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Star 55
Operating Manual
Star 55
LARSEN & TOUBRO LIMITED
Star 55
8 channel multiparameter color monitor
OPERATING MANUAL
Star 55
CAT NO. : 3-86-020-0009-83 ISSUED : Oct 2007 Rev. : 0
© 2007 Larsen & Toubro Limited
All rights reserved
Technological upgradation is a continuous process at L&T. Hence, the specifications mentioned in this
manual are subject to change without any prior notice. The contents in this manual are strictly not
to be reproduced in any form, by any method, for any purpose.
Introduction
Congratulations on becoming one of the proud
customers of L&T Medical’s multiparameter color
monitor Star 55.
Star 55
Left blank intentionally
Table Of Contents
Exemptions . . . . . . . . . . . . . . . . . i
Copyright . . . . . . . . . . . . . . . . . . i
Standards . . . . . . . . . . . . . . . . . i
Disposal Instructions . . . . . . . . . . . . . . i
Caution . . . . . . . . . . . . . . . . . . ii
WARNING . . . . . . . . . . . . . . . . . iii
Indication For Use . . . . . . . . . . . . . . . iv
Handling Precautions . . . . . . . . . . . . . . v
Symbols . . . . . . . . . . . . . . . . . . vii
Abbreviations & Acronyms . . . . . . . . . . . . . ix
2. Application Guide . . . . . . . . . . . . . . . . 2
• ECG . . . . . . . . . . . . . . . . . . . 2.1
• ST Segment Analysis . . . . . . . . . . . . . . 2.6
• Respiration . . . . . . . . . . . . . . . . . 2.8
• Temperature . . . . . . . . . . . . . . . . . 2.9
• Pulse Oximetry . . . . . . . . . . . . . . . . 2.10
• Non Invasive Blood Pressure . . . . . . . . . . . . 2.13
• Invasive Blood Pressure (Optional) . . . . . . . . . . 2.15
• Capnography (Optional) . . . . . . . . . . . . . 2.18
4. Parameter Setting . . . . . . . . . . . . . . . . 4
• ECG . . . . . . . . . . . . . . . . . . . 4.1
• ST Segment . . . . . . . . . . . . . . . . . 4.4
Star 55
• Respiration . . . . . . . . . . . . . . . . . . 4.6
• Temperature . . . . . . . . . . . . . . . . 4.7
• SpO 2 . . . . . . . . . . . . . . . . . . . 4.8
• NIBP . . . . . . . . . . . . . . . . . . . 4.9
• Capnography (Optional) . . . . . . . . . . . . . 4.11
• IBP (Optional) . . . . . . . . . . . . . . . . 4.13
• Drug cal . . . . . . . . . . . . . . . . . . 4.17
5. System Functions . . . . . . . . . . . . . . . . 5
• System Functions . . . . . . . . . . . . . . . 5.2
• Menu . . . . . . . . . . . . . . . . . . . 5.3
• Trend . . . . . . . . . . . . . . . . . . . 5.8
• Display . . . . . . . . . . . . . . . . . . 5.13
• Volume . . . . . . . . . . . . . . . . . . 5.15
• Recall . . . . . . . . . . . . . . . . . . 5.16
• Autoset . . . . . . . . . . . . . . . . . . 5.18
7. Accessories . . . . . . . . . . . . . . . . . . 7
• ECG . . . . . . . . . . . . . . . . . . . 7.1
• Respiration . . . . . . . . . . . . . . . . . . 7.1
• Temperature . . . . . . . . . . . . . . . . 7.2
• Pulse Oximetry . . . . . . . . . . . . . . . . 7.3
• NIBP . . . . . . . . . . . . . . . . . . . 7.4
• CO 2 (Optional) . . . . . . . . . . . . . . . . 7.5
• IBP (Optional). . . . . . . . . . . . . . . . . 7.7
• Grounding cable . . . . . . . . . . . . . . . . 7.7
Copyright
L&T owns all rights to the manual and intends to maintain this manual as confidential.
L&T also seeks to maintain this manual as a copyright. This manual is to be used
solely for the purpose of reference, operation and maintenance of L&T equipment.
The contents of this manual are proprietary. Reproduction or distribution of any part
of this manual in any form is prohibited.
Due to continuous updating of technology, the specifications, as well as information
in this manual, are subject to change without prior notice.
All information in this manual is believed to be correct. L&T shall not be liable for
errors contained herein with the performance or use of this manual.
Standards
This equipment has been designed to meet the following International standards:
Class 1 equipment requirement of IEC 60601-1.
EMI/EMC requirements as per IEC 60601-1-2.
IEC 60601-2-27 requirements for ECG.
IEC 60601-2-30 requirements for NIBP.
IEC 60601-2-34 requirements for IBP.
IEC 60601-1-8 requirements for alarm systems.
IEC 60601-2-49 requirements for multifunction patient monitor systems.
ISO 9919 requirements for SpO2.
ISO 21647 requirements for CO2.
AAMI EC 13 for ECG.
AAMI SP 10 for NIBP.
Regulatory Requirement
" United States law restricts this device to sale or use by or on the order of a physician"
Disposal Instructions
• Follow the local regulations and procedures for the disposal of unit and battery.
i Star 55
Caution
Cautions are intended to alert you to the importance of following correct operating
procedures to prevent the risk of damage to the system.
z Electrical installation of the room or the building in which the equipment is to be used,
should comply with regulations specified by the country in which the equipment is to be
used.
z If earthing arrangements are suspected, the monitor must be connected to a mains line
with proper earth connection to ensure correct readings.
z The equipment should be used in accordance with the "instruction for use" provided by
L&T and as specified on the rear panel of the monitor.
z If any function of the monitor fails, then consult L&T Medical authorized service engineer.
z Failure to meet ventilation requirement may cause equipment failure and intern jeopardise
the functions of automated monitoring. Do not place equipment in an enclosed area that
could restrict heat dissipation from the front or rear of the unit.
z Keep pacemaker patients under close observation. Rate meters may continue to count
the pacemaker rate during cardiac arrest and some arrhythmia.
z This equipment is meant for use by qualified medical personnel only.
z For the disposal of battery after its life, follow the local regulations and procedures.
ii
WARNING
WARNINGs are intended to alert you to the importance of following correct operating
procedures where risk of injury to the patient or system user exists.
z All modifications and repairs should be carried out by authorized L&T personnel or
authorized agents.
z Alarms:
Adjusting the alarm volume to a low level or switching OFF alarms during patient
monitoring may result in alarm conditions going unnoticed. Hence do not rely
fully on audible alarm.
The most reliable method of patient monitoring combines close personal surveillance
with correct operation of monitoring equipment.
z After AC power is resumed keep the monitor ON for 16 hours to charge the battery, if
low battery indicator is displayed.
z When 'low battery' indication comes on screen, connect the unit to main supply and keep the
unit for charging.
z Use only L&T approved accessories and batteries.
z Do not use damaged cables/sensors, cuffs and contaminated accessories.
z Do not rely fully on apnea, arrhythmia detection and alarms.
z When several equipment of different companies/makes are interconnected through the
same mains power distribution line, the summation of the resulting leakage
currents may exceed the maximum limits.
z Explosion hazards are possible if used in the presence of flammable anesthetics.
z For continued protection against fire hazard, use fuses of only specified type and rating.
z 'Electrical shock hazard'. Do not remove cover. Refer to qualified personnel for servicing.
z Patient safety and performance of this unit when connected to patients undergoing magnetic
resonance diagnostic procedures is unknown. It is advice that all sensors and cables
used with this unit should be removed from patient during such procedures.
z L&T medical does not assume responsibility for damage to the equipment caused by
improperly ventilated cabinets, improper or faulty power or insufficient wall strength incase
of wall mounted units.
z Do not use the machine with nuclear spin tomography (MRT, NMR, NMT) as the function of the
machine may be disturbed.
z Pay extra attention if the parts of the equipment are provided with protections against burning the
patient when used with High Frequency (HF) surgical equipment.
z Observe extreme caution when a defibrillator is used on a patient. Do not touch any part
of patient, table or monitor when a defibrillator is in use.
iii Star 55
Indication for use
The Star 55 multiparameter patient monitoring system is intended to monitor a single
adult, pediatric or neonatal patient's vital signs at the bedside or during intra-hospital
transport along with the appropriate accessories mentioned / supplied with the unit.
Vital signs parameter include ECG (3 lead /5 lead), SpO2, Respiration, Invasive (IBP1-
IBP4) and Non Invasive Blood Pressure and Capnography (CO 2). It can also display the
digital values of HR/PR, SpO2, RR, Invasive and Non-invasive Blood Pressure (Systolic,
Diastolic and Mean), EtCO2, FiCO2 and temperature readings. Star 55 can be used to
calculate the drug dosage and to display Oxygen Cardio Respirograph.
The user, responsible to interpret the monitored data made available, will be a professional
health care provider. The device, which can also be used as a portable device, permits
patient monitoring with adjustable alarm limits as well as visible and audible alarm signals.
The monitor is not intended for home use.
iv
Handling precautions
This monitor is intended for use by only qualified medical personnel.
Please read these precautions thoroughly before attempting to operate this monitor.
1. For effective use of monitor , operation of the unit must be fully understood.
z The monitor should be placed on an even, level floor. Vibration and mechanical
shock should be avoided even during moving.
z Avoid placing in an area where chemicals are stored or where there is danger
of gas leakage.
3. Before Operation
z Pay extra attention when the monitor is in combination with other instruments
to avoid misdiagnosis or other problems.
z All circuitry used for direct patient connection must be doubly checked.
v Star 55
4. During Operation
z Both the monitor and the patient must receive constant, careful attention.
z Turn power OFF or remove electrodes and cables when necessary to assure
patient's safety.
z Avoid direct contact between the monitor and the patient.
z Extra care should be taken when the monitor is in use with the HF Surgical
Equipment.
Note:
The applied parts of NIBP and CO2 are protected against HF surgical
burns and the applied parts of ECG, SpO2, IBP and Temperature are not
protected.
vi
Symbols
Logo
Unit ON indicator
Equipotential ground
Alarm Acknowledge
vii Star 55
Monitor ON/OFF
Recorder ON/OFF
Freeze/Defreeze
Goto
Stand By
Home
CO2 Pump
NIBP Trend
PR Source selection
NIBP Timer
Left Navigator
Selection Key
Right Navigator
viii
Acronyms and Abbreviations
FLT Fault.
CHECK HR Displayed Heart Rate may not be valid (More than 30 BPM diff).
PR Pulse Rate.
RR Respiration Rate.
ARRHY Arrhythmia
ix Star 55
CNS Central Nursing Station
PA Physiological Alarm
TA Technical Alarm
NA No Alarm
X
1
DI
SP
LA
CO Y, C
N O
A N NEC N T R
D OL
O U TION S,
TP S
UT
S
1 Star 55
Notes :
Left blank intentionally
Star 55
15 17 20
16
18
19 21
1 234 5 6 7 8 9 10 11 12 13 14
1.1
Front panel description
1 Monitor ON/OFF switch To switch ON or switch OFF the monitor (Unit should
be connected to the mains supply or to the internal
battery).
2 Mains Indicator Amber color LED turns ON when monitor is connected
to Mains.
3 Remote Sensor To sense the remote signals.
4 Monitor ON indicators Green LED ON indicates Monitor ON.
Amber LED OFF and Green LED ON indicates unit
is ON in battery operation mode.
5 Alarm suspend/ On pressing this key all audio alarms are muted or
Acknowledge suspended. When Audio/Visual alarms are indicated
by the unit, this key acts as alarm ackowledge key.
6 NIBP Start/Stop This key is used to start/stop the NIBP mesurement.
7 Freeze/Defreeze This key is used to Freeze/Defreeze the screen.
8 Record This key is used to Start/Stop recorder.
9 Goto This key used as a short cut key for Menu option.
10 ' Zero' This key is used to make invasive blood pressure
value zero. (Ensure that the IBP transducer is
connected to the unit).
11 CO2 pump This key is used to ON CO2 pump when in use and
OFF when not in use.
12 Stand By To toggle between Stand By and ON.
13 Home To go back directly to the Main screen, from any
other screen.
14 Optical Encoder This is a special rotating knob used for multipurpose
applications. Rotating the optical encoder in clockwise
or anti-clockwise direction, moves the cursor
(highlighted rectangular block) right or left in the Menu
area of the screen. Pressing the optical encoder
selects the particular function.
15 Message Display Area Displays error messages.
16 Waveform Display Area Displays waveforms. Maximum 8 channel.
17 Alarm Indicator Gives flashing Yellow color indication for cable /
accessory related alarms like cable coming off patient
and flashing Red color indication for patient related
1.2 Star 55
alarms, e.g. when the value of any parameter being
monitored goes above or below the set alarm limits.
Audio frequency [AAMI 4.1.2.1(i)]:
Red alarm : 1.7 K Hz
Yellow alarm : 1.4 K Hz
Video frequency :
Red alarm : 2 Hz (250ms ON, 250ms OFF)
Yellow alarm : 0.5 Hz ( 1s ON, 1s OFF)
Fixed 3 minutes realarm facility is present.
Crossed bell indication for alarm silence.
18 Parameter/Numeric Displays numerical values for all parameters.
19 Menu Display Area Displays Main menus.
20 Battery status Area Displays the status of the battery.
21 Non display parameters Displays the alarm of non display parameter
1.3
Left blank intentionally
1.4 Star 55
1
3
1.5
Rear panel description
Connector Function
CIC Connectors
Connector Description
* Future upgrade
1.6 Star 55
4
1
5
6
2 7
3
10
1.7
Left side panel description
Connector Function
* Future upgrade
1.8 Star 55
1
1.9
Right side panel description
Connector Function
1.10 Star 55
Procedure to connect and disconnect the
detachable connectors
Power Cord
Connect Disconnect
b) Hold the unit with one hand b) Hold the unit with one hand
and insert the power cord into and gently pullout the head of
the slot provided on the rear the power cord from the unit
panel of the Unit as shown in as shown in Figure 1.6.
Figure 1.5.
ECG
Connect Disconnect
Allign the notch of the ECG cable Hold the unit with one hand
connector with the connector and gently pullout the ECG cable
slot on the side panel of the connector as shown in Figure 1.8.
Unit and insert the cable as
shown in Figure 1.7.
Note
Follow similar procedure to connect/disconnect SpO2 and IBP connectors to/from their
Follow similar procedure to connect/disconnect IBP connectors to/from their respective
respective slots on the front panel of the unit
slots on the side panel of the unit
1.11
Temperature
Connect Disconnect
NIBP
Connect Disconnect
Insert the NIBP connector in the Press the NIBP connector on the
slot provided on the side panel side panel of the unit and remove
of the unit as shown in Figure1.11. connector as shown in Figure1.12.
1.12 Star 55
CO2
Connect Disconnect
a) Open the CO 2 inlet shutter in the a) Turn the CO2 Filterline connector
direction as shown in the unit. in anticlockwise direction to
b) Insert and turn the CO2 Filterline unlock as shown in Figure1.14.
connector in clockwise direction b) Gently pull out the CO2 connector
to lock as shown in Figure 1.13. as close the inlet shutter.
Grounding Cable
Connect Disconnect
a) Insert the grounding connector a) Hold the unit with one hand and
in the slot provided on the pull out the connector as shown
rear panel as shown in the in the Figure.1.16.
Figure.1.15.
1.13
Recorder
Green LED
Red LED
Feed Key
Figure 1.17
Function
ii. Trend data recording : The status of any three parameters can be selected
for recording in tabular format.
iii. NIBP data recording : The status of NIBP along with any two other parameters
can be selected for recording in tabular format.
1.14 Star 55
i. Delayed recording ii. Trend data recording iii. NIBP data recording
- - - - - - - DELAYED - - - - - - - - - - - - - TABULAR TREND - - - - - - - - - - - - - - - NIBP TREND - - - - - - - - -
1.15
Remote
Figure 1.21
21 hotkeys along with stand by key and an LED is provided on the wireless
hand-held remote. The remote can be used parallely with the internal keyboard,
over a maximum distance of 20 feet.
Note
Use the remote in straight line with the remote sensor to avoid changes in other
patient monitors (55 series) kept near by.
1.16 Star 55
Left blank intentionally
2
AP
PL
IC
GU AT
IO
ID N
E
2 Star 55
Notes :
ECG
ELECTRODE PLACEMENT (3 LEAD):
INTRODUCTION
For continuous, stable ECG monitoring which is not disturbed by the patient's
LA
RAare put on the patient's chest.
movement, the electrodes The following section
describes various modified ECG leads which are similar to the standard 12
ECG leads. LL
Figure 2.2 Lead I Figure 2.3 Lead II Figure 2.4 Lead III
2.1 Star 55
ELECTRODE PLACEMENT (5 LEAD)
Chest electrode positions
C1 (V1) : Fourth intercostal space at
the right border of the
sternum
C2 (V2) : Fourth intercostal space at the
left border of the sternum
C3 (V3) : Halfway between C2 (V2) and
C4 (V4)
C4 (V4) : Fifth intercostal space of the
left midclavicular line.
Figure 2.5
C5 (V5) : Left anterior axillary line at the
same level as C4 (V4).
C6 (V6) : Left midaxillary at the same
level as C4 (V4).
2.2
Bipolar Limb Leads Unipolar Limb Leads Unipolar Chest Leads
Figure 2.6 Lead I Figure 2.7 Lead aVR Figure 2.8 Lead V1-6
Note
Place the electrodes on the patient before the electrode cable is plugged into the monitor.
Special consideration should be given to electrode placement when an electrosurgical
unit is to be used. The active electrodes should be equidistant from the proposed cutting
line, but situated as far away as possible. The conductive parts of Electrodes and
associated connectors for applied parts, including the Neutral Electrode, should not
contact other conductive parts including Earth. Care should be taken to ensure that the
diathermy return plate is clean and makes good contact with patient. Though spikes
may be observed in the ECG trace when diathermy is used on the patient, there is
instantaneous recovery of the ECG trace when diathermy electrodes are removed from
the patient.
Always ensure ECG cables are properly placed to avoid which may cause interference
signals resembling cardiac waveforms, from other equipment.
Poor ECG trace can occur due to dry electrodes. To rectify, remove the electrodes,
apply gel and reattach with new tape (Replace incase of disposable electrodes).
This monitor meets the safety requirements for direct cardiac monitoring.
2.3 Star 55
Steps for application of ECG electrodes :
Proper skin preparation is necessary for good quality signal pick up and display. Please
follow the guidelines as listed below:
1. Wash electrode site and shave surface hair.
2. Gently rub skin surface with a prep pad to remove outer epidermal layer.
3. Thoroughly clean site with soap and water, depending on your patient's skin type
and sensitivity.
4. Allow site to dry thoroughly.
5. Check the expiry date on the electrode package. Ensure that the electrode gel is fresh
before placing the electrode on the patient.
6. Use one electrode brand for all electrodes placed on a single patient. Mixing electrode
brands may cause a fuzzy base line or a lead fault message.
7. Place an electrode on a flat, nonmuscular area to avoid motion artifact.
8. Procedure for applying the electrodes may vary with the type of electrode:
• Wet gel type-press down along the edge of the electrode so that all edges adhere
firmly to the skin. Do not press central contact area of electrode.
• Solid gel type-begin by pressing on the gelled area, then apply pressure toward
outside of electrode.
9. Replace the electrodes at least every 48 hours.
10. Reusable ECG electrodes can be applied after applying a little bit of ECG gel on the
cup of the electrodes and then securing the electrode at site using sticking tape or
suitable adhesive tape.
11. Fasten the electrode leads with surgical tape (with an extra length of wire between
the tape and the electrode) as shown in the Figure 2.13.
Figure 2.13
12. In operation theatres, please ensure that the disinfecting/cleaning solutions do not
come in contact with ECG electrodes.
2.4
Clinical Limitations :
• Shivering patients or patients giving exceptionally low signals can be difficult to
monitor.
• Although the monitor is provided with exceptionally good filters against the effects of
electrosurgery, this technique can affect readings.
• Defibrillation causes temporary disruption of the waveform display.
• Patients with burns may need special needle electrodes.
Star55 has 3 lead / 5 lead ECG options for monitoring ECG. L&T offers either of these
cables:
• 3 lead ECG cable (I, II, III) of Berned Ritcher make.
• 5 lead ECG cable (I, II, III, aVR, aVL, aVF, V) of Berned Ritcher make.
2.5 Star 55
ST Segment Analysis
Peak R
ST segment interval
ST selection
P T
ISO line
ST depression
Q
S
Isoelectric point -80 ms 120 ms
(Default) ST point (Default)
Figure 2.14
ST segment indicates elevation and depression of ST segment from ISO electric baseline
which reflects the vital information of patient’s cardiac function for myocardial ischemia (i.e.
imbalance between oxygen supply and requirement in myocardium) ST elevation or devia-
tion more than 1.0 mm requires immediate medical attention.
2.6
ST analysis with 5 lead ECG cable
Simultaneously any three selected leads can be analyzed out of seven (I, II, III, aVR, aVF, aVL,
V) Lead II and V gives maximum information therefore lead II and V is preferred.
ISO point
It is ISO electric point which provides the baseline for the measurement. By default ISO
electric point is 80 ms from R peak.
ST point
ST point is the measurement point where ST analysis is required. By default ST point is
measured at 100 ms from R peak.
Note
The algorithm used in ST segment analysis is tested for the accuracy of the ST
segment data. Clinician has to determine the significance of the ST segment changes.
2.7 Star 55
RESPIRATION
(When sourced from ECG cable)
Tests of respiratory functions are carried out for various reasons, including the
assessment of lung disease, monitoring the condition of patients under anesthesia
or under intensive care and the investigation of normal lung physiology.
The body, in particular the brain requires a constant supply of blood with dissolved
oxygen and carbon dioxide of around 100 and 40 mmHg respectively. For maximum
efficiency, perfect matching of air and blood flow is required in each of the lungs'
alveolar compartments, with overall ventilation rate of 18-20 breaths per minute.
There are several ways to measure respiration. In Star 55, respiration can be
measured either through Capnography or ECG. Priority is given to Capnography.
If Capnography option is not provided then respiration is measured from ECG.
When measured from ECG, respiration measurement is based on impedance
pneumography. This method comprises of passing a low current, high frequency
carrier signal between two ECG electrodes on either side of the chest wall. The
impedance or resistance of the chest changes as the lungs expand and contract
and as the volume of air in the lung changes. The change in impedance creates
a change in voltage across the carrier signal which is interpreted as a breath and
displayed as an analog waveform. Respiration Rate is displayed as a digital value.
The ECG electrodes are to be placed as shown in the diagram below. However,
in order to improve the respiration measurement, it is found useful to move the
Right Arm electrode (R) within the area shown in the Figure 2.15.
Figure 2.15
Respiration can be monitored through same ECG cables (3/5 lead) or through
Capnography. Priority for respiration is given to Capnography, if the option is
installed.
2.8
TEMPERATURE
The three zones most commonly used for measuring temperature are:
o
1. Rectal (typically 37 C)
o
2. Oral (typically 37 C)
o
3. Axillary (underarm) (typically 36 C)
Note
Apply gauze piece and sticking plaster to cover temperature sensor of YSI 409A (tape-
on skin) for better results.
2.9 Star 55
PULSE OXIMETRY
When the light from the LEDs is transmitted through the blood and the various
tissue components, a portion of it is absorbed . The photodiode in the sensor
measures the light that is transmitted, and this measurement is used to determine
how much light was absorbed.
With each heart beat, a pulse of oxygenated arterial blood flows to the sensor site.
This oxygenated haemoglobin differs from deoxygenated haemoglobin in the amount
of red and infrared light that it absorbs. The Star 55 measures absorption of both red
and infrared light and uses those measurements to determine the percentage of
functional haemoglobin that is saturated with oxygen.
Initially, light absorption is determined when the pulsatile blood is not present. This
measurement indicates the amount of light absorbed by tissue and nonpulsatile
blood absorption that does not change substantially during the pulse. This is
analogous to the reference measurement of a spectrophotometer. Absorption is
then measured when the pulsatile blood is present. In that measurement, light
absorption at both wavelengths is changed by the presence of the pulsatile, arterial
blood. The Star 55 then corrects the measurement obtained during the pulsatile flow for
the amount of light that was absorbed at the initial measurement. The ratio of the correct
absorption at each wavelength is then used to determine functional oxygen saturation.
2.10
SpO 2 SENSORS
WARNING
Use only L&T approved sensors. Use of sensors by other manufacturers may result
in improper oximeter performance.
SELECTING A SENSOR
z Prepare the application site, remove nailpolish, clean surface area of contact
and apply the oxygen transducer using the sensor application guide of pulse
oximetry transducer.
z The perfusion indicator fills up the bar and plethysmographic waveform will be
displayed accompanied by an audible beep and numerical values of SpO2 and
PR (pulse rate) are displayed on the screen. ( In case ECG is not connected).
Note
Do not connect the SpO2 sensor and non-invasive blood pressure cuffs to the same
limb of the patient.
2.11 Star 55
PERFORMANCE CONSIDERATION
To ensure optimal performance, use an appropriate sensor. Apply the sensor as per the
manufacturer's instructions. Keep the sensor site at the level of the patient's heart and
observe the Warnings and Cautions indicated in the sensor's booklet (manufacturer's
instructions booklet).
If excessive ambient light is present, cover the sensor site with opaque material.
Light sources that can affect performance includes surgical lights, especially those
with a xenon light source, flourescent lights, infrared heating lamps and direct
sunlight.
z Move the cables of the Star 55 and the cautery unit as far as possible.
z Plug the Star 55 and cautery unit into different mains socket.
z Move the sensor away from the cautery site and ground plate as much as
possible.
z Check whether the sensor is dry and firmly attached.
z Avoid criss-crossing of Cautery cables with Star 55 monitor cables
2.12
NON INVASIVE BLOOD PRESSURE
Preparation for NIBP monitoring :
1. Place the patient in supine position and connect the BP cuff to the arm.
2. If the cuff is not placed at level of the heart then the pressure values obtained
will not reflect the true physiological pressure.
Note
Accuracy of NIBP performance / results depends on patients pre clinical condition and
the technique used (oscillometric method of calculating NIBP).
1. Place the limb in such a way to minimize stretching and avoid weight exertion on
affected nerves.
2 Select a measurement interval that provides adequate venous drainage during cuff
deflation.
3. The limb on which the cuff is connected must be inspected periodically in order to
detect venostasis.
4. An accurate BP determination might be difficult if the patient has irregular cardiac
rhythm.
5. Cuff size selection is a very important criteria to get accurate blood pressure readings.
6. Avoid compression or restriction of the NIBP pressure tube.
Note
Cuffs become soft after use. They sometimes develop folds which are permanent
and hence leave temporary marks on the limb. Any cuffs that exhibit this effect
should be replaced.
If NIBP is used with SpO 2, (PR) pulse rate is derived from SpO2 sensor.
If NIBP, SpO2 and ECG all three are connected to patient; then heart rate (HR) is
derived from ECG.
Do not measure NIBP continuously, as it might result in prolonged impairment of the
blood circulation of the patient.
2.13 Star 55
Caution
Extreme caution must be taken when NIBP is set to STAT mode for all types of
patients. Reports have been made of nerve injury occurring during use of automatically
cycled blood pressure measurements.
Caution
For NIBP measurements :
z The cuff selected must fit the upper limb properly and must overlap to encircle
the limb on which it is applied. There should not be any air gap in between the
cuff and the limb. It can be fastened using the VELCRO strap.
z The usual application sites of the cuff is the brachial artery. The right size of
cuff should be wrapped around the arm to achieve the best result.
z The cuff is designed to inflate only when it is wrapped on the limbs. Do not
inflate the cuff when not supported by the extremity.
WARNING
The cuff should not be applied on a limb being used for an intravenous infusion.
2.14
INVASIVE BLOOD PRESSURE
The results of IBP are observed to be the more accurate, when compared with
indirect technique (NIBP) there are some distinct advantages of IBP over NIBP
like accessibility of various locations for measuring pressure in body.
Patient preparation :
Note
The following actions apply to Medex make 'Logical' transducers only. (For
other transducer types, refer to the manufacturers recommended assembly
instruction)
1. Turn ON the monitor and plug in the pressure cable, or cables in case of
double pressure option.
2. It is vital that blood clots are not allowed to form in the catheter. This is
achieved by continuous flushing with the saline solution. The rate of flow
is limited to 3 to 5 ml/hr by a flushing device, which does not alter the
pressure being recorded. Prepare the pressure line and transducer by
flushing saline solution through the system. Ensure that the system is
free of air bubbles. (Even small bubbles will distort reading)
4. Connect the patient catheter to the pressure line, making sure that no air
is trapped.
5. Position the transducer so that it is in line with site at which blood pressure
is to be measured. Usually this is where the catheter tip is placed. (For
eg., in centrally located catheters, the tip is generally considered to be in
the mid-chest position. The transducer level is then set to corresponding
to the patient's mid-chest level).
2.15 Star 55
6. Close the pressure line to the patient and open the transducer venting
stopcock to atmosphere. Zero the monitor by pressing zero soft key ( ).
7. Select appropriate averaging time from SETUP menu. SLOW, NORMAL and
FAST options are provided.
8. Close the venting stopcock to atmosphere, and open the stopcock to the
patient.
2.16
Figure 2.16
2.17 Star 55
CAPNOGRAPHY
Theory of operation
The principle of Capnography is based on the absorption of infrared radiation
by CO 2. The technique is known as non-dispersive infrared absorption technique.
The spectral region is particularly appropriate for measuring carbon dioxide
because it has a strong absorption band in the near Infrared wavelength. CO 2
selectively absorbs specific wavelengths of Infrared light. The main part of the
system is CO 2 bench, which consist of one IR source and detector. A sample
of patient's expired gas that consists of CO 2, Water vapors, Nitrogen, Anaesthetic
Agents, etc. is drawn from a lightweight T-piece through a sample line into the
CO 2 bench. Expired air is aspirated into measuring chamber (CO 2 bench) by a
small pump. The amount of light passing through a sample cell varies according
to the concentration of CO 2 in the sample cell. When concentration of CO 2 in
sample cell is high, more light is absorbed by the sample and therefore a small
amount of light reaches the detector as compared to low concentration of CO 2 .
The amount of light absorbed is proportional to the concentration of CO 2 . The
CO 2 concentration measured by the monitor is usually expressed as end tidal
concentration of CO 2 (EtCO 2 ), expressed in terms of mmHg or percentage (%)
or Kilopascal (Kpa).
Figure 2.17
2.18
End tidal CO 2 is the concentration of CO 2 measured at the end of tidal volume
expired (Point D in above diagram).
C - D : The expiratory plateau i.e. the period during which the level of
CO 2 in the lungs ceases to increase significantly.
Figure 2.18
2.19 Star 55
from pulmonary blood to alveolar gas space. CO 2 diffuses into this space because
continuous breathing keeps CO 2 concentration in alveoli lower than that in
pulmonary circulation. During exhalation, gas leaving lungs mixes thoroughly,
so Capnograph measures average concentration of CO 2 from all the alveoli.
Capnography gives an excellent pictures of respiratory process.
Technology Used
Capnography measurement is done with the help of microstream technology
in this unit.
Microstream Capnography
In microstream capnography method, the optical sensor is incorporated in
the module. Gas sample is aspirated from the patient at a flow rate of 50
ml/min with the help of FilterLine (connected to endotrachial tube with the
help of ‘T’ connector or directly from nose with the help of Nasal prongs)
and is given to module. The CO 2 measurement takes place at the CO 2 bench.
After the measurement, the waste gas exhausted from the rear panel.
2.20
Respiration Rate
The respiration rate is defined as the average rate of the patient's last 8
significant measured breaths. During the first 8 breaths the respiration rate
is calculated by averaging the available data. The module measures the RR
in range of 0 to 150 bpm.
Initialization Time
The module requires a typically a time of 30 seconds before entering into the
first operating mode. During this time, the module completes self test and
initialization procedures required for proper operation of the module.
The module prevents the triggering of an auto zero in the following situations:
z In case of purging until the end of this state.
z 20 seconds to 3 minutes from the last detected breath.
z While wait up to 5 minutes for host auto zero enable command.
2.21 Star 55
Leak Tightness
The leak rate of the module flow system is less than 40 mBr per minute
when a 30% vacuum is invoked on the flow system.
Purge
The module performs a purging whenever it detects an occlusion in the
FilterLine or in the airway adapter. The module informs the host of the purge
situation by setting the "Purging in progress" bit in the Wave Message While
purging, the CO 2 values are invalid. The duration of the purging is up to 30
seconds.
The module recovers from occlusion when FilterLine is replaced. The module
then shifts to initialization mode for typically less than 5 seconds and then goes
to normal measurement mode.
Definitions
Breath : A rise and fall in the carbon-
dioxide concentration of at least
one percent carbon-dioxide is no
less than 0.4 seconds.
One inhalation + One exhalation
= One Breath.
2.22
End Tidal Carbon-dioxide (EtCO 2 ) : The level of CO 2 in the airway at
the end of expiration. In L&T's
Capnography one breath is the
sampling interval, therefore
monitor will report the CO 2 level at
the end-respiration point of each
breath.
Machine Preparation
1. Switch ON the unit.
2. Make sure the patient connection to the unit with the help of FilterLine
and T Connector.
3. Machine takes approx. 30 seconds for its initialization. During this
time sensor gets warm up and ‘INITIALIZING MODULE’ message will
appear on the screen.
4. Then monitor will perform Auto Zero (if required) and ‘AUTO ZERO’
message will appear on the screen.
5. Monitor is ready for Capnography monitoring.
Patient Preparation
1. Prepare the patient (Refer Figure 2.19 and Figure 2.20) for CO 2
measurement. Use recommended accessories.
2. Screw up one end of the ‘T’ Connector to the unit through Filter Line.
Use proper types for adults and neonatal accessories.
2.23 Star 55
Figure 2.19 Patient with ‘T’ Figure 2.20 Patient with Nasal
connector connected to Prong (Adult & Paediatric nasal
Endotrachial tube. prongs are available).
Caution
Following accessories are provided for Capnography along with Star 55 monitor.
z Capno Line
- Adult
- Paediatric
- Infant - Neonate
z Filter Line
- Adult / Paediatric
- H set Adult / Paediatrc
- H set Infant / Neonatal
WARNING
CO2 accessories are for single use only, use new accessories for new patients.
2.24
3
OP
ER
AT
MA A N ION
IN D S
SC
RE
EN
3 Star 55
Notes :
OPERATION
Connect the unit to a mains supply socket with a proper ground / earthing
connection.
3.1 Star 55
MAIN SCREEN 1
Figure 3.1
Note
Main screen when maximum i.e. eight waveforms are present.
3.2
MAIN SCREEN 2
Figure 3.2
Note
Main screen when ST segment is ON in 5 lead ECG cable.
3.3 Star 55
MAIN SCREEN 3
Figure 3.3
Note
Main screen when maximum ECG waveforms are present.
3.4
MAIN SCREEN 4
Figure 3.4
Note
Main screen when single ECG waveform and three digital fields are present.
3.5 Star 55
Menu Trend Display Volume Recall Autoset
3.6
Alarm Record Parameter 3
CO2
Timer Exit Exit
RESP
NIBP Exit
TEMP
EXIT ID ECG Filt Mode Duration
Bed No Waveform Speed Scroll Display
New Patient First Name RESP Speed Clear Exit
Patient Mode Last Name Default Exit
Patient CLR Resolution
Age Pacer Det Display
Exit Display
Sex PR Source Edit
Confirm Exit
Weight Alarm Vol Exit
Cancel
Height Beep Vol Parameter 1
Clear All Limit Display Parameter 2
Save ST Display
Exit Exit Exit Exit
Menu Select this to go to Monitor settings / System functions.
Trend Select this to retrieve the data of the patients recorded.
Display Select this to choose different display formats.
Volume Select this to set and vary alarm volume and beep volume.
Recall Select this to recall alarm, ECG, arrhythmia and ST trend.
Autoset Select this to set alarm limits automatically for all the
parameters except NIBP.
ECG :
HR/PR high limit = (Present HR/PR) x 8/10 +76
HR/PR low limit = (Present HR/PR) x 8/10 +2
SpO2 :
SpO2 high limit = 100
SpO2 low limit = (Present SpO2 Value -8) or 80
whichever is greater.
IBP :
Systolic high limit = Present Systolic value +8
Systolic low limit = Present Systolic value -8
Diastolic high limit = Present Diastolic value +8
Diastolic low limit = Present Diastolic value -8
Respiration :
Respiration high limit = Present Respiration rate +5
Respiration low limit = Present Respiration rate -5
Temperature :
T1 high limit = Present T1 value +2
T1 low limit = Present T1 value –2
3.7 Star 55
Capnography :
EtCO 2 high limit = Present value +5
EtCO 2 low limit = Present value -5
FiCO 2 high limit = Present value +2
FiCO 2 low limit = 0
ST :
ST high limit = Present value +2
ST low limit = Present value -2
WARNING
Check if the current alarm preset value is appropriate, prior to use on each patient.
3.8
Setting Date Time Commn ST EN Arrhy EN Demo Exit
3.9
Start Cal Italian
Unit
Exit Bhahasa
Default Setting NIBP Russian
Non Disp ParaAlm Latched
CO2 German
Exit Non Latched
TEMP Chinese
Exit
ST Exit
Audio/Led ON Height
Hospital
During Self Test (Start-up Sequence)
Star 55
Exit Exit
Special Function Adjustment Menu Is Displayed If Optical Encoder Is Pressed
SETTING : Select this to view/modify different monitor settings.
Date Format : Select this to choose different date formats from the list.
SpO2 for NIBP : Select this to enable/disable SpO2 monitoring during NIBP
measurement.
Alarm Type : Select this to choose either latched or Non latched as Alarm type.
o
Unit : Select this to choose the measurement unit for the
parameter from the list. The different parameters and
the units in the list are as given below.
Parameters Unit
NIBP mmHg and kPa
CO2 mmHg, kPa and Vol%
Temp Centigrade and Fahrenheit
ST mm and mV
Height Inches and Cms
Weight Kg and lb
IBP mmHg and Kpa
Default Setting : Select this to set monitor for Hospital or Factory setting as
default in real time screen.
* Future upgrade
3.10
Hospital Setting : Press ALARM ACK and HOME keys simultaneously in set up
screen to store required display settings. Select Hospital in
Default setting.
Factory Setting : Select facotry in Default setting. Default Factory settings are
as follows.
ECG:
Alarm : Disable
Gain : 1mV
Lead : II
Trace Speed : 25 mm/sec
HR Upper Limit : 150 (A)*160(P)* 80(N)*
HR Lower Limit : 50(A) 60(P) 80(N)
Pacer : OFF
SpO2:
Alarm : Disable
Gain : X1
Response : Normal
Trace Speed : 25 mm/sec
HR Upper Limit : 100(A) 100(P) 100(N)
HR Lower Limit : 85(A) 85(P) 85(N)
CO2:
Alarm : Disable
Scale : 20
Unit : mmHg
Trace Speed : 12.5 mm/sec
EtCO2 Upper Limit : 40(A) 40(P) 40(N)
EtCO2 Lower Limit : 25(A) 25(P) 25(N)
FiCO2 Upper Limit : 4(A) 4(P) 4(N)
RR Upper Limit : 30(A) 100(P) 100(N)
RR Upper Limit : 10(A) 10(P) 50(N)
No Breath : 30 sec(A) 30 sec(N) (If enabled)
3.11 Star 55
NIBP:
Alarm : Disable
Mode : Manual
Auto Timer : 2 min
SYS Upper Limit : 150(A) 135(P) 120(N)
SYS Lower Limit : 95(A) 95(P) 50(N)
DIA Upper Limit : 100(A) 100(P) 80(N)
DIA Lower Limit : 65(A) 65(P) 20(N)
Unit : mmHg
Temp:
Alarm : Disable
Unit : °F
Upper Limit ; 104.0(A) 104.0(N)
Lower Limit : 89.6(A) 89.6(N)
Resp:
Alarm : Disable
Gain : X4
No Breath : Disable
Apnea Timer : 30 sec
RR Upper Limit : 30(A) 100(P) 100(N)
RR Lower Limit : 10(A) 10(P) 50(N)
Resp Speed : 12.5 mm/sec
ST:
Alarm : OFF
Lead : II (For 3 Lead), III and V (For 5 Lead)
* A - Adult
P - Paediatric
N - Neonatal
3.12
IBP:
General:
3.13 Star 55
CO2 pump will be ON.
Rec ON Ala will be OFF.
Tabular Trend resolution will be 30 sec.
Graphical trend scale will be 2 Hrs.
Resp Source will be RA-LA for respiration.
Resp will be CO2 for CO2 module.
Display will be in Format1 for 3/5 lead ECG cable.
In setup (Service, Production and User) settings will not change.
Non Disp Para Alm : Select this to choose either Audio/LED ON or Audio/LED OFF
alarm for non display parameter.
DATE : Select this to set year, month and date from numeric keypad.
EXIT : Select this to save and exit from the Configuration mode.
* Future upgrade
3.14
4
PA
R AM
SE ET
TT ER
IN
G
4 Star 55
Notes:
ECG
When ECG option is selected in the Main screen, ECG Setup window will pop-up on
the screen as shown in Figure 4.1.
Figure 4.1
Lead : When Lead is selected depending upon the cable mode chosen
3/5 Lead setup window will appear as shown in Figure 4.2 and
4.3. Select any one of the leads in 3 Lead setup and select any
number of leads in 5 lead setup based on the selection of
number of ECG waveforms in display format.
Figure 4.2
Figure 4.3
OK : Select this to save the settings and exit from Lead setup.
Exit : Select this to exit from the Lead setup without saving the settings.
Gain : Allows the user to change the amplitude of the ECG waveform in scales
X0.2, X0.5, X0.75, X1, X2, X5.
X0.2 will provide the lowest amplitude and X5 will have maximum
amplitude.
4.1 Star 55
Alarm : Select this to Enable or Disable HR alarm detection from the
drop down list.
High Limit : Select this to set upper alarm limits for HR from Numeric keypad
as shown in Figure 4.4 (To use this function ensure that HR
alarm is enabled).
Figure 4.4
Low limit : Select this to set lower alarm limits for HR from the Numeric keypad
(To use this function ensure that HR alarm is enabled).
Cal : Allows the user to enable (switch ON) or disable (switch OFF)
Cal option. When it is selected square pulses of 1mV will be
displayed.
Figure 4.5
4.2
OK : Select this to save the settings and exit from Arrhy setup.
Exit : Select this to exit from Arrhy setup without saving the settings.
Note
Flashing heart in parameter display area indicates valid QRS/Pulse detection. ECG
speed ( 12.5/25/50 mm/sec) and ECG Mode (Mon/Diag./OT) options are provided in
SETUP menu and displays value after window averaging of last eight QRS peaks.
4.3
Star 55
ST
When ST is selected in the Main screen, based on the Lead selection of ECG
menu ST Setup window will pop-up on the screen as shown in Figure 4.6 and 4.7.
Figure 4.8
OK : Select this to save the settings and exit from Lead setup.
Exit : Select this to exit from the Lead setup without saving the settings.
High Limit : Select this to set upper alarm limits for ST alarm from Numeric
keypad (To use this function, ensure that alarm is enabled).
Low limit : Select this to set lower alarm limits for ST alarm from Numeric
keypad (To use this function, ensure that alarm is enabled).
4.4
Note
In 5 Lead Setup screen High Limit and Low Limit of all the three ST segment can
be seen.
Mark : Select this to enter ST 3/5 Lead Mark Setup menu appears as
shown in Figure 4.9 and 4.10.
ISO : Select this to mark the Iso Electric Point using optical encoder.
The default value is 82.5 msec.
ST : Select this to mark the Iso Electric Point using optical encoder.
The default value is 122.5 msec.
Exit : Select this to exit from ST 3/5 Lead Mark Setup menu.
Note
When setting ST analysis ON, the monitor will select ‘Diagnostic’ mode. User can
set it to ‘Monitor’ or ‘OT’ mode as required. It is recommended to view the ST
analysis in ‘Diagnostic’ mode.
4.5
Star 55
RESP (When sourced from ECG cable)
When RESP is selected in the Main screen, Resp setup window will pop-up on the
screen as shown in Figure 4.11.
Figure 4.11
Alarm : Select this to enable / disable the alarm from the drop down list.
High Limit : Select this to set upper alarm limits for Respiration Rate from
Numeric keypad (To use this function, ensure that alarm is
enabled).
Low Limit : Select this to set lower alarm limits for Respiration Rate from
Numeric keypad (To use this function, ensure that alarm is enabled).
The last set gain level is saved in memory. This setting will remain even when
the unit is switched OFF.
RR Source : Select this to choose the source for Respiration rate between
RA-LA and RA-LL.
Figure 4.12
Alarm : Select this to enable (switch ON) or disable (switch OFF) the
Temperature alarm from the drop down list.
High Limit : Select this to set upper alarm limit for Temperature alarm
from Numeric keypad (To use this function, ensure that
alarm is enabled).
Low Limit : Select this to set lower alarm limit for Temperature alarm
from Numeric keypad (To use this function, ensure that
alarm is enabled).
4.7 Star 55
SpO2
When SpO2 is selected in the main screen, SpO2 setup window will pop-up on the
screen as shown in Figure 4.13.
Figure 4.13
Response : Select this to set the response mode for SpO2 readings from
the drop down list.
Norm : Preferred for adults.
Alarm : Select this to enable (switch ON) or disable (switch OFF) the
SpO 2 alarm by drop down list.
High Limit : Select this to set upper alarm limits of SpO2 from Numeric
keypad (To use this function, ensure that alarm is enabled).
Low Limit : Select this to set lower alarm limits of SpO2 from Numeric
keypad (To use this function, ensure that alarm is enabled).
Gain : Allows the user to change the amplitude of the SpO2 waveform
in scales of X1 and X0.5.
4.8
NIBP
When NIBP is selected in the main screen, NIBP Setup window will pop-up on the
screen as shown in Figure 4.14.
Figure 4.14
Alarm : Select this to enable (switch ON) or disable (switch OFF) the
NIBP alarm.
Sys High Limit : Select this to set upper alarm limit for Systolic alarm from Numeric
keypad ( To use this function, ensure that alarm is enabled).
4.9 Star 55
Sys Low Limit : Select this to set lower alarm limit for Systolic alarm from Numeric
keypad ( To use this function, ensure that alarm is enabled).
Dia High Limit : Select this to set upper alarm limit for Diastolic alarm from Numeric
keypad ( To use this function, ensure that alarm is enabled).
Dia Low Limit : Select this to set lower alarm limit for Diastolic alarm from Numeric
keypad ( To use this function, ensure that alarm is enabled).
Note
In NIBP auto mode, time left before the next measurement is displayed at
the timer display area. Time displayed is decremented every minute.
4.10
CAPNOGRAPHY (Optional)
When CO2 is selected in the main screen, CO2 setup window will pop-up on the screen
as shown in Figure 4.15.
Figure 4.15
RR Alarm : Select this to enable / disable the RR alarm from the drop down list.
CO2 Alarm : Select this to enable / disable the CO2 alarm from the drop down list.
RR High Limit : Select this to set upper alarm limit for RR alarm from Numeric
keypad (To use this function, ensure that RR alarm is enabled).
RR Low Limit : Select this to set lower alarm limit for RR alarm from Numeric
keypad (To use this function, ensure that RR alarm is enabled).
FiCO2 High Limit : Select this to set upper alarm limit for FiCO2 alarm from Numeric
keypad (To use this function, ensure that CO2 alarm is enabled).
EtCO2 High Limit : Select this to set upper alarm limit for EtCO2 alarm from Numeric
keypad (To use this function, ensure that CO2 alarm is enabled).
EtCO2 Low Limit : Select this to set lower alarm limit for EtCO2 alarm from Numeric
keypad (To use this function, ensure that CO 2 alarm is enabled).
4.11
Star 55
Scale : Select this to change the amplitude of the CO waveform in
2
scales 20, 40, 60, 80 or 100 mmHg from the drop down list.
RR Source : Select this to choose the source of Respiration either from the
CO2 (if connected) or from ECG (RA-LA or RA-LL).
4.12
IBP (Optional)
When IBP is selected in the main screen, IBP Setup window will pop up on the
screen as shown in Figure 4.16.
Figure 4.16
Alarm : Select this to Enable/Disable alarm from the drop down list.
Sys High Limit : Select this to set upper alarm limits for Systolic value (To use
this function, ensure that RR alarm is enabled).
Sys Low Limit : Select this to set lower alarm limits for Systolic value (To use
this function, ensure that RR alarm is enabled).
Dia High Limit : Select this to set upper alarm limits for Diastolic value (To use
this function, ensure that RR alarm is enabled)
Dia Low Limit : Select this to set lower alarm limits for Diastolic value (To use
this function, ensure that RR alarm is enabled)
Scale : Select this to choose scale from the drop down list.
Label : Select this to choose label for pressure waveform from the
drop down list.
Add Label : Select this to add label through Alpha English keyboard.
CAL : Select this to get cal pulse of 100mmHg. Press this key again
to come out of this mode. This function can be used to
ascertain accuracy of IBP detection circuit.
4.13 Star 55
CAL FAC : Select this to calibrate the IBP transducer.
1. Press 'CAL' (machine will introduce 100mmHg CAL signal)
2. Press 'CAL FAC' and adjust display to read 100mmHg.
3. Press 'CAL' again to come out of calibration mode.
Note
This is not a routine procedure and needs to be carried out only in case of major
discrepancies in IBP readings which might be due to ageing effect in reusable
transducers.
Mean Size : Select this to choose the size of the mean value from the drop
down list.
IBP Average : Select this to choose the rate at which the display of averaging
of IBP readings from the drop down list.
NORM : Averaging of IBP readings shall be done at the rate of 6 beats.
SLOW : Averaging of IBP readings shall be done at the rate of 8 Beats.
FAST : Averaging of IBP readings shall be done at the rate of 4 Beats
EXIT : Select this to save and exit from the IBP SETUP menu.
DETAILED INFORMATION :
1. Before the start of using a new pressure measurement, it is necessary
to ZERO the transducer to atmospheric pressure. Sometimes it is also
necessary to ZERO the transducer during the pressure measurement,
if required, for better results.
Zeroing Procedure :
To ensure accurate pressure readings, the transducer must be zeroed
to atmospheric pressure.
Note
The transducer must be “ZEROED” whenever the “ZERO” message
is displayed.
• Close the pressure line to the patient. Open the transducer to air
(atmospheric pressure).
4.14
• The transducer should be placed at the level of the heart (approximately
mid axillary line).
• Press 'ZERO' key on the front panel. IBP zero window will appear. Press
OK to confirm zeroing. Wait until '0' is displayed in parameter display
area. Transducer zeroing is now completed.
• All pressure channels or desired pressure channel can be zeroed in
IBP ZERO menu.
4.15 Star 55
The table below identifies the labels available
Label :
IBP Invasive Blood Pressure
ICP Intracranial Pressure
CVP Central Venous Pressure
PAP Pulmonary Artery Pressure
LAP Left Atrial Pressure
RAP Right Atrial Pressure
LVP Left Ventricular Pressure
ART Arterial Blood Pressure
P C W Pulmonary Capillary Wedge Pressure
6 To change label, select the IBP option from the main screen using
Optical Encoder key and choose LABEL.
7 Rotate the encoder either clockwise or anti-clockwise and press it to
select the desired label.
8 Change of IBP labels will change the gain and default alarm limits for
systolic/diastolic pressure.
9 Adjust pressure range/waveform size:
The pressure waveform size can be adjusted by selecting a different
pressure gain/scale.You can adjust waveform size by selecting the
pressure gain by pressing the GAIN option in IBP menu.
10 Scales available – Auto, 300, 240, 200, 180, 150, 120, 100, 80, 60, 30,
20,10 and 5.
4.16
DRUG CAL
When DRUG CAL is selected in the main screen, DRUG CAL Setup window will
pop up on the screen as shown in Figure 4.17.
Figure 4.17
Drug : Select this to choose the Drug from the drop down list.
Weight : Select this to enter the Weight of the patient from the Numeric
keypad if limits are enabled. If the weight is already entered in the
PATIENT INFO, same value will be set here.
Note
When drug and weight is selected default values are set in all other fields. User
can change the values if required.
Amount : Select this to enter the Amount of the drug from the the Numeric keypad.
Volume : Select this to enter the Volume of the drug from the Numeric keypad.
Conc : Select this to enter the Concentration of the drug from the Numeric
keypad
Dose/min : Select this to enter the Drug Dosage per min from the Numeric
keypad
Dose/hr : Select this to enter the Drug Dosage per hour from the Numeric
keypad
4.17
Star 55
Dose/kg/min : Select this to enter the Drug Dosage per kg per min from the
Numeric keypad
Dose/kg/hr : Select this to enter the Drug Dosage per kg per hour from the
Numeric keypad
INF Rate : Select this to enter the Infusion rate from the Numeric keypad
Drip Rate : Select this to enter the Drip rate from the Numeric keypad.
Drop Size : Select this to enter the Drop size from the numeric keypad.
Figure 4.18
: Select this to go to the previous page.
4.18
Amount Unit : Select this to set or change the Amount unit. Selecting a
new unit will reset all the fields.
Add Drug : Select this to add customized drugs other than system default
drugs. When this is selected, Add New Drug window will pop up as
shown in Figure 4.19.
Figure 4.19
Drug Name : Select this to enter the new drug from the Alpha
English keyboard. The maximum no.of drugs and
maximum characters can be entered is 10.
Unit : Select this to choose the unit for amount from the drop
down list.
Note:
Two fields among amount, volume and concentration of drug, one among
1) Dose/min
2) Dose/hr
3) Dose/Kg/min
4) Dose/Kg/hr
5) Duration
6) Drip Rate
is mandatory and also ‘DROP SIZE’ field should be entered to calculate
and display the other values.
4.19
Star 55
Left blank intentionally
5
SY
FU ST
NC EM
TIO
NS
5
Star 55
Notes :
Menu Trend Display Volume Recall Autoset
5.1
Timer Exit Exit
RESP
NIBP Exit
TEMP
EXIT ID ECG Filt Mode Duration
Bed No Waveform Speed Scroll Display
New Patient First Name RESP Speed Clear Exit
Patient Mode Last Name Default Exit
Patient CLR Resolution
Age Pacer Det Display
Exit Display
Sex PR Source Edit
Confirm Exit
Weight Alarm Vol Exit
Cancel
Height Beep Vol Parameter 1
Clear All Limit Display Parameter 2
Save ST Display
Exit Exit Exit Exit
Star 55
System Functions
Volume : Select this to adjust the Alarm Volume and Beep Volume.
Autoset : Select this to set alarm limits automatically for all parameters
except NIBP.
5.2
Menu
Pat Info : Select this to get Patient Info Menu to enter patient details.
Figure 5.1
New Patient : Select New Patient menu, Star55 displays new patient
entry panel as shown below.
Figure 5.2
ID : Select this to enter patient’s identification number from the
Alpha-Numeric keypad.
Bed No : Select this to enter patient’s bed number from Alpha English
key board.
First Name : Select this to enter patient’s first name from Alpha English
keyboard (Maximum 9 characters).
Last Name : Select this to enter patient’s last name from Alpha English
keyboard (Maximum 9 characters).
Age : Select this to enter patient’s age from Numeric keypad. The
age will be in years for adults and days for neonates.
5.3
Star 55
Sex : Select this to enter patient’s sex from drop down list.
Weight : Select this to enter patients’s weight from Numeric keypad.
Height : Select this to enter patient’s height from Numeric keypad.
Clear All : Select this to reset entered data.
Save : Select this to save the entered data.
Exit : Select this to return to the patient info menu.
Patient Mode : Select this to choose Adult, Neonate or Pediatric mode from
drop down list.
Patient CLR : Select this to clear all recorded trend data of selected patient
from drop down list. Confirmation window will be displayed.
System : Select this to view all system information and alarm information.
Note
No changes can be made in system Info screen
All Info : Select this to view the information about the settings of the
monitor.
Alarm Info : Select this to view the information about the status of alarm
conditions. [Enable/ Disable, limits (High and Low)] and the unit of
all the parameters.
5.4
Mode : Select this to choose Direct, Delayed or Continuous recording
from drop down list.
Figure 5.3
Direct : Select this to record real time data for 8 seconds after pressing
recorder hot key.
Delayed : Select this to record 8 seconds (previous 6 seconds and real
time 2 seconds) after pressing recorder hot key.
Continuous : Select this to record real time data for 30 seconds after pressing
recorder hot key.
Timer : Select this to choose the time interval between two consecutive
recordings.
Color : Select this to choose the color of the parameter from the color box.
5.5
Star 55
Setup : Select this to set the general settings. Star55 displays the Setup
menu as shown below.
Figure 5.4
ECG Filt Mode : Select this to choose the bandwidths for ECG monitoring from
drop down list.
MON ( Monitoring - 0.5 Hz to 120 Hz)
DIAG ( Diagnostic - 0.05 Hz to 120 Hz)
OT (0.5 - 20 Hz)
Waveform Speed : Select this choose the waveform speed for all parameters except
CO2 / RESP from drop down list.
RESP Speed : Select this choose the waveform speed of CO2 / RESP from drop
down list.
Pacer Det : Select this to choose pacer detection ON/OFF from drop down list.
PR Source : Select this to choose PR Source either IBP, NIBP or SpO2 from drop
down list.
Alarm Vol : Select this to adjust alarm volume. Star55 displays volume menu.
5.6
: Select this to increase the alarm volume.
Beep Vol : Select this to adjust beep volume. Star55 displays volume menu.
: Select this to increase the beep volume.
Limit Display : Select this to enable / disable the display alarm limits.
5.7
Star 55
Trend
Figure 5.5
Display : Select this to view the graphical trend of the parameters selected.
Star55 displays Graphical Trend screen as shown in Figure 5.6.
Scroll : Select this to scroll through the graphical trend.
Zoom : Select this to view the zoomed graphical trend.
Exit : Select this to return to the Graphical Trend Duration menu.
5.8
Tachy High
Figure 5.6
Figure 5.7
Rec : Select this to record the current page of the tabular trend.
Exit : Select this to return to the Tabular Resolution menu.
5.9
Star 55
Exit : Select this to return to the Trend menu.
NIBP : Select this to view the stored NIBP readings along with parameters
selected.
Parameter1 : Select this to choose any one of the parameters for which the trend
data required from the drop down list.
Parameter2 : Select this to choose any one of the parameters for which the trend
data required from the drop down list.
Figure 5.8
5.10
OXYCRG : Select this to view graphic summary of 3 specific vital signs
- ECG (HR), SPO2, RESPIRATION (RR) of 2sec
duration.
Figure 5.9
5.11
Star 55
Patient : Select this to choose patient ID for which the trend data is required
from drop down list.
5.12
Display
Standard : Select this to set the standard display format which includes
ECG, cascaded ECG, Respiration/CO2, SpO2, Temperature and
NIBP.
User1 - User6 : Select this to view or edit pre configured user defined display
formats.
Five main display formats can be configured by the user.
* Format 1 - Displays 8 parameter waveforms.
* Format 2 - Displays 7 waveforms and maximum 4 digital values.
* Format 3 - Displays 4 - 6 waveforms and 2 - 3 digital values.
* Format 4 - Displays 1 - 3 waveforms and 4 - 6 digital values.
* Format 5 - Displays 1 - 3 waveforms and 1 - 3 digital values.
Note
Figure 5.10
5.13
Star 55
Format 1 : Select eight parameters in the waveform field1 to field 8 from the dropdown
list. Select the number of ECG waveforms from the dropdown list.
Format 2 : Select seven parameters in the waveform field1 to field 7 from the
dropdown list. Select the number of ECG waveforms from the dropdown
list. Select the number of digital values1, 2, 3, or 4 in row1 and select the
parameters in the digital fields from the dropdown list.
Format 3 : Select 4 - 6 parameters in the waveform field 1 to field 6 from the drop
down list. Select the number of ECG waveforms from the dropdown
list. Select the number of digital values 2, 3, (LW, SW) and (SW, LW) in
row 1 and select the parameters in the digital fields from the drop down list.
Format 4 : Select 1 - 3 parameters in the waveform field 1 to field 3 from the drop
down list. Select the number of ECG waveforms from the drop down list.
Select the number of digital values 2, 3, (LW, SW) and (SW, LW) in
row 1 and row 2 and select the parameters in the digital fields from the
drop down list.
Format 5 : Select 1 - 3 parameters in the waveform field 1 to field 3 from the drop
down list. Select the number of ECG waveforms from the drop down list.
Select the number of digital values 1,2, 3 row 1 and select the parameters
in the digital fields from the drop down list.
Note
IBP Overlap : Select this to set 2 or 3 IBP waveform for overlap from the IBP overlap
window.
5.14
Volume
Figure 5.11
Alarm Vol : Select this to adjust alarm volume. Star55 displays volume menu.
: Select this to increase the alarm volume.
Beep Vol : Select this to adjust beep volume. Star55 displays volume menu.
: Select this to increase the beep volume.
5.15
Star 55
Recall
Alarm : Select this to recall last 24 patient related alarm conditions in tabular format
as shown below. High alarm values and the message “Asystole” is displayed
in red color and low alarm values are displayed in violet color.
Figure 5.12
ECG : Select this to recall -30sec of freezed ECG waveforms with heart
rate. Each 30 sec strip stores in the form of 5 individual strips. Each
individual strip duration will be 6 sec. There will be maximum
of eight pages with five strips in each page.
5.16
Figure 5.13
5.17
Star 55
Figure 5.14
Figure 5.15
Autoset
Select this to set alarm limits for all the parameters (except for NIBP) .
5.18
6
MA
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6 Star 55
Notes :
Routine Maintenance
L&T products have been designed to operate continuously with minimum
maintenance.
However, in order to ensure better performance and safety, the routine maintenance
should be performed. A summarized schedule and full details of maintenance is
covered in this section.
Caution
Maintenance involving removal of the outer case or access covers must not be
attempted by the operator, but referred to a qualified L&T medical's representative.
A B
6.1 Star 55
Action Details
1B) Leads, sensor and probes should be carefully checked for any signs of
damage. Damaged leads should be replaced. Do not attempt to repair.
2B) All accessories must be cleaned before use. Following precautions must
be observed while cleaning and sterilizing of accessories.
Cleaning
WARNING
ECG:
a. ECG leads should be cleaned with a cloth slightly moistened with soap water.
Always allow the cable to dry thoroughly before use.
b. Clean blood from all external surfaces.
NIBP :
a. Cuffs - reusable may be cleaned in any of the two ways.
1) Sponge the outer surface of the cuff with a moist cloth.
2) Remove the cuff's bladder. Wash the cuff in water with soap or detergent /
disinfectant. Rinse the cuff and allow it to air dry.
b. Hoses - clean the hose by wiping it with a cloth moistened with soap water.
WARNING
Do not immerse the hose of NIBP in any liquid.
Do not use phenol - based cleaner for cleaning NIBP cuffs and hose.
Note
6.2
Sterilization
ECG:
a Clean as detailed above.
. b Wrap the connector lead in a polythene bag to prevent moisture penetration.
c. Loosely coil the cable to avoid any kinks.
d. Wrap cable in the recommended way for ethylene oxide sterilization.
NIBP :
WARNING
Do not steam autoclave the hose and cuff of NIBP. Use ethylene oxide gas only for
sterilization.
3A) Isolate equipment from mains supply before cleaning. Clean the case and front
panel with a soft cloth lightly moistened with warm soap water. Use only mild
soaps or detergents. Allow the machine to dry thoroughly before use. Do not
use chemicals or abrasive cleaning agents.
4A) Inspect the power cord for any signs of damage to cable or connectors. If
damaged, replace with a L&T replacement part. Do not attempt to repair.
5A) Isolate monitor from the mains supply. Switch ON the monitor, and observe
the green LED. If green LED is ON, the battery status is acceptable and no
further action is required.
If the green LED is flashing with LOW BATTERY indication, connect monitor
to mains supply. Leave the unit for charging. If low battery indication still remains
on the screen, refer the monitor to service personnel for battery replacement.
Caution
6.3 Star 55
6AB) Connect the power cable to the mains supply, switch ON the monitor and
check the following:
Adjustment of alarm volume.
Adjustment of Beep volume.
Adjustment of alarm limits. Enabling and disabling of individual alarms.
Operation of alarm functions.
Operation of recorder functions (optional).
Operation of fault function (patient cable disconnected).
Selection of trace speed for ECG, IBP, RESP, SpO2 and CO 2.
Selection of waveform parameters.
Selection of graphical/tabular trend view.
Selection of ECG, Resp, SpO2, IBP and CO2 gains.
Selection of ECG arrhythmias.
Selection of SpO2 response.
Selection of IBP label.
Selection of no breath detect duration.
0 0
Selection of TEMP unit (either C or F).
Selection of NIBP mode.
Return all adjustments to the desired settings after the checks.
7B) Perform the following checks to ensure that the monitor is calibrated correctly.
i. ECG
• Select CAL option from the menu list of ECG and observe the display.
• Square pulses will be produced of 1mV / 1 cm amplitude.
Note
ECG CAL is associated for II, III and V leads for 5 lead and lead II and III for 3 lead
ECG cable.
ii. TEMPERATURE
• Select CAL option from the menu list of TEMP and observe the display.
• 0
T will read 98.6 F.
6.4
Capnography Maintenance Schedule
• Use specified accessories only.
• Check the accessories before use.
• Sample line is disposable and for single use only.
• Incase of any water condensation in sample line, replace the sample
line with a new one.
• CO2 module should be calibrated once in a year or 4000 hours of usage, which
ever is earlier. This calibration should be done by authorized L&T personnel.
Battery Replacement
Call L&T authorized service personnel for battery replacement.
Press Press
Figure 6.1
Step 2 : Remove empty paper spool by pulling it out gently.
Step 3 : Insert new paper roll into the paper holder with the sensitive (shiny) side
of the paper facing the print head at the top of the recorder.
Step 4 : Unroll approximately 4 inches of paper.
Step 5 : Align the paper across the top of the metal bar.
Step 6 : Holding the paper in place, close the recorder cover.
Step 7 : To ensure that the paper is aligned properly and has not been pinched in the
recorder, pull the loose edge out a couple of inches. If the paper jams, open
the recorder cover and return to Step 5.
6.5 Star 55
Left blank intentionally
7
AC
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SS
OR
IES
7 Star 55
Notes:
ECG
Star 55 offers 3 lead and 5 lead ECG monitoring facility.
• 3 lead ECG cable (I, II, III) ( Refer figure 7.1 )
• 5 lead ECG cable (I, II, III, aVR, aVL, aVF, V) ( Refer figure 7.2 )
Figure 7.1 : 3 Lead ECG Cable Figure 7.2 : 5 Lead ECG Cable*
Respiration
Respiration can be monitored through same ECG cables 3/5 lead or through
Capnography. Priority for respiration is given to Capnography, if the option is installed.
Figure 7.3 : 3 Lead ECG Figure 7.4 : 5 Lead ECG Figure 7.5 : Adult / Paediatric
Cable Cable Filter line
* Optional
7.1 Star 55
Temperature
L&T Star 55 is compatible with YSI 400 series of temperature probes.
YSI 401 : Rectal/Esophageal temperature probe (Adult) (Refer Figure 7.6)
YSI 402 : Rectal/Esophageal temperature probe (Neonatal) (Refer Figure 7.7)
YSI 409A : Tape-on skin probe (Refer Figure 7.8)
* Optional
7.2
Pulse Oximetry
Accessories for Pulse Oximeter
• DS 100™ (DURA SENSOR) from NELLCOR for adults application (patients above 40 Kg)
(Refer Figure 7.9)
• DURA Y™ for universal application (patients above 1 Kg to 80 Kg) (Refer Figure 7.10)
• Extension cable (Refer Figure 7.11)
* Optional
7.3 Star 55
Non Invasive Blood Pressure
NIBP basic configuration comprises of following accessories:
• Adult cuff (14 cm x 37 cm) (Reusable) (Refer Figure 7.12 )
• Child cuff (9 cm x 27 cm) (Reusable) (Refer Figure 7.13 )
• Neonate cuff (3 cm x 9 cm) (Disposable) (Refer Figure 7.14 )
• Hose tube (3 meters) (Reusable) (Refer Figure 7.15 )
7.4
Capnography (Optional)
Following accessories are provided for Capnography (Microstream) along with
Star 55 monitor.
• Capno Line
- Adult (Refer Figure 7.16)
- Paediatric (Refer Figure 7.17)
- Infant - Neonate (Refer Figure 7.18)
7.5 Star 55
• Filter Line
- Adult / Paediatric (Refer Figure 7.19)
- H set Adult / Paediatric (Refer Figure 7.20)
- H set Infant / Neonatal (Refer Figure 7.21)
7.6
Invasive Blood Pressure (Optional)
Following accessories can be used for measuring IBP:
z Disposable Blood Pressure Transducer (Medex) (Refer Figure7.22)
z Reusable Blood Pressure Transducer (Medex)
z Reusable Interface Cable (Refer Figure 7.23)
Grounding Cable
This cable is used for grounding the unit (Refer Figure 7.24)
7.7 Star 55
Left Blank Intentionally
8
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8 Star 55
Notes:
Troubleshooting Chart
8.1 Star 55
Problems Cause Corrective Action
After NIBP measurement Cuff not connected properly. Check cuff for proper connection
is taken, unit displays (- -) and position. The cuff must be
in NIBP readings box. properly wrapped around the
limb and must not be loosely
attached.
Temperature alarms not Alarm is disabled Enable the alarm.
responding
Not recording and red Recorder paper roll Insert recorder paper roll.
indicator in recorder module empty.
is blinking.
Recorder cover is open Close the recorder cover.
Recorder module not Call L&T authorized service
connected. personnel.
8.2
Error Messages
Problem Cause Corrective Action Alarm Type
ECG
Patient HR / PR value Patient needs medical
exceeding higher alarm attention (Acknowledge
limit. the alarm). Reset the
limit, if require. PA
Patient HR / PR value Patient needs medical
below the lower alarm attention (Acknowledge
limit. the alarm). Reset the
limit, if require. PA
Check HR The difference between Patient needs medical
PR from SpO2 and HR attention.
from ECG is more than NA
30 BPM.
HR-RR coincidence The difference between Patient needs medical
HR and RR is less than attention.
30 BPM. NA
Communication Module not responding. Call L&T authorized
Error service personnel. TA
Leads OFF Cable not connected Connect the cable
properly to the unit. properly to the unit. TA
Fault messages Respective leads are Connect respective
i. LA Fault disconnected from the leads properly.
ii. RA Fault patient.
iii. LL Fault
iv. RL Fault
v. CL Fault TA
Respiration
Patient RR value Patient needs medical
exceeding higher alarm attention. (Acknowledge
limit. the alarm). Reset the
limit, if require. PA
Patient RR value below Patient needs medical
the lower alarm limit. attention (Acknowledge
the alarm). Reset the
limit, if require. PA
Fault RA-LA or RA-LL leads Connect the leads
are not connected properly to the patient.
properly to the patient. TA
8.3 Star 55
Problem Cause Corrective Action Alarm Type
Temperature
Patient Temperature Patient needs medical
value exceeding higher attention (Acknowledge
alarm limit. the alarm). Reset the
limit, if require. PA
Patient Temperature Patient needs medical
value below the lower attention (Acknowledge
alarm limit. the alarm). Reset the
limit, if require. PA
OFF Cable not connected Connect the cable
properly to the unit. properly to the unit. TA
-?- Range has exceeded. Patient needs medical
attention. NA
SpO2
Patient SpO2 value Patient needs medical
exceeding higher alarm attention (Acknowledge
limit. the alarm). Reset the
limit, if require. PA
Patient SpO2 value below Patient needs medical
the lower alarm limit. attention (Acknowledge
the alarm). Reset the
limit, if require. PA
Check Probe Site Sensor not connected Connect the sensor
properly to the patient. properly to the patient. PA
Sensor OFF Cable not connected Connect the cable
properly to the unit. properly to the unit. TA
Communication Module not Call L&T authorized
Error responding. service personnel. TA
8.4
Problem Cause Corrective Action Alarm Type
NIBP
Patient systolic pressure Patient needs medical
value exceeding higher attention (Acknowledge
alarm limit. the alarm). Reset the
limit, if require. PA
Patient systolic pressure Patient needs medical
value below the lower attention (Acknowledge
alarm limit. the alarm). Reset the
limit, if require. PA
Patient diastolic pressure Patient needs medical
value exceeding higher attention (Acknowledge
alarm limit. the alarm). Reset the
limit, if require. PA
Patient diastolic pressure Patient needs medical
value below the lower attention (Acknowledge
alarm limit. the alarm). Reset the
limit, if require. PA
Time Exceeded Measurement time Restart the NIBP
exceeded. measurement. TA
Air leak Removal of NIBP tube Check the connections
from the unit. and tighten if required.
Leakage in tube or cuff. Replace the tube or cuff
if required. TA
Pneumatic Bent or block in NIBP Replace the tube if
Blockage tube. required. TA
Over Pressure Use of inappropriate Use the appropriate cuff.
cuff. TA
Loose Cuff Cuff is loosely wrapped. Wrap the cuff properly. TA
Cuff Position Error Cuff placement is not at Place the cuff in proper
the proper position. position. TA
Communication Module not Call L&T authorized
Error responding. service personnel. TA
Star 55
8.5
Problem Cause Corrective Action Alarm Type
CO2
Patient EtCO2 value Patient needs medical
exceeding higher alarm attention (Acknowledge
limit. the alarm). Reset the
limit, if require. PA
Patient EtCO2 value Patient needs medical
below the lower alarm attention (Acknowledge
limit. the alarm). Reset the
limit, if require. PA
Patient FiCO2 value Patient needs medical
exceeding higher alarm attention (Acknowledge
limit. the alarm). Reset the
limit, if require. PA
CO2 No tubing Sample line not Connect sample line to
connected to the unit. the unit. TA
CO2 Purging Sample line blocked. Change the sample line. TA
Change sample Purging continues for Change the sample line.
line more than 30 Sec. TA
No breath RR is zero. Patient needs medical
attention (Acknowledge
the alarm). Reset the
limit, if require. PA
IBP
Patient systolic pressure Patient needs medical
value exceeding higher attention (Acknowledge
alarm limit. the alarm). Reset the
limit, if require. PA
Patient systolic pressure Patient needs medical
value below the lower attention (Acknowledge
alarm limit. the alarm). Reset the
limit, if require. PA
Patient diastolic pressure Patient needs medical
value exceeding higher attention (Acknowledge
alarm limit. the alarm). Reset the
limit, if require. PA
Patient diastolic pressure Patient needs medical
value below the lower attention (Acknowledge
alarm limit. the alarm). Reset the
limit, if require. PA
8.6
Note
Physiological Alarms (PA) and Technical Alarms (TA) are should be treated as
High Priority and Medium Priority alarms respectively.
Physiological Alarms will appear in case of Power down and Power failure.
8.7 Star 55
PROBLEMS OBSERVED DURING
ECG MONITORING
PATIENT RELATED
A. INVOLUNTARY MOVEMENT
Figure 8.1
IDENTIFICATION :
Muscle movement near the electrodes generates myoelectricity or additional
background electrical patterns. Notice the irregular height and width of the spikes
(Refer Figure 8.1).
CORRECTIVE ACTION :
Involuntary movement is usually a result of patient discomfort and is caused by
chill or muscle tremors, coughing or other nervous reactions. Assuring the patient
that the procedure will not hurt and setting his mind at ease will help relieve
natural anxieties. Ensure the room temperature is warm enough for the patient.
B. VOLUNTARY MOVEMENT
Figure 8.2
8.8
IDENTIFICATION :
Gross body movement will cause base line deviation. The signal will be present
but, there will be baseline wanders. Myoelectricity may be present as well
(Refer Figure 8.2).
CORRECTIVE ACTION :
The patient should be comfortable and relaxed. Again, reassuring the patient
that the monitoring will not hurt him, will restore confidence. Usually voluntary
movement is of short duration. Normal ECG waveform will return when
movement stops. If severe artifact results from slightest body movements,
check the electrode application.
Figure 8.3
IDENTIFICATION :
Failure to prep a patient with oily skin will cause low amplitude, wandering base
line and 60/50 Hz frequency interference. Poor skin preparation may not show
problems immediately, but effects the signal in long term monitoring
(Refer Figure 8.3)
CORRECTIVE ACTION :
Cleaning the body oils and dead tissues are essential for proper adhesion and
contact of electrodes. The prep area should includes the electrodes site under
the adhesive as well as the contact area. Preferred scrub solutions for skin
preparation are : abrasion, special detergent solutions and saline wash. While
using solutions, ensure that the area is dried before the application of electrodes.
8.9 Star 55
ELECTRODES RELATED
A. LOOSE ELECTRODE
Figure 8.4
PLACEMENT ON BONY AREA :
Electrode placed on a bony area will show abrupt base line deviation or complete
loss of signal. A loose electrode usually have a full amplitude signal with several
artifacts. It also happens if electrodes are not placed properly (Refer Figure 8.4).
CORRECTIVE ACTION :
Electrodes should be placed on fleshy areas which will help to place electrodes
properly. Check that the patient cables are not pulling the electrodes and the
electrode is attached properly to the body of the patient.
Figure 8.5
This signal usually degenerates with time. Characteristics such as low amplitude,
diphasic QRS complexes, 60/50 Hz frequency interference and base line wander
will usually be present (Refer Figure 8.5).
8.10
CORRECTIVE ACTION :
Check the electrode to make sure that the electrolyte is moist and is in sufficient
quantity and is in proper contact with the electrode and skin.
EQUIPMENT RELATED
A. POOR CONNECTION
Figure 8.6
IDENTIFICATION :
Poor connection will indicate muscle artifact on entire trace (Refer Figure 8.6).
CORRECTIVE ACTION :
Check lead wires, junction of cable and electrode to ensure proper connection.
Figure 8.7
IDENTIFICATION :
Broken lead wire or completely detached electrode will cause pure 60/50 Hz
frequency interference. The QRS complex is almost masked by the extremely
wide base line ( Refer Figure 8.7 ).
8.11 Star 55
CORRECTIVE ACTION :
Check the lead wires, cables and connections. Replace with new cable if
required. The use of shielded cables is recommended, to protect lead wires
from interfering current.
C. BAD GROUNDING
Figure 8.8
IDENTIFICATION :
Bad grounding may cause 60/50 Hz frequency interference which is
distinguishable because of wide base line (Refer Figure 8.8).
CORRECTIVE ACTION :
Bad grounding may also create a shock hazard. If grounding is doubtful,
request for an electrical maintenance check. TV sets, electrical cords and
fluorescent bed lamps near the bed may also cause 60/50 Hz frequency
interference.
D. STATIC ELECTRICITY
Figure 8.9
8.12
IDENTIFICATION :
Static electricity may throw the trace off the screen abruptly. The trace will
gradually recentre itself within few seconds ( Refer Figure 8.9).
CORRECTIVE ACTION :
Synthetic fabrics in bed sheets and clothing may generate static electricity.
This can disturb the trace abruptly without patient movement, especially
when cables without proper shieldings are used.
Star 55
8.13
CO 2 TYPICAL WAVEFORMS
Normal Waveform:
The “normal” capnogram provides a waveform of changing levels of
expired CO 2 ( Refer Figure 8.10).
Figure 8.10
The letters A - E indicate the phase of the respiration cycle:
Cardiogenic Oscillations:
Cardiogenic oscillations appears during the final phase of the alveolar
plateau and during the descending limb (Refer Figure 8.11). They are caused
by the heart beating against the lungs.
Figure 8.11
8.14
Characteristics:
a. Rhythmic and equal to heart rate
b. May be observed in pediatric patients, mechanically ventilated at low
respiratory rates with prolonged expiratory times.
Hyperventilation:
An decrease in the level of the End Tidal CO2 from previous levels (Refer Figure 8.12).
Figure 8.12
Possible Causes:
a. Increase in respiratory rate
b. Increase in Tidal Volume
c. Decrease in metabolic rate.
d. Fall in body temperature
NOTE:
Exponentially decrease in CO 2 can also be because of cardiac arrest or
severe hypotension (massive bleeding).
Hypoventilation:
An increase in the level of the End Tidal CO2 from previous levels (Refer Figure 8.13).
Figure 8.13
Possible Causes:
a. Decrease in respiratory rate
b. Decrease in tidal Volume
c. Increase in metabollic rate
d. Rapid rise in body temperature (malignant hyperthermia)
8.15 Star 55
Muscle Relaxants:
Clefts are seen in the final third portion of the alveolar plateau. They
appear when the action of the muscle relaxants are affected by
spontaneous ventilation (Refer Figure 8.14).
Figure 8.14
Characteristics:
a. Depth of the cleft is inversely proportional to the degree of drug activity
b. Position fairly constant on same patient but may not be present in every
capnogram.
Rebreathing:
Rebreathing is characterized by an elevation in the baseline with a
corresponding increase in End Tidal CO 2 . It indicates the rebreathing of
the previously exhaled CO 2 (Refer Figure 8.15)
Figure 8.15
Possible Causes:
a. Insufficient expiratory time
b. Faulty expiratory valve
c. Inadequate inspiratory flow
d. Malfunction of a CO 2 absorber system
e. Partial rebreathing circuits.
8.16
Obstruction in Breathing Circuit or Airway:
An obstruction to the expiratory gas flow noted as a change in the slope
of the ascending limb of the capnogram. The expiratory portion may
diminish without a plateau (Refer Figure 8.16)
Figure 8.16
Possible Causes:
a. Partial obstruction in the expiratory limb of the breathing circuit
b. Presence of a foreign body in the upper airway
c. Partially kinked or occluded artificial airway
d. Herniated endotracheal / tracheostomy tube cuff
e. Bronchospasm
Figure 8.17
Waveform Evaluation:
a. Any obstruction will cause an abrupt change in the ascending limb
resulting in either a diminished plateau or no plateau. EtCO 2 and slope
will depend on the degree of obstruction ( Refer Figure 8.17).
Figure 8.18
Star 55
8.17
Possible Causes:
a. A leaky or deflated endotracheal or tracheostomy cuff
b. An artificial airway that is too small for the patient
Figure 8.19
Waveform Evaluation:
a. A normal capnogram is the best available evidence that the Et tube is
correctly positioned and that ventilation is occurring. When the Et tube
is placed in the Esophagus, either no CO 2 is sensed or any small transient
capnograms are present ( Refer Figure 8.19 ).
Figure 8.20
Waveform Evaluation:
a. Baseline elevated
b. Sloping descending limb of capnogram
c. Allows patient to rebirth exhaled gas ( Refer Figure 8.20 ).
Paediatric Capnogram
Figure 8.21
Typical Capnogram for a Paediatric Patient ( Refer Figure 8.21 ).
8.18
9
TE
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Star 55
9
Notes :
1. EQUIPMENT CLASSIFICATION
Mode of operation : Continuous
Type of protection
against electric shocks : Class1
Degree of protection : Type CF for ECG, IBP, Temperature and Respiration
against electric Shock Type BF- Capnography, NIBP and SpO2
(All with defib protection)
Degree of protection against
hazards of explosion : Not protected
Degree of protection against
ingress of liquids : Drip Proof - IPX1
3. BATTERY
Type : 14.8 V (4AH / 8AH) Lithium ion
No. of battery : One pack
Two packs
Charging time (min) : 8 Hrs (one pack)
Discharge time : 2/4 hrs
9.1 Star 55
For 4 hrs backup:
Two packs fully charged new batteries at 25 0C.
Discharge condition:
ECG, RESP, SpO2, Temp, NIBP running at 15 min interval without CO2 and recorder
printing.
Low battery indication voltage : 13.3 +/- 0.2V
Battery cut-off voltage : 12.2 +/- 0.2V
INDICATOR:
Green LED ON and Yellow LED OFF indicates battery operation.
Green LED ON and Yellow LED ON indicates mains operation and battery charging.
NOTE
4. CONTROLS
Front Panel : 1 switch for unit ON/OFF control
9 specific function switches.
1 optical encoder with switch.
5. DISPLAY
Display : 12.1 " TFT display (800X600)
Trace Speed : 12.5,25,50mm/sec. for ECG, SpO2, IBP.
6.25,12.5,25 mm/sec. for Respiration
and CO2.
9.2
Waveform : 8 waveform display. one standard and six user
selectable format. Waveform and Digital fields
are individually selectable and can be stored.
9.3 Star 55
6. TRENDS
Data storage : 5 sec for 72 hours
Graphical trend view resolution : 30sec, 1min, 3min, 4.5min, 6min, 12min and
18 min.
Tabular trend view resolution : 5sec, 10sec, 15sec, 30sec, 1min, 2min, 4min
and 8min.
9.4
Storage of ECG strips 8 ECG strips (strip duration depends on the
sweep selected for ECG) what ever is appearing
on the display at that moment will be stored)
ECG strip recording is possible.
Auto Setting Of Alarms : Provided for HR, SpO2, IBP, RR, EtCO2, FiCO2,
ST and TEMP.
9.5 Star 55
Rear panel : Standard 3-pin IEC power connector.
Live and neutral lines protected by fuse.
8. ECG
Input : Isolated and floating 3/5 leads (depending on
ECG cables). Protected against surges produced
by Electro-Surgical and defibrillator potentials.
Cascade option available.
Input impedance : >2.5 MOhms at 10Hz
CMRR : <15mm (max.) (Allowable noise for 3V p-p
applied sine wave of 20Hz)
Patient applied risk current : < 10uA (Isolated Normal condition)
50uA (Isolated single fault condition)
Patient isolation risk current : < N/A (Isolated Normal condition)
50uA (Isolated single fault condition)
Overload recovery : < 8 Sec
Fault indication : Individual lead fault indication on screen
Calibration : Cal indicator for all the gains in lead II, III and V
for 5 lead ECG cable and lead II and III for 3
lead ECG cable.
Patient isolation : 4KV rms (for 1 minute- isolated Normal
condition)
Band width : 0.5 - 120 Hz for Monitoring mode
0.05 - 120 Hz for Diagnostic mode
0.5 - 20 Hz for OT mode
Gain : X0.2, X0.5, X0.75, X1, X2, X5 mV - User
selectable
Tall T Wave rejection : Up to 1.2mV or QRS amplitude (whichever
is higher)
QRS beep volume Control : 12 steps (Off to maximum)
Beep source : User selectable beep source from ECG/IBP/
SPO2/NIBP
Leads : 3 leads for 3 lead cable.
5 leads for 5 lead cable
QRS Indicator : Beep and flashing heart symbol for every QRS
complex detected.
9.6
9. Heart Rate
Range : 20-350 BPM
Accuracy : 2BPM or 2% which ever is greater
Source of HR : ECG, SpO2, NIBP and IBP.
HR alarms : Adjustable alarm limits
Min - 18 to 336 BPM.
Max - 38 to 356 BPM
4 seconds delay for HR alarms
3 seconds R-R interval triggers systole
alarms if selected in Arrhythmia menu.
Time to alarm for Tachy : 5 sec
Heart rate meter response time : Change from 80 to 120 BPM (6 to 7 sec).
Change from 80 to 40 BPM (6 to 8 sec).
Arrhythmias Detected : Irregular, Skip beat, Tachycardia, Bradycardia,
Asystole
Pacemaker pulse rejection capability: When pacer is ON the monitor will display
the HR for all single and double pacemaker
pulses either 150 or 250 msec part with a
pulse width of 0.1 to 2msec and amplitudes
±2 mV to ±500 mV without overshoot.
Note
9.7 Star 55
ST point : 122.5ms from QRS peak (Default) any point in the
range of 0 to 200ms from QRS peak (user
selectable).
Marker resolution : 2.5ms.
Alarms : Alarm limits adjustable in the range
High : -8 to 12
Low : -12 to -8
Method of measurement : Cyclic
Note
9.8
12. Temperature:
Inputs : Isolated and floating
Leakage Current : <10 µA at 240V AC, 50 Hz
Measurement Range : 0 0C - 50 0C
Scale value : Displays direct readings of Temperature
input. ‘∆T’ value displayed in place of T2
Warm up : <10 min (Excluding probe)
Accuracy : ±0.2 0C or ±0.4 0F
Alarms : Temperature limits adjustable
Upper : 3.0 0C to 57.0 0C
Lower : 1.0 0C to 55.0 0C
Unit : C or 0F user selectable
0
9.9 Star 55
Pulse rate range : 20 to 230 BPM
Accuracy (+ 1 Std. Dev.) : +3 BPM
RR : 0-150 BPM
Units : mmHg or kPa or Vol %.
Scale : 20, 40, 60 or 80 mmHg or 2.6, 5.3, 8, 11
kPa/Vol%
Flow rate : 50 ml/min
Warm up time : 40 sec (Typical)
Alarms :
EtCO2
Upper : 10 - 105 mmHg
Lower : 0 - 95 mmHg
FiCO2
Upper : 2 - 22 mmHg
RR
Upper : 10 - 155 BPM
Lower : 0 - 145 BPM
Accuracy : 0-70 (±1) BPM
71-120 (±2) BPM
121-150 (±3) BPM
9.10
Calibration :
Zero calibration : Automatically performed by the module.
Indicated to the user through a message
on the screen.
Note
15. NIBP:
Method : Oscillometric
Display : Systolic, Diastolic and Mean
Modes of measurement : Manual, Auto and Stat mode
• In Auto mode, intervals of 2, 3, 4, 5, 10, 15, 30, 60 and 90 minutes are user
selectable
• In Stat mode, unit will take as many readings as possible in 5 minutes
• Duration between measurements is 10-12 sec
Unit (User selectable) : mmHg or kPa
Range : 20 - 250 mmHg
Accuracy : +5 mmHg with a standard deviation no
greater than 8 mmHg
Cuffs : Single quick connect hose
Auto zero : Zero pressure reference is automatically
established after every reading
Cuff inflation
Initial inflation
Adult : 160 mmHg
Neonates : 90 mmHg
Pediatric : 120 mmHg
9.11 Star 55
Subsequent inflation approximately 30 mmHg greater than previous systolic pressure
Cuff deflation : Automatic
Alarms : Adjustable alarm limits (for both Sys and Dia)
Upper : 20 to 260 mmHg
Lower : 10 to 250 mmHg
Safety features :
Automatic deflation if, cuff pressure exceed.
• 300 mmHg (Adult and Pediatric mode)
• 150 mmHg (Neonate mode)
• Measurement time exceeds more than one minute to deflate.
9.12
Pressure ranges : 5,10,20,30,60,80,100,150,180,200,240,300,AUTO mmHg
Measurement range : -40 to 300mmHg
Calibration : 100mmHg signal injected into the screen.
Alarms : Adjustable alarm limits.
PR range : 30-350 BPM
Accuracy : +/- 3 BPM
9.13 Star 55
18. Alarms:
Accessory alarms : Audio (Alarm beep), Visual (Flashing
Yellow LED) and message indication
Patient alarms : Audio (Alarm beep), visual (Flashing Red
LED alarms) and message indication
Re-alarm : 3 min after an alarm is acknowledged
Alarms suspend : Continuous Yellow LED to indicate “Alarms
Suspend” condition with display of alarm
cross mark.
Alarm volume control : 12 steps (min to high)
19 Outputs:
ECG Sync : Provides 5V P-P pulse for synchronizing
with defibrillator
Analog : 15 pin D-type sub connector (Female)
(Future Upgrade)
External monitor : 15 pin D-type sub connector (Female)
(Future Upgrade)
RS485 communication : USB type
Ethernet : RJ45 type (Future Upgrade)
Nurse call : Stereo phono jack
PC Dump : 9 pin D-type, dumping of all real time data.
Software upgrade : USB type
9.14
20. Recorder:
Recorder : Two channel
• Make : Woosim (Port - P40)
• Printing method : Thermal recording
• Dot density : 203 DPI
• Paper Width : 58 mm
• Printing Width : 48 mm
• Speed : 25 mm/sec
Recording modes : Direct, Delayed / Continuous modes
On red alarm
Recording duration : Direct : 8 sec
Delayed : -6 to +2 sec
Continuous : 30 sec
On alarm : -6 to +2 sec
21. Communication:
CNS Interface : Communicating with Skyline (L&T’s CNS -
Future Upgrade)
USB : USB connector
Ethernet port : RJ45 connector (Future Upgrade)
PCDUMP : Dumping of all trend data (9-pin D-type)
22. General:
Dimensions (H * W * D) : 280 mm * 320 mm * 158 mm
Weight : 5.5 Kg (approx) with battery and recorder,
without accessories
Mounting option : GCX option
Operating temperature : 5 to 40 0C
Operating humidity : 10 to 90% RH (Non condensing)
Storage and Transportation : -10 to 50 0C
temperature
Storage and Transportation : 0 to 90% RH (Non condensing)
humidity
Operating pressure : 500 to 760 mmHg
Storage pressure : 500 to 760 mmHg
9.15 Star 55
23. Accessories Supported:
ECG/Respiration : 3 lead cable with electrodes
SpO2 : DS (Dura sensor) 100A (Adult)
Oxy-A / N (Adult / Neonate) (Optional)
Dura Y (Universal) – ear clip (Optional)
NIBP : Tuff-Cuff reusable blood pressure cuffs
(Infant to large adult sizes)
IBP : Disposable Transducer kit (Baxter, Abbott,
Medex) and IBP cable (optional)
Temperature (Optional) : YSI 400 series temperature probes
CO2 : Microstream filter lines
Remote (Optional) : Infrared
24. Standards:
Designed to confirm to the following international standards
Class 1 equipment requirement of IEC 60601-1.
EMI/EMC requirements as per IEC 60601-1-2.
IEC 60601-2-27 requirements for ECG.
IEC 60601-2-30 requirements for NIBP.
IEC 60601-2-34 requirements for IBP.
IEC 60601-1-8 requirements for alarm systems.
IEC 60601-2-49 requirements for multifunction patient monitor systems.
ISO 9919 requirements for SpO2.
ISO 21647 requirements for CO2.
AAMI EC 13 for ECG.
AAMI SP 10 for NIBP.
9.16
10
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10 Star 55
Notes :
WARRANTY AND WARRANTY SERVICE
L&T warrants its Medical equipment against only manufacturing defects for a period of
12 (Twelve) months from the date of installation or 13 (Thirteen) months from the date
of despatch from L&T whichever is earlier, unless specified otherwise by separate
document from L&T.
During the warranty, L&T will, at its option, either repair or replace the defective
components / assemblies free of charge. The defective part shall be sent duly packed
to L&T's concerned office / service station at purchaser's cost including freight, insurance
and forwarding charges. Other claims, particularly for compensation, are excluded.
The warranty shall be valid only if installation and repairs are carried out by L&T's
Engineer or Authorised Service Franchisee.
L&T shall not be liable for any special or consequential damages of any kind or nature.
L&T will not be liable in any manner for use of or failure in the performance of other
equipment to which the product is attached / connected.
Star 55
10.1
10.2
Star 55
11.3
LARSEN & TOUBRO LIMITED
MEDICAL EQUIPMENT & SYSTEMS
(Annexe Building, Gate No. 7) Telephone : 91 22 67051223
P.O. Box No. 8901 : 91 22 67053223
Saki Vihar Road, Telefax : 91 22 67051276
Powai (E), E-mail : ebg-med@lntebg.com
Mumbai - 400 072 Website : WW.LNTMEDICAL.com