11.8.4.3 Organ Dose Modulation (ODM)

By modulating the X-ray tube current as a function of X-ray tube angle, Organ Dose Modulation (ODM)
enables targeted reduction of the X-ray tube current towards the anterior surface of the patient,
providing enhanced dose reduction to radio-sensitive organs of the patient while maintaining overall
image quality.
11.8.4.4 AEC with Cardiac Modes

SmartmA modulates X-ray tube mA to account for specific patient anatomy based on clinical task and
data gathered from the scout image. You input the desired image quality (Noise Index) and the system
adjusts the mA to achieve this within the ECG-based mA profile.
11.8.4.5 SmartHelical
SmartHelical is integrated into all GE CT systems. It decreases image noise as measured by pixel
standard deviation.
11.8.4.6 Advanced Artifact Reduction (AAR)

A filter that significantly reduces streaking artifacts when highly absorbent objects are in the field of
view (example: large shoulders). AAR is automatically enabled as needed.
11.8.4.7 Adaptive Statistical Iterative Recon (ASiR-V)

The next generation ASiR-V is a reconstruction technology that may allow for reduced mA in the
acquisition of diagnostic images thus, enabling the physician to reduce the patient dose depending on
the clinical task, patient size, anatomical location, and clinical practice.
11.8.4.8 kV Assist/Auto Prescription

kV Assist optimizes kV and NI/mA to optimize CNR at or below the baseline dose for the patient size
and clinical task.
patient size and works with SmartmA to optimize dose and image quality.

Scan
Auto Prescription is a profile-driven feature that selects scan parameters defined for a patient by
patient size and works with SmartmA to optimize dose and image quality. It uses the scout to evaluate
patient attenuation to calculate patient size and a kV/mA table for selecting kV, mA, SFOV, and ASiR-V
level for the protocol.
11.8.4.9 Auto Gating

Auto Gating is a feature designed to optimize ECG-gated acquisition settings based on an assessment
of patient heart rate and variability, primarily focused on exams of the coronary arteries. Auto Gating
workflow provides the capability to record heart rate statistics during a breath hold to determine the
acquisition settings best suited for the heart rate characterization of the patient.
11.8.4.10 Dose Reports

CTDIvol, DLP and Dose Efficiency are displayed during the scan prescription and provide patient dose
information. The CTDIvol, DLP, and phantom size used to calculate dose are automatically saved once
you end the exam. The Dose Report is saved as a DICOM secondary capture image in Series 999. This
series can be filmed, archived, and networked after the scan is completed.
DICOM Structured Dose Report generates a CT Dose Report, which can enable tracking of dose for the
patient by the hospital radiation tracking system or HIS/RIS. The Dose Report is saved as a DICOM SR
Object in Series 997.
11.8.5 View the Dose Report

CTDIvol, DLP, and Dose Efficiency are displayed during the scan prescription to provide patient dose
information.
11.8.5.1 Prerequisites
Before DICOM Structured Dose Report is turned on, confirm that your PACS or other receiving station
supports structured reports.
Contact your service representative to enable DICOM SR Dose Report.
11.8.5.2 Dose Report Generation

After closing the exam:
• The CTDIvol, DLP, and Phantom size used to calculated dose are automatically saved.
• DICOM Structured Dose Report generates a CT Dose Report which can enable tracking of the
patient’s dose information with the hospital radiation tracking system or HIS/RIS.
• If configured, the DICOM SR Dose Report is saved as part of the patient's exam in Series 997.
The DICOM SR Dose Report cannot be opened on the scanner. It can be reviewed and printed
using the Reporting Tool on the Advantage Windows workstation or any station that can read a
DICOM Structured Report. It cannot be saved to DVD or CD on the Advantage Workstation (AW)
system (4.4 or lower).
• The Dose Report is saved as a secondary capture image in Series 999. It can be archived and
networked after the scan is completed.

Scan
NOTE
If you edit patient information for an exam, the Dose SR report will be excluded from
the edited patient information due to the format of the files. Dose Report Series 999
will be updated using the edited information.
11.8.6 Dose Information

Figure 220 Dose Information
Number Description
1 Dose Display area
2 Dose Report

Scan Applications
12 Scan Applications
12.1 Overview
NOTICE

ON THIS SYSTEM.
The following applications can be applied in Scan. If an application is not available, it may not be
included with your system options.
12.2 ASiR-V
12.2.1 ASiRTM-V Theory
ASiR-V is a reconstruction technique that enables reduction in image noise (standard deviation), streak
artifact at low signal condition and improvement in LCD (Low Contrast Detectability), while preserving
the structure details in the image.
ASiR-V can be used to reduce the image noise (standard deviation) and streak artifact in diagnostic
images and thereby reduce the dose required for routine imaging.
The scanner allows you to select levels of ASiR-V.
These “levels” provide a varying degree of noise removal from the images. As shown in 10% and 50%
MTF performance MTF remains constant as the ASiR-V level is increased.

Scan Applications
Figure 221 10% and 50% MTF performance
Figure 222 Filtered Back Projection compared to 100% ASiR-V
If manual mA is selected, the software does not make mA adjustment automatically when ASiR-V is
enabled. These changes need to be calculated using the following tables to make changes to manual
mA values. Refer to mA adjustment factor and Return to a value for a non-ASiR protocol for guidance in
making parameter step adjustments during ASiR-V evaluation process.

Scan Applications
Before using ASiR-V, the site physicist, in collaboration with the radiologist, should conduct image
quality evaluations with varying degrees of ASiR-V and different scan techniques, both at routine dose
and decreased dose. This should be done using your site’s preferred method and phantoms. Using this
information, an appropriate starting point for ASiR-V level and diagnostic scanning techniques can be
incorporated into your site’s protocols.
A general guideline for parameter step adjustment is:
Dose Reduction increments of about 20% ASiR-V level increments of 10%.
Whether ASiR-V is used for dose reduction or image quality improvement, parameter settings
should be made in steps and then reviewed for diagnostic image quality until the desired clinically
appropriate image quality is achieved.
12.2.2 Dose adjustment Factor - Manual mA method

When using standard reconstruction algorithm, use the following chart to calculate dose reduction for
mA based on the ASiR-V level selected.
The mA Adjustment Factors in mA adjustment factor are intended to help you enter the mA settings
in manual mA protocols. These factors were derived based on calculating the relative difference in
measured noise standard deviation (SD) with Filtered Back Projection (FBP) and ASiR-V on a 20 cm
water phantom taken by 0.625 mm thickness and 25 cm DFOV with Large Body SFOV.
Table 101 mA adjustment factor
ASiR-V Normal
10% 0.87
20% 0.74
30% 0.63
40% 0.52
50% 0.44
60% 0.35
70% 0.29
80% 0.23
90% 0.18
100% 0.14
For example, if 40% ASiR-V is selected, multiply the mA displayed in the mA control screen by 0.52, as
indicated in mA adjustment factor to obtain the new mA for protocol using ASiR-V, that needs to be
entered into the mA field on the mA control screen.
Multiply the Noise Index or manual mA values that were adjusted for an ASiR-V applied protocol by the
adjustment factors in Return to a value for a non-ASiR protocol.
Use the following factors to return any manual mA values adjusted for ASiR-V to non- ASiR-V value.

Scan Applications
Table 102 Return to a value for a non-ASiR protocol
ASiR Level Return to non-ASiR manual mA value
10% 1.15
20% 1.35
30% 1.59
40% 1.92
50% 2.27
60% 2.86
70% 3.45
80% 4.35
90% 5.56
100% 7.14
12.2.3 Reconstruction
Reconstruction of ASiR-V images involves defining the level of noise reduction desired for the
parameters used for various applications. Image reconstruction is a blending of the original images
and a percentage of an ASiR-V image. There are 10 blending levels available that are the amount of
noise reduction based on the maximum of the 100% image reconstructed with the original image data.
Reconstruction of ASiR-V images can be prescribed retrospectively in Retro Recon. A New Series should
be selected for each reconstruction of the data with ASiR-V applied so comparisons and identification
of series with ASiR-V can be made more easily.
ASiR-V is located on the Primary and secondary recon settings collection. ASiR-V Setup Selection is 0%
to 100%.
12.2.4 ASiR-V Image annotation

ASiR-V level and mode are annotated on the image using a character string that defines the mode and
level. It is displayed in the upper‐left corner of the image next to the Recon Type.
The annotation logic is as follows:
• AR - ASiR-V reconstruction
• 10 - 100, which is the percentage of the 100 % ASiR-V image that was blended with the original to
reduce the noise in the ASiR-V images.
For example, AR60 denotes ASiR-V reconstruction mode with 60% of the 100% ASiR-V was blended
with the original image.

Scan Applications
NOTE
ASiR-V annotation information is not displayed in Advantage Workstation (AW)
applications on the operator console.
12.2.5 Acquire a scan

Use this procedure to acquire data where ASiR-V noise reduction reconstruction will be used. ASiR-V is
a reconstruction technique designed to reduce pixel-noise standard deviation in clinical images while
preserving the structure details in the image. The ASiR-V noise reduction technique may let you reduce
the X-ray dose, while maintaining acceptable image noise levels, or it can be used to improve images
with an unacceptable level of noise. ASiR-V is prescribed in 10 percent increments for 10 percent to 100
percent. ASiR-V mode is annotated AR xx.
Keep the following in mind when selecting an ASiR-V recon mode: ASiR-V is not compatible with any of
the real time interactive image modes such as Smart Prep.
Scan with ASiR-V
1. Prescribe the scan.
2. To enable ASiR-V and select an ASiR-V level in percentage open the Primary Recon settings
collection by clicking the Primary Recon title or icon. Click ASiR-V.
3. Select the desired ASiR-V percentage level or use SmartmA.
If you want to use ASiR-V to maintain image quality but reduce dose, from the kV and mA Control
settings collection, reduce mA.
4. Start the scan.
12.3 SmartPrep
SmartPrep™ allows intermittent monitoring of IV contrast enhancement in one particular section of
anatomy that is in the area of interest. The contrast flow is monitored by low-dose scans until the
contrast enhancement reaches the preferred point and you initiate the diagnostic scan or the Dynamic
Transition level has been reached.
You can add SmartPrep to a group of any scan type.
A SmartPrep prescription is a series with a SmartPrep task enabled. Only one SmartPrep task may be
added to a series. If a scout series is included in the study prior to the SmartPrep series, the scout
may be used to determine the monitor location. The series will contain the SmartPrep task and the
prescription for the contrast enhanced scans to be taken when the contrast enhancement level is
reached. These scans are referred to as the diagnostic scans.
If SmartPrep is enabled for a series, the system cancels the AutoView display for any images in the
recon queue when the SmartPrep series is started. These images are selected from the browser for
review once they have been reconstructed. Only images from the series with SmartPrep and those
after the SmartPrep series are displayed in AutoView viewport.
There are three phases to a SmartPrep scan.

Scan Applications
• Baseline phase — A single unenhanced image is acquired in the anatomy where the monitoring
occurs and the Region of Interest (ROI) is established.
• Monitor phase — Uses the ROI defined in the baseline phase to display a graph that helps
you determine the peak enhancement value. Up to 40 low-dose scans can be taken during the
injection of IV contrast.
• Scan phase — Acquires the data based on the scan setup parameters. You start the scan when the
contrast is at the peak on the curve or by when a preset Hounsfield value is reached.
You do not need to set SmartPrep parameters each time you use SmartPrep. The parameters can
be included in any protocol using SmartPrep. SmartPrep parameters allow for checking the contrast
enhancement both visually and graphically.
You can use Protocol Management to set up SmartPrep, including the ability to set the Dynamic
Transition enable/disable field.
12.3.1 SmartPrep Workflow

SmartPrep exams do not follow the same flow as other exams. The process begins when you add a
SmartPrep task to a series and ends when you delete the SmartPrep task, select Revisit Settings, select
Done Scanning, or the first diagnostic scan is completed.
The following is a typical workflow for a SmartScan study.
1. Start a study with a SmartPrep task
2. Confirm and take the scout scan.
3. Setup the diagnostic scan.
4. Execute the SmartPrep task.
a. Set up the SmartPrep scan.
b. Take the baseline scan. (baseline phase)
c. Set the monitor phase ROI(s).
d. Set the transition region of interest (ROI) — optional.
e. Perform the monitoring phase.
f. Transition to the diagnostic scan phase.
5. Perform diagnostic scanning. (scan phase)
6. Display the resulting report.
12.3.2 SmartPrep Windows/Elements

This section describes the SmartPrep windows and the buttons, viewports and tools they contain.
12.3.2.1 SmartPrep Baseline Setup window

Click on the SmartPrep task to open the SmartPrep baseline setup window. The window also displays
when you confirm the associated diagnostic scan.

Scan Applications
Figure 223 SmartPrep baseline setup
Element Description
Scan Timeline The Scan Timeline for SmartPrep is shown above the viewport and in-
cludes a minimum of three sections and some number of delays:
• Delay - Represented as a circle with the time of the delay shown
underneath.
• SP Baseline - First rectangular section under the SP label and repre-
sents the baseline scan.
• SP Monitor - Second rectangular section and represents the monitor
scan. The timeline represents a single monitor scan. As scans are
taken, the timeline will fill and then clear for the next monitor scan.
You can edit the Baseline and Monitor collection values by clicking
Revisit Settings.
• Diagnostic Scan - Third rectangular section and represents the diag-
nostic scan for the SmartPrep series. When this is a multi-group
series, a rectangular section is shown for each group.
Scout Image The last scout image taken at the current landmark is shown with a cut line
that will allow the monitor location to be specified. Moving the cut line will
correspondingly change the Monitor Location in the Baseline & Monitor
Collection.

Scan Applications
Settings Collections The collections for the SmartPrep parameters are located just below the
Scan Timeline.
SmartPrep has two collections:
• Contrast Collection - Allows contrast data to be specified for the
study. In this area you can: enable or disable the integrated injector,
set manual IV contrast (if Integrated Injector is disabled), and set oral
contrast values.
The contrast collection should have the same settings that were con-
firmed in the Baseline settings screen except that the injector will be
disabled if it was enabled and the retake monitor option was selected
after the injector started. You can choose to re-enable the injector.
The contrast agent and its concentration are associated with the
series. All groups in a series that has contrast will have the same val-
ues for agent and concentration if contrast is enabled for the series.
Contrast can be enabled for any series except a Scout.
The volume of the contrast injected is associated with a series. Once
contrast is injected in a series in an exam, all subsequent series are
considered contrast series.
Refer to Enter contrast descriptions for more information .
• Baseline and Monitor Collection - Allows setup of the parameters
controlling the Baseline and Monitor scans. See Set up a SmartPrep
series for more information.
The prescription for the baseline scan and for the monitor scans must
be the same, unless the monitor scan is below 0.35s, then the rota-
tion speed of the baseline scan will be 0.35s and mA is automatically
adjusted to maintain mAs of the monitoring scan.
Revisit Settings The Revisit Settings button, available from any of the SmartPrep steps, is
active when the scan is paused or aborted or when 40 scans have been
taken in the monitor phase.
You can edit the Baseline and Monitor collection values by clicking Revisit
Settings.
When you select Revisit Settings:
• The diagnostic scan task is unconfirmed.
• If no baseline scan had been taken, the SmartPrep task is un-confirmed.
• If a baseline scan had been taken, the SmartPrep task is marked as
skipped.
NOTE
Once the SmartPrep task is skipped you can no longer change
SmartPrep parameters. To enable SmartPrep again for the ser-
ies, duplicate the current scan series task, delete the unscan-
ned original diagnostic scan and confirm the duplicated scan.
• The diagnostic task is selected and the settings displayed.

Scan Applications
Skip to Diagnostic Skip the monitor phase and go directly into the diagnostic scan. If you click
Skip to Diagnostic to transition to the diagnostic scan, the SmartPrep task
is set to skipped.
Acquire Baseline Continue to the step of taking the Baseline Scan.
Figure 224 SmartPrep baseline setup collections

Scan Applications
Figure 225 SmartPrep scan timeline
Table 103 Scan timeline segments
1 SP baseline
2 Delay
3 SP monitor
4 Diagnostic scan
12.3.2.2 Monitor Phase Setup window

This window displays after the baseline scan is completed.
Figure 226 Monitor Phase setup with 1 region of interest (ROI) deposited and Dynamic Transition
selected

Scan Applications
Element Description
Baseline Image The baseline image displays allowing ROIs to be placed on the image.
ROI Placement Use these tools to put ROIs on the baseline image. You may place from 0
to 3 ROIs on the image. You can drag ROIs in the Anterior/Posterior and
Right/Left directions. You can also resize them.
Hide (Show) ROIs — Hide or show graphics (ROIs)
Box ROI, Elipse ROI — Deposit up to three ROIs total with any combina-
tion of box and ellipse.
Explicit Magnify — 0.5, 1.0, 1.5, 2.0, or enter a different value.
Erase — Erase or delete selected ROI.
Dynamic Transition ROI Select the ROI to be used as the dynamic transition ROI. This can be Off
or any one.
The system sets the first ROI you add as the transition ROI if Dynamic
Transition is enabled.
The system sets the first ROI as the transition ROI when you enable
Dynamic Transition, either using the Enable Dynamic Transition button
or when changing this value in the Baseline or Monitor Collection, and
there is at least one ROI present.
If the transition ROI is deleted and there is at least one remaining ROI, the
new ROI #1 will be set as the transition ROI. If the last ROI is deleted, the
transition selection is set to “None”.
Retake Baseline Selecting the Retake Baseline will return to the SmartPrep Setup win-
dow.
Begin Monitoring Select to begin the monitor scanning phase of the exam
12.3.2.3 Monitor Phase window

This window displays during the Monitor Phase.

Scan Applications
Figure 227 Monitor Phase scan
Element Description
Baseline Image The baseline image with the ROIs that have been set will display on the
lower right side of the window.
Monitor Image The latest image from the monitor phase that corresponds to the image
used to calculate the HU level on the Enhancement Chart and Enhance-
ment Graph is shown in the upper right viewport. The ROIs that were set
are shown on this image.

Scan Applications
Enhancement Graph The timeline on the Enhancement Graph is shown in seconds. Scroll to
show the latest points when the time expands beyond the number of
seconds that can fit in the viewer. The zero point is the time that the
Start Scan button was pressed. All points are relative to this time even if
there is a pause in scanning. The time for each data point is the midpoint
of the scan time for the scan from which the HU level is calculated. The
HU level is calculated for each ROI and is shown relative to the HU level
of the corresponding ROI that was on the baseline image. If an ROI is
selected as the transition ROI, that is shown in yellow.
The x-axis displays time. The y-axis displays relative HU level -relative
to the HU level in the ROI on the baseline scan. A separate line for each
ROI is shown on the graph with a point for each monitor scan. A white
horizontal line indicating the enhancement threshold that was set in the
SmartPrep setup is also shown. This provides a visual indication of when
the level on an ROI reaches or exceeds this level.
Enhancement Chart The data in the Enhancement chart is the same as the data shown on
the graph. The Elapsed time is the time since the Start Scan button
was pushed. If the scan is paused, no empty rows are added to this
table. When more rows are needed than what fits on the view, the data
is scrolled down so that the latest is visible. The latest data is always
shown on the bottom.
Dynamic Transition On the top row of the Enhancement Graph is a check box that allows
Dynamic Transition to be disabled. This displays only if an ROI has been
designated as the transition ROI.
Real Time Information At the bottom of the window is the Real Time Information, showing
Patient Handling, Scanning and Injector Status information. The Injector
Status information is available only when Integrated Injector is enabled.
Pause Will pause the current monitor scanning. When paused, the options to
Skip to Diagnostics, Resume, or Revisit Settings will be available.
Begin Scan Now Whether or not Dynamic Transition is enabled, the Begin Scan Now
button is available. Use this button to start the Diagnostic Scan.
Retake Monitor Selecting the Retake Monitor will return to the SmartPrep Setup window.

Scan Applications
Figure 228 Monitor Phase scan paused

Scan Applications
Figure 229 Monitor Phase — Maximum of 40 monitor scans reached
12.3.3 Set up a SmartPrep series

Use this procedure to set up a SmartPrep series.
1. Add a SmartPrep sub-step for a selected series by selecting the diagnostic group to which the
SmartPrep task is to be added and using the right mouse menu to add a SmartPrep task to the
end of the task list for the series.

Scan Applications
Figure 230 SmartPrep option on the right mouse menu
2. If the diagnostic scan tasks are not confirmed, confirm the settings for these groups. After the last
is confirmed, the SmartPrep Setup window opens.
NOTE
Once Confirm for the diagnostic scan is selected, recon is moved to SmartPrep
mode and the system places any active reconstruction jobs in the pending state. Do
not select Confirm until all images that are needed have completed reconstruction.
The Acquire Baseline will be insensitive until recon is ready for SmartPrep scanning.
3. From the scout localizer on the display monitor, click and drag the slice line to define the Monitor
location. Alternatively, type in the S/I location in the Monitor Location text field in the Baseline
and Monitor Collection, for example, S110.
4. Expand the Baseline and Monitor Collection and enter the following values:

Scan Applications
Figure 231 SmartPrep baseline setup collections
•
• Baseline mA is the mA used during the Baseline Phase. Baseline scan rotation speed and
mA are automatically adjusted if the monitoring scan is faster than 0.35s. The baseline mA is
adjusted to maintain mAs at 0.35s.
• kV is a non-editable field and is the same as the value set for the first diagnostic scan. If this
needs to be changed, go back to the Diagnostic scan task and change the settings there.
• Monitoring Delay (0 to 60 seconds in 1-second increments) sets the time before monitoring
scans begin. The time varies based on the anatomy being monitored.
• Monitoring Inter Scan Delay (1 to 60 seconds in 1-second increments) sets the time
between monitoring scans.

Scan Applications
• Enhancement Threshold (0 to 1,000 in steps of 1) sets the bar on the graph to

monitor threshold enhancement. When Dynamic Transition is On, the Scan Phase starts
automatically when the HU value of the Transition ROI reaches the Enhancement Threshold.
This is the magnitude of the change in HU level with respect to the HU level in the baseline
scan.
• Auto Minimum sets the Diagnostic Delay to the minimum value possible, taking into
consideration location of the monitor phase, start phase location, and Auto Voice pre-
message length. When Auto Minimum is set, the Diagnostic Delay value is read only. Use
this to see the minimum delay value for your specific scan.
• Diagnostic Delay, (up to 60 seconds in one-second increments) typically set to the minimum
value (automatic) for arterial studies and 10 seconds or longer for venous studies. The
minimum value is constrained to the time needed to move the table and play the Auto
Voice message. The minimum for scans without Auto Voice and no table move is about 1.1
seconds.
• Allow enough time to deliver breathing instructions if you are not using Auto Voice.
• The minimum time may vary if Auto Voice is on and depending on the monitor location
relative to the start location.
• Auto Voice is available if Auto Voice is prescribed in the diagnostic scan. If Auto Voice is
enabled for the series, the pre-message will be played as part of the diagnostic delay. The
diagnostic delay will be increased to accommodate the length of the Auto Voice message.
Auto voice is not editable from the Baseline setup screen. Make any changes to it in the
diagnostic settings.
5. Set the contrast settings. If the integrated injector option is enabled, see the Enhanced Xtream
Injector section in this chapter. If the integrated injector option is not enabled, see the Enter
Contrast Description section in the Scan chapter.
6. From the SmartPrep Setup window, click Acquire Baseline.
NOTE
Acquire Baseline will be insensitive until recon is ready for SmartPrep scanning.
7. Review and respond to the potential alert message that indicates that the projected dose
efficiency had fallen below 70%.
8. Proceed to Acquire a scan without Dynamic Transition or Acquire a scan with Dynamic Transition.
12.3.4 Acquire a scan without Dynamic Transition

To acquire contrast-enhanced images with a bolus tracking technique without Dynamic Transition,
follow these steps:
12.3.4.1 Baseline Phase without Dynamic Transition

The baseline scan is taken as a standard axial scan with one rotation and one image and allows you to
establish an area to monitor contrast enhancement.

Scan Applications
1. After the SmartPrep settings are confirmed, the Baseline scan is taken. When the Baseline scan is
complete, the Monitor Phase Setup window displays.
2. Review the values on the Scan Timeline for the monitor and scan phases.
3. If the baseline scan is not correct (for example if the patient moved or the scan location is not
right), click Retake Baseline and return to Set up a SmartPrep series.
NOTE
Changes to the Contrast collection, Monitor Delay, Monitor Inter Scan Delay,
Enhancement Threshold, Auto Minimum or Diagnostic Delay can be made without
having to click Revisit Settings on the Monitor Phase Setup window.
4. Press Move to Scan to advance the table to the monitoring location.
6. Once the scan is complete, from the reconstructed image on the display monitor, click Ellipse ROI
or Box ROI to place a maximum of three ROIs over areas of interest. Monitor ROIs are colored
blue.
For example, if scanning a liver, place an ROI in liver parenchyma away from vessels, if evaluating
a vessel place the ROI over the vessel.
Figure 232 SmartPrep ROI placement tools
Use, as needed, the zoom, roam, display normal, hide/show graphics, erase, or explicit mag
(factor range: 0.5 to 2.0) from the SmartPrep display control panel.
7. Click Begin Monitoring to continue to the Monitor Phase.
NOTE
The following parameters can be changed after the baseline scan has been taken
and before the Monitor Phase is started:
• All parameters in the Contrast collection
• Monitor Delay, Monitor Inter Scan Delay, Enhancement Threshold, Auto
Minimum On/Off or Diagnostic Delay.
12.3.4.2 Monitor Phase without Dynamic Transition

The Monitor phase acquires images at the monitoring location during the delivery of intravenous
iodinated contrast material and graphically displays the images, charts the enhancement thresholds,
and clock with the time since monitoring began. Use the contrast graph, contrast table, and/or
monitor images to determine when the diagnostic scan can begin.

Scan Applications
1. After the Monitor scan settings are confirmed, the Start Scan button begins to flash.
2. Simultaneously press Start Scan and start the IV contrast injection. A maximum of 40 monitoring
scans is available. Move To Scan is typically not required since the last scan was at the baseline
location.
NOTE
If using an integrated injector, the step to start the IV contrast injection is not
needed as the command will be sent by the scanner to the injector to start the
injection.
3. The system waits the time set in the Monitoring Delay area, then begins acquiring images at the
time set for the interscan delay (ISD). The total SmartPrep monitor scan time shows next to the
elapsed timer. The ISD countdown displays on the Real Time Information area at the bottom of
the Monitor Phase window.
4. Using the tools on the Monitor Phase window (refer to Monitor Phase window) to determine when
the contrast has reached a sufficient level to take the diagnostic scan. When this occurs, use the
Begin Scan Now button to transition to the Scan Phase (refer to Scan Phase - Diagnostic Scan .
12.3.5 Acquire a scan with Dynamic Transition

Use these steps to acquire contrast-enhanced images with a bolus tracking technique with Dynamic
Transition.
12.3.5.1 Baseline Phase with Dynamic Transition

The Baseline phase acquires one non-contrast scan and allows you to establish an area to monitor
contrast enhancement.
1. After the SmartPrep settings are confirmed, the Baseline scan is taken. After the Baseline scan is
complete, the Monitor Phase Setup window displays.
2. Review the values on the Scan timeline for the monitor and scan phases.
3. Press Move to Scan to advance the table to the monitoring location.
5. In the case that the baseline scan is not correct (for example if the patient moved or the scan
location is not right), click Retake Baseline and return to Setup a SmartPrep series.
6. Once the scan is complete, from the reconstructed image on the display monitor, click Ellipse ROI
or Box ROI to place a maximum of three ROIs over areas of interest. Monitor ROIs are colored
blue.
For example, if scanning a liver, place an ROI in liver parenchyma away from vessels, if evaluating
a vessel place the ROI over the vessel.

Scan Applications
Figure 233 SmartPrep ROI placement tools
Use, as needed, the zoom, roam, display normal, hide/show graphics, erase, or explicit mag
(factor range: 0.5 to 2.0) from the SmartPrep display control panel.
7. Select one of the ROIs to be used for the dynamic transition. The dynamic transition ROI is
colored orange-yellow.
8. Click Begin Monitoring to continue to the Monitor Phase.
12.3.5.2 Monitor Phase with Dynamic Transition

The Monitor phase acquires images at the monitoring location during the delivery of intravenous
iodinated contrast material and graphically displays the images, charts the enhancement thresholds,
and clock with the time since monitoring began. The contrast graph, contrast table, and/or monitor
images can be used by the technologist to determine that the diagnostic scan can begin.
1. After the Monitor scan settings are confirmed, the Start Scan button will begin to flash.
2. Simultaneously press Start Scan and start the IV contrast injection. A maximum of 40 monitoring
scans are available. Move To Scan is typically not required since the last scan was at the baseline
location.
NOTE
If using an integrated injector, the step to start the IV contrast injection is not
needed as the command will be sent by the scanner to the injector to start the
injection.
3. The system waits the time set in the Monitoring Delay area and then begins acquiring images at
the time set for the ISD. The total SmartPrep monitor scan time and Interscan Delay time between
monitor images is displayed on the Real Time Information screen on the Monitor Phase screen.
4. Use the tools on the Monitor Phase window (refer to Monitor Phase window) to determine when
to switch to the diagnostic scan phase. In all the viewports with ROI information, the Dynamic
Transition ROI will be visually distinct from the other ROIs.
5. The system will auto-transition when the HU Enhancement level has been reached on the ROI
selected as the transition ROI.
6. Using the tools on the Monitor Phase window, monitor the progress of the contrast.
a. If it looks like the dynamic transition will happen too early, uncheck the Dynamic Transition
checkbox to disable this function. Once this is done, you must click Begin Scan Now to
transition to the diagnostic scan.

Scan Applications
b. If it looks like the dynamic transition will happen too late, click Begin Scan Now to transition
to the diagnostic scan. If you click Skip to Diagnostic to transition to the diagnostic scan, the
SmartPrep task is marked as skipped. Clicking Begin Scan Now sets the SmartPrep task to
completed.
12.3.6 Retake Monitor

The Retake Monitor option is available when paused or aborted during the monitor scanning or when
all 40 scans are completed. This option returns you to the monitor setup screen with the ROIs still in
place and selected for Dynamic Transition. All parameters are in the same state as when the last Begin
Monitor was chosen except that the monitor delay will be set to 0 and the injector option will be set to
Off, if it was on and the injector started. You can re-enable the injector if a re-injection is needed.
12.3.7 Scan Phase — Diagnostic Scan

The Scan Phase is the start of the actual scan prescription following the Monitor Phase.
1. After you clicked Begin Scan Now or Dynamic Transition has occurred, deliver the first breath hold
instructions if Auto Voice Pre-Message is not turned on.
2. The system will:
a. Move to the scan prescription start location (no need to press Move to Scan).
b. Play the Auto Voice message at the appropriate time if Auto Voice Pre-Message is turned on.
c. Start the scan (no need to press Start Scan).
d. Save an image of the last monitoring phase screen including the images, graphs, and table
and save in series 99 for the study.
e. Save the baseline image and monitoring images in series 201. If an extra monitoring phase
was added, this will be in series 202.
3. When the scan is complete close the study by clicking Done Scanning. The Reports step displays.
See the Reports section for more information.
12.4 Smart Prep with Auto ROI (Option)

Related to Product Differences
Auto ROI is a protocol driven feature that uses the patient’s scout scan to set the Baseline scan
location and the Baseline axial image to set the Monitor Scan ROI based on recognition of anatomical
landmarks from validscout and axial images. Enabling Auto ROIin SmartPrep settings and prescribing
a supported Diagnostic Region allows the system to determine and display the initial Baseline scan
location to the technologist. After the Baseline scan is acquired, the ROI is placed on the Baseline axial
image. The technologist must review and accept the parameters or make necessary adjustments prior
to confirming the Baseline location and the MonitorROIon the Baseline axial image.
Auto ROI is only valid when all the following criteria are met:
• Adult protocol with SmartPrep Enabled
• The plane of the scout image should include 0° or 180° plane

Scan Applications
• SmartPrep Scan Group must include a valid Diagnostic Regionthat supports Auto ROI
Diagnostic Region:
• Thoracic - Pulmonary
• Thoracic - Aorta
• Cardiac
• Abdomen
• Pelvis
12.4.1 Auto ROI Workflow Overview

1. In Protocol Management, Set Auto ROI to On or Off and Diagnostic Region with SmartPrep
enabled group. .
2. In Auto ROI Management, set Auto ROI Preference and Offset if needed.
3. Select Auto ROI enabled Protocol, Scan scouts, and then click Continue.
4. Click SmartPrep, one purple baseline is positioned automatically on the scout, with indicator
message below the scout image.
5. Confirm setting and click Acquire Baseline.
6. One purple ROI is set on the Aorta or Pulmonary automatically, with an indicator message below
the monitor slice image.
7. Begin Monitoring, and then finish the scan.
NOTE
1. When the user modifies the baseline or monitor ROI position manually, the color of the
modified baseline or ROI changes from purple to blue.
2. If Dynamic Transition is turned on with a single ROI, the ROI sets as yellow even with
Auto ROI ON.
The accuracy of Baseline and ROI location predicted by Auto ROI might be affected by internal
and external interference. Make sure the predications by Auto ROI are reviewed or make necessary
adjustments prior to confirming the baseline location on scout images and Monitor ROI on the
baseline axial image.
When Auto ROI is enabled, an indicator message will be shown below the scout image with
baseline location and Baseline Axial image for the Monitor ROI set up. Baseline location is set by
Auto ROI. Verify Baseline location and adjust manually if needed. ROI position is set by Auto ROI. Verify
ROI position and adjust manually if needed.

Scan Applications
Figure 234 Baseline position
Figure 235 Monitor ROI position
Following goes in section in Protocol Management.
12.4.1.1 AutoROI (Option) Settings in Protocol Management

1. SelectAdultbody scan protocol with SmartPrep and select Edit.
2. In SmartPrep task, set Auto ROI to On or Off.
3. In Diagnostic Region, select the desired anatomical region from the pull down.

Scan Applications
12.4.1.2 Auto ROI Management

In Auto ROI Management, set Auto ROI Preference and Offset per clinical usage.

Scan Applications
Figure 236 Auto ROI Management
1. From the Mode Menu, select Protocol Management, then select Auto ROI Management
2. For each Diagnostic Region enter the desired Offset for the Baseline location in mm.
The offset range is S80 to I80. No decimal is allowed.
The default offset value is S0.
3. For Abdomen set the Baseline Preference and for Cardiac set the Monitor ROI Preference.
The default baseline selection of Abdomen is Top of diaphragm.
The default Monitor ROI for Cardiac is Descending Aorta.
4. Click Save
12.5 Enhanced Xtream Injector

The Enhanced Xtream Injector provides synchronization of the start of the scan and the start of the
contrast injector using the start scan button on the Scan Control Interface or the gantry controls. The
Enhanced Xtream Injector also allows setting of the contrast injector parameters within the CT scan

Scan Applications
protocol and creation of an Injector Report at End Exam of what was delivered by the injector. The
system and injector are operated independently after the start scan button is pressed on the system.
The supported injectors are CiA425 compliant and are compliant with the Class 4 injector as defined
in CiA425. Only the Medrad Stellant D and Nemoto DualShot Alpha / DualShot GC/GXV injectors
are supported. Connecting any other injector will disable the ability to use the integrated injector
capabilities.
12.5.1 About Enhanced Xtream Injector
12.5.1.1 Indications for use

The Enhanced Xtream Injector option is designed to facilitate contrast-enhanced CT imaging by
connecting the system with a compatible injector. When used, pressing one single start button at the
system allows the user to start the CT scan synchronized with the injector.
The Enhanced Xtream Injector option is based on the protocol contained in the CiA425 standard and
allows this injector to operate with multiple GE systems that have the modified software and hardware
interface required for the CiA425 communication protocol built into them. This device is only the
communication protocol and bus interface needed to communicate with a 510(k) cleared injector that
is compatible with the CiA425 standard.
NOTE
This option is only the communication protocol and bus interface needed to
communicate with a validated compatible OEM injector (availability may vary
regionally).
12.5.1.2 Protocol considerations

Injection parameters can be included in scan protocols when the Enhanced Xtream Injector option is
installed. Patient size and conditions should be taken into consideration for the parameters set in the
protocol.

Scan Applications
12.5.2 Enhanced Xtream Injector window

1. From the Contrast collection, select Enhanced Xtream Injector and click On.
2. Open the Injector Settings window by clicking the icon next to the Injector Settings field. The
injector parameters can also be defined in Protocol Management.

Scan Applications
Figure 237 Injector Phases window

Scan Applications
Table 104 Injector Phases window components
Icon name Icon Description
Up to six phases are available depending on

Phase
the injector.
Injection delay can be set in increments of

seconds.
• 0 no delay prior to the injection of this
phase.
• 1 to max — injection delay of the injec-
Inj. Delay (s) tor in seconds prior to the start of this
phase. This is a timed pause.
• Hold — the injection for this phase is
started from the injector by pressing
the start button. This is only valid for
phases two through five.
Select the type of injection: Saline, Contrast

or Contrast-Saline.
Type
Selecting Contrast-Saline opens the Ratio
fields.
Available only when Contrast-Saline is se-

lected in Type. The upper frame is for con-
trast, the lower frame if for Saline. The range
is 5:95 and 95:5.
Ratio (%) When mixed phase is set from CT user in-
terface, the indication of ratio on Injector
Monitor is dismissed. If you want to set the
ratio on Injector Monitor, those buttons are
displayed.
The pressure limit value sets the limit at

which when reached will stop the injection.
NOTE
Pressure Limit A Red Alert is shown for a PSI val-
ue of 350 when injector is MedRad.
This is due to an error in the con-
version of PSI to kPA to PSI. Enter
325 PSI to clear the alert.

Scan Applications
Injector Phases window components continued

Icon name Icon Description
Contrast
Saline
(Not Displayed The system displays the remaining volume
when En- of contrast media and saline.
hanced
Xtream Injec-
tor is Off.)
Get Injector
Parameters Selecting Get Injector Parameters retrieves
(Not Displayed the values currently set on the injector and
when En- displays them in the Injector Settings popo-
hanced ver. Click Apply to choose these values or
Xtream Injec- click Cancel to return to the original values.
tor is Off.)
Add Phase Adds a phase.
Delete Phase Deletes a phase.
Clicking Apply when the injector is armed,

disarms the injector, but the parameters will
Apply NOT be updated on the injector. Open the
popover again and click Apply to update the
parameters.
Parameter values are not updated and re-

Cancel main at the values present when the pop up
window is opened.
NOTE
There is no Xtream Injector button for Scout scans.
12.5.3 Contrast report

An Enhanced Xtream Injector contrast report detailing the contrast agent used, injection phase, delay,
phase type, rate, volume and duration is automatically saved when you select Done Scanning. The
contrast report is saved as Series 996. It can be archived and transmitted over a network. The values
saved for rate, volume and duration are the actual values achieved by the injector, not the prescribed
values.

Scan Applications
Figure 238 Enhanced Xtream Injector contrast report text page
NOTE
Selecting Done Scanning before the Injection Complete message posted on the injector
may result in the Injector Report not being created.
12.5.4 Set up the Enhanced Xtream Injector

NOTICE

ON THIS SYSTEM.
Before you start

• A cable from the injector must be connected to the gantry.
• Confirm that the injector is connected to the system and power is on.

Scan Applications
• Setup the syringes.

• Prepare the Injector as described in the injector operator manual.
To set up the Enhanced Xtream Injector after the patient and the injector are prepared, follow these
steps. Review the injector status messages.
1. Prepare the injector.
2. From the Contrast collection, select Enhanced Xtream Injector from the IV Contrast field drop-
down menu.
• The button turns on and synchronizes the start of the scan and injector.
• IV contrast is automatically turned on when Enhanced Xtream Injector is turned on.
3. Set injector settings on the Injector Settings window. To open this window, click the icon next to
the Injector Settings field. The injector parameters can also be defined in Protocol Management.
4. Click Apply on the Injector Settings window when you have adjusted the settings.
5. From the Scan Settings screen, set the scan parameters.
• If there is an alert next to the Contrast Collection, check and resolve the injector parameters
on the system or the Injector. Confirm Settings is only active when both the system and the
injector are ready. Some errors may require a power cycle of the injector to resolve.
• Complete any required fields and note the injector status information on the Scan Progress
screen.
7. Press Start Scan to start the scan and injection.
NOTE
IF YOU STOP THE SCAN OR THE SYSTEM ABORTS, THE SCAN THE INJECTOR DOES
NOT STOP. -OR- IF YOU STOP THE INJECTOR OR THE INJECTOR ABORTS, THE
SYSTEM DOES NOT STOP SCANNING.
If either of these scenarios occur, verify the remaining volume to be injected before
resuming the injection or scan. You may need to update parameters on the Scan
Settings screen.
NOTE
If you have the Enhanced Xtream Injector option, after you end the exam, a contrast
report is saved as Series 996.
12.6 SmartStep
SmartStep is a mode of scanning designed to be used by the clinician during interventional
procedures. SmartStep uses the Hand-Held Controller and foot switch.
The Radiologist or Physician usually inserts a needle or catheter into a patient and then needs to see
images showing the position of the needle or catheter.

Scan Applications
Both single-slice (1i) and triple-slice (3i) imaging modes are selectable by the user at scan prescription.
1i mode is available at 5 mm and 10 mm aperture modes, and 3i imaging modes can be selected from
overlapped and non-overlapped 3i mode at 5 mm, 10 mm and 20 mm aperture modes.
Table 105 Slice Thickness Table
Detector Coverage 1i (mm) Overlap 3i (mm) Non-Overlap 3i (mm)
5 5 2.5 1.25 + 2.5 + 1.25
10 10 5 2.5 + 5 + 2.5
20 N/A 10 5 + 10 + 5
Overlap mode
Non Overlap mode
Only the 0.5 second rotation scan time is available for SmartStep. The Soft, Stnd, Detail, Lung, Bone
and Bone Plus recon types are available for reconstructions.
12.6.1 Workflow overview

During the system preparation phase, the foot pedal and HHC are connected so that the clinician can
make exposures, view images, and move the cradle during the SmartStep exam.

Scan Applications
Once the patient has been prepared for the interventional procedure, the image acquisition is setup in
the SmartStep mode.
During the SmartStep scan, the clinician can view the images and use the HHC to adjust window width
and level.
12.6.2 Prepare for an exam

NOTE
Prior to beginning the exam ensure that you know the settings in the Interventional
system preferences. See 22.3.13 Set Interventional Preferences on page 980
Use this procedure to prepare the system for a SmartStep scan. During this phase, the foot pedal and
HHC are connected so that the clinician can make exposures, view images, and move the cradle during
the SmartStep exam.
1. From the gantry’s front access plates, plug in the foot switch and HHC on the clinician’s side.
• Place the foot pedal and HHC on the gantry side from which the clinician works.
• The foot pedal is active as long as the system is prepped and ready for scan. Do NOT make
unwanted exposures by accidentally stepping on the foot pedal.
• See Hand-Held Controller to set the SmartStep W/L values used with the HHC.
Figure 239 Access plate is located on the front side of the gantry
1 HHC outlet
2 Foot switch outlet

Scan Applications
Table 106 Proper connection of HHC and foot switch
Engaging
Push the plug straight into the receptacle.
Latched
Once firmly latched, connection cannot be bro-
ken by pulling on the cable or any other compo-
nent part other than the outer release sleeve.
Disengaging
Disengage the connector by a single, straight
pull on the outer release sleeve. This first disen-
gages the latches, then withdraws the plug from
the receptacle.
• Close the access plate cover once you have plugged in the foot switch and HHC.
2. Install the flouro pan.

a. Remove the patient pad from the cradle and set aside.
b. Orient the cradle handle adaptor plate (fluoro pan), and position the velcro on the adapter
plate with the velcro on the cradle. This prevents slippage during the manual positioning.
c. Return the patient pad to the cradle.
d. Slide the HHC holder and cradle handle onto the cradle adapter plate. Orient them such that
the knurled knobs face away from the cradle.
e. Secure the holder and handle into place by tightening the knurled knobs.
NOTE
The cradle handle may have some small lateral movement. This is normal.
3. Position the ceiling-suspended, in-room display monitor so the clinician can view the images.
Care should be taken in positioning the in-room monitor so that it does not interfere with patient
loading and unloading.
Additional considerations when adjusting the in-room display monitor: Note that in references to
the system below, the system includes the monitor, spring arm and extension arm.
a. When the spring arm and the extension arm are positioned at 180° to each other (see figure
below), the attachment cannot be moved in the direction of the ceiling column. Repeated

Scan Applications
exertion of a force of greater than 25 Neutons may cause damage to the attachment.
b. Move the system only by the handle provided. Always hold the system firmly until you have
finished moving it. Never allow the arms to swing outward in an uncontrolled manner.
c. Do not overload the system beyond the maximum weight marked on the system.
d. Do not stand or work beneath the system.
e. The manufacturer must be immediately informed of any damage caused to the system. The
system must not be used until the damage has been rectified. Disconnect the system from
the mains. Do not stand or work beneath the system.
f. GE is not responsible for unauthorized or inappropriate handling of or changes to the system.
Unauthorized changes to the system may adversely affect on the smooth operation, safety
and reliability of the system.
4. Prepare the patient and supplies (for example biopsy tray) for the procedure.
a. Follow your departmental procedure for patient preparation.
b. Give the patient breathing instructions.
12.6.3 Set up the scan

NOTE
PLEASE REFER TO THE SAFETY SECTION FOR IMPORTANT SAFETY INFORMATION

Once the patient has been prepared for the interventional procedure, follow these steps to set up the
image acquisition in the SmartStep mode.
1. Select a protocol that contains an interventional series or Select Create a new interventional
series from the scan task list.
2. Position the patient and set the patient orientation and patient position settings to match in the
Patient Position Area in all series.
3. Proceed with scout and any additional planning series.

Scan Applications
4. Select the interventional series to set parameters of the interventional exposures.

The scan mode and rotation speed are automatically set. SmartStep and rotation speed is 0.5s.
These cannot be changed.
Figure 240 SmartStep settings collections
5. Click Start Location and type the initial image location where you want to start. The + and -
symbols may be substituted for S1 and I2. S = + and I = -.
Alternately, set the start location, DFOV, R/L and A/P center graphically from the Show Localizer
viewport.
6. Click SFOV and type the desired scan field of view value.
7. Click kV and select the desired kV value.
8. Click mA and select or type the desired mA value.
NOTE
Maximum mA is 300mA for systems with a Quanitx 160 tube.
9. Click Slice Mode and select 1i or 3i.
10. Click Recon Mode and select Overlap or Non Overlap (Overlap or Non Overlap is valid only if 3i
Mode is selected).
• Overlap mode provides 3 images of the same slice thickness with data overlap between each
slice.
• Non Overlap mode provides 3 images with asymmetric slice thickness where the center slice
is thicker than the outside slices.

Scan Applications
11. Click Thickness and select desired thickness. Thickness selection shown in SmartStep settings
collections.
12. Click Exposure Time and type an exposure time. Exposure Time is the maximum allowable
cumulative exposure time in the SmartView scan, which may be set up to 90 seconds.
13. Click Bump Distance and type the distance you want the cradle to bump in or out. The default
Bump Distance is half of the selected Slice Thickness.
14. Click Confirm, which displays the warning message, "This series contains one or more groups
with multiple scans at the same tomographic plane, i.e., the same location. Do you wish to
continue?"
15. Click Continue.
16. Proceed to Acquire a scan Acquire a scan.
12.6.4 GraphicRx with Axial System Preference

Table 107 SmartStep Localizer buttons
Set Scan Center Location and Window/Level
Maximize/Minimize Viewport
Show/Hide FOV ROI
Display Previous Series
Display Next Series

NOTE
Previously queued reconstructions will be paused until you exit SmartStep.
12.6.5.1 Prerequisite
• Verify that the foot switch and the HHC devices are plugged into the gantry.
• If you want to enable the alignment lights during a SmartStep procedure, use the button on the
HHC. If the Alignment Light button is selected on the gantry controls, the gantry decelerates and
stops.
• The SmartStep Remaining time and Accumulative time message areas on the in-room monitor
update with each step of the SmartStep scan procedure. If the remaining time is 0, a message
displays on the in-room monitor instructing you to re-prescribe the interventional scan.

Scan Applications
12.6.5.2 Scan
1. Press Prep from either the HHC or from the Scan progress screen.
Screen messages:
• "PRESS PREP"
• "PREP in PROGRESS" once Prep is selected
NOTE
Prep may fail to complete or an exposure cannot be made if the table transporter
is not at the full-in position. The HHC is not able to move the cradle past the table
transporter position. Manually move the cradle to the full-in position.
2. From the HHC, press Move to Start Location.
The Light Emitting Diode (LED) display is illuminated by the Move to Start Location button when
the table is not at the prescribed scan location for the first scan or at the last scanned location for
subsequent scans.
3. Press the foot pedal to make a single rotation exposure. The Prep LED on the HHC flashes while
the system is prepping.
Screen messages:
• "READY TO SCAN" indicates you can press foot pedal
• "XRAY ON" displays when scan is active
4. Release the foot pedal when the exposure is finished. Following each rotation, you must release
the foot pedal before you can scan again.
• Screen message:
"RELEASE PEDAL" displays if the exposure pedal is not released.
• Cradle Release can be used to freely move the cradle in/out of the gantry.
5. Repeat steps 1 through 4 as needed to complete the SmartStep scan.

6. Proceed to Display images. The next scan is initiated only when all images are displayed.
12.6.5.3 Dose Check during Interventional (SmartStep) Scans

Like non-interventional series, Dose Check for a SmartStep series is based on the estimated dose for
the series when you select Confirm Settings. Thus, if a Dose Check Notification Value or Alert Value is
exceeded for a SmartStep series, the user would see the Dose Check Notification Confirmation or Dose
Check Alert Confirmation screen only once prior to beginning scanning of the SmartStep series. This is
to prevent interruption during interventional scanning by avoiding excessive Dose Check Confirmation
screens.

Scan Applications
12.6.5.4 SmartStep Dose Display

CTDIvol mGy displays the CTDIvol information for the Z location with the highest accumulated dose in
the current imaging range during the SmartStep procedure.
For example, the illustration below a helical scan with CTDIvol of 10mGy acquired prior to SmartStep
with additional SmartStep scans acquired during the interventional series using SmartStep mode.
SmartStep group one contributes a CTDIvol of 5mGy to a different region. 15 mGy will become the
highest accumulated dose. A SmartStep group two contributes a CTDIvol of 5 mGy and overlaps with
the previous regions. 20 mGy will because the highest accumulated dose. A SmartStep group three
contributes a CTDIvol of 5 mGy adjacent to the SmartStep group two. 15 mGy will become the highest
accumulated dose. A SmartStep group four contributes a CTDIvol of 5 mGy outside of the regions. 5
mGy will become the highest accumulated dose.
Figure 241 SmartStep Dose display example
*The position resolution on CT gantry display is 0.5 mm, the table position resolution is more accurate
than 0.5 mm. A very small overlap between SmartStep Group 2 and Group 3 may not be recognized
from the CT gantry display, the accumulated dose will be 15 mGy pre scan and 20 mGy post scan in
this case.
12.6.6 SmartStep Display screen

The SmartStep Display screen has one or three interventional viewports that automatically update
each time an exposure is made with the foot pedal. The images are displayed superior to inferior.
Images are displayed superior to inferior if Fixed Viewport Order is set as system preference or in the
order set on the Viewport Orientation widget, if configurable.

Scan Applications
Figure 242 SmartStep Display screen — 1 interventional viewport
Figure 243 SmartStep Display screen — 3 interventional viewports

Scan Applications
Number Description
1, 2, 3 The interventional viewports automatically update each time an exposure is made

with the foot pedal. Viewport order is configurable using the Viewpoint Orientation
widget in Quick Settings.
4 Reference viewport. If a scout series was acquired, the most recent scout image
displays automatically. Can be changed to any selected image for this patient. Line
on scout illustrates the planned scan location and last scanned location.
5 Viewport Order Graphic illustrates the order and the recon mode. RAS Compass
displays the RAS coordinates for the image based on patient position/ orientation
and flip and rotate settings.
6 Reference Viewport. Axial images displayed on GraphicRx viewport are automati-

cally copied to this reference viewport when Confirm Settings is clicked. Can be
changed to any selected image for this patient.
7 Remaining Time
8 Accumulative Time
9 Exposure State Indicators:

• Ready to Prep
• Prep in Progress
• Ready to Scan
• X-ray On
• X-ray Off
• X-ray Time Expired
Operator Message Indicators

• Press PREP
• Press Pedal
• Release Pedal
• Re-prescribe Interventional Scan
10 Dose indicators:
• Max CTDIvol (mGy) in Scan Coverage - for the current location
• DLP (mGy/cm)- for the entire exam
11 Table Latch Indicator Illuminated when table has been unlatched
NOTE
The total accumulated exposure time for all SmartStep scan groups and series displays
on the Dose Text page.

Scan Applications
NOTE
For the safety of SmartStep exams, you can only expose the patient for 90 seconds per
session.
Control panel
See Display SmartStep images to view the display functions for manipulating an image.
12.6.7 Display images

One or three interventional viewports automatically update on the SmartStep Display screen each
time an exposure is made with the foot pedal. Use the W/L button on the HHC to view images with
different W/L values.
NOTE
HHC image operation is not available if the foot pedal is pressed.
1. From reference viewport hover menu, click .
2. From the File Manager, select the desired Exam and Series.
3. Click Accept to display the selected image.
4. Select any tool from the SmartStep control panel to manipulate the image.
Table 108 SmartStep display functions
Icon Name Function
Add Line ROI Add graphics to measure Distance
Add Angle ROI Add graphics to measure Angle
Add Ellipse ROI Add Ellipse ROI graphics
Add Annotation Add Annotation graphics
Maintain Maintains graphics from image to image
Erase All Graphics Erase All Graphics
Open reference image browser and load refer-

Load Reference Image
ence Image
Blank Viewport Clear loaded images from the reference viewport

Scan Applications
NOTE
Scan data from a SmartStep series cannot be reconstructed retrospectively.
12.7 GSI
12.7.1 GSI Overview

GSI is licensed for use with a GE X-ray tube. Use of a third party X-ray tube will require an additional
license for this feature.
Gemstone™ Spectral Imaging (GSI) enables the acquisition, reconstruction, and visualization of
spectral or GSI imaging.
Spectral images may provide additional clinical information about material composition. In addition,
images generated by the projection-based material decomposition algorithm have reduced beam-
hardening and metal induced artifacts.
The key technologies of the Gemstone Spectral Acquisition Imaging include:
• Fast energy switching providing data from two different kVp energies
• Projection-based reconstruction algorithms for generating monochromatic images
• Generation of Material Density (MD) Images that provide addition information over
monochromatic imaging
• Native Generation of Material Suppressed Iodine (MSI) / Virtual Unenhanced (VUE) images
• Native Generation of Material Pairs including: Water, Iodine, Calcium, Uric Acid, HydroxyApatite
(HAP), and Fat
• Application of GSI MAR, a metal artifact reducing algorithm to help to restore artifacts caused by
dense objects in the patient.
12.7.2 Material Density and Monochromatic images

• The two X-ray energies are acquired in an interleaved fashion by rapid switching of the energy
levels at the generator.
• Because the two energy levels are acquired simultaneously, mis-registration between the
resulting two data sets due to patient or organ motion are virtually eliminated. After acquiring
data at the two targeted energy levels, the energy dependent material attenuation can be
leveraged to generate Monochromatic images or pairs of Material Density images. These images
may provide additional diagnostic information, such as the differentiation of iodinated contrast
from calcified lesions. Material density and monochromatic images may also significantly reduce
beam hardening and metal-induced artifacts.

Scan Applications
12.7.3 Quality Check images

The GSI Quality Check image is a DICOM kVp image where all standard image corrections have not
been applied. This image allows you to assess/determine the scan coverage and completeness of the
exam prior to the image generation of the Monochromatic images.
12.7.4 KVP-Like images

The kvp-like images are intended for the novice user to GSI. These images are made to choose the keV
level that will most look like what a 100 or 120 KVp images would look like. The keV level are chosen
based on the scan field of view (SFOV). The table below shows the keV level that is chosen based on
KVp-like level and SFOV.
SFOV 100 kVp 120 kVp
Medium 66 73
Large 68 74
NOTE
HU values between kVp-like and true single kVp scans may not be exactly the same since
values can vary based on patient size and scan settings.
kVp-like images should be used as a guide to choosing the keV. Users may find another
keV that works best.
12.7.5 High kVp images

High KVP images are created with the full single energy reconstruction algorithm using the high kVp
data.
12.7.6 GSI MAR images

The GSI MAR images have been shown to reduce photon starvation artifacts caused by metal
implantations in the spine, hips, extremities, and shoulders. When using MAR, reconstruct the
data with and without MAR for comparative image review. In addition, high keV (100 to 140 keV)
monochromatic reconstructions may aid in assessing the shape and size of metal implantations. MAR
performance is suboptimal when metal is outside of the body, and in situations where there is a rapid
change of shape of dense anatomical structure in the path of small metal objects, such as aneurysm
clips in the head.
Effective MAR for GSI imaging requires that the following conditions are satisfied: The entire metal
object must be fully contained in the volume that is being scanned. Patient anatomy must not extend
beyond the 50 cm scan field-of-view. Patients should be centered within the SFOV with respect to
isocenter to ensure optimal image quality. Avoid using MAR reconstruction mode when portions of the
patient extend beyond the SFOV. The image interval is greater than or equal to 0.3125mm.
Reconstruction changes have been implemented to minimize the out of field artifact. ROI
measurements at the edge of the SFOV will not be accurate where there is anatomy outside the
SFOV.

Scan Applications
CAUTION
GSI MAR IMAGES SHOULD BE REVIEWED WITH BOTH GSI MAR APPLIED
AND NOT APPLIED TO HAVE A COMPARISON BETWEEN THE NATIVE IMAGE
AND THE IMAGE WITH METAL REMOVED.
12.7.7 Kidney stone evaluation with GSI

A study was conducted by Kulkarni, Sahani et al. (MGH), to characterize the urinary tract stones
in phantom and patients using Gemstone Spectral Imaging (GSI). Twenty stones of pure crystalline
composition [Uric acid (UA), struvite, cystine, and calcium oxalate monohydrate (COM)] were assessed
in a phantom as well as 11 patients (age 39 to 67 years) with urinary tract stones were evaluated.
An initial low dose unenhanced CT (kV - 120, Min mA -150, Max mA -450, NI - 26, slice thicknesses -
5 mm) followed by a targeted GSI acquisition on a Discovery CT 750 HD system (GE) was performed.
UA and non-UA stones were defined using a two-material decomposition (MD-Iodine/Water) algorithm.
The stone HU was also studied to determine its performance in predicting the composition. Ex-vivo
analysis of the stone using polarized microscopy with infrared spectrophotometry served as the gold
standard.
Of the 59 verified stones (phantom = 20 and patients = 39, mean size - 6 mm) there were 16 UA and 43
non-UA type.
The material density (MD) images were 100% sensitive and accurate in characterizing UA versus
non-UA stones. In patients, Effective Z identified 83% of calcium stones (n = 24) and in stones of
mixed type it accurately identified the dominant composition. The HU measurements alone were
71% sensitive and 69% accurate in characterizing the UA stones. GSI can provide accurate adjunct
information that may predict UA and from non-UA stone composition in-vitro and in-vivo.
GSI provides information of the chemical composition of renal calculi by calculation and graphical
display of the spectrum of effective atomic number. GSI kidney stone characterization provides
additional information to aid in the characterization of uric acid versus non-uric acid stones. It is
intended to be used as an adjunct to current standard methods for evaluating stone etiology and
composition. Characterization of kidney stones should be performed on non-contrasted exams using
information from the material density images and the effective atomic number displays
12.7.8 GSI Profile Editor

Use the GSI Profile Editor to create, edit and customize user GSI profiles and map these profiles to a
Clinical Category and Clinical Identifier.
Each profile consists of GSI preset families which define the scan settings and Recon settings available.
Each profile in the GSI Profile Editor has a unique name and consists of scan settings, recon settings
and a description. The GSI Profile Editor has two types of profiles:
• GE Reference Profiles. These are provided by GE and come as templates within the GSI Profile
Editor. GE Reference Profiles cannot be edited or deleted, but they can be copied.
• User Profiles. These are created by a user with appropriate privileges for the GSI Profile Editor.
User Profiles can be copied, edited, renamed or deleted.

Scan Applications
When you copy a GE Reference Profile, it is given a unique name. The copied, renamed profile is now a
User Profile and can be edited, renamed and deleted, as well.
Figure 244 GSI Profile Editor
12.7.8.1 Create a new profile/Copy a profile

You create a new profile by copying an existing profile.
1. Right-click on the profile that you would like to copy and select Copy from the drop-down menu.
You can copy both GE Reference and User Profiles.
2. Enter a unique profile name in the pop up that appears.
3. Click Save.
12.7.8.2 Rename a profile

You can rename only User Profiles, not GE Reference Profiles.

Scan Applications
1. Select the User tab on the Main Page under the search bar.
2. Right-click on the profile you would like to rename and select Rename from the drop-down menu.
3. Enter a new, unique name for the profile in the pop up that appears.
4. Click Save.
12.7.8.3 Delete a profile

You can delete only User Profiles, not GE Reference Profiles.

Scan Applications
1. Select the User tab on the Main Page under the search bar.
2. Right-click on the profile you would like to delete and select Delete from the drop-down menu.
3. Confirm the deletion by clicking the Delete button that appears in the pop up.
12.7.8.4 Edit a profile

You can edit only User Profiles, not GE Reference Profiles. To edit a GE Reference Profile, make a copy
of the GE Reference Profile, then edit the copy. You can edit a profile’s description, scan settings and/or
its recon settings.
To edit the profile’s description, click inside the Description box and enter the description you want.
12.7.8.4.1 Edit scan settings

The Scan Settings consist of groups of Preset Families. Each Preset Family is a unique combination
of SFOV, focal spot, collimation, rotation speed and pitch. The top Preset Family is considered the
primary Preset Family.
Edit an existing Preset Family:
To edit an existing Preset Family, select Head or Body. With Head
selected only the preset families with Head SFOV will be displayed. Make

Scan Applications
a new selection in one of the three drop-down menus per Preset Family.
Add a new Preset Family

To add a new Preset Family, click the Add button at the top right corner of the Scan Settings screen.
A unique Preset Family is added which you can now edit. The Add button is disabled once no more
unique Preset Families exist.
A profile cannot contain any duplicate scan settings. The system will notify you if duplicate settings
exist.

Scan Applications
Change the order of the Preset Families

1. Hover your mouse over the Preset Family you would like to move. The Preset Family becomes
blue highlighted.
2. Click and hold the mouse button on the highlighted Preset Family
3. While pressing the mouse button, drag the Preset Family to the new location in the order.
4. Release the mouse button.
Delete a Preset Family

a. Click the X on the right side of the Preset Family next to the Pitch field. When duplicate preset
families are added to a profile, the preset families are outlined in red and the Save button is disabled.
12.7.8.4.2 Edit recon settings

The Recon Settings consist of individual recons. Each recon has all or a subset of the following fields:
• Name
• Image Type
• Recon Type
• keV
• MAR
• Data File
Allows the user to manipulate keV data through various monochromatic energies for post
processing work.
• ASiR-V
• Window Width
• Window Level
• Image Enhance Filter
Table 109 GSI Head and Body Settings
Body Settings Head Settings
WW WL WW WL
Monochromatic 400 40 800 150
Water(Iodine) 300 1000 90 125
Iodine(Water) 150 50 115 40
Water(Calcium) 300 1000 300 1000
Calcium(Water) 250 50 250 50
Calcium(Iodine) 200 800 100 800

Scan Applications
GSI Head and Body Settings continued

Body Settings Head Settings
WW WL WW WL
Iodine(Calcium) 250 -500 250 -500
Uric Acid (HAP) 350 1100 - -
HAP(Uric Acid) 300 10 - -
Uric Acid (Calcium) 365 1065 - -
Calcium(Uric Acid) 125 12 - -
HAP (Iodine) 130 660 130 660
Iodine(HAP) 150 -180 150 -180
HAP (Water) 500 150 500 150
Water(HAP) 300 1000 300 1000
Fat(Iodine) 300 1000 - -
Iodine(Fat) 155 40 - -
Fat(Water) 750 50 - -
Water(Fat) 750 250 - -
Add a new Recon

Click the Add button at the top right corner of the Recon Settings screen. A new default recon is added.

Scan Applications
NOTE
Only 10 GSI-specific tasks can be defined in the profile.
Figure 245 GSI profile neuro recon settings
Copy a Recon
1. Find the recon you want from any GE Reference or User Profile.
2. Click the Copy button at the right side of the recon to copy a single recon or click the Copy button
at the top of the recon settings window to copy all of the recons.
3. Return to the profile where you would like to add the copied recon.

Scan Applications
4. Click the Paste button at the top right corner of the Recon Settings screen. The copied recon is
appended to the current profile’s Recon Settings.
5. (Optional) Rename the copied recon.
Copy all Recons

Use this procedure to Copy All recons from a GE or User GSI Profile.
1. Find the recon(s) to be copied from either a GE Reference GSI profile or a User profile.
2. Click the Copy button on the Recon Settings label.
3. Click the User GSI profile you wish to copy the recons to.
4. Click the Paste button to copy the recons.
Delete a Recon
1. Find the recon to be deleted.
2. Click the Delete button at the far right side of the recon.
3. Confirm the deletion by clicking the Delete button in the pop up that appears.
Edit an existing Recon

You can edit an existing Recon by changing the prescription settings inside the recon.
Change the order of the Recon settings
1. Hover your mouse over the setting you would like to move. The row becomes blue highlighted.
2. Click and hold the mouse button on the highlighted setting.
3. While pressing the mouse button, drag the recon setting to the new location in the order.
4. Release the mouse button.
12.7.8.5 Map a Profile to a Clinical Identifier

You can map a profile to a Clinical Identifier on the Clinical Identifier to Profile Mapping page.
Navigate to this page by clicking the Clinical Identifier to Profile Mapping button on the navigation
bar at the top of the screen. You must click Save before closing the Profile Editor for all changes to be
saved.

Scan Applications
Figure 246 Clinical Identifier to Profile Mapping
1. Filter the list of Clinical Identifiers using the box on the right of the Clinical Identifier to Profile
Mapping page.
You can filter the list by any combination of Clinical Category, Clinical ID and Profile. You can
change the filter using the drop-down menus or clear all filters using the Clear All Filters button.

Scan Applications
2. The center box, Current Profile Mapping shows current mappings between Clinical Identifiers
and profiles. Click on a row of this list to select a Clinical Identifier you want reassign/unassign to
a particular profile. You can also select all clinical identifiers using the Select All button or clear all
selections using the Clear All Selections button.
Once you make or change an assignment, the filtered list contains the changed records.
12.7.9 GSI Assist mA Mode

When GSI Assist mA Mode is selected, the system will select a GSI acquisition mode and mA based on
the patient attenuation from the scout, noise index value based on a non-GSI protocol, Clinical task
category and Clinical Identifier.
GSI Assist mA Mode is designed to provide assistance in the selection of a GSI acquisition mode
with similar dose to a non-GSI scan using a noise index value based on a non-GSI scan. The optimal
acquisition mode and mA is selected based on the patient’s size, Clinical Identifier and Noise Index.
GSI Assist mA Mode is available only for head and body scanning (not recommended for pediatrics).
12.7.10 GSI Profiles

GSI scanning is organized into a set of GSI Profiles that provide the user with an optimized set of
scanning techniques based on a clinical task. There are a set of GSI profiles provided with the system,
and the user may define profiles utilizing the GSI Profile Editor.
GSI profiles are mapped to Clinical Identifier.
NOTE
Use of appropriate CID is critical to image quality for the following specific recon tasks:
• Gout analysis images must use CID Extremity.
• Gout Non-contrast head images must use CID Neuro.RoutineHead.

Scan Applications
Table 110 GSI Profile Overview (Performix™ HDw)
GE GSI Description Scan Parameters Preset Family Order Recon Parameters

Profile
GE Head Intended for head con- SFOV: Head Head/ Large/ 70 keV Stnd AR40 100/40
Contrast trast Collimations: 40 40mm/0.8/ 0.516 Iodine(Water) Stnd AR40
Primary imaging fac- mm Head/ Large/ 115/40
tors: Pitches: 0.516, 40mm/0.8/ 0.984 Water(Iodine) Stnd
Low Contrast Detectabil- 0.984 Head/ Large/ AR4090/1025
ity Rotation Speeds: 40mm/1.0/ 0.516
Spatial Resolution 0.5, 0.8, 1.0 Head/ Large/
Secondary imaging fac- Scan Type: Helical 40mm/1.0/ 0.984
tor: Head/ Large/
MD Accuracy 40mm/0.5/ 0.516
Head/ Large/
40mm/0.5/ 0.984
GE Head Intended for head non- SFOV: Head Head/ Large/ 70 keV Stnd AR40 100/40
NC contrast Collimations: 40 40mm/0.8/ 0.516 70 keV Bone AR40
Primary imaging fac- mm Head/ Large/ 2000/350
tors: Pitches: 0.516, 40mm/0.8/ 0.984 Iodine(Water) Stnd AR40
Low Contrast Detectabil- 0.984 Head/ Large/ 115/40
ity Rotation Speeds: 40mm/1.0/ 0.516 Water (Iodine) Stnd AR40
Spatial Resolution 0.5, 0.8, 1.0 Head/ Large/ 90/1025
Secondary imaging fac- Scan Type: Helical 40mm/1.0/ 0.984
tor: Head/ Large/
MD Accuracy 40mm/0.5/ 0.516
Head/ Large/
40mm/0.5/ 0.984
GE Head Intended for head CTA SFOV: Head Head/ Large/ 70 keV Stnd AR40 800/150
CTA Primary imaging fac- Collimations: 40 40mm/0.5/ 0.516 Water(Iodine) Stnd AR40
tors: mm Head/ Large/ 90/1025
Low Contrast Detectabil- Pitches: 0.516, 40mm/0.5/ 0.984 Iodine(Water) Stnd AR40
ity 0.984 Head/ Large/ 115/40
Spatial Resolution Rotation Speeds: 40mm/0.8/ 0.516
Secondary imaging fac- 0.5, 0.8 Head/ Large/

tor: Scan Type: Helical 40mm/0.8/ 0.984
MD Accuracy

Scan Applications
GSI Profile Overview (Performix™ HDw) continued

Profile
GE Head Intended for head and SFOV: Head Head/ Large/ 70 keV Stnd AR40 800/150
Neck CTA neck CTA Collimations: 40 40mm/0.5/ 0.984 55 keV Stnd AR40 800/150
Primary imaging fac- mm Head/ Large/ Water(Iodine) Stnd AR40
tors: Pitches: 0.984 40mm/0.8/ 0.984 90/1025
Low Contrast Detectabil- Rotation Speeds: Head/ Large/ Iodine(Water) Stnd AR40
ity 0.5, 0.8, 1.0 40mm/1.0/ 0.984 115/40
Spatial Resolution Scan Type: Helical
Secondary imaging fac-
tor:
MD Accuracy
GE Soft Intended for Soft Tissue SFOV: Large Large Body/ Large/ 70 keV Stnd AR40: 400/40
Tissue Neck protocols. Collimations: 80 80 mm/ 0.8/ 0.992 55 keV Stnd AR40: 630/75
Neck Primary imaging fac- mm Large Body/ Large/ Iodine(Water) Stnd AR40:
tors: Contrast Timing Pitches: 0.992 80mm/1.0/ 0.992 150/50
Low Contrast Detectabil- Large Body/ X-Large/ Water(Iodine) Stnd AR40:
ity. Rotation Speeds:
0.8 , 1.0 80mm/0.8/ 0.992 300/1000
Secondary Imaging Large Body/ X-
factors: Artifact Reduc- Scan Type: Helical VUE Stnd AR40: 400/40
Large /80mm//1.0/
tion 0.992
GE Neck Intended for Circle of SFOV: Large Large Body/ Large/ 70 keV Stnd AR40: 800/150
CTA Willis Carotids protocols. Collimations: 80 80 mm/0.5/ 0.992 Iodine(Water) Stnd AR40:
Primary imaging mm Large Body/ Large/ 150/50
factors: Pitches: 0.992 80 mm/0.6/ 0.992 Water(Iodine) Stnd AR40:
Spatial resolution Rotation Speeds: Large Body/ Large/ 300/1000
Contrast Timing 0.5, 0.6, 0.8 80 mm/0.8/ 0.992
Artifact Reduction Scan Type: Helical

Secondary imaging
factor:
Material Density Accura-
cy

Scan Applications

Profile
GE Chest Intended for PE studies SFOV: Large Large Body/ Large/ 70 keV Stnd AR40: 400/40
CTA and general Chest CTA Collimations: 80 80 mm/0.5/ 0.992 50 keV Stnd AR40: 630/75
protocols. mm Large Body/ Large/ Iodine(Water) Stnd AR40:
Primary imaging Pitches: 0.508, 80 mm/0.6/ 0.992 150/50
factors: 0.992 Large Body/ Large/ Water(Iodine) Stnd AR40:
Temporal resolution Rotation Speeds: 80 mm/0.8/ 0.992 300/1000
Spatial resolution 0.5, 0.6, 0.8 Large Body/ Large/
Contrast timing/CNR Scan Type: Helical 80 mm/0.5/ 0.508
Secondary imaging
factors:
cy
Z coverage
GE Fast Intended for PE studies SFOV: Large Large Body/ Large/ 70 keV Stnd AR40: 400/40
Chest and general Chest CTA Collimations: 80 80 mm/0.5/ 1.531 50 keV Stnd AR40: 630/75
protocols. mm Large Body/ Large/ Iodine(Water) Stnd
Primary imaging Pitches: 1.375, 80 mm/0.6/ 1.531 AR40:150/50
factors: 1.531 Large Body/ Large/ Water(Iodine) Stnd AR40:
Temporal resolution Rotation Speeds: 80 mm/0.6/ 1.375 300/1000
Spatial resolution 0.5, 0.6, 0.8 Large Body/ Large/
Contrast timing/CNR Scan Type: Helical 80 mm/0.8/ 1.375
Secondary imaging
factors:
cy
Z coverage
GE Abdo- Intended for Kidney SFOV: Large Large Body/ 70 keV Stnd AR40: 400/40
men NC Stone protocols. Collimations: 80 Large/80 mm/ 0.8/ Water(Iodine) Stnd AR40:
Primary imaging factor: mm 0.992 300/1000
Material density accura- Pitches: 0.508, Large Body/ Iodine(Water) Stnd AR40:
cy 0.992 Large/80 mm/0.5/ 150/50
0.508
Rotation Speeds: Uric Acid(Calcium)Stnd
0.5, 0.8, 1.0 Large Body/ AR40: 160/1045
Large/80 mm/1.0/
Scan Type: Helical 0.992

Scan Applications

Profile
GE Rou- Intended for Routine SFOV: Large Large Body/ 70 keV Stnd AR40: 400/40
tine Ab- Abdominal/Pelvis proto- Collimations: 80 Large/80 mm/ 0.6/ 50 keV Stnd AR40: 600/40
domen cols. mm 0.992
Contrast Iodine(Water) Stnd AR40:
Primary imaging Pitches: 0.508, Large Body/ 150/50
factors: 0.992 Large/80 mm/ 0.8/
0.992 Water(Iodine) Stnd AR40:
Low/appropriate dose Rotation Speeds: 300/1000
General consistent im- 0.5, 0.6, 0.8, 1.0 Large Body/
Large/80 mm/0.6/ VUE Stnd AR40: 400/40
age quality Scan Type: Helical 0.508
Secondary imaging
factors: Large Body/
Large/80 mm/0.5/
Spatial Resolution 0.508
MD Accuracy Large Body/
Large/80 mm/0.8/
0.508
Large Body/
Large/80 mm/1.0/
0.992
Large Body/
Large/80 mm/1.0/
0.508
GE Abdo- Intended for multi- SFOV: Large Large Body/ 70 keV Stnd AR40: 400/40
men phase liver protocols. Collimations: 80 Large/80 mm/0.8/ 50 keV Stnd AR40: 600/40
Contrast Primary imaging mm 0.992
Iodine(Water) Stnd AR40:
factors: Pitches: 0.508, Large Body/ X- 150/50
Contrast timing/CNR 0.992 Large/80 mm/0.8/
Low Contrast Detectabil- Rotation Speeds: 300/1000
ity 0.5, 0.8, 1.0 Large Body/
Large/80 mm/0.5/ Fat(Iodine) Stnd AR40:
Material Density Accura- XL Focal Spot in- 0.508 300/1000
cy cluded VUE Stnd AR40: 400/40
Large Body/
Scan Type: Helical Large/80 mm/1.0/
0.992
Large Body/ X-
Large/80 mm/1.0/
0.992

Scan Applications

Profile
GE Fast Intended for Routine Ab- SFOV: Large Large Body/ 70 keV Stnd AR40: 400/40
Abdo- dominal / Pelvis proto- Collimations: 80 Large/80 mm/0.6/ 50 keV Stnd AR40: 600/40
men cols. mm 1.375
Primary imaging Pitches: 1.375, Large Body/ 150/50
factors: 1.531 Large/80 mm/0.6/
Low/appropriate dose Rotation Speeds: 300/1000
general consistent im- 0.6, 0.8 Large Body/
age quality XL Focal Spot in- 1.375
Secondary imaging cluded
factors: Large Body/ X-
MD Accuracy Large Body/
Large/80 mm/0.8/
1.531
Large Body/ X-
Large/80 mm/0.8/
1.531
GE Abdo- Intended for general Ab- SFOV: Large Large Body/ 70 keV Stnd AR40: 400/40
men CTA dominal CTA protocols. Collimations: 80 Large/80 mm/0.6/ 55 keV Stnd AR40:
Primary imaging mm 0.992 1000/250
factors: Pitches: 0.992, Large Body/ Iodine(Water) Stnd AR40:
Contrast timing/CNR 1.375, 1.531 Large/80 mm/0.8/ 150/50
0.992
Z coverage Rotation Speeds: Water(Iodine) Stnd AR40:
0.6, 0.8 Large Body/ X- 300/1000
Secondary imaging Large/80 mm/0.8/
factors: XL Focal Spot in- 0.992 VUE Stnd AR40: 400/40
Spatial resolution cluded
Large Body/
Temporal resolution Scan Type: Helical Large/80 mm/0.8/
1.531
Large Body/
Large/80 mm/0.6/
1.375
Large Body/ X-
Large/80 mm/0.8/
1.531

Scan Applications

Profile
GE Run- Intended for Runoff pro- SFOV: Large Large Body/ 70 keV Stnd AR40: 800/150
off CTA tocols where outrunning Collimations: 40 Large/40 mm/0.5/ 55 keV Stnd AR40:
the contrast bolus is a mm 0.984 1000/250
concern. Large Body/
Pitch: 0.984 Iodine(Water) Stnd AR40:
Primary imaging Large/40 mm/0.6/ 150/50
factors: Rotation Speeds: 0.984
0.5,0.6, 0.8, 1.0 Water(Iodine) Stnd AR40:
Contrast Timing Large Body/ 300/100
Z Coverage Iodine(Calcium) Stnd
0.984
Secondary imaging AR40: 150/-180
Large/40 mm/1.0/ Calcium(Iodine) Stnd
Spatial resolution 0.984 AR40: 130/660
Temporal Resolution
GE Run- Intended for long z cov- SFOV: Large Large Body/ 70 keV Stnd AR40: 800/150
off CTA erage runoff protocols Collimations: 80 Large/80 mm /0.5/ 55 keV Stnd AR40:
Plus where outrunning the mm 0.992 1000/250
contrast bolus is a con- Large Body/
cern. Pitches: 0.992 Iodine(Water) Stnd AR40:
Large/80 mm/0.6/ 150/50
Primary imaging Rotation Speeds: 0.992
factors: 0.5,0.6, 0.8, 1.0 Water(Iodine) Stnd AR40:
Large Body/ 300/1000
Contrast Timing XL Focal Spot in- Large/80 mm/0.8/
cluded 0.992 Iodine(Calcium) Stnd
Z Coverage AR40: 150/-180
Scan Type: Helical Large Body/
Secondary imaging Calcium(Iodine) Stnd
factors: Large/80 mm/1.0/
0.992 AR40: 130/660
Spatial resolution
Large Body/ X-
Temporal Resolution Large/80 mm/0.5/
0.992
Large Body/ X-
Large/80 mm/0.6/
0.992

Scan Applications

Profile
GE CTA Intended for CTA proto- SFOV: Large Large Body/ 70 keV Stnd AR40: 800/150
General cols where outrunning Collimations: 40 Large/40 mm/0.6/ 55 keV Stnd AR40:
the contrast bolus is a mm. 80 mm 0.984 1000/250
Pitches: 0.984, Iodine(Water) Stnd AR40:
Primary imaging 0.516, 0.992 Large/40 mm/0.8/ 150/50
factors: 0.984
Rotation Speeds: Water(Iodine) Stnd AR40:
Contrast Timing 0.5,0.6, 0.8, 1.0 Large Body/ 300/1000
Z Coverage Large/40 mm/1.0/
Scan Type: Helical 0.984 Iodine(Calcium) Stnd
Temporal Resolution Large Body/
Large/40 mm/0.8/
0.516
Large Body/
Large/80 mm/0.8/
0.992
Large Body/
Large/80 mm/0.5/
0.992

Scan Applications

Profile
GE CTA Intended for CTA proto- SFOV: Large Large Body/ 70 keV Stnd AR40: 800/150
General cols where outrunning Collimations: 80 Large/80 mm/0.5/ 55 keV Stnd AR40:
Plus the contrast bolus is a mm 0.992 1000/250
Pitches: 0.508, Iodine(Water) Stnd AR40:
Primary imaging 0.992, 1.375 Large/80 mm/0.6/ 150/50
factors: 0.992
Rotation Speeds: Water(Iodine) Stnd AR40:
Contrast Timing 0.5,0.6, 0.8, 1.0 Large Body/ 300/1000
Z Coverage Large/80 mm/0.8/
Scan Type: Helical 0.992 Iodine(Calcium) Stnd
Temporal Resolution Large Body/
Large/80 mm/0.6/
0.508
Large Body/
Large/80 mm/0.8/
0.508
Large Body/
Large/80 mm/1.0/
0.508
Large Body/
Large/80 mm/0.5/
1.375
Large Body/
Large/80 mm/0.6/
1.375

Scan Applications

Profile
GE Body Intended for Body proto- SFOV: Large Large Body/ 70 keV Stnd AR40: 400/40
Artifac- cols with metal implants Collimation: 80 Large/80 mm/0.8/ 70 keV MAR On Stnd AR40:
tRed and stents. mm 0.992 400/40
Primary imaging Pitches: 0.508, Large Body/ X- 110 keV Bone AR0:
factors: 0.992 Large/80 mm/0.8/ 2000/350
Contrast timing/CNR 0.992
Rotation Speeds: 110 keV MAR On Bone AR0:
Z coverage 0.5, 0.8, 1.0 Large Body/ 2000/350
Large/80 mm/0.5/
Secondary imaging XL Focal Spot in- 0.508
factors: cluded
Large Body/
Spatial resolution Scan Type: Helical Large/80 mm/1.0/
Temporal resolution 0.992
Large Body/X-
Large/80 mm/1.0/
0.992
Large Body/
Large/80 mm/1.0/
0.508
GE MSK Intended for Spine and SFOV: Large Large Body/ 70 keV Stnd AR40: 400/40
NC Arti- general MSK protocols. . Collimations: 40 Large/80 mm/0.6/ 70 keV MAR On Stnd AR40:
factRed Primary imaging mm, 80 mm 0.508 400/40 110
factors: Pitches: 0.508, Large Body/ keV Bone Plus AR40:
Spatial Resolution 0.516, 0.984 Large/40 mm/0.8/ 2000/350
0.516
Artifact Reduction Rotation Speeds: 110 keV MAR On Bone Plus
0.6, 0.8, 1.0 Large Body/ AR40: 2000/350
Secondary imaging Large/40 mm/1.0/
factor: Scan Type: Helical 0.516
Low Contrast Detectabil- Large Body/
ity Large/40 mm/0.8/
0.984
Large Body/
Large/40 mm/1.0/
0.984
Large Body/
Large/80 mm/1.0/
0.508

Scan Applications

Profile
GE Ex- Intended for Extremity SFOV: Medium Medium Body/ 70 keV Stnd AR40: 400/40
tremity protocols as an optional Collimations: 40 Large/40 mm/0.5/ 110 keV Bone AR40:
approach. mm 0.516 2000/350
Primary imaging Pitches: 0.516, Medium Body/ 125 keV Bone AR40:
factors: 0.984 Large/40 mm/0.6/ 2000/350
Rotation Speeds:
Artifact Reduction 0.5, 0.6, 0.8, 1.0 Medium Body/
Large/40 mm/0.5/
Secondary imaging Scan Type: Helical 0.984
factor:
Medium Body/
Low Contrast Detectabil- Large/40 mm/0.6/
ity 0.984
Medium Body/
Large/40 mm/0.8/
0.984
Medium Body/
Large/40 mm/1.0/
0.984
GE Gout Intended for Gout proto- SFOV: Medium Medium Body/ 70 keV Stnd AR40
cols as an optional ap- Collimations: 40 Large/40 110 keV Bone AR40
proach. Primary imaging mm mm/0.5/0.516
factors include Spatial Uric Acid(HAP) Stnd AR40
Pitches: 0.516, Medium Body/
Resolution and Artifact Large/40 HAP(Uric Acid) Stnd AR40
Reduction. Low Contrast 0.984
mm/0.6/0.516
Detectability is a Secon- Rotation Speeds:
dary imaging factor. Medium Body/
0.5, 0.6, 0.8, 1.0 Large/40
Scan Type: Helical mm/0.5/0.984
Medium Body/
Large/40
mm/0.6/0.984
Medium Body/
Large/40
mm/0.8/0.984
Medium Body/
Large/40
mm/1.0/0.984

Scan Applications

Profile
GE Body GE Ref Body All for 40 SFOV: Large Large Body/ 70 keV Data File On Stnd
40 mm mm collimation Collimations: 40 Large/40 mm/0.5/ AR40: 400/40
All mm 0.516 55 keV Stnd AR40:
Pitches: 0.516, Large Body/ 1000/250
0.994, 1.375 Large/40 mm/0.6/ 110 keV Bone AR40:
0.516 2000/350
Rotation Speeds:
0.5, 0.6, 0.8, 1.0 Large Body/ 110 keV Mar On Bone
Large/40 mm/0.8/ AR40: 2000/350
Scan Type: Helical, 0.516
Axial Iodine(Water) Stnd AR40:
Large Body/ 150/50
Large/40 mm/1.0/
300/1000
Large Body/
0.984 High kVp Stnd AR40:
Large Body/ 400/40
Large/40 mm/0.6/ 120 kVp Like Stnd AR40:
0.984 400/40
Large Body/
Large/40 mm/0.8/
0.984
Large Body/
Large/40 mm/1.0/
0.984
Large Body/
Large/40 mm/0.5/
1.375
Large Body/
Large/40 mm/0.6/
1.375
Large Body/
Large/40
mm/0.8/1.375
Large Body/
Large/40 mm/1.0/
1.375
Large Body/
Large/40 mm/0.5/
Axial
Large Body/
Large/40 mm/0.6/
Axial

Scan Applications

Profile
Large Body/
Large/40 mm/0.8/
Axial
Large Body/
Large/40 mm/1.0/
Axial
GE Body GE Ref Body All for 80 SFOV: Large Large Body/ 70 keV Data File On Stnd
80 mm mm collimation Collimations: 80 Large/80 mm/0.5/ AR40: 400/40
All mm 0.508 55 keV Stnd AR40:
Pitches: 0.508, Large Body/ 1000/250
0.992, 1.375, 1.531 Large/80 mm/0.6/ 110 keV Bone AR40:
0.508 2000/350
Rotation Speeds:
0.5, 0.6, 0.8, 1.0 Large Body/ 110 keV Mar On Bone
Large/80 mm/0.8/ AR40: 2000/350
Scan Type: Helical 0.508
Large Body/ 150/50
Large/80 mm/1.0/
300/1000
Large Body/
0.992 High kVp Stnd AR40:
Large Body/ 400/40
Large/80 mm/0.6/ 120 kVp Like Stnd AR40:
0.992 400/40
Large Body/
Large/80 mm/0.8/
0.992
Large Body/
Large/80 mm/1.0/
0.992
Large Body/
Large/80 mm/0.5/
1.375
Large Body/
Large/80 mm/0.6/
1.375
Large Body/
Large/80 mm/0.8/
1.375
Large Body/
Large/80 mm/1.0/
1.375

Scan Applications

Profile
Large Body/
Large/80 mm/0.5 /
1.531
Large Body/
Large/80 mm/0.6/
1.531
Large Body/
Large/80 mm/0.8/
1.531
Large Body/
Large/80 mm/1.0/
1.531
Large Body/ X-
Large/80 mm/0.5/
0.508
Large Body/ X-
Large/80 mm/0.6/
0.508
Large Body/ X-
Large/80 mm/0.8/
0.508
Large Body/ X-
Large/80 mm/1.0/
0.508
Large Body/ X-
Large/80 mm/0.5/
0.992
Large Body/ X-
Large/80 mm/0.6/
0.992
Large Body/ X-
Large/80 mm/0.8/
0.992
Large Body/ X-
Large/80 mm/1.0/
0.992
Large Body/ X-
Large/80 mm/0.5/
1.375
Large Body/ X-
Large/80 mm/0.6/
1.375

Scan Applications

Profile
Large Body/ X-
Large/80 mm/0.8/
1.375
Large Body/ X-
Large/80 mm/1.0/
1.375
Large Body/ X-
Large/80 mm/0.5 /
1.531
Large Body/ X-
Large/80 mm/0.6/
1.531
Large Body/ X-
Large/80 mm/0.8/
1.531
Large Body/ X-
Large/80 mm/1.0/
1.531
Table 111 GE GSI Profile Mapping
GE GSI Profile Category.CID Mapping
GE Head Contrast Neuro.Routine Head w Contrast
GE Head NC Neuro.Routine Head
GE Head CTA Neuro.COW
GE Head Neck CTA Neuro.CTA
GE Soft Tissue Neck Neuro.Soft Tissue Neck
GE Neck CTA Neuro.Carotids
GE Chest CTA Thoracic.Aorta

Thoracic.PE
Thoracic.CTA
Extremity.Upper Extremity CTA
GE Fast Chest Not mapped
GE Abdomen NC Abdominal.Renal Stone

Abdominal.Colonography

Scan Applications
GE GSI Profile Mapping continued

GE Routine Abdomen Contrast Thoracic. Chest Abd Pelvis

Abdominal.Abd Pelvis
Abdominal.Pelvis
Abdominal.Abd Pelvis w Contrast
Abdominal.Urogram
Pelvis.Pelvis
Pelvis.Cystogram
Pelvis.Pelvis w Contrast
GE Abdomen Contrast Thoracic.Routine Chest

Thoracic.Chest Abd
Abdominal.Abdomen
Abdominal.Abdomen w Contrast
Abdominal.Renal
Abdominal.Pancreas
Abdominal.Multiphase Liver
Abdominal.Tumor Perfusion
GE Fast Abdomen Not mapped
GE Abdomen CTA Abdominal.CTA
GE Runoff CTA Abdominal.Runoff

Extremity.Lower Extremity CTA
GE Runoff CTA Plus Not mapped
GE CTA General Not mapped
GE CTA General Plus Not mapped
GE Body ArtifactRed Not mapped

Scan Applications
GE GSI Profile Mapping continued

GE MSK NC ArtifactRed Spine.General

Spine.Cervical
Spine.Thoracic
Spine.Lumbar
Spine.Thoracic and Lumbar
Spine.Complete
Abdominal.Bony Pelvis
Pelvis.General
Pelvis.Bony Pelvis
Pelvis.Hip
Pelvis.Sacroilliac
Extremity.General
Extremity.Upper
Extremity Extremity.Shoulder
Extremity Extremity.Lower
Extremity.Scapula
Extremity.Elbow
Extremity.Wrist Extremity.Knee
Extremity.Ankle
GE Extremity Not mapped
GE Gout Extremity.Gout
GE Body 40 mm All Not mapped
GE Body 80 mm All Thoracic.General

Abdominal.General

Scan Applications
Table 112 GSI Preset Families
Rotati Pitches Supported Annotated CTDIw

on mA
Axial CTDIw =
Time
SFOV/ Focal Spot/ Collimation CTDIvol
Helical CTDIw/
pitch = CTDIvol
280 15.51
320 17.90
365 20.31
Head/Large/40mm 0.5 0.516/0.984
405 22.69
445 25.08
485 27.44
280 18.38
320 21.22
360 24.10
Head/Large/40mm 0.6 0.516/0.984
400 26.94
440 29.76
480 32.61
275 23.9
315 27.67
355 31.48
Head/Large/40mm 0.8 0.516/0.984
395 35.22
435 38.93
475 42.68
270 29.55
315 34.26
355 38.97
Head/Large/40mm 1 0.516/0.984
395 43.63
435 48.27
475 52.92

Scan Applications
GSI Preset Families continued

on mA
Axial CTDIw =
Time
Helical CTDIw/
pitch = CTDIvol
200 4.69
240 5.75
280 6.82
320 7.89
LARGE BODY/LARGE/80 mm 0.5 0.508/0.992/1.375/1.531
365 8.96
405 10.02
445 11.09
485 12.15
195 5.54
235 6.8
280 8.08
320 9.35
360 10.63
400 11.89
440 13.15
480 14.44
190 7.09
230 8.76
275 10.4
315 12.06
355 13.75
400 15.39
435 17.04
480 18.7
185 8.73
230 10.79
270 12.84
315 14.9
LARGE BODY/LARGE/80 mm 1 0.508/0.992/1.375/1.531
355 16.97
395 19.01
435 21.04
475 23.09

Scan Applications

on mA
Axial CTDIw =
Time
Helical CTDIw/
pitch = CTDIvol
530 13.27
LARGE BODY/-X-LARGE/80 mm 0.5 0.508/0.992/1.375/1.531
579 14.4
525 15.78
LARGE BODY/-X-LARGE/80 mm 0.6 0.508/0.992/1.375/1.531
565 17.08
520 20.46
LARGE BODY/-X-LARGE/80 mm
0.8 0.508/0.992/1.375/1.531 560 22.1
520 25.23
LARGE BODY/-X-LARGE/80 mm 1 0.508/0.992/1.375/1.531
560 27.3
200 4.8
240 5.89
280 6.98
320 8.08
LARGE BODY/LARGE/40 mm 0.5 0.516/0.984/1.375 Axial
365 9.18
405 10.27
455 11.36
485 12.44
195 5.66
235 6.96
280 8.26
320 9.56
360 10.86
400 12.16
440 13.44
480 14.74

Scan Applications

on mA
Axial CTDIw =
Time
Helical CTDIw/
pitch = CTDIvol
190 7.25
230 8.95
275 10.63
315 12.32
355 14.03
400 15.72
440 17.39
480 19.07
185 8.93
230 11.02
270 13.11
315 15.22
LARGE BODY/LARGE/40 mm 1 0.516/0.984/1.375 Axial
355 17.33
395 19.42
435 21.5
475 23.59
280 7.63
320 8.82
365 10.01
MEDIUM BODY/LARGE/40 mm 0.5 0.516/0.984/1.375
405 11.2
445 12.37
485 13.55
280 9.01
320 10.42
360 11.84
400 13.25
440 14.64
480 16.05

Scan Applications

on mA
Axial CTDIw =
Time
Helical CTDIw/
pitch = CTDIvol
275 11.57
315 13.4
355 15.26
400 17.08
440 18.9
480 20.72
270 14.26
315 16.54
355 18.82
MEDIUM BODY/LARGE/40 mm 1 0.516/0.984/1.375
395 21.08
435 23.24
475 25.6
* Note CTDIvol will change according to pitch settings

GSI Assist is selected in the kV/mA collection from the scan settings screen Refer to GSI Assist mA mode
settings and GSI Manual Settings.
If a Scout is available and GSI Assist mA Mode is enabled, the system selects the GSI acquisition mode
to best meet the Noise Index set in the protocol.
If a Scout is not available, GSI Manual mA mode will be selected and the initial GSI preset family
defined for the Clinical Category and Clinical Identifier will be selected. The user may change the mA
value.
12.7.11 GSI Manual

GSI Manual allows the user to select any GSI Profile which contains a GSI Family (Rotation Speed,
Pitch, Focal Spot, Aperature, SFOV). mA value can then be selected to match dose to a prior scan.
When the mA mode is GSI Manual, the GSI Profile selected in kV and mA collection does not determine
the recon settings. Recon settings are applied based on Clinical Category and Clinical Identifier
selected in the Anatomy Selection collection in secondary recon settings. The recon settings used are
for the GSI Profile mapped to the Clinical Category and Clinical Identifier defined in GSI Profile Editor.
Refer to Clinical Identifiers for this mapping.

Scan Applications
12.7.12 ASiR-V in conjunction with GSI data

ASiR-V works in a similar manner to single KV ASiR. It applies a level of volumetric noise reduction
to the images based on the level chosen. Levels of 0 to 100 percent in 10–percent intervals may be
chosen. Levels above 50% will not adjust the GSI Assist settings.
NOTE
When choosing GSI ASiR-V greater than 50%, care should be taken to ensure dose levels
are high enough based on clinical intent.
12.7.13 GSI Annotation

• QC or Quality Check
• MD label, material and basis pair, and MD unit for Material Density images
• Mono for Monochromatic image with keV (40 - 140)
• M to indicate MAR was selected
• The Recon Mode is annotated + for Plus
12.7.14 GSI Recon
12.7.14.1 GSI QC Recon

QC images are generated for every GSI acquisition. These are high kVp images where all standard
image corrections have not been applied. GSI QC images will not be auto-transferred.
12.7.14.2 Primary Recon

The Primary Recon is prescribed in the Scan Settings window on the scan monitor. Refer to Recon
Parameter descriptions in the Scan chapter.
12.7.14.3 GSI Assist Link/CID Link

Pre-scan or post scan Secondary Recons can be linked or unlinked to the recon settings contained in
the GSI Profile mapped to the selected Clinical Category and Clinical Identifier or direct selection of a
GSI profile by turning off CID Link. This streamlines the GSI workflow by automatically pre-populating
secondary recon prescriptions with parameters settings (GSI image type, Data File, MAR On/Off) that
are appropriate for the Clinical indication.
When the GSI mA mode is GSI Assist and GSI Assist Link is turned On, the recon settings will be those
defined for the GSI Profile mapped to the Clinical Category selected in the Patient Collection and
Clinical Identifier selected in Anatomy Collection. These two settings determine the GSI Profile that
will be used as defined in the GSI Profile Editor GSI Profile to Clinical Identifier mapping. Alternatively,
a GSI Profile can be selected directly by turning CID Link off.

Scan Applications
The Clinical Category and Clinical Identifier will populate in secondary recon Anatomy Selection to the
same selection as the Patient Collection Clinical Category and Clinical Identifier in the scan Anatomy
Selection when a secondary GSI Recon is added. You can select a different Clinical Category and
Clinical Identifier by turning Off GSI Assist Link.
When the GSI mA mode is GSI Manual and GSI Assist Link is turned On, recon settings are applied
based on Clinical Category and Clinical Identifier selected in Anatomy Selection in secondary recon
settings. The recon settings used are for the GSI Profile mapped to the Clinical Category and Clinical
Identifier defined in GSI Profile Editor. See Clinical Identifiers for this mapping.
12.7.14.4 GSI Recon Task Settings

Pre-scan or post scan secondary GSI recons will display a common parameters task as indicated by
and GSI specific recon tasks.
NOTE
A GSI-specific recon task cannot be duplicated. To create an additional GSI-specific
recon, duplicate the common parameter task and assign the GSI-specific recon task the
desired image type.
Common parameters are the same across all GSI specific recon tasks and include the following:
Recon Settings:
• Thickness
• Recon Options
• IQ Enhance
• Interval
• Flip/Rotate
Anatomy Selection:
• Start
• End
• Number of images
• DFOV
• A/P Center
• R/L Center
• Clinical Identifier

Scan Applications
NOTE
Use of appropriate CID is critical to image quality for the following specific recon
tasks:
• Gout analysis images must use CID extremity.gout
• Non-contrast head images must use CID neuro.routinehead.
GSI recon-specific parameters include the following:

Recon Settings:
• GSI Image Type
• GSI Image type specific parameters
• Recon Type
• ASiR-V
• DLIR
• Window Width
• Window Level
Output Options — series description

Transfer Options — host selection
NOTE
Only 10 GSI-specific tasks can be added in each secondary recon.
NOTE
DLIR for GSI can be prescribed only if the Recon Type is Standard and if the interval is
equal to or one half the slice thickness. DLIR for GSI may not be prescribed under the
following conditions:
• SFOV is Head or Cardiac
• GSI Image Type is High kVP
• Scan Range is less than 40 mm
NOTE
Three levels of Enhanced Contrast are available for GSI: EB1, EB2, and EB3. Enhanced
Contrast for GSI may be prescribed only under the following conditions:
• SFOV is Head, Small Head, or Ped Head
• Recon Type is Stnd or Soft
• GSI Image Type is Monochromatic 70 keV, 65 keV, or 60 keV
• DataFile is OFF

Scan Applications
12.8 Volume Shuttle (Axial)
12.8.1 Overview
NOTICE

ON THIS SYSTEM.
The following applications can be applied in Scan. If an application is not available, it may not be
included with your system options.
Volume Shuttle is specially designed for perfusion scanning and can extend the coverage of
tissue imaged, thus dispersing the dose over a wider area and decreasing peak skin dose. The
temporal sampling rate is reduced for any specific anatomic location compared with continuous and
intermittent exposure modes where the table remains stationary. The user must ensure that the
sampling frequency remains adequate for the post-processing software.
In axial shuttle mode, scanning is performed at two adjacent axial locations by moving the table
between X-ray exposures, thereby increasing the amount of anatomy that is imaged. As with
intermittent scanning, the X-rays are not turned on continuously, and thus peak skin dose and overall
delivered X-ray radiation dose are reduced (compared with continuous mode), while overall exam time
remains the same.
12.8.2 Volume Shuttle Theory

Shuttle Mode Imaging is a scanner capability that allows for extended longitudinal coverage by
shuttling the patient back and forth during the scan. VolumeShuttle (Axial) provides extended
perfusion and dynamic CT angiography coverage beyond conventional cine scanning. Since the
patient is transported back and forth between two adjacent scan locations, the sample interval is
increased.
Volume Shuttle Mode achieves an 80 mm wide coverage, all within a single scan and contrast injection.
There are two scans and two table moves for one pass, the timing of one pass with specific gantry
rotation speed I called Min Time Between Passes (MTBP) and
The ISD is fixed to 0.96 sec for manual mA mode, and 1.5sec for SmartmA mode.

Scan Applications
The table control algorithm for Volume Shuttle Mode has been optimized to provide the shortest
possible transit time between the two locations. The average sample interval is 2.92 seconds (0.5sec
rot) or less, even for large patients (up to 181 kg / 400 lbs.), and easily meets the time sampling
requirements described previously.
Another benefit of Volume Shuttle data is that it can be reconstructed to thin slice sections, e.g. 0.625
mm thick. The resulting images can be used as a dynamic 4D CT angiogram. The table “Two” position
is available only with 40 mm detector coverage axial mode.

Scan Applications
If the temporal sampling period extends beyond 3.2 seconds, there may be errors present in the data
when processed by Head CT Perfusion. There is pop-up to notify the operator the MTBP is larger than
3.2 seconds together with warning scan at the same location after clicking Confirm.

Scan Applications
SmartmA will increase the MTBP beyond the 3.2 seconds and extend the temporal sampling period.
If the MTBP is smaller than 3.2 seconds, only a message indicating multiple scans at same location
displays.
ODM / Auto prescription is not compatible with VolumeShuttle.

Scan Applications
12.8.4 Reconstruction
There is no QC image for Axial Shuttle to secure the timing performance, and the Autoview is enabled
with diagnostic level images for he user. The user can monitor the Autoview images, if no contrast
agent during the exposure, pause or stop the scan to save the doses.
12.8.5 Working with an Injector and Axial Shuttle

Refer to Enhanced Xtream Injector

1. Set up the patient's information.
2. Set up and position the patient.
Position the patient to a head-first orientation.
Make sure the patient is securely positioned.

Scan Applications
Wrap the table straps around the body to prevent the arms from dragging on the table that might
interfere with table travel in/out of the gantry.
3. From the Protocol Selection window, select a protocol and click Accept.
4. Acquire a scout.
5. From the Scan Settings window, click Continue.
6. Click Scan Type, then select Axial.
7. For Rotation Time, click 0.5.
Rotation time should be 0.5 seconds to meet temporal sampling requirements for perfusion
processing.
8. Click Coverage Speed.
9. Select Two as the Table position
10. Set the Detector Coverage to 40mm.
For the Start/End Location, the coverage is limited to 80 mm.
The Number of Images is determined by the settings in Thick/Speed.
Set the Slice Thickness to 5 mm. Prospectively only 2.5 and 5 mm slices can be reconstructed.
Thinner slices can be created in Secondary Recon.
Set the Coverage time or Number of Passes to the desired value to meet clinical requirements. At
least 13 passes are needed. The maximum number of passes is 60.
Set the SFOV, as needed.
For kV, click 80.
Set the mA to 500.
11. Set the Timing parameters, as needed.
Set the Prep Delay to 5.
The user can find the total elapsed time by checking Total Scan Time.


Scan Applications

Lung Cancer Screening
13 Lung Cancer Screening
13.1 Indications for Use

Scanners with the Lung Cancer Screening Option installed are indicated for using low-dose CT for
lung cancer screening. The screening must be performed within the established inclusion criteria
of programs/protocols that have been approved and published by either a governmental body or
professional medical society.
Refer to the clinical literature, including the results of the National Lung Screening Trial (The New
England Journal of Medicine, 2011; 365:395-409) and subsequent literature for additional information.
13.2 Lung Cancer Screening Overview

CT Lung Cancer Screening has been performed and scientifically analyzed in several large clinical
trials globally. The trial results were positive toward the conclusion that CT Lung Cancer Screening
provides benefit to certain at risk populations taking into account smoking history and age, using
low-dose protocols. The outcome of these trials provided valuable information for the United States
Preventative Services Task Force and, subsequently, the Center for Medicare and Medicaid Services
(CMS) decision on lung cancer screening.
• I-ELCAP (International Early Cancer Action Program) - The New England Journal of Medicine,
October 26, 2006
• NLST (National Lung Screening Trial) - The New England Journal of Medicine, August 4, 2011
• USPSTF (US Preventative Service Task Force) - Annals of Internal Medicine, March 4, 2014
• CMS (Centers for Medicare and Medicaid Services) - Decision Memo for Screening for Lung Cancer
with Low Dose Computed Tomography (LDCT) (CAG-00439N), February 5, 2015
Below is a description of each of the above mentioned trials and decisions.
13.2.1 I-ELCAP (International Early Lung Cancer Action Program)

The I-ELCAP trial was a multi-center, multi-national trial that screened 31,567 asymptomatic persons
at risk for lung cancer using low-dose CT from 1993 through 2005, and from 1994 through 2005. 27,456
repeat screenings were performed 7 to 18 months after the previous screening.
I-ELCAP was designed to determine the difference in proportion of early stage disease between two
methods of early diagnosis (chest radiography and low-dose Computed Tomography-CT) as measured
by the increase in the proportion of Stage I diagnoses following a well-defined regimen of screening.
This regimen of screening recommended and defined the further workup of findings on the CT scan
before the subsequent round of screening. The regimen is critical as it embodies the concept that
screening is a clinical diagnostic process, not simply a standalone test. The study determined that CT
screening according to the I-ELCAP regimen can detect clinical Stage I lung cancer in a high proportion of
persons when it is curable by surgery.

By pooling the data collected under this protocol from many national and international institutions,
I-ELCAP was able to show, in several 2006 publications that:
1. Lung cancers diagnosed under screening were typically small, including small-cell cell
carcinomas.
2. The estimated cure rate of patients whose lung cancer was diagnosed under screening.
After long-term follow-up of 31,456 asymptomatic participants, 484 of whom had lung cancer
diagnosed under CT screening of which 414 (86%) had clinical Stage I disease, the estimated overall
cure rate for the 484 patients diagnosed under CT screening was 80% (95% CI: 74% - 85%).
In addition to the above, findings from this study and its protocol that included only high risk patients,
the following other conclusions were made.
CT screening creates a counseling opportunity that results in greater smoking cessation.
The cost of CT screening for lung cancer compares favorably with breast, cervical and colon cancer
screenings.
Research is ongoing, incorporating larger pools of patient data to reaffirm early findings and suggest
new directions for future research and recommendations.
13.2.2 NLST (National Lung Screening Trial)

The NSLT enrolled 53,454 persons at high risk for lung cancer at 33 medical centers in the United
States, from August 2002 through April 2004. Participants were randomly assigned to undergo three
annual screenings with either low-dose CT (26,722 participants) or single-view PA (posterior-anterior)
chest radiography (26,732). Screening took place from August 2002 through September 2007. Data
were collected on cases of lung cancer and deaths from lung cancer that occurred through December
31, 2009.
Eligible participants were between 55 and 74 years of age at the time of randomization, had a history
of cigarette smoking of at least 30 pack-years, and, if former smokers, had quit within the previous 15
years. Persons who had previously received a diagnosis of lung cancer, had undergone chest CT within
18 months before enrollment, had hemoptysis, or had an unexplained weight loss of more than 6.8 kg
(15 lb) in the preceding year were excluded.
The NLST compared two ways of detecting lung cancer: low-dose helical Computed Tomography
(CT)—often referred to as spiral CT—and standard chest X-ray. Helical CT uses X-rays to obtain a
multiple-image scan of the entire chest, while a standard chest X-ray produces a single image of the
whole chest in which anatomic structures overlie one another.
The study found a relative reduction in mortality from lung cancer with low-dose CT screening
compared to chest radiography of 20.0% (95% CI, 6.8 to 26.7; P = 0.004). Additionally, the rate of death
from any cause was reduced in the low-dose CT group, as compared with the radiography group, by
6.7% (95% CI, 1.2 to 13.6; P = 0.02).
Adenocarcinomas and squamous cell carcinomas were detected more frequently at an earlier stage
by low-dose helical CT compared to chest radiography. Small-cell lung cancers, which are very
aggressive, were infrequently detected at early stages by low-dose helical CT or chest X- ray.

13.2.3 USPSTF (U.S. Preventative Services Task Force)

The U.S. Preventive Services Task Force is an independent group of national experts in prevention and
evidence-based medicine. The Task Force works to improve the health of all Americans by making
evidence-based recommendations about clinical preventive services such as: screenings, counseling
services, preventive medications. Their recommendations are based on a rigorous review of existing
peer-reviewed evidence.
These recommendations apply only to people who have no signs or symptoms of the specific disease
or condition that the screening, counseling or preventive medication targets.
Recommendations address only services offered in the primary care setting or services referred by a
primary care clinician.
Through acts of the U.S. Congress, the U.S. Department of Health & Human Services’ Agency for
Healthcare Research and Quality (AHRQ) has been authorized to convene the Task Force and to provide
ongoing scientific, administrative, and dissemination support to the Task Force.
The USPSTF recommends annual screening for lung cancer with low-dose computed tomography in
adults aged 55 to 80 years who have a 30 pack-year smoking history and currently smoke or have quit
within the past 15 years. Screening should be discontinued once a person has not smoked for 15 years
or develops a health problem that substantially limits life expectancy or the ability or willingness to
have curative lung surgery. It received a B grade.
13.2.4 Centers for Medicare and Medicaid Services (CMS)

When making national coverage determinations concerning additional preventive services, CMS
applies the statutory criteria in the Social Security Act and associated regulations, and evaluates
relevant clinical evidence to determine whether or not the service is reasonable and necessary for the
prevention or early detection of illness or disability, is recommended with a grade of “A” or “B” by the
USPSTF, and is appropriate for individuals entitled to benefits under Part A or enrolled under Part B of
the Medicare program.
CMS uses the initial public comments to inform its proposed national coverage determination. CMS
responds in detail to the public comments on a proposed national coverage determination when
issuing the final national coverage determination.
CMS’s February 5, 2015 Final National Coverage Determination on Screening for Lung Cancer with Low
Dose Computed Tomography (LDCT) determined
that the evidence is sufficient to add a lung cancer screening counseling and shared decision
making visit, and for appropriate beneficiaries, annual screening for lung cancer with low-
dose computed tomography (LDCT), as an additional preventive service benefit under the
Medicare program.
It has a comprehensive list of criteria that must be met, part of which is the Beneficiary Eligibility
Criteria:
• Age 55 – 77 years
• Asymptomatic (no signs or symptoms of lung cancer)

• Tobacco smoking history of at least 30 pack-years (one pack-year = smoking one pack per day for
one year; 1 pack = 20 cigarettes)
• Current smoker or one who has quit smoking within the last 15 years; and receives a written order
for LDCT lung cancer screening that meets certain criteria.
In conclusion, these studies and analyses provided valuable information on the importance of low-
dose Lung Cancer Screening for high risk individuals when performed within the established inclusion
criteria of programs/protocols that have been approved and published by either governmental body
or professional medical society.
13.3 Appropriateness and Inclusion Criteria

Additional information concerning criteria for patient eligibility for Low-Dose CT Lung Cancer
Screening and protocol definition can be found in material provided by the following organizations in
their guidance documents:
• www.aapm.orgAmerican Associations of Physicists in Medicine Lung Screening Protocols –
Provides direction on dose and protocols for various CT systems.
• www.ACR.orgAmerican College of Radiology Lung Screening Resources – Provides overview of
the ACR accreditation requirements for Lung Cancer Screening sites.
• www.ACR.orgACR Practice Parameters for Performance and Reporting of Lung Cancer
Screening Thoracic Computed Tomography (CT) – Provides overview of the ACR accreditation
requirements for Lung Cancer Screening sites.
• www.cms.govCenter of Medicare and Medicaide Services – Decision memo for Screening of Lung
Cancer with Low Dose – Provides patient eligibility, reading radiologist eligibility criteria, and
radiology site eligibility criteria.
• www.uspreventiveservicestaskforce.orgUS Preventative Services Task Force: Screen for Lung
Cancer: US Preventive Services Task Force Recommendation Statement – Provides information
which includes patient eligibility, recommendations, risk assessment, screening tests, treatment,
balance of benefits and harm, and other relevant USPSTF recommendations.
• www.nccn.orgNational Comprehensive Cancer Network – NCCN Clinical Practice Guidelines in
Oncology – Lung Cancer Screening. These are valuable resources for you to refer to when creating
and implementing a Lung Cancer Screening
It is advised that you refer to these references when establishing a Lung Cancer Screening program at
your institution and developing CT protocols for Lung Cancer Screening.
13.3.1 Patient Eligibility

Patient eligibility is determined by the specific established inclusion criteria of programs/ protocols
that have been approved and published by either a governmental body or professional medical
society that your site is following. Current (as of publication date of this manual) examples of patient
eligibility requirements from the USPSTF and CMS are as follows:
The USPSTF recommends annual screening for lung cancer with low-dose computed tomography in
adults aged 55 to 80 years who have a 30 pack-year smoking history and currently smoke or have quit
within the past 15 years. Screening should be discontinued once a person has not smoked for 15 years

or develops a health problem that substantially limits life expectancy or the ability or willingness to
have curative lung surgery.
The CMS Beneficiary Eligibility Criteria is:
• Age 55 – 77 years;
• Asymptomatic (no signs or symptoms of lung cancer);
• Tobacco smoking history of at least 30 pack-years (one pack-year = smoking one pack per day for
one year; 1 pack = 20 cigarettes);
• Current smoker or one who has quit smoking within the last 15 years; and
• Receives a written order for LDCT lung cancer screening that meets certain criteria
13.4 GE Lung Cancer Screening Protocol

Considerations
GE provides a Lung Cancer Screening Protocol Option that includes Lung Cancer Screening (LCS)
protocols within the GE Reference Protocols provided with the CT Scanner.
The LCS protocols have been evaluated via Contrast to Noise Ratio and Visual Inspection on phantoms
to provide sufficient image quality for Low Dose CT Lung Cancer Screening Use. These protocols are for
adults who meet the eligibility criteria for lung cancer screening. The LCS protocols provide acquisition
parameters for small, medium and large patients based on the sizing provided by AAPM.
Table 113 Patient Sizing Chart provided by AAPM
Patient Size Approximate Weight Approximate Weight Approximate CTDIvol

(kg) (lb) (mGy)
Small 50-70 110-155 0.25 - 2.8
Average 70-90 155-200 0.5 - 4.3
Large 90-120 200-265 1.0 – 5.6
LCS protocols are designed and intended as a starting point. They should be reviewed with your
Radiologist, Physicist and Radiation Safety Officers prior to clinical use and should be monitored as
revised as needed to meet the clinical needs of your department and the Lung Cancer Screening
program protocol that your site is following.
The Lung Cancer Screening Option installs three size based protocols in the GE Reference Protocols.
To customize LSC protocols follow instructions in Protocol Management to create user protocols by
copying and pasting a GE Reference Lung Cancer Screening protocol into User Protocols.

NOTE
Use of doses substantially below those found in the GE CT Low Dose Lung Cancer
Screening reference protocols may not produce clinically acceptable image quality,
primarily due to high image noise and low signal strength. Several other CT image
quality metrics may be affected as well, such as: CT Number Accuracy, CT Number
Uniformity, MTF, Visual Resolution (Image Artifacts), Noise Power Spectrum, Slice
Thickness and Contrast to Noise Ratio (CNR). The protocols defined in the Reference
Protocol Guide have been evaluated via CNR and Visual Inspection on phantoms to
provide sufficient image quality for Low Dose CT Lung Cancer Screening use.
When evaluating or changing Lung Cancer Screening Protocols consider the following:
Follow your department Quality Assurance guidelines. For more information, review the Quality
Assurance chapter in the Technical Reference Manual for your system. No additional QA procedures
are required for Lung Cancer Screening use beyond those provided in the Technical Reference Manual
or specified in your department's QA procedures
13.4.1 Acquisition and Reconstruction Guidelines

AAPM recommendation of a single end inspiration breath hold acquisition and acquisition guidelines
for acquiring data for Low-Dose CT Lung Cancer Screening with regard to important factors in
the protocol for kV, mA, pitch, rotation time, and slice thickness. Recommendations for image
reconstruction image thickness of ≤2.5mm with ≤1mm preferred. Reconstruction of coronal and
sagittal reformation as well as MIPS may be helpful and encouraged.
Each protocol will need to have reconstructions built for physicians’ preferred reading slice thickness
to build reformat images from lung and mediastinal reconstruction algorithms. Direct Multi-Planar
Recon (DMPR) can be included in the protocol to automatically create reformatted images in sagittal
and coronal planes in average and MIP format.
GE Lung Cancer Screening Reference Protocols are provided for Manual mA mode.
13.4.2 Dose Guidelines

CMS indicates for a patient of 5’7” and approximately 155 pounds (which is also AAPM’s definition of
an average patient), the CTDIvol should be ≤3.0 mGy (milligray) measured using the 32cm diameter
CTDI phantom for a scan range of 250 mm with appropriate reduction in CTDIvol for smaller patients
and increases in CTDIvol for larger patients.
AAPM provides information depending on patient size such as the approximate CDTIvol as shown
above; they recommend using AEC or a manual method to account for patient size:
Examples of manual adjustment may include (but are not limited to): Starting protocol parameters are
provided in the GE Reference Protocols provided with Lung Cancer Screening option.
• Reducing the mAs for small patients (defined below) by 50%
• Increasing the mAs for large patients (defined below) by 50-100%
Each site needs to establish dose guidelines for patient size.

13.4.3 Automatic Exposure Control

The GE LSC protocols are set up with manual mA. If you choose to create LCS protocols utilizing
auto exposure control (AEC) features SmartmA or SmartmA with ODM, scan parameters including
AEC parameters must be chosen to carefully balance patient radiation dose and image performance.
The CDTIvol values should be reviewed for patients to ensure target dose level is being achieved for
different patient sizes. Adjustment to mA and NI values may be needed to ensure the scan meets the
radiologist’s IQ criteria and lung cancer screening needs.
It is also important to note that if SmartmA is included in the protocol, the CTDIvol that is initially
displayed when the protocol is loaded is based on what the manual mA is set at if SmartmA
would be turned off. This is because in order to provide an accurate prediction of the CTDIvol for
a SmartmA acquisition, the information from the last scout taken must be used. The displayed CTDIvol
is automatically updated once the scout is taken for SmartmA scans. SmartmA may be used. However,
attention should be given to the CTDIvol for smaller patients and patients whose AP diameter is
much smaller than the RL diameter where overall dose could be reduced significantly from the target
CTDIvol.
13.4.4 Noise Reduction Features

Noise Reduction Features, such as Adaptive Statistical Iterative Reconstruction (ASiR-V), Deep Learning
Image Reconstruction (DLIR), can be applied to Lung Cancer protocols. ASiR-V and DLIR are compatible
with Lung Cancer Screening protocols. However, it is recommended no further dose reduction beyond
that provided in the reference protocol should be prescribed if ASiR-V or DLIR is applied. This is
because at the very low doses, and hence low signal strength and high noise, used in CT Lung Cancer
Screening, ASiR-V or DLIR are close to their technical design limits for enabling further dose reduction.
However, both ASiR-V and DLIR are able to improve image quality, especially the contrast-to-noise
ratio, at these dose levels.
13.4.5 Enabling Dose Check Notification

Dose Check is a feature that provides the ability to display a notification to the user if the dose exceeds
a predetermined CTDIvol value prescribed in the protocol.
Given the low-dose requirement for performing CT Lung Cancer Screening exams, GE suggests
enabling Notification Values and setting the Notification Value to a factor of 2 for the CTDIvol,
inherently contained in our Lung Cancer Screening protocols. The ultimate decision for setting
Notification Values is a clinical one that must be made by the site.
If the Notification Value is exceeded, the CTDIvol and/or DLP is highlighted in the Dose Information
area. At the confirm prompt, the user is prompted for a Diagnostic Reason to be able to continue
scanning. The Diagnostic Reason is recorded in the Dose Check Logs for review by the Dose Check
Administrator.
13.4.6 Considerations for Acquisition and Post-Processing Patient

Scanning
Several points need to be taken into consideration when scanning for Lung Cancer Screening: .

• Patient Positioning and Centering

Patient Centering is important for SmartmA. It enables the system to correctly calculate the
mA needed for a scan. If using Automatic Exposure Control (SmartmA) and the patient is more
than 2 cm off isocenter, adjust the patient position to the table height recommended by patient
centering and repeat the scout in a new series.
• Breathing Instructions
AutoVoice instructions should be given so the patient is holding their breath in inspiration.
Consider using AutoVoice option Preset Delay Time for patients who need more time to hold their
breath. The Preset Delay Time will delay X-Ray ON 0-7 seconds after the AutoVoice message is
completed, allowing patients more time to follow the breathing instructions and may result in
less exams with breathing motion.
13.4.7 Image Analysis Technical Considerations

WARNING DEPENDING ON WW/WL SETTINGS, OBJECTS MAY DISPLAY DIFFERENTLY. CHECK WL/WW
BEFORE DEPOSITING MEASUREMENT POINTS. CAUTION When performing measurements using the
Basic Display software tools, the user shall be aware of the various factors that limit the accuracy
of the results. The accuracy of measurements obtained with on-view graphics depends on various
factors, in particular the size of the ROI being measured. The rotation angle of a graphic (e.g., ellipse)
also affects accuracy. • Using a straight line segment or straight line distance graphic, measurement
accuracy for the displayed length is equal to +/– one image pixel size. • Using angle graphics,
measurement accuracy depends on the length of the segments, and improves as the length of the
segments increases. As an example, for an angle measured between segments, which are 100x the
image pixel size, the measurement accuracy of the displayed angle value is equal to +/– 1 degree.
CAUTION Distance measurements are valid only if all trace segments are longer than the inter-slice
distance. 2D Measurements • Distance measurements are accurate to within the inter-slice distance. •
Angles measured between segments at least five times larger than the inter-slice distance are accurate
to ten degrees. Accuracy improves with the length of the segment. When you place the measurement
points yourself, the apparent diameter can differ by one or more pixels depending on the W/L settings,
thereby adding another factor of uncertainty. Making a Measurement 1. Select the desired series from
the Image Browser. 2. Open Exam 3. Select viewport to display images 4. Page through the images
and identify the axial image showing the widest diameter of nodule. 5. Select Measure/Annotate to
measure the distance and angle between two points. 6. Select and position each handle to set the
measurement points. 7. Obtain the value of the measurement in the ROI result area of the viewport
13.4.7.1 Nodule Sizing

Several points need to be taken into consideration when sizing nodules using the measurement tools
available on your CT system.
CAUTION
WHEN PERFORMING MEASUREMENTS USING THE BASIC VIEWER DISPLAY

SOFTWARE TOOLS, THE USER SHALL BE AWARE OF THE VARIOUS FACTORS
THAT DETERMINE THE ACCURACY OF RESULTS.

CAUTION
USING A STRAIGHT LINE SEGMENT OR STRAIGHT LINE DISTANCE GRAPHIC,

MEASUREMENT ACCURACY FOR THE DISPLAYED LENGTH IS EQUAL TO +/–
ONE IMAGE PIXEL SIZE. ACCURACY OF ON-VIEW MEASUREMENTS
13.4.7.2 Accuracy of On-View Measurements
WARNING
DEPENDING ON WW/WL SETTINGS, OBJECTS MAY DISPLAY DIFFERENTLY.

CHECK WL/WW BEFORE DEPOSITING MEASUREMENT POINTS.
CAUTION
WHEN PERFORMING MEASUREMENTS USING THE BASIC DISPLAY

SOFTWARE TOOLS, THE USER SHALL BE AWARE OF THE VARIOUS FACTORS
THAT LIMIT THE ACCURACY OF THE RESULTS.
The accuracy of measurements obtained with on-view graphics depends on various factors, in
particular the size of the ROI being measured. The rotation angle of a graphic (e.g., ellipse) also
affects accuracy.
• Using a straight line segment or straight line distance graphic, measurement accuracy for the
displayed length is equal to +/– one image pixel size.
• Using angle graphics, measurement accuracy depends on the length of the segments, and
improves as the length of the segments increases. As an example, for an angle measured between
segments, which are 100x the image pixel size, the measurement accuracy of the displayed angle
value is equal to +/– 1 degree.
CAUTION
DISTANCE MEASUREMENTS ARE VALID ONLY IF ALL TRACE SEGMENTS ARE

LONGER THAN THE INTER-SLICE DISTANCE.
2D Measurements
• Distance measurements are accurate to within the inter-slice distance.
• Angles measured between segments at least five times larger than the inter-slice distance are
accurate to ten degrees. Accuracy improves with the length of the segment.
When you place the measurement points yourself, the apparent diameter can differ by one or more
pixels depending on the W/L settings, thereby adding another factor of uncertainty.
Making a Measurement

1. Select the desired series from the Image Browser.

2. Open Exam.
3. Select viewport to display images
4. Page through the images and identify the axial image showing the widest diameter of nodule.
5. Select Measure/Annotate to measure the distance and angle between two points.
6. Select and position each handle to set the measurement points.
7. Obtain the value of the measurement in the ROI result area of the viewport.

Cardiac
14 Cardiac
14.1 Overview
This chapter covers Cardiac scanning in depth. This includes Calcium scoring scan, patient prep, ECG
setup and testing, scan parameters as well as cardiac profiles and some post processing options.
14.2 Patient preparation and set up before Scanning

Follow these steps to prepare the patient for the cardiac exam.
14.2.1 Consent Forms

If a consent form is required, review the form with the patient and get a signature.
14.2.2 Exam Prep Instructions

Advise the patient of the following:
• Fast for four hours prior to the exam.
• No caffeine 12 hours prior to the exam.
• No cardiovascular exercise prior to the exam.
• Thoroughly explain all phases of the scan before you start the exam to keep the patient as calm as
possible.
Administration of Beta Blockers and/or Sublingual Nitroglycern Spray can be used according to your
site's policy.
Please refer to the Society of Cardiovascular CT Guidelines at www.scct.org for more patient
preparation information.
14.2.3 Breathing instructions

Diagnostic cardiac images are dependent on the patient’s heart rate during the data acquisition; a
calm patient keeps the heart rate steady with a repeatable rhythm. Therefore, breathing instructions
are critical for a successful cardiac scan.
Follow these breathing instruction guidelines:
• Deliver the same instructions for each series starting with the scout scan.
• Program cardiac breathing instructions with Auto Voice to deliver consistent breathing
instructions.
• The voice instructions should be 10 seconds or longer so that the patient is breathing slowly.
• After you say, "take a breath in and hold it," allow 3 to 5 seconds of silence before you click the
Stop recording button. This gives the patient enough time to hold his breath before the scan

Cardiac
starts and for the heart rate to stabilize before the scan. This time prevents the patient from
breathing in during data acquisition, which results in image motion.
• Use the Preset Delay feature in Auto Voice to program an additional 1–7 seconds prior to X-ray On,
as needed for each patient.
• The scan time for the contrast enhanced cardiac gated acquisition is approximately 1 second for
a single scan location that covers the entire heart. The heart rate stabilizes 2–7 seconds after a
breath hold. Therefore, have the patient start the breath hold 3–5 seconds prior to X-ray exposure.
Watch the ECG waveform display so you can determine when the patient's heart rate stabilizes
within the breath hold. Adjust your breath hold instructions to achieve as stable of a heart rate as
possible during the contrast enhanced cardiac gated scan.
• According to your physician and site's policy, deliver 2–4 liters of oxygen via nasal cannula if the
patient has difficulty holding his breath. This can help lower the heart rate.
• Practice the breathing instructions with the patient.
14.2.3.1 Automatically record the heart rate during breath hold

Auto Gating requires that the heart rate be recorded during a patient breath hold to provide profile
feedback. Use this procedure to automatically record the patient's heart rate and variability during the
Scout, Timing Bolus, Calcium Scoring (Smart Score), or other CT scan series.
A recording of at least 5 seconds is required to gather enough data to evaluate the heart rate and
variability. The breath hold duration for the scan must be at least as long as the Breath Hold Recording
Length setting or the recording will not be used.
3. From the System Preferences window, click the ECG tab.
4. In the Breath Record Length area, adjust the time. Valid recording lengths are 5–15 seconds.
The system will apply the Breath Hold Recording Length time and the Auto Voice message
prescribed in Auto Voice.
• If no message is selected, an Auto Voice message will not be played and you will need to
provide manual breathing instructions.
• The breathing commands should be the same as those given for the contrast enhanced scan.
NOTE
The patient’s heart rate is automatically recorded during the Scout, Timing Bolus,
Calcium Scoring (Smart Score), or other CT scan series as long as the scan duration
is at least as long as the breath hold duration.
NOTE
Auto Gating uses the patient’s heart rate prior to the breath hold recording up to the
Irregular Beat Window Length. The system preset is set to 60 seconds.
5. Click Save.

Cardiac
14.2.3.2 Manually record the heart rate during breath hold

Auto Gating requires that the heart rate be recorded during a patient breath hold to provide profile
feedback. Use this procedure to manually record the patient's heart rate and variability when other
compatible series with breath holds cannot be used, or the patient’s heart range has changed
significantly.
This method may be useful when using Smart Prep instead of a Timing Bolus to initiate the scan
at optimal contrast enhancement. You may also initiate a practice breath hold recording when the
patient’s heart rate changes or any time prior to the contrast enhanced scan.
A recording of at least 5 seconds is required to gather enough data to evaluate the heart rate and
variability. The breath hold duration for the scan must be at least as long as the Breath Hold Recording
Length setting or the recording will not be used.
4. In the Breath Record Length area, adjust the time. Valid recording lengths are 5–15 seconds.
The system will apply the Breath Hold Recording Length time and the Auto Voice message
prescribed in Auto Voice.
• If no message is selected, an Auto Voice message will not be played and you will need to
provide manual breathing instructions.
• The breathing commands should be the same as those given for the contrast enhanced scan.
NOTE
The patient’s heart rate is automatically recorded during the Scout, Timing Bolus,
Calcium Scoring (Smart Score), or other CT scan series as long as the scan duration
is at least as long as the breath hold duration.
5. Click Apply or Save.
6. Click Record New HR from the Acquisition Window and Heart Rate widget with Auto Gating “on”.
• The system indicates Recording Prep while the selected Auto Voice message plays, giving
pre-message breathing instructions.
• The system indicates Recording in blue while the Heart Rate is being recorded.
• When recording is completed, Auto Voice plays the post-message breathing instructions.
7. A jump point is added to the viewer. Click the jump point to review the recorded trace.
NOTE
If a patient's heart rate characteristics have changed, use Record to re-record the
heart rate during a breath hold and generate new scan settings.

Cardiac
14.2.3.3 Manual Mode Breath Hold

In some cases, the patient may not be able to hold their breath. Use this procedure to manually enter
the patient’s heart rate, variability and irregular beats.
1. From the Gating Based “On” window, select Manual.
The Manual window opens with presets for heart rate, variability and irregular beats.
2. Edit these parameters based on the patient’s heart rate.
14.2.4 IV setup and contrast

• To conserve CT table time, set up the patient IV line outside the scan room.
• Explain the contrast injection and potential effects, even if the patient has had a previous contrast
injection. Reassure the patient that what he feels during the injection is normal and to remain
relaxed during the scan. An informed patient is a calm, less anxious patient.
• Have the injector loaded with contrast by a trained person authorized by your site. The total
volume and contrast strength is site dependent.
• For single-barrel injectors: load with contrast.
• For dual-barrel injectors: load one syringe with contrast media and one syringe with saline.
14.2.5 Attach ECG electrodes to the patient

Use this procedure to attach electrodes to the patient for an ECG-gated scan. Use of a patient
grounding strap further improves the ECG waveform signal quality for ECG-gated scans. This can be
used optionally, but should not replace the recommended process for patient preparation.
1. Bring the patient into the scan room.
2. Verify that you have a signed consent form, if needed.
3. Transfer the patient to the CT table.
• Position the patient supine, feet first.
• Landmark the patient at the sternal notch.
4. Review the ECG trigger device status on the gantry display.

Make sure the selected ECG trigger device is connected and active.
NOTE
If the gantry display shows ICM is disconnected, even though it is connected, clear
the connection status alert by selecting Cardiac settings from the gantry display
menu. Select a menu selection such as Active Lead and change the setting. The
disconnection alert will then clear.

Cardiac
Display Icon Description
Internal ECG trigger device is selected.
External ECG trigger device is selected.
NOTE
You can change the selected ECG trigger device (internal or external) from the tool
menu on the gantry display. See Gantry Display on page 580.
5. Place the patient grounding strap on the patient’s wrist. The strap should have direct contact with
the patient’s skin.
6. Connect the grounding strap cable from the grounding point behind the integrated cardiac
module to the patient grounding wrist strap.
7. Trim any excess hair at ECG electrode placement site, if needed.
8. Place the patient’s arms above their head and elevate with pillows or sponges.
Do not place the arms flat on the table or gantry. This position can limit vessel flow and cause arm
and shoulder motion. As the table moves into the gantry during the scan, it tends to cause the
patient to arch his back, raising the chest and causing incorrect registration artifacts.
9. With the patient's arms above their head, place the RA and LA electrodes, midline of the clavicle
bone & also below the clavicle bone. Do not place any electrodes over muscle, scar tissue, or hair
for the following reasons:
• Muscle: The ECG can register muscle electrical activity due to the above head arm position.
Help the patient relax his arms and reduce shoulder muscle fatigue.
• Scar tissue: This is denser than normal tissue, which makes it difficult to get a good signal.
If the patient has scar tissue in the shoulder area, place the electrode out onto the patient's
arm. In the chest area, place the electrode where there is no scar tissue.
• Hair: Electrodes placed over a very hairy area do not allow good skin contact. If necessary,
shave a 4 inch square area for electrode placement.
10. To remove any lotion or oils, gently scrub the electrode location with cotton gauze until the skin is
a healthy pink. Do not use alcohol to prepare the electrode area.
To ensure proper skin preparation and ensure good ECG signal quality, GE recommends using
Nuprep® skin prep gel to prepare the patient’s skin prior to placing the ECG electrodes. Nuprep®
gel strips away the top layer of skin and moistens the underlying skin layer, which lowers the
patient’s skin impedance while minimizing patient discomfort. Follow the instructions for use
provided with Nuprep® gel.
11. With the patient in the scan position (arms above the head), apply the ECG electrodes and leads
to the patient no more than 5–10 minutes before the scan.

Cardiac
Follow these guidelines:

• Use GE recommended electrodes: AccuScan-EG™ by Nissha Medical Technologies. Electrode
ordering information is found on the top of the IVY monitor or in the Integrated Cardiac
Module (ICM) Operator Manual. Using other electrodes can result in gating errors that can
lead to non-diagnostic images. GE requires high chloride, radio-lucent ECG electrodes.
• Use electrodes made for short-term monitoring (for example: exercise monitoring). Do not
use electrodes used for long-term monitoring.
• Always use new ECG electrodes (radiotranslucent with silver/silver chloride) with a fresh
gel pad. Dry or expired electrodes can result in poor signal conduction that can cause
intermittent triggering.
• Keep the electrodes as far away as possible from the scan field of view.
• Place the two upper electrodes directly on the middle portion of the patient's clavicle. Move
the electrodes towards the arms to produce a better signal, if needed.
• Place the two lower electrodes at the bottom of the rib cage.
Figure 247 Recommended Electrode Placement
Electrode Description
RA US (white); EU (red)
LA US (black); EU (yellow)
RL US (green); EU (black)
LL US (red); EU (green)
12. Review the ECG waveform. Ensure the patient’s heart rate is within allowable system limits for
scanning: 30–200 beats per minute.
a. If the internal ECG trigger device is selected and active, you can display the ECG status area
by selecting the ECG waveform icon using the back, forward and enter keys on the gantry.
b. If the external ECG trigger device is selected and active, the ECG waveform will display on the
external device only. It will not display on the gantry display.

Cardiac
13. If the ECG waveform looks noisy and/or improper R-peak triggering occurs at any time prior to
the diagnostic scan series, use the impedance measurement utility on the ECG trigger device to
ensure proper electrode connection. See Check Electrode Impedance on page 581.
Reposition any electrodes with poor electrode connection and recheck the impedance value.
After repositioning any electrodes, initiate another impedance measurement. Repeat this process
until all electrodes indicate successful impedance measurements.
14. Check the waveform. The more abnormal the waveform, the less chance for a successful cardiac
exam. A calm patient keeps the heart rate steady with a repeatable rhythm. A significantly varying
heart rate can result in non-diagnostic images. A low and stable heart rate typically allows for a
high-quality study with low radiation dose.
Figure 248 Normal Waveform
Figure 249 Noisy ECG Trace (extra trigger at #4)
Figure 250 Elevated T-wave (causing double trigger)

Cardiac
Figure 251 ECG Trace (premature beat arrhythmia at trigger #3)
15. Complete these activities to improve the ECG trace, if needed.

• Check the cable connections.
• If the external ECG trigger device is selected, position it away from the table and gantry to
minimize sensitivity to noise.
• Consider an alternative electrode placement: remove electrodes, prep the patient again
using Nuprep® gel, apply fresh electrodes, and repeat the impedance check.
• Check default electrode selection on the active ECG trigger device.
14.2.5.1 Adjust ECG Trigger Device Settings
14.2.5.1.1 User Console

The user console allows you to select an internal or external ECG trigger device, and adjust the internal
ECG trigger device settings.
4. Make any adjustments or changes.
Internal ECG trigger device settings:
• Active Lead: lead I, lead II, lead III or auto
• ECG Waveform Filter: enabled or disabled
• ECG Simulator: enabled or disabled; if enabled, the heart rate is simulated
• ECG Waveform: gain level or auto
• Pacer Detection: enabled or disabled
14.2.5.1.2 Gantry Display

The gantry display allows you to select an internal or external ECG trigger device and adjust the
internal ECG trigger device settings.

Cardiac
1. Using the back, forward and enter keys on the gantry, select the ECG settings icon on the gantry
display.
2. Select the ECG trigger device, and adjust the ECG settings as needed.
Internal ECG trigger device settings that can be edited include:
• Active Lead: lead I, lead II, lead III or auto
• ECG Waveform Auto Display: enabled or disabled
• Alternatively, Active Lead Selection can be changed from the gantry display.
a. Press the forward or back arrow on the gantry controls to select the Active Lead
Selection button .
b. Press Enter.
c. Press Enter until the desired lead is displayed.
NOTE
If the external ECG trigger device is selected, all other menu options are disabled.
See accompanying user documentation for instructions.
14.2.5.1.3 External ECG Trigger Device

For information on the external ECG trigger device settings, see accompanying user documentation for
instructions.
14.2.6 Check Electrode Impedance

You may initiate an ECG electrode impedance check from the system if the internal ECG trigger device
is selected. For information and instructions on checking electrode impedance using an external ECG
trigger device, see accompanying user documentation for instructions.
14.2.6.1 Initiating Electrode Impedance Check

User Console
The user console allows you to initiate an impedance measurement, if the internal ECG trigger device
is selected and active.
1. Right-click on the ECG waveform in an active patient study.
2. Select Test Electrode Impedance.
Gantry Display
The gantry display allows you to initiate an impedance measurement, if the internal ECG trigger device
is selected and active.
1. From the gantry display, select the Check Impedance icon.

Cardiac
2. The impedance check automatically runs.
You can also initiate an impedance measurement in the following way.

1. From the gantry display, select the ECG Settings menu.
2. Select Test Electrode Impedance.
14.2.6.2 Electrode Impedance Check Results

The system displays the electrode impedance check results on both the user console and the gantry
display. Measurements are displayed with a color indicating whether the measurement is within the
allowed threshold.
On the gantry display:
• Green indicates a good electrode connection.
• Red indicates a poor electrode connection.
Figure 252 Good and Poor Electrode Connections and Active Lead
NOTE
Lead I (LA & RA): is going to tell you about the top portion of the heart.
Lead II (RA & LL): is going to tell you about the right side of the heart (Right Ventricle &
Right Atrium).
Lead III (LL & LA): is going to tell you about the left side of the heart (Left Ventricle & Left
Atrium).
Lead RL: is a reference point used by all lead types. It is imperative that proper patient
prep is adhered to ensure best outcomes.
On the scan monitor:
The ECG trace will indicate the lead to check.

Cardiac
Figure 253

Cardiac
In the Waveform Filter area, select On or Off.
The following message will also be displayed:
Click Run Impedance Check to check the signal again, or click Override to ignore the low signal
condition for the rest of the exam. Reposition any ECG electrodes that fail the impedance check.
NOTE
Override may cause erratic triggering and possibly a scan abort. Use Override only
when absolutely necessary.
14.2.7 Cardiac Phase Background

Use this information to learn about cardiac phases.

Cardiac
Figure 254 ECG Waveform
Number Description
1 R-wave to R-wave interval
2 R-peak 75% default
3 Reconstruction window
• Systole, cardiac contraction, is from R-peak to T-wave.

• Diastole, cardiac relaxation, is from T-wave to R-peak.
R-wave to R-wave Interval

The R-wave to R-wave Interval is the time from the R-peak of one heart cycle to the R-peak of the next
heart cycle. The R-peak is used to predict where the targeted phase for reconstruction occurs and then
acquire/reconstruct images at that period of time during the heart cycle.
Phase Location (R-Peak Delay (%))
The cardiac phase location is defined as a period in time in the cardiac cycle. The Acquisition Window
Range setting (2) controls when the CT system will acquire data. Data is acquired so that images can
be reconstructed at all of the specified phases. (3) Refers to the center of the reconstruction window in
terms of a percentage distance between any two successive R-peaks given from the ECG.
The cardiac phase location is defined as the time interval from the R-wave to the center of the
reconstruction window (3). It is usually desirable to reconstruct images at the phase that has the
least amount of cardiac motion. The phase location can be changed to identify where the least
amount of cardiac motion occurs. For lower heart rates, the most common location is in the middle of
diastole, typically around 75%, but as heart rate increases or varies this location may change. It is not
uncommon for higher heart rates to have better image quality at the end of systolic portion, typically
around 45%.

Cardiac
14.2.8 Display an ECG Trace on the operator console

The ECG Trace component is displayed near the top of the scan monitor. It shows the real-time heart
rate, recent min and max heart rates, the ECG Trace, the procedure duration, user-selectable jump
points to show the live ECG or one of up to three breath-hold ECG recordings. The statistics of the last
recording, indicated by a white dot, are used to set the Auto Gating parameters. Click on Live to return
to the live ECG.
Figure 255 ECG Trace component
When Auto Gating is “On”, scan settings in the ECG and Gating collection are automatically updated
when a patient breath hold ECG is recorded. These settings are indicated by a white dot, and are
highlighted when an update occurs.
The ECG Trace is automatically displayed on the Scan Settings window when an ECG-gated scan mode
is selected.
For scan modes that are not ECG-gated, the ECG Trace is displayed when the ECG option is "On" in the
ECG and Gating collection. Note this can be preset for each series in a protocol.
Place the cursor in the ECG Trace viewer and right-click to display the Statistics menu.
• Select Reset Statistics to reset or clear the current statistics if the patient's heart rate has
changed. This step may be desired if there has been a change in the patient's heart rate or if a
modification of the electrodes or leads has caused changes to the waveform.
• Select Preferences to open the Stats Preferences window. From the Stats Preferences window,
select values for any of the following options:
• Select Stats Window to define the moving window of time during which the heart rate
statistics are calculated (Min, Avg, Max). Heart rate is a real-time heart rate. Minimum HR
is the minimum heart rate detected within the time frame you specify. Maximum HR is the
maximum heart rate detected within the time frame you specify. Average HR is the heart
rate averaged within the time frame you specify. The default is 30 seconds and the allowable
range is 5–60 seconds.
• Click Apply.
14.3 Cardiac Scan Parameters

Use these parameters to select Cardiac Scan Type and to review and setup Primary Recon and any
Secondary Recons.
14.3.1 Scan Type

1. From the Scan Settings window, click the Scan Type collection.

Cardiac
2. Select Cardiac.
3. Click Apply.
14.3.2 Primary Recon

From the Scan Settings window, click the Primary Recon collection and make any changes as needed.
See Cardiac Recon for more details.
14.3.3 Secondary Recon

From the image monitor, in the Reconstruction and Image Processing area, you can edit, add, or
delete Secondary Recons.
Left‐clicking on an existing recon task or adding a new one opens the editing panel to the right of the
task list.
Any needed recon setting changes can be made within the editing panel.
See Set ECG Preferences for details on setting ECG and Gating parameters.
Table 114 Secondary Recon Cardiac Phase Type Selection
Cardiac Phase Type Selection User Interface Description
ECG Acquisition Parts Prescrip- ECG prescription with three (3)

tion acquisition parts at a stable
heart rate of 80 BPM with Widen
for SnapShot Freeze enabled.
Center Phase (1) A recon will occur at the cen-

ter of Acquisition Window Part 1
(e.g. 75% R).
Center Phase (All) Recons will occur at all acquisi-

tion parts > 50% peak mA (e.g.
48% R & 75% R).

Cardiac
Secondary Recon Cardiac Phase Type Selection continued

Cardiac Phase Type Selection User Interface Description
Earliest to Latest A multi-phase recon within the

acquisition parts > 50% peak mA
(e.g. 40–55% R, 70–80% R).
Earliest to Latest (All) A multi-phase recon within all

acquired data (e.g. 5–95% R).
Smart Phase A phase of the least motion with-

in the earliest acquisition part >
50% of peak mA (e.g. within end-
systole).
Smart Phase (All) A phase of the least motion with-

in each acquisition part > 50% of
peak mA (e.g. systole & diastole).
After the scan, additional cardiac phase type selections are available. See Cardiac Recon for more
details.
14.3.4 One Heart Cycle recon

The One Heart Cycle recon option will restrict the system to reconstruct one heart cycle of data and
label the images between 0–99%.

Cardiac
Figure 256 One Heart Cycle Recon
In the example shown above, a 1 beat acquisition was performed, with available phases from 15–
110%. Enabling the One Heart Cycle option will cause the annotated phases to always be between
1–99%, or in this example, 0–95% by 5% intervals.

Cardiac
14.3.5 Cardiac Scan Modes
14.3.5.1 Cardiac Axial

• Use Cardiac Axial imaging for low dose cardiac or cardiovascular imaging when the system data
acquisition timing will use the patient’s ECG signal.
• Cardiac Axial imaging can acquire data at one or multiple cardiac phases or phase ranges within a
single cardiac cycle.
• Cardiac Axial imaging can be used to simultaneously acquire images of cardiac function by
imaging at a low dose throughout one complete cardiac cycle.
• Cardiac Axial imaging can be used to obtain images during consecutive cardiac cycles.
• Cardiac Axial imaging with AutoGating uses a patient’s heart rate and heart rate variation to
determine the patient-specific cardiac scan duration, providing robust acquisition of the cardiac
phases that will be most useful for clinical assessment.
• Cardiac Axial imaging incorporates automatic adjustment of the system collimation to acquire
low dose cardiac scans within a single heartbeat, and to acquire larger scan ranges with
automated, dose-optimized collimation with a minimum number of interscan table position
boundaries.
• Cardiac Axial imaging is used for non-contrast calcium score scans.
Recommended setting for calcium scoring, including Agatston (AJ-130), calcium volume and
calcium mass: GE CACS Auto Gating Profile, 120 kV, 0.28 s/rotation, 2.5 mm slice thickness, 160
mm coverage, 25 cm DFOV, Noise Index = 20, with an ASiR-V level of 50%. A manual mA of 300 for a
medium-sized patient may be used in place of specifying a Noise Index.
• The system will support heart rates from 30–200 beats per minute, but imaging cardiac patients
with arrhythmias, mechanical dysfunction, or higher heart rates may lead to images that are
degraded because of motion, which may compromise diagnostic quality.
14.3.6 Cardiac scan modes (for helical 40mm only)

Cardiac
14.3.6.1 SnapShot Segment
Figure 257 ECG & Gating collection with Cardiac Helical
• Cardiac Helical is a lower pitch helical scan and is available for cardiac applications in conjunction
with the Cardiac Helical option. In this scanning mode, heart rate monitoring is performed during
the helical acquisition and the associated EKG gating information is stored with the scan mode
such that a cardiac gated SnapShot reconstruction algorithm can be applied for prospective and
retrospective images. SnapShot reconstruction is used to minimize the motion of the heart in the
resultant images. The pitch factor for the cardiac helical scan is determined by the system and is
a function of the patient heart rate and scan speed. Pitch factor table at different scan speed is in
table xxx
Scan Speed BPM Pitch factor
0.28s 30-52 0.14
53-60 0.16
61-68 0.18
69-74 0.2
75-80 0.22
81-86 0.24
87-92 0.26

Cardiac
(continued)
Scan Speed BPM Pitch factor
93-99 0.28
100+ 0.3
Rotation Speed BPM Pitch factor
0.35s 30-40 0.16
41-49 0.18
50-57 0.2
58-65 0.22
66-70 0.24
71-75 0.26
76-80 0.28
81-85 0.3
86+ 0.32
• When using Cardiac Helical at higher heart rates, not all coronary vessels may be motion free at
all phases. If the heart rate change is less than 15 BPM, at least 1 phase will have vessel motion
frozen.
• When using Cardiac Helical with higher heart rates, consider generating the following on an AW
system: Secondary Recon with Temporal Enhance and post processing with SnapShot Freeze.
• Images acquired with Cardiac Helical are annotated SSEG.
• It is an acquisition and reconstruction method used to generate retrospectively ECG-gated images
using data from one cardiac cycle in a half-scan reconstruction technique.
Figure 258 SnapShot Segment, 1 = one cardiac cycle

Cardiac
14.3.6.2 Widen for SSF

Enabling this feature directs the system to acquire data so a SSF image may be generated at the
specified cardiac phases or times. For background information about R-wave, R-wave to R-wave, and
% phase. This adds 80 msec before and after the targeted reconstruction phase. For example, turning
on Widen for SSF adds 80 msec of X-ray on time before and after the targeted phase location.
Figure 259 Widen for SSF in Acquisition Window
14.3.6.3 HR Variation Allowance

The phases acquired within the Acquisition Window are only accurate to the extent that the real-time
predicted heart rate is close to the actual heart rate. The HR Variation Allowance ensures that the
prescribed phases will be acquired as long as the heart rate, in beats per minute, does not jump by
more than the HR Variation Allowance value.
For Cardiac Helical scan mode, HR Variance Allowance is used to extend the high mA duration. It
ensures that the prescribed high mA phase window will be acquired as long as the heart rate, in beats
per minute, does not jump by more than the HR Variation Allowance Value.
For example, if the HR Variation Allowance is 5 BPM, and the real-time predicted heart rate is 60 BPM,
then the system will ensure that the prescribed phases or prescribed high mA phases (for Cardiac
Helical) will be acquired so long as the actual heart rate during the beat when data is being acquired is
between 55 (= 60 –5) and 65 (= 60 + 5) BPM.
A typical value will be the heart rate variation measured during the previous breath hold.

Cardiac
For very low heart rates, such as below 50–55 BPM, it may be possible to reduce this value when doing
mid-diastolic (for example, 75%) imaging, as the quiescent duration is long enough that acquisition of
the exact prescribed phase may not be required.
Allowed values are 0 to 10 BPM.
Figure 260 HR Variation Allowance in Acquisition Window
14.3.6.4 Adaptive Gating

Adaptive Gating tells the system to avoid scanning during beats that are immediately after an early
beat. The system will delay the exposure due to early beats at most two times during a scan group.
Adaptive Gating is typically turned on when functional information is desired, as the beat after an
early beat will not typically be representative of the patient’s cardiac function, or when it is important
to avoid or reduce incorrect registrations between neighboring images acquired with multiple table
positions.
Set Adaptive Gating to “Off” to allow scanning during compensatory, or unusually long beats which
may occur immediately after early beats.
14.3.7 Anatomy Selection

The user sets the start and end location of the cardiac scan, either graphically or using a numerical
entry. The system determines the minimum number of exposures and the smallest collimation or
collimations that will cover the prescribed region to minimize both scan time and dose.
For systems with up to 160 mm coverage, hearts can typically be acquired using a single exposure.
Scans that require the aortic arch or scans of coronary artery bypass graft (CABG) patients will typically
require two exposures. In this case, the system also optimizes to place the entire heart within a large
inferior-sided scan with a smaller superior-sided scan. For systems with up to 80 mm coverage more
exposures are needed to cover the heart.

Cardiac
The user inputs the top and bottom of the region where imaging is required. The system generates
scan prescription parameters that will cover these top and bottom locations out to the edge of the
DFOV specified for the primary reconstruction. Additional image slices will also be reconstructed
above and below these locations to the extent allowed by the geometry of the system. The first and
last image locations are displayed, and these values can be indirectly changed by specifying where full
field of view images are required.
14.3.7.1 Considerations
The advanced, wide coverage system is able to generate high temporal-resolution images throughout
most of the imaged volume. Additionally, the system generates images with excellent spatial
resolution but with increased susceptibility to motion artifact in the outer radial portions of several of
the first and last images. For this reason, we recommend that the scanned region extend at least 1 cm
beyond the heart in all directions.
14.3.8 Cardiac Modulated mA

The goal of Cardiac AEC modulation with the cardiac scan modes, similar to AEC modulation for
non-cardiac modes, is to deliver a patient exposure that is appropriate to the combination of the
patient attenuation and the diagnostic imaging task. In AEC with Cardiac mode, the advantages of
patient-specific exposure modulation control, and the scanning and image reconstruction techniques
unique to cardiac imaging mode combine to enable low dose cardiac imaging of the patient.
Similar to other AEC-related scan modes, a scout of the patient is required when using AEC with
Cardiac modes. The AEC feature then uses the patient attenuation information extracted from the
scout and combines this unique information with the user-prescribed scan parameters contained in
the protocol to derive an appropriate scan technique. Similar to standard AEC mode, a user-prescribed
Noise Index is the scan parameter input that plays the major role in determining the final patient
exposure solution derived by the feature. In general, a higher Noise Index results in a reconstructed
image dataset with higher overall image noise but at a lower patient exposure; conversely, a lower
Noise Index results in lower overall image noise but at the cost of generally higher overall patient
exposure. The user must balance the competing requirements of image noise and patient dose to
arrive at a Noise Index that accomplishes the diagnostic imaging task at a dose that is as low as
reasonably achievable.
In ECG-gated mA modulation for cardiac, the AEC algorithm determines the required peak mA of the
exposure profile to satisfy the user requested Noise Index for the reconstructed image. The peak value
is derived from the patient attenuation information extracted from the scout projections, combined
with the user requested scan parameters.
The AEC algorithm recognizes the fact that the user is in cardiac mode and adjusts the scan technique
for an equivalent non-cardiac AEC scan to account for the unique challenges imposed by cardiac scan
acquisition and reconstruction techniques.
See Scan chapter for detailed information on non-Cardiac AEC.
14.3.9 Auto Gating

Auto Gating is a feature designed to optimize ECG-gated acquisition settings based on an assessment
of patient heart rate and variability, primarily focused on exams of the coronary arteries. The Auto

Cardiac
Gating workflow provides the capability to record heart rate statistics during a breath hold to
determine the acquisition settings best suited for the heart rate characteristics of the patient.
For example, at higher heart rates, end-systolic phases are usually preferred due to the lack of a
diastasis period in mid-diastole. Auto Gating automatically uses heart-rate specific acquisition settings
(called “profiles”) from predetermined lookup tables.
A patient's heart rate can change over the course of a cardiac examination and result in suboptimal
results if adjustments are not made prior to the diagnostic cardiac CT scan. A patient's heart rate
should be assessed throughout an exam to watch for heart rate changes.
Consider the following factors that can impact a patient's heart rate during Coronary CT Angiography
(CCTA). These factors should remain consistent between the practice breath hold and the gated
cardiac exam to ensure that the pre-scan heart rate assessment is accurate.
• Breath Hold Technique — end inspiration, mid inspiration, suspended breathing, et cetera
• Time Delay — after the breath hold command
• Contrast — total volume, injection rate
• Beta Blockers — oral and or IV
• Vasodilators — can lead to slight increase in heart rate
• Patient aspects — sex, age, electrophysiological disease, cardiac function issues
14.3.9.1 Auto Gating

When Auto Gating is enabled, the system uses the heart rate measurements from the most recent
breath hold recording with the Auto Gating Profile table, to automatically prescribe the data
acquisition timing. The ECG recording that is used for Auto Gating is indicated by a white dot next
to the name of the recording, to the immediate right of the ECG trace window. Similar white dots are
next to the settings that are specified by the Auto Gating feature.
Figure 261 Auto Gating HR Measurements

Cardiac
Number Description
1 Live ECG Trace
2 Breath-hold ECG recording
3 Diagnostic scan
4 Auto Gating optimized ECG settings applied
5 Up to “Irregular Window Length” seconds of ECG Trace
The Acquisition Window Parts, described below, set the desired areas of the cardiac cycle to be
imaged and thus determine the overall exposure time of the scan(s). The kV and mA Control settings
determine the mA values as a function of the heart cycle and thus determine the dose of the scan(s).
14.3.9.1.1 Gating Based On

This setting shows the heart rate calculations based on the most recent ECG recording /Irregular
Beat window and the associated average heart rate. When no ECG recording exists, the values for
parameters normally specified by the Auto Gating feature come directly from the scan protocol
definition. You can change the Auto Gating Profile at this point in the workflow, if needed. If a different
Auto Gating Profile is desired, you must change it from the Auto Gating window.
14.3.9.2 Auto Gating Considerations
Table 115 Auto Gating — Typical Clinical Scenarios
Scenario Acquired Phase Ranges Patient to Patient SnapShot Freeze

Variability for Optimal (SSF) Motion Cor-
Phase rection Helpful
Low Lower Uncommon

Heart Rate
75%
Moderate Moderate to High Sometimes

Heart Rate
70%-80%

Cardiac
Auto Gating — Typical Clinical Scenarios continued

Scenario Acquired Phase Ranges Patient to Patient SnapShot Freeze
Variability for Optimal (SSF) Motion Cor-
Phase rection Helpful
Intermediate Very High Commonly

Heart Rate
40%-80%
High High Frequently

Heart Rate
40%-55%
14.3.9.3 Auto Gating Profiles

GE provides 11 Auto Gating Profiles as defined in Auto Gating Profiles. GE Profiles can be copied and
used as a basis for a User Profile, but cannot be edited, renamed or deleted.
To view the settings for a GE Profile or to create a User Profile, see Auto Gating Configuration.

Cardiac
Table 116 Auto Gating Profiles
GE Profile Summary Details
Targets phases with

the least motion
changes based on
heart rate and heart
rate variability.
Mid-diastolic
• For low heart
rates, mid-dia-
stole is targeted.
Nominal • For intermediate
CCTA heart rates (70s
to mid-80s BPM),
mid-diastole
Mid-diastolic + End-systolic and end-systolic
are targeted.
• For higher heart
rates, only end-
systolic is target-
ed.
End-systolic
Tighter acquisition
window. Only targets
mid-diastole or end-
systolic; never both.
73 BPM
Immediate transition
from mid-diastole to
Narrow end-systolic (73 BPM).
Peak End-diastolic range
is slightly narrower
41-53% compared to
Low Dose CCTA. This
profile is should be
used in conjunction
with 0.234s option.
73 BPM Tighter acquisition

Low Dose
CCTA
Immediate transition
end-systolic (73 BPM).

Cardiac
Auto Gating Profiles continued

GE Profile Summary Details
Extra Large Similar to Nominal

0.35 s/rot may be utilized up to a higher heart rate limit (80 BPM).
Pt CCTA CCTA profile.
73 BPM Tighter acquisition

General mid-diastole or end-
Cardiovas- systolic; never both.
cular Immediate transition
Tighter acquisition
76 BPM window. Only targets
CACS Immediate transition
No usage of 0.35 s/
rot.
Nominal CCTA profile

plus an additional
CCTA w Fcn low mA part that
spans a 5-95% inter-
val.
1 or 2 high mA peaks for CCTA, plus additional low mA full-cycle peak.
81 BPM Very tight acquisition

window. No mid-di-
GE Pedia- astolic + end-systol-
tric Mor- ic heart rate range.
phology Immediate transition
Acquisition of one full

heart cycle at full mA.
GE Whole
Heart Cycle Targets one full heart
beat acquired from R-
peak to R-peak.
14.3.9.4 Auto Gating Acquisition Settings

Auto Gating generates suggested scan settings using the selected profile based on the patient's
recorded heart rate, the patient’s heart rate prior to the breath hold recording up to the Irregular

Cardiac
Beat Window Length, and selected Auto Gating profile (GE Adult Coronary). The system preset for
the Irregular Beat Window is set to 60 seconds. Auto Gating uses the patient's recorded heart rate
information to predict the heart rate behavior during a CCTA scan to optimize the parameters for
each patient. You can acquire a recording automatically during scan acquisition (timing bolus, calcium
scoring series, etc.) or manually during a practice breath hold by using the Record New HR option in
the Acquisition Window and Heart Rate widget.
NOTE
Irregular Beat Window Length is set in System Preferences on the ECG tab.
Figure 262 Acquisition Window and Heart Rate widget
An alert message will be given under the following conditions:

• The recorded median heart rate is more than 30 BPM from the current real-time heart rate
average.
• The heart rate range/variability measured is greater than 40 BPM.
• There is no breath hold recording present.
• When there is an alert set in the profile.
See Automatically record the heart rate during breath hold.

See Manually record the heart rate during breath hold.
14.3.10 Graphic Prescription (Graphic Rx) Detailed View

See Adjust the Graphic Rx for how to use Graphic Rx to adjust scan and recon coverage. When using
Graphic Rx for a cardiac exam, click the Detailed View button , to show a graphical illustration of
the areas within each group that have optimal temporal resolution and full field of view, and areas
with reduced temporal resolution.
Detailed View On:
Graphic Rx groups display the group color in areas where the image regions have optimal temporal
resolution and a green color to indicate image regions that have reduced temporal resolution, where
these images are more susceptible to motion artifacts.

Cardiac
Figure 263 Detailed View On Single Group

Cardiac
Figure 264 Detailed View On Multiple Group
14.3.11 Scan Overlap

The system applies a small amount of overlap when scanning neighboring regions. The amount of
overlap is controllable from the Coverage Speed collection.

Cardiac
• Minimum will generate images with some susceptibility to motion artifacts in the outer region of
axial slices near the table position boundary. This is the pre-populated setting in the GE Reference
protocols.
• More overlap will generate images with optimal temporal resolution, and hence, minimal
susceptibility to motion artifacts throughout the axial slices near the table position boundary.
The increased overlap results in a higher dose scan than Minimum.
14.3.12 Single Table Position

When the Single Table Position setting (see Coverage Speed) is set to One, the system constrains the
scan range to the maximum detector coverage. Set this option to One or More to enable longer scan
ranges or on systems with up to 80 mm coverage.
14.3.13 Set the ECG and Gating settings

The ECG and Gating settings control the timing for when the scan data will be acquired.
When you select ECG and Gating from the Scan Settings window, the window displayed will depend
on the scan type selected.
Figure 265 ECG and Gating collection
• The heart icon on the gantry display indicates that the internal monitor is connected to the
gantry.
• The instantaneous BPM heart rate is shown on the user console and gantry display.
• If the heart rate does not display and a lead off message is displayed, follow these guidelines:
• Check Gating box to view the ECG trace on the scan monitor.
• Check electrode placement. Consider an alternative placement to improve the cardiac
signal.

Cardiac
14.3.13.1 Acquisition Window Part 1

This setting directs the system to acquire data so that an image may be generated at specified cardiac
phases or times. For background information about R-wave, R-wave to R-wave, and % phase, see
Cardiac Phase Background.
While preparing to acquire scan data, after each R-wave is detected, the system predicts the heart rate
of the upcoming beat to be the same as the last previously measured regular beat. The system begins
to acquire scan data from about half a rotation before the first required phase or time, continuing to
acquire scan data until about half a rotation after the last required phase or time. For example, at a
gantry rotation time of 280 ms and a real-time predicted heart rate of 60, corresponding to an R-wave
to R-wave time of 1000 ms, an Acquisition Window of 75% would result in scan data acquisition from
about 610 ms (= 1000 * 75% - 280/2) to about 890 ms (= 1000 * 75% + 280/2).
The system sets the minimum data acquisition so that SnapShot Freeze images can be generated for at
least one cardiac phase.
Although scan data is acquired for a duration of at least one complete rotation, the temporal
resolution is, on average, half of the gantry rotation time (for example, 140 ms when the gantry
rotation time is 280 ms). The additional data is used for the outer few slices, and for image quality
improvements throughout the volume. The tube current (mA) is typically modulated to 20% for the
outer views so the additional image information can be provided with minimal increase in patient
dose.
A range can be specified (for example, 70% – 80%), indicating that the system should acquire data
so that all phases in the range can be reconstructed, assuming that the actual heart rate variation is
within the limits specified by the HR Variation Allowance parameter (described below).
A time value is used to specify an absolute time after the R-wave. For example, a value of 250 ms will
acquire scan data centered 250 ms after an R-wave, which may be useful, for example, for imaging
patients prior to electrophysiology procedures.
A number of heart beats may also be specified for acquisition (1, 2, or 3). In this acquisition mode,
the system will start the exposure immediately following a detected R-peak and terminate it following
the R-peak corresponding to the number of beats prescribed by the user. If an abnormal early beat is
detected during the exposure, and Smart Arrythmia Management is ON and mA is 100% of peak mA,
the system will automatically extend the exposure by one additional heartbeat, but the system will
never extend the exposure by more than one additional beat.
Figure 266 One Heartbeat Acquisition
The exposure starts immediately following the R-peak and terminates following the next R-peak such
that a full heart cycle can be reconstructed. Robustly covers heart rates down to 30 BPM. If a early beat
is encountered during the exposure, the exposure will be extended for one additional beat. If multiple
early beats are detected, the exposure is extended for one beat total.

Cardiac
The phases, time, or beats to be acquired are shown graphically in the Acquisition Window and Heart
Rate widget.
Allowed values for the Acquisition Window are from 0 – 300%, 0 –1000 ms, or 1–3 beats. A typical
value is 75%, typically corresponding to mid-diastole. Values greater than 100% are for phases to be
acquired from the following beat, most commonly used for Acquisition Window Part 2 or Acquisition
Window Part 3.
Set the mA value for this Acquisition Window to a percentage of the value specified in the kV and mA
Control setting. Lower values reduce dose, but will also increase the amount of noise in the images.
The mA value set here is the 100% level for Acquisition Window Part 2 or Acquisition Window Part 3
below.
If acquiring data for multiple purposes (coronary, function, et cetera), Coronary Assessment
acquisitions should be prescribed in Acquisition Window Part 1.
Widen for SnapShot Freeze (SSF)
Set the Widen for SnapShot Freeze gating parameter to “On” to ensure that the system will acquire
sufficient data to support SnapShot Freeze processing at all of the prescribed phases or times.
For example, if Acquisition Window Part 1 is 70%–80% and the Widen for SSF gating setting is
enabled, then as long as the heart rate is within HR Variation Allowance of the predicted heart rate, the
system will be able to generate images to support SnapShot Freeze processing at both a 70% and 80%
target phase, and any target phase in between.
Applying this parameter to a part of the Acquisition Window can result in a slightly larger data
acquisition window. To reduce patient dose, this parameter should not be applied to the part or parts
of the Acquisition Window that will not be used for coronary assessment.

A second data Acquisition Window can be used to acquire additional cardiac phases during the same
heart cycle used for Acquisition Window Part 1.
For example, a value of 45%, or a range of 45%–50%, would acquire scan data near the end-systole.
A one heart beat prescription would acquire scan data to generate all phases of the cardiac cycle,
which may be useful for functional assessment of the heart. A significantly lower mA value, such as
20%, significantly reduces the tube current except where higher tube current is required by other
acquisition windows. Wide reconstructed slices, such as 2.5 mm instead of the 0.625 mm typically
used to assess coronaries, reduces the amount of increased noise that otherwise would be seen in
functional images.
A range of 60% –150% would acquire data from early-diastole (60%) through the end-diastole (100%)
and continuing to the end-systole in the following beat (150%). Phases reconstructed every 10%
would then show an entire heartbeat and would allow an ejection fraction calculation based on an
end-diastolic measurement followed by the subsequent end-systolic measurement.
Allowed values for the mA % are 10%–100%. A typical value is 100%, indicating that the system uses
the mA value specified in the Scan chapter, kV and mA Control section.
For additional details, see the Cardiac Modulated mA section in this chapter and the Scan chapter, kV
and mA Control section.

Cardiac

A third data acquisition window can be used to acquire additional cardiac phases during the same
heart cycle used for Acquisition Window Part 1.
For example, if Acquisition Window, Part 1 is used to acquire 75%, and Acquisition Window Part 2 is
used to acquire 45%, then Acquisition Window Part 3 can be used to acquire functional images from
30%–120%. When combined with a lower mA, such as 20%, this allows the acquisition of functional
images for relatively little additional dose.
Allowed values are the same as for Acquisition Window Part 2. Allowed values for the mA % are
10%–100%.
14.3.13.4 HR Variation Allowance

The phases acquired within the Acquisition Window are only accurate to the extent that the real-time
predicted heart rate is close to the actual heart rate. The HR Variation Allowance ensures that the
prescribed phases will be acquired as long as the heart rate, in beats per minute, does not jump by
more than the HR Variation Allowance value.
For example, if the HR Variation Allowance is 3 BPM, and the real-time predicted heart rate is 60 BPM,
then the system will ensure that the prescribed phases will be acquired so long as the actual heart rate
during the beat when data is being acquired is between 57 (= 60 – 3) and 63 (= 60 + 3) BPM.
A typical value will be the heart rate variation measured during the previous breath hold.
For very low heart rates, such as below 50–55 BPM, it may be possible to reduce this value when doing
mid-diastolic (for example, 75%) imaging, as the quiescent duration is long enough that acquisition of
the exact prescribed phase may not be required.
Allowed values are 0 to 10 BPM.
14.3.13.5 Smart Arrhythmia Management

Turning “On” Smart Arrhythmia Management enables the system to automatically rescan exposures
where the prescribed cardiac phases were not successfully acquired. While this may double the dose
for some patients with irregular heart rates, having two acquisitions increases the chances that at
least one of the scans will be diagnostic, using the same contrast injection. Patients without heart rate
irregularities during scanning will not have any increased dose.
A typical value is “On” for most types of scans, but it may be turned off for very dose-sensitive patients
or for time-resolved studies such as dynamic perfusion.
Smart Arrhythmia Management may be enabled only for scans where the maximum phase
prescription is less than 150% and where the number of passes is set to 1.
The system limits the number of automatic rescans to 1 per location and 2 per scan series. Automatic
rescans are disabled if ECG signal is lost during scanning and R-peaks are being simulated.
NOTE
The system limits the number of automatic rescans to 1 per location and 2 per scan
series.

Cardiac
14.3.13.6 Adaptive Gating

Adaptive Gating tells the system to avoid scanning during beats that are immediately after an early
beat. The system will delay the exposure due to early beats at most two times during a scan group.
Adaptive Gating is typically turned on when functional information is desired, as the beat after an
early beat will not typically be representative of the patient’s cardiac function, or when it is important
to avoid or reduce incorrect registrations between neighboring images acquired with multiple table
positions.
Set Adaptive Gating to “Off” to allow scanning during compensatory, or unusually long beats which
may occur immediately after early beats.
14.3.13.7 Coverage Speed
14.3.13.7.1 Detector Coverage (mm)

The detector coverage of the scan, or of the series of scans, is shown. To edit a value in a multi-table
position scan, first split the group into individual scans, then change the detector coverage to the
desired value. Note that this will disable the automatic determination of the detector coverage based
on your numerically or graphically specified end location.
14.3.13.7.2 Single Table Position

When Table Positions is set to “One”, the feature restricts the system to acquiring data at a single
axial location. When the system cannot fully cover the user-prescribed scan region, at the field of view
specified in the primary reconstruction, an alert will be displayed by the Anatomy Selection scan start
and end parameters, indicating that the scan range has been restricted by the Coverage Speed: Table
Positions: One. To allow a larger scan range with multiple table positions, change the value to One or
More.
14.3.13.7.3 Number of Passes

The number of times that the system runs the prescription defined in the Anatomy Selection and ECG
and Gating settings. For example, changing the value from 1 to 2 will result in two passes, and will
double the patient dose.
This parameter is useful for generating multiple passes of a region, such as for viewing the dynamic
changes in contrast.
NOTE
Smart Arrhythmia Management may be enabled only if the number of passes is set to 1.
14.3.13.7.4 Minimum Time Between Passes

The system adds a delay between each pass so that generated images will be separated by this
amount of time. When the acquisitions are ECG-gated, the minimum time between passes is 0.8
seconds.

Cardiac
14.4 Cardiac Study Workflow
14.4.1 Acquire a scout scan

Use this procedure to acquire a scout scan series for the cardiac protocol.
1. From the scan monitor, open the Patient Schedule drawer.
2. Select the patient to be scanned and double left‐click or click Select Patient.
3. Enter the patient's information.
4. Start or connect the IV line to the contrast tubing.
5. Review the contrast effects with the patient.
6. Attach the electrodes to the patient, if you have not already done so.
See Attach ECG electrodes to the patient for details.
NOTE
Do not scan until you have an acceptable cardiac waveform and heart rate.
7. Secure both IV tubing and ECG cables. Make sure that the cables do not dangle from the table.
ECG lead wire movement during the scan can result in a degraded signal.
8. Review breathing instructions with the patient.
9. From the Protocol Selection window, select a cardiac protocol and click Accept.
10. From the Scan Settings window, review the current settings and click Confirm Settings.
NOTE
When a 90° or 270° azimuth scout is acquired, the system will assess patient
centering. If the patient is centered, a single orange line will display on the image. If
the patient is off‐centered greater than 2 cm, the system will display the table height
location and an up or down arrow to indicate the elevation needed to reach that
height. Use the gantry control to press and hold the indicated button along with the
fast button to move the table to the recommended height.
12. Deliver the breathing and table movement instructions.
14. Repeat steps 11–13 to acquire an orthogonal scout scan.
15. Proceed to Acquire a heart localizer or calcium score scan (optional, but recommended) on
page 610.

Cardiac
14.4.2 Acquire a heart localizer or calcium score scan (optional,

but recommended)
Use this procedure to acquire Axial images that can be used to determine the start and end locations
for the heart scan, and to determine the location for the contrast bolus tracking scan.
2. Choose one of the following options:
• Option 1: Gated localizer for calcium scoring
a. Make sure the scan type is Cardiac.
b. For calcium scoring recommended scan settings, see Cardiac Scan Parameters.
c. Adjust the position of the Graphic Rx region to fully cover the heart.
• Option 2: Ungated localizer
a. Maker sure the scan type is Helical.
b. Recommended settings: 120 kV, 0.5 seconds, 60 mA (100 mA for large patients), 1.375:1
pitch, 55 table speed, 40 mm detector coverage.
c. Position the localizer lines to cover just the heart, approximately from the carina to 2 cm
below the apex of the heart.
Figure 267 Heart Localizer
3. Evaluate the ECG waveform for heart rate stability.

6. Deliver breathing and table movement instructions. Give the patient the same breathing
instruction that they have practiced.

Cardiac
8. Continue on the Scan Settings window to one of the following procedures:

• Acquire a manual bolus timing scan and acquire a contrast enhanced cardiac scan.
• Acquire a contrast enhanced cardiac scan using Smart Prep.
NOTE
Override may inhibit the ability to start the scan, cause erratic triggering, or result in
the scan being acquired using simulated R-peaks if the patient's ECG R-peak signal
is lost during the scan.
14.4.3 SmartPrep Workflow

SmartPrep exams do not follow the same flow as other exams. The process begins when you add
a SmartPrep task to a series and ends when you delete the SmartPrep task, select Revisit Settings,
select Done Scanning, or the first diagnostic scan is completed.
The following is a typical workflow for a SmartPrep study.
1. Start a study with a SmartPrep task.
2. Confirm and take the scout scan.
3. Setup the diagnostic scan.
4. Execute the SmartPrep task.
a. Set up the SmartPrep scan.
b. Take the baseline scan. (baseline phase).
c. Set the monitor phase ROI(s).
d. Set the transition region of interest (ROI) — optional.
e. Perform the monitoring phase.
f. Transition to the diagnostic scan phase.
5. Perform diagnostic scanning. (scan phase)
6. Display the resulting report.
14.4.4 Acquire a Timing Bolus (optional)

Use this procedure to calculate the bolus transit timing to determine when to start the contrast
injection to capture the arterial phase. Omit this step if Smart Prep will be used.
Recommended settings: 120 kV, 1 rev/s, 50 mA, 5 s prep delay, 1 s ISD, 5 mm/1i
2. Place the localizer line one centimeter below the carina and just above the base of the heart, the
optimal location to find the ascending aorta for a timed contrast injection.

Cardiac
Figure 268 Localizer scan location for timed bolus injection
3. Evaluate the ECG waveform for heart rate stability.

From the Scan Settings window, check that the ECG is reported out in the ECG and Gating
collection, or open the ECG and Gating collection and turn on ECG Gating.
5. Deliver breath hold instructions identical to the instructions you will use for the cardiac gated
series. See breathing instructions for more details.
7. Start the injector.
• If using the Integrated Injector option: The injector is started automatically when Start Scan
is pressed.
• If not using the Integrated Injector option: Simultaneously press Start the Injector and Start
Scan.
8. Observe the heart rate during the scan.

9. Click the viewport with the reconstructed test bolus images. Review the images and identify the
image with contrast in the ascending aorta.
10. From the image monitor, open the Measure / Annotate collection and select MIROI.
11. From the MIROI Analysis window, select Ellipse ROI.
12. Click and drag the ROI to the ascending aorta.
13. Size the ROI to fit completely inside the aorta.
14. Click Plot.
15. Use the graph to calculate the bolus timing.

Cardiac
Figure 269 MIROI graph
Number Description
1 first tick mark
2 pre-scan delay time
NOTE
Elapsed time represents the time from the first non-scout image acquired in the
exam.
a. Count each tick mark to the peak of the curve.
b. Multiply the number of tick marks by two.
c. Add 5 seconds for prep group delay.
• This time represents the time it takes for the contrast once injected to reach the aortic
root where the coronary arteries branch off (Time to Peak enhancement).
• If you use the GE reference protocol, image number one is at 5 seconds and the tick
marks are 2 seconds apart, as shown in the graph above.
d. Add 3–4 seconds to allow for filling of the distal coronary vessels. The minimum total time
should be set to 24 seconds or greater.
In the example below, total time = 24 seconds. The value will be entered in the Prep Group
Delay fields in the Timing collection on the Scan Settings window, for the contrast enhanced
cardiac scan.
• (7 tick marks × 2 = 14 seconds)
• (+5 for prep group delay = 19 seconds for peak enhancement time)

Cardiac
• (+4 for distal filling of vessels = 23 seconds)

• (+1 additional delay to make total delay 24 seconds or greater = 24 seconds)
NOTE
If total time >= 24 seconds, no additional delay is required.
16. Click Continue to proceed to the next procedure.
14.4.5 Acquire a contrast enhanced cardiac scan

Use this procedure to acquire the contrast enhanced cardiac scan. This is the final scan before
transferring the images to the Advantage Windows Workstation.
1. Confirm the ECG trace is strong and stable.
2. Select the SFOV:
NOTE
When a Cardiac SFOV is selected, dose is computed based on a 32 cm phantom.
SFOV Default (cm) Upper Limit (cm)
Cardiac Small 25 32
Cardiac Medium 25 36
Cardiac Large 25 50
Ped Body 25 32
3. Position the scan lines to cover the complete heart from approximately 1 cm superior to the left
main coronary artery ostium to 1 cm inferior to the apex of the heart.
4. Confirm that a cardiac scan mode is selected.
5. Review the heart rate measurements made during the breath hold recording, and the ECG and
Gating settings that were adjusted based on those measurements. If you have not recorded a
breath hold recording, do so now.
6. Review the ECG and Gating settings.
• The data acquisition windows/parts indicate the portion or portions of the cardiac cycle that
will be imaged.
• When using Auto Gating, the acquisition windows/parts will change depending on the
patient's heart rate during the most recent ECG recording during a breath hold.
7. Smart Arrhythmia Management

• If your cardiac protocol or AutoGating profile is setup to use Smart Arrhythmia Management,
then the system may automatically rescan an exposure when an arrhythmia is detected
during scanning, to increase the likelihood for a clinically successful scan. The Auto Gating
Profile determines if this setting is enabled or disabled. The user has the ability to change
this setting by disabling Auto Gating and changing the Arrhytmia Management setting.

Cardiac
• The expected dose and number of scans are shown assuming no rescans are required, which
is the nominal case.
• This value can be changed after setting Auto Gating to “Off”. Change this value if it is not
appropriate.
8. Enter the prep delay that you determined from the MIROI timing bolus scan. The typical prep
delay time is Peak + 9 seconds, assuming the time bolus scan had a prep delay of 5 seconds.
9. The primary reconstruction for the scan series and may influence scan parameters. If needed,
prescribe additional secondary reconstructions.
10. From the Contrast collection, enter the contrast description and amount for the IV Contrast
setting.
Alternatively, you may choose one of any preset items from the list.
11. Program the contrast injector.
• The protocol to use varies depending on the contrast type, patient size, and injector
capability.
• Consider adjusting the volume of contrast on the second phase to ensure a 6 second range
from the end of the contrast injection to the start of X-ray on. This delay time ensures that
if using saline, you are getting the advantage of the saline bolus in the right chamber. If you
start the scan too soon, you will not see enough saline flush through the SVC. If you start the
scan too late, you will completely flush out the right chamber.
• The time delay from the end of the contrast injection (3) to the start of the scan (5) should not
exceed 6 seconds.
• Skip the next step if Smart Prep is not selected.
Figure 270 Time Delay
Number Description
1 22 second prep delay
2 Phase 1
3 Phase 2
4 Saline for 10 seconds
5 X-ray on

Cardiac
12. See the Scan Applications chapter; Smart Prep section for more details.
Typical Smart Prep parameters for cardiac scans:
• mA = 40–60
• Monitoring Delay = 10.0 seconds
• Monitoring Inter-Scan Delay (ISD) = 1.7 seconds produces an image every 2.0 seconds
• Enhancement Threshold = 150
• Diagnostic Delay = Auto Minimum or desired delay time
13. Arm the injector.

15. Give the patient the same breathing instructions as the previous series. See Breathing Instructions
for more details.
17. Start the injector.
• If using the Integrated Injector option: The injector is started automatically when Start Scan
is pressed.
• If not using the Integrated Injector option: Simultaneously press Start the Injector and Start
Scan.
NOTE
In the event patient ECG R-peaks signal is lost after pressing Start Scan the system
proceeds with scanning using simulated R-peaks corresponding to the last recorded
patient heart rate. The system displays a message indicating this condition in the
real time alerts patient handling window. If the user does not wish to proceed with
scanning using simulated R-peaks they may pause or abort the scan. Refer to Check
Electrode Impedence for troubleshooting poor ECG signal.
14.5 Cardiac Recon
14.5.1 Cardiac QC Recon

QC images will be generated for Cardiac acquisitions. For exams with multiple axial acquisitions, it
may skip displaying a QC image as the next rotation’s QC image is ready for display. All images will be
displayed in the reconstruction viewports on the right monitor. The reconstruction phase is the center
of the first acquisition window. The Cardiac QC images will not be auto-transferred.
14.5.2 Primary Recon

The Primary Recon is prescribed in the Scan Settings window on the scan monitor. The available recon
options are the same as those for pre-scan Secondary Recons.

Cardiac
14.5.3 Recon Link to Auto Gating

Pre-scan Secondary Recons can be linked or unlinked to Auto Gating. This allows Auto Gating to
streamline the cardiac workflow by automatically pre-populating secondary recon prescriptions with
parameters settings (phase location and utilization of Smart Phase and/or SSF) that are appropriate
for the given heart rate.
When Auto Gating is “On” and a recon is linked to Auto Gating, the phase prescription method and
SnapShot Freeze (SSF) recon flag will be set by Auto Gating and it can not be edited.
14.5.4 Prescribing Basic Cardiac Secondary Recons

Use this procedure to prescribe cardiac secondary reconstructions pre-scan or post-scan.
• Cardiac Axial acquisitions allow reconstruction during a portion of the R-to-R interval. The
amount of data acquired is controlled by cardiac phases prescribed in the acquisition.
• See Add reconstruction for details on adding a recon from raw scan data.
1. From the image monitor, in the Reconstruction and Imaging Processing area, select the
secondary recon task and click Add Recon.
2. The window displays all of the recon settings available for the secondary reconstruction.
3. Optional:
Type the Start and End locations that fall within the range of the selected group. Add an S (+) or I
(-) prefix to the location.
4. Optional:
Click Thickness and enter a thickness that populates all groups.
• If you only need to change the thickness for one group, or only one of multiple groups, select
the thickness area for that group.
• The original detector configuration at which the patient was scanned affects how you can
change the slice thickness. The thickness in black is available for reconstruction.
5. Optional:
Click DFOV and type a DFOV value.
The system defaults to the DFOV used for the scan acquisition.
6. Optional:
Click R/L Center. Type an offset value. Use one of the following methods to determine the offset
value:
Place the real-time cursor in an image and view the upper‐left corner for the RAS coordinates.
7. Optional:
Click A/P Center and enter an offset value.
8. Optional:
Click Recon Type and select the algorithm.

Cardiac
9. From the ECG and Gating settings collection, click the Recon mode for the phase prescription
method.
This allows you to select the phases of the cardiac cycle from which images are created.
• Single Phase (post-scan only): User specified single %, ms or beats value and interval to be
used for reconstruction.
• Multi-phase (post-scan only): User specified range of %, ms or beats values to be used for
reconstruction.
• Center Phase (1): A reconstruction will occur at the center of acquisition part 1.
• Center Phase (all): Reconstructions will occur at the center of acquisition part 1 and at any
additional acquisition parts with mA greater than 50% of peak mA.
• Smart Phase: A reconstruction that automatically selects the phase of least motion within
the earliest acquisition part with mA greater than 50% of peak mA (e.g. if acquisition parts of
70-80% and 40-50% are prescribed, then the 40-50% range will be evaluated).
• Smart Phase (All): A reconstruction that automatically selects the phase of least motion
within each acquisition part with mA greater than 50% of peak mA (e.g. if acquisition parts of
70-80% and 40-50% are prescribed, then the 70-80% and 40-50% ranges will be evaluated).
• Earliest to Latest: A multi-phase reconstruction based on the scan prescription with a user-
defined increment.
• Earliest to Latest (All): A multi-phase reconstruction adapted to the available data acquired
with a user-defined increment.
The manual options, Single Phase, Multi-phase and Smart Phase, for defining the reconstruction
timing relative to the cardiac cycle, are only available after the scan has been acquired. Smart
Phase -- manual is helpful when you would like the system to search for the phase of least motion
within an explicit phase range.
A typical Multi-phase prescription is 70–80% in 5% intervals, which is applied to all available heart
cycles during X-ray ON. To adjust Smart Phase manually, see Smart Phase.
10. In ECG and Gating settings, select the mode (Single Phase, Multi-phase, et cetera) and enter the
desired phase(s) for reconstruction.
• %R displays standard phase percent reconstruction
• +ms displays absolute millisecond reconstruction
• -ms displays reverse absolute millisecond reconstruction
11. For Multi-phase, enter the Start phase, End phase, and Interval to reconstruct.
• The recommended reconstruction phases are 70–80% with a 5% increment.
• If you are acquiring a functional imaging exam for ejection fraction and wall motion,
prescribe phases from 5–95% in increments of 10% and consider reconstructing the data
with a 2.5 mm thickness.
• One Heart Cycle recon option will restrict the system to only reconstruct one heart cycle of
data and label the images between 0-99%.

Cardiac
• Enabling the Cardiac Multiphase Fixed Interval Recon option in the system preferences will
ensure that multiphase reconstructions using Earliest to Latest or Earliest to Latest (all) recon
types are integer multiples of the prescribed phase interval. For example, if the option is
enabled and a 5% interval is selected, the system will always reconstruct multiples of 5 – 0%,
5%, 10%, 15% etc.
12. Click Apply to close the Phase Selection dialog box.
NOTE
A DICOM compliant ECG trace image is automatically saved after each primary and
secondary image reconstruction request. These traces are saved in a dedicated Series
labeled as 599.
Use these images only as a record of the trace used to the generate images. The images
should not to be used for diagnostic purposes.
14.5.5 Smart Phase

While AutoGating helps determine the appropriate cardiac phase range to be acquired (given patient
heart rate and variability), the Smart Phase feature can be utilized following the cardiac scan to
determine the optimal phase location for coronary imaging within the acquired range. The automated
Smart Phase feature is particularly helpful on coronary exams where the user might otherwise have
to prescribe an earliest-to-latest multiphase reconstruction and manually search for a best phase,
including irregular heart beat scenarios that utilized msec-based fixed-delay triggering.
Smart Phase can also be used in conjunction with SnapShot Freeze where a lowest motion target
phase is first automatically selected as a starting point for subsequent motion correction. This is
particularly advantageous for challenging high heart rate exams that might otherwise be difficult to
process at a nominal (45% for example) target phase location.
The user can select three modes of Smart Phase: Smart Phase, Smart Phase-All, and Smart Phase
Manual. Descriptions of each of these modes can be found in step 9 of section 14.6.4.
If any of the three Smart Phase modes is selected as the phase type, a Smart Phase Region will also
be set. This field prescribes the region of the heart which will be used for Smart Phase processing
and should be selected to include the mid-proximal region of the heart including the right coronary
artery (RCA), left coronary artery (LCA), and left circumflex (LCX). An Auto solution is provided to assist
in identifying which table location will most likely contain these vessels of the heart. The user should
always confirm the Smart Phase Region aligns with the proper heart anatomy after the scan has been
acquired as a failure to do so may result in a sub-optimal phase being selected. In the event the
Auto solution does not adequately cover the proper heart anatomy the user will have the ability to
manually select a scan location.

Cardiac
Shown above is the Smart Phase recon collection when viewed in Protocol Management. Similar to
the manual Phase Type options, Smart Phase Region will be user configurable only after the scan
has been acquired. When the recon collection is observed either in protocol management or prior to
acquiring the scan (e.g. during scan setup) Smart Phase Region will be constrained to Auto and Region
Selected will not be displayed on the UI.
As depicted below, when the recon collection is viewed post-scan the Smart Phase Region and Region
Selected fields are both displayed. The Smart Phase Region will have selectable dropdown values

Cardiac
of Auto in addition to the total number of table locations scanned. The values listed correlate to the
chronological order of table locations scanned. The Region Selected field is also displayed indicating
the corresponding z-locations for the selected SmartPhase Region. If Auto is selected this field also
displays the corresponding scan number.

Cardiac
14.5.6 Interactive ECG Editor

Use these procedures to visually interact with cardiac reconstruction timing relative to the ECG trace.
This allows you to adjust gating information such as R-peak trigger time and reconstruction timing
relative to the ECG trace.
Considerations
If the accession number is not in the image header, it may cause the series to be listed as a separate
exam. If so, reconcile the exam on the PACS.
1. Select a patient and exam for reconstruction and image processing; this will open the exam on
the image monitor.
2. Select the Series desired for reconstruction.
3. Make edits to R-peak triggers or reconstruction timing on the ECG trace.
Figure 271 ECG Editor window
Table 117 ECG Editor window
Number Description
Heart rate statistics are displayed: minimum, maximum, average heart rates and
1
number of irregular beats.
Secondary reconstructions parameters are displayed: start phase, end phase, and
2
interval.
The trigger point on the ECG Trace for each R-peak is displayed, as well as the X-ray on
3
interval, and the image reconstruction timing when images will be generated.
4 Click the Save icon to save your modified trigger locations with exam information.
5 Click the Restore icon to restore the original ECG Trace information for the acquisition.
Click the Measure icon to measure, in msec, the distance between two defined points
6
on the waveform. Place the cursor on the trace and click and drag right or left.

Cardiac
ECG Editor window continued

Number Description
Click the Magnify icon or the Minimize icon to magnify or minimize the ECG wave-
7
form.
8 Click and drag the navigation bar to view the selected portion of the waveform.
Purple indicates simulated R-peak. If the R-wave trigger timeout occurs after “start
scan” has been pressed – either during the prep delay, during a SmartPrep monitor
scan or after ECG-gating has been enabled - the system will begin simulating R-peaks
9
based on the last known patient heart rate as measured by the system. Cardiac scan
will continue using the simulating R-peaks. Simulated R-peaks will be colored as
purple in the ECG Editor window.
14.5.7 Graphically adjust reconstruction timing

Use this procedure to move or reposition image reconstruction timing within a single heart cycle.
Method
Place the cursor over the recon location and click, drag, and drop to the new location.
The annotation in the reconstruction location indicates the % or ms where images will be
reconstructed.
For all cardiac scan types, the recon window cannot be moved outside of its current X-ray on interval.
14.5.8 Insert, delete, or move an R-peak trigger

Use this procedure if gating issues occur during the scan or if the system does not trigger accurately at
the R-peak of the ECG trace.
Insert, remove, or move a trigger to normalize a heart cycle when a trigger occurs at an unwanted
location. This can be due to abnormal ECG waveform patterns, external noise interference, or a low
amplitude trace.
1. Open a prior ECG-gated scan series in the Reconstruction and Image Processing area on the
image monitor.
2. To insert a trigger, place the cursor anywhere on the ECG trace where you want to insert it and
right-click Insert R-peak Trigger.
An additional trigger will display on the ECG trace.
3. To delete a trigger point on the ECG trace and to normalize the heart cycle, place the cursor on the
trigger and right-click Delete R-peak Trigger.
4. To move a trigger, place the cursor over the trigger and click and drag it to the new location.
5. If the cardiac scan acquisition was completed using simulated R-peaks, the R-peaks are displayed
on the Series 599 image in purple, as opposed to the non-simulated R-peaks displayed in white.

Cardiac
14.5.9 Switching between Smart Arrhythmia Management

Exposures
Primary recon and any pre-scan secondary recons will be reconstructed from the last successful scan.
• Unsuccessful scans without enough views will be colored red. No reconstructions can be made
from this data.
• Unsuccessful scans (scans that do not include the phase range prescribed) will be colored gray.
Reconstructions can be made from this data.
• Successful scans will be colored green. Reconstructions can be made from this data.
1. Place the cursor in the ECG Editor, and right-click and select Switch Scan.
2. The reconstruction window moves from one acquisition to the other acquisition.
14.5.10 Display secondary recon images
14.5.10.1 Cardiac image annotation

SSCIN (Secondary Cardiac Axial — single sector image)
14.5.10.2 Edited cardiac image annotation

Image where the ECG trace has been edited, are annotated with an “E” placed before the scan type,
e.g. E/SSCIN.
E/SSCIN (Secondary Cardiac Axial — single sector image)
14.5.10.3 Cardiac negative phase image annotation

When a reconstructed image has an actual % phase value less than 0%, the image phase is annotated
as 0%.
14.5.10.4 Cardiac prescribed/actual annotation

The system reconstructed phase may be different from the prescribed phase. This can happen if there
is significant heart rate variation during the acquisition.
In these cases the image will be annotated with the prescribed phase followed by the actual phase.
Example: 25% ( 80%) where 25% is prescribed and 80% is actual phase reconstructed.
14.6 SnapShot Freeze

The SnapShot Freeze (SSF) feature can be utilized to reduce coronary artery motion artifacts that may
occur in cardiac exams. SSF is an available recon option with cardiac axial scanning, for both Hi Res
and non-Hi Res acquisition modes.

Cardiac
When SSF reconstruction is selected, a special 3-phase image series is generated for subsequent
motion correction processing on the AW workstation (or AW Server) with the CardIQ Xpress Process
application.
SSF is prescribed at a specified target phase location appropriate for coronary imaging. In the case of
higher heart rate exams, you may, for example, wish to prescribe SSF at both a 75% R-to-R target phase
(mid-diastole) as well as a ~45% R-to-R target location (approximate end-systole).
All Cardiac Axial scan acquisitions are inherently SSF compatible, meaning that for at least the target
phase location corresponding to the center of the acquisition window, SSF is available. However, when
prescribing an acquisition with a given phase range (70-80% R-to-R for example), if coronary motion
correction is also desired across this full phase range, ensure that Widen for SSF is explicitly enabled
as part of the scan Acquisition Window prescription (Otherwise, in the example above, SSF recon may
only be available at the 75% phase location.).
Constraints
SnapShot Freeze is not available with the following:
• Cardiac Axial PLUS mode reconstruction
• 0.625 Z, overlapped reconstruction 2.5 mm
• DFOV < 15cm
• ASiR-V 90-100%
• Multi-phase reconstruction
• Multiple scans at the same location
• Unlinked groups
• 1024 Matrix
Considerations
• Appropriate cardiac target phase selection (mid-diastole and/or end-systole) is essential for
optimal performance.
• Ensure a sufficient acquisition phase range for the anticipated SSF target phase(s). For ease of
use, utilize the Widen for SSF option within Auto Gating.
• For a single-beat/single-table position acquisition, position the heart well within the wide-
coverage Cardiac Axial scan.
• For an acquisition series that requires more than one axial scan location given clinical coverage
needs (perhaps a bypass graft assessment for example), ensure that the native coronaries are well
within the coverage of one axial scan to prevent having a higher motion vessel near an axial scan
boundary.
• Avoid an excessive image noise level. Select the appropriate kV / mA technique (using the AEC
Noise Index parameter) for optimal performance, and utilize ASiR-V as needed.
• Select a recon type that is appropriate for coronary imaging.
• Poor contrast opacification of the coronary vessels (low or non-uniform HU enhancement from
poor or missed bolus, venous contamination, et cetera) can result in sub-optimal SnapShot
Freeze motion correction.

Cardiac
• Streak artifacts from surgical clips, pacemaker lead wires, etc., in close proximity to the
coronaries, can result in sub-optimal SnapShot Freeze motion correction.
• Utilize targeted reconstruction to maximize pixel resolution; however the prescribed DFOV should
allow for at least 2 cm of tissue between the edge of the DFOV and the heart. Do not “over-zoom”.
• As SnapShot Freeze targets coronary motion, for an acquisition series with a scan range
significantly longer than the heart itself, select only the axial scan location(s) containing the
heart to streamline subsequent SSF motion correction processing.
• Millisecond-based phase prescription and the ECG Editor are fully compatible with SnapShot
Freeze. Utilize as needed.
Prescribe SnapShot Freeze for a Secondary Recon

Use this procedure to prescribe SnapShot Freeze for a Secondary Recon to reduce motion in the
coronary vessels. SnapShot Freeze is only available for single phase and center phase recon options.
NOTE
SnapShot Freeze is not available for a Primary Recon.
1. From the image monitor, in the Reconstruction and Imaging Processing area, select the
appropriate Secondary Recon task (prescribed as part of the protocol) or add a Secondary Recon
task using Add a Recon.
2. Click on an existing Secondary Recon task or add a new one to open the editing panel to the right
of the task list.
• Adjust Thickness and Images per rotation as needed.
• ASIR-V can be adjusted by clicking on the recon settings ASiR-V % menu.
• Adjust any other parameters as needed.
3. Open the Anatomy Selection collection to adjust the recon Start Location, End Location, DFOV,
A/P Center offset, and R/L Center offset as needed.
• The DFOV has to be at least 15 cm.
• The prescribed DFOV should allow for at least 2 cm of tissue between the edge of the DFOV
and the heart.
4. Open the ECG and Gating collection.

• Select SnapShot Freeze to “On”.
• Select Phase Type as needed.
• Select Phase percent or percents as needed and click Apply.
5. To automatically transfer this series for motion reduction processing with SnapShot Freeze, open
Transfer Options and select the desired hosts. AW or AWS with CardIQ Xpress to process with
SnapShot Freeze.

View Images
15 View Images
15.1 Overview
You view images through a series of viewports and access images using the File Manager. You can
also view and work with images and set image-viewing preferences on the Reconstruction and Image
Processing window. This window is available during the scan session and when accessing raw scan
data via Scan Data Manager.
15.1.1 Viewports Overview

Images display on a series of viewing areas called viewports, located on both the scan monitor (left)
and the image monitor (right).
Viewports on the scan display are used during the scanning process. Viewports on the image monitor
are used during image processing and when accessing images through the File Manager.
A viewport becomes active or receives primary focus by clicking on it. At that point, the border around
the image turns blue. You can window level, magnify and perform other image manipulation functions
without affecting other images currently displayed on the screen.
Any viewport can be expanded to double size by clicking the Expand icon on the hover menu for
the viewport. To return the viewport to its normal size, click the same icon.
To expand a viewport in File Manager, click the Expand button above the viewport . Click the
Minimize button to return to return the viewport to its normal size.

View Images
Table 118 Scan Monitor Viewports (left monitor)
These viewports: Are used for:
Scout Acquisition viewports These viewports display scout images as they are acquired. The acquired scout
images alternate between these viewports.
By default, the most recent scout image appears in the bottom viewport.
On the bottom viewport, you can select next or previous series to see different
scout series in the exam.
Auto-View viewport The Auto-View viewport displays the quality control image being acquired in
real-time as each volume is being reconstructed.
You can page through these images.
Quality control images are displayed in this viewport as the volume is created.
This allows you to ensure the images being acquired are adequate, without
having to wait for a full reconstruction to complete. QC images are marked
“QC/Quality Check”.
Navigation viewport Quality control images are displayed in this viewport if they are acquired. QC
images are marked “QC/Quality Check.”
Table 119 Image Monitor Viewports (right monitor)
Pagable auto-view viewports The pagable auto-view viewport dis-

plays recon Images.
Recons Reformats
By default, the top left viewport auto-
views primary and secondary recon
images.
You can set up the behavior of these
viewports when you set up the proto-
col, or you can configure their behav-
ior through the recon or reformat set-
up screens.
These viewports display only if you
are not running some other task like
reformat or volume viewer.

View Images
Image Monitor Viewports (right monitor) continued

Navigation viewports The top right, lower right and low-

er left viewports on the image moni-
tor are navigation viewports. In these
viewports, you can load and navigate
through any finished recon/reformat
image set from the image-processing
list.
Each of the three viewports can show
a different series.
Hover your mouse over the top of
these viewports to display a tool-
bar containing frequently used image
tools.
Hover your mouse over the right of
these viewports to display a scroll bar.
Click and drag to show the images in
the series.
15.1.2 File Manager Overview

The File Manager features a large viewing area to display images. File Manager lists the exams stored
on the console. This list is known as the browser. The browser is broken down into examinations,
series and images.
• The exam listing includes patient name, date, description of the exam and the network and
archive status by exam. You can customize the information displayed on the exam list. Refer to
Configuring the Exam List in the Data Management chapter.
• The series area lists the series that comprise the exam. The series number is listed here, as well as
the series type, name and number of images. You can customize the information displayed on the
series list. Refer to Configuring the Series List in the Data Management chapter.
• The image display/image list contains information related to images that comprise the selected
series. This function provides a list of all the exams on the system disk available for viewing.
15.1.3 Reconstruction and Image Processing Overview

The Reconstruction and Image Processing Task List provides an overview of what image processing
is required for a protocol/exam. It allows you to manage all image processing activities from one

View Images
window, including set up, monitoring and transferring. It also allows you to view the images created
for any image-processing series.
Several image-processing tasks work only with raw or unprocessed scan data. For this reason the
Reconstruction and Image Processing Task List and its functionality is available during the initial scan
session, when it opens on the right monitor. You also access the Reconstruction and Image Processing
Task List by opening an exam in the File Manager.
15.1.4 Additional Considerations

If a power failure occurs during a prospective image reconstruction, any images reconstructed prior
to the power failure are not displayed in the browser/patient list and are not saved in the database.
Type an exam/series/image number in the Accelerator Line, and then select another exam from the
browser to refresh it. There may be a slight delay. If this action fails, reboot the system. If that fails, use
post-scan secondary reconstruction to generate the images. There is no need to rescan the patient.
15.2 Image Display
15.2.1 Access images in File Manager

To open File Manager to access browser applications, follow the steps below.
File Manager is always accessible on the image monitor (right monitor).
1. On the image monitor, click the File Manager “drawer”. (You do not have to click the File Manager
icon – just click the drawer labeled with the File Manager icon .
Figure 272 Opening File Manager
2. From the Exam List, double-click the exam you want to view. The exam opens in a patient session
tab, and the File Manager drawer closes. Alternatively, click the Select Patient icon to the left of
the patient’s name, or right-click the exam and then click Open Exam.
NOTE
If the exam fails to open or a error dialog is shown, try opening the exam from the
Scan Data Manager. See Add reconstruction in Data Management.

View Images
Figure 273 Sections of the File Manager Drawer
1 Controls area 3 Series list
2 Exam list 4 Image display/Image list
Refer to the File Manager section of the Data Management chapter for information sorting the Exam list
and on setting which columns display on the list.
15.2.1.1 Selecting images in File Manager

1. From the display monitor, open the File Manager drawer.
2. From the Exam list, select the patient name.
3. The Series list shows the series for the selected patient. Select the series you want to view.
4. The series loads into the Image viewport on the bottom right side of the right monitor.
5. Hover your cursor over the right of the viewport to reveal the scroll bar at the right of the
viewport.
By default, the first image in the series is displayed. To scroll through the images in the series,
click and drag the slider on the scroll bar.

View Images
Figure 274 File Manager viewport controls
1 Image list icon 3 Maximize image icon
2 Toolbar containing frequently used tools 4 Images scroll bar – click and drag to show the
images in the series

View Images
Figure 275 Right mouse menu on the File Manager viewport
Table 120 File Manager viewport menu items
Page — click this icon to use the left mouse button to page through the images.
Pan/Roam — click this icon to use the left mouse button to pan and move around the
image in the viewport.
Zoom— click this icon to use the left mouse button to zoom in and out on the image
in the viewport.
Window width/Window level — click this icon to use the left mouse button to adjust
the window width and window level of the image in the viewport.
NOTE
WW and WL values are not propagated to images that have already
been displayed in the File Manager Viewer. This occurs if WW and WL
are changed before all images in the series have been loaded into the
memory. Wait for 5-10 seconds before changing WW and WL, especially
for data sets of more than 1000 images.
Annotation Level — Full, Partial, No, Custom
Display Normal — Return all images in series to original zoom

View Images
Reset All — Return all images in series to original zoom and orientation
Copy All — Copy all ROIs and user annotations applied to the image
Paste All — Paste ROIs and user annotations applied to the image
Erase All — Erase all annotation on all images in the series
Screen Save — Take an electronic photograph of everything on the image in primary

focus. The system saves it as a screen capture in a new series under the exam.
Save State — Save the state of the image and create a gray scale presentation state
(GSPS).
NOTE
Scout images that have had a Save State applied are rotated 90 degrees
even if no rotation has been selected for the Save State. The image RAS
annotation is indicated correctly.
15.2.1.2 Selecting Images using keyboard commands

Hover your cursor over a viewport to activate the keyboard controls for that viewport. If you are not
hovering over a viewport, the selected viewport is active. If you have more than one selected viewport,
all selected viewports are affected by the keyboard commands.
Table 121 Keyboard commands for viewports
This key: Does this:
Page up PgUp Displays the previous image in the series
Page down PgDn Displays the next image in the series
Left arrow ← and Right arrow → Left arrow decreases and Right arrow increases window
width
Up arrow ↑ and Down arrow ↓ Up arrow increases and Down arrow decreases window
level
F5 Return to previous W/L
F6 through F11 Window/Level presets
Control-s Cntrl-s Saves the currently displayed image as a screen capture

*Hovering over a viewport does not affect the function of these keys.

View Images
15.2.2 Access images from the Reconstruction and Image

Processing window
The Reconstruction and Image Processing Task List opens on the image monitor when you open the
exam. You can also access The Reconstruction and Image Processing Task List from Scan Data Manager
in File Manager.
Figure 276 Reconstruction and Image Processing window — image controls
1 Image tool sets 2 Active viewport highlighted in blue
3 Hover-over top of viewport to display tool- 4 Images scroll bar – click and drag to show the images
bar in the series

View Images
Figure 277 Reconstruction and Image Processing viewport controls
1 Toolbar containing frequently used tools 2 Images scroll bar – click and drag to show the images
in the series

View Images
Figure 278 Right mouse menu on the Reconstruction and Image Processing viewport
Table 122 Reconstruction and Image Processing viewport menu items
Annotation Level — Full, Partial, No, Custom
Display Normal — Return all images in series to original zoom
Reset All — Return all images in series to original zoom and orientation
Copy All — Copy all ROIs and user annotations applied to the image
Paste All — Paste ROIs and user annotations applied to the image
Erase All — Erase all annotation on all images in the series
Screen Save — Take an electronic photograph of everything on the image in primary

focus. The system saves it as a screen capture in a new series under the exam.
Save State — Save the state of the image and create a gray scale presentation state
(GSPS)

View Images
15.2.3 Selecting viewports for images in the Reconstruction and

Image Processing Task List
The viewport selection button displays after the anatomy label . Use this control to indicate in
which viewport each image series is to be displayed. In Protocol Management you can enter the
setting for each reconstruction or image processing set of images. Mouse over the icon to enlarge it,
then click on the viewport in which you want to view the recon or reformat series.
NOTE
Window Width (WW) and Window Level (WL) values do not change in any viewports
except the Auto View Viewport once Auto View starts until the recon task is complete.
This is because the cursor focus is locked to the Auto View Viewport when recon is
active. Wait until recon completes to change the WW and WL.
Figure 279 Viewport selector in Reconstruction and Image Processing Task List
15.2.3.1 Auto-View
The upper left viewport will always auto view the primary and secondary recons unless the recon
Clinical ID is Stroke.Perfusion. Once reconstruction of the volume is complete images will display
automatically in the viewport.
15.2.3.2 Viewport Priority

The priority for images being displayed in the viewports:
1. Upper left viewport, displays secondary images automatically after the reconstruction of the
volume is complete.
2. Any image assigned to a viewport using a viewport selection button.
3. Primary recon will only be displayed if image display has been selected for the recon.
15.2.4 View images in a cine loop

Use this procedure to view images in a cine loop, which is useful for tracking flow in same-location
scans taken with contrast or with motion such as flexing an elbow.

View Images
Figure 280 Cine loop controls
NOTE
Paging series with an unequal number of images does not keep paging synchronized. To
view individual series use the Next/Prior Series arrows from the hover menu bar.
1. From the Reconstruction and Image Processing window, load the series you want to view into a
viewport.

View Images
2. From the viewport control panel, click the arrow next to Export, then click the Cine icon .
3. In the Cine area, click the Play icon , which uses all the default settings. Alternatively,
make selections from the Cine area.
To do this: Use this setting: Icon:
Define the range of slices in the Check Play All to play all of the
cine display images in the series, or click Play
Range and enter the image num-
bers in the From and To fields.
Define the image interval Typically, leave this value set to 1

(the default value). When display-
ing a multi-phase series in cine,
enter the number representing
the number of phases in the im-
age range.
Select a viewing mode Click the Loop icon to view the Loop icon
series from start to end, then
from start to end. For example, Rock icon
if there are 20 images in the ser-
ies, the images display 1-20, 1–
20, 1-20, and so on.
Click the Rock icon to view the
series from start to end, and then
end to start. For example, if there
are 20 images in the series, the
images display 1-20, 20-1, 1-20,
and so on.
Play the cine loop forward and Click the Play icon to play the Play icon
backward cine loop.
Pause the cine loop Click the Pause icon. Pause icon
Go to the end of the cine loop Click the End icon. End icon
Go to the beginning of the cine Click the Beginning icon. Beginning icon
loop

View Images
(continued)
To do this: Use this setting: Icon:
Step forward through the cine Click the Step Forward icon. Step Forward icon
loop, one image at a time
Step backward through the cine Click the Step Backward icon. Step Backward icon
loop, one image at a time
NOTE
To change the series, load the new series into the viewport.
15.2.5 View a reference image

Use this procedure to view a reference image:
1. From the Viewport Control Panel, click the arrow next to Image Display.
2. Click Reference Image On icon file ref_Image_on_icon.png.
To turn Off the Reference image:

1. From the viewport control panel, click the arrow next to Image Display.
2. Click the Reference Image off icon. file ref_image_off_icon.png
15.3 Image Tools

You can modify images many ways using the image tools, available when accessing images on the
Reconstruction and Image Processing Task List
15.3.1 Display normal

Use this procedure to restore an image to its original size and orientation. This feature removes all
filters, magnification factors, orientation changes and graphics.
1. Hover over the top of the viewport to display the viewport control panel.
2. Click the Display Normal icon .
You can also select Display Normal from the right mouse button menu on the viewport.
15.3.2 Edge, smoothing and lung enhancement filters

The edge and smoothing filters enhance anatomical structure without additional reconstruction time.
Edge Enhancement filters sharpen the image and are useful for filming bone windows. There are
six levels of Edge Enhancement: E1, E2, E21, E22, E23 and E3. E1 applies the least amount of

View Images
enhancement and E3 applies the most. When these filters are used, the image is annotated with E1, E2,
E21, E22, E23 or E3.
The smoothing filters decrease the appearance of noisy images or enhance low-contrast areas when
filming soft tissue. There are five Smoothing filters, S1, S11, S2, S22 and S3. S1 applies the least
amount of smoothing and S3 applies the most. When these filters are used, the images is annotated
with S1, S11, S2, S22, or S3.
The Lung Enhancement filter is designed specifically to use when filming lung windows. When the
Lung Enhancement filter is applied, the image is annotated with lu.
Figure 281 Image filters

View Images
15.3.2.1 Considerations
• Smoothing and edge filters are not additive. Only one filter may be applied to an image at a time.
Applying a new filter negates the previously applied values.
• A new series is not created for the filtered images.
• Filters are applied to image data only.
NOTE
It is recommended to use Clinical Identifier Neuro Routine Head, Neuro Routine
Head with Contrast, Stroke.Routine Head, Stroke Routine Head with Contrast,
Trauma Routine Head, or Trauma Routine Head with Contrast to enable Head-
specific filters that reduce artifact near the bone brain interface.
15.3.2.2 Applying filters

1. From the viewport control panel, click the arrow next to Image Display, then the Filters icon
.
2. Select a filter type.

• Click E1, E2 or E3 for edge enhancement.
• Click LU for lung enhancement.
• Click S1, S2 or S3 for smoothing.
3. To turn off the filters, click None for the filter type.
Alternatively, click the Display Normal icon from the Image Display set of tools.
15.3.3 Gray Scale Enhancement

Gray Scale Enhancement (GSE) changes the slope and gamma curve of an image. It can be used in
head studies to improve the bone/brain interface, which helps with gray/white matter differentiation.
There are three levels of GSE: G1, G2, and G3. G1 applies the least amount of enhancement and G3
applies the most. The GSE filter selected is applied to all images in the series. When you apply this
filter, the image is annotated with G1, G2, or G3 just above the vertical tick mark scale on the right side
of the image.

View Images
Figure 282 Gray scale enhancement filter
1. From the viewport control panel, click the arrow next to Image Display, then click the Filters icon
.
2. Under Gray Scale Filter, click G1, G2 or G3.

3. To turn off GSE, click None for the filter type.
Alternatively, click the Display Normal icon from the Image Display set of tools.

View Images
15.3.4 Flip/rotate images

Use this procedure to change the orientation of a displayed image.
Figure 283 Flip/rotate tools
2. Click the icon corresponding to how you want to reorient the image.
To reorient the image in this direction: Click this icon:
Flip the image top-to-bottom
Flip the image left‐to‐right

View Images
(continued)
To reorient the image in this direction: Click this icon:
Rotate the image 90° to the left (counterclockwise)
Rotate the image 90° to the right (clockwise)
3. To return the image to its normal orientation, click the Display Normal icon from the Image
Display set of tools.
NOTE
Display Normal does not affect the orientation of secondary focus viewports. Put the
viewport in primary focus and select Display Normal again.
15.3.5 DICOM Gray Scale Presentation State (GSPS) objects

DICOM Gray Scale Presentation State (GSPS) is a DICOM object which saves a range of images, WW,
WL, roam, zoom, image flip and graphic annotations such as image annotation and measurement
graphics. This object is then sent to a review station along with the source images. When the object
is viewed, images are presented in the form that was displayed on the scanner. A GSPS object can be
viewed only on CT scanners or remote hosts that support DICOM GSPS objects. Not all PACS systems
support GSPS.
15.3.5.1 Create a GSPS object

1. In a viewport, modify the image using any of the following features:
• Window Width and Window Level
• Roam
• Zoom
• Flip
• Rotate
• Graphics such as ROI, measure distance, and image annotation
2. From the viewport control panel, click the arrow next to Export, then click the Save State icon
.
The GSPS object will be saved as series 10,000 for the current exam.
15.3.5.2 View a GSPS object

1. Select the GSPS object in File Manager. The images display in the Image Viewport in File Manager.
2. Use the image tools to modify the image.

View Images
3. To view additional GSPS objects in the series, click the Image List icon and select the
desired GSPS from the list, then select the image view icon .
15.3.6 Magnify or minify an image

To zoom in (magnify) or zoom out (minify) an image, right-click and drag the image in a viewport.
15.3.7 Apply a matte

Use the matte procedure to eliminate unwanted information on or around an image. There are two
types of matte: rectangular and elliptical. The size of the matte is adjustable.
15.3.7.1 Place a matte

From the command line use the Short Cut command.
The following table shows some shortcuts for placing mattes.
To do this: Type or click:
Place an elliptical matte Type ematte in the Command box and press Enter.
Place a rectangular matte Type rmatte in the Command box and press Enter.
To propagate the matte to all images in the series, type prop a in the Command box and press Enter.
15.3.7.2 Move, resize, hide, or delete a matte

1. To resize the matte, click and drag the open red box in the lower right corner of the matte.
2. To move the matte, click and drag anywhere outside the matte.
3. To delete or hide the matte:
a. From the viewport control panel, click the arrow next to Measure/Annotate.
b. To remove the matte, click Erase selected graphics .
c. To hide the matte, click Hide Graphics .
NOTE
To remove all graphics from a viewport, click the Remove all Graphics icon
on the viewport right mouse menu.
15.3.8 Move images within a viewport

You can reposition images in a viewport. All images in the series will be moved.

View Images
Hold down the Control (Ctrl key), and right-click in the viewport, and drag the image to the desired
position.
15.3.9 Inverse the video display

To invert the video display between black/white and white/black, type inv in the command line.
To return the image to its normal display, type inv again.
15.3.10 Adjust the W/L

Use one of the following methods to adjust the W/L to control the image brightness and contrast.
15.3.10.1 Mouse
1. Place the cursor over any viewport.
2. To adjust only the window’s width, middle-click and drag the mouse:
• to the right to widen the window width (make the image gray).
• to the left to narrow the window width (make the image more black and white).
3. To adjust the window level, middle-click and drag the mouse:

• up to darken the image.
• down to brighten the image.
4. Middle-click and drag diagonally to change both the window width and the level.
15.3.10.2 Function keys

You can use the F5 - F11 function keys to apply preset W/L values. The W/L values are defined from
System Preferences Viewers.
1. Press one of the function keys (F6 through F11) to activate the preset window.
2. Press F5 to reset the window level to the previous setting.
Figure 284 Function keys

View Images
15.4 Measurements
Figure 285 Measure/Annotate tools
15.4.1 Measure a density reading

Use these procedures to obtain information on areas of anatomy and pathology.
1. From the viewport control panel, click the arrow next to Measure/Annotate.
2. Select the Rectangular ROI , Ellipse ROI or Draw free hand ROI .
NOTE
Freehand ROI shows distance statistics, not ROI statistics. Use Ellipse or Box ROI for
ROI statistics.

View Images
NOTE
The Ellipse ROI button is also available from the hover menu bar which appears
when you hover your cursor over a viewport.
3. Position the cursor on the image and click to deposit the insertion point.
• For Draw free hand ROI, move the solid blue box to the start point. Press and hold Shift, then
click and drag to define the area for the trace.
• For Rectangular ROI or Ellipse ROI, click and drag on the small box in the upper-right corner
of the ROI to resize or click the ROI number and drag to a new location.
4. Click Erase selected graphics to erase selected measurements.
15.4.2 Use MIROI density reading to calculate bolus timing

Use this procedure to calculate the scan delay for a contrast enhanced exam.
Scale for HU, there are two selections.
• Absolute: has an actual Hounsfield Unit number for each ROI plotted on the graph.
• Relative: the ROI measured for the first image is set to zero and the change from zero is plotted for
the rest of the images.
1. From the viewport control panel, click the arrow next to Measure/Annotate to display
measurement icons.
2. Click the MIROI button to open the MIROI controls window.
3. Define the region of interest using either the eillipse ROI button or the rect ROI button.
4. Click and drag the ROI to the anatomy of interest. Size the ROI to fit completely inside the aorta.
5. Click Plot.
6. Use the graph to calculate the scan delay.

View Images
7. Optionally, screen save the graph. Right click and select Screen Save
Figure 286 MIROI graph
NOTE
Elapsed time represents the time from the first non-scout image acquired in the exam.
15.4.3 Add a grid

Use these procedures to place a grid (matrix) over the primary image to measure anatomy or
pathology on an image.
1. From the viewport control panel, click the arrow next to Measure/Annotate, then click the Grid
icon.
2. Click and drag the center point of the grid to move it.
3. To remove the grid, click the Grid icon again.

View Images
15.4.4 Measure distance

Use these procedures to activate a measure tool to obtain information, distances, and areas of
anatomy or pathology. Multiple measurements can be added to the image, but only up to three
measurement statistics can be displayed on a single image.
2. Click the Add Line ROI icon.
NOTE
You can click the Add Line ROI icon from the viewport hover bar, which displays
3. Click and drag either end point of the start and end locations to adjust the line segment size.
4. Click the arrow next to Image Display. Select ROI Text page.
• This is useful when more than three measurements are on a viewport.
• You can screen save Text page ROI.
5. Click the Erase Graphics icon to erase all display objects.
15.4.5 Report a cursor

Use this procedure to display cursor statistics and Right Anterior Superior (RAS) coordinates for a
single pixel.
2. Click the Report Cursor icon .
NOTE
You can click the Report Cursor icon from the viewport hover menu, which displays
3. Click Report Cursor again to turn it off.
15.5 Additional Image Tools

15.5.1 Annotate an image
Use this procedure to add annotation to your images, which allows you to comment for labeling
purposes or draw attention to a specific area of interest.
1. Click on the viewport to which you want to add annotation.

View Images
3. Click the Annotate button .
4. Move the mouse to the selected viewport and enter the text.
• To move the annotation, click on the blue box and drag.
• To move the end of the line, click and drag the arrowhead.
• To remove the line, click and drag it into the box.
5. Click the Annotate icon to add another annotation.
6. Click theErase all graphics icon on the viewport toolbar to remove all annotations.
Figure 287 Add annotation

View Images
15.5.2 View an exam or series text page

Use this procedure to view patient and scan parameter information.
2. Click the Text Pages .
3. Click either the Exam Textpage, Series Textpage or ROI Textpage button.
4. Click the Save as Secondary Image icon to save the displayed information to series 98.
You can also right click on the image, then click Screen Save.
5. Use arrow keys to navigate between multiple pages.

6. Click Quit.
15.5.3 Hide, show, or remove graphics

Use this procedure to temporarily remove added annotation and graphic objects on an image then
re-display them.
1. To hide measurements, such as ROIs:
a. From the viewport control panel, click the arrow next to Measure/Annotate .
b. Click the Hide Graphics icon .
2. To remove measurements, select the measurement, then click the Erase Selected Graphics. icon
or press the Delete button on the keyboard.

View Images
3. To hide graphics:
a. Select the annotation you want to hide.
b. Click Hide Graphics icon .
c. To remove graphics, click theErase all graphics icon on the viewport toolbar.
15.5.4 Save an image screen

Screen Save is an electronic photograph of an image. Screen Save saves everything that is on the
image in primary focus. This includes zoom, cursors, measurements, flip or annotation. You can use
Screen Save to save images when anatomy or pathology has been measured. The screen saved images
are listed on the patient list browser as series number 99, and called SSave for the series type.
The images can be archived and networked. However, these images have image processing
restrictions, and any annotation on the image cannot be removed once the screen has been saved.
NOTE
Screen Save images are not PPS aware. Images created in Reformat, 3D, and Navigator
are not PPS aware. Image types INPR is posted in the PPS column in the browser even
though PPS is not enabled.
1. From the viewport control panel, click Export.
2. Click the Save as Secondary Image icon to save the displayed information to Series 99.
You can also right click on the image, then click Screen Save.

View Images
15.5.5 Cross-reference images on a scout

Use this feature to view lines on the scout image representing previously scanned locations.
In the Command box, type xr <series number> <image set>: <interval>, where:
• series number is an appropriate series number to be cross-referenced
• image set is a consecutive group of image numbers within the series
• interval is the interval of scan plane lines to be displayed. 2 equals every other image, 3
equals every third image, and so on.
For example, if you wanted to display lines showing previously scanned locations for the third series,
images 1 through 20, with the lines appearing on every third image, you would type: xr 3 1–20:3
into the Accelerator Line, and then press Enter.
15.5.6 Command Line

The Command box lets you enter command-line instructions for various functions that apply to all
active viewports.
1. To view a list of all available commands, type ? in the Command box and press Enter.
2. To enter a command, type the command and press Enter.
• The command is applied to all selected viewports. As next and prior images are selected, the
command applies to those images.
• Image selection from the Command box does not function if the primary viewport contains
an MIROI plot. Use prior/next series selection buttons from the viewport hover menu.
• On the left monitor access the command line by maximizing the viewport.
The table below lists available commands with descriptions and their applicable applications.
Table 123 Accelerator commands
Image moni-
Scan moni-
Scan monitor (right)
tor (left),
Command / Description tor (left) patient ses-
scout view-
viewport sion view-
port
port
ac
Applies custom annotation to the image displayed as defined by X X X
Display Preferences settings.
af
X X X
Restores full annotation to the image displayed.
an
X X X
Removes all annotation from the image displayed.

View Images
Accelerator commands continued

Image moni-
Scan moni-
tor (left),
scout view-
viewport sion view-
port
port
ang
Creates an angle type measurement cursor by explicitly describing X X X
the end points of the lines that make up the cursor.
ap
Applies partial annotation to the image displayed as defined by X X X
Display Preferences dialog box on Exam Rx screen.
arrow <on> or <off>

Displays or removes an arrow cursor from a text annotation box for X X X
user annotation.
dist
X X X
A measure distance line will appear on the screen.
eag
X X X
Removes all graphics from the selected image.
eg
X X X
Removes selected graphics from the selected image.
el
X X X
Creates an ellipse type measurement cursor.
ematte
Displays an elliptical black matte or mask around the image. Size is
adjustable with the mouse by a left click and drag on the red open X X X
box. Position is adjustable by a click and drag on the edge of the
matte or the red solid box.
fi <filter name> filter names: e1; e2; e21; e22; e23; e3; lung; (for
edge enhancement) s1; s11; s2; s21; s3; (for smoothing filters)
and none
Apply/remove edge enhancement and smoothing filters on selec-
ted images. Edge enhancement filter names are, from least sharp- X X
ening to most: e1, e2, e3, lung; smoothing filters are named s1,
s2, s3. Entering the command fi e1 applies the least image sharp-
ening,; entering fi lung applies the most. For example: fi e1, fi e2, fi
e3, fi lung, fi s1, fi s2, fi s3, fi none.
flr
X X X
Flips the image left/right.

View Images

Image moni-
Scan moni-
tor (left),
scout view-
viewport sion view-
port
port
flrtb
X X X
Flips the image left/right and top/bottom.
ftb
X X X
Flips the image top/bottom.
fo <rows>< columns>
For example: fo 4 3
Formats the display screen as specified by rows and columns. The X
above example displays images across the screen in four rows and
three columns, or common twelve-on-one.
freehand
Displays a small solid red box that can be used to draw a freehand
trace for an ROI. You must click on the image where you want to X X X
start. Then select the red box while holding Shift on the keyboard
and move the mouse cursor around the screen to draw the trace.
gse <filter name>

filter names: g1; g2; g3; none
Gray scale enhancement increases the apparent contrast of the X X
image without changing the window/ level settings. Useful for
enhancing low contrast structures. For example: gse g1, gse g2, gse
g3, gse none).
grid <on> or <off>

X X X
(Displays or removes a ruled grid on the image.
hg
Hides all graphics on the selected image. The undo function is X X X
show graphics.
inv
X X X
Reverses the blacks and whites on the image.
ns
Displays the first image of the next series from the displayed exam X
in the selected viewport.
no
Restores the image display to display normal mode: removes all X X X
zoom, filter, pan, annotations etc. applied to the viewport. Displays
the image from the disk as created.

View Images

Image moni-
Scan moni-
tor (left),
scout view-
viewport sion view-
port
port
nori
X
Takes reference image off of selected image.
noria
X
Takes reference image off all images in the selected series.
noxr
X
Removes cross-reference lines from the image display.
pa [<start> <end>] [<rate>]

Activates cine paging. For the start and end values, enter the first
and last images you want to page thru. For rate, enter the number X X
of images per second to page through, with the maximum being
60.
pi <interval>
Allows you to set the interval for paging. The pa command must be X X
used prior to setting paging interval.
pm <spatial/temporal>
Allows you to change the mode for paging. Selecting temporal will X X
display the images in a loop mode. Spatial will display images in a
back-and-forth mode.
ps
Displays first image of the previous series of the displayed exam in X
the selected viewport.
prop <range>
range: a= all images in series; s = series; i = image range (1-15)
For example,: prop a or prop i 1-15)
Displays selected graphics on the specified images. The “i” is lower
X X X
case sensitive. In the first example, the graphic displays on all
images called into the viewport until cleared by another command
(such as erase graphics) or a different series is displayed in the
viewport. In the second example, the graphic is applied only to
images 1 through 15 in the current series.
rc
Displays (reports) current mouse cursor location in pixel coordi- X X X
nates, and a single pixel ROI reading.

View Images

Image moni-
Scan moni-
tor (left),
scout view-
viewport sion view-
port
port
rect
X X X
Creates a rectangle measurement cursor. Used for ROI.
ri
X
Puts a reference image on the selected image.
ria
X
Puts a reference image on all images in the series.
rl
X X X
Rotates the image 90 degrees counterclockwise.
rmatte
Displays a rectangular, black matte or mask around the image.
You can adjust the by clicking and dragging the red open box. You X X X
can adjust the position by a clicking and dragging the edge of the
matte or the red solid box.
rr
X X X
Rotates the image 90 degrees clockwise.
rs
X X X
Reset image to initial display parameters.
scnsave
Captures the selected image exactly as it is displayed, and creates
a new image with a series number of 99 on the system disk that in- X
cludes all graphics and display factors applied to the image and/or
viewport at the time of capture.
scroll <dx><dy>
X X X
Scroll images by delta x and delta y pixels.
sg
Shows, or re-displays all graphics on the selected image which X X X
were hidden with the hide graphics command.
siw
X X X
Applies default window width and level setting to the display.

View Images

Image moni-
Scan moni-
tor (left),
scout view-
viewport sion view-
port
port
ss [<first image> <last image>]

Saves the image orientation, W/L values, graphics, and filter and
GSE values of a range of images that you can set. Typing ss by itself X
will save settings for the entire series. A GrayScale Presentation
State Object is also created and saved to the data base.
tpe
X
Displays text page for the exam.
tm <on> or <off>
Displays or removes horizontal and vertical tick marks (rulers) X X X
along the border of the image.
tmh <on> or <off>

Displays or removes only horizontal tick marks (rulers) along the X X X
border of the image.
tmv <on> or <off>

Displays or removes only vertical tick marks (rulers) along the X X X
border of the image.
tpr
Displays a text page for the image in the primary viewport which X
lists all the ROI cursors and their statistics.
tps
X
Displays text page for the exam/series.
ua
X X X
Displays specified text in a user annotation field on the image.
wl <level>
X X X
Applies specified window-level setting to the display.
ww <width>
X X X
Applies specified window-width setting to the display.
xr <series number> <image set> : <interval>

Example: xr S3 1–20 :3
Series number: an appropriate series number to be cross-refer- X
enced. image set: a consecutive group of image numbers within
the series. interval: the interval of images to be filmed: two equals
every other image, three equals every third image, etc.

View Images

Image moni-
Scan moni-
tor (left),
scout view-
viewport sion view-
port
port
xra <series number> <image set> : <interval>

Used to add additional cross-referenced groups or series to a
scout which already has a cross-reference on it. series number:
an appropriate series number to be cross-referenced. image set: X
a consecutive group of image numbers within the series. interval:
the interval of scan plane lines to be displayed: two equals every
other image, three equals every third image, etc.
zo <factor>
Factor: magnification factor
Magnifies the image by the factor specified. For example, zo 1.5 X X X
displays the image one and one half times larger than its display
size.
autofit
X X X
Returns or sets zoom to a factor of one.
15.6 User Preferences

You can choose customized settings for annotation, tick marks, grid, right-mouse button use,
series binding, and window/level presets. You set many image-display preferences on the Viewport
Preferences window, part of System Preferences. Access System Preferences from the Mode icon at
the top of the Image Monitor.
Refer to Set Viewport Preferences for more information.

View Images
Figure 288 Viewport Preferences
15.6.1 Set annotation preferences

You set an annotation level by right mouse clicking an image, selecting annotation level from the
menu and choosing a level.

View Images
Figure 289 Right mouse menu on image to set annotation level — image at full annotation

View Images
Figure 290 Image at partial annotation

View Images
Figure 291 Image with no annotation
You set the default annotation level from the Viewports tab of System Preferences. Refer to Set
Viewport Preferences for more information.
15.6.2 Set series binding preferences

You can toggle series binding on and off using the Series Binding button on the right side of the
viewport control panel. The system series binding setting for the viewport until you click the button to
change the setting.

View Images
Figure 292 Series binding on
Figure 293 Toolbar with series binding off
You set the default series binding from the Viewports tab of System Preferences. Refer Set Viewport
Preferences to for more information.

View Images

Display Applications
16 Display Applications
16.1 Overview
NOTICE
THE FOLLOWING DISPLAY APPLICATIONS CAN BE USED WITH SCANNED

IMAGES.
Add/Subtract
Direct Multi Planar Reformat (DMPR)
Exam Split
16.2 Add/Subtract
Considerations:
• Add/Subtract can process a maximum of 1,000 images. To select a range of images, select the first
image in the range, hold the shift key and select the last image in the range.
• Add/Subtract images are displayed in the series type column of the Series list as either processing
pairs (Proc) or combination (Comb).
• Proc is the result of processing pairs of images that have identical locations in the patient’s
body. Proc series can be used like any other series of acquisition images, for example,
geometrical measurements, reformatting, 3D reconstructions, etc.
• Comb is the result of a combination of images having different locations in the patient’s
body. The absolute anatomical coordinates accompanying Comb series are not accurate
and therefore only relative geometrical measurements (for example, distance, angle or area)
made within a resulting image are accurate.
16.2.1 Add/Subtract basic terminology

Term Definition
Image addition Adds image intensity values pixel by pixel and is useful for adding thin slices
together to get a thicker slice.
Image subtraction Subtracts image intensity values pixel by pixel and is useful to evaluate con-
trasted vessels.
NOTE
Patient movement and breathing between the images can affect
the quality of the subtraction.

Maximum pixel value extrac- Locates maximum image-intensity values pixel by pixel. This is useful for
tion contrasted vessels or calcifications.
Minimum pixel value extrac- Locates minimum image intensity values pixel by pixel. Useful when evaluat-
tion ing soft tissue.
Binding Series Creates a new series consisting of copies of selected images from one or more
existing series. Useful if you have images in two separate series and want
them in one series to perform 3D or Reformat.
NOTE
Save State information is not maintained in the new series gener-
ated with Binding Series.
Accept negative pixels Allows negative pixel values in the resulting image, otherwise all negative pixel
values are set to zero.
Ratio slider When both Select Set buttons are used during addition or subtraction, equal
weighting is applied to the two pixels in each pair. You can change that with
the Ratio slider.
Disable Normalization Performs a pixel-by-pixel addition or subtraction. The images are not normal-
ized.
16.2.2 Add/Subtract and Image Combination window

In File Manager, highlight the exam you want to work with, right click and select Add/Sub.
Alternatively, highlight the series you want to work with, right click and select Open with, then
Add/Sub. You can do the same for individual images. Highlight the image you want to work with, right
click and select Open with, then Add/Sub

Figure 294 Accessing Add/Subtract from File Manager exam list
Figure 295 Accessing Add/Subtract from File Manager series list

Figure 296 Accessing Add/Subtract from File Manager image list
Figure 297 Add/Subtract window

Figure 298 Image Combination area
Element Description
Select Set (1) Defines the first image set.
Select Set (2) Defines the second image set.
Equal (=) Runs the process and generates the new images.
Ratio slider Adjusts the pixel weighting ratio between the two sets. The slider is available only
during addition and subtraction when both Select Set buttons are selected.
Save Series Displays the current series and starting image number of the saved series. By
default, images resulting from subsequent operations are added onto the end of the
same series unless you click New Save Series.
Enter the name of the series in the Description field.
Figure 299 Save Series area
New Save Series Places images resulting from subsequent operations into a new series in the File
Manager series list for this exam. If you do not select this option, the images are
saved in the current saved series.
Mode
Figure 300 Mode buttons
Button Description
Max Creates a new series that finds the highest corresponding signal intensity values in the
selected set or sets of images.

Plus (+) Creates a new series that adds the image intensity values of the selected image sets.
Minus (-) Creates a new series that subtracts the image intensity values of the selected image sets.
Min Creates a new series that finds the lowest corresponding signal intensity values in the
selected set or sets of images.
Bind Creates a new series that consists of copies of the selected images from one or more existing
series.
Accept Negative Pixels

Allows negative pixel values in the images. If not enabled, all negative pixel values are set to zero. This
operation is useful on pre- and post-contrast studies of the same slice location. This checkbox displays
only when you press the minus button.
Figure 301 Add/Subtract window with Minus mode button selected showing Accept Negative
Pixel box
Disable Normalization
Performs a pixel-by-pixel addition or subtraction. The images are not normalized.
• Disable Normalization is available for both addition and subtraction.
• If Accept Negative Pixels is not selected the negative pixels are scaled to zero and the resultant
images are clipped to 16–bits if they go beyond the bounds of 16–bit images.
• If both Accept Negative Pixels and Disable Normalization are selected, then Add/Subtract accepts
input of negative pixels and performs a true pixel-by-pixel subtraction. A message displays if any
overflow beyond the 16–bit image size occurs.
Clear Selection
Clears the values associated with the Select Set buttons.

16.2.3 Add/subtract images

To create a new image set, for example add thin slices together or subtract pre/post contrast series,
follow the steps below. Processed images will be annotated with the date.
1. In File Manager, highlight the exam you want to work with, right click and select Add/Sub to open
the Image Combination window. Alternatively, highlight the series you want to work with, right
click and select Open with, then Add/Sub.
2. Select the images.
• If one set is selected, each operation produces one resulting image.
• If two sets are selected, images in the two sets are paired according to physical location in
the patient’s body. Unpaired images are ignored.
3. On the Image Combination window, click the left Select Set.

4. If you are adding/subtracting two sets of images, select the second set of images, and click the
right Select Set.
• By default, equal weighting is applied to the pixels in each pair, but you can use the Ratio
slider to change the weighting values.
• Drag the slider to the left to increase the pixel weighting of the images on the left Select Set
button. Drag the slider to the right to increase the pixel weighting of the images on the right
Select Set button.
5. Click + or -.
6. For subtraction, click Accept Negative Pixels unless you want the negative pixel values set to 0 in
the resulting image.
7. Typically, use the system provided series number.
8. Click = (equal sign) to generate the images in the exam defined by the left Select Set button.
9. To repeat the add/subtract procedure with a new series number and description, click New Save
Series.
16.2.4 Bind series

To combine images from different series to create a new series, follow the steps below. Processed
images will be annotated with the date.
3. Click the left Select Set button.
4. Click the right Select Set button.
5. Click Bind.

Use the system-provided series number, or enter a new series number in the Save Series field and
a name in the Description field.
6. Click = to generate the images in the exam defined by the left Select Set button.
7. To repeat the add/subtract procedure with a new series number and description, click New Save
Series.
16.2.5 Create images with min/max values

To create a new image using only the minimum or maximum CT numbers, follow the steps below. The
resulting images are annotated with the day on which the addition/subtraction was performed.
3. Click the left Select Set button.
4. Click Min (minimum) or Max (maximum).
5. Typically, use the system-provided series number.
6. Click = (equal).
7. Optional: Click New Save Series to repeat the add/subtract procedure with a new series number
and description.
16.3 Direct Multi Planar Reformat (DMPR)

Direct Multi Planar Reformat (DMPR) allows you to move from the usual 2D image review mode to
a prospective 3D image review mode in the axial, sagittal, coronal and oblique planes. You can also
automatically create batch reformats using predefined reformat protocols and network reformatted
images to selected reading locations, reducing total exam time and increasing productivity.
DMPR displays images in anatomical orientation where anterior is at the top, posterior is at the
bottom, right is on the left and left is on the right. For example, if you have a data set where the patient
was scanned prone, the image display is automatically set to this orientation.
Reformat protocols can be applied in three ways:
• Automatically – the reformat protocol is defined before the scan takes place and runs after the
source images have reconstructed.
• Semi-automatically – the reformat protocol is defined before the scan takes place but requires
manual prescription of the slices before it is run.
• Manually – the reformat protocol is defined after the scan is acquired.
No matter how reformats are applied, they appear in the Reconstruction and Image Processing Task
List.
DMPR allows for:

• visualization of multi-planar volumes

• creation of multi-planar reformat batch images
• visualization of multi-planar batches
• networking of multi-planar batch images
• archiving of multi-planar batch images
Applications of DMPR include:

• fast review of scan prescription
• combined with AutoView for trauma imaging and automated multiplanar reformat protocols
• surgical planning assessment of trauma
• CT angiography
• as a supplement for other diagnostic information
To combine groups, the following parameters must be identical within each group:
• Scan Type
• Thickness
• Interval
• DFOV
• R/L Center
• A/P Center
Once the recon and multi-planar reformat batch images are created, the Reconstruction and Image
Processing Task List allows you to select and view image sets.
Considerations
• Each group must be contiguous to be able to be combined with the prior group in a DMPR
session. DMPR can be prescribed with primary and secondary recons. DMPR reformats are limited
to 2,000 images. Additional reformat protocols can be added from the Volume Viewer Reformat
application which can be accessed with the File Manager.
• Any scans acquired after scanning has completed on the original scan group using Add Group
are not added to the DMPR session unless Link was selected for the original scan group prior to
scanning. Remember to include all of the desired coverage area in the original scan prescription.
• If the patient orientation is prescribed as Decubitus (right or left), you will observe that the Paging
slider for the sagittal image will scroll images in DMPR coronal viewport and vice versa. This
is because in Decubitus orientation, patient’s sagittals and coronals are switched. Hence, the
DMPR sagittal viewport contains the coronals from patient’s reference axis, and the DMPR coronal
viewport contains the sagittals from the patient’s reference axis.
• Make sure the interval between groups is appropriate to support DMPR in secondary recons 2-10
if the slice thickness prescribed for the groups in primary recon 1 is different.

16.3.1 Reformat Tools panel

To display the Reformat Tools panel, select or create a reformat task from the Reconstruction and
Image Processing task list.

Figure 302 Reformat Tools panel

16.3.1.1 Icons
On the Reconstruction and Image Processing task list, an icon identifies a reformat task.
This icon: Identifies a reformat task:
Any reformat task
16.3.1.2 Reformat processing order

Reformats are processed in order whether they are automatically run or manually run. One does not
interrupt the other.
16.3.1.3 Processing and transfer status indicators

The process and transfer status of recons and reformats is shown by changing the fields showing the
task name.
Indicator: Means:
Processing has not started, reconstruction

has not been added to the recon queue
Processing has not started, but reconstruc-

tion has been added to the recon queue
Currently processing
Completed processing, not transferred
Transfer in progress
Transfer completed
Processing failure or invalid task
16.3.1.4 Reformat Settings panel

From the Reconstruction and Image Processing Task List, select a reformat task to display the
Reformat Settings panel.
NOTE
The settings for the reformat are contained in sections on the Reformat Settings panel.
These sections are collapsible. When these sections are collapsed, the current settings
for the reformat are shown on the collapsed panel.

Figure 303 Reformat Settings panel
1 Protocol section (opened) 3 Output Options section (collapsed)
2 Batch Options section (collapsed) 4 Transfer Options section (collapsed)

16.3.1.4.1 Protocol settings
Table 124 Protocol settings
For this setting: Select or set:
Type Protocol allows selecting a protocol from a anatomi-

Protocol and Manual cal category. Manual uses a generic set of reformat
parameters.
Anatomy Available only when Protocol selected. Selects the

anatomical category to select a reformat protocol
from. GE Reference Reformat protocols are stored in
the General category.
Protocol Name Available only when Protocol selected.

Select the protocol.
This setting affects the settings available in the Batch
Options section.
Model Available only when Manual selected. Selects the

model type or generic protocol that will be applied.
Two selections are available Oblique and Rotation.
Oblique – Produces sagittal, coronal, or off‐axis (obli-
que) images from CT data.
Rotate – Creates multiple images of an anatomical
region by rotating around a single axis at a specified
angle. This is used for vascular structures, such as
pulmonary veins.
16.3.1.4.2 Batch Options

The Batch Options change depending on the type of series being used in the reformat.
Table 125 Oblique settings
Model This setting is read-only (set in the Protocol settings)
Matrix Size Select the Matrix Size.
Number of images Set the number of images to include in the reformat.

This number updates based on slice thickness, slice
interval, and the start and end locations.

Oblique settings continued

Slice thickness Set the slice thickness.
NOTE
The minimum thickness is limited to the
pxiel size of the recon series from which
the DMPR is prescribed. Refer to 23.6 Image
Display on page 1025
Interval Set the slice interval.
NOTE
The minimum interval is limited to the pix-
el size of the recon series from which the
DMPR is prescribed. Refer to 23.6 Image Dis-
play on page 1025
FOV Set the field of view. The value is specified in centime-

ters (cm).
NOTE
FOV is limited to be less than or equal to
the FOV of the recon series from which the
DMPR is prescribed.
Rendering Mode Select the rendering mode.
WW Select the window-width.
WL Select the window-level.
Table 126 Rotate settings
Model This setting is read-only (set in the Protocol settings)
Matrix Size Select the Matrix Size
Number of images Set the number of images. This value updates based
on slice thickness, angle between images and start
and end location.
Angle between images Set the angle between images.

Rotate settings continued

Slice Thickness Set the slice thickness.
NOTE
The minimum thickness is limited to the
pxiel size of the recon series from which
the DMPR is prescribed. Refer to 23.6 Image
Display on page 1025
FOV Set the field of view
Rendering Mode Select the rendering mode.
WW Select the window width.
WL Select the window-level.
Preview tool
Before you save or print a batch, you can preview what the batch will look like using the Preview tool
in the Batch Options section of the Reformat Settings panel.
Figure 304 Preview tool

1 Play/Pause button 3 Preview mode buttons Toggle between loop

and rock
2 Click through images button 4 Preview speed selector
16.3.1.4.3 Output Options
Table 127 Output options
Series Description You can enter a description for the series in this field.
If you do not enter a description, the series will take
the name of the pre-selected protocol. If you are
not using a pre-selected protocol, the series will take
the name “Processed Images”. The Series Description
will always match the Series Description on the Re-
construction and Image Processing Task List for that
reformat.
Reference Image Indicate whether to include a reference image, an

optional image created as part of the batch reformat
image series.
16.3.1.4.4 Transfer options

The Transfer options allow you to send the completed reformats to network hosts. You can transfer a
single series or task or multiple series and tasks or you can transfer entire exams.
Each image series can be prescribed individually to transfer data to any network or archive host after
the image series has been fully created by clicking on the image series task bar to display the settings
for that task, and then opening the data transfer settings.
Figure 305 Transfer options

Table 128 Transfer options
Host name Select the hosts to which you want to send the refor-
mat when it is complete.
Host default level Standard Selects the priority level of the host. Standard priority
is sent after any High priority entries
Host default level High Indicates the Hosts default priority as set in Sys-
tem Preferences/Networking. Highest priority jobs are
sent as high as long as the maximum number of jobs
for a destination has not been reached
Host default level Low Indicates the Hosts default priority as set in System
Preferences/Networking. Lowest priority jobs are sent
after any Standard or High Priority jobs
Host default level Override Overrides the default priority of the host to High.
Highest priority jobs are sent as high as long as the
maximum number of jobs for a destination has not
been reached.
Figure 306 Transfer options — set transfer time
Select the option corresponding to how you want to send the reformat. Select either Series Complete
or Images Reconstructed
The default is to send each series as reconstruction for it is complete. However, for exams that take a
long time to reconstruct, you can transfer each image as soon as it is reconstructed.
Transferring an exam
You can transfer the entire exam and exam level reports using the button next to each protocol name.
This sends all series in the exam to the selected network locations when:
• You press Done Scanning or Close Exam and
• All recons are complete and
• All reformats are complete

Figure 307 Transferring an exam
Stopping a transfer
Cancel a transfer before it begins by unchecking the box next to that location. Once a transfer has
started, it cannot be stopped. Once a file transfer has taken place to a selected host, you can no longer
uncheck the selected host box.
16.3.1.4.5 Auto-Run/Run button

The Auto-Run/Run button is at the bottom of the Reformat Settings panel. This button takes on one of
two states, depending on the state of the reformat.

When the button is in this state: The reformat is in this state: Clicking the button does this:
Auto-Run You are prescribing the reformat If the button is grayed out, select
task. the appropriate protocol from the
Protocol section.
Click the button to autorun the re-
format after recon data has been
acquired.
Run The recon data is available, but the Click the button to run the refor-
reformat has not been run. mat.
This button is grayed out if you
have not selected a protocol or de-
fined a batch reformat manually,
or an Auto Batch has been run.
16.3.2 Reformat planning
16.3.2.1 Automatic reformat

For an automatic reformat, no images are acquired before planning the reformat.
1. From the Reconstruction and Image Processing Task List, click the down arrow on the series you
want to reformat.
2. Select the protocol you want to use from the Reformat Settings panel.
3. Check the Auto Run box in the lower right of the window to enable auto run. DMPR images will be
generated automatically.
NOTE
If Close Exam is selected from the Patient Session, any DMPR with Auto Run enabled
will not generate images. If Auto Run is desired, do not close the Patient Session
until the DMPR Task has completed.

WARNING
SYSTEM HAS DETECTED REFORMAT AUTO RUN JOBS FOR THIS EXAM.
AUTO RUN JOBS IN PROGRESS OR QUEUED WILL NOT COMPLETE AND
REFORMAT AUTO RUN JOBS NOT QUEUED WILL NOT QUEUE IF CLOSE
EXAM IS SELECTED. CLICK RESUME EXAM TO KEEP THE EXAM SESSION
OPEN TO COMPLETE AUTO RUN REFORMAT JOBS THEN SELECT CLOSE
EXAM ONCE ALL REFORMAT JOBS HAVE COMPLETED.
16.3.2.2 Semi-automatic reformat

want to reformat.
2. Select the protocol you want to use from the Reformat Settings panel. Adjust the settings for the
protocol. Auto Run is not selected.
3. After the source images have been reconstructed, select the reformat task.
4. Adjust the prescription parameters.
5. Click Run.
16.3.2.3 Manual reformat

For a manual reformat, the recon data is available.

want to reformat.
2. Select the protocol (or generic batch) you want to use from the Reformat Settings panel. Adjust
the settings for the protocol.
3. The default reformat views appear in the viewports: left upper viewport-oblique, left lower
viewport-sagittal, right upper viewport-axial, right lower viewport-coronal. If a protocol has been
selected, batch lines appear on the views.
4. Enter the batch prescription parameters and graphically adjust the location.
5. Click Run.
NOTE
Once a Batch is run, it cannot be modified or re-run. Add a new reformat task to create
additional Batch Reformat image sets.
16.3.2.4 Graphic object for oblique reformats

The graphic object used for planning an oblique reformat allows you to move the entire plan in the
recon scan area, extend coverage in any plane, adjust the FOV and rotate the reformat angle.
This graphic object can be used on any of the multiplanar volume views for manual reformats.
Figure 308 Graphic object – oblique reformats

1 Handle to extend coverage, number of images 3 Handle to move the entire reformat plan
in any plane
2 Handle to rotate the reformat angle 4 Handle to adjust the FOV in any plane. IN sagittal
or coronal planes the FOV handle adjusts the magni-
fication of the view, not the z location range.
5 Numbers showing start and end of reformat: 1

represents the starting point. “N” is the ending
point
16.3.2.5 Graphic object for rotate reformats

The graphic object used for planning a rotate reformat allows you to move the entire plan in the recon
scan area, change where the rotation will take place and where the start and end of the reformat will
be.
Figure 309 Graphic object – rotate reformats
1 Handle to move the entire reformat plan 3 Numbers showing start and end of reformat
2 Handle to change the angle between the slices 4 Handle to change the range of numbers be-
tween start and end of reformat

16.3.2.6 Modify active (yellow) annotation

All active (yellow) annotations on the image indicate adjustable fields. Yellow Numerical values
can also be adjusted with left/right‐click to decrease/increase values. Refer to Modify active (red)
annotation in the Reformat chapter for more information.
Figure 310
16.3.2.7 3D cursor
Use the 3D cursor to point to the same location in all viewports.
Place the 3D cursor by clicking a viewport and dragging the cursor into position, or you can move the
mouse over an area and press the Shift key.

Figure 311 3D cursor (shown with arrows)
16.4 Exam Split

Exam Split gives you the capability to divide a series of patient images into separate groups. These
new smaller image groups can be networked to desired reading stations for multiple "reads" and
multiple billings on select patient exams.
Exam Split creates a new exam of images for each accession number or procedure code to which
ranges of images are assigned. The split images are automatically installed in the File Manager and
transfered to any remote hosts selected.
Exam Split allows you to split images from a single acquisition and assign them to a Requested
Procedure ID or accession number retrospectively.

Retrospectively procedures from the HIS/RIS that were not selected at scan time can be selected.
NOTE
Exam Split requires that a worklist server be configured.
16.4.1 Selecting exams to be split

At scan time, select all patient records you want available to split in Patient Schedule.
1. From the scan monitor, open Patient Schedule.
2. From the Patient Schedule window, select the patient exams to which you want to apply Exam
Split once the images are reconstructed. You can select a maximum of 15 procedures.
Figure 312 Patient Schedule with exams selected for split
3. Click Select Patient.

When the patient record opens, only the description of the last exam selected
displays. The system stores the others and they will be available during the split.
NOTE
If multiple accession numbers are selected, lowest accession number selected is listed in
the image header. The accession number is stored in a different DICOM field (0040, 0275)
when multiple records are selected. Use Exam Split to send images to the PACS with the
associated accession number for a particular procedure.

16.4.2 Configure hosts for exam split

Use this procedure to configure available hosts to select from in Exam Split. Remote hosts must first
be configured in Network Configuration from the File Manager (refer to Configure Network Hosts
window).
Figure 313 Hosts Selection
1. From File Manager select an exam.

2. Right click and select Exam Split.
3. Click Settings .
4. From the Default host dropdown menu, select the desired host. This is the host to which images
are always sent.
5. Click the box next to the name you wish to have available for selection in the Split window Hosts
dropdown menu.

16.4.3 Split exams when the scan is completed

Use this procedure to split a series into separate groups that can then be used for multiple reads and
billing.
1. Complete an exam where multiple Requested Procedure ID or Accession Numbers are available in
the Patient Schedule. Procedures can be added post scan as long as the procedure is listed in the
Patient Schedule and was created on the HIS/RIS.
NOTE
Patient information added manually and Saved to Schedule using New Patient icon
cannot be selected in Exam Split.
2. In File Manager, highlight the examwant to work with, right click and select Open With, then
select Exam Split.
Figure 314 Accessing Exam Split from File Manager exam list

Figure 315 Exam Split window
Screen Element Description
1 Patient Information Displays patient name, date of birth
2 Host selection settings. Sets default host and other

remote hosts for selection in split set up.
3 Split set up Select series and or images to assign to procedure for

splitting.
4 Procedures to split to Procedures selected at scan time by accession number

to split to.
5 Add procedure for splitting

(continued)
Screen Element Description
6 Select host destination for split images to be sent
7 Opens image range selection and edit series descrip-

tion
8 Initiate split and transfer of images
9 Split progress status
10 Not assigned to procedure/accession number
3. From the Exam Split window, confirm that the desired procedures are listed.
4. To add a procedure, select .
5. Check the procedure you want to add in the Select column.

6. Select the images to assign to each procedure. To assign entire series, place a check under the
procedure to assign to for the entire series.
7. To assign a smaller range of images to a procedure, select .
8. Type the first image number and last image number desired or adjust the slider bar to select
range.

9. Select icon to edit the series description if desired. Click in the series description area
and type the desired text.
10. Select to check any additional hosts to send the split images to. To
configure hosts refer to Configure hosts for exam split.

11. Select to process the split and send the images to the selected destinations.
12. If another Split is desired, select Close and repeat steps 2 through 10.
16.5 Prospective Exam Split

Prospective Exam Split allows you to specify how to split images from a scan into separate requested
procedures/accession numbers prior to performing the scan. This capability is especially useful in
cases of full body trauma or for chest, abdomen and pelvis exams. If the operator is not sure which
body parts to scan, he/she can scan large portions of the patient, usually the head, neck, chest,
abdomen and spine, and have the images go to separate exams.
You select the requested procedures/accession number from the Patient Schedule. During the scan,
the system forwards them to the PACS or other reading station. Prospective Exam Split works with
primary, secondary and reformatted images. DMPR or reformatted images inherit the requested
procedure that is assigned to the recon from which they are generated. Scout images and dose
reports are all associated with the primary requested procedure. ECG Trace secondary capture image
Series 599 are associated with the procedure selected for the Series utilizing Cardiac scan type. The
system designates the exam with the lowest accession number as the primary requested procedure.
To transfer these items to other workstations, use Retrospective Exam Split. Refer to Exam Split for
more information

When you build a protocol you can save a pre-configured procedure code for the protocol in the
Recon Output Option settings. When scanning, if there is a pre-configured procedure code for the
protocol, the system compares the recon procedure code prescription with the patient study code. If
they match, the procedure code displays in the Requested Procedure field.
If the recon procedure code prescription and patient study code do not match, the pre-configured
procedure code displays in the Requested Procedure field and the field is outlined in red. In either
case, you can select a different accession number from the patient information in RIS.
You enter, edit and delete pre-configured procedure codes in Set Exam Split Preferences. You can also
use this function to import recently scanned exam procedures for use as pre-configured procedure
codes.
16.5.1 Enabling Prospective Exam Split

Retrospective Exam Split Mode must be set to HES in Exam Split Preferences to use Prospective Exam
Split. Refer to Set Exam Split Preferences in the System Management chapter for more information.
When PPS (Performed Procedure Step) is enabled and multiple worklist entries are selected (i.e.
Prospective Exam Split), a single PPS event will be sent using the details of lowest selected accession
number.
You enable Prospective Exam Split for a protocol in Protocol Management. In the Output Options
group, set Exam Split to On.
16.5.2 Splitting exams prior to scanning

In Patient Schedule select the requested procedures you want sent to a different workstation for
analysis. The patient name, birth date and ID must be the same for each exam.
1. From the scan monitor, open [Patient Schedule].
2. Enter multiple exams for the same patient name/patient ID, one for each body part to be scanned.
For example, select one for Head, one for Chest and one for Abdomen/Pelvis.
Figure 316 Patient Schedule showing 3 exams for same patient
3. Highlight all three exams in Patient Schedule, then click Select Patient. You will not be able to
open multiple exams if the patient names, birth dates and IDs are not identical.

4. Select the protocols for each exam. In this case, select a Head protocol and a Chest/Abdomen/
Pelvis protocol.
5. Run the scout scan. Add a secondary reconstruction to the scout scans for each accession number
in the exam that you want to attach the scouts.
Figure 317 Adding a secondary reconstruction
6. For each recon group to be sent to another workstation, in the Output Options group:
a. Set Exam Split to On.
b. In the Requested Procedure, select the name of the procedure to be sent to the other
workstation. The procedures come from the procedures you entered in Step 2.
Figure 318 Output Options showing Exam Split set to On with drop-down list of
procedures

You can leave the Requested Procedure field blank. If there is a pre-configured procedure
code for the recon group and it matches the patient study code, it displays in the field.
If the pre-configured procedure code and patient study code do not match, the field is
outlined in red. You can override the alert or select a different accession number from the
patient information in RIS.
c. In the Transfer Options group, click on the network host to which the exam is to be
transferred.
7. Scan the remaining groups.
8. Dose reports will be automatically added to each procedure selected.

16.6 Advanced Processing

Advanced Processing allows you to prescribe post processing application task on Edison server.
Prescribing Advanced Processing task from the scan session.
NOTE
Applications available for Advanced Processing follow the Authorized Product Matrix
Manual.
1. From the Reconstruction and Image Processing Task List, click the down arrow on the series on
which you want to use Advanced Processing.

2. Select Add Application.
3. Select the application you want to use from the Advanced Processing panel. Check the Auto Run
box in the lower right of the window to enable auto run if needed.

Filming
17 Filming
17.1 Overview
The Film Composer is the interface with your camera that allows you to manually film images.
The available film formats are determined by your camera. This section presents the procedures
necessary to successfully film images. To configure a DICOM or Post Script printer contact your service
representative.
17.2 Film Composer

Film composer is launched from scan/review sessions and the system status area.
Figure 319 Film Composer Icon on system status area
17.2.1 Tools on the Film Composer
17.2.1.1 Maximized/Minimized Film Composer

The film composer has two modes (Maximized mode and Minimized mode) and the mode can be
switched by the Maximize or Minimize button. Only the maximized mode has the Tool panel at upper
left window.

Filming
Figure 320 Maximized/Minimized Film Composer
ICON Functions
1 Change to minimized mode
2 Change to maximized mode
3 Close Film Composer
NOTE
Any images added in the Film
Compser will be removed when the
composer is closed. Make sure to
print images if desired prior to clos-
ing the composer.
4 Printer selection
5 Print Options setup
6 Layout Selection

Filming
7 Add new page
8 Delete current page

Delete all pages
9 Print all pages

Print current page
10 Print Status messages

Filming
17.2.1.2 Print Options Setup
Figure 321 Print Options Setup

Filming
Auto Clear Clear images from the film composer automatically when the print
finishes.
Show ESI ESI is displayed instead of DICOM or Screen Capture image.
No of Copies Number of sets for filming
Favorite Layouts Three favorite layouts can be defined (1x1 to 8x8), and the buttons are
displayed. Click on the Layout icon to set.
Film Size and Orientation Sets the film size and orientation to use for the printer selected.
NOTE
The film size and film orientation used will be the last size
and orientation used when the Filmer is opened again.
Expose Order Order of insert images, “Left/Right Top/Bottom” or “Right/Left Bot-

tom/Top” is selectable.
NOTE
Expose Order is applied only to the current page. You need
to set the expose order on each individual page.
Custom Layout Sets user-defined custom layout.
Layout Setting Sets Favorite Layout format and base format for Custom layouts. Click
and drag on the grid to select the desired format.
Auto Print Not active at this time.
17.2.1.3 Custom Layout

Pre-defined custom layout is selectable. And, user can create new custom layout.

Filming
Create a Custom Layout

1. Click Custom Layout Load/Create/Save .
2. Click Create/Save Layout.

3. Click Layout Settings .
4. Click and drag to set number of rows and columns for the base format.
5. Click on the film frame you want to resize.
6. Click and drag the yellow line to resize.
7. Repeat with the other film frames until you have the design you want.
8. Enter a name for the layout.
9. Click Save Layout.
Figure 322 Create Custom Layout

Filming
17.2.1.4 Tools on the viewport

The viewport of Film Composer supports the keyboard operation for the selected image as follows.
• Ctrl + x --- cut the image
• Ctrl + c --- copy the image
• Ctrl + v --- paste the image
• Delete --- delete the image
The viewport of Film Composer supports the image drag and drop by mouse operation to change the
frame in the page.
Figure 323 Pull-down menu on each viewport
The viewport of Film Composer supports the pull-down menu by pressing right mouse button as
follows.

Filming
Function Definition/Action
Cut Image Cuts the image in the frame and moves to clip board.
Copy Image Copies image to the clip board.
Paste Image Pastes last image cut or copied to the frame.
Delete Image Removes the image in the frame.
Insert Image Inserts the last image cut or copied into the frame.
Reset All Resets any magnification applied to the image frame.
Auto Pack Images When checked, assures that blank frames are at the end of the last
sheet when images are deleted automatically and removes blank
frames on layout change to all pages.
Remove Frame Removes the image in the frame.
Add Frame Adds a frame and shifts image frames.
Annotation Level Sets the Annotation Level of the film frame. Selections are Full,
Partial, No Annotation or Custom Annotation.
Pack Images Pack Page Fills in blank frames on a single sheet and places blank
frames at the end of the sheet.
Pack All Page Fills in blank frames on all sheets and places blank
frames at the end of the last sheet.
Cross Reference Selections are None or series to Cross Reference.
17.3 Filming
17.3.1 Filming from Navigation Viewport in Scan/Review Session

The inserted image becomes the screen capture to support the copy of a graphic object on the images
if it exists.
17.3.1.1 Load an image to the Film Composer

One selected image on the Navigation Viewport in Scan/Review session is inserted into the Film
Composer viewport by using F1 key on the keyboard.
17.3.1.2 Load images in a series to the Film Composer

Print Series setup screen is opened by using F4 key on the keyboard or clicking on Print Series button
at Filming.

Filming
Figure 324 Print Series button and the setup screen
Film format selection • As is --- Keep the current Film Composer format
• Customize --- Apply the selected format (1x1 to 8x8)
Image Selection Select All for all images in the series or select Images From to indicate image
numbers to be printed.
Only 500 images can be loaded at a time. If the number of images in the series
exceeds 500, select multiple image ranges to film all images in the series.
Interval Select an Interval to print the images.
Filming Status Status of images populating the film composer is shown.
Load images Specified images are loaded onto the Film Composer.
17.3.2 Filming from File Manager

The inserted images are DICOM format.
NOTE
The graphic objects are added on the film frame when added from the Film Manager,
they are not copied.
17.3.2.1 Load an image to the Film Composer

Selected images in the List View in the File Manager are inserted into the Film Composer viewport by
drag-and-drop mouse operation.

Filming
17.3.2.2 Load images in a series to the Film Composer

When the exam or series list is dragged and dropped, all images in the exam or series are inserted into
the File Manager.
• By selecting the menu in the exam or series list, all the images in the exam or series are inserted
into the Film Composer and the Film Composer opens if it is closed.
• By selecting the menu in the image list, the selected image in the image list is inserted into the
Film Composer and the Film Composer opens if it is closed.
17.3.3 Filming from Navigation Viewport in Scan/Review Session

and File Manager
The images can be inserted from File Manager and from the Navigation Viewport into the same page.
i.e. DICOM and Screen Capture can be mixed in the same page.
17.3.4 Scout Image with Cross Reference Line

In Scan/Review Session, the Cross reference line can be added on the scout image by using the xr
command. The scout image is inserted into the Film Composer by F1 or F4 (Print series).
When the images are inserted from File Manager to Film Composer and the inserted exam contains the
Scout and non-Scout series, Cross reference lines can be added on the scout image.
• To draw a cross reference line on the scout image right mouse click, select Cross Reference, then
select the series for which reference lines needs to be drawn.
• Cross reference lines are drawn only for the images loaded into the film composer.
• When the axial image is deleted/added the cross reference lines are refreshed after selecting
Cross Reference/Series again.
• When the scout images and axial images are inserted by selecting at Exam level, Cross reference
line is automatically added to all scouts.
Cross Reference can be disabled or enabled from one pull-down menu of right mouse click by
selecting None.
17.4 Tools in Maximized Film Composer

There are four categories on the Tool panel (Display, Measure, Annotate, Analyze) on the Maximized
Film Composer. The tools are enabled when the images are added from File Manager (DICOM). The
tools are disabled when the images are added from the Navigation Viewport in the Scan/Recon
Session (Screen Capture).
17.4.1 Display Tools

The Display Tools support the functions in the table below.

Filming
Figure 325 Display Tools Collections
NOTE
The first 5 tools (excluding 1 settings button) on this panel are set by the system and
cannot be changed. The user can select a maximum of another 19 tools from the
settings options available under this panel.

Filming
Figure 326 My Tools Settings Menu

Filming
Figure 327 User can select multiple icons to display by default

Filming
Figure 328 Max number of filmer icons allowed
Icon Functions
Flip image top to bottom
Flip image left to right
Rotate Left by 90 degrees
Rotate Right by 90 degrees
Apply grid
Display Normal

Filming
Add Annotation
Apply Vertical Tick Mark
Apply Horizontal Tick Mark
Apply color map
Apply elliptic matte
Apply rectangle matte
Invert video
Propagate ROI
Flip and Rotate Images
Reference Image All Off/On
Figure 329 Color Map Selections

Filming
Figure 330 Propagated ROI
Figure 331 Flip and Rotate Images

Filming
17.4.1.1 Reference Image

The last scout image in the exam is displayed as thumbnail image when Reference Image All is
selected. The cross reference is displayed on the reference image. The Reference Image displays in the
film frame only when the format is no larger than 3x3.
Figure 332 Reference Image
17.4.2 Measure
The Measure Tools collections support the functions in the table below.

Filming
Figure 333 Measure Tools Collections
Icon Functions
Report cursor
Add Line ROI (Measure Distance)
Add Angle ROI (Measure Angle)
Add Ellipse ROI
Add Rectangular ROI
Erase All Graphics
Erase Selected Graphics
Hide/Show Graphics
17.4.3 Annotate
The Annotate Tools collections support the functions in the table below.

Filming
Figure 334 Annotate Tools Collections
Icon Functions
Screen Annotation Settings
Large Font Annotation Settings
Figure 335 Screen Annotation Settings

Filming
Figure 336 Customize Annotation

Filming
Figure 337 Large Front Annotation
17.4.4 Analyze
The Analyze Tools collections support the functions in the table below.
Figure 338 Analyze Tools Collections
Icon Functions
Apply filters

Filming
Figure 339 Filters (Edge and Smooth Filter, Grayscale Filter)
17.5 Filming Status

The Filming status for the exam can be displayed in the File Manager as Printed (F) status when images
are filmed from the File Manager viewer only.
The Filming status icon can show the status below.
• Full --- All Images except Dose SR are printed.
• Partial--- Partial Images except Dose SR are printed.
• Not Printed (No Icon)
The Filming status for the series can be displayed in the File Manager as Filmed status when images
are filmed from the File Manager viewer only.
The Filming status icon can show the status below.
• Full --- All or Partial images are printed.
Figure 340 Filming Status in File Manager (Left: Exam Level, Right: Series Level)

Filming
17.6 Exam Mix Case Support with Warning Attention

When images from different exams are inserted in the film composer, a pop-up appears to warn of
mixed patient exams. If No is selected, the insert is canceled. If Yes is selected, the image insert is
performed.
Figure 341 Warning Attention for the Exam Mix

Filming

Reformat
18 Reformat
18.1 Overview
Use the Reformat software, launched from File Manager, to display and manipulate Reformat data
sets.
NOTICE

ON THIS SYSTEM.
18.1.1 Indications for use

Volume Viewer is a medical diagnosis software that allows the processing, review, analysis, and
communication of 3D reconstructed images and their relationship with originally acquired images for
CT, MR, X-ray Angio, and PET scanning devices. The combination of acquired images, reconstructed
images, annotations, and measurements performed by the clinician are intended to provide to the
referring physician clinically relevant information for diagnosis, surgery, and treatment planning.
18.1.2 User profile

As with any medical imaging process, only qualified personnel should use this equipment. You must
be aware of the limitations of the basic imaging modality and of ensuing image processing. This
includes understanding the limitations of the initial series acquisition, image processing technology
used, and image display methods.
18.1.3 Requirements for Reformat

Certain requirements need to be met before you can perform reformat.
• A valid image set for reformat must have the same:
• Matrix size
• Display center
• Orientation
• Four or more images must be selected before selecting Reformat.

• Tilt acquisitions are not supported for right and left decubitus patient orientation.
• You cannot have two images with identical locations.
• Spacing must be less than 10 mm.
• The image set can only include axial, sagittal, or coronal images.

Reformat
• Different Display Field Of Views and Gantry Tilts can be loaded, however you have to select
between different sources of images to view them. The source annotation is located in the upper‐
left corner of the image. You can change between sources by clicking on the red annotation.
• If Volume Viewer hangs, simultaneously press Alt and X to clear the issue.
• If a message is displayed indicating images are too far apart or failed to build a reformat model for
series with a large number of images, wait several seconds and launch Reformat again. When the
series has a large number of images, the system may not have identified how many images are in
the series before Reformat tries to start.
• Reformat does not include the slice location for axial images. If axial slice location is needed,
generate the images in DMPR or generate secondary recons of the data.
18.2 Reformat
Reformatting allows you to define and display cross-sections of a 2D stack or 3D volume of image data
that are oriented differently from the original acquisition images.
A baseline view is a basic axial, coronal or sagittal view. Of these, the acquisition view displays
the images in the acquisition plane of the original image set, the other two are the corresponding
orthogonally reformatted views. They can be moved to show any location in the 3D volume, but
remain aligned parallel to the three main axes of the Right Anterior Superior (RAS) coordinate system.
An oblique view is a plane reformatted view that can be both moved and rotated to any location and
orientation within the 3D volume.
If a feature of interest extends beyond a single plane, standard baseline or oblique view reformatting
cannot show the entire feature no matter how you position the oblique plane. To create a single view
that includes the entire feature, use curved reformatting to create a curved cross-section.
Depending on system configuration, the system supports Volume Share 5 Applications on console and
Volume Share 7 Applications on console. User instructions for Volume Share 7 Application on console
are found by selecting Learning Solutions, then selecting AWS.
18.2.1 Open Reformat

1. From the File Manager, select the desired exam / series / images to reformat.
• To select a subset of images, press Shift and simultaneously click the first and last image.
• To select specific images, press Ctrl and simultaneously click individual items.
2. Right-click on the desired exam / series / image and click Reformat.

• An oblique, axial, sagittal, and coronal are displayed in the four viewports.
• My Tools tab can be customized to display any display icons. Therefore, the instructions in
this chapter are for accessing a particular icon from the tab on which it originated. On your
system, the icon may be on your My Tools tab.

Reformat
3. Change the view type by selecting a view type from the red annotation.
18.2.2 Use the Reformat Image Controls for Volume Share 5

Applications
The Image Controls display when you start Reformat.
Figure 342 Image Control area
Click an icon on the top row to set the action of the left mouse button when placed over the image.
Changing the selection in the Image Control area updates the on-view Mouse Modes menu selection.
The icons can be in one of three states:
1. Selected (depressed)
2. Unselected (light blue)
3. Unavailable (grey)
18.2.2.1 Rotate freehand or page images

1. Click the Page/Rotate icon to activate a freehand rotation or to page through images.
2. Click and drag to rotate 3D/Oblique views and page axial/sagittal/coronal views.
No rotation handle is displayed on 3D/Oblique views when this mode is selected.
18.2.2.2 Zoom (magnify) images

1. Click the Zoom icon to activate zoom mode.
2. Click and drag to zoom the image in or out.

Reformat
18.2.2.3 Roam (pan) images

1. Click the Roam icon to activate a roaming mode.
2. Click and drag the image to move it up and down and left and right (only applicable if the image
has been zoomed in).
18.2.2.4 Select objects

Click the Select icon to activate the selection mode.
18.2.2.5 W/L images

1. Click the W/L icon to activate the W/L mode.
2. Click and drag over an image to adjust the window width (left‐right motion) or the window level
(up-down motion).
18.2.2.6 Change the image orientation
Click an image orientation icon to change the plane or a 3D or oblique reformat image.
Table 129 Orientation controls
Button Description
S Superior
I Inferior
A Anterior
P Posterior
L Left
R Right

Reformat
18.2.2.7 Activate the Oblique mode
The Multi Oblique Mode button (left) displays three oblique planes defined by three adjustable color
axis (orange, green, blue).
1. Adjust any axis to update the two other oblique planes.
2. Click again to deactivate the Multi Oblique mode, which keeps the orientations defined in oblique
viewports.
The Single Oblique Mode button (right) displays a line cursor in Reformat, which is used to define a
new plane.
1. Set the function of one viewport to Oblique.
2. Make another viewport primary and then click the Single Oblique Mode button.
A solid yellow line appears, which represents the plane of the Oblique reformat.
3. Place the cursor on the solid yellow line and click and drag it to tilt the yellow line to the desired
plane.
18.2.3 Use the Reformat Image Controls for Volume Share 7

Applications
The Image Controls display when you start Reformat.
Figure 343 Image Control area
Click an icon to set the action. A user can do this by Left‐clicking the mouse button when placed over
the icon of interest.
The icons can be in one of three states:
1. Selected (Highlighted blue background)
2. Unselected (No Highlighted blue background)
3. Unavailable (grey)

Reformat
Figure 344 Additional actions within Docking Station
-The user can click the down arrow to visualize more icons within the docking station.
-The user can Left‐click the mouse on an icon, continue holding it down and drag it within the docking
station, to a new location for further customization.
Figure 345 Customize Docking Stations with Icons
-If the user wants to display additional icons to be immediately visualized within the docking station,
not immediately observed by clicking the down arrow; please perform the following:
1. Preferences
2. ToolBar

Reformat
3. All docking stations will now display. Select additional icons via the check box so they are added
to the active use docking stations.
4. Once finished, click the X on the top right of the window as changes will be immediate.
18.2.3.1 Rotate freehand or page images

1. Click the Page/Rotate icon to activate a freehand rotation or to page through images.
2. Click and drag to rotate 3D/Oblique views and page axial/sagittal/coronal views.
No rotation handle is displayed on 3D/Oblique views when this mode is selected.
18.2.3.2 Zoom (magnify) images

1. Click the Zoom icon to activate zoom mode.
2. Click and drag to zoom the image in or out.
18.2.3.3 Roam (pan) images

1. Click the Roam icon to activate a roaming mode.
2. Click and drag the image to move it up and down and left and right (only applicable if the image
has been zoomed in).
18.2.3.4 Select objects

Click the Select icon to activate the selection mode.
18.2.3.5 W/L images

1. Click the W/L icon to activate the W/L mode.
2. Click and drag over an image to adjust the window width (left‐right motion) or the window level
(up-down motion).

Reformat
18.2.3.6 Change the image orientation
Locate the Visualization docking station. Click an image orientation icon to change the plane, 3D or an
oblique reformat image.
Table 130 Orientation controls
Button Description
S Superior
I Inferior
A Anterior
P Posterior
L Left
R Right
18.2.3.7 Activate the Oblique mode
The Multi Oblique Mode button (left) displays three oblique planes defined by three adjustable color
axis (orange, green, blue).
1. Adjust any axis to update the two other oblique planes.
2. Click again to deactivate the Multi Oblique mode, which keeps the orientations defined in oblique
viewports.
The Single Oblique Mode button (right) displays a line cursor in Reformat, which is used to define a
new plane.
1. Set the function of one viewport to Oblique.
2. Make another viewport primary and then click the Single Oblique Mode button.
A solid yellow line appears, which represents the plane of the Oblique reformat.
3. Place the cursor on the solid yellow line and click and drag it to tilt the yellow line to the desired
plane.

Reformat
18.2.4 Use the keyboard shortcuts

Figure 346 Keyboard
Table 131 Keyboard shortcuts
Indicator/Key Description
Film keys Press F1 - F4 for manual filming with the Manual Film Composer.
Preset Window Width/Window Level

Press F5 - F11 for preset Window Width and Window Level.
Keys
Page Up / Page Down Keys
Press these keys to scan through the images in a viewport.
Window Width / Window Level Con-

trol Keys
Press these keys to change the WW/WL settings for images in a viewer.
The Up/Down arrow keys increase/decrease the window level, respec-
tively. The Right/Left arrow keys increase/decrease the window width,
respectively.
Tab Press Tab to swap between image control modes.
Space Bar Press the Space Bar to show/hide the MyTools palette.
Press Ctrl and simultaneously move the mouse to page through the
Ctrl Key + moving the mouse
slices.
Shift Press Shift to place the cursor at the mouse location.
Press Shift and simultaneously click and drag to draw a trace line as
Shift + click and drag
you move the mouse.

Reformat
Keyboard shortcuts continued

Indicator/Key Description
Alt Press Alt and click to edit a trace area.
Alt + s Press Alt and s simultaneously to save the image as you name it.
18.2.5 Use the right-click functions

Place the cursor over the viewport and right-click to display the on-view menu. Move the cursor down
the menu until your choice is selected. Not all choices are available under all conditions.
Table 132 Right-click menu selections
Menu Selection Description
Save Image - saves the image as a DICOM image.

Save Image As - saves the image and assigns it a description.
Save Save All Images - saves all images displayed on the screen, individually, as DICOM
images.
Save Screen - saves all images displayed on the screen as DICOM images, as a 4:1
layout.
Save to Report (if ap- Save Image to Report - sends the selected image to the Report Tool.
plicable) Send Screen to Report - sends the whole screen to the Report Tool.
Hide 3D cursor - removes the 3D cursor from the screen. Toggles back with Show 3D
cursor.
Hide Cross-References -
Show all planes -
Reference image - displays a small reference image showing the plane orientation
Display Properties and position of the current image.
Lock orientation - locks image orientation (3D and 2D oblique only). It is not possible
to change the orientation with the mouse in the locked view.
Center on cursor - centers the image on the cursor.
Center on FOV - centers the image on the FOV.
Center on object - centers the image on an object (useful after segmentation).
No Annotation - hides all annotations including the right and left markers.
Full Annotation - shows all annotations. This option is available when full annota-
tions are not shown.
Partial Annotation - hides or shows part of the image annotations (scan parameters).
Annotations
Custom Annotation - shows the annotations that have been checked in the Annota-
tion tab of the Display panel.
User Graphics - shows only the user graphics (including measurements and annota-
tions).

Reformat
Right-click menu selections continued

Menu Selection Description
When a trace has been defined with the Display Trace tool, this option is available.
Create trace - create a trace on the image.
Trace Clear last point - deletes the last point deposited.
Clear trace - deletes all points.
Lock cursor to trace - locks the 3D cursor on the trace.
Left Mouse: Paging/Rotation

Left Mouse: Zooming
Left Mouse: Roaming
Mouse Modes
Left Mouse: Selection
Left Mouse: Opacity/WW-WL
Left Mouse: Mag. Glass
Enlarge Changes the view to Full Screen.
Returns the object back to the center of the viewport. Use this tool if there are blank
Reset Pointer
viewports.
The cursor must be centered on an active ROI to view this menu.

Delete ROI - deletes the active ROI.
Delete all ROIs - deletes all ROIs.
ROI Edit ROI's label - allows you to change the ROI's label. There is a maximum of 10
characters.
Duplicate - duplicates the active ROI.
Hide/Show Statistics - hides or shows the ROI statistics.
18.3 Display
In most respects, a 3D display view is like any other view. You can adjust window width and level
as required, zoom, and scroll the image. You can add text annotations and change the color of the
displayed object. In theory, you can also perform measurements or define and perform a scalpel cut
on a 3D view since you can mark points and create traces on it. In practice, this is highly inadvisable,
because on the 3D view you have no indication how deep into the 3D object the 3D cursor is located,
and the result may not be at all what you wanted or expected.
A 3D view is different in that it displays an image of the 3D model (which may consist of one or more 3D
objects), and that you can manipulate this 3D model.
On a 3D view, you can:
• Rotate and tilt the 3D model in all directions.
• Define one or more cut planes and display the 3D model with part of it removed, showing a cross
section of the 3D model at the location of the cut plane.

Reformat
• Place a spherical shutter (mask) on the view to show only an essential part of the model, with the
remainder masked out.
• Use colors, in particular to distinguish merged 3D models in merged 3D views.
• Extract a 3D object or volume of interest from the original 3D models using the Segment tools.
18.3.1 Annotation
There are two types of annotation:
• System annotation which is automatically supplied by the system and is always displayed in the
same place. The type and amount of annotation displayed can be modified but not moved.
• User annotation which is annotation you add. This annotation can be text or measurements and
can be placed anywhere on the viewport.
Text annotation
You can add notes and comments directly on the views, and use a marker with the annotation to point
out anatomical features. User text annotations can be edited, moved or deleted as necessary. When
images are saved, any annotations shown on the images are saved with them.
Preset annotation
Preset annotations are those which have already been created and saved for future use. These
annotations can consist of text or text with measurement annotations. The preset measurement
annotations vary depending on the current protocol. In addition to the supplied default annotations
supplied, you can create and save annotations.
Measurement annotation
You can create and view various measurements (voxel value, distance, angle, area, volume) on the
views. Like text annotations, they can be moved, deleted or edited as necessary.
18.3.2 ROI
The Region of Interest (ROI) tools exist in 2D and 3D. Several shapes are available to measure a region
of interest in any view plane/volume: circle, elliptic, rectangle, and cubic for 3D ROIs. You can use the
ROI tools to obtain information, volumes, areas and statistics of anatomy or pathology. The ROI tools
allow you to:
• measure the pixel intensity value at a specific point on the image
• display the area or volume
• display the mean, standard deviation and minimum and maximum pixel values within the ROI
In order to perform measurements on an image that can be expressed in absolute values (mm), the
image must be calibrated, i.e. the relationship between image pixels and true anatomical distance in
the patient’s body (the scale factor) must be known. For images such as CT and MR this information
is automatically recorded during image acquisition and stored with the image. Measurements on such
images can therefore be expressed directly in mm, using the patient-based Right Anterior Superior
(RAS) coordinate system.

Reformat
18.3.3 Modify active (red) annotation

All active (red) annotations on the image indicate adjustable fields. Red Numerical values can also
be adjusted with left/right‐click to decrease/increase values. Other red annotations can be modified
selecting options from a menu. The selections vary based on the application launched and the
selected view.
Figure 347 Active annotation

Reformat
Table 133 Active annotation
No. Annotation Description
Right-click and select a view type from the menu to change the plane
or select a 3D model. The type of view displayed in each of the four
1 Plane or View Type views of the viewing area is determined by the selected protocol. During
image processing, you can change the view at any time using the active
annotations.
Middle-click and drag horizontally to scroll through the images or click

Scan Location to increment and right-click to decrement an image at a time. Alterna-
2
Image Location tively, you can use the left and right arrow keys on the keyboard to move
through the image set. Scan location is not available on 3D views.
Middle-click the drag horizontally to real-time magnify the image or click

to increment and right-click to decrement the mag factor. The maximum
zoom factor (ratio between acquisition DFOV and actual DFOV) is 8.0.
DFOV You cannot increase the DFOV beyond the original value, unless the
height of the stack of images (number of images × slice thickness) is
larger than the DFOV. In that case, you can zoom up to the height of the
stack of images (zoom factor < 1.0).
Smooth 1 to 3, Edge 1 to 3, and Lung filters are 2D display filters and are
available only on Axial, Sagittal, Coronal, and Oblique viewports.
Smooth 3D Plus is a 3D anisotropic filter that smoothes the whole vol-
ume. It can be applied on any 2D or 3D viewport.
3 NOTICE
THE FILTER EFFECT IS PURELY VISUAL AND ANY

STATISTICS PERFORMED ON A FILTERED IMAGE
Image Filter WILL BE PERFORMED ON ORIGINAL VOLUMES (NON
FILTERED)
NOTE
CT Filters can be applied on thick slabs only when rendering
is set to “Average”.
NOTE
CT Display filters can be combined with Cardiac filters when
in Cardiac applications.
4 Image Roam Click and move the image within the viewport.
Middle-click and drag horizontally to real-time change the slice thick-

5 Slice Thickness ness or click to increment and right-click to decrement the slice thick-
ness (2D images).

Reformat
Active annotation continued

No. Annotation Description
Middle-click and drag vertically and horizontally to real-time change the

W/L. Alternatively, move the mouse over the annotation and type in a
Window Width and Win-
6 new value or right-click to display the W/L Preset menu. To modify the
dow Level
W/L of the reference images, middle- click and hold on the reference
image and move the mouse.
Click or right-click and select Show or Hide to show/hide the patient

7 Patient Name
name.
18.3.4 Review Controller screen

The Review Controller screen contains display short cuts. The image selection sliders can appear on
the left or the right side of the image.

Reformat
Figure 348 Review Controller

Reformat
Table 134 Review Controller functions
No. Function Description
1 Maneuver Docking Stations The Main Docking Station control panel (signified by the black dots
& the yellow arrow pointing to it), can be Left‐mouse clicked and
held down to new locations. The user can place the Main Docking
station as:
1. Top justified
2. Left justified
3. Bottom justified
4. Right justified
2 Paging Direction/Speed a = Click and drag either side button to change the Thickness of the
MIP image. Slice thickness adjustment is not available on 3D views.
b = Click and drag the middle slider to page through the image set.
To page, you can also press Ctrl and click and drag the mouse up
and down.
3 Bookmarks Allows you to navigate to an image that has a graphic.
18.3.5 Toolbar
The Preferences, Toolbar selection tab contains the following tools.

Reformat
Figure 349 Preferences Toolbar Screen
Table 135 Display icons
Icon Description
Arrow Tool Deposits an arrow on the screen. Click and drag the end of the arrow to re-size and rotate
it. Click and drag anywhere on the arrow to move it.
Report Cursor Deposits a point on the viewports to display a RAS coordinate and vector ROI at the
current cursor position.

Reformat
Display icons continued

Icon Description
2D ROIs Displays statistics as average, minimum and maximum voxel values, standard deviation,
and area within the 2D ROI.
• Elliptic ROI
• Rectangular ROI
3D ROIs Displays statistics as average, minimum and maximum voxel values, standard deviation,
and volume within the 3D ROI.
The 3D color ROI provides the ability to colorize voxels inside the ROI based on ranges of
voxel value. Additional Statistics such as volume can be calculated for each colored area.
• Sphere ROI
• 3D Box ROI
Annotation Opens the Annotate control panel, which allows you to use predefined annotations on
the views or create new annotation.
Many of the options are linked to measurement tools. For example, the Distance Annota-
tion allows you to link an annotation with a measurement (e.g., Stenosis: xx.x mm).
Preset Annotation Opens the Preset Annotation control panel, which allows you to place preset annotations
on an image.
Straight Distance Opens the Measure Distance control panel, which allows you to perform measurements
on an image.
Measure Angle Opens the 2D Angle control panel, which allows you to deposit thee points on an image.
Measure Volume Opens the Volume control panel, which allows you to deposit a point to obtain a volume
measurement.
Set Color Opens the Set Color control panel, which allows selection of a color map or custom color
to apply to non-VR viewports.
Trace Opens the Trace control panel, which allows you to create and manipulate a curved
reformation, a Profile, or an X-Section.
Rotate/Translate Opens the Rotate/Translate control panel, which you can set rotation by degree and
direction and translation by distance.

Reformat
Display icons continued

Icon Description
Integrated Regis- Integrated Registration is not supported on the CT console.

tration
Link/Unlink Opens the Link/Unlink control panel, which allows you to unlink multiple volumes to
allow manual registration adjustment.
Cine Opens the Cine control panel, which allows you to automatically page through all of the
slices of a single phase series or control a 4D Cine of multiphase series.
MPR/3D Opens the MPR/3D control panel, which guides you through the creation of 3D or multi-
planar image views. From this panel you can adjust slab thickness and select render
modes such as MIP, Average, MinIP, and Volume Rendering.
18.3.6 Export Summary Table screen

In order to use this feature, within the Measure / Annotate Docking Station, a user must select either
the: Auto-Counter, Sphere ROI or 3D Box ROI icon.
In this example:
1. The 3D Box ROI icon was used and it provided the following default look:

Reformat
2. The user right clicked on the 3D Box ROI and the pop-up menu displayed. Navigate down to 'Color
Coded Display: Activate" and left click now.

Reformat
3. You will now see the ROI box fill with different colors representing different Housfield Units.

Reformat
4. Navigate to the Export Docking Station and select: Summary Table icon. You will now be able to
see the summary table display with the ROI information data set.
-Right click on the ROI entry and ensure to click "Color Coded" with a left click of the mouse.

Reformat
5. You will now see the summary table display data specific to your ROI.
18.3.7 ROI Preferences screen

From the Review Controller, click the ROI icon to display the ROI Preferences screen.

Reformat
Table 136 ROI selections
Function Name Description
Copy Sets the display of the ROI on one or all viewports for the images.
Statistics Allows any combination of minimum, maximum, average, standard deviation and vol-
ume values.
Size Type in a height, width and depth. There is no depth for the sphere ROI. This will become
the default size of the ROI, but it can be modified directly on the image.
18.3.8 Annotate an image

Use this procedure to add specific and unique annotation to an image or apply a pre-set annotation
that is saved on your system.
1. Open Reformat.
2. Click the Display tab.
3. Click the Annotate icon .
4. On the Annotate screen, click the annotation type (simple, linked, or measure).
5. Place the cursor on the image and click to deposit the cursor and default text.
6. Enter new text in the Annotation text screen.
18.3.9 Save preset annotation

Use this procedure to add a custom pre-set annotation to the Preset Annotation list.
1. Open Reformat.
2. From the Display tab, click the Annotate icon .
3. On the Annotate screen, type text in the Annotation Text field.

The preset name automatically fills in with part of the text from the annotation text field.
4. Change the preset name.
5. Select the text.
6. Press Backspace.
7. Type in a new name.
8. Click Use for other anatomy if you want the annotation available for other anatomies or Use for
other protocol if you want the annotation available for other protocols.
9. Click Save as preset to add annotation to preset annotation list.

Reformat
18.3.10 Measure
Use these procedures to activate a measure tool to obtain information, distances, and areas of
anatomy or pathology.
1. Open Reformat.
3. Follow one of the measure procedures below.
18.3.10.1 Measure distance

1. Click the Straight Distance icon .
2. After the user clicks the Straight Distance icon and places it on a viewport, right clicking on the
line itself now shows the following:
• Color
• Select from the seven default colors
• Thickness
• The user can select from 1px, 3px or 5px.
• Show/Hide
• Hide Statistics
• Hide ID
• Float stat attached to ROI

This will now place the measurement in the lower right hand corner of the viewport.
3. Click an image at the start of measurement.

4. Move cursor to end point of measurement and click.
5. View the measurement results.
18.3.10.2 Measure angle

1. Click the Measure Angle icon .
2. Click an image three times to deposit three points.

3. Click and drag the squares to adjust the points.
4. View the measurement results.

Reformat
18.3.10.3 Measure volume

1. Click the 3D ROI icon .
2. Click an image to deposit the 3D ROI on an object of interest.

3. Click any of the corners to size the volume.
4. View the area measurement results.
18.3.11 Manage Colormaps

Use this procedure to manage Colormaps on reformatted images.
1. Open Reformat.
3. Click the 3D ROI with color icon .
4. Click the image to deposit the ROI.

5. Click the color ramp displayed on the left side of the image to open the Export Docking Station -
Summary Table icon screen.
6. Click the Statistics tab to view range percentages for each color.
7. Change the values of the ROI on the viewport.
a. Click the Configuration tab to change the values of the ROI on the viewport.
b. Click a value in the Min Value column, and type a new value.
c. Click a value in the Max Value column and type a new value.
d. Click a Range name column text box to type a name.
8. To change a color in the color ramp, select a color in the Color column.
a. From the Select new color screen, drag the cursor over a color on the color wheel.
b. View the Current selected color.
c. Click Apply.
9. To add or remove a color in the color ramp, click Add or Remove.
10. Click the Presets tab to load and save Colormap presets.
11. Click Save to save setting adjusted in the Configuration tab.

Reformat
12. To load a color map preset, select the color ramp preset from the menu.
13. Click OK.
18.3.12 Add an ROI

Use this procedure to add an ROI on an image to obtain information, volumes, areas, and statistics of
anatomy or pathology. The ROI allows you to:
• measure the pixel intensity value at a specific point on the image
• display the area or volume
• display the mean, standard deviation, and minimum and maximum pixel values within the ROI
1. Open Reformat.
3. Select the desired ROI tool.
3D color ROI is available one color MR or multi-color CT.
4. Define your preferences on the ROI panel.
a. Choose an ROI propagation option.
• Select One Volume to view the ROI on only the viewport on which the ROI is displayed.
• Select All Volumes to view the ROI and statistics on all viewports.
b. Select one or more Statistic options to view any combination of minimum, maximum,
average, standard deviation and area (2D) or volume (3D).
c. Explicitly adjust the size of the ROI.
• For 2D ROIs, type a diameter in the Vertical and Horizontal Diameter fields.
• For 3D VOIs, type a VOI size for the XY-plane and Z-axis depth.
• The sphere VOI does not have a depth entry.
5. Click the desired anatomy to deposit the ROI.

6. Click and drag an ROI corner to adjust the size.
7. View the ROI measurements.
8. To hide the ROI statistics, click on the edge of the ROI to make it active, then right-click the center
of the ROI, and select Hide Statistics.
NOTE
To delete the ROI, right-click on the ROI and select Delete ROI.
18.4 View Types

The following table contains the available view types in Reformat and their function.

Reformat
Table 137 View Types
View Type Function
Displays the volume in 3D with different rendering. Default

3D rendering is high density MIP. Other modes are available
from the rendering mode red annotation.
Volume Rendered (VR) Displays the volume in 3D color rendering.
An image plane representing a cross-sectional slice of anato-

Axial
my.
An image plane dividing the body into left and right por-
Sagittal
tions.
An image plane through the body, dividing it into anterior

Coronal
and posterior portions (lengthwise).
An image plane that has been tilted through the body rather
Oblique
than following the long axis. It can look like a axial image.
A 3D image plane created by defining points along an ana-

Oblique 3D
tomical feature.
An image plane created by defining points along an anatom-

Curved
ical feature.
Profile A graph showing CT number intensity across a location.
A graph showing the percentage of occurrence and numeri-

cal statistics of each voxel intensity value in an object and
Histogram (3D data) total object volume. It also determines boundaries around
a class of similar voxel intensities and can highlight pixel
values. Statistics are not valid for 2D data.
A histogram (graph) showing the percentage of occurrence

and numerical statistics, and area calculations in a user-de-
X Section fined surface area on a reformatted slice. It also determines
boundaries around the class of similar pixel intensity values
in this area.
18.4.1 Create a Curved view

Use this procedure to display a reformat of a curved, complex view of tortuous vessels or organs. The
curved view does not need to lie along a single orthogonal or oblique plane but can follow anatomical
lines.
1. Open Reformat.
2. In one of the viewports, right-click on the view type active annotation and select Curved.
3. On an axial, sagittal, or coronal image, press and hold Shift as you deposit points along the
anatomy.

Reformat
4. As you trace, the curved image updates automatically in the curved reformat viewport.
18.4.2 Create an X Section Histogram view

A histogram graph shows the percentage of occurrence of each voxel value, either in a user-defined
surface area on a reformatted slice (cross-section histogram) or in the entire 3D object (volume
histogram). It also determines boundaries around the class of similar voxel intensities.
1. Open Reformat.
2. In one of the viewports, right-click on the view type active annotation and select Histogram or X
Section.
• If you select a view type of histogram, you will immediately view a volume histogram which
includes the entire 3D model. No other action is required. Place the cursor on the voxel
reference line and hold Shift. The image displays the range of voxel class boundary lines by
highlighting them in green.
• If you select a view type of X Section, the view will display Undefined histogram until you
start to define the trace.
• Both the volume and cross-section histograms contain the same information with the
exception of the name and measurement units. Cross-section histograms show total area,
while volume histograms show the total volume for the entire object without cut planes.
3. For a cross-section (X Section) histogram, in the viewport containing the anatomy of interest,
press Shift and simultaneously click the image to deposit points on the area of interest to create a
trace.
NOTE
The histogram values and statistics are those of the current 3D model, not those of
the original exam. If the 3D model contains only a given range of voxel values, only
voxels within that range will appear in the histograms. Statistics and computed values
of surface area or volume displayed on the histograms are subject to the same accuracy
limitations as other on-view measurements. This tool can be used for cross-section and
volume measurements of specific anatomic features if the feature to be measured can
be clearly defined by a range (class) of voxel values.
18.4.3 Create an MPVR view

Use this procedure to create an Multi-Projection Volume Reformation (MPVR) view. This type of thick
slab reformatted image is often used to see vessels in Computed Tomography Angiography (CTA)
scans.
1. Open Reformat.
2. Click the red annotation in the upper‐left corner of the viewport and select 3D or MIP render
mode. The selections available are dependent on the view type.
MIP is used most often in CTA models to demonstrate the most intense voxels.
3. Click the Oblique Mode icon .

Reformat
4. Click and drag the yellow line on the image.

5. Place the cursor over the red thickness annotation to do one the following options.
• Type the desired thickness and press Enter.
• Middle-click and drag to the desired thickness.
18.4.4 Create a Profile view

A profile graph shows the voxel value along a 3D trace (profile). This allows you to analyze the
voxel value distribution of a 3D object in various ways, as an aid in setting up 3D processing (e.g.,
thresholding).
1. Open Reformat.
2. Select the Profile Layout preset, if available.
3. In one of the viewports, right-click the view type active annotation and select Profile.
4. On an axial, sagittal, or coronal image, press and hold Shift as you deposit points along the
anatomy.
As you trace, the profile view displays the pixel intensity along the trace.
5. On the profile view:
• The horizontal axis is the position in millimeters along the trace and the vertical axis is the
pixel intensity values as a function of that position.
• Press Shift to display the pixel intensity from the location of the 3D cursor. Click and drag the
white line to move it, which in turn, moves the cursor on the image.
• View the displayed statistics.
18.5 Volume Render

Volume Rendering uses the concept of Opacity. For different density levels, each voxel transmits a
certain amount of light, which is reflected on the following voxel, and only the residual light reaches
the following layer. The resulting image is the total sum of the reflection from each layer of tissue
through which the light has passed. The effect of using Volume Rendering on a dataset is that it
makes highly opaque objects more visible and at the same time it makes less opaque objects more
transparent.

Reformat
Figure 350 Opacity Curve
Letter Description
(A) Ramp up
(B) Lower threshold
(C) Upper threshold
Figure 351 Opacity Levels and Associated Light

Reformat
Description
Left = Structures presenting density value associated with high opacity reflect light:
they are visible.
Right: = Structures presenting density value associated with low opacity transmit light:
they are translucent.
18.5.1 Up ramp VR adjustments

• To decrease background noise, increase the value of the lower threshold.
• To increase visualization of soft tissues structures, decrease the value of the lower threshold.
• Max opacity can be reduced: structures become more translucent.
Threshold Values constant: (50 to 800); Opacity values are changed.
Figure 352 Opacity Values
Description
Left = 100%
Middle = 50%
Right = 25%
Opacity Values constant: (100); Threshold values are changed.
Figure 353 Threshold Values (Left to Right)

Reformat
Description
-200 Low Threshold
-100 Low Threshold
0 Low Threshold
50 Low Threshold
100 Low Threshold
18.5.2 Surface rendering

Surface Rendering is similar to Volume Rendering except that it first separates the Volume of Interest
(VOI) from the original data set and then it creates the rendered image.
Figure 354 Surface Rendering
18.5.3 Render modes

The Render modes consist of Volume Rendering, HD MIP, MIP, Min IP, Ray Sum, and Integral.
Table 138 Render modes
Mode Function
Exists only if the model was built using volume mode and is used to display the surface of a
Volume Rendering
model.
Displays the model using the High Definition Maximum Intensity Projection mode. The mode
HD MIP is identical to the MIP mode as described below, except that image definition is greater but
the system speed is slower.
Weighted MIP Displays MIP rendering enhancing front voxels and fading voxels in the back.

Reformat
Render modes continued

Mode Function
Displays the model using the Maximum Intensity Projection mode. In this mode, the density
MIP
of each point on the screen is the maximum density along a line perpendicular to the screen.
Displays the model using the Minimum Intensity Pixel mode. In this mode, the density of
Min IP
each point on the screen in the minimum density along a line perpendicular to the screen.
Displays the model by summing the model’s intensity along lines perpendicular to the
Ray Sum
screen. This mode simulates conventional radiography images.
Displays only the surface of the model, but the density of each surface point is equal to the
Integral
sum of densities along a shallow depth below the displayed surface point.
18.5.4 VR Controls screen

From the Visualization Docking Station, click the "Advanced VR Settings" icon and the VR Controls
screen will appear.

Reformat
Figure 355 VR Controls screen

Reformat
Table 139 ROI selections
Ramp Defines the opacity curve shape.

• Step: surface type rendering displaying structures with high voxel values.
• Ramp-up: displays structures with high values typically vessels and bone.
• Ramp-down: displays structure with low values typically airways.
• Plateau: displays structures within a given range.
• Valley: use with cut plane to create endo-luminal view.
• Attach mode: used to apply multiple plateau ramps attaching colors to ranges of
voxel values.
Enhance Contours Enhances boundaries of structures. This is useful to display vessels or orthopedic
cases.
Transparency Makes internal objects transparent and makes objects boundaries more visible.
Zoom Zoom in or out to modify the range of voxel values displayed.
Histogram Displays the voxel distribution (number of voxels per voxel value) in the image. Peaks
correspond to voxel values that are highly represented in the image.
Vertical Red Line Represents the numerical value of the voxel at the location of the 3D cursor. Moving
the 3D cursor on the image will change the location of the red line.
White box Represents the Opacity Threshold values. When using Ramp-up shape:
• Drag the lower white box to the right to remove soft tissue from an exam to
modify the maximum opacity of voxels.
• Click the upper white box at the top of the ramp and drag up or down to modify
the opacity of all visible voxels.
Blue Box Allows you to shift the whole ramp. Click and drag the solid blue box on the ramp to
change the upper and lower values of the ramp.
Red Box Represents the scale of voxel values. Click and drag the box left or right to shift the
display.
• Zoom in or out with the Zoom icons upper-right corner.
• Right-click the main control to return to the original zoom.
VR Ramp Represents the voxel opacity in the VR images as a function of the voxel values. It
means that voxels with identical value will have the same opacity.
Color Activates the color. An unchecked box displays the VR in black and white.
Partial Volume Filter Attenuates the partial volume by associating partial volume voxels with adjacent
voxels that represent the more opaque object. It improves the visibility of structures
that would otherwise be hidden by partial volume voxels and improves the color
coding of voxels in color mode.

Reformat
ROI selections continued

Active Color Use to select the active color. Click the square color button below the ramp (the
triangle above the color gets black). Click Active Color to change the color.
Transition • Smooth: shaded transition from one color to the next.

• Step: all voxels inside the value range display the same color. When Step is
selected small white diamonds indicating range borders display. Click the dia-
monds to adjust precisely range of values that are assigned to each color.
Brightness The amount of light displayed in the model. Type in a value greater than 100 to
increase the light in the model.
18.5.5 Create a multi-VR object

You can merge multiple objects into a multiple VR model into a single view or model to perform more
complex VR views with multiple object segmentation and visualization.
1. Open Reformat.
2. First, the user must change a viewport to 3D. Second, the user must navigate to the Visualization
Docking Station and click the "Multi-Objects" icon.
3. Click the Auto Select icon .
4. Select the desired structure.

• Small Vessels - segments vessels below a 5 mm diameter.
• Any Structure - segments vessels greater than a 5 mm diameter and soft tissues growing
from a seed point.
• Bones - segments bony structures growing from a seed point.
5. Click Add.
6. Click Yes to clear the upper‐left viewport.
7. From any 2D view, click and hold on the object you want to add.
A green filter will fill the object while this object is being reconstructed in the upper‐left viewport.
8. In a viewport, right-click and select Mouse Modes > Left Mouse: Selection.
9. Drag the VR viewport and drop it on the viewport of the isolated object where the message, Drop
here to reassign views displays.
10. From the Tools section, click the VR tab.
11. From the Visualization Docking Station, click the Multi Objects icon .

Reformat
12. On the Multi-Object panel, hover over the objects.

The corresponding object appears in the left window.
13. Select an object to adjust its transparency.
14. Click the Eye icon to hide or show the corresponding object on the active viewport.
18.6 Segmentation
To display a specific feature within the image, you can define what part of the exam data should be
visible, and what part should not. The main Segment tools include:
• Threshold: To extract a region of interest by selecting a range of voxel values that represents a
specific tissue or anatomical feature.
• Scalpel: To perform cuts in the 3D volume to define the region of interest.
• Paint: To mark the region of interest with colored paint and then display only this region.
• Auto Select: To select an object and add it on or remove it from the selected view.
The process of removing structures is sometimes referred to as volume segmentation because the 3D
volume is segmented, or split, in two parts: the volume of interest that is currently displayed, and the
remainder that is removed from view.
After volume segmentation, the displayed part of the 3D model consists of one or more 3D objects. A
3D object is a part of the 3D model that is separate from other parts. Two 3D objects are separate if
there is at least one voxel width of empty space between them.
Sometimes two seemingly separate objects still act as one, because they are still connected
somewhere by a bridge of voxels. It is also possible that a seemingly single object turns out to consist
of two or more parts, separated by narrow gaps. The tools on the Advanced Processing screen can
help you to deal with these effects.
18.6.1 Segment Docking Station

The Segmentation Docking Station tab contains Advanced Processing tools used to refine segmented
objects or combine them using Boolean operations. Before using the tools, perform an initial
segmentation with any of the Segment tools.
When a tool is clicked, a control panel for that tool displays.
Figure 356 Segment tab

Reformat
Table 140 Segment selections
Auto Select Allows you to select an object and add or remove it from the selected view.
Auto Contour Click the center of the structure or use the click and drag method to define a
diameter. Adjust contour if needed. Accept and Measure. Click Auto Contour icon
again to initiate a new contour.
Threshold Opens a screen from which you extract a region of interest by selecting a range of
voxel values that represents a specific tissue or anatomical feature.
Remove Object Opens a screen from which you remove or keep isolated objects or display
removed structures.
Scalpel Cut outside or inside region. Opens a screen from which you cut the 3D volume,
split an object into separate object, define a volume of interest or remove part of
the 3D volume.
Paint on Slices Opens a screen from which you trace contours on the baseline (axial, sagittal
and coronal) views, to outline and mark the region of interest on the slices that
intersect the region.
Quick Paint Opens a screen from which you paint with an adjustable sphere-shaped cursor
on reformatted slices to define the volume of interest.
Advanced Processing Opens the Advanced Processing screen that consolidates many advanced seg-
menting processes.
One Click AVA The One Click AVA button is activated with VesselIQ Xpress licenses and allows
vessel tracking in one click.
Two Click AVA The Two Click AVA button is activated with VesselIQ Xpress licenses and allows
vessel tracking in two clicks.
18.6.2 Scalpel control panel

From the Segment tab, click the Scalpel icon to display the Scalpel control panel.

Reformat
Figure 357 Scalpel control panel
Table 141 Scalpel selections
Cut Inside Click and drag around the object of interest and then click the appropriate
button to either cut inside or outside the trace. The trace may appear either red
or green.
Cut Outside Saves the current settings as a new VR preset.
Cut On Trace Applies the cut along the trace.
Clear Clears the latest trace.
Cut Depth Allows changing the Scalpel from a restricted depth defined by the text field or
an Infinite depth.
Apply to all volumes Applies the action to all volumes.
Undo Undoes the last operation performed. If the view on which the last operation
was performed is changed, the possibility of undoing the last operation is
permanently lost.
Keep Object Keeps all the voxels that are attached to the object of interest under the cursor.
18.6.3 Advanced Processing panel

From Reformat, click the Segment tab and then click Advanced Processing. Advance Processing
consolidates many processes: dilate, erode, filters, subtraction methods, close gaps/open bridges,
close holds, and extract surface.

Reformat
Figure 358 Advanced Processing panel
Table 142 Advanced Processing selections
Determines the number of layers you want to add or remove. Change the value by
Size in Voxels
using the slider or by typing in a value.
Add one or more layers (20 maximum) of voxels to the surface of the current 3D
Dilate objects. This feature can restore voxels that were removed by operations like thresh-
olding, erosion, or opening bridges.
Removes one or more layers (20 maximum) of voxels from the surface of the current 3D
Erode
objects.

Reformat
Fills in the gaps and connects the adjacent features. Adjacent features in the 3D
volume that appear to consist of a single object may be composed of more than one
3D object when you try to use Keep Object or Remove Object. This can be caused
by the presence of narrow gaps, often only a few voxels in size, that separate the
features. This mostly occurs when using thresholding to define a feature of interest,
when the threshold setting is marginal. You can try to modify the threshold setting or
alternatively use Close Gaps to fill in the gaps and connect the adjacent features. You
set the size in voxels of the gaps you want filled in.
This function resembles the Dilate function, but only gaps up to the specified size are
Close Gaps filled in; the rest of the objects are not dilated.
This function consists of performing a dilation followed by an erosion. Since erosion
does not totally remove the voxels added by dilation, some small gaps or holes are
filled in. A closing size of N is obtained by N dilations followed by N erosions. This
means that small gaps or holes having one of their X, Y, or Z dimensions less than 2N
are filled in. For example, a closing size of 3 is obtained by three dilations followed by
three erosions. This means that small gaps having one of their three dimensions less
than six are filled in.
Open Bridges describes the opposite function.
Removes residual bridges and separates adjacent features in the 3D volume. You set
the size in voxels of the bridges you want removed. This function resembles the Erode
function, but only the bridges up to the specified size are eroded.
This function consists of an erosion followed by a dilation. Since dilation does not
totally restore the voxels removed by erosion, some fine structures remain eroded. An
Open Bridges
opening size of N is obtained by N erosions followed by N dilations. Fine structures
having one of their X, Y, or Z dimensions less than 2N are removed. For example,
an opening size of 3 is obtained by three erosions followed by three dilations. Fine
structures having one of their three dimensions less than six are removed.
Close Gaps describes the opposite function.
Resets any such inner holes to the original voxel values. When using thresholding, this
can result in holes appearing inside the 3D volume (i.e., closed spaces inside the 3D
volume where the voxel value is outside the selected range).
By default, the voxel value inside such inner holes will be set to the same value as the
Close Holes
outside of the 3D volume (empty space).
If you have used the Scalpel or Paint tools to remove part of the 3D model, any holes
enclosed within the 3D volume resulting from these operations will also be re-filled
when you use this feature.
Removes all data from the inside of the current 3D objects, leaving only the surface.
Since the inside of the objects no longer contain any data, little if any further process-
ing is possible.
Use this function to speed up the display after you have fully defined your region or
Extract Surface objects of interest; e.g., during rotation or batch filming, or to modify 3D shading. Enter
a surface thickness of at least 2 to guarantee connectivity information for any further
operations such as selecting or removing objects. With a value of 1, the result appears
visually correct, but the surface is too thin to be considered as one or more coherent
objects.

Reformat
Intersection keeps only the voxels that exist in the same location in both objects. The
Intersection
values of the resulting voxels are those of the original object in the primary view.
Set Addition keeps all the voxels that exist in either of the objects. If a voxel belongs
to both objects, its value in the primary view is kept. Use Set Addition to combine
structures obtained using different processing tools. For example, you may need differ‐
ent tools and settings to process a vessel from the left side of the patient and another
Set Addition vessel from the right side. By treating the two vessels separately and storing the results
in the Save/Recall panel, you can optimize the processing for each side.
After recalling both from the Save/Recall panel in two separate views, the set addition
operation allows you to join and display them as a single object.
Set Subtraction removes all the voxels in the primary view that also exist in the
secondary view. In other words, the secondary view is subtracted from the primary
view.
Using a set operation on the data from two 3D models results in a single object (3D
model). As an example, you can start by using thresholding to select the entire hip
bone structure and store the result in the Save/Recall panel. Next, isolate and select
Set Subtraction only the femur (using paint or scalpel) and store the result separately. Subtracting the
femur from the complete bone structure may now allow you to see the extent of a hip
bone fracture that was obscured by the femur.
This is different from the merge operations, which allow you to display more than one
3D model at the same time and show their spatial relation by means of cut planes and
different levels of transparency. Merge operations are strictly a display feature; they do
not combine the separate 3D models.
Filter Floaters allow you to remove small residual objects in the 3D model that can
Filter Floaters
appear after thresholding, usually resulting from noise in the original image set.
Undo Undo becomes active after you have performed an action.
Place the cursor over pixels representing the pixel intensities you want to keep. Keep
Keep Object
Object keeps all pixels with the selected intensity; all other pixels are discarded.
18.6.4 Combine segmented objects

Use this procedure to combine 3D segmented objects together.
1. Open Reformat.
2. Select and view the images to be used for combining objects.
All objects must originate from the same master volume.
3. From the Tools section, click the Segmentation Docking Station.
4. Perform segmentation to generate objects to combine using any segmentation technique
(Threshold, Auto Select, Paint, etc.).
5. Display objects to combine in separate views.
6. In a viewport, right-click and select Mouse Modes > Left Mouse: Deposit Points icon.
7. Double-click to isolate first view of interest.
8. Single-click to isolate second view of interest.

Reformat
• Views of interest display red and green borders. Other views should not have color borders.
• To adjust red and green borders, click the view to set red, the other view will turn green.
9. Select an operation (results of the operation display in the red views).

10. Click the Segmentation Docking Station -> Advanced Processing Icon
11. The Advanced Processing panel will now display, perform one of the following functions.
• Click the Subtraction icon to remove all the voxels in the primary view that also exist
in the secondary view.

Before subtracting, make sure the borders of the view are displayed as: Red - Green = Red.

Reformat
• Click the Intersection icon to keep only the voxels that exist in the same location in
both objects.
• Click the Addition icon to keep all the voxels that exist in either of the objects.
18.6.5 Paint On Slices

Use this procedure to draw contours of the structure of interest on different slices. The volume to keep
will be interpolated based of the defined contours.
1. Open Reformat.
2. From the Tools section, click the Segment tab.
3. From the Segment panel, click the Paint On Slices icon .
4. Move the 3D cursor to the edge of the feature of interest.

5. Optional: Click Edge Attraction to automatically refine the drawn contours, adjusting them to
nearby structure edges.
6. Press Shift and click to deposit the cursor.
7. Click and drag the 3D cursor to define the area.
When the mouse button is released, the first and last points connect.
8. Move to the next slice on which you want to paint.

Reformat
• It is not necessary to define contours on every slice.

• The contours interpolates to the intermediate slices.
9. Repeat the process until your reach the last slice containing the structure to contour.
10. Click Apply.
Figure 359 Paint on slices
18.6.6 Add/Remove anatomy with Auto Select

Use this procedure to automatically remove anatomy from reformatted images.
1. Open Reformat.
2. From the Tools section, click the Segment tab.
3. From the Segment panel, click the Auto Select icon .
4. Select a tool for segmenting.

• Click Small Vessels for vessels less than 5 mm. Click once to fill and track vessel.
• Click Any Structure for vessels greater than 5 mm or soft tissue. Click and hold until area of
interest is filled.
• Click Bones to segment bones.

Reformat
• Click Pick from VR.
5. Click Add or Remove depending on the desired outcome.

6. Scroll through the axial images at minimum slice thickness.
If any vessels are contoured in green, put the cursor on the missing vessel in the 2D view and click
and hold until the area of interest is filled.
7. Repeat steps to complete all missing vessels.
Figure 360 Auto Select
18.6.7 Remove Object

Removes small residual objects in the 3D model that can appear after thresholding, usually resulting
from noise in the original image set.
1. Open Reformat.
2. Navigate to the Segmentation Docking Station
3. Click on the Remove Object icon.
4. You will now see the Remove Object panel display.

Reformat
-For example, click on Remove Object.

-Next, click on parts of the image you want to be removed.
18.6.8 Threshold an image

Use this procedure to threshold the image and keep only voxels within a specified range of value.
1. Open Reformat.
2. Click on the Segmentation Docking Station
3. Click the Threshold icon .
4. Select the desired image from which you want to threshold.

5. From the Threshold panel, use one of the following methods to adjust the threshold range of
voxel values.
• Click and drag the Min. and Max. Threshold sliders.
• Type a minimum and maximum value in the Min. and Max. fields.
• Click Bone or Air to apply preset threshold values.
6. Click Apply Threshold to display only the part of the 3D volume with voxel values inside the set
range.
7. To further refine segmentation, select the object on the viewport and choose to remove or keep
the object.
• Click Remove Object to remove all voxels connected to the object.
• Click Keep Object to remove all objects not connected to the object.

Reformat
Figure 361 Threshold
18.7 Batch
The Batch function allows you to rapidly set up a set of regularly spaced images, preview the set as an
animated sequence (batch loop) and film and save it.
18.7.1 Batch types

A batch can be one of the following types:
• Parallel oblique batch: a series of parallel oblique slices along a common center line
• Radial oblique batch: a series of oblique slices generated radially around a common axis
• 3D batch: a series of 3D images obtained by rotating a 3D object around an axis
• Batch loop: a series of 3D images obtained by rotating a 3D object in a continuous mode
A batch loop allows you to rotate the 3D model, to adjust the display speed and to stop it in any
position. You can select the number of views making up the loop, the FOV to use, etc. A batch
image set can be viewed step-by-step or as a batch loop. It can be filmed, and/or saved on the
image disk as a new series in the exam. To set up a batch you typically start with a batch protocol.
A default batch protocol is provided for each of the three types of batches. You can use these as a
starting point for your own custom batch protocols which you can save and re-use.
18.7.2 Batch protocol

To set up a batch you typically start with a batch protocol. A default batch protocol is provided for
each of the three types of batches. You can use these as a starting point for your own custom batch
protocols which you can save and re-use.

Reformat
A batch protocol defines:

• Batch mode: oblique or rotation.
• Number of views and spacing between views (mm or degrees).
• Spacing between views.
• Display field of view.
• Slice thickness (and render mode for thick slices).
• Output mode: this can be preview only, film, archive, film + archive, filmer images or filmer
movies. If you select film mode, you can also define the film layout.
When creating and saving your own custom batch protocol, you have two options:
• Add it to the list of existing batch protocols for the current loading/processing protocol.
• Combine it with the current loading/processing protocol to create a new loading/processing
protocol. Create a custom multiple-batch protocol by combing two or more batch protocol
setups.
18.7.3 Preview, film, or save a batch

Once you have defined the batch, you can:
• Preview the resulting batch as an animated sequence (batch loop). The controls allow you to set
the display rate (frames per second), to pause and restart the sequence, and to move through the
set step-by-step.
• Film the batch, i.e., send image set to a hardcopy device such as a laser camera.
• Save the batch on the image disk of the workstation. A new series is created in the current exam
and can be used later for viewing and/or processing.
18.7.4 Export Docking Station

Figure 362 Export Docking Station icon set
Batch Creates rotation, loop or oblique batch images based on your prescription.
Movie Creates a comprehensive movie including different rotations, zoom and pan of the
volume.

Reformat
QTVR Not applicable in reformat.
Quick Export Exports in a single click a batch of rotations of a 3D view or a full batch of contiguous
images for 2D images.
NOTE
Video Export does not work on the Operators Console.
Save Image Saves selected image with user-selected format.
Save State Saves current status of Volume Viewer (3D Model, displays, ROIs) as an additional
series of the exam. A One-Touch protocol entitled Save State will appear in the
Application field providing the ability to restore Volume Viewer State.
Save/Recall Opens a clipboard where you can drag and drop objects for temporary storage
within the current Volume Viewer session.
Film/Save options Saves format type and other film options.
Summary Table The summary table is a standard Volume Viewer feature which automatically cap-
tures measurements as they are made during a VV session. The summary table
is optimized in advanced applications to provide a user friendly display of the
statistics.
Statistics can be compared over time to a reference date, which can be easily
modified and will display the percentage of change on comparison measurements.
18.7.5 Batch screen

Click the Film/Save tab and then click Batch to display the Batch screen.

Reformat
Figure 363 Batch screen — Loop tab Figure 364 Batch screen — Oblique tab

Reformat
Figure 365 Batch screen — Rotate tab
Prescription mode • Oblique displays a set of lines to define the reformat planes.
• Rotation defines projection planes. The defined planes rotate 180°.
• Loop defines the first and last slices of your projection planes that can be set to
any degree of rotation.
The displayed values are those of the current protocol and can be modified. The text
fields change depending on the mode you select (oblique, rotation or loop).
Copies Appears only if Print or Print & Save are selected as an Output mode. Enter a value in
the text field.

Reformat
Output Modes • > Print > allows filming of the projection images and makes the Format and
Reference Image buttons available. Select a film format and select the film that
you want the reference image to appear on.
• > Save > creates a new series in the browser. The series type is determined from
the Film/Save Options screen. Note that if Color Save has been turned on from
the Film/Save Options screen, the projections will be saved as SSAVE images
even if Rfmt is selected as the image type. Screen saves cannot be filtered or
measured.
• > Filmer Images > drops all generated images into the filmer (AW only).
• > Print/Save > allows for both filming the generated images and saving a new
series to the browser.
• > Filmer Movie > drops the generated images in the filmer as a movie to be
exported as .mpeg or .avi image type.
Format Appears only if Print or Print & Save are selected as an Output mode. The Format
menu allows you to make a format selection.
Reference Image Appears if Print or Print & Save are selected as an Output mode. Select which film
you want the reference image to appear on: the first film, all films, or no film. The
reference image is the first image of a rotation that has the following items displayed
on it: number of views, rotation degrees, and the direction arrows icon.
Apply to • > Current Volume > – Apply to the displayed volume.

• > Phases of this Series > or Series of this Exam – Apply to all phases in a series
selected or all series in the exam selected.
• > All Volumes of all Exams > – Apply to all volumes of all exams selected.
Preview Displays the planes in a movie prior to filming or saving the images.
OK Saves and previews the images simultaneously. If Save or Print & Save is the selected
as output mode, a new series is created in the Patient List.
Advanced Allows you add a new batch step for oblique or rotation. Click the arrow button and set
the parameters as desired.

Reformat
18.7.6 Export Images screen

Figure 366 Preferences -> Export Tab Menu
Element Description
Current Description Choose either an existing description from the drop-down box, or be prompted to enter
a new description before saving. Each new description gets stored in the drop-down
box.

Reformat
Format • Color saves non-VR images in Color SCPT. Due to DICOM format restrictions, Win-
dow Level and Width of color SCPT images cannot be modified. It is then recom-
mended to unselect this option to be able to perform windowing adjustments
when reading saved images in PACS or other DICOM viewers.
• Color (VR images) saves VR images in Color SCPT.
• Hide Cursor on Copies saves images with cursor hidden.
• Key Image Note when checked, all saved images are referenced into a single Key
Image series (DICOM standard) when exiting Volume Viewer. This Key Image series
can be opened in the Viewer or any compatible PACS or other workstation (all
referenced images must be pushed on a remote host).
• Save State: saves the current status of Volume Viewer (3D Model, displays, ROIs…)
at the same time as saving the image. This Saved State can be used later on to
restore the Volume Viewer State.
• Force Saving Square Images: When sending rectangular viewport, adjusts the
image in a square format (no resize but adding space around image). This option is
mainly used for PACS or other DICOM systems not supporting rectangle images.
• High Definition: Saves the image in high resolution.
• Save as Reformatted or PJN: Images saved under these formats contain geomet-
rical information so that they can be reloaded in 3D software and freely windowed.
• Check Save as Reformatted or PJN to save images in this format every time it is
possible. Images saved under these formats contain geometrical information so
that they can be reloaded in 3D software and freely windowed. Click the link [when
possible] to display the list of image types that can be saved as Reformatted and
PJN according to DICOM requirements.
Uncheck the option Save as Reformatted or PJN to benefit from Color and Save State
capabilities every time you save an image.
Color and Save State options are not compatible with Reformatted DICOM format.
These settings cannot apply to images which were saved as Reformatted.
18.7.7 Film/Save Options screen

Click the Film/Save tab and then click Film/Save Options to display the Film/Save Options screen.

Reformat
Figure 367 Film/Save Options screen
Select Printer Printer options are displayed in the menu. Note that the camera selected from this menu
can be different from the camera selected from the Film Composer.
Current Batch De- Allows you to use the Patient List series description name for the saved series. Select Ask
scription for description when you want to be prompted to provide a description.
FOV is a multiple Enter a multiple by which the FOV is changed when clicking on the red DFOV annotation.
of For example, if the FOV is set to 130, the FOV is adjusted as a multiple of 130 – 6.5 mm/13
mm/26 mm. It is not possible to set the DFOV higher than the acquired FOV or lower than
a DFOV of 8 mm.

Reformat
Format • Color Save (non-VR Images) - saves non-Volume Rendered images in color.
• Color Save (VR Images) - saves Volume Rendered images in color.
• Hide Cursor on Copies - hides or shows the cursor on the saved or filmed image.
• High Definition - films images along the Z direction in high definition.
Image Type for Re- When saving reformatted images, you can select the image type. The image type deter-
format mines functions that can be performed on the image and how the annotations are
stored.
SCPT:
• Allows W/L adjustments of saved images.
• Saves only annotation (system or user entered) that is currently visible on the view.
These annotations are part of the image: they can no longer be edited or deleted.
Reformatted:
• Allows W/L adjustments, measurements, and filtering of saved images.
• Automatically saves all system annotations with the view, even if they are hidden
at the moment that you save the image. However, the user annotations (text and
measurements) are saved only if they are shown at the moment that you save the
image.
18.7.8 Set up a batch oblique

Use Batch Oblique to define a set of oblique planes adjusting settings (range, angle, position) from a
grid on a reference image.
1. Open Reformat.
2. Export Docking Station, select the Batch icon.
3. Click the Oblique tab to display a grid used to define the oblique planes.
4. Type a value for the Number of Images, Spacing Between Images, Slice Thickness, Mode
(Average, MIP, MIN, VR), and FOV.
5. Select the desired output mode from the menu.
• Choose Print to send generated images to the default printer (setup the Format and the
display of a Reference Image).
• Choose Save to save generated images in a new series in the browser.
• Choose Print/Save to film the generated images from a default printer and save them in a
new series.
6. Click OK.
The Spacing between views and slice thickness can be set independently of each other creating a
gap, contiguous or overlapped images.

Reformat
Figure 368 Oblique tool
Number Description
1 Add slice handle
2 Tilt handle
3 Move handle
18.7.9 Batch film images

Use this procedure to set up a batch rotation of images to film/save.
1. Open Reformat.
3. From the Batch panel, click the Rotate tab.
18.7.9.1 Rotate 360° 3D images

1. Click the appropriate arrow to indicate rotation direction.
Figure 369 Rotation direction
2. Type in the number of images or angle between images in the appropriate field.

Reformat
Modifying one of these parameters updates the other.

3. Type in the FOV.
new series.
5. Click OK.
18.7.9.2 Radial planes on 2D views

1. From the Export Docking Station, Batch Icon - Protocol drop-down menu, select Fan.
2. Adjust the center of radial slices (A), first radial plane location (B), and the number of radial planes
(C) on the 2D reference image.
Figure 370 Radial prescription
3. Enter the Number of Images, Spacing Between Images, Slice Thickness, Rendering Mode, and
FOV.
new series.
5. Click OK.

Reformat
18.7.10 Save a curved parallel plane or rotating curve batch

Use this procedure to set up a Loop batch for a curved parallel plane or rotating curved batch.
1. Open Reformat.
3. From the Batch panel, click the Loop tab.
4. Prescribe one of the following.
• For a curved parallel plane batch:
• Scroll to the first image to be saved and click Set Start.
• Scroll to the last image to be saved and click Set End.
• For a rotating curved batch:

• Adjust the angle of the first image from the Angle active annotation on the curved
viewport and click Set Start.
• Set the angle of the last image and click Set End.
5. Type the number of images to be saved.

6. Press Enter.
7. To save the new series, set Output to Save.
8. Click OK.

Data Management
19 Data Management
19.1 Overview
The File Manager allows you to manage your acquired images. This section contains information on
how to save, restore, delete and network images using File Manager. It also includes procedures on
how to make an anonymous patient and edit patient data.
File Manager has four sections:
• A Controls Area, which allows you to select databases, search databases, and access functions
that you can use on exams.
• The Exam List, which shows the exams in the selected database. Status information for exams is
also provided here.
• The Series List, which shows the series and image information for the exams selected in the Exam
List. Status information for series and images is provided here.
• A navigation viewport, which shows images you select from the Series List.
19.2 File Manager

To open File Manager to access browser applications, follow the steps below. This procedure uses
Image Viewer as an example.
File Manager is always accessible on the right monitor.
On the right (display) monitor, click the File Manager “drawer”. (You do not have to click the File
Manager icon – just click the drawer that is labeled with the File Manager icon .
Figure 371 Opening File Manager

Data Management
Figure 372 Sections of the File Manager Drawer
1 Controls area 3 Series list
2 Exam list 4 Image display/Image list
You can resize these areas in relation to one another.

Place your cursor over the line you want to move. Click and drag the line between the exam list and
the series list and the line between the series list and the images list. The images will shrink/enlarge as
the area is reduced/increased.
The system will use the new sizes the next time the drawer opens and following system restart.
19.2.1 Controls area

The controls area of the File Manager has a set of controls that allow you to change the source
database, search the database and launch applications.

Data Management
Figure 373 Controls area of the File Manager
1 Source menu – select the database you 3 Search box – typing a string of characters
are using in this box will search for that string in
any of the searchable fields of the source
2 Applications – gives you shortcuts to database
launching applications
19.2.1.1 Local/Remote Exam List Selection

The Local/Remote Exam List Selection controls the contents of the Exam List and displays the host
database or archive to which you are currently connected. The default source list is the local database
of your scanner.
19.2.1.2 Search box

To help you find an exam, you can type a character string to find into the search box.
When you type a character string into the search box, the system searches:
• patient names (in any part of the name)
• patient IDs
• exam IDs
• exam description
Search results appear in the exam list. The exam list changes color to indicate that you are looking at a
filtered list.
Figure 374 Filtered exam list

Data Management
To remove the filter, click the Close icon in the search box. The filter is also removed if you close
the File Manager, or if you choose a different source database.
19.2.1.3 Source menu

When you click on a network or media device in the Source menu, the Exam List displays the exams
from the selected source. You can also access the list of network sources by clicking the down arrow on
the right of the Source menu box or by accessing the Configured Network Hosts window.
Figure 375 Source menu
NOTE
When selecting the USB device from the Source Menu, the USB may fail to be read. To
read the USB, select Media Creator from the File Manager controls area, close Media
Creator and select USB from File Manager Source Menu.
19.2.1.4 Application icons

The controls area displays application icons. The applications available depend on the options
purchased for your system.
To change the icons displayed in the control area, right-click in the control area and select the icons
you want to display. Up to seven icons can be displayed. If you choose to display more than seven, an
arrow icon displays indicating more choices.
Figure 376 Control area icon selection

Data Management
Table 143 Application icons
Icon Description
DICOM Header — displays a listing of the image DICOM fields.
Media Creator – save DICOM images to media.
Data Export – save images in non-DICOM formats.
Scan File Manager — List of scan files available for reconstruction.
Network Manager – show the network and archive queues.
Network Settings – set up network locations.
19.2.1.5 Recycle Bin

When images are deleted using the right-click selection, they are initially moved to the Recycle Bin.
Images can be restored back to the local disk. The Recycle Bin can hold up to 10,000 images. You
cannot delete further images until the bin has available space. The Recycle Bin icon indicates how full
the Recycle Bin is.
Table 144 Recycle Bin status icons
This Recycle Bin

icon:
Indicates: The Recycle Bin The Recycle Bin The Recycle Bin The Recycle Bin The Recycle Bin
is between 0% is between 13% is between 38% is between 63% is between 89%
and 12% full and 37% full and 62% full and 88% full and 100% full
1200 images 1201-3700 im- 3701-6200 im- 6201-8800 im- 8801-10,000 im-
ages ages ages ages
To see the contents of the Recycle Bin, click the Recycle Bin icon.

Data Management
Figure 377 Recycle Bin
To perform this action: Do this:
Restore an exam from the Recycle Bin Highlight the exam and then click Restore
Delete an exam from the Recycle Bin Highlight the exam and then click Delete
Delete all exams from the Recycle Bin Click Empty Recycle Bin
19.2.2 Exam list

The exam list contains all current and previous exams still stored on the console. An exam appears in
this list once the first image is created and stored in the database from the first step in the Task List.
Figure 378 Exam list
19.2.2.1 Exam list columns

By default, the following columns are displayed:
• Exam tab status

Data Management
• Patient name (in the format configured for the system) (last name, first name or first name last
name).
• Exam description
• Patient ID
• Exam networked flag
• Exam archived flag
• Examination date
You can configure the Exam list to display these additional columns:
• Exam ID
• Accession number
• Referring physician
• Examination time
• Patient name in ideographic form (certain locations only)
• PPS flag – this flag is displayed if PPS commands have been sent (available only at sites where
PPS has been configured)
See Configuring the Exam List on page 802 for information about configuring, arranging, and resizing
the columns displayed in the Exam list.
19.2.2.1.1 Exam status column

The first column of the Exam list shows icons representing the status of exams.
Table 145 Exam list status icons
This icon: Indicates:
The exam is for the patient currently on the table.

To bring the exam tab to the front, click the icon or double-click the exam.
The exam is open in a tab, but the patient is not on the table. (For example, the patient scan is
complete and the patient is no longer on the table, but you are performing image processing
tasks.)
To bring the exam tab to the front, click the icon or double-click the exam.
The exam is closed.

To open the exam, click the icon or double-click the exam.
The tab will show the scan task list and the dose report, and the current state of image
processing. Images will be displayed if assigned to a display viewport.
Image processing is not completed, but the tab for the exam is closed.
If the exam was aborted before image processing was complete, you can reopen the exam and
continue with image processing.

Data Management
Exam list status icons continued

The exam is being pulled from a remote network host, a DVD, or USB media.
The exam is paused for remote network or archive.
19.2.2.1.2 Network Status icons

The Network Status column shows the network state of exams.
Table 146 Network Status icons
No icon The exam has not been networked.
All series in the exam have been networked.
A network transfer is in progress for the exam.
There was an error when attempting to network the exam.

The icon displays if there is an error in transferring to any network location.
Click the icon to open the network queue manager.
The exam has been partially networked. (One or more series in the exam have been net-
worked.)
A network transfer is paused.
NOTE
The icons change depending on the language used in the user interface.
Hovering over a network status icon displays a pop-up list showing the destinations to which the exam
was networked. The list is limited to 10 destinations.
Figure 379 Network destinations pop-up list

Data Management
Destinations to which there has been a network error are shown in red.
For partially networked exams, see the network status flags in the Series list for information about
where the series in the exams are networked.
19.2.2.1.3 Archive Status icons

The Archive Status column shows the archive state of exams.
Table 147 Archive Status icons
No icon The exam has not been archived.
An archive is in progress for the exam.
All series in the exam have been archived.
The exam has been partially archived. (One or more series in the exam have been archived.)
There was an error while attempting to archive the exam.

If the archive is a network archive, click the icon to open the network queue manager.
An archive is paused for the exam.
NOTE
The icons change depending on the language used in the user interface.
19.2.2.2 Right mouse options in the exam list

Right clicking your mouse while the cursor is over an exam, brings up a menu of tasks you can perform
on the exam.

Data Management
Figure 380 Right mouse menu on exam list
• Open Exam — Select to open exam in the Reconstruction and Image Processing Task List. You can
also do this by double clicking an exam in the exam list.
• Send Exam To — Send the exam to another device on the network. Available devices display in a
drop-down menu
• Anonymize Patient — Select to remove identifying information from the images of this exam.
• Edit Patient — Select to open the patient record for updates/changes.
• Exam Split — Select to open an Exam Split session, allowing you to "split" a series of patient
images into separate groups. Refer to Exam Split in the Display Applications chapter for more
information.
• Add/Sub — Select to access the Add Subtract function. Refer toAdd Subtract in the Display
Applications chapter for more information.
• Reformat — Select to access the Reformat function. Refer to Reformat for more information.
• Additional image processing options— Select to access additional image processing functions.
Additional options purchased will be listed on the menu.
• Send PPS — Select either complete or discontinue the performed procedure step (PPS) for a
patient. Refer to Performed Procedure Step (PPS) on page 803 for more information.
• Delete Exam — Select to delete the highlighted exam. Refer to Deleting exams on
page 801Deleting Exams for more information.

Data Management
19.2.2.3 Sorting the Exam List

You can sort the Exam List by any displayed column. Click a column heading to sort the list by that
column.
Figure 381 Exam list column headings
NOTE
Changes to the sort order are retained, even after a reboot.
You can change the order of columns (except for the Name column) by clicking and
dragging the column headings.
19.2.2.4 Deleting exams

To delete an exam, right-click the exam in the Exam List and then click Delete Exam. Alternately, you
can select the exam and then press the Delete key.
The system asks you to confirm that you want to delete the exam.
You can delete more than one exam at a time. Shift‐click exams to select a contiguous list of exams, or
Control-click to select exams one by one.
When you delete an exam using the right-click selection, the system checks to see if the Recycle Bin is
full. If the Recycle Bin has enough space, deleted exams are moved to the Recycle Bin.
If there is not enough space in the Recycle Bin to hold the deleted exams, the system posts a message.
The Recycle Bin can hold up to 10,000 images.
To permanently delete exams without moving them temporarily to the Recycle Bin, highlight the
exams you want to delete, press and hold Shift and then press Delete .
NOTE
There are some conditions that prevent you from deleting exams:
• The exam is for the patient on the table
• The exam is open in a tab
• The exam has open processing
• Networking or archiving for the exam is in process
If you try to delete an exam that has any of the above conditions, the system displays a
message informing you why the exam cannot be deleted.

Data Management
19.2.2.5 Configuring the Exam List
19.2.2.5.1 Choosing which columns to display

You can change which columns are displayed in the Exam List. Right-click on any column heading
(except the Network column), and select the columns you want to display from the pop-up list.
Figure 382 Exam List – choosing columns to display
19.2.2.5.2 Changing the width of columns

To change the width of columns in the Exam List, click and drag the right edge of the column heading.
NOTE
You cannot change the width of columns that show only icons.
19.2.2.5.3 Changing the order of columns

You can change the order of the columns in the Exam List by clicking and dragging the column
headings.
The first column (Exam Status) cannot be moved.
Figure 383 Exam List – changing column order

Data Management
19.2.2.6 Keyboard shortcuts

The following shortcuts apply when working with the Exam List:
• The Delete key deletes the selected items. The system will prompt you to confirm any deletions.
• To permanently delete exams, press and hold Shift and then press Delete.
• Simultaneously press Ctrl and A to select all items in the Exam List.
• To select a contiguous range of items, select the first item, press Shift, and then select the last
item.
• To select a non-contiguous range of items, select the first item, press Ctrl, and then select the rest
of the items you want to select.
19.2.2.7 Performed Procedure Step (PPS)

Performed Procedure Step (PPS) communicates to PACS and HIS/RIS after a procedure is complete.
It improves the transfer of data to PACS by providing a complete message when all data has been
transferred.
When PPS is enabled and multiple worklist entries are selected (i.e. Prospective Exam Split), a single
PPS event will be sent using the details of lowest selected accession number.
If the PPS column is displayed, the PPS icon appears when PPS is completed for an exam.
19.2.2.7.1 PPS Column

You can set your exam list to include the PPS state of each exam by selecting PPS flag from the exam
list column chooser drop-down menu. There are three states of exam status:
• COMP ends the exam and PPS. You can annotate an image or add a series, such as a screen
save, but you should not edit the patient information once it is in this state. If you edit the exam
(through Edit Patient Data), the exam is no longer recognized by the HIS/RIS system as the exam it
requested. This status annotates the exam as COMP.
• DISC notifies the HIS/RIS that you are aborting the PPS. Use this only if the images you acquired
were unacceptable or were not for the correct patient. This status annotates the exam as DISC.
• DEFER does not end PPS. You can still post-process and edit the patient information. However,
once it is in this state, if you edit the exam (through Edit Patient Data), the exam is no longer
recognized by the HIS/RIS system as the exam it requested.
19.2.2.7.2 Send PPS for an exam

Selecting PPS from the browser menu bar displays a window and allows you to Complete or
Discontinue the PPS on the patient. This status annotates the exam as INPR.

Data Management
19.2.3 Series list

The Series List shows the series and image information for exams in the database. It appears on the
right side of the right monitor. When you select an exam in the Exam List, the Series List updates to
show the Final Dose Report and all series associated with the exam.
If you select a series that contains images from the Series List, the images are previewed in the
viewport directly below the Series List.
Figure 384 Series list
The Series List sorts the series in an exam by the series number, although you can sort the columns by
any of the columns. The series types are indicated with text labels.
Table 148 Series labels
This label: Indicates:
SCOUT Scout: acquired scan data that can be viewed, W/L, measured, and so on.
PROSP Prospective: acquired scan data that can be viewed, W/L, measured, and so on.
COMB Combined: result of a combination of image data that can be W/L. Produced by Add/Sub from
images at different locations.
SSAVE Screen Save: screen capture data that can be W/L. Produced by the Viewer, 3D, and Reformat
applications.
Dose Report: generated by each exam if Dose Report is enabled on the system. CDTIvol, DLP,
and Dose Efficiency displays during scan prescription and provides patient dose information.
PROC Processed: post-processed data that can be W/L and measured. Produced by Add/Sub from
images at the same location.
REFMT Reformat: post-processed data that can be W/L, filtered, and measured.
3D Three-dimensional: post-processed data that can be W/L. Produced by Volume Analysis.

Data Management
Series labels continued

This label: Indicates:
SR Structured Report: generated by each exam if Structured Dose Report is enabled on the
system. A CT Dose Report can enable tracking of dose for the patient by the hospital radiation
tracking system/HIS/RIS.
GSPS Gray Scale Presentation State: produced by the Viewer to be used in conjunction with
the original series to capture presentation information (W/L, flip, rotate, zoom). It can be
networked to review stations that support this DICOM type.
RETRO Retrospective: reconstructed data post-scan.
19.2.3.1 Sorting the Series List

By default, Series List sorts by series number. To sort on a different column, click the column heading.
19.2.3.2 Deleting series and images

To delete a series or image, right-click the item in the Series List and then click Delete Series or Delete
Image. Alternately, you can select the item and then press the Delete or Shift and Delete to delete the
series or image permanently.
The system asks you to confirm that you want to delete the item.
You can delete more than one item at a time. Shift‐click items to select a contiguous list of items, or
Control-click to select items one-by-one.
When you delete a series or image, the system checks to see if the Recycle Bin is full. If the Recycle Bin
has enough space, deleted items are moved to the Recycle Bin.
If there is not enough space in the Recycle Bin to hold the deleted items, the system warns you that the
items will be permanently deleted and asks you to confirm that you want to delete the items.
To permanently delete exams without moving them temporarily to the Recycle Bin, highlight the
series or images you want to delete, press and hold Shift and then press Delete .
19.2.3.3 Configuring the Series List
19.2.3.3.1 Choosing which columns to display

You can change which columns are displayed in the Series List classic view. Right-click on any column
heading, and select the columns you want to display from the pop-up list.
By default, the Series List has the following columns:
• Series type
• Series name
• Series number
• Number of images
• Networked

Data Management
Additional columns you can display in the Series List include:

• Archived
• PPS Status
19.2.3.3.2 Changing the width of columns

To change the width of columns in the Series List classic view, click and drag the right edge of the
column heading.
19.2.3.3.3 Changing the order of columns

You can change the order of the columns in the Series List classic view by clicking and dragging the
column headings.
19.2.3.4 Keyboard shortcuts

The following shortcuts apply when working with the Series List:
• The Delete key deletes the selected items. The system will prompt you to confirm any deletions.
• To permanently delete series or images, press and hold Shift and then press Delete.
• Simultaneously press Ctrl and A to select all items in the Series List.
• To select a contiguous range of items, select the first item, press Shift, and then select the last
item.
• To select a non-contiguous range of items, select the first item, press Ctrl, and then select the rest
of the items you want to select.
19.3 Job Management Screen

From File Manager, click the Network Management icon .

Data Management
Figure 385 Job Management window
Jobs Menu
Figure 386 Jobs Menu
The Show jobs menu filters the list of Registered jobs and Completed jobs displayed in the tables. The
selections include:
• All jobs
• All PPS jobs (only for sites with PPS, HIS or RIS systems)

Data Management
• All Network jobs

• All Archive jobs
• Network push
• Network retrieve
• Archive record (Not Applicable)
• Archive restore (Not Applicable)
• Remote archive
Job Queue
The Job Queue area displays the list of registered jobs as defined from the Show All Jobs menu.
Click and drag the edges of each title in the menu bar to expand or contract the field.
Click on the arrow and select the job type by which you want to filter the list.
The job status types include:
• Paused — indicates that stops the progress of a transmission
• Failed
• Running — indicates the job is active
Figure 387 Queue list
Completed Jobs
The Completed Jobs area displays when a successful transfer is completed the job is listed. The most
recent job is listed at the top of the list.
Click Clear to remove all jobs from the Completed Jobs list.
Figure 388 Completed Jobs
Queue Controls

Data Management
• Click Pause to place the selected items in the list into a paused state. To resume the job, select the
item and click Resume/Retry.
• Click Resume/Retry to initiate the job of the selected items in the list.
• Click Delete to remove a transmission from the Registered Jobs list. A pop-up requires your
confirmation for deletion.
• Click Clear to delete all items from the Completed Jobs list.
See View the Backlog/Queue.

Network History
The Network History tab lists the jobs that have been transferred. The entries are listed by how the job
was queued for transfer, i.e., by exam, series, or image.
See Check the Network History.
Figure 389 Network History
19.4 Archive/Network
Archive
The CT Scanner is intended for short-term storage of data only and does not act as an Archive.
An archive device is a network device set up as an archive destination by your service personnel. When
an image is archived, the icon in the Archive column of the Exam List and Series List indicates that it
has been archived. The archive flag does not display when an image is saved to a CD, USB or DVD.
There are two methods of archiving. You can manually archive images, which allows you to save only
those specified by you. You can also automatically archive images. In this case, all exams are auto
archived upon scan completion.

Data Management
The archive and network status columns on the Exam List and Series List contains information
regarding archive or network status.
When saving images to a remote archive device such as a PACS, items queued to be saved to the device
will be listed in the Job Management window.
The archive status is displayed in the Job Management window and in the status area of the window.
Network
Networks link image acquisition systems and workstations together, providing a way to quickly
and easily transfer images between your scanner, remote workstations, and other image acquisition
systems. You may view images that are supported by your scanner from any station, or view images
from other stations networked to your scanner.
You can network images between your system and any DICOM compatible device. Images transferred
from your system can be automatically networked upon reconstruction or manually networked upon
your initiation. You may also get images from another networked device. Before networking images,
check to see that there is enough room on the receiving system's disk to accommodate the images
being transferred.
Network status information is displayed on the Job Management window in the Feature Status area.
NOTE
Images cannot be sent to an IRIX-based CT system.
Archive/Network queues: Job Management
The archive and network queues are viewed from the Job Management window. When you choose to
view an archive or network job, the queues provide a snapshot of the status of the archive or network
tasks occurring on the system. You are able to pause, resume and delete the archive and network
tasks.
The Job Management window also provides a history of archive and network events. The list allows
you to check and verify that an exam, series or image has been sent to an archive or network node. If
an entire exam or series has been selected, only one transfer is executed and one entry is displayed
in the queue. If specific series or images have been selected, a separate transfer is executed and a
separate entry is displayed for each selection. When saving images to a remote archive device such
as a PACS, items queued to be saved remotely will be listed in the Archive Queue under the Remote
archive list.
NOTE
After a system crash or reboot, check the queue status and restart, if necessary. The
restore and save queues are maintained even after a shutdown has been performed.
19.4.1 Configure Network Hosts window

You access the Configure Network Hosts window by clicking the Network Settings icon on the File
Manager control bar.

Data Management
Figure 390 Configure Network Hosts
19.4.1.1 Configured Hosts list

The Configured Hosts area lists of all the archive and network nodes.
Figure 391 Configured Hosts list

Data Management
You can also view the configured remote networks from the Source menu above the Exam List in File
Manager,
19.4.1.2 Remote Host Information
Figure 392 Remote Host Information
• Host Name: The name given to the network node of the currently selected node. This name is
typically entered by the service engineer.
• Display Name: The name that is shown in both the source menu and Archive and Network
destinations.
• IP Address: The location of the node within the network. You must enter the IP (Internet
Protocol) address correctly or the connection cannot be made. Your service engineer can help
you determine the IP address.
• Port: A predetermined number specific to the type of host and the protocol used. Your service
engineer can provide you with this number.
• AE title: This title is provided by the service engineer.
• Comments: A space to enter text that is associated with the selected node.
19.4.1.3 Archive Node Settings

Select the Archive Node option to place the selected node in the Archive destinations. Only devices or
nodes that have this option checked can be used as an archive device. Not all hosts can be used as
archive nodes (for example, another CT system cannot be used as an archive node, but a PACS system
can be used as an archive node).

Data Management
To be a successful archive node, the node must meet certain DICOM requirements so that when the
data is transferred from the host system to the node, the DICOM handshake can be successful. The
remote host must be a DICOM storage permit provider. This is not necessary for networking images.
The same handshake is not required.
The storage commitment host details are populated from the selected Remote Host Information area.
These fields can be edited
Figure 393 Archive Node Settings box
19.4.1.4 SCU and SCP Services

The Services area contains settings for SCU and SCP.
Figure 394 Services Area

Data Management
In the SCU Settings area:

• Select Query Retrieve to ping and retrieve images from the currently selected node.
• Select Custom Search to filter the patient list of the selected node. When you select the current
node from the Source menu on the File Manager control bar, the Filter Data window displays.
In the SCP Settings area:

• Select Allow Query to give the currently selected remote node the ability to query your host
system.
• Select Allow to Retrieve to give the currently selected remote node the ability to retrieve from
your host system.
• Select Allow to Send to give the currently selected remote node the ability to send to your host
system.
Save
Click Save to save the settings for the currently selected node.
19.4.2 Working with archive nodes and network hosts
19.4.2.1 Add or Edit a Host

1. Click the Network Settings icon to open the Configure Network Hosts window.
2. Click Add next to the Configured Hosts list.

3. In the Remote Host Information area, complete all fields.
4. If the host is an archive, check the Archive Node box.
5. To send encrypted data to a TLS capable DICOM network host, Click the checkbox next to the lock
symbol.
NOTE
Both the CT Scanner and the receiving network host must have applicable
certification. See Certificate Management for DICOM over TLS to install certificates
on the CT Scanner.
6. In the Services area, select your options.
7. Click Save to save the settings for the currently selected node.
8. Click OK.
19.4.2.2 Remove Nodes from the Configuration Host List

1. From the Configured Hosts list, select the node you want to remove.
2. Click Remove.
3. Click Yes at the confirmation prompt.

Data Management
19.4.2.3 Ping a Remote Host

1. From theConfigured Hosts list, select the node you want to ping.
2. Click Ping.
3. Click OK to the message prompt.
If a failure occurs, read the prompt to help determine the cause of the failure.
19.4.3 Certificate Management for DICOM over TLS

Certification is required for DICOM over TLS transfer. Certificate Management is designed for
organizing public and private SSL certificates. It allows application on the scanner desktop to connect
to the external servers securely using the SSL/TLS certificates that are imported into the Certificate
Management application. This allows certificates to imported, configured, viewed and deleted.
19.4.3.1 Generate Host Certificates and Save to USB :

Generate Host Certificates
1. Login as EA3 Admin.
2. Open an xterm.
3. Run the following command as root:
# openssl req -newkey rsa:2048 -nodes -keyout hostkey.pem -x509
-days 365 -out hostcert.pem
NOTE
During openssl command execution, the user must enter input for each item:
• Country Name (2 letter code) [AU]:
• State or Province Name (full name) [Some-State]:
• Locality Name (eg, city) []:
• Organization Name (i.e. company) [Internet Widgits Pty Ltd]:
• Organizational Unit Name (i.e, section) []: e.g. CT
• Common Name (i.e. server FQDN or YOUR name) []: e.g. hostname
• Email Address []:
When this command is run two certificates are generated.

1. hostkey.pem -- Private Key (can be used in Device/Server itself)
2. hostcert.pem – Public Certificate (can be used to connect other devices)
Copy the certificates into USB

mountUSB

Data Management
cd /USB
copy <path to certificates> /USB
19.4.3.2 Import Host Certificates with USB:

Launch Certificate Management
1. Login to EA3/HIPAA authentication page in the administrator role or GE service role
2. From System Utilities menu, select Service, to open the service desktop.
3. From the Utilities tab, select Security Center.
4. Select the Certificate Management GUI menu item from the Application tab.
Figure 395 Certificate Management
NOTE
The Application tab is not displayed when the current user is not in the EA3 admin or GE
Service role.
The host certificate needs to be imported using USB.
Click the Import host certificate button. The following screen displays:

Data Management
Figure 396 Certificate Management- Import Host Certificate
1. Enter the certificate name.

2. Select USB from the dropdown menu.
3. Select the private key from the dropdown menu.
4. Select the certificate content from dropdown menu and click Submit.
If the certificate imported successfully, a message displays indicating so. The imported certificates
display in the table as shown below:

Data Management
Figure 397 Certificate Management- Imported Host Certificate
19.4.3.3 Import Third Party Certificates:

Third-Party certificates can be imported using USB or URL. Click on the Import Third party certificate
button to open the following screen:
Figure 398 Certificate Management- Import Third party Certificate
Steps to import third party certificate using USB:

1. Enter certificate name.
2. Select USB from the dropdown menu.
3. Select the certificate content from the dropdown menu and click Submit.
Steps to import third party certificate using URL:

1. Provide certificate name.

Data Management
2. Provide certificate URL.
19.4.3.4 Configuring Certificate to Applications:

To configure certificates, click on Configure Certificate. Select the certificate and check the checkbox
to which application that particular certificate should be configured.
Figure 399 Configure Certificate -based on selection
Once complete, a message displays indicating the configuration was successful.

Refreshing the table shows the applications configured to particular certificates.
Figure 400 Configured Certificate
View certificate screen:

Clicking on the View icon of any certificate displays the certificate.

Data Management
Figure 401 View Configured Certificates
Delete certificate screen:

Clicking on the Delete icon of any certificate opens a Delete Certificate confirmation window.
Figure 402 Delete Configured Certificates
Click Confirm to delete the certificate. Certificates configured to an application will not be deleted. An
error message displays in this case.

Data Management
Figure 403 Message during deletion of Configured Certificates
NOTE
Attempting to import an existing certificate brings up the error message “Certificate
Name already Exists hence failed to save”.
19.4.4 Malware Protection
19.4.4.1 Overview
Anti-virus is a software used to prevent, detect and remove malware/viruses.
McAfee Endpoint Security for Linux Threat Prevention as an option. Once installed, the Antivirus
software starts protecting your CT system from threats. The software uses the latest anti-malware
engine from McAfee.
When enabled, the software checks for viruses, trojans, unwanted programs and other threats by
scanning files and folders on local drives, network-mounted volumes and removable media whenever
a file is created or accessed. On-Access scans are disabled by default for performance reasons.
You can also run scans on demand. An on-demand scan can be initiated from the Security Center by
clicking the Antivirus menu item in the left navigation area.
McAfee Endpoint Security (ENSL) is installed when AntiMalware_McAfee_standalone or
AntiMalware_McAfee_EPO option is installed. ENSL can be configured to work in the two modes:
Managed mode (i.e., with ePO Server) or Standalone mode (i.e., without ePO server). For managed
systems, the ePO administrator configures and manage the protection configuration policies using
these servers.
• McAfee® ePolicy Orchestrator® (McAfee ePO™)
• McAfee® ePolicy Orchestrator® Cloud (McAfee ePO™ Cloud)
Following are the acronyms used in this section:

Data Management
• DAT - McAfee DAT Signature Database

• ENSL - McAfee Endpoint Security for Linux
• EPO - McAfee ePolicy Orchestrator
• MSA - McAfee Security Agent
ENSL provides the following Virus Scan methods.

• Custom On-Demand Scan
Custom On-Demand scan must be scheduled from EPO. It schedules a task defined by the user to
scan on files and directories at specific times.
• On-Access Scan
This type of scan is disabled because it causes high system load and affects CT functionalities.
• Policy-Based On-Demand Scan client tasks
Run a Quick Scan or Full Scan on the client from McAfee ePO. Configure the behavior of these
scans in the policy settings for an on-demand scan.
To integrate with ePO, additional configuration procedure is required in EPO side. Server-side
procedure/methods for configuration of ePO Server are not in scope of this document and need
to refer to McAfee Installation / Product Guide for details.
When ePO Server is configured, Virus signature database (DAT) should be updated or scheduled using
ePO. Virus scans should also be scheduled from the ePO Server
NOTE
ANTIVIRUS SCANS ON CT SCANNERS ARE COMPUTE INTENSIVE AND TAKES SIGNIFICANT

AMOUNT CPU, MEMORY AND DISK RESOURCES THAT CAN POTENTIALLY INTERFERE
WITH NORMAL OPERATING FUNCTIONS OF CT SCANNERS INCLUDING BUT NOT LIMITED
TO SCAN ACQUISITION, CALIBRATIONS AND IMAGE RECONSTRUCTIONS. USERS MIGHT
PERCEIVE SIGNIFICANT SLOWNESS OF THE SYSTEM IF ANTIVIRUS SCANS ARE RUN IN
THE BACKGROUND. IT IS RECOMMENDED TO NOT RUN ANTIVIRUS SCANNING WHEN
THE SYSTEM IS USED FOR NORMAL CLINICAL OPERATIONS. THE IT OR HOSPITAL
ADMINISTRATOR RESPONSIBLE FOR ANTIVIRUS SCANS MUST COORDINATE WITH
TECHNOLOGISTS/USERS OF THE CT SCANNERS FOR PROPER DOWNTIME TO COMPLETE
ANTIVIRUS SCANS.
When a user starts a patient scanning session by clicking Accept and if the system
detects an antivirus scan in the background, the system will first stop the antivirus scan
before proceeding into patient scanning session.
19.4.4.2 Standalone license mode (when ePO server does not exist)
Installation of Anti-Malware solution
When the AntiMalware_McAfee_standalone option is installed, McAfee Endpoint Security (ENSL) is
installed by default with a full license.
Launching McAfee Agent in Stand-alone Mode

Data Management
1. Login as user with Administrator privileges in EA3 2.

2. Launch Antivirus UI from Security Center. Click on the Antivirus Non-EPO setup tab.
Figure 404 Launching Antivirus application in Stand-alone mode
NOTE
Antivirus version installed on the console may be different from that shown above.
Stand-alone Mode Cron jobs
When the AntiMalware_McAfee_standalone option is installed, a weekly cron job is scheduled to run
the antivirus scans and engine and DAT updates.
The user can specify the antivirus scan time by running /usr/g/scripts/
schedule_antivirus.sh. The default scan time is 3:00 AM every Friday.

Data Management
Start Anti-virus scan manually

1. Login to EA3 as a user with Administrator or GE service privileges.
2. From the System Utilities menu, select Service to open the service desktop application.
3. From the Utilities tab, select Security Center.
4. Select the Antivirus UI sub-menu item from the Application menu.
5. Click the Antivirus Scan tab on the Antivirus UI.
6. Click Start Scan. The Anti-virus scan is now running.
Figure 405 Start Anti-virus scan in Standalone mode
The Anti-virus scan will take about 30 minutes to an hour or more, based on system available
resources. Wait to complete anti-virus scan.

Data Management
When the scan is complete. the message Antivirus scan is completed is shown in the Status
Information pane.
Figure 406 Anti-virus scan completed in Standalone mode

Data Management
If a virus is detected during the scan, the system displays

the message WARNING: VIRUSES WERE DETECTED. Call GE Service.
Update the Anti-virus cron schedule

1. Launch Security Center and expand the Antivirus accordion by clicking on it. I twill show the
current cron schedule for Antivirus scan.
2. Click on the Pencil icon to edit schedule, opening the Edit Job Schedule window.
Figure 407 Anti-virus cron job schedule
3. Click on the Occurs dropdown menu in Edit Job Schedule and choose the occurrence.
4. Based on the occurrence selected, choose time accordingly.

Data Management
5. Click on Submit in Edit Job Schedule. The system Successfully updated displays when the
cronjob has been updated or displays a message on why the update failed.
19.4.5 Local DB Retrieve Exams, Series, or Images

Use these steps to restore exams, series, or images to your system from a remote host.
1. On the right monitor, open the File Manager.
2. From the Source menu, select the remote host from which you want to retrieve images.
• If the host is not available, a message appears. Click OK.
• The host must be configured to receive a query. Check the SCP Settings on the Configure
Network Hosts window to verify that all the SCP settings have been checked (Allow to query,
Allow to retrieve, Allow to send). You may need to add the CT system to the remote service as
a network destination.
3. To find the exam you want to restore:

a. In File Manager, enter a search string into the Search box.
The filtered Exam List displays.
b. To return to the non-filtered Exam List, click the close icon in the Search box.
4. From the Exam List, select the exam you want to retrieve.
If you are selecting series or images, select them from the Series List.
NOTE
You can select more than one exam, series, or image. Shift‐click to select a
contiguous list, or Control-click to select items one-by-one.
You cannot retrieve series or images from different exams in the same transfer. Select the series
or images you want to retrieve from an exam, start the retrieval, and then transfer the series or
images from the other exam.
5. To retrieve exams, right click the exam, then click Retrieve Exam.
To retrieve series, right click the series, then click Retrieve Series.
To retrieve images, right click the images, then click Retrieve Images.
6. The selected items transfer to your system.
The system indicates that exam transfers are taking place with an animated icon next to the
exams. The system status bar shows the progress of the transfer. You can check the status of the
transfer using the Job Management window.
• Jobs are performed on a first-come, first-served basis.
• When the data has been transferred to the local database, the Archive flag is set for the
transferred data.
• When the data has been successfully transferred to a network host, the Networked flag is set
for the data.

Data Management
• Hover the cursor over the Archive or Networked flag to see more information.
NOTE
If there is an error in retrieving an exam, it will be indicated in the local Exam List
with a red icon. Click the icon to open the Job Management screen.
19.4.6 Manually Send Exam, Series or Images

Follow these steps to send an exam, series, or image to a an archive or network host as an alternative
to auto archive.
1. On the right monitor, open the File Manager.
2. From the Exam List, select the exam, series, or images you want to send.
If you are selecting series or images, select them from the Series List.
NOTE
You can select more than one exam, series, or image. Shift‐click to select a
contiguous list, or Control-click to select items one-by-one.
You cannot send series or images from different exams in the same transfer. Select the series
or images you want to retrieve from an exam, start the retrieval, and then transfer the series or
images from the other exam.
3. To send to a non-archive host, right-click the selected item, click Send Exam To (or Send Series To
or Send Image To, and then click the host name.
The data transfer process begins.
4. To send to an archive, right click the selected item and then click Archive Exam (or Archive Series,
or Archive Image). If there is more than one archive available on your network, select the archive.
5. View the Job Management window or the archive and network status in the Feature Status area to
view the state of the images as they are transferred to the archive or network host.
• Jobs are performed on a first-come, first-served basis.
• When saving images to a remote archive device such as a PACS, items queued are performed
on a first-come, first-served basis.
• When the data has been successfully transferred to an archive device, the Archive flag is set
for the data.
• When the data has been successfully transferred to a network host, the Networked flag is set
for the data.
• Hover the cursor over the Archive or Networked flag to see more information.
19.4.7 View the Backlog/Queue

Follow these steps to view a backlog of archive or network activity or to delete an archive or network
job.

Data Management
1. Click the Job Management icon on the File Manager toolbar.
2. On the Job Manager tab, click the down arrow button on the Show Jobs box and select an
option to refine the lists.

3. From the Job Queue, select the jobs you would like to change.
• Click an individual item.
• Press Shift and simultaneously click the first and last item.
• Press Ctrl and simultaneously click individual items.
4. Choose one of the following job actions:

• Click Pause to pause the selected items.
• Click Retry/Resume to initiate the job for the selected items.
• Click Delete to remove a transmission from the queue. A message confirms the deletion.
• Click Clear to delete Completed Jobs from the list.
5. 6. Click Close.
Delete Jobs from the Completed Jobs List

1. Click the Job Management icon on the File Manager toolbar.
2. On the Job Manager tab, click Clear to remove the selected jobs from the list.
3. Click Close.
19.4.8 Eject (Detach) Media

To make sure a removable media device is in a safe state, it need to be ejected (detached) before you
remove it from the system.
Follow these steps to eject (detach) a CD, DVD, or USB drive.
1. Insert a CD, DVD, or USB drive into the appropriate drive.
2. Check the Archive/Network backlog to verify that all image transfer from the device is complete.
3. From the File Manager, click the Eject button , next to the Source menu on the File
Manager toolbar.
4. The system asks which device you want to eject. Select the device, and then click Eject.
5. The system displays a message when it is safe to remove the device.
6. In the case of DVD and CD drives, the drive will open. If you have ejected a USB device, unplug the
USB device.

Data Management
19.4.9 Check the Network History

1. Click the Job Management icon on the File Manager toolbar, then click the Network History
tab.
2. In the log, locate the network history you want to view.
Entries are listed how the job was queued for transfer. If by Exam, then only the exam number
is listed. If by Series, then the exam and series are listed. If by Image, then the exam, series, and
image are listed.
3. Enter a specific exam, series or image number into the Search ESI or Host field.
The history file opens for all matches to the exam, series or images.
4. Click the Refresh icon to update the network history log.
5. Click Close.
19.4.10 Workarounds
• Images archived on an Advantage Windows system may fail to restore on the system. Use Network
to transfer images from the Advantage Windows to the system.
• If the system is unable to read the media, remove the write protect and see if the system is able to
recover the media to access the data.
19.5 CD, DVD and USB Interchange

CD, DVD and USB interchange is used to write or recall images from a Compact Disc-Recordable (CD-R)
or Digital Versatile Disc-Recordable (DVD-R) in a Digital Imaging and Communications in Medicine
(DICOM) format. Optionally, a DICOM viewer may be stored on the media so the images can be viewed
on a personal computer.
Only CD -R or DVD -R media can be used for CD/DVD/USB Interchange. For CD-R, write speed should be
at least 4X and storage size of 700 MB. The media is write once and all selections must be queued at
the same time. Approximately 7,000 images can be stored to a 4.7 GB DVD-R.
In order to view the information placed on media using CD/DVD/USB interchange. The first time the
reader of the Interchange media tries to access the data, the security setting in Advanced Settings
on the PC must be set to "Allow active contents from CDs to run on My Computer.” A log file is
created on the PC used to read the media, which tracks the reading of the media to record issues for
troubleshooting. The log file is limited to six files and overwrites data once the limit is reached.
NOTE
CD/DVD/USB interchange is available for writing DICOM images onto the compatible
media listed in Table 149 on page 831. It is not considered a method for long-term
image storage.

Data Management
Media and Device Requirements

The following table lists the recommended CD-R and DVD-R manufacturers that have been qualified by
GE Healthcare. Other high-quality CD-R and DVD-R media may also work, but GEHC has qualified only
the media types shown below.
Table 149 Recommended media
CD-R DVD-R
Sony 650 - 700 M CD-R Verbatim 4.7 GB 4X Commercial
Maxwell 4.7 GB 1X-4X
Sony 1X-4X Compatible 4G
TDK 4.7 GB Commercial
Pay attention to the following declarations about media and operation requirements when you use
CDs and DVDs.
• Only supports single layered CD-R and DVD-R media. No other media types are supported,
including but not limited to DVD-RW.
• Dual layered CD-R and DVD-R media are not supported.
• Only supports 700 MB single layer CD-R media.
• Only supports 4.7 GB single layer DVD-R media.
Pay attention to the following considerations about USB devices:

• USB devices can be flash drives or USB hard drives which use external power.
• By DICOM standards, the format of USB device must be VFAT.
• There are no USB capacity limitations.
• You can erase data from the USB device with your PC.
• Before writing to the USB device, the system checks the USB capacity and the size of the data
being written.
Operation Requirements
Pay attention to the following operation requirements for CD/DVD/USB interchange.
• Only supports single-write session. Multi-session mode is not supported.
• Cannot append write data to media that has already been written.
• CD/DVD/USB interchange is NOT INTENDED for archive or backup purposes! These features make
only “temporary copies” for interchange purposes. GEHC will not “recover” any interchange
media (it should just be burned again if necessary using patient data restored from authorized/
provided archive media).
• It is advised to not write to CD/DVD/USB interchange media during a scan operation.
• It is advised to not open post-processing applications requiring high computer usage while
writing to CD/DVD/USB.

Data Management
19.5.1 Media Creator

From File Manager, click the Media Creator icon .
NOTE
USB must be conditioned to FAT32 file type before media copying begins.
Figure 408 Media Creator Window

Data Management
Table 150 Media Creator selections
Icon Name Description
Add When an exam is selected in the Exam List,

click Add to add it to the exam to the list.
Select a single or multiple series and click
Add to add the selected series to the list.
Remove Click to delete selected items in the list.
Eject Click to eject the CD or DVD from the drive.

Eject also makes it safe to detach a USB
device from the drive.
Refresh Click to update the contents of Select Me-

dia menu.
Media menu Displays the CD/DVD drives and USB

drives.
Include Image When selected, a Viewer is saved with the

Viewer image to the identified device (CD/DVD or
USB).
Verify Data Verifies the data on CD/DVD or USB after a

recording.
Disk Capacity The Total display shows the size of the

items that have been added to the list. It
updates as you add more items.
Copy Click to begin the copy.
Stop Click to halt the copy process.
Quit Click to close the Media Creator window
19.5.2 How to Handle CDs and DVDs

Recordable CDs (CD-R) are more sensitive to damage than conventional CD-ROMs that you may be
familiar with. Follow the handling suggestions below.

Data Management
NOTICE
TO AVOID IMAGE LOSS, NEVER TOUCH THE RECORDING SURFACE OF A

RECORDABLE CD (CD-R). HANDLE THE DISK ONLY BY THE OUTER EDGE OR
CENTRAL HOLE. DO NOT PLACE THE CD FACE DOWN ON A HARD SURFACE.
FINGERPRINTS OR SCRATCHES WILL MAKE THE DISK UNUSABLE.
• Store the disc in a protective case. Proper storage helps protect the data from damage due to
scratches on the disc surface.
• Do not leave the disc in direct sunlight or in a hot, humid environment. These conditions can warp
and damage the disc.
• Use only a felt tip permanent pen when labeling. Write only on the clear, inner diameter of the
disk (or the printed area of a CD-R). Never use a ballpoint or hard point pen. Do not use adhesive
labels.
• Use a soft, lint-free cloth to remove spots, dust, or fingerprints from the disc. Always wipe from
the center to the outside edge of the disc. Do not wipe the disc in a circular motion.
• Do not use any chemical-based cleaners. These can damage the disc.
• Do not use the CD/DVD/USB interchange program to permanently store your data. If the
CD/DVD/USB is damaged there is no recovery of the data.
19.5.3 Save Images

NOTICE

ON THIS SYSTEM.
Use these steps to save images from your system to a CD, DVD or USB device.
You can record DICOM image data to either a blank, compatible CD/DVD that is placed in the CD/DVD
read/write external drive or to a USB device inserted into one of the USB ports. If saving to CD/DVD,
once you close the drawer with the CD/DVD in it, wait until the CD/DVD drive light turns off. This is an
indication that the CD-R or DVD-R is spinning up to speed.
• Images may copy very slowly or may fail to copy to USB from Media Creator. Use a USB3.0 device
with a write speed of greater than or equal to 45 mb/s. The USB must be formatted in VFAT
or FAT32 format. Format the USB on a system running Windows. If the system does not allow
formatting the USB, download a tool such as HP USB Disk Storage Format Tool.
• Data on a CD-R and DVD-R can be recorded only in a single session. Data on USB can be recorded
in multiple sessions. All image data that you want to record must be selected beforehand. The
data will be recorded in a single pass. It is not possible to add data on a CD-R, DVD-R or USB.
• Image data can also be recorded in Portable Document Format (PDF) or HTML format by using the
Data Export function.

Data Management
• You can load images on a USB that already has data on it. The system informs you that the USB
contains data and asks How would you like to proceed? You can either select Append Data to add
the images to the USB or Delete Data and Continue to erase the data from the USB and add the
images.
• Do not connect two USB devices at the same time for save/restore of scan data.
• The following information will be displayed for CT images: Hospital Name, Patient Name, Date
of Birth, Acquisition Date, Exam/Series/Image information, Anatomical Reference, Slice Location,
DFOV, Recon Algorithm, Series Description, kV, mA Noise Index Values, Pitch, Rotation Time, Tilt,
Slice Thickness, Scan Time of Day, RAS coordinates, and WW/WL values.
1. Insert the media to which you want to copy.

2. From File Manager, click the Media Creator icon .
3. From the Media Creator window, select the media type from the Media menu.
If you opened the Media Creator window before you inserted a device into a drive, click the
Refresh icon to update the Select Media menu.
Figure 409 Media Menu
4. To save a Viewer with the images, select Include Image Viewer.

If you do not select Include Image Viewer, you will not be able to view the images on a PC or
laptop. The purpose of saving the images without the Viewer is to transport them to another
compatible system.
Figure 410 Include Image Viewer Option

Data Management
5. Select the desired exams or series from the File Manager.

• Press and hold Shift and click the first and last item.
6. From the Media Creator window, click Add.

• The selected exam/series/images are added to the Media Creator list.
• The Total Size display updates as more exams/series/images are added to the list. Toggle
Include Image Viewer on/off to see updated Total Size display.
• A message displays if the size of the exams/series/images exceeds the space on the CD/DVD
or USB device.
• You cannot add the same exam to the window more than once. A message displays that you
have entered the same patient more than once. Remove one of the exams.
7. Clear exams or series from the Media Creator list.

a. From the Media Creator window, select the series and/or exams you wish to clear.
• Press Ctrl and simultaneously click individual items to remove non-contiguous items on
the list.
• Press Shift and simultaneously click the first and last item to remove contiguous items
on the list.
b. Click Remove.
8. Click the Write icon to start the recording process.
• Do not begin recording until all desired series have been added to the list. You cannot record
more data to the CD-R or DVD-R once you have started the recording process.
• The progress bar (1) and message bar (2) displays messages indicate the progression of the
copy activity.
Figure 411 Progress Bar and Message Area

Data Management
• Error prompts may appear if the media is damaged, if the media contains corrupted or
unsupported data or the files are too large for a single media, etc.
• The progress bar displays 100% and a message appears in the message area when recording
is completed.
• Very large data sets can take a very long time (more than one hour) to copy to CD. If you
change your mind about copying the files to CD/DVD, you can stop copying and start it over
at a time more convenient. Click Exit to cancel the copy process and upon clicking OK to the
confirmation prompt, the copy process is stopped and the Media Creator window closes. An
alternative is to click Cancel.
9. Once the recording is finished, click the Exit icon .
• If you click Exit before the save process has completed, a confirmation prompt appears. If
you confirm the Exit, then the save process is canceled.
• The Cancel icon stops burning data.
10. From File Manager, click the Media Creator icon .
View the progress bar to note if the burning process is finished.

11. When the contents have been burned to the media, a message posts in the Message area. It is now
safe to remove the CD/DVD or USB.
12. Click the Eject icon to remove the media from the drive.
• The CD/DVD drive automatically opens when the CD/DVD save is finished. Only click Eject to
stop the CD/DVD save process.
• Removing the USB device without ejecting it can results in errors that may require the device
to be reformatted.
• Do not remove the USB device during copy process. Make sure you first Stop the copy
process before you remove the device from the drive.

Data Management
19.5.4 Restore Images

Follow the steps below to restore images from a CD, DVD or USB device to your system.
1. Place a CD-R or DVD-R in the CD/DVD external drive or place a USB device into one of the USB
drives. Wait until the drive light turns off, which is an indication that the CD-R or DVD-R is spinning
up to speed.
2. From the File Manager Source menu, select the drive that has the CD, DVD, or USB.
3. From the File Manager, select the exam, series or images to restore.
• Press Shift and simultaneously click the first and last item.
4. To retrieve exams, right click the exam, then click Retrieve Exam.
To retrieve series, right-click the series and then click Retrieve Series.
To retrieve images, right-click the images and then click Retrieve Images.
5. To view the restore process status, see the View the Backlog/Queue procedure.
6. After the restore process completes, click the Eject icon (next to the Source list in File
Manager).
19.5.5 View Images on a PC

The Media Viewer is loaded, if selected, onto a CD-R or DVD-R that is burned from the CD/DVD/USB
program. Follow these steps to view images from a CD or DVD.
Figure 412 Media Viewer
1. Load a recorded CD-R or DVD-R into the drive of your PC or laptop.

Data Management
The CD Viewer automatically launches. If an Auto Play window displays, click Run CDViewer.exe.
2. Click Accept to the license agreement.
3. From the DataSelector, select an exam and wait until the data is loaded.
Your PC or laptop must contain Java run time environment as JRE1.5_14 or higher version. If not,
the Java, bundled with the application, is installed on demand.
4. Select a series to view.
5. Use the Media Viewer image controls, located at the top of the Media Viewer, to manipulate the
images.
Table 151 Media Viewer Image Controls
Icon Description
Adds an angle measurement on the selected viewport.
Adds a line measurement on the selected viewport.
Adds an ellipse ROI on the selected viewport.
Adds a rectangle ROI on the selected viewport.
Hides/Shows a grid on the selected viewport.
Hides/Shows a horizontal tick mark for all viewports.
Hides/Shows a vertical tick mark for all viewports.
Adds user annotation on the selected viewport.
Erase All Graphics (right-click menu), removes all the Graphics (ROIs, User
Annotation, Grid) from the selected viewport.
Flips the image left to right on the selected viewport.
Flips the image top to bottom on the selected viewport.
Rotates the image counter-clockwise by 90° on the selected viewport.
Rotates the image clock-wise by 90° on the selected viewport.
Zoom (right-click menu), selects the left mouse drag operation as zoom.

Data Management
Roam (right-click menu), selects the left mouse drag operation as roam.
Window/Level (right-click menu), selects the left mouse drag operation as

window/level.
Display normal (right-click menu), resets image operations on the selected

viewport.
Viewer format adjusts viewport format.
Turns the window annotation off/on.
Inverts Grayscale for selected viewport.
Starts cine or movie.
Stops cine or movie.
Save to my PC Right-click menu item, exports the image of the selected viewport to the local
system in JPEG/PNG format.
Hides/Shows the Data Selector panel.
19.5.6 Remove DVD RAM Cartridge

Use this procedure to remove media from a DVD RAM cartridge for use in the Peripheral Media Tower
(PMT) equipped with a single DVD multimedia drive.
• For use with Operator Console utilizing a single bay Peripheral Media Tower (PMT) (DVD-
Multimedia drive only).
• DVD-Multimedia drives cannot accept cartridge type DVD-RAM media. Use the following
procedure for removing the DVD-RAM media from the cartridge if so equipped.
• Handle bare DVD-RAM media with care. Do not touch the recording surface. Fingerprints, dirt,
dust and scratches on the recording surface can destroy previously recorded data and prevent
recording of additional data.
• If required, use only approved CD/DVD media disk cleaning solution (not supplied) to clean any
disks that become contaminated with fingerprints, dirt and dust. Do not use alcohol, antistatic or
other cleaning solutions.
• Take care with placing bare DVD-RAM media without cartridge.
• Always return a DVD-RAM media to its cartridge for storage.

Data Management
NOTE
In the case of double-sided DVD-RAM media, take care to insert the media back into
cartridge with the same orientation as it was removed. If media is inserted upside down,
any labeling on the cartridge will not be consistent with data on the disk.
Follow the procedure and precautions outlined below to remove the disc from the cartridge.
1. Remove the disc.
a. Push and remove the cartridge-locking pin with a sharp-tipped object, such as a ballpoint
pen.
b. Open the cover by pushing the sharp-tipped object into the gap on the left‐front side of the
cartridge.
2. Do not touch the recording surface. Fingerprints, dirt, dust and scratches on the recording surface
can destroy previously recorded data and prevent recording of additional data.
3. Open the cover with care. If you damage the cover, you may not be able to close it again.
4. Use a felt-tipped marker to write on the label. Never stick a new label on a disc.
5. Clean dirty discs only with the special DVD-RAM disc cleaner and cleaning fluid (not included).
6. Always return a disc to its cartridge for storage.
7. Make sure the printed side of the shutter and the printed side of the disc is facing the same side
when returning the disc to its cartridge. Also, note the setting of the write-protect tab.
8. Place bare DVD-RAM media back in cartridge for storage.
9. Close cartridge lid once DVD-RAM media is fully inserted into cartridge.
Figure 413 DVD RAM Removal

Data Management
19.6 Data Export

Data Export allows you to store images on a CD-R or USB device as JPEG, PNG, AVI, MPEG, or MOV
formats.
The files can only be burned to a CD-R and only one report can be burned at a time. Once a CD-R has
been burned, you cannot add more reports at a later time. It is not a re-writable process.
The JPEG, PNG, AVI, MPEG, or MOV images can be viewed from a PC or laptop with a Windows 2000 or
XP operating system using Internet Explorer 5.5 or later.
There are two tabs on the Data Export window:
• Compose tab — allows you to define the compression factor, annotation level, W/L, zoom, scroll,
and output format for the series you want to export.
• Export tab — allows you to view a list of all the examinations and series you have in the Data
Export program.
• You can compose a series and then export it to a CD or USB at a later date.
• Examinations and series stay in the Export program until they are actively deleted.
19.6.1 Compose Tab

From the File Manager, click the Data Export icon .

Data Management
Figure 414 Compose Tab
Selection
Displays the patient name, exam and series number, the number of images in the series, the file size of
the images with the current compression selection and matrix size.

Data Management
Figure 415 Selection Area
Conversion Format
Click the Conversion Format drop-down menu to select the image format for the currently selected
data set. Format choices include: JPEG, PNG, AVI, MPEG, and MOV. AVI, MPEG, and MOV are all
movie-type formats. Choose the format that is compatible with the movie player on your PC or laptop.
Compression Factor and Image/Sec
Move the Compression Factor slider to choose a compression value for JPEG and MPEGs. The lower
the number, the less the compression, the higher the image quality but the larger the file.
Select an Image/Sec rate for the movie play back speed. It is only applicable for MPEG, AVI, or MOV
files.
Figure 416 Compression Factor and Image/Sec
Image Range Selection

In the Image Range Selection area, choose the images you want to place in the designated folder. For
example, if you have a multi-phase series selected and all you want is the first phase in the MPEG, then
select the range of images representing phase one of your data set.

Data Management
Figure 417 Image Range Selection
Annotation
In the Annotation area, choose the level of annotation for the images: none, full, partial (a subset of
the full annotation, or custom. Click Customize to turn on specific annotation fields.
NOTE
DMPR viewports will show image annotation even if the annotation level is set to None
in the system preferences.
Figure 418 Annotation
Series + or -
Click Series + or - to navigate through a series within the exam.
Select Propagate Image Operations to apply the image manipulations (W/L, zoom, scroll) you have
performed on all images forward from the currently displayed image within a series.

Data Management
Figure 419 Series Area
Play/Stop
Click Play to preview the MPEG, AVI, or MOV file.
Click Stop to quit playing the movie.
Image Viewport
The image viewport displays the current images by scrolling through them in a cine loop. Press Page
Up and Page Down to scroll through the images.
Image Conversion
Figure 420 Image Conversion
• In the Report Name menu field, select or enter a name to display at the top of the report. The
name also appears in the Export Data list. Typically the patient’s name and type of file are entered
as the report name. There can be no spaces or characters other than alpha numeric.
• In the Folder Name menu field, select or enter the name of the folder where you want to file the
report name. From the Export tab, you can view the data listed within each folder. The data within
a folder is sorted by file type. For example, if you added 10 JPEGs from the T1 series and 20 JPEGs
from the T2 series you will see a list of 30 JPEGs in that folder. If you want these JPEGs separated,
you must place them in separate folders.
• Select Save Preferences to save the changes you have made on Data Export screen.
• Select Anonymous to have the patient’s name replaced with Anonymous and the exam number
when the images are added to the report.
• Click Add to Report to add the current data set to the report from which you can burn the
information to a CD-R. A Data Conversion progress window displays the status.
• Click Cancel if you want to stop the data conversion.
19.6.2 Export Tab

From the File Manager, click the Data Export icon . Click the Export tab.

Data Management
Figure 421 Export Tab
Report Name List

Contains all the report names in the database.
Click the Delete icon to remove selected items from the list. Items remain on the list after you
click Quit Data Export until they have been deleted through this method.
Figure 422 Report Name List

Data Management
Folder Name List

Identifies all the folders associated with the report name. Check the file size to make sure you can
store it on a single CD-R or USB.
Figure 423 Folder Name List
Click Move to Report to move the selected item to a destination of your choice. For example, you can
select an item in the Type list and add it to a particular folder in the Folder list. The folder size is listed.
click Quit until they have been deleted through this method.
Type Name List
Contains of all the file types within the selected folder. Keep in mind that the only items displayed in
the list are the item types. If, for example, you added 20 T1 JPEG images to Folder 1 and then added
another 20 T2 JPEG images to Folder 1, the number of JPEGs in folder 1 is 40. The quantity and size of
each data type is listed.
Figure 424 Type Name List
Image Name List

Contains of all the images within the selected file type.

Data Management
Figure 425 Image Name List
Enter Report Name

In the Enter Report Name field, select the report that you are going to export.
Type in a comment that appears on the report. Do not apply a carriage return when typing. The text
will wrap automatically for the finished report.
Figure 426 Report Name
Conversion Formats
In the Conversion Format area, choose a file type. Typically select HTML.
In the Media Label field, enter a name for the CD.
Figure 427 Conversion Format
Media Type
Select the media type to export the data as.
Figure 428 Media Type Destination

Data Management
Media information
This area of the Data Export tab changes based on the media selection.
Figure 429 Media Information
Click the Select USB Disk menu to select a specific USB device if more than one device is inserted into
the USB ports.
Click Refresh to update the Select USB Disk menu if you insert another USB device into a second port
after you have opened the Data Export window.
The Total Disk Space, Free Disk Space, and Total Data Size fields provide information about the
selected USB device. Verify that you have sufficient space on the device before you click Save.
Click Save to start the transfer process.
Click Close to close this area of the Data Export window.
19.6.3 Compose a Report

1. From the File Manager, select the series you want to export.
Only one series can be exported at a time.
2. From the File Manager, click the Data Export icon .
Click Compose if it is not selected.

3. Review the images in the Compose image viewport.
• Middle-click and drag to adjust the W/L.
• Right-click and drag to adjust zoom factor.
• Click and drag to scroll.
• Press Page Up or Page Down to navigate through the images.
• Click Play to view the images in a cine loop.

Data Management
4. Click the Conversion Format menu and select an image format that is compatible with the movie
player on your PC.
5. In the Image Range Selection area, choose the image range.
If you want a subset of the images, select Custom, and then type the range in the text box.
6. Move the Compression Factor slider to select a value.
The smaller the number, the higher the image quality and the larger the file size.
7. In the Annotation area, choose your desired annotation display format.
If you want the patient name to be displayed as Anonymous with the exam number, select
Anonymous.
8. Once you are satisfied with the image appearance (W/L, zoom, scroll), select Propagate Image
Operations.
9. Enter a name for both the report and the folder (only use alpha numeric characters, no spaces).
10. Click Add to Report.
If you change your mind and decide not to add the data to the report, click Cancel from the
progress bar screen.
11. To add another data set to the report, repeat these steps.
12. Click the Export tab to export the report (for details see Export a Report) or click Quit to exit Data
Export.
19.6.4 Export a Report

This procedure assumes that you have composed a report in Data Export.
1. From the File Manager, select the series you want to export. Only one series can be exported at a
time.
2. From the File Manager, click the Data Export icon .
3. Click the Export tab.

4. From the Export Report Name list, select a report.
5. From the Folder Name, Type Name, and Image Name lists, select a data set.
6. Optional: Type a message in the Comment field. Do not press Enter, the system will adjust the text
for the final report.
7. Choose a Conversion format, typically HTML.
8. To create a CD:
a. Insert a compatible CD-R into the DVD-RW drive.
• This is not the drive housed in the computer cabinet but rather the box that houses the
CD/DVD drives located on the desk.
• The only compatible media for Data Export is CD-R 700 MB with at least 4X write speed.
DVDR is not supported. If a DVD-R is placed in the drive, the system will write to this

Data Management
media, but the integrity of the data cannot be guaranteed and the time for the system to
recognize the media will be excessive.
b. Carefully seat the media in the drive. Wait until the drive has sensed the media and the drive
light goes off, then click Create CD.
c. Click OK.
When the CD writing step is completed, the CD ejects from the drive.
d. Click OK to the CD Written Successful prompt.
9. To copy the data to a USB drive:
a. Select a USB device.
b. Click Save.
10. Click Quit.
• Reports stay listed in the Export tab until you remove them.
• Consider how long you will want to keep the file in the program based on if you need to burn
another CD or USB.
19.6.5 View a Report on a PC

1. Place the CD or USB in the appropriate drive of a PC running Windows 2000 or XP.
2. If the report does not open automatically:
• Click on the My Computer icon and open your CD or USB drive.
• Click INDEX to open the file. The report opens in an Internet browser.
3. 3. When finished, select File > Close.

4. Remove the CD or USB from the drive.
19.6.6 Delete Items

1. From the Data Export window , click the Export tab.
2. From the Export tab, select an item from Report, Folder, Type, or Image list.
3. Click the Delete icon .
4. Click Quit.
19.7 Patient Data

Removal of Patient Information

Data Management
The Anonymize Patient feature assists you in removing patient identifiers by electronically removing
certain exam information and replacing it with anonymous information. An anonymous patient can be
created by exam, series or image.
Two modes are available for you to remove patient identifiers:
• Full mode removes most patient identifiers from an exam, image or series. However, the use
of Full mode does not guarantee exams, series, or images will be rendered anonymous in
compliance with applicable data privacy laws. Review the exam, series, or image data processed
by the feature to ensure compliance with applicable data privacy laws before sharing the
information with third parties.
• Partial mode removes a subset of patient identifiers including, but not limited to, patient name,
patient ID, patient date of birth and patient age. Site name, exam and series descriptions remain
unchanged.
Anonymization occurs after the patient has been scanned, so you must enter a name when you start a
new patient.
The default level of annotation for Anonymize Patient is set in the Image Database tab of the System
Preferences.
NOTE
Screen save images, such as Exam or Series text pages or Contrast Report text pages
are not anonymized, and are not included in the exam if anonymize by exam has been
selected.
Table 152 Fields removed from exams, series, or images using Full or Partial Anonymous modes
Field Full mode Partial mode
Exam Number ANON or ANONYMIZED ANON or ANONYMIZED
Patient ID ANON or ANONYMIZED ANON or ANONYMIZED
Patient Name ANON or ANONYMIZED ANON or ANONYMIZED
Exam Description ANON or ANONYMIZED Shown
Series Description ANON or ANONYMIZED Shown
Birth Date Removed Removed
Age Removed Removed
Weight Removed Removed
Operator Name Removed Removed
Site Name Removed Shown
Sex Blank Blank
Referring Physician Blank Blank
Referring Physician Blank Blank

Data Management
Anonymizing an exam is useful when:

• your radiologist wants to take the films to a conference
• you have scanned a test patient or volunteer and do not want the name displayed
• anytime you do not want the patient’s name on the films (For example, films that are in a
marketing display or in a trade show.)
• anytime you send images to GE
Edit Patient Information

Edit Patient allows you to edit certain patient information once the exam has been completed. You can
only edit exams that were created on your system.
You cannot access Edit Patient if the exam you want to edit is currently in use. An exam is currently in
use if the Patient Session tab, Network Send, Archive Save, 3D, Reformat, Navigator or Image Viewer is
active. If you try to use Edit Patient when an exam is currently in use, which means the exam is on the
archive or network queue, an error message displays.
• Use Edit Patient during idle times in network receive, active recon, or archive restore. The system
may hang if Edit Patient is started while the following operations are in progress:
• Network Receive
• Prospective or Retrospective reconstruction
• Archive Restore
• You cannot edit contrast or patient weight.

• Edit Patient will not update scan data files or completed patient information.
• Check that additional series or images are not in the recycle bin. Move any series or images in the
recycle bin back to the local disk or empty them from the bin.
• If you edit an exam that has a saved 3D model, the 3D model is deleted from the exam. If you edit
an exam and you have the 3D model selected when you select Edit Patient, you will not be able to
edit the exam.
• There must be sufficient disk space available.
• All images should be reconstructed before editing. Scan data cannot be edited, only images. All
remove images and post-processing (screen saves, reformat, 3D surface) should be done after
editing. All images created before the edit do not contain the edited information.
• Any DICOM secondary screen captures such as text pages, screen saved image, Smart Prep and
ECG Trace screen saves will be deleted from the exam with Edit Patient Data.
Edit Patient Data Window

From the File Manager, right-click on the exam and then select Edit Patient Info .

Data Management
Figure 430 Edit Patient Data window

Data Management
• If the text field is empty, click in the field, and enter the new data.
• If the field contains data, place your cursor in the field and select the text you want to change.
Once selected, either press Delete or enter new data.
• If you make an error, you can reset the individual text box or all the text boxes. Click Reset
Selected Value or Reset All Values. The Exam Number field cannot be edited.
• When entering data in the Birthdate field, the month, day, and year can be separated by a hyphen
(-), forward slash (/), comma (,) or period (.). The year must contain four digits.
Edit Patient Data

Follow these steps to edit or add patient information.
1. From the Exam List in the File Manager, select the exam to be edited.
• Only one exam number can be selected.
• The exam must be closed or ended.

• Exams can be edited multiple times.
• You can edit only exams created on your system.
• Edit Patient is not accessible if the exam you want to edit is currently in use. An exam is
currently in use if New Patient, Network/Archive/Film queues, Save, 3D, Reformat, Denta
Scan, Navigator, viewport, AutoFilm queue or Image Viewer is active. An error message
displays.
2. Right-click on the exam and then select Edit Patient Info.

3. At the alert window, click Accept to continue.
4. From the Edit Patient Data window, edit the text fields.
• Click the text you want to edit and enter your changes.

Data Management
• The Exam Number field cannot be edited.

• Edit Patient is not accessible if the exam is in use.
5. Click Save when you are satisfied with the changes and you have entered your initials in the
Edited By field. A confirmation window opens.
6. At the confirmation window, click Accept.
• A percentage countdown menu displays until Edit Patient is closed and the Patient
Information Edit Log is updated.
• It takes approximately two minutes to update a 100-image exam.
• The original exam is replaced with the edited exam and is indicated by e+1 in the description
field. The number indicates how many times the exam has been edited.
Make a Patient Anonymous

Use this procedure to remove certain exam information. An Anonymous Patient can be created by
exam, series, or image. To set the annotation level to Full or Partial, see the Set the anonymize patient
annotation level procedure.
1. From the File Manager, right-click on the exam and then select Anonymize Patient.
2. Verify that there is enough disk space to create an anonymous patient exam.
A progress bar displays the process’s status.
Install a SMPTE Pattern

Follow these steps to install a SMPTE pattern to view BRH or quality assurance images. Once installed
the images are in exam 1000, which can be selected from the Exam List. The patient Name is listed as
SMPTE.
1. Click the Utilities icon on the image monitor, select Service, then Service Tools to open the
Service Desktop.
2. Click the Image Quality tab.
3. Click Install SMPTE Image from the menu tree on the left of the window.

Data Management
Figure 431 Install SMPTE image
Display a DICOM Header

Follow these steps to open a DICOM image header in a floating window. The window displays all image
DICOM header information, including the DICOM tag, value, and description.
1. From the File Manager, select the exam.
2. From the Series List, select an image.
3. From the File Manager control area, click the DICOM header icon .
A window opens with the DICOM header information.
NOTE
Refer to the DICOM Conformance Statement for the system.
19.8 Scan Data Manager

Scan data
During a scan, x-rays pass through the patient’s anatomy with each rotation of the gantry and strike
the detectors. The signal from the detectors is converted to an analog signal that is then captured as
part of the scan file. This is the scan data (or raw data). The scan data contains all of the information
gathered during an exposure.
Lock scan data
As patient exams and scans are performed on the system, the raw scan data is saved to a database.
By default, the scan data from the earlier scans is deleted to make room for the data from newer
scans. However, it may be necessary to retain (lock) the scan data for reconstruction at a later time or
perform additional reconstructions.

Data Management
Unlock scan data

Once scan files are no longer needed, you can unlock them so they can be overwritten with new data.
Unlocked scan data files are overwritten as the system requires space for new scan data files.
Save scan data
You can save scan data to USB media if scan data needs to be retained for an indefinite time or sent
elsewhere for diagnostic review.
Scan data may be saved to a USB hard drive.
You can restore saved scan data back to the system database for later reconstruction.
NOTE
USB must be conditioned to FAT32 file type before before saving scan data to USB. A
prompt will ask the user if the USB can be converted to EXT3/EXT4 file type before and
saving of system state backup to USB occurs.
19.5.3 Save Images on page 834:"USB3.0 device with a write speed of greater than or
equal to 45 mb/s
NOTE
Only scan data from a Revolution™ CT system can be restored on a Revolution™ CT
system. Restoring and processing scan data from sources other than the Revolution™ CT
scanner is not authorized for clinical use since safety and effectiveness have not been
established.
The system overwrites the oldest scan files on the system when restoring scan data.
When you restore scan data, the system locks scan files to make sure the system does
not overwrite them. You will have to manually unlock scan files when they are no longer
needed.
Scan Data Manager
From the File Manager control panel, click the Scan Data Manager icon .

Data Management
Figure 432 Scan Data Manager
1 Controls area 3 Progress Bar
2 Scan Data Exam list 4 Series Information
5 Group Information
You can sort all three of the areas on Scan Data Manager by column heading to help find the records
you need. Click a column heading to sort the table by that heading. Click the heading again to reverse
the display order.
The Controls contains the Source menu and a search box. Selecting anything other than Scan Data
from the Source menu will close the Scan Data Management window. You can type a search string into
the Search box to find exams (this is like searching for exams in the File Manager).
The Exam List contains a list of exams for which there is scan data available. This list works similarly to
the Exam List in the File Manager.
There is a Locked status column that indicates which exams (or partial exams) have been locked
against automatic deletion.

Data Management
Table 153 Locked column status flags
This flag: Means:
Blank (no flag) The exam is unlocked and will be deleted when the system requires space for data
from new scans.
The scan data for the exam is locked against automatic deletion.
Part of the exam scan data has been locked against automatic deletion.
19.8.1 Locking and unlocking scan data

You can lock scan data to prevent the system from automatically deleting it when it needs space for
new exams and scans. When you are finished with the scan data from an exam or series, you can
unlock it.
1. In File Manager, highlight any exam to activate the control panel icons.
2. From the File Manager control panel, click the Scan Data Manager icon .
3. In the Scan Data Manager, highlight the exam, series, and scan for which you want to lock or
unlock scan data. Hold down the Control key while selecting to choose multiple records.
4. To lock the scan data for the item, right click Lock Scan Data. To unlock scan data, right click
Unlock Scan Data.
19.8.2 Deleting scan data

Scan Data Manager deletes raw scan data that is not locked as space is required for new data. To
ensure that raw scan data is preserved, save it to a USB device. Refer to 19.8.5 Save full or anonymized
raw scan data on page 862
19.8.3 Deleting scan data from USB device

You can remove obsolete scan data from the USB device to make space for new data while not erasing
all the scan data on the USB device.
1. Plug in the USB device to the console.
2. Select USB Drive from the drop-down menu at the left of the controls area of Scan Data Manager.
3. In the Scan Data Manager, highlight the exam, series, and scan you want to delete. Hold down the
Control key while selecting to choose multiple records.

Data Management
4. Right click and select Delete Scan Data
19.8.4 Add reconstruction

You can add a new reconstruction from the raw scan data.
3. In the Scan Data Manager, right-click the exam, series, or group for which you want to add a new
reconstruction.
4. Click Open Exam Session.
5. The Reconstruction and Post Processing window opens. The item you selected in the Scan Data
Manager will be selected in the task list. Use the task list to create the reconstruction (as you
would do after a scan).
The Exam Summary page opens on the Scan Display (as it does at the completion of a scan).
19.8.5 Save full or anonymized raw scan data

To save raw scan data, you can send it to a USB. You can send the full scan data, or an anonymized
version of the data.
Sending anonymized data does not guaranty that data will be rendered anonymous in compliance
with applicable data privacy laws. Review the scan data before sharing the data with third parties to
ensure compliance with applicable privacy laws or regulations.
Raw data saved anonymously and then restored will reconstruct with patient identifying information
removed.
If you select a scan file for saving, you cannot select it for another process while it is in the save queue.
NOTE
Scan must be idle when you start this procedure. Each cardiac, non-Hi Res scan file
takes approximately 5 minutes to save, if it was a 0.28 second scan. Scan times can be
longer based on the length of the exposure.
Make sure the selected scan files do not exceed the space available on the USB.
1. Connect a USB device to the USB port on the front of the media tower or the front of the operator
console computer.

Data Management
4. Highlight the exam/series you wish to save anonymously. Hold down the Control key while
selecting to choose multiple records.
5. Right click and select Send Scan Data As.
6. Select Anonimized Copy or Full Copy.
NOTE
Make sure the USB to which you are sending the data has enough disk space to store
the data. The system does not check disk space before sending.
NOTE
If USB fails to mount, a message is displayed. This may indicate that the USB is not
formatted to the required format. Use the following steps to format the USB From
the display monitor:
a. Click Troubleshooting, then Unix Shell. A Unix Shell window opens.
b. At the prompt, enter the operating system password for ctuser.
NOTE
If your system is configured in a language other than English, the
Unix Shell may show unreadable text when first opened. Enter the
operating system password for ctuser.
c. Type mkfsUSB and press Enter. Depending on the size of the USB it may take
some time for the formatting to complete.
d. When the prompt returns, disconnect the USB
e. Click the X in the upper corner of the Unix Shell window to close it.
f. Return to step 1.
7. Click Close to exit.
8. Once the save is complete to the USB device, exit Scan Data Manager and disconnect the USB
device. Then, resume scanning.

Data Management
NOTE
If a patient exam session is in the scanning state and you select Save or Restore, a
message displays indicating that the Scan Resource cannot be acquired.
“Could not acquire Scan Hardware Resource. This may have occurred due to one of the
following:
• Scan Data Save or Restore is in progress
• Daily Prep is in progress
• Service scanning tools are in use
• Scanning Session is open
Please wait for completion or cancel the job or queue in progress by the application. If
this is not the case, please perform a Scan Hardware Reset from the Service Tools menu.
If problem persists, please contact your service representative.”
NOTE
See Fields removed from exams, series, or images using Full or Partial Anonymous
modes (page 19-47) to view the data that is removed.
19.8.6 Restore Data

You can restore saved scan data back to the system database for later reconstruction.
If you select a scan file to be restored, you cannot select it for another process while it is in the restore
queue.
NOTE
Only scan data from a Revolution™ CT system can be restored on a Revolution™ CT
system. Restoring and processing scan data from sources other than the Revolution™ CT
scanner is not authorized for clinical use since safety and effectiveness have not been
established.
The system overwrites the oldest scan files on the system when restoring scan data.
When you restore scan data, the system locks scan files to make sure the system does
not overwrite them. You will have to manually unlock scan files when they are no longer
needed.
1. Select USB Drive from the drop-down menu at the left of the controls area of Scan Data Manager.
2. Highlight the exam, series or group you want to restore. Hold down the Control key while
selecting to choose multiple records.

Data Management
3. Right click and select Restore and Lock Scan Data.
4. When you no longer need the data, unlock it to allow the system to overwrite it to conserve space.
Refer to 19.8.1 Locking and unlocking scan data on page 861
NOTE
If a patient exam session is in the scanning state and you select Save or Restore, a
message displays indicating that the Scan Resource cannot be acquired.
“Could not acquire Scan Hardware Resource. This may have occurred due to one of the
following:
• Scan Data Save or Restore is in progress
• Daily Prep is in progress
• Service scanning tools are in use
• Scanning Session is open
Please wait for completion or cancel the job or queue in progress by the application. If
this is not the case, please perform a Scan Hardware Reset from the Service Tools menu.
If problem persists, please contact your service representative.”
19.8.7 Pausing, Resuming or Canceling a save or restore

You can pause, resume or cancel a save or restore process.
Clicking the Pause button at the right of the controls area of Scan Data Manager completes the current
scan file, then pauses from processing additional files in the queue.
Clicking the Resume button resumes saving or restoring files in the queue.
Selecting Cancel, finishes the current scan file then clears the rest of the jobs from the queue.
19.8.8 Open Exam Session

You can click on a record to open an Exam Session for any exam, series or group on the Scan Data
Manager window.
1. In the Scan Data Manager, highlight the exam, series or group for which you want to open the
session.

Data Management
2. Right click and select Open Exam Session.
19.9 Recon Management
19.9.1 Recon Management concepts

This section provides the information you need to view reconstruction progress and manage
reconstruction jobs.
The system status dashboard Recon Status Card will show the number of active reconstruction tasks
and the number of suspended reconstruction tasks. The icon is green when there are no suspended
tasks and orange when there is one or more suspended tasks. Access Recon Management by clicking
the Recon Management icon at the top left of the image (right) monitor, then selecting Recon
Management.
Recon Status Card - no suspended tasks
Recon Status Card - suspended tasks

Data Management
Figure 433 Recon Management window
19.9.2 General Recon Management Window

The General Recon Management window displays all currently active reconstruction jobs. You can
review progress here with the % Complete indication.
19.9.2.1 Suspended entries

Sometimes the system for a variety of reasons may not be able to complete the reconstruction
of a particular image. The General Recon Management window provides the ability to attempt to
unsuspend and restart suspended reconstruction jobs.
19.9.2.2 Deleting Reconstruction Jobs

There may be circumstances where you want to delete a reconstruction job before it completes.
Secondary reconstruction jobs may be deleted in the General reconstruction window.
19.9.3 Completed Recon Management Window

The Completed Recon Management window is a quick way to see which reconstruction jobs are
completed.

Data Management
19.10 Reconstruction and Image Processing Task List

The Reconstruction and Image Processing Task List provides the ability to define additional image
processing tasks during the scan process, including recons and manual and automatic reformats, in
one central place. It also allows the display those image sets and the monitoring of both the creation
and transfer of the image sets.
You can set up these tasks directly before scanning a series, set up all post-processing before doing
any scans or scan the patient first, then set up the image processing.
If you modify the tasks on the scan task list on the left monitor, the corresponding changes are made
on the Reconstruction and Image Processing Task List. For example, if you copy/paste a scan series,
that new series and all of its associated recons and reformats is also copied onto the Reconstruction
and Image Processing Task List. Similarly, if you delete a scan series from the scan task list, that series
and all of its associated recons and reformats is also deleted from the Reconstruction and Image
Processing Task List.
19.10.1 Reconstruction and Image Processing Task List window

Data Management
Figure 434 Reconstruction and Image Processing Task List
Table 154 Reconstruction and Image Processing Task List components
1 Primary recon for first scan series — the first recon listed under each scan series, identified with a triangle
in the upper left corner of its task bar
2 First reformat for first scan series
3 Secondary recon for second scan series
4 Reconstruction and transfer settings

Data Management
5 Image tools
6 For multi-group acquisitions, a label to the right of the recon bar indicates the part of the scanned anatomy
the recon covers. Reformats and AW tasks do not have an anatomy label.
If the recon start and end points correspond exactly with the entire scan acquisition (including all scan
groups if there are multiple groups) the label All displays.
If the recon start and end points correspond exactly with a single scan group, the label is G# (e.g. G1 or G2)
where # is the scan group number.
The Reconstruction and Image Processing Task List opens on the Image Display when you open the
exam and organizes image processing tasks in relation to the scan series set up in the Scan Display
scan task list. Under each image processing scan series are the recons, reformats and AW tool bars that
can be prescribed via protocol or before or after an exam.
The Reconstruction and Image Processing Task List also opens when you open an exam in a tab via File
Manager.
19.10.2 Reconstruction in the Reconstruction and Image

Processing Task List
A recon is any primary or secondary reconstruction of a scan. In a multi-group scan, it may cover a
single group or multiple groups or any part of the groups. Primary Recon settings are prescribed in the
scan settings on the Scan Display, and are not editable from the task list. However, you can change a
primary recon’s output and transfer options from the Reconstruction and Image Processing Task List.
19.10.2.1 Reconstruction queue priority order

When utilizing Xtream Stroke and Xtream ER/Trauma options reconstruction priority has different
behavior based on the Clinical Identifier selected for the reconstruction.
When the Clinical Identifier is Stroke.Perfusion or Trauma.General, these reconstructions will always
have the highest priority and will be moved to top of the image reconstruction priority after any
pending scout or Smart Prep reconstructions are completed.
19.10.2.2 Adding a recon

The Reconstruction and Image Processing Task List provides the ability to add secondary recon tasks
that were not prescribed as part of the protocol.
1. Click Add Recon.
2. Select either Add All Anatomy Recon or Add G0 Recon (Group 1). A new recon task is added at
the bottom of the list of recons, highlighted and opened to display its settings. The values in this
recon inherit the setting from the primary recon.

Data Management
Figure 435 Add recon menu
NOTE
If scan data for a series no longer exists, the Add Recon button is disabled.
If the scan is already completed, the primary recons are reconstructed and you pressed Continue to
start any secondary recons for this primary recon, when the new secondary recon is created, you must
click Run to start/queue the recon. You can also start/queue the recon by closing the panel.
The new recon is processed last on the recon list once scan data is available.
19.10.2.3 Duplicate a recon

Use the recon context menu to
• Delete the selected recon and all sub-tasks, as long as the recon has not yet been acquired.
• Duplicate the current recon to create a new one. This copies and pastes this recon, selects the
new recon and opens the recon tool to allow you to make any changes to it.
• Create a new reformat based upon the recon image data.
Right click the series bar, then select Duplicate Recon.
Figure 436 Duplicate recon
19.10.2.4 Editing/viewing a secondary recon task

You can edit recon tasks that were prescribed as part of the protocol and have not yet been put in the
recon queue. You can also edit the settings for newly added tasks. If it has been performed, you can
only view these options. Clicking on an existing secondary recon task or adding a new one, opens the
editing panel.

Data Management
NOTE
Primary recon settings are not editable on the Image Display, only on the Scan Display
19.10.3 Reformatting in the Reconstruction and Image Processing

Task List
Refer to the Direct Multi Planar Reformat (DMPR) section of the Scan Application chapter for
information on using the reformat tools, including a description of the Processing and Transfer Status
Indicators.
19.10.4 Series Numbering

The system uses the following series numbering schemes:
System Condition Series Numbering
Primary Recons 1–89
Pre or post scan Secondary Recons 301-389

401-489
Smart Prep 201-289
DMPR 601-689
701-789
801-889
Text Pages 98
(exam, series, roi)
Secondary Capture 99
SmartPrep Report 299
Cardiac ECG trace per recon 599
Contrast Report 996
Dose SR 997
Dose SC 999
NOTE
For primary or secondary recons and DMPR that exceed the number of series allocated,
any additional series will go into Series 1001+.

Data Management
19.10.5 Selecting viewports for images in the Reconstruction and

Image Processing Task List
As soon as any image exists for an image series, the viewport selection button displays after the
anatomy label . Use this control to indicate in which viewport each image series is to be displayed.
Mouse over the icon to enlarge it, then click on the viewport in which you want to view the recon or
reformat series.
Figure 437 Viewport selector in Reconstruction and Image Processing Task List
19.10.5.1 Auto-View
The upper left viewport will autoview each primary and secondary recon unless the Clinical ID is
Stroke.Perfusion.
Autoview does not display every single image on systems with Xtream Recon, as images are
reconstructed in bursts of more than one image. Use the right monitor review viewport to review
all images.
19.10.5.2 Series Binding

If you have series binding in the viewports, and use it or the next/previous series buttons to change the
series displayed within the viewport.
19.10.5.3 Expanded Mode

When you have expanded any of the 4 512x512 viewports to 1024x1024 mode, so that a single
viewport takes up the full viewport area, the viewport control button changes to a single button, and
only a single series at a time can be displayed.
19.10.5.4 Viewport Priority

The priority for images being displayed in the viewports:
1. Any task (recon, reformat or AW) opened by clicking on a task bar.
2. Any reformat auto-view by volume – where DMPR is set to show the entire volume in all 4
viewports as it is being acquired and built.
3. Any standard auto-view set up for a reconstruction or reformat task, where the auto-view is
displayed in the upper left viewport.

Data Management
4. Any image assigned to a viewport using a viewport selection button.
19.10.6 Image Tools Column

The right column of the list includes a menu of image-related tools and options.
Refer to the View Images chapter for information on using the image-related tools and options.

Data Management
Figure 438 Reconstruction and Image Processing Task List — image tools

Data Management
19.10.7 Output Options

Figure 439 Output Options
Table 155 Output options
Auto-view Enables the automatic display of reconstructed im-

ages in the upper left view port. This is the viewport
indicated with the green box.
Series Description You can enter a description for the series in this field.
If you do not enter a description, the series will take
the name of the primary reconstruction’s series de-
scription.
Exam Split Select On to enable selection of the Requested Proce-

dure that this reconstruction should be assigned to.
Any DMPR or reformat images from this reconstruc-
tion will be assigned to this procedure as well.
Requested Procedure If Prospective Exam Split is set to On, select which

requested procedure the image reconstruction is as-
signed to from the drop-down list of available proce-
dures. The available procedures come from the work-
list entries you selected from the patient schedule.
19.10.8 Data Transfer

You can prescribe a transfer of the data of an individual image series to any network or archive host
after the image series has been fully created. Click on the image series task bar to display the settings
for that task, then open the data transfer settings.
Refer to the DMPR section of the Display Applications chapter for information on transferring images.

Data Management
Figure 440 Transfer Options

Data Management

Protocols
20 Protocols
20.1 Overview
A protocol is a series of pre-programmed scan and recon parameters used for imaging a particular part
of the body. The system is equipped with a set of GE Adult and GE Pediatric Reference Protocols that
can be used for common types of examinations. You can use these protocols or modify them to fit
particular clinical needs. Protocols are used as a basis for routine or established procedures. Refer to
known sources for techniques and dose information for viable parameters, as proper techniques must
be used to ensure patient safety and image quality.
A protocol must be selected to initiate the scanning sequence. Once chosen for use, any protocol
may have any parameters modified as needed for individual case purposes. Any protocol parameter
in the individual exam may be adjusted without affecting the established protocol. If an established
protocol has a parameter or parameters you wish to permanently change, this can be done through
the Protocol Management feature.
Protocol Management provides a place to create established protocols with preset scan and recon
parameters for a specific clinical exam. This saves time when prescribing scan parameters for each
patient. Each series can be viewed, and scan values may be changed to see the effect on other values
or other available options. When building protocols, care should be taken to think about the order
and importance of getting reconstructed images to a physician review station (IE workstation or PACS).
This is extremely important, especially when building protocols that will be used in a trauma setting.
You must have permissions to access Protocol Management. Permissions are enforced by a user
authentication window.
Protocol Management also provides a structure to organize the presentation of the protocols on the
protocol selection screen that will aid in protocol selection at scan time.
Protocols can be saved and restored via System State, Protocol Exchange or IPM Services. It is
recommended to save Protocols, Autovoice and Display preferences when protocol changes are made.

Protocols
In order to save to USB the Protocols, Autovoice, Display preferences & etc; use at least USB 3.0 for fast
writing speeds, otherwise the user will see the message.
NOTE
USB must be conditioned to FAT32 file type before before a system state backup is
started. A prompt will ask the user if the USB can be converted to EXT3/EXT4 file type
before saving of system state backup to USB occurs.
Finally, insert a new Hyperlink back up to Section 18.5.3 Save Images: "USB3.0 device
with a write speed of greater than or equal to 45 mb/s
If System State is used to restore protocols with Intelligent Protocoling selected, do not select Dismiss
and Restart. Instead perform system restart from Mode > Power Management > Restart.
NOTE
Do not restore protocols from a system with a Quantix 160 tube to a system with a
Performix™ HDw tube. Protocols and Profiles are not backward compatible to older
software releases.
20.2 Manage Protocols

20.2.1 Enter Protocol Management
2. Click Protocol Management, then click Protocol Management again.

Protocols
Figure 441 Protocol Selection window
20.2.2 Protocol Selector Screen

1. Select Protocol Category and Anatomy from the drop-down menus
2. There are eight protocol categories:
• Adult: Defined by your site for adult patients. These protocols are custom protocols that your
radiologist or physician likes to use.
• GE Reference Adult: A set of predefined protocols for adult patients that cannot be modified
but can be copied and used. These protocols are factory installed. They have been developed
in collaboration with clinical partners to provide users with a convenient and clinical relevant
starting point for tailoring your departmental protocols.
• Pediatric: Defined by your site for pediatric patients. These protocols are custom protocols
that your radiologist or physician likes to use.

Protocols
• GE Reference Pediatric: A set of predefined protocols for pediatric patients that cannot be
modified but can be copied and used. These protocols are factory installed. They have been
developed in collaboration with clinical partners to provide users with a convenient and
clinical relevant starting point for tailoring your departmental protocols.
• Recently Scanned Protocols: A copy of the last 90 protocols reside exactly as they were used.
These protocols can be copied and used but cannot be modified or deleted.
• Service: Used by a service representative.
• GE Service: A set of predefined protocols for use by a GE service representative.
• Manufacturing: Used by a manufacturing representative.
3. Anatomical Selector (Drop-down menu or Anatomical Figure)

Within the Adult, GE Adult, Pediatric and GE Pediatric categories, protocols can be assigned to 1 of
10 anatomies. Each Anatomy has space for 90 protocols.
• Head
• Orbit
• Neck
• Upper Extremity
• Spine
• Chest
• Abdomen
• Pelvis
• Lower Extremity
• Miscellaneous
If you wish to edit pediatric protocols, click Pediatric.

For color coded pediatric anatomical areas, there is space for 90 protocols in each of the different
weight classifications.
NOTE
Head, Orbit, and Miscellaneous are not color coded.
4. Protocol numbers consist of two parts. The first part is based on the Category and anatomical
region and the second number is numerically assigned as it is saved to that region.
User area numbers: Adults = 1 to 10, Pediatrics = 11 to 20, Service = 90
GE area numbers: Adults = 21 to 30, Pediatrics = 31 to 40, Service =40, Recently Scanned =50, and
Manufacturing= 60
To see protocol numbers, right-click in the upper right corner of the Protocol Selection window
and select Protocol Numbers.
5. Search – the user can search by protocol number or protocol name. This will filter the list of
protocols displayed.

Protocols
6. Favorites
Displays protocols tagged as favorite within a protocol region at the top of the list of protocols.
To Manage Favorites:
• Add a protocol to favorites. Select an anatomical region, right-click on a desired protocol in
the all protocol list and click Add to Favorites.
• Remove a protocol from favorites. Select an anatomical region, right-click on a desired
protocol in the favorites list and click Remove from Favorites.
NOTE
Protocols marked as Favorites when copied are marked as favorites when
pasted into any anatomical category. If you do not wish the newly pasted
protocol to be a favorite, right click on the protocol name and select Remove
from Favorite. refer to the Define a User Protocol section of the user manual.
7. Protocol Tags
Within the Adult and Pediatric categories, protocols can be tagged as Draft, Radiation Therapy,
Research and/or Trauma.
To add Tags:
a. Select an anatomical area, right-click on a desired protocol and select Tags.
b. The list of Tags displays,
c. Click on the desired tag. Note multiple tags can be selected.
d. Once all desired Tags selected, click on the protocol name.
e. Tags selected will be listed in
To delete Tags
a. Select an anatomical area, right-click on a desired protocol and select Tags.
b. The list of Tags displays,
c. Click on the desired tag. Note multiple tags can be selected.
d. Once all desired tags are deleted, click on the protocol name.
NOTE
Protocols marked with Tags when copied retain the Tags when pasted into any
anatomical category. If you do not wish the newly pasted protocol to be tagged,
follow Delete Tags prior to copying the protocol.
8. All
Displays all protocols in the anatomical region in this list of protocols. Unless the search feature is
activated.

Protocols
9. Sort Protocols
Right-click in the upper right to display the sort menu.
Check the box to display protocol numbers.

Select the radial button for the preferred sort method, Alphabetically, by Protocol Number or
Custom Sort.
When Custom Sort is selected, separators can be added to the displayed protocol list. To add a
space above a protocol, select the protocol, right-click and select Add Separator. To remove a
separator, select the line with the separator, right-click and select Remove Separator.
When Custom Sort is selected, the protocol list may be re-arranged. Left‐click on a
protocol or left click and shift to select multiple protocols and drag the protocol(s) up or
down, drop to place the protocol(s) in the list. This is particularly useful when creating
new protocols that need to be inserted into the existing protocol list. Optionally, you
can then re-number the protocols within an anatomy after the list has been rearranged.
20.2.3 Define a User Protocol

Use this procedure to change the established user protocols on the system.

Protocols
NOTE
GE Reference protocols are read-only and cannot be edited.
1. Several option packages may be purchased and installed on your system, including the setup of
various protocols. You need to have some understanding of their functions to use them in your
protocols. These options include Cardiac Scan modes and 3D Dose Modulation. Please review
Scan and Recon Parameters prior to building protocols.
5. From the Protocol Selection window, use the category and anatomical selector or the search field
to identify the starting protocol to edit or create a new protocol. You can create a new protocol
by copying and pasting a starting protocol or by editing a protocol with the Save As option. It is
recommended to use the Edit and Save As option to create pediatric protocols in the different
color weight categories.
6. Copy and Paste a starting protocol:
NOTE
Protocols marked as Favorites when copied are marked as favorites when pasted
into any anatomical category. If you do not wish the newly pasted protocol to be a
favorite, right click on the protocol name and select Remove from Favorite. refer to
the Define a User Protocol section of the user manual.
a. Click the desired category and anatomy selections to view that protocol list.
b. Select the protocol to be copied.
c. Right-click and select Copy.
d. Select the anatomical category as the destination to paste the protocol.
e. Right-click in the protocol list area and select Paste
f. Rename the protocol as needed.
i. Click the protocol.
ii. Right-click and select Rename to enter the New name.
iii. Click OK.
7. Select a protocol you wish to edit.
8. Click Edit if you are making changes to an existing protocol.
9. From the Scan Settings window, you will be able to define the scan acquisition, recon and image
processing tasks, and set the desired scan and recon parameters within each task for the clinical
intent of the protocol. You will be able to enable Prospective Exam Split with pre-configured
procedure codes and set the transfer options for each image series as well as the exam. You will
be able to set notification values for dose check for each protocol. These settings are described
throughout this manual. Please review how they will impact the protocol before use.

Protocols
Dose values displayed in the Dose Display area of the Scan Settings window use the Manual
mA and Manual kV values, and for Cardiac scans the baseline SFOV is defined in the protocol to
calculate the CTDIvol and DLP. The SmartmA, SmartmA ODM or Cardiac Modulation settings are
not used.
10. Click Changes Complete, then click the appropriate button for the desired result.
• Exit without Save - will close the edit session. No changes will be made to the protocol.
• Save- to save the changes to the current protocol
• Save As - will save changed as a new protocol, You will be prompted to enter the settings for
the new protocol in the Protocol Save window.
11. In the Protocol Save window, enter the desired settings for the new protocol. Enter Protocol
Name, select the Protocol Category, and Anatomy from the drop-down menu. Note that when
the Category is Pediatric, and the selected Anatomy region supports weight-based protocols, you
will need to make a Color Selection.
Figure 442 Protocol Save window
20.2.4 Delete a Protocol

Use this procedure to delete a protocol from your user defined protocol list. This keeps your protocol
list current by deleting any unnecessary protocols.
NOTE
Only protocols in the Adult or Pediatric categories can be deleted.

Protocols

4. From the Protocol Selection window, select either the Adult or Pediatric protocol category.
5. Click the desired anatomical body part to view that protocol list.
6. Select the protocol you want to delete.
7. Right-click and select Delete.
8. Click Yes to confirm the deletion.
20.3 Protocol Management with kV Assist/Auto

Prescription
NOTE
Auto Prescription will replace kV Assist in a future software release. GE strongly
recommends that you begin to modify your protocols to utilize Auto Prescription.
Your kV Assist Protocols will continue to work. However, when modifying any protocol utilizing kV
Assist, a message will be displayed to encourage implementing Auto Prescription. In addition, kV
Assist will be an available selection in kV mode only when the protocol being edited already utilizes kV
Assist.
20.3.1 Considerations when enabling Auto Prescription in a

Protocol
Auto Prescription is a profile-driven feature. The settings within the profile will impact how the settings
are changed at scan time for the patient being scanned in relation to the Reference Size Patient. It
is important to determine which Auto Prescription Profile to use. GE provides a set of GE Adult Auto
Prescription Profiles that can used for common types of examinations and clinical tasks. You can use
these profiles, or you can modify them for particular clinical needs. See Creating a Auto Prescription
Profile.
Any protocol with kV Assist 1.0 will need to be edited to change the kV mode to Manual kV or Auto
Prescription. For Manual kV, refer to .
Table 156 GE Auto Prescription Profile Descriptions
Profile Name Description
GE Thorax (Adult) This profile is intended for use during routine thoracic scans for evaluation of chest
region for abnormalities.
GE Small Ves- This profile is intended for use during non-gated Thoracic CTA scans for evaluation of
sel Thoracic CTA small thoracic vasculature (e.g., Pulmonary Embolism).
(Adult)

Protocols
GE Auto Prescription Profile Descriptions continued

Profile Name Description
GE Large Ves- This profile is intended for use during non-gated Thoracic CTA scans for evaluation of
sel Thoracic CTA large thoracic vasculature (e.g., Thoracic Aorta).
(Adult)
GE CCTA (Adult) This profile is intended for use during prospectively gated Cardiac axial scans for
evaluation of coronary arteries.
GE CCTA Hi Res This profile is intended for use during prospectively gated Cardiac axial scans utilizing
(Adult) HiRes scan mode for evaluation of coronary arteries.
GE Abd/Pel (Adult) This profile is intended for use during routine Abdomen Pelvis scans for evaluation of
abnormalities of abdominal and pelvic structures.
GE Small Vessel This profile is intended for use during body CTA for evaluation of small abdominal
Body CTA (Adult) vasculature.
GE Large Vessel This profile is intended for use during body CTA for evaluation of abdominal aortic
Body CTA (Adult) aneurysm and other large abdominal vasculature.
GE L/T Spine (Adult) This profile is intended for evaluation of soft tissue and bony structures of the lumbar or
thoracic spine.
GE High Pitch Thor- This profile is intended for use during routine thoracic scans using high pitch for
ax (Adult) evaluation of chest region for abnormalities.
GE High Pitch Thor- This profile is intended for use during Thoracic CTA scans using high pitch for evaluation
ax CTA (Adult) of thoracic vasculature (e.g., Pulmonary Embolism).
GE Runoff (Adult) This profile is intended for use during runoff scans for evaluation of vascular structures
of abdomen, femurs and lower extremities
GE CAP (Pediatric) This profile is intended for use during routine pediatric Chest, Abdomen and Pelvis
scans for evaluation of abnormalities of abdominal, pelvic, and thoracic structures
GE Gated Thoracic This profile is intended for use during gated Thoracic CTA scans for evaluation of small
CTA (Adult) and large thoracic vasculature.
Table 157 GE Auto Prescription Profile Settings
Profile Name Clinical SANI Be- SANI Min Max kV Min Max Rota- Pitch
Task low Ref Above Ref Size Size mA mA tion
Size Size (AP + (AP + Time
Lat) Lat) [s]
(* denotes kV for Reference Size Patient)
GE Thorax ST+C Large De- Small In- 39 45 70 220 500 0.5 -

(Adult) High crease crease
45 54 80 100 600 0.5 -
54 64 100* 100 720 0.5 -

Protocols
GE Auto Prescription Profile Settings continued

Lat) Lat) [s]
64 70 120 100 740 0.5 -
70 96 120 100 740 0.7 -
GE Small Ves- ST+C Large De- Small In- 39 42 70 100 500 0.35 -
sel Thoracic High crease crease
CTA (Adult) 42 54 80 100 600 0.35 -
54 64 100* 100 720 0.35 -
64 70 120 100 740 0.35 -
70 96 120 100 740 0.6 -
GE Large Vessel ST+C Large De- Small In- 39 42 70 100 500 0.35 -
Thoracic CTA High crease crease
(Adult) 42 58 80 100 600 0.35 -
58 68 100* 100 720 0.35 -
68 70 120 100 740 0.35 -
70 96 120 100 740 0.5 -
GE CCTA ST+C Small De- Constant 39 47 70 100 500 - -

(Adult) High crease
47 55 80 100 600 - -
55 65 100* 100 720 - -
65 96 120 100 740 - -
GE CCTA Hi Res ST+C Small De- Constant 39 57 100 100 475 - -

(Adult) High crease
57 70 120* 100 405 - -
GE Abd/Pel ST+C Large De- Very Small 39 50 80 250 600 0.5 0.992
(Adult) Low crease Increase
50 56 100 100 720 0.5 0.992
56 70 120* 100 740 0.5 0.992
70 96 120 100 740 0.6 0.508
GE Small Ves- Angio Large De- Small In- 39 47 70 220 500 0.5 -
sel Body CTA crease crease
(Adult) 47 52 80 100 600 0.5 -
52 60 100* 100 720 0.5 -

Protocols

Lat) Lat) [s]
60 68 120 100 740 0.5 -
68 96 120 100 740 0.7 -
GE Large Vessel Angio Large De- Small In- 39 52 70 220 500 0.5 -
Body CTA crease crease
(Adult) 52 60 80* 100 600 0.5 -
60 64 100 100 720 0.5 -
64 70 120 100 740 0.5 -
70 96 120 100 600 0.7 -
GE L/T Spine ST+C Constant Constant 39 58 100 50 720 0.7 0.992

(Adult) Low
58 96 120* 90 450 1 0.508
GE High Pitch ST+C Large De- Small In- 39 45 70 300 500 0.35 -
Thorax (Adult) High crease crease
45 54 80 100 600 0.35 -
54 64 100* 100 720 0.35 -
64 70 120 100 740 0.35 -
70 96 120 100 740 0.5 -
GE High Pitch ST+C Small De- Large In- 39 46 80 100 600 0.35 -
Thorax CTA High crease crease
(Adult) 46 50 100 100 720 0.35 -
50 58 120* 100 740 0.35 -
58 96 120 100 740 0.5 -
GE Runoff ST+C Constant Constant 39 47 80 365 600 - -

(Adult) High
47 56 100 200 700 - -
56 96 120* 150 700 - -
GE CAP (Pedia- ST+C Large De- Small In- 0 31 70 80 500 0.28 -

tric) Low crease crease
31 54 80 90 600 0.35 -
54 96 100* 110 710 0.35 -

Protocols

Lat) Lat) [s]
GE Gated ST+C Very Small Very Large 39 44 80 100 600 0.28 -

Thoracic CTA High Decrease Increase
(Adult) 44 54 100 100 720 0.28 -
54 96 120 100 740 0.35 -
Auto Prescription can only be enabled when the mA mode is SmartmA or SmartmA ODM. It is
important that Noise Index, minimum mA and maximum mA settings be appropriate for the kV of the
Reference Size Patient in the Auto Prescription Profile that will be used (Noise Index Values). The kV
setting for manual kV mode should be set to same value as the kV for the Reference Size Patient.
In protocol management, parameters within the Reference Size Patient Range of the Scan Profile are
displayed in the protocol. Dose display is based on the settings for Manual kV mode and Manual mA
mode. As Auto Prescription can be overridden at scan time, the settings in the protocol should be set
for manual kV mode to be the same as the Reference Size Patient Range settings in the kV Profile.
NI Set in Protocol: Auto Prescription adjusts NI for changes in technique based on Size Adjusted NI
(SANI) strength setting and Clinical Task settings in the kV Profile.
NI set in Profile: The NI in the corresponding Patient Size Range will be applied.
20.3.2 Build a protocol with Auto Prescription

Use this procedure to enable Auto Prescription in a protocol.
NOTE
Because Auto Prescription can be overridden at scan time, first set the technique in
manual mA and manual kV mode that is intended for the Reference Size Patient.
4. From the Protocol Selection window, create a new protocol or select a protocol to edit.
6. Set the Scout parameters. A scout scan is required for using Auto Prescription.
7. Set the scan parameters for each group.
a. From the Scan Settings window, set the kV Mode and mA Mode to manual and set the
parameters:
• mA
• kV

Protocols
• Slice Thickness
• Rotation Time
• Pitch
• SFOV
• ASIR V
• WW
• WL
to match the settings of the Reference Size Patient in the planned kV Profile.
b. Click mA mode and change to SmartmA or SmartmA ODM. Set the minimum mA and
maximum mA to match the Reference Size Patient in the planned kV Profile. Set the Noise
Index based on the Reference kV, slice thickness, anatomy and clinical task.
c. Click kV Mode, select Auto Prescription.
d. Select the Auto Prescription Profile- each group can have a different kV Profile.
Once you select a Auto Prescription profile in Protocol Mangement, the kV is set to the
Reference kV of the profile. If the Reference kV of the profile is different than the kV that
was set before selecting the profile, the system automatically adjusts the prescribed NI for
the Reference kV. This is done to maintain a similar a Contrast-to-Noise Ratio, based on the
clinical task from the profile, as the previous kV and NI. The system will display a yellow
notification banner, and the user has the option to keep the recommended adjusted NI or to
revert to the previous NI.
At this point, all parameters specified within the kV Profile will be designated with a white dot.
In Protocol Management the values displayed are from the Reference Size Patient Range, at scan
time these will adjust based on the patient size calculated from the scout scan.
8. Auto WW/WL of WW/ WL is set to ON automatically for primary and secondary recons when kV
Mode is Auto Prescription unless the original protocol had set the Auto WW/WL to Off.
Click Primary Recon Settings Collection to set Auto WW/WL to OFF for the primary recon, which
will automatically disable Auto WW/WL for all secondary recons associated with this group.
Click Secondary Recon Settings Collection to set Auto WW/WL to OFF for individual secondary
recons.
9. For scans with multiple groups where timing between groups is critical for a successful exam,
click Timing and set Group Delay Lock to Enabled. This results in an alert at scan time if any
factors such as SFOV, rotation time or pitch increase the intergroup delay by 5 seconds over the
protocol delay value.
10. Continue with specifying the parameters for the series.
11. Verify the remaining parameters for the subsequent series in the protocol.
12. Save the protocol.

Protocols
20.3.3 Auto Prescription Profile Editor

The Auto Prescription Profile Editor has two types of profiles:
• GE Reference Profiles The system is equipped with a set of GE Adult Reference Profiles that
include common types of clinical tasks. You can use these profiles or modify them to fit a
particular clinical need. The patient size ranges and settings can be reviewed when the GE
Reference Tab is selected. GE Reference Profiles cannot be edited or deleted, but may be copied
to use as the basis for a user profile.
• User Profiles These are created by a user with appropriate privileges for the Auto Prescription
Profile Editor. User Profiles are editable and can be copied, renamed or deleted via the right click
menu.
Each Auto Prescription profile consists of a unique name, a description, the Noise Index mode and
applicable settings: Slice Thickness or Size Adjusted Noise Index strength and Clinical Task, minimum
and maximum values defining the patient size ranges, and scan settings applicable to a specified size
range.
Figure 443 Auto Prescription Profile Editor

Protocols
20.3.4 Create Auto Prescription User Profile

NOTE
The GE Reference Profiles are designed to provide the optimal image quality at the
lowest radiation dose across patient size. While customers can create their own custom
profiles, changing the settings from the GE Reference Profiles may result in non-optimal
dose and/or image quality.
1. From the image monitor, click , then Protocol Management > Auto Prescription Profile Editor.
Enter Log in credentials.
2. Select GE Reference or User to view the list of existing profiles.
3. Select a profile to display the settings within the profile. GE profiles are read only. User profiles
are editable.
4. Right Click to:
• Copy (GE or User Profile) - Enter Profile Name and Save will create a new user profile.
• Rename (User Profile Only) - Enter Profile Name and Save will rename the selected profile.
• Delete (User Profile Only) - Select Delete and Save if you are sure you want to delete the
profile.
• Select Cancel in any of these options to return to the profile list.
5. Create the desired number of Patient Size Ranges for the profile.
The ranges are continuous (max of one range always equals min of the next range) and will adjust
accordingly as ranges are added and/or deleted.
Ensure that the size ranges are accurate for intended patient population.
a. Click [+] to add or [X] to delete until the correct number of size ranges are displayed, up to a
maximum of 9 size ranges.
b. Click the drop down to select the Patient Size Units you want to use to set the minimum
and maximum size values. Note that Weight and BMI can be used for viewing and editing.
However, the protocol cannot be saved with these units. The values will be converted when
changing between units.
• Dw ( cm)
• AP+ Lat ( cm)
• AP ( cm)
• Lat ( cm)
• Weight ( kg)
• Weight ( lbs)
• BMI
c. Enter the Minimum (MIN) and Maximum (MAX) size values to create the Patient Size Range.

Protocols
Min value Max Value
Dw: 9.9 46.5
AP: 0 41.63
AP_Lat: 0 96.31
Lat: 0 58.51
Weight(lbs): 0 364.34
Weight(kg): 0 165.27
BMI: 0 57.78
6. Select where the Noise Index should be managed for Auto Prescription. This setting is in the
window Where do you want to set Noise Index? See description below for Setting NI in Protocol
or Setting NI in Profile.
A. Setting NI in Protocol
Auto Prescription will update the NI in accordance with the kV selected at scan time to maintain
a consistent CNR relative to that which would be achieved for the Reference Patient Size. The
level of NI adjustment is determined by Size Adjusted Noise Index (SANI) settings and the Selected
Clinical Task.
Figure 444 Auto Prescription User Profile - setting NI in Protocol
a. Ensure that the NI in the protocol is appropriate for the kV and scan settings for the Reference
Size Patient Size Range.

Protocols
b. Determine if you would like to adjust NI strength for patients smaller or larger than the
Reference Patient Size and by how much.
Smaller than Reference Patient Size Larger than Reference Patient Size
No Change No Change
Small Decrease Small Increase
Moderate Decrease Moderate Increase
Large Decrease Large Increase
c. Select the Clinical Task. The drop down is in order from the smallest to largest NI adjustment
across kV.
B. Setting NI in Profile

Protocols
Figure 445 Auto Prescription User Profile - setting NI in Profile
a. In the window What is your Primary Recon slice thickness?, set the Slice Thickness for the
Primary Recon (this will only appear when Setting NI in Profile.
b. Enter the NI value in each patient size range.
7. In the window What additional parameters do you want to change with Patient Size?, click all
parameters that will be set for each Patient Size Range, SFOV, Rotation Time, Pitch and/or ASIR-V.
8. Select individual parameters that you would like to specify for a specific size:
SFOV, ASIR-V, Rotation Time, Noise Index, Pitch
9. For each size range enter the values for kV, minimum mA, maximum mA, NI if NI Set in Profile
is selected, and any other settings clicked from the other parameters window. During scanning,
patient size will be calculated from the scout scan and the settings from the applicable Patient
Size Range will be applied to the scanning protocol.
Note that minimum and maximum mA values default to the minimum and maximum mA for the
selected kV. If alternate values are entered to limit the mA range, ensure that they are appropriate
for the technique parameters prescribed within that Patient Size Range.
10. Save. See Build a protocol with Auto Prescription.
kV Assist recommendations for kV and NI/mA are optimized based upon typical clinical tasks or
scanning and imaging conditions.
20.3.5 Considerations when enabling kV Assist

kV Assist may not be available on future software releases.

Protocols
kV Assist does not utilize profiles, all settings must be set within in protocol.
kV Assist can be used with manual mA, Smart mA or SmartmA with ODM. It is important that mA
or Noise Index and minimum/ maximum mA values set within the protocol be appropriate for the
baseline kV for an average size patient.
20.3.6 Build a protocol with kV Assist

Use this procedure to build a kV Assist enabled protocol and define the baseline Manual kV, Noise
Index, or Manual mA values in the protocol.
NOTE
Because Auto Prescription can be overridden at scan time, first set the technique in
manual mA and manual kV mode that is intended for the Reference Size Patient.
4. From the Protocol Selection window, select a protocol to edit that has kV Assist enabled.
6. Set the Scout parameters. A scout scan is required for using kV Assist.
7. Set the Axial scan parameters.
a. From the Scan Settings window, set the baseline parameters for Noise Index, Mode, Slice
Thickness, Rotation Time, Pitch and SFOV.
b. From the Scan Settings window, open the kV and mA Control collection and then click kV
and set the baseline Manual kV value.
c. From the kV Mode area, select kV Assist.
d. Select a clinical task.
e. Select a Minimum kV and Maximum kV value to define the kV range. Set a Baseline kV. This
selection allows the user to avoid using tube voltages that are too low or too high.
NOTE
The Baseline kV must be within the kV range. When the Baseline kV is changed
to less than the Minimum kV, Minimum kV is lowered to the Baseline kV value.
Conversely, when the Baseline kV is raised to a value higher than the Maximum
kV and Maximum kV are increased to the baseline value.
f. Note that Auto WW/WL of WW/ WL is set to ON automatically when kV Mode is kV Assist
unless the original protocol had set the Auto WW/WL to Off. Click Primary Recon Settings
Collection to set Auto WW/WL to OFF.
8. Continue with specifying the parameters for the series.
10. Save the protocol.

Protocols
20.4 SmartPlan Settings in Protocol Management
20.4.1 SmartPlan Overview

SmartPlan is a protocol driven feature that uses the patient’s scout scan to set scan and recon range,
DFOV, A/P & R/L center based on recognition of anatomical landmarks from valid scout images.
Enabling SmartPlan in the protocol and prescribing a supported Clinical Category, Clinical Identifier
Pair (CID) allows the system to determine and display the initial scan or recon range settings to
the technologist for each group. The technologist must review and accept the parameters or make
necessary adjustments prior to confirming the scan prescription.
20.4.2 SmartPlan Theory

SmartPlan is designed to identify anatomical landmarks within a scout image for the supported
anatomical regions. When enabled within a group, SmartPlan uses the prescribed CID to determine
which anatomical landmarks to look for and then sets the Start, End and when enabled, the DFOV,
AP Centering and RL Centering for each group based on identified landmark locations plus system
defined or user defined margin. To set user defined margins see SmartPlan Management.
SmartPlan is designed to identify the initial scan range settings for the following anatomical regions:
• Single Anatomy:
• Head
• Chest
• Abdomen
• Pelvis
• Combination anatomies:
• Chest + Abdomen
• Abdomen + Pelvis
• Chest + Abdomen + Pelvis
SmartPlan can only be applied to head, chest, abdomen and pelvis regions based on the supported
CID.
NOTE
If a head, neck, chest, abdomen and pelvis is to be scanned in a single group, do not
enable SmartPlan. In these cases, select the scan range manually.
20.4.3 Enabling SmartPlan

SmartPlan can only be enabled in Protocol Management. The SmartPlan settings are not displayed
and cannot be enabled at scan time.

Protocols
1. From , click Protocol Management.

2. Select the protocol and click Edit.
3. Open Patient Position area to set Patient Orientation/Position.
SmartPlan supports Head first or Feet first orientation.
For Neuro scans, SmartPlan is valid only when the patient position is Supine.
For Thoracic, Abdominal, or Pelvis scans, SmartPlan is valid only when the patient position is
Supine or Prone.
Decubitus patient position is not valid with SmartPlan.
4. Ensure that a scout series is prescribed and includes valid scout for the intended anatomy. If
more than one valid scout is acquired, the system will use the last valid scout for the SmartPlan
processing.
Scout Plane:
For all anatomies, both an AP and lateral scout are desired, however SmartPlan only requires a
single scout to run.
A lateral scout (90° /270° azimuth) is mandatory for Neuro CIDs.
An AP scout (0°/180° azimuth) is mandatory for Thoracic, Abdominal, and Pelvis CID’s.
Scan Coverage:
The scan range needs to include the anatomical landmarks
Neuro: top of skull, base of skull, forehead and back of head
Thoracic: bilateral lung apex, both costophrenic angles, both axillary soft tissue
Abdominal: top of diaphragm, iliac crest, bilateral soft tissue
Pelvis: superior border of iliac crest, ischial tuberosity, bilateral soft tissue
5. For each group and secondary recon that you would like to enable SmartPlan

Protocols
a. Open the Anatomy Selection Collection
b. Enter Start (Full FOV Start), End (Full FOV End), DFOV, A/P center and R/L center based on the
series landmark setting in case SmartPlan does not run at scan time due to invalid scout or
inability to identify anatomical landmarks.
NOTE
SmartPlan cannot be enabled if Copy Forward (“d” duplicate) is entered in Start
or End Location. DFOV/Center Adjust cannot be enabled when Copy Forward
(“d” duplicate) is entered in DFOV, A/P center or R/L center.
c. Click Clinical Identifier and select a supported clinical category/clinical identifier pair for the
desired SmartPlan anatomical region. Refer to Table 158 on page 902.
d. Click SmartPlan and set to On.
e. Click Center Adjust set to On or Off.
f. Click DFOV Adjust set to On or Off.
NOTE
Center Adjust and DFOV Adjust will default to ON for all CID categories except
Neuro. When CID Categrory is Neuro, Center Adjust defaults to ON, and DFOV
Adjust defaults to OFF.

Protocols
Table 158 SmartPlan supported Clinical Identifiers
Supported CID SmartPlan Region Superior Margin Inferior Margin

Clinical Category. Clini-
cal Identifier Pair
Neuro.General Head top of head foramen magnum
Neuro.Routine Head Head top of head foramen magnum
Neuro.Routine Head w Head top of head foramen magnum

Contrast
Neuro.CTA Head top of head foramen magnum
Neuro.COW Head top of head foramen magnum
Neuro.Perfusion Head top of head foramen magnum
Neuro.Dynamic CTA Head top of head foramen magnum
Neuro.Tumor Perfusion Head top of head foramen magnum
Stroke.General Head top of head foramen magnum
Stroke.Routine Head Head top of head foramen magnum
Stroke.Routine Head w Head top of head foramen magnum

Contrast
Stroke.CTA Head top of head foramen magnum
Stroke.Perfusion Head top of head foramen magnum
Stroke.Dynamic CTA Head top of head foramen magnum
Cardiac.Gated Chest Chest bilateral lung apex adrenals
Cardiac.Triple Ruleout Chest bilateral lung apex adrenals
Cardiac.PE Chest bilateral lung apex adrenals
Thoracic.General Chest bilateral lung apex adrenals
Thoracic.Routine Chest Chest bilateral lung apex adrenals
Thoracic.Hires Chest Chest bilateral lung apex adrenals
Thoracic.Lung Nodule Chest bilateral lung apex adrenals
Thoracic.Chest Abd Chest + Abdomen bilateral lung apex iliac crest
Thoracic.Aorta Chest bilateral lung apex celiac artery
Thoracic.PE Chest bilateral lung apex adrenals
Thoracic.Chest Abd Pelvis Chest + Abdomen + Pelvis bilateral lung apex ischial tuberosity

Protocols
SmartPlan supported Clinical Identifiers continued

cal Identifier Pair
Thoracic.Lung Airway Lung bilateral lung apex costophrenic angles
Thoracic.Lung Parenchy- Lung bilateral lung apex costophrenic angles

ma
Thoracic.Respiratory Gat- Lung bilateral lung apex adrenals

ed
Thoracic.CTA Chest bilateral lung apex adrenals
Thoracic.Tumor Perfu- Lung bilateral lung apex costophrenic angles

sion
Abdominal.General Abdomen top of diaphragm iliac crest
Abdominal.Abdomen Abdomen top of diaphragm iliac crest
Abdominal.Abdomen w Abdomen top of diaphragm iliac crest

Contrast
Abdominal.Renal Stone Abdomen + Pelvis top of diaphragm ischial tuberosity
Abdominal.Colonography Abdomen + Pelvis top of diaphragm ischial tuberosity
Abdominal.Abd Pelvis Abdomen + Pelvis top of diaphragm ischial tuberosity
Abdominal.Pelvis Pelvis iliac crest ischial tuberosity
Abdominal.Bony Pelvis Pelvis iliac crest ischial tuberosity
Abdominal.CTA Abdomen + Pelvis top of diaphragm ischial tuberosity
Abdominal.Renal Abdomen top of diaphragm iliac crest
Abdominal.Pancreas Abdomen top of diaphragm iliac crest
Abdominal.Tumor Perfu- Abdomen top of diaphragm iliac crest

sion
Abdominal.Abd Pelvis w Abdomen + Pelvis top of diaphragm ischial tuberosity

Contrast
Abdominal.Urogram Abdomen + Pelvis top of diaphragm ischial tuberosity
Pelvis.General Pelvis iliac crest ischial tuberosity
Pelvis.Pelvis Pelvis iliac crest ischial tuberosity
Pelvis.Bony Pelvis Pelvis iliac crest lessor trochanter of fe-

mur

Protocols
SmartPlan supported Clinical Identifiers continued

cal Identifier Pair
Pelvis.Hip Pelvis iliac crest lessor trochanter of fe-

mur
Pelvis.Sacroilliac Pelvis iliac crest lessor trochanter of fe-

mur
Pelvis.Urogram Pelvis iliac crest ischial tuberosity
Pelvis.Cystogram Pelvis iliac crest ischial tuberosity
Pelvis.Pelvis w Contrast Pelvis iliac crest ischial tuberosity
20.4.4 SmartPlan Management

SmartPlan Management allows customization of the margins for a selected SmartPlan Profile.
The user may adjust any of the following values within a SmartPlan Profile:
• Superior Offset
• Inferior Offset
• DFOV Adjust
A SmartPlan Profile defines coverage settings based on clinical intent as defined by the clinical
identifier mapping; any changes to the offsets will be applied to all associated CIDs, as described in
table above SmartPlan supported Clinical Identifiers.

Protocols
Figure 446 SmartPlan Management Profile Editor
1. Select , click Protocol Management > SmartPlan Management.

2. Enter User Name and Password with Standard User Access if prompted. (See Access Controls if
needed)
3. Determine which SmartPlan Profile to adjust.
4. Click on the desired SmartPlan Profile. Only one SmartPlan Profile can be selected at a time.
5. Hover over the oval with the number to view the list of applicable CIDs that will be impacted by
any changes.
6. If desired, click in Superior Offset, enter S or + and a value between 0 and 80 to move the offset
superior, or I or - and a value between 0 and 80 to move the offset inferior to the Superior Margin
Anatomy. The display will show S or I. Note if S/I or +/- are not entered, the system defaults to
superior and will display S.
7. If desired, click in Inferior Offset, enter S or + and a value between 0 and 80 to move the offset
superior, or I or - and a value between 0 and 80 to move the offset inferior to the Inferior Margin
Anatomy. The display will show S or I. Note if S/I or +/- are not entered, the system defaults to
superior and will display S.

Protocols
8. If desired, click in DFOV Adjust, enter + for wider or - for narrower and a value between 0 and 5
cm.
NOTE
if + or – are not entered, the setting will widen the DFOV and display +.
9. Click Save.
NOTE
Clicking X without Save closes the window without saving the edited values.
GE SmartPlan Region User defined SmartPlan Region (Superior 2 cm offset

of Inferior Margin)
20.5 Auto ROI (Option) Settings in Protocol

Management
1. Select an Adult body scan protocol with SmartPrep and select Edit.
2. In SmartPrep task, set Auto ROI to On or Off.
3. In Diagnostic Region, select the desired anatomical region from the drop-down menu.

Protocols
20.6 Auto ROI (Option) Management

Use Auto ROI Management to set Auto ROI Preferences and Offsets per clinical usage.

Protocols
Figure 447 Auto ROI Management
1. From the Mode Menu, select Protocol Management, then select Auto ROI Management.
2. For each Diagnostic Region enter the desired Offset for the Baseline location in mm.
• The offset range is S80 to I80. No decimal is allowed.
• The default offset value is S0.
3. For the Abdomen set the Baseline Preference and for Cardiac set the Monitor ROI Preference.
• The default baseline selection of Abdomen is Top of diaphragm.
• The default Monitor ROI for Cardiac is Descending Aorta.
4. Click Save.

Protocols
20.7 Auto Voice Management

Figure 448 Auto Voice Management window
20.7.1 Add an Auto Voice language

Use this procedure to add an Auto Voice language.
2. Click Protocol Management, then Auto Voice Management.
The Auto Voice Management window opens.
3. Select Add Language from the drop-down menu.
• A window will display to enter the new Language Name. The name has to be unique from
the others already in the list.
• After a name is added, the Message Record window will display.

Protocols
Figure 449 Message Record window
4. Enter Type and Description and follow Steps 4-9 of 20.7.4 Record an Auto Voice message on
page 911.
NOTE
To save a language, at least one message set must be recorded within the language.
20.7.2 Delete an Auto Voice language

Use this procedure to delete user-defined languages.
2. Click Protocol Management, then Auto Voice Management.
3. Select the language to delete.
4. Select Delete Language from the drop-down menu.
• The language will not be deleted if it is a factory installed language.
• Deleting the language will remove all user-defined Auto Voice messages.
20.7.3 Copy an Auto Voice Language

Use this procedure to copy a language.

Protocols
1. From the image monitor, click the Mode icon.

2. Click Protocol Management, then Auto Voice Management. The Auto Voice Management
window opens.
3. Select the language to copy.
4. Select Copy Language from the drop-down menu.
5. Enter the Destination Language Name and click OK. This must be a unique name. The new
language will be listed containing all recorded messages from original language.
20.7.4 Record an Auto Voice message

The system has three pre-recorded voice message sets in 26 selectable languages that cannot be
deleted.
Use this procedure to record up to 17 additional voice messages (for each language) on your system.
2. Click Protocol Management, then Auto Voice Management
3. To record a message, select Add Message from the drop-down menu.
• The new message will be created with the Auto Voice message list for the selected language.
• Every new message must have a Type and Description entered.
Each language is limited to one recorded message of each type:
• Inspiration *
• Expiration *
• Suspension *
• Hyperventilation
• Cardiac Hyperventilation
• Lung Expiration
• One
• Two
• Three
• Slow Exhale
• Shallow Inspiration
• Shallow Expiration
• Expiration with cough
• Free Breathing
• No swallow
• No Valsalva

Protocols
• Valsalva
• Don’t Move
• User 1
• User 2
*These are pre-recorded messages sets within each factory installed language.
• The Description should be easily identifiable (example - Mary S. Inspiration); this helps
identify whose voice is being used and the content of the message.
4. Select Pre.
5. Click Record and begin the pre-message.
• Click and hold Record until you are ready to begin your message. Normally, you are recording
a pre-message first (example - “Take in a breath and hold it.”). When you release the mouse
button, the recording starts.
• Begin your message right away.
• Speak clearly into the microphone located on the scan control interface.
6. Click Stop as soon as you finish speaking.

• If you make a mistake, simply click Stop and repeat these steps.
• Try to start and stop the recording as quickly as possible to avoid adding time to the
beginning or end of a message.
7. Select Post.
8. Click Record and begin the post-message.
9. Click Save.
NOTE
An Auto Voice message can only be saved if both a pre-message and post-message
are recorded.
10. To hear a recorded message, select the pre-message or post-message and click Play in the Auto
Voice Message area.
20.7.5 Delete an Auto Voice message

You may need to remove old or unwanted messages from the system as employees change or as
different languages are required. Use this procedure to delete an Auto Voice message.
2. Click Protocol Management, then Auto Voice Management
3. From the Auto Voice Management window, select the titled message you want to delete.

Protocols
NOTE
The three pre-recorded messages cannot be deleted.
4. Click Delete Message from the drop-down menu.
20.8 Auto Gating Configuration

Use this workflow to setup a cardiac protocol which uses Auto Gating. Cardiac protocols can be built
using GE provided profiles or user profiles.
• Set up a user profile or choose a GE provided profile using the Auto Gating Configuration tool.
• Build a cardiac protocol using the Auto Gating Configuration tool.
20.8.1 Set up a User Profile

2. Click Protocol Management, then click Auto Gating Configuration.
The Auto Gating Configuration window is displayed and allows you to configure acquisition
settings based on the patient's heart rate and variation. The bottom half of the window lets you
define scan settings for the selected Heart Rate and HR Rhythm categories in the top half of the
window. These heart rate ranges and scan settings can be edited for the selected user profile.
Figure 450 Steps to complete Auto Gating Configuration

Protocols
3. Select a GE Profile or User Profile from the Profile drop-down menu.

There are 11 GE profiles. GE Profiles can be copied and used as a basis for a User Profile. GE
profiles cannot be edited, renamed or deleted.
• GE CACS
• GE CCTA
• GE CCTA with Function
• GE CV w CCTA Group
• GE Gen CardioVasc
• GE Low Dose CCTA
• GE Pediatric Morphology
• GE Stress Perf Compare
• GE Whole Heart Cycle
• GE XXL
• GE Narrow Peak
4. Click Copy and in the Profile Name field, type or edit the name of the profile.
Once saved, any User Profile can be renamed by selecting the profile and clicking Rename or
deleted by clicking Delete.
5. Within the profile you may set individual settings for a given heart rate and heart rate rhythm
which are customizable via the table. Define the Average Heart Rate (BPM) andHR Rhythm
categories in the table, click on the box for each setting and enter text.
6. Define the Heart Rate Rhythm Thresholds. These thresholds define how Auto Gating will
categorize the patient’s heart rate based on the breath hold recording.
• Variable Beat to Beat Threshold: Max beat to beat variability before the HR Rhythm is
classified as “Variable”.
• Irregular Threshold: Max number of irregular beats before the HR Rhythm is classified as
“Irregular”.
• Highly Irregular Threshold: Max number of irregular beats before the HR Rhythm is classified
as “Highly Irregular”.
• Arrhythmia Rescan Threshold (%): The percent error from the prescribed phase location
before the system rescans when the acquisition part is in percent R-to-R. If the user
prescribed the acquisition window in milliseconds after R-peak, then the system will only
rescan if there is significant R-peak variation during the exposure (approximately 30% beat-
to-beat variation).
• Arrythmia Rescan Delay (s): Defines how long the system must wait after the first exposure
before reattempting a rescan. Some users may wish for the system to rescan as soon as
possible to avoid contrast washout, while in other cases the user may wish to use a longer
delay as a chance for the heart rate to stabilize.

Protocols
7. Define the Average Heart Rate (BPM) ranges. Click on the gray box at the top of each column and
edit the value. The value in the box needs to be greater than the previous cell and less than the
next cell. To expand the range of HR values, edit the last few HR values to 199, 198 and 197; then
edit the other columns. The heart rate range supported is 30-200 BPM.
8. Click in a cell within the table, to define the ECG Gated Scan Settings for a given HR Range and
Rhythm. This cell will be blue.
9. Edit the Scan Settings below the table.
The title bar of the Scan Settings area is updated with the exact boundaries selected in the
Average Heart Rate (BPM) / Heart Rate Rhythm category table.
Whenever the setting cannot be edited, it is disabled.
10. When all desired settings are entered. Click Save.
Table 159 Cardiac Scan Settings for 80 mm and 160 mm systems
Name Description
Slowest Allowable Rota- Slowest gantry speed that would be suggested if prescribed Noise Index
tion Speed cannot be achieved by SmartmA
Acquisition Part1 Defines the phases of the cardiac cycle that will be acquire during the scan,
Acquisition Part2 and the relative mA (%) that will be applied for each part of the cardiac
cycle.
Acquisition Part3
Acquisition Parts can be defined in R-R %, ms offset from prior R-peak, or
number of heart beats (1, 2, or 3).
Widen for SSF Enabling this feature directs the system to acquire data so a SSF image may
be generated at the specified cardiac phases or times.
For background information about R-wave, R-wave to R-wave, and % phase,
see the Cardiac Phase Background section.
HR Variation Type HRVar- Inputs to calculate HR Variation Amount in BPM.

iation Amount HR Variation Type: Select Scale Factor or Absolute Value.
For low heart rate patients there are typically multiple quiescent phases (i.e.
where the heart is mostly at rest) to achieve sufficient image quality. As a
result, for dose efficiency, it is common to reduce the amount of padding
prescribed for heart rate variability. This is accomplished in the auto gating
profile (for low BPM scenarios) by using a scale factor of 0.8 or 0.6 for the
heart rate variability tolerance. For further information, please reference the
Apex 2.5 user manual Section 19.8.1 Set up a User Profile, Figure 450 on
page 913.
HR Variation Amount: Values are applied as scale factor if Scale Factor
is selected or as absolute values in BPM if Absolute Valueis selected.
HR Variation Allowance defines the additional X-ray on interval that will be
applied to the scan to accommodate a possible discrepancy between the
predicted heart rate and the actual heart rate when the system is acquiring
data.

Protocols
Cardiac Scan Settings for 80 mm and 160 mm systems continued

Name Description
Adaptive Gating A feature used to avoid scanning during the beat immediately after an irreg-
ular (short) beat. The system continuously monitors the R-peak Triggers in
real-time.
If the system detects an irregular beat, it pauses to avoid scanning during
the subsequent beat. The system then resumes scanning when the ECG
trace returns to normal.
Smart Arrhythmia Man- Turning On Smart Arrhythmia Management enables the system to automat-
agement ically rescan exposures where the prescribed cardiac phases were not suc-
cessfully acquired. While this may double the dose for some patients with
irregular heart rates, having two acquisitions increases the chances that at
least one of the scans will be diagnostic, using the same contrast injection.
Patients without heart rate irregularities during scanning will not have any
increased dose.
Secondary Recon Phase Prescan Secondary Recon Phase Type.

Type
SecondaryRecon SSF Prescan Secondary ReconSSF
Display Alert Set alert level: None, Alert or Severe.
Alert Message Key Determines the message to be displayed.
Alert Message Displays the alert message as read-only.
Table 160 Cardiac Scan Settings for 40 mm systems
Name Description
Scan mode The Scan mode area allows you to define the scan mode for Cardiac Axial and
Cardiac Helical scans.
Slowest Allowable Rota- Slowest gantry speed that would be suggested if prescribed Noise Index can
tion Speed not be achieved by SmartmA.
Acquisition Part1 Defines the high mA and low mA phases of the cardiac cycle that will be
Acquisition Part2 acquired during the scan, and the relative mA (%) that will be applied for
each part of the cardiac cycle.
Acquisition Part3
Acquisition Parts 1 or 2 can be defined in R-R %, ms offset from prior R-peak.
Acquisition Parts 3 is always defined as 0-100 R-R % and can’t change.

Protocols
Cardiac Scan Settings for 40 mm systems continued

Name Description
HR Variation Type HRVar- Inputs to calculate HR Variation Amount in BPM.

iation Amount HR Variation Type: Select Scale Factor or Absolute Value.
HR Variation Amount: Values are applied as scale factor if Scale Factor is
selected or as absolute values in BPM if Absolute Value is selected.
HR Variation Allowance defines the additional high mA on interval that will
be applied to the scan to accommodate a possible discrepancy between the
predicted heart rate and the actual heart rate when the system is acquiring
data.
Secondary Recon Phase Prescan Secondary Recon Phase Type.

Type
SecondaryRecon SSF Prescan Secondary Recon SSF
20.8.2 Build a cardiac protocol using Auto Gating

Use this procedure to build a cardiac protocol using Auto Gating.
Considerations
GE cardiac protocols that use Auto Gating are set to a GE defined profile. Auto Gating automatically
provides suggested settings based on the selected profile for any ECG-gated acquisition, if an ECG
recording has been done.
2. Click Protocol Management.
3. From the Protocol Selection window, click Chest and select an existing cardiac protocol.
4. Click Edit to add Auto Gating to an existing protocol.
a. From the Scan Setting window, click ECG and Gating.
b. Click Auto Gating.
c. Select On and a default profile will be displayed. Select the Auto Gating Profile that is
appropriate for the clinical intent of the protocol.
d. Click Apply.
e. Click Gating Based On and make sure it is set to Latest Recording.
f. Click Apply.
5. Continue setting the rest of the ECG and Gating parameters for the protocol.
7. Click Save or Save As to save the protocol.

Protocols
20.9 Protocol Exchange

Use Protocol Exchange to move protocols from one system to another via USB device. You can export
or import individual or groups of protocols.
When you transfer a protocol, all profiles related to the protocol are included in the import or export.
These include Auto Voice profiles, contrast profiles, GSI profiles and Auto Gating profiles.
Protocol Exchange includes a means to resolve protocol name and ID conflicts between imported
protocols and existing protocols.
Figure 451 Protocol Exchange Login

Protocols
20.9.1 Filter Protocols

Use the Filters box on the Protocol Exchange screen to narrow your search for the protocols you want
to import or export.
1. Select either adult or pediatric from the first drop-down list.
2. Select a region of anatomy from the second drop-down list or click on an area of the graphic
below to select an anatomic region.
You can also do a free-text search to find a specific protocol using the box labeled Type Protocol
Name.

Protocols
Figure 452 Protocol Exchange Filter

Protocols
20.9.2 Export Protocol

NOTE
The USB device must contain an EXT file system.
1. Insert a USB device into the system.
2. From the image monitor, click , select Protocol Management > Protocol Exchange.
3. Click the Export button on the Protocol Exchange main screen.
4. Click the protocols you want to export on the Available Protocols column. The protocols you
select display in the Selected Protocols column on the right of the screen.
5. Click the Export Select button. The protocols are copied onto the USB device.
Figure 453 Protocol Exchange Export
20.9.3 Import Protocol

3. Click the Import button on the Protocol Exchange main screen.

Protocols
Figure 454 Data Source select
4. Select the data source from which you want to import. The protocols on the USB device display in
the Available Protocols column.
5. Click the protocols you want to import on the Available Protocols column. The protocols you
select display in the Selected Protocols column on the right of the screen.
6. Click the Import Select button.
7. Resolve any naming conflicts using the prompts displayed.

Protocols
Figure 455 Protocol Exchange Import
20.9.4 Export All Protocols

NOTE
3. Enter User Name and password to log into Protocol Exchange.
4. Click the Export All button on the Protocol Exchange main screen. The prompt All user protocols
will be exported. Click on ‘Continue’ to proceed displays.
5. Click the Continue button.

Protocols
Figure 456 Protocol Exchange Export All
20.9.5 Replace All Protocols

NOTE
3. Enter User Name and password to log into Protocol Exchange.
4. Click the Replace All button on the Protocol Exchange main screen.
5. Click the Data Source that contains an Export All. All protocols from the Export All data source
display in the Selected Protocols column on the right of the screen.
6. Click the Continue button.

Protocols
Figure 457 Protocol Exchange Replace All
20.10 IPM Service

Imaging Protocol Manager (IPM) is a cloud-based protocol management software solution that
helps to maintain and standardize protocols at a centralized location by creating protocol libraries,
standardizing imaging workflow, identifying protocol variation, and increasing protocol compliance to
improve quality of care, operational efficiency, and an optimized patient experience.
IPM allows protocols to be sent (pushed) from the cloud to a connected CT device. Revolution™ CT’s
base software contains the connection kit to securely connect to the IPM cloud server. When protocols
have been pushed to the device, cloud icon will be displayed on the System Status area on the
right monitor. To view the menu, click . The menu will display the number of IPM pushes that

Protocols
have occurred since the last since the last time the system was restarted. The pushed protocols will
automatically be installed to the device upon the next system restart.
Figure 458 IPM Cloud Status
The cloud protocols are considered the master and will overwrite all protocols on the CT device.
If it is necessary to revert to prior version of protocols on the device, login to Protocol Exchange,
click Replace All, and select the desired backup from the list under Select Protocols to Import, Click
Continue on the Replace All pop-up window.
To interact with IPM service requires setting the Cloud Connectivity System Preferences. System
Preferences settings include entering the URL and Advanced Settings to Activate connection to the
cloud. Once activated, the device preferences can be changed to disconnect or re-enroll. During

Protocols
activation or re-enrollment, the system will require user logon and password. Contact your service
representative to Activate, or Re-enroll the CT device to the cloud.
Figure 459 System Preferences- Cloud Connectivity
20.11 GSI Profile Editor

RELATED TOPICS
GSI Profile Editor on page 521

Protocols

Access Controls
21 Access Controls
21.1 Security Overview

Today, most countries have enacted data privacy laws to protect against the unauthorized access and
use of health information.
Examples of global privacy laws are:
• Health Insurance Portability and Accountability Act (HIPAA)
• Directive 95/46/EC on Data Protection (Data Protection Directive)
• Personal Information Protection and Electronic Documents Act (PIPEDA)
• NEMA XR 26-2012 Access Controls for Computed Tomography: Identification, Interlocks and Logs
GE has a long-standing reputation for providing customizable, clinical solutions that protect the
privacy and security of your organization’s unique clinical workflow, as well as your patient’s
confidentiality.
Make sure to understand the intended use of the product when determining privacy risk relative to
patient care and safety. GE is very concerned with providing the best care to patients, and in some
cases, we have determined that patient care is more important than the risk to privacy. In these cases,
GE takes every precaution to minimize privacy risk.
Security and privacy are maintained across a healthcare system. Any product that is placed into an
uncontrolled environment will not be secure and cannot protect privacy. GE designs systems to be
implemented in a “secure environment”. A secure environment is based on multiple layers of security,
a concept known as “defense in depth”.
It is the healthcare enterprise's responsibility to ensure the product is installed and operated in a safe
and secure manner.
21.1.1 Network Security

GE strongly recommends that medical information systems are operated in a secure network
environment that is protected from unauthorized intrusion. There are many effective techniques
for isolating and protecting medical information systems, including implementing firewall protection,
demilitarized zones (DMZs), Virtual Local Area Networks (VLANs) and network enclaves.
For example, a best practice is to place firewalls between departments, as well as at a DMZ
(Demilitarized Zone) between all extranets, and the external internet access point. In this example,
a radiology firewall may allow DICOM and HL7 protocol traffic through, but no other protocols. These
DICOM and HL7 protocols would be blocked at the DMZ and again at the internet firewall.
21.1.2 Privacy & Security Controls on the System

There are several features found on the system that help provide Privacy & Security protections.
Access control that include user account creation and assigning privileges for user authentication.

Access Controls
Audit Logging and Accountability Controls that support security surveillance and privacy and security
investigations and reporting.
De-identification (anonymization and pseudonymization) capabilities to limit privacy and security
risks to sensitive information.
Firewall protections that block unauthorized incoming network connections.
Use of a commercial network vulnerability scan tool to identify high risk vulnerabilities that are
mitigated prior to release of the CT system software. The tool probes all TCP/IP and UDP/IP ports on
the system looking for known vulnerabilities.
21.1.3 Personal Information Collected by the Product

The CT system collects the following types of information for the purposes of creating diagnostic
images:
• Patient demographic information
• Personal or protected health information
• Facility information
• Provider information
• Machine data
The CT system protects this information by access controls and retains this information until the user
removes it.
The details of all personal information collected by the product and how it is used is described in
the DICOM Conformance Statements and IHE Integration statements. These are found at the following
URLs:
http://ge.com/dicom
http://ge.com/ihe
http://ge.com/hl7
21.1.4 Inbound Firewall Configuration

All inbound network connections are blocked, Open to DICOM server(s) configured on the system ed
by the CT system’s internal firewall, with the exemptions listed in the table below.
Local Port 4006 Open to DICOM server, DICOM Storage Service SCP
Local Port 22 Optional, Secure Shell
21.1.5 Removable Media Privacy

Data stored on removable media is stored unencrypted. As this data could contain personal
information (PI) / protected health information (PHI), removable media and the content on removable
media must be handled according to applicable regulations and guidelines for handling personal
information (PI) / protected health information (PHI).

Access Controls
21.1.6 Removable Media Security

CD/DVD/USB flash drives containing malware may infect the CT system. It is the healthcare
enterprise's responsibility to prevent use of unauthorized external media to prevent malware, such as
computer viruses.
21.1.7 Long Term Storage of Privacy Data

The system supports interconnections to external storage systems. This includes connections to
DICOM servers. Personal information (PI) / protected health information (PHI) should not be kept
on the CT system for extended timeframes. The data stored on the interconnected system must be
secured on the external storage system (outside the scope of the CT system).
21.2 Application Access Controls
21.2.1 Introduction
Access Controls using EA3 requires logging in to the system and logging out when you are done
scanning for a period of time. If you do not log out, the system will log you out and you will need to log
back in.
Access Controls using EA3 contains the following user permissions after logging in:
• GE Service – Can perform all functions
• Administrator – Can set up, add or delete users and view the Audit Log
• Standard User – Can perform scanning functions and modify protocols
• Limited User – Can perform all scanning functions
NOTE
Emergency User login has Limited User permissions. When logged in as an Emergency
User you are limited to scanning 5 exams. The system will log you out and require you to
log back into the system again.
When adding users to local databases certain rules apply.
You must use the following guidelines:
• Users/Groups:
• Lower case letters and numbers only
• Cannot start with a number
• No limit on length
• Passwords:
• Must be at least eight characters long; no null characters and no more than 63 characters.
• Can contain uppercase letters, numbers and special characters

Access Controls
• Cannot contain include a palindrome or logon name.
Access Controls is an option that can be enabled or disabled by setting the Access Control preference
in System Preferences.
If the authentication login screen is turned off, then security of system may be compromised.
Disabling the access control feature greatly reduces the control of access to sensitive information
on the CT system.
21.2.2 Users and groups

Every person with system permissions is a user. Users are set up by administrators. Administrators may
be IT personnel in an enterprise environment, or a site manager or lead technologist in a standalone
environment. Administrators add new users and assigns users to groups, which determines system
access levels and privileges. For example, a person named Sue Smith could belong to a group called
technologists, radiologists, administrators, or any combination.
21.2.3 Groups and privileges

The group to which a person belongs has certain privileges. If you do not have an enterprise system,
the assignment of group privileges is probably limited to those who have administrator privileges and
those who do not. Additionally, permission for protocol editing may be assigned to groups. If your
system is set up for enterprise log on, your IT person or administrator will use more of the features.
21.2.4 Open EA3

Use this procedure to open the EA3 user interface.
1. From the image display, click .
The EA3 Administration window opens.
Figure 460 EA3 Administration Window

Access Controls
3. Type your Username and Password and click Login.
NOTE
Ask your administrator or GE Service for a Username and Password.
To configure EA3, you must have administrative privileges.
4. From the Local Users or Groups tab, select a user or group.

• Only one user and group can be in context at a time. If you choose multiple users, the system
selects the top user in the selected list. Once a user or group is in context, you can make any
necessary modifications to that user or group.
• If there are no users or groups, then there no items in context. All of the buttons in the center
panel are disabled until a user or group is added.
Figure 461 Local Users and Groups
21.2.5 Configure local users

Use this procedure to add or remove users, change user groups, change usernames and passwords,
lock or unlock users, prompt users to change their passwords at next login, et cetera.

Access Controls
1.
Open EA3 on page 932.

2. From the Local Users tab, enter the desired parameters.

Access Controls
Field Description
• The number of failed log on attempts before your ac-

count is locked for a specific number of minutes.
• If your account is locked, you cannot log on, even if
you provide the correct Username and Password. Either
the specified amount of time must pass, or an adminis-
Max Logon Attempts Before trator must unlock the account before you can log on
Lock again. Locking only applies to local users. Locking for
enterprise users is managed by the enterprise server.
• If the administrator locks your account, the lock time
duration does not apply. The account is locked until the
administrator unlocks it.
• The number of minutes your account is locked after the

maximum number of failed log on attempts.
Lock Duration (Minutes)
• The account can become locked due to failed log on
attempts or by the administrator.
• Minimum Password length is 8 characters. Enter a value

between 8 and 14.
• If a password is already less than the minimum length,
setting this value has no effect. For example, if your
password is 8 characters, and the minimum length is
changed to 10 characters, the 8 character password is
Minimum Password Length still valid. However, the next time you change the pass-
word, you must choose a new password that is 10 char-
acters or greater.
• Minimum password length only applies to local users.
Minimum password length for enterprise users is man-
aged by the enterprise server.
Enable or disable advanced password rules. Your password must

contain 1 number, 1 uppercase letter, 1 lowercase letter, and 1 non-
alphanumeric special character and cannot contain 3 consecutive
Advanced Password Rules characters or a space.
Does not contain palindrome, white space, logon name or consec-
utive same characters.
3. Click Apply Configuration to accept the configuration changes.

Click Restore Configuration to undo any configuration changes not yet applied.
• If there was a problem with the changes (such as an invalid value or an issue contacting the
backend servlet) an error message displays with a description of the error.
• If the changes were successful, a brief message displays indicating that the changes were
applied.

Access Controls
21.2.6 Add a local user

Use this procedure to add a local user.
1. Open EA3 on page 932.
• User ID
• Full Name
• Password
Figure 462 Add User Window
4. Click Add User.

If an error occurs, a message displays and the changes are not applied in the database. Correct
the errors and try again.
Common errors include:
• Username and Password cannot be the same. Change either the Username or Password.
• Password does not meet the minimum length criteria. Choose a longer Password.
• Password and Confirm Password do not match. Make sure these entries match.
User Restricted Fields

Some text fields and buttons on the Local Users tab are not selectable under certain conditions.
The following roles, users or groups have one or more of these criteria, and cannot be modified.
• Roles: GE Service, Administrator, Standard User, Limited User, DC Administrator , AV Exceeding
User, FullSWInstaller and SPInstaller.
• Users: root, ctuser , insite

Access Controls
• Permanent: If a user is permanent, he can never be removed. When a permanent user is in

context, Remove User is disabled.
• Content Not Editable: If a user is identified as such, their group memberships cannot be
changed. When a “content not editable” user is in context, Add To Groups and Remove From
Groups are disabled.
• Password Not Changeable: If a user is identified as such, their password cannot be changed;
Change Password is disabled.
NOTE
“In context” is a HIPAA term indicating that all selections and buttons in the center panel
apply to the selected user or group.
21.2.7 Add a local group

Use these procedures to add a group.
3. From the Add Local Group window, type a unique Group Name.
If an error occurs a message displays, and the changes are not applied in the database. Correct
• Group Name already exists in the database. Try another Group Name.
• Application session timed out. Begin another session.
Figure 463 Add Local Group Window
4. Click Add Group.

The group is highlighted in the Local Groups list area. All selections and buttons in the center
panel apply to the highlighted group.
5. To change a group's role, select a Roles option and click Apply Roles.

Access Controls
21.2.7.1 Add memberships

2. From the Groups tab, select a group in the Local Groups area.
3. From the Group Members area, click Add Membership.
A panel lists all the users that are eligible to be added to the selected group.
4. Select the users to add to the group.
If no users are eligible to be added to the group, an error message displays.
5. Click Add To Group.
21.2.7.2 Group Restricted Fields

Some text fields and buttons on the Groups tab are not selectable under the certain conditions.
The following roles, users or groups have one or more of these criteria, and cannot be modified.
• Roles: GE Service, Administrator, Standard User and Limited User, DC Administrator and AV
Exceeding User
• Users: root, ctuser, insite
• Permanent: If a group is permanent, it can never be removed. When a permanent group is in
context, Remove Group is disabled.
• Content Not Editable: If a group is identified as such, its group memberships cannot be
added or deleted. When a “content not editable” group is in context, users cannot be
removed or added from the group, and the group name does not display when you click
Remove From Group or Add to Group.
• Password Not Changeable: If a group is identified as such, the roles associated with that
group cannot be changed. This property does not have a direct impact on what you can do
on the Local Users tab.
NOTE
“In context” is a HIPAA term indicating that all selections and buttons in the center panel
apply to the selected user or group.
21.2.8 Add an enterprise group

Use this procedure to add an enterprise group.
2. From the Groups tab, click Add Enterprise Group.
3. From the Add Enterprise Group window, type a unique Group Name.
If an error occurs a message displays, and the changes are not applied in the database. Correct

Access Controls

• Group Name already exists in the database. Try another Group Name.
• Application session timed out. Begin another session.
Figure 464 Add Enterprise Group Window
4. Click Add Group.

• This action does not add an enterprise group, rather it provides EA3 the ability to manage
roles for that group that already exists on the enterprise directory server. For example, if you
add a group All Employees as an enterprise group to EA3, and assign that group with the
Standard User role, then any enterprise user that logs in through EA3 and belongs to the All
Employees group has the Standard User role.
• You cannot manage group memberships for enterprise groups. This is managed by the
enterprise directory server, not EA3. Therefore, whenever an enterprise group is in context,
both Add Membership and Remove Membership are blocked. This does not mean that no
one belongs to enterprise groups, rather that this is managed by the enterprise directory
server and not EA3.
• Once an enterprise group is added, it is automatically highlighted in the Enterprise Groups
list box and is in context. “In context” is a HIPAA term indicating that all selections and
buttons in the center panel apply to the selected user or group.
21.2.9 Add or remove a user from a group

Use this procedure to add or remove groups listed in the Groups list.
2. Select the Local Users tab.
3. In the Local Users area, select the user you want to modify.
The groups from which this user is currently a member are listed in the Groups area.
4. In the Groups area, click Add To Groups or Remove From Groups.

Access Controls
Figure 465 Groups Area
5. Select the group to add or remove for the user.

6. Click Add Membership or Remove Membership.
Figure 466 Add Membership List

Access Controls
Figure 467 Remove Membership List
21.2.10 Change a user's full name

Use this procedure to change a user's name.
2. From the Local Users tab, select a user.
3. Click Change Name.
4. From the Change Name window, type a new Full Name.
Figure 468 Change Name Window
5. Click Confirm Change.
21.2.11 Change Application Password

Use this procedures to change a user's password.

Access Controls

3. Click Change Password.
4. From the Change Password window, enter a new Password that complies with the password
rules on the EA3 Local User Tab.
• When Advanced Password Rules are not configured, the password must be the minimum
length setting and can contain uppercase letters, numbers, and special characters.
When Advanced Password Rules are configured, the password must be the minimum length
setting and contain 1 uppercase, 1 lowercase, 1 number, and 1 special character and cannot
contain 3 repeating characters or a space.
• A password cannot include the username, contain a palindrome or be easily guessed.
Figure 469 Change Password Window
5. Click Confirm Change.

An error message displays if the password does not meet the minimum length criteria or the
password rules. The password must meet the password rules to be changed.

Access Controls
21.2.12 Change password from Login

Any user can change their password from the Login Menu.
1. Click Change Password from the Login Menu.
2. Enter Old Password.
3. Enter New Password that complies to password rules in New Password and Confirm Password
4. Click OK. An error message displays if the password does not meet the minimum length criteria or
the password rules. The password must meet the password rules to be changed.
21.2.13 Prompt a user to change password

Use this procedure if you are an administrator to prompt a user to change his password on next login.
1. From the Local Users tab, select a local user.
2. From the bottom of the Local Users tab, select the Change Password on Next Login option.
3. Click Apply Configuration.
• The next time the user logs in, he will be required to enter a new Password.
• Once the new password is entered, the Change Password on Next Login option is
deselected.
21.2.14 Lock or unlock a user

Use this procedure to lock or unlock a user from login privileges.
3. From the bottom of the Local Users tab, select the Locked option.
• When Locked is selected, the user is locked from login, even if he has valid login credentials.
• If Emergency User is enabled on your system, the locked user can still login as an Emergency
User.
4. Click Apply Configuration.
21.2.15 Remove a user, group, or membership

Use these procedures to remove a user, group, or membership.
21.2.15.1 Remove a user


Access Controls
3. Click Remove User.

4. From the Confirm Removal window, click Confirm Removal.
Figure 470 Confirm Removal Window
21.2.15.2 Remove a group

2. From the Groups tab, select a group.
3. Click Remove Group.
4. From the Confirm Removal window, click Confirm Removal.
Figure 471 Confirm Removal Window
21.2.15.3 Remove a membership

2. From the Groups tab, select a group.
3. Click Remove Membership.
• A panel lists all the users eligible for removal from the highlighted group. Select the users you
want to remove.
• If no users are eligible to be removed from this group, an error message displays.
4. Click Remove From Group.

Access Controls
Figure 472 Remove Users From Group Window
21.2.16 Configure EA3 properties

Use this procedure to configure EA3 application properties.
2. From the Application tab, select the desired parameters.

Access Controls
Figure 473 Application Tab

Access Controls
Field Description
• Enable or disable authorization.

• If authorization is enabled, anyone logging in through
EA3 (both local and enterprise users) must have a role.
Enable Authorization Anyone without a role is denied access.
• The user role does not matter for logging in through
EA3, however, other EA3 client applications may restrict
which roles can login.
• Enable or disable emergency access.

• If EA3 is used in GUI mode, this determines whether or
not the Emergency Login button displays.
Emergency Logon Allowed • If disabled, emergency user access is prevented.
• When logged in as an Emergency User you are limited
to scanning 5 exams. The system will log you out and
require you to log back into the system again.
• The roles assigned to the emergency user.

Emergency Roles • The defaults allow an administrator to assign a
Standard User role, Limited User role, or both roles.
Configurable delay after When password entered is not valid for user name and sign in fails,
authentication failure this is the time delay until the user can attempt to sign in again.
(Seconds) Time can be between 0 and 120 seconds.
• The minutes that must pass without any user activity

before a timeout is generated.
• When a timeout is generated, the EA3 Login window is
displayed.
Inactivity Timeout (Minutes) • This value can be any positive integer or 0. If the value is
0, there is no inactivity timeout, regardless of how much
time has passed.
• When the system is in the scanning state the system will
not automatically log off.
Enable or disable to display the username of the last user logged in

Display Last Logon Name
to the EA3 Login window.
Under certain circumstances or error conditions, a user can be

Administrator Message prompted to contact an administrator. This field allows the admin-
istrator to specify contact details and a custom message.
The text displayed to any user logging in as an Emergency User.

Emergency Prompt The user is prompted to enter information; usually their actual
name.
Custom Message to display on Enter text for a custom message to display to any user on the login
login page screen.

Access Controls

Click Restore Configuration to undo any changes not yet applied.
• If there was a problem with the changes (such as an invalid value or a problem contacting the
backend servlet) an error message displays with a description of the error.
• If the changes are successful, a brief message displays indicating that the changes were
applied.
21.2.17 Configure the Enterprise tab

Use this procedure to configure the properties needed to make a connection to an enterprise directory
server (MSAD, Novell, et cetera). The Enterprise tab is used by the site’s IT or GE Service personnel.
It provides connectivity to the site’s user database. If you do not have a network established in your
hospital or clinic, this tab is not used.
2. From the Enterprise tab, select the desired parameters.

Access Controls
Figure 474 Enterprise Tab

Access Controls
Field Description
• Login authorization.
Enable Enterprise • If unchecked, only local EA3 users can login.
Authentication • If checked, both local users and enterprise EA3 users can
login; the local EA3 user database is tried first.
• Enables enterprise users to be cached once they suc-

cessfully login.
• If the enterprise directory server is not available due to
network or other issues, the following scenarios occur:
• If checked, a local record of an enterprise user is
Cache Enterprise Users
kept and you can login.
• If unchecked, an enterprise user is denied access.
• Hashed passwords are cached; the actual pass-
word is not cached.
• Time the EA3 login process waits for a response from the
enterprise directory server.
• There is frequently a network latency when connecting
to servers, which is dependent on your network configu-
ration.
Enterprise Authentication
Latency (Seconds) • If the amount of time is reached without a response
from the enterprise directory server, the EA3 login proc-
ess returns a failed login. A value of 5 seconds is usually
enough time to allow a properly configured directory
server to respond, without causing undue user incon-
venience.
3. Modify the properties in the text fields provided to allow an enterprise directory server
connection.
NOTE
Use SSL must be checked for a secure LDAP connection.
21.2.18 Auto configuration

2. From the Enterprise tab, click Auto-detect Server Name.
• The system searches for the server name of the enterprise directory server.

Access Controls
• If the DNS allows service lookups, EA3 executes an auto-detection with the enterprise
directory server. If it cannot find the server, it is not an error. Continue with these steps
to configure the server.
3. In the Server Configuration area, type the Server Name/IP of the enterprise directory server that
EA3 should connect to.
The system must have DNS enabled or static information in a hosts file (/etc/hosts).
4. Select the Authentication Type that the enterprise directory server supports.
• For a Microsoft Active Directory Server, typically select Kerberos.
For a Novell eDirectory Server, typically select LDAP.
If you do not know this information, check with the owner of the enterprise directory server.
• If the enterprise directory server supports SSL connections, select the Use SSL option.
• If you use LDAP authentication without SSL, passwords are not sent securely. This is not
recommended. An alert is posted for this configuration. With Kerberos and non-SSL, the
authentication is encrypted, but the LDAP traffic is not.
5. Click Test Connection to test if the machine can connect to the enterprise directory server.
• If the connection is successful, CONNECTION OK is displayed next to Test Connection.
• If the connection is unsuccessful, CONNECTION BAD is displayed next to Test Connection.
This indicates there is a problem connecting to the enterprise directory server.
Check the following:
• Server Name/IP
• If the system has DNS running.
• If the system can resolve the Server Name/IP.
6. Once the Test Connection is successful, select the Server Type for the enterprise directory server
(Microsoft Active Directory, Novell eDirectory, et cetera).
7. Click Generate Defaults to populate the Realm Name, Format, DN, Login Attribute, First Name
Attribute, Last Name Attribute, and Group Attribute fields with default values for the enterprise
directory server type.
• If the enterprise directory type is MSAD, both the Realm Name and the DN are populated.
• If the enterprise directory type is eDirectory, the Realm Name is left blank. If you are
configuring an enterprise directory server that is not MSAD or Novell eDirectory, the
configuration must be done manually. Get the correct LDAP property information from the
owner of the enterprise directory server.
• If this is a non-MSAD, non-eDirectory server, or is a server with a non-default configuration,
manually change properties, as needed.
8. Enter a Username and Password for a user that resides on the enterprise directory server.
9. Click Login to see if the login is successful.

Access Controls
• The First Name, Last Name, and any Group Memberships for the user are displayed. If First
Name, Last Name, or Group Memberships are not found, a warning is posted indicating:
• The LDAP properties are not configured correctly (First Name Attribute, Last Name
Attribute, and/or Group Attribute).
• The user does not have a First Name, Last Name, or any Group Memberships configured
on the enterprise directory server.
• If you get these warnings, contact the owner of the enterprise directory server to verify it is
configured properly.
• If the test login was successful and you’re satisfied with the First Name, Last Name, or any
Group Memberships information, the enterprise directory server is configured properly.

21.2.19 Manual configuration

Use this information to connect to an enterprise directory server other than MSAD, Novell eDirectory,
or any other system that has a custom configuration. The following LDAP definitions are for
configuration properties that may need to be manually selected.
Field Description
Set to domain or dn.
• domain is the MSAD way of doing LDAP authentication (<user-

Id>@<realm name>).
Format • dn is the eDirectory way of doing LDAP authentication; most
other directory servers use (loginAttribute=<userId>,<ldap
base dn>). If you are connecting to a non-MSAD directory
server, you will more than likely use dn.
• The LDAP base DN of the LDAP server to which you are con-
necting.
• Typically this is the fully qualified domain name separated by
DN clusters of DC=.
• For example, if the fully qualified domain name of the direc-
tory server is example.com, it is likely that the DN is DC=exam-
ple,DC=com.
• The LDAP attribute to be used for the unique user identifier;

the username to login.
• Set to the unique identifier your server uses.
Login Attribute
• On MSAD it is: sAMAccountName
• On eDirectory, it is typically: cn

Access Controls
(continued)
Field Description
First Name Attribute The LDAP attribute used for the user's first name.
Last Name Attribute The LDAP attribute used for the user's last name.
• The LDAP attribute used to find group memberships for the

user.
• On MSAD, it is memberOf.
Group Attribute
NOTE
EA3 finds all instances of this attribute (not just the first,
like it does for other attributes). If a user belongs to
more than one group, EA3 finds all memberships.
NOTE
Regarding LDAP parameter configurations, EA3 finds the first instance of the configured
attribute for a user, except for Group Membership. If you configure the First Name
Attribute to be an attribute listed multiple times, EA3 assumes the first one found during
an LDAP query is the correct First Name. For Group Membership, EA3 finds all instances
of that attribute.
Save changes
• No changes are saved to EA3 on a tab unless you click Apply Configuration before you navigate to
another tab, or click Confirmation. If there is more than one Apply Configuration on a tab, click
the one associated with the data you changed (buttons are grouped with the data they manage in
a bordered panel).
• Click Apply Configuration or Restore Configuration.
Within 5 seconds a message indicates whether the changes were saved or not, respectively:
• Enable Authorization
• Limited User
• Inactivity Timeout (Minutes)
• Emergency Prompt
• Apply Configuration
21.3 Operating System (OS) Access Controls

The Operating System Access Controls are independent of Application Access Controls. The user
names, root and ctuser, are used in both OS Access and Application Access control systems. Each
access control system allows maintaining passwords, therefore the same user name may have
different passwords to login to the operating system or login to the CT Scanner.

Access Controls
The user accounts for the OS are root, ctuser and insite. These are user accounts that have embedded
permissions.
These OS user accounts have default passwords, that are set during software installation by the
service representative and should be provided to your user with administrator role. Passwords are
reset to the default values when software is installed and will need to be set again.
NOTE
The Applications Menu is not displayed when the current user does not have
Administrator or GE Service role.
To Change the OS password
1. From the Utilities Menu, select Service to open the service desktop.
2. Select Utilities Tab, select Security Center.
3. Select Application.
4. Select OS Password Change.
5. Select the user account (root, ctuser or insite) from User Name drop-down menu.
6. Enter the Old Password
7. Enter the New Password that complies with OS password strength rules in New Password and
Retype New Password.
OS Password Strength Rules
• Update the 8 characters including 1 upper case, 1 lower case, 1 numeric, 1 special character
and cannot contain 3 repeating characters.
• The default passwords cannot be used.
• Note that the reuse of a password is prohibited for 5 password changes.
8. Click Submit. A message will be displayed to indicate Password Changed Successfully or why the
password change was not accepted.
To reset an OS Password (this should only be used when the password is unknown)
1. From the Utilities Menu, select Service to open the service desktop.
2. Select the Utilities tab, then select Security Center.
3. Select Applications, select OS Password Reset.
4. Select User Name from the dropdown menu (root, ctuser, insite).
5. Enter the New Password that complies with OS password strength rules in New Password and
Retype New Password.
OS Password Strength Rules
• All passwords must have a minimum of 8 (normal) alphanumeric characters.
• All passwords must have at least one uppercase alphabetic character
• All passwords must have at least one lowercase alphabetic character
• All passwords must have at least one numeric character

Access Controls
• All passwords must have at least one non-alphanumeric special character

• Passwords must not contain more than three consecutive repeating characters
• The default passwords cannot be used
NOTE
The reuse of a password is prohibited for 5 password changes.
6. Select Submit.
7. Close Security Center when Done.

Access Controls

System Management
22 System Management
22.1 Overview
Use these procedures for system management level functions.
22.2 System Tools
22.2.1 Using Message Viewer

2. From the Utilities menu, click System Tools, then Message Viewer.
The Current Messages window opens.
3. Click one of the following options:
• Clear: Removes the message displayed in the message area.
• View Log: Opens the system log for more detailed information about messages and errors.
Click Select Viewing Level, select the type of messages to display: User for user messages or
Class A for service messages and click OK.
• Close: Closes the message window.
• Memo: Allows you to leave a note in the message log for the service engineer.
22.2.2 Save Cyber Security Audit Logs

2. From the Utilities menu, click System Tools, then Save Cybersecurity Audit Logs. The message
Remove all other USB media and connect only the USB media where you want to backup
Cybersecurity Audit Logs displays.

System Management
3. Remove all other media devices attached to the system, insert USB and click on Save to USB
button. The message Please wait for some time while storing Cybersecurity Audit logs into USB
media should display.
NOTE
If the USB media does not have enough disk space, the message Connected USB
media does not have enough free space to copy Cybersecurity Audit Logs. Please
clean up data from USB media or connect another USB media displays.
Once the audit logs are saved completely, following message Export to USB is complete displays
and all the archived audit logs (/var/log/audit/auditlogs) will be deleted from the system.
The audit logs will be copied in the following directory on the USB: 5. NOTE
/<mountdir>/ cslogs_<hostname>
4. Remove the USB drive.

System Management
NOTE
If the save to USB fails, the message below displays the next time the audit log size is
checked.
Audit Log data is near maximum number of records that can be stored on system.
To prevent audit log data from being over-written, please insert a USB media into the
USB port on the computer and select Save Now or select Save Later to do this at a
later time by selecting Tools, System Tools, Save Cybersecurity Audit Logs.
Failure to save the audit logs may result in the permanent loss of some audit log
records.
NOTE
All the logs that are saved to USB are deleted from the local system.
22.2.3 Apply Product Network Filters

Product Network Filters allow you to place a site firewall in front of the CT scanner. Filters may be
configured to restrict which computers may access the system and which system services are allowed
to be controlled by other devices trying to access the operator console such as ftp, telnet and rlogin.
This access is determined by configuring IP addresses allowed to access the system. DICOM access
to the system can also be configured. The system default is for no services enabled, no IP addresses
authorized and DICOM port 4006 enabled.
Consult your Field Engineer and your IT Department to configure Product Network Filters.
22.2.4 Find system software version information and third party

software license
Use this procedure to find a license for a third party software option.
2. From the Utilities menu, click Service, then Service Tools.

System Management
3. From the Service Desktop, click the Utilities icon.

4. From the Utilities/Tools folder, click Legal Notice.
The system displays the list of licensed third party software.
5. Select the desired software to display the license.
NOTE
For system software version information, select Revolution-CT-SW.
22.3 System Preferences
22.3.1 Introduction
The following preference require a system restart to take effect:
• Enable Access Control
• Calling AE Title setting on
• Simultaneous Transfer Mode
• Simultaneous Transfer Per Host
• All settings in Performed Procedure Step Preference tab
22.3.2 Set General Preferences

Use these procedure to set general system preferences.
3. From the System Preferences window, click the General tab.

System Management
Figure 475 General Tab
22.3.2.1 Set Screensaver Time

1. In the Screensaver Time area, click and drag the slider to set the amount of time the system must
remain idle before the screensaver becomes active.
2. Click Save to save the new preference, or Save and Close to additionally close the System
Preferences window.
22.3.2.2 Set the Scan Room Playback Volume

1. In the Scan Room Playback Volume area, click and drag the slider to set the volume level.
Preferences window.
22.3.2.3 Set Auto Alignment Light

1. In the Auto Alignment Light area, select On or Off.
Preferences window.

System Management
22.3.2.4 Preset Patient Load Positions enabled

1. In the Preset Patient Load positions enabled, select On of Off. Refer to Use the Load/Unload
foot pedals on page 207.
2. Click Save to save the new preferences or Save and Close to additionally close the System
Preferences window.
22.3.2.5 Set the Extended Hounsfield Units (HU)

1. In the Extended HU area, select On or Off.
Preferences window.
22.3.2.6 Time to Peak mA [minutes]

Use this procedure to set Time to Peak mA value preference for Condition Now mode. The Time to
Peak mA Value can be set between 1 and 19 minutes. In general, using a shorter time to Peak mA value
is preferable. This time should be based on the time from when patient arrives in CT room, until the
prescribed diagnostic scan is done.
3. From the System Preferences window, click the General tab.

System Management
Figure 476 Time to Peak mA (minutes)
Set Time to Peak mA (minutes)

1. In the Time to Peak mA (minutes) area, click and drag the slider to set the time.
Figure 477 Time to Peak mA (minutes) slider
Preferences window.
22.3.3 Set Access Control Preferences

3. From the System Preferences window, click the Access Control tab.

System Management
Figure 478 Access Control Tab
4. In the Enable Access Control area, click Yes or No.

5. Click Save to save the new preferences, or Save and Close to additionally close the System
Preferences window.
6. The System will perform a System Restart when Save or Save and Close is selected.
22.3.4 Set Viewport Preferences

Use this procedure to set viewport display preferences.
3. From the System Preferences window, click the Viewports tab.

System Management
Figure 479 Viewport Tab
22.3.4.1 Set annotation preferences

Use this procedure to set the default font size and level for image annotations.
1. In the Image Annotation Viewers area, select a preferred annotation level:
• No Annotation
• Partial Annotation
• Full Annotation
• Custom Annotation
Click Customize to select specific annotations to display, then click OK.
NOTE
DMPR viewports will show image annotation even if the annotation level is set to No
Annotation in the Viewport System Preferences.

System Management
Figure 480 Customize Image Annotation Viewers
To view annotations in a larger font, click Customize Large Font and select the specific
annotation group to enlarge.
NOTE
The system preset is set to Full Annotation.
Preferences window.
22.3.4.2 Set Window Width / Window Level Presets

Use this procedure to set W/L preset values and define shortcut keys.
1. In the Window Width/Window Level Preset area, under Name, enter anatomical names for each
desired W/L preset.
2. In the WW and WL area, enter preset values for each anatomical name.
Preferences window.
22.3.4.3 Set Series Binding

Use this procedure to set the default series binding.
1. In the Series Binding area, select On or Off.

System Management
• On : To page through all series in an exam.

• Off: To page through only the current series in an exam.
Preferences window.
22.3.4.4 Set Tick Marks

Use this procedure to set default tick marks to display.
1. In the Tick Mark area, select default tick marks to display:
• Vertical & Horizontal: To show side and bottom tick marks.
• Vertical: To show side only tick marks.
• Horizontal: To show bottom only tick marks.
• None: To show no tick marks.
Preferences window.
22.3.4.5 Set Grid

Use this procedure to customize the default grid display.
1. In the Grid area, set the following parameters:
a. Matrix Lines : Select On or Off.
b. Lines: Select Dotted or Solid.
c. Type spacing values for Grid Spacing, Line Spacing, Tick Mark Spacing and Tick Mark
Length.
Preferences window.
22.3.4.6 Set Show Localizer Group Color

This preference allows to the user to differentiate groups within Graphic Rx Show Localizer. The
chosen color palette is applied to both Graphic Rx viewports and secondary reconstructions.
Color indication is also displayed on each group task in the Series scan task list and the group in
primary focus is indicated with the color in the group tab of the scan settiings.
Classic is the standard blue tones and remains the default setting. The Bright, Soft-Toned and Pastel
color palettes allow for up to 6 groups to each have a distinct color. If more than 6 groups are applied,
then groups 7 and above are colored the same as group 1 for their respective color palette.

System Management
Figure 481 Group Color - Soft- Figure 482 Group Color - Figure 483 Group Color -
toned Bright Pastel
Figure 484 Scan task list color Figure 485 Group tab scan settings
Follow this procedure to customize the color scheme used for show localizer groups.

System Management
1. In the Show Localizer Group Color select one of the following parameters: Classic: standard
blue tones. This is the default setting. Bright: 6-color vibrant palette, Soft-Toned: 6-color muted
palette, Pastel: 6-color pastel palette
2. Click Save to save the new preference or Save and Close to additionally close the System
Preferences window.
22.3.5 Set Patient Data Entry Preferences

Use this procedure to set patient data entry preferences.
3. From the System Preferences window, click the Patient Data Entry tab.
Figure 486 Patient Data Entry Tab
Patient Data Entry Presets

Refer to the following to add, edit or delete:
• Referring Physician
• Radiologist

System Management
• Operator
The procedures to add, edit or delete are the same for these presets.
NOTE
The following characters cannot be used in the first or last name field for Referring
Physician, Radiologist and Operator: =, /, ^
22.3.5.1 Add Patient Data Entry Preset

1. Click Add New….
2. Enter name or description in the provided field.
Click in each field and type any other desired information.
NOTE
Selecting another Preferences tab will save any entered information.
Preferences window.
22.3.5.2 Edit Patient Data Entry Preset

1. Click preset name in the list to highlight it.
2. Edit the name or description.
Preferences window.
22.3.5.3 Delete Patient Data Entry Preset

1. Click the preset’s name in the list to highlight it.
2. Click next to the name.
3. Click OK to confirm you want to delete the preset.

Preferences window.
22.3.6 Set Image Database Preferences

Patient de-identification or anonymizing an exam electronically removes certain exam information
and replaces it with anonymous information. There are two levels to anonymizing patient information:
Full and Partial.
Use this procedure to set the annotation level for patient anonymize.

System Management

3. From the System Preferences window, click the Image Database tab.
Figure 487 Image Database Tab
4. In the Anonymize Patient Image Annotation Level area, select: Full or Partial mode.
NOTE
Full mode is the most HIPAA-compliant.
For detailed information on how to anonymize patient data, see Patient Data.
22.3.7 Set Networking Preferences

Use this procedure to set Networking Preferences. This tab controls how exams, series or images are
transferred to other host systems on the network configured to archive or read this data.
You identify and configure these network hosts using Configure Network Hosts on the Network
Settings menu.

System Management
3. From the System Preferences window, click the Networking tab.
Figure 488 Networking Preferences Tab
22.3.7.1 Set the Simultaneous Transfer Mode

Simultaneous Transfer Mode allows multiple concurrent transfers of exams, series or images to other
hosts on the network configured for reading or archiving this data. By default it is set to On.
1. Click the On button to allow concurrent transfers or click Off to allow only one transfer at a time.
Preferences window.
22.3.7.2 Set the Simultaneous Transfer Per Host

The Simultaneous Transfer Per Host field indicates the number of transfers that can occur
concurrently. You can choose to transfer 1, 2 or 3 concurrent transfers. The default is 2.
1. Click the 1, 2 or 3 buttons to set the number of concurrent transfers.
Preferences window.

System Management
If you select a new choice, the system needs to restart.
22.3.7.3 Set High Priority Hosts

Use the two drop-down menus to indicate the hosts on the network that take first and second priority
when transferring exams, series or images.
1. Click the first drop-down box to display the list of configured network hosts. Select the host that is
to have top priority for data transfers.
2. Click the second drop-down box to display the list of configured network hosts. Select the host
that is to have second priority for data transfers.
Preferences window.
22.3.7.4 Set Low Priority Hosts

Use the two drop-down menus to indicate the hosts on the network that have a lower priority when
transferring data.
1. Click the first drop-down box to display the list of configured network hosts. Select the host that is
to have low priority for data transfers.
2. Click the second drop-down box to display the list of configured network hosts. Select the host
that is to have low priority for data transfers.
Preferences window.
22.3.8 Set Exam Split Preferences

When you build a protocol you can save a pre-configured RIS procedure code for the protocol.
Use this procedure to add new RIS procedure codes to associate with protocols for use with
Prospective Exam Split. You can also edit, synchronize or remove the procedure codes. In addition,
you can import the most recent RIS procedure codes from the scanner database.
1. From the display monitor, click .
2. From the System Preferences window, click the Exam Split tab.

System Management
Figure 489 Exam Split
3. Click Add Requested Procedure to enter a new RIS description. Click Save. The new procedure
can now be associated with a protocol for use with Prospective Exam Split.
4. Click Import Recent Procedures to import the most recent RIS procedure codes from the scanner
database. Click Save. The new procedures can now be used with Prospective Exam Split.
22.3.9 Set Protocol Selection Preferences

Use this procedure to modify the maximum age for a pediatric protocol. This is the age that will
automatically display for pediatric protocols.
3. From the System Preferences window, click the Protocol Selection tab.

System Management
Figure 490 Protocol Selection Tab
4. In the Maximum Pediatric Age area, select an age.
NOTE
The system preset is 18 years old.
Preferences window.
22.3.10 Set Contrast Management Preferences

Use this procedure to set units for pressure injection, and what contrast agents can be selected.
3. From the System Preferences window, click the Contrast Management tab.

System Management
Figure 491 Contrast Preferences tab
22.3.10.1 Set Units for Injector Pressure

Choose the units of measure for contrast injector pressure.
1. Click PSI for pounds per square inch, the default value, kg/cm2 for kilogram per square
centimeter or kPA for kilopascal.
Preferences window.
22.3.10.2 Set the List of Available Agents

Use this section to create and maintain a list of contrast agents and agent/concentrations that can be
selected at scan time. These entries pre-populate the IV and Oral Contrast Agent UI in the scan user
interface. You can enter up to 99 agents and 99 agent/concentration combinations. The agent name
can be up to 64 characters.
1. For IV Contrast:
a. Add an agent by typing a name in the Agent field, then enter a concentration (in mg/ml) for
the agent. Click the Add button.

System Management
b. Edit an existing entry by selecting the entry on the list, then making changes to the name in
the Agent field or the value in the Concentration field.
c. Delete an entry by selecting the entry in the list then clicking the X next to the entry.
2. For Oral Contrast:
a. Add an agent by typing a name in the Agent field, then enter a concentration (in mg/ml) for
the agent. Click the Add button.
b. Edit an existing entry by selecting the entry on the list, then making changes to the name in
the Agent field or the value in the Concentration field.
c. Delete an entry by selecting the entry in the list then clicking the X next to the entry.
Preferences window.
22.3.11 Set Patient Handling Preferences

Use this tab to set the scout table speed.
3. From the System Preferences window, click the Patient Handling tab.
4. Indicate whether the Scout Table Speed is to be set at 100 mm/s, the default value, or 200 mm/s.
NOTE
200mm/s is available only if the Fast Scout option in installed.

System Management
Figure 492 Patient Handling tab
22.3.12 Set ECG Preferences

Use this procedure to set the ECG device preferences.

System Management
Figure 493 ECG Tab
4. In the ECG Device area, select Internal or External.

5. If Internal is selected, see the Integrated Cardiac Module Operator Manual for information on the
settings described in 5–9 below.
6. In the Active Lead area, select Lead I, Lead II, Lead III or Auto.
7. In the Waveform Filter area, select On or Off.
The filter is used to suppress 50 or 60Hz interference from nearby AC power sources. With the
filter turned on, typically less noise is observed on ECG traces, as long as proper patient prep is
followed.
Refer to Figure 252 on page 582
8. In the Gain area, select 1X, 2X, 4X, 8X or Sets the ECG "R" wave to predetermined amplitude.
This will change the amount of amplification applied to a waveform signal. Depending on which
the user selects, the height and depth of the cardiac waveform signal will change.
A selection of 1x will appear more 'zoomed out' compared to a selection of 8x 'more zoomed in.
9. In the Impedance Sensitivity area, select High (50 kΩ), Medium (25 kΩ) or Low (10 kΩ).
10. In the Pacer Detect area, select On or Off.
11. The following settings are for the ECG trace displayed on the scan monitor. See the Cardiac
chapter for more details.

System Management
12. In the Statistics Window Length area, enter a value for seconds (0–99).
13. In the Irregular Beat Window Length area, enter a value for seconds (0–999).
NOTE
The system default is set to 60 seconds. Decrease this value to 30-45 seconds if you
want Auto Gating to use a smaller time window for heart rate measurements.
14. In the Breathhold Record Length area, enter a value for seconds (0–99).
15. In the Cardiac Multiphase Fixed Interval Recon field, select On to activate the feature, or set to
Off, the default value.
Preferences window.
22.3.13 Set Interventional Preferences

3. From the System Preferences window, click the Interventional tab.
Figure 494 Interventional Tab
4. In the WW and WL area, enter a label, a window width value and a window level value.

System Management
5. In the Viewpoint Display Orientation area, click Fixed or Configurable.

The fixed 3i viewport order is always |Head| Center |Feet|.
The configurable 3i viewport order is set based on the side of the table on which the
interventionalist is standing and the patient’s orientation on the table.
6. In the Graphic Rx Plane area, click Scout or Axial.
Scout: Interventional GraphicRx viewport shall show Scout images with the same landmark.
Axial: Interventional GraphicRx viewport shall show Axial images with the same landmark.
Preferences window.
22.3.14 Set Scan Room Display Preferences

Scan Room Display Preferences let you set the information that appear on the gantry display during
the scan.
3. From the System Preferences window, click the Scan Room Display tab.

System Management
Figure 495 Scan Room Display tab
22.3.14.1 Patient Name

1. Select On to show the Patient Name on the display. This is the default setting. Select Off to keep
the Patient Name off of the display.
Preferences window.
22.3.14.2 Patient ID
1. Select On to show the Patient ID on the display. This is the default setting. Select Off to keep the
Patient ID off of the display.
Preferences window.

System Management
22.3.14.3 Patient Age

1. Select Age to display the patient’s age in years on the display. This is the default value. Select
Date of Birth to display the patient’s date of birth. Select Off to keep the patient’s age off of the
display.
Preferences window.
22.3.14.4 Patient Sex

1. Select On to show the Patient Sex on the display. This is the default setting. Select Off to keep the
Patient Sex off of the display.
Preferences window.
22.3.14.5 Protocol Information

1. Select On to show the selected protocol on the display. This is the default setting. Select Off to
keep the protocol off of the display.
Preferences window.
22.3.14.6 Patient Default Character Type

1. Select Alphabetic to display patient information in alphabetic characters. This is the default
value. Select Ideographic to display patient information in ideographic form. Select Phonetic to
display patient information in phonetic form.
Preferences window.
22.3.15 Set Lighting Preferences

Use these procedures to set system lighting preferences.
3. From the System Preferences window, click the Lighting tab.

System Management
Figure 496 Lighting Tab
4. In the Accent Lights area, select On or Off.

5. In the Bore Lights area, select On or Off.
6. In the Bore Light Intensity area, click and drag the slider to set the brightness level.
Preferences window.
22.3.16 Set PPS Preferences

3. From the System Preferences window, click the PPS tab.

System Management
Figure 497 PPS Tab
4. In the PPS Enable area, click Yes or No.

5. Enter the following connectivity data: SCP AE Title, SCP Host Name, SCP IP and SCP Port.
Preferences window.
22.3.17 Set Patient Schedule

3. From the System Preferences window, click the Patient Schedule tab.

System Management
Figure 498 Patient Schedule
4. The Calling AE (Application Entity) title is used when opening the association to the HIS/RIS. This
AE will also be used in the Scheduled Station AE Title (0040,0001) tag in the C-FIND request if ‘This
System’ option is selected in the Schedule Refresh Setup menu refer to Setting up the HIS/RIS
Refresh.
The calling AE title for the CT system is used by the Patient Schedule application when a Modality
Worklist C-FIND request is performed. If the local system's calling AE title does not match the
expected AE in the remote HIS/RIS configuration (or the local system is not configured on the
remote HIS/RIS), the remote HIS/RIS may fail to return worklist entries to the local system.
Preferences window.
6. Click >Troubleshooting > Restart Application to enable Scheduler SCU Configuration.
22.3.18 Set the Patient Information Display

1. In the Patient Information Display area, select On or Off.
Preferences window.

System Management
22.3.19 Set Intelligent Protocoling Preferences

This functionality is available only when the Intelligent Protocoling option is installed.
3. From the System Preferences window, click the Intelligent Protocoling tab.
4. In the Worklist key select a DICOM tag from the dropdown menu.
Work with the site medical record system administrator to identify the DICOM tag that is most
meaningful and unique for the clinical intent of the exam.
The default setting is: Requested Procedure Description (0x0032, 0x1060)
Available selections:
• Requested Procedure ID (0x0040, 0x1001)
• Requested Procedure Code Sequence value (0x0032, 0x1064)
• Requested Procedure Description (0x0032, 0x1060)
• Requested Procedure Comments (0x0040, 0x1400)
• Scheduled Procedure Step Description (0x0040, 0x0007)
• Scheduled Procedure Step Code Sequence Value (0x0040, 0x0008)
• Scheduled Procedure Step ID (0x0040, 0x0009)
5. Set Autoselect Protocols to either On or Off from the dropdown menu.

If set to Off, the default value, all suggested protocols display in the Suggested Protocols and no
protocol is automatically selected.
If set to On, suggested protocols that have been selected at least 20 times for a given Requested
Procedure entry and have a high confidence over the next most commonly selected protocol will
be automatically selected and displayed in the Suggested Protocol area.
If set to On, the system selects a protocol and displays it in the Selected protocols area, if
a protocol has been selected at least 20 times for a given modality worklist entry and the
confidence is 30 percent higher than the next highest protocol.

System Management
NOTE
Only recommended protocols from adult protocols display when the adult selector
is displayed and only recommended protocols from pediatric protocols display
when the pediatric selector is displayed.
If the AutoSelect protocol preference is set to On, and a protocol has been selected
at least 20 times for a given modality worklist entry and the confidence is 30 percent
higher than the next highest protocol, the system selects a protocol and displays it
in the Selected Protocols area. The user can click Accept to use this protocol(s) for a
patient scan. Prior to selecting Accept, read and verify the protocol name(s) selected
are the protocols desired for the exam. If not, use the X icon next to the protocol
name to delete a protocol that is not desired and select the desired protocol(s) from
any protocol per select a protocol.
22.3.20 Set Cloud Connectivity


3. From the System Preferences window, click the Cloud Connectivity tab.
Figure 499 Cloud Connectivity tab

System Management
Preferences window.
22.3.21 Set Related Protocol

Use these procedures to modify how the related protocols are defined. Related protocols capability is
available only when using Exam Workflow on the Gantry Display.

3. From the System Preferences window, click the Related Protocols tab.
From the Related Protocols tab the user can configure key words (lexicon), including contrast type and
anatomies. These are used to match related protocols based on Exam Description and protocol names.
Six contrast types are defined:
• Non-Contrast
• Regular Contrast
• CTP (CT Perfusion)
• CTU (CT Urography)
• CTV (CT Venography)
• CTA (CT Angiography)
The anatomies are defined as 2-level tree structures in the lexicon.

In the second level of each category, a few anatomies which belong to that category are added. For
example, circle of Willis and Trauma Head are defined as second-level anatomies under the Head
category. For each contrast type, category or anatomy, their thesaurus (alias or abbreviation) are
added in Context column to increase the matching possibility. The omitted terms are used as exclusion
phrase in the matching algorithm. For example, feet first will not be considered in a search a foot scan
protocol.
The user can customize the lexicon based on the GE-provided default lexicon:
• Add or remove a thesaurus of a contrast type (in the Context area for that contrast type).
• Add or remove a thesaurus of an anatomy (in the Context area for that anatomy).
• Add or remove an anatomy, either an anatomy category or the anatomy under a category.
Different anatomies’ names need to be different.
• Add or remove an exclusion phrase in the "Omitted Terms".
22.3.21.1 Set Anatomies

Use this procedure to add a new Category/Anatomy thesaurus.

System Management

4. Click the Anatomys tab.
5. In the Category window, click + , a new category is added.
6. Double click to edit the category name.
7. In the Anatomys window, click + , a new anatomy is added.
8. Double click to edit the anatomy name.
9. In the Context window, click +, a new context is added
10. Double click to edit the context name.
Preferences window.
Figure 500 Set Anatomies
22.3.21.2 Set Contrast Type


System Management

4. Click the Contrast Type tab.
5. In Context window, click + , a new context is added.
6. Double click to edit context name.
Preferences window.
Figure 501 Set Contrast Type
22.3.21.3 Set Omitted Terms


4. Click the Omitted Terms tab.
5. In the Context window, click + , a new context is added.

System Management
6. Double click to edit context name.

Preferences window.
Figure 502 Set Omitted Terms
22.3.21.4 Delete Anatomies, Contrast Type and Omitted Terms


4. Click the tab (Anatomys, Contrast Type, Omitted Terms) you wish to delete from.
5. In the associated window, highlight the term you wish to delete.
6. Click -(minus sign), to delete the term.
Preferences window.

System Management
22.3.21.5 Export and Import the lexicon

Export the lexicon

4. Click Export and select the desired output location.
• Local: The lexicon will be saved to the CT file system.
• USB: The lexicon will be saved to the USB device.
5. Input the desired file name in the File name field, and then click Ok to save. If you select USB,
insert USB device first and then click Ok to save.
6. Click Ok to close the dialog message.
Import the lexicon


4. Click Import and select the desired location, then click Ok.
• Local: The lexicon will be restored from Local (CT file system)
• USB: The lexicon will be restored from USB device.
• Default: The system default lexicon will be restored, select one of the following supported
languages: English, Italian, French, Portuguese, Danish, Finnish, German, Spanish, Dutch,
Norwegian, or Swedish.
5. Select the lexicon you want to restore, then click Ok. An attention message displays.
6. Select Continue to restore the lexicon. This restarts the application. Or select Cancel to leave the
lexicon unchanged.
22.4 System Troubleshooting
22.4.1 Open a Unix shell

Use this procedure to display a Unix shell. This area is used by your service personnel.
2. Click Troubleshooting, then Unix Shell.

System Management
A Unix Shell window will open. At the prompt, enter the operating system password for ctuser.
NOTE
If your system is configured in a language other than English, the Unix Shell may
show unreadable text when first opened. Enter the operating system password for
ctuser.
3. Click the X in the upper corner of the Unix Shell window to close it.
22.4.2 Collect Data with SPR Snap

Use this procedure to capture SPR information on the system.
NOTE
Do not initiate an SPR Snap if the system is actively collecting data with X-ray on.
2. Click Troubleshooting, then SPR Snap.

A user message will be displayed. Warning: Do not execute during acquisition! Complete current
acquisition before proceeding. Select OK to Continue.
If you need to continue scanning patients click Cancel and collect the data at the next available
time.
Click OK to continue. An attention message will open to indicate the SPR Snap is in progress.
Attention: SPRsnap is in progress. Do not start any scan acquisition until the snap is complete.

System Management
3. When SPR Snap is finished, the sprsnap window will close. The SPR information will be stored
in the following system directory: /service/SPRSnaps/ for (Z440, P520 host computers with
a service partition) or /usr/g/service/log/SPRSnaps/ (Z420 older computers without a
service partition), and can be retrieved be your service representative. Note the directory location
for future use.
4. Click Cancel to stop data collection. Proceed with urgent scanning need and then repeat steps for
Collect Data with SPR Snap.
22.4.3 System Time Adjustment Tool

Use this procedure to adjust the system time.
1. From the display monitor, click
2. Click Troubleshooting, then System Time Adjustment Tool.

3. As this tool needs Application software shutdown, if you proceed to the system time adjustment,
click OK.
Figure 503 System Time Adjustment Tool attention

System Management
ATTENTION
System Time Adjustment Tool needs application software shutdown, and system
reboot after completing time adjustment.
Before application shutdown, please close any open Exam tab sessions and
complete pending recon jobs. Failure to do so will resume in the loss of data
currently in progress.
Please click the "OK" button to proceed the tool, and it takes approx 30sec, to
complete application shutdown.
4. The System Time Adjustment Tool screen is posted.
Figure 504 System Time Adjustment Tool screen
5. Set new time by using arrows or manual input from the keyboard.
6. Click Accept to exit.
NOTE
New Time needs to be in the Available Time Range. If it is outside of the range,
another popup window will be posted. Click Accept to exit.
Figure 505 Attention screen
ATTENTION
Invalid time, Please try again.

System Management
NOTE
If the system is connected to NTP Server, the message below is displayed.
Figure 506 Attention screen
ATTENTION
NTP (Time Server) is configured. System Time Adjustment Tool is not available.
22.4.4 Restart an Application

Use this procedure to restart the system when the Patient Exam Session has become non responsive.
2. Click Troubleshooting, then Restart Application.

A restart of the system software will be performed.
22.4.5 Close Volume Viewer / Reformat

Use this procedure to close the Volume Viewer or Reformat application when it is not fully closed
by selecting Exit. The screen may display a blank area of the screen that represents a portion of the
Volume Viewer or Reformat menu.
2. Click Troubleshooting, then Close Volume Viewer / Reformat.

The blank area on the screen will be removed once the application is fully closed.
22.4.6 Fast Cal with GSI Refresh

Use this procedure for troubleshooting purposes when GSI QA specification results have failed or if
artifacts are seen in QA phantom images when Fast Cal with GSI Refresh has not been run in the last 7
days.

System Management
2. Click Troubleshooting, then Fast Cal with GSI Refresh. The Service-Calibration Tools window
opens.
3. Click Run.
4. When Fast Cal with GSI Refresh is complete, perform a quality assurance scan.
22.4.7 Xtream Camera Reset

Use this procedure when the Xtream camera is not responding to reset the camera connection.
2. Click Troubleshooting, then Xtream Camera Reset. The Reset in Progress dialog opens. After
approximately 10 seconds the message Xtream Camera Connection Reset successfully displays.
22.4.8 Use iLinq

Use iLinq to access GE Online Center engineers and Answerline Applications Specialists.
The iLinq tools are designed so you can get information yourself, rather than having to always rely on a
FE or an Online Center Engineer. The Applications Self Help feature provides automated expert advice
from a database of application problems and solutions.
• Answer questions — Top 10 FAQs.
• Search the Knowledge Database.
• Share the knowledge with coworkers by saving the results.
If InSite is running the Remote Safety test, New Patient does not open. To access New Patient:
• Call InSite and request they abort the test
• Navigate to the Service Desktop and select CleanUp option to cancel the test in progress
22.4.8.1 Launch iLinq

2. Click Troubleshooting, then iLinq.

The iLinq desktop will open.
22.4.8.2 Terminate iLinq remote connection

Use this procedure to terminate an iLinq connection when a GE representative initiated the
connection.
1. Click New Patient.
A message is posted that the scan hardware resource is not available.
2. Wait three minutes and click New Patient again to begin scanning.

System Management
22.4.9 Enabling Tip Virtual Assist (TVA)

2. Click Troubleshooting, then TiP Virtual Assist. The Tip Virtual Assist desktop will open.

System Management
3. Once the GE Representative has launched a virtual assist

program, you will be prompted to allow remote control.

System Management
4. Click Accept to allow access with GE default password or click Change Session Password to
generate a Password specific to this session.
5. Click Cancel to decline remote access.

System Management

General Information
23 General Information
23.1 Introduction
This section provides a simple introduction to CT, or Computed Tomography, for people with no
detailed physics or medical diagnostic education.
23.1.1 System Components

The system components are also described in the User Manual.
23.1.2 Emergency Stop

Emergency Stop procedures are described in the Safety chapter.
23.1.3 CT Description
Computed tomography (CT) is a medical imaging method employing tomography created by
computer processing. Digital geometry processing is used to generate a three-dimensional image
of the inside of an object from a large series of two-dimensional X-ray images taken around a single
axial of rotation. The word "tomography" is derived from the Greek tomos (slice) and graphein (to
write). Computed tomography is known as computed axial tomography (CAT or CT scan).
CT produces a volume of data, which can be manipulated, through a process known as windowing,
in order to demonstrate various bodily structures based on their ability to block the X- ray/Röntgen
beam. Although historically the images generated were in the axial or transverse plane, orthogonal
to the long axis of the body, modern scanners allow this volume of data to be reformatted in various
planes or even as volumetric (3D) representations of structures.
23.2 CT Operation Theory

The CT Scanner consists of the following subcomponents:
• X-ray source
• CT Detector
• Gantry
• Power Distribution Unit
• Table
• System Cabinet
• Scanner Desktop

General Information
23.2.1 X-ray Source

The source and detector components are housed on a gantry with a cylindrical patient bore. An X- ray
tube that is part of the source subcomponent is housed on the rotating gantry, diametrically opposite
to the detector. The high voltage generator is the second part of the X-ray source. It provides high
voltage to the X-ray tube across the anode and the cathode, along with current to the filament, which
is part of the cathode
The X-ray tube contains filaments, a cathode and an anode. The filament provides the electrons that
create X-rays. The X-ray system generates a current that heats the filament until electrons start to
“boil off” and break away from the filament. We refer to the filament current as “mA.” Increasing the
mA increases the number of electrons that become available to make X-ray. Higher concentrations of
electrons improve image resolution.
The X-ray system creates a high voltage, or kV, potential between the cathode and anode. The negative
charge on the cathode repels the electrons that boil off the filament. The positive charge on the anode
attracts the negatively charged electrons. The electrons strike the rotating anode target and displace
electrons in the target material. This interaction creates heat and X-ray photons. The target rotates to
help spread the heat over a larger area. Increasing the kV increases the electron strike speed, which in
turn increases the intensity or “hardness” of the X-ray photon beam.
The X-ray tube's heat capacity and dissipation can determine the frequency and length of CT
Exposures, or limit the mA. A Helical or Cine exposure can last up to 60 seconds and axial exposures
last from 0.28 to 1.0 seconds.
The X-ray system provides focal spots S, L and XL that are automatically selected by the system based
on kV, mA and exposure time. Refer to the Revolution™ CT, Revolution™ CT ES TRM, Chapter 7, System
Specifications, Section 6, CT System X-ray Tube Ratings for the maximum tube power limits.
23.2.2 CT Detector
The CT Detector is a wide coverage cone beam detector with multiple detector rows along the
longitudinal plane. The Detector channels are arranged as an arc diametrically opposite to the X- ray
tube on the rotating CT gantry. The detector consists of a scintillator that converts X-rays into light,
diodes for light conversion into current and analog to digital converter that converts the current into
digital signal. The Data Acquisition System (DAS) samples each detector cell up to about 2496 times
per gantry rotation, amplifies and quantifies the current from the cells and transmits the resultant
data to the scanner desktop.
256 rows = 256 (for 160 mm configured systems) or 128 rows = 128 (for 80 mm configured systems)
or 64 rows=64 (for 40 mm configured systems) unique physical cell locations in Z-axis. Detector cell
segregation in the Z-axis provides 3-D post-patient collimation.
23.2.3 Gantry
The stationary and rotating structure and drive system which controls the rotation and angular
positioning of the Detector and X-ray Source.
Variable rotation scan speeds (0.28, 0.35, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0 seconds per rotation).

General Information
23.2.4 Power Distribution Unit

The Power Distribution Unit, or PDU, distributes power to the rotating gantry, patient table and
scanner desktop.
23.2.5 Table
The Table provides support and vertical/longitudinal motion of the patient relative to the CT
scanner. The Table also mechanically houses and electrically interfaces to the integrated ECG
unit. This subcomponent includes patient positioning and support accessories (pads, straps, poles,
headholders) as well as foot pedals.
23.2.6 System Cabinet

The System Cabinet subcomponent provides pre-processing, image reconstruction and scout image
construction operations on data available from scan data management. It includes both the software
and computer hardware for image generation and scan data acquisition.
23.2.7 Scanner Desktop

The Scanner Desktop provides the software user interface in the control room of the scanning suite
for all system operations. It governs system operation and workflow until the user confirms a scan
prescription (resuming control after scan completes), and includes both the software and scanner
desktop hardware.

General Information
Figure 507 CT System Illustration
Table 161 CT System Description
Number Description
1 X-ray must reach the detector’s

reference channels at the edges of
the Scan Field of View (SFOV)
2 X-ray Tube
3 Centered Patient
4 Gantry Opening
5 Detector DAS
23.3 General Information

23.3.1 Gantry Coordinate System
X, Y, Z: Scanner gantry coordinate system:
• X=Tangent to circle of rotation.

General Information
• Y=Radial (from isocenter toward tube focal spot).

• Z=Longitudinal (in/out of the scan plane).
Figure 508 Gantry Coordinate System
Table 162 Scanner Geometry
Parameter
Isocenter height 1026 mm
Focal spot to isocenter 625.6 mm
Focal spot to detector 1097.6 mm
SFOV 500 mm
Gantry bore diameter 795 mm

General Information
23.3.2 Patient Scanning

Table 163 Table Scan Length
Scan Scan Length (mm)
NG2000 Table NG2000V Table NG1700V Table
Scout Scans 2000 mm 2000 mm 1700 mm
Axial/Cardiac Scans 2000 mm 2000 mm 1700 mm
Helical Scans 1850 mm 1850 mm 1550 mm
NOTE
Helical scan range varies based on the helical pitch and gantry rotation speed selected.
23.3.3 Table Capacity

Standard Weight Capacity Table – Table maximum capacity is 227 kg (500 lbs)
Heavy Weight Capacity Table – Table maximum capacity is 306 kg (675 lbs)
23.4 Network
23.4.1 Purpose of Revolution™ CT, Revolution™ CT ES Scanner

Connection to Network
The Revolution™ CT, Revolution™ CT ES Scanner is intended to be connected to a network in order to
support the following functionality:
• DICOM services to retrieve images from other DICOM-compliant machines
• DICOM services to push images to other DICOM-compliant machines
• DICOM services to query for images on other DICOM-compliant machines
• DICOM services to confirm that images have been permanently stored on a DICOM-compliant
machine
• DICOM services to get DICOM modality worklist information from a remote hospital or radiology
department information system computer
• DICOM services to allow a Modality Performed Procedure Step to be communicated to the
Hospital/Radiology information system
• DICOM services to verify the remote DICOM system is connected properly to the scanner device
• Services to provide authentication and authorization against Enterprise directory servers
All of the above features are optional on the Revolution™ CT, Revolution™ CT ES Scanner.

General Information
23.4.2 Network Interface Technical Specifications

Connection Name: Hospital network port
Physical network connection type: IEEE 802.3-1998 1000/100/10 BaseT Ethernet
Speeds and duplex modes supported: 10Mbps, 100Mbps, and 1Gbps half and full duplex
Auto-negotiate
Default IP Address (from factory): IP Address – 192.9.101.1

Subnet Mask – 255.255.255.0
Gateway – empty
IP addressing: IPv4 static
QoS Support: n/a
23.4.3 Network Information Flows Specifications

Flow Name DICOM image retrieve
Network Connection on device Hospital network port
Usage Type/Function/Purpose Get a DICOM image or set of images from a network

device
Licensed/optional/required optional
Communication Partner Device/IP Address/Network Any network device supporting the DICOM application
layer protocol(s) listed below
Middle Layer Protocols TCP/IP
Application Layer Protocol and Encoding CT Image Storage

MR Image Storage
X-Ray Radiation Dose SR – CT Radiation Dose
RT Structure Set Storage
Positron Emission Tomography Image Storage
Ports (default) 4006
Traffic characterization and bandwidth requirements On demand, local user initiated. The bandwidth is
dependent on the local site.
Latency max n/a
Flow Name DICOM image push

General Information
Usage Type/Function/Purpose Send a DICOM image or a set of images to a network

device
Application Layer Protocol and Encoding CT Image Storage

MR Image Storage
Grayscale Softcopy Presentation Sate Storage
X-Ray Radiation Dose SR – CT Radiation Dose
RT Structure Set Storage
Positron Emission Tomography Image Storage
Traffic Characterization and Bandwidth Requirements On demand, local user initiated. The bandwidth is
Latency Max n/a
Flow Name DICOM image query
Usage Type/Function/Purpose Find a list of DICOM images from a network device
Application Layer Protocol and Encoding Study Root Query/Retrieve Information Model - FIND
Study Root Query/Retrieve Information Model - MOVE
Latency Max n/a
Flow Name DICOM Storage Commit
Usage Type/Function/Purpose Used to confirm that local DICOM images have been
permanently stored on a remote DICOM device

General Information
Application Layer Protocol and Encoding Storage Commitment Push Model SOP Class
Latency Max n/a
Flow Name DICOM Modality Worklist Information
Usage Type/Function/Purpose Transfer patient information for HIS/RIS system to CT

scanner
Application Layer Protocol and Encoding Basic Modality Worklist Information Model – FIND
SOP Class
Latency Max n/a
Flow Name Modality Performed Procedure Step
Usage Type/Function/Purpose Send a report about a performed patient exam to the

HIS/RIS system
Application Layer Protocol and Encoding Modality Performed Procedure Step SOP Class

General Information
Latency Max n/a
Flow Name Enterprise Authentication / Authorization
Usage Type/Function/Purpose Authenticate local user against Enterprise Server
Application Layer Protocol and Encoding Microsoft Active Directory / Novell eDirectroy
Ports (default) 3002, 3003, 3004, 6386
Latency Max n/a
23.4.4 Required characteristics and configuration for network

support of Revolution™ CT, Revolution™ CT ES Scanner
specifications
The network must meet the specific requirements above for all traffic flows associated with the subset
of features, use cases and workflow required by the responsible organization’s users.
In addition, the network must be “flat” (limited to a single IP broadcast domain).
23.4.4.1 Remote Host Parameters

You access the Configure Network Hosts window by clicking the Network Settings icon on the File
Manager control bar. You can also view the configured remote networks from the Source menu above
the Exam List in File Manager.
• Host Name: The name given to the network node of the currently selected node. This name is
typically entered by the service engineer.
• Display Name: The name that is shown in both the source menu and Archive and Network
destinations.
• IP Address: The location of the node within the network. You must enter the IP (Internet
Protocol) address correctly or the connection cannot be made. Your service engineer can help
you determine the IP address.

General Information
• Port: A predetermined number specific to the type of host and the protocol used. Your service
engineer can provide you with this number.
• AE title: This title is provided by the service engineer.
• Comments: A space to enter text that is associated with the selected node.
23.4.4.2 Archive Node Settings

Select the Archive Node option to place the selected node in the Archive destinations. Only devices or
nodes that have this option checked can be used as an archive device. Not all hosts can be used as
archive nodes (for example, another CT system cannot be used as an archive node, but a PACS system
can be used as an archive node).
To be a successful archive node, the node must meet certain DICOM requirements so that when the
data is transferred from the host system to the node, the DICOM handshake can be successful. This is
not necessary for networking images. The same handshake is not required.
The storage commitment host details are populated from the selected Remote Host Information area.
These fields can be edited.
23.4.5 Network Compatibility

The BrightSpeed Series, LightSpeed QX/i, Plus, Ultra, RT, RT16, Xtra, Pro16, Pro32, VCT, Optima CT660,
Optima CT520, Optima CT540, Optima CT580, Discovery CT590, Discovery™ CT750 HD and Revolution™
CT, Revolution™ CT ES image formats are DICOM. This image format may only be transferred between
systems using a DICOM network protocol. The receiving station must support DICOM receive for the CT
scanner’s images to be transferred (send or receive) to it.
Use the following table for network compatibility. The table lists the network protocol to use and the
features available for that system. The far left column lists the system the user is at (from).

General Information
Table 164 Network Compatibility
To
BrightSpeed HiSpeed CT/i HiSpeed 3rd Party

Series, Bright- NX/i, X/i, or DICOM Sta-
Speed Select QX/i tion
Series, Light-
Speed™ QX/i,
Plus, Ultra, RT,
RT16, Xtra,
Pro16, Pro32/
From VCT. Revolu-
tion™ CT, Revo-
lution™ CT ES,
Discovery™
CT750HD, Opti-
ma CT660, Opti-
ma CT520, Opti-
ma CT540, Opti-
ma CT580, Dis-
covery CT590,
Revolution EVO
BrightSpeed DICOM DICOM DICOM DICOM*

Series, Query Query Query Query**
BrightSpeed
Select Series, Send Send Send Send
LightSpeed™ Receive Receive Receive Receive**
QX/i, Plus, Ultra,
RT, RT16, Xtra,
Pro16, Pro32/
VCT.Revolution™
CT, Revolution™
CT ES,
Discovery™
CT750HD,
Optima CT660,
Optima CT520,
Optima CT540,
Optima CT580,
Discovery CT590,
Revolution EVO
HiSpeed CT/i DICOM DICOM DICOM DICOM*

Query Query Query Query**
Send Send Send Send
Receive Receive Receive Receive**

General Information
Network Compatibility continued

To
BrightSpeed HiSpeed CT/i HiSpeed 3rd Party

Series, Bright- NX/i, X/i, or DICOM Sta-
Speed Select QX/i tion
Series, Light-
Speed™ QX/i,
Plus, Ultra, RT,
RT16, Xtra,
Pro16, Pro32/
From VCT. Revolu-
tion™ CT, Revo-
lution™ CT ES,
Discovery™
CT750HD, Opti-
ma CT660, Opti-
ma CT520, Opti-
ma CT540, Opti-
ma CT580, Dis-
covery CT590,
Revolution EVO
HiSpeed DICOM DICOM DICOM DICOM*

FX/i, DX/I, LX/i Query Query Query Query**
Send Send Send Send
3rd Party DICOM DICOM DICOM DICOM DICOM*

Station Query Query Query Query**
Send Send Send Send
* Some 3rd party stations use the ODINA network protocol. In this case use DICOM protocol and port
number 104.
** Query capability is available only if station is a query retrieve provider.
NOTE
LightSpeed™ VCT, LightSpeed™ Pro32, BrightSpeed based systems do not support
Advantage Network Protocol.

General Information
Table 165 Advantage Windows Network Compatibility
From
AW 1.X AW 2.X AW 3.X AW4.X BrightSpeed Series,
BrightSpeed Select
Series, LightSpeed
QX/i, Plus, Ultra, RT,
RT16, Xtra, Pro16,
Pro32/VCT Select,
VCT/VCT XT or Rev-
olution™ CT, Revo-
lution™ CT ES, Dis-
covery™ CT750HD,
Optima CT660, Op-
tima CT520, Opti-
ma CT540, Optima
CT580, Discovery
CT590, Revolution
EVO
BrightSpeed Series, DICOM DICOM DICOM DICOM DICOM

BrightSpeed Select Send Send Send Query Query
Series, LightSpeed
QX/i, Plus, Ultra, Send Send
RT, RT16, Xtra, Receive Receive
Pro16, Pro32/VCT
Select, VCT/VCT XT
or Revolution™ CT,
Revolution™ CT ES,
Discovery™ CT750
HD, Optima CT660, ,
Optima CT520,
Optima CT540,
Optima CT580,
Discovery CT590,
Revolution EVO
AW 1.X SdC Net SdC Net SdC Net SdC Net DICOM
Query Query Query Query Query
Send Send Send Send Send
Receive Receive Receive Receive Receive

General Information
Advantage Windows Network Compatibility continued

From
AW 1.X AW 2.X AW 3.X AW4.X BrightSpeed Series,
BrightSpeed Select
Series, LightSpeed
QX/i, Plus, Ultra, RT,
RT16, Xtra, Pro16,
Pro32/VCT Select,
VCT/VCT XT or Rev-
olution™ CT, Revo-
lution™ CT ES, Dis-
covery™ CT750HD,
Optima CT660, Op-
tima CT520, Opti-
ma CT540, Optima
CT580, Discovery
CT590, Revolution
EVO
V1 V2 V3 Query Query
Query Query Query Send Send
Send Send Send Receive Receive
Receive Receive Receive
NOTE
Advantage Windows systems do not support Query Retrieve provider. Send images from
the Advantage Windows to the BrightSpeed Series, LightSpeed™ QX/i, LightSpeed™ Plus,
LightSpeed™ Ultra, LightSpeed™ Pro16, LightSpeed™ Pro32/VCT Select, LightSpeed™
VCT/VCT XT, Revolution™ CT, Revolution™ CT ES, Discovery™ CT750HD, Optima CT660,
Optima CT580, Optima CT520, Optima CT540, Discovery CT590.
23.4.6 Hazardous Situations Due to Failure of IT—network

Archived or networked data corrupted during transfer, write, or restore can cause the following
hazardous siutations:
Archived radiation imaging data is unavailable or lost after diagnostic reading or review. Imaging data
is unavailable or lost before diagnostic reading or review.
Connection of the CT to an IT-network that includes other equipment could result in previously
unidentified risks to patients, operators, or third parties. The responsible organization should identify,
analyze, evaluate and control these risks. Subsequent changes to the IT-network could introduce
new risks and require additional analysis; and changes to the IT-network include, changes in the

General Information
IT-network configuration, connection of additional items to the IT-network, disconnecting items

from the IT-network, update of equipment connected to the IT-network; and upgrade of equipment
connected to the IT-network.
23.5 System Operational Modes
23.5.1 Overview
The system provides powerful data collection capability with following scan modes:
• Scout
• Axial
• Cine
• Helical
• Cardiac Axial
• Gemstone Spectral Imaging (GSI)
• SmartStep
23.5.2 Scout
Scout imaging is used for anatomical location in conjunction with scan and recon prescription, to
provide an anatomical cross-reference for axial images, and to provide quick feedback to the user as to
the anatomy scanned.
Scout supports the following features:
• Selectable kV (70, 80, 100, 120, 140 kV)
• Tube current limited to 250 mA with Focal Spot L
• Approximately 100 mm/s table speed, with option Fast Scout preference 200 mm/s
• Detector coverage: 5 mm
• Scout orientation: 0, 90, 180, 270 degrees
23.5.3 Axial
Axial imaging features include:
• All kV and mA stations available, dependent on generator and tube limitations.
• Rotation times: 0.28, 0.35, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0 second
• Detector coverage: 5, 40, 80, 100, 120, 140, 160 mm
• Variable image thickness selections: 0.625, 0.625z, 1.25z, 2.5z, 5.0z overlapped, 1.25, 1.25i, 2.5, 5.0
mm
• Sample rates: 984 Hz-8571Hz

General Information
• Revolution™ CT, Revolution™ CT ES can acquire up to 512 axial slices per rotation on the 160 mm
system, Revolution™ CT, Revolution™ CT ES can acquire up to 256 axial slices per rotation on the
80 mm system
23.5.4 Cine
Cine imaging features include:
• All kV and mA stations available, dependent on generator and tube limitations
• Maximum scan time: 60 seconds
• Rotation times: 0.28, 0.35, 0.5, 1.0 second
• Detector coverage: 40, 80, 100, 120, 140, 160 mm
• Variable image thickness selections: 0.625, 1.25, 2.5, and 5.0 mm
• Sample rates: 984 Hz-8571Hz
• Revolution™ CT, Revolution™ CT ES can acquire up to 512 axial slices per rotation
23.5.5 VolumeShuttle™ (Axial)

VolumeShuttle™ (Axial) mode is a repetitive axial scan mode, where the table shuttles (moves back
and forth) between two adjacent axial locations with minimal interscan delay. No gaps are allowed
with VolumeShuttle™ (Axial) mode.
23.5.6 Helical
Helical imaging features:
• All kV and mA stations available, dependent on generator and tube limitations
• Rotation times: 0.28, 0.35, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0 second
• Detector coverage: 40 mm, 80 mm
• Variable image thickness selections: 0.625, 1.25, 2.5, 3.75, and 5.0 mm
• Sample rates: 984 Hz-8571 Hz
• Pitches: 0.508:1, 0.516:1, 0.984:1, 0.992:1, 1.375:1 and 1.531:1
Helical Image Interval

The system has the ability to generate diagnostic images at small spacing for helical scan mode.
Images can be reconstructed at a minimum interval of 10% of the reconstructed slice thickness. The
average number of slices (images) per gantry rotation is calculated by dividing the total number of
reconstructed slices (images) by the number of rotations during the data acquisition.

General Information
23.5.7 Cardiac Axial

Cardiovascular imaging utilizes ECG-gating to target specific phases of the cardiac cycle, and a
weighted reconstruction algorithm to increase temporal resolution. In this mode, projection data
is acquired for at least one rotation, with an effective image temporal resolution of approximately half
of the gantry rotation time.
Cardiac Axial acquisition is a prospectively ECG-gated scan mode, where the heart rate is monitored
and the R-Peak triggers the acquisition of data for a specified range of phases in the cardiac cycle
(using R-peak to R-peak phase percent or ms after R-peak). The system coverage of up to 160 mm at
one table location is enough to cover many cardiovascular applications in a single scan. However, if
more than one table location is required, the system will determine required collimations and table
locations based on user specified scan range, scan field of view, the primary recon display field of view
(DFOV), and image offsets (A/P and R/L). The system also allows the user to control the amount of scan
overlap based on user selection (min, medium, or full) to balance image quality and dose (see User
Manual for description of these settings).
The Heart Rate Variation Allowance parameter (specified in BPM, typically based on the maximum
beat to beat variation during a short breath-hold) can be used to increase the scan duration in order
to ensure requested phases are acquired in the presence of heart rate variation. A low and stable heart
rate will allow the shortest scan duration, which will minimize patient dose.
Cardiac Axial imaging features include:
• Scan speed of 0.28 or 0.35 seconds
• Compatible with Hi Res mode
All kV and mA stations available, dependent on generator and tube limitations
• Compatible with SmartmA (See Automatic Exposure Control)
• Image thickness of 0.625 mm or 2.5 mm.
• Reconstruction algorithms optimized to cardiac imaging
23.5.8 ECG-Modulated mA
23.5.8.1 Electrocardiograph Tube Current Modulation

Modulating tube current (mA) based on an electrocardiograph (ECG) signal is a technical innovation
that significantly reduces radiation dose for cardiovascular imaging applications. The concept is based
on the fundamental principles of cardiac CT imaging.
23.5.8.2 ECG-Modulated mA Theory

The motion of the heart has always been challenging for diagnostic imaging of the heart and
surrounding areas. Motion can cause blurring and mis-registration artifacts in images. Heart motion
increases with a patient’s heart rate and for some heart rates there may not be one single optimal
phase of the heart cycle which minimizes motion for all coronary arteries. For this reason, the CT
system allows the user to set up a cardiac acquisition window with up to 3 independent parts for

General Information
imaging different periods of the heart cycle. The user may specify phases of the heart cycle to acquire
and the relative tube current level for each part of the acquisition window. The system responds
to the patient’s heart rate and modulates the tube current to acquire the cardiac phases requested
by the user. This tube current modulation, in conjunction with prospective ECG gating of the X-ray
exposure, allows the system to acquire the requested cardiac phases while minimizing dose to the
patient. If Auto Gating is enabled, the system will automatically adjust the scan parameters based on
the patient’s heart rate and heart rate variability during scan prescription. This allows the system to
intelligently respond to heart rate changes and optimize the scan parameters prior to acquisition.
The tube current utilized for cardiac acquisition window part 1 (100% mA) may be set by the user
manually or automatically by the system (see Auto mA) based on the user specified Noise Index (NI).
In addition to the user-specified ECG-based mA modulation, the system will also modulate the tube
current during each cardiac acquisition phase to minimize patient dose. Although projection data is
acquired for a duration of at least one complete rotation, the temporal resolution is, on average, half
of the gantry rotation time (e.g. 140 ms when the gantry rotation time is 280 ms). The additional
projection data beyond 140 ms is used for the outer few slices, and for image quality improvements
throughout the volume. The system typically modulates the tube current (mA) to 20% for the outer
views, so that the additional image information can be provided with minimal increase in patient
dose.
Example 1: Coronary Imaging for 75BPM Patient
Description: Acquire systolic and diastolic phases of the heart cycle
• Acq. Window Part 1: 70-80% R-to-R, 100% of specified mA (based on Auto mA or prescribed
manual mA)
• Acq. Window Part 2: 40-50% R-to-R, 100% of specified mA
Figure 509 Example 1
Example 1, dark grey indicates the approximate range of phases available for image recon at 100% mA;
light grey indicates full range of phases available for recon, with increasing image noise as the recon
phase moves further away from the 100% mA ranges at 40-50% and 70-80%
Example 2: Coronary + Functional Imaging for 60BPM Patient:
Description: Acquire low-noise coronary images at diastole and lower dose data for functional
assessment over the full cardiac cycle.
• Acq. Window Part 1: 75% R-to-R, 100% of specified mA
• Acq. Window Part 2: 0-95% R-to-R, 20% of specified mA

General Information
Figure 510 Example 2
Example 2, dark grey indicates approximate range of phases available for image recon at 100% mA and
20% mA
In the event that the patient should experience a premature ventricular contraction (PVC) or other
irregular heart rhythm, there is the possibility that low noise images could become shifted from the
prescribed phases.
23.5.9 SmartTrack
The purpose of SmartTrack (also known as z-axis tracking, or beam tracking) is to follow the focal
spot so that we can keep the most uniform part of the X-ray beam and the narrowest possible beam
on the detector to reduce dose and still avoid artifacts. The focal spot moves in the z-axis due to
thermal changes in the tube and mechanical forces during gantry rotation. In order to maintain the
narrowest possible beam, the system employs a closed loop control system called "Z-Axis Tracking".
The closed loop control system uses measured beam position data from the detector to position the
collimator cams in real time. Each blade is automatically and independently adjusted for optimal
beam performance1.
1T.Toth, et al., "A dose reduction X-ray beam positioning system for high-speed multi-slice CT
scanners", Medical Physics, Vol 27, No.12, (Dec 2000)
23.5.10 Gemstone Spectral Imaging

NOTE
Gemstone Spectral Imaging (GSI) is licensed for use with a GE X-ray tube. Use of a third
party X-ray tube will require an additional license for this feature.
Gemstone Spectral Imaging is a novel dual energy scan mode that uses two nearly simultaneous scans
at two different energy levels to generate material characterization information. The X-ray tube kV
determines the average energy level of the X-ray beam. By acquiring data of an object at different
energy levels, data with different attenuation values corresponding to the energy levels is generated.
This data can be utilized to identify material-specific differences in attenuation in terms of Water,
Iodine, Calcium, Uric Acid, Fat and Hydroxyapatite (HAP) basis-pair images, allowing monochromatic
and material representations.
Dual Energy scanning has been researched for several years in conventional X-ray Imaging as well
as CT imaging. The earlier methods include sequential Axial/Cine scans and dual source scans. Both
earlier methods suffer from the inability to temporally register the high and low energy data leading to
artifacts in the images. The system cycles or switches the kV from high to low at a very fast switching
rate of up to 4.8kHz and utilizes the fast response of the GE Gemstone Detector to capture the two data

General Information
sets that are temporally registered to within micro-seconds. The acquisition of the two kV samples that
are temporally well registered, provides the ability to use the feature for a broad range of applications.
Gemstone Spectral Imaging has the following image quality benefits and capabilities:
• Improved Beam Hardening performance - Streaking and shading artifacts in traditional CT
imaging, which is caused by the presence of bone or metal, is mitigated when using Gemstone
Spectral Imaging.
• Improved Contrast Visualization - The Gemstone Spectral Imaging feature allows for improved
contrast visualization by providing the capability to visualize the data at lower derived
monochromatic spectral energy settings.
• Virtual Contrast Subtraction - The Gemstone Spectral Imaging feature allows for virtual
"subtraction" of virtual non-contrast like images.
• Iodine/Calcium Separation - The Gemstone Spectral Imaging feature enhances CT Angiographic
capabilities to better discern the differences between contrast opacified vessels and surrounding
bone structures.
The Gemstone Spectral Imaging features provides better accuracy and sensitivity of identification of
materials and may lead to new uses or applications that require more accurate quantification than
achievable with current CT imaging.
Figure 511 Gemstone Spectral Imaging
The feature has the ability to generate multiple image representations including:
• Material Basis Pair Images (in mg/cm3, μg/cm3)
• Monochromatic – Data File Images – Contains Transform Data
• kVp-like Images – A monochromatic image made guided based on choosing the keV level that will
look most like a 100 or 120 kVp image

General Information
• Monochromatic Images
• High kVp Images
• QC High kVp Images
• VUE
With the rapid switching of the kV values, it is helpful to think of the data as "Mean Low Energy" and
"Mean High Energy". The concept of Mean Energy is illustrated in the figure below. As the CT detector
integrates the signal during one sample or one view, the kV value for each view will also be an integral
of the rise and fall curves as illustrated.
Figure 512 Mean Energy during GSI scan
Two important specifications that are impacted by the non-static beam energy are X-ray dose
reporting and kV accuracy. X-ray dose measurements using the standard CTDIw metric will be
performed using a scan with the rapid kV switching. A separate set of CTDI100 measurements have
been defined and reported in the Dosimetry section. Further, since the kV is rapidly switched view by
view, an accuracy specification has been defined for the GSI modes.
23.5.11 SmartStep
SmartStep imaging is designed to be used by the Radiologist or Physician during interventional
procedures using the integrated Hand Held Controller (HHC) and foot switch.
SmartStep imaging features include:
• All kV and mA stations available, dependent on generator and tube limitations.
• SmartStep scan mode does not use Focal Spot XL.
• Rotation times: 0.5 second

General Information
• Detector coverage: 5, 10, 20 mm

• Variable image thickness selections:
• 20mm Detector Coverage: 1i: N/A, Overlap 3i: 10mm, Non-Overlap 3i: 5+10+5mm
• 10 mm Dectector Coverage: 1i: 10 mm, Overlap 3i: 5 mm, Non-Overlap 3i: 2.5+5+2.5 mm
• 5mm Detector Coverage: 1i: 5 mm, Overlap 3i: 2.5 mm, Non-overlap 3i: 1.25+2.5+1.25 mm
• Sample rate: 984 Hz
23.6 Image Display

The left monitor LCD has two viewports in a matrix of 512 x 512 picture elements, or pixels. The right
monitor LCD displays a matrix of 1024 x 1024 pixels. The 1024 display can be further divided into up to
4 viewports of 512 x 512 pixels. Each pixel displays one of the 256 available shades of gray.
Figure 513 Monitor examples
The Revolution™ CT, Revolution™ CT ES system reconstructs axial and continuous images of 512 x 512
pixels. Images from other scanners may display 64, 128, 320, or 1024 pixel image matrices.
The amount of anatomy represented by each pixel equals the Display Field of View diameter in mm
divided by the matrix width/height.
The system assigns a unique CT number value, originally called a Hounsfield Unit, to each pixel.
The two dimensional pixel represents a three dimensional portion of patient tissue. The pixel value
represents the proportional amount of X-ray beam that passed through anatomy and entered the
detector.
23.6.1 CT Number
Image reconstruction supports two ranges of pixel CT Numbers, the "normal range" and an "extended
range".
• Normal Range is -1024 to 3071
• Extended Range is -31743 to 31743
However, the system display supports pixels with a range of -32,767 to +32,767.

General Information
The system references CT number zero to water and CT number -1000 to Air. Lung and fat have
negative pixel values and normally appear black. A CT number over 200 represents dense material like
contrast agent, calcium, bone, and normally appears white.
Inverse Video reverses video white to black, but pixel values remain the same.
Variables that can affect CT Number accuracy:
• Partial volume effects of anatomy
• Scans acquired with IV or oral contrast agents
• X-ray tube deterioration
• Improperly calibrated system (poorly centered phantom, used wrong phantom, replaced current
calibration files with extremely old Cal files)
• Beam hardening due to patient anatomy, especially bone.
To reduce CT Number variations:

• Warm up the X-ray tube whenever the system recommends it; make sure the tube design matches
the software configuration parameters
• Center the patient anatomy of interest in the gantry opening. Select an SFOV that encompasses
the patient.
• Acquire comparable images with similar scan and reconstruction choices.
• Maintain consistent table height throughout the exam.
• Test image quality on a regular basis to provide the numerical data to track system performance
over time.
To decrease the potential for misdiagnosis:

• Use ROI to compare pathology to surrounding tissue
• Scan structures with slice thicknesses about one-half the thickness of the lesion or less.
Example: Prescribe scan thickness of 5 mm or less to scan a lesion with a 10 mm thickness. (Display an
axial image and use the Measure Distance and ROI functions to determine the size of the pathology.)
Center ROI measurements over the midpoint of the pathology to minimize partial volume effects.
The mixture of tissue types, such as fat with tissue within the same voxel (a pixel with depth), varying
patient sizes, differences between CT machines and X-ray tubes, all lead to CT number variance. In a
well calibrated scanner, water has a CT number that ranges from -3 to +3. The CT number remains
uniform across all kV settings. However, as the X-ray tube ages, kV decreases and pixel values become
less dependable.
The Window Width and Window Level for GSI images will vary depending on the keV selected
compared to non-GSI images. Place an ROI on an anatomical area and note the mean value. Set
the Window Level to the mean value and adjust the Window Width to the desired viewing level.
23.6.2 Pixels
The anatomic image consists of rows and columns of small, square, picture elements called pixels. The
monitor displays 1,048,576 pixels in a matrix of 1024 horizontal rows of 1024 pixels. Add number of

General Information
viewports selected for viewing to determine the number of pixels used for display in each viewport.
The monitor pixel size remains the same, but the amount of anatomy the pixels represent varies with
the scan and display field of view (SFOV & DFOV). A pixel also represents a specific anatomic area. The
system identifies each two dimensional pixel by its location, area and value.
23.6.3 Pixel Coordinates

Describe pixel location two ways.
• Matrix Coordinates: Upper left pixel = (0,0);
Lower right pixel = (511,511);
Pixel in center of matrix = (255,255);
Pixel ten columns to the right = (10,0)
Figure 514 RAS Coordinates Schematic
NOTE
The illustration above represents a 512 x 512 matrix viewport.
• RAS: Anatomic distance from the center of the landmark slice

General Information
Target the image; decrease the DFOV diameter. Center the reconstruction on coordinates other than
the SFOV center.
Magnifying and targeting can displace the central SFOV pixel from the central monitor pixel. Look at
the DFOV coordinates and magnification annotation to find the SFOV center, or display the grid. The
grid always appears over the pixel in the center of the DFOV Matrix (coordinate 255,255).
23.6.4 RAS Coordinates

These three distances in millimeters appear on the upper left of the viewport on which the mouse
cursor is on, when Continuous Report Cursor is selected.
• The pixel with the R/L and A/P coordinates closest to zero, represents the SFOV center. The S/I
coordinate always equals the table location at isocenter.
• Coordinates transition from R to L, A to P, and S to I, to show relationships between current
location, landmark location, and isocenter.
Figure 515 RAS Coordinates Schematic
Table 166
Right: Coordinate location falls to the patient's right of the mid-sagittal

plane (right of isocenter)
Left: Coordinate location falls to the patient's left of the mid-sagittal

plane (left of isocenter)
Anterior Coordinate location falls above the mid-coronal plane (above

isocenter)
Posterior: Coordinate location falls below the mid-coronal plane (below

isocenter)

General Information
Inferior: Scan location falls between the selected landmark and patient's
feet
Superior: Scan location falls between the selected landmark and patient's
head
The DFOV and matrix determine pixel size.

A reconstructed pixel size is determined by dividing the Display FOV (in mm) by the reconstruction
matrix size. You may magnify pixels up to eight times the reconstructed size, or minify them to one
half size. The anatomic area represented by each monitor pixel decreases as the magnification factor
increases; anatomic area/monitor pixel increases as the magnification factor decreases.
Table 167
Pixel Size in millimeters
DFOV in cm 512 x 512 1024 x 1024
5 0.10 0.05
10 0.20 0.10
15 0.29 0.15
20 0.39 0.20
22 0.43 0.22
25 0.49 0.25
30 0.59 0.30
35 0.68 0.34
40 0.78 0.39
45 0.88 0.44
50 0.98 0.49
The DFOV determines the anatomic area imaged by a single reconstruction.

• Area equals pr2 (Area = 3.14 x radius x radius)
• The 50 cm FOV has a 25 cm radius, so its area equals 1963 cm2.
• The ROI or magnification factor determines the anatomic area covered by a magnified image.
Example: A monitor pixel represents 0.5 by 0.5 mm. Magnify pixel size by 2. Each monitor pixel now
represents 0.25 by 0.25 mm of anatomy.

General Information
Figure 516 Pixel Size and DFOV Illustration
23.6.5 Pixels and CT Numbers

Besides anatomic location and area, each CT pixel also represents a CT number, which in turn
indicates tissue density.
• An ROI averages the values of the enclosed pixels, and displays the resulting Mean value.
• Standard Deviation describes the difference between the minimum and maximum ROI value.
• A large ROI provides a larger, more accurate statistical sample than a small ROI.
An image pixel represents a three dimensional volume, or voxel. It represents anatomy with a
location, an area, and a pixel (density) value. The system flattens the 0.625, 1.25, 2.5, 3.75, and 5
mm scan thickness into a two dimensional screen image. If a pixel represents a variety of tissues,
the system averages the contents to produce an averaged, rather than accurate, pixel value. Uniform
tissues (within the voxel) produce fairly accurate pixel values.
CT pixel shading shows relative density. Denser materials weaken X-ray and produce whiter pixels.
(Assumes Inverse Video OFF)
Reformat displays non axial planes created from contiguous pixels extracted from multiple images.
3D locates similar pixel values within contiguous images, and generates a mathematical model to
produce images that appear three dimensional. BMD samples pixel values to estimate bone or tissue
density.
Reconstruction assigns one value to every image pixel. CT uses pixel values of -32767 to +32767.
MR uses pixel values of +16,000. The screen pixel translates the assigned value into one of the 256

General Information
shades of gray. Vary the gray scale window width and level to select anatomy for display. Window
Width determines the quantity of gray pixel values. Window Level selects the center Window Width
pixel value.
Example: Two windows may contain identical widths of 100 values, but display completely different
anatomy, because one has a level of -100 and the other has a level of 150.
23.6.6 Window Width

The system uses 256 gray shades to display 63,486 CT pixel values. The Window Width selection
determines the number of CT values represented by each shade of gray. A narrow window assigns
fewer pixels to each gray level than a wide window.
Example: WW = 256 System assigns one pixel value to each gray shade WW = 2560 System assigns ten
pixel values to each gray shade.
23.6.7 Window Level

The Level equals the CT number value of pixel in the center of the Window Width range. The Level
value receives the middle shade of gray. The system displays pixel values that fall between the center
and upper window level as gray to off white. It displays pixel values that fall between the center and
lower window values as gray to charcoal. When you change the level, the window width moves up
and down the CT number line. The CT values change with Window Level, but the Window Width and
number of pixels per gray level don’t change.
Inverse Video reverses display conventions. Dense or high numbers are portrayed as black rather than
white.
23.7 Scout Based Attenuation Characterization

A patient’s size, shape and density define the attenuation characteristics seen by the X-rays. An
understanding of the desired image quality (noise and contrast) and the attenuation characteristics of
the region being scanned can be used to determine the required scan technique factors (kVp and mA).
Automatic characterization of the patient’s attenuation can enable a CT system to aid the user in
determining the scan technique factors required to achieve the desired image quality. The scout image
is a measurement of the distribution of the attenuation for the patient. This distribution of attenuation
can be analyzed to give a metric of total attenuation (or patient size) and a metric of patient shape.
One size metric that can be used is Water Equivalent Diameter, Dw. This is the diameter of a uniform
cylinder of water that gives the same total attenuation as the patient. Although Dw assumes a circular
water object, patients are rarely circular. Most anatomical regions, however, can be approximated as
ovals. Therefore, in addition to Dw, it is beneficial to have a shape metric to indicate how non-circular
the anatomy is. One shape metric is the Oval Ratio, OR. The OR is the ratio of the major and minor
diameters, with a value of 1 indicating a circle. Together, these two metrics can be determined at
every location over the selected scan range of the patient to create a 3D characterization of the
attenuation. This information can then be used by different applications, such as SmartmA, kV Assist,
Auto Prescription and GSI Assist.
The following are some examples of phantom images and their representative Dw and OR
characterizations:

General Information
Figure 517 35cm Polyethylene Phantom with Water Equivalent Diameter = 33.6cm (OR=1)
Figure 518 20x32cm Polyethylene Phantom shown with overlay indicating: Left - Water
Equivalent Diameter = 24.3 cm (OR=1) and Right - Ellipse based on Dw and OR (OR=1.58)

General Information
Figure 519 Thorax Phantom shown with overlay indicating: Left - Water Equivalent Diameter =
22.1cm (OR=1) and Right - Ellipse based on Dw and OR (OR=1.08)
Figure 520 Large Thorax Phantom shown with overlay indicating: Left - Water Equivalent
Diameter = 33.8cm (OR=1) and Right - Ellipse based on Dw and OR (OR=1.14)
Since these metrics are dependent on the attenuation distribution, Dw and OR measurements can
vary across the entire anatomical region. In an anatomical area like the abdomen, which contains little
air pockets, the Dw is similar to the average physical diameter of the patient. But for an area like the
chest, which contains the lungs, Dw may be significantly smaller than the average diameter.
An example of this behavior can be seen in the figure below of a scout torso phantom with the
measured Dw and OR at different locations.

General Information
Figure 521 Scout of Torso Phantom in Lateral View (middle) with measured Water Equivalent
Diameter (top) and (bottom) Oval Ratio Torso images from the scout are shown with their
representative Dw and OR characterizations.
Figure 522 Torso Phantom shown with overlay indicating: Left - Water Equivalent Diameter =

General Information
Figure 523 Torso Phantom shown with overlay indicating: Left - Water Equivalent Diameter =

General Information

Operator Messages
Appendix A Operator Messages
A.1 Operator Messages

This appendix lists user messages that are posted to the user interface. These message are displayed
in one or more of the following areas.

Operator Messages
Areas where messages are posted to the user interface
Attention pop up dialog. Message area (1) and message history pull down (2) of
the System Status Area on the image monitor.
Real Time information area (1) of the scan progress Scan Settings parameter alerts.
screen on the left monitor.

Operator Messages
(continued)
Areas where messages are posted to the user interface
Gantry Display
Table 168 Gantry Hardware Operator Messages
Num- English Operator Message Translated Operator Message

ber
Command to disable Gantry rotation failed. Command to disable Gantry rotation failed.
1 Power to Gantry rotation has been removed. Power to Gantry rotation has been removed.
See service log for details. See service log for details.
Covers Open. Covers Open.

Please ensure that the gantry covers are closed. Please ensure that the gantry covers are closed.
2
If problem persists, contact your service repre- If problem persists, contact your service repre-
sentative. sentative.
E-stop System Failure. E-stop System Failure.

3
Please contact your service representative. Please contact your service representative.
Gantry Rotation Hardware Unavailable. Gantry Rotation Hardware Unavailable.

Select Resume to retry the scan. Select Resume to retry the scan.
4 If unable to Resume, please perform a Scan Hard- If unable to Resume, please perform a Scan Hard-
ware Reset from the Service Tools menu. ware Reset from the Service Tools menu.
Gantry Rotation Hardware Unavailable. Gantry Rotation Hardware Unavailable.

Please wait for gantry rotation to stop, then select Please wait for gantry rotation to stop, then select
Resume to retry the scan. If unable to Resume, Resume to retry the scan. If unable to Resume,
5 perform a Scan Hardware Reset from the Service perform a Scan Hardware Reset from the Service
Tools menu. Tools menu.

Operator Messages
Gantry Hardware Operator Messages continued

ber
Gantry Rotation is Not Available. Gantry Rotation is Not Available.

Please perform a Scan Hardware Reset from the Please perform a Scan Hardware Reset from the
6 Service Tools menu. Service Tools menu.
Gantry Hardware is unavailable. Gantry Hardware is unavailable.

Gantry Hardware Unavailable. Gantry Hardware Unavailable.

Please select Resume to retry the scan. If unable Please select Resume to retry the scan. If unable
to Resume, select Done Scanning and perform to Resume, select Done Scanning and perform
8 a Scan Hardware Reset from the Service Tools a Scan Hardware Reset from the Service Tools
menu. menu.


Please select Done Scanning and perform a Scan Please select Done Scanning and perform a Scan
10 Hardware Reset from the Service Tools menu. Hardware Reset from the Service Tools menu.
System rotating power unavailable. System rotating power unavailable.

11 Scanning is not possible. Scanning is not possible.
System rotating power unavailable. System rotating power unavailable.

Scanning is not possible. Scanning is not possible.
12 Please perform a Scan Hardware Reset from the Please perform a Scan Hardware Reset from the
Service Tools menu. Service Tools menu.

Operator Messages

ber
System X-ray power unavailable. System X-ray power unavailable.

13 Scanning is not possible. Scanning is not possible.
Gantry is too hot to operate. Contact your service Gantry is too hot to operate. Contact your service
14 representative to determine cause of overheat- representative to determine cause of overheat-
ing. ing.
Gantry Thermal Hardware Unavailable. Gantry Thermal Hardware Unavailable.

If problem persists, please contact your service If problem persists, please contact your service
representative. representative.
Gantry Hardware Unavailable. Gantry Hardware Unavailable.

Scan hardware is too hot to operate. Scanning Scan hardware is too hot to operate. Scanning
may be available after 30 minutes of cooling. may be available after 30 minutes of cooling.
17
Contact your service representative to determine Contact your service representative to determine
cause of overheating. cause of overheating.
Control panel on gantry front left is disconnected. Control panel on gantry front left is disconnected.
18
Please use alternative gantry control panel. Please use alternative gantry control panel.
Control panel on gantry front right is disconnec- Control panel on gantry front right is disconnec-
19
ted. Please use alternative gantry control panel. ted. Please use alternative gantry control panel.
Control panel on gantry rear left is disconnected. Control panel on gantry rear left is disconnected.
20
Please use alternative gantry control panel. Please use alternative gantry control panel.
Control panel on gantry rear right is disconnec- Control panel on gantry rear right is disconnec-
21
ted. Please use alternative gantry control panel. ted. Please use alternative gantry control panel.

Operator Messages

ber
X-Ray Tube is not in optimal operating state. X-Ray Tube is not in optimal operating state.
Maximum mA allowed will be limited for the ex- Maximum mA allowed will be limited for the ex-
am which may impact image quality. am which may impact image quality.
GSI acquisition cannot be confirmed until Tube GSI acquisition cannot be confirmed until Tube
22 Warm-up is completed. Warm-up is completed.
Select Done Scanning, if available. Select Done Scanning, if available.
Select Tools, Daily Prep, Tube Warm-up and com- Select Tools, Daily Prep, Tube Warm-up and com-
plete Tube Warm-up to enable full mA range ca- plete Tube Warm-up to enable full mA range ca-
pability and GSI acquisition. pability and GSI acquisition.
X-Ray Tube is not in optimal operating state. X-Ray Tube is not in optimal operating state.
Maximum mA allowed will be limited for the ex- Maximum mA allowed will be limited for the ex-
am which may impact image quality. am which may impact image quality.
23 Select Done Scanning, if available. Select Done Scanning, if available.
Select Tools, Daily Prep, Tube Warm-up and com- Select Tools, Daily Prep, Tube Warm-up and com-
plete Tube Warm-up to enable full mA range ca- plete Tube Warm-up to enable full mA range ca-
pability. pability.
System detected problem with detection compo- System detected problem with detection compo-
nent. nent.
24 Please run Fast Calibration. Please run Fast Calibration.
If problem persists contact your service represen- If problem persists contact your service represen-
tative. tative.
Detector thermal control has detected a system Detector thermal control has detected a system
pressure that has exceeded a pressure limit or pressure that has exceeded a pressure limit or
25
has lost all pressure sensors. System is entering has lost all pressure sensors. System is entering
protect mode and will shut down. protect mode and will shut down.
System configuration mismatch. Patient scanning System configuration mismatch. Patient scanning
26 will be disabled. will be disabled.
Table 169 Acquire Scan Operator Messages

ber
SPRsnap is in progress. Do not start any scan SPRsnap is in progress. Do not start any scan
1
acquisition until the snap is complete. acquisition until the snap is complete.
Do not execute during acquisition! Complete cur- Do not execute during acquisition! Complete cur-
2 rent acquisition before proceeding. Select OK to rent acquisition before proceeding. Select OK to
Continue. Continue.

Operator Messages
Acquire Scan Operator Messages continued

ber
Data Collection Hardware Unavailable. Data Collection Hardware Unavailable.

Data Collection Hardware configured incorrectly. Data Collection Hardware configured incorrectly.
4 Slip ring miswired. Slip ring miswired.
Data Collection Hardware Unavailable. Data Collection Hardware Unavailable.

The scan database is corrupted. The scan database is corrupted.

If you continue to use the system you might prop- If you continue to use the system you might prop-
agate the corruption. Please perform a System agate the corruption. Please perform a System
6 Restart from the Mode menu in order to automat- Restart from the Mode menu in order to automat-
ically recover the database. ically recover the database.
Unable to reserve scan data. Unable to reserve scan data.

7 Please perform a System Restart from the Mode Please perform a System Restart from the Mode
menu. menu.
Acquired data is corrupt. Acquired data is corrupt.

8 Scanning will be disabled. Scanning will be disabled.
Failed to start exposure due to system problem. Failed to start exposure due to system problem.
Scan time out. Scan time out.
9
Actual dose information for the scanned group Actual dose information for the scanned group
unavailable, recorded dose has been estimated unavailable, recorded dose has been estimated
10 from the scan prescription. from the scan prescription.
Firmware reset occurred. Please wait until reset is Firmware reset occurred. Please wait until reset is
11
completed. completed.

Operator Messages

ber
12 Landmark not set. Landmark not set.
13 Prescribed interscan delay not met. Prescribed interscan delay not met.
Real Time Display error. Real Time Display error.

Displayed indication may be inconsistent with ac- Displayed indication may be inconsistent with ac-
14
tual system state. tual system state.
System configuration data is invalid or corrupt. System configuration data is invalid or corrupt.
Please perform a System Restart from the Mode Please perform a System Restart from the Mode
15 menu. menu.
Unable to verify system configuration. Unable to verify system configuration.

Patient Scanning may be possible with degraded Patient Scanning may be possible with degraded
16
performance and/or functionality. performance and/or functionality.
The system configuration has changed since the The system configuration has changed since the
system was started. system was started.
17
menu. menu.
System could not detect ECG Triggers. System could not detect ECG Triggers.
18
Please check ECG lead connection. Please check ECG lead connection.
System detected software error during scanning. System detected software error during scanning.
19 menu. menu.
System is recovering after serious error, please System is recovering after serious error, please
20 check suspended image reconstructions in the check suspended image reconstructions in the
queue. queue.
Table position detected outside of scan start and Table position detected outside of scan start and
end positions during AEC scan. end positions during AEC scan.
21

Operator Messages

ber
X-ray exposure terminated by backup timer in- X-ray exposure terminated by backup timer in-
22 stead of normal control. stead of normal control.
Pause failed. Please retry Pause, press Stop Scan, Pause failed. Please retry Pause, press Stop Scan,
23
or press E-stop. or press E-stop.
24 Stop Scan failed. Please retry or press E-stop. Stop Scan failed. Please retry or press E-stop.
Laser alignment lights are automatically turned Laser alignment lights are automatically turned
25
off during scanning. off during scanning.
Scan has completed but the injection is still in Scan has completed but the injection is still in
26
progress. progress.
Cannot open a new review session while on scan Cannot open a new review session while on scan
progress screen. Please complete the scan in pro- progress screen. Please complete the scan in pro-
27 gress and then open the desired session. gress and then open the desired session.
Close if any of the following application(s) are Close if any of the following application(s) are
running: running:
Protocol Management is not available while in an Protocol Management is not available while in an
active scan session. active scan session.
28
running: running:
Auto Gating Management is not available while in Auto Gating Management is not available while in
an active scan session. an active scan session.
29
running: running:
Auto Voice management is not available while in Auto Voice management is not available while in
30
running: running:
User Admin application is not available while in User Admin application is not available while in
31
running: running:
Dose Check Management is not available while in Dose Check Management is not available while in
32
running: running:

Operator Messages

ber
Audit Tool application is not available while in an Audit Tool application is not available while in an
33
running: running:
Switch User cannot be completed at this time. Switch User cannot be completed at this time.
Please complete the scan in progress and then Please complete the scan in progress and then
34 switch users. switch users.
running: running:
Fast Cal application is not available while in an Fast Cal application is not available while in an
35
running: running:
Scan cannot be resumed as a irrecoverable sys- Scan cannot be resumed as a irrecoverable sys-
tem error has occurred. tem error has occurred.
36
Please select Done Scanning and start a new pa- Please select Done Scanning and start a new pa-
tient session or restart the system. tient session or restart the system.
37 QC Recon Job Failed. QC Recon Job Failed.
Image Generation unavailable. Image Generation unavailable.

Further scanning or reconstructions cannot be Further scanning or reconstructions cannot be
38 performed. Restart the system. performed. Restart the system.
Low ECG signal. Verify the following: Low ECG signal. Verify the following:
• Select the lead with the highest amplitude, • Select the lead with the highest amplitude,
typically Lead II or AUTO. typically Lead II or AUTO.
• The proper placement of the ECG electro- • The proper placement of the ECG electro-
des. The ECG electrodes may need to be des. The ECG electrodes may need to be
repositioned. repositioned.
39 • The ECG electrodes still have moist conduc- • The ECG electrodes still have moist conduc-
tive gel. tive gel.
• Perform impedance test to check ECG sig- • Perform impedance test to check ECG sig-
nal. nal.
Override may cause erratic triggering and possi- Override may cause erratic triggering and possi-
bly a scan abort. Override only when absolutely bly a scan abort. Override only when absolutely
necessary. necessary.
40 Low signal warning has been overridden by user. Low signal warning has been overridden by user.

Operator Messages

ber
Queuing of Auto Transfer jobs failed. Please trans- Queuing of Auto Transfer jobs failed. Please trans-
fer images, series or exam manually from the File fer images, series or exam manually from the File
41 Manager. Please perform Application Restart from Manager. Please perform Application Restart from
the Troubleshooting menu to restart the Auto the Troubleshooting menu to restart the Auto
Transfer application. Transfer application.
One of the following fields contains a character One of the following fields contains a character
42
that is not supported. that is not supported.
Could not acquire Scan Hardware Resource. Could not acquire Scan Hardware Resource.
This may have occurred due to one of the follow- This may have occurred due to one of the follow-
ing: ing:
• Scan Data Save or Restore is in progress • Scan Data Save or Restore is in progress
43 • Daily Prep is in progress • Daily Prep is in progress
• Service scanning tools are in use • Service scanning tools are in use
• Scanning Session is open • Scanning Session is open
Please wait for completion or cancel the job or Please wait for completion or cancel the job or
queue in progress by the application. queue in progress by the application.
Dynamic Transition is enabled and there is no Dynamic Transition is enabled and there is no
dynamic transition ROI selected. Please add an dynamic transition ROI selected. Please add an
44
ROI to the baseline image or disable dynamic ROI to the baseline image or disable dynamic
transition in the Baseline and Monitor Collection transition in the Baseline and Monitor Collection
You are about to exit the SmartPrep workflow. You are about to exit the SmartPrep workflow.
If you exit and still want to include a SmartPrep If you exit and still want to include a SmartPrep
45 phase, you will need to duplicate the series and phase, you will need to duplicate the series and
delete the un-scanned group in the current ser- delete the un-scanned group in the current ser-
ies. Are you sure you want to continue? ies. Are you sure you want to continue?
Post processing application is open. Please close Post processing application is open. Please close
46 the post processing application to enable Con- the post processing application to enable Con-
firm Settings. firm Settings.
Reconstruction System error occurred. Please Reconstruction System error occurred. Please
47 wait for the following number of seconds for the wait for the following number of seconds for the
recovery: recovery:
Integrated Hand-held controller connection error. Integrated Hand-held controller connection error.
48
Please check the connection. Please check the connection.
49
50

Operator Messages

ber
51
Interventional Foot pedal connection error. Interventional Foot pedal connection error.
52
Interventional Foot Pedal Stuck. Please check the Interventional Foot Pedal Stuck. Please check the
53
foot pedal. foot pedal.
Abnormal heart beat detected during Smart Ar- Abnormal heart beat detected during Smart Ar-
rhythmia Management Scan. System reacquiring rhythmia Management Scan. System reacquiring
54
scan. Review the ECG Editor in the secondary scan. Review the ECG Editor in the secondary
recon for details. recon for details.
Lost connection with the X-Ray foot Pedal. Lost connection with the X-Ray foot Pedal.
Check that the pedal is connected. Check that the pedal is connected.
If it is and problem persists, Revisit Settings, de- If it is and problem persists, Revisit Settings, de-
55 lete any unscanned interventional groups or ser- lete any unscanned interventional groups or ser-
ies to continue with non-interventional scans. ies to continue with non-interventional scans.
If problem still persists, contact your service rep- If problem still persists, contact your service rep-
resentative. resentative.
System has detected the X-Ray foot Pedal has System has detected the X-Ray foot Pedal has
been depressed for more than 10 seconds. been depressed for more than 10 seconds.
Check that the foot pedal is not depressed. Check that the foot pedal is not depressed.
56 If it is not and problem persists, delete any un- If it is not and problem persists, delete any un-
scanned interventional groups or series to con- scanned interventional groups or series to con-
tinue with non-interventional scans. tinue with non-interventional scans.
Unrecognized System Configuration detected. Pa- Unrecognized System Configuration detected. Pa-
tient Scanning may still be possible with poten- tient Scanning may still be possible with poten-
57 tially degraded performance and/or functionality. tially degraded performance and/or functionality.
SmartPlan does not support Secondary Recon- SmartPlan does not support Secondary Recon-
58 structions associated with linked groups. Please structions associated with linked groups. Please
use Copy Forward or Unlink the primary groups. use Copy Forward or Unlink the primary groups.
SmartPlan Clinical Category Clinical Identifier SmartPlan Clinical Category Clinical Identifier
pair selection is incompatible with selected pa- pair selection is incompatible with selected pa-
59 tient position. Please select a different patient tient position. Please select a different patient
position in the Patient Collection or change the position in the Patient Collection or change the
SmartPlan setting SmartPlan setting

Operator Messages

ber
Copy Forward and SmartPlan cannot be enabled Copy Forward and SmartPlan cannot be enabled
60 together. Please select only one of SmartPlan and together. Please select only one of SmartPlan and
Copy Forward. Copy Forward.
SmartPlan CID selection has automatically SmartPlan CID selection has automatically
61 changed the setting of SmartPlan DFOV/Center changed the setting of SmartPlan DFOV/Center
Adjust. Please confirm the setting. Adjust. Please confirm the setting.
SmartPlan was unable to determine the location SmartPlan was unable to determine the location
of the anatomy requested by Clinical Category of the anatomy requested by Clinical Category
62
Clinical Identifier pair. Please adjust scan range Clinical Identifier pair. Please adjust scan range
manually. manually.
SmartPlan does not support the selected Clini- SmartPlan does not support the selected Clini-
cal Category Clinical Identifier pair. Please select cal Category Clinical Identifier pair. Please select
63
a supported Clinical Category Clinical Identifier a supported Clinical Category Clinical Identifier
pair. pair.
Lost connection with the Integrated Hand-held Lost connection with the Integrated Hand-held
Controller: Controller:
Check that the controller is connected. Check that the controller is connected.
64 If it is and problem persists, Revisit Settings de- If it is and problem persists, Revisit Settings de-
lete any unscanned interventional groups or ser- lete any unscanned interventional groups or ser-
ies to continue with non-interventional scans. ies to continue with non-interventional scans.
The scan database encountered an error. The scan database encountered an error.
65
Please restart applications to recover. Please restart applications to recover.
Image Generation was NOT ready. Image Generation was NOT ready.
Press Resume. Press Resume.
66 If problem persists, Pause Scan, Revisit Settings, If problem persists, Pause Scan, Revisit Settings,
Confirm Settings, and press Prep Confirm Settings, and press Prep
DLIR processing cannot be applied with the cur- DLIR processing cannot be applied with the cur-
rently selected recon type. rently selected recon type.
67
Please select a compatible recon type to enable Please select a compatible recon type to enable
the selection of DLIR processing. the selection of DLIR processing.

Operator Messages

ber
DLIR processing cannot be applied in combina- DLIR processing cannot be applied in combina-
tion with 0.625mm thickness, pitch 0.5 and Full tion with 0.625mm thickness, pitch 0.5 and Full
68 Recon mode. Recon mode.
Please select Plus Recon Mode, or a different slice Please select Plus Recon Mode, or a different slice
thickness in order to enable DLIR processing. thickness in order to enable DLIR processing.
DLIR processing cannot be enabled when the DLIR processing cannot be enabled when the
scan range is less than 40mm. scan range is less than 40mm.
69
Set the scan range to 40mm or greater to enable Set the scan range to 40mm or greater to enable
DLIR processing. DLIR processing.
Table 170 Scan Set Up Operator Messages

ber
Patient orientation/position has changed from Patient orientation/position has changed from
the previous series. the previous series.
1 Please verify the orientation/position of this ser- Please verify the orientation/position of this ser-
ies is as intended or change the orientation/posi- ies is as intended or change the orientation/posi-
tion, if needed. tion, if needed.
The table landmark has been changed. This The table landmark has been changed. This
changes the location of all scans you have pre- changes the location of all scans you have pre-
2
scribed. Double check all scans locations before scribed. Double check all scans locations before
you start scanning. you start scanning.
Dynamic Transition in Smart Prep is ON. Sys- Dynamic Transition in Smart Prep is ON. Sys-
tem will automatically transition into Scan Phase tem will automatically transition into Scan Phase
3 when enhancement level for Transition ROI rea- when enhancement level for Transition ROI rea-
ches the HU value set for threshold. Please con- ches the HU value set for threshold. Please con-
firm that the Transition ROI is set appropriately. firm that the Transition ROI is set appropriately.
Image generation failed, scanning is paused: Use Image generation failed, scanning is paused: Use
4 the elapsed time to determine when to select the elapsed time to determine when to select
Begin Scan Now. Begin Scan Now.
The baseline location has changed. The baseline location has changed.
You may proceed, but ROIs and dynamic transi- You may proceed, but ROIs and dynamic transi-
5 tion will be disabled. If you wish to use ROIs, tion will be disabled. If you wish to use ROIs,
please select [Retake Baseline] to acquire a new please select [Retake Baseline] to acquire a new
baseline image. baseline image.
The baseline location has changed. Dynamic The baseline location has changed. Dynamic
Transition is disabled. Transition is disabled.
6 Use the Monitor images to determine the transi- Use the Monitor images to determine the transi-
tion or select [Revisit Settings] to start a new tion or select [Revisit Settings] to start a new
Smart Prep series. Smart Prep series.

Operator Messages
Scan Set Up Operator Messages continued

ber
Injector is not armed. Please arm the injector or Injector is not armed. Please arm the injector or
7 select Disable the Injector from the Contrast col- select Disable the Injector from the Contrast col-
lection. lection.
The injector is not communicating or is not in the The injector is not communicating or is not in the
right state. right state.
Please cycle power on the injector or disable the Please cycle power on the injector or disable the
8
Injector in the Contrast collection. Injector in the Contrast collection.
If the problem persists, contact your service rep- If the problem persists, contact your service rep-
There is a mismatch with the Injector settings. There is a mismatch with the Injector settings.
9 Please check the injection settings in the Contrast Please check the injection settings in the Contrast
collection. collection.
Please select Revisit Settings and check Injector Please select Revisit Settings and check Injector
10 settings or disable the Injector from the Contrast settings or disable the Injector from the Contrast
collection. collection.
Injector is not ready. Please cycle power on the Injector is not ready. Please cycle power on the
11 injector or select Injector Off to disable the Injec- injector or select Injector Off to disable the Injec-
tor from the Contrast collection. tor from the Contrast collection.
Internal communication error. Internal communication error.

System detected internal communication error. System detected internal communication error.
Please select [Done Scanning] or [Close Exam] Please select [Done Scanning] or [Close Exam]
and perform a Scan Hardware Reset from the and perform a Scan Hardware Reset from the
ODM has been disabled. Verify Noise Index, Min ODM has been disabled. Verify Noise Index, Min
mA/Max mA, resultant CTDIvol and DLP meet the mA/Max mA, resultant CTDIvol and DLP meet the
14
clinical goal of the acquisition and follow the ra- clinical goal of the acquisition and follow the ra-
diation exposure guidelines for your department. diation exposure guidelines for your department.
Projected noise index is less than the prescribed Projected noise index is less than the prescribed
15 noise index. Review and reduce minimum mA, if noise index. Review and reduce minimum mA, if
appropriate. appropriate.

Operator Messages

ber
SmartmA, ODM and kV Assist unavailable due SmartmA, ODM and kV Assist unavailable due
to patient orientation/position mismatch. Scan a to patient orientation/position mismatch. Scan a
16
scout with the same patient orientation/position scout with the same patient orientation/position
or Manual mA and kV must be set. or Manual mA and kV must be set.
SmartmA, ODM, and kV Assist unavailable due SmartmA, ODM, and kV Assist unavailable due
to new landmark. Scan a scout with the current to new landmark. Scan a scout with the current
17
landmark if appropriate or Manual mA and kV landmark if appropriate or Manual mA and kV
must be set. must be set.
kV Assist mode has been enabled. kV Assist mode has been enabled.
Verify kV, Noise Index, Min mA/Max mA, or kV, Verify kV, Noise Index, Min mA/Max mA, or kV,
18 Manual mA values and resultant CTDIvol and DLP Manual mA values and resultant CTDIvol and DLP
meet the clinical goal for the acquisition and fol- meet the clinical goal for the acquisition and fol-
low the radiation exposure guidelines for your low the radiation exposure guidelines for your
department. department.
Manual kV mode enabled or kV Assist baseline (kV Manual kV mode enabled or kV Assist baseline
Assist Delta) has been enabled. has been enabled.
Verify kV, Noise Index, Min mA/Max mA, or kV, Verify kV, Noise Index, Min mA/Max mA, or kV,
19 Manual mA values and resultant CTDIvol and DLP Manual mA values and resultant CTDIvol and DLP
meet the clinical goal for the acquisition and fol- meet the clinical goal for the acquisition and fol-
Manual mA mode has been enabled. Verify the Manual mA mode has been enabled. Verify the
prescribed mA and resultant CTDIvol and DLP prescribed mA and resultant CTDIvol and DLP
20 meet the clinical goal for the acquisition and fol- meet the clinical goal for the acquisition and fol-
Prescribed NI cannot be achieved with selected Prescribed NI cannot be achieved with selected
29
scan parameters. scan parameters.
SmartmA has been enabled. Verify the Noise In- SmartmA has been enabled. Verify the Noise In-
dex, Min mA/Max mA values and resultant CTDIvol dex, Min mA/Max mA values and resultant CTDIvol
30 and DLP meet the clinical goal for the acquisition and DLP meet the clinical goal for the acquisition
and follow the radiation exposure guidelines for and follow the radiation exposure guidelines for
your department. your department.
SmartmA with ODM has been enabled. Verify the SmartmA with ODM has been enabled. Verify the
Noise Index, Min mA/Max mA, ODM range and Noise Index, Min mA/Max mA, ODM range and
31 the resultant CTDIvol and DLP meet the clinical the resultant CTDIvol and DLP meet the clinical
goal for the acquisition and follow the radiation goal for the acquisition and follow the radiation
exposure guidelines for your department. exposure guidelines for your department.
32 Early Beat Avoidance disabled. Early Beat Avoidance disabled.
33 Irregular heart beats detected prior to scan. Irregular heart beats detected prior to scan.

Operator Messages

ber
Preparing to scan extremely high heart rate with Preparing to scan extremely high heart rate with
34 highly irregular beats. Verify the heart rate is valid highly irregular beats. Verify the heart rate is valid
for clinical indication. for clinical indication.
Preparing to scan extremely high heart rate with Preparing to scan extremely high heart rate with
35 irregular beats. Verify the heart rate is valid for irregular beats. Verify the heart rate is valid for
clinical indication. clinical indication.
Preparing to scan high heart rate with highly ir- Preparing to scan high heart rate with highly ir-
36 regular beats. Verify the heart rate is valid for regular beats. Verify the heart rate is valid for
Preparing to scan high heart rate with irregular Preparing to scan high heart rate with irregular
37 beats. Verify the heart rate is valid for clinical beats. Verify the heart rate is valid for clinical
indication. indication.
Preparing to scan intermediate heart rate with Preparing to scan intermediate heart rate with
highly irregular beats using narrow phase range. highly irregular beats using narrow phase range.
38
Verify that the acquisition phase range is valid for Verify that the acquisition phase range is valid for
Preparing to scan intermediate heart rate with Preparing to scan intermediate heart rate with
irregular beats using narrow phase range. Verify irregular beats using narrow phase range. Verify
39
that the acquisition phase range is valid for clini- that the acquisition phase range is valid for clini-
cal indication. cal indication.
Preparing to scan with extremely high and varia- Preparing to scan with extremely high and varia-
40 ble heart rate. Verify the heart rate is valid for ble heart rate. Verify the heart rate is valid for
Preparing to scan with extremely high heart rate. Preparing to scan with extremely high heart rate.
41
Verify the heart rate is valid for clinical indication. Verify the heart rate is valid for clinical indication.
There are still scan tasks to be completed. Done There are still scan tasks to be completed. Done
42 Scanning will end the scanning portion of this Scanning will end the scanning portion of this
exam. Are you sure you are done scanning? exam. Are you sure you are done scanning?
Tube temperature is too cold. Warm-up is nee- Tube temperature is too cold. Warm-up is nee-
43
ded. ded.
Attention Attention
An unrecognized tube has been installed on the An unrecognized tube has been installed on the
system. system.
44 Fast Calibration techniques are designed specifi- Fast Calibration techniques are designed specifi-
cally for GE tubes and GE cannot guarantee that cally for GE tubes and GE cannot guarantee that
the performance of the system will meet specifi- the performance of the system will meet specifi-
cations with an unrecognized tube. cations with an unrecognized tube.

Operator Messages

ber
An unrecognized X-Ray tube has been installed on An unrecognized X-Ray tube has been installed on
the system. the system.
GE cannot assure that system performance will GE cannot assure that system performance will
conform to specifications. conform to specifications.
45
Advisory messages will be posted to the operator Advisory messages will be posted to the operator
about an unrecognized tube during tube warm- about an unrecognized tube during tube warm-
up, during Fast Calibration, and in the dose re- up, during Fast Calibration, and in the dose re-
port. port.
Gantry balance sensing hardware unavailable. Gantry balance sensing hardware unavailable.
46 Fast Cal and Detailed Cal will not be possible. Fast Cal and Detailed Cal will not be possible.
Patient Name, ID or Date of Birth is mismatched. Patient Name, ID or Date of Birth is mismatched.
47 Please edit the patient information on the RIS, Please edit the patient information on the RIS,
refresh the list and retry. refresh the list and retry.
Cannot start a New Patient scan session while in Cannot start a New Patient scan session while in
48
running: running:
Cannot switch patient sessions while on the scan Cannot switch patient sessions while on the scan
progress screen. progress screen.
49
running: running:
Patient Information currently displayed is from a Patient Information currently displayed is from a
previous selection in the Patient Schedule or a previous selection in the Patient Schedule or a
manual entry. manual entry.
50
Select the X at the top of the New Patient tab Select the X at the top of the New Patient tab
and then re-enter patient information manually and then re-enter patient information manually
or from the Patient Schedule or from the Patient Schedule
This scan prescription has selected one of the op- This scan prescription has selected one of the op-
tions for Recon based ACR Image Flip and Rotate. tions for Recon based ACR Image Flip and Rotate.
51 Please ensure that this desired orientation is dis- Please ensure that this desired orientation is dis-
played appropriately on all remote viewing devi- played appropriately on all remote viewing devi-
ces. ces.
Maximum number of exam sessions are currently Maximum number of exam sessions are currently
open. open.
Please complete, as needed, at least one exam Please complete, as needed, at least one exam
52
session. session.
Once a session is closed, start a new patient ses- Once a session is closed, start a new patient ses-
sion. sion.

Operator Messages

ber
Integrated Hand-held Controller is not connec- Integrated Hand-held Controller is not connec-
53 ted. Please check the connection to enable Con- ted. Please check the connection to enable Con-
firm Settings. firm Settings.
The Integrated Hand-held Controller hardware is The Integrated Hand-held Controller hardware is
unavailable. Remove the Interventional series to unavailable. Remove the Interventional series to
54
continue. If problem persists, contact your serv- continue. If problem persists, contact your serv-
ice representative ice representative
Integrated Hand-held controller hardware is un- Integrated Hand-held controller hardware is un-
55 available. Please contact your service representa- available. Please contact your service representa-
tive. tive.
Scan Center Location is outside table limits. Enter Scan Center Location is outside table limits. Enter
56 a location within table limits, or set a different a location within table limits, or set a different
landmark to enable Confirm Settings. landmark to enable Confirm Settings.
Exposure time is less than the minimum limit 1.0 Exposure time is less than the minimum limit 1.0
s. s.
57
Select Revisit Settings and Adjust the Total Expo- Select Revisit Settings and Adjust the Total Expo-
sure time. sure time.
SmartStep software option is not installed, inter- SmartStep software option is not installed, inter-
ventional series is disabled in the protocol. to ventional series is disabled in the protocol. to
continue scanning delete the Interventional ser- continue scanning delete the Interventional ser-
58 ies. ies.
Please contact your service representative to veri- Please contact your service representative to veri-
fy your configuration. fy your configuration.
System is not ready to perform the Interventional System is not ready to perform the Interventional
series. Select [Confirm Settings] again. If problem series. Select [Confirm Settings] again. If problem
59
persists, please select [Done Scanning] and then persists, please select [Done Scanning] and then
select System Restart from the Mode menu. select System Restart from the Mode menu.
System is not ready to perform the Intervention- System is not ready to perform the Intervention-
al series. Please select [Prep] again. If problem al series. Please select [Prep] again. If problem
60
persists, select [Done Scanning] and then select persists, select [Done Scanning] and then select
System Restart from the Mode menu. System Restart from the Mode menu.
System is not functional. Please select Revisit System is not functional. Please select Revisit
Settings and select Confirm Settings to continue. Settings and select Confirm Settings to continue.
61
If problem persists, select Done Scanning and If problem persists, select Done Scanning and
then select System Restart from the Mode menu. then select System Restart from the Mode menu.
The following installed option keys are not valid The following installed option keys are not valid
with the detected system configuration and will with the detected system configuration and will
62 be disabled. be disabled.
Please review any protocols utilizing these op- Please review any protocols utilizing these op-
tions to ensure they are still clinically relevant tions to ensure they are still clinically relevant

Operator Messages

ber
The group delay has increased from the protocol The group delay has increased from the protocol
value. Changing SFOV and or rotation time be- value. Changing SFOV and or rotation time be-
tween groups can cause large group delays which tween groups can cause large group delays which
63 may negatively affect contrast timing. Please re- may negatively affect contrast timing. Please re-
view and type the desired group delay value. If view and type the desired group delay value. If
changes between these parameters are desired, changes between these parameters are desired,
then turn Off Lock Group Delay. then turn Off Lock Group Delay.
Lock Group Delay has been turned Off. Please Lock Group Delay has been turned Off. Please
64 review the Group Delay value in the Timing Col- review the Group Delay value in the Timing Col-
lection. lection.
Image Enhance Filters are not compatible with Image Enhance Filters are not compatible with
Snapshot Freeze image reconstruction. Set Image Snapshot Freeze image reconstruction. Set Image
65 Enhance Filters to “None” in Recon Options or Enhance Filters to “None” in Recon Options or
turn Off Snap Shot Freeze in ECG and Gating Set- turn Off Snap Shot Freeze in ECG and Gating Set-
tings in secondary recon. tings in secondary recon.
No valid solutions available. Please select a dif- No valid solutions available. Please select a dif-
ferent clinical category from the Patient Collec- ferent clinical category from the Patient Collec-
66 tion, then select an appropriate Clinical Identifier tion, then select an appropriate Clinical Identifier
or change the mA Mode to GSI Manual and select or change the mA Mode to GSI Manual and select
a valid GSI Profile a valid GSI Profile
Invalid GSI prescription: Invalid GSI prescription:

Adjust to a valid prescription within the GSI Im- Adjust to a valid prescription within the GSI Im-
67
age Quality Widget age Quality Widget
Invalid Parameter = Invalid Parameter =
Invalid GSI profile, Please select a different clin- Invalid GSI profile, Please select a different clin-
ical category from the Patient Collection, then ical category from the Patient Collection, then
68 select an appropriate Clinical Identifier or change select an appropriate Clinical Identifier or change
the mA Mode to GSI Manual and select a valid GSI the mA Mode to GSI Manual and select a valid GSI
Profile Profile
GSI Assist has been enabled. Verify the Noise GSI Assist has been enabled. Verify the Noise
Index and resultant CTDIvol and DLP meet the Index and resultant CTDIvol and DLP meet the
69
clinical goal for the acquisition and follow the ra- clinical goal for the acquisition and follow the ra-
diation exposure guidelines for your department. diation exposure guidelines for your department.
GSI Manual mA mode has been enabled. Verify GSI Manual mA mode has been enabled. Verify
the GSI Settings and resultant CTDIvol and DLP the GSI Settings and resultant CTDIvol and DLP
70 meet the clinical goal for the acquisition and fol- meet the clinical goal for the acquisition and fol-
department department
Intervals less than 0.3125 are not supported with Intervals less than 0.3125 are not supported with
71
MAR, Turn off MAR or select an interval >= 0.3125 MAR, Turn off MAR or select an interval >= 0.3125

Operator Messages

ber
Currently selected GSI Profile does not have %s Currently selected GSI Profile does not have %s
scan type included. Change the scan type or se- scan type included. Change the scan type or se-
72
lect a GSI Profile that contains the scan type de- lect a GSI Profile that contains the scan type de-
sired. sired.
Image Enhance Filters are not compatible with Image Enhance Filters are not compatible with
GSI Data File. Set Image Enhance Filters to GSI Data File. Set Image Enhance Filters to
73
“None” in Recon Options or turn off Data File in “None” in Recon Options or turn off Data File in
primary or secondary recon. primary or secondary recon.
Table 171 Table Operator Messages

ber
Table received an invalid request. Please retry Table received an invalid request. Please retry
positioning the table. positioning the table.
1 If problem persists, select Done Scanning and If problem persists, select Done Scanning and
perform a Scan Hardware Reset from the Service perform a Scan Hardware Reset from the Service
Table did not reach position. Please retry posi- Table did not reach position. Please retry posi-
tioning the table. tioning the table.
2 If problem persists, select Done Scanning and If problem persists, select Done Scanning and
perform a Scan Hardware Reset from the Service perform a Scan Hardware Reset from the Service
Table motion is unavailable. Table motion is unavailable.

Table motion is unavailable. Table motion is unavailable.

Serious error detected during table operation. Serious error detected during table operation.
Please stop all table motions immediately using Please stop all table motions immediately using
E-stop. E-stop.
5 Please select Done Scanning and perform a Scan Please select Done Scanning and perform a Scan
Hardware Reset from the Service Tools menu. Hardware Reset from the Service Tools menu.

Operator Messages
Table Operator Messages continued

ber
Table is in service mode. Table is in service mode.
6 All table motion shall be controlled from the table All table motion shall be controlled from the table
service panel. Gantry control panels will be disa- service panel. Gantry control panels will be disa-
bled. bled.
An error was detected in the table firmware. An An error was detected in the table firmware. An
auto-recovery will be attempted. If the problem auto-recovery will be attempted. If the problem
7
persists, please contact your service representa- persists, please contact your service representa-
tive. tive.
Table has entered a fault state due to the repea- Table has entered a fault state due to the repea-
ted occurrence of the indicator listed below. ted occurrence of the indicator listed below.
Try to recover by pressing the Emergency Stop Try to recover by pressing the Emergency Stop
8
button and then the Driver Recovery button. button and then the Driver Recovery button.
If the problem persists, please contact your serv- If the problem persists, please contact your serv-
ice representative. ice representative.
Table 172 General System Operator Messages

ber
Can't establish Insite connection. Please check Can't establish Insite connection. Please check
1
your network configuration. your network configuration.
Image database is corrupted. Image database is corrupted.

2 menu. menu.
System firewall is not working or not configured. System firewall is not working or not configured.
3
System is vulnerable to security threats. System is vulnerable to security threats.
System detected a mismatch on the displayed System detected a mismatch on the displayed
information. information.
4
If the problem persists, please perform a Scan If the problem persists, please perform a Scan
Hardware Reset from the Service Tools menu. Hardware Reset from the Service Tools menu.
System detected internal communication error. System detected internal communication error.
5 Please perform a Scan Hardware Reset from the Please perform a Scan Hardware Reset from the
Service Tools menu. If problem persists, contact Service Tools menu. If problem persists, contact
your service representative. your service representative.
Low image space. Please remove images and Low image space. Please remove images and
6
empty the recycle bin. empty the recycle bin.

Operator Messages
General System Operator Messages continued

ber
To run SPR Snap first press Revisit Settings. To run SPR Snap first press Revisit Settings.
7 Close if any of the following application(s) are Close if any of the following application(s) are
running: running:
The currently logged user does not have a role The currently logged user does not have a role
8
assigned. assigned.
Image Database is full. Image Database is full.

Please select the exam(s), series or images, press Please select the exam(s), series or images, press
and hold Shift and then press Delete. and hold Shift and then press Delete.
9 If this does not resolve the issue, please perform If this does not resolve the issue, please perform
a System Restart from the Mode menu. a System Restart from the Mode menu.
Recon self test found reconstruction errors. Recon self test found reconstruction errors.
10
Please contact service Please contact service
Unable to verify system functionality on startup. Unable to verify system functionality on startup.
11 menu. menu.
If the problem persists, please contact your serv- If the problem persists, please contact your serv-
ice representative. ice representative.
One, or more components failed to report their One, or more components failed to report their
configuration. configuration.
Assuming previous configuration. Assuming previous configuration.
12 Please perform a System Restart from the Mode Please perform a System Restart from the Mode
menu. menu.

Operator Messages

Abbreviations
Appendix B Abbreviations
B.1 Abbreviations
Table 173 Abbreviations
Abbreviations Acronym
AW Advantage Workstation
CFR Code of Federal Regulations
cm Centimeter
CT Computed Tomography
CTDI Computed Tomography Dose In-

dex
DAS Data Acquisition System
DFOV Display Field of View
DICOM Digital Imaging and Communica-

tion in Medicine
DLP Dose Length Product
ECG Electro cardiogram
EMC Electro-magnetic Compatibility
EMI Electro-magnetic Immunity
FDA Food and Drug Administration
FWHM Full Width Half Maximum
FWTM Full Width Tenth Maximum
GSI Gemstone Spectral Imaging
HAP Hydroxyapatite
HU Hounsfield Units
HV High Voltage
IEC International Electro-technical

Commission
ISO Iso-center
IV Intra-venous

Abbreviations
Abbreviations continued
keV kilo-electronvolts (unit of energy

for GSI monochromatic images)
kg Kilogram
kV kilo-volts
kW kilo-watts
LCD Liquid Crystal Display
lb Pound
LCD Low Contrast Detectability
mA milli-amps
MAR Metal Artifact Reduction
MD Material Density
MDC Main Disconnect Control
mGy Milligray
ml Milliliter
mm Millimeter
MPR Multiplanar Reconstruction
ms millisecond
MTF Modulation Transfer Function
NCRP National Council on Radiation

Protection and Measurements
NIST National Institute of Standards

and Technology
PDU Power Distribution Unit
PM Planned Maintenance
PMMA Poly-methyl methacrylate
QA Quality Assurance
QEF Quality Equivalent Filtration
QSR Quality System Regulation
ROI Region of Interest

Abbreviations
Abbreviations continued
SATA Serial Advance Technology Attach-

ment
SCI Scan Control Interface
SFOV Scan Field of View
SSP Slice Sensitivity Profile
UL Underwriters’ Laboratories
VUE Virtual Unenhanced
WL Window Level
WW Window Width

Abbreviations

Units of Measure
Appendix C Units of Measure
C.1 Units of Measure

This appendix lists the units of measure used in this manual.
Table 174 Patient Information/Patient Schedule
Data Unit Symbol
Weight Kilogram kg
Weight Pounds lb
Height Centimeter cm
Height Inches in
Table 175 Scan Settings Window numeric indications
Data Unit Symbol
Rotation Time Second s
Slice Thickness Millimeter mm
Interval Millimeter mm
kV (Tube Voltage) Kilovolt kV
mA (Tube Current) Milliampere mA
Total Exposure Time Second s
Prep Group Second s
ISD Second s
Cine Duration Second s
DFOV Centimeter cm
R/L Center Millimeter mm
A/P Center Millimeter mm
CTDIvol Milligray mGy
DLP Milligray centimeter mGy cm
Phantom Size Centimeter cm

Units of Measure
Beam Collimation Millimeter mm
Axial Thickness Millimeter mm
Table 176 Smart Prep Setting
Data Unit Symbol
Monitoring Delay Second s
Monitoring Inter Scan Delay Second s
Diagnostic Delay Second s
mA (Tube Current) Milliampere mA
Table 177 Enhance Xtream Injector Setting
Data Unit Symbol
Inj. Delay Second s
Flow Rate Milliliter/Second ml/(s)
Duration Second s
Pressure Limit Kilopascal kPa
Remaining Contrast Media Milliliter ml
Remaining Saline Milliliter ml
Table 178 Auto Voice and Breathing Lights Selection
Data Unit Symbol
Preset Delay Time Second s
Table 179 Routine Display Tools — List/Select
Data Unit Symbol
im Ctr S-I Millimeter mm
Thick Millimeter mm
Gantry Degree °
Im Ctr R-L Millimeter mm
Im Ctr A-P Millimeter mm
SFOV Centimeter cm

Units of Measure
DFOV Centimeter or Millimeter cm or mm
Midscan Seconds s
Table 180 Exam Pg / Series Pg
Data Unit Symbol
Height Centimeter cm
Weight Kilogram kg
Table 181 Display result on an image for Image Measurements - Ellipse ROI / Box ROI / Trace ROI
Data Unit Symbol
a (Area) Square Millimeters mm2
Distance Millimeter mm
Angle Degree °
Table 182 Measure Angle
Data Unit Symbol
Angle Degree °
Table 183 Scan Progress Window numeric indications Data Unit
Data Unit Symbol
kV Kilovolt kV
mA Milliampere mA
Time Second s
Thk Millimeter mm
Table 184 File Manager numeric indications
Data Unit Symbol
Im Ctr S-I Millimeter mm
Thick Millimeter mm
Gantry Degree °
Im Ctr R-L Millimeter mm
Im Ctr A-P Millimeter mm
SFOV Centimeter cm

Units of Measure
DFOV Centimeter or Millimeter cm or mm
Midscan Seconds s
Table 185 Batch Control Panels for Reformat / 3D Data Unit
Data Unit Symbol
Spacing between images Millimeter mm
Slice Thickness Millimeter mm
FOV Centimeter cm
Angle between images Degree °
Table 186 Image Annotation numeric indications
Data Unit Symbol
DFOV Centimeter cm
kV Kilovolt kV
mA Milliampere mA
Thickness Millimeter mm
Rotation Speed Second s
L/R/A/P/S/I indication Millimeter mm

Lexicon
Appendix D Lexicon
D.1 Lexicon
For the CT technologist who operates multiple scanner models, perhaps from multiple manufacturers,
the variability in names for important scan acquisition and reconstruction parameters can lead to
confusion, reduced comfort and an increased potential for error. The intent of this CT terminology
lexicon is to allow users to translate important CT acquisition and reconstruction terms between
different manufacturers' systems.
The following tables provide the SABMI (Scout Adjusted Body Mass Index) terminology for GE and is a
result of the AAPM CT Terminology working group. It identifies relevant from established lexicon (e.g.,
Radlex and DICOM) and other relevant literature published.
The AAPM website will provide updates when changes in standardization of terminology occur. Visit
www.aapm.org, search CT Protocols, and select Lexicon for full listing of terminology across various
manufactures of CT equipment.
The generic descriptions or terms in the first column are intended to orient the user to the relevant
concepts; they are not consensus "preferred terms." The generic descriptions are not based on any
single existing or pending terminology standard; however the references cited below were consulted
in developing the generic descriptions.
A number of individuals and groups have advocated for terminology standardization in CT, including
at a March 30-31, 2010 FDA (Food and Drug Administration) public meeting entitled "Device
Improvements to Reduce Unnecessary Radiation Exposure from Medical Imaging" (transcripts
available at the FDA website: www.fda.gov in Medical Devices). Participants proposed a cooperative
effort among professional organizations (AAPM, ASRT, ACR, etc.), industry, and the FDA.
D.1.1 Scan acquisition and user interface basics on page 1070 Scan acquisition and user interface
basics
D.1.2 Dose modulation and reduction tools on page 1071 Dose modulation and reduction tools
D.1.3 Multi-slice detector geometry on page 1071 Multi-slice detector geometry
D.1.4 Image reconstruction and display on page 1072 Image reconstruction and display
D.1.5 Contrast media tools on page 1073 Contrast media tools
D.1.6 Multi-planar formats and 3D processing on page 1074 Multi-planar formats and 3D processing
D.1.7 Service and application tools on page 1074 Service and application tools
D.1.8 Workflow on page 1074 Workflow

Lexicon
D.1.1 Scan acquisition and user interface basics

Table 187 Scan acquisition and user interface terms
Generic description GE names
The portion of the user interface where scans are prescribed Scan Settings
Other portions of the user interface, such as where reconstructed images are Patient tabs or File Manager
viewed
CT localizer radiograph (i.e. the scanned projection radiograph, often ac- Scout
quired by the CT system to allow the user to prescribe the start and end
locations of the scan range)
Axial scan mode: Data acquisition while the patient table remains stationary; Axial
the table position may be incremented between X-ray exposures to collect
data over a longer z axis range.
Helical or Spiral scan mode: Data acquisition while the patient table is Helical
continuously moving along the z axis.
Dynamic scan mode - single detector width: Data acquisition at multiple Cine or zero interval Axial
time points over the same anatomic location(s) while the patient table re-
mains stationary; X-ray exposure can be continuous or intermittent
Dynamic scan mode - multiple detector widths: Data acquisition at multi- Not used on this system
ple time points over the same anatomic location(s) while the patient table
cycles back and forth between designated start and end locations in order
image a region wider than the detector
Interventional CT - Intermittent X-ray exposures Not used on this system
Interventional CT - Continuous X-ray exposures Not used on this system
Table increment (mm) per 360 degree rotation of the X-ray tube (axial scan Scan Interval
mode)
Table feed per 360 degree rotation of the X-ray tube (helical scan mode) Speed (mm/rot)
Field of measurement: Diameter of the circular region within the scan plane Scan Field of View (SFOV, cm)
over which projection data are collected. Nominally equal to the diameter of
the primary beam at isocenter in the axial plane.
Tube current: Number of electrons accelerated across an X-ray tube per unit mA
time, expressed in units of milliampere (mA)
Tube current-time product: The product of tube current and exposure time Shown as read only in the
per rotation, expressed in units of milliampere • seconds (mAs). In axial scan mA mode menu under Rela-
mode, this is equal to tube current × (scan angle ÷ 360) × rotation time. In ted Settings
helical scan mode, this is equal to tube current × rotation time.

Lexicon
Scan acquisition and user interface terms continued

Generic description GE names
Effective tube current-time product: In helical scan mode, this is the prod- Not used on this system
uct of tube current and rotation time (expressed in units of milliampere •
seconds (mAs) ÷ pitch)
Tube potential: The electric potential applied across an X-ray tube to acceler- kV
ate electrons towards a target material, expressed in units of kilovolts (kV)
Pitch: Unitless parameter used to describe the table travel during helical CT; Pitch
equal to table travel (mm) per gantry rotation ÷ total nominal beam width
(mm)
Automated patient instructions Auto Voice
D.1.2 Dose modulation and reduction tools

Table 188 Dose modulation and reduction tool terms
Generic description GE name
Automatic exposure control (AEC): A scanner feature that automatically Available in SmartmA
adapts the X-ray tube current to the overall patient size to achieve a specified
level of image quality
Angular tube current modulation Organ Dose Modulation
Longitudinal tube current modulation Not used on this system
Angular and longitudinal tube current modulation SmartmA (x, y, z)
ECG-based tube current modulation Cardiac Modulated
Image quality reference parameter for AEC Noise Index
D.1.3 Multi-slice detector geometry

Table 189 Multi-slice detector geometry terms
Multi-slice detector array design Fixed
Detector configuration Detector Configuration

Lexicon
Multi-slice detector geometry terms continued

Detector rows (N) and slice thickness (T) selection console screen image
Figure 524 Detector Coverage and Slice Thickness
D.1.4 Image reconstruction and display

Table 190 Image reconstruction and display terms
Window width: Range of CT numbers (maximum - minimum) that are distrib- Window Width
uted over the viewable grey scale of the display device or film
Window center: The CT number in the center of the viewable grey scale Window Level
Reconstruction field of view: Width of the square region mapped to the Display Field of View (DFOV)
reconstructed image matrix (cm)
Prescribing the reconstruction parameters prior to scan acquisition Primary and Secondary recon
Prescribing the reconstruction parameters after scan acquisition Post Scan Secondary recon
Reconstruction property that determines sharpness or smoothness of image Algorithm

in the axial plane
Helical interpolation options to achieve a wider or narrower section sensitivi- Full (narrower) or Plus (wider)
ty profile mode
Nominal width of reconstructed image along the z-axis Thickness (mm)
Distance between two consecutive reconstructed images Interval
Fast but lower-quality reconstructed images for rapid review of entire exam Quality Check

Lexicon
Image reconstruction and display terms continued

Off‐center reconstruction coordinates RL Center;

AP Center
Flip or rotate the image orientation Flip/rotate
Image modifications to alter sharpness or smoothness (done in image space Image Filters
without reconstructing images)
D.1.5 Contrast media tools

Table 191 Contrast media tool terms
Bolus tracking: Scanner feature to automatically initiate a prescribed axial, Smart Prep
helical or dynamic scan when a threshold level of contrast enhancement is
reached at a specified region of interest
Test Bolus: Scan mode used to measure the contrast transit time using a Take axial scans at zero table
small injection of contrast media feed and process with MIROI
Time-attenuation curve (TAC): Graph of the contrast enhancement versus Smart Prep graph or MIROI
time graph
Threshold: CT number (HU) where bolus tracking tool will trigger the system Transition ROI Threshold
to begin the scan
Scanner feature used to quantitatively evaluate the TAC MIROI (multiple image region
of interest)
Monitoring delay: Time from injection to the start of monitoring scans (Time Monitoring Delay
1 in figure below)
Monitoring interval: Time between consecutive monitoring scans to (Time 2 Monitor ISD (InterScan Delay)
in figure below)
Scan delay: Time from when threshold is reached and prescribed axial, Diagnostic delay
helical or dynamic scan begins (Time 3 in figure below)

Lexicon
D.1.6 Multi-planar formats and 3D processing

Table 192 Multi-planar formats and 3D processing terms
Reformatted image at an oblique plane (not an axial, coronal, or sagittal) Oblique reformat
Saving images at various viewing angles about a volume or surface rendered Batch Loop
object
Saving images at various planes through a volume Batch Reformat
Surface-rendered object 3D
Volume-rendered object Volume Rendered image (VR)
D.1.7 Service and application tools

Table 193 Service and application tool terms
X-ray tube warm up Tube Warm-up (tube warm

up)
Daily calibrations Fast Cals (done in daily prep)
Application information Learning Solutions or User

Manual
Application support assistance Insite or Ilinq
D.1.8 Workflow
Table 194 Workflow terms
Scheduled (but not yet scanned) patient list is called Patient Schedule
Already scanned patient list is called File Manager
User comments or text added to an image is called User annotation
Filming tools are called Not used on this system
Data page summarizing scan parameters, CTDIvol and DLP Exam Text Page, Series Text
Page, or Dose SC
Sorting patient list Click column to sort

Lexicon
D.1.9 References
IEC 60601-2-44 ed3.0 (2009-02) Medical electrical equipment – Part 2-44: Particular requirements for
the basic safety and essential performance of X-ray equipment for computed tomography.
Kalra, M. K. and S. Saini. 2006. Standardized nomenclature and description of CT scanning techniques.
Radiology 241, 657-660.
National Electrical Manufacturer's Organization. 2009. Digital Imaging and Communications in
Medicine (DICOM). (Downloadable from: www.nema.org)
RadLex Tree Browser (www.radlex.org)
Weber, N. M., C. L. Siegle, J. E. Miller, M. K. Hudson, J. M. Kofler, M. R. Bruesewitz, and C. H.
McCollough. How to be a "multi-lingual" CT technologist: understanding scan parameters from
different manufacturers’ equipment. 2004 RSNA Annual Meeting poster (www.mayo.edu in Research).
Weigold, W.G., et al. 2011. Standardized Medical Terminology for Cardiac Computed Tomography: A
Report of the Society of Cardiovascular Computed Tomography. Journal of Cardiovascular Computed
Tomography (downloadable from: www.scct.org in Documents).

Lexicon

Dose Information Reference
Appendix E Dose Information Reference
E.1 Dose Information Reference

Table 195 User Manual
Chapter Section
Safety Radiation Safety
Pediatrics and Small Patients Radiation Exposure

Pediatric and Small Patient Scans
Large Patient Large Patient
Dose Check All sections
Scan Scan Theory

Scan Parameters
Additional Scan Features
Scan Applications ASiR-V
Cardiac Cardiac Scan Parameters

Cardiac Modulated mA
Protocols kV Assist/Auto Prescription Settings

Dose Reporting in Protocol Management
General Information ECG-Modulated mA

SmartTrack
Scout Based Attenuation Characterization
Table 196 Technical Reference Manual
Chapter Section
Safety Radiation Safety
Dose and Performance All sections

Dose Information Reference
General Information ECG-Modulated mA

SmartTrack
Scout Based Attenuation Characterization
CT Perfusion
Total Scan Time
Automatic Exposure Control
Slice Thickness Reference Noise Index and Noise Index Values
SmartmA/ODM
kV Assist/Auto Prescription
CT Acceptance Testing Dose

Changes Impacting Dose or Dose Display/Reporting
Appendix F Changes Impacting Dose or Dose

Display/Reporting
F.1 Changes Impacting Dose or Dose Display/

Reporting
F.1.1 Display of Z-Location with Highest Max Z-Location CTDIvol

If Max Z-Location CTDIvol exceeds the AV value of CTDIvol, the Z position is displayed in () (parenthesis)
next to that value in Dose Information area on the Scan Settings screen ( on page 1079). Within a
contiguous scan range where multiple locations may have the same Max Z-location CTDIvol value, the
mid-point of that scan range is displayed.
For cases where multiple locations from more than one separate scan range have the same Max Z
Location CTDIvol value, the mid-point of the most superior scan range is displayed. An example is given
in on page 1080. See section x.x for more information on Max Z-Location CTDIvol

F.1.2 Optimizing ODM on Revolution Apex

The anterior angular region during which mA is reduced for ODM scans has been narrowed on
Revolution Apex systems to optimize image quality (Figure 525 on page 1081). Relative to the previous
release, ODM scans on Revolution Apex may yield:
• lower image noise
• improved image texture
• less streaking
• small increase in CTDIvol
Estimates of the maximum CTDIvol increase and measured noise decrease are shown in Table x.
Note that the actual differences in CTDIvol, noise, and image texture/artifacts relative to the previous
release are dependent on the scanned anatomy and scan technique. Table x: Estimates of maximum
difference in CTDIvol and measured noise of current ODM relative to previous release.

Figure 525 ODM angular region for body scans before and after the change.
Table 197 Estimates of maximum difference in CTDIvol and measured noise of current ODM
relative to previous release
Scan Technique Maximum Estimated Difference Estimated Difference in Meas-

in CTDIvol (Current relative to ured Noise (Current relative to
Previous) Previous)
Body / Axial or Helical Pitch 0.5 / +1.2% -0.8%

1.0s +
Body / Axial or Helical Pitch 0.5 / +5.4% -3.8%

0.28s
Body / Axial or Helical Pitch +0.5% -0.3%

non-0.5/ 1.0s
Body / Axial or Helical Pitch +2.8% -1.8%

non-0.5/ 0.28s
Head / 1.0s +0.3% -0.2%
Head / 0.28s +2.7% -1.6%
F.1.3 Update to Auto Prescription Size Adjusted Noise Index

Strength Settings
Auto Prescription previously offered five Size Adjusted Noise Index (SANI) strength settings
• No Change

• Very Small Decrease/Increase

• Small Decrease/Increase
• Moderate Decrease/Increase
• Large Decrease/Increase
With this release, an additional SANI strength setting is introduced. The level of noise adjustment with
patient size for this new setting is between that of the previous “Small” and “Moderate” settings. The
names of the SANI settings have been updated according to the table below.
Name of Size Adjusted Noise Index Strength Set- New Name for this Size Adjusted Noise Index
ting in Previous Release Strength Setting in Current Release
No Change No Change (Same as previous)
Very Small Decrease/Increase Very Small Decrease/Increase (Same as previous)
Small Decrease/Increase Small Decrease/Increase (Same as previous)
(No previous strength setting available) Moderate Increase/Decrease
Moderate Decrease/Increase Large Decrease/Increase
Large Decrease/Increase Very Large Decrease/Increase
Auto Prescription GE Reference Profiles and User Profiles that previously used “Moderate” or “Large”
SANI settings will automatically update to show “Large” or “Very Large” SANI setting, respectively.
Note that this is only a change in the name of the SANI settings relative to the previous release, and
importantly, the underlying Noise Index adjustment behavior, and thus dose behavior, will remain the
same as before.
For example, assume a User Profile was set up in the previous release with the following SANI settings
T
• SANI Below Reference Patient Size = Moderate Decrease
• SANI Above Reference Patient Size = Large Increase
hen this profile will be automatically updated in the current release to show the following SANI
settings:
• SANI Below Reference Patient Size = Large Decrease
• SANI Above Reference Patient Size = Very Large Increase
The Noise Index adjustment across patient size and resultant dose at scan time will remain the same
as the previous release; only the name of these two settings has changed.
F.1.4 Dose Impact of Auto Prescription GE Reference Profile

Changes
Some GE Reference Profiles for Auto Prescription have been updated to allow for additional dose and
improved image quality for larger patients, as shown in Table y

Scanner Auto Prescription GE Reference Change Description and Estimat-

Profile ed Dose Impact
Revolution CT, Revolution CT ES GE Small Vessel Thoracic CTA Increase rotation time of largest
(Adult) patient size range from 0.5s to 0.6s
to allow ~20% more dose and im-
proved image quality for patients
larger than 75cm AP + LAT
Revolution Apex GE Abd/Pel (Adult) Use new “Moderate Increase” Size

Adjusted Noise Index Setting for
patients larger than reference pa-
tient size to allow more dose
and improved image quality for pa-
tients larger than 60cm AP + LAT
• 60-70cm AP + LAT, ~5-15%
dose increase
• 70-80cm AP + LAT, ~15-35%
dose increase
• > 80cm AP + LAT, 30-40% dose
increase


Manufacturer
GE HealthCare
3000 North Grandview Blvd
Waukesha,WI 53188 USA
www.gehealthcare.com

23MW17.xx Revolution CT Revolution CT ES User Manual - UM - 5951015-1EN - 1

Uploaded by

Document Information

Original Description:

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

23MW17.xx Revolution CT Revolution CT ES User Manual - UM - 5951015-1EN - 1

Uploaded by

Copyright:

Available Formats

Revolution™ CT, Revolution™ CT ES

5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES i

5 Pediatrics and Small Patients . . . . . . . . . . . . . . . . . . . . 125

ii Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

6 Large Patient . . . . . . . . . . . . . . . . . . . . . . . . . . 135

7 Dose Check . . . . . . . . . . . . . . . . . . . . . . . . . . . 139

5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES iii

9 Startup and Shutdown . . . . . . . . . . . . . . . . . . . . . . . 233

10 Patient Schedule . . . . . . . . . . . . . . . . . . . . . . . . 255

iv Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES v

12 Scan Applications . . . . . . . . . . . . . . . . . . . . . . . . 475

vi Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

13 Lung Cancer Screening . . . . . . . . . . . . . . . . . . . . . . 563

5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES vii

15 View Images . . . . . . . . . . . . . . . . . . . . . . . . . . 627

viii Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

16 Display Applications . . . . . . . . . . . . . . . . . . . . . . . 669

5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES ix

x Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

19 Data Management . . . . . . . . . . . . . . . . . . . . . . . . 791

5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES xi

21 Access Controls . . . . . . . . . . . . . . . . . . . . . . . . . 929

xii Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

22 System Management . . . . . . . . . . . . . . . . . . . . . . . 957

5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES xiii

23 General Information . . . . . . . . . . . . . . . . . . . . . . .1003

Appendix A Operator Messages. . . . . . . . . . . . . . . . . . . . .1037

Appendix B Abbreviations . . . . . . . . . . . . . . . . . . . . . .1061

Appendix C Units of Measure . . . . . . . . . . . . . . . . . . . . .1065

Appendix D Lexicon. . . . . . . . . . . . . . . . . . . . . . . . .1069

xiv Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

Appendix F Changes Impacting Dose or Dose Display/Reporting . . . . . . . . .1079

5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES xv

Revision Date Reason for Change

1 August 2023 Initial release

5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES xvii

1.2 User Documentation

Accessing User Documentation

5951015-1EN Revision 1 Revolution™ CT, Revolution™ CT ES 1

To start the user information:

2. AWS User Manual

To exit the user information:

1.3 GE Approved Accessories, Components and

Table 1 GE Approved Accessories

SmartStep Kit (includes hand controller and foot- GE 5149705-4

Axial Head Holder 2115996-4

Coronal Head Holder 2115990-3

Cradle Extender 2115993-4

2 Revolution™ CT, Revolution™ CT ES 5951015-1EN Revision 1

Table 2 GE Approved Components

Partial UPS* Eaton Powerware 9355-15-14GE

External Hard Drive Seagate 2 TB USB 2.0/3.0

Bar Code Reader Honeywell 1300G

GE CT Flat Tabletop AAPM TG-66 Kit GE 5924000

Patient grounding strap Wrist band GE 5788434

SmartStep Monitor Boom (includes LCD monitor and GE 5115174-30, GE 5115174-33

Water Phantom 5432878

Metalless Compatible Phantom Holder 2331933-2

Carrying case for Phantom 5537763

Cradle Pad for Revolution 5433273 46-278986P2 (part of 46-229452G1)

Extender Pad 5122945-5