Philips V200 User Manual

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Respironics V200 Ventilator
Operator’s Manual
1057983 50
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For Technical Support and Customer Service, contact:
USA and Canada: 1-800-345-6443 or 724-387-4000 Respironics Europe, Africa, Middle East: +33-1-47-52-30-00 Respironics Asia Pacific: +852-3194-2280 Facsimile: 724-387-5012
Respironics California, Inc. 2271 Cosmos Court Carlsbad, CA 92011
Email and web addresses
service@philips.com clinical@philips.com www.philips.com\healthcare
Authorized European address
Respironics Deutschland GmbH
EC REP
Gewerbestrasse 17 D-82211 Herrsching Germany +49-8-15-29-30-60
© 2009 Respironics and its affiliates. All rights reserved.
This work is protected under T itle 17 of the United States copyright code and is the sole property of Respironics. No part of this document may be copied or otherwise reproduced, or stored in any electronic information retrieval system, except as specifically permitted under United States copyright law, without the prior written consent of Respironics.
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Table of Contents
1. Introduction and Intended Use. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-1
2. Warnings, Cautions, and Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1
Summary of Warnings, Cautions, and Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1
3. Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
4. Getting Started . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1
Unpacking . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1
Inspection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
List of Parts and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
Repacking. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
Ventilator Positioning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
Backup Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
Inspiratory Bacteria Filter Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-16
Heated Expiratory Bacteria Filter Installation . . . . . . . . . . . . . . . . . . . . . . . . . 4-18
Oxygen Source Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-20
Patient Circuit Flex Arm Installati on . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-22
5. Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1
Back Panel Connections and Control s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1
Connecting AC Power Cord . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Power On/Off. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
Entering Diagnostic Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
User Configuration Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-7
Backup Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-11
Extended Self Test (EST) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-12
6. Connecting Additional Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-1
Communication Interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-1
Connecting Serial Communications Devices . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
Connecting Remote Alarm Port . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
Connecting Humidifier. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3
Connecting the Patient Circuit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-5
Connecting the Analog Port . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7
7. Operating Theory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-1
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-1
System Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-1
Ventilator Breath Types . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-1
Ventilation Modes Common to VCV and PCV. . . . . . . . . . . . . . . . . . . . . . . . . . . 7-3
Ventilation Modes Common to NPPV . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-6
Emergency Modes of Ventilation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-7
REF 1057983 A Respironics V200 Ventilator Operator’s Manual iii
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8. Operating Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-1
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-1
The Front Panel. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3
Ventilator Screens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-11
Settings Screens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-14
Selecting a New Ventilation Breath Type (VCV, PCV, or NPPV). . . . . . . . . . . . . . 8-23
Selecting the Mode (A/C-SIMV-CPAP or Spont-Spont/T) . . . . . . . . . . . . . . . . . . 8-26
Apnea Ventilation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-27
Patient Data Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-28
Monitor Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-29
Special Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-31
Preoperational Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-32
Alarm Testing Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-34
Where To Go For Help . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-34
9. Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-1
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-1
Visual Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-1
Audible Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2
Alarm Reset . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-3
Alert Messages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-4
Alarm Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-9
10. Care and Maintenance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-1
General Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-1
Cleaning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-1
Sterilization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-2
Bacteria Filters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-4
Periodic Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-7
Storage. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-10
Repairs. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-10
11. Diagnostics. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-1
Entering Diagnostic Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-2
Diagnostic Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-3
Extended Self Test (EST) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-4
Self Test. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-10
12. Technical Specifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-1
Breath Types. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-1
Modes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-1
Volume Ventilation Settings, Ranges and Resolution . . . . . . . . . . . . . . . . . . . . . 12-1
Pressure Control Ventilation Settings, Ranges and Resolution . . . . . . . . . . . . . . 12-2
Non-Invasive Positive Pressure Ventilation Settings, Ranges and Resolution . . . . 12-3
Apnea Ventilation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-3
Value Entry Message . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-4
iv Respironics V200 Ventilator Operator’s Manual REF 1057983 A
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Patient Data Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-5
Front Panel Keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-6
Level Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-7
Calculated Values from Expiratory Hold Maneuver. . . . . . . . . . . . . . . . . . . . . . 12-7
Interface Ports . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-7
Environmental Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-8
Environmental Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-8
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-8
Connectors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-9
Filters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-10
Measuring and Display Devices. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-10
AC Power and Battery Indicators. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-10
Leakage Current . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-11
Compliance and Approvals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-11
Power Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-11
Dimensions and Weights . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-12
Electromagnetic Compatibility Declaration . . . . . . . . . . . . . . . . . . . . . . . . . . 12-12
Pneumatic System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-17
Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-18
13. Options and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-1
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-1
Oxygen Sensor Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-3
Assemble O2 Sensor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-3
Attaching the Sensor to the Ventilator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-4
Warranty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-5
O
Sensor Tee. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-5
2
External Battery Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-7
Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-8
Power Consumption Sequence . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-8
External Battery/Backup Battery Operation. . . . . . . . . . . . . . . . . . . . . . . . . . . 13-8
Battery Capacity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-10
Battery Charging . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-10
Testing. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-11
Battery Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-11
Warranty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-12
Oxygen Manifold Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-13
Kit Contents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-13
Assembly Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-14
Replacement Parts: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-17
Using the Manifold . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-17
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Graphics. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-19
Starting Graphics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-19
Using Graphics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-19
Replotting and Scrolling. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-20
Rescaling the Display. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-20
Freeze Feature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-22
Save and Overlay Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-23
Inspiratory Area. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-24
Alarms During Graphics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-25
Communications Option (Com1) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-27
Print Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-27
VueLink Compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-29
Configuring the VueLink Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-30
Analog Output (Chart Recorder) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-36
RS-232 Communications Option 2 (Com2) . . . . . . . . . . . . . . . . . . . . . . . . . . 13-39
RS-232 Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-39
Commands Transmitted to the Ventilator . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-40
Transmission of Data from the Ventilator . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-40
SNDA<CR>, Send Variable Length Ventilator Settings Report . . . . . . . . . . . . . 13-40
Respiratory Mechanics Option. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-51
Accessing Respiratory Mechanics Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-51
Vital Capacity Maneuver. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-52
MIP/P0.1 Maneuver. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-54
Static C and R Maneuver . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-56
Alarms and Error Messages. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-58
Compliance (C) and Resistance (R) Computations. . . . . . . . . . . . . . . . . . . . . . 13-65
Trending Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-69
Accessing Trending Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-69
Selecting Parameters for Display. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-72
Using the Manual Rescale Function . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-74
Changing the Cursor Position . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-74
Selecting the Time Scale . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-75
Using the +2 Hrs/-2 Hrs buttons. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-76
Using the Zoom Function. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-76
Using the Rescale Button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-76
Using the View 1/View 2 buttons. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-77
Using the Clear button. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-77
Alarms during Trending . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-77
PCMCIA Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-77
Trending Not Available. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-78
Specifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-78
vi Respironics V200 Ventilator Operator’s Manual REF 1057983 A
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Contents
Flow-Trak® Option. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-83
On the Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-84
Breath Delivery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-85
Inspiratory Hold. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-85
Respiratory Mechanics. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-85
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-86
Respiratory Profile Monitor Interface ( NICO-Esprit) Option. . . . . . . . . . . . . . . . 13-87
System Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-87
Hardware Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-88
RS-232 Communications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-91
Trended NICO Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-92
Troubleshooting. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-96
Neonatal Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-97
System Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-97
Changing Patient Types . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-98
Percent Leak. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-101
Patient Leak Values . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-102
Speaking Mode Option. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-103
Warnings, Cautions, and Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-103
Patient Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-104
Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-106
Starting Speaking Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-106
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-109
Displayed Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-111
Trended Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-112
Discontinue Speaking Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-115
Auto-Trak Sensitivity™. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-117
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-117
Compatible Patient Interfaces. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-117
How to Select Auto-Trak. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-118
Turning Auto-Trak Off . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-121
Triggering and Cycling with Auto-Trak . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-121
Leak Detection and Compensation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13-121
REF 1057983 A Respironics V200 Ventilator Operator’s Manual vii
Page 8
Contents
A. RS-232 Communications Protocol. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-1
RS-232 Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-1
Commands Transmitted to the Ventilator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-1
Transmission of Data from the Ventilator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-1
Ventilator Report Command and Response (VRP T) . . . . . . . . . . . . . . . . . . . . . . . A-1
Volume Control Ventilation Settings Report (VCVS) . . . . . . . . . . . . . . . . . . . . . . A-11
Pressure Control Ventilation Settings Report (PCVS) . . . . . . . . . . . . . . . . . . . . . A-14
Non-Invasive Positive Pressure Ventilation Settings Report (NPVS). . . . . . . . . . . A-16
Patient Data Report (PTDT) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-18
Alarm Status Report (ALRM) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-21
Unrecognized Commands. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-24
B. Customer Service & Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-1
Customer Service. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-1
Warranty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-1
Options and Accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-2
C. Alarm Testing Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-1
Glossary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Glossary-1
Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Index-1
viii Respironics V200 Ventilator Operator’s Manual REF 1057983 A
Page 9

Chapter 1. Introduction and Intended Use

The Respironics V200 Ventilator is a microprocessor-controlled, electrically powered mechanical ventilator. It is intended for use by qualified medical personnel to provide continuous or intermittent ventilatory support for adult, pediatric, and neonatal patients as prescribed by a physician. The ventilator is intended for use in either invasive or non-invasive applications in institutional environments.
The Respironics V200 Ventilator meets applicable safety requirements, consensus guidelines, U.S.A. regulatory statutes, and international regulatory standards for life support/mechanical ve ntilation devices.
Please read this manual thoroughly and become familiar with the ventilator's operation before using it on a patient. For additional information about accessories or related equipment, such as humidifiers and remote alarm systems, refer to the appropriate instruction manual prior to operating the accessory with the ventilator.
Advanced troubleshooting, calibration, and maintenance instructions are included in the Esprit /V200 Ventilator Service Manual, P/N 580- 1000-02. All maintenance and repair work should be performed by qualified biomedical technicians who have received appropriate training and authorization to provide maintenance, repair, and service for the ventilator.
WARNING: Patients on life-support equipment should be visually monitored by
competent medical personnel, since life-threatening circumstances may arise that may not activate alarms. Heed all appropriate alarms and follow the instructions and warnings in this operator’s manual. Always check life­support equipment for proper operation before use.
WARNING: Do not use in the presence of flammable anesthetics. Possible explosion
hazard.
CAUTION: Federal law (USA) restricts this device to sale by or on the order of a
physician.
NOTE: Follow the setup instructions in this manual before placing the
Respironics V200 Ventilator into service. If you have questions, contact Respironics Customer Service at 1-800-345-644
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 1-1
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Chapter 1
Introduction and Intended Use
(This page is intentionally blank.)
1-2 Respironics V200 Ventilator Operator’s Manual REF 1057983 A
Page 11

Chapter 2. Warnings, Cautions, and Notes

Throughout this manual the following definitions apply:
WARNING: A condition that could cause injury to a patient or operator if the operating
instructions in this manual are not followed correctly.
CAUTION: A condition that could cause damage to, or shorten the service life of,
the Respironics V200 Ventilator.
NOTE: Important information concerning the construction or operation of the
Respironics V200 Ventilator.
Additional Warnings, Cautions, and Notes pertaining to options and accessories are included in the documentation for each option or accessory. Refer to Chapter 13, “Options and Accessories”.

Summary of Warnings, Cautions, and Notes

Warnings

Patients on life-support equipment should be visually monitored by competent medical personnel, since life-threatening circumstances may arise that may not activate alarms. Heed all appropriate alarms and follow the instructions and warnings in this operator’s manual. Always check life-support equipment for proper operation before use.
Do not use in the presence of flammable anesthetics. Possible explosion hazard.
One person alone should not attempt to lift the ventilator or remove it from the shipping carton or the cart. At least two people are required to avoid possible personal injury or damage to the equipment.
To reduce the chance of contamination or infection, always use an inspiratory and expiratory filte r when the ventilator is in operation. Refer to manufacturer’s instructions and follow institutional infection control guidelines when replacing the inspiratory and expiratory filter.
Do not use anti-static or conductive hoses or conductive patient tubing.
The expiratory filter housing may be hot ventilator immediately after use. Wait 15 minutes after turning off
if removed from the
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 2-1
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Chapter 2
Warnings, Cautions, and Notes
ventilator power before removing the heated expiratory bacteria filter. Exercise caution when handling the filter housing.
All oxygen connections should be carefully inspected to ensure that leaks are not present. Excessive leaks can result in higher than normal ambient oxygen concentrations and create a potentially hazardous oxygen-enriched environment.
Worn/frayed oxygen hoses or oxygen hoses contaminated by hydrocarbon greases or oils should not be used since an oxygen leak or intense fire could result.
Care in the routing of the oxygen inlet hose should be exercised to ensure it is not exposed to mechanisms that could cause damage by cutting or heating/melting.
The cover plate for the PCMCIA slot at the back of the ventilator must be replaced after the adapter and card are installed. This is to protect the ventilator.
AC power is applied to the humidifier from the ventilator humidifier outlet (only available on 100-120 VAC ventilators). Under no circumstances does the Respironics V200 Ventilator provide control for the humidifier. To ensure patient safety, it is important that any humidifier used with the ventilator include an acceptable temperature control and monitoring mechanism, as well as a temperature display and appropriate alarm capabilities (refer to ISO 8185).
To avoid electrical shock hazard, connect the ventilator to a properly grounded AC power outlet.
The ventilator front panel LEDs will indicate the power source that is being used. If the ventilator is plugged in and the MAINS LED is not lit, either the circuit breaker is off or the wall power outlet is not functioning.
The two circuit breakers (MAINS/Humidifier) located on the back of the ventilator are covered to prevent unintentional ventilator power-off. Do not use the circuit breaker to power the ventilator on/off. The power switch is located on the front of the ventilator below the front panel.
Always turn the ventilator power OFF before connecting additional equipment.
Use only Respironics approved cables when connecting to the remote alarm port. Be sure to fully insert the cable into the remote alarm port and into the remote alarm.
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Chapter 2
Warnings, Cautions, and Notes
When using the Re mote Alarm Port be sure to fully test the
Remote Alarm Port and cable by:
• Verifying that annunciated alarms on the ventilator are also annunciated on the remote alarm.
• Verifying that disconnecting the cable from the Remote. Alarm port results in an alarm notification at the Remote Alarm.
• Verifying that disconnecting the cable from the remote alarm results in an alarm notification at the Remote Alarm.
Ensure that an alternative means of ventilation (that is, a resuscitator or similar device) is available while the ventilator is in use on a patient.
The ventilator complies with the requirements of IEC 601-1-2 (EMC collateral standard), including the E-field susceptibility requirements at a level of 10 volts per meter. However, even at this level of immunity, certain transmitting devices (cellular phones, walkie-talkies, etc.) emit radio frequencies that could disrupt ventilator operation if operated in a range too close to the ventilator.
DO NOT operate the ventilator in a Magnetic Resonance Imaging (MRI) environment.
V ent Inop is a serious condition, which is indicated by both visual and audible alarms. If the ventilator is attached to a patient when Vent Inop occurs, the patient must be supported with another means of life support ventilation.
When the battery low indicator is flashing red, operation of the ventilator from battery power should be discontinued.
For patient safety the HIP Limit Setting should be set as close to the peak inspiratory pressure as patient conditions allow.
DO NOT perform the preoperational procedure when the ventilator is on a patient.
You wi ll be warned if the compliance is 9.0 ml/cmH
O (hPa) or
2
larger. Patients should not be put on a patient circuit that does not meet this requirement.
A high priority, visual and audible alarm indicates a potentially life-threatening condition and immediate response is required.
When the safety valve open indicator is lit, the ventilator d o es not provide any ventilatory support to the patient. Immediately use a backup means of ventilatory support.
Visually monitor the patient and ventilator during the Alarm Silence period to ensure that alarms do not go undetected. Allowing alarm conditions to continue without interventi on may result in harm to the patient and/or ventil ator.
Do not expose expiratory and inspiratory bacteria filters or reusable patient tubing to ETO gas.
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 2-3
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Chapter 2
Warnings, Cautions, and Notes
Disposable or single-patient filters must be discarded between patients. Do not chemically disinfect or expose single patient use bacteria filters to ETO gas.
The patient must be disconnected from the ventilator before entering the Diagnostic Mode since normal ventilation is suspended.
Do not use a ventilator that has failed SST without verifying operational readiness by other means. Doing so may place a patient at risk.
Never initiate SST while the patient is connected to the ventilator. The high airway pressures generated during SST can injure a patient.
Never initiate EST while the patient is connected to the ventilator. The high airway pressures and gas flows generated during EST can injure a patient.
Do not use a ventilator that has failed EST without verifying operational readiness by other means. Doing so may place a patient at risk.
Remove the ventilator from service and contact trained service personnel if any diagnostic codes appear with the exception of: 1, 3, 2000, 3000, 5000, 5002, 8003, or 8004.
Use of a ventilator that has not passed SST or EST is against the strongest recommendation of Respironics.
Please contact Respironics Customer Service at 1-800-345-6443 or consult your service manual if any diagnostic codes are encountered.
When connecting a humidifier to the humidifier outlet (available only on 100-120 VAC ventilators) allowable leakage current values may be exceeded.
The use of accessories, cables, and transducers other than those specified may result in increased EM emissions or decreased immunity of the system.
We recommend that you use an oxygen monitor that complies with ISO-7767; Oxygen Monitors or Monitoring Patient Breathing Mixtures - Safety Requirements. This requirement ensures that the desired fraction of inspired oxygen (FiO2) is delivered to the patient.
The batteries (backup battery) in the battery compartment are non-spillable sealed lead acid. Recycle or dispose of bat ter ies properly.
Do not connect the DC power cord from the backup battery while the Respironics V200 is functioning as a ventilator. Always turn the Power On/Off switch to off ( ).
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Cautions

Chapter 2
Warnings, Cautions, and Notes
Backup battery operating life may be affected by battery age and
the number of times it has been discharged and recharged. Over time the battery will degenerate and will not provide the same amount of operating time per charge that is available from a fully charged new battery. Use only the Respironics backup battery P/ N 1059956.
Titrate the EPAP level such that the masks air entrainment valve
(if present) remains closed to room air. Always evaluate and monitor patient condition when ad justing EPAP or other settings.
The backlight lamps in the monitor display contain mercury,
which must be recycled or disposed of in accordance with local, state, or federal laws. (Within this system, the backlight lamps in the monitor display contain mercury.)
Federal law (U SA) restrict s this device to sale by or on the order of
a physician.
Be sure to check all exterior parts of the ventilator. Problems
found during inspection should be corrected and/or reported to Respironics before using the ventilator.
Always ship the ventilator using the original packing material. If
the original material is not available, contac t your Respironics representative to order replacement s.
Do not operate the ventilator without a properly functioning
expiratory filter and heater. Doing so may cause damage to delicate ventilator components, such as the expiratory flow sensor, which may lead to inaccurate spirometry or a Vent Inop condition.
The ventilator oxygen filter should be replaced annually as a part
of preventive maintenance.
The PCMCIA card should only be removed by trained service
personnel once power to the ventilator is off.
To avoid the possibility of damage t o the ventilator, do not connect
a humidifier whose maximum rati ng exc eed s 3 am ps. Ensure tha t the humidifier power cord is free from defects and any obvious wear, and is properly grounded. A hu mi difier connection is only available on 100-120VAC ventilators.
Before connecting the ventilator to the AC power source, ensure
that the total electrical load does not exceed the ampere rating of the AC branch circuit, especially when using the ventilator with other electrical equipment. An AC branch circuit includes all outlets serviced by a single circuit breaker. If the maximum current drain through a branch circuit exceeds the circuit breaker’s rating, the branch circuit will open, causing the
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 2-5
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Chapter 2
Warnings, Cautions, and Notes
ventilator to lose power. For further information, consult a service technician or a trained biomedical technician.
The ventilator is shipped with a power cord that complies with electrical safety standards. Do not use substitute power cords unless specifically instructed to do so by an authorized distributor or qualified personnel. Do not modify the power cord or connect it with electrical extension cords or outlet adapters.
To prevent the risk of excessive leakage due to external equipment being connected to the ventilator via the communication ports, a means for external separation of the conductive earth paths must be provided.
All equipment used and connected to the ventilator communications ports (analog, parallel, and serial) must comply with the medical electrical equipment (IEC601-1) or other applicable standards.
The remote alarm port is intended to connect only to SELV (safety extra low voltage and ungrounded system with basic insulation to ground), in accordance with IEC60601-1. To prevent damage to the remote alarm, the signal input should not exceed the maximum rating of 24 VAC or 36 VDC at 500 mA with a minimum current of 1 mA.
Failure to protect the expiratory filter from damage by using inappropriate patient circuit configurations may cause damage to delicate ventilator components, such as the expiratory flow sensor, which may lead to inaccurate spirometry or a Vent Inop condition.
If clinical conditions do not require setting the HIP Limit above 60 cmH cmH
O, we recommend the setting normally be adjusted to 60
2
O or less in order to prolong the operating life of the blower
2
and to maximize backup battery run time.
The ventilator alarm indicators and the Alerts insert should be monitored closely during the Alarm Silence period to ensure that unexpected alarms are noticed.
If an alarm persists for no apparent reason, contact Respironics Customer Service at 1-800-345-6443.
Care should be taken when cleaning the touch display. (Refer to Figure 8-2 on page page 8-3). A soft moist cloth should be used that does not drip water and/or soap solution when in contact with the display. After cleaning and rinsing with a damp cloth, remove all moisture with a dry, soft cloth. Never allow solutions of any kind to collect on the bottom bezel of the display. Never use a brush or device that can cause abrasion to clean the touch display or its bezel; they will cause irreparable damage.
Do not remove any screws from the cooling filter area. Removing screws from this area will result in damage to internal components.
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Chapter 2
Warnings, Cautions, and Notes
Follow the detergent manufacturer’s instructions. Exposure to
detergent solution stronger than necessary can shorten the useful life of the product. Rinse parts thoroughly to remove all detergent residues. Wipe parts dry. Detergent residue can cause blemishes or fine cracks, especially on parts exposed to elevated temperatures during sterilization.
Autoclavable parts will withstand repeated steam autoclaving at
temperatures not to exceed 135° C (275ºF).
DO NOT autoclave the ventilator.
Formaldehyde, phenol-based, and quaternary ammonium
compound (QUATS) disinfectants are not recommended because these agents can cause cracking and crazing of plastic parts. Exposure of components to disinfectant concentrations stronger than required or for excessive time may shorten product life. Parts should be thoroughly rinsed and dried to prevent spotting and blemishes when exposed to elevated temperatures.
DO NOT allow liquid to penetr ate the ventilator rear or front panel.
DO NOT attempt to sterilize the ventilator by exposing to ETO gas. DO NOT steam-autoclave.
Troubleshooting and repair should be performed only by a
qualified service technician.
If the optional external O
sensor is in-line, it must be calibrated
2
during EST.
Diagnostic codes should only be cleared by qualified personnel.
To prevent contamination of the O
sensor, always locate it
2
between the ventilator gas output port and the inspiratory bacteria filter.
•PVC O
(P/N 8-100498-00) and Ultem® (P/N 1020380) Sensor
2
Tees cannot be autoclaved or chemically disinfected.
When inserting the battery tray into the cart’s center column,
make sure not to crimp cable connections between the battery tray and cart.
The backup battery is designed to be charged only by the
Respironics V200 Ventilator. Under no circumstances should an attempt be made to charge it in any other way.
If the ventilator will not be used for 30 days or more, the backup
battery should be preserved. Either disconnect the backup battery from the ventilator or keep the ventilator plugged into an active electrical outlet.
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 2-7
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Chapter 2
Warnings, Cautions, and Notes

Notes

Follow the setup instructions in this manual before placing the Respironics V200 Ventilator into service. If you have questions, contact Respironics Customer Service at 1-800-345-644
Save the shipping container in case the backup battery has to be returned to Respironics.
We recommend that before using the ventilator for the first time, wipe the exterior clean and disinfect or sterilize its components according to the instructions in Chapter 10, “Care and Maintenance” or the component manufacturer’s instructions.
Follow institutional infection control guidelines when rep lacing the inspiratory or expiratory bacteria filter.
When adding attachments or other components or subassemblies to the breathing system, for example, an HME or humidifier, ensure that the inspiratory and expiratory resistances (measured at the patient connection port) do not exceed 6 cmH
O (hPa) at a
2
flow of 60 L/min for adults, 30L/min for pediatrics.
High humidity and aerosol medications may reduce expiratory filter life, increase expiratory resistance, and/or cause filter damage. Review ventilator patient graphics frequently for changes in expiratory resistance. Consult filter manufacturer recommendations regarding duration of use, maintenance, and removal and disposal of expiratory filter.
The ventilator should only be connected to an appropriate medical grade 100% O
gas source capable of delivering a regulated 40 to
2
90 PSIG (276-620 kPa).
The ventilator is shipped with the appropriate gas fittings and hoses for the intended environment, i.e. DISS (U.S.A . and Canada), Ohmeda (Germany), NIST (UK), Air Liquide (France), SIS (Australia).
All volumes entered into the ventilator are assumed to be BTPS (Body Te mperature atmospheric Pressure Saturated (with H
2
O)) volumes unless otherwise noted. All volumes reported by the ventilator are reported as BTPS volumes. All pressures are assumed to be relative to atmospheric pressure unless otherwise noted.
The Air Inlet Filter houses a reusable foam filter that should be periodically cleaned. Refer to Chapter 10, “Care and Maintenance”, for more information on filter changes.
Unless the Mains Circuit Breaker is turned OFF, electrical power is applied to the ventilator even though the front panel switch is in the OFF position. With the Mains Circuit Breaker ON, if the backup battery is connected, the ventilator will charge the battery if it requires a charge.
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Chapter 2
Warnings, Cautions, and Notes
To disconnect the ventilator from MAINS power, remove the AC
plug from the wall power receptacle. The MAIN switch/circuit breaker is covered to prevent unintentional ventilator turn off.
If the operator sets the %O
indicator does not light. The 100% O the 100% O
front panel key has been pressed.
2
The ventilator selects its power source based on the following
prioritization: AC power (if present), external battery, then backup battery.
The ventilator may automatically reset certain types of alarm
conditions once the causes of the alarms are corrected. After an automatic reset, the ventilator will clear the audible alarm and will display a Low Urgency Alarm alert in the Alert Message Insert to inform the operator that an alarm condition existed. When this situation occurs, use ALARM RESET to clear the visual alarm indicator.
For optimal performance and battery life of a newly purchased
backup battery, establish full backup battery charge by plugging the ventilator into AC power for eight (8) hours maximum, or until the charging indicator light turns off, and then unplug the unit.
setting to 100%, the 100% O2
2
indicator only lights when
2
To monitor backup battery performance and life, run the ventilator
on battery power for at least 20 minutes at typical settings once a month. Recharge the battery when the test is complete.
If the 100% O
available, the Low O 100% O
2
key is pressed and a 100% O2 gas source is not
2
alarm will be active for the two-minute
2
delivery period.
Manual breaths are not permitted during the inspiratory phase of a
breath (whether manual or spontaneous). Pressing the MANUAL BREATH key during these times will not result in the delivery of a manual breath.
Some settings buttons appear active despite the fact they are not
being used in the ACTIVE MODE. This is because the setting is used in Apnea Ventilation or when manual inspiration is pressed. The operator should always choose a value for an active button that is appropriate for the patient being ventilated.
When the active mode is set to NPPV, the HIP Limit Setting will
automatically be adjusted to 10 cmH
O above the current IPAP
2
setting.
Pt. Leak only appears on Patient Data block on Settings screen.
The V200 Ventilator keeps a distinct set of alarm limits for each
ventilation breath type (VCV, PCV and NPPV).
Any of the changes made in the screen shown in Figure 8-18, do
not take effect until the operator switches to the new ventilation breath type (in this case Pressure Control).
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 2-9
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Chapter 2
Warnings, Cautions, and Notes
If the EXP HOLD key is held continuousl y, and the expiratory hold maneuver exceeds 5 seconds, the ventilator automatically terminates the expiratory hold maneuver and begins a new inspiratory period.
If Auto PEEP as calculated in Equation 1: Aut o-PEEP = Expiratory Pause Pressure – End Expiratory Pressure, is negative, Auto-PEEP will be displayed as “—.”
All components of the patient circuit must not have leaks in order to pass SST.
If time is found to be incorrect more than once in the preoperational procedure, an internal battery may have to be replaced. Contact qualified service personnel or call Respironics Customer Service at 1-800-345-6443.
Because conditions and practices in health care institutions vary, this manual can only describe general guidelines. It is the user’s responsibility to ensure the validity and effectiveness of the methods used.
Because some environments cause a quicker collection of lint and dust than others, inspect and clean the fan filters more often than every 250 hours if necessary.
The “Hardware” function and EST in the Diagnostics Mode should only be run by qualified personnel.
A “restart” is an infrequent event.
The gas return port on the ventilator is a cylindrical port which requires mating to a specified expiratory filter to seal the expiratory limb.
The humidifier power connection is available only on 100-120V AC ventilators.
Record O
sensor manufacturing or warranty numbers and
2
installation date for future reference. Save manufacturers instruction about end of life replacement.
To ensure accurate O
monitoring, check O2 sensors periodically
2
and replace as per manufacturer specification.
Sensor performance and expected operating life information is outlined in the sensor manufacturer’s instructions for use. Thoroughly review all O
sensor instructions prior to installation
2
and use with the Respironics V200 Ventilator.
•O
sensor calibration is performed during EST. If recalibration of
2
the O
sensor is required, follow the instructions in “Extend e d
2
Self Test (EST)” on page 11-4 for running EST.
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Chapter 2
Warnings, Cautions, and Notes
Medical electrical equipment needs special precautions regarding
EMC and needs to be installed and put into service according to the EMC information provided in Chapter 12, “Technical Specifications”.
Speaking Mode is available ONLY in invasive ventilation mode.
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 2-11
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Chapter 2
Warnings, Cautions, and Notes
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2-12 Respironics V200 Ventilator Operator’s Manual REF 1057983 A
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Chapter 3. Symbols

The following symbols appear on the Respironics V200 V entilator, accessories, documentation, and packaging. Additional symbols pertaining to options and accessories are included in the documentation for each option or accessory. Refer to Chapter 13, “Options and Accessories”.
Symbol Description
Symbols
READ THE USER MANUAL OR ACCOMPANYING DOCUMENTS
ATTENTION
ON condition for part of the equipment. When pressed, the ventilator will operate from the MAINS voltage if connected or from the backup battery if the battery charge is within operating specifications.
OFF condition for part of the equipment
PROTECTIVE EARTH (ground)
POTENTIAL EQUALIZATION CONNECTOR used to connect the equipment to an electrical installation earth busbar
TYPE B applied part, which indicates equipment that provides a particular degree of protection against electric shock, particularly with regards to allowable leakage current and of the protective earth connection
SUITABLE FOR ALTERNATING CURRENT
DIRECT CURRENT
DRIP PROOF Chart recorder ANALOG OUTPUT. Pin 12 signals an unsilenced high or
medium urgency alarm: 0 VDC= active alarm, 1.5 VDC = no alarm or silenced alarm. (Voltage signal for flow and pressure reserved for futur e use.)
DC BATTERY CONNECTION
Table 3-1: Symbols (Sheet 1 of 5)
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 3-1
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Chapter 3
Symbols
Symbols (Continued)
Symbol Description
DC BATTERY CONNECTION
HOT SURFACE warning
EUROPEAN CONFORMITY
REMOTE ALARM connection
RS-232 serial output
PARALLEL PORT printer connection
ALARM SILENCE (Silences alarm for two minutes)
BRIGHTNESS ADJUST
AUDIO ALARM VOLUME CONTROL
ACCEPT
ALARM RESET
100% OXYGEN
Located between the ALARM RESET and 100% O2 buttons, this symbol indicates that the two keys (ALARM RESET AND 100% O must be pressed simultaneously for approximately five seconds to enter Diagnostic Mode
2)
Table 3-1: Symbols (Sheet 2 of 5)
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Symbol Description
MANUAL BREATH
EXPIRATORY HOLD
SCREEN LOCK
(Symbol version of the front panel only) Illuminates yellow to indicate backup battery IN USE (backup)
Chapter 3
Symbols
Symbols (Continued)
(Symbol version of the front panel only) llluminates yellow to indicate backup battery CHARGING
(Symbol version of the front panel only) Flashes red to indicate that the backup battery is LOW
(Symbol version of the front panel only) MAINS battery indicator
(Symbol version of the front panel only) EXTERNAL BATTERY is in use
DANGEROUS VOLTAGE—electrical shock hazard
The portion of the circuit breaker that must be pushed in to turn the CIRCUIT BREAKER OFF
The portion of the circuit breaker that must be pushed in to turn the CIRCUIT BREAKER ON
CANADIAN STANDARDS ASSOCIATION approval.
DATE OF MANUFACTURE
MANUF ACTURER
Table 3-1: Symbols (Sheet 3 of 5)
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Chapter 3
Symbols
Symbol Description
The product must be disposed of in accordance with the WEEE directive.
SEALED, NON-SPILLABLE LEAD ACID BATTERY. MUST BE RECYCLED
Pb
SEALED, NON-SPILLABLE LEAD-ACID BATTERY. MUST BE
Pb
RECYCLED
RECYCLE
Symbols (Continued)
-20C
500-1060 hPa
THIS SIDE UP
AT LEAST TWO PEOPLE ARE REQUIRED TO LIFT THE VENTILATOR TO AVOID POSSIBLE PERSONAL INJURY OR DAMAGE TO THE EQUIPMENT.
KEEP DRY
LIMIT TEMPERATURE TO BETWEEN-20 AND 60 ºC (-4 AND 140 ºF)
+60C
FRAGILE
Table 3-1: Symbols (Sheet 4 of 5)
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Symbol Description
STORE AT 10%-95% RELATIVE HUMIDITY
%
10-95
Do not stack > 2 high
2
Chapter 3
Symbols
Symbols (Continued)
Table 3-1: Symbols (Sheet 5 of 5)
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 3-5
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Chapter 3
Symbols
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3-6 Respironics V200 Ventilator Operator’s Manual REF 1057983 A
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Chapter 4. Getting Started

Unpacking The Respironics V200 Ventilator has been carefully packaged to assure safe

shipping. In addition, the packing container has been designed for easy unpacking. Do not discard packing materials.
Before unpacking the ventilator, examine the shipping carton(s) for visible damage. If the shipping carton(s) arrives damaged or if you suspect the contents are damaged, contact the carrier for an inspection report. If any damage is evident, we recommend that you photograph the carton(s) before the shipment is unpacked. Report any damage to the shi pping container or ventilator to your local authorized Respironics distributor and to the carrier.
Save all packing material after removing the ventilator. In the event that the ventilator or backup battery needs to be repacked and reshipped, use the original packing material or order replacement material from a Respironics representative.
NOTE: The contents of the shipping carton may vary.
Top Foam Insert
Respironics V200 Ventilator
Center Foam Insert
Bottom Foam Insert
Figure 4-1: Unpacking/Repacking the Ventilator
WARNING: One person alone should not attempt to lift the ventilator or remove it from
the shipping carton or the cart. At least two people are required to avoid possible personal injury or damage to the equipment.
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 4-1
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Getting Started
NOTE: Medical electrical equipment needs special precautions regarding EMC
and needs to be installed and put into service according to the EMC information provided in Chapter 12, “Technical Specifications”.

Unpacking Instructions

Refer to Figure 4-1.
Tools Required: Box knife
1. Using a box knife, cut a slit in packaging tape on top of shipping carton.
2. Remove accessories box and optional flex arm box (not shown).
3. Remove top foam insert from inside carton.
4. Roll the plastic shipping bag (not shown) off the ventilator.
5. Gently lift ventilator from the bag and carton.
6. Remove patient circuit package (not shown).
7. Store carton, foam insert, and plastic bag in safe place for possible future use.

Inspection After unpacking the ventilator, inspect its cabinet exterior for damage,

including cracks and scratches or blemishes. Inspect the front panel for scratches, chips, abrasions or other deformities.
CAUTION: Be sure to check all exterior parts of the ventilator. Problems found
during inspection should be corrected and/or reported to Respironics before using the ventilator.

List of Parts and Accessories

Using the packing list that accompanies the ventilator, take an inventory of the entire shipment before assembling the ventilator. In case of discrepancies, immediately contact Respironics Customer Service at 1-800-345-6443.
The Esprit/V200 Ventilator Service Manual, P/N 580-1000-02, is available for qualified personnel. It includes block diagrams, components parts lists, descriptions, calibration instructions, and ot her information that will assist appropriately qualified personnel to repair those parts of the equipment that are designated by the manufacturer as repairable. For more information contact Respironics Customer Service at 1-800-345-6443.
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NOTE: We recommend that before using the ventilator for the first time, wipe
the exterior clean and disinfect or sterilize its components according to the instructions in Chapter 10, “Care and Maintenance” or the component manufacturer’s instructions.

Repacking Should the ventilator need to be returned to Respironics for servicing, or

shipped elsewhere for any reason, instructions for repacking are listed below. The following instructions should be followed closely to avoid damage to the ventilator.
WARNING: One person alone should not attempt to lift the ventilator or remove it from
the shipping carton or the cart. At least two people are required to avoid possible personal injury or damage to the equipment.
CAUTION: Always ship the ventilator using the original packing material. If the
original material is not available, contact your Respironics representative to order replacements.

Repacking Instructions

Refer to Figure 4-1.
Tools Required: Heavy duty packaging tape
1. Open carton so that bottom foam insert is facing up.
2. Place backup battery in the bottom foam insert if it is being shipped.
3. Place center foam insert into box on top of the bottom foam insert.
4. If you are also shipping the flex arm, place it in its box (not shown)
and place the box in the bottom of the center foam insert.
5. Remove all power cords and accessory items from the ventilator.
6. Set the open ventilator shipping bag (not shown) in the box on the
middle foam insert.
7. Gently place the ventilator into the open bag. Check to ensure that the
ventilator is firmly positioned into bottom foam insert. Close plastic bag over the ventilator.
8. Replace accessories box (not shown) in the center foam insert beside
the ventilator (if also being shipped).
9. Place top foam insert onto ventilator. Ensure snug fit.
10. Close top flaps of carton and seal with heavy-duty packaging tape.
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 4-3
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Getting Started

Ventilator Positioning For information about mounting the ventilator on a table top, see the Esprit

Operator’s Manual (580-1000-01). If the ventilator is on a cart, lock the cart wheels as needed as shown in Figure
4-2.
Figure 4-2: Locking Ventilator Wheel

Backup Battery The ventilator will automatically switch to operating on backup battery power when

the AC power fails or the system is disconnected from AC mains power. A fully charged backup battery will operate the ventilator for approximately 30 minutes, dependent upon the specific ventilator setting.
WARNING: The batteries (backup battery) in the battery compartment are non-spillable
sealed lead acid. Recycle or dispose of batteries properly.
WARNING: Do not connect the DC power cord from the backup battery while the
Respironics V200 is functioning as a ventilator. Always turn the Po wer On/ Off switch to off ( ).
WARNING: Backup battery operating life may be affected by battery age and the number
of times it has been discharged and recharged. Over time the battery will degenerate and will not provide the same amount of operating time per charge that is available from a fully charged new battery. Use only the Respironics backup battery P/ N 1059956.
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Chapter 4
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Backup Battery Removal and Installation

Required Tool: Philips screwdriver Remove the backup battery from the internal packaging material and shipping
bag. Do not discard packing materials until the backup battery has been installed on the ventilator and its operation has been confirmed.
NOTE: Save the shipping container in case the backup battery has to be returned
to Respironics.
Figure 4-3 illustrates the backup battery assembly.
Figure 4-3: Backup Battery
1. Before the backup battery is installed, disconnect AC power and any
attached equipment. Disconnect the backup battery cable connector from the rear panel of the ventilator by rotating the connector's collar nut counterclockwise while pulling back on the connector.
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Figure 4-4: Disconnecting the Battery Cable
2. Remove the rear cable channel cover from the cart by gently prying it back from the top of the center column, freeing it from the column.
Rear cable channel cover
Figure 4-5: Removing the Rear Cable Channel Cover
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3. Loosen the ventilator mounting screws (4) from the underside of the
cart, and remove the ventilator from the cart.
WARNING: One person alone should not attempt to lift the ventilator or remove it from the
shipping carton or the cart. At least two people are required to avoid possible personal injury or damage to the equipment.
Mounting screws
Figure 4-6: Removing the Ventilator from the Cart
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 4-7
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Chapter 4
Getting Started
4. Remove the screws (4) holding the battery tray to the cart.
Battery tray mounting screws
Figure 4-7: Removing the Battery Tray
5. Gently pull up the battery tray and remove it from the cart.
Figure 4-8: Removing the Battery Tray
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6. If a battery is present in the battery tray, disconnect the old battery
from the battery tray’s cable.
Figure 4-9: Disconnecting the Old Battery from the Battery Tray’s Cable
7. Undo the straps, remove the old battery if present, and place the new
battery in the battery tray.
Figure 4-10: Inserting Battery Into Tray
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Getting Started
8. Position the D ring on the straps as shown below.
NOTE: If the D rings are not positioned properly, the excess strap will interfere
with the tray’s channel guide.
Figure 4-11: Positioning the D Rings on the Battery Straps
9. Connect the battery to the battery tray’s cable.
Figure 4-12: Connecting the Battery to the Battery Tray’s Cable
10. Insert the battery tray into the cart’s center column by mating the battery tray’s channel guide to the tray’s channel guide of the center column.
CAUTION: When inserting the battery tray into the cart’s center column, make sure
not to crimp cable connections between the battery tray and cart.
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Figure 4-13: Installing the Battery Tray
11. Slide the battery halfway down the center column, and insert the
circular right angle battery connector into the cutout. Pull the cable downward as the tray is fully inserted into the cart's center column.
Figure 4-14: Inserting the Circular Right Angle Battery Connector Into the Cutout
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12. Fasten the battery tray to the cart using the 4 screws used when the tray was removed.
Battery tray mounting screws
Figure 4-15: Battery Tray Mounting Screws
13. Set the ventilator back on the cart, ensuring that the four ventilator feet meet the four circular recesses on the top of the cart. Tighten the four mounting screws that were loosened in step 3 .
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14. Routing the backup battery cable from the tray between the rear of the
ventilator and the rear handle of the cart, connect the cable to the circular battery connector on the back of the ventilator. Snap the rear channel cover back into place.
Battery backup connector
Figure 4-16: Backup Battery Connector
15. Plug the ventilator into an AC outlet.
16. Allow the backup battery to charge as required (see “Battery
Charging” on page 4-15).
17. When charging is complete, attach a patient circuit
and turn the
ventilator on in the diagnostics mode. Select the User Config touch key and enable the Backup Battery confirmation feature (refer to Chapter 5, “Backup Battery”).
18. Run SST (refer to Chapter 11, “Diagnostics”).
19. After SST has been successfully completed, exit the diagnostics mode
and power up the ventilator in the normal ventilation mode.
20. While the ventilator is cycling, unplug the AC power from the wall.
21. The ventilator should continue ventilation without interruption of any
kind.
22. The ventilator should have the “In Use” indicator (text version of front
panel) or the battery symbol (symbol version of the front panel) on and a non-silenceable, non-resettable audible alarm should sound every 60 seconds. "Backup Battery On" is displayed while the ventilator consumes power from the backup battery.
23. Plug the AC wall power back in and the ventilator should continue
ventilation without interruption of any kind.
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Getting Started

Backup Battery Operation

When the backup battery is attached and the Respironics V200 Ventilator is op­erating in normal ventilation mode an ytim e there is a loss of AC power, the ven­tilator will automatically switch to battery pow er a nd c on tinue ventilation without interruption. Whenever the ventilator is powered by th e backu p battery, it will generate a non-silenceable, non-resettable alarm that creates an alarm sound every 60 seconds. During this state, the front panel indicator labeled “In Use” (text version of the front panel as shown in Figure 4-17), or the battery symbol (symbol version of the front panel as shown in Figure 4-18) will illuminate yellow continuously. In addition, "Backup Battery On" is displayed.
Figure 4-17: Backup Battery Front Panel Indicators — Text Version
Figure 4-18: Backup Battery Front Panel Indicators — Symbol Version
Operation will continue in this state until the battery capacit y is nearly ex pend­ed. When the battery has only about 5 minutes of operation left, an audible, nonresetable, HIGH priority alarm will sound. When this happens, the red, front panel indicator labeled “Low” (text version of the front panel as shown in Figure 4-17), or the low battery symbol (symbol version of the front pan­el as shown in Figure 4-18) and the high priority alarm LED will flash continu­ously. In addition, "Low Backup Battery" is displayed.
WARNING: When the battery low indicator is flashing red, operation of the ventilator
from the battery power should be discontinued.
When power is finally depleted, the ventilator will open the Safety Valve a nd terminate ventilation in an orderly fashion. In this state, the front panel dis­plays "Backup Battery Depleted-Connect AC & Cycle Power." The backup alarm emits a continuous tone, the high priority alarm LED flashes, and the Safety Valve, V ent Inop, and Battery Low front panel indicators remain lit until power from the Backup Battery is completely gone.

Battery Capacity

There is a great deal of variability in the power consumption of the ventilator depending on altitude, ventilator settings, and the age and amount of charge on the backup battery. These parameters will determine the exact amount of time the ventilator can operate from the backup battery.
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Battery Charging

When the ventilator is plugged into a viable AC supply, it will charge the backup battery if the Mains Circuit Breaker is on and the machine is operating as a ventilator, or in diagnostic mode or the Power ON/OFF switch is OFF Charging time will depend on the amount of charge the batteries require. A fully discharged backup battery will be fully recharged within 10 hours. If the backup battery does not reach a full charge within 10 hours, contact Respironics Customer Service. While the ventilator is charging, the front panel indicator labeled “Charging” (text version of the front panel as shown in Figure 4-17) or the charging battery symbol (symbol version of the front panel as shown in Figure 4-18) will be on continuously. When the backup battery is fully charged, the indicator will turn off.
NOTE: For optimal performance and battery life of a newly purchased backup
battery, establish full backup battery charge by plugging the ventilator into AC power for eight (8) hours maximum, or until the charging indicator light turns off, and then unplug the unit.
( ).
NOTE: To monitor backup battery performance and life, run the ventilator on
battery power for at least 20 minutes at typical settings once a month. Recharge the battery when the test is complete.
CAUTION: The backup battery is designed to be charged only by the Respironics
V200 Ventilator . Under no circumstances should an attempt be made to charge it in any other way.
CAUTION: If the ventilator will not be used for 30 days or more, the backup battery
should be preserved. Either disconnect the backup battery from the ventilator or keep the ventilator plugged into an active electrical outlet.

Warranty

Respironics warrants the backup battery to be free from defects in material and workmanship for a period of one year from the date of purchase, provided that the unit is operated under conditions of normal use as described in this operator’s manual.
At its discretion, Respironics will make replacements, repairs or issue credits for equipment or parts that are found to be defective.
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 4-15
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Inspiratory Bacteria Filter Installation

The inspiratory bacteria filter (4) in Figure 4-19, mounts on the gas outlet port (1) located in the lower right corner on the front of the ventilator. If the optional O (1) before the inspiratory bacteria filter is connected. For more information regarding the optional O Accessories”.
sensor (2) will be used, it will be connected to the gas outlet port
2
sensor, refer to Chapter 13, “Options and
2
5
4
3
2
1
Flow
5
Figure 4-19: Inserting Disposable Inspiratory Bacteria Filter
4
3
2
1
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WARNING: To reduce the chance of contamination or infection, always use an
inspiratory and expiratory filter when the ventilator is in operation. Refer to manufacturer’s instructions and follow institutional infection control guidelines when replacing the inspiratory and expiratory filter.
WARNING: Do not use anti-static or conductive hoses or conductive patient tubing.
NOTE: Follow institutional infection control guidelines when replacing the
inspiratory or expiratory bacteria filter.
NOTE: When adding attachments or other components or subassemblies to the
breathing system, for example, an HME or humidifier, ensure that the inspiratory and expiratory resistances (measured at the patient connection port) do not exceed 6 cmH adults, 30L/min for pediatrics.

Inspiratory Bacteria Filter Installation Instructions

Refer to Figure 4-19.
1. Locate the gas outlet port (1) on the front panel.
2. If the optional O
port (1).
3. Remove the inspiratory bacteria filter from the filter package and
inspect for cracks or potential leaks. Discard the filter if it is cracked, has moisture inside, or is otherwise unserv iceable.
4. Some bacteria filters provide an arrow or other mark to indicate the
direction of flow. The flow indicator should be pointed away from the ventilator, toward the patient circuit connection Insert inspiratory filter inlet (4) into either
the optional O or
the gas outlet port (1) if the optional O
5. Connect inspiratory limb of patient circuit (5) to bacteria filter (4).
sensor (2) will be used, connect it to the gas outlet
2
sensor (2) using the 22mm connector (3 )
2
O (hPa) at a flow of 60 L/min for
2
sensor (2) is not used.
2
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Heated Expiratory Bacteria Filter Installation

Figure 4-20: Installing Expiratory Bacteria Filter
WARNING: The expiratory filter housing may be hot if removed from the ventilator
immediately after use. Wait 15 minutes after turning off ventilator power before removing the heated expiratory bacteria filter. Exercise caution when handling the filter housing.
CAUTION: Do not operate the ventilator without a properly functioning expiratory
filter and heater. Doing so may cause damage to delicate ventilator components, such as the expiratory flow sensor, which may lead to inaccurate spirometry or a Vent Inop condition.
WARNING: Vent Inop is a serious condition, which is indicated by both visual and
audible alarms. If the ventilator is attached to a patient when Vent Inop occurs, the patient must be supported with another means of life support ventilation.
NOTE: Follow institutional infection control guidelines when replacing the
inspiratory or expiratory bacteria filter.
NOTE: When adding attachments or other components or subassemblies to the
breathing system, for example, an HME or humidifier, ensure that the inspiratory and expiratory resistances (measured at the patient connection port) do not exceed 6 cmH2O (hPa) at a flow of 60 L/min for adults, 30L/min for pediatrics.

Heated Expiratory Bacteria Filter Installation Instructions

Refer to Figure 4-20.
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1. Locate the heated expiratory bacteria filter (1) and receiving compartment (6) in the lower center of front panel.
2. Turn knob (2) counterclockwise to unlatch retaining bracket (3).
3. Open retaining bracket (3) by pulling it out and away from the ventilator.
4. Use tabs (4) to gently pull the heater housing (5) away from the ventilator.
5. Ensure that ventilator has been turned off for 15 minutes. If not, allow the heater housing (5) to cool before touching it with fingers.
6. Gently remove the heater housing (5). Tap filter input port (7) if the filter does not come out easily.
7. Insert the new expiratory bacteria filter (1) into the heater housing (5).
8. Reinstall housing (5) and filter (1) into receiving com partment (6), then close retaining bracket (3).
9. Ensure that the retaining bracket (3) is securely closed and turn knob (2) clockwise to secure latch.
10. Connect the exhalation limb and water collection system of the patient circuit (not shown) to the inlet port of the exhalation filter (7).
NOTE: High humidity and aerosol medications may reduce expiratory filter life,
increase expiratory resistance, and/or cause filter damage. Review ventilator patient graphics frequently for changes in expiratory resistance. Consult filter manufacturer recommendations regarding duration of use, maintenance, and removal and disposal of expiratory filter.
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 4-19
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Oxygen Source Connection

Figure 4-21: O2 Gas Connections and Filter
WARNING: All oxygen connections should be carefully inspected to ensure that leaks
are not present. Excessive leaks can result in higher than normal ambient oxygen concentrations and create a potentially hazardous oxygen-enriched environment.
WARNING: Worn/frayed oxygen hoses or oxygen hoses contaminated by hydrocarbon
greases or oils should not be used since an oxygen leak or intense fire could result.
WARNING: Care in the routing of the oxygen inlet hose should be exercised to ensure it
is not exposed to mechanisms that could cause damage by cutting or heating/melting.
CAUTION: The ventilator oxygen filter should be replaced annually as a part of
preventive maintenance.
NOTE: The ventilator should only be connected to an appropriate medical
grade 100% O PSIG (276-620 kPa).
NOTE: The ventilator is shipped with the appropriate gas fittings and hoses for
the intended environment, i.e. DISS (U.S.A. and Canada), Ohmeda (Germany), NIST (UK), Air Liquide (France), SIS (Australia).
gas source capable of delivering a regulated 40 to 90
2
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Oxygen Source Connection Instructions

Refer to Figure 4-21.
1. Locate the O of the rear panel.
2. Ensure that the O the ventilator. Inspect the bowl (1) for cracks or potential leaks. Ensure all connections are tight.
3. Inspect the O mate (4).
4. Check the oxygen gas supply. Clean, adjust pressure, and drain condensate from any water traps, filters, or regulators in the O lines.
5. Connect O connector (4).
6. If gas source is not already turned on, turn it on and verify that no O gas is leaking.
filter with water trap (1) located in the lower left corner
2
filter and water trap (1) are properly attached to
2
hose (2), hose connector (3) and the hose connector
2
gas connector (3) to the ventilator O2 filter with DISS hose
2
Chapter 4
supply
2
2
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Getting Started

Patient Circuit Flex Arm Installation

A patient circuit flex arm is provided for use on the ventilator. The patient circuit flex arm may be installed on either the left or right side rail on the cart.
3
1
2
5
4
Figure 4-22: Patient Circuit Flex Arm Installation

Patient Circuit Flex Arm Installation Instructions

Refer to Figure 4-22.
1. Slide flex arm bracket (1) on to the side rail of the cart (one per side).
2. Tighten black screw knob (2) on flex arm bracket.
3. Insert base of flex arm (3) into flex arm bracket and tighten.
4. Place patient circuit hose clamp (4) into the flex arm clamp (5) and tighten.
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Chapter 5. Setup

C

Back Panel Connections and Controls

1.RS-232
Serial Port
2. Remote Alarm Nurse Call
3. Parallel Printer Port
4. PCMCIA Card Slot
5. Analog Port
6. DC Battery
Connector
17. Cooling Fan
Inlet
16. Potential Equalization
Connection
15. O
Inlet
2
Filter and
Water Trap
14. O
Inlet
2
Connector
13. Elapsed Time Meter
1. 232 Serial Port: Connection source for devices capable of serial
2. Remote Alarm Nurse Call: Connection source for remote alarm devices.
3. Parallel Printer Port: For use with the Communications Option. Refer to
4. PCMCIA Card Slot: (PC Card) For use with the T rending Option. Refer to
7. AC Inlet 8 Humidifier A
Circuit Breaker
9. Circuit Breaker Cover (not shown)
10. Mains Circuit Breaker
11. Humidifier AC Outlet
12. Air Inlet Duct and Filter
Figure 5-1: Back Panel
communication. Refer to Chapter 6, “Connecting Additional Equipment”.
Chapter 13, “Options and Accessories”.
Chapter 13, “Options and Accessories”.
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WARNING: The cover plate for the PCMCIA slot at the back of the ventilator must be
replaced after the adapter and card are installed. This is to protect the ventilator.
CAUTION: The PCMCIA card should only be removed by trained service personnel
once power to the ventilator is off.
5. Analog Port: Pin 12 signals an unsilenced high or medium urgency alarm. Other pins are used by the Communications Option. Refer to Chapter 13, “Options and Accessories”.
6. DC Battery Connector: Connection source for battery power cord.
7. AC Inlet: Connection for AC power cord.
8. Humidifier AC Circuit Breaker: Circuit breaker for AC power applied to a humidifier.
WARNING: AC power is applied to the humidifier from the ventilator humidifier outlet
(only available on 100-120 VAC ventilators). Under no circumstances does the Respironics V200 Ventilator provide control for the humidifier . T o ensure patient safety, it is important that any humidifier used with the ventilator include an acceptable temperature control and monitoring mechanism, as well as a temperature display and appropriate alarm capabilities (refer to ISO 8185).
CAUTION: To avoid the possibility of damage to the ventilator, do not connect a
humidifier whose maximum rating exceeds 3 amps. Ensure that the humidifier power cord is free from defects and any obvious wear , and is properly grounded. A humidifier connection is only available on 100­120VAC ventilators.
9. Circuit Breaker Cover: Circuit breaker cover (not shown) protects the Humidifier AC Circuit Breaker and Mains Circuit Breaker switches.
10. Mains Circuit Breaker: Circuit breaker for main AC circuit.
11. Humidifier AC Outlet: Connection for Humidifier AC power cord.
12. Air Inlet Duct and Filter: Filters room air drawn into the ventilator internal air source.
13. Elapsed Time Meter: Records time when the Power On/Off Switch is on ().
14. O
Inlet Connector: Connection for oxygen hoses.
2
15. O
Inlet Filter and Water Trap: Filters oxygen entering the ventilator.
2
16. Potential Equalization Connection: Common grounding point.
17. Cooling Fan Inlet: Allows cooling air to enter the ventilator.
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NOTE: All volumes entered into the ventilator are assumed to be BTPS (Body
Temperature atmospheric Pressure Saturated (with H2O)) volumes unless otherwise noted. All volumes reported by the ventilator are reported as BTPS volumes. All pressures are assumed to be relative to atmospheric pressure unless otherwise noted.

Connecting AC Power Cord

NOTE:
The Air Inlet Filter houses a reusable foam filter that should be periodically cleaned. Refer to Chapter 10, “Care and Maintenance”, for more information on filter changes.
2
3
1
Circuit Breaker Cover not shown.
Figure 5-2: AC Power Cord Retaining Bracket
WARNING: To avoid electrical shock hazard, connect the ventilator to a properly
grounded AC power outlet.
CAUTION: Before connecting the ventilator to the AC power source, ensure that the
total electrical load does not exceed the ampere rating of the AC branch circuit, especially when using the ventilator with other electrical equipment. An AC branch circuit includes all outlets serviced by a single circuit breaker. If the maximum current drain through a branch circuit exceeds the circuit breaker’s rating, the branch circuit will open, causing the ventilator to lose power. For further information, consult a service technician or a trained biomedical technician.
CAUTION: The ventilator is shipped with a power cord that complies with electrical
safety standards. Do not use substitute power cords unless specifically instructed to do so by an authorized distributor or qualified personnel. Do not modify the power cord or connect it with electrical extension cords or outlet adapters.
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Setup

Connecting AC Power Cord Instructions

Refer to Figure 5-2.
Tools Required: Small Phillips screwdriver
1. Ensure that the ventilator is properly positioned on a secure table top, wall mount, or pedestal.
2. Connect the AC Power Cord (1) to the AC inlet (3) located on the rear panel. (Refer to Figure 5-1.)
3. After cord is fully inserted, tighten the retaining bracket screw (2) so that the power cord cannot be inadvertently disconnected from the ventilator.

Power On/Off The ON/OFF ( / ) switch is located in the lower portion of the front panel,

and is recessed to avoid inadvertent access. When the switch is in OFF ( ) position, the ventilato r does not provide
mechanical ventilation. If the AC plug is connected and the Mains circuit breaker (refer to Figure 5-1) is ON ( ), AC power is active and the green Mains circuit indicator on the front panel, is illuminated.
Vent
Inop
Safety Valve
Power On/ Off Switch
Figure 5-3: On/Off Switch
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Turning the Ventilator On

1. Ensure that the Mains Circuit Breaker (refer to Figure 5-1), located on
the ventilator back panel, is in the ON ( ) position.
2. For 120V applications, if a humidifier is attached to the ven tilator,
ensure that the Humidifier AC Circuit Breaker (refer to Figure 5-1), located on the ventilator back panel, is in the ON ( ) position. A humidifier connection is only available on 100-120VAC ventilators.
3. Press the Power ON/OFF switch to the ON ( ) position (left side up).
WARNING: The ventilator front panel LEDs will indicate the power source that is being
used. If the ventilator is plugged in and the MAINS LED is not lit, either the circuit breaker is off or the wall power outlet is not functioning.

Turning the Ventilator Off

1. Press the Power ON/OFF Switch to the OFF ( ) position (right side
up).

Entering Diagnostic Mode

WARNING: The two circuit breakers (MAINS/Humidifier) located on the back of the
ventilator are covered to prevent unintentional ventilator power-off. Do not use the circuit breaker to power the ventilator on/off. The power switch is located on the front of the ventilator below the front panel.
NOTE: Unless the Mains Circuit Breaker is turned OFF, electrical power is
applied to the ventilator even though the front panel switch is in the OFF position. With the Mains Circuit Breaker ON, if the backup battery is connected, the ventilator will charge the battery if it requires a charge.
NOTE: To disconnect the ventilator from MAINS power, remove the AC plug
from the wall power receptacle. The MAIN switch/circuit breaker is covered to prevent unintentional ventilator turn off.
The Diagnostic Mode is used for:
1. Running tests of the operation of the ventilator that can only be run
when a patient is not attached to the machine.
2. Setting altitude, time and date, and circuit compliance.
3. Other more detailed service/maintenance functions.
4. Calibration of inline Oxygen Sensor, during EST only.
Some of these functions are discussed in detail in Chapter 12, “Technical Specifications”. The functions of the Diagnostic Mode that are used to make the machine ready for use as a ventilator when it is first put into service are explained here.
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Entering Diagnostic Mode

1. To access the Diagnostic Mode, simultaneously press the ALARM RESET and 100% O seconds while turning the ventilator power on. The following message will appear on the screen:
Figure 5-4: Warning in Diagnostic Mode
2. Press the OK button to enter the Diagnostic Mode. The following screen appears:
keys on the front panel for approximately five
2
Figure 5-5: Main Screen in Diagnostic Mode
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User Configuration Screen

The buttons across the top and bottom bars are used to select the Diagnostic Mode functions. To set up the machine for the first time for operation as a ventilator, USER CONFIG should be selected. When this button is pressed, the following screen appears.
Figure 5-6: User Configuration Screen
The User Configuration screen allows the operator to:
Set the date and time
Activate or deactivate the automatic patient circuit compliance
compensation feature
Set the proper altitude
Set 24 Hrs/AM PM time display
Activate or deactivate backup battery check at startup

Date and Time

The real-time clock and calendar will last for approximately 2.5 years. When the ventilator is received, the clock’s time will have to be changed to that of the existing time zone. The date should be checked and changed if necessary.

Setting Date and Time Format

To set time (Figure 5-8) or date (Figure 5-7):
1. Press the desired date or time button (month, day, year, hour, minute,
second).
2. When the window insert appears, press the INCREASE or DECREASE
button, or rotate the control knob to change the value of the selected parameter.
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3. Press the ACCEPT butt on to confirm the change and return to the User Config screen. Press the CANCEL button to leave the value unchanged.
Window insert to change the value of Month
Figure 5-7: Setting the Date
Window insert to change the value of Hour
Figure 5-8: Setting the Time
4. After the date and time values have been set, the changes will be shown on the screen.
5. Press the APPLY DATE and APPLY TIME buttons to activate the change.
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Apply Date
button
Apply Time button
Figure 5-9: User Configuration Screen After Date and Time are Set
Chapter 5
Setup
6. The 24 HR CLOCK button allows the operator or technician to set the
displayed time in an AM/PM (e.g., 1:15 PM) or 24 Hr. (e.g., 13:15) format. When the 24 HR CLOCK button has a white background, time is displayed in the 24 Hr. format; when it has a gray background, time is displayed in the AM/PM format.
7. Press the 24 HR CLOCK button to toggle between AM/PM and 24 Hr.
formats. Observe the time display in the lower right hand corner of the diagnostic screen to confirm the format.

Altitude

The User Configuration screen in the Diagnostic Mode is used to input the altitude of the location of the ventilator. To enter Diagnostic Mode, follow th e instructions “Entering Diagnostic Mode” on page 5-6. At Figure 5-5 select USER CONFIG and the screen in Figure 5-10 appears. Pressing the ALTITUDE button enables you to set the altitude to that of the present geographical location of the ventilator. This factor ensures a more accurate tidal volume delivery.

Setting Altitude

To adjust the altitude:
1. Verify the altitude using an altimeter, if available , or estimate the
altitude in feet (or meters) above sea level.
2. Press the ALTITUDE button.
3. When the window insert appears, select either feet or meters. Press
the INCREASE or DECREASE button, or rotate the control knob, to change the value. The longer the increase and decrease are touched, the faster the value will change.
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4. Press ACCEPT to accept the changed value. Press the CANCEL button to leave the value unchanged.
Window insert to change the value of Altitude
Figure 5-10: Setting Altitude

Enabling/Disabling Tubing Compliance

The operator can activate or deactivate “tubing compliance compensation” in the User Configuration screen. To enter Diagnostic Mode, follow the instructions for “Entering Diagnostic Mode” on page 5-6. At Figure 5-5, select USER CONFIG and the screen in Figure 5-11 appears.
Figure 5-11: Compliance Activated
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You can have the ventilator compensate the volumes delivered in volume controlled, mandatory breaths with the tubing compliance volume by activating the COMPLIANCE button (Figure 5-11). Circuit compliance is activated when this button has a white background. When the function is activated the exhaled volumes reported by the ventilator will also be tubing compliance compensated.
Backup Battery You can have the ventilator confirm the backup battery is connected each time
that the machine powers on. Pressing the BKUP BATTERY button (Figure 5-
12) allows this confirmation feature, which is identified by an active button
with a white background.

Backup Battery

(confirm at startup) button active
Figure 5-12: Backup Battery Activated
From then on when the machine powers on, it searches for a backup battery . If the backup battery is connected to the ventilator, the startup is normal. If the backup battery is not connected, the ventilator displays a message at startup and a 5002 Diagnostic Code will be logged.
Figure 5-13: No Backup Battery Connected message
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Press the OK button to clear the message from the screen. You may continue to use the ventilator without the backup battery or power off the ventilator and reconnect the backup battery.
WARNING: Always turn the ventilator power OFF before connecting additional
equipment.
To turn this feature off, enter Diagno stic Mode and deactivate the messaging feature by pressing the BKUP BATTERY button.
1. Power off the ventilator.
2. Power on the ventilator while holding down the ALARM RESET and 100% O
3. A message appears on the ventilator screen asking the user to ‘Verify that the patient is disconnected prior to proceeding.’ Press OK to enter Diagnostic Mode.
4. Once you’ve entered Diagnostic Mode, select USER CONFIG button, which takes you to the User Config screen.
5. Press the BKUP BATTERY button. The background color should return to blue signifying that this feature has been deactivated.
keys simultaneously for approximately 5 seconds.
2

Extended Self Test (EST)

We recommend that you run an Extended Self Test (EST) upon receipt of the ventilator to ensure that there has been no shipping damage to the system. We also recommend that you run EST betwee n patients to verify the overall functional integrity of the ventilator. Refer to chapter 11 for instructions on running EST.
If EST was run successfully and all configuration information has been entered, the ventilator is ready to be used. Follow the recommended “Preoperational Procedure” on page 8-32 once a patient has been selected.
To exit the Diagnostics Mode you must turn the Power On/Off switch OFF ( ) and then turn it ON ( ).
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Chapter 6. Connecting Additional Equipment

Communication Interface

WARNING: Always turn the ventilator power OFF before connecting additional
equipment.
CAUTION: T o prevent the risk of excessive leakage due to external equipment being
connected to the ventilator via the communication ports, a means for external separation of the conductive earth paths must be provided.
CAUTION: All equipment used and connected to the ventilator communications
ports (analog, parallel, and serial) must comply with the medical electrical equipment (IEC601-1) or other applicable standards.
The ventilator provides three communications interfaces: one serial RS-232 port, an analog output port, and a parallel port. (The parallel port is reserved for use by the Communications Option.)
Remote Alarm
Serial
AnalogParallel
AC Power Cord
Circuit Breaker (cover not shown)
Humidifier AC Outlet
Figure 6-1: Ports and Outlets on the Rear Panel
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Connecting Additional Equipment

Connecting Serial Communications Devices

Connecting Remote Alarm Port

The serial port is designed to transmit data on a one device to one device serial communications channel. In the connection between the two devices, the ventilator assumes the “slave” role and responds to commands transmitted to it via the serial port by the external “master.” The serial communications port uses a standard RS-232, null modem, pin configuration. The ventilator assumes the serial communications is set up for:
19,200 bits/second baud rate
8 data bits
no parity bit
1 stop bit
The ventilator is sent commands that are 4 ASCII characters from the external device and responds with a fixed format message. The commands and the responses are specified in Appendix A, “RS-232 Communications Protocol”.
The ventilator is equipped with a remote alarm port enabling ventilator alarm conditions to be sounded at remote locations away from the ventilator. Pressing ALARM SILENCE deactivates the remote alarm. The ventilator signals an alarm using a normally open or normally closed relay contact. The de­energized state of the relay represents an alarm state (any Medium or High Priority alarm) and the energized state represents no alarms.
The remote alarm port is a standard ¼ inch, female, phono jack (ring, tip, sleeve) connector.
Remote alarm
RingNO
TipNC SleeveCommon
Figure 6-2: Remote Alarm Port
The port is configured to work with the Normally Open (NO), Normally Closed (NC), and Respironics (LifeCare) systems. Each requires specific cabling identified in Table 6-1:.
connector & cable
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Connecting Additional Equipment
Remote Alarm Cable Kits
System Part Number
Remote Alarm Cable Kit (Normally Open Protocol) 1003741 Remote Alarm Cable Kit (Normally Closed Protocol) 1003742 Remote Alarm Cable Kit — Respironics (LifeCare) 1003743
Table 6-1: Remote Alarm Cable Kits
WARNING: Use only Respironics approved cables when connecting to the remote alarm
port. Be sure to fully insert the cable into the remote alarm port and into the remote alarm.
WARNING: When using the Remote Alarm Port, be sure to fully test the Remote Alarm
Port and cable by:
Verifying that annunciated alarms on the ventilator are also annunciated on the remote alarm.
Verifying that disconnecting the cable from the Remote Alarm port results in an alarm notification at the Remote Alarm.
Verifying that disconnecting the cable from the remote alarm results in an alarm notification at the Remote Alarm.

Connecting Humidifier

CAUTION: The remote alarm port is intended to connect only to SELV (safety extra
low voltage and ungrounded system with basic insulation to ground), in accordance with IEC60601-1. To prevent damage to the remote alarm, the signal input should not exceed the maximum rating of 24 VAC or 36 VDC at 500 mA with a minimum current of 1 mA.
We recommend only those humidifiers that comply with ISO 8185 fo r use on the ventilator.
You should consult with the manufacturer(s) of the active humidification system (humidifier and patient circuit components) for their most recent recommendations regarding circuit configurations. Additionally, unless specifically contraindicated by th es e manufacturers’ recommendations, we recommend the use of a drop-down tube and water collection vial (water trap) placed between the expiratory filter and the expiratory limb of the patient circuit. This is necessary to prevent damage to the expiratory filter. Refe rence P/N 1006241 Water Collection System, or equivalent.
CAUTION: Failure to protect the expiratory filter from damage by using inappropriate
patient circuit configurations may cause damage to delicate ventilator components, such as the expiratory flow sensor , which may lead to inaccurate spirometry or a Vent Inop condition.
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WARNING: Vent Inop is a serious condition, which is indicated by both visua l and audible
When connecting a humidifier to the patient circuit, follow the setup procedure supplied by the humidifier manufacturer . The following steps should be followed to electrically connect the humidifier to the ventilator (for 100­120 VAC ventilators). For ventilators using voltage other than 100-120 VAC, the humidifier must be connected to another AC outlet.
alarms. If the ventilator is attached to a patient when Vent Inop occurs, the patient must be supported with another means of life support ventilation.
1. Remove the cover of the humidifier AC power outlet on the back of the ventilator (Figure 6-3).
(Circuit Breaker Cover not shown)
Humidifier AC Outlet Cover
Figure 6-3: Humidifier AC Outlet Cover
2. Connect the humidifier AC plug to the humidifier AC power outlet.
(Circuit Breaker Cover not shown)
Humidifier AC Plug
Figure 6-4: Humidifier AC Plug
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3. Run any test procedures recommended by the h umidifier
manufacturer before the ventilator and humidifier are used on a patient.
WARNING: AC power is applied to the humidifier from the ventilator humidifier outlet
(only available on 100-120 VAC ventilators). Under no circumstances does the Respironics V200 Ventilator provide control for the humidifier . T o ensure patient safety, it is important that any humidifier used with the ventilator include an acceptable temperature control and monitoring mechanism, as well as a temperature display and appropriate alarm capabilities (refer to ISO 8185).

Connecting the Patient Circuit

1. The humidifier should be connected between the inspiratory bacteria
filter (Figure 6-5) and the inspiratory limb of the patient circuit that leads to the patient wye (Figure 6-6).
2. Follow steps illustrated by Figure 6-5, Figure 6-6, and Figure 6-7.
Figure 6-5: Ventilator Gas Outlet Port to Humidifier Patient Circuit Connection
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Figure 6-6: Humidifier Outlet to Patient Wye Connection
Figure 6-7: Expiratory Limb of Patient Circuit to Water Trap Connection (Shows Down
Tube between Ventilator and Water Trap)
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When connecting a patient circuit without a humidifier (for example, when using a heat and moisture exchanger), refer to Figure 6-8.

Connecting the Analog Port

Figure 6-8: Patient Circuit Connections Without Humidifier
The analog output port adds a second remote alarm output. Pin 12 (fourth pin from the top left is pin 12) signals an unsilenced high or medium urgency alarm:
0 VDC = active alarm
1.5 VDC = no alarm or silenced alarm
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The Communications option provides additional signals on this port. Refer to Chapter 13, “Options and Accessories”.
Analog Port
(Circuit breaker cover not shown)
Figure 6-9: Analog Port
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Chapter 7. Operating Theory

Introduction This chapter describes the ventilator’s breath delivery capabilities. It includes

a system overview and descriptions of the ventilation modes and available breath types. For descriptions of button settings and general operating instructions, refer to Chapter 8, “Operating Instructions”.

System Overview The ventilator is a microprocessor-controlled ventilator capable of delivering a

mixture of air and oxygen to a patient’s lungs in a predetermined manner to augment or replace the work normally performed by the patient’s respiratory system. The ventilator performs breath delivery via two different patient interfaces:
endotracheal tube or tracheostomy tube (invasive ventilation)
face mask, nasal mask, nasal pillows, or mouthpiece with a seal (non-
invasive ventilation)

Ventilator Breath Types

The ventilator provides the following ventilation breath types:
Volume Control Ventilation (VCV) – invasive ventilation
Pressure Control Ventilation (PCV) – invasive ventilation
Non-Invasive Positive Pressure Ventilation (NPPV) – non-invasive
ventilation
During mechanical ventilation, the operator selects one of the ventilation modes. The selected ventilation breath type, along with the selected mode, the patient breathing effort, and the ventilator settings determine the type of breath delivered. Each ventilation breath type has its own settings, alarms, and monitor screens. (Refer to Chapter 8, “Operating Instruct ions”.)

Volume Control Ventilation (VCV)

In Volume Control Ventilation, breaths may be controlled by the ventilator (mandatory) or triggered by the patient (spontaneous). When controlled by the ventilator, breaths will be flow controlled and time cycled, thus delivering an operator (TIDAL VOLUME) set volume. In Volume Control Ventilation, the flow pattern can be selected between square and descending ramp waveforms. Refer to Figure 7-1.
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Figure 7-1: Volume Control Ventilation (VCV) Waveform

Pressure Control Ventilation (PCV)

In Pressure Control Ventilation, breaths may be controlled by the ventilator (mandatory) or by the patient (spontaneous). When controlled by the ventilator , breaths are pressure limited and time cycled, resulting in an operator set (PRESSURE) pressure being delivered for an operator set (I-TIME) period of time. Refer to Figure 7-2.
Figure 7-2: Pressure Control Ventilation (PCV) Waveform
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Ventilation Modes Common to VCV and PCV

In Volume Control Ventilation and Pressure Control Ventilation, the operator can select between ventilation modes of Assist/Control, SIMV, and CPAP.

Assist Control Ventilation (A/C)

With the Assist/Control mode (refer to Figure 7-1 or Figure 7-2), a minimal rate and tidal volume (or inspiratory pressure) are set by the operator. The patient can trigger the ventila tor at a more rapid rate, but the operator set tidal volume (or inspiratory pressure) is delivered during each breath. The ventilator delivers only mandatory breaths. Assisted breaths may be either pressure or flow triggered. If the trigger setting is adjusted so that the patient cannot trigger the ventilator, all breaths will be delivered by the ventilator at the operator set rate and tidal volume (or pressure).

Synchronized Intermittent Mandatory Ventilation (SIMV)

SIMV is a ventilation mode where the patient is allowed to breathe spontaneously and the machine attempts to deliver volume (VCV) or pressure (PCV) mandatory breaths in synchrony with the patient’s effort at the operator set rate and volume (or pressure). This is accomplished by a combination of spontaneous and mandatory windows that open and close. The type of breath delivered depends upon whether the event during the window is patient initiated, operator initiated or time initiated. This logic is illustrated in Table 7­1: “SIMV Logic”.
SIMV Logic
Current SIMV State Inputs Ventilator Response
Mand Window
Mand Window
Spont Window
Spont Window
Spont Window
Time Trigger (breath period timer expires)
Patient Trigger; Operator Trigger
Patient Trigger Deliver a spontaneous breath using
Operator Trigger Deliver a mandatory breath using operator
Time Trigger (breath period elapses)
Deliver mandatory breath using operator settings for mandatory breath type; Restart breath period
Deliver mandatory breath using operator settings for mandatory breath type
operator settings for spontaneous breath type
settings for mandatory breath type Restart breath period timer Mand
Table 7-1: SIMV Logic
Next SIMV State
Mand Window
Spont Window
Spont Window
Spont Window
Window
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Continuous Positive Airway Pressure (CPAP)

CPAP is a spontaneous mode of ventilation. No mandatory breaths are delivered. Throughout the breath cycle, an opera tor set pressure is provided. The level of pressure delivered during CPAP is the baseline pressure, or PEEP (Positive end Expiratory Pressure). Refer to Figure 7-3.
Figure 7-3: Continuous Positive Airway Pressure (CPAP)

Pressure Support Ventilation (PSV)

In Pressure Support Ventilation, the patient’s spontaneous efforts are assisted by the ventilator at an operator set level of inspiratory pressure. Inspiration is initiated by the patient and terminated when the inspiratory flow falls below an operator set percentage of the peak flow during this breath. During Pressure Support, the patient determines the respiratory rate, and the patient and ventilator determine the inspiratory time and tidal volume. Refer to Figure 7-4.
Figure 7-4: Pressure Support Ventilation (PSV)
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Positive End Expiratory Pressure (PEEP)

The PEEP pressure is the operator set baseline pressure maintained during exhalation. All breaths are referenced to this baseline pressure and the resulting pressure is in addition to the baseline pressure. Refer to Figure 7-5.
Figure 7-5: Positive End Expiratory Pressure (PEEP)

Rise Time Setting

Rise Time applies to all pressure targeted breaths — PSV, PCV, and IPAP in NPPV. The operator can adjust the velocity of pressurization to better match the patient’s demand for flow. Refer to Figure 7-6.
Figure 7-6: Rise Time

Patient Initiated Breath Triggering

Patient initiated breaths can be flow or pressure triggered in A/C, SIMV, CPAP for Pressure or Volume breath types, or flow triggered in NPPV. The pressure trigger level determines the amount of pressure below the baseline pressure that the patient must create in order fo r the ventilator to deliver a breath. The Flow Trigger level is the amount of flow that the patient must inspire from the base flow in order for the ventilator to deliver a breath.
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Patient Leak Display

Estimated patient leak (Pt Leak) is displayed in LPM and updated at each breath. Pt Leak is the average leak rate during a breath (delivered volume minus exhaled volume divided by the breath time).
Pt Leak is estimated breath by breath. If the physical characteristics of the leak change, there will be a corresponding change in the actual leak flow, which will be detected and leak estimation will be updated in subsequent breaths. Physical characteristics of leaks are determined by a number of factors, for example, the size and shape of the leak (such as a gap in the seal between the mask and face). Leaks that may occur during invasive ventilation are usually undesirable and are not compensated to allow easier leak detection.

Ventilation Modes Common to NPPV

Non-Invasive Positive Pressure Ventilation (NPPV)

In Non-Invasive Ventilation, gas is delivered to the patient via a nasal mask, full face mask, nasal pillows, or mouthpiece with a lip seal. The operator determines whether the mode is totall y spon taneous (Spont Ventilation Mode) or spontaneous with a backup rate (Spont/T Ventilation Mode).

Spontaneous Ventilation Mode (Spont)

In Spontaneous Ventilation Mode, the operator sets the pressure during exhalation (EPAP) and the target pressure during inspiration (IPAP). The patient triggers the breath based on the Flow Trigger setting. Exhalation is determined by the setting E-Trigger , which is a percentage of peak flow during the breath. Refer to Figure 7-7.

Spontaneous/Timed Ventilation Mode (Spont/T)

In the Spontaneous/Timed Ventilation Mode, the patient can breathe spontaneously, or receive machined controlled breaths. The machine controlled breaths are delivered for a set inspiratory time at a set breath rate. In Spont/T mode, every patient initiated breath is spontaneous and restarts the breath period timer. If the patient triggers a breath before the breath period elapses, the ventilator delivers a spontaneous supported breath (based upon the settings). If the breath period elapses without a patient trigger, the ventilator delivers a ventilator initiated mandatory breath at the set IPAP level. Patient initiated, time cycled breaths are not delivered in Spont/T mode. Refer to Figure 7-7.
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Emergency Modes of Ventilation

Figure 7-7: Spont/T Mode
The ventilator has the following two emergency modes of ventilation that are entered in response to certain alarm conditions:
Apnea Ventilation
Safety Valve Open

Apnea Ventilation

Apnea ventilation provides an emergency mode of ventilation if the ventilator does not deliver a breath for an operator set interval of time. The apnea time can be set between 10 and 60 seconds. Upon entering this mode of ventilation, the ventilator will alarm and immediately start using the Apnea Rate setting specified by the operator. In PCV and VCV, the ventilator will begin delivering breaths in Assist/Control (A/C), but with the operator set Apnea Rate. In NPPV, the ve ntilator will deliver only machine controlled breaths either at the operator set Apnea Rate or in response to patient effort. In Apnea ventilation, the alarms used are the ones used for machine controlled breaths for the ventilation breath type (VCV, PCV and NPPV) the ventilator was using when Apnea occurred.
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Parameters Used in Apnea Ventilation, Settings, and Alarm Limits
VCV PCV NPPV
Settings
Alarm Limits
Tidal Volume Peak Flow PEEP I-Trigger (pressure/flow) Flow pattern O2 % Insp Hold Apnea Rate
High Pressure Low Insp Pressure Low PEEP Low Mandatory Tidal Volume High Rate High Exhaled Minute Volume Low Exhaled Minute Volume
Table 7-2: Parameters Used in Apnea V entilation, Settings, and Alarm Limits
Inhalation Pressure Inhalation Time PEEP I-Trigger (pressure/flow) Rise Time O2 % Apnea Rate
High Pressure Low Insp Pressure Low PEEP Low Mandatory Tidal Volume High Rate High Exhaled Minute Volume Low Exhaled Minute Volume
IPAP EPAP Inhalation Time Rise Time I-Trigger (flow) E-Cycle O2% Apnea Rate
Low Pressure Low EPAP Low Tidal Volume High Rate Low Exhaled Minute Volume High Leak
The ventilator will reset out of Apnea Ventilation if the operator presses the Alarm Reset button, or if the patient triggers two successive breaths.

Safety Valve Open (SVO)

Safety valve open is an emergency mode of ventilation that allows the patient to breathe through the system whenever any of the following occur:
1. An occlusion is detected. (The ventilator resumes normal breathe delivery if the occlusion is removed.)
2. Loss of both the air supply and the oxygen supply occurs. (The ventilator resumes normal breath delivery if the gas supply is made available.)
3. The Ventilator Inoperative state (Vent InOp) is entered due to a hardware malfunction that prevents breath delivery. (The ventilator will not resume normal breath delivery in this case. Call for service.)
During SVO:
1. The safety valve is opened,
2. The exhalation valve is opened,
3. The air and oxygen valves remain closed,
4. A high priority alarm is activated,
5. The Safety Valve Open indicator is illuminated,
6. The Normal indicator is turned off.
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Overview

Chapter 8. Operating Instructions

WARNING: Ensure that an alternative means of ventilation (that is, a resuscitator or
similar device) is available while the ventilator is in use on a patient.
WARNING: The ventilator complies with the requirements of IEC 601-1-2 (EMC
collateral standard), including the E-field susceptibility requirements at a level of 10 volts per meter. However, even at this level of immunity, certain transmitting devices (cellular phones, walkie-talkies, etc.) emit radio frequencies that could disrupt ventilator operation if operated in a range too close to the ventilator.
WARNING: DO NOT operate the ventilator in a Magnetic Resonance Imaging (MRI)
environment.
There are three ventilation breath types:
Volume Control Ventilation (VCV)
Pressure Control Ventilation (PCV)
Non-Invasive Ventilation (NPPV)
Each has mandatory or machine controlled breaths and each has patient controlled or spontaneous breaths.
Each ventilation breath type has its own settings that are mutually exclusive from the other ventilation modes.
1
In VCV, you can select either A/C, SIMV, or CPAP mode.
In PCV, you can select either A/C, SIMV, or CPAP mode.
In NPPV, you can select Spont/T or Spont mode.
Alarms are specific to the ventilation breath type. Alarm limits in one ventilation breath type are mutually exclusive from the alarm limits of the other ventilation breath types.
The ventilator is easy to use because all mode settings and alarm limits are selected using the same three-step process:
1. Select the parameter to be changed by pressing the associated button.
The screen shown in Figure 8-1 appears.
1. Set O2 and patient type are exceptions that can be changed only in the active mode and
applies to all modes.
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Digital value of setting to be changed
Increase bar, the farther from the middle the bar is pushed the faster the value changes. Similarly for the decrease bar.
Figure 8-1: Entering Settings and Alarm Parameters
2. Press the INCREASE bar or DECREASE bar until the desired value appears in the digital window, or use the front panel control knob to increase or decrease the displayed value.
3. Press the ACCEP T button (or FRONT PANEL ACCEPT key) to enter the value and return to the previous display. Press the CANCEL button to leave the value unchanged.
NOTE: All volumes entered into the ventilator are assumed to be BTPS (Body
Temperature atmospheric Pressure Saturated (with H unless otherwise noted. All volumes reported by the ventilator are reported as BTPS volumes. All pressures are assumed to be relative to atmospheric pressure unless otherwise noted.
O)) volumes
2
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The Front Panel The text version of the ventilator’s front panel includes the indicators and

controls shown in Figure 8-2. The symbol version of the front panel is shown in Figure 8-3.
Alarm Status Indicators
Touch Display
Power Status Indicators Front Panel Keys
Level Controls
Power On/Off Switch
Ven t Inop
Safety Valve
Figure 8-2: Front Panel — Text Version
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Alarm Status Indicators
Touch Display
Power Status Indicators Front Panel Keys
Level Controls
Power On/Off Switch
Ven t
Inop
Safety Valve
Figure 8-3: Front Panel — Symbol Version
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Alarm Status Indicators

The alarm status indicators located at the top of the ventilator alert you to the ventilator’s alarm conditions. (Refer to Chapter 9, “Alarms” for more detailed descriptions.)
Normal Alarm Med/LowAlarm High
VENT INOP
Figure 8-4: Alarm Status Indicators
SAFETY VALVE
Alarm Status Indicators
Alarm Indicator Status Description
Normal Green No active or auto reset alarm condition exists. High Flashing red A high priority alarm condition exists. Med/Low Flashing
yellow Continuous
yellow
Vent Inop Red (active) The ventilator is not capable of supporting
A medium priority alarm condition exists. A low priority alarm condition exists. In addition,
indicates auto reset conditions
mechanical ventilation and requires service. During Vent Inop, the ventilator opens the safety valve to enable the patient to breathe room air spontaneously. The ventilator also discontinues detection of new alarm conditions during Vent Inop.
WARNING: Vent Inop is a serious condition, which is
indicated by both visual and audible alarms. If the ventilator is attached to a patient when Vent Inop occurs, the patient must be supported with another means of life support ventilation.
Safety Valve Red (active) The safety valve is open and the ventilator is not in
operation. This is a high priority alarm condition. When the Safety Valve indicator is illuminated, the ventilator is not providing ventilatory support to the patient. The safety valve opens to allow the patient to breathe spontaneously through the ventilator circuit. The patient must be capable of creating a spontaneous breath in order to breathe through the safety valve.
Table 8-1: Alarm Status Indicators
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Power Status Indicators

Power status indicators alert you to the status of the backup battery. The text version of the power status indicators is shown in Figure 8-5. The symbol version of the power status indicators is shown in Figure 8-6.
NOTE: The ventilator selects its power source based on the following
prioritization: AC power (if present), external battery, then backup battery.
Figure 8-5: Power Status Indicators — Text Version
Figure 8-6: Power Status Indicators — Symbol Version
Power Status Indicators
Battery Indicator Status Description
In Use Yellow (active) The ventilator is running on backup battery
power. The backup battery is used when there is no AC power and no other battery is available.
Charging Yellow (active) The backup battery is charging. The battery
should not be considered a fully charged power source when this indicator is illuminated. The Charging indicator will stay on for the duration of the charging cycle, which can last up to ten hours. Once the battery has fully charged, the Charging indicator will turn off.
Low Flashing red The backup battery has approximately 5
minutes of power remaining.
WARNING: When the battery low indicator is
flashing red, operation of the ventilator from battery power should be discontinued.
Table 8-2: Power Status Indicators (Sheet 1 of 2)
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Power Status Indicators (Continued)
Battery Indicator Status Description
Mains Green The ventilator is connected to an AC power
source and the rear panel Mains circuit breaker is on ( I ).
Ext. Battery Yellow Continuously illuminated when the external
battery is in use. NOTE: The external battery is an optional
accessory. See “Options and Accessories” on page 13-1 for more information.
Table 8-2: Power Status Indicators (Sheet 2 of 2)
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Front Panel Keys

The front panel keys enable you to initiate ventilator functions. The keys that include an indicator ( ) also provide operational status of the function that it performs. The text version of the front panel keys is shown in Figure 8-7. The symbol version of the front panel keys is shown in Figure 8-8. (Refer to Chapter 9, “Alarms” for more detailed information on the alarm keys and buttons).
Figure 8-7: Front Panel Keys — Text Version
Figure 8-8: Front Panel Keys — Symbol Version
Key Symbol Definition Description
Screen Lock
Accept Function: Enables you to accept selected settings on the front panel
Function: Locks and unlocks the graphic display (touch screen). When the screen lock is activated, all on-screen buttons are disabled until the touch screen is unlocked. This prevents inadvertent setting and display changes via the touch screen. MANUAL BREATH, 100% O2, EXP. HOLD, ALARM RESET, and ALARM SILENCE keys are still active keys.
Indicator: Illuminates green when active.
graphical display.
Table 8-3: Front Panel Keys (Sheet 1 of 3)
Front Panel Keys
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Front Panel Keys (Continued)
Key Symbol Definition Description
Alarm Silence
Alarm Reset
Function: Disables the audio alarm for two minutes. When Alarm Silence is pressed before the end of a two-minute period, the two-minute timer is reset. Alarms that cannot be silenced are listed in Table 9-1: “Alarm Alert Messages” on page 9-5.
Indicator: Illuminated yellow when the audible alarm has been disabled; is active and stays on for two minutes when the ALARM SILENCE button is pressed. If ALARM SILENCE is active, and a new alarm condition occurs, which involves exceeding an active alarm limit, the visual alarm functions will be active. (Refer to “Alarm Silence” on page 9-2.) ALARM RESET clears ALARM SILENCE. If a medium or high priority alarm exists after ALARM RESET clears ALARM SILENCE, the audible alarm will begin.
Function: Clears the visual indicator for auto reset alarms, certain active alarms (see “Alarm Reset” on page 9-3), and reset of apnea ventilation back to the active mode of ventilation (see “Apnea Ventilation” on page 8-
27). Alarm Reset also terminates ALARM SILENCE.
Chapter 8
Operating Instructions
100% O
NOTE: The ventilator may automatically reset certain types of alarm
conditions once the causes of the alarms are corrected. After an automatic reset, the ventilator will clear the audible alarm and will display a Low Urgency Alarm alert in the Alert Message Insert to inform the operator that an alarm condition existed. When this situation occurs, use ALARM RESET to clear the visual alarm indicator.
Function: Press once to deliver 100% O2 to the patient for two minutes.
2
Subsequent button presses will reset the timer to two minutes. NOTE: If the 100% O
available, the Low O
delivery period.
O
2
key is pressed and a 100% O2 gas source is not
2
alarm will be active for the two-minute 100%
2
Indicator: Illuminated green; is active only when the 100% O2 front panel button has been pressed and the ventilator is delivering 100% O patient; remains on for the duration of 100% O
NOTE: If the operator sets the %O
setting to 100%, the 100% O2
2
indicator does not light. The 100% O the 100% O
front panel key has been pressed..
2
delivery (two minutes).
2
indicator only lights when
2
Table 8-3: Front Panel Keys (Sheet 2 of 3)
to the
2
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Key Symbol Definition Description
Manual Breath
Expiratory Hold
Front Panel Keys (Continued)
Function: Delivers an operator-initiated, mandatory (OIM) breath. Delivery of the breath is based on the current ventilation breath type settings.
NOTE: Manual breaths are not permitted during the inspiratory phase of a
breath (whether manual or spontaneous). Pressing the MANUAL BREATH key during these times will not result in the delivery of a manual breath.
Enables calculations of Auto-PEEP from an expiratory hold maneuver. (See “Special Procedures” on page 8-31.)
Table 8-3: Front Panel Keys (Sheet 3 of 3)

Front Panel Level Controls

The front panel level controls enable you to adjust ventilator settings, brightness, and volume.
Front Panel Controls
Control Definition Description
Adjust Control
Display Brightness
Audible Alarm Volume
On/Off Switch
Used in conjunction with the front panel graphical display and touch screen to enter operator-selected values for ventilator settings and alarms.
Increases or decreases the brightness of the touch screen display
Increases or decreases the audible alarm volume. The minimum audible alarm volume is dictated by international standards. The audible alarm volume control will not turn the audible alarm volume lower than the minimum decibel level dictated by these standards. It is not possible to turn the audible alarm volume off.
Located near the front panel, the On/Off switch is recessed to avoid inadvertent or accidental access. When the switch is in off ( ) position, the ventilator does not provide mechanical ventilation, although AC power is active and the green Mains indicator is illuminated.
Table 8-4: Front Panel Controls
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Ventilator Screens Front Panel Touch Display

The front panel display allows you to select ventilation modes, breath types, settings, alarms, and access patient data. The front panel display is a touch screen that lets you select settings and data so you can monitor the status of the patient, ventilator, and control ventilator operation.
There are two different categories of screens:
Ventilator Screens that appear when the machine is functioning as a
ventilator
Diagnostic Screens that appear when the machine is not functioning
as a ventilator and is running internal tests
(Refer to Chapter 11, “Diagnostics”, for more information about displaying ventilator diagnostic information.).

Common Ventilator Screen Components

Except for the patient data screen, sc reen configurations are determined by the selected ventilation breath type. Figure 8-9 shows the elements that are common to all ventilator (non-diagnostic) screens: the top bar , bottom bar , and manometer.
Chapter 8
Operating Instructions
To p Bar
Manometer
Bottom Bar
Figure 8-9: Elements Common to All Operational Screens (VCV settings shown)
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Figure 8-10 shows the top bar and describes its bu ttons.
Active Mode: push to display the settings for the active ventilation mode and breath type.
Figure 8-11 shows the bottom bar and describes its butto ns.
VCV Settings: push to display VCV settings screen, which allows you to view and change settings for volume controlled ventilation.
Active Alarms: push to show current alarm settings for the active ventilation mode and breath type.
Patient Data: push to show the Patient Data screen.
Monitor: push to display the monitor screen (ventilator settings and patient data).
Figure 8-10: Top Bar (common to all operational screens)
NPPV Settings: push to display NPPV settings screen, which allows you to view and change settings for noninvasive positive pressure ventilation.
Respiratory Mechanics button: selects
option if installed.
Graphics button: selects
option if installed.
PCV Settings: push to display PCV settings screen, which allows you to view and change settings for pressure controlled ventilation.
Option: for use in the future.
Printer: Available if Communications option is installed.
Figure 8-11: Bottom Bar (common to all operational screens)
Buttons in the bottom bar have two states, “selected” and “not selected”. In the “selected” state, the button has a white background and black letters (see VCV SETTINGS in Figure 8-11). In the “not-selected” state the button has a gray background and black letters (see PCV SETTINGS, and NPPV SETTINGS in Figure 8-11). In the upper bar the buttons PATIENT DATA, ALARM SETTINGS, and MONITOR are also the “selected/not-selected” type.
When one of these “selected/not-selected” buttons is selected, it indicates that the screen is being used to display the information described by the name of the button on the screen. Making a setting screen “sele cted” (for a breath type that is not active), is the first step to activa te that ventilation breath type (Refer to “Selecting a New Ventilation Breath Type (VCV, PCV, or NPPV)” on page 8-23.)
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Figure 8-12 shows the real time manometer displays.
Chapter 8
Operating Instructions
Waveform: airway pressure versus time
Upper limit of real time display determined by High Pressure alarm setting
Zero pressure line
Indicator
High pressure alarm setting ­press this button to modify HIP.
Breath Indicator
Manometer with Waveform Manometer only
(for mode setting screens)
Figure 8-12: Manometer (common to operational screens)
Table 8-5: “Breath Indicator” describes the breath indicator.
Breath Indicator
Breath Symbol Description
Mand Operator or ventilator triggered mandatory breath. Assist Patient triggered mandatory breath. Plateau Inspiratory hold, can be set at the end of the inspiratory phase of
a VCV breath type.
Support Patient triggered spontaneous breath with PSV>0 or IPAP>EPAP. Spont Patient triggered spontaneous breath, PSV=0 or IPAP = EPAP. Exhale Indicates exhalation phase of any breath.
Table 8-5: Breath Indicator
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Pressing the HIP indicator on the screen (Figure 8-12) will
HIP
immediately allow the operator to modify the high pressure limit for
VCV or PCV. In NPPV, the high pressure limit is automatically set to 10 cmH manometer in NPPV.
O (hPa) above IPAP. The HIP indicator does not appear near the
2

Settings Screens The buttons in the middle of the settings and alarm limit screens all have two

states: active and inactive. Active settings have a gray background with black letters (Figure 8-13). An active setting is currently being used to control ventilation or as an alarm limit. Inactive setting buttons have a gray background with gray letters. Inactive settings are not currently being used to control ventilation or as an alarm limit. In both states the button can be pressed and an insert window will appear that will allow the operator to change the value of the setting (Figure 8-1).
NOTE: Some settings buttons appear active despite the fact they are
not being used in the ACTIVE MODE. This is because the setting is used in Apnea Ventilation or when manual inspiration is pressed. The operator should always choose a value for an active button that is appropriate for the patient being ventilated..
Pressing the ACTIVE MODE button displays the settings screen for the currently selected ventilation breath type and mode (Chapter 7, “Operating Theory”, for more information on ventilation modes, breath types, and controls).
For example, in Figure 8-13 the current breath type is VCV and the mode is A/ C. Because A/C does not allow the ventilator to deliver any spontaneous breaths, any settings that apply to spontaneous breaths are not active and are grayed out. In Figure 8-13, PSV is grayed out, indicating that it isn’t active, but you can still push this button and change the PSV valu e. The PSV value will become active only if the SIMV or CPAP mode is selected.
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Ventilation mode: A/C, SIMV, or CPAP. Spont or Spont/T are available during NPPV
Chapter 8
Operating Instructions
Ventilation control settings: VCV, PCV, or NPPV
Figure 8-13: VCV Settings Screen (VCV active)

Selecting Settings

Follow these steps to adjust ventilator control settings:
1. Push VCV SETTINGS, PCV SETTINGS, or NPPV SETTINGS.
2. Push the button for the control settings you want to select. The ventilator displays the current value for that parameter in an insert that allows the operator to adjust the settings value. (Figure 8-14).
3. Press the bar to increase or decrease the setting to the value you want or use the front panel knob to adjust the value of the setting.
4. Press the screen ACCEPT button or the front panel ACCEPT button to activate the new setting or CANCEL to leave the setting unchanged.
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Push this bar to increase the value
Push this bar to decrease the value
Press CANCEL to leave the setting unchanged
Current or new value displayed digitally and graphically
Press ACCEPT to activate the new setting
Figure 8-14: Changing a Setting
When a value is entered, as shown in Figure 8-14, the ventilator checks to assure that the value has been accepted by the operator, is within limits, and will not cause other settings to be out of limits. If the new value causes these limits to be exceeded, a diagnostic message will be displayed. (Refer to “V alue Entry Message” on page 12-4 for more details about the diagnostic messages).

Selecting Alarm Limits

Follow these steps to adjust currently active alarm limits:
1. Push ALARM SETTINGS. The ventilator displays the alarm limits for the currently active ventilation mode (Figure 8-15).
2. Push the button for the alarm limit you want to adjust. The ventilator displays the current value for that alarm limit in a display insert, similar to Figure 8-14.
3. Press the bar or use the front panel knob to adjust the value.
4. Press ACCEPT to activate the new alarm limit or CANCEL to leave it unchanged.
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Push button of alarm you want to adjust
Chapter 8
Operating Instructions
Active ventilation mode and breath type button displayed
Indicates this screen is for VCV alarms
Figure 8-15: Setting Alarm Limits That Are Currently Active
The High Pressure Alarm Setting may be accessed through the Alarms Settings Screen or through the HIP Indicator adjacent to the manometer in the PCV and VCV Settings, Alarm Settings, Patient Data, and Monitor Screens.
WARNING: For patient safety the HIP Limit Setting should be set as close to the peak
inspiratory pressure as patient conditions allow.
CAUTION: If clinical conditions do not require setting the HIP Limit above 60
O, we recommend the setting normally be adjusted to 60 cmH2O
cmH
2
or less in order to prolong the operating life of the blower and to maximize backup battery run time.
NOTE: When the active mode is set to NPPV, the HIP Limit Setting will
automatically be adjusted to 10 cmH
Follow these steps to adjust alarm limits that are not currently active
O above the current IPAP setting.
2
:
1. Depending on the alarm limits you wish to review, push the VCV
SETTINGS, PCV SETTINGS, or NPPV SETTINGS button that has a gray background and black letters (not active).
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ACTIVATE button
Figure 8-16: PCV Setting while NPPV is the active breath type
2. From the control settings screen, push the ACTIVATE button. Refer to Figure 8-16. The ventilator displays a prompt insert (Figure 8-17).
Figure 8-17: Change Breath Type Insert Window for PCV
3. Select the REVIEW ALARMS button to display the alarm settings for PCV (Figure 8-18).
4. Notice that all the alarm buttons (Figure 8-18) are grayed out, indicating that the alarm limits are not currently active. The ventilator displays the current value for that set of alarm limits. Push the button for the alarm limit you want to adjust.
NOTE: The ventilator keeps a distinct set of alarm limits for each
ventilation breath type (VCV, PCV and NPPV).
5. Press the bar or use the front panel knob to adjust the value (as shown in Figure 8-14).
6. Press ACCEPT to activate the new alarm limit or CANCEL to leave it unchanged.
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Grayed out buttons indicate that the alarm limits are not active
Push button of alarm setting to adjust
Press this ACTIVATE button to switch to the ventilation breath type indicated. The ventilation breath type on this button indicates which alarm set is shown on this
Chapter 8
Operating Instructions
Figure 8-18: Setting Alarm Limits That Are Not Currently Active
NOTE: Any of the changes made in the screen shown in Figu re 8-18, do
not take effect until the operator switches to the new ventilation breath type (in this case Pressure Control).

Selecting Waveforms (VCV only)

Two inspiratory flow wave forms for mandatory VCV breaths are available: descending ramp and square wave (Figure 8-19). The selected waveform is highlighted and defines the inspiratory flow for all mandatory VCV breaths, whether they are initiated by the patient, the ventilator, or the operator. The waveform selection is not applicable to PCV or NPPV.
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Descending ramp and square wave act as mutually exclusive select/non-select buttons.
Push this button to select descending ramp waveform
Figure 8-19: Selecting Waveforms (descending ramp selected)
Push this button to select square waveform

Selecting Adult/Pediatric Buttons

You can conf igure ventilati on for adult or pediatric patients (Figure 8-20) from the active ventilation type screen. Selecting adult or pediatric tailors the ventilator’s breath delivery algorithms to the selected adult/pediatric patient type. Selecting adult or pediatric does not change how the screens work, and does not change ventilator or alarm settings. The patient type selection determines flow output at various rise time settings for PCV, PSV, and IPAP. In addition, the “I-Time too long” alarms and time out for spontaneous breaths are set to 3.5 seconds for the adult setting and 2.5 seconds for the pediatric setting. Peak flow is limited to 100 LPM in all pressure-based breaths when using the pediatric setting.
Push this button to select controls
Figure 8-20: Selecting Adult/Pediatric Controls (adult selected)
Push this button to select pediatric controls
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Selecting the Inspiratory Trigger (I-Trigger)

The I-Trigger setting determines how inspiratory effort is detected (by measuring a drop in airway pressure or an increase in patient inspiratory flow) and when inspiration begins.
In VCV and PCV, you can select a pressure or flow I-Trigger.
In NPPV, the I-Trigger is always Flow.
Follow these steps to set the I-Tri gger:
1. Push the VCV SETTINGS, PCV SETTINGS, or NPPV SETTINGS button.
2. Push the I-TRIGGER button. The inspiratory trigger window insert
(Figure 8-21) appears.
3. In VCV and PCV : select Pressure or Flow . (Because only the flow trigger
is available in NPPV, the Pressure and Flow buttons do not appear in this insert in NPPV.)
4. Adjust and change the value as described above.
You can select Pressure or Flow in VCV or PCV. In NPPV, only Flow I- Trigger is available (these buttons do not appear).
Figure 8-21: Inspiratory Trigger Window

Settings with Calculated Values

Certain window inserts that are used to modify values of settings can also have calculated results in them (Figure 8-22).
When the settings window insert being displayed is VCV Rate, the calculated minute volume that results from the rate and tidal volume setting s is displayed along with the rate value. This is also the case when the tidal volume setting window insert is displayed. When the setting window insert for PCV Rate is
REF 1057983 A Respironics V200 Ventilator Operator’s Manual 8-21
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Chapter 8
Operating Instructions
displayed, the calculated value for the I:E ratio that will result from the PCV rate value is also displayed.
When the setting window insert for VCV Apnea Rate is displayed, the calculated minute ventilation that will exist if the ventilator goes into Apnea Ventilation in VCV is shown. When the setting window insert for PCV Ap nea Rate is displayed, the I:E Ratio shown is the I:E Ratio that will exist if the ventilator goes into Apnea Ventilation in PCV.
PCV Settings Window Insert VCV Settings Window Insert
Setting to be changed on the top.
Setting that is calculated as the setting above changes, below.
I:E Ratio is the parameter that is calculated and displayed in certain PCV setting window inserts. These are PCV Rate, PCV I-T ime, and PCV
Figure 8-22: Settings Window Inserts With Calculated Results
VE is the parameter that is calculated and displayed in certain VCV setting window inserts. These

Rate and Apnea Rate Settings Relationship

For all breath types, VCV, PCV, and NPPV, the ventilator ensures the Apnea Rate setting is equal to or greater than the set Rate up to 20 BPM. When set rate is equal to the Apnea Rate and less than 20 BPM increasing the Set Rate increases the Apnea Rate equally up to 20 BPM. Above 20 BPM the Apnea Rate can be greater than or less than the Set Rate, down to 20 BPM.
8-22 Respironics V200 Ventilator Operator’s Manual REF 1057983 A
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