Puritan Bennett 740, 760, 700 User Manual

.........................................................................
Operator’s Manual
Part No. G-061874-00 Rev. D September 2000
Copyright Information
Copyright 2000 Mallinckrodt Inc. EasyCart, EasyNeb, 740, 760, and 700 Series are trademarks of Mallinckrodt Inc. All rights reserved. The 700 Series (including the 740 proprietary information, covered by one or more of the following U.S. Patents and foreign equivalents: 5,524,615; 5,540,222; 5,596,984; 5,632,270; 5,664,560; and 5,673,689.
The information contained in this manual is the sole property of Mallinckrodt Inc. and may not be duplicated without permission. This manual may be revised or replaced by Mallinckrodt Inc. at any time and without notice. You should ensure that you have the most current applicable version of this manual; if in doubt, contact the Technical Publications Department of Mallinckrodt Inc. While the information set forth herein is believed to be accurate, it is not a substitute for the exercise of professional judgment.
The ventilator should be operated and serviced only by trained professionals. Mallinckrodt’s sole responsibility with respect to the ventilator, and its use, is as stated in the limited warranty provided.
Nothing in this manual shall limit or restrict in any way Mallinckrodt’s right to revise or otherwise change or modify the equipment (including its software) described herein, without notice. In the absence of an express, written agreement to the contrary, Mallinckrodt Inc. has no obligation to furnish any such revisions, changes, or modifications to the owner or user of the equipment (including its software) described herein.
Ô
and 760Ôventilators) are manufactured in accordance with Mallinckrodt
Ô
Ventilator System
Definitions
This manual uses these special indicators to convey information of a specific nature:
Warning
Indicates a condition that can endanger the patient or the ventilator operator.
Caution
Indicates a condition that can damage the equipment.
NOTE:
Indicates points of particular emphasis that make operation of the ventilator more efficient or convenient.
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Warnings, cautions, and notes
Please take the time to familiarize yourself with the following safety considerations, special handling requirements, and regulations that govern the use of the 700 Series Ventilator System.
Warning
To avoid an electrical shock hazard while servicing the ventilator, be sure to remove all power to the ventilator by disconnecting the power source and turning off all ventilator power switches.
Warning
To avoid a fire hazard, keep matches, lighted cigarettes, and all other sources of ignition (e.g., flammable anesthetics and/or heaters) away from the ventilator and oxygen hoses.
Do not use oxygen hoses that are worn, frayed, or contaminated by combustible materials such as grease or oils. (Textiles, oils, and other combustibles are easily ignited and burn with great intensity in air enriched with oxygen.)
In case of fire or a burning smell, immediately disconnect the ventilator from the oxygen supply and electrical power source.
Warning
Patients on life-support equipment should be appropriately monitored by competent medical personnel and suitable monitoring devices.
The 700 Series Ventilator is not intended to be a comprehensive monitoring device and does not activate alarms for all types of dangerous conditions for patients on life-support equipment.
Warning
Check the ventilator periodically as outlined in the service manual; do not use if defective. Immediately replace parts that are broken, missing, obviously worn, distorted, or contaminated.
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Warning
An alternative source of ventilation should always be available when using the 700 Series Ventilator System.
Warning
To ensure proper servicing and avoid the possibility of physical injury, only qualified personnel should attempt to service or make authorized modifications to the ventilator.
The user of this product shall have sole responsibility for any ventilator malfunction due to operation or maintenance performed by anyone not trained by Mallinckrodt staff.
Warning
For a thorough understanding of ventilator operations, be sure to read the 700 Series Ventilator System Operator's Manual in its entirety before attempting to use the system.
Warning
Before activating any part of the ventilator, be sure to check the equipment for proper operation and, if appropriate, run the self­diagnostic short self test (SST) program described in this manual.
Caution
U.S. Federal law restricts this device to sale by or on the order of a physician.
Warranty
The 700 Series Ventilator System is warranted against defects in material and workmanship in accordance with Mallinckrodt Medical Equipment Warranty for a period of one year from the time of sale. To ensure the validity of the warranty, be sure to keep a maintenance record.
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M
Year of manufacture
The 700 Series Ventilator System’s year of manufacture is indicated by the fifth and sixth digits of the serial number which is located at the lower edge of the ventilator front panel.
Manufacturer
anufactured by
Nellcor Puritan Bennett Ireland A subsidiary of Mallinckrodt Inc. Mervue, Galway, Ireland
Phone: +353.91.753.771 Fax: +353.91.753.922
European Headquarters
Mallinckrodt Europe BV Hambakenwetering 1 5231 DD ’s-Hertogenbosch The Netherlands
Phone: +31.73.6485200 Fax: +31.73.6410915
Electromagnetic susceptibility
The 700 Series Ventilator System complies with the requirements of IEC 60601­1-2 (EMC Collateral Standard), which includes E-field susceptibility and ESD requirements. However, even though the device is compliant at the levels of immunity specified in the standard, certain transmitting devices (cellular phones, walkie-talkies, cordless phones, paging transmitters, etc.) emit radio frequencies that could interrupt ventilator operation if located in a range too close to the ventilator. It is difficult to determine when the field strength of these devices becomes excessive. Practitioners should be aware that radio frequency emissions are additive, and that the ventilator must be located a sufficient distance from transmitting devices to avoid interruption. Do not operate the ventilator in a magnetic resonance imaging (MRI) environment. The Alarm handling section of this manual describes possible ventilator alarms and what to do if they occur. Consult with your institution’s biomedical engineering department in case of interrupted ventilator operation, and before relocating any life support equipment.
Customer assistance
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For further assistance contact your local Mallinckrodt representative.
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Contents
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1 Introduction
1.1 Functionaldescription ......................................1-2
1.2 Symbolsandlabels ........................................1-8
1.3 Keyboard ...............................................1-13
1.3.1 VENTILATORSETTINGS .......................... 1-14
1.3.2 PATIENTDATA .................................. 1-24
1.3.3 VENTILATORSTATUS ............................1-28
2 Setting up the ventilator
2.1 Connectingandusinginternalandexternalbatteries ..............2-2
2.2 Connectingtheelectricalsupply............................... 2-6
2.3 Connecting the oxygen supply . . . . . . . . ........................ 2-8
2.4 Connectingtheventilatorbreathingcircuit ...................... 2-10
2.5 Installingthecollectorvial .................................. 2-13
2.6 Installingtheflexarm ......................................2-14
2.7 Installingthehumidifier..................................... 2-16
2.8 Usingtheventilatorcart ....................................2-17
3 Getting started
3.1 Poweringuptheventilator ...................................3-1
3.2 Selectingventilatorsettings .................................. 3-4
3.3 Viewingandchangingalarmsettings...........................3-6
3.4 Enteringandexitingstandbymode ............................ 3-8
4 Self tests (SST and EST)
4.1 Shortselftest(SST) ........................................ 4-3
4.2 Extended self test (EST) . . . . . . . . . . . . ....................... 4-13
5 Once ventilation begins
5.1 Changingsettings:aquickreview .............................5-1
5.1.1 Changingsettings.................................. 5-1
5.1.2 SwitchingbetweenVCV,PCV,andPSV ................ 5-2
5.1.3 Changingthemode ................................5-2
5.2 Viewingandchangingalarmsettings:aquickreview .............. 5-3
5.3 Adjustingapneaparameters ................................. 5-4
5.3.1 Adjustingtheapneainterval ..........................5-6
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5.4 Viewingpatientdata........................................ 5-6
5.5 The 100% O2 and MANUAL INSP keys . . . . . .................. 5-10
5.6 The EXP PAUSE and INSP PAUSE keys (760 only) ............. 5-11
6 The MENU key
6.1 Moreactivealarms......................................... 6-5
6.2 Autoresetalarms .......................................... 6-6
6.3 Selftests ................................................ 6-7
6.4 Usersettings ............................................. 6-7
6.4.1 Endotrachealtube ................................. 6-7
6.4.2 Humidifiertype .................................... 6-8
6.4.3 Dateandtimeset .................................. 6-8
6.4.4 Apneainterval(Ta)................................. 6-9
6.4.5 VCVflowpattern .................................. 6-9
6.4.6 Speakingvalvesetup .............................. 6-10
6.4.7 Alarmvolume .................................... 6-16
6.4.8 PCVtimingsetting ................................ 6-16
6.4.9 VolumeLEDbar.................................. 6-16
6.5 Oxygensensor........................................... 6-17
6.6 Standby mode . . . . . . . . . . . . ............................... 6-19
6.7 Batteryinfo ............................................. 6-20
6.8 Softwarerevision ......................................... 6-20
6.9 Servicesummary ......................................... 6-21
6.10 Nebulizer .............................................. 6-21
Contents
7 Alarm handling
7.1 Autoresetalarms .......................................... 7-3
7.2 Alarmsilence ............................................. 7-3
7.3 Alarmreset............................................... 7-4
7.4 Clinicalandtechnicalalarms ................................. 7-5
7.5 Poweralarm............................................. 7-17
7.5.1 LossofACPower ................................ 7-17
7.5.2 LossofPower ................................... 7-18
Appendix A Maintenance
A.1 Cleaning,disinfection,andsterilization .........................A-2
A.1.1 Cleaning: general guidelines . . . . . . ...................A-4
A.1.2 Disinfectionandsterilization .........................A-4
A.2 Preventivemaintenance ....................................A-5
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A.2.1 Daily or as required:
inspiratoryandexpiratorybacteriafilters.............. A-8
A.2.2 Dailyorasrequired:collectorvial .................... A-8
A.2.3 Dailyorasrequired:in-linewatertraps ................ A-9
A.2.4 Asnecessary:oxygensensorcalibration............... A-9
A.2.5 Every 250 hours (or 1 month of use): cooling fan filter . . . A-10 A.2.6 Every 1000 hours (or 3 months of use): air intake filter . . . A-11
A.2.7 Every2years:devicechecks ...................... A-12
A.2.8 Storage ....................................... A-13
A.2.9 Repacking ..................................... A-13
Appendix B Part numbers
Appendix C Specifications
C.1 Physical ................................................ C-2
C.2 Environmental ........................................... C-3
C.3 Power ................................................. C-3
C.4 Complianceandapprovals ................................. C-5
C.5 Technical ............................................... C-5
Appendix D Breath delivery
D.1 A/Cmode ............................................... D-3
D.2 SPONTmode ........................................... D-3
D.3 SIMVmode ............................................. D-4
D.3.1 Breathtiming .................................... D-4
Appendix E Alarm testing
Appendix F Pneumatic schematic
Appendix G Glossary
Index
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Figures
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Figure 1-1 Block diagram: 700 Series Ventilatorfunction ............1-5
Figure 1-2 740 VentilatorSystemkeyboard......................1-13
Figure 1-3 760 VentilatorSystemkeyboard......................1-14
Figure2-1 Liftingtheventilator ................................ 2-2
Figure2-2 Internalbatterychargeindicator ....................... 2-3
Figure2-3 Pluggingtheexternalbatteryintotheventilator .......... 2-5
Figure2-4 Disconnectingtheexternalbattery .....................2-6
Figure2-5 Connectingtheventilatorpowercord ................... 2-7
Figure2-6 Storingthepowercordontheventilator ................. 2-7
Figure2-7 Connectingtheoxygensupply ........................ 2-9
Figure2-8 Connectingtheventilatorbreathingcircuit ..............2-12
Figure2-9 Installingthecollectorvial .......................... 2-13
Figure2-10 Installingtheflexarm ..............................2-14
Figure2-11 Shorteningtheflexarm ............................ 2-15
Figure2-12 Installingthehumidifier ............................2-16
Figure2-13 Lockingandunlockingthecart’sfrontwheels ...........2-17
Figure3-1 Turningthepowerswitchon(the“I”position)............. 3-2
Figure5-1 Viewingpatientdata ................................5-8
Figure 5-2 Volume bar graph (760 Ventilatoronly) ................. 5-9
Figure 6-1 Using the More active alarms menu function
to view active alarms 6-5
Figure 6-2 Using the Autoreset alarms menu function
to view autoreset alarms 6-6
Figure7-1 Viewingactivealarms ..............................7-2
FigureA-1 Removing/replacingthecollectorvial .................. A-9
FigureA-2 Coolingfancover ................................ A-10
FigureA-3 Airintakefilter ................................... A-12
FigureB-1 Ventilatoraccessories ............................. B-9
Figure C-1 Recommended ventilator breathing circuit configurations . . C-8
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Figures
FigureD-1 Flowwaveform ................................... D-2
FigureD-2 SIMVbreathperiodintervals ........................ D-4
Figure D-3 Synchronizing breath intervals with patient effort . . . . . . . . . D-5
FigureD-4 SpontaneousbreathsduringSIMV ................... D-5
FigureD-5 MandatorybreathsduringSIMV...................... D-5
FigureD-6 ManualinspirationduringSIMV ...................... D-6
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Ta bl e s
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Table 1-1 Mode/breath type availability on 740/760 Ventilators ........1-2
Table 1-2 Changes to current settings in occlusion cycling mode . . . . . . . 1-7
Table 1-3 700 Series Ventilator keyboards: VENTILATOR SETTINGS . 1-15
Table 1-4 700 Series Ventilatorkeyboards:PATIENTDATA .........1-24
Table 1-5 700 Series Ventilator keyboards: VENTILATOR STATUS . . . 1-29
Table 4-1 700 Series Ventilatorselftests .........................4-2
Table4-2 SSTsequenceoftests................................4-9
Table4-3 OverallSSTresults .................................4-12
Table4-4 ESThardwarerequirements ..........................4-13
Table4-5 ESTsetupmessages................................ 4-14
Table4-6 ESTtestsequence..................................4-16
Table4-7 KeyfunctionsduringEST ............................ 4-21
Table4-8 PromptsduringEST.................................4-22
Table4-9 ESTcompletionstatus ..............................4-23
Table5-1 Breathtypeavailability ................................5-2
Table6-1 Menufunctionsummary............................... 6-2
Table7-1 Clinicalalarms ...................................... 7-5
Table7-2 Technicalalarms ...................................7-12
TableA-1 Cleaning,disinfection,andsterilization .................. A-3
TableA-2 Preventivemaintenanceschedule ..................... A-7
TableB-1 Ventilatoraccessories ............................... B-2
TableC-1 Physicalspecifications ............................... C-2
TableC-2 Environmentalspecifications .......................... C-3
TableC-3 Powerspecifications ................................ C-3
TableC-4 Complianceandapprovals ........................... C-5
TableC-5 Technicalspecifications .............................. C-5
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Tables
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SECTION
Introduction 1
1
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The 700 Series Ventilator System (including the 740 and 760 Ventilators) provides respiratory support for a wide range of pediatric to adult patients for a wide variety of clinical conditions. The ventilator’s mixing technique allows it to ventilate critically ill patients at adjustable oxygen concentrations without the need for a blender, compressor, or hospital-grade wall air.
The 700 Series Ventilator System can be mains- or battery-powered. Each ventilator includes two microcontrollers: one for breath delivery (which controls ventilation), and one for the user interface (which monitors ventilator and patient data). Each microcontroller verifies that the other is functioning properly. Using two independent microcontrollers in this fashion prevents a single fault from causing a simultaneous failure of controlling and monitoring functions.
The 700 Series Ventilator System supplies mandatory or spontaneous breaths with a piston-based pneumatic system. Table 1-1 summarizes the modes and breath types offered by the 740 and 760 Ventilators. Mandatory breaths can be
volume control ventilation (VCV, available on 740 and 760 Ventilators) or pressure control ventilation (PCV, available on the 760 Ventilator only). VCV
delivers breaths to the patient at a preset tidal volume, peak flow, waveform, and oxygen concentration at a minimum respiratory rate. PCV delivers breaths to the patient at a preset inspiratory pressure, I:E ratio or inspiratory time, rise time factor (how quickly inspiratory pressure rises to achieve the set inspiratory pressure), and oxygen concentration at a minimum respiratory rate. A spontaneous breath allows the patient inspiratory flows of up to 300 L/min, with or without pressure support ventilation (PSV). On the 760 Ventilator, you can set the rise time factor and exhalation flow sensitivity (that is, the point at which the ventilator cycles from inspiration to exhalation) in PSV.
The ventilator begins apnea ventilation if no breath (patient- , ventilator-, or operator-initiated) is delivered within the selected apnea interval. Apnea ventilation is active during all modes. On the 740 Ventilator, only VCV breaths are available in apnea ventilation. On the 760 Ventilator, VCV or PCV breaths are available in apnea ventilation.
The 760 Ventilator also offers the ability to perform respiratory mechanics calculations and maneuvers as a standard feature using the EXP PAUSE (to
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1 Introduction
calculate auto-PEEP) and INSP PAUSE (to calculate patient resistance and compliance) keys.
Table 1-1: Mode/breath type availability on 740/760 Ventilators
Mode/breath type 740 Ventilator 760 Ventilator
VCV breath type
PCV breath type
PSV breath type (support pressure setting)
PSV (rise time factor and exhalation sensitivity settings)
SIMV mode
Apnea ventilation (VCV breath type)
Apnea ventilation (choice of VCV or PCV breath type)
Respiratory mechanics (EXP PAUSE and INSP PAUSE)
••
This manual tells you how to operate and perform simple maintenance for the 700 Series Ventilator. Mallinckrodt recommends that you become familiar with this
manual and accompanying labels before attempting to operate or maintain the ventilator. If you need additional copies of this manual, contact your Mallinckrodt representative.
To ensure optimum performance of the 700 Series Ventilator System, Mallinckrodt recommends that a qualified service technician perform periodic maintenance on the ventilator. For more information, contact your Mallinckrodt representative.
1.1 Functional description
By pressing keys and turning the knob on the ventilator keyboard, the operator gives initial instructions and data to the ventilator (Figure 1-1). The user interface microcontroller processes this information and
1-2
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stores it in the ventilator’s memory. The breath delivery microcontroller uses this stored information to control and monitor the flow of gas to and from the patient.
The 700 Series Ventilator uses a flow trigger to recognize patient effort. The trigger monitors flow from the piston during exhalation. When the patient inhales, patient circuit pressure drops very slightly below end-expiratory pressure. At the same time, the piston moves forward to deliver flow to the ventilator breathing circuit and maintain the preset PEEP/CPAP level. The level of flow depends on the patient’s effort. If this flow exceeds the user-set level, the ventilator triggers. By design, the ventilator attempts to maintain PEEP in the presence of a circuit leak. Since a leak drives the piston to deliver flow to make up for pressure losses, a circuit leak can require an increase in the flow trigger level to avoid autocycling.
During exhalation, the ventilator’s piston retracts and draws air and oxygen into the cylinder. The ventilator uses room air, which means the ventilator can operate without a compressor or wall air source. Room air enters the ventilator through a protected user-replaceable air intake filter just inside the ventilator cabinet. This filter captures airborne particles.
Oxygen from a cylinder or wall supply enters the ventilator through a hose and oxygen fitting (the fitting is available in several versions). Once inside the ventilator, the oxygen is regulated to a pressure the ventilator can use, then mixed with air, according to the selected % O
The flow-triggered piston/cylinder system and motor controller circuit control the flow of gas to the patient. On the 760 Ventilator in PCV or PSV, the rate of flow is also determined by the preset rise time factor. This system is designed with a minute gap (about the size of a thin sheet of paper) between the piston and the cylinder wall. This design eliminates the friction between the piston and cylinder, allowing it to respond more rapidly than a “sealed” system.
.
2
A small amount of gas leaks through the gap between the piston and cylinder. Ventilator software and a continuous forward motion of the piston compensate for this leak.
The piston delivers the mixed air and oxygen through the inspiratory manifold system, and out to the patient. The oxygen concentration and temperature of the delivered gas are monitored here, using a galvanic oxygen sensor and a thermistor. The galvanic sensor generates a voltage proportional to the partial pressure of oxygen, from which the oxygen concentration is calculated. The ventilator alarms if the monitored oxygen concentration is more than ten percentage points above or below the % O
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setting. The inspiratory manifold
2
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1 Introduction
system also includes a safety valve to relieve patient pressure if necessary (for example, if the ventilator breathing circuit is kinked or occluded).
The patient system includes the components external to the ventilator that route gas between the ventilator and the patient. These components include the inspiratory filter (which protects against contamination between the ventilator and patient), a humidification device, ventilator breathing circuit (the tubing through which the gas travels), collector vial (which protects the exhalation system from moisture in the exhaled gas, and can be emptied without losing circuit PEEP), and an expiratory filter (which limits the bacteria in the patient’s exhaled gas from escaping to room air or contaminating the ventilator).
1-4
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+
-
740 Ventilator
Keyboard
Regulator
Piston/cylinder
system
Exhalation/
PEEP/CPAP
system
Filter
Oxygen
Room air
Inspiration manifold
Inspiratory filter
Gas intake system
Expiratory
filter
Humidification device
Collector
vial
Ventilator breathing circuit (inspiratory limb)
Patient
Ventilator breathing
circuit (expiratory limb)
7-00017
Figure 1-1. Block diagram: 700 Series Ventilator function
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1 Introduction
The heated exhalation system monitors the flow of the patient’s exhaled gas using a differential pressure transducer. The patient exhales through the exhalation valve. During exhalation, the PEEP/CPAP system maintains user-selected pressure in the ventilator breathing circuit.
Throughout the respiratory cycle, pressure transducers monitor inspiratory, expiratory, and atmospheric pressures. The temperatures of the pneumatic compartment and inspiratory gas are also monitored. Information from these transducers is continuously used to update the calculations that control ventilation. (Appendix F provides a diagram of the ventilator’s pneumatic system and ventilator breathing circuit.)
Power to operate the ventilator comes from ac mains (wall) or battery power. The power supply is designed to protect against excessive voltages, temperatures, or current draws. A power cord retainer prevents the cord from accidental disconnection.
The ventilator includes an internal battery, and accommodates an optional external battery. Depending on the ventilator settings, battery backup power can be supplied for up to 2 ½ the external battery. Both batteries are recharged during operation from ac power. If both are installed, the external battery is used first when ac power is not present. If the external battery is depleted or not installed, the internal battery supplies power to the ventilator when ac power is not available. The keyboard indicates the source of power and battery charge level of the internal battery at all times.
hours using the internal battery, and up to 7 hours using
1-6
Emergency modes: The ventilator declares a ventilator inoperative (VENT INOP) condition if a hardware failure or critical software error that could compromise
safe ventilation occurs. In case of a ventilator inoperative condition, the VENT INOP indicator lights and the ventilator enters the safety valve open (SVO) state. To correct a ventilator inoperative condition, the ventilator must be turned off, then powered on again; at power-on, the operator must run extended self-test (EST). The ventilator must pass EST before normal ventilation can resume.
The safety valve allows the patient to breathe room air unassisted when the ventilator is in the SVO state. The ventilator remains in the SVO state until power-on self-test (POST) verifies that power levels to the ventilator are acceptable and that the motor controller and microcontrollers are functioning correctly, and until the user has confirmed ventilator settings.
If the ventilator enters the SVO state and POST is not running, the SAFETY VALVE OPEN indicator lights and a high-priority alarm sounds. The ventilator enters the SVO state if it detects a hardware or software failure that could
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compromise safe ventilation. In case of a malfunction that prevents software from opening the safety valve, there is also an analog circuit that opens the safety valve when system pressure exceeds 115 cmH
If the ventilator detects an occlusion or a continuous high inspiratory pressure condition, it opens the safety and exhalation valves to vent excess pressure, then shuts them and begins occlusion cycling mode. In occlusion cycling mode the ventilator uses current settings except for those summarized in Table 1-2. If the ventilator again detects an occlusion or continuous high pressure condition, it again opens the safety and exhalation valves then resumes occlusion cycling mode. If the operator presses the alarm reset key or the ventilator does not detect an occlusion or continuous high pressure condition, it reverts to normal ventilation using the most recently accepted settings.
Table 1-2: Changes to current settings in occlusion cycling mode
Setting Change to setting
O (113 hPa).
2
HIGH PRESSURE alarm (VCV breath type)
PEEP (all modes) Set to 0 cmH2O
(all modes) Set to 100%
%O
2
SPONT mode (PSV breath type)
SUPPORT PRESSURE (PSV breath type)
SUPPORT PRESSURE (PCV breath type)
RISE TIME FACTOR (PCV breath type)
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Setto30cmH
Breaths are delivered at a rate of 12/min with an inspiratory time of 2 seconds.
If less than 15 cmH If 15 cmH
If less than 15 cmH If 15 cmH2O or above: the current setting is used (no change).
Set to 70%
O
2
O:setto15cmH2O.
2
O or above: the current setting is used (no change).
2
O:setto15cmH2O.
2
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1 Introduction
1.2 Symbols and labels
These symbols and labels appear on the 700 Series Ventilator System:
Power switch positions per IEC 601-1.”Irepresents ON position; “O represents OFF position.
7-00421
Refer to manual per IEC 601-1. When this symbol appears on product, it means Refer to documentation for information.
7-00418
Potential equalization point, per IEC 601-1
7-00416
External battery connection
7-00426
Circuit breaker
1-8
7-00414
Serial number
SN
ac current
7-00427
Type B equipment, per IEC 601-1
7-00415
Indicates the degree of protection provided by enclosure (drip-proof).
IPX1
7-00403
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Signifies compliance with the Medical Device Directive, 93/42/EEC
7-00412
CSA and NRTL (Nationally Recognized Testing Laboratory) certification, granted by CSA
8-00417
The TUV Rheinland logo signifies TUV Rheinland Type Test approval to Annex III of the Medical Device Directive
7-00420
Exhaust port connector
EXHAUST
Inspiratory limb connector
TO
PATI EN T
Expiratory limb connector
FROM
PATI EN T
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1 Introduction
Oxygen inlet port label
O
2
.
V
max
61006
Air intake label
61010
Cooling fan label
General life support equipment warning label
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61009
61011
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740 Ventilator back panel label
61012
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1 Introduction
760 Ventilator back panel label
1-12
61952
700 Series Ventilator Operators Manual G-061874-00 Rev. D (09/00)
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Introduction 1
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1.3 Keyboard
Caution
To avoid damaging the keyboard, do not press on it with sharp objects.
The keyboard (Figure 1-2 shows the 740 keyboard and Figure 1-3 shows the 760 keyboard) is grouped into three sections:
VENTILATOR SETTINGS: Where you set breath delivery variables.
PATIENT DATA: Where you set alarm limits and view the monitored pressures, breath timing, and volumes.
VENTILATOR STATUS: Where you see the alarm status and operating condition of the ventilator.
Patient data Ventilator status
Ventilator settings
Figure 1-2. 740 Ventilator System keyboard
G-061874-00 Rev. D (09/00) 700 Series Ventilator Operators Manual
7-00048
1-13
1 Introduction
Patient data Ventilator status
1-14
Ventilator settings
7-00123
Figure 1-3. 760 Ventilator System keyboard
1.3.1 VENTILATOR SETTINGS
The VENTILATOR SETTINGS section of the keyboard allows you to select the ventilation mode, breath type, and settings. For more detail on ventilation modes and breath delivery, see Appendix D.
To change the mode and settings, select the mode, then the breath type, and then the ventilator settings. The keys flash during setup and mode changes to ensure that you review all pertinent settings. The keyboard is designed to minimize accidental or unintentional changes.
Table 1-3 summarizes the functions of the keys, knob, and indicators in the VENTILATOR SETTINGS section of the keyboard. Ventilator settings are also limited by these breath delivery boundaries:
I:E ratio £ 4:1 for PCV (760 Ventilator only), £ 3:1 for all other breath types
Inspiratory time = 0.2 to 8 seconds (excluding plateau)
Expiratory time ³ 0.2 seconds
700 Series Ventilator Operators Manual G-061874-00 Rev. D (09/00)
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Introduction 1
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PEEP/CPAP + SUPPORT PRESSURE or INSPIRATORY PRESSURE £ 80 cmH
O (80 hPa)
2
NOTE:
Maximum SUPPORT PRESSURE is 70 cmH INSPIRATORY PRESSURE is 80 cmH
2
SUPPORT PRESSURE or INSPIRATORY PRESSURE + PEEP/CPAP < HIGH PRESSURE - 2 cmH
O(2hPa)
2
HIGH PRESSURE (in A/C and SIMV modes) > PEEP/CPAP + 7cmH
O(7hPa)
2
HIGH PRESSURE (in SPONT mode) > PEEP/CPAP + SUPPORT PRESSURE + 2 cmH
O(2hPa)
2
HIGH PRESSURE > LOW INSP PRESSURE
Minute volume £ 50 L/min at an I:E ratio of 2:1
Table 1-3: 700 Series Ventilator keyboards: VENTILATOR SETTINGS
O.
O, maximum
2
Key/indicator Specifies... Range
Mode/breath type settings
A/C Assist/control mode VCV (volume control ventilation)
and PCV (pressure control ventilation) breath types.
(PCV available on 760 Ventilator only.)
SIMV Synchronous intermittent
mandatory ventilation mode
SPONT Spontaneous mode PSV breath type
VCV VCV breath type VCV available on 740 and 760
PCV PCV breath type PCV available on 760 Ventilator
G-061874-00 Rev. D (09/00) 700 Series Ventilator Operators Manual
VCV, PCV (760 only), and PSV (pressure support ventilation) breath types.
Ventilators in A/C or SIMV modes.
only in A/C or SIMV modes.
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1 Introduction
Table 1-3: 700 Series Ventilator keyboards: VENTILATOR SETTINGS (continued)
Key/indicator Specifies... Range
PSV PSV breath type PSV available in SIMV or
SPONT modes.
Mandatory (VCV) settings
RESPIRATORY RATE
TIDAL VOLUME
PEAK FLOW Maximum flow of gas delivered
PLATEAU (s) Length of inspiratory pause after a
Mandatory (PCV) settings (760 Ventilator only)
RESPIRATORY RATE
The minimum number of mandatory breaths the patient receives per minute. During apnea ventilation the minimum RESPIRATORY RATE setting is 6 / minute.
Volume delivered to the patient during a mandatory breath, compliance-compensated and corrected to body temperature and pressure, saturated (BTPS).
during a mandatory breath (BTPS). (Combined with tidal volume, peak flow defines the active portion of inspiratory time.)
mandatory breath has been delivered, during which no gas is delivered.
The minimum number of mandatory breaths the patient receives per minute. During apnea ventilation the minimum RESPIRATORY RATE setting is 6 / minute.
1to70/minute Accuracy: ± (0.1 + 1%) /minute
40 to 2000 ml Accuracy: ± (10 ml + 10% of
setting)
3to150L/min Accuracy: ± (5 + 10% of setting)
L/min
0.0to2.0second Accuracy: ± 0.05 second
1to70/minute Accuracy: ± (0.1 + 1%) /minute
INSPIRATORY PRESSURE (760 only)
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Pressure above PEEP during the inspiratory phase of a PCV breath.
700 Series Ventilator Operators Manual G-061874-00 Rev. D (09/00)
5to80cmH Accuracy: ± (3 + 2.5% of setting)
O
cmH
2
O(5to80hPa)
2
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