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Dr Farooq Ghani
• Lab Automation
Farooq Ghani, M.D.,Ph.D
Director, Bayer HealthCare
Tarrytown, New York
Online
Connectivity
& Barcoding The FUTURE of
Clinical Laboratory Me dicine
Blood Whole
Samples blood ~25 % Hematology
~ 90 %
Automation ~ 10 %
• “The first rule of any technology
used in an organization is that
The applied
automation FUTURE to anof efficient
operation will magnify the
Clinical Laboratory
efficiency. The second is Me dicine
that
automation applied to an inefficient
operation will magnify the
inefficiency”
Farooq Ghani, M.D.,Ph.D
Director, Bayer HealthCare
Tarrytown, New York
Bill Gates
Increase
Capacity
Reduce Faster
Errors Laboratory TAT
Automation
Space Personnel
Utilization Optimisation
Turnaround Time
Testing
13%
Delivery
4% Sorting
Frontend 6%
Documentation 52%
5% Accessioning
Troubleshooting 27%
4%
Loading Aliquoting
4% 15%
Centrifugation
Resulting 4%
18%
High Gain Opportunities
Goal: Reduce Costs and Turnaround Time
17 Steps
• Samples manually logged
into laboratory
Fewer steps equal
• Verification of Collection
at LIS
faster, more consistent
Costs • Load individual tubes into
turnaround
& centrifuge
• Centrifuge Samples
TAT • Unload each tube from
centrifuge
• Split samples for separate
9 Steps
workstation
• Distribute samples to each
workstation • Samples manually logged
• Visualize Serum Indices into laboratory
• Check QC • Verification of Collection
5 Steps
• Load sample tube on wheel at LIS
• Results validated and • Load racks into centrifuge
verified at LIS • Centrifuge samples
• Samples Stored • Unload racks from • Samples placed into inlet
3 Steps
• Delta Checking centrifuge station
• Program tests not validated • Place racks on analyzer • Place racks on analyzer
• Rerun tests not validated • Rerun tests not validated • Rerun test not validated • Samples placed into inlet
• Identify samples for reflex • Identify samples for reflex • Reflex Testing station
testing testing automatically • Review by exception
• Reflex Testing • Reflex Testing • Samples stored • Samples stored
Productivity Increases
Steps Automated
in the Diagnostic Laboratory
Post-Analytical Pre-Analytical
prepare order
collect sample
transport to lab
Sample retrieval
accession sample
store samples
Analytical
Solutions to Streamline the Process
EDTA Pre-Analytics Track
tubes Informatics Tube Storage & Retrieval
X X X X X X X
Sort
Receive Sample Label
into lab Load Unload Aliquot Sort
tubes Decap aliquot
centrifuge centrifuge
tubes
X
Load in
Input Queue Pre-Analytics (100% of tubes / >50% of labor) Walk to
analyzers
X X X X X X X X
Walk Verify/
Store Archive Recap Unload Rerun Locate Verify
to storage Manage
racks tubes tubes analyzers exceptions exceptions at LIS
area exceptions
X X X X XX X Find
tube
Load on
analyzer
Verify at
LIS
Unload
analyzer
Process Mapping
• Analyze your processes
• Identify opportunities
• Eliminate waste
Metrics for Success
• Testing • TAT
• Test/Tube • Tube Arrival
12,000
Volume
Stated
Estimated Annual IA Volume by Order/Assay
35%
California Hospital Medical Center
Tests per Tube Distribution
Jan. 3 through 10, 2005 60
California Hospital Medical Center
Total Samples by Hour - Thursday, Jan 6, 2005
318 Routine, 238 STAT
30.00
Analysis
Histogram of Sample TAT: Order to Result Verified
USL 60.00
33%
10,244
STAT Routine Mean 76.21 Cp -0.16
Extrapolated Routine Median Cpk
53
62.89 -0.16
10,000
30% STAT 50
Pp -0.11
48
25.00
8,475
27%
Ppk -0.11
46
Number of Orders per Year
Cpm 0.15
8,000
7,150
Stdev 48.24
25%
40 20.00 Max 255.59
21%
Number of Samples
Min 25.16
36
20%
Zbench
34
6,000 -0.34
Number
20% CpkU
Frequency
-0.16
4,420
15.00
4,160
30
32
13
3,692
3,700
27
15%
3,484
ZTarget 0.22
26
51
4,000
3,075
25
25
%Defects
45
15% 0.59
23
23
2,525
2,450
2,350
2,274
%Expected 0.63
21
21
10.00
19
19
1,716
DPMO
8
20 586206.90
9
1,392
30
7
1,196
1,200
2,000
17
17
17
Expected
10
631608.88
7
10%
15
936
8%
825
676
12
VANCORDM 0 572
8
468
7%
450
468
357
364
9
5.00
1 12
275
306
300
7%
260
208
156
156
160
156
6%
6%
104
104
100
52
52
52
52
10
41
23
11
7
0
13
0 10
20
15
4%
4%
18
2 8
5%
17
4%
HEPFPNL
FREET3
CARBAM
HBSAB
HBSAG
HCYST-ARUP
RUBG-NHMC
BNP
CKMB
PSA
TROPONIN
FT4
HCGQL
16
16
HCGQN
MYOGLOBIN
TSH
T3
T4
CK
VANCOT
VANCOP
FOLATE
3%
3%
3%
14
14
3%
2%
13
5
2%
5 05
2%
2%
8
11
2%
2%
11
10
0.00
2%
1%
1%
1%
1%
1%
1%
9
1%
1%
8
1%
1%
1%
0%
0%
0%
0%
0%
0%
0%
0%
0%
0%
6
0%
-3.647656257 25.156249993 53.960156243 82.764062493 111.567968743 140.371874993 169.175781243 197.979687493 226.783593743 255.587499993
4
3
2
2
0% 0 to to to to to to to to to to
25.156249993 53.960156243 82.764062493 111.567968743 140.371874993 169.175781243 197.979687493 226.783593743 255.587499993 284.391406243
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23
Order/Assay Number of Tests per Tube Hour of Day Minutes
100%
At Risk 60
40
60%
TAT (min)
30
44%
40%
31%
30%
29%
20
26%
14%
13%
20%
13%
10
11%
10%
8%
6%
6%
4%
2%
2%
2%
2%
2%
1%
1%
1%
0%
0%
0% 0
0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 0:00 3:00 6:00 9:00 12:00 15:00 18:00 21:00 0:00
The FUTURE of
Clinical Laboratory Me dicine
The FUTURE of
Clinical Laboratory Me dicine
Tubes (thousands) %
5 100
The FUTURE of
4 Clinical
$1,600
savings
75 Laboratory Me dicine
3 98%
50 reduction
2
25
1 Farooq Ghani, M.D.,Ph.D
Director, Bayer HealthCare
Tarrytown, New York
Primary tubes Aliquots
Source: ACM
Individual results may vary.
Technology Adoption Life Cycle
100
75
50
25
0
The FUTURE of
Clinical Laboratory Me dicine