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Prosim™ 2/3: Users Manual
Prosim™ 2/3: Users Manual
Prosim™ 2/3: Users Manual
Users Manual
FBC 0038
January 2013, Rev. 1
© 2013 Fluke Corporation. All rights reserved. Specifications are subject to change without notice.
All product names are trademarks of their respective companies.
Warranty and Product Support
Fluke Biomedical warrants this instrument against defects in materials and workmanship for one year from the date of original
purchase OR two years if at the end of your first year you send the instrument to a Fluke Biomedical service center for
calibration. You will be charged our customary fee for such calibration. During the warranty period, we will repair or at our
option replace, at no charge, a product that proves to be defective, provided you return the product, shipping prepaid, to Fluke
Biomedical. This warranty covers the original purchaser only and is not transferable. The warranty does not apply if the
product has been damaged by accident or misuse or has been serviced or modified by anyone other than an authorized Fluke
Biomedical service facility. NO OTHER WARRANTIES, SUCH AS FITNESS FOR A PARTICULAR PURPOSE, ARE
EXPRESSED OR IMPLIED. FLUKE SHALL NOT BE LIABLE FOR ANY SPECIAL, INDIRECT, INCIDENTAL OR
CONSEQUENTIAL DAMAGES OR LOSSES, INCLUDING LOSS OF DATA, ARISING FROM ANY CAUSE OR THEORY.
This warranty covers only serialized products and their accessory items that bear a distinct serial number tag. Recalibration of
instruments is not covered under the warranty.
This warranty gives you specific legal rights and you may also have other rights that vary in different jurisdictions. Since some
jurisdictions do not allow the exclusion or limitation of an implied warranty or of incidental or consequential damages, this
limitation of liability may not apply to you. If any provision of this warranty is held invalid or unenforceable by a court or other
decision-maker of competent jurisdiction, such holding will not affect the validity or enforceability of any other provision.
7/07
Notices
All Rights Reserved
Copyright 2012, Fluke Biomedical. No part of this publication may be reproduced, transmitted, transcribed, stored in a retrieval system, or translated into any
language without the written permission of Fluke Biomedical.
Copyright Release
Fluke Biomedical agrees to a limited copyright release that allows you to reproduce manuals and other printed materials for use in service training programs and
other technical publications. If you would like other reproductions or distributions, submit a written request to Fluke Biomedical.
Technical Support
For application support or answers to technical questions, either email techservices@flukebiomedical.com or call 1-800- 850-4608 or 1-440-248-9300. In
Europe, email techsupport.emea@flukebiomedical.com or call +31-40-2965314.
Claims
Our routine method of shipment is via common carrier, FOB origin. Upon delivery, if physical damage is found, retain all packing materials in their original
condition and contact the carrier immediately to file a claim. If the instrument is delivered in good physical condition but does not operate within specifications, or
if there are any other problems not caused by shipping damage, please contact Fluke Biomedical or your local sales representative.
In the U.S.A.:
Cleveland Calibration Lab
Tel: 1-800-850-4608 x2564
Email: globalcal@flukebiomedical.com
In Asia:
Everett Calibration Lab
Tel: +425-446-6945
Email: service.international@fluke.com
To ensure the accuracy of the Product is maintained at a high level, Fluke Biomedical recommends the product be calibrated at least once every
12 months. Calibration must be done by qualified personnel. Contact your local Fluke Biomedical representative for calibration.
Certification
This instrument was thoroughly tested and inspected. It was found to meet Fluke Biomedical’s manufacturing specifications when it was shipped from the
factory. Calibration measurements are traceable to the National Institute of Standards and Technology (NIST). Devices for which there are no NIST calibration
standards are measured against in-house performance standards using accepted test procedures.
WARNING
Unauthorized user modifications or application beyond the published specifications may result in electrical shock hazards or improper operation. Fluke
Biomedical will not be responsible for any injuries sustained due to unauthorized equipment modifications.
Restrictions and Liabilities
Information in this document is subject to change and does not represent a commitment by Fluke Biomedical. Changes made to the information in
this document will be incorporated in new editions of the publication. No responsibility is assumed by Fluke Biomedical for the use or reliability of
software or equipment that is not supplied by Fluke Biomedical, or by its affiliated dealers.
Manufacturing Location
The ProSim™ 2/3 Vital Signs Simulator is manufactured at Fluke Biomedical, 6920 Seaway Blvd., Everett, WA, U.S.A.
Table of Contents
Title Page
Introduction .................................................................................................................... 1
Safety Information.......................................................................................................... 1
Accessories ................................................................................................................... 4
Product Familiarization .................................................................................................. 5
Battery Eliminator .......................................................................................................... 8
How to Turn On the Product .......................................................................................... 8
Operation ....................................................................................................................... 9
Cardiac Functions .......................................................................................................... 10
ECG Functions.......................................................................................................... 10
Pacemaker Signals ................................................................................................... 13
Arrhythmia Function .................................................................................................. 13
ECG Tests ................................................................................................................ 14
How to Set a Performance Wave Output ............................................................. 14
R-Wave Detection Test ........................................................................................ 14
Blood Pressure Function ........................................................................................... 15
How to Set the BP Sensitivity ............................................................................... 15
How to Set Up a BP Channel ............................................................................... 15
Dynamic BP Waveforms ...................................................................................... 15
How to Add a Respiration Artifact to the BP Waveform ....................................... 17
Cardiac Output .......................................................................................................... 17
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List of Tables
1. Symbols ................................................................................................................................ 3
2. Standard Accessories ........................................................................................................... 4
3. Optional Accessories ............................................................................................................ 4
4. Front-Panel Controls and Connectors .................................................................................. 6
5. Top-Panel Connectors .......................................................................................................... 7
6. Product Functions ................................................................................................................. 9
7. Dynamic BP Waveforms by BP Channel .............................................................................. 16
8. Error Codes .......................................................................................................................... 27
9. Product Control States and Modes ....................................................................................... 28
10. General Commands .............................................................................................................. 28
11. ECG Function Commands .................................................................................................... 28
12. Pacemaker Waveform Commands ....................................................................................... 30
13. Arrhythmia Function Commands .......................................................................................... 31
14. ECG Test Commands ........................................................................................................... 33
15. Respiration Function Commands .......................................................................................... 35
16. Blood Pressure Function Commands ................................................................................... 37
17. Other Function Commands ................................................................................................... 40
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iv
List of Figures
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Introduction Table 1 is a list of symbols used on the Product and in this
manual.
Warning
Warning
To prevent possible electrical shock, fire, or
personal injury, read all safety information To prevent possible electrical shock, fire, or
before you use the Product. personal injury:
The ProSim™ 2 and ProSim™ 3 Vital Signs Simulators • Use the Product only as specified, or the
(the Product) are electronic signal sources used to protection supplied by the Product can be
measure the performance of patient monitors. The Product compromised.
simulates: • Do not connect the Product to a patient or
• ECG (with and without arrhythmias) equipment connected to a patient. The
• Respiration Product is intended for equipment analysis
only. Do not use the Product for
• Blood pressure
diagnostics, treatment, or other capacity
• Temperature
where the Product touches a patient.
• Cardiac output (ProSim 3 only)
• Fetal/Maternal ECG and IUP (ProSim 3 only) • Remove the batteries if the Product is not
used for an extended period of time, or if
The ProSim™ 3 is shown in all illustrations. stored in temperatures above 50 °C. If the
Safety Information batteries are not removed, battery leakage
can damage the Product.
A Warning identifies conditions and procedures that are
• Replace the batteries when the low battery
dangerous to the user. A Caution identifies conditions and
procedures that can cause damage to the Product or the indicator shows to prevent incorrect
equipment under test. measurements.
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Users Manual
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Vital Signs Simulator
Safety Information
Table 1. Symbols
Symbol Description Symbol Description
Important information. Refer to manual. Hazardous Voltage
Conforms to relevant North American Safety
Conforms to European Union directives Standards.
Conforms to relevant Australian EMC
Battery
requirements
This product complies with the WEEE
Directive (2002/96/EC) marking requirements.
The affixed label indicates that you must not
discard this electrical/electronic product in
domestic household waste. Product Category:
Conforms to relevant South Korean EMC
Standards
With reference to the equipment types in the
WEEE Directive Annex I, this product is
classed as category 9 "Monitoring and Control
Instrumentation" product. Do not dispose of
this product as unsorted municipal waste. Go
to Fluke’s website for recycling information.
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ProSim™ 2/3
Users Manual
Accessories
Available Product Accessories are shown in Tables 2 and 3.
Table 2. Standard Accessories
Item Fluke Biomedical Part Number
ProSim 2/3 Safety Information 4308669
ProSim 2/3 Users Manual CD 4253822
IBP Cable, Unterminated 2392173
ProSim 2/3 Carrying Case 2248623
CI-3 Cable Assembly (Cardiac Output Box), 3010-0289FG 2392199
USB Mini-B Cable 1671807
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Vital Signs Simulator
Product Familiarization
Product Familiarization
Table 4 is a list of controls and connectors on the Product shown in Figure 1.
8 7 6
hal001.eps
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Vital Signs Simulator
Product Familiarization
1
2
hal006.eps
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hal007.bmp
hal022.eps
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Vital Signs Simulator
Operation
Figure 5. Home Screen 1. Push the navigation buttons to move the highlight to a
function. Figure 6 shows the cardiac output icon
Operation highlighted.
All Product functions are shown in the home screen. See
Figure 5. To set parameters for a function, push the
navigation buttons (, , , ) to move the highlight to a
function icon. Push . Table 6 is a list of Product
functions shown in the home screen.
hal005.bmp
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2. Push . The cardiac output screen in Figure 7 highlight to Home and push . The home screen
shows in the display. shows all the Product functions. See Figure 5.
An alternative to the Home screen is to use the Prev and
Next selections. The software lets you move through the
Product functions sequentially. The function sequence is:
ECG, Respiration, Blood Pressure, Arrhythmias,
Performance Wave, Pacemaker Wave, Temperature,
Cardiac Output, Fetal Maternal, and Setup.
For example, look at the Cardiac Output screen in
Figure 7. When you move the highlight to Prev and push
, the display shows the Temperature screen. When
you highlight Next and push in the Cardiac Output
screen, the display shows the Fetal/Maternal screen.
hal003.eps Cardiac Functions
Figure 7. Cardiac Output Screen The cardiac functions of the Product are ECG, Arrhythmia,
3. To set the injection temperature, push to move the Blood Pressure, Pacemaker, Cardiac Output, and
highlight to the INJ Temp value. Performance Waves.
4. Push or to change the value for the highlighted ECG Functions
parameter. The adjusted simulated value changes the The ECG function of the Product lets you set five
output signal immediately. parameters of an ECG waveform: Rate, Amplitude, Patient
All parameter values in the Product are set with this Type, ST, and Artifact. Figure 9 shows a typical setup for
procedure. For the parameters that cannot be set, the an ECG test on a patient monitor.
highlight will not move to the value of that parameter. To set an ECG parameter:
There are two procedures to move between Product 1. In the Home screen, push the navigation buttons to
functions. When the home screen is not shown in the move the highlight to ECG .
display, Prev, Home, and Next show along the bottom of
the display. To move to the home screen, move the 2. Push to show the ECG screen in Figure 8 in the
display.
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Vital Signs Simulator
Cardiac Functions
hal004.bmp
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ProSim™ 2/3
Users Manual
Patient
Monitor ProSim 2/3
ECG
Cable
hal030.eps
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Vital Signs Simulator
Cardiac Functions
Pacemaker Signals
The Product can simulate heart signals with pacemaker
control signals. To set the waveform, amplitude, and width
of the pacemaker signal:
1. In the Home screen, push the navigation buttons to
highlight PACE .
2. Push to show the Pacemaker Waves screen in
the display.
3. Use the parameter selection procedure described in
the Operation section to set the parameters of the
pacemaker signal.
hal009.bmp
See the detailed specifications for the range of parameter Figure 10. Arrhythmia Screen
values.
The simulated arrhythmias are grouped into four
Arrhythmia Function categories: Supraventricular, Premature, Ventricular,
The Product can simulate heart arrhythmias. To start an and Conduction Defect. See the specifications to learn
ECG arrhythmia simulation: the arrhythmias in each group.
1. In the Home screen, push the navigation buttons to 3. Push or to move the highlight to an arrhythmia
highlight ARRY . group icon.
2. Push to show the Arrhythmias screen in the 4. Push .
display. See Figure 10. 5. Use the parameter selection procedure described in
the Operation section to set the arrhythmia.
When the type parameter has been set to an arrhythmia,
the group icon of the group the arrhythmia belongs to has
a thicker border around it.
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ProSim™ 2/3
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Vital Signs Simulator
Cardiac Functions
Blood Pressure Function 5. Before you start the BP simulation, you must set the
The Product simulates dynamic Blood Pressure (BP) simulated pressure to 0 mmHg. Push the navigation
waveforms that synchronize with all normal sinus rhythm buttons to highlight ZERO .
rates and track all simulated arrhythmias. You can set 6. Push . The static pressure parameter is set to
each of the four BP channels independently. Each channel 0 mmHg and the dynamic and artifact variables are set
simulates a bridge pressure transducer. A respiration to Off.
artifact can be injected into each BP channel waveform.
7. Zero the patient monitor to set the baseline for future
How to Set the BP Sensitivity simulations.
The sensitivity of the four BP channels must be set to 8. Use the parameter selection procedure described in
match the sensitivity of the patient monitor. To set BP the Operation section to set the Blood Pressure
channel sensitivity: channel parameters.
1. In the Home screen, push the navigation buttons to
highlight SETUP .
Dynamic BP Waveforms
The Dynamic parameter is used to simulate the various
2. Push to show the Setup screen in the display. pressures that are found around the heart and associated
3. Use the parameter selection procedure described in blood vessels. The dynamic waveforms have a normal
the Operation section to set the BP Sense parameter. sinus rhythm at 80 bpm. Only the systolic and diastolic
pressures change for each dynamic waveform.
How to Set Up a BP Channel All the dynamic waveforms are not available on all four BP
To set up one of the four BP channels: channels. Table 7 is a list of the dynamic BP waveforms
1. In the Home screen, push the navigation buttons to with a check to indicate which BP channel each waveform
highlight BP . can be set on.
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ProSim™ 2/3
Users Manual
Procedure
In Swanz-
Right Ventricle 25/00 √ √ √ √
Ganz
Pulmonary Artery 25/10 √ √ √
Pulmonary Wedge 10/2 √ √ √
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Vital Signs Simulator
Cardiac Functions
How to Add a Respiration Artifact to the BP connector is for catheter blood temperature (BT) and is
standard on most monitors.
Waveform
When the dynamic parameter for a blood pressure channel Note
is set to a value other than off, the Product will let you This 3-pin catheter BT connector is compatible
move the highlight to the artifact parameter. With the with the standard Baxter (Edwards) BT catheter
highlight on the artifact value, push or to toggle the and equivalent catheters available from other
value between on and off. manufacturers such as Viggo-SpectraMed and
Abbott (Sorenson).
Each BP channel has a different range of pressure change
due to the respiration artifact. The larger 4-pin connector supplies the simulated injectate
temperature. The 10-turn 100 kΩ potentiometer enables
Cardiac Output adjustment of the injectate temperature to 0 °C or 24 °C.
The Cardiac Output function electronically simulates the
The 4-pin IT thermistors connector is not standard on all
dynamic temperature changes of blood that is cooled by
monitors. A general function connector that you can
an injectate.
connect to the device under test (DUT) injectate cable is
Note also available.
Cardiac output measurement devices that use the Note
Fick dye injection, Doppler ultrasonography, and
A DUT cardiac output cable changed for this test
bioimpedance are not addressed or intended for
must not be used in clinical applications.
this Product.
Cardiac-Output Test Set Up
To simulate cardiac output with the Product, a CI-3
adapter is necessary to connect the monitor to the
Product. The adapter is shown in Figure 11. Note that the
injectate temperature thermistor has to be cut off at the
EUT cable to install the general-purpose connector.
This module has connections for the cardiac output
measurement under test and simulates the injectate
temperature (IT) thermistors at 0 °C or 24 °C. Of the two
connectors on the CI-3 module/cable, the smaller 3-pin
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ProSim™ 2/3
Users Manual
hal010.eps
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Vital Signs Simulator
Cardiac Functions
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ProSim™ 2/3
Users Manual
Patient
Monitor
ProSim 2/3
Blood
Temperature
Connection
70
6 0 50 40
hal057.eps
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Vital Signs Simulator
Cardiac Functions
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ProSim™ 2/3
Users Manual
To set a periodic FHR with IUP: 4. Push the navigation buttons to highlight START .
1. If the Fetal Maternal screen shows in the display, go to 5. Push to start the test. If the Period parameter is
step 3. If not, go to the Home screen of the Product set to Manual, the simulation stops automatically after
and push the navigation buttons to highlight FE/MA . the IUP wave stops. Each time you push
another IUP wave starts. If not set to Manual, the IUP
2. Push to show the Fetal Maternal screen.
wave repeats at the frequency set in the Period
3. Use the parameter selection procedure to set the FHR, parameter until the simulation is stopped.
IUP, and Period parameters
To stop the simulation, highlight STOP and push .
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Vital Signs Simulator
Cardiac Functions
Fetal Monitor
IBP Channel 4
ProSim 2/3
Fetal ECG
Input
Intrauterine
Blood Pressure
Input
BP Cable
Jumper
Wires
Maternal Thigh
Reference Plate
Fetal Scalp
Electrode
hal058.eps
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Vital Signs Simulator
Other Functions
ProSim 2/3
Temperature
Cable
Patient
Monitor
hal038.eps
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ProSim™ 2/3
Users Manual
ProSim 2/3
USB Port
Mini Series
B Connector
hal060.eps
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Vital Signs Simulator
Remote Operation
When connected to a PC with a Windows operating command is not accepted by the Product, an error code
system, the Product will communicate through a PC COM shown in Table 8 is sent to the PC.
port. Make sure the COM port parameters are set to:
Table 8. Error Codes
• 9600 Baud
• No Parity Error Code Description
• 8 data bits ERR=00 No commands allowed at this time
• 1 stop bit
• Hardware handshake set to off ERR=01 Unknown command
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Remote Operation
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Vital Signs Simulator
Remote Operation
Table 12. Pacemaker Waveform Commands (cont.) Table 13. Arrhythmia Function Commands
Action Command Action Command
[1]
Amplitude Supraventricular
1 mV PA1 Atrial fibrillation, coarse AF1
2 mV PA2 Atrial fibrillation, fine AF2
5 mV PA5 Atrial flutter AFL
10 mV PA10 Sinus arrhythmia SINA
[1]
Width Missed beat MB80
0.1 mV PA0.1 Atrial tachycardia ATC
0.5 mV PA0.5 Paroxysmal atrial tachycardia PAT
1.0 mV PA1.0 Nodal rhythm NOD
1.5 mV PA1.5 Supraventricular tachycardia SVT
2 mV PA2.0 Premature
1. Set the Pacemaker waveform before you set amplitude and width. Premature atrial contraction PAC
Arrhythmia Functions Premature nodal contraction PNC
Table 13 is a list of the commands to simulate arrhythmias.
Premature vent contraction left
These waveforms are grouped by supraventricular PVC1S
(PVC1), standard
arrhythmia, premature arrhythmia, ventricular arrhythmia,
and conduction defect.
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Vital Signs Simulator
Remote Operation
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Vital Signs Simulator
Remote Operation
Table 14. ECG Test Commands (cont.) Table 15. Respiration Function Commands
Action Command Action Command
R-Wave Amplitude (cont.) Lead
0.40 mV RWA0.40 Lead LA RLLA
0.45 mV RWA0.45 Lead LL RLLL
0.50 mV RWA0.50 Baseline
1.00 mV RWA1.00 500 Ω RB500
1.50 mV RWA1.50 1000 Ω RB1000
2.00 mV RWA2.00 1500 Ω RB1500
2.50 mV RWA2.50 2000 Ω RB2000
3.00 mV RWA3.00 Rate
3.50 mV RWA3.50 0 BrPM RR0
4.00 mV RWA4.00 15 BrPM RR15
4.50 mV RWA4.50 20 BrPM RR20
5.00 mV RWA5.00 30 BrPM RR30
5.50 mV RWA5.50 40 BrPM RR40
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Vital Signs Simulator
Remote Operation
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Vital Signs Simulator
Remote Operation
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Vital Signs Simulator
Maintenance
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ProSim™ 2/3
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Battery Replacement
Warning
To prevent possible electrical shock, fire, or
personal injury:
• Remove batteries to prevent battery
leakage and damage to the Product if it is
not used for an extended period.
• Be sure that the battery polarity is correct
to prevent battery leakage.
• Batteries contain hazardous chemicals that
can cause burns or explode. If exposure to
chemicals occurs, clean with water and get
medical aid.
When the charge in the batteries becomes low, a warning hal008.eps
will show in the display. Replace the batteries immediately. Figure 16. Battery Replacement
To replace the batteries:
1. Turn off the Product and remove all test leads.
2. Slide the battery door off on the rear of the Product.
See Figure 16.
3. Remove the two 9-volt batteries and replace them with
new ones. Use the correct battery orientation.
4. Install the battery door.
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Vital Signs Simulator
General Specifications
General Specifications
Power .........................................................................Two 9-V alkaline batteries (IEC 6LR61, NEDA 1604A). Optional battery eliminator: 15 Vdc, 1.5 mA
Battery Life ................................................................8 hours minimum
Display .......................................................................LCD Greyscale Display
Size.............................................................................14.0 cm x 20.6 cm x 4.5 cm (5.5 in x 8.2 in x 1.8 in)
Weight ........................................................................0.47 kg (1 lb 4 oz)
Temperature
Storage ................................................................-25 °C to +50 °C (-13 °F to +122 °F)
Operation .............................................................10 °C to 40 °C (50 °F to 104 °F)
Humidity ....................................................................10 % to 80 % non-condensing
Altitude ......................................................................2000 m (6,562 ft)
Safety .........................................................................IEC 61010-1, Pollution degree 2
Electromagnetic Environment .................................IEC 61326-1, Portable
EMC ............................................................................Applies to use in Korea only. Class A equipment (Industrial Broadcasting & Communication Equipment)
[1]
[1] This Product meets requirements for industrial (Class A) electromagnetic wave equipment and the
seller or user should take notice of it. This equipment is intended for use in business environments and
is not to be used in homes.
Detailed Specifications
ECG Waveform
ECG Reference..........................................................The ECG amplitudes specified are for Lead II, from the baseline to the peak of the R wave. All other
leads are proportional in percentage per:
Lead I ..................................................................70 %
Lead II .................................................................100 %
Lead III ................................................................30 %
Lead V1 ...............................................................24 %
Lead V2 ...............................................................48 %
Lead V3 ...............................................................100 %
Lead V4 ...............................................................120 %
Lead V5 ...............................................................112 %
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ProSim™ 2/3
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Lead V6 .............................................................. 80 %
Normal Sinus Rhythm ............................................. 12-lead configuration with independent outputs referenced to right leg (RL). Output to 10 Universal ECG
Jacks, color-coded to AHA and IEC Standards.
Amplitude ................................................................. 0.05 mV to 0.45 mV (0.05 mV steps), 0.5 mV to 5.5 mV (0.5 mV steps)
Amplitude Accuracy ................................................ ±2 % of setting Lead II. All other leads ±5 %
ECG Rate .................................................................. 30, 40, 45, 60, 80, 90, 100, 120, 140, 160, 180, 200, 220, 240, 260, 280, and 300 BPM
Rate Accuracy .......................................................... ±1 % of setting
ECG Waveform Selection........................................ Adult (80 ms) or pediatric (40 ms) QRS duration
Artifact (Superimposed) .......................................... 50 and 60 Hz, muscle, baseline wander, respiration
ST-Segment Elevation ............................................. Adult mode only. -0.8 mV to +0.8 mV (0.1 mV steps) Additional steps: +0.05 mV and -0.05 mV
Power-On Default ..................................................... 80 BPM, 1.0 mV, adult QRS, ST-segment elevation of 0 mV, and a P-R interval of 0.16 seconds
Pacemaker Waveform
Pacer-Pulse Amplitude ............................................ 0 (off), 1, 2, 5, 10 mV ±10 % for lead II (reference lead) with other leads proportional as for performance
waves.
Pacer-Pulse Width ................................................... 0.1, 0.5, 1.0, 1.5, 2.0 ms ±5 %
Pacing Rate .............................................................. 75 BPM
Paced Arrhythmias .................................................. Atrial 80 BPM
Asynchronous 75 BPM
Demand with frequent sinus beats
Demand with occasional sinus beats
Atrio-Ventricular sequential
Noncapture (one time)
Nonfunction
Power-On Default ..................................................... Off
Arrhythmia
Baseline NSR ........................................................... 80 BPM
PVC Focus ................................................................ Left focus, standard timing (except where specified)
Supraventricular Arrhythmia .................................. Atrial fibrillation (coarse or fine), atrial flutter, sinus arrhythmia, missed beat (one time), atrial tachycardia,
paroxysmal atrial tachycardia, nodal rhythm, and supraventricular tachycardia
Premature Arrhythmia ............................................. (All one-time events) Premature atrial contraction (PAC), premature nodal contraction (PNC), PVC1 left
ventricular, PVC1 left ventricular – early, PVC1 left ventricular – R on T, PVC2 right ventricular, PVC2
right ventricular – early, PVC2 right ventricular – R on T, and multifocal PVCs
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Vital Signs Simulator
Detailed Specifications
Ventricular Arrhythmia .............................................PVCs (6, 12, or 24 per minute), frequent multifocal PVCs, bigeminy, trigeminy, multiple PVCs (one-time
run of 2, 5, or 11 PVCs), ventricular tachycardia, ventricular fibrillation (coarse or fine), and asystole
Conduction Defect ....................................................First-, second-, or third-degree AV block and right- or left-bundle-branch block
Power-On Default......................................................None (off)
ECG-Performance-Tests
Amplitude ..................................................................0.05 mV to 0.45 mV (0.05 mV steps)
0.5 mV to 5.5 mV (0.5 mV steps)
Pulse Wave ................................................................30 BPM, 60 BPM, with 60 ms pulse width
Square Wave .............................................................2.0, 0.125 Hz
Triangle Wave ...........................................................2.0, 2.5 Hz
Sine Wave ..................................................................0.5, 5, 10, 40, 50, 60, 100 Hz
R-wave-Detection Waveform ...................................Haver-Triangle
R-wave Rate ..............................................................30, 60, 80, 120, 200, and 250 BPM
R-wave Width ............................................................20 ms to 200 ms (10 ms steps)
Additional Steps: 8, 10, and 12 ms
Rate Accuracy ...........................................................±1 %
Amplitude Accuracy .................................................±2 %, Lead II (Exception: ±5 % for R waves ≤20 ms)
Power-On Default .....................................................None (off)
Respiration
Rate ............................................................................0 (OFF), 15, 20, 30, 40, 60, 80, 100, 120 BrPM
Impedance Variations (Δ Ω) .....................................0.2, 0.5, 1, or 3 Ω peak-to-peak variation of lead impedance
Delta Accuracy ..........................................................±10 %
Baseline .....................................................................500, 1000, 1500, 2000 Ω, Leads I, II, III
Accuracy Baseline ....................................................±5 %
Respiration Lead.......................................................LA or LL
Apnea Selection ........................................................OFF, 12, 22, or 32 seconds (one-time events), or continuous (Apnea ON = respiration OFF)
Power-On Default......................................................20 BrPM, delta 1.0 Ω, 1000-Ω baseline
Blood Pressure
Input/output Impedance ...........................................300 Ω ±10 %
Exciter Input Range ..................................................2.0 V to 16.0 V rms
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Vital Signs Simulator
Detailed Specifications
Temperature
Temperature ..............................................................0 °C (32 °F), 24 °C (75.2 °F), 37 °C (98.6 °F), and 40 °C (104 °F)
Accuracy....................................................................±0.1 °C
Compatibility .............................................................Yellow Springs, Inc. (YSI) Series 400 and 700
Output Connector .....................................................DIN 4-pin
Power-On Default......................................................0 °C (42 °F)
47
ProSim™ 2/3
Users Manual
Computer Setup
USB Device Upstream Port ..................................... Mini-B connector for control by a computer
Baud Rate ................................................................. 9600
Parity ......................................................................... None
Stop Bits ................................................................... 1
Data Bits ................................................................... 8
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