Zoll Ventilators Guide

EMV+® Ventilator Operator’s Guide
906-0731-01-05 Rev G
The issue date for the ZOLL EMV+ Ventilator Operator’s Guide (REF 906-0731-01-05 Rev G) is
March 2024.
Copyright © 2024 ZOLL Medical Corporation. All rights reserved. ZOLL, EMV+, and Smart Help are
trademarks and/or registered trademarks of ZOLL Medical Corporation in the United States and/or other
countries. All other trademarks are the property of their respective owners.
Masimo Pulse Oximeter
This device uses Masimo SET® technology to provide continuous pulse oximeter and heart rate monitoring and
is covered under one or more of the following U.S.A. patents: 5,758,644, 5,823,950, 6,011,986, 6,157,850,
6,263,222, 6,501,975 and other applicable patents listed at www.masimo.com/patents.htm.
Limited Copyright Release
Permission is hereby granted to any military/governmental agency to reproduce all materials furnished herein
for use in a military/governmental service training program and/or other technical training program.
ZOLL Medical Corporation
269 Mill Road
Chelmsford, MA USA
01824-4105
ZOLL International Holding B.V.
Einsteinweg 8A
6662 PW Elst
Netherlands
ZOLL Medical Switzerland AG
Baarerstrasse 8
6300 Zug
Switzerland
0123
Contents
Contents
Chapter 1
General Information
Product Description ............................................................................................................ 1-1
How to Use this Guide ........................................................................................................ 1-1
Operator’s Guide Updates .................................................................................................. 1-2
Unpacking........................................................................................................................... 1-2
Assembly ............................................................................................................................ 1-2
Product Symbols................................................................................................................. 1-2
Symbols on the Ventilator Graphical User Interface ........................................................... 1-6
Conventions ........................................................................................................................ 1-8
Abbreviations ...................................................................................................................... 1-9
Indications for Use ............................................................................................................ 1-11
Ventilation ................................................................................................................. 1-11
Pulse Oximetry (SpO2) ............................................................................................. 1-11
Features .................................................................................................................... 1-11
Warnings........................................................................................................................... 1-12
General ..................................................................................................................... 1-12
Ventilator ................................................................................................................... 1-12
Pulse Oximeter ......................................................................................................... 1-13
Batteries .................................................................................................................... 1-14
User Safety ............................................................................................................... 1-14
Patient Safety ........................................................................................................... 1-14
MR Conditional Equipment ....................................................................................... 1-15
Cautions .................................................................................................................... 1-16
FDA Tracking Requirements ............................................................................................. 1-16
Notification of Adverse Events .................................................................................. 1-17
Software License .............................................................................................................. 1-17
NO IMPLIED LICENSE ...................................................................................... 1-17
Limited Warranty ....................................................................................................... 1-17
Technical Support ............................................................................................................. 1-18
Returning a Ventilator for ZOLL Service ............................................................ 1-19
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Chapter 2
Product Overview
Ventilator Description .......................................................................................................... 2-2
Main Features ............................................................................................................. 2-2
Controls and Indicators ............................................................................................... 2-3
Controls ............................................................................................................... 2-4
Indicators ............................................................................................................. 2-4
Display Screen ............................................................................................................ 2-4
Message Area ...................................................................................................... 2-5
Parameter Windows ............................................................................................ 2-5
Shared Icon Area ................................................................................................. 2-5
Auxiliary Parameter Boxes .................................................................................. 2-5
Fresh Gas/Emergency Air Intake and Attachments .................................................... 2-6
Oxygen Reservoir Kit (Optional) .......................................................................... 2-6
Top Panel ................................................................................................................... 2-7
Pulse Oximeter Compatibility ...................................................................................... 2-8
Power Sources ........................................................................................................... 2-8
Operating Using External DC Power ................................................................... 2-8
Operating Using Battery Power ........................................................................... 2-8
Pneumatic Design ....................................................................................................... 2-9
Oxygen Input: High Pressure Gas Supply ........................................................................ 2-10
High Pressure Oxygen Supply Hose ................................................................. 2-10
Patient Circuits.................................................................................................................. 2-12
Intended Use ............................................................................................................ 2-13
Use of Heat and Moisture Exchangers ..................................................................... 2-13
Attaching a Patient Circuit to the Ventilator .............................................................. 2-14
Specifications ............................................................................................................ 2-15
Pediatric/Adult, 6 ft (1.82 m) Patient Circuit ....................................................... 2-15
Pediatric/Adult, 12 ft (3.7 m) Patient Circuit ....................................................... 2-15
Infant/Pediatric, 6 ft (1.82 m) Patient Circuit ...................................................... 2-15
Infant/Pediatric, 12 ft (3.7 m) Patient Circuit ...................................................... 2-16
Reusable Circuit ................................................................................................ 2-16
Chapter 3
Setting Up the Ventilator
1. Attach the Patient Circuit ................................................................................................ 3-2
2. Attach the High Pressure Oxygen Supply (Optional) ...................................................... 3-3
3. Inspect Fresh Gas/Emergency Air Intake Filters ............................................................ 3-4
4. Connect Fresh Gas/Emergency Air Intake Attachments (Optional) ................................ 3-4
Oxygen Reservoir Kit .................................................................................................. 3-4
Bacterial/Viral (BV) Filter ............................................................................................ 3-6
Chemical/Biological C2A1 Filter ................................................................................. 3-6
5. Select the Ventilator’s Power Source.............................................................................. 3-6
Connecting the Power Supply .................................................................................... 3-7
6. Turn On the Ventilator..................................................................................................... 3-8
7. Select Start Menu Option................................................................................................ 3-8
8. Change Operating Mode (Optional)................................................................................ 3-9
9. Change Parameter Values............................................................................................ 3-10
10. Perform Operational Test ............................................................................................ 3-10
11. Attach the Pulse Oximeter (Optional).......................................................................... 3-11
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12. Attach Patient.............................................................................................................. 3-12
Chapter 4
Using the Ventilator
Operating Mode Availability ................................................................................................ 4-2
Initial Operation with Default Parameter Settings ............................................................... 4-3
Default Parameter Settings for Adult, Pediatric and Mask CPAP ............................... 4-3
Adult Default Parameter Setting Values .............................................................. 4-3
Making a Choice From the Start Menu ....................................................................... 4-4
Changing Parameter Settings............................................................................................. 4-5
Navigating the Parameter Windows Using Parameter Buttons .................................. 4-6
Changing a Parameter Setting ................................................................................... 4-7
Example 1 — Changing a Primary Parameter ..................................................... 4-7
Example 2 — Changing a Secondary Parameter ................................................ 4-7
Example 3— Changing a Context Menu Parameter ............................................ 4-7
Saving Changed Parameters for Future Use...................................................................... 4-8
Using the Last Settings Enabled on the Ventilator.............................................................. 4-8
Mode Parameter Window Options ...................................................................................... 4-9
Primary Parameter ...................................................................................................... 4-9
Secondary Parameters and Alarm Thresholds/Limits ................................................ 4-9
Breath Target ....................................................................................................... 4-9
Leak Compensation ........................................................................................... 4-10
Context Menu ........................................................................................................... 4-10
Mode Parameter Window Reference ........................................................................ 4-11
BPM Parameter Window Options ..................................................................................... 4-12
Secondary Parameters and Alarm Thresholds/Limits .............................................. 4-12
Context Menu ........................................................................................................... 4-12
Control Parameter (I:E or Ti) ............................................................................. 4-13
Rise Time ........................................................................................................... 4-13
Cycle Off % Parameter ...................................................................................... 4-14
Spont Ti Limit Parameter ................................................................................... 4-14
BPM Parameter Window Reference ......................................................................... 4-15
Vt Parameter Window Options ......................................................................................... 4-16
Secondary Parameters and Alarm Thresholds/Limits .............................................. 4-16
Context Menu ........................................................................................................... 4-17
Vt Parameter Window Reference ............................................................................. 4-18
PIP Parameter Window Options ....................................................................................... 4-18
Secondary Parameters and Alarm Thresholds/Limits .............................................. 4-18
Context Menu ........................................................................................................... 4-19
PIP Parameter Window Reference ........................................................................... 4-20
FIO2 Parameter Window Options ..................................................................................... 4-21
Secondary Parameters and Alarm Thresholds/Limits .............................................. 4-21
Context Menu ........................................................................................................... 4-21
FIO2 Parameter Window Reference ......................................................................... 4-22
SpO2 Parameter Window Options.................................................................................... 4-22
Secondary Parameters and Alarm Thresholds/Limits .............................................. 4-23
Context Menu ........................................................................................................... 4-23
SpO2 Parameter Window Reference ....................................................................... 4-24
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HR (Heart Rate) ................................................................................................................ 4-25
Secondary Parameters and Alarm Thresholds/Limits .............................................. 4-25
Context Menu ........................................................................................................... 4-25
HR Parameter Window Reference ........................................................................... 4-26
Manual Breath .................................................................................................................. 4-27
Plateau Pressure .............................................................................................................. 4-27
Plateau Pressure Maneuver ..................................................................................... 4-27
Popup Messages .............................................................................................................. 4-28
Popup Message List ................................................................................................. 4-29
Transitions ........................................................................................................................ 4-36
Using the Menu................................................................................................................. 4-37
Alarm Configuration .................................................................................................. 4-37
Powerup .................................................................................................................... 4-37
Specifying Powerup Settings ............................................................................. 4-38
Specifying Custom Settings ............................................................................... 4-38
Specifying a Language ...................................................................................... 4-38
LCD Contrast ............................................................................................................ 4-38
LCD Brightness ......................................................................................................... 4-39
UTC Offset ................................................................................................................ 4-39
Unit Info .................................................................................................................... 4-40
Alarm History ............................................................................................................ 4-40
Chapter 5
Alarms
Alarm Overview .................................................................................................................. 5-1
Muting Alarms ..................................................................................................................... 5-3
Alarm Priorities ................................................................................................................... 5-3
High Priority ......................................................................................................... 5-3
Medium Priority .................................................................................................... 5-3
Low Priority (Advisory) ......................................................................................... 5-3
Popup Messages ................................................................................................................ 5-4
Alarm Types ........................................................................................................................ 5-4
Patient Safety Alarm Type .......................................................................................... 5-4
Environmental and Use Alarm Types ......................................................................... 5-7
Complete Power Failure ............................................................................................. 5-9
Self-Check Alarm Types ............................................................................................. 5-9
Managing Alarms .............................................................................................................. 5-11
Alarm Muting ............................................................................................................. 5-12
Start Up Muting .................................................................................................. 5-12
Preemptive Muting ............................................................................................. 5-12
Disabling Alarms from the Alarm Configuration Menu .............................................. 5-14
Patient Detect Mode ................................................................................................. 5-14
Backup Modes .......................................................................................................... 5-15
Apnea Backup Mode ......................................................................................... 5-15
Alarm Summary ................................................................................................................ 5-16
High Priority Alarms .................................................................................................. 5-16
Medium Priority Alarms ............................................................................................. 5-22
Low Priority Alarms ................................................................................................... 5-31
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Chapter 6
Operating Environments
Extending Battery Runtime when External Power is Unavailable....................................... 6-1
Using the Ventilator in Transport Environments.................................................................. 6-2
Using the Ventilator in Harsh Environments ....................................................................... 6-2
Airborne Particulates .................................................................................................. 6-2
Extreme Temperature Environments .......................................................................... 6-2
Operating at High Temperatures ......................................................................... 6-3
Operating at Low Temperatures .......................................................................... 6-3
Altitude ........................................................................................................................ 6-3
Rain and Snow ........................................................................................................... 6-4
Using the Ventilator in Hazardous Environments ............................................................... 6-4
Bacterial/Viral Filter Use ............................................................................................. 6-4
Chemical/Biological Filter Use .................................................................................... 6-5
Check Valve on Patient Circuit when in Hazardous Environments ............................ 6-5
Using the Ventilator in an MRI Environment ....................................................................... 6-6
Chapter 7
Maintenance
Inspecting the Ventilator ..................................................................................................... 7-1
Cleaning.............................................................................................................................. 7-2
Post-Contaminated Environment Cleaning ................................................................. 7-2
Fresh Gas/Emergency Air Intake Filters ............................................................................. 7-3
Inspecting and Replacing the Foam Filter .................................................................. 7-3
Inspecting and Replacing the Disk Filter .................................................................... 7-3
Replacing Ventilator Filters ................................................................................................. 7-4
Replacing the Foam Filter ........................................................................................... 7-4
Replacing the Disk Filter ............................................................................................. 7-4
Battery Maintenance ........................................................................................................... 7-6
Battery Storage................................................................................................................... 7-7
Battery Replacement and Shipping Regulations ........................................................ 7-7
Ventilator Storage ............................................................................................................... 7-8
Calibration Checks.............................................................................................................. 7-8
Pulse Oximeter Check ........................................................................................................ 7-8
Electrical Safety Check ....................................................................................................... 7-8
Troubleshooting .................................................................................................................. 7-9
Appendix A
Specifications
General ...............................................................................................................................A-1
Pulse Oximeter ...................................................................................................................A-4
Device Classification...........................................................................................................A-4
Emissions and Immunity Compliance .................................................................................A-5
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Appendix B Accessories
Appendix C Pulse Oximeter Principles
Pulse Oximeter Signaling ...................................................................................................C-1
Successful Monitoring for SpO2, PR and Pi ...............................................................C-2
Functional Oxygen Saturation (SpO2) ........................................................................C-2
Pulse Oximeter Operation ..................................................................................................C-2
Understanding Alarm Response Delay ...............................................................................C-3
Appendix D Troubleshooting Patient Circuits
Troubleshooting Procedure.................................................................................................D-1
Index
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Chapter 1
General Information
This chapter provides general information about the ZOLL® EMV+ ® ventilator and the ZOLL
EMV+ Ventilator Operator’s Guide, which we provide with this product. Specifically, this
chapter provides:
A brief description of the ventilator.
Information about this manual (EMV+ Ventilator Operator’s Guide).
A table that describes the symbols that appear on the ventilator and in this manual.
Ventilator Indications for Use.
A list of Warnings and Cautions regarding the use of the ventilator.
Information regarding FDA tracking requirements, and the product’s warranty and software
license.
• How to contact ZOLL Medical Corporation for service to this product.
•
•
•
•
•
•
Product Description
The ZOLL EMV+ ventilator is a small, extremely durable, full-featured portable mechanical
ventilator designed to operate in hospitals or severe and under-resourced environments. They
can be used in prehospital, aeromedical, field hospital and hospital settings.
How to Use this Guide
The ZOLL EMV+ Ventilator Operator’s Guide provides information that users need for the
safe and effective use and care of the ventilator. It is important that all persons using this device
read and understand all the information contained within.
Please thoroughly read the warnings section.
Procedures for device care are located in Chapter 7, “Maintenance”.
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Chapter 1 General Information
Operator’s Guide Updates
An issue or revision date for this manual is shown on the front cover. If more than 3 years have
elapsed since this date, contact ZOLL Medical Corporation to determine if additional product
information updates are available.
All users should carefully review each manual update to understand its significance and then
file it in its appropriate section within this manual for subsequent reference.
Product documentation is available through the ZOLL web site at www.zoll.com. From the
Products menu, choose Product Manuals.
Unpacking
Carefully inspect each container for damage. If the shipping container or cushion material is
damaged, keep it until the contents have been checked for completeness and the device has
been checked for mechanical and electrical integrity. If the contents are incomplete, if there is
mechanical damage, or if the ventilator does not pass its Self-Check test when turned on,
U.S.A. customers should call ZOLL Medical Corporation (1-978-421-9655). Customers
outside of the U.S.A. should contact the nearest ZOLL authorized representative. If the
shipping container is damaged, also notify the carrier. If there is no apparent sign of mechanical
damage, read instructions contained within this manual before attempting operation.
Assembly
The device only requires that you attach the breathing circuit to begin ventilation using either
battery or external power. Both the ventilator and breathing circuit are supplied clean and are
ready for use on a patient.
Product Symbols
The following symbols appear on a ventilator or in this manual:
Symbol
Description
Off
On
Direct Current: Identifies the location to connect external DC Power.
Mute / Cancel: Identifies button which mutes the active alarms or cancels
the parameter selection.
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Chapter 1 General Information
Symbol
Description
Accept /Select: Identifies button which accepts the parameter selection.
ESD: Warns that connector pins should not be touched.
Identifies the dial that allows the selection of parameter values.
Do Not Re-Use: This item should not be re-used.
Do Not Discard: Follow all governing regulations regarding the disposal
of any part of this medical device.
Serial Number: Numbers following “SN” indicate the serial number.
Defibrillation Proof: Indicates the degree of protection against electrical
shock.
BF Symbol: Protection against electric shock, Type B with floating
(F-type) parts.
MR Symbol: Identifies the use of the device’s ability to perform in a MRI
environment.
Power Input Orientation: Locates the DC input identifying its point of
insertion.
Manufacturer: This symbol identifies the name and address of the
manufacturer.
Manufacturer Date: Manufacturer Date Symbol identifies the device’s
date of manufacture.
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Chapter 1 General Information
Symbol
Description
Consult Instruction: Consult the instructions for use or operation manual.
Refer to instruction manual.
Menu icon. This icon identifies the button that, when pressed, displays a
menu of options that you can select to configure the ventilator.
280 - 600 kPa High Pressure O2 Connector (top faceplate icon).
O2 (40
- 87 PSIG)
Maximum Operational Flow Rate: 100 l/m (liters per minute).
HAUST
NOT OCC
Exhalation Valve (top faceplate icon).
Exhaust Do Not Occlude (top faceplate icon).
Transducer (top faceplate icon).
Gas Output -- Patient Circuit Connector (top faceplate icon).
Contains Phthalates
Non-Sterile
Indicates the entity importing the medical device into the locale.
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Symbol
Description
Indicates the authorized representative in the European Community
Indicates the authorized representative in Switzerland.
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Chapter 1 General Information
Symbols on the Ventilator Graphical User Interface
The following symbols appear on the ventilator’s Graphical User Interface (GUI):
Symbol
Description
Heart: Provides indication that the pulse oximeter is in use.
Alarm Bell Outline: Identifies alarm limit settings; Identifies the on-screen
alarms.
Alarm Bell: Identifies the number of off-screen alarms.
+
O2 reservoir mode is in use.
LC
Leak Compensation (LC) feature is ON.
LC
Leak Compensation Feature is OFF.
___
Patient Detect Mode: Backup Ventilation Started.
__
Not receiving a reading from the pulse oximeter.
Warning: High Priority Alarm Active.
Caution: Medium Priority Alarm Active.
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Symbol
Description
Attention: Low Priority Alarm Active.
Mute: Active Alarm Audible Signal Muted.
Speaker: Active Alarm Audible Signal.
Oxygen Supply: Oxygen Supply Connected.
External Power: Indicates the device is operating using an external
power source.
No External Power: Indicates the device is operating without an external
power source.
Internal Battery: Provides indication of battery capacity and charging.
EXT
BATT
Indicates that an external battery is powering the ventilator.
No Internal Battery: Indicates when internal battery is not an available
power source.
Head with Mask: the device is in the non-invasive positive pressure
ventilation modes, CPAP or BL, with Leak Compensation turned on.
off
on
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Feature OFF -- feature or alarm not selected.
Feature ON -- feature or alarm has been selected.
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Chapter 1 General Information
Symbol
Description
srch
Search (Pulse oximeter searching for a patient signal.)
stby
Standby (Pulse oximeter in standby.).
Conventions
This guide uses the following conventions:
• Within text, the names and labels for physical buttons and soft-keys appear in boldface type
(for example, “Press the Accept button”).
• Within text, system and alarm messages which display on the screen appear with initial
capitalization. For example, External Power Failure).
Warning!
Warning statements alert you to conditions or actions that can result in personal injury
or death.
Caution
Caution statements alert you to conditions or actions that can result in damage to the device.
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Chapter 1 General Information
Abbreviations
A/C - Assist/Control
ID - Internal Diameter
AEV - Automatic Electrical Ventilator
IPAP - Inspiratory Positive Airway Pressure.
ACLS - Advanced Cardiac Life Support
L - Liters
ALS - Advanced Life Support
LC - Leak Compensation
ATLS - Advanced Trauma Life Support
LCD - Liquid Crystal Display
ACV - Assist-Control Ventilation
LED - Light Emitting Diode
AMC - Alarm Message Center
LPM - Liters Per Minute (flow)
APOD - Advanced Probe Off Detection
l/min - liters per minute (minute volume)
ATPD - Ambient Temperature and Pressure Dry
ml - Milliliters
b/min - Beats Per Minute
mm - Millimeter
B/V - Bacterial/Viral Filter
MRI - Magnetic Resonance Imaging
BL - Bilevel positive airway pressure
O2 - Oxygen
BPM - Breaths per Minute
Paw - Airway Pressure
cm H2O - Centimeters of Water
PEEP - Positive End Expiratory Pressure
CPAP - Continuous Positive Airway Pressure
PIP - Peak Inspiratory Pressure
CPR - Cardiopulmonary Resuscitation
PPV - Positive-Pressure Ventilation
CPU- Central Processor Unit
PS - Pressure Support
CT - Tubing Compliance
psig - Pounds per Square Inch Gage
dBA - Decibel
RF - Radio Frequency
DISS - Diameter Index Safety System
RGA # - Returned-Goods-Authorization number
EMC - Electromagnetic Compatibility
RTC - Real Time Clock
EMV - Emergency Medical Ventilator
SIMV - Synchronized Intermittent Mandatory
Ventilation
EPAP - Expiratory Positive Airway Pressure
SPM - Smart Pneumatic Module
ESD - Electrostatic Discharge
SpO2 - Oxyhemoglobin Saturation,%
FIO2 - Fraction of Inspired Oxygen
USP - United States Pharmacopoeia
HME - Heat and Moisture Exchanger
VAC - Volts AC
HMEF - Heat and Moisture Exchanger/Bacterial Viral
filter combined
VDC - Volts DC
hPa - Hectopascal
VT - Tidal Volume
HP O2 - High Pressure Oxygen
WOB – Work Of Breathing
Hz - Hertz (as in frequency, cycles per second)
I:E- Inspiratory/Expiratory Ratio
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Chapter 1 General Information
Indications for Use
Ventilation
The ZOLL EMV+ ventilator is indicated for use in the management of infant through adult
patients weighing ≥ 5kg with acute or chronic respiratory failure or during resuscitation by
providing continuous positive-pressure ventilation. ZOLL ventilators are appropriate for use in
hospitals, outside the hospital, during transport and in severe environments where they may be
exposed to rain, dust, rough handling, and extremes in temperature and humidity. With an
appropriate third-party filter in place, they may be operated in environments where chemical
and/or biological toxins are present. When marked with an “MRI conditional” label, the ZOLL
ventilators are suitable for use in an MRI environment with appropriate precautions. ZOLL
ventilators are intended for use by skilled care providers with knowledge of mechanical
ventilation, emergency medical services (EMS) personnel with a basic knowledge of
mechanical ventilation, and by first responders under the direction of skilled medical care
providers.
Pulse Oximetry (SpO2)
The ZOLL EMV+ ventilator pulse oximeter with Masimo SET® technology is intended for use
for continuous noninvasive monitoring of the oxygen saturation of arterial hemoglobin (SpO2),
and pulse rate. The pulse SpO2 oximeter and accessories are indicated for use with adult and
pediatric patients during both no motion and motion conditions, and for patients who are well
or poorly perfused, in hospitals, hospital-type facilities, or in mobile environments.
Features
• Portable ventilator that you can use in the hospital, aeromedical and ground transport, mass
casualty situations, and extreme environments.
• Multiple modes of ventilation for use with acute or chronic respiratory failure in both
intubated and non-intubated patients.
• Intuitive user interface minimizes user training and protects existing settings from
inadvertent contact and manipulation.
• Smart Help® messages guide the user through on-screen commands when responding to
•
•
•
•
•
•
•
•
1-10
alarms.
Lightweight < 4.4 kg — for easy transport.
Rechargeable battery provides over 10 hours of operation (at factory default with pulse
oximeter operating).
Operating temperature range for extreme conditions: -26 to 55 °C.
Altitude compensation from 110 to 37.6 kPa (-2,250 to 25,000 ft).
Self-contained system able to operate with or without external oxygen.
Gas manifold design allows operation with both high and low-pressure oxygen sources. All
oxygen is delivered to the patient breathing circuit.
Sealed gas path with chemical/biological filter connected to assure safe breathing gas
supply.
Case and control panel protects components from weather and fluids.
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Warnings
General
• The ZOLL EMV+ ventilator is intended for use by qualified personnel only. You should
•
•
•
•
read this manual before using the device.
Before using a ventilator on a patient, you must test the device in its normal configuration to
ensure proper operation.
Do not modify this equipment without authorization of the manufacturer.
This operator’s guide is not meant to supersede any controlling operating procedure
regarding the safe use of assisted ventilation.
Follow all governing regulations regarding the disposal of any part of this medical device,
the handling of materials contaminated by body fluids, and shipment of the Li-ION
batteries.
Ventilator
• The EMV+ ventilator can operate from its internal battery or from an external power source.
When using external power, position the power cord to avoid accidental disconnect.
• The use of accessories and cables other than those sold by ZOLL may result in increased
•
•
•
•
•
•
emissions or decreased immunity of this device.
Portable and mobile RF communication equipment may affect the performance of this
device. We describe the EMC performance for this device in Appendix A Specifications of
this guide.
ZOLL ventilators may cause radio interference or may disrupt the operation of nearby
equipment. It may be necessary to take mitigation measures, such as re-orienting or
relocating of the device or shielding the location.
Do not connect to an electrical outlet controlled by a wall switch or dimmer.
The protection against defibrillator depends on the use of accessories (including Pulse
Oximeter) that are specified by ZOLL.
Grounding:
• Do not under any circumstances remove the grounding conductor from the power
plug.
• Do not use extension cords or adapters of any type. The power cord and plug must
be intact and undamaged.
• If there is any doubt about the integrity of the protective earth conductor or power
supply, operate on internal battery power.
As with all medical equipment, carefully route the patient circuit, patient cabling, and
external power cords to reduce the possibility of patient entanglement or strangulation.
The product design includes materials with phthalates in the pressure lines of
both the manifold design and patient circuit. Patient mask accessories used
with the device also are made with materials containing phthalates. Phthalates
are NOT present in the inspiratory line (blue hose/tube) of the patient circuit.
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Chapter 1 General Information
• Do not use in MRI environment unless MRI marking is present.
• Do not operate the ventilator on a patient when the USB port is connected to any other
device (the USB port is only for servicing the ventilator).
• The ZOLL-supplied patient circuit’s labeling provides the resistance and compliance values
for the circuits under normal operating conditions. If added accessories are used
(e.g. HME, filters etc.), you should assure they do not degrade the performance of the
device.
Pulse Oximeter
• Do not use the pulse oximeter as an apnea monitor.
• A pulse oximeter should be considered an early warning device. As a trend towards patient
•
•
•
•
1-12
deoxygenation is indicated, blood samples should be analyzed by a laboratory co-oximeter
to completely understand the patient’s condition.
Measurements: if the accuracy of any measurement does not seem reasonable, first check
the patient’s vital signs by alternate means and then check the pulse oximeter for proper
functioning.
Inaccurate measurements may be caused by:
• Incorrect sensor application or use.
• Significant levels of dysfunctional hemoglobin (e.g. carboxyhemoglobin or
methemoglobin).
• Intra-vascular dyes such as indocyanine green or methylene blue.
• Exposure to excessive illumination, such as surgical lamps (especially ones with a
xenon light source), bilirubin lamps, fluorescent lights, infrared heating lamps, or
direct sunlight (exposure to excessive illumination can be corrected by covering the
sensor with a dark or opaque material).
• Excessive patient movement.
• Venous pulsations.
• Placement of a sensor on an extremity with a blood pressure cuff, arterial catheter,
or intravascular line.
• The pulse oximeter is defibrillator-proof. The pulse oximeter can be used during
defibrillation, but the readings may be inaccurate for a short time.
Interfering Substances: carboxyhemoglobin may erroneously increase readings. The level of
increase is approximately equal to the amount of carboxyhemoglobin present. Dyes, or any
substance containing dyes, that change usual arterial pigmentation may cause erroneous
readings.
Alarms: Check alarm limits each time the pulse oximeter is used to ensure that they are
appropriate for the patient being monitored.
Loss of pulse signal can occur in any of the following situations:
• The sensor is too tight.
• Excessive illumination from light sources such as a surgical lamp, a bilirubin lamp,
or sunlight.
• A blood pressure cuff is inflated on the same extremity as the one with an SpO2
sensor attached.
• The patient has hypotension, severe vascoconstriction, severe anemia, or
hypothermia.
• Arterial occlusion proximal to the sensor.
• The patient is in cardiac arrest or is in shock.
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• Sensors:
Before use, carefully read the Masimo LNCS® sensor directions for use.
Use only Masimo oximetry sensors for SpO2 measurements. Other oxygen
transducers (sensors) may cause improper performance.
• Tissue damage can be caused by incorrect application or use of an LNCS sensor for
example, by wrapping the sensor too tightly. Inspect the sensor site as directed in
the sensor Directions for Use to ensure skin integrity and correct positioning and
adhesion of the sensor. When operating at extreme temperatures, take care not to
apply the sensor with excessive pressure and monitor application to prevent tissue
damage.
• Do not damage LNCS sensors. Do not use an LNCS sensor with exposed optical
components. Do not immerse the sensor in water, solvents, or cleaning solutions
(The sensors and connectors are not waterproof). Do not sterilize by irradiation,
steam, or ethylene oxide. See the cleaning instructions in the directions for reusable
Masimo LNCS sensors.
• Do not use damaged patient cables. Do not immerse the patient cables in water,
solvents, or cleaning solutions (the patient cables are not waterproof). Do not
sterilize by irradiation, steam, or ethylene oxide. See the cleaning instructions in
the directions for reusable Masimo patient cables.
• Do not use the pulse oximeter sensor during magnetic resonance imaging (MRI) scanning.
Inducing current could potentially cause burns. The pulse oximeter may affect the MRI
image and the MRI unit may affect the accuracy of the dosimetry measurements.
•
•
Batteries
• Only use the power supply provided with the device. Use of any other power supply could
cause damage or create a fire and/or destroy the battery and device.
• If you witness a battery or the battery compartment starting to balloon, swell up, smoke, or
feel excessively hot, turn off the device, disconnect external power, and observe it in a safe
place for approximately 15 minutes and send the device for service. Never puncture or
disassemble the battery packs or cells.
User Safety
• Electric shock hazard: Do not remove equipment covers. You may only perform
•
•
•
•
•
•
maintenance procedures specifically described in this manual. Refer all servicing to
ZOLL or a ZOLL-authorized service center.
Possible explosion hazard if used in the presence of flammable anesthetics or other
flammable substances in combination with air, oxygen-enriched environments, or nitrous
oxide.
This device is not intended for use in explosive atmospheres.
Pins of connectors identified with the ESD warning symbol should not be touched. Always
use precautionary procedures with ESD-sensitive connections.
Power source installation must only be carried out by qualified service personnel
Verify integrity of the external power source
Connect and verify that the fixed equipment is connected to the power source
Patient Safety
• To ensure patient electrical isolation, connect only to other equipment with electronically
isolated circuits.
• Do not place the device or external power supply in any position that might cause it to fall
on the patient. Do not lift the device by the power cord, patient circuit, or pulse oximeter
patient cable.
• Never service the ventilator while in use with a patient.
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MR Conditional Equipment
• Failure to follow all instructions can result in MRI artifacts, injury to the patient or
user, or malfunction of the device.
• You must follow all safety procedures that are in effect for the MRI Environment. Do
not use the ventilator in an MRI Environment with greater than 3T magnetic force.
• You must secure the device to a suitable MRI-compatible cart -- ZOLL MRI Roll
Stand; Optional IV Arm Assembly.
• You must place the ventilator behind the 130 Gauss field line (approximately 2
meters to the bore opening of a 3T MRI magnet).
• The ventilator must be attended by a person with no other responsibility than
monitoring the device and patient while in the MRI Environment.
• You must visually monitor the ventilator for alarms at all times -- during imaging,
the alarms may not be audible beyond the area immediately adjacent to the MRI.
• Danger! Possible Missile Projection.
• DO NOT position any person between the bore entrance and an unsecured cart or
device.
• Lock the wheels when the rolling stand is in place.
• We recommend that you tether the rolling stand in place when in the MRI
Environment.
• Place the ventilator and stand in its position before the patient is positioned on the
scanner table and advanced into the bore.
• Remove the patient from the MRI Environment before removing the ventilator and
roll stand.
• Unapproved device apparatus shall NOT be allowed in the MRI Environment,
including:
• Pulse Oximeters sensors and cabling.
• External AC/DC Power Supply.
• Rolling Cart Breathing Circuit Arm.
• Active Humidification and associated support apparatus.
• Ensure proper configuration of the ventilator.
• DO NOT attach the pulse oximeter sensor to the patient and remove it from the
device.
• The ventilator should run only on battery power in the MRI Environment
-- DO NOT use an external AC/DC power supply.
• The ventilator’s battery should be fully charged before entering the MRI
Environment.
• Oxygen Supply -- an aluminum, non-magnetic cylinder and oxygen hose must
provide the oxygen supply.
• Ensure proper operation of the ventilator’s breathing system.
• 12 ft patient circuits are available for use with the ventilator -- the additional length
enables a suitable separation between the ventilator and the bore opening.
(Adult/Pediatric Wye Patient Circuit; Pediatric/Infant Wye Patient Circuit).
• The extended tubing length of a 12 ft patient circuit can result in loss of volume due
to additional tubing compressibility.
-- Set the Tubing Compliance (CT) to OFF and ensure that the patient is
receiving correct tidal volume.
• DO NOT use the 12 ft circuit with PEEP settings below 5 cm H2O (hPa).
• Ensure that the ventilator is able to maintain PEEP -- for patients with short
expiratory times, the additional tubing length of the 12 ft circuit may affect system
behavior.
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Cautions
• Inspect the circuit every day to ensure that there is no damage or wear that could affect its
performance. Remove fluid or other biological material from the circuit or replace the
circuit following the local standard of care.
• Federal law restricts this device to sale by or on the order of a physician.
• Only qualified biomedical equipment technicians should service the device.
• Internal components are susceptible to damage from static discharge. Do not remove device
covers.
• Possession or purchase of this device does not convey any expressed or implied license to
use the device with unauthorized sensors or cables which would, alone, or in combination
with this device fall within the scope of one or more of the patients related to this device.
ZOLL cannot ensure the proper functioning of this device if it is used with unauthorized
sensors, cables, or patient circuits.
FDA Tracking Requirements
U.S. Federal Law (21 CFR 821) requires the tracking of ventilators. Under this law, owners
of this ventilator must notify ZOLL Medical Corporation if this product is
• Received
• Lost, stolen, or destroyed
• Donated, resold, or otherwise distributed to a different organization
If any such event occurs, contact ZOLL Medical Corporation in writing with the following
information:
• Originator's organization – Company name, address, contact name, and contact phone
number
• Model number, and serial number of the ventilator
• Disposition of the ventilator (for example, received, lost, stolen, destroyed, distributed to
another organization), new location and/or organization (if known and different from
originator’s organization) – company name, address, contact name, and contact phone
number
• Date when the change took effect
Please address the information to:
ZOLL Medical Corporation
Attn: Tracking Coordinator
269 Mill Road
Chelmsford, MA 01824-04105
Fax: (978) 421-0007
Telephone: (978) 421-9655
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Chapter 1 General Information
Notification of Adverse Events
As a health care provider, you may have responsibilities under the Safe Medical Devices Act
(SMDA), for reporting to ZOLL Medical Corporation, and possibly to the FDA, the occurrence
of certain events.
These events, described in 21 CFR Part 803, include device-related death and serious injury or
illness. In addition, as part of our Quality Assurance Program, ZOLL Medical Corporation
requests to be notified of device failures or malfunctions. This information is required to ensure
that ZOLL Medical Corporation provides only the highest quality products.
Software License
Note:
Read this Operator’s Guide and License agreement carefully before operating a
ZOLL ventilator product.
Software incorporated into the system is protected by copyright laws and international
copyright treaties as well as other intellectual property laws and treaties. This software is
licensed, not sold. By taking delivery of and using this system, the Purchaser signifies
agreement to and acceptance of the following terms and conditions:
1. Grant of License: In consideration of payment of the software license fee which is part of
the price paid for this product, ZOLL Medical Corporation grants the Purchaser a
nonexclusive license, without right to sublicense, to use the system software in object-code
form only.
2. Ownership of Software/Firmware: Title to, ownership of, and all rights and interests in the
system software and all copies thereof remain at all times vested in the manufacturer, and
Licensors to ZOLL Medical Corporation and they do not pass to purchaser.
3. Assignment: Purchaser agrees not to assign, sublicense, or otherwise transfer or share its
rights under the license without the express written permission of ZOLL Medical
Corporation.
4. Use Restrictions: As the Purchaser, you may physically transfer the products from one
location to another provided that the software/firmware is not copied. You may not disclose,
publish, translate, release, or distribute copies of the software/firmware to others. You may
not modify, adapt, translate, reverse engineer, decompile, crosscompile, disassemble, or
create derivative works based on the software/firmware.
NO IMPLIED LICENSE
Possession or purchase of this device does not convey any express or implied license to use the
device with replacement parts which would, alone, or in combination with this device, fall
within the scope of one or more of the patents relating to this device.
Limited Warranty
ZOLL warrants the device to be free from all defects in material and workmanship for a period
of one (1) year from the date of delivery to the original purchaser.
During the warranty period, ZOLL will repair or replace the device or any part which upon
examination is shown to be defective. At its sole discretion, ZOLL may choose to supply a new
or equivalent replacement product or refund the amount of the purchase price (on the date sold
by ZOLL). To qualify for such repair, replacement, or refund, the defective device must be
returned to the ZOLL Service Center within thirty (30) days from the date that the defect is
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discovered. This warranty does not apply if the device has been repaired or modified without
the authorization of ZOLL or if the damage was caused by incorrect (off-label) use, negligence,
or an accident.
Batteries, which by their nature are consumable and subjected to environmental extremes, will
be warranted only for a period of ninety (90) days. Accessories, also consumable in usage, such
as connecting hose and breathing circuits, are not warranted.
DISCLAIMER OF IMPLIED & OTHER WARRANTIES:
THE PRECEDING WARRANTY IS THE EXCLUSIVE WARRANTY AND ZOLL MAKES
NO OTHER WARRANTY OR REPRESENTATION OF ANY KIND WHATSOEVER,
EXPRESS OR IMPLIED, WITH RESPECT TO MERCHANTABILITY, FITNESS FOR A
PARTICULAR PURPOSE, OR ANY OTHER MATTER. THE REMEDIES STATED IN THIS
DOCUMENT WILL BE THE EXCLUSIVE REMEDIES AVAILABLE TO THE
CUSTOMER FOR ANY DEFECTS OR FOR DAMAGES RESULTING FROM ANY
CAUSE WHATSOEVER AND WITHOUT LIMITATION.
ZOLL WILL NOT IN ANY EVENT BE LIABLE TO THE CUSTOMER FOR
CONSEQUENTIAL OR INCIDENTAL DAMAGES OF ANY KIND, WHETHER FOR
DEFECTIVE OR NONCONFORMING PRODUCTS, BREACH OR REPUDIATION OF
ANY TERM OR CONDITION OF THIS DOCUMENT, NEGLIGENCE, OR ANY OTHER
REASON.
Technical Support
If the ventilator requires service, contact the ZOLL Technical Support Department.
For customers In the U.S.A.
For customers outside the U.S.A.
Telephone
Call the nearest authorized ZOLL Medical Corporation
representative.
1-800-348-9011
1-978-421-9655
Email
[email protected]
To locate an authorized service center, contact:
ZOLL Medical Corporation
269 Mill Road
Chelmsford, MA 01824
Telephone: 1-978-421-9655
[email protected]
When requesting support, please provide the following information to the support
representative:
•
•
•
•
•
Ventilator serial number
Description of the problem, and service code if available
Department using the equipment and name of the person to contact
Purchase order to allow tracking of loan equipment
Purchase order for a device with an expired warranty
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Chapter 1 General Information
Returning a Ventilator for ZOLL Service
Before sending a ventilator to the ZOLL Technical Support Department for repair, obtain a
service request (SR) number from the service representative.
The Li-ion battery should remain inside the ventilator. Follow directions provided on the return
authorization form.
Pack the ventilator with its power supply in the original shipping containers
(if available) or equivalent packaging. Be sure the assigned service request (SR) number
appears on each package and follow the Shipping Regulations as described in Chapter 7 of this
manual.
Return the device to:
.
For customers
Return the device to
In the U.S.A.
ZOLL Medical Corporation
269 Mill Road
Chelmsford, MA 01824
Attention: Technical Support Department (SR number)
Telephone: 1-978-421-9655
In Canada
ZOLL Medical Canada Inc.
1750 Sismet Road, Unit #1
Mississauga, ON L4W 1R6
Attention: Technical Support Department (SR number)
Telephone: 1-866-442-1011
In other locations
The nearest authorized ZOLL Medical Corporation
representative.
To locate an authorized service center, contact the
International Sales Department at:
ZOLL Medical Corporation
269 Mill Road
Chelmsford, MA 01824-4105
Telephone: 1-978-421-9655
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Chapter 2
Product Overview
This chapter describes the ZOLL EMV+ ventilator and provides more detailed descriptions of
the following:
•
•
•
•
•
•
•
•
•
•
•
•
Operating modes support
Manual Breath and Pressure Plateau support
Main features
Controls and indicators
Display screen
Fresh Gas/Emergency Air Intake and attachments
Top Panel
Pulse Oximeter compatibility
Power sources
Pneumatic design
Oxygen Input
Patient circuits
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Chapter 2 Product Overview
Ventilator Description
The sections that follow provide a description of the ZOLL EMV+ ventilator.
Main Features
Figure 2-1 shows the ventilator’s main features.
Gas Output
External Power USB Connector
Input Connector
Gas Output Cap (Red)
Oxygen
Inlet
Pulse
Oximeter
Connector
Fresh Gas/Emergency
Air Intake
Status
Indicator
LED Array
LCD
Display
Alarm Message
Center / Waveform
Window
Handle
Battery
Compartment
Control
Panel
Figure 2-1 Main Features
2-2
Item
Location Description
Oxygen Inlet
Top
Enables connection to an external high pressure oxygen
source.
Gas Output
Top
Enables connection of the patient circuit.
Gas Output Cap (RED)
Top
The ventilator is shipped with a red cap covering the
Gas Output to protect it from dust and other
contaminants. The cap should be saved and reused
when the ventilator is stored or not in use.
Status Indicator LED Array
Top
Lights to indicate ventilator status and a visible alarm
indicator.
External Power Input
Connector
Top
Enables connection to an external power source.
USB Connector
Top
Enables connection to a USB compatible device for
servicing the ventilator.
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Item
Location Description
Pulse Oximeter Connector
Top
Enables connection to a pulse oximeter sensor
LCD Display
Front
Displays settings, ventilation data, and alarm information.
Alarm Message Center
Front
Displays active alarms and alarm mitigation information.
Control Panel
Front
Provides user access to the ventilator settings.
Battery Compartment
Bottom
Holds the ventilator’s rechargeable Li-ion battery.
Fresh Gas/Emergency Air
Intake
Side
Enables the ventilator internal compressor to use ambient
air and acts as an anti-asphyxia valve.
Handle
Side
Controls and Indicators
The ventilator controls and indicators (shown in Figure 2-2) facilitate ease of use and visibility
in all operating environments.
LCD Display
LED Array
Menu
Button
Parameter
Buttons
Mute/Cancel
Button
Accept
Button
Manual Breath/
Plateau Pressure
Button (Pressure Plateau
Power
Switch
feature not available on
all Models)
Selection Dial
Figure 2-2 Controls and Indicators
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Chapter 2 Product Overview
Controls
The ventilator’s controls consist of the following:
Control
Function
Power Switch
Enables the user to turn the ventilator ON and OFF.
Parameter Buttons
Enables the user to access primary parameters, secondary parameters
and context menus associated with a primary parameter (if applicable),
and then modify settings using the Selection Dial).
Menu Button
Enables the user to access the Menu.
Selection Dial
Enables the user to set values for a chosen (highlighted) Primary
Parameter, Secondary Parameter, Context Menu item, and Menu item.
Values accelerate with speed of turning.
Mute/Cancel Button
The Mute/Cancel button mutes the audible alarm allowing the user time
to change parameters. It can also be used to cancel parameter entries.
Accept Button
The Accept button allows the user to accept parameter value settings,
acknowledge popup messages, and accept menu choices.
Manual Breath Button/
Plateau Pressure
Enables the user to deliver a manual breath and measure Plateau
Pressure.
Note: The button is labeled “Manual Breath / P Plat”.
Indicators
The ventilator’s indicators consist of the following:
Indicator
Description
LCD Display
Displays settings, patient data, and alarm information.
LED Array
Indicates operational status (Red, Yellow, or Green).
Display Screen
The ventilator’s display screen has four functional areas as shown in Figure 2-3:
Alarm Message Center/Waveform Window
Parameter Windows
Shared Icon Area
Auxiliary Parameter Boxes.
These functional areas are discussed in the following sections.
•
•
•
•
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Alarm Message
Center / Waveform Window
Parameter Windows
Shared Icon Area
Auxiliary Parameter Boxes
Figure 2-3 Display Screen Functional Areas
Message Area
The display screen’s message area can display the following:
• Airway Pressure and Pleth Waveform Plots -- Under normal operation (as in the example
above), the message area displays plots for airway pressure and, when the pulse oximeter is
connected, the Pleth waveform. When a plot is necessary to facilitate a parameter
adjustment, the message area displays both the plot and the parameter’s context menu.
• Menus -- Displays the Menu after you press the Menu button on the ventilator’s control
panel, or displays a parameter’s context menu (which appears after you press and hold the
associated parameter button on the control panel).
• Alarms -- When an alarms occur, the message area displays Smart Help™ messages that
identify the alarms and describe possible causes and actions that you can take in response.
• Popup Windows -- Display information that assists you when adjusting parameter values.
Parameter Windows
Each parameter window displays its primary parameter and associated secondary parameters,
that can include, associated parameters and alarm limits.
Two types of values appear in a parameter window.
• Solid text is used for primary and secondary parameter values you can adjust.
• Outlined text is used for patient-dependent measured values.
Chapter 4, “Using the Ventilator” contains more information and instructions for adjusting
parameter values.
Shared Icon Area
Directly below the message area, the device displays icons that indicate
•
•
•
•
The ventilator’s power source (operating on external power or its battery)
The battery charging status
An oxygen supply is attached
Alarms are muted or audible
Auxiliary Parameter Boxes
Some parameters have values that the ventilator displays in the parameter boxes at the bottom
of the display screen. You can adjust these values using the parameter’s context menu.
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Chapter 2 Product Overview
Fresh Gas/Emergency Air Intake and Attachments
The Fresh Gas/Emergency Air Intake is located on the side of the ventilator as shown in
Figure 2-4.
Fresh Gas/Emergency Air
Intake
Figure 2-4 Fresh Gas/Emergency Air Intake
The Fresh Gas/Emergency Air Intake allows ambient air into the device’s internal compressor.
The intake also acts as an anti-asphyxia valve that enables the patient to breathe ambient air
should the ventilator fail. The Fresh Gas/Emergency Air Intake contains a particulate filter and
permits the user to connect either a bacteria/viral or a chemical/biological filter depending on
ambient conditions.
An Oxygen Reservoir Kit is attached to the Fresh Gas/Emergency Air Intake to allow low flow
oxygen use with the ventilator to provide supplemental oxygen to patients, an ISO 5362
compliant breathing bag is attached with to a manifold which is connected to a low flow
oxygen source (either an oxygen flow meter or oxygen concentrator).
Oxygen is delivered through the Fresh Gas/Emergency Air Intake when the device's internal
compressor cycles to deliver a breath.
Oxygen Reservoir Kit (Optional)
The Oxygen Reservoir Kit serves the following purposes:
• Acts as a reservoir, collecting oxygen during the expiratory phase of ventilation.
• Provides an interface to the ventilator and the attachment of the low-flow oxygen supply
hose.
• Provides an inlet in the event the low-flow oxygen supply fails or the tidal volume is greater
than the supplied oxygen.
See Chapter 3 for more information about using low flow oxygen sources.
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Figure 2-5 Ventilator with O2 Reservoir Kit
Top Panel
The oxygen hose, patient circuit, external power, and pulse oximeter attach to the top panel of
the ventilator. The USB port is only used when servicing the device.The ventilator top panel
appears as shown in Figure 2-6.
Gas
Output
High Pressure
Oxygen Input
Transducer
(Patient Airway
Pressure)
Gas Output
Cap (Red)
Power Cord
Connector
(External AC/DC
Power)
Fresh Gas/ Emergency
Air Intake
Exhaust
Exhalation
Valve
USB Port
(Service Use Only)
Pulse Oximeter
Connector
Figure 2-6 Top Panel
Note:
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The ventilator is shipped with a red cap covering the Gas Output (called out in
Figure 2-6) to protect it from dust and other contaminants. The red cap should be saved
and reused when the ventilator is stored or not in use.
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Chapter 2 Product Overview
Pulse Oximeter Compatibility
The ventilator can accommodate an optional connection of external Masimo Pulse Oximeter.
When the appropriate sensor is connected, the pulse oximeter provides continuous noninvasive
monitoring of the oxyhemoglobin saturation (SpO2) and pulse rate (measured by the SpO2
sensor) for adult, pediatric and infant patients.
The Masimo LNCS series of probes are approved for use with the ventilator. The Accessory
table in Appendix A lists the sensors which are available for use with the ventilator.
Power Sources
The ventilator can operate using external power or it can operate powered by its internal Li-ion
battery.
The external AC/DC Power cable is a universal supply that can operate with an input of
100 to 240 VAC 50/60 Hz. The external supply can also power the device when provided with
a 400 Hz input.
The external AC/DC Power cable that ZOLL provides with the ventilator delivers a DC input to
the device of 24 V at 4.2 A. When this external power source is present, the ventilator
automatically charges its internal battery while operating.
Only use the external power supply provided with the ventilator when connecting to AC power.
The device is docked when connected to a power supply that is attached to a wall, bench, or
fixed location. Use Power Supply Holder Kit to dock the ventilator.
Operating Using External DC Power
The ventilator can also operate using external DC power. When connected to a standard vehicle
DC outlet using either the 12 or 28 VDC Power Cable that ZOLL offers, the ventilator
automatically charges its internal battery while operating. The input DC supply is monitored
and the ventilator issues alarms for the following conditions:
Insufficient current
High voltage
Disconnect/ low voltage
DC reversed
Note: The input connector of the ventilator accepts DC voltages between 11.8 to 30.3 VDC.
•
•
•
•
Caution
When using the standard vehicle DC outlet, do not jump start the vehicle during operation of the
ventilator.
Operating Using Battery Power
When an external power failure occurs, the ventilator automatically switches to its internal
battery for operating power and activates the External Power Fault alarm; there is no
interruption in operation. When external power returns, operating power automatically
switches to the external power source and the following symbol displays on the ventilator
screen as shown in Figure 2-7.
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Figure 2-7 External Power GUI Symbol
In the event that the ventilator needs to be shutdown, turn the POWER switch to the OFF (“O”)
position. If this fails to work or puts the patient or user at possible risk, disconnect the device
from the external power source.
Pneumatic Design
The ventilator includes an oxygen valve and a compressor to provide the appropriate gas
mixture for the patient. The system includes transducers for pressure measurements including
O2 input supply and barometric pressure.
The Wye circuit is part of the ventilator’s pneumatic system. The inspiratory side of the wye
circuit provides gas to the patient. The expiratory side exhausts directly to atmosphere without
returning to the ventilator. The ventilator pneumatically controls the exhalation valve (to
maintain PEEP) and a transducer within the ventilator measures the airway pressure.
The ventilator breath transitions from expiratory to inspiratory phase is triggered by patient
effort (negative pressure) or time. The breaths are time or flow cycled and can either be
pressure or volume (flow) targeted.
Figure 2-8 depicts a diagram of the ventilator’s pneumatic design.
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Chapter 2 Product Overview
Figure 2-8 Pneumatic Design
Oxygen Input: High Pressure Gas Supply
An external high pressure gas source connects to the ventilator using the high pressure oxygen
input port. The device attaches to a regulated medical grade (USP) O2 system or O2 cylinder
supply of 40 to 87 psig (280 to 600 kPa). Maximum flow rate of the oxygen supply is 100 liters
per minute. The Oxygen Input fitting (See Figure 2-9) has a male oxygen Diameter Index
Safety System (DISS) thread.
Note:
If external oxygen is connected, the oxygen pressure must be at least 41 psig (± 2 psig)
(283 kPa (± 14 kPa)) at the time the ventilator performs its Self-Check after turning on
the ventilator.
High Pressure Oxygen Supply Hose
A standard oxygen hose is available for connecting the ventilator to a high pressure oxygen
source. (Also see Chapter 6 “Operating Environments”). Hoses are available from ZOLL, or a
suitable alternative as described below can be used as indicated.
High Pressure Oxygen Hose for compliance with ISO standard (ISO STANDARD 5359)
2-10
Ventilator Side
Connections
Hose Attributes
Supply Side Connections
DISS
1.8 m (maximum 6.1 m) Green or White
(as determined by local regulations)
non-conductive
Quick Disconnect, DISS, etc.
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External Gas Sources
Bottled Oxygen
Regulated
55 psig
(3.8) Output
-OR-
55 psig
(3.8 bar) Output
OXYGEN
OXYGEN
High Pressure Hose
D.I.S.S. X.D.I.S.S.
12 VDC 24 VDC
AC/DC
POWER POWER
POWER
CONVERTOR CABLE CABLE
Low O๜ /O๜ concentrator
To Fresh
Gas/Emergency
Air Intake
3-Liter
Reservoir
Figure 2-9 Ventilator Gas Sources
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Chapter 2 Product Overview
Patient Circuits
The ventilator can use 6 ft or 12 ft patient circuits (see Figure 2-10) to support adult, pediatric,
and infant patients.
Note:
Troubleshooting information regarding patient circuits is found in Appendix D.
Figure 2-10 Patient Circuits
ZOLL provides the following circuit types:
• Pediatric/Adult, 6 ft and 12 ft
• Infant/Pediatric, 6 ft and 12 ft
• Reusable Adult, 120 cm only
Caution
2-12
Always dispose of disposable circuits after single patient use following the institutional
guidelines for biologically contaminated material. Reusing a disposable circuit can result in
cross contamination between patients.
Follow all product labeling for sterilization and use of the reusable circuit.
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Chapter 2 Product Overview
Intended Use
The pediatric/adult patient circuits are intended for use when delivering tidal volume from
200 ml to Adult.
The infant/pediatric patient circuit is intended for use when delivering tidal volume from
50 ml to 300 ml.
Warning!
Patient circuits marked as such are non-sterile and intended for Single Patient Use Only
Caution
During use the circuit may come into contact with biohazard material. Handle carefully to avoid
cross-contamination.
Not intended for use with heated humidifier.
Note:
ZOLL Medical Corporation recommends that you examine the patient circuit on a
daily basis for damage or wear, such as cracking, discoloration, or disfigurement. If
there is any sign of physical degradation or if the ventilator has patient circuit alarm
conditions replace the patient circuit.
Use of Heat and Moisture Exchangers
Heat and Moisture Exchangers (HMEs) can be used with the device. The HME provides heat
and moisture to the inspired gas by recycling the heat and moisture contained in the patient's
exhaled gas. While HMEs may not be suitable for all applications, they facilitate portability in
a way that conventional humidifiers cannot. The device can be used with an optional HME or
an optional HME/bacterial viral filter (HMEF). Be sure to follow all instructions provided by
the manufacturer.
Note:
Use of the HME will cause a slight increase in the inspiratory and expiratory
resistance. Always monitor the patient and adjust the ventilator as needed.
ZOLL does not offer a heated humidification option for the device.
Warning!
Users should use the appropriate HME for the patient's size. Failure to do so can result
in excessive dead space and lead to hypercapnia and hypoxia.
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Chapter 2 Product Overview
Attaching a Patient Circuit to the Ventilator
Figure 2-11 shows how to attach a patient circuit to the ventilator.
Inspiratory Line
(Hose/Tube)
Exhalation Line
(Hose/Tube)
Inspiratory Line
(Hose/Tube)
Exhalation Line
(Hose/Tube)
Figure 2-11 Patient Circuit Attachment
The list that follows identifies the circuit connections.
Connection
2-14
Symbol on the Ventilator
Description
Inspiratory Line
(Hose/Tube)
Gas Output
Pressure Line (Green)
Transducer
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Chapter 2 Product Overview
Connection
Symbol on the Ventilator
Description
Exhalation Line (Clear)
Exhalation Valve
Oxygen In
High Pressure Oxygen
Outlet
Exhaust
Do Not Occlude
Specifications
Note:
1 cm H2O equals.98 hPa.
Pediatric/Adult, 6 ft (1.82 m) Patient Circuit
The Pediatric/Adult, 6 ft (1.82 m) patient circuit has the following specifications:
• Internal Diameter: 22 mm
• Inspiratory Resistance: RINSP @ 30 Lpm: 0.01 cm H2O/l/min
• Expiratory Resistance: REXP @ 30 Lpm: 0.10 cm H2O/l/min
• Tubing Compliance: CT @ 60 cm H2O: 1.6 ml/cm H20
• Dead Space: 22 ml
• Maximum Working Pressure: 100 cm H20
Pediatric/Adult, 12 ft (3.7 m) Patient Circuit
The Pediatric/Adult, 12 ft patient circuit has the following specifications:
• Internal Diameter: 22 mm
• Inspiratory Resistance: RINSP @ 30 Lpm: 0.02 cm H2O/l/min
• Expiratory Resistance: REXP @ 30 Lpm: 0.10 cm H2O/l/min
• Tubing Compliance: CT @ 60 cm H2O: 2.8 ml/cm H2O
• Dead Space: 22 ml
• Maximum Working Pressure: 100 cm H2O
Infant/Pediatric, 6 ft (1.82 m) Patient Circuit
The Infant/Pediatric, 6 ft (1.82 m) patient circuit has the following specifications:
• Internal Diameter: 10 mm
• Inspiratory Resistance: RINSP @ 15 Lpm: 0.11 cm H2O/l/min
• Expiratory Resistance: REXP @ 15 Lpm: 0.17 cm H2O/l/min
• Tubing Compliance: CT @ 60 cm H2O: 0.5 ml/cm H2O
• Dead Space: 4.2 ml
• Maximum Working Pressure: 100 cm H2O
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Chapter 2 Product Overview
Infant/Pediatric, 12 ft (3.7 m) Patient Circuit
The Infant/Pediatric, 12 ft (3.7 m) patient circuit has the following specifications:
• Internal Diameter: 10 mm
• Inspiratory Resistance: RINSP @ 15 Lpm: 0.17 cm H2O/l/min*
• Expiratory Resistance: REXP @ 15 Lpm: 0.17 cm H2O/l/min
• Tubing Compliance: CT @ 60 cm H2O : 0.8 ml/cm H2O
• Dead Space: 4.2 ml
• Maximum Working Pressure: 100 cm H2O
Note:
The extended length of the tubing in the 12 ft (3.7 m) circuit results in a higher RINSP
compared to the 6 ft (1.82 m) circuit.
Reusable Circuit
See product labeling insert for all specifications.
Warning!
Compressible volume can significantly decrease the delivered tidal volume. When
managing patients at risk, always correct for compressible volume Use the Vt Context
Menu to adjust Tubing Compliance and Compressible Volume Measurements.
Warning!
Do not use the 12 ft circuit with PEEP settings below 5 cm H2O (hPa).
Warning!
Given the additional length of the 12 ft circuit, the system may not be able to trap PEEP
in patients with short expiatory time. Always ensure that the device is performing as
required.
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Chapter 3
Setting Up the Ventilator
This chapter describes how to set up the ventilator. It lists the tasks required to set up the
ventilator for safe, effective use, and describes each task in detail.
Warning!
You must properly set up the ventilator before use. Failure to do so can result in
inadequate care or death of the patient.
To set up the ventilator, you must perform the following tasks:
1. Attach the patient circuit
2. Attach the high pressure oxygen supply (optional)
3. Inspect Fresh Gas/Emergency Air Intake filters
4. Connect Fresh Gas/Emergency Air Intake attachments (optional)
5. Select the ventilator’s power source
6. Turn on the ventilator
7. Select Start Up default configurations
8. Change the operating mode (optional)
9. Change parameter values
10. Perform an operational test
11. Attach the pulse oximeter (optional)
12. Attach patient
We describe how to perform these tasks in the following sections of this chapter.
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Chapter 3 Setting Up the Ventilator
Warning!
Always follow physicians orders and local protocols that includes preparations to
manually ventilate (bag) the patient. Ensure there is a functioning Bag Valve Mask
available to support the patient in the event of a ventilator failure. DO NOT start up the
ventilator with the patient attached.
1. Attach the Patient Circuit
Select the correct patient circuit for the patient and environment (as we describe in the previous
chapter). Always follow the instructions included with the circuit. Attach the patient circuit to
the ventilator’s top panel as follows. See Figure 3-1.
1. Remove the red cap covering the Gas Output, then connect the patient circuit (22 mm
corrugated hose) to the ventilator’s Gas Output
2. Connect the green 4.76 mm ID airway pressure line to the pressure transducer
3. Connect the clear 6.35 mm ID exhalation valve control line to the exhalation valve fitting.
4. Connect the oxygen hose to the Oxygen Input connector.
Note:
Note:
The patient circuit recommended temperature range for use is -40 to 70 °C.
The ventilator is shipped with a red cap covering the Gas Output (called out in
Figure 2-6) to protect it from dust and other contaminants. The red cap should be saved
and reused when the ventilator is stored or not in use.
Oyxgen Hose to
Oxygen Input
Connector
Green Oxygen Hose
to Green Transducer
Connector (Airway Pressure)
Corrugated Tubing to
Gas Output Connector
Remove Red
Gas Output Cap
(If Present)
Clear Hose to
Exhalation Valve
Connector
Pulse Oximeter Cable to
Pulse Oximeter Connector
(Optional)
Figure 3-1 Patient Circuit Device Connections
Warning!
3-2
Adult patients should only be ventilated with Pediatric/Adult circuits. Infant patients
should only be ventilated with Infant/Pediatric circuits.
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Chapter 3 Setting Up the Ventilator
Warning!
ZOLL recommends the use of the patient circuits that ZOLL offers for the ventilator. If
circuits with different resistance/compliance are used or additional accessories are
placed in line with the circuit, you must use the appropriate compliance factors for the
new circuit, and make sure the dead space volume of the added accessories are
considered so that the device delivers an effective tidal volume to the patient.
Warning!
Use of a facemask adds dead space, always ensure the dead space of the system (patient
circuit plus facemask) is appropriate for the patient you are supporting.
2. Attach the High Pressure Oxygen Supply (Optional)
Since the ventilator includes an internal compressor, the attachment of a high pressure oxygen
supply is optional. Review the high pressure supply requirements that we describe in Chapter 2,
and use the oxygen hose to attach the ventilator’s oxygen inlet to the high pressure O2 source.
The ventilator oxygen inlet is shown in Figure 3-2.
Warning!
Use only with medical-grade (USP) oxygen. When using with an oxygen cylinder, the
cylinder must be secured. The O2 hose is either colored green or white, depending on
country specifications.
Oxygen
Inlet
Figure 3-2 Oxygen Inlet
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Chapter 3 Setting Up the Ventilator
3. Inspect Fresh Gas/Emergency Air Intake Filters
The Fresh Gas/Emergency Air Intake provides the gas path for the ventilator’s internal
compressor. Two built-in filters protect the compressor and patient from particulate matter (a
removable foam filter and a Fresh Gas/Emergency Air Intake disk filter).
The ventilator’s Fresh Gas/Emergency Air Intake is shown in Figure 3-3. Inspect the filters
and, if dirty, replace them (See the section, “Replacing Ventilator Filters” in Chapter 7.
Fresh Gas/Emergency Air
Intake
Figure 3-3 Fresh Gas/Emergency Air Intake
Warning!
Never block the Fresh Gas/ Emergency Air Intake, free flow of air is required during
compressor operation or in the event of device failure to allow spontaneous breathing.
The Fresh Gas/Emergency Air Intake also acts as an anti-asphyxia port in the event of a
ventilator failure.
4. Connect Fresh Gas/Emergency Air Intake Attachments
(Optional)
The operating environment of the ventilator may require you to connect the following
attachments to the Fresh Gas/Emergency Air Intake:
Oxygen Reservoir Kit
If the ventilator will use oxygen from low-flow sources, you may choose to attach an Oxygen
Breathing Bag (compliant with ISO 5362). Follow these steps:
1. Press the Menu button and use the Dial to choose O2 Reservoir “On”. This tells the
ventilator that the reservoir is attached and prevents the Intake Restricted alarm from
sounding.
2. Attach the Oxygen Reservoir Kit to the Fresh Gas/Emergency Air Intake. This port is located
in the side of the ventilator. It will be necessary to use a 22 mm male-to-male adapter (with
hose barb) with 731 Series Ventilators.
3. Connect the O2 supply tubing between the O2 source and the hose barb on the adapter.
4. Adjust the O2 flow to achieve an acceptable O2 saturation.
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Chapter 3 Setting Up the Ventilator
Note:
Warning!
The assembly will function when the reservoir bag is hanging down or lying
horizontally provided the bag does not fall in such a way that occludes the neck of the
bag. The ventilator will sound a low priority Intake Restricted alarm if the menu has
not been changed (see “1”above). Operating with the alarm active does not affect the
ability of the ventilator to deliver breaths at the current settings. It is to alert the user
that a restriction has been detected at the inlet. Always allow 5 to 10 minutes between
adjustments to assure the patient oxygenation has stabilized. This is very important
when decreasing the O2 supply where it may take several minutes for a patient to
stabilize at the new O2 flow. Never use O2 flows > 10-12 liters/min. Flows greater than
this can cause the baseline pressure to drift, waste oxygen, and may cause an AutoPEEP alarm.
Always monitor the patient's oxygenation using a pulse oximeter. The O2 flow from a
concentrator or other O2 source may not be adequate to achieve the desired SPO2
target. Failure to follow the Instructions and WARNINGS provided with the O2
Reservoir could result in an adverse effect on the patient.
Note:
Due to the slight difference between the densities of air and O2, the tidal volume will
decrease slightly as O2 is entrained. The worst case is a < 10% decrease in tidal
volume when the entrained O2 results in FIO2 of 100%.
The table below shows both the affect on tidal volume and the resultant FIO2 supply
rate.
Ventilator
AC 12, Vt 700, PEEP 5, I:E 1:2.5
O2 Flow
0
1
2
3
4
5
6
7
8
FIO2
21
30
38
48
57
70
80
89
100
Vt (set)
740
732
725
718
711
703
691
689
682
Vt (actual)
700
692
685
678
671
663
651
649
642
0
-1.1
-2.1
-3.1
-4.1
-5.3
-7.0
-7.3
-8.3
% Chg
AC 12, Vt 500, PEEP 5, I:E 1:2.5
O2 Flow
0
1
2
3
4
5
6
FIO2
21
30
43
56
69
89
100
Vt (set)
527
523
514
506
502
493
486
Vt (actual)
500
496
487
479
475
466
459
% Chg
0
-0.8
-2.6
-4.2
-5.0
-6.8
-8.2
AC 18, Vt300, PEEP 5, I:E 1:2.5
O2 Flow
0
1
2
3
4
5
6
FIO2
21
32
47
62
76
96
100
Vt (set)
312
307
303
299
298
291
287
Vt (actual)
300
295
291
287
286
279
275
% Chg
0
-1.7
-3.0
-4.3
-4.7
-7.0
-8.3
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Chapter 3 Setting Up the Ventilator
Bacterial/Viral (BV) Filter
If the ventilator will operate in an environment where the patient is at risk from cross
contamination or airborne pathogens, you may choose to attach a BV filter (See Chapter 6,
“Operating Environments” for more information on this filter).
Chemical/Biological C2A1 Filter
If the ventilator will operate in a contaminated environment, you may choose to attach a
chemical/biological C2A1 filter obtained from a Chemical/Biological Filter supplier.
Connect the filter canister directly to the device or use an approved adapter.
Note:
Warning!
ZOLL does not offer this filter. (See Chapter 6, “Operating Environments” for more
information on this filter).
Always monitor the patient and ventilator when using external filters or the external O2
reservoir. Changing modes can trigger false compressor failure alarms when the
device’s parameter configurations requires very high air flow.
5. Select the Ventilator’s Power Source
The ventilator can run using one of the following power sources:
• Fully charged, the battery provides 10 hours of operation at factory default settings with
pulse oximeter operating at 25 °C.
• External AC/DC Power Supply that ZOLL provides (100 to 240 VAC 50/60 and 400 Hz
with an IEC 320 style AC input connector. The AC/DC Power Supply provides a DC output
of 24 V at 4.2 A.
• External DC power from a standard vehicle DC outlet using either the 12 or 28 VDC Power
Cable that ZOLL provides to connect the ventilator to the DC outlet. The ventilator’s input
connector accepts DC voltages between 11.8 to 30.0 VDC.
The ventilator uses external power when available rather than its internal battery pack. When an
acceptable external power source is present, the ventilator automatically charges the internal
battery while the device operates. When an external power failure occurs, the device
automatically switches to its internal battery for operating power and activates the
External Power Fault alarm; there is no interruption in operation or loss of any alarms. When
external power returns, operating power automatically switches from internal power to the
external source.
In the event that the device needs to be shutdown, turn the Power switch to the OFF (“O”)
position. If this fails to work or puts the patient or user at possible risk, disconnect the device
from the mains power.
To connect the ventilator to an external power source, connect an AC/DC Power Supply plug to
the device’s External Power Input and an acceptable electrical outlet.
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Connecting the Power Supply
Connect the external power cable to the ventilator as described in Figure 3-4 and Figure 3-5.
Figure 3-4 Connecting and Disconnecting the Power Supply
Warning!
If the power supply, power cable, or power connection plugs are damaged or become
damaged during use, immediately disconnect the power cable from external power and
the device.
Caution
Do not twist the power cable connection plug. Pinch the plug and slide up to release the safety
latches. Failure to do so may damage the power connection plug and prevent it from functioning.
Figure 3-5 Power Supply Latching
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Chapter 3 Setting Up the Ventilator
6. Turn On the Ventilator
To turn on the ventilator, turn the Power switch to “I”. Figure 3-6 shows the location of the
ventilator’s power switch.
Power Switch
Figure 3-6 Power Switch
After turning on the ventilator, the device performs its Self-Check test, which checks for alarm
conditions and the operation of the pneumatic system, internal communications, and power
system. After completing the Self-Check test, the ventilator waits for the user to select a
starting configuration before it begins to operate. Once operation begins, the ventilator
continuously monitors for alarm conditions.
During normal start-up, the ventilator’s alarms are muted for 2 minutes (120 seconds) to allow
you to connect the patient circuit, pulse oximeter, adjust ventilator settings, and perform an
operational test without distraction. The start-up mute self clears when there are not any active
medium priority alarms and no unmuted low priority alarms for a period of 15 seconds.
Warning!
Always start the ventilator, select the patient settings, ensure operation, and then
connect the patient. Always manually ventilate the patient when they are not connected
to the ventilator.
7. Select Start Menu Option
When you turn on the ventilator, the Start Menu appears, from which you choose an appropriate
starting configuration for the patient. You can select from these patient defaults:
Adult
Pediatric
Mask CPAP -- Continuous Positive Airway Pressure (CPAP)
Custom -- Values saved in a previous session
Last Settings -- Values set for the last patient treated before turning OFF the ventilator
Note: Gas flow at start up is used to detect the patient in event proper procedures are not
followed.
•
•
•
•
•
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Warning!
Default settings are intended to speed the configuration of the ventilator. Particular
care should be taken to adjust the ventilator appropriately before ventilating infants
and children. The ventilator should always be adjusted before placing the patient on the
ventilator.
The predefined configurations (Adult, Pediatric, Mask CPAP) are default settings defined
within the specified use. The Custom default can be used to define a configuration that supports
your use and/or patient population. See Chapter 4 for more information.
To select the device’s default parameter values, highlight one of the above settings in the Start
Menu and press the Accept button. To operate with parameter values that differ from the
default values, use the device’s parameter buttons (see the “Changing Parameter Values”
section later in this chapter).
Note:
Warning!
You can configure the ventilator to automatically select Adult parameter defaults at
start up from the start config submenu from the menu.
Never use the CPAP and BL mode on a patient that is NOT spontaneously breathing
and/or may stop spontaneous breathing. CPAP and BL are intended for ventilatory
support, NOT ventilation.
When noninvasive CPAP and BL with LC is used, the head with mask icon appears in the
location used by the speaker/mute icons. Low and Medium priority alarms cause this head with
mask icon to disappear. It reappears when low priority alarms are muted.
When Medium priority alarms are muted, the muted speaker icon appears.
8. Change Operating Mode (Optional)
The ventilator offers four operating modes that you can use to manage the patient (active
modes, AC and SIMV can provide either pressure or targeted ventilation): See, “Chapter 4
Using the Ventilator” for detailed instructions.
• AC (Assist/Control) -- The patient receives either controlled or assisted breaths. When the
patient triggers an assisted breath, the patient receives a breath based on either the volume or
pressure target.
• SIMV (Synchronized Intermittent Mandatory Ventilation)-- The patient receives controlled
breaths based on the set breathing rate. Spontaneous breaths are either unsupported demand
flow or supported using Pressure Support.
Note: SIMV mode is an optional mode and might not be available on your ventilator.
• CPAP (Continuous Positive Airway Pressure) -- The patient receives constant positive
airway pressure while breathing spontaneously. Spontaneous breaths are either demand flow
or supported using Pressure Support.
• BL (Bilevel) -- the ventilator provides two pressure settings to assist patients breathing
spontaneously: a higher inspired pressure (IPAP) and a lower expiratory pressure (EPAP).
To select the operating mode, press the Mode parameter button, turn the Dial to highlight the
mode you want to use, and press the Accept button.
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Chapter 3 Setting Up the Ventilator
When transitioning from active ventilation to CPAP/BL modes, or from CPAP/BL with LC
mode to active ventilation, the following parameter/alarm limit may be adjusted:
•
•
•
•
•
•
•
•
Warning!
Low BPM alarm
High BPM alarm
Low Airway Pressure alarm
PEEP
VT High Limit
VT Low Limit
Rise Time
Pressure Support
The transition into CPAP or BL automatically adjusts the rise time and always needs to
be checked since the setting might need further adjustment. Before using the ventilator
with an infant or small child, you should always configure the ventilator appropriately
before attaching the patient and monitor the patient to ensure optimal support.
Note:
The Patient Detect alarm triggers when you connect the patient to the ventilator while
the Start Menu is still active. To resolve the alarm, you must select a mode of
ventilation and configure the device appropriately for the patient. In addition, you
should perform the Operational Test procedure before reconnecting the patient to the
device.
9. Change Parameter Values
If the patient requires parameter values that differ from the default values, you can use the
parameter buttons to change these values. To change the parameter values, press the parameter
buttons to highlight the primary parameter and secondary parameter values, or press and hold
the parameter button to display the parameter’s context menu. Use the Dial to adjust the value
of the highlighted parameter. Press the Accept button to implement the change.
Warning!
The alarm limits must be appropriate for the patient being ventilated. If a parameter is
changed, adjust the high and low alarm limit to bracket the new value.
10. Perform Operational Test
Before attaching the patient to the ventilator, you should perform an Operational Test to ensure
that the breathing circuit is properly attached and that the primary patient safety alarms, such as
PATIENT DISCONNECT and AIRWAY PRESSURE HIGH are functioning properly.
To perform the operational test procedure, do the following:
a. Press the Manual Breath button; gas should flow out of the patient connection each time
the button is pressed.
b. Close the patient port with a clean gloved hand. The High Airway Pressure Limit alarm
should activate after 2 breaths that reach the PIP High Limit.
If the Airway Pressure High alarm fails to activate, check to determine that all of the circuit
connections are secure, the exhalation valve is closing during inhalation, and that the High
Airway Pressure Limit is set to 35 cm H2O (hPa) or less.
c. After a breath or two, release the patient port while allowing the ventilator to operate. The
Patient Disconnect alarm should activate.
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Chapter 3 Setting Up the Ventilator
d. Partially close the patient port to reset the Patient Disconnect alarm.
e. With no other alarms occurring, remove external power from the ventilator. The External
Power Low/Disconnect alarms should activate. Reconnect external power to reset alarms.
If either the High Airway Pressure, Patient Disconnect, or External Power Low/Disconnect
alarms fail to activate, continue to manually ventilate the patient, check the patient circuit
for leaks or a faulty exhalation valve and repeat the operational test.
If operating using the internal battery, verify that the Battery icon indicates sufficient available
battery capacity remains to support the anticipated duration of operation. If not, begin
ventilation and find an alternate source of power.
Warning!
Until you have determined that the ventilator is functioning properly and that the
ventilator parameters are set correctly for the patient, do not connect the patient to the
ventilator.
11. Attach the Pulse Oximeter (Optional)
The pulse oximeter operates in all ventilator modes when its cable and sensor are properly
attached to the SpO2 connector (during start up, the pulse oximeter is on standby -- the SpO2
and HR parameter windows display stby).
To operate the pulse oximeter, connect the sensor to the patient and the cable to the SpO2
connector on the top of the ventilator as shown in the Figure 3-7.
Pulse Oximeter
Probe Connection
Figure 3-7 Connecting the Pulse Oximeter Sensor
Monitoring begins automatically when a valid patient signal is detected for greater than
10 seconds. For more information about the Masimo pulse oximetry technology that the
ventilator uses, see Appendix C, Pulse Oximeter Principles.
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Chapter 3 Setting Up the Ventilator
12. Attach Patient
After you confirm that the ventilator is operating correctly, detach the test lung (if used in the
Operational Test) from the patient circuit. Attach the patient airway (endotracheal tube,
supraglottic airway or tracheotomy tubes) or mask to the patient circuit connection port.
Note:
If there are circuit-related alarms during set up or initial use, such as Disconnect, PEEP
Leak, Low Airway Pressure, or Auto PEEP, check all circuit connections and the
exhalation valve.
Caution
When patient conditions require a PEEP = 0, ensure the exhalation valve is in the upright
position. The orientation of this valve position may impact the ability to deliver the intended tidal
volume for small volumes or slow rise times.
Warning!
Never leave the patient unattended.
Warning!
Always ensure that there is an alternate means of providing mechanical ventilation.
A bag-valve resuscitator and an appropriate mask for the patient being ventilated
should be immediately available.
Warning!
Do not connect the patient to the ventilator until you determine that the ventilator is
functioning properly and that the ventilator parameters are set correctly for the
patient.
Warning!
Do not connect anything to the USB connection. The USB connection does not provide
any signal output or input to the user. The USB connection is a tooled access used
during service of the device.
Patient Circuit
Endotracheal
Tube (ETT)
Figure 3-8 Attaching the Patient
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Chapter 4
Using the Ventilator
This chapter describes how to use a ZOLL ventilator. Effective operation of the ventilator
requires understanding of the following topics:
•
•
•
•
•
•
•
•
•
•
•
•
•
•
Operating mode availability by ventilator model
Initial operation with default (predefined) parameter settings
Changing parameter settings
Saving custom configurations for future use
Using the last settings enabled on the ventilator
Mode Parameter Window Options
BPM Parameter Window Options
Vt Parameter Window Options
PIP Parameter Window Options
FIO2 Parameter Window Options
SpO2 Parameter Window Options
HR Parameter Window Options
Popup Messages
Using the Menu
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Chapter 4 Using the Ventilator
Operating Mode Availability
Mode availability is dependent on your ZOLL ventilator model. The table that follows provides
information on mode availability for ZOLL ventilator models.
Ventilator Model
Modes
Supported
Leak
Compensation
Target
Pressure
Support
Regional
Mode
Reference***
EMV+
EMV+ MR
AC(V)
Off (Default)
Volume
No
VC-CMV
AC(P)
Off (Default)
Pressure
No
PC-CMV
SIMV (V)
Off (Default)
Volume
Yes
VC-IMV
SIMV (P)
Off (Default)
Pressure
Yes
PC-IMV
CPAP*
On (Default)**
Pressure
Yes
PC-CSV
BL*
On (Default)**
Pressure
Yes
PC-CSV
* Spontaneously Breathing Patient Mode
** When Mask CPAP selected from Startup Menu
*** Outside of the United States
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Initial Operation with Default Parameter Settings
After turning on the ventilator, the ventilator goes through a Self-Check (a set of system tests
and checks). If the Self-Check passes, the LED array turns green and the Start Menu displays,
indicating that the ventilator is operational.
The Start Menu enables the user to choose between predefined ventilator parameter settings
(for adult patients, pediatric patients, patients requiring Mask CPAP), a previously saved set of
Custom parameter settings, or the parameter settings last used during ventilator operation. The
Start Menu choices include:
Warning!
Choice
Description
Adult
Preset ventilation parameter settings for adult patients.
Pediatric
Preset ventilation parameter settings for pediatric patients.
Mask CPAP
Preset ventilation parameter settings for Mask CPAP (Continuous
Positive Airway Pressure) ventilation.
Custom
Ventilation parameter settings previously saved by a user.
Last Settings
The settings enabled on the ventilator during its last use (but not
saved as Custom Settings by the user).
Do not connect patient to the ventilator while the Start Menu is active.
Default Parameter Settings for Adult, Pediatric and Mask CPAP
Default parameter settings might be localized to meet country-specific specifications. The
standard factory default settings for Adult, Pediatric, and Mask CPAP are as follows:
Adult Default Parameter Setting Values
Parameter
Default Setting Value
Mode
AC (V)
BPM
12
I:E
1:3
VT
450
PEEP
5
PIP Limit
35
FIO2
21
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Pediatric Default Parameter Setting Values
Parameter
Default Setting Values
Mode
SIMV (P)*
AC(P)
BPM
20
20
Ti
0.6
0.6
PIP
20
20
PEEP
4
4
PIP Limit
30
30
FIO2
21
21
* SIMV (V) and SIMV (P) modes are not available on all ventilator models. See
“Operating Mode Support” in Chapter 2 for more information.
Mask CPAP Default Parameter Setting Values
Parameter
Default Setting Value
Mode
CPAP
Backup BPM
12
Backup I:E
1:3
Backup PIP
20
PEEP
5
PIP Limit
30
FIO2
21
Making a Choice From the Start Menu
Choose the option that is most is appropriate for the patient. With the Start Menu displayed,
follow these steps:
1. Turn the Dial to highlight your choice. For example, to choose the Mask CPAP default, turn
the Dial until Mask CPAP highlights.
2. Press the Accept button to enable your choice. The ventilator begins operation with the
choice you made. For initial set-up, see Chapter 3.
Note:
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The ventilator provides a 120-second alarm mute it automatically clears as described
above to allow the provider time to adjust parameter settings for the patient.
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Changing Parameter Settings
The ventilator helps you to manage the patient by organizing ventilator parameters in groups
that are accessed through parameter windows on the right side of the display screen.
A button corresponding to each window, enables you to select and set parameters.
Parameter Group Item
Description
Primary Parameter
The primary parameter setting accessed and controlled through the
parameter window. These are labeled with large font as: HR,
SPO2,FIO2, PIP, Vt, BPM, and Mode.
Secondary Parameters and
Alarm Thresholds/Limits
Secondary parameters associated with the primary parameter and
alarm thresholds for alarms associated with the primary parameter,
(small font).
Context Menu
Additional settings that further adjust the performance of the device
related to the primary parameter.
Parameters controlled by the user appear as solid text (or a solid symbol) in either the parameter
window or auxiliary boxes. Parameters dependent on the patient appear as outlined text in the
parameter window. Figure 4-1 shows parameter windows.
Solid
Symbol
Solid
Text
Outlined
Outlined
Text
Text
Auxiliary
Boxes
Figure 4-1 Parameter Windows and Auxiliary Boxes
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Figure 4-2 shows the buttons associated with parameter windows.
Parameter
Buttons
Figure 4-2 Parameter Buttons
Navigating the Parameter Windows Using Parameter Buttons
Parameter values are accessed with a parameter button as follows:
• Single Press: highlights the primary parameter for the chosen parameter window
• Multiple Presses: highlights secondary parameters and alarm limits. (Multiple presses
highlight secondary parameters moving in a clockwise direction)
• Press and Hold: opens the context menu (for those primary parameters that have a context
menu). Turning the Dial highlights context menu items.
Note: If you attempt to set parameter values that are outside the typical clinical range of
settings, the ventilator displays popup messages that ask if you are sure you would like
to set the parameter to that value. We describe popup messages in more detail later in
this chapter. To set the parameter above the limit, you must press the Accept button,
and then adjust the values and press the Accept button again.
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Changing a Parameter Setting
To change a parameter, follow these steps.
1. Access the parameter you intend to change using the parameter buttons as described in the
previous sections.
2. Press the Accept button to highlight your choice. Multiple presses are required for secondary
parameters.
3. Turn the Dial to adjust the parameter value
4. Press the Accept button to enable your choice.
The examples that follow describe how to change a primary parameter, secondary parameter,
and a context menu parameter.
Example 1 — Changing a Primary Parameter
In Example 1, the ventilator is operating with the default Adult parameters. The user wants to
change the Mode from AC (Adult Default) to CPAP.
To change the Mode parameter from AC to CPAP, follow these steps:
1. Press the Mode parameter button once.
2. Turn the Dial until the Mode parameter window displays CPAP.
3. Press the Accept button.
Example 2 — Changing a Secondary Parameter
In Example 2, the ventilator is operating with the default Adult parameters and user wants to
adjust the PEEP secondary parameter setting from 5 (the adult default setting) to
7 cm H2O (hPa).
To change the secondary parameter PEEP setting from 5 to 7, follow these steps:
1. Press the PIP parameter button until PEEP is highlighted.
2. Turn the Dial until the PEEP setting is 7 as displayed in the PIP parameter window.
3. Press the Accept button.
Example 3— Changing a Context Menu Parameter
In Example 3, the ventilator is operating with the default Adult parameters and user wants to
change the Masimo Pulse Oximeter Sensitivity from Norm (normal) which is the adult default
setting – to Max (maximum).
To change the Sensitivity setting from Norm to Max, follow these steps:
1. Press and hold the HR or SpO2 parameter button until the Masimo context menu displays.
2. Release the parameter button, then turn the Dial until the Sensitivity choice highlights, then
press the Accept button. The Sensitivity setting highlights.
3. Turn the Dial until the setting changes to Max (maximum).
4. Press the Accept button.
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Saving Changed Parameters for Future Use
When you change parameters, you can save them for future use through the Custom Settings
Menu option.
To save changed parameters for future use, follow these steps.
1. With the ventilator turned on, make the desired parameter changes using the parameter
buttons, Dial and Accept button.
2. Press Menu button.
3. Using the Dial, highlight Powerup Settings, and then press the Accept button.
4. Use Dial to highlight Custom Settings, then press the Accept button to highlight Save, and
then press the Accept button again to save the changed parameters.
To use or confirm that the changed parameters are saved as Custom settings, follow these steps:
1. Turn on the ventilator.
2. When the Start up Menu displays, turn the Dial to highlight Custom Settings, and then press
the Accept button.
3. The ventilator displays the custom parameter settings in the parameter windows.
Warning!
The Custom and Last Setting options save the current configuration of the ventilator.
Always ensure that the both the ventilation settings and alarm limits are appropriate
for the patient.
Using the Last Settings Enabled on the Ventilator
The ventilator preserves the last setting used on the ventilator (even if they were not saved as
Custom Setting). To use the last settings, do the following:
1. Turn ON the ventilator, wait for the Self-Check to complete, and the Start Menu to display.
2. Turn the Dial to highlight the Last Settings choice.
3. Press the Accept button to enable your choice.
The ventilator begins operation with the last settings used.
Warning!
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Last Settings uses all of the parameters including alarms. You must ensure that both the
setting and alarms are appropriate for the patient.
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Mode Parameter Window Options
The ventilator allows you to select different ventilation modes to optimally manage the patient.
Primary Parameter
The Mode parameter window has four primary parameter choices.
• AC (Assist/Control) -- The patient receives either controlled or assisted breaths. When the
patient triggers an assisted breath, they receive a breath based on either the volume or
pressure target.
• SIMV (Synchronized Intermittent Mandatory Ventilation) -- The patient receives
controlled breaths based on the set breathing rate. Spontaneous breaths are either
unsupported demand flow or supported using Pressure Support.
Note: SIMV mode is an optional mode and might not be available on your ventilator.
• CPAP (Continuous Positive Airway Pressure) -- The patient receives constant positive
airway pressure while breathing spontaneously. Spontaneous breaths are either demand flow
or supported using Pressure Support.
• BL (Bilevel) -- the ventilator provides two pressure settings to assist patients breathing
spontaneously: a higher inspiratory pressure (IPAP) and a lower expiratory pressure
(EPAP).
Secondary Parameters and Alarm Thresholds/Limits
The Mode parameter window has two secondary parameter choices.
• Breath target
• Leak Compensation
Breath Target
• Volume targeting (V) -- assures a constant volume is delivered to the patient in the
inspiratory time using a constant flow. During volume targeting, the PIP parameter appears
as outlined text.
• Pressure targeting (P) -- provides a constant airway pressure for the duration of the
inspiratory time using a decelerating flow pattern. During pressure targeting, the Vt
parameter appears as outlined text.
To set (or change) the Breath Target, follow these steps:
1. Press the Mode parameter button twice to highlight the Breath Target parameter
2. Use the Dial to switch between V (Volume Targeting) and P (Pressure Targeting)
3. Press the Accept. button.
Note:
Please note that tidal volume cannot be adjusted in pressure-targeted ventilation. You
may have to adjust PIP to maintain desired tidal volume.
To adjust the PIP target in Pressure Targeted ventilation, follow these steps:
1. Press the PIP parameter button.
2. Use the Dial to set the desired PIP target value.
3. Press the Accept button.
In pressure target ventilation, setting the high and low tidal volume limits protect against leaks
and ensures delivery of a minimum tidal volume.
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Warning!
During pressure-targeted ventilation, always set the high tidal volume just above the
patient's maximum tidal volume. In the event of disconnection or decannulation, the
increase in volume will trigger the alarm.
Leak Compensation
Leak Compensation (LC) is available in all pressure-targeted ventilation modes for fullfeatured ventilators or limited to start up settings (see Operating Modes Availability table
above). Leak compensation and provides flow during the expiratory phase to maintain the
baseline pressure caused by a leaking airway or facemask. Leak compensation can
accommodate leaks in the range of 0 to 30 liters per minute.
To activate leak compensation, follow these steps:
1. Press the Mode parameter button twice. The “No Leak Compensation” icon highlights.
2. Turn the Dial to turn leak compensation ON. A pop-up message appears asking for
confirmation.
3. Press the Accept button to activate Leak Compensation.
To avoid nuisance alarms in patients with active leaks, Leak Compensation suppresses the
following alarms:
• Low Airway Pressure (SC: 2071)
• High Tidal Volume (SC: 2072)
• Low Tidal Volume (SC: 2073)
Note:
Note:
Once the patient is stable on CPAP or BL, the suppressed alarms should be set to
ensure safe ventilation of the patient. When in BL or CPAP modes, the Insufficient
Flow alarm (SC: 2095) triggers when the patient's inspiratory flow is greater than
100 lpm for two concurrent breaths. The user may choose to decrease the magnitude of
the trigger pressure (from default setting of -2 to -1 or -.5 cm H2O) and decrease the
Rise Time to 1 so that the flow reaches the maximum in the shortest amount of time.
When LC is available at start up, the user may choose to turn off the feature while in
CPAP or BL mode. LC is no longer available until the user restarts the ventilator.
Context Menu
The Apnea Backup context menu is accessible when the primary parameter is set to CPAP or
BL modes.
Pressing and holding the Mode parameter button in CPAP or BL Modes displays the menu. The
menu displays:
• PIP Target
• BPM
• I:E
Apnea Backup default settings are PIP target of 20, BPM 12, I:E (1:3), these settings should be
adjusted for the patient you are supporting in CPAP or BL modes.
When Apnea ventilation is enabled, the ventilator provides pressure targeted breaths at the
default Apnea settings or the provider can chose to change the settings. Apnea Backup is
triggered using the BPM Low Limit setting.
If the low breath limit is set to 4 and a breath is not detected every 15 seconds the ventilator will
begin ventilating at the Apnea Backup settings and trigger an alarm. In CPAP or BL modes,
Apnea Backup is automatic.
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To adjust or change any Apnea Backup settings,
1. From the menu, use the Dial to highlight the parameter to change, and then press the Accept
button (The current highlighted parameter value highlights).
2. Use the Dial to set the desired value
3. Press Accept to enable the change.
Mode Parameter Window Reference
The following table provides a reference to the primary parameters, secondary parameters, and
context menu parameters and other options for the Mode parameter window.
Mode Parameter Window
Options/Range
Availability/Notes
AC
Primary Parameter
Mode
SIMV
Optional mode*
CPAP
BL
Breath Target
Secondary Parameters
LC
(Leak Compensation)
Alarms
None
Measured Value
None
(V) or (P)
ON or OFF
(Default OFF)
AC (P) and SIMV(P)
modes
OFF
BL Mode
Default ON
CPAP Mode
Mode Context Menu
Apnea Backup
Context menu is available
in CPAP and BL Modes
BPM
1 to 80
PIP
10 to 80
I:E, Ti
1:99, 0.1 to 3
Control selected in context
BPM context menu
* SIMV mode is an optional mode and might not be available on your ventilator.
Warning!
Apnea Backup settings are appropriate for most adult patients. For small adult and
pediatric patients, adjust the Apnea Backup settings so that they are appropriate for the
patient.
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BPM Parameter Window Options
The BPM (Breathes Per Minute) parameter window defines the number of breaths per minute
delivered by the ventilator, as well as other parameters related to breath timing.
For AC and SIMV ventilation modes, the BPM parameter displays the setting as solid text. The
BPM parameter range is 0 to 80.
The BPM measured range is from 0 to 99.9
When CPAP and BL mode are used the primary parameter is the patient's breathing rate, shown
in the outlined text.
Assisted and controlled breaths are time-triggered and time-cycled. Spontaneous breathes are
patient triggered and flow cycled.
Secondary Parameters and Alarm Thresholds/Limits
The secondary parameters for the BPM parameter window are the following:
• BPM High Limit (number immediately below the Alarm Bell symbol)
• BPM Low Limit (lower number below the Alarm Bell symbol)
• Control Parameter (I:E ratio or Ti)
Note:
Display of I:E or Ti in the BPM parameter window is determined by the Control
Parameter setting in the BPM context menu
The BPM High Limit can be set from 20 to 99 or to OFF.
The BPM Low Limit can be set from 2 to 40.
To change the BPM High Limit or BPM Low Limit secondary parameter setting, follow these
steps:
1. Press the BPM parameter button until the BPM High Limit or BPM Low Limit secondary
parameter highlights..
2. Turn the Dial to the desired limit setting.
3. Press the Accept button.
To change the Control parameter setting, follow these steps:
1. Press the BPM parameter button until the I:E or Ti secondary parameter highlights.
2. Turn the Dial to change the setting (either I:E or Ti).
3. Press the Accept button.
Context Menu
Pressing and holding the BPM parameter button brings up the BPM context menu. Different
parameters associated with the BPM can be adjusted in this context menu. The menu offers the
option of changing the following:
•
•
•
•
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Control Parameter (I:E or Ti)
Rise Time (when pressure targeted breathes are available)
Cycle Off %
Spont Ti Limit
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Control Parameter (I:E or Ti)
The control parameter allows you to select between I:E ratio and Ti. The control parameter you
select is displayed in the parameter window and the parameter you are measuring is always
calculated and shown in the auxiliary boxes.
For AC and SIMV ventilation modes, control breaths are time-triggered and
time-cycled. The ventilator uses the inspiratory time (Ti) parameter setting to terminate the
breath being delivered.
For volume targeted breaths, the Ti parameter is used to determine the constant flow rate of the
delivered breath. Popup messages are triggered to alert the user if inappropriate settings are
selected.
The default inspiratory/expiratory control parameter is I:E ratio unless the pediatric default is
selected. The ventilator automatically calculates the inspiratory time, and displays it when the
I:E ratio is controlled, and it calculates the I:E ratio when the inspiratory time is used. Both are
always displayed on the screen.
I:E Ratio may be adjusted so that inspiration time is longer than expiration time (referred to as
inverse I:E with a range from 4.0:1 to 1.0:1, whereas normal I:E is from 1:1.0 to 1:99). Going
inverse requires a popup confirmation due to the potential for harm when this setting is
inappropriate for the patient’s condition.
Inverse I:E ratio is not available on all devices.
Rise Time
Rise Time allows the user to adjust the time it takes to reach the full inspiratory flow and Peak
Inspiratory Pressure (PIP) during pressure targeted breathing. The Rise Time displays in the
auxiliary boxes at the bottom of the display (See Figure 4-1). Use the PIP waveform as a
reference when adjusting the Rise Time for the patient. Rise time is available in these
ventilation modes:
AC (P)
SIMV (V or P)
CPAP
BL
When Pressure Support is enabled, you can adjust the time it takes to reach the PIP, where 1 is
the shortest and 10 is the longest. You should reassess and readjust the Rise Time settings after
the patient is placed on the ventilator and initially stabilized. To minimize patient's work of
breathing and potential for pressure overshoots, the following should be considered when
setting the Rise Time:
•
•
•
•
Patient tidal volume
Patient repiratory pattern
Patient's comfort
Patient's flow demand
Patient's lung mechanics - resistance and compliance
Rise Time for a passive lung is driven primarily by airway resistance, and is fairly independent
of compliance.
•
•
•
•
•
Increasing Rise Time also decreases the maximum flow from the ventilator to allow for the
management of infant and pediatric patients.
Note:
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An adult patient with high resistance may benefit from a Rise Time setting of 3 to 4 for
optimal breath delivery. Rise Times of 8 to 10 are optimized for infants and are flow
limited. (The infant circuit is not intended for flows > 60 LPM.)
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Chapter 4 Using the Ventilator
Cycle Off % Parameter
For flow cycled breaths, the ventilator transitions from inspiratory to expiratory phase when the
flow drops below a set percentage of the peak flow. The default is 25% of peak flow with a
range of 10 to 70% Cycle Off % is typically used during noninvasive ventilation to ensure the
breath cycles in synchrony with the patient. Some patients may have difficulty cycling due to
their lung mechanics or a bag that prevents the flow from reaching the cycle flow rate. When
this happens, spontaneous breathe may time cycle causing asynchrony.
You can adjust the Cycle Off% value to account for patient leaks and weak respiratory effort.
Users must carefully assess the patient's response when adjusting the Cycle Off % to avoid
cycle asynchrony and patient discomfort
Note:
The longest duration of a spontaneous breath is 5 seconds. At the end of this time, the
ventilator ends flow and opens the exhalation valve.
If there is no leak, increasing the Cycle Off % parameter causes breaths to cycle sooner, and
deliver less volume. If you set the Cycle Off % parameter too high, the breath ends early
relative to patient effort, which may lead to the triggering of a second breath.
Spont Ti Limit Parameter
The Spontaneous Inspiration Time (Spont Ti) Limit parameter provides an additional method to
limit the duration of spontaneous breaths in the presence of a leak or weak respiratory effort.
The parameter provides an inspiratory time limit for spontaneous breaths.
Adult default is 3.00 sec, Pediatric default is 2.00 sec, and Mask CPAP default is 3.00 sec.
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BPM Parameter Window Reference
The following table provides the options and ranges for the BPM parameters:
BPM Parameter Window
Primary Parameter
Options/Range
BPM
Availability/Notes
1 to 80
Breaths per minute
Secondary Parameters
Ti (sec)
or
I:E
Ti 0.3 to 3.0
or
I:E 1:1 to 1:99
Ti 0.1 to 5.0
or
I:E 4:1 to 1:99
Alarm Limits
BPM High
20 to 99, OFF
BPM Low
2 to 99
l/min
0 to 99
Control
Parameter
Default I:E
I:E or Ti (sec)
The control value is shown
in the parameter window,
the dependent value is
shown in the Auxiliary Box.
Rise Time -
Pediatric Default 5
1 to 10
Auxiliary Box
Auxiliary Box
Measured Value
BPM Context Menu
Mask CPAP Default 3
Cycle Off %
(% Cycle )
Default 25%
10 to 70%
Spont Ti Limit
Default
Adult = 3.00
Infant = 2.00
Mask CPAP = 3.00
0.30 to 4.00
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Chapter 4 Using the Ventilator
Vt Parameter Window Options
The Vt parameter defines the volume (ml) delivered to the lung with each breath. Tidal volume
is calculated by integrating the flow over the inspiratory time. During volume targeted
breathing, pressing the Vt parameter button highlights the currently set tidal volume and
enables it to be changed. When breathing is pressure targeted, the delivered tidal volume is
shown as outlined text and is based on the PIP and patient’s pulmonary mechanics.
Warning!
In CPAP and BL, a Vt that is lower than anticipated may be an indication that the
patient is not able to adequately ventilate. The minimum tidal volume during
volume-targeted ventilation is 50 ml.
Note:
Warning!
In CPAP, the Vt delivered and Vmin may be overestimates of the true volume going to
the patient when leaks are present. The O2 Use values accurately display the O2 use,
though the amount used is more than if no leak was present.
If significant leaks are present during CPAP and BL modes, the Vt delivered and Vmin
shown may be overestimates of what is actually being delivered to the patient. The
adequacy of ventilation should be assessed using an alternate method.
Secondary Parameters and Alarm Thresholds/Limits
The secondary parameters for the Vt parameter window are the following:
• Vt High Limit (lower number below the alarm bell)
• Vt Low Limit (number below the Vt High Limit)
Note:
The Vt High Limit and Vt Low Limit are not presented during volume targeted
ventilation because the ventilator automatically alarms if two consecutive breathes are
out of range.
The Vt High Limit can be set from 50 to 2000 (ml). The Vt Low Limit can be set to OFF, or it
can be set from 5 to 500 (ml).
The Vt High Limit parameter cannot be adjusted below the primary parameter Vt setting or the
Vt Low Limit setting and attempting to do so generates a conflict popup message.
The Vt High Limit parameter is used to limit the delivered tidal volume during pressure
targeted breaths. If two consecutive breaths are limited by the setting of this parameter, the
High Tidal Volume alarm (SC: 2072) is triggered. The Vt Low Limit parameter setting is used
to trigger the Low Tidal Volume alarm (SC: 2073).
Warning!
During pressure targeted breathing with infant and pediatric patients, always set the
high tidal volume limit just above the desired tidal volume. Doing this ensures an alarm
in the event of a leak or decanulation.
To change a limit setting, follow these steps:
1. Press the Vt parameter button more than once until the desired Vt limit setting highlights.
2. Turn the Dial until the desired value is reached.
3. Press the Accept button to enable the change.
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Context Menu
Pressing and holding the Vt parameter button brings up the Vt context menu that includes:
Compliance
Adult
Infant
Compliance Volume
The tubing compliance can be set to off, adult, or infant.
•
•
•
•
Users can chose to use the adult or infant circuit defaults for the standard ZOLL adult/pediatric
and infant/pediatric patient circuits. Compliance for reusable circuit should be adjusted
according to circuit labeling.
The patient circuit is part of the breathing system of the ventilator. Tubing compliance of the
circuit is a physical property that affects the tidal volume delivered to the patient. The ventilator
allows you to adjust the compliance value of the circuit (see Chapter 6 for more information).
Tubing compliance is adjustable and a different compliance value can be entered for each
circuit type by selecting either of the menu items. The range is limited for the adult patient
circuits from 0 to 3.5 ml/cm H2O and from 0 to 2 ml/cm H2O for the infant circuits to prevent a
selection beyond the range of the standard circuits.
In order to prevent inappropriate or unsafe use of this feature, the tubing compliance
compensation is turned OFF at startup.
Adult and Infant settings correspond to the standard WYE patient circuit used. Adult CT range
is between 0 and 3.50 ml/cm H2O (default of 1.60 ml/cm H2O), and the Infant CT range is
between 0 and 2.00 ml/cm H2O (default of .5 ml/cm H2O).
During volume targeted breathes the ventilator corrects for the loss due to CT by adding the
correction to the set Vt ensuring that the set volume is delivered to the patient. During pressure
targeted breaths the compensation volume is subtracted from the displayed Vt to indicate the
volume delivered to the patient.
To change a Vt context menu setting, follow these steps:
1. Press and hold the Vt parameter button until the Vt context menu displays.
2. Release the Vt parameter button, then turn the Dial until the context menu item you want to
change highlights, then press the Accept button. The current setting for the context menu
parameter highlights.
3. Turn the Dial to change the value of the parameter.
4. Press the Accept button.
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Vt Parameter Window Reference
The following table provides the options and ranges for the Vt window parameters:
Vt Parameter Window
Primary Parameter
Vt
Options/Range
Availability/Notes
50 to 2000
Volume Target: Control Setting
ml
Secondary Parameters
Alarm Limits
Pressure Target: Measured
None
High Vt
50 to 2000, Off
Low Vt
5 to 500, Off
Limits are not present during
volume targeted ventilation
Vt Context Menu
Tubing Compliance (CT) Default: Off
OFF, Adult, Infant
Auxiliary Box
Adult
Default: 1.60
0 to 3.50
Infant
Default: 0.50
0 to 2.00
User entered values are not
retained when the ventilator is
turned OFF
Compliance Volume
(ml)
(Measured value)
0 to 349
PIP Parameter Window Options
The PIP (Peak Inspiratory Pressure) parameter window displays and/or controls airway
pressure. The breath target determines if the PIP value is a measurement or a control setting
(solid text). When PIP is a control setting, the user can adjust PIP from 10 to 80 cm H20.
Note:
When the user attempts to set a PIP value greater than 60 cm H2O (hPa), a popup
message displays prompting for a confirmation before values above 60 cm H20 (hPa)
are available.
During pressure targeted ventilation, the PIP parameter is displayed as solid text.
During volume targeted ventilation, the PIP primary parameter is a measurement and displays
as outlined text.
Positive End Expiratory Pressure (PEEP) is the baseline pressure maintained above
atmospheric pressure at the end of exhalation to prevent alveolar collapse and improve gas
exchange.
For BL mode, the ventilator provides noninvasive ventilation with the ability to manage the
patient by adjusting the IPAP and EPAP parameters. IPAP is adjustable from
6 to 60 cm H2O (hPa), EPAP is adjustable from 3 to 30 cm H2O (hPa).
Secondary Parameters and Alarm Thresholds/Limits
In pressure targeted ventilation mode, the following secondary parameters are available.
•
•
•
•
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PIP High Limit
PIP Low Limit
PEEP
PS (Available for SIMV(P), CPAP, and BL)
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For the PIP High Limit and PIP Low Limit, the user can set the PIP High Limit from 20 to 100
cm H20 (hPa). For the PIP Low Limit from 3 to 35 cm H20 (hPa), or turn the PIP Low Limit to
OFF.
Note:
Warning!
PEEP cannot be set within 5 cm H20 (hPa) of the PIP High Limit setting.
Set the PIP Low Limit to be at least PEEP +5. This reduces the likelihood of not
detecting a kinked hose. Setting the PIP Low Limit just below the PIP can also serve to
detect leaks and patient circuit as a PIP compensated disconnected threshold.
To change an a PIP secondary parameter, follow these steps:
1. Press the PIP parameter button more than once until desired alarm threshold highlights in
the PIP parameter window.
2. Turn the Dial to set a parameter value.
3. Press the Accept button.
Context Menu
The PIP context menu provides the user the ability to adjust the pressure needed to trigger a
breath minimizing the work of breathing and prevent auto-triggering in the presence of leaks
and very high motion environment.
When ventilating infants and other patients with weak inspiratory effort, the trigger threshold
may need to be adjusted. To reduce the work required for the patient to trigger a breath,
decrease the magnitude.
To prevent auto-triggering, the magnitude of the trigger pressure may need to be increased.
(This should be done with caution as it will increase the work of breathing and may lead to
asynchrony.)
The Spontaneous/Assisted Breath Trigger is preset to -2.0 cm H2O (hPa) and can be adjusted
from -6.0 to -0.5 cm H2O (hPa) below the baseline (PEEP) pressure. To initiate a spontaneous
or assisted breath, the patient must generate -2.0 cm H2O (hPa). When the pressure drop is
detected, an assisted breath is delivered. The trigger automatically adjusts when the PEEP is
changed. The set Trigger Level threshold displays on the bottom of the screen.
Warning!
Set the trigger level so as to minimize the patient's inspiratory effort and prevent
autotriggering. When ventilating infants and other patients with weak inspiratory
effort, lower the trigger threshold magnitude (> -2 cm H2O (hPa) to reduce the work
required for the patient to trigger a breath. If a large leak is present while ventilating in
CPAP or BL with LC turned on, the trigger threshold magnitude may need to be
increased to prevent auto-triggering with the variable baseline pressure.
Airway pressure measurements are also displayed. The Airway Pressure waveform
(0 to 100 cm H2O (hPa)) is plotted over time with indications of the PEEP and PIP high limit.
See Figure 4-1. The Mean Airway Pressure (MAP) measurement (0 to 99.9 cm H2O (hPa)) is
provided in the auxiliary box area of the ventilator display.
To change a the Trigger Level in the PIP context menu, follow these steps:
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1. Press and hold the PIP parameter button until the PIP context menu displays.
2. Release the PIP parameter button, then turn the Dial until the Trigger Level highlights, then
press the Accept button. The current setting for the context menu parameter highlights.
3. Turn the Dial to adjust the value of the parameter.
4. Press the Accept button.
Note:
The scale of the Airway Pressure waveform varies based on the PIP High Limit. If the
waveform is too small the PIP High limit maybe set too high.
PIP Parameter Window Reference
The following table provides the options and ranges for the PIP parameter window.
PIP Parameter Window
Primary Parameter
PIP
Options/Range
Availability/Notes
10 to 80
Volume Target:
Measurement
Pressure Target: Control
Setting
PIP values greater than
60 cm H2O (hPa) require
the user to perform a
separate confirmation.
Secondary Parameters
Alarm Limits
Measured Value
0 to 30
AC and SIMV*
3 to 30
CPAP
PS
0 to 60 cm H20
Spontaneous Breaths
(SIMV* and CPAP)
EPAP
3 to 30
IPAP
6 to 60
High PIP
20 to 100
Low PIP
3 to 35, Off
Mean Airway
Pressure
0 to 99.9
PEEP
BL
PEEP cannot be within
5 cm H2O (hPa) of the PIP
High Limit setting.
MAP
Paw Waveform
0 to 100
Default: -2
-6 to -0.5
PIP Context Menu
Breath Trigger
(Assisted, Spontaneous)
Adjustment Increments:0.5
* SIMV mode is an optional mode and might not be available on your ventilator.
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FIO2 Parameter Window Options
The FIO2 (Fraction of Inspired Oxygen) parameter window manages oxygen delivery. Pressing
the FIO2 parameter button highlights the current FIO2 value so that you can adjust it using the
Dial. The default value at start up is 21% whether oxygen is present or not.
If an FIO2 value greater than 21% is saved as a custom default or the last setting, the ventilator
begins with that saved FIO2 value if high-pressure oxygen is present. If high-pressure oxygen is
not present, the ventilator begins operation with FIO2 = 21% and the Low O2 Supply Fault
alarm is not activated to prevent a nuisance alarm.
The secondary display in the parameter window is O2 Use1. This value indicates the flow of
high pressure oxygen (l/min) consumed with the current FIO2 setting to support the patient
(from 0 to 99.9 l/minute). This value can be used to calculate the time of useful O2 flow from an
O2 cylinder: Flow time (min) = cylinder volume (l) /O2 flow (l/min). O2 Reservoir use is
indicated on the display with a plus “+” sign next to the FIO2 value. See Chapter 3 for more
information.
Note:
The “O2 Use” parameter does not calculate low flow oxygen only high pressure
oxygen use is calculated.
Secondary Parameters and Alarm Thresholds/Limits
There are no secondary parameters for the FIO2 parameter window.
Context Menu
Access the FIO2 context menu to turn the O2 Reservoir ON or OFF.
Note:
The O2 reservoir feature ON can be used for following:
When using the O2 Reservoir for low flow oxygen
• In a high vibration environment
• When using biological or chemical filters.
When the O2 reservoir feature is on 21+ displays in the FIO2 parameter window indicating that
O2 is coming from a low-pressure external source. In addition, it also disables the Gas Intake
Restricted alarm (SC: 3031) that can trigger due to the small resistance caused by the reservoir.
This feature is used to eliminate nuisance alarms caused by the restriction of the external filter
or extremely high vibration. To turn the O2 Reservoir feature ON or OFF from the FIO2 context
menu, follow these steps:
•
1. Press and hold the FIO2 parameter button until the FIO2 context menu displays.
2. Release the FIO2 parameter button, then turn the Dial until O2 Reservoir highlights, then
press the Accept button. The current setting for the O2 Reservoir parameter highlights.
3. Turn the Dial to change the setting to ON or OFF.
4. Press the Accept button.
1. O2 Use = ((FIO2-0.21)/0.79)*Minute Volume where FIO2 is represented as a fraction and minute
volume is the actual minute volume (controlled and spontaneous breaths * tidal volume).
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FIO2 Parameter Window Reference
The following table lists the options and ranges for the FIO2 parameter window:
FIO2 Parameter Window
Primary Parameter
Options/Range Availability/Notes
21 to 100
FIO2
%
Primary Parameter
FiO2 +
21
Demonstrates O2 reservoir
mode is in use.
Secondary Parameters
None
Alarm Limits
None
Measured Value
O2 Use (L/min)
0 to 99.9
Shows when High Pressure
Oxygen Supply is present and
the consumption of flow.
Default: OFF
OFF/ON
“+” icon indicates when “ON” for
low pressure O2
FIO2 Context Menu
O2 Reservoir
SpO2 Parameter Window Options
The SpO2 parameter window controls the Masimo Pulse Oximeter used in the ventilator. The
SpO2 measurement (0 to 100%) is shown in the parameter window and the Pleth waveform is
plotted when the sensor is used. The parameter window displays a “--”.
Note: The pulse oximeter operates only when the ventilator is providing ventilation.
The following conditions can affect the pulse oximeter reading:
• The sensor is too tight.
• There is excessive illumination from light sources such as a surgical lamp, a bilirubin lamp,
or sunlight.
• A blood pressure cuff is inflated on the same extremity as the one with a SpO2 sensor
attached.
Poor perfusion
The patient has hypotension, severe vasoconstriction, severe anemia, or hypothermia.
There is an arterial occlusion proximal to the sensor.
The patient is in cardiac arrest or is in shock.
Patient movement
Nail polish or finger pigment
Carbon monoxide poisoning
The SpO2 display is active only when the pulse oximeter is connected. The pulse oximeter is in
standby (and displays STBY in the parameter window) when:
•
•
•
•
•
•
•
• No SpO2 sensor is connected
• The sensor is off the patient during start up
• You place the pulse oximeter in standby
Note:
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You can place the pulse oximeter in standby only when the probe is disconnected from
the patient. A valid signal automatically brings the pulse oximeter out of standby.
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Secondary Parameters and Alarm Thresholds/Limits
Pressing the SpO2 parameter button highlights the SpO2 Low Limit secondary parameter and
enables its setting to be changed. The SpO2 Low Limit is the only secondary parameter for the
SpO2 parameter. The default SpO2 Low Limit setting at start up is 94%.
The SpO2Low Limit is adjustable from 86% to 99% or can be set to OFF.
To change an SpO2 Low Limit secondary parameter setting, follow these steps:
1. Press the SpO2 parameter button until the SpO2 Low Limit highlights.
2. Turn the Dial to adjust the setting (%).
3. Press the Accept button.
Context Menu
The Masimo context menu is the same for both the SpO2 and HR parameter windows.The
menu provides for the following pulse oximeter controls:
Standby
Pulse Ox
Fast SAT
Sensitivity
APOD
Averaging
Signal Strength
Signal IQ
The menu allows for the Pulse Oximeter monitoring to be placed in standby. It also provides
options to turn on the fast SAT, adjust Sensitivity, and other Masimo specific parameters, see
the table below for additional details.
•
•
•
•
•
•
•
•
To change a menu setting, follow these steps:
1. Press and hold the SpO2 parameter button until the Context menu displays, then release the
button.
2. Turn the Dial until the Context menu item you want to change highlights, then press the
Accept button. The current setting for the selected item highlights.
3. Turn the Dial to adjust the value of the parameter.
4. Press the Accept button.
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SpO2 Parameter Window Reference
The following table provides the options and ranges for the SpO2 Masimo context menu.
SpO2 Parameter Window
Primary Parameter
Options/Range Availability/Notes
0 to 100
SpO2
Measurement only
%
Secondary Parameters
None
Alarm Limits
SpO2 Low Limit
Measured Value
Pleth Waveform
86 to 99, Off
Default: 94%
Masimo Context Menu
4-24
Pulse Ox
Default: Standby
Standby, Off,
On
Fast SAT
Default: Off
Off, On
Fast SAT enables rapid tracking
of arterial oxygen saturation
changes by minimizing the
averaging. This mode is
clinically applicable during
procedures when detecting
rapid changes in SpO2 is
paramount such as induction,
intubation, and sleep studies.
Sensitivity
Norm
Max, Norm
Norm adjusts the pleth signal
sensitivity. Max interprets and
displays data for even the
weakest of signals. Max is
recommended during
procedures and when clinician
and patient contact is
continuous.
APOD
Off
Off, On
When on, this mode improves
detection of the “probe off
patient” condition, but reduces
the ability to acquire a reading
on patients of low perfusion.
Averaging
8 Seconds
2 to 4, 4 to 6, 8,
10, 12, 16
Seconds
Adjusts the SpO2 and HR
averaging durations.
Signal Strength
Measured Value
0 to 20
Current signal strength value,
not adjustable. A value of zero
indicates that no measurement
is available. This value helps
clinicians place sensors on the
optimal site.
Signal IQ
Measured Value
Bar Graph
Bar graph displays the relative
reliability of the pulse oximeter
signal.
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HR (Heart Rate)
The HR parameter window displays the patient’s heart rate when the pulse oximeter is working
and the sensor is attached. The HR measurement (0 to 240 beats per minute) is shown in the
parameter window and the Pleth waveform is plotted when the pulse oximeter is used. During
monitoring “--” displays when the sensor does not detect a measurement. The heart icon blinks
at the pulse rate.
Secondary Parameters and Alarm Thresholds/Limits
The secondary parameters for the HR parameter window are the following:
• HR High Limit (adjustable from 80 to 240 beats per minute (or OFF)
• HR Low Limit (adjustable from 30 to 79 beats per minute (or OFF)
To change an alarm threshold setting, follow these steps:
1. Press the HR parameter button more than once until desired limit setting highlights.
2. Turn the Dial to adjust the value of the parameter.
3. Press the Accept button.
Context Menu
The menu supports both HR and SpO2 parameter windows. The menu provides for the
following pulse oximeter controls:
Standby
Pulse Ox
Fast SAT
Sensitivity
APOD
Averaging
Signal Strength
Signal IQ
The menu allows for the Pulse Oximeter monitoring to be placed in standby. It also provides
options to turn on the fast SAT, adjust Sensitivity, and other Masimo specific parameters, see
table below for additional details.
•
•
•
•
•
•
•
•
To change a menu setting, follow these steps:
1. Press and hold the HR parameter button until the menu displays.
2. Release the HR parameter button, turn the Dial until the Context menu item you want to
change highlights, then press the Accept button. The current setting for the context menu
parameter highlights.
3. Turn the Dial to change the setting to the desired value.
4. Press the Accept button.
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HR Parameter Window Reference
The following table gives the options and ranges for the HR parameter:
HR Parameter Window
Options/Range Availability/Notes
Primary Parameter
HR
b/min
Secondary Parameters
None
0 to 255
Measurement - Heart icon
blinks at the pulse rate
HR High Limit
80 to 240, OFF
HR Low Limit
30 to 79, OFF
Pulse Ox
Default: Standby
Standby, Off,
On
Fast SAT
Default: Off
Off, On
Fast SAT enables rapid tracking
of arterial oxygen saturation
changes by minimizing the
averaging. This mode is
clinically applicable during
procedures when detecting
rapid changes in SpO2 is
paramount such as induction,
intubation, and sleep studies.
Sensitivity
Norm
Max, Norm
Norm adjusts the pleth signal
sensitivity. Max interprets and
displays data for even the
weakest of signals. Max is
recommended during
procedures and when clinician
and patient contact is
continuous.
APOD
Off
Off, On
When on, this mode improves
detection of the “probe off
patient” condition, but reduces
the ability to acquire a reading
on patients of low perfusion.
Averaging
8 Seconds
2 to 4, 4 to 6, 8,
10, 12, 16
Seconds
Adjusts the SpO2 and HR
averaging durations.
Signal Strength
Measured Value
0 to 20
Current signal strength value,
not adjustable. A value of zero
indicates that no measurement
is available. This value helps
clinicians place sensors on
optimal sites
Signal IQ
Measured Value
Bar Graph
Bar graph displays the relative
reliability of the pulse oximeter
signal.
Alarm Limits
Masimo Context Menu
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Manual Breath
The Manual Breath button enables the user to deliver a manual breath to a patient when pressed
during the expiratory phase and then only after the airway pressure drops to the PEEP target.
The effect of the manual breath button depends on the ventilation mode set on the ventilator.
• In AC and SIMV*, a button press will deliver a mandatory breath defined by the settings.
• In CPAP and BL, it delivers a mandatory breath based on the Apnea Backup settings.
Figure 4-3 shows the Manual Breath Button on the EMV+ ventilator.
Note:
Note:
If the ventilator supports the Plateau Pressure option, the button is labeled “Manual
Breath/ P Plat”.
SIMV mode is an optional mode and might not be available on your ventilator.
Plateau Pressure
Plateau pressure (P Plat) is the pressure applied to small airways and alveoli. It is measured
during an inspiratory pause on the ventilator. Current clinical practice seeks to maintain the
plateau pressure < 28-30 cm H2O (hPa) to prevent excessive pressure in the lung.
Note:
Plateau Pressure is an optional feature on the ventilator. If the ventilator supports the
Plateau Pressure option, the Manual Breath button is labeled “Manual Breath/ P Plat”
(see Figure 4-3).When Plateau Pressure is available on the EMV+ ventilator, the
Manual Breath button performs two functions:
• Allow the user to deliver a manual breath
• Enables the user to perform a plateau pressure maneuver.
Plateau Pressure Maneuver
To perform a P Plat maneuver, press and hold the Manual Breath button during the inspiratory
period. The maneuver is used during volume targeted breath. During pressure targeted
breathing the PIP typically represents to alveolar pressure as flow decelerates to 0 l/min at the
end of inspiration.
Holding the button past the end of inspiration during a mandatory breath causes the ventilator
to delay opening the exhalation valve for as long as the button is held (up to 3 seconds).
During this period the ventilator measures the pressure while there is no gas flow. At the end of
the period the exhalation valve opens and the device continues normal operation while the P
plat is displayed for ~20s
The activation of a new alarm or pressing the Mute/Cancel button also clears the Plateau
Pressure measurement.
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Manual Breath Button
Note: If the ventilator supports
Plateau Pressure the button is
labeled Manual Breath/P Plat
Figure 4-3 Manual Breath/Pressure Plateau Button
Popup Messages
To prevent the setting of parameter values that are outside the typical clinical range of settings,
the ventilator presents popup messages that ask if you are sure you would like to set the
parameter beyond the typical range. A sample popup message is shown in Figure 4-4.
When a message occurs, you are asked to press the Accept button before you can adjust a
parameter beyond the typical range. Popup messages are also used to alert you that certain
settings are not permitted or possible based on the current parameter settings. In addition,
popup messages can call for you to press the Accept button to acknowledge that you are
entering configurations where certain alarms are being suppressed, turned “off”, and/or
canceled.
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Popup
Message
Figure 4-4 Popup Message Example
In addition to addressing setting conflicts, popup messages are used for confirmation (for
example, alarms). These messages also appear whenever you attempt to adjust the ventilator in
a way that is outside clinical norms or is outside its performance range.
Popup messages also appear when you are required to confirm their action before you proceed.
For example, setting the BPM Low Limit setting below 4 would allow for 15 second apnea
periods and would, in essence, disable the alarm for some patients. If the desired value is
outside the performance range, the popup message alerts you to why you cannot make the
change. (Example: trying to set the PEEP level greater than the PIP setting).
A list of all popup messages follows.
Popup Message List
Popup/Information/Message
Requested Compressor Flow Too Low
Popup message triggers when the rate/tidal volume/FIO2 combination requires a flow that is less
than the flow capability of the compressor. Resolution involves changing a setting to increase the
flow required from the compressor if possible. Note: this condition is only possible with infant setting
and for FIO2 < 25% at very low tidal volume with long inspiratory time.
Message: Reduce FiO2 , increase BPM, reduce I Time, or increase Vt
Requested Compressor Flow Too High
Popup message triggers when the user attempts to adjust the ventilator so that flow from the
compressor is > 100 l/min.
Message: Cannot exceed 100 LPM total flow
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Popup/Information/Message
Requested O2 Flow Too Low
Popup message triggers when the rate/tidal volume/FIO2 combination requires a flow that is less
than the flow capability of the O2 valve. Resolution involves changing a setting to increase the flow
required from the O2 valve if possible.
Note: This condition is only possible with infant setting and for FIO2 < 25%.
Message: Increase FiO2 , increase BPM, reduce I Time, or increase Vt
Requested O2 Flow Too High
Popup message triggers when the user attempts to adjust the ventilator so that flow from the O2
valve
is > 100 l/min.
Message: Cannot exceed 100 LPM total flow
Total Requested Flow Too High
Popup message triggers when the user attempts to adjust the ventilator so that the combined flow
from the compressor and O2 valve is > 100 l/min.
Message: Cannot exceed 100 LPM total flow
Total Requested Flow Too Low
Popup message triggers when the user attempts to adjust the ventilator so that combined flow from
the compressor and O2 valve is < 2 l/min.
Message: Cannot flow less than 2 LPM total flow
Alarm Disable
Popup message triggers when the user attempts to adjust to disable an alarm by setting the value
to 0 or the maximum value which would render the alarm essentially off.
Message: Confirmation required -- press accept key to disable alarm
BPM Setting Conflict
Popup message triggers when the user attempts to set the BPM to a value that would result in an
inspiratory time (I Time) > 3 seconds.
Message: I Time cannot exceed 3 seconds
BPM Setting Conflict
Popup message triggers when the user attempts to set the BPM to a value that would result in an
inspiratory time (I Time) > 5 seconds during inverse I:E ratio ventilation.
Message: I Time cannot exceed 5 seconds with inverse I:E
E Time Range Exception
Popup message triggers when the user attempts to set the BPM to a value that would result in an
expiratory time (E Time) < 0.3 seconds.
Message: E Time must be greater than 0.3 seconds
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Popup/Information/Message
I:E Setting Conflict
Popup message triggers when the user attempts to transition from AC mode using an inverse I:E
ratio to another mode where inverse I:E is not allowed.
Message: Inverse I:E only allowed in AC - Mode change will reset I:E to 1:3
I:E Setting Conflict
Popup message triggers when the user attempts to set an inverse I:E ratio in an mode other than
Assist/Control (AC).
Message: Inverse I:E Not Allowed
BPM Setting Conflict
Popup message triggers when the user attempts to set a BPM rate that will result in an I:E ratio >
1:99.
Message: I:E > 1:99 not allowed
I Time Range Exception
Popup message triggers when the user attempts to set inspiratory time (I Time) > 3 seconds during
standard I:E ratio ventilation
Message: I Time cannot exceed 3 seconds
I Time Range Exception
Popup message triggers when the user attempts to SET inspiratory time (I Time) > 5 seconds
during inverse I:E ratio ventilation.
Message: I Time cannot exceed 5 seconds with inverse I:E
I Time Range Exception
Popup message triggers when the user attempts to set an inspiratory time (I Time) < 0.1 seconds.
Message: I Time must be greater than 0.1 seconds
I:E Range Exception
Popup message triggers when the user attempts to set an inverse I:E ratio < 4:1.
Message: I:E < 4:1 not allowed
I:E Range Exception
Popup message triggers when the user attempts to set an I:E ratio > 1:99.
Message: I:E > 1:99 not allowed
Vt Limit Conflict
Popup message triggers when the user attempts to set Vt lower than the Vt Low Limit secondary
parameter setting.
Message: Cannot adjust Vt Set below Vt Low Alarm
Vt Limit Conflict
Popup message triggers when the user attempts to set the Vt higher than the Vt High
Limit.secondary parameter setting.
Message: Cannot adjust Vt Set above Vt High Limit
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Popup/Information/Message
High Vt Setting
Popup message triggers when the user attempts to set Vt > 1000 ml. To do this, the user must
press the Accept button and then continue to set a value > 1000 ml followed by Accept again to
confirm the setting change.
Message: Confirmation required -- press accept key to allow Vt > 1000ml
PEEP Setting Conflict
Popup message triggers when the user attempts to set the PEEP setting ≤ 5 cm H2O (hPa) below
the PIP High pressure limit.
Message: Cannot adjust PEEP target to within 5 of PIP High Limits
PEEP Setting Conflict
Popup message triggers when the user attempts to configure the ventilator so that the PEEP plus
the pressure support (PS) are > the PIP High pressure limit.
Message: PEEP + PS cannot be greater than PIP High Limit
PEEP Backup Setting Conflict
Popup message triggers when the user attempts to set the PEEP setting ≤ 5 cm H2O (hPa) below
the Apnea Backup PIP pressure during CPAP or BL mode ventilation.
Message: Cannot adjust PEEP target to within 5 of backup PIP target
PEEP Setting Conflict
Popup message triggers when the user attempts to set the PEEP ≤ 5 cm H2O (hPa) below PIP
pressure.
Message: Cannot adjust PEEP target to within 5 of PIP target
PEEP+PS Setting Conflict
Popup message triggers when the user attempts to set a combination of PEEP and PS that is
< 3 cm H2O (hPa).
Message: Cannot adjust PEEP+PS below 3
High Pressure Target Setting
Popup message triggers when the user attempts to set the PIP pressure > 60 cm H2O (hPa) . To do
this, the user must press the Accept button and then continue to set a value > 60 cm H2O (hPa)
followed by Accept again to confirm the setting change.
Message: Confirmation required -- press accept key to exceed 60 cm H2O (hPa)
PIP Setting Conflict
Popup message triggers when the user attempts to set the PIP target ≤ 5 of PEEP pressure.
Message: Cannot adjust PIP target to less than 5 more than PEEP
PIP Setting Conflict
Popup message triggers when the user attempts to set the PIP > the PIP High pressure limit.
Message: Cannot adjust PIP target higher than PIP High Limit
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Popup/Information/Message
BPM Limit Conflict
Popup message triggers when the user attempts to set the BPM High Limit < the BPM Low Limit.
Message: Cannot adjust high limit lower than low limit
Low Breath Rate Setting
Popup message triggers when the user attempts to set the BPM < 6 bpm. Doing this could, in
effect, disable the alarm for some patients. To do this, the user must press the Accept button and
then continue to set a value < 6 bpm followed by Accept again to confirm the setting change.
Message: Confirmation required -- press accept key for values below 6 BPM
BPM Limit Conflict
Popup message triggers when the user attempts to set the BPM Low Limit > the BPM High limit.
Message: Cannot adjust low limit higher than high limit
Vt Limit Conflict
Popup message triggers when the user attempts to set the Vt High Limit < the Vt Low Limit.
Message: Cannot adjust high limit lower than low limit
Vt Limit Backup Setting Conflict
Popup message triggers during CPAP or BL mode when the user attempts to set the Vt High Limit <
the Vt setting in the Apnea Backup settings.
Message: Cannot adjust high limit lower than Backup Vt Setting
Vt Limit Conflict
Popup message triggers when the user attempts to set the Vt High Limit < the Vt setting.
Message: Cannot adjust high limit lower than Vt Setting
High Vt Limit Setting
Popup message triggers when the user attempts to set the Vt limit > 1500 ml. Doing this could, in
effect, disable the alarm for some patients. To do this, the user must press the Accept button and
then continue to set a value > 1500 ml followed by Accept again to confirm the setting change.
Message: Confirmation required -- press accept key for values above 1500ml
Vt Limit Conflict
Popup message triggers when the user attempts to set the Vt Low Limit > Vt High Limit.
Message: Cannot adjust low limit higher than high limit
Vt Limit Conflict
Popup message triggers during SIMV (V) when the user attempts to set the Vt Low Limit > the
current Vt.
Message: Cannot adjust low limit higher than Vt Setting
Vt Limit Backup Setting Conflict
Popup message triggers during CPAP or BL mode when the user attempts to set the Vt Low Limit >
the Vt setting in the Apnea Backup settings.
Message: Cannot adjust low limit higher than Backup Vt Setting.
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Popup/Information/Message
High Pressure Limit Setting
Popup message triggers when the user attempts to set the PIP > 60 cm H2O (hPa). To do this, the
user must press the Accept button and then continue to set a PIP > 60 cm H2O (hPa) followed by
Accept again to confirm the setting change.
Message: Confirmation required -- press accept key to exceed 60 cm H2O (hPa)
PIP Limit Conflict
Popup message triggers when the user attempts to set the PIP High Limit < the PIP Low Limit.
Message: Cannot adjust high limit lower than low limit
PIP Limit Backup Setting Conflict
Popup message triggers during CPAP or BL mode when the user attempts to set the PIP High Limit
< Apnea Backup PIP limit.
Message: Cannot adjust high limit lower than backup PIP target
PIP Limit Conflict
Popup message triggers when the user attempts to set the PIP High Limit < the PIP Low Limit.
Message: Cannot adjust high limit lower than PIP target
PIP Limit Conflict
Popup message triggers when the user attempts to set the PIP High Limit < the combination of PS
and PEEP pressures.
Message: Cannot adjust high limit lower than PS + PEEP
PIP Limit Conflict
Popup message triggers when the user attempts to set the PIP Low Limit > the PIP High Limit.
Message: Cannot adjust low limit higher than high limit
Heart Rate Limit Conflict
Popup message triggers when the user attempts to set the HR High Limit < the HR Low Limit.
Message: Cannot adjust high limit lower than low limit
Heart Rate Limit Conflict
Popup message triggers when the user attempts to set the HR Low Limit > the HR High Limit.
Message: Cannot adjust low limit higher than high limit
PS Conflict
Popup message triggers when the user attempts to set the PS > the PIP High Limit - PEEP
pressure.
Message: Cannot adjust PS higher than PIP High Limit - PEEP
Leak Comp.
Popup message triggers when the user attempts to initiate leak compensation (LC). To do this, the
user must press the Accept button and then select LC followed by Accept again to confirm the
setting change.
Message: Some Alarms Disabled! Configure Alarms for Patient!
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Popup/Information/Message
Mode Conflict
Popup message triggers when the user attempts to initiate leak compensation (LC) during volume
targeted ventilation. Note: LC is only available during pressure targeted ventilation.
Message: Cannot select Volume targeted control breaths with Leak Compensation on -- first turn
Leak Compensation off
Inverse I:E
Popup message triggers when the user attempts to set an inverse I:E ratio. To do this, the user
must press the Accept button and then adjust the I:E ratio to the desired inverse value and press
Accept again to confirm the setting change.
Message: Confirmation required -- press accept key to allow inverse I:E
Excessive Volume for Infant Circuit
Popup message triggers when the user attempts to set a Vt > 300 ml when the tubing compliance
compensation is set to Pediatric.
Message: Press accept to confirm use of adult circuit
Insufficient Volume for Adult/Ped Circuit
Popup message triggers when the user attempts to set a Vt < 200 ml when the tubing compliance
compensation is set to Adult.
Message: Press accept to confirm use of infant circuit
High PEEP Setting
Popup message triggers during CPAP mode when the user attempts to set the PEEP > 15 cm H2O
(hPa) To do this, the user must press the Accept button and then adjust PEEP to the desired value
and press Accept again to confirm the setting change.
Message: Confirmation required -- press accept key to allow PEEP above 15
High EPAP Setting
Popup message triggers during BL mode when the user attempts to set the EPAP > 15 cm H2O
(hPa). To do this, the user must press the Accept button and then adjust PEEP to the desired value
and press Accept again to confirm the setting change.
Message: Confirmation required -- press accept key to allow EPAP above 15
EPAP Setting Conflict
Popup message triggers during BL mode when the user attempts to set the EPAP < 3 cm H2O
(hPa) below the IPAP target.
Message: Cannot adjust EPAP target to within 3 of IPAP target
EPAP Setting Conflict
Popup message triggers during BL mode when the user attempts to set the EPAP < 5 cm H2O
(hPa) below the Apnea Backup PIP target.
Message: Cannot adjust EPAP target to within 5 of backup PIP
PIP Limit Conflict
Popup message triggers during BL mode when the user attempts to set the PIP Limit) < the IPAP
target.
Message: Cannot adjust high limit lower than IPAP target
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Popup/Information/Message
IPAP Setting Conflict
Popup message triggers during BL mode when the user attempts to set the IPAP < 3 cm H2O
(hPa) above the EPAP setting.
Message: Cannot adjust IPAP target to less than 3 more than EPAP
IPAP Setting Conflict
Popup message triggers during BL mode when the user attempts to set the IPAP < the PIP limit.
Message: Cannot adjust IPAP target higher than PIP High Limit
High IPAP Setting
Popup message triggers during BL mode when the user attempts to set the IPAP > 30 cm H2O
(hPa).To do this, the user must press the Accept button and then adjust IPAP to the desired value
and press Accept again to confirm the setting change.
Message: Confirmation required -- press accept key to allow IPAP above 30 cm H2O (hPa)
High PEEP+PS Setting
Popup message triggers in CPAP mode when the user attempts to set the combination of PEEP +
PS < 30 cm H2O. To do this, the user must press the Accept button and then adjust PEEP or PS to
the desired value and press Accept again to confirm the setting change.
Message: Confirmation required -- press accept key to allow PEEP+PS above 30 cm H2O (hPa)
High Pressure Limit Setting
Popup message triggers when the Start Menu is active and the user selects either the Custom or
Last Setting options and the PIP High Limit is >35 cm H2O. When the user selects one of the
options where this is true, the popup message is triggered requiring the user to provide additional
conformation, pressing Accept, to initiate ventilation with the option.
Message: Confirmation required -- press accept key to recall limit setting above 35 cm H2O (hPa)
Transitions
Transitioning between modes or between volume and pressure targeting the device may adjust
or set any of the following parameters:
BPM, BPM High Limit, BPM Low Limit
VT, VT High Limit, VT Low Limit
PIP, PIP High Limit, PIP Low Limit
PEEP
PS / IPAP
I:E Ratio / Ti
Rise Time
LC
These parameters are adjusted or populated to safely transition the settings that were not
available in the previous mode. After changing the mode or ventilation target, the parameters
and alarm limits should be adjusted to be appropriate for the patient being ventilated. It is
recommended to adjust the parameters and alarm limits by window moving in order up the
device from the Mode parameter window.
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•
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•
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•
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Warning!
The alarm limits must be appropriate for the patient being ventilated. If a parameter is
changed, adjust the high and low alarm limit to bracket selected value.
Warning!
The transition into CPAP or BL automatically adjusts the rise time and always needs to
be checked since the setting might need further adjustment. Before using the ventilator
with an infant or small child, you should always configure the ventilator appropriately
before attaching the patient and monitor the patient to ensure optimal support.
Using the Menu
The Menu button displays the Menu, which allows you to change various ventilator options,
such as the contrast or brightness of the Display Screen (LCD Contrast/LCD Brightness).
When you press the Menu button, the Menu appears:
•
•
•
•
•
•
•
Alarm Config
Powerup Settings
LCD Contrast
LCD Brightness
UTC Offset
Unit Info
Alarm History
Alarm Configuration
Selecting Alarm Configuration allows the user to enable or disable the audible and visible alerts
associated with specific alarms to prevent nuisance alarms.
Refer to, “Managing Alarms” in Chapter 5.
Powerup
You can configure how the ventilator starts (powers up) based on your use or patient
population. The Powerup settings include:
Powerup Setting
(Option)
Setting Choices
Powerup
Adult, Pediatric, or Start Menu
Custom Settings
Saves the currently set operating parameters
Language
English, Language Option
In addition to controlling how the ventilator starts up, the Powerup settings sub-menu also
allows the user to save the current ventilator configuration for use as the Custom starting
configuration and which language will be used when the ventilator is turned ON.
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Specifying Powerup Settings
To configure new Powerup settings, follow these steps:
1. Press the Menu button to display the menu, then turn the Dial to highlight the Powerup
settings.
2. Press the Accept button. The following list of configurable items with
Powerup highlighted displays.
• Powerup
• Custom Settings
• Language
3. Press the Accept button, then turn the Dial to the desired starting configuration.
• Adult Settings
• Pediatric Settings
• Start Menu
4. Press the Accept button to confirm the new starting configuration.
5. Press the Mute/Cancel button to return to the Menu.
6. Press the Mute/Cancel button again to return to the configured Powerup setting (Start menu,
Adult, or Pediatric).
Specifying Custom Settings
To save the current configuration parameter settings (if different than Adult or Pediatric default
parameter settings) for use at start up, follow these steps:
1. Press the Menu button, then turn the Dial to Powerup Settings, then press the Accept
button.
2. Turn the Dial to highlight the Custom Settings choice, and then press the Accept button
(Save becomes highlighted).
3. Press the Accept button again to save the current parameter settings.
4. Press the Mute/Cancel button to return to the menu.
5. Press the Mute/Cancel button again to return to the configured Powerup setting (Start Menu,
Adult, or Pediatric).
Specifying a Language
The ventilator is provided with the English language and a local language. (This feature is
limited to ventilators with multiple languages.).
LCD Contrast
The LCD Contrast submenu allows the user to adjust the contrast of the ventilator display
screen to optimize visibility in the current lighting environment. Given the use environment, the
ventilator automatically compensates for the temperature changes that can effect LCD performance.
However, in temperatures outside its performance specification of- 26 to 55 °C, or when the ventilator
temperature is rapidly changing (warm storage into a very cold environment) the contrast can fade making
viewing difficult.
To adjust the LCD screen contrast, follow these steps:
1. Press the Menu button to display the Menu.
2. Turn the Dial to highlight LCD Contrast, and then press the Accept button.
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3. Turn the Dial clockwise to increase contrast (counterclockwise to decrease it) while watching
the LCD screen to determine the best contrast value based on visibility, then press the Accept
button to set the new contrast value.
4. Press the Mute/Cancel button to return to the Menu.
Note:
The contrast value is saved between uses. This may require adjusting the contrast value
when the temperature is within the ventilator’s operating range or with the next use.
In the event the LCD is not viewable due to extreme temperature conditions there is a
short cut to the contrast control. Press and hold the Menu button for 2 to 3 seconds.
Doing this, jumps the menu highlight directly to the contrast control where the contrast
can be adjust as described above.
LCD Brightness
The LCD Brightness control allows the user to adjust the brightness of the LCD display screen
and LED Array to optimize visibility in the current lighting environment.
The initial numerical value is 25. The brightness ranges from 0 to 32.
To adjust the brightness, follow these steps:
1. Press the Menu button to display the menu.
2. Turn the Dial to highlight LCD Brightness, and then press the Accept button.
3. Turn the Dial clockwise to increase brightness (counterclockwise to decrease it) while
watching the LCD screen and LED Array to determine the best brightness value based on
visibility, then press the Accept button to set the new brightness value.
4. Press the Mute/Cancel button to return to the Menu.
UTC Offset
The UTC Offset control allows the user to set the ventilator clock to match the local time zone
relative to Coordinated Universal Time (UTC). Matching the local time zone through the
UTC Offset setting allows an accurate time record of events recorded in the alarm log.
Before setting the UTC Offset, the user must know the UTC Offset value for your timezone.
When determining the UTC Offset value, remember to consider variances for Daylight Saving
Time (DST).
Once set, the setting is retained until:
• You change the setting (required for daylight savings time)
• The ventilator is serviced.
To adjust the UTC Offset, follow these steps:
1. Press the Menu button to display the Menu.
2. Turn the Dial to highlight UTC Offset, and then press the Accept button.
3. Turn the Dial clockwise or counterclockwise to find the offset value for your timezone, then
press the Accept button to set the new contrast value.
4. Press the Mute/Cancel button to return to the Menu.
Note:
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The UTC offset changes the time (min/max of 12 hrs). This offset is only applied to the
time, not to the date stored in the device.
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Chapter 4 Using the Ventilator
Unit Info
The Unit Info choice allows the user to view the following information about the ventilator as
follows:
Item
Description
Use Statistics
Provides access to ventilator usage in hours and minutes.
Date
The current calendar date
Cal Date
Last date the calibration was checked
PM Cycle
Annual
SPM SW Rev
Software revision of the Smart Pneumatic Module
SPM SN
Serial number of the Smart Pneumatic Module
SPM Model
Smart Pneumatic Module model
EMV Soft Rev
Software revision of the ventilator model
Device SN
Serial number of the ventilator model
Device Model
Ventilator model
To view unit information for the ventilator, follow these steps:
1. Press the Menu button to display the Menu.
2. Turn the Dial to highlight Unit Info, and then press the Accept button. The list of
information displays with Use Statistics highlighted.
3. Press the Accept button to display ventilator usage in hours and minutes (hh:mm)
4. Press the Mute/Cancel button to return to the Menu.
Alarm History
The Alarm History provides a list of the alarm messages generated by the ventilator during use.
The history holds a maximum of 256 events.
Note: Power cycling does not clear the alarm history.
Each list entry provides the following information
•
•
•
•
•
•
4-40
The Alarm Name
The Service Code
The calendar date when the event was entered
Whether the alarm is set or cleared
The time (24hr) when the event was entered
The log entry number <NNN> The higher the number the more recent the alarm message
event was logged
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To display the Alarm History, follow these steps:
1. Press the Menu button to display the Menu.
2. Turn the Dial to highlight Alarm History, and then press the Accept button. The most recent
history entry displays.
3. Turn the Dial counterclockwise to view earlier entries. Turn the Dial clockwise to view more
recent entries.
4. Press the Mute/Cancel button to return to the Menu.
5. Press the Mute/Cancel button again to return to the user interface.
The alarm condition is not logged when alarm is active but not displayed (due to other higher
priority alarm indication as explained in the Alarms Chapter of this manual), or if the alarm is
disabled in the alarm configuration the condition is not logged.
The "Complete Power Failure" alarm occurs when no power is provided to the ventilator
(See Chapter 5). This alarm is not triggered by software and is not recorded in the alarm log.
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Chapter 5
Alarms
This chapter provides a detailed description and comprehensive reference for ZOLL
ventilator’s alarms. This chapter addresses the following:
• Describes alarm types and priorities
• Provides a comprehensive list of alarms
Alarm Overview
To safeguard the patient, the ventilator continuously monitors the patient, device, and
environment to ensure that all the systems are functioning as intended. When device detects a
problem, it triggers an alarm to alert the user and displays a Smart Help message to assist the
user in resolving the alarm. Smart Help presents a multi-line message in the upper left-hand
corner of the display screen.
This screen area is the Alarm Message Center (AMC) and the following information displays in
it.
• The alarm name
• SmartHelp information which is a series of instructions to help you resolve the alarm.
The ventilator prioritizes alarms based on the risk to the patient and always presents the alarm
with the greatest risk to the patient first. All SmartHelp messages are context-based and suggest
what is causing the alarm, as well as show how it can be resolved.
The Alarm Message Center (AMC) contains the information and instructions for all active
alarms, as shown in Figure 5-1.
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Chapter 5 Alarms
A
B
C
D
E
F
Figure 5-1 Smart Help Alarm Display
A. Alarm Name: describes the type or cause of the alarm. When more than one alarm occurs at
the same time, the device prioritizes the alarms based on the highest risk to the patient.
B. Mitigation/Resolution: prioritized instructions that give more information about the nature
of the alarm and describe how to resolve the alarm state.
C. If Not Resolved Instructions: instructions for what to do you cannot resolve the alarm
state. The instruction is always shown in the following format **Message...**.
D. Alarm Icons: for each active alarm, an alarm bell appears. When multiple alarms are active,
the number of bells corresponds to the number of alarms. The alarm in the AMC is
displayed as the solid bell. To view each active alarm, turn the Dial to scroll through all
active alarms. The plot icon is also in this list. It allows you to see the current waveform to
better assess the nature of the failure. A maximum of five alarms can be displayed without
the plot icon.
E. Service Code (SC): each alarm has a 4 digit number associated with it, which helps the user
indicate the specific alarm when communicating with technical support. Service Codes
appear in the following format:
1###
High Priority Alarm
2###
Medium Priority Alarm
3###
Low Priority Alarm
F. Attention Warning Icon: identifies the severity of the alarm: Low, Medium, or High
priority. See the Symbols table in Chapter 1 for the appearance of the warning triangle for
each of these three alarms.
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Chapter 5 Alarms
Muting Alarms
During device operation, the mute behavior depends on the alarm priority (see section below).
There are other mute behaviors used by the alarm system. See “Managing Alarms” for
Preemptive Mute and Startup Mute descriptions.
Warning!
Use in High Noise Environments — in high noise environments, you may be inclined not
to mute the alarm while addressing the problem. Not pressing Mute limits the user's
ability to resolve the alarm because with each breath the alarm is re-triggered and any
parameter changes you are attempting are canceled as the alarm re-triggers.
Alarm Priorities
Alarm priorities define the operational status of the device and its ability to provide mechanical
ventilation. The alarm priorities are as follows:
High Priority
Mechanical ventilation under user control is no longer possible. This alarm priority requires
immediate intervention indicated by fast red blinking alarm LED and audio signal. This
includes system failure alarms where the CPU has failed and a backup has taken over to sound
the audible and visual alarms. It can also occur when the device is turned on and there is no
internal or external power source.
Pressing the Mute/Cancel button has no effect on a high priority alarm. The alarm can only be
silenced by turning off the ventilator. Some alarms can be resolved by turning the ventilator off,
then on again.
Medium Priority
Mechanical ventilation is active or is possible (maybe for a finite period of time) but, there is a
failure or fault with the patient, ventilator circuit, a pneumatic subsystem, or pulse oximeter.
This alarm priority requires immediate intervention by the user indicated by a slow red blinking
alarm LED and audio signal.
Pressing the Mute/Cancel button mutes medium priority alarms for 30 seconds. If the alarm
trigger still exists after 30 seconds, the audible alarm recurs until you mute it again for another
30 second period or the alarm is resolved.
Low Priority (Advisory)
Safe mechanical ventilation is active but, there is a fault that you must be aware of to ensure
safe management of the patient or ventilator. Low priority alarms present with both an audible
and yellow alarm LED signal (slow blink) alerting you to the condition.
Pressing the Mute/Cancel button cancels the audible signal. If the alarm is not resolved, the
yellow LED remains illuminated to remind you of the fault or failure.
Note:
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Some Low Priority alarms are canceled and the Alarm LED turns green when you
push the Mute/Cancel button. For others, the audible alarm is canceled but the Alarm
LED stays yellow to remind you that the device is operating in a state that needs
monitoring.
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Chapter 5 Alarms
Popup Messages
As described in Chapter 4, popup messages are used to help the user make alarm adjustments
and prevent unintended adjustment of the device. See Chapter 4 for a list of popup messages.
Alarm Types
Alarm types are identified to provide a framework for the alarm scheme and titles. The alarm
indication may be due to patient conditions, breathing circuit conditions, device conditions, or
environment. For a list of all alarms, with descriptions of ventilator behavior and mitigation
actions see Alarm Summary section later in this chapter.
The alarm types are:
• Patient Safety — address the ventilation of the patient and their respiratory effort. Patient
Safety alarm types also includes: pulse oximetry monitoring and circuit/exhalation valve
issues.
• Environmental and Use — address the device inputs: external power, battery, high pressure
O2 supply, and the fresh gas intake. Environmental and Use alarm types also includes:
ambient and device temperature, barometric pressure, and altitude.
• Self Check — address the performance of the device systems and include:
• Internal Communication (Comm): faults/failures of inter-device communication,
cyclic redundancy checking, or processor-related issues
• Pneumatic Sensor: faults/failures of the pneumotachographs that measure gas flow
or the pressure transducers.
• Pneumatic System: faults/failures of the compressor or O2 supply valve.
• Power System: faults/failures of the power system that render the device unable to
operate from external power or charge/operate from the internal rechargeable
battery.
• Pulse Oximeter Module: faults/failures of the pulse oximeter module that are not
related to monitoring of the patient, a fault or failure of the module.
• Preventive Maintenance: alarms that occur when device is due for preventive
maintenance.
Patient Safety Alarm Type
The ventilation mode determines whether parameters are controlled by the user. As a result, the
alarms monitoring the patient safety behave differently based on the ventilation mode. Patient
safety alarms may be muted or turned off if the use determines this is appropriate for the
management of the patient.
Note:
Popup messages are used to prevent inadvertent setting of alarm limits at their extreme
which could limit the effectiveness of the alarm.
The table below lists alarms related to patient safety, describes default settings and adjustable
ranges in different ventilation modes and provides the Service Code (SC) number for each
alarm. Alarm settings are retained if set prior to power loss and can be retrieved by following
the Using the Last Setting instructions in Chapter 4.
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Chapter 5 Alarms
Alarm Name
Adjustable Range, Default
Airway Pressure High
20 to 100 (>60 requires confirmation)
Service Code
2070
Default: Adult:35 Pediatric: 30
Low Airway Pressure
3 to 35, OFF (with popup confirmation; 3
without confirmation)
2071
Default: 10 in AC, SIMV
Default: OFF in CPAP or BL
See transition and feature notes in
Chapter 4.
High Tidal Volume
0 to 2000, OFF (with popup confirmation;
2000 without confirmation)
(Vt High)
2072
Default: Adult: N/A Pediatric: 500
(ml)
Default: OFF in CPAP or BL
See transition and feature notes in
Chapter 4.
Low Tidal Volume
0 to 2000, OFF (with popup confirmation;
0 without confirmation)
(Vt Low)
2073
Default: Adult: N/A Pediatric: 500
(ml)
Default: OFF in CPAP or BL
See transition and feature notes in
Chapter 4.
High Breath Rate
20 to 99, OFF (with popup confirmation;
99 without confirmation)
2074
Default: Adult: 25 Pediatric: 30
Low Breath Rate/Apnea
2 to 25 (with popup confirmation below 6)
2075
Apnea
Default: Adult: 8 Pediatric: 10
2076
PEEP Leak
Not adjustable, OFF (with Alarm Menu)
2090
Insufficient Flow
Not adjustable
2095
Spont. Breath PIP High
20 to 100
2170
Default = Adult:35 Pediatric: 30
Spont. Breath PIP Low
3 to 35, OFF (with popup confirmation; 3
without confirmation)
2171
Default: 10 in AC, SIMV
Default: OFF in CPAP or BL
See transition and feature notes in
Chapter 4.
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Chapter 5 Alarms
Alarm Name
Adjustable Range, Default
Service Code
Spont. Breath-VT High
0 to 2000, OFF (with popup confirmation;
2000 without confirmation)
2172
Default: Adult: N/A Pediatric: 500
Default: OFF in CPAP or BL
See transition and feature notes in
Chapter 4.
Spont. Breath-VT Low
0 to 2000, OFF (with popup Confirmation;
0 without confirmation)
2173
Default: Adult: N/A Pediatric: 500
Default: OFF in CPAP or BL
See transition and feature notes in
Chapter 4.
Inspiratory Demand
Not adjustable, OFF (with Alarm Menu)
3092
Auto-PEEP
Not adjustable, OFF (with Alarm Menu)
3091
Patient Disconnect
Not adjustable
2100
Exhalation System Failure
Not adjustable
1060
Exhalation System Failure
Not adjustable
1061
Exhalation System Fault
Not adjustable
2062
Self Check Failure
(Pneumatic Sensor: Autocal)
Not adjustable
1051
Self Check Fault
(Pneumatic Sensor: Airway
Pressure)
Not adjustable
2053
Tubing Compliance Fault
Not adjustable
3073
Patient Safety Alarms Related to Use of a Pulse Oximeter
The primary use of the ventilator is to provide patient ventilation: however, the ventilator has
an integrated pulse oximeter. The pulse oximeter operates only when the ventilator is
ventilating. When there is an issue with the SpO2 or HR signals or the value is outside of the
alarm limits the device triggers alarms as identified in the table below.
Note:
5-6
Pulse oximetry is not available when the Start Menu is active, only after ventilation is
started.
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Alarm Name
Adjustable Range, Default
Service Code
Pulse Ox Sensor Off Patient
Not adjustable, OFF (with alarm
menu)
2314
SpO2 Low
86 to 99, (with popup confirmation; 86
without confirmation)
2401
Default: 94
Heart Rate High
80 to 240, OFF (with popup
confirmation; 240 without
confirmation)
2410
Default: Adult: 120 Pediatric: 150
Heart Rate Low
30 to 79, OFF (with popup
confirmation; 30 without confirmation)
2411
Default: 40
Pulse Ox Sensor Not Connected
Not adjustable
3310
Defective Pulse Ox Sensor
Not adjustable, OFF
3311
Pulse Search
Not adjustable, OFF
3312
Pulse Ox Signal Interference
Not adjustable, OFF
3313
Ambient Light Fault
Not adjustable, OFF
3315
Invalid Pulse Ox Sensor
Not adjustable, OFF
3316
Low SpO2 Perfusion
Not adjustable, OFF
3317
3318
Environmental and Use Alarm Types
Environmental and Use alarms result from a ventilator fault or failure (for example, the
ventilator’s battery is drained) or from a change in use (for example, an external O2 tank
requires replacement).
Note:
The alarm priority is dependent on whether an alternate power or gas source is
available
These alarms clear when the environmental or use condition is corrected. (for example, external
power is supplied or external O2 is restored)
Note:
Environmental and Use alarms cannot be preemptively muted or muted at Start Up.
Additionally, these alarms cannot be turned OFF or adjusted. The user must correct the
cause of the alarm or change the therapy.
The table that follows lists the Environmental and Use alarms. They are grouped based on their
condition and effect on the ventilator.
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Chapter 5 Alarms
Environmental and Use
Alarm Types
Alarm Group
Service Code(s)
Battery State of Charge
1430
2430
3430
3431
Battery Charge Fault/Failure
2423
3423
Battery
3422
Nearly Too Hot for discharge
2450
3450
Too hot for charge/discharge w/ external power
3451
3452
Power Fault/Failure
Climatic Environment
Fault
Too Cold for charge
3453
External Power Failure
3431
Insufficient Current
3442
High Voltage
3441
DC Power Reversed
3444
Disconnect/Low Voltage
3421
Altitude Too High/Low
3131
3132
Temperature Too High/Low
3140
3141
Low O2 Supply Failure/ Fault
O2 Supply
1020
2020
High O2 Supply Failure/Fault
1041
3041
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Chapter 5 Alarms
Environmental and Use
Alarm Types
Alarm Group
Service Code(s)
1030
Gas Intake Fault
Gas Intake Blocked or Restricted
2030
3030
3031
Complete Power Failure
In event the ventilator is operating and it detects that there is no internal power and there is no
external power the device will issue a “Complete Power Failure” alarm for two minutes. For
this alarm there is no LCD indication, the Red LED blinks, and the buzzer sounds for two
minutes. The alarm clears with a user acknowledgment of turning the power switch to OFF.
This alarm is not recorded in the alarm history file. All other alarms are recorded in the alarm
history file prior to the complete power failure.
Self-Check Alarm Types
During power up, the ventilator goes through a Self-Check Test (a set of system tests and
checks). When the Self-Check passes, the LED array turns green and the Start Menu displays,
indicating that the ventilator is operational.
If the Self-Check does not pass, then one or more Self-Check alarms present to identify the
nature of the problem.
Warning!
Unresolved Self-Check alarms alert the user to issues with the device that can affect its
performance. Users should carefully consider the risk of using the device with these
alarms before using it with a patient.
Note:
The alarm priority is dependent on whether an alternate power or gas source is
detected.
The device continually self-monitors to ensure hardware functionality and minimize software
errors. A Self-Check alarm is triggered when a fault or failure condition is detected. These
alarms clear when the condition reported by the alarm is corrected. (for example, an internal
communication failure.)
Note: Self-Check alarms cannot be preemptively muted or muted at Start Up.
The table that follows lists the Self-Check alarms.
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Chapter 5 Alarms
Self Check Alarm Types
Group(s)
Internal COMM CPU - SPM
Related Service
Code(s)
1176
1173
Internal COMM CPU
1471
1475
Communication
Internal COMM SPM
1175
1472
1474
Compressor Flow Path (Failure/Faults)
1001
2001
3001
Internal COMM Compressor (Failure/Faults)
1002
2002
3002
O2 Valve Failure
1010
O2 Flow Path (Failure/Faults)
1011
2011
3011
Pneumatic System Failure
Internal COMM Valve (Failure/Faults)
1012
2012
3012
3172
Sensor/Transducers/Cal file Failures
1003
1052
1174
Sensor and Transducers Faults
3143
3130
3032
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Chapter 5 Alarms
Self Check Alarm Types
Power System Fault/
Failure
Group(s)
Related Service
Code(s)
5V Bus Compromised
1172
No Back Up power available Input Protection
Circuit Failure
2421
Internal COMM Battery Faults
2455
Back Up power available
3455
Internal COMM Power Components Fault
3470
Internal OEM Board (In Use/Not in Use)
2300
3300
Pulse Ox - Module Failure
Internal COMM (In Use/Not in Use)
2301
3301
PM Due
3120
• 1year
• Stockpile I
• Stockpile II
Preventive Maintenance
(PM)
Note:
Firmware Compatibility faults (during device
service only)
1480
Serial Number Compatibility faults (during
device service only)
3480
RTC Battery Low (Checked at start up)
3110
Power Cycle Needed
3121
It is possible that an internal communication failure may due to a software condition
rather than a hardware failure. When this occurs the alarm may be cleared with a
power cycle (turn the device OFF and then back ON). If the condition persists then the
device should be returned to service.
Managing Alarms
Alarms are indicated both audibly (through the buzzer and visually through the LED array (red,
yellow), and in the LCD with alarm bell icons, title, and Service Code (SC). As indicated
above, each alarm is also indicated with Smart Help in the AMC which provide several steps to
resolve or mitigate the alarm. The AMC also contains “If Not Resolved” instructions which are
at the end of the AMC and surrounded by asterisk. These contain instructions on how to
manage the patient if the Mitigation/Resolution Instructions and user actions do not resolve the
alarm. The example below shows an “If Not Resolved” instruction.
**Contact Service Center**
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Chapter 5 Alarms
Based on the types of alarms (Patient Safety, Environmental and Use, and Self Check) and their
effect on the patient and/or device (high, medium, low) alarms are prioritized and presented to
the user in the order that most effects the patient. In this way, the user is prompted to address
the issue or issues that most effect the safety of the patient. This grouping is to provide a
framework to identify the alarm conditions.
The AMC accommodates the display of up to 5 active alarms. The alarms are displayed in
order of priority and rank. Only the highest priority alarm or set of alarms are displayed at one
time. For example, if three medium and one high priority alarms are present in the system only
the high priority alarm will be displayed until it is resolved. The medium priority alarms will
then be displayed if they are still present in the system. In addition to the priority, each alarm is
ranked according to the severity of risk to the patient. Only the five highest ranked alarms will
be displayed on the screen. If six or more alarms are present in the system, the lowest rank and
priority will not be displayed in the AMC. Additionally, only alarms that are set and displayed
in the system can be reviewed in the Alarm History Menu. Lower priority and rank alarms that
resolve before the displayed higher alarms will not be logged in the Alarm History Menu. See
Chapter 4 for instructions on viewing the Alarm History Menu.
When there are multiple alarms, you can control which alarm is displayed by selecting its
associated icon. If the alarms are Low Priority, then the Pleth and Pressure/Time plots appear
permanently on the screen when the alarms are muted. If the alarms are Medium Priority, the
ventilator cycles through each Medium Priority Alarm every 20 seconds. You can use the
selection dial to select a particular Medium Priority Alarm and/or Plot for 20 seconds, after
which, cycling resumes. New alarms can overwrite the screen at any time based on their
priority.
Alarm Muting
Start Up Muting
At start up, the ventilator suspends active patient safety alarms, with the exception of those
alarms that could affect the performance of the device. This prevents nuisance alarms during
start up while you configure the ventilator. When the Start Menu is used, the 2-minute
countdown starts once you select a start option. Once the patient is connected, the mute cancels
automatically after 15 seconds when there are no active alarms.
Note:
When the Start Menu is not used as the powerup option, the 120 seconds mute begins
immediately following the Self Check and cancels as described above.
Preemptive Muting
To prevent excessive noise in the patient care environment, alarms shown below can be
preemptively muted for 30 seconds. This enables you to prevent the audible alarm, by pressing
the Mute button, before initiating a procedure that could trigger an alarm.
Note:
5-12
During this preemptive mute of this audible alarm, the LED alarm light and alarm
message are still indicated.
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Chapter 5 Alarms
Service Code
Alarm Name
2062
Exhalation System Fault
2070
Airway Pressure High
2071
Low Airway Pressure
2072
High Tidal Volume
2073
Low Tidal Volume
2074
High Breath Rate
2075
Low Breath Rate/Apnea
2076
Apnea
2090
PEEP Leak
2095
Insufficient Flow
2100
Patient Disconnect
2170
Spont. Breath PIP High
2171
Spont. Breath PIP Low
2172
Spont. Breath-VT High
2173
Spont. Breath-VT Low
2300
Self Check Fault (Pulse Ox Module Failed)
2301
Self Check Fault (Internal COMM: Pulse Ox Module)
2314
Pulse Ox Sensor Off Patient
2401
SpO2 Low
2410
Heart Rate High
2411
Heart Rate Low
3300
Self Check Fault (Pulse Ox Module Not Available, SpO2 /HR Not Available
(MS2011SB Failure-Monitor Not In Use)
3301
Self Check Fault (Pulse Ox Module Not Available, SpO2 /HR Not Available
(Pulse Ox Module Failure, SpO2 /HR Not Available)
3310
Pulse Ox Sensor Not Connected
3311
Defective Pulse Ox Sensor
3312
Pulse Search
3313
Pulse Ox Signal Interference (External Signal Interfering With Measurement)
3315
Ambient Light Fault
3316
Invalid Pulse Ox Sensor
3317
Low SpO2 Perfusion
3318
Low SpO2 Perfusion
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Chapter 5 Alarms
Disabling Alarms from the Alarm Configuration Menu
There are clinical situations where an alarm occurs, and in the user’s clinical judgment, this
alarm is a nuisance that does not affect the safe management of the patient.
The ventilator allows a series of alarms to be disabled for the duration of the current use. These
alarms are listed in the following table:
Alarm Name
Service Code
Auto PEEP
3091
PEEP Leak
2090
PM Due
3120
RTC Battery Low
3110
Inspiratory Demand
3092
Intake Restricted
3031
Constraints
To avoid nuisance alarms, the Auto-PEEP
alarm is disabled at start up.
The user can choose to activate the alarm if
they believe the patient is at risk of Auto-PEEP.
Alarms that have occurred in the current
operating session can be canceled.
To disable an alarm, press the Menu button and use the Dial to scroll to the alarm configuration
menu. Press the Accept button. Then scroll down to the alarm that is to be disabled using the
Dial and press the Accept. Use the Dial to select off, and then press the Accept to complete the
change.
Alarms that have occurred in the current operating session can be canceled.
Alarms which have not occurred since turn on are indicated with a “--”.
Disabled alarms are not be saved in the User Settings for the next session.
All disabled alarms reappear (if appropriate) when the ventilator is next used. (As an
example, the Self Check Fault (Calibration Due) (SC: 3480), reappears in the next operating
session.)
Note: To avoid nuisance alarms, the Auto-PEEP alarm (SC: 3091) is disabled at start up.
The user can choose to activate the alarm if they believe the patient is at risk of
Auto-PEEP.
•
•
•
•
Patient Detect Mode
When powering on the device with the Start Menu, the device has a Patient Detected (PD)
alarm to detect if a patient connected to the device is in a non-ventilating state. The device
detects pressure changes which reflect the following conditions:
• Infant through adult patients with no inspiratory effort
• Infant through adult patients with active inspiratory effort
• Infant through adults with patient circuits connected to masks.
In the event a patient is detected before a Start Menu option is made, a medium priority alarm is
displayed to indicate that a patient is connected to a non-ventilating device.
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Chapter 5 Alarms
While in PD mode, low and medium priority alarms mute behavior is maintained. Triggered
low and medium priority alarms will display. When muted or resolved the start menu will
display again. PD mode has no affect on high priority alarms.
The device immediately starts ventilating with the setting described in the table below:
Note:
When the Patient Detect alarm is active the Mode Parameter window displays "---".
The is done to encourage the user to configure the ventilator appropriately for the
patient.
While in PD Mode, Battery and Power, Environmental, and Self check alarms are detected and
displayed when present in the device. Only the following selected patient safety alarm
conditions are detected:
•
•
•
•
SC: 2110 - Patient Detected
SC: 2062 - Exhalation System Fault
SC: 1060 - Exhalation System Failure
SC: 1061 - Exhalation System Failure
Backup Modes
In the event of certain internal system failures, a backup mode takes control to continue
ventilating and alerts the user with audible and visual alarms. While in backup mode the device
continues to ventilate with the currents settings that were in use before the failure. Changes to
the device settings are not possible. The backup mode is activated with all internal COMM
failure alarms. (SC: 1173,1471, 1472, 1474, and 1475)
While in backup mode, if any of the following conditions are detected for three consecutive
breaths, the device will switch to a pressure targeted configuration, see table below, to continue
support of the patient and prevent excessive airway pressure:
• Airway Pressure High (SC: 2070)
• Patient Disconnect (SC: 2100)
• Auto-PEEP (SC: 3091)
Note:
Since the priority of these conditions are lower priority than the initial failure causing
backup mode, these alarms will not be visible in the AMC.
The Mitigation/Resolution Instructions for the individual alarms should be followed to manage
the patient and device if Backup is active.
Apnea Backup Mode
Apnea Backup is activated when the Apnea alarm (SC: 2076) is triggered during CPAP or BL
mode. The alarm triggers when the spontaneous breathing rate is less than the BPM Low Limit
setting. Apnea Backup settings should be configured for the individual patient’s needs. This is
done in the Mode context menu when either CPAP or BL is the mode. Chapter 4 contains
detailed information on editing the Mode context menu along with the default settings and
setting ranges.
Additionally, the Manual Breath button delivers a single breath when pressed, using the current
Apnea Backup settings for a mandatory breath in CPAP and BL modes.
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Chapter 5 Alarms
Backup
Apnea
PD Mode
AC(P)
SIMV(P)
AC(P)
BPM
12
12
14
I:E
1:4
1:3
1:3
PIP
20
20
20
PEEP
5
As Set
5
Rise Time
5
As Set
6
PIP High
25
As Set
25
PIP Low
3
As Set
10
Vt High
700
As Set
750
As Set
250
Vt Low
FIO2
As Set
As Set
21
Trigger
-2 cm H2O (hPa)
As Set
-2 cm H2O (hPa)
Alarm Summary
A list of all ventilator alarms follows and is divided into three categories:
• High Priority
• Medium Priority
• Low Priority
Alarms in each list are provided in numerical order based on their Service Code.
High Priority Alarms
Service
Code
Alarm Name
Description / Mitigation/Resolution / If Not Resolved Instructions
1001
Self Check Failure
Description: Alarm triggers when the compressor fails to operate or fails to
provide the flow required to deliver a breath and high pressure O2 is not available
to provide ventilation.
Mitigation/ Resolution: Pneumatic System: Compressor, Manually
Ventilate Patient, Connect 55 psig/380 kPa O2, Restart Ventilator with
O2,
If Not Resolved: **Contact Service Center**
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Chapter 5 Alarms
Service
Code
Alarm Name
Description / Mitigation/Resolution / If Not Resolved Instructions
1002
Self Check Failure
Description: Alarm triggers when communication between the compressor
controller and Smart Pneumatic Module (SPM) is lost and high pressure O2 is
not available to provide ventilation.
Mitigation/ Resolution: Pneumatic System: Compressor, Manually
Ventilate Patient, Connect 55 psig/380 kPa O2, Restart Ventilator with
O2,
If Not Resolved: **Contact Service Center**
1003
Self Check Failure
Description: Alarm triggers when the flow from the first breath is ± 20% of the
expected flow for the tidal volume at start up. This unusually low RPM is a
symptom of a dirty flow screen which cannot be serviced by the user.
Mitigation/ Resolution: Pneumatic Sensor: Pneumotach, Manually
Ventilate Patient,
If Not Resolved: **Contact Service Center**
1010
Self Check Failure
Description: Alarm triggers when the O2 valve fails in the open position which
results in continuous inspiratory flow. When this occurs the device automatically
opens the exhalation valve to prevent pressure from accumulating in the circuit
and ventilation stops.
Mitigation/ Resolution: Pneumatic System: O2 Valve, Manually Ventilate
Patient,
If Not Resolved: **Contact Service Center**
1011
Self Check Failure
Description: Alarm occurs when the signal to the O2 valve is not delivering the
required flow rate and the compressor is not available to provide ventilation.
Mitigation/ Resolution: Pneumatic System: O2 Valve, Manually Ventilate
Patient,
If Not Resolved: **Contact Service Center**
1012
Self Check Failure
Description: Alarm occurs when the communication between the O2 valve and
the SPM fails and the compressor is not available to provide ventilation.
Mitigation/ Resolution: Pneumatic System: O2 Valve, Manually Ventilate
Patient,
If Not Resolved: **Contact Service Center**
1020
Low O2 Supply
Failure
Description: Alarm occurs when the O2 supply pressure is < 35 psig (241 kPa)
and the compressor is not available to support ventilation. If the O2 source can
be restored the device should be cycled off then on to reset. By design the
device will not reestablish O2 operation unless the supply pressure is ≥ 40 psig
(276 kPa). If the supply pressure is between 40 and 87 psig (276 to 600 kPa) the
user should check the hose connections for leaks. Occasionally, this alarm can
be caused by a regulator that provides a static pressure within range but is not
able to provide the flow necessary to meet the patient flow demand.
Mitigation/ Resolution: Manually Ventilate Patient, Connect 55 psig/380
kPa O2, Restart, Check O2 Supply for Leaks, Replace Regulator,
If Not Resolved: **Contact Service Center**
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Chapter 5 Alarms
Service
Code
Alarm Name
Description / Mitigation/Resolution / If Not Resolved Instructions
1030
Gas Intake Failure
Description: Alarm occurs when the Fresh Gas/Emergency Air Inlet is blocked
so that the compressor is not able to deliver flow sufficient for the current settings
and high pressure O2 is not available to support ventilation. The user should
clear the blockage and restart the ventilator. A false alarm can be triggered in
very high vibration environments.
Mitigation/ Resolution: Manually Ventilate Patient, Clear Blocked Intake,
Connect 55 psig/380 kPa O2, Restart Ventilator
If Not Resolved: **Contact Service Center**
1041
High O2 Supply
Failure
Description: Alarm triggers when the O2 supply pressure is > 87 psig (600 kPa).
Pressures above 87 psig (600 kPa) can result in a failure, harm to the patient
and/or damage to the device. While the patient is manually ventilated the user or
assistant should seek to reduce the O2 supply pressure. Sometimes this requires
changing the regulator which is not functioning as required. If the pressure
cannot be reduced and a low flow device like a flow meter is available the user
can provide supplemental O2 via the optional low flow O2 reservoir. To clear the
alarm the device should be turned off and then restarted with supply pressure in
the appropriate range (40 to 87 psig, 276 to 600 kPa) or without the high
pressure O2 source connected.
Mitigation/ Resolution: Manually Ventilate Patient, Decrease O2 to 55
psig/380 kPa, Replace Regulator, Connect Low Flow O2, Restart
If Not Resolved: **Contact Service Center**
1051
Self Check Failure
Description: Alarm triggers when the autocal procedure is not able to zero the
airway pressure transducer to ambient pressure. When this occurs, manually
ventilate the patient, replace the ventilator and contact the service center for
additional information. Note: a false alarm can be triggered during operation in
very high vibration environments when the device is not mounted correctly. If this
could be the cause, restart the ventilator and continue operation if no alarms are
triggered.
Mitigation/ Resolution: Pneumatic Sensor: Autocal, Manually Ventilate
Patient
If Not Resolved: **Contact Service Center**
1052
Self Check Failure
Communication between the airway pressure sensor and SPM is lost. When this
happens, manually ventilate the patient, replace the ventilator and contact the
service center for additional information.
Mitigation/ Resolution: Pneumatic Sensor: Airway Pressure, Manually
Ventilate Patient
If Not Resolved: **Contact Service Center**
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Chapter 5 Alarms
Service
Code
Alarm Name
Description / Mitigation/Resolution / If Not Resolved Instructions
1060
Exhalation System
Failure
Description: Alarm occurs when the PIP fails to return to the baseline pressure
for 3 consecutive breaths, indicating that the exhalation control valve has failed.
When triggered, the device stops ventilating and attempts to discharge the
pressure in the breathing circuit to atmosphere. This failure may be caused by a
significant blockage of the exhalation valve or an occlusion/kink in the exhalation
valve tube. If possible, the user should replace the breathing circuit and restart
the ventilator. If this does not resolve the failure, replace the ventilator and contact
the service center for additional information.
Mitigation/ Resolution: Patient Can Not Exhale, Manually Ventilate
Patient, Check for Kinked Hose/Tube, Replace Circuit and Restart
If Not Resolved: **Contact Service Center**
1061
Exhalation System
Failure
The airway pressure, PIP, is > 40 cm H2O (hPa), the PIP High Limit (when PIP
High Limit is < 35 cm H2O (hPa)) for > 5 seconds, or when the PIP is
> 75 cm H2O (hPa) for > 1.5 seconds. When this happens, the device stops
ventilating and attempts to discharge the pressure in the breathing circuit to
atmosphere. This failure may be caused by a significant blockage of the
exhalation valve or an occlusion/kink in the exhalation valve tube. If possible, the
user should replace the breathing circuit and restart the ventilator. If this does not
resolve the problem, replace the ventilator and contact the service center for
additional information.
Mitigation/ Resolution: Patient Can Not Exhale, Manually Ventilate
Patient, Check for Kinked Hose/Tube, Replace Circuit and Restart
If Not Resolved: **Contact Service Center**
1172
Self Check Failure
Description: Alarm occurs when the 5 VDC power bus fails to provide the
required voltage. If this failure occurs, the user should manually ventilate the
patient, replace the ventilator and contact the service center for additional
information.
Mitigation/ Resolution: Pneumatic Sensor: Autocal, Manually Ventilate
Patient
If Not Resolved: **Contact Service Center**
1173
Self Check Failure
Description: Alarm occurs when communication fails between one of the
subcomponents and the host processor. If this failure occurs, remove
(disconnect) the external power supply, turn OFF the ventilator, then turn it back
ON (providing time to allow the ventilator to rest). If the ventilator starts with a
Self-Check failure, or if the alarm continues, then the user should manually
ventilate the patient, replace the ventilator and contact the service center for
additional information.
Mitigation/ Resolution: Internal COMM, Manually Ventilate Patient,
Backup Ventilator Started
If Not Resolved: **Contact Service Center**
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Chapter 5 Alarms
Service
Code
Alarm Name
Description / Mitigation/Resolution / If Not Resolved Instructions
1174
Self Check Failure
Description: Alarm occurs when the device is not able to calibrate one or more
transducers and is no longer able to operate safely. If this failure occurs, the user
should manually ventilate the patient, replace the ventilator, and contact the
service center for additional information.
Mitigation/ Resolution: Pneumatic Sensor: Transducer, Manually
Ventilate Patient, Restart Ventilator
If Not Resolved: **Contact Service Center**
1175
Self Check Failure
Description: Alarm triggers when the internal communication bus and the host
are not able to communicate with the subassemblies. If this failure occurs,
remove (disconnect) the external power supply, turn OFF the ventilator, then turn
it back ON (providing time to allow the ventilator to rest). If the ventilator starts
with a Self-Check failure, or if the alarm continues, then the user should
manually ventilate the patient, replace the ventilator and contact the service
center for additional information.
Mitigation/ Resolution: Internal COMM, Manually Ventilate Patient
If Not Resolved: **Contact Service Center**
1176
Self Check Failure
Description: Alarm triggers when the calibration file fails its integrity check. The
user should manually ventilate the patient, replace the ventilator and contact the
service center for additional information.
Mitigation/ Resolution: Internal COMM, Manually Ventilate Patient
If Not Resolved: **Contact Service Center**
1420
Self Check:
Complete Power
Failure
Description: Alarm triggers when power is lost from both the internal battery and
an external source during operation. When this occurs, the LCD blanks (no
power for operation), the audible alarm pulses rapidly, and the visual alarm
flashes rapidly. This alarm will last approximately two minutes. If the device can
be recharged after the failure and there are no other issues it can be returned to
service. If there are any questions, contact the service center for additional
information. See the section titled, “Complete Power Failure”, earlier in this
chapter.
Mitigation/ Resolution: No LCD Display
1430
Drained Battery
Description: Alarm triggers when the internal battery power drops below the
amount required to provide ventilation and external power is not connected.
When this occurs there is enough power to operate the user interface and
provide information to the user. The user should be manually ventilate the patient
while an external source of power is sought. To cancel the alarm and begin
operation with external power the device must be turned off and then back on.
Mitigation/ Resolution: Manually Ventilate Patient, Connect External
Power
If Not Resolved: **Contact Service Center**
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Service
Code
Alarm Name
Description / Mitigation/Resolution / If Not Resolved Instructions
1471
Self Check Failure
Description: Alarm triggers when the device is no longer able to communicate
with the User Interface Module (UIM) and the interface controls. When this
occurs ventilation continues at the current settings or the backup mode settings
and the high priority alarm sounds. When this failure occurs, remove
(disconnect) the external power supply, turn OFF the ventilator, then turn it back
ON (providing time to allow the ventilator to rest). If the ventilator starts with a
Self-Check failure, or if the alarm continues, then the user should manually
ventilate the patient, replace the ventilator and contact the service center for
additional information.
Mitigation/ Resolution: Internal COMM, Manually Ventilate Patient
If Not Resolved: **Contact Service Center**
1472
Self Check Failure
Description: Alarm triggers when the device is no longer able to communicate
with the Smart Pneumatic Module (SPM). When this occurs ventilation continues
at the current settings or the backup mode settings and the high priority alarm
sounds. The user should manually ventilate the patient, replace the ventilator
and contact the service center for additional information.
Mitigation/ Resolution: Internal COMM, Manually Ventilate Patient
If Not Resolved: **Contact Service Center**
1474
Self Check Failure
Description: Alarm triggers when cyclic redundancy checking between the
device and SPM fails. When this occurs ventilation continues at the current
setting or the backup mode settings and the high priority alarm sounds. The user
should manually ventilate the patient, replace the ventilator and contact the
service center for additional information.
Mitigation/Infor: Internal COMM, Manually Ventilate Patient
If Not Resolved: **Contact Service Center**
1475
Self Check Failure
Description: Alarm triggers when the device has lost communication with the
contrast control and in most instances the content of the LCD is not visible.
When this occurs ventilation continues at the current settings or the backup
mode setting and the high priority alarm sounds. The user should manually
ventilate the patient, replace the ventilator and contact the service center for
additional information.
Mitigation/ Resolution: Internal COMM, Manually Ventilate Patient,
Backup Ventilator Started
If Not Resolved: **Contact Service Center**
1480
Self Check Failure
Description: Alarm triggers when the device and SPM software loads are not
compatible. This alarm is typically associated with an SPM change where the
technician failed to update the device and SPM to the current software revision.
Ventilation is provided using the backup mode settings. The user should
manually ventilate the patient, replace the ventilator and contact the service
center for additional information.
Mitigation/ Resolution: Firmware Mismatch, Manually Ventilate Patient,
Software Compatibility Failure
If Not Resolved: **Contact Service Center**
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Chapter 5 Alarms
Medium Priority Alarms
Service
Code
Alarm Name
Mitigation/Resolution
2001
Self Check Fault
Description: Alarm triggers when the communication between the compressor
and the SPM fails and high pressure O2 is available to provide ventilation. The
alarm will continue to sound as a medium priority alarm until the user
acknowledges that ventilation is being provided using O2 by setting the FIO2 to
100%. At this time the priority changes to low priority. While operating in this
state the user should ensure an adequate supply of O2. Failure to maintain the
O2 supply will result in a high priority alarm.
Mitigation/ Resolution: Pneumatic System: Compressor, Operation
Switched to O2 Supply, Set FIO2 to 100%, Monitor O2 Supply
If Not Resolved: **Contact Service Center**
2002
Self Check Fault
Description: Alarm triggers when the communication between the O2 valve and
the SPM fails and the compressor is available to provide ventilation. The alarm
will continue to sound as a medium priority alarm until the user acknowledges
that ventilation is being provided using the compressor by setting the FIO2 to
21%. At this time the alarm priority changes to low. While operating in this state
the user should monitor the SpO2 to ensure that adequate oxygenation is
maintained. If low flow O2 is available it can be entrained through the Fresh Gas/
Emergency Air Intake port using the optional O2 reservoir. Maintain an
acceptable SpO2 by adjusting the O2 supply up or down to increase or decrease
the amount of O2 delivered to the patient.
Mitigation/ Resolution: Pneumatic System: Compressor, Operation
Switched to O2 Supply, Set FIO2 to 100%, Monitor O2 Supply
If Not Resolved: **Contact Service Center**
2011
Self Check Fault
Description: Alarm triggers when the signal to the O2 valve is outside of the
calibration range for the required flow rate and the compressor is available to
provide ventilation. The medium priority alarm will continue until the user
acknowledges that ventilation is being provided using the compressor by setting
the FIO2 to 21%. At this time the alarm priority changes to low priority. While
operating in this state the user should monitor the SpO2 to ensure that adequate
oxygenation is maintained. If low flow O2 is available it can be entrained through
the Fresh Gas/Emergency Air Intake port using the optional O2 reservoir.
Maintain an acceptable SpO2 by adjusting the O2 supply up or down to increase
or decrease the amount of O2 delivered to the patient.
Mitigation/ Resolution: Pneumatic System: O2 Valve, Operation
Switched to Compressor, Connect Low Flow O2, Monitor SpO2
If Not Resolved: **Contact Service Center**
5-22
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution
2012
Self Check Fault
Description: Alarm triggers when the communication between the O2 valve and
the SPM fails and the compressor is available to provide ventilation. The alarm
will continue to sound as a medium priority alarm until the user acknowledges
that ventilation is being provided using the compressor by setting the FIO2 to
21%. At this time the alarm priority changes to low. While operating in this state
the user should monitor the SpO2 to ensure that adequate oxygenation is
maintained. If low flow O2 is available it can be entrained through the Fresh Gas/
Emergency Air Intake port using the optional O2 reservoir. Maintain an
acceptable SpO2 by adjusting the O2 supply up or down to increase or decrease
the amount of O2 delivered to the patient.
Mitigation/ Resolution: Pneumatic System O2 Valve, Set FIO2 To 21%,
Connect Low Flow O2, Monitor SpO2
If Not Resolved: **Contact Service Center**
2020
Low O2 Supply
Fault
Description: Alarm triggers when the O2 supply pressure is < 35 psig (241 kPa)
and the compressor is able to support ventilation. When this occurs the device
begins ventilation using the compressor. The alarm will continue to sound as a
medium priority alarm until the user acknowledges that ventilation is being
provided using the compressor by setting the FIO2 to 21%. The alarm will cancel
completely when the user sets FIO2 to 21%.
Note: The device works with or without external O2. If O2 is connected the device
will restart O2 operation unless the supply pressure is ≥ 40 psig (276 kPa). This
is done to prevent continuous cycling between alarms during the inspiratory
phase and no alarm during the expiratory phases. If low flow O2 is available it
can be entrained through the Fresh Gas/Emergency Air Intake port using the
optional O2 reservoir. Maintain an acceptable SpO2 by adjusting the O2 supply
up or down to increase or decrease the amount of O2 delivered to the patient.
Mitigation/ Resolution: Operation Switched to Compressor, Check O2
Supply Pressure, Check/Replace Regulator, Set FIO2 to 21%. Connect
Low Flow O2, Monitor SpO2
If Not Resolved: **Contact Service Center**
2030
Gas Intake Fault
Description: Alarm triggers when the Fresh Gas/Emergency Air Inlet is blocked
so that the compressor is not able to deliver a breath within ±10% of the current
settings and high pressure O2 is available to support ventilation. When this
occurs the ventilator immediately switches to O2 powered ventilation. To clear
the alarm first set the FIO2 to 100% to acknowledge that the patient is being
ventilated at 100%, clear the blockage and then set the FIO2 back to the original
value. Once the blockage has been cleared operation with the compressor will
restart. If the blockage cannot be cleared, the alarm will resound, continue
ventilation with FIO2 set to 100% and ensure an adequate supply of O2 . NOTE:
A high vibration environment can trigger this alarm. If necessary, the user can
activate the O2 Reservoir mode while continuing to operate normally. This will
suppress the alarm.
Mitigation/ Resolution: Operation Switched to O2 Supply, Clear Blocked
Intake, Set FIO2 to 100%, Monitor SpO2, Monitor O2
If Not Resolved: **Contact Service Center**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution
2053
Self Check Fault
Description: Alarm triggers when the expiratory time is < 170 ms for 3
consecutive breaths. When this occurs the device attempts to reestablish a
baseline by momentarily setting PEEP to 0 cm H2O (hPa) and suspending
triggered breaths. This interruption lasts no longer than 2 breath cycles. The user
should also check for leaks in the hose and tubes, patient airway and exhalation
valve. If recalibration is successful the alarm will automatically cancel. If the
device does not reset, manually ventilated the patient, replace the ventilator and
contact the service center for additional information.
Mitigation/ Resolution: Pneumatic Sensor: Airway Pressure, Check
Circuit for Leaks/Disconnects, Check Tube Placement/Cuff
If Not Resolved: **Contact Service Center**
2062
Exhalation System
Fault
Description: Alarm triggers when the airway pressure, PIP, measured at the end
of expiration is > 5 cm H2O (hPa) above the baseline pressure, PEEP. This is
typically caused by a restriction of the exhalation valve or an occlusion/kink in
one or more of the breathing circuit tubes or hose. If the breathing circuit tubes
appear to be intact the circuit should be replaced to eliminate the possibility of a
bad exhalation valve. If the condition does not resolve the user should manually
ventilate the patient, replace the ventilator and contact the service center for
additional information.
Mitigation/ Resolution: Check Patient Exhalation, Check Circuit for
Kinked Hose/Tube, Check for Blocked Exhalation Valve, Replace
Circuit, Replace/Service Ventilator
If Not Resolved: **Manually Ventilate Patient**
2070
Airway Pressure
High
Description: Alarm triggers when the airway pressure, PIP, is > the high airway
pressure limit for 2 consecutive breaths. When the limit is reached, the flow
decelerates to keep the PIP below the airway pressure for the duration of the
breath (inspiratory time). The user should check for kinks or blockage of the
breathing circuit, exhalation valve or patient airway. In some instances the cause
can be an accumulation of secretions in the airway which will require suctioning
to clear. The user should also assess if the patient is fighting the ventilator,
asynchrony, or if the high airway pressure limit is set too low.
Mitigation/ Resolution: Pressure Exceeds Limit Setting, Check Circuit for
Kinked Hose/Tube, Check for Airway Obstruction, Suction Airway if
Necessary, Check High PIP Limit Setting
If Not Resolved: **Manually Ventilate Patient**
2071
Low Airway
Pressure
Description: Alarm triggers when the airway pressure, PIP, is < the low airway
pressure limit for 2 consecutive breaths. The user should check for leaks/
disconnects in the breathing circuit, patient airway or a failure of the exhalation
valve. The user should also assess if the patient is breathing with the ventilator,
the PIP or tidal volume are set too low, or if the low airway pressure limit is set
too high. If a replacement is available, the user should replace the breathing
circuit. If these mitigations do not resolve the alarm condition, replace the
ventilator and contact the service center for more information.
Mitigation/ Resolution: Check Patient Connection, Check Circuit For
Loose Hose/Tube, Check Exhalation Valve, Check Tube Placement/
Cuff, Check Low Limit Setting
If Not Resolved: **Manually Ventilate Patient**
5-24
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution
2072
High Tidal Volume
Description: Alarm triggers during pressure targeted ventilation when the
delivered tidal volume exceeds the user defined limit for 2 consecutive breaths.
This can be caused by a leak in the patient connection or breathing circuit. When
the ventilator is not able to reach the pressure target flow increases to
compensate which leads to a high delivered tidal volume. It is critical to set this
alarm with infant and pediatric patients given that the high resistance airways
used with these patients can provide a false airway pressure even when the
patient has extubated or decannulated. The user should check for leaks/
disconnects in the breathing circuit, patient airway or a failure of the exhalation
valve. Users should also assess if the patient is anxious and breathing deeply or
if the high tidal volume limit is set too low. If a replacement is available the user
should replace the breathing circuit.
Mitigation/ Resolution: Check Patient Connection, Check Circuit For
Loose Hose/Tube, Check Exhalation Valve, Check Tube Placement/
Cuff, Check High Limit Setting
If Not Resolved: **Monitor Patient**
2073
Low Tidal Volume
Description: Alarm triggers during pressure targeted ventilation when the
delivered tidal volume does not reach the user defined limit for 2 consecutive
breaths. When this occurs flow decelerates to maintain the airway pressure at
airway pressure limit for the duration of the breath (inspiratory time). If the PIP
setting is set properly the breath should be greater than the low limit, provided it
is set correctly. The user should check for kinks or blockage of the breathing
circuit or patient airway. In some instances the cause can be an accumulation of
secretions in the airway which will require suctioning to clear. The user should
also assess if the patient is fighting the ventilator, asynchrony, or if the PIP target
is set too low.
Mitigation/ Resolution: Check Circuit For Kinked Hose/Tube, Check For
Airway Obstruction, Suction Airway If Necessary, Check Low Limit
Setting,
If Not Resolved: **Manually Ventilate Patient**
2074
High Breath Rate
Description: Alarm triggers when the actual breathing rate (set rate plus
spontaneous patient rate) exceeds the high alarm limit. This can be caused by
the patient breathing too fast due to anxiety or pending respiratory failure. It can
also be caused by autotriggering due to a leak or the when the spontaneous/
assisted breath trigger is set too close to the baseline pressure, PEEP. The user
should check for leaks/disconnects in the breathing circuit, patient airway or a
failure of the exhalation valve. The user should also assess if the patient is
anxious and breathing deeply or if the high tidal volume limit is set too low. If a
replacement is available the user should replace the breathing circuit.
Mitigation/ Resolution: Check For Loose Circuit Connection, Check
Trigger Setting, Check High Alarm Limit Setting
If Not Resolved: **Consult Physician**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution
2075
Low Breath Rate/
Apnea
Description: Alarm triggers when the actual breathing rate (set rate plus
spontaneous patient rate) is less than the low alarm limit. This can be caused by
the patient not breathing or breathing at a rate less than the limit. If the
spontaneous/assisted breath trigger is not sensitive enough the patient may not
be able to trigger breaths. The user should also determine if the low rate is set
too high for the patient.
Mitigation/ Resolution: Check Patient for Spontaneous Breathing, Adjust
Breath Trigger, Check Low Alarm Limit Setting, Increase Ventilation
Support
If Not Resolved: **Manually Ventilate Patient**
2076
Apnea
Description: Alarm triggers when the spontaneous breathing rate is less than
the low alarm limit. This alarm only occurs in noninvasive ventilation, CPAP and
BL modes. The alarm can be caused by the patient not breathing or breathing at
a rate less than the limit. The apnea backup ventilation starts automatically when
the alarm is triggered. The user should select an active mode of ventilation, AC
or SIMV, to support the patient.
Mitigation/ Resolution: Apnea Backup Ventilation Started, Set Mode to
AC or SIMV, Set Rate and Tidal Volume/Pressure Target
If Not Resolved: **Manually Ventilate Patient**
2090
PEEP Leak
Description: Alarm triggers when the airway pressure drops below the PEEP
setting by 2 cm H2O (hPa) during the expiratory phase of the breath. This can be
caused by a leak in the breathing circuit, exhalation valve or patient airway. The
user should check the breathing circuit and exhalation valve to ensure that all
connections are tight. If the circuit appears damaged or is suspect it should be
replaced. The user should also check if there is a cuff leak from the patient’s
airway or mask. If these mitigations do not resolve the alarm the user can choose
to use leak compensation to provide additional flow during the expiratory phase
to compensate for the leak. If you still cannot compensate for the leak, consult
the attending physician. If this fails replace the ventilator and contact the service
center for more information.
Mitigation/ Resolution: Check Patient Connection, Check for Loose
Circuit Connection, Check Exhalation Valve, Check Tube Placement/
Cuff, Disable Alarm
If Not Resolved: **Replace Circuit**
2095
Insufficient Flow
Description: Alarm triggers when the pressure target is not reached during the
inspiratory period during pressure targeted ventilation. Typically this can occur
when the Rise Time is set too low for the patient and their respiratory mechanics.
Decrease the Rise Time and check the circuit and exhalation valve for leaks or
disconnects. If the flow cannot be adjusted appropriately then the patient should
be ventilated using volume targeted ventilation.
Mitigation/ Resolution: Pressure Target Not Met, Decrease Rise Time,
Press/Hold BPM Button, Consult Physician
If Not Resolved: **Ventilate With Volume Target**
5-26
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906-0731-01-05 Rev G
Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution
2100
Patient Disconnect
Description: Alarm triggers when the airway pressure fails to exceed the PEEP
setting by ~ 7 cm H2O (hPa) When this occurs the user should check the patient
connection, breathing circuit connections and the exhalation valve. At times this
alarm can be caused by the patient breathing with the ventilator during
inspiration which prevents the PIP from passing the minimum pressure.
Mitigation/ Resolution: Check Patient Connection, Check Circuit for
Loose Hose/Tube, Check Exhalation Valve, Check Patient, Replace
Circuit
If Not Resolved: **Manually Ventilate Patient**
2110
Patient Detected
An alarm triggers when you connect the patient to the ventilator while the Start
Menu is active. To resolve the alarm, you must select a mode of ventilation and
configure the device appropriately for the patient. In addition, you should perform
the Operational Test procedure before reconnecting the patient to the device.
Mitigation/ Resolution: Backup Ventilation Started, Set Mode (AC, SIMV,
CPAP, BL), Configure Other Settings
If Not Resolved: **Manually Ventilate Patient and Restart**
2170
Spont. Breath PIP
High
Description: Alarm triggers when the airway pressure, PIP, exceeds the High
PIP Limit Setting during 2 consecutive spontaneous breaths. The user should
quickly check for kinked hoses/ tubes and check for airway obstruction.
Suctioned the patient if necessary. The user should also check if the High PIP
limit is set correctly of if the pressure support (PS) level is set too high.
Mitigation/ Resolution: Pressure Exceeds Limit Setting, Check Circuit for
Kinked Hose/Tube, Check for Airway Obstruction, Suction Airway if
Necessary, Check High Limit Setting
If Not Resolved: **Manually Ventilate Patient**
2171
Spont. Breath PIP
Low
Description: Alarm triggers when the airway pressure, PIP, exceeds the Low
PIP Limit Setting during 2 consecutive spontaneous breaths. The user should
quickly check circuit for loose hoses/ tubes and also check the exhalation valve
and the tube placement/ cuff. The user should also check if the Low PIP Limit is
set correctly.
Mitigation/ Resolution: Check Patient Connection, Check Circuit for
Loose Hose/Tube, Check Exhalation Valve, Check Tube Placement/
Cuff, Check Low Limit Setting
If Not Resolved: **Manually Ventilate Patient**
2172
Spont. Breath Vt
High
Description: Alarm triggers when the high VT Limit is exceeded during 2
consecutive spontaneous breaths. The user should check: the patient
connection, airway placement, breathing circuit for loose hoses/ tubes and also
check the exhalation valve. The user should also check if the High VT Limit is set
correctly.
Mitigation/ Resolution: Check Patient Connection, Check Circuit for
Loose Hose/Tube, Check Exhalation Valve, Check Tube Placement/
Cuff, Check Limit Setting
If Not Resolved: **Monitor Patient**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution
2173
Spont. Breath Vt
Low
Description: Alarm triggers when the Low VT Limit Setting is not achieved
during 2 consecutive spontaneous breaths. When this occurs, the user should
quickly check for kinked hoses/ tubes and check for airway obstruction. The
patient should be suctioned if necessary. The user should also check if the Low
VT limit is set correctly.
Mitigation/ Resolution: Check Circuit for Kinked Hose/Tube, Check for
Airway Obstruction, Suction Airway if Necessary, Check Low Limit
Setting
If Not Resolved: **Manually Ventilate Patient**
2300
Self Check Fault
Description: Alarm triggers when the pulse oximeter module fails while in use.
The user cannot resolve this fault. When the alarm is active “-- --” displays in the
HR and SpO2 windows. Pressing the Mute/Cancel button silences the audible
alarm for 30 seconds. To resolve the alarm, remove the probe from the device
and put the pulse oximeter in standby “stby”. Contact the service center for
additional information.
Mitigation/ Resolution: Pulse Ox Module, Internal Failure, SpO2 /HR Not
Available from Pulse Ox, Turn Off Pulse Ox, Remove SpO2 Cable From
Ventilator
If Not Resolved: **Contact Service Center**
2301
Self Check Fault
Description: Alarm triggers when the communication between the pulse
oximeter module and device fails. When this occurs the user must turn off the
pulse oximeter monitor to end the alarm condition through the SpO2 Context
menu while also removing the probe from the device. When this is done “stby“
displays in the parameter windows for SpO2 and HR as those parameters are no
longer available. When appropriate the user should replace the ventilator and
contact the service center for additional information.
Mitigation/ Resolution: Internal COMM: Pulse Ox Module, SpO2 /HR Not
Available from Pulse Ox, Turn Off Pulse Ox, Remove SpO2 Cable from
Ventilator
If Not Resolved: **Contact Service Center**
2314
Pulse Ox Sensor
Off Patient
Description: Alarm triggers when a pulse oximeter sensor loses the patient
signal. The most common cause is when the sensor disconnects from the patient
or is misaligned with the sensor site. This alarm can also be caused by poor
perfusion at the sensor site which doesn’t provide an adequate signal. In these
cases try another site. Replace the sensor if another sensor is available. If the
alarm condition cannot be resolved the user should remove the sensor from the
patient and put the pulse oximetry monitor in standby “stby”.
Mitigation/ Resolution: Check Pulse Ox Sensor Site, Check Patient for
Peripheral Pulse, Change Placement, Check Sensor Operation, Replace
Sensor,
If Not Resolved: **Turn Off Pulse Ox Monitoring**
5-28
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906-0731-01-05 Rev G
Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution
2401
SpO2 Low
Description: Alarm triggers whenever the SpO2 value drops below the Low
SpO2 Limit. The default value for the limit is 94%. Corrective actions are
increasing oxygenation by increasing the FIO2 or PEEP settings. PEEP should
only be changed based on consultation with the attending physician. When using
low flow O2 the user should increase the flow of O2 to the low flow O2 reservoir.
Mitigation/ Resolution: SpO2 Below Limit, Increase FIO2, Check O2
Supply, Increase PEEP Per Physician
If Not Resolved: **Consult Physician**
2410
Heart Rate High
Description: Alarm triggers when the heart rate is greater than the High Heart
Rate Limit. The default value for the limit is 120 beats/minute. The user should
consult with the attending physician on how best to reduce the heart rate to an
acceptable level.
Mitigation/ Resolution: Heart Rate Above Limit, Check High Limit Setting
If Not Resolved: **Consult Physician**
2411
Heart Rate Low
Description: Alarm triggers when the heart rate is less than the Low Heart Rate
Limit. The default value for the limit is 40 beats/minute. The user should consult
with the attending physician on how best to increase the heart rate to an
acceptable level.
Mitigation/ Resolution: Heart Rate Below Limit, Check Low Limit Setting
If Not Resolved: **Consult Physician**
2421
Self Check Fault
Description: Alarm triggers when there is a failure of the input protection circuit
and the device is able to operate. The alarm will continue until the device is
turned off. The user can mute the alarm for 30 seconds by pushing the Mute/
Cancel button. The user should replace the ventilator and contact the service
center for additional information.
Mitigation/ Resolution: Power System, Power System Needs Repair,
Internal Battery Operation, Monitor Battery% Charge
If Not Resolved: **Contact Service Center**
2423
Self Check Fault
Description: Alarm triggers when the internal power circuit has failed and
external power is connected but cannot be used. The fault cannot be repaired by
the user. Pressing the Mute/Cancel button silences the audible alarm for 30
seconds. Replace the ventilator and contact the service center for additional
information.
Mitigation/ Resolution: Power System, Power System Needs Repair,
Internal Battery Operation, Monitor Battery% Charge
If Not Resolved: **Contact Service Center**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution
2430
Nearly Drained
Battery
Description: Alarm triggers when the device detects that there is ≤ 5 minutes of
battery operation remaining and external power is not connected. The user
should immediately seek a source of external power and/or plan to provide
manual ventilation. Attaching external power will immediately clear the alarm
though a low priority alarm will remain until the internal battery has recharged so
that the device can provide 30 minutes of operating time. This will take
approximately 5 to 10 minutes. If recharging the battery does not resolve the
issue, contact the service center for additional information.
Mitigation/ Resolution: ≤ 5 Minutes Operation, Connect External Power,
Ensure Ability to Manually Ventilate
If Not Resolved: **Contact Service Center**
2450
Battery Discharge
Fault
Alarm triggers when the battery temperature reaches 70 °C which is
5 °C from its maximum operating temperature using the internal battery and
external power is not connected. When the battery temperature reaches
75 °C the battery will shut down to prevent failure and the device will sound a
high priority alarm and shutdown. If possible the user should provide a source of
external power which will allow operation to continue at the current and higher
temperatures. In addition, the device should be removed from the soft case
which acts as insulation. Shading the patient and ventilator from direct sunlight
may also help reduce the battery temperature.
Mitigation/ Resolution: Battery Within 5 °Cof High Limit, Remove Padded
Case, Ensure External Power Available, Ensure Ability to Manually
Ventilate
If Not Resolved: **Move To Cooler Location**
2455
Battery Fault
Description: Alarm triggers when the device is not able to communicate with the
internal battery. When this occurs the device does not know the current charge of
the battery and operation could stop at any time. To continue operation and the
user should connect external power and ensure the ability to manually ventilate
the patient. When external power is connected the alarm priority decreases to
Low Priority, replace the ventilator and contact the service center.
Mitigation/ Resolution: Battery Communication, Connect External Power,
Ensure Ability to Manually Ventilate Patient
If Not Resolved: **Contact Service Center**
5-30
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906-0731-01-05 Rev G
Chapter 5 Alarms
Low Priority Alarms
Service
Code
Alarm Name
Mitigation/Resolution Instructions
3001
Self Check Fault
Description: Alarm triggers when the compressor fails to operate or fails to
provide the flow required to deliver a breath within ±10% of the current settings,
high pressure O2 is available to provide ventilation and the user has set the FIO2
to 100%. While operating in this state the user should ensure an adequate
supply of O2. Failure to maintain the O2 supply will result in a high priority alarm.
The user cannot repair the compressor, replace the ventilator and contact the
service center for additional information.
Mitigation/ Resolution: Pneumatic System: Compressor, Ensure 55 psig/
380 kPa O2, O2 Operation Only
If Not Resolved: **Contact Service Center**
3002
Self Check Fault
Description: Alarm triggers when communication between the compressor
controller and SPM is lost, high pressure O2 is available to provide ventilation
and the user has set the FIO2 to 100%. While operating in this state the user
should ensure an adequate supply of O2. Failure to maintain the O2 supply will
result in a high priority alarm and loss of ventilation. The user cannot repair the
device, replace the ventilator and contact the service center for additional
information.
Mitigation/ Resolution: Pneumatic System: Compressor, Ensure 55 psig/
380 kPa O2 Supply, O2 Operation Only
If Not Resolved: **Contact Service Center**
3011
Self Check Fault
Description: Alarm triggers when the signal to the O2 valve is outside of the
calibration range for the required flow rate, the compressor is available to provide
ventilation and the user has acknowledged that ventilation is being provided
using the compressor by setting the FIO2 to 21%. While operating in this state
the user should monitor the SpO2 to ensure that adequate oxygenation is
maintained. If low flow O2 is available it can be entrained through the Fresh Gas/
Emergency Air Inlet port using the optional O2 reservoir. Maintain an acceptable
SpO2 by adjusting the O2 supply up or down to increase or decrease the amount
of O2 delivered to the patient. The user cannot repair the O2 valve, replace the
ventilator and contact the service center for additional information.
Mitigation/ Resolution: Pneumatic System: O2 Valve, Compressor
Operation Only!, Keep FIO2 at 21%, Connect Low Flow O2, Monitor
SpO2
If Not Resolved: **Contact Service Center**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution Instructions
3012
Self Check Fault
Description: Alarm triggers when communication between the O2 valve and
SPM is lost, the compressor is available to provide ventilation and the user has
set the FIO2 to 21%. While operating in this state the user should monitor the
SpO2 to ensure that adequate oxygenation is maintained. If low flow O2 is
available it can be entrained through the Fresh Gas/Emergency Air Inlet port
using the optional O2 reservoir. Maintain an acceptable SpO2 by adjusting the O2
supply up or down to increase or decrease the amount of O2 delivered to the
patient. The user cannot repair the O2 valve, replace the ventilator and contact
the service center for additional information.
Mitigation/ Resolution: Pneumatic System: O2 Valve, Compressor
Operation Only!, Keep FIO2 at 21%, Connect Low Flow O2, Monitor
SpO2
If Not Resolved: **Contact Service Center**
3030
Gas Intake Fault
Description: Alarm triggers when the Fresh Gas/Emergency Air Inlet is blocked
so that the compressor is not able to deliver breaths within ±10% of the current
settings, high pressure O2 is available to support ventilation and the user has set
the FIO2 to 100%. To clear the alarm, clear the blockage and set the FIO2 back
to the original value. If the blockage is cleared operation with the compressor will
restart. If the blockage is not cleared, the alarm will resound, set the FIO2 to
100%, continue ventilation and ensure an adequate supply of O2. It is possible
for this alarm to be a false alarm that is triggered in a very high vibration
environment or if the device is not mounted correctly. If the alarm does not
resolve contact the service center for additional information.
Mitigation/ Resolution: O2 Supply Operation, Clear Blocked Intake,
Reset FIO2 to Previous, Monitor SpO2
If Not Resolved: **Contact Service Center**
3031
Intake Restricted
Description: Alarm triggers when the Fresh Gas/Emergency Air Inlet is blocked
but is still capable of delivering breaths within ±10% of the current settings. This
could be caused by an external blockage or a dirty/wet external or internal filter. If
the blockage is cleared the alarm will automatically cancel. Refer to instructions
for changing the internal filters. If the problem does not resolve contact the
service center for additional information. On rare occasions, this alarm can be
triggered by a patient with a very high inspiratory demand. In this case decrease
the rise time or shorten the inspiratory time to increase the inspiratory flow rate.
Mitigation/ Resolution: Clear Fresh Gas Intake, Check Filter for Moisture
or Dirt, OR, Manage Settings / Inspiratory Demand
If Not Resolved: **Manually Ventilate Patient**
3032
Self Check Fault
Description: Alarm triggers when communication between the Fresh Gas/
Emergency Air Inlet pressure sensor is lost. Normal operation can continue but,
if the condition is not cleared by powering off and restarting the device should be
replaced when appropriate as. When used during this alarm condition the user
should be sure to keep the Fresh Gas/Emergency Air Inlet clear and ensure that
external filters are checked regularly.
Mitigation/ Resolution: Pneumatic Sensor, Ventilator Operating, Unable
to Detect Inlet Obstruction
If Not Resolved: **Contact Service Center**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution Instructions
3041
High O2 Supply
Fault
Description: Alarm triggers when the high pressure O2 supply is ≥ 80 psig
(552 kPa) and < 87 psig (600 kPa). The alarm automatically cancels when the
supply pressure is < 80 psig (552 kPa). Pressure above 87 psig (600kPa) could
result in a catastrophic failure, harm to the patient and/or damage to the device.
The user should reduce the O2 supply pressure, sometimes this requires
replacing the regulator that is not functioning correctly. If the pressure cannot be
reduced and a low flow device like a flow meter is available the user can provide
supplemental O2 via the optional low flow O2 reservoir. If not, the user should
monitor the O2 supply pressure and ensure that the pressure does not rise
further.
Mitigation/ Resolution: Decrease O2 Supply Pressure, Replace
Regulator, Connect Low Flow O2, Monitor SpO2
If Not Resolved: **Monitor O2 Supply Pressure**
3073
Tubing Compliance
Fault
Description: Alarm is triggered when the tubing compliance correction shows
that it is > the set tidal volume indicating that the patient may not be receiving the
appropriate tidal volume. In this case the user should assess the patient and
settings. Consult the attending physician if there are questions about how to
configure the ventilator correctly to support the patient.
Mitigation/ Resolution: Calculated Compliance Volume Larger than
Delivered Volume, Check Tubing Compliance vs. Circuit
3091
Auto-PEEP
Description: Alarm triggers when the exhaled flow from the patient continues
throughout the expiratory period causing the expiratory control valve to cycle
throughout the period to maintain the baseline pressure. When this occurs the
user should increase the expiratory period by decreasing the inspiratory time,
decreasing the breathing rate or both. The physician should also be consulted as
this alarm is an indication that AutoPEEP is occurring. Note: at startup, this alarm
is off. The user can choose to activate the alarm if they believe the patient is at
risk of AutoPEEP using the Alarm Configuration submenu that is access using
the Menu.
Mitigation/ Resolution: Increase Expiratory Time, Decrease Inspiratory
Time, Decrease Respiratory Rate, Disable Alarm,
If Not Resolved: **Consult Physician**
3092
Inspiratory Demand
Description: Alarm triggers when the end-inspiratory pressure is < -1.0 cm H2O
(hPa) for 3 consecutive breaths. This can occur due to changes in the patient’s
status, where the patient attempts to inhale more gas than what is currently set.
When this occurs, the user should note if the patient is breathing or fighting with
the ventilator. The user should increase the flow rate (by decreasing the
inspiratory time) and/or reduce the rise time. The physician should be consulted.
Mitigation/ Resolution: Patient May be Breathing with the Ventilator,
Increase I Time and/or Decrease Rise Time, Check Patient and Circuit
for Leaks, Disable Alarm
If Not Resolved: **Consult Physician**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution Instructions
3110
RTC Battery Low
Description: Alarm triggers when the real-time clock (RTC) battery is < ~2.5
VDC. The alarm condition is checked at start up and if this alarm occurs the
device is safe to operate but the user should replace the device when
appropriate and consult the service center for additional information. The user
cannot change the RTC battery. The RTC battery provides power for the clock
that tracks the local time. It is replaced every 4 years during preventive
maintenance.
Mitigation/ Resolution: Vent Fully Functional
If Not Resolved: **Contact Service Center**
3120
PM Due
Description: Alarm triggers at start up when the preselected number of days has
elapsed since the last calibration. When appropriate the device should be
replaced and sent for preventive maintenance. The low priority message serves
as a reminder. Calibration is due every 365 days or 730 days for devices
configured for stockpile use (check with your organization regarding the
configuration of your device). Users should schedule the device for service as
soon as possible. Users can suspend the yellow alarm notification for the current
use by turning the alarm off using the Alarm Configuration submenu in the Menu.
Mitigation/ Resolution: Preventive Maintenance Due, Ventilator
Functioning with No Faults
If Not Resolved: **When Appropriate, Contact Service Center**
3121
Power Cycle
Needed
This alarm occurs when the device has been running continuously for 30 days. In
order to check the flow pneumotach, which is done a startup, the user should
manually ventilate the patient and cycle the power. Once this is done the user
can select the Last Settings options from the Start Menu and continue operation
if not faults are detected during the self check. If nonoperating alarms occur,
contact the service center for additional information.
Mitigation/ Resolution: Power-on Self Checks are Due, When
Appropriate, Power Off Then On, Verify Proper Settings
If Not Resolved: **Review Manual For Additional Information**
3130
Self Check Fault
Description: Alarm triggers when the ambient pressure transducer fails. When
this occurs, the device is no longer able to automatically compensate for
changes in altitude especially in situations where the ambient pressure could
change rapidly as during transport by air. When this alarm is active during
aeromedical transport the user should ventilate using pressure targeting if the
ventilator cannot be replaced. Users should also monitor chest rise and breath
sounds to ensure adequate ventilation.
Mitigation/ Resolution: Sensor: Barometer, Altitude Compensation
Disabled, Maintain Airway Pressure, Check Patient Chest Rise, Avoid
Use At Varying Altitude
If Not Resolved: **Contact Service Center**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution Instructions
3131
Excessive Altitude
Description: Alarm triggers when the ambient pressure transducer detects an
altitude > 25,000 ft. Beyond this altitude compensation remains fixed at the
25,000 ft compensation level. The user should monitor the airway pressure and
reduce the tidal volume as altitude increases though, there is very little change in
performance over this altitude. Where possible cabin pressure should be
maintained in the compensated range.
Mitigation/ Resolution: Beyond Altitude Compensation Limit, Maintain
Airway Pressure, Check Patient Chest Rise, Monitor Ventilator/Patient
If Not Resolved: **Reduce Altitude/ Pressurize Cabin if Possible**
3132
Low Altitude
Description: Alarm triggers when the ambient pressure transducer detects an
altitude of -2,000 ft below sea level. This can be caused by use in a subterranean
rescue operation or mistaken use in a hyperbaric chamber.
Note: The device is not intended for use in hyperbaric chambers or at hyperbaric
pressures.
Mitigation/ Resolution: High Barometric Pressure Detected, Beyond
Compensation Limit, Maintain Airway Pressure, Check Patient Chest
Rise, Monitor Patient and Ventilator
If Not Resolved: **Reduce Ambient Pressure**
3140
Ambient
Temperature Fault
Description: Alarm triggers when the ambient temperature exceeds the normal
operating range, > 55 °Cfor the ventilator. The device allows operation at these
temperatures but alerts the user to the condition. Operating above the specified
range can affect the longevity of the internal battery and the duration of operating
time. When operating at high temperatures the user should remove the padded
case which insulates and increases the ventilator’s internal temperature.
Mitigation/ Resolution: High Temperature Detected, Remove Padded
Case
If Not Resolved: **Monitor Patient and Ventilator**
3141
Ambient
Temperature Fault
Description: Alarm triggers when the ambient temperature falls below the
normal operating range < -10 °C for the ventilator. The device allows operation at
these temperatures but alerts the user to the condition. Operating below the
specified range can affect the longevity of the internal battery and the duration of
operating time. At extreme cold temperatures operating time can be significantly
reduced. When operating at low temperatures always use the padded case
which insulates and increases the ventilator’s internal temperature.
Mitigation/ Resolution: Low Temperature Detected, Use Padded Case
If Not Resolved: **Monitor Patient and Ventilator**
3143
Self Check Fault
Description: Alarm triggers when there is failure of the internal temperature
sensors. When this occurs the sensors are no longer able to detect when the
device is operating outside of its specified temperature range, and the user
should replace the ventilator and contact the service center for additional
information.
Mitigation/ Resolution: Environmental Sensor: Temperature, Ventilator
Operating, Service Required
If Not Resolved: **Contact Service Center**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution Instructions
3172
Self Check Fault
Description: Alarm triggers when the device is not able to zero the airway
pressure transducer during the autocal cycle. When this occurs the device is still
able to monitor the airway pressure safely. Large changes in temperature should
be avoided which can affect the calibration of the transducer. This alarm can also
be triggered when the device is exposed to excessive vibration and/or is
mounted in a vehicle in a manner that increases its exposure to vibration. If the
alarm continues, replace the ventilator and contact the service center for
additional information.
Mitigation/ Resolution: Pneumatic Sensor: Autocal, Reduce Vibration if
Possible, Avoid Temperature Changes, Autocal Suspended
If Not Resolved: **Contact Service Center**
3300
Self Check Fault
Description: Alarm triggers when the pulse oximeter module fails and the user
has turned off pulse oximeter monitoring acknowledging the condition. When this
is done “stby“ appears in the parameter windows for SpO2 and HR as those
parameters are no longer available. When appropriate the user should replace
the ventilator and contact the service center for additional information.
Mitigation/ Resolution: Pulse Ox Module Not Available, SpO2 /HR Not
Available
If Not Resolved: **Contact Service Center**
3301
Self Check Fault
Description: Alarm triggers when the communication between the pulse
oximeter module and device fails and the user has turned off pulse oximeter
monitoring acknowledging the condition. When this is done “stby“ appears in the
parameter windows for SpO2 and HR as those parameters are no longer
available. When appropriate the user should replace the ventilator and contact
the service center for additional information.
Mitigation/ Resolution: Internal COMM: Pulse Ox, Pulse Ox Module
Failure, SpO2/HR Not Available
If Not Resolved: **Contact Service Center**
3310
Pulse Ox Sensor
Not Connected
Description: Alarm triggers when the pulse oximeter detects that no SpO2
sensor is connected after a period of successful operation. NOTE: During start
up the device automatically detects if a sensor is connected. If it is, the device
begins operation with the pulse oximeter active. If no sensor is detected the
device turns off this function. If the sensor is properly connected this failure can
also be the result of a broken or defective sensor. If the alarm condition cannot
be resolved the user should remove the sensor and turn off pulse oximetry
monitoring using the SpO2 Context menu to put the monitor in standby. Contact
the service center for additional information.
Mitigation/ Resolution: Check Pulse Ox Sensor, Check Sensor/Ventilator
Connection, Reinsert Sensor, Replace Cable/Sensor, Replace Sensor
If Not Resolved: **Contact Service Center**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution Instructions
3311
Defective Pulse Ox
Sensor
Description: Alarm triggers when the pulse oximeter cannot identify the
connected sensor or the sensor has failed. Causes for this alarm include: broken
sensor cable, inoperative sensor LEDs and/or faulty detector. If the alarm
condition cannot be resolved the user should suspend pulse oximetry monitoring
by placing it in standby “stby” using the SpO2 Context menu.
Mitigation/ Resolution: Check Pulse Ox Sensor, Check Sensor/ Ventilator
Connection, Reinsert Sensor, Cable/Sensor Damaged?, Replace
Sensor
If Not Resolved: **Turn Off Pulse Ox Monitoring**
3312
Pulse Search
Description: Alarm triggers when the pulse oximeter is searching for a pulse
signal. If a value is not displayed within 30 seconds disconnect and reconnect
sensor and reapply to the patient. If pulse search continues, relocate it to a site
that may have better perfusion. Replace the sensor if another sensor is
available. If the alarm condition cannot be resolved the user should suspend
pulse oximetry monitoring by placing it in standby “stby”.
Mitigation/ Resolution: Please Wait Acquiring Signal, Check Sensor
Placement, Change Placement of Probe, Minimize Patient Movement,
Check Sensor Operation/Replace
If Not Resolved: **Turn Off Pulse Ox Monitoring**
3313
Pulse Ox Signal
Interference
Description: Alarm triggers when an outside signal or energy source prevents
accurate reading by the device. When this occurs the patient should be moved
from the location or pulse oximeter turned off.
Mitigation/ Resolution: External Signal Interfering With Measurement,
Remove Patient From Location
If Not Resolved: **Turn Off Pulse Ox Monitoring**
3315
Ambient Light Fault
Description: Alarm triggers when there is too much ambient light on the SpO2
sensor or there is inadequate tissue covering the sensor detector. Most often this
alarm condition can be resolved by shielding the sensor from ambient light.
Mitigation/ Resolution: Too Much Ambient Light, Shield Sensor From
Light, Change Sensor Placement, Check Sensor Operation, Replace
Sensor
If Not Resolved: **Turn Off Pulse Ox Monitoring**
3316
Invalid Pulse Ox
Sensor
Description: Alarm triggers when the pulse oximeter does not recognize the
connected sensor, i.e. a non-Masimo sensor. The alarm can also occur when
there is a broken sensor cable, inoperative LEDs, a fault is detected and/or the
sensor has failed. To resolve the alarm condition the sensor should be replaced.
If the alarm condition cannot be resolved the user should turn off pulse oximetry
monitoring by placing it in standby “stby”.
Mitigation/ Resolution: Replace Sensor
If Not Resolved: **Turn Off Pulse Ox Monitoring**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution Instructions
3317
Low SpO2
Perfusion
Description: Alarm triggers whenever the amplitude of the arterial pulsation is
weak. Low perfusion typically occurs in patients with poor circulation or when the
sensor is applied to the same limb as the noninvasive blood pressure (NIBP)
cuff. To resolve the alarm condition, move the sensor to a better perfused site or
to another limb if the interference is from the NIBP cuff.
Mitigation/ Resolution: Pulse Signal Weak, Check Sensor Placement,
Change Sensor Placement, Check Sensor Operation
If Not Resolved: **Turn Off Pulse Ox Monitoring**
3318
Low SpO2
Perfusion
Description: Alarm triggers when the pulse oximeter determines the quality of
the input signal is low due to excessive motion or artifact. To resolve the alarm
minimize patient movement and make sure the sensor is properly applied.
Mitigation/ Resolution: Signal Artifact, Minimize Patient Movement,
Check Sensor Placement, Check Sensor Operation
If Not Resolved: **Turn Off Pulse Ox Monitoring**
3421
External Power Low
/ Disconnect
Description: Alarm triggers when the external power (either AC or DC) drops
below minimum level (~11 VDC as supplied by either the AC/DC Power Supply
or a direct DC source) or power is intentionally disconnected. Since the device
operates with either external power or using its internal battery this is a low
priority alarm that clears when the user presses the Mute/Cancel button.
Pressing the Mute/Cancel button is the user’s acknowledgment that the device is
operating on internal battery. If this alarm occurs and the user believes that the
device is still connected to external power the user should investigate the
external power source and contact the service center for additional information.
Mitigation/ Resolution: Internal Battery Operation, Check Power
Connection/Supply, Monitor Battery Status
If Not Resolved: **Contact Service Center**
3422
Battery Fault
Description: Alarm triggers when the internal battery has been removed or
communication between the battery and CPU has failed. When external power is
applied the device is capable of operation however, loss of external power will
result in loss of ventilation and a high priority alarm. Operating in this state
should only be done when no other alternatives are available.
Mitigation/ Resolution: Battery Power Not Available, DO NOT Remove
External Power!, Maintain External Power
If Not Resolved: **Contact Service Center**
3423
Battery Charging
Fault
Description: Alarm triggers when the battery charging circuit fails. When this
alarm is active, the battery cannot be charged. The device can only run with
external power. If power is lost, ventilation will stop and a high priority alarm will
trigger. Operating in this state should only be done when no other alternatives
are available. Contact the service center for additional information.
Mitigation/ Resolution: Ventilator Operating, Power System Needs Repair,
Battery Cannot Charge, Maintain External Power
If Not Resolved: **Contact Service Center**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution Instructions
3430
Low Battery
Description: Alarm triggers when the device detects that there is < 30 minutes
of battery operation remaining and no external power is connected. The user
should seek a source of external power and/or plan to provide manual
ventilation. Attaching external power will immediately clear the alarm however,
SC: 3431 will occur in its place, see below.
Mitigation/ Resolution: < 30 Minutes Operation, Connect External Power,
Ensure Ability to Manually Ventilate
If Not Resolved: **Contact Service Center**
3431
Low Battery
Description: Alarm triggers when external power is connected to a device that
has an internal battery that has drained to a low battery status. The device is
warning the user that in the event of an external power failure the device has <
30 minutes of backup. This alarm will resolve when the internal battery charge
has > 30 minutes of operation. The user must maintain constant monitoring of
the device and the patient during this period.
Mitigation/ Resolution: < 30 Minutes Operation, Operating With External
Power, Continue Charging With External Power, Ensure Ability To
Manually Ventilate
If Not Resolved: **Contact Service Center**
3441
External Power
Fault
Description: Alarm triggers when the supplied DC power is > 33 VDC. When
this occurs the device automatically switches to operation using the internal
battery. If the supplied voltage drops to < 30 VDC the device automatically
returns to operation using external power. If the external power source is known
to be good then the AC/DC Power Supply may be faulty and need replacement.
Contact the service center for additional information.
Mitigation/ Resolution: External Voltage Too High, Internal Battery
Operation, Check/Replace Power Supply
If Not Resolved: **Remove DC Connection**
3442
External Power
Fault
Description: Alarm triggers when the external power supply has insufficient
current. When this occurs the device automatically switches to operation using
the internal battery. If the external power source is known to be good then the
AC/DC Power Supply may be faulty and need replacement. Contact the service
center for additional information.
Mitigation/ Resolution: External Power Insufficient Current, Internal
Battery Operation, Check/Replace Power Supply
If Not Resolved: **Remove DC Connection**
3444
External Power
Fault
Description: Alarm triggers when the voltage polarity is reversed when the
device is attached to an external DC source. When this occurs the device
automatically switches to operation using the internal battery. This condition is
most likely caused by a faulty DC source. The user should seek an alternate
power source.
Mitigation/ Resolution: DC Voltage Reversed, Internal Battery Operation,
Disconnect Power Source
If Not Resolved: **Replace Power Source**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution Instructions
3450
Battery Discharge
Fault
Description: Alarm triggers when the battery temperature reaches 70 °C
which is 5 °C from its maximum operating temperature and external power is
connected. When the battery temperature reaches 75 °C
the battery will shut down to prevent failure. When this occurs the device will
continue operation using external power only. The device should be removed
from the padded case which acts as insulation. Shading the patient and ventilator
from direct sunlight may also help reduce the battery temperature.
Mitigation/ Resolution: Battery Within 5 °C of High Limit, Remove
Padded Case, Continue External Power Operation, Shade Patient and
Ventilator
If Not Resolved: **Move To Cooler Location**
3451
Battery Discharge
Fault
Description: Alarm triggers when the battery temperature reaches ≥ 75 °C
and external power is connected. Discharging the battery beyond this
temperature could destroy the battery and damage the device. During the alarm
condition the device will continue operation using external power. The device
should be removed from the padded case which acts as insulation. Shading the
patient and ventilator from direct sunlight may also help reduce the battery
temperature.
Mitigation/ Resolution: Battery Too Hot to Discharge, Do NOT Remove
External Power!, Remove Padded Case, Ensure Ability to Manually
Ventilate Patient
If Not Resolved: **Move To Cooler Location**
3452
Battery Charging
Fault
Description: Alarm triggers when the battery temperature is > 45 °C. Charging
the battery above this temperature could destroy the battery and damage the
device. During the alarm condition the device continues to operate using external
power and if external power is lost the device will operate using internal battery
power. The device should be removed from the padded case which acts as
insulation. Shading the patient and ventilator from direct sunlight may also help
reduce the battery temperature.
Mitigation/ Resolution: High Battery Temperature, Battery Does Not
Charge When It is Too Hot, Ensure External Power Available, Remove
Padded Case, Shade Patient and Ventilator
If Not Resolved: **Move To Cooler Location**
3453
Battery Charging
Fault
Description: Alarm triggers when the battery temperature is ≤ 0 °C. Charging
the battery below this temperature could destroy the battery and damage the
device. During the alarm condition the device continues to operate using external
power and if external power is lost the device will operate using internal battery
power. The padded case should be used because it provides insulation.
Mitigation/ Resolution: Battery Too Cold To Charge, Ensure External
Power Available, Use Padded Case
If Not Resolved: **Move to Warmer Location**
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Chapter 5 Alarms
Service
Code
Alarm Name
Mitigation/Resolution Instructions
3455
Battery Fault
Description: Alarm triggers when the device is not able to communicate with the
internal battery and external power is connected. To continue operation, the
device must remain connected external power. Use in this state should only be
done if there are no other alternatives. Contact the service center for additional
information.
Mitigation/ Resolution: Battery Communication, Do Not Remove External
Power, Ensure Ability to Manually Ventilate Patient
If Not Resolved: **Contact Service Center**
3470
Self Check Fault
Description: Alarm triggers when the device is no longer able to communicate
with the Power Interface Module (PIM). When this occurs the user should
monitor operation continuously, replace the ventilator when possible and ensure
the ability to manually ventilate the patient. Contact the service center for
additional information.
Mitigation/ Resolution: Power System, Power Management Fault, Ensure
the Ability to Manually Ventilate the Patient, Monitor Power Source
If Not Resolved: **Replace/Service Ventilator**
3480
Self Check Fault
Description: Alarm triggers when the device software detects that it has not
been calibrated with the SPM that is inside the device. This fault occurs when the
biomedical technician fails to recalibrate the device following an SPM change or
service. When this occurs the device should be replaced when appropriate and
sent to the service center.
Mitigation/ Resolution: Serial Number Mismatch, Hardware Compatibility
Failure, Update Calibration Records
If Not Resolved: **Replace/Service Ventilator**
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Chapter 6
Operating Environments
This chapter describes how to operate a ZOLL ventilator outside of a hospital environment.
The types of environments that we describe are:
•
•
•
•
•
Extending Battery Runtime
Transport environments
Harsh environments – prehospital and transport
Hazardous environments – in the presence of chemical and/or biological toxins
MRI environments – during MRI (magnetic resonance imaging) treatment
Extending Battery Runtime when External Power is
Unavailable
In environments where access to external power is not available, ZOLL testing demonstrates
that operators can extend internal battery runtime up to 20% by adjusting screen brightness
(See Chapter 4 for information on adjusting screen brightness). The table below lists ZOLL
testing battery runtime results for a new, fully charged battery at various levels of screen
brightness.
Ventilator Screen Brightness Setting
Approximate Fully-Charged Battery Runtime*
25 (Default)
10 Hours
16
11 hours
8
12 hours
* Testing conducted with ventilator operating with default adult settings
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Chapter 6 Operating Environments
Using the Ventilator in Transport Environments
The ventilator is designed to be used in the field and transport environments with include road
ambulances, fixed wing and rotary wing transport vehicles. The ventilator is intended to
operate on battery during transport.
Using the Ventilator in Harsh Environments
The ventilator is designed to operate in harsh prehospital environments and during air and
ground transport. In order to safely manage the patient, you must understand the operating
characteristics of the ventilator and diligently monitor the patient and device in these
environments. The device continuously monitors environmental conditions (temperature and
ambient pressure) and when it detects extreme environments, the device alerts you with a Low
Priority alarm which defines the operating condition and prompts your actions. Low Priority
alarms are advisory and you should remember that the device is operating as designed.
Airborne Particulates
Under normal operating conditions, the internal 2-stage filtration system protects the gas flow
path from particulates entrained through the Fresh Gas/Emergency Air Intake. However, when
operating in areas where fine dust or dirt is airborne due to wind or vehicle movement, you
should use a disposable bacterial/viral filter to preserve the internal filter. Using disposable
filters prevents you from having to change the ventilator’s internal filters and provides
additional protection to the internal gas path component. Visually inspect the filter for dust/dirt
build up for extended operation in harsh environments, you should change the filter as it
becomes dirty.
The primary effect of entrained particles is on the operation of the flow pneumotach used to
control the gas delivered to the patient. Dirt on the pneumotach screens affects the device’s
calibration. Cleaning the screens requires a biomedical technician to disassemble the device
and ultrasonically clean the screens. Using a filter in dusty environments prevents having to
remove the device from service for cleaning. In addition to using the filter, you can also keep
the device in the soft case, which will protect the device case and the LCD from being
scratched or damaged. It is also easier to clean the padded case following use in a dusty/dirty
environment than the device.
Caution
When the ventilator is deployed in dusty environments, but not in use, be sure to cover the Gas
Output using the red cap, provided by ZOLL, that covered the Gas Output when the ventilator
shipped.
Extreme Temperature Environments
The ventilator’s recommended operating range is from 0 to 40 °C. However, the ventilator can
operate over the extended range of with limitations on battery use (charge and runtime), and
can operate over the range of -26 to 55 °C during emergency situations.
For temperatures > 45 °C and < 0 °C the Li-ION batteries stop charging to prevent damage
through excessive heat building. To ensure maximum operating time, the device automatically
monitors the battery temperature and charges it whenever it is safe.
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Chapter 6 Operating Environments
Operating at High Temperatures
When operating the ventilator at high temperatures, you may observe alarm conditions
associated with Li-ION battery performance:
Note:
If the device is stored ready for use at the temperature extremes, users should note the
battery charging and discharging conditions identified below.
Charging — If operating using external power, the device may trigger an alarm when the
battery reaches its high charge temperature limit of45 °C (. At this temperature Li-ION
batteries stop charging to prevent damage through excessive heat building.
Compliance is a physical characteristic of the patient circuit that varies with temperature. The
circuit becomes more compliant as the temperature rises. The ventilator allows you to increase
the automatic compliance value when operating in hot environments via the main menu.
When operating at high temperatures, you should remove the device from its padded case,
which allows the device to pass heat into the surrounding environment.
Operating at Low Temperatures
When operating the ventilator at low temperatures, you may observe alarm conditions
associated with Li-ION battery performance:
Charging — If operating using external power, the device may issue an alarm when the battery
reaches its low charge temperature limit of 0 °C (.
Compliance is a physical characteristic of the patient circuit that varies with temperature. The
circuit becomes less compliant as the temperature drops. The ventilator allows you to decrease
the compliance value when operating in cold environments.
The O2 Valve operating performance can be affected by extremely low temperatures.
Consequently, at low temperatures, you should monitor the patient to ensure that the patient is
receiving adequate tidal volume and monitor the patient’s SpO2 readings.
At temperature ~ - 26 °C ( you may have to run the device for a few minutes to exercise the O2
Valve before attaching the ventilator to the patient.
When operating at low temperatures, you can improve performance by operating the device in
the padded case, which insulates the device and allows it to retain heat generated by the
compressor, circuit boards, and AC/DC Power Supply.
Altitude
ZOLL ventilators are designed to operate from 110 to 37.6 kPa (-2,250 to 25,000 ft). An
absolute barometric pressure sensor monitors ambient pressure and the device uses this
information to continuously correct the output of the device to maintain the ventilation
parameters. When the altitude is > 25,000 ft, the device activates a Low Priority alarm. When
this occurs, you should monitor the peak inspiratory pressure (PIP) and adjust the tidal volume
to maintain the PIP and monitor breath sounds and chest excursion to assure the device
maintains adequate ventilation. The tidal volume increases as altitude increases, so you should
look to prevent over-pressurization of the lung when the altitude increases beyond
> 25,000 ft. If changes are made above > 25,000 ft, you should revert to the initial settings once
operation resumes in the compensated range (the LED will turn from yellow to green).
Warning!
The device is not intended for hyperbaric operation. Use in a hyperbaric chamber can
result in harm to the patient and/or damage to the device.
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Chapter 6 Operating Environments
Rain and Snow
You should prevent exposing the device to rain or snow. Use the optional padded case provided
with the ventilator to protect it from rain and snow. The device is capable of operating in these
conditions if you keep the device in the padded case and use the rain flap that is provided with
the padded case. Under these conditions battery operation is required. and the Pulse Oximeter
patient cables are not connected to the device.The padded case and rain flap prevent rain and
snow from puddling on any of the device’s surfaces. In cases of driving rain, where water could
possibly enter the device’s compressor, you can use a bacterial/viral filter to protect the
compressor inlet.
Using the Ventilator in Hazardous Environments
You can use the ventilator in environments where chemical and/or biological toxins are present.
To do this safely, all gas delivered to the patient comes from either a pressurized medical-grade
O2 source and/or filtered ambient air entrained through the Fresh Gas/Emergency Air Intake.
You can choose between a bacterial/viral filter and a C2A1 Chemical/Biological filter based on
the direction of the Medical Control Officer. Hazardous environment filters are shown in
Figure 6-1.
To prevent the patient from breathing contaminated ambient air in the event of a ventilator
failure, the device contains an internal antiasphyxia valve that allows the patient to inspire gas
through the external filter. While this design assures that no contaminated gas reaches the
patient, you must ensure that nothing blocks the input of the external filter.
Warning!
The Medical Control Officer and/or Incident Commander should determine which, if
any, external filter is used based on the potential hazard.
Warning!
You must ensure that nothing blocks the inlet of the external filter; failure to do so could
prevent the patient from breathing and cause a ventilator failure.
Bacterial/Viral Filter Use
You can use Bacterial/Viral (B/V) filters in environments where the patient is at risk from cross
contamination of airborne pathogens. When used in accordance with the manufacturer’s
instructions, these filters can help prevent inhalation of infectious matter. In dusty
environments, you can also use the B/V filters to prevent entrainment of particulate matter that
could affect the ventilator’s pneumatic components. To use a bacterial/viral filter, insert the
filter's male 22 mm conical fitting into the Fresh Gas/Emergency Air Intake.
Warning!
6-4
If filters have been exposed to biological matter, dispose of them following the Universal
Precaution procedures for your facility.
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Chapter 6 Operating Environments
Chemical/Biological Filter Use
ZOLL ventilators are designed to allow attachment of chemical/biological filter/canister (type
C2A11) for use in contaminated environments. The Fresh Gas/Emergency Air Intake fitting
allows for attachment of standard Rd 40 x 1/7 threads. A complete description of this standard
can be found in BS EN 148-1:1999 Respiratory protective devices - Threads for face pieces.
Fresh Gas/Emergency Air Intake
Bacterial/Viral Filter
C2A1 Chemical/Biological Filter
Figure 6-1 Hazardous Environment Filters
Note:
ZOLL does not offer a C2A1 Chemical/Biological filter. This filter can be obtained
from a Chemical/Biological filter supplier.
Check Valve on Patient Circuit when in Hazardous Environments
When operating in a hazardous situation where a chemical/biological filter is in use, you should
use a check valve to prevent hazardous gas from entering the patient circuit. The exhalation
valve on the patient circuit is not adequate to protect patients if they rapidly inhale/exhale as the
valve may not fully close in time to prevent hazardous gas entrainment.
Also, if the PEEP is set low, patients may inhale faster than the flow is delivered which could
cause hazardous gas entrainment. Consequently, a Check Valve is required to protect patients.
Warning!
The device is shipped with both the pediatric/adult and infant/pediatric single limb
circuits. A check valve is required with these patient circuits when operating in
chemical/biological environments. The correct mating of the check valve with the
patient circuit is shown in Figure 6-2. Users who anticipate use in these environments
should also stock the check valve.
1. A 3M C2A1 canister (3M St. Paul, MN) was used in our validation testing to represent the class of filters
generically known as C2A1 under the NSN number 4240-01-361-1319. These tests confirmed the
performance of the ventilator when operating with these devices as a class. Use of the 3M canister does not
constitute endorsement or recommendation of the 3M device. Use and selection of the appropriate filter
should always be under the direction of the Incident Commander.
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Chapter 6 Operating Environments
Figure 6-2 Check Valve Connection To Patient Circuit
Using the Ventilator in an MRI Environment
You can use ventilator in an MRI environment using a ZOLL MRI Roll Stand with an
Aluminum IV Support Arm. To securely mount the ventilator, tighten the knob on the back
plate of the roll stand to hold the ventilator in position, then lock the roll stand wheels
(we also recommend that you tether the rolling stand in place). See Figure 6-3.
Ventilator secured
onto roll stand
Aluminum IV arm
Wheels locked in position
Figure 6-3 Ventilator Mounted on MRI Rolling Stand With IV Support Arm
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Chapter 6 Operating Environments
Warning!
Use only ZOLL ventilators marked with the MR Conditional symbol in an MRI
environment. Figure 6-4 shows the MR Conditional label and describes the location of it
on ventilator models supporting MRI environments. Figure 6-5 shows an example of
MR Conditional label placement the Z Vent ventilator model.
Before using the ventilator in an MRI environment, it is important that you read and
understand all warnings in the “MR Conditional Equipment” section of Chapter 1
Warning!
The ventilator must be placed behind the 130 Gauss line.
ZOLL offers 12 ft (3.7 m) patient circuits to accommodate the length required to place the
ventilator behind the 130 Gauss line.
Warning!
The use of longer breathing circuits may increase the risk of self-triggering ventilator
breaths. Reducing the pressure trigger sensitivity may solve this problem.
Figure 6-4 Conditional MR Label
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Chapter 6 Operating Environments
MRI Label
MR
Figure 6-5 Example: Conditional MR Label Placement on EMV+ Ventilator
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Chapter 7
Maintenance
This chapter describes how to maintain a ventilator to ensure its optimum working condition
and readiness for immediate use. Specifically, this chapter describes how to:
Inspect the device
Clean the device
Replace intake filters, as necessary
Store the device
Troubleshoot operational problems
In addition to the activities that we describe in this chapter, it is also important to perform
preventative maintenance, replacing worn or defective components, as necessary. Only
ZOLL-trained and certified personnel should perform preventative maintenance using
ZOLL’s Remote Calibration System (RCS) system.
•
•
•
•
•
Inspecting the Ventilator
You should perform the following physical inspections of the ventilator on a regular basis:
• Ensure that the ventilator is clean and free of visible damage.
• Inspect all accessories and connectors for signs of damage or excessive wear. Replace worn
or defective items.
• Examine high pressure hoses for cracking, discoloration, or disfigurement. Examine end
connection fittings for damaged threads and sharp edges. Replace worn or defective hoses
– Do Not attempt to repair hoses.
• Examine the ventilator circuits for damage or wear including cracking or discoloration. If
there are signs of physical degradation or the ventilator trigger circuit related alarms, replace
the patient circuit.
• Examine the Fresh Gas/Emergency Air Intake filters and replace them if dirty, damaged, or
clogged.
• Inspect the external AC/DC adapter, line cords, and DC power cables for wear or damage.
Replace if worn or damaged.
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Chapter 7 Maintenance
Configuration and firmware information appears on the display screen after powering on the
device. Additional device information is available through the Menu (select Unit Info),
including the device’s calibration date. For most customers, the ventilator operates on an annual
preventative maintenance cycle, and the device issues a low priority alarm to remind you when
calibration is due.
Note:
The alarm is based on a countdown timer. It does not indicate an issue with the
ventilator, only that 365 days have passed and you should schedule preventative
maintenance.
Cleaning
Keep the ventilator and its accessories clean at all times. Never allow grease or oil to enter the
system or coat its components.
Clean the device at regular intervals and maintain up-to-date records of inspections, cleaning,
and maintenance.
Take care to prevent liquids from entering the ventilator. Never submerge the ventilator and
avoid using excessive amounts of water that might enter the device. Dry all exposed parts
following use in wet environments.
Clean the device’s housing and hose connections with a damp, soapy cloth.
For general decontamination and cleaning, apply a 10% bleach solution with a damp cloth.
Do not clean the device with abrasives or chlorinated hydrocarbon cleansers, which damage the
housing and interface lens.
After cleaning, thoroughly dry the device with a lint-free cloth. Make sure that all exposed
surfaces are cleaned and dried.
Warning!
Never use oil or grease of any kind with oxygen or compressed gas equipment.
Post-Contaminated Environment Cleaning
If you have used the ventilator in an environment where it may have been exposed to
contamination from a hazardous materials accident, mass epidemic, or weapon of mass
destruction, we recommend that you follow these guidelines:
1. Always follow the decontamination procedures specified by the local Incident Command
Safety Officer.
2. You should clean and decontaminate the equipment as soon as possible after use. Personnel
should always wear the appropriate Personal Protective Equipment while decontaminating
equipment.
3. Review the cleaning instructions that we provide in the previous section.
4. Since the potential list of contaminants that the ventilator might be exposed to is so large, it
is difficult to provide an appropriate cleaning method for each type of exposure. An effective
cleaning agent for one type of exposure may not be effective with another. Cleaning and
sterilizing practices may vary between institutions. We suggest that each facility have in
place a procedure for the cleaning and disinfection of its medical equipment and that these
procedures to be consulted for further guidance.
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Chapter 7 Maintenance
Fresh Gas/Emergency Air Intake Filters
The Fresh Gas/Emergency Air Intake (located on the right side of the ventilator) has a two
stage filtering system: an easily accessible foam filter protects a second disk filter. As we
describe in Chapter 6, “Operating Environments,” additional filter protection may be necessary
when operating the device in extreme environments. These filters are replaced every year
during the preventative maintenance performed by a ZOLL authorized service center.
Inspecting and Replacing the Foam Filter
When used in dusty environments, you should inspect and replace, if necessary, the device’s
foam filter.
Remove the filter using a pair of tweezers or similar tool. Examine the filter for dirt, lint, or
general wear. Replace the foam filter, if necessary. DO NOT attempt to clean the filter.
Caution
Do not operate the compressor without a filter in place.
Inspecting and Replacing the Disk Filter
The Fresh Gas/Emergency Air Intake Disk Filter is located behind the Foam Filter. This filter
provides a second level of filtration to the ambient air that is delivered to the patient. You must
check this filter periodically and replace it if necessary. The ventilator triggers an alarm when
the combination of foam filter and disk filter become dirty. This alarm indicates that the device
is still able to deliver the correct tidal volume but one or more of its filters needs replacement.
You can visually inspect the Fresh Gas/Emergency Air Intake Disk Filter after the Foam Filter
is removed. If the filter appears discolored, replaced it.
Warning!
If filters are exposed to biological matter, dispose of them following Universal
Precaution procedures for your facility.
Caution
There are no user serviceable parts except the filter components above. Opening the case can
damage the ventilator.
Caution
When used in dusty/dirty environments, you should check the foam and disk filters, and replace
them as needed. This prevents particle build up on the transducer screen and the need to take the
device out of service for maintenance by a service technician.
Note:
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Do not attempt to clean this filter and do not operate the internal compressor without a
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Chapter 7 Maintenance
Replacing Ventilator Filters
Tools needed:
Hemostat or tweezers
Torque Driver (with #2 Phillips Bit)
Warning!
Before attempting to replace filters, make sure that external power is disconnected and
that the ventilator’s power switch is set to “OFF”.
Replacing the Foam Filter
The Foam Filter is located inside the
Fresh Gas/ Emergency Air Intake.
Foam Filter
1. Carefully remove the Foam Filter using a hemostat
or tweezers.
DO NOT reuse or attempt to clean the old filter.
2. Replace the Foam Filter with a new filter.
Lightly tap the new filter into place. The top of
the filter should reside approximately
19 mm to 22 mm below the height of the
22 mm female connector that is part of
the Fresh Gas/ Emergency Air Intake.
Replacing the Disk Filter
1. Remove the four (4) 8-32 x 3 Phillips
Flat Head screws that secure the Fresh
Gas/ Emergency Air Intake assembly
to the cover.
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Chapter 7 Maintenance
2. Lift the two (2) segments of the Compressor Inlet
Fitting Assembly away from the device. If the two
segments come apart, do not lose the gasket that seats
between the parts.
Alignment Pins
The Disk Filter is now exposed. Do not
remove the filter at this time.
Disk
Filter
3. Examine the surface of the Disk Filter.
Do not replace the Disk Filter if it isn’t
discolored. If the Disk Filter is discolored,
replace the filter.
4.
Remove the Disk Filter using the hemostat or
tweezers and replace it with a new, clean
filter. Make sure that the filter sits flat on the
shoulder in its recessed area.
5. Insert the lower segment of the
Compressor
Inlet Fitting Assembly into the device,
making sure that its alignment pin mates.
Shoulder
Alignment
Hole
6. Set the upper segment of the Compressor Inlet Fitting Assembly into the lower segment,
making sure that its alignment pin mates.
7. Secure the Compressor Inlet Fitting Assembly to the device by equally tightening each
of the four (4) 8-32 x 3 Phillips Flat Head screws. Tighten screws to 1.6 Nm.
Momentarily turn the device’s Power switch to its on position “I” to confirm operating
power, then turn the device’s Power switch to its off position “O”.
8. Test the operation of the ventilator using a patient circuit and test lung
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Chapter 7 Maintenance
Battery Maintenance
The ventilator uses a rechargeable Li-ION battery, which offers a wide operating temperature
range, and long operating time. Avoid exposing the battery to direct sunlight or heat sources.
Following the guidelines that we describe in this chapter prevents premature charge depletion
and reduction of the battery’s life.
Observe the warnings and cautions and that follow for safe use of the battery:
Warning!
If you witness a battery or the battery compartment starting to balloon, swell up,
smoke, or feel excessively hot, manually ventilate the patient, turn off the device,
disconnect external power, and observe it in a safe place for approximately 15 minutes
and send the device for service. Never puncture or disassemble the battery packs or
cells.
Caution
Only use the power supply provided with the device. Use of any other power supply could cause
damage or create a fire and/or destroy the battery and ventilator.
Caution
Never attempt to completely discharge the battery by shorting it or some other method and never
ship the battery in a completely discharged state.
Caution
During continuous, uninterrupted use (> 100 hours), you should disconnect the ventilator from
AC power for 30 seconds to allow the battery to run diagnostics while the battery is discharging.
Note:
The ventilator continuously monitors the available power sources; occasionally a false
Low Priority power alarm can be triggered for approximately 1 second. These false
alarms immediately clear themselves.
When operating from battery always monitor the battery charge state via the battery icon that
provides both a graphical and numeric indication of the remaining battery power. The ventilator
monitors temperature and controls the charging and discharging of the battery under the
following conditions:
• Best operating conditions are 15 to 40 °C
• - 20 to 60 °C for discharging
• 0 to 45 °C for charging
The battery rapidly recharges to 90% of its runtime in approximately 2 hours. It takes
approximately another 2 hours of trickle-charging to top off the battery to 100% of its runtime.
While in use, continuous connection to external power operates the ventilator and ensures a
fully charged battery. While off continuous connection to external powerfully charges the
battery.
Note:
Note:
7-6
When connected to power for an extended period of time (> 30 days), the device
indication may drop below 100% stored charge which allows the battery to perform
diagnostics. To reset, power cycle by removing and reconnecting the connection to
external power. Once this is done, the battery will recharge back to 100% in a few
minutes.
If when operating on battery power the device shuts down due to loss of power,
connect external power and power cycle the device to restore function.
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Chapter 7 Maintenance
Battery Storage
Li-ion batteries discharge during storage. Higher temperatures (above 20 °C) reduce the battery
storage life.
Follow these rules to ensure the best storage life of the ventilator’s batteries:
• Always store the ventilator with the battery fully charged. DO NOT store the ventilator with
the batteries discharged.
• For long-term storage, the optimum storage temperature range is -15 to 21 °C . Avoid
exposing the battery to direct sunlight or heat sources. It is not recommended to store
batteries at high temperatures (above 40 °C ).
• If long-term storage/non-use is common, recharge the device every six months; this ensures
that the battery charge is maintained at 80% capacity or better.
• When batteries are in extended storage, you should charge them at recommended intervals.
There is no need to store the device continuously connect to power. This can shorten the
useful life of the battery.
Ambient Storage Temperature
Recharge Interval
20 °C
12 months
20 to 30 °C
6 months
30 to 40 °C
3 months
Note:
Caution
When charging in the storage case, be advised that the battery may stop charging if
ambient temperature is above 40 °C, even though the device is still connected to
external power. Under these conditions, battery temperature can get considerably
hotter than the ambient temperature. Charging automatically starts when the battery
temperature drops below 45 °C.
DO NOT store the ventilator with batteries in a discharged condition.
Battery Replacement and Shipping Regulations
Only trained technicians at an authorized ZOLL Service Center can replace the ventilator’s
battery. Contact your local service center for return instructions and please note the following:
• Shipping of the ventilator’s battery should always use proper State of Charge (SOC), which
must never exceed 30%. The ventilator’s Rechargeable Li-Ion battery follows these and
other important regulations, which IATA/DOT UN 38.3 mandates.
• The ventilator’s battery is less than 100 Wh, and thus is Classified as Class 9 Exempt and
does not require Class 9 labeling or marking.
• Always check all applicable local, national, and international regulations before transporting
a Lithium-Ion battery.
• Transporting an end-of-life, damaged, or recalled battery may, in certain cases, be
specifically limited or prohibited.
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Chapter 7 Maintenance
Ventilator Storage
For optimal prolonged storage, you should store the ventilator indoors and follow the battery
storage recommendations described in this chapter.
The environment should be clean and out of direct sunlight. For storage in uncontrolled
environments, remove batteries from ventilator if temperatures might exceed the battery
storage temperature limits described in the section above.
The Gas Output port should be covered using the red Gas Output cap provided with the
ventilator at shipment.
Following 6 months (or longer) of continuous storage or non-use, inspect the device, perform
an Operational Test, and recharge the device’s batteries before attempting to use it with a
patient.
If the device has been stored in non-controlled environments (such as a vehicle), allow the
device sufficient time (three hours) to stabilize to a temperature within its specified operating
range. The ventilator is available with transit and carry case options. Follow the instructions
that we provide with the transit or carry case.
Calibration Checks
The ventilator continuously performs a self check to monitor the pneumatic system.
The ventilator’s calibration is checked as part of the annual service procedure. You should send
the ventilator for preventative maintenance:
• Every 12 months.
• Whenever significant usage or rough handling warrants a shorter period between
preventative maintenance inspections.
• Whenever you suspect the device is not functioning properly.
• Following mass deployment before the device is returned to storage.
If the ventilator fails the self-check, restart the device, if it fails again, it should be returned to
ZOLL or an authorized Service Center for calibration.
Pulse Oximeter Check
A Masimo pulse oximeter tester is available to confirm operation of the HR and SpO2
functions. The recommended tester is directly available from Masimo (PN 1593).
Note:
A functional tester cannot be used to assess the accuracy of a pulse oximeter probe or a
pulse oximeter monitor.
Electrical Safety Check
The ventilator’s power system has an internal protection system that continuously monitors the
device. In event of a fault or failure condition. the device triggers an alarm.
The ventilator is double insulated, and is categorized as IEC60601-1 Class I equipment.
The ventilator’s electrical safety design is not dependent on earth grounding as the means of
protection.
Safety checks include:
• Patient leakage
• DC HiPot testing
• Defibrillator applied parts testing
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Chapter 7 Maintenance
Troubleshooting
You can quickly address common problems by following the Smart Help instructions. Should
the device fail to operate properly, verify the integrity of all accessories, ventilator circuits, and
fitting connections. Check all control panel settings and follow the alarm mitigation
instructions provided in the Smart Help message(s).
Verify that the Fresh Gas/Emergency Air Intake disk filter and foam filter are not clogged or
dirty. Check for operating power from the internal battery and external power sources.
If the actions above do not resolve an operating problem, service is required. Note the service
code number(s) and contact the closest authorized ZOLL Service Center or the ZOLL
Customer Service Department ([email protected]).
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Appendix A
Specifications
General
Parameter
Operating Range
Operating Modes
AC, SIMV, CPAP with and without Pressure Support, BL Mode, and Leak
Compensation for Invasive and Noninvasive ventilation
Breath Target
Volume or Pressure
Flow Rate
0 to 100 LPM at 40 cm H2O (40 hPa)
Breath Rate
1 to 80 BPM ± 1 BPM over the interval
Setting Resolution: 1 BPM
Measurement: 1 to 90 BPM ± 1 BPM over the interval
Inspiratory Time (Ti)
Setting: 0 to 3 ± 0.1 sec for I:E from 1:1 to 1:99
0 to 5 ± 0.1 sec for I:E from 4.0:1 to 1:99 (Inverse I:E)
Setting resolution: 0.05 s
Tidal Volume
Setting: 50 to 2000 ml
Resolution: 10 ml (above 100 ml), 5 ml (below 100 ml)
Measurement: 50 ml to 2000 ml ± (5 ml + 10%) ATPD
FIO2
21 to 100% ± (3% of full scale ± 10% of setting)
PEEP/EPAP
Setting: 0 to 30 cm H2O (30 hPa)
Setting Resolution: 1 cm H2O (hPa)
Reading: 0 to 30 cm H2O ± (2 cm H2O + 8% of reading) or,
0 to 30 hPa ± (2 hPa + 8% of reading)
Peak Inspiratory Pressure
(PIP)
Setting: 0 to 80 cm H2O (0 to 80 hPa)
Setting Resolution: 1 cm H2O (hPa)
Reading: 0 to 99 cm H2O ± (2 cm H2O + 8% of reading) or
0 to 99 hPa ± (2 hPa + 8% of reading)
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Specifications
Parameter
Operating Range
Pressure Support (PS)/
IPAP
Setting: 0 to 60 cm H2O (kPa)
Setting Resolution: 1 cm H2O (kPa)
Reading: 0 to 60 cm H2O ± (2 cm H2O + 8% of reading) or,
0 to 60 kPa ± (2 kPa + 8% of reading)
Mean Airway Pressure
(MAP)
(0 to 99.9 cm H2O ± (2 cm H2O + 8% of reading) or,
(0 to 99.9 hPa ± (2 hPa + 8% of reading)
Airway Pressure High
Limit
Setting: 20 to 100 cm H2O (20 to 100 hPa)
Setting Resolution: 1 cm H2O (hPa)
Airway Pressure Low
Limit
Setting: Off, 3 to 35 cm H2O (3 to 35 hPa)
Setting Resolution: 1 cm H2O (hPa)
Breath Trigger
Setting: -6.0 to -0.5 cm H2O (-6.0 to -0.5 hPa)
Setting Resolution: .5 cm H2O (5 hPa)
Airway Pressure
Waveform
0 to 99 cm H2O ± (2 cm H2O + 8% of reading) or,
0 to 99 hPa ± (2 hPa + 8% of reading)
Minute Volume
0 to 99.9 liters per minute (trend)
Oxygen Input Pressure
Nominal: 55 psig (380 kPa)
Extreme Range: 40 to 87 psig (280 to 600 kPa)**
LED Status/Alarm
Indicator
Red, Yellow, and Green
Alarm Volume
82 dBA @ 1 meter
Noise Level
~60 dBA when measured at 1 meter (operating at default settings using the
compressor only)
Operating Voltages
AC Supply: 100 to 240 VAC (50/60 and 400 Hz) -- use only the AC/DC power supply
that ZOLL provides with the ventilator.
DC Supply: Nominal 12.5 to 28.0 VDC (accepts DC voltages between
11.8 to 30 VDC).
Operating Time
Internal Battery
10 hours at default settings*
Ventilator Temperature
Ranges*
Standard Operating Temperature: 14 °F to 104 °F (-10 °C to 40 °C)
Extended Operating Temperature: 9 °F to 120 °F (-13 °C to 49 °C)
Extreme Operating Temperature: 13 °F to 131 °F (-26 °C to 55 °C)
Battery Temperature
Ranges
Battery Charge: 32 °F to 113 °F (0 °C to 45 °C)
Battery Discharge: -4 to 140 °F (-20 to 60 °C)
Size
8.0” Wide X 12.5” High X 4.5” Deep (20.3 cm Wide X 31.8 cm High X 11.4 cm Deep)
Weight
~9.7 lbs (4.4 kg)
Altitude
Standard Altitude: 110 to 70 kPa (-2.250 ft to 10000 ft)
Extended Altitude: 70 to 57.2 kPa (10000 ft to 15000 ft)
Extreme Altitude: 57.2 to 37.6 kPa (15000 ft to 25,000 ft)
Extreme Operational
Humidity
15% to 95% non-condensing
Transport and Storage
Temperature: -40 °F to 158 °F (-40 °C to 70 °C)
Humidity: 15 to 95% RH (non-condensing)
Vibration
IEC 60068-2-6, IEC 60068-2-34, IEC 60068-2-36, IEC 60068-2-64
Shock
IEC 60068-2-27
Bump
IEC 60068-2-29
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Specifications
Parameter
Operating Range
Road Ambulance
EN 1789
EN 1789:2007+A2:2014 Medical vehicles and their equipment. Road ambulances.
(Sections applicable to medical device)
Commercial Aircraft
RTCA/DO-160G
Environmental Conditions and Test Procedures for Airborne Equipment Vibration
(Section 8): Fixed wing Category S and Helicopter Category U2, Zones 1&2
EMC (Section 21): Category M, Conducted and Radiated emissions
Shock/Vibration
MIL SRD 810G, Method 514.6, Procedure I:Jet Aircraft, Fixed Wing, and Rotary Wing
* No degradation of performance due to extended or extreme temperature environments. See Chapter 6 for battery
alarm indications and battery limitations.
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Specifications
Pulse Oximeter
Parameter
Specification
Range
Saturation (% SpO2):1% to 100%
Pulse Rate (bpm): 25 to 240
Perfusion: 0.02% to 20%
Accuracy
Saturation (% SpO2) - During No Motion Conditions:
Adults, Pediatrics: 70%-100% ± 2 digits, 0%-69% unspecified
Neonates: 70%-100% ± 3 digits, 0%-69% unspecified
Saturation (% SpO2) - During Motion Conditions
Adults, Pediatrics: 70%-100% ± 3 digits, 0%-69% unspecified
Neonates: 70%-100% ± 3 digits, 0%-69% unspecified
Pulse Rate (bpm)
Pulse Rate (bpm) - During No Motion Conditions:
Adults, Pediatric, Neonates: 5 to 240 ± 3 digits
Pulse Rate (bpm) - During Motion Conditions
Adults, Pediatric, Neonates: 5 to 240 ± 5 digits
Resolution
Saturation (% SpO2): 1%, Pulse Rate (bpm): 1
Low Perfusion
Performance
>0.02% Pulse Amplitude Saturation (% SpO2) ± 2 digits
and% Transmission >5% Pulse Rate ± 3 digits
Interfering Substances
Carboxyhemoglobin may erroneously increase readings. The level of
increase is approximately equal to the amount of carboxyhemoglobin
present. Dyes, or any substance containing dyes, that change usual
arterial pigmentation may cause erroneous readings.
Device Classification
The following table describes the ventilator’s device classification:
Category
A-4
Classification
Type of Protection against
Electric Shock
The medical power supply (which contains the system's safety
barrier) is labeled as Class I.
Degree of Protection against
Electric Shock
Applied Parts
The ventilator circuit is Type BF applied part.
The pulse oximeter is Type BF Defibrillation Proof Applied Part.
Degree of Protection against
Harmful Ingress of Water
IPX4: Splash-proof equipment rating, include:
• Padded case with rain flap
• Bacterial/viral filter to protect the compressor
Method of Sterilization or
Disinfection
O2 Supply hoses and connections should be wiped with a
damp, soapy cloth and thoroughly dried with a
lint-free cloth. The device’s housing should also be cleaned as
necessary with a damp, soapy cloth and throughly dried with a
lint-free cloth. Do not clean with abrasives or chlorinated
hydrocarbon cleansers.
Ventilator circuits are only for single use. Follow all IFU
instructions.
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906-0731-01-05 Rev G
Specifications
Category
Classification
Degree of Safety of Application in Equipment not suitable for use in presence of Flammable
the presence of a Flammable
Anesthetic Mixture of Air or with Oxygen or Nitrous Oxide
Anesthetic Mixture with Air or with
Oxygen or Nitrous Oxide
Mode of Operation
Continuous Operation
Emissions and Immunity Compliance
The device meets the electromagnetic tests as specified by regulations. The following tables
provide guidance as to the environments in which you can operate the device.
Emissions test
Compliance
Electromagnetic environment-guidance
RF emissions
CISPR 11
Group 1
The ventilator used RF energy only for their internal function.
Therefore, their RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
RF emissions
CISPR 11
Class A
Harmonic emissions
IEF 61000-3-2
Class A
The ventilator is suitable for use in all establishments other than
domestic and those directly connected to the public
low-voltage power supply network that supplies buildings used
for domestic purposes.
Voltage
fluctuations/flicker
emissions
IEC 61000-3-3
Complies
The ventilator is intended for use in the electromagnetic environment specified below. The
customer or user of the ventilator should ensure that they are used in such an environment.
Immunity Test
Test level
Compliance level
Electromagnetic environment-guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
± 6 kV contact
± 8 kV air
± 6 kV contact
± 8 kV air
Floors should be wood, concrete, or
ceramic tile. If floors are covered with
synthetic material, the relative humidity
should be at least 30%.
Electrical fast
transient/burst
IEC 61000-4-4
± 2 kV for power
supply lines
± 1 kV for
input/output lines
± 2 kV for power
supply lines
± 1 kV for
input/output lines
Mains power quality should be that of a
typical commercial or hospital
environment.
Surge
IEC 61000-4-5
± 1 kV line(s) to line(s)
± 2 kV line(s) to earth
± 1 kV line(s) to line(s)
± 2 kV line(s) to earth
Mains power quality should be that of a
typical commercial or hospital
environment.
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A-5
Specifications
Immunity Test
Test level
Compliance level
Electromagnetic environment-guidance
Voltage dips, short
interruptions, and
voltage variations
on power supply
input lines
IEC 61000-4-11
< 5% UT
(> 95% dip in UT)
for 0.5 cycles
40% UT
(60% dip in UT)
for 5 cycles
70% UT
(30% dip in UT)
for 25 cycles
< 5% UT
(> 95% dip in UT)
for 5 sec
< 5% UT
(> 95% dip in UT)
for 0.5 cycles
40% UT
(60% dip in UT)
for 5 cycles
70% UT
(30% dip in UT)
for 25 cycles
< 5% UT
(> 95% dip in UT)
for 5 sec
Mains power quality should be that of a
typical commercial or hospital
environment. If the user of the ventilator
requires continued operation during
power mains interruptions, it is
recommended that the ventilator be
powered from an uninterruptible power
supply or a battery.
Power frequency
(50/60) magnetic
field IEC 6100-4-8
3 A/m
3 A/m
Power frequency magnetic fields should
be at levels characteristic of a typical
location at a typical commercial or
hospital environment.
For devices labeled for MR
environments, follow the specific
directions that ZOLL provides.
Note:
UT is the AC mains voltage prior to application of the test level
Immunity Test
Test level
Compliance level
Electromagnetic environment-guidance
Portable and mobile RF
communications equipment should be
used no closer to any part of the
ventilator, including cables, then the
recommended separation distance
calculated from the equation applicable
to the frequency of the transmitter.
Recommended separation distance
Conducted RF
IEC 61000-4-6
A-6
3 Vrms
150 kHz to 80 MHz
outside ISM bandsa
3V
d = 1.17 √P
10 Vrms
150 kHz to 80MHz
outside ISM bandsa
10 V
d = 1.12 √P
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906-0731-01-05 Rev G
Specifications
Immunity Test
Test level
Compliance level
Electromagnetic environment-guidance
Radiated RF
IEC 61000-4-3
10 V/m
80 MHz to 2.5 GHz
20 V/m
d = 0.6 √P 80 MHz to 800 MHz
d = 1.15 √P 800 MHz to 2.5 MHz
Where P is the maximum output power
rating of the transmitter in watts (W)
according to the transmitter
manufacturer and d is the
recommended separation distance in
meters (m).b
Field strengths from fixed RF
transmitters, as determined by an
electromagnetic site surveyc, should be
less than the compliance level in each
frequency range.d
Interference may occurring the vicinity
of equipment marked with the following
symbol:
Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects, and people.
a. The ISM (industrial, scientific, and medical) bands between 150 kHz and 80 MHz are 6.765 MHz to 6.795 MHz; 13.553
MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz.
b. The compliance levels in the ISM frequency bands between 150 kHz and 80 MHz and in the frequency range 80 MHz to 2.5
GHz are intended to decrease the likelihood that mobile/portable communications equipment could cause interference if it is
inadvertently brought into patient areas. For this reason, an additional factor of 10/3 has been incorporated into the formula
used in calculating the recommended separation distance for transmitters in these frequency ranges.
c. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios,
amateur radio, AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To assess the
electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the ventilator is used exceeds the applicable RF compliance level above, the
ventilator should be observed to
verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or
relocating the ventilator.
d. Over the frequency range 150 kHz to 80 MHz, field strength should be less than 3 V/m.
Recommended separation distances between portable and mobile RF communications equipment and the
ventilator (device). The device is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. You can help prevent electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communication equipment (transmitters) and the ventilator as
recommended below, according to the maximum output power of the communication equipment.
Rated maximum output power
of transmitter (W)
Separation distance according to frequency of transmitter (m)
150 kHz to 80 MHz
outside ISM bands
d = 1.17 √P
150 kHz to 80
MHz in ISM bands
d = 1.12 √P
80 MHz to 800
MHz
d = 0.6 √P
800 MHz to 2.5
GHz
d = 1.15 √P
0.01
0.117
0.12
0.06
0.115
0.1
0.37
0.38
0.19
0.36
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A-7
Specifications
Recommended separation distances between portable and mobile RF communications equipment and the
ventilator (device). The device is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. You can help prevent electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communication equipment (transmitters) and the ventilator as
recommended below, according to the maximum output power of the communication equipment.
1
1.17
1.2
0.6
1.15
10
3.7
3.8
1.9
3.6
100
11.7
12
6
11.5
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in
meters (m) can be determined using the equation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
Note 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency applies.
Note 2: The ISM (industrial, scientific, and medical) bands between 150 kHz and 80 MHz are 6.765 MHz to 6.795
MHz; 13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz.
Note 3: An additional factor of 10/3 has been incorporated into the formula used in calculating the recommended
separation distance for transmitters in the ISM frequency bands between 150 kHz and 80 MHz and in the
frequency range of 80 MHz to 2.5 GHz to decrease the likelihood that mobile/portable communications
equipment could cause interference if it is inadvertently brought into patient areas.
Note 4: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption
and reflection from structures, objects, and people.
A-8
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906-0731-01-05 Rev G
Appendix B
Accessories
The following accessories are available for use with a ZOLL ventilator. To order any of these
items, contact ZOLL or your local distributor.
Part Description
3 Liter O2 Reservoir Kit
AC Power line cord, (US Hospital Grade)
AC Power line cord, 6 ft (United States Version)
AC/DC Power Supply and Line Cord with NEMA 5-15P termination
AC/DC Power Supply, 100-240 VAC, 100 W, 24 V, 4.2 A, IEC 320 Plug
Adapter, Metered Dose Inhaler, Adult
Adapter, Metered Dose Inhaler, Adult (Case of 25)
Adapter, Metered Dose Inhaler, Pediatric/Infant
Adapter, Metered Dose Inhaler, Pediatric/Infant (Case of 25)
Battery Pack
Breathing Circuit support arm for Rolling Cart (ferrous, not for MRI use)
Cable, 18”, Pulse Oximeter, Disposable, Finger Sensor, Adult
Cable, 18”, Pulse Oximeter, Disposable, Finger Sensor, Pediatric
Cable, 3 ft, Masimo Adult Ear Sensor, LNCS Type DC-1, Adult Sensor to DB9 Male
Note: All LNCS Masimo cables are approved for use with the ZOLL ventilators
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B-1
Accessories
Part Description
Cable, 3 ft, Masimo SET Oximeter, LNCS Type DC-1, Adult Digit Sensor to DB9 Male, Single
Patient
Note: All LNCS Masimo cables are approved for use with the ZOLL ventilators
Cable, 3 ft, Masimo SET Oximeter, LNCS Type DC-1, Adult Digit Sensor to DB9 Male
Note: All LNCS Masimo cables are approved for use with the ZOLL ventilators
Cable, 3 ft, Masimo SET Oximeter, LNCS Type DC-1, Pediatric Digit Sensor to DB9 Male, Single
Patient
Note: All LNCS Masimo cables are approved for use with the ZOLL ventilators
Cable, 3 ft, Masimo SET Oximeter, LNCS Type Inf/Inf-3, Infant Sensor to DB9 Male
Cable, 3 ft, Pulse Oximeter, Reusable, Finger Sensor, Pediatric
Cable, 4 ft, Masimo LNCS Patient Cable Type LNC-4, DB9 Female to Male
Note: All LNCS Masimo cables are approved for use with the ZOLL ventilators
Cable, 6 ft, BS 546 (UK-SA) Plug Right Angle
Cable, 6 ft, Continental Europe CEE 7/7 to IEC-60320-C5 2.5 Amp Connector
Carry-all Case with AC Receptacle
Carry-all Case with Foam Inserts, without AC Receptacle
Case, Transit Carry
Case, Transit Carry, with AC Bulkhead & USB Connectors
Case, Transit Carry, with AC Bulkhead Connector
Case, Transit Carry, with Wheels & Pull-Out Handle
Case, Transit Carry, with Wheels & Pull-Out Handle, AC Bulkhead Connector
CCLAW (Critical Care Litter Attachment Widget) Mounting Bracket
Check Valve Kit
Circuit (reusable)
Circuit (reusable) (Case of 10)
Circuit, 12 ft, Vent, Single Limb, Infant/Pediatric (disposable)
Circuit, 12 ft, Vent, Single Limb, Infant/Pediatric (disposable) (Case of 10)
Circuit, 12 ft, Vent, Single Limb, Pediatric/Adult (disposable)
Circuit, 12 ft, Vent, Single Limb, Pediatric/Adult (disposable) (Case of 10)
Circuit, 6 ft, Vent, Single Limb, Infant/Pediatric (disposable)
Circuit, 6 ft, Vent, Single Limb, Infant/Pediatric (disposable) (Case of 20)
Circuit, 6 ft, Vent, Single Limb, Pediatric/Adult (disposable)
Circuit, 6 ft, Vent, Single Limb, Pediatric/Adult (disposable) (Case of 15)
Cord set, 6 ft, IEC 60320-C5 Plug to Country-Specific Connector (Contact factory for complete part
number for each country)
B-2
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906-0731-01-05 Rev G
Accessories
Part Description
DC Power Cable, 12 VDC. Ambulance
DC Power Cable, 28 VDC, Military Vehicle
Extension Cord 8 ft US Hospital Grade Female Plug to Country-Specific Connector
(Contact factory for complete part number for each country)
Extension Cord Assembly, AS 3112 (Australian) Plug to US Hospital Grade Plug
Filter, Bacterial/Viral (B/V)
Filter, Disk, B/V, Emergency Air Intake (replaceable part/service item)
Filter, HME/B/V, Heat and Moisture Exchanger
Gas Output Cap (Package of 10)
Harness, Mask, Universal
Harness, Mask, Universal (Case of 10)
Heat and Moisture Exchanger/Bacterial and Viral Filter (HMF), Adult, Dead-space ≤ 75ml
Heat and Moisture Exchanger/Bacterial and Viral Filter (HMF), Adult, Dead-space ≤ 75ml
(Case of 25)
Heat and Moisture Exchanger/Bacterial and Viral Filter (HMF), Infant
Heat and Moisture Exchanger/Bacterial and Viral Filter (HMF), Infant (Case of 25)
Heat and Moisture Exchanger/Bacterial and Viral Filter (HMF), Pediatric (Case of 25)
Heat and Moisture Exchanger/Bacterial and Viral Filter (HMF), Pediatric, Dead-space ≤ 25ml
High pressure Oxygen Hose, DISS x DISS, oxygen, 6’
IV support arm for Rolling Cart (aluminum, MRI safe)
Mask, CPAP, #1, Small Infant
Mask, CPAP, #2, Infant
Mask, CPAP, #2, Infant (Case of 20)
Mask, CPAP, #2, Infant (Case of 40)
Mask, CPAP, #3, Small Child
Mask, CPAP, #3, Small Child (Case of 20)
Mask, CPAP, #3, Small Child (Case of 40)
Mask, CPAP, #4, Child
Mask, CPAP, #4, Child (Case of 20)
Mask, CPAP, #4, Child with harness
Mask, CPAP, #4, Child with Harness (Case of 20)
Mask, CPAP, #4, Child with Harness (Case of 50)
Mask, CPAP, #5, Adult
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B-3
Accessories
Part Description
Mask, CPAP, #5, Adult (Case of 20)
Mask, CPAP, #5, Adult with Harness
Mask, CPAP, #5, Adult with Harness (Case of 20)
Mask, CPAP, #5, Adult with Harness (Case of 50)
Mask, CPAP, #6, Large Adult
Mask, CPAP, #6, Large Adult (Case of 20)
Mask, CPAP, #6, Large Adult with Harness
Mask, CPAP, #6, Large Adult with Harness (Case of 20)
Mask, CPAP, #6, Large Adult with Harness (Case of 50)
MRI conditional Rolling Cart
Non-MRI Rolling Cart
Padded Carry Case, Tan, for ventilator and accessories
Power Supply Holder Kit
Removable foam compressor inlet filter (replaceable part/service item)
Test Lung, plastic/silicone
B-4
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Appendix C
Pulse Oximeter Principles
The Masimo SET® MS board pulse oximeter is based on these principles.
1.Oxyhemoglobin and deoxyhemoglobin differ in their absorption of red and infrared light
(spectrophotometer).
2.The volume of arterial blood in tissue and the light absorbed by the blood changes during
the pulse (plethysmography). Therefore, the amount of light absorbed by the varying
quantities of arterial blood changes as well.
3.Arterio-venous shunting is highly variable and that fluctuating absorbance by venous blood
is a major component of noise during the pulse.
Information about wavelength range can be especially useful to clinicians, see Pulse Oximeter
Operation below.
Pulse Oximeter Signaling
Figure C-1 illustrates pulse oximeter signaling.
Note:
Figure C-1 is intended for conceptual purposes only.
Figure C-1 Example of Pulse Oximeter Signaling
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C-1
Pulse Oximeter Principles
Successful Monitoring for SpO2, PR and Pi
Stability of the SpO2 readings may be a good indicator of signal validity. Although stability is a
relative term, experience will provide a good feeling for changes that are artifactual or
physiological and the speed, timing, and behavior of each.
The stability of the readings over time is affected by the averaging time being used. The longer
the averaging time, the more stable the readings tend to become. This is due to a dampened
response as the signal is averaged over a longer period of time than during shorter averaging
times. However, longer averaging times delay the response of the oximeter and reduce the
measured variations of SpO2 and pulse rate.
Functional Oxygen Saturation (SpO2)
The pulse oximeter is calibrated to measure and display functional oxygen saturation (SpO2 ):
the amount of oxyhemoglobin expressed as a percentage of the hemoglobin that is available to
transport oxygen.
Note:
Dyshemoglobins are not capable of transporting oxygen, but are recognized as
oxygenated hemoglobins by conventional pulse oximetry.
Pulse Oximeter Operation
The Masimo SET MS board pulse oximeter as well as traditional pulse oximetry determines
SpO2 by passing red and infrared light into a capillary bed and measuring changes in light
absorption during the pulsatile cycle. Red and infrared light-emitting diodes (LEDs) in
oximetry sensors serve as the light sources, a photodiode serves as the photodetector. The
optical output power of the pulse oximeter is < 15mW radiant power at 50mA pulsed.
Traditional pulse oximetry assumes that all pulsations in the light absorbance are caused by
oscillations in the arterial blood volume. This assumes that the blood flow in the region of the
sensor passes entirely through the capillary bed rather than through any arterio-venous shunts.
The traditional pulse oximeter calculates the ratio of pulsatile absorbance (AC) to the mean
absorbance (DC) at each of two wavelengths, 660 nm (red) and 905 nm (infrared):
S(660) = AC(660)/DC(660)
S(905) = AC(905)/DC(905)
The oximeter then calculates the ratio of these two arterial pulse-added absorbance signals:
R = S(660)/S(905)
This value of R is used to find the saturation SpO2 in a look-up table built into the oximeter’s
software. The values in the look-up table are based upon human blood studies against a
laboratory co-oximeter on healthy adult volunteers in induced hypoxia studies.
The Masimo SET MS board pulse oximeter assumes that arterio-venous shunting is highly
variable and that fluctuating absorbance by venous blood is the major component of noise
during the pulse. The MS board decomposes S(660) and S(905) into an arterial signal plus a
noise component and calculates the ratio of the arterial signals without the noise:
S(660) = S1 + N1
S(905) = S2 + N2
R = S1/S2
Again, R is the ratio of two arterial pulse-added absorbance signals and its value is used to find
the saturation SpO2 in an empirically derived equation into the oximeter’s software. The values
in the empirically derived equation are based upon human blood studies against a laboratory
co-oximeter on healthy adult volunteers in induced hypoxia studies.
C-2
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Pulse Oximeter Principles
The above equations are combined and a noise reference (N’) is determined:
N’ = S(660) - S(905) x R
If there is no noise, N’ = 0: then S(660) = S(905) x R, which is the same relationship for
traditional pulse oximeter.
The equation for the noise reference is based on the value of R, the value being sought to
determine the SpO2. The MS board software sweeps through possible values of R that
correspond to SpO2 values between 1% and 100% and generates an N’ value for each of these
R-values. The S(660) and S(905) signals are processed with each possible N’ noise reference
through an adaptive correlation canceler (ACC), which yields an output power for each
possible value of R (i.e., each possible SpO2 from 1% to 100%). The result is a Discrete
Saturation Transform (DST™) plot of relative output power versus possible SpO2 value as
shown in the following figure where R corresponds to SpO2 = 97%:
Figure C-2 Pulse Oximeter Discrete Saturation Transformation
The DST plot has two peaks: the peak corresponding to the higher saturation is selected as the
SpO2 value. This entire sequence is repeated once every two seconds on the most recent four
seconds of raw data. The MS board SpO2 therefore corresponds to a running average of arterial
hemoglobin that is updated every two seconds.
Sensors are designed as Surfaces Devices with skin contact for prolonged contact duration,
>24hrs to 30days, as defined in ISO 10993-1. All patient contacting materials have passed ISO
10993-1 for cytotoxicity, sensitization, and irritation or intracutaneous reactivity tests.
Sensors are designed not to exceed 41 °C based on a maximum operating temperature of 35 °C.
Understanding Alarm Response Delay
As with any pulse oximeter equipment, the audible and visual alarms are subject to alarm
response delay, which is composed of Alarm Condition Delay and Alarm Signal Generation
Delay. Alarm Condition Delay is the time from the occurrence of the triggering event to when
the alarm system determines the alarm condition exists. While Alarm Signal Generation Delay
is the time from the onset of an alarm condition to the generation of its alarm signal. Figure C-3
is a simplified illustration of the concept of alarm response delay and does not reflect actual
lengths of delays.
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C-3
Pulse Oximeter Principles
Figure C-3 Alarm Response Delay (Concept)
The Alarm Condition Delay is graphically represented as t1-t1 in the figure above to show the
delay due to processing and averaging.
The Alarm Signal Generation Delay is graphically represented as t3 -t1 in the figure above to
show the delay due to alarm system strategy and communication time.
The overall alarm system delay time is graphically represented as t3 -t1.
C-4
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906-0731-01-05 Rev G
Appendix D
Troubleshooting Patient
Circuits
This appendix provides information on troubleshooting patient circuits.
Troubleshooting Procedure
If there are circuit-related alarms during set up or initial use, such as Disconnect, PEEP Leak,
Low Airway Pressure, or Auto-PEEP, check all circuit connections and the exhalation valve.
If the exhalation valve is not performing, manually ventilate the patient and perform the
following procedure:
1. Using a hemostat or a tongue blade, carefully open the exhalation valve as we show in
Figure D-1. Remove the top cover first, and then remove the silicon diaphragm. Place the
silicon diaphragm in a clean area on disposable circuits only. Do not attempt to the
following procedure on a reusable circuit.
Figure D-1 Removing Silicon Diaphragm -- Pediatric/Adult Patient Circuit
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D-1
Troubleshooting Patient Circuits
2. Examine the silicon diaphragm for kinks, cuts, holes, or inconsistencies in the material. See
Figure D-2.
If the diaphragm is kinked, relax the silicone diaphragm with your fingers, ensuring that there
are no longer any kinks (this usually takes a few seconds).
If the diaphragm has a hole or cuts, replace the patient Circuit.
Figure D-2 Examining the Patient Circuit’s Silicone Diaphragm
3. Carefully re-seat the silicone diaphragm in the exhalation valve seat. Tap around the silicone
diaphragm lightly to ensure that kinks do not develop when closing the exhalation valve. See
Figure D-3.
4. Locate the top of the exhalation valve, taking care not to touch the silicone diaphragm. Ensure
that the barbed end with tubing is pointing into the FLOW direction. Apply enough pressure
to snap the exhalation valve cover in place.
Figure D-3 Closing Exhalation Valve Cover
5. Test the patient circuit with a test lung before using it with a patient. If it fails to perform,
replace the patient circuit.
D-2
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Index
A
Abbreviations table 1-9
Accessories B-1 – B-4
Alarm configuration 4-37
Alarm History 4-40
Alarm Overview 5-1 – 5-2
Alarm Priorities 5-3
Alarm Summary 5-16 – 5-41
High Priority Alarms 5-16
Low Priority Alarms 5-31
Medium Priority Alarms 5-22
Alarm Types 5-4 – 5-11
Environmental and Use 5-7
Patient Safety 5-4
Self-Check 5-9
Assembly Information 1-2
Attaching a Patient Circuit to the Ventilator 2-14
B
Backup 5-15
Backup Mode
Apnea Backup Mode 5-15
Backup Modes 5-15
Battery
Maintenance 7-6
Storage 7-7
BPM Parameters
Alarm Thresholds 4-12
BPM Parameter Group Reference 4-15
Context Menu 4-12
Primary Parameter 4-12
Secondary Parameters 4-12
C
Cautions 1-16
Controls and Indicators 2-3 – 2-5
Conventions used in guide 1-8
D
Default Parameter Settings 4-3 – 4-4
Device Classification A-4
Disabling Alarms 5-14
Display Screen 2-4
E
Emissions A-5
Environmental and Use Alarms 5-7
Extending Battery Runtime 6-1
F
FDA Tracking 1-16
FIO2 Parameters
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Alarm Thresholds 4-21
Context Menu 4-21
FIO2 Parameter Group Reference 4-22
Primary Parameter 4-21
Secondary Parameters 4-21
Fresh Gas Intake and Attachments 2-6
G
Guide Updates
How to Obtain 1-2
Information about 1-2
H
Harsh Environment Operation
Airborne Particulates 6-2
Altitude 6-3
Extreme Temperature Environments 6-2
Rain and Snow 6-4
Hazardous Environment Filters 6-4 – 6-6
Bacterial/Viral 6-4
Change/Insertion 7-4 – 7-5
Check Valve on Patient Circuit 6-5
Chemical/Biological 6-5
Foam Filter 7-3
Fresh Gas/Emergency Air Intake Disk Filter 7-3
Replacing 7-4 – 7-5
Heat and Moisture Exchangers 2-13
High Pressure Gas Supply 2-10
High Priority Alarms 5-16
How to Use this Guide 1-1
HR Parameters
Alarm Thresholds 4-25
Context Menu 4-25
HR Parameter Group Reference 4-26
Primary Parameter 4-25
Secondary Parameters 4-25
I
Immunity Compliance A-5
Indications for Use 1-11
L
LCD Brightness 4-39
LCD Contrast 4-38
Limited Warranty 1-17
Low Priority Alarms 5-31
M
Main Features 2-2
Maintenance
Calibration Checks 7-8
General Cleaning 7-2
ZOLL EMV+ Ventilator Operator’s Guide
Index-1
Index
Inspecting 7-1
Post-Contaminated Environment Cleaning 7-2
Managing Alarms 5-11 – 5-15
Backup Modes 5-15
Disabling Alarms 5-14
Patient Detect Mode 5-14
Preemptive Muting 5-12
Start Up Muting 5-12
Manual Breath 4-27
Medium Priority Alarms 5-22
Mode Parameters
Alarm Thresholds 4-9
Context Menu 4-10
Mode Parameter Group Reference 4-11
Primary Parameter 4-9
Secondary Parameters 4-9
MRI Environments 6-6 – 6-7
MRI Environments, Using the Ventilator 6-6
Muting Alarms 5-3
N
Notification of Adverse Events 1-17
O
Operation
Changing Parameter Settings 4-7
Default Parameter Settings 4-3 – 4-4
Making Choices form the Start Menu 4-4
Modes of 3-9
Saving Changed Parameters 4-8
Using Last Settings Enabled on Ventilator 4-8
P
Parameter Groups
BPM Parameters 4-12 – 4-15
FIO2 Parameters 4-21 – 4-22
HR Parameters 4-25 – 4-26
Mode Parameters 4-9 – 4-11
PIP Parameters 4-18 – 4-20
SpO2 Parameters 4-22 – 4-24
Vt Parameters 4-16 – 4-18
Patient Circuits 2-12 – 2-16
Attaching Circuit to Ventilator 2-14
description 2-12
Intended Use with Ventilator 2-13
Specifications 2-15
Troubleshooting D-1 – D-2
Use with Heat and Moisture Exchangers 2-13
Patient Detect Mode 5-14
Patient Safety Alarms 5-4
Related to Use of a Pulse Oximeter 5-6
PIP Parameters
Alarm Thresholds 4-18
Context Menu 4-19
PIP Parameter Group Reference 4-20
Primary Parameter 4-18
Secondary Parameters 4-18
Plateau Pressure 4-27
Plateau Pressure Maneuver 4-27
Pneumatic Design 2-9
Pop Up Messages 4-29 – 4-36
Power Connections 3-7
Power Sources
Operating Using Battery Power 2-8
Index-2
Operating Using External DC Power 2-8
Powerup 4-37
Preemptive Muting 5-12
Pulse Oximeter
Principles C-1 – C-3
Pulse Oximeter Compatibility 2-8
Pulse Oximeter Specifications A-4
S
Setting up the Ventilator 3-1 – 3-12
Attaching a Patient 3-12
Attaching an Optional Pulse Oximeter 3-11
Attaching Optional High Pressure Oxygen Supply 3-3
Attaching the Patient Circuit 3-2
Changing Parameter Values 3-10
Connecting Fresh Gas Intake Attachments 3-4
Inspecting Fresh Gas Intake Filters 3-4
Performing an Operational Test 3-10
Powering ON the ventilator 3-8
Selecting a Power Source 3-6
Selecting an Operating Mode (Optional) 3-9
Selecting Start Menu Option 3-8
Summary of Steps 3-1
Software License 1-17
Specifications A-1 – A-8
Patient Circuits 2-15
SpO2 Parameters
Alarm Thresholds 4-23
Context Menu 4-23
Primary Parameter 4-22
Secondary Parameters 4-23
SpO2 Parameter Group Reference 4-24
Start Up Muting 5-12
Storage 7-7
Symbols
in graphical user interface 1-6 – 1-8
on product 1-2 – 1-4
T
Technical Support 1-18 – 1-19
Top Panel 2-7
Transitions 4-36
Transport Environments, Using the Ventilator 6-2
U
Unit Info 4-40
Unpacking the Ventilator 1-2
Using the Main Menu
Alarm configuration 4-37
Alarm History 4-40
LCD brightness 4-39
LCD Contrast 4-38
Powerup 4-37
Unit Info 4-40
UTC Offset 4-39
UTC Offset 4-39
V
Ventilator Description 2-2 – 2-10
Controls and Indicators 2-3
Display Screen 2-4
Fresh Gas Intake and Attachments 2-6
Main Features 2-2
Pneumatic Design 2-9
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906-0731-01-05 Rev G
Index
Power Sources 2-8
Pulse Oximeter Compatibility 2-8
Top Panel 2-7
Vt Parameters
Alarm Thresholds 4-16
Context Menu 4-17
Primary Parameter 4-16
Secondary Parameters 4-16
Vt Parameter Group Reference 4-18
W
Warnings 1-12 – 1-15
Batteries 1-14
General 1-12
MR Conditional 1-15
Patient Safety 1-14
Pulse Oximeter 1-13 – 1-14
User Safety 1-14
Ventilator 1-12 – 1-13
906-0731-01-05 Rev G
ZOLL EMV+ Ventilator Operator’s Guide
Index-3
Index
Index-4
www.zoll.com
906-0731-01-05 Rev G
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