Philips Intellivue MP5 User manual

INSTRUCTIONS FOR USE

IntelliVue Patient Monitor

MP5
Release G.0 with Software Revision G.0x.xx
Patient Monitoring
Part Number M8105-9001C Printed in Germany 09/08 4512 610 29031
M8105-9001C
1Table Of Contents
1 Installation 1
Installation Checklist 1 Unpacking and Checking the Shipment 2 Mounting the Monitor 3 Connecting the Monitor to AC Mains 3 Checking Out The Monitor 3 Loading Paper 4 Operating the Monitor 5 Setting the Date and Time 6 Checking Country-Specific Default Settings 6 Handing Over the Monitor 6
2 Basic Operation 9
Introducing the Monitor 9 Operating and Navigating 13 Operating Modes 19 Understanding Screens 20 Using the XDS Remote Display (not MP5T) 21 Using the Visitor Screen 21 Understanding Profiles 22 Understanding Settings 24 Adjusting a Measurement Wave 25 Freezing Waves 26 Using Labels 27 Entering Measurements Manually 29 Changing Monitor Settings 29 Checking Your Monitor Revision 30 Getting Started 30 Disconnecting from Power 32 Networked Monitoring 32 Using the MP5 with a Host Monitor 33
3 What’s New? 35
What’s New in Release G.0? 35 What’s New in Release F.0? 36
4 Alarms 39
Visual Alarm Indicators 40 Audible Alarm Indicators 41 Acknowledging Alarms 43 Pausing or Switching Off Alarms 44 Alarm Limits 45 Reviewing Alarms 50
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Latching Alarms 52 Testing Alarms 52 Alarm Behavior at On/Off 53 Alarm Recordings 53
5 Patient Alarms and INOPs 55
Patient Alarm Messages 55 Technical Alarm Messages (INOPs) 61
6 Managing Patients 85
Admitting a Patient 85 Quick Admitting a Patient 87 Editing Patient Information 87 Discharging a Patient 88 Transferring Patients 89 Care Groups 92
7 ECG, Arrhythmia, ST and QT Monitoring 99
Skin Preparation for Electrode Placement 99 Connecting ECG Cables 99 Selecting the Primary and Secondary ECG Leads 100 Checking Paced Status 100 Understanding the ECG Display 100 Monitoring Paced Patients 101 Changing the Size of the ECG Wave 103 Changing the Volume of the QRS Tone 103 Changing the ECG Filter Settings 104 Selecting Positions of Va and Vb Chest Leads (for 6-lead placement) 104 Choosing EASI or Standard Lead Placement 105 About ECG Leads 105 ECG Lead Fallback 106 ECG Lead Placements 106 Capture 12-Lead 110 EASI ECG Lead Placement 111 ECG and Arrhythmia Alarm Overview 112 Using ECG Alarms 113 ECG Safety Information 114 About Arrhythmia Monitoring 115 Switching Arrhythmia Analysis On and Off 116 Choosing an ECG Lead for Arrhythmia Monitoring 116 Understanding the Arrhythmia Display 117 Arrhythmia Relearning 120 Arrhythmia Alarms 121 About ST Monitoring 127 Switching ST On and Off 127 Understanding the ST Display 128
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Updating ST Baseline Snippets 129 Recording ST Segments 130 About the ST Measurement Points 130 ST Alarms 132 Viewing ST Maps 133 About QT/QTc Interval Monitoring 137 QT Alarms 140 Switching QT Monitoring On and Off 141
8 Monitoring Pulse Rate 143
Entering the Setup Pulse Menu 143 System Pulse Source 143 Switching Pulse On and Off 144 Using Pulse Alarms 144
9 Monitoring Respiration Rate (Resp) 147
Lead Placement for Monitoring Resp 147 Understanding the Resp Display 148 Changing Resp Detection Modes 148 Changing the Size of the Respiration Wave 149 Changing the Speed of the Respiration Wave 150 Using Resp Alarms 150 Changing the Apnea Alarm Delay 150 Resp Safety Information 150
10 Monitoring SpO
SpO2 Sensors 153 Applying the Sensor 153 Connecting SpO2 Cables 154 Measuring SpO SpO2 Signal Quality Indicator (Fast SpO2 only) 155 Assessing a Suspicious SpO2 Reading 155 Changing the Averaging Time 156 Setting the Measurement Mode 156 Understanding SpO2 Alarms 156 Pleth Wave 157 Perfusion Numeric 158 Perfusion Change Indicator 158 Setting SpO2/Pleth as Pulse Source 158 Setting Up Tone Modulation 158 Setting the QRS Volume 159
2
2
154
11 Monitoring NBP 161
Introducing the Oscillometric NBP Measurement 161 Preparing to Measure NBP 162 Starting and Stopping Measurements 164
153
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Enabling Automatic Mode and Setting Repetition Time 165 Enabling Sequence Mode and Setting Up The Sequence 165 Choosing the NBP Alarm Source 166 Switching Pulse from NBP On/Off 166 Assisting Venous Puncture 167 Calibrating NBP 167
12 Measuring Predictive Temperature 169
Making a Temperature Measurement 169
13 Monitoring Temperature 173
Making a Temp Measurement 173 Calculating Temp Difference 174
14 Monitoring Invasive Pressure 175
Setting up the Pressure Measurement 175 Zeroing the Pressure Transducer 176 Adjusting the Calibration Factor 178 Displaying a Mean Pressure Value Only 178 Changing the Pressure Wave Scale 178 Optimizing the Waveform 179 Using the Wave Cursor 179 Non-Physiological Artifact Suppression 179 Choosing the Pressure Alarm Source 179 Calibrating Reusable Transducer CPJ840J6 181 Calculating Cerebral Perfusion 182 Calculating Pulse Pressure Variation 182
15 Monitoring Carbon Dioxide 185
Using the CO2 Measurement 186 Measuring Microstream CO Setting up all CO2 Measurements 190
2
189
16 Assigning Two Devices to One Patient 195
How Can You Combine Devices? 195 Functions Available When the Telemetry Data Window is Displayed 199 Functions Available For Devices Connected Via SRR 200 General Telemetry-related Functions 201 Use Models With Telemetry 202
17 Enhancing Telemetry Monitoring with the Monitor 205
18 Tre nd s 207
Viewing Trends 207 Setting Up Trends 210 Documenting Trends 213
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Trends Databases 214 Screen Trends 215
19 High Resolution Trend Waves 219
OxyCRG 219 Printing Hi-Res Trend Wave Reports 219 Hi-Res Trend Wave Recordings 220
20 Event Surveillance 221
Event Episodes 221 Events Pop-Up Keys 222 Event Triggers 222 The Events Database 224 Viewing Events 224 Annotating Events 226 Documenting Events 226
21 ProtocolWatch 231
Severe Sepsis Screening 231
22 Recording 237
Starting and Stopping Recordings 237 Overview of Recording Types 238 All ECG Waves Recordings 239 Creating and Changing Recordings Templates 239 Changing ECG Wave Gain 240 Recording Priorities 241 Sample Recording Strip 241 Reloading Paper 243 Recorder Status Messages 243
23 Printing Patient Reports 245
Starting Report Printouts 245 Stopping Reports Printouts 246 Setting Up Reports 246 Setting Up Individual Print Jobs 248 Checking Printer Settings 249 Printing a Test Report 249 Switching Printers On Or Off for Reports 249 Dashed Lines on Reports 249 Unavailable Printer: Re-routing Reports 249 Checking Report Status and Printing Manually 250 Printer Status Messages 251 Sample Report Printouts 252
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24 Using the Drug Calculator 257
Accessing the Drug Calculator 257 Performing Drug Calculations 258 Charting Infusion Progress 260 Using the Titration Table 260 Documenting Drug Calculations 260
25 Using the Timer 261
Viewing the Timer 261 Timer Setup Pop-up Keys 261 Setting Up Timers 262 Displaying a Timer On The Main Screen 263 Displaying A Clock On The Main Screen 264
26 Laboratory Data 265
Viewing Received Data 265
27 Care and Cleaning 267
General Points 267 Cleaning the Monitor 268 Disinfecting the Monitor 268 Sterilizing the Monitor 268 Cleaning, Sterilizing and Disinfecting Monitoring Accessories 269 Cleaning and Disinfecting the Predictive Temperature Accessories 269 Cleaning Batteries and the Battery Compartment 269
28 Using Batteries 271
Battery Power Indicators 271 Checking Battery Charge 274 Replacing a Battery 274 Optimizing Battery Performance 274 Battery Safety Information 275
29 Maintenance and Troubleshooting 277
Inspecting the Equipment and Accessories 277 Inspecting the Cables and Cords 277 Maintenance Task and Test Schedule 278 Troubleshooting 279 Disposing of the Monitor 279 Disposing of Empty Calibration Gas Cylinders 279
30 Accessories 281
ECG/Resp Accessories 281 NBP Accessories 285 Invasive Pressure Accessories 286 SpO2 Accessories 287
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Temperature Accessories 291 Predictive Temperature Accessories 291 Mainstream CO2 Accessories 292 Sidestream CO2 Accessories 292 Microstream CO2 Accessories 292 Recorder Accessories 293 Cable for Direct Connection of a Telemetry Device 294 Battery Accessories 294
31 Installation and Specifications 295
Intended Use 295 Manufacturer’s Information 296 Symbols 296 Installation Safety Information 298 Altitude Setting 300 Monitor Safety Specifications 300 EMC And Radio Regulatory Compliance 301 Out-Of-Hospital Transport - Standards Compliance 302 Monitor Performance Specifications 304 M4605A Battery Specifications 308 Measurement Specifications 309 Safety and Performance Tests 321
32 Default Settings Appendix 327
Country-Specific Default Settings 327 Alarm and Measurement Default Settings 333 Alarm Default Settings 333 ECG, Arrhythmia, ST and QT Default Settings 334 Pulse Default Settings 337 Respiration Default Settings 337 SpO2 Default Settings 338 NBP Default Settings 339 Temperature Default Settings 339 Predictive Temperature Default Settings 340 Invasive Pressure Default Settings 340 CO2 Default Settings 342
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1Installation

Installation should be carried out by qualified service personnel, either by the hospital’s biomedical department, or by Philips Support.
If you have purchased a “customer-installable bundle”, it is assumed that your own hospital personnel will install and, if necessary, configure the monitor. You can contact Philips Support for assistance if required; any assistance will be associated with additional costs.
For mechanical and electrical installation, you need technically qualified personnel with a knowledge of english. Additionally, for monitor configuration, you need clinically qualified personnel with a knowledge of the use environment. For further information on Installation, refer to the Service Guide.
WARNING • Monitor configuration settings must be specified by authorized hospital personnel.
• For installation of the monitor as part of a system, always refer to the Service Guide.
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• As the first step in preparing the monitor for use, follow the installation instructions given in this chapter.

Installation Checklist

Use this checklist to document your installation.
Step Ta s k Check Box
1 Perform initial inspection of delivery, unpack and check the shipment (see
“Unpacking and Checking the Shipment” on page 2)
2 Mount the monitor as appropriate for your installation (see “Mounting the
Monitor” on page 3)
3 Connect the monitor to AC mains using the supplied power cord (see
“Connecting the Monitor to AC Mains” on page 3)
4 Perform Visual, Power On and Functional test blocks (see “Checking Out
The Monitor” on page 3)
5 Perform Safety Tests, if required by local laws and regulations (see “Checking
Out The Monitor” on page 3)
6 Load paper into the recorder, if present (see “Loading Paper” on page 4)
when Task
Done
1
1 Installation Unpacking and Checking the Shipment
Step Ta s k Check Box
when Task
Done
7 Check/set the time and date (see “Setting the Date and Time” on page 6) 8 Check that the country-specific default settings are appropriate (see
“Checking Country-Specific Default Settings” on page 6)
9 Perform System Test as necessary (see the Service Guide)

Unpacking and Checking the Shipment

The monitor and any supporting options ordered are supplied packed in protective shipping cartons.

Initial Inspection

Before unpacking, check the packaging and ensure that there are no signs of mishandling or damage. Open the package carefully and remove the monitor and accessories.
Check that the contents are complete and that the correct options and accessories have been delivered.
System Components, Accessories and Supplies Comments
Monitor with options as ordered 1 ECG accessories optional NBP accessories 1 SpO2 accessories optional Pressure accessories optional Temperature accessories optional Predictive Temperature accessories optional CO2 Accessories optional Recorder paper optional Powercord 1 Telemetry Interface cable optional Measurement Link (MSL) cable optional Instructions for Use 1 Quick Guide 1 Documentation CD-ROM (includes Service Guide and Instructions
for Use)

Claims for Damage

If the shipping cartons are damaged, contact the carrier.
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If any of the equipment is damaged, contact both the carrier and your local Philips service organization for repair or replacement arrangements.
2
Mounting the Monitor 1 Installation

Repacking

Retain the original packing carton and material, in case you need to return equipment to Philips for service. If you no longer have the original packing materials, Philips can advise you on alternatives.

Mounting the Monitor

The monitor can be rested on a flat surface, hung on the bed rail, or mounted on a wall. See the Service Guide for details.

Connecting the Monitor to AC Mains

The monitor has a wide-range power supply that allows you to operate the monitor from an AC (alternating current) power source of 100 V to 240 V (± 10%) and 50 to 60 Hz (± 5%).
WARNING • Always use the supplied power cord with the earthed mains plug to connect the monitor to an
earthed AC mains socket. Never adapt the mains plug from the power supply to fit an unearthed AC mains socket.
• Do not use AC mains extension cords or multiple portable socket-outlets. If a multiple portable socket-outlet without an approved isolation transformer is used, the interruption of its protective earthing may result in enclosure leakage currents equal to the sum of the individual earth leakage currents, so exceeding allowable limits.
• Do not connect any devices that are not supported as part of a system.
• Any non-medical device placed and operated in the patient’s vicinity must be powered via an approved isolation transformer that ensures mechanical fixing of the power cords and covering of any unused power outlets.

Checking Out The Monitor

The following table defines which tests and inspections need to be performed, and when they are required.
Te s t Test or Inspection to be Performed
Visual Inspect the monitor, measurement accessories and cables for any damage.
Are they free of damage?
Power On Power on the monitor. Does it start up successfully without errors? Do all alarm
lamps light up during power up? After start up the monitor sounds a tone, and you can see the monitoring main screen (normally with measurement wave channels and numeric positions).
Functionality Test After power up, touch the blue Main Screen key at the bottom right of the
screen to test the Touchscreen. The key should turn light blue then after several seconds return to its standard blue color.
3
1 Installation Loading Paper
Te s t Test or Inspection to be Performed
Safety Tests (1) to (4) Perform safety tests (1) to (4), as described in the Service Guide, for standalone
devices if required by local laws and regulations, and each time you combine equipment to form a system, or exchange system components.
safety tests and procedures are described in the Service Guide. These safety tests are derived from international standards but may not always be sufficient to meet local requirements.
System Perform the system test according to IEC 60601-1-1, if applicable, after
combining equipment to form a system (see the Service Guide).
For test and inspection information regarding repairs, upgrades and all other service events, refer to the Service Guide.
Details of the

Loading Paper

1 Use the latch on the right side of the recorder door to pull the door open.
2 Remove the empty core.
3 Insert a new roll and secure it in place on the paper holder. The paper
feeds from the bottom of the roll and over the top of the recorder door. Recommended paper: M4816A and M4817A.
4 With at least one inch of paper extending beyond the edge of the door,
swing the recorder door up and push it firmly closed.
5 To test if paper is loaded correctly, start a recording. If no printing appears, paper may be loaded
backwards. Try reloading the paper.
4
Operating the Monitor 1 Installation

Operating the Monitor

To complete installation you will need to operate the monitor. Here is a short introduction for those not experienced with IntelliVue monitors.
1 Switch on the monitor. After start-up the
monitor display will become active. You operate the monitor using the touch screen.
3 Touch again to select an item on the menu and
work through the menu activities.
2 Touch something on the screen to enter a
menu. Touching the time, as shown here, brings you to the date and time menu needed for the next section.
4 You can touch numerics, waves and any
item on the screen, to get you to the corresponding menu.
5 If you cannot find a menu by touching the
screen you can always use the Main Setup key which will get you to all menus on the monitor
5
1 Installation Setting the Date and Time

Setting the Date and Time

To set the date and time:
1 Select the Date, Time screen element from the monitor’s info line to enter the Date, Time
menu.
2 Select, in turn, the Year, Month, Day, Hour (in 24 hour format, only) and Minute as
necessary. Select the correct values from the pop-up list.
3 Select Store Date, Time to change the date and time.
If your monitor is connected to an Information Center, the date and time are automatically taken from this.
Once it is set, the internal clock retains the setting even when you switch off the monitor.

Checking Country-Specific Default Settings

Some settings are made in the factory to match the typical requirements in a specific country. Line frequency, units for weight and height, and ECG cable colors (AAMI or IEC) have been set to appropriate values. If you suspect that these settings may not match your institution’s requirements, check the settings and change them if necessary as described in the Configuration Guide.
WARNING Before starting monitoring, check that the current configuration meets your requirements, especially
patient category, alarm limits and paced setting.
If you need to enter configuration mode:
1 In the Main Setup menu, select Operating Modes. 2 Select Config and enter the passcode.
The passcode for configuration mode is given in the monitor’s service documentation.
The monitor displays Config at the right hand side of the status line and in the center of the Screen while you are in configuration mode.
Before you leave configuration mode, always be sure to store any changes you made. You must store changes made to each Settings Block and to each Profile, individually. As it may be difficult to remember whether the settings you changed belong to a Monitor Settings block or a Measurement Settings block, we recommend that you store each block before you leave configuration mode.
To leave configuration mode:
In the Main Setup menu, select Operating Modes and then select Monitoring.

Handing Over the Monitor

If you are handing over the monitor to the end-users directly after configuration, make sure that it is in Monitoring mode.
Ensure that the users have access to the following documentation delivered with the monitor:
• Instructions for Use (this book) - for more detailed questions during use
• Quick Guide - for quick reminders during use
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Handing Over the Monitor 1 Installation
Additionally, we recommend working through the Training Guide for self-training on the monitor before use (not available in all languages). The part number is M8105-944XB, where X is a digit dependent on the language. The English training guide is M8105-9441B. An English training video, M8000-9451E, is also available.
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1 Installation Handing Over the Monitor
8
2

2Basic Operation

These Instructions for Use are for clinical professionals using the IntelliVue MP5 and MP5T (M8105A and M8105AT) patient monitors.
This basic operation section gives you an overview of the monitor and its functions. It tells you how to perform tasks that are common to all measurements (such as entering data, switching a measurement on and off, setting up and adjusting wave speeds, working with profiles). The alarms section gives an overview of alarms. The remaining sections tell you how to perform individual measurements, and how to care for and maintain the equipment.
Familiarize yourself with all instructions including warnings and cautions before starting to monitor patients. Read and keep the Instructions for Use that come with any accessories, as these contain important information about care and cleaning that is not repeated here.
This guide describes all features and options. Your monitor may not have all of them; they are not all available in all geographies. Your monitor is highly configurable. What you see on the screen, how the menus appear and so forth, depends on the way it has been tailored for your hospital and may not be exactly as shown here. In particular for the MP5T, refer to the table on the following page to see which sections of this guide are applicable to your monitor.
In this guide:
•A warning alerts you to a potential serious outcome, adverse event or safety hazard. Failure to observe a warning may result in death or serious injury to the user or patient.
•A caution alerts you to where special care is necessary for the safe and effective use of the product. Failure to observe a caution may result in minor or moderate personal injury or damage to the product or other property, and possibly in a remote risk of more serious injury.
Monitor refers to the entire patient monitor. Display refers to the physical display unit. Display Screen and Screen refer to everything you see on monitor’s display, such as measurements, alarms, patient data and so forth.

Introducing the Monitor

The MP5 monitor provides a comprehensive set of basic physiological measurements: NBP, SpO2, and optionally ECG, invasive blood pressure, predictive temperature, standard temperature and CO Through networking it provides information integration, documentation and information access. The MP5 can be used with adult, pediatric and neonatal patients in a hospital and transport environment.
.
2
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2 Basic Operation Introducing the Monitor
The monitor stores data in trend and event databases. You can see tabular trends (vital signs) and document them on a central printer. You can view measurement trend graphs, with up to three measurements combined in each graph, to help you identify changes in the patient’s physiological condition. You can view fast-changing measurement trends with beat to beat resolution and see up to four high resolution trend segments.
The MP5 monitor can also be connected to another IntelliVue patient monitor (MP20 to MP90), where it acts as a multi-measurement module (MMS), acquiring measurements for the host monitor. When connected to a host monitor, the host controls the MP5 including all alarm functionality. No alarms are available on the MP5, and the alarm lamps are controlled by the host. You can recognize when an MP5 is connected to a host monitor by the following indication on the screen:
Companion Mode
Companion Mode
No Alarm Display
When the MP5 is disconnected from the original host monitor, it continues to monitor the patient as a stand-alone monitor with all settings and data. On connection to a new host monitor, the MP5 resumes its role as MMS, transferring all settings and data, ensuring fully continuous monitoring. When the MP5 is connected to a host monitor it still requires batteries or AC power; it also cannot charge its batteries via the host monitor’s AC connection.
The MP5T monitor is intended for use together with a telemetry device. It has no ECG measurement of its own but does have NBP and optionally SpO
and predictive temperature. When the telemetry
2
device is directly connected to the MP5T, the measurements from the MP5T are transmitted with those from the telemetry device (ECG and optionally SpO
) to the Information Center. The MP5T
2
alone has no network capability (no direct wired or wireless connection to the Information Center).
The following comparison table shows in detail the differences between MP5 and MP5T:
Functionality (including optional features) MP5 MP5T
ECG 3 SpO
2
NBP 33 Predictive Temperature 33 Te m p e r at u r e 3 Invasive Pressure 3 Carbon Dioxide 3 Direct Telemetry Connection 33 ECG Output signal 3 LAN networking capability 3 WLAN networking capability 3 Short range radio interface 3 IntelliVue Instrument Telemetry networking capability 3 Severe Sepsis Screening 3 OxyCRG high resolution trend 3 Neonatal event review 3 Integrated recorder 33 Drug Calculator 33
33
1
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Introducing the Monitor 2 Basic Operation
Functionality (including optional features) MP5 MP5T
Gas monitor support 3 Connection to a host monitor (companion mode) 3 Connection to an external display 3 Nurse call capability 3
1.MP5 options without ECG do not have an ECG output signal
The MP5/MP5T patient monitor has an 8.4-inch TFT LCD flat panel SVGA display. You operate the monitor with the Touchscreen. There is an optional built-in recorder.
11
2 Basic Operation Introducing the Monitor

MP5/MP5T Major Parts and Keys

1
3
4
5
2
US measurement connectors
Pressure and Temp
Noninvasive Pressure
SpO
1 Color-coded alarm lamps 2 Alarms off lamp 3 Measurement connectors (see
below)
4 Predictive Temperature Unit 5 ECG out (not MP5T and MP5
options without ECG)
6 On/Standby Switch 7 Indicator LEDs
7
6
2
ECG/ Respiration
Telemetry device
CO
2
International measurement connectors
Pressure and Temp
Noninvasive Pressure
SpO
2
MP5(T) front panel
1
2
3
4
12 3 4
ECG/ Respiration
Telemetry device
On/Standby switch On/Standby/Error LED - green when monitor is
switched on, red if there is a problem with the monitor Battery status LED - green, yellow or red, see Battery
section for details AC power operation LED - green when the monitor is
connected to AC power (mains)
12
Operating and Navigating 2 Basic Operation

Operating and Navigating

Everything you need to operate the monitor is contained on its screen. Almost every element on the screen is interactive. Screen elements include measurement numerics, waveforms, screen keys, information fields, alarms fields and menus:
1
2
3
4
5
678
9
Bed 3
Doe, John Adult
3 Waves A
ALARMS PAUSED 2:59
II
1mv
HR
Pleth
Resp
1Ohm
NBP
Sys.
Auto 10 min
NBP
mmHg
SpO
RR
2
Pulse
Temp
Local Recorder out of paper
10
Repeat
Time
status line - shows information and messages prompting you for action
10
close all open menus and windows and return to main screen
11
enter Main Setup menu
12
scroll right to display more SmartKeys
13
SmartKeys - these change according to your monitor’s configuration
14
scroll left to display more SmartKeys
15
Pause Alarms - pauses alarm indicators. Pause duration depends on monitor
16
configuration. If pause duration is infinite, this key is labeled Alarms Off. Select again to immediately re-enable alarm indicators.
17
Pause
Alarms
16
Silence
Monitor information line Other screen elements
network connection indicator
1
(documented in Information Center Instructions for Use)
bed label
2
patient identification
3
patient category
4
paced status
5
date and time
6
current screen name/enter
7
change screen menu
Start/
Stop
15 14
Delayed
Record
Vitals
Trend
Default Profile
End Case
Main
Setup
13 12
hrs
Main
Screen
11
13
2 Basic Operation Operating and Navigating
Monitor information line Other screen elements
adjust alarm volume/level
8
indicator
alarm status area - shows active
9
alarm messages
Silence - acknowledges all active alarms by switching off audible alarm indicators and
17
lamps permanently or temporarily, if alarm reminder (ReAlarm) is configured on.

Selecting Screen Elements

Touch a screen element to get to the actions linked to that element. For example, touch the Patient Identification element to call up the Patient Demographics window, or touch the HR numeric to call up the Setup ECG menu. Touch the ECG wave segment to call up the ECG lead menu.

Using the Setup Menu

Setup
Alarm Messages
Alarm Limits
Alarm Volume
My Care Group
Change Screen
Profiles
Admit/Dischrg
Paced No
Network
Bed Information
Date, Time

Disabling Touchscreen Operation

To temporarily disable touchscreen operation of the monitor, press and hold the
Main Screen permanent key. A padlock will appear on the Main Screen permanent key.
The elements at the top of the Screen are grouped together for ease of navigation. Touch any item at the top of the Screen to open the Setup menu; then touch the element you want.
Press and hold the Main Screen permanent key again to re-enable the touchscreen operation.

Moving Windows

You can move windows and menus using the Touchscreen. To move a window
1 Select the title of the window and keep your finger on the title.
2 Move your finger on the Touchscreen to move the window.
3 Take your finger off the screen to place the window in the final position.
Not all locations on the screen can be a target position, a window cannot overlap the monitor info line, the alarms and INOPs or the status line.
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Operating and Navigating 2 Basic Operation

Using Keys

The monitor has three different types of keys.
Perma nent Ke y s
A permanent key is a graphical key that remains on the screen all the time to give you fast access to functions.
SmartKeys
Pause Alarms
configuration. If pause duration is infinite, this key is labeled Alarms Off.
- pauses alarm indicators. Pause duration depends on monitor
Select again to immediately re-enable alarm indicators.
Silence - acknowledges all active alarms by switching off audible alarm indicators
and lamps.
Main Screen - close all open menus and windows and return to the main screen.
Main Setup - enter main setup menu.
A SmartKey is a configurable graphical key, located at the bottom of the main screen. It gives you fast access to functions. The selection of SmartKeys available on your monitor depends on your monitor configuration and on the options purchased.
enter profile menu, or revert to default profile
change Screen, or revert to default screen
access timers
freeze waves quick admit a patient
set alarm limits
change alarm volume end case to discharge a patient
change QRS volume
previous Screen
enter patient identification menu to admit/discharge/transfer
view information for patients in other beds
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2 Basic Operation Operating and Navigating
enter standby mode - suspends patient monitoring. All waves and numerics disappear from the display. All settings
change screen brightness (not for
independent displays) and patient data information are retained.
review beat labels (annotate arrhythmia wave)
re-learn arrhythmia
change amplitude (size) of ECG wave access wedge procedure window
- start/stop manual NBP measurement
- start auto series
- stop current automatic measurement
start/stop NBP STAT measurement
within series
stop automatic or STAT NBP
measurement and measurement series
start NBP measurement and
stop current NBP measurement measurement series
start veni puncture (inflate cuff to
start NBP STAT measurement subdiastolic pressure)
set the NBP repeat time
start a delayed recording
zero invasive pressure transducer
access pop-up recording keys
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access Vital Signs recording key
access Select Waves recording key
set wide automatic alarm limits set narrow automatic alarm limits
switch CO
pump off access neonatal event review
2
review vital signs trend review graph trend
access the calculator access the Drug Calculator
gas analyzer - exit standby mode suppress zero for all gas measurements
Operating and Navigating 2 Basic Operation
Pop-Up Keys
unpair equipment and continue central monitoring with the monitor
start 12-Lead Capture (only available if Information Center is connected)
set standard or EASI lead placement access patient reports
new lead setup manual data entry
access ProtocolWatch start/stop car seat assessment record
open the histogram window open unit conversion window
unpair equipment and continue central
monitoring with the telemetry device
access ST Map application
Pop-up keys are task-related graphical keys that appear automatically on the monitor screen when required. For example, the confirm pop-up key appears only when you need to confirm a change.

Using the On-Screen Keyboard

Use this as you would a conventional keyboard. Enter the information by selecting one character after another. Use the Shift and capital Lock keys to access uppercase letters. Use the Back key to delete single characters, or use the Clr key to delete entire entries. Select Enter to confirm what you have entered and close the on-screen keyboard.
17
2 Basic Operation Operating and Navigating

Using the On-Screen Calculator

You can use the on-screen calculator to perform any of the standard operations for which you would normally use a handheld calculator.
To access the on-screen calculator, select the
Calculator SmartKey, or select Main Setup
-> Calculations -> Calculator.
Calculator
MR
MC
M+ Back
C/CE
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Operating Modes 2 Basic Operation

Operating Modes

When you switch the monitor on, it starts up in monitoring mode. To change to a different mode:
1 Select the Main Setup menu.
2 Select Operating Modes and choose the mode you require.
Your monitor has four operating modes. Some are passcode protected.
Monitoring Mode: This is the normal, every day working mode that you use for monitoring patients. You can change elements such as alarm limits, patient category and so forth. When you discharge the patient, these elements return to their default values. Changes can be stored permanently only in Configuration Mode. You may see items, such as some menu options or the altitude setting, that are visible but ‘grayed out’ so that you can neither select nor change them. These are for your information and can be changed only in Configuration Mode.
Demonstration Mode: Passcode protected, this is for demonstration purposes only. You must not change into Demonstration Mode during monitoring. In Demonstration Mode, all stored trend information is deleted from the monitor’s memory.
Configuration Mode: Passcode protected, this mode is for personnel trained in configuration tasks. These tasks are described in the Configuration Guide. During installation the monitor is configured for use in your environment. This configuration defines the default settings you work with when you switch on, the number of waves you see and so forth.
Service Mode: Passcode protected, this is for trained service personnel.
When the monitor is in Demonstration Mode, Configuration Mode, or Service Mode, this is indicated by a box with the mode name in the center of the Screen and a symbol in the bottom right-hand corner. Select this field to change to a different mode.
When an MP5 is connected to a host monitor (Companion Mode is indicated):
• The MP5 will adopt the operating mode of the host monitor:
• You cannot change the operating mode at the MP5.

Standby Mode

Standby mode can be used when you want to temporarily interrupt monitoring. To enter Standby mode,
select Main Setup, followed by Monitor Standby.
The monitor enters Standby mode automatically after the End Case function is used to discharge a patient.
Standby suspends patient monitoring. All waves and numerics disappear from the display but all settings and patient data information are retained. A special Standby screen is displayed. This can be configured to a moving image or a blank screen. If a patient location is entered at the Information Center, this will also be displayed on the Standby screen (availability depends on Information Center revision).
Config
select the Monitor Standby SmartKey or
To resume monitoring,
19
2 Basic Operation Understanding Screens
Select anything on the screen or press any key.
If you connect an MP5 that is powered on (and not in Standby) to a host monitor in Standby mode, the host will leave Standby mode. When connected to a host monitor, with both the host and the MP5 in Standby mode, leaving Standby on the MP5 will also make the host leave Standby.

Understanding Screens

Your monitor comes with a set of preconfigured Screens, optimized for common monitoring scenarios such as OR adult, or ICU neonatal. A Screen defines the overall selection, size and position of waves, numerics and SmartKeys on the monitor screen when you switch on. You can easily switch between different Screens during monitoring. Screens do NOT affect alarm settings, patient category and so forth.

Switching to a Different Screen

1 To switch to a different Screen, select the monitor info line and then Change
Screen in the Setup Menu, or select the Change Screen SmartKey.
2 Choose the new Screen from the pop-up list.

Changing a Screen’s Content

If you do not want to change the entire Screen content, but only some parts of it, you can substitute individual waves, numerics, high-res waves, or trends. Be aware that these changes cannot be stored permanently in Monitoring Mode.
To change the selection of elements on a Screen,
1 Select the element you want to change. 2 From the menu that appears, select Change Wave, Change Numeric, or
Change HiResTrend, and then select the wave or numeric you want, or select the high­resolution trend wave you want from the list of available waves.
If you do not see Change Numeric in the menu, this Screen may be configured to always display the numeric beside its wave. Changing the wave will automatically change the numeric.
The changed Screen is shown with an asterisk in the monitor info line.
20
Using the XDS Remote Display (not MP5T) 2 Basic Operation
In the Change Screen menu, the changed Screen is shown linked to the original Screen and marked with an asterisk.
Up to three modified Screens can be accessed via the Change Screen menu.
To recall Screens, either
select the name of the Screen in the
Change Screen menu
or
use the previous/next arrows at the top of the
Change Screen menu to move back and forth in the Screen history. The ten most recently-used Screens including up to three modified Screens can be accessed.
After a patient discharge, the monitor’s default Screen is shown. Modified Screens are still available in the Change Screen menu.
If the monitor is switched off and then on again, modified Screens are erased from the monitor’s memory and cannot be recalled. If a modified Screen was the last active Screen when the monitor was switched off, it is retained (unless Automat. Default is configured to Yes).
Change Screen
3 Waves A
Split Screen A
Graph Trends
Vital Signs B
Vital Signs A
Vital Signs A*

Using the XDS Remote Display (not MP5T)

Using the IntelliVue XDS solution it is possible to view an independent monitor screen on an external display. The XDS solution consists of a medical grade PC-based hardware platform, XDS application software and the XDS connectivity option on the monitor. Depending on the configuration you can also operate the monitor from the external display. The XDS must be connected to the same Local Area Network (LAN) as the monitor.
It is also possible to use an existing PC, connected to the same LAN, to host the XDS Application software.
For more details, including limitations and restrictions, refer to the Instructions for Use for the XDS Application.

Using the Visitor Screen

If a visitor Screen is configured for your monitor, you can use it to clear the screen of all waves and numerics but continue to monitor the patient with active alarms and trend storage at the bedside and Information Center. You can change the name of the visitor Screen in Configuration Mode.
To activate this Screen,
1 Select the monitor info line to open the Setup menu
2 Select Change Screen
3 Select the name of the visitor Screen configured for your monitor from the list of available Screens.
To select a Screen with waves and numerics again,
21
2 Basic Operation Understanding Profiles
Select any element on the Screen to open the Screen menu and select a screen from the list.

Understanding Profiles

Profiles are predefined monitor configurations. They let you change the configuration of the whole monitor so you can adapt it to different monitoring situations. The changes that occur when you change a complete profile are more far reaching than those made when you change a Screen. Screens affect only what is shown on the display. Profiles affect all monitor and measurement settings.
The settings that are defined by Profiles are grouped into three categories. Each category offers a choice of ‘settings blocks’ customized for specific monitoring situations. These categories are:
Display (screens) – Each profile can have a choice of many different predefined screens. If you are using a second
display, each display can have its own individual screen selection. When you change the profile, the screen selection configured for the new profile becomes active.
• Measurement Settings
– Each profile can have a choice of different predefined measurement settings. These relate directly
to individual measurements, for example, measurement on/off, measurement color, alarms limits, NBP alarm source, NBP repeat time, temperature unit (°F or °C), pressure unit (mmHg or kPa).
• Monitor Settings
– Each profile can have a choice of different predefined monitor settings. These relate to the
monitor as a whole; for example, display brightness, alarms off/paused, alarm volume, QRS tone volume, tone modulation, prompt tone volume, wave speed, resp wave speed, pulse source.
Profiles
Profile : Profile A
Patient Category: Adult
Paced : No
Display : S-014
Measmt. Settings:Measurement A
Monitor Settings: Monitor A
Profiles Menu, showing current settings
Measurement A
Measurement B
Measurement C
Measurement D
Available choices in measurement menu
22
You can change from one complete profile to another or swap individual settings blocks (display screen/monitor settings/measurement settings) to change a subset of a profile. Changes you make to any element within the settings blocks are not saved when you discharge the patient, unless you save them in Configuration Mode.
Depending on your monitor configuration, when you switch on or discharge a patient the monitor either continues with the previous profile, or resets to the default profile configured for that monitor.
Understanding Profiles 2 Basic Operation
WARNING If you switch to a different profile, the patient category and paced status normally change to the setting
specified in the new profile. However some profiles may be setup to leave the patient category and paced status unchanged. Always check the patient category, paced status, and all alarms and settings, when you change profiles.
When you leave Demonstration Mode, the monitor uses the default profile.
23
2 Basic Operation Understanding Settings

Swapping a Complete Profile

1 Select the monitor info line and then Profiles in the Setup menu, or select the
Profiles SmartKey.
2 In the Profiles menu, select Profile.
3 Chose a profile from the pop-up list.
4 Confirm your selection.

Swapping a Settings Block

1 Select the monitor info line and then Profiles in the Setup menu, or select the
Profiles SmartKey.
2 In the Profiles menu, select Display or Measmnt. Settings or
Monitor Settings to call up a list of the settings blocks in each category.
3 Choose a settings block from the pop-up list.
4 Confirm your selection.

Default Profile

Your monitor has a default profile that it uses when you leave Demonstration, or Service modes, or when you discharge a patient. This profile is indicated by a diamond .

Locked Profiles

Some profiles are locked, so that you cannot change them, even in Configuration Mode. These are indicated by this lock symbol.

Understanding Settings

Each aspect of how the monitor works and looks is defined by a setting. There are a number of different categories of settings, including,
Screen Settings, to define the selection and appearance of elements on each individual Screen
Measurement settings, to define settings unique to each measurement, for example, high and low
alarm limits
Monitor settings, including settings that affect more than one measurement or Screen and define general aspects of how the monitor works, for example, alarm volume, reports and recordings, and display brightness.
You must be aware that, although many settings can be changed in Monitoring Mode, permanent changes to settings can only be done in the monitor’s Configuration Mode. All settings are reset to the stored defaults:
24
• when you discharge a patient
• when you load a Profile
Adjusting a Measurement Wave 2 Basic Operation
• when the monitor is switched off for more than one minute (if Automat. Default is set to Yes).

Changing Measurement Settings

Each measurement has a setup menu in which you can adjust all of its settings. You can enter a setup menu:
• via the measurement numeric - select the measurement numeric to enter its setup menu. For example, to enter the Setup ECG menu, select the HR (heart rate) numeric.
•via the Main Setup permanent key- if you want to setup a measurement when the measurement is switched off, use the Main Setup permanent key and select Measurements. Then select the measurement name from the popup list. With this permanent key you can access any setup menu in the monitor.
• via the Measurement Selection key.

Switching a Measurement On and Off

When a measurement is off, its waves and numerics are removed from the monitor’s screen. The monitor stops data acquisition and alarming for this measurement.
1 Enter the measurement’s setup menu and select the measurement. 2 Select the measurement name to toggle between on and off. The screen display indicates the active
setting.

Adjusting a Measurement Wave

To quickly adjust wave-related measurement settings (such as speed or size), select the
measurement wave itself. This displays the measurement Wave menu, which has only wave-related measurement settings.

Changing Wave Speeds

Lowering the wave speed compresses the wave and lets you view a longer time period. Increasing the speed expands the waveform, giving you a more detailed view.
The monitor distinguishes two groups of wave speed settings,
RespiratorySpeed, for all respiratory waves: CO
Global Speed, for all waves not included in the other group.

Changing the Wave Group Speed

The wave speed group setting defines the speed of all the waves in the group.
, Resp. anesthetic agents and O
2
2
To change the wave speed of a wave speed group,
1 Select Main Setup -> User Interface
2 Select Global Speed or RespiratorySpeed, as required
3 Select a value from the list of available speeds.
25
2 Basic Operation Freezing Waves

Changing Wave Speed for a Channel

To change the wave speed of an individual wave channel,
1 Enter the Wave menu for a measurement by selecting its wave. 2 Select Change Speed.
3 To set the speed to the wave group speed, select RespiratorySpeed or Global Speed.
To set an individual channel speed, select a numeric value from the list of available speeds. This overrides the wave group speed setting and sets the speed for the individual wave channel on the monitor Screen. The wave channel speed is independent of the wave (label) depicted in the channel, if you change the wave, the new wave will retain the set channel speed.

Freezing Waves

You can freeze waves on the screen and measure parts of the wave using cursors. The waves are frozen with a history of 20 seconds so that you can go back and measure what you have seen.

Freezing An Individual Wave

To freeze a wave,
1 Enter the Wave menu for the measurement by selecting the wave on the screen. 2 Select Freeze Wave.
The realtime wave is replaced with the frozen wave.

Freezing All Waves

To freeze all waves on the screen,
1 Select the Freeze Waves SmartKey.
All realtime waves are replaced with frozen waves.

Measuring Frozen Waves

To measure a frozen wave,
1 Select the frozen wave.
This automatically positions the vertical cursor. The cursor can be repositioned by touching the required point on the wave, or
2 Use the up/down arrow keys to activate and move the horizontal cursor.
The horizontal cursor measures the wave value, which is displayed above the cursor line. If the wave is a pressure wave, the cursor value can be stored as a systolic, diastolic or mean pressure value and if the pressure wave is a PAP wave, it can also be stored as a PAWP value. The stored value appears in the trend database as a manually entered value. To return to the vertical cursor use the <> pop-up key.

Changing The Wave Speed

Lowering the wave speed compresses the wave and lets you view a longer time period. Increasing the speed expands the waveform, giving you a more detailed view.
26
Using Labels 2 Basic Operation
To change the wave speed:
1 Select the frozen wave.
2 Select Change Speed.
3 Select a speed from the list.

Updating The Frozen Wave

To update the wave, that is freeze the current wave:
1 Select the frozen wave. 2 Select Freeze Again.

Releasing Frozen Waves

To release frozen waves,
1 Select a frozen wave. 2 Select Unfreeze Waves.
All frozen waves are released.

Using Labels

Depending on the monitor options purchased, you may be able to measure two invasive pressures and temperatures simultaneously. The monitor uses labels to distinguish between them. The default settings defined in the profile (such as measurement color, wave scale, and alarm settings) are stored within each label. When you assign a label to a measurement, the monitor automatically applies these default settings to the measurement. The labels assigned are used throughout the monitor, in reports, recordings, and in trends.

Changing Measurement Labels (e.g. Pressure)

To change a measurement label of a measurement with multiple labels (invasive pressure or temperature),
1 Enter the Wave menu of the measurement.
2 Select Label.
3 Choose a label from the list.
The monitor automatically applies the scale, color, etc. settings stored in the Profile for the label you select. You can change scale settings in Monitoring Mode, but color can only be changed in the monitor’s Configuration Mode.
Any labels already being used in the monitor are shown “grayed-out” in the list and cannot be selected.

Resolving Label Conflicts

Each label must be unique, that is, it can only be assigned once. If you have a gas monitor connected to the monitor there is a potential conflict with the CO
Depending on your configuration, the monitor will either
label.
2
27
2 Basic Operation Using Labels
• display the Measurement Selection window automatically for you to resolve the conflict
• take no action, you must enter the Measurement Selection window and resolve the conflict
measurement selection key
All the currently available measurements are depicted in the Measurement Selection window. If a measurement label is causing a label conflict it is shown in red.
WARNING When an MP5 with an active measurement, say SpO
measurement already active, the SpO
measurement on the MP5 is deactivated and the
2
Meas. DEACTIVATED INOP is displayed. The measurement can only be reactivated if the MP5 is disconnected from the host monitor. The label conflict can be resolved on the host monitor like any other label conflict.
When the MP5 is connected to a host monitor, the Measurement Selection window can be opened, but only the measurement Setup key is functional. Derived measurements are not active and cannot be activated, but become active again when the MP5 is disconnected from the host monitor. Resolve any label conflicts at the host monitor.
To resolve a label conflict,
1 Select the measurement selection key or select Main Setup -> Measurement Selection
to display the Measurement Selection window.
2 Select the measurement to be deactivated.
3 Select the De-activate pop-up key to disable the conflicting measurement. When the
measurement has been deactivated the question marks under the measurement selection key will be replaced by XXX.

Label Compatibility

When a new measurement is introduced, or new labels for an existing measurement, these labels will not be shown on older Information Centers, and consequently not on the Overview screen sourced from the Information Center.
, is connected to a host monitor with the same
2
28
When a patient is transferred from a monitor with these new labels to one with an older software revision, the labels will be replaced with a generic label for that measurement. The settings for that generic label will then be used.
Entering Measurements Manually 2 Basic Operation
If it is critical that the measurement labels are available at the Information Center and after transfers, the older monitors and the Information Center must be upgraded to the appropriate software revision.

Entering Measurements Manually

You can enter values into the monitor that have been measured with other equipment or manually (for example, manual temperatures, lab values). These values are then stored in the database, included in trends and reports, and passed on to the Information Center and central charting systems. There is no alarm functionality for manually entered measurements.
To enter values,
1 Select the Enter Values SmartKey or select Main Setup -> Enter MeasValues
2 Select the measurement you want to enter values for. The Edit <Measurement> window will
open.
3 If the measurement is switched off, switch it on by selecting the label.
4 Select Value and enter the value.
5 Select Date/Time to enter the date and time for the value. The default is always the current date
and time.
6 For compound labels, for example ABPs, ABPd and ABPm, select the Format field to select
whether all values are required or a single value.
7 Select Confirm.
When a manually entered value has been configured to display as a numeric on the screen, you can also enter a new value for this measurement by selecting the numeric, then selecting Enter MeasValues.
Manually entered measurement values are marked with a * on the display, in trends, and so forth. Each measurement has a defined measurement interval after which a value becomes invalid (no value is then displayed). Values can be entered up to two hours after they have been measured or up to the measurement interval, if this is shorter.
The list of measurement labels which appears in the Manual Entry window is set in Configuration Mode.
No values can be entered manually on the MP5 when it is connected to a host monitor.

Switching Manually Entered Measurements On and Off

To switch a manually entered measurement on or off,
1 Select the Enter Values SmartKey or select Main Setup -> Enter MeasValues
2 Select the measurement you want to switch on or off.
3 Select the measurement label field to switch between On and Off

Changing Monitor Settings

To change monitor settings such as brightness, or QRS tone volume, select the Main Setup
permanent key and then select User Interface to enter a submenu where you can change these settings.
29
2 Basic Operation Checking Your Monitor Revision

Adjusting the Screen Brightness

1 Select the Brightness SmartKey.
2 Select the appropriate setting for the screen brightness. 10 is the brightest, 1 is the least
bright. Optimum is suitable for most monitoring locations and optimizes power usage for battery powered monitors.
Your monitor may be configured with a lower brightness for Standby mode and also for transport to conserve battery power. These settings can only be changed in the monitor’s Configuration Mode.

Adjusting Touch Tone Volume

The touch tone volume is the tone you hear when you select any field on the monitor screen. To adjust the touch tone volume,
1 In the Main Setup menu, select User Interface
2 Select Touch ToneVolume, then select the appropriate setting for the touch tone volume: 10 is
the loudest and 1 is the quietest. Selecting zero switches the touch tone volume off.

Setting the Date and Time

If your monitor is connected to an Information Center, the date and time are automatically taken from this. Once it is set, the internal clock retains the setting even when you switch off the monitor.
1 Select the Date, Time screen element from the monitor’s info line to enter the Date, Time
menu.
2 Select, in turn, the Year, Month, Day, Hour (in 24 hour format, only) and Minute as
necessary. Select the correct values from the pop-up list.
3 Select Store Date, Time to change the date and time.

Checking Your Monitor Revision

1 Select Main Setup -> Revision to open the Monitor Revision menu.
2 From the Monitor Revision menu, select the monitor component for which you need
revision information.

Getting Started

Once you understand the basic operation principles and have completed the Training Program, you can get ready for monitoring.

Inspecting the Monitor

WARNING If the monitor is mechanically damaged, or if it is not working properly, do not use it for any
monitoring procedure on a patient. Contact your service personnel.
1 Before you start to make measurements, carry out the following checks on the monitor.
– Check for any mechanical damage.
30
Getting Started 2 Basic Operation
– Check all the external cables, plug-ins and accessories.
2 Plug the power cord into the AC power source. If you are using battery power, ensure that the
battery has sufficient power for monitoring. When you use a battery for the first time, you must charge it, following the instructions given in the section on Charging Batteries.
3 Check all the functions of the instrument that you need to monitor the patient, and ensure that the
instrument is in good working order.

Switching On

Press the on/off switch on the monitor for one second. The monitor performs a self test and is then
ready to use. If you see a message such as CO starting monitoring that measurement.
SENSOR WARMUP wait until it disappears before
2

Power On/Power Off Behavior

The general rules determining the behavior of the monitor when connected to, or disconnected from power are as follows:
• A monitor that was switched on prior to a temporary power loss switches on again when power is restored.
• A monitor that was switched off prior to a temporary power loss remains off when power is restored.
• When AC mains power is lost, a battery powered monitor continues to run without interruption on battery power.
• The MP5 switches on automatically when connected to a running host monitor.
• When the MP5 is disconnected from a running host monitor, it continues to run without interruption on battery power.

Setting up the Measurements

1 Decide which measurements you want to make. 2 Connect the required patient cables and sensors. The connectors are color-coded to the patient
cables and sensors for easy identification.
WARNING When connecting devices for acquiring measurements, always position cables and tubing carefully to
avoid entanglement or potential strangulation.

Starting Monitoring

After you switch on the monitor,
1 Admit your patient to the monitor.
2 Check that the profile, alarm limits, alarm and QRS volumes, patient category and paced status
and so forth are appropriate for your patient. Change them if necessary.
3 Refer to the appropriate measurement section for details of how to perform the measurements you
require.
31
2 Basic Operation Disconnecting from Power
WARNING During MR imaging, remove all transducers, sensors and cables from the patient. Induced currents
could cause burns.

Disconnecting from Power

The On/Standby switch does not disconnect the monitor from the ac power source. To disconnect, unplug the power cable.

Monitoring After a Power Failure

If the monitor is without power for less than one minute, monitoring will resume with all active settings unchanged. If the monitor is without power for more than one minute, the behavior depends on your configuration. If Automat. Default is set to Yes, the default profile will be loaded when power is restored. If Automat. Default is set to No, all active settings are retained, if power is restored within 48 hours. The Automat. Default setting is made in Configuration Mode.

Networked Monitoring

You can connect your monitor to an Information Center on a network. This can be done using one of the optional interfaces:
• Standard wired LAN
• Wireless LAN
• IntelliVue Instrument Telemetry System (IIT)
WARNING Do not connect patient monitors to the standard hospital network.
Additionally, when the MP5 is equipped with IIT and declared at the Information Center as a telemetry device, it allows data continuity when paired to a host monitor. After disconnection from the host monitor, it continues to monitor the patient during transport and provides continuous data to the same sector on the Information Center. (See the Instructions for Use for your host monitor for viewing telemetry data on the host.)
If your monitor is connected to a network, a network symbol is displayed in the upper left corner next to the bed label. To see details about the Care Group, the monitoring equipment, and technical information about the network, select the monitor info line to enter the Setup menu, then select Bed Information.
Be aware that some network-based functions may be limited for monitors on wireless networks in comparison to those on wired networks.
Printout functionality and data export are not guaranteed when using a standard hospital network.
32
Using the MP5 with a Host Monitor 2 Basic Operation

Using the MP5 with a Host Monitor

Host monitors that can support the MP5 as a multi-measurement module require software revision F.00.00 or higher. When you connect an MP5 to a host monitor, an integrated system is formed for monitoring a single patient. The following general observations and considerations apply to such a system:
• The host monitor is the “master” of the system, and you have full control over all the system’s operation only from the host monitor.
• Functions you can operate on the MP5 are restricted to measurements originating in that device. If you try to operate controls that are disabled, you are prompted by the message “Not available in Companion Mode”.
• Depending on how it is configured, your host monitor can determine whether the user interface of a connected MP5 is completely disabled or not, and what is displayed (a standard main screen, or a blank screen similar to the Standby screen indicating “Companion Mode”).
This is controlled by two monitor settings that are applied to the MP5 on connection. You can change the settings in Configuration Mode.
• Some general settings, such as line frequency, QRS sound, ECG lead colors, from the host monitor are applied to the MP5 on connection. When disconnected from the host, the MP5 applies its own settings again.
• No audible alarms are available on an MP5 when connected to a host monitor. The only visual alarm indication is provided by the alarm lamps which are controlled by the host monitor. Alarms become active again as soon as the MP5 is disconnected from the host monitor.
• The host monitor is the master of all ADT information. ADT operations on the MP5 are disabled, and any pending actions on the MP5 (for example, admit or end case) are cancelled.
• The date and time of the MP5 is synchronized with that of the host monitor.
• Event surveillance in the MP5 is disabled. Main Setup menu operations and SmartKeys are disabled. While connected to host monitor, no new events are detected in the MP5, and no events are deleted. There is no transfer of stored events from the MP5 to the host monitor. After disconnection from the host monitor, event surveillance is enabled again in the MP5, and new events are detected.
The MP5 is connected to the host monitor using the measurement link (MSL) cable:
33
2 Basic Operation Using the MP5 with a Host Monitor
34
This section lists the most important new features and improvements to the monitor and its user interface introduced with each release. Further information is provided in other sections of this book.
You may not have all of these features, depending on the monitor configuration purchased by your hospital.

What’s New in Release G.0?

Short Range Radio Interface for MP5
A short range radio interface is now available for the MP5 monitor. This allows a telemetry transceiver with a short range radio adapter to be assigned to the monitor resulting in a direct connection, as an alternative to the cable connection. The measurement data from the telemetry transceiver appear directly on the monitor screen with a minimal delay and are combined with the monitor data in one sector at the Information Center.
3

3What’s New?

Product Options Without ECG
The monitor now has several options, with varying measurement combinations, without an ECG measurement.
Microstream CO
The Microstream CO
Histogram Trend
Trended values can also be viewed in the form of a histogram. The SpO histograms or realtime histograms with 1 second samples.
Car Seat Assessment Record
In Event Surveillance, in the NER group, you can run a Car Seat Assessment Record (CAR). This is a special period of event surveillance for neonates during a car seat test. During the CAR period a realtime SpO
IntelliVue XDS Solution
Using the IntelliVue XDS solution it is possible to view an independent monitor screen on an external display. The XDS solution consists of a medical grade PC-based hardware platform, XDS application software and the XDS connectivity option on the monitor. Depending on the configuration you can also operate the monitor from the external display. The XDS must be connected to the same Local Area Network (LAN) as the monitor.
It is also possible to use an existing PC, connected to the same LAN, to host the XDS Application software.
in MP5
2
measurement method is now available in MP 5 monitors.
2
histogram is also generated with 1 second samples.
2
histograms can be trend
2
35
3What’s New? What’s New in Release F.0?
New Fields in the Admission Form
A Middle Name field is now available in the admission form - whether it appears is configurable. Two additional ID fields, Lifetime Id and Encounter Id, can also be configured to appear and their names can be customized to fit hospital requirements.
Enhancements
SpO
2
Additional SpO
New manual measurement mode when telemetry devices are connected via a short range radio link.
Labels - SpO2pr and SpO2po labels have been added.
2
• Signal Quality Indicator displayed with the SpO
ECG Enhancements
•New */**Afib yellow alarm when an atrial fibrillation waveform is detected.
QT View window - shows current wave and baseline wave with Q and T points marked so that you can verify that the QT algorithm detects correct Q and T points.

What’s New in Release F.0?

The SSC Sepsis protocol is now available on the MP5 in the form of the screening option. If a patient has been screened on arrival with an MP5, then transferred to Intensive Care when Sepsis is confirmed, the current state, the settings and the log from the SSC Sepsis Protocol can be transferred from the MP5 by connecting it to the new monitor.
QT/QTc Interval Monitoring
QT interval monitoring is used to assist in the detection of prolonged QT interval syndrome. The QT interval is measured and the heart-rate corrected QT value, QTc, is calculated. The monitor also provides a QTc value which tracks variation in the QT interval in relation to a baseline value. High alarm limits can be set for QTc and QTc enabling alarm notification.
Manual Data Entry
Measurement values (for example lab data or manually measured temperatures) can be entered manually into the monitor and stored in the database. They can then be used for trends, reports and also be displayed as a numeric on screen, if required.
numerics.
2
36
Horizon Trend Enhancements
The trend indicator arrow indicates how the patient trend has developed in a set time period. This period is now configurable and can be set to 10 minutes, 5 minutes or 2 minutes. The horizon (or baseline) can now be set to a range or to a specific value.
Connecting an MP5 to a Monitor (Companion Mode is indicated)
The MP5 monitor can be connected to one of the MP20 to MP90 monitors (then called the host monitor) and used like an MMS. This provides monitoring continuity in transport situations allowing measurement data and patient demographics from the MP5 to be transferred to another monitor. When the MP5 is connected to a host monitor, no alarms will be announced on the MP5.
Pairing MP5 with another IntelliVue Monitor
The MP5 (with IIT) can be declared as a telemetry device at the Information Center and paired with another monitor. The data from the MP5 will then be shown on the same sector on the Information Center as that from the other monitor.
What’s New in Release F.0? 3What’s New?
Sending Data To An Information Center Via A Telemetry Device
For the MP5T monitor, or an MP5 monitor without a connection to an Information Center, a small set of monitoring data can be sent from the monitor to the Information Center via a connected telemetry device.
NBP - Programmable Measurement Sequence
Up to four measurement cycles can be set up which will run consecutively. For each cycle you can set the number of measurements and the interval between them. By setting the last cycle to run continuously you can have regular measurements continue after the sequence has run.
New Printing Options For Reports
Reports can now also be printed via an external PC-based print server or to an internal print database, when no printer is available (for example, during transport). As soon as a printer becomes available, the reports stored in the database will print automatically.
Manual Pairing At Monitor
Previously, devices could only be manually paired at the Information Center. You can now pair devices at the monitor as long as the monitor is already connected to the Information Center.
Moving Windows And Menus
Windows and menus can now be moved on the monitor screen. Using touch or a mouse you can select the title of a window and then “drag” it across the screen. Some positions on the screen are not allowed, such as ones overlapping the alarm field or the monitor info line.
Invasive Pressure Changes
Wave cursor - A cursor is now available on the realtime pressure wave to allow you to define a position
and store the corresponding value.
Reduced alarm limit steps in lower ranges - The alarm limits setting in 2 mmHg steps is now possible in ranges up to 50 mmHg (previously up to 30 mmHg).
New Patient Check
The monitor can be configured to ask you in certain situations: after a specified power-off period, after a specified standby period and when no basic vitals (HR, RR, Pulse, SpO
, NBP) have been measured
2
for a specified period, whether a new patient is now being monitored. By selecting the Yes pop-up key you can discharge the previous patient and reset settings.
New Smart Keys
A SmartKey is available for New Lead Setup when a new ECG lead set with fewer leads than previously is being used.
Better Visibility Of Gridlines
The brightness of the gridlines on the realtime waves has been increased for better visibility.
37
3What’s New? What’s New in Release F.0?
38
4

4Alarms

The alarm information here applies to all measurements. Measurement-specific alarm information is discussed in the sections on individual measurements.
The monitor has two different types of alarm: patient alarms and INOPs.
Patient Alarms are red and yellow alarms. A red alarm indicates a high priority patient alarm such as a potentially life threatening situation (for example, asystole). A yellow alarm indicates a lower priority patient alarm (for example, a respiration alarm limit violation). Additionally there are short yellow alarms, most of which are specific to arrhythmia-related patient conditions (for example, ventricular bigeminy).
INOPs are technical alarms, they indicate that the monitor cannot measure or detect alarm conditions reliably. If an INOP interrupts monitoring and alarm detection (for example, LEADS OFF), the monitor places a question mark in place of the measurement numeric and an audible indicator tone will be sounded. INOPs without this audible indicator indicate that there may a problem with the reliability of the data, but that monitoring is not interrupted.
Most INOPs are light blue, however there are a small number of INOPS which are always yellow or red to indicate a severity corresponding to red and yellow alarms. The following INOPs can also be configured as red or yellow INOPs to provide a severity indication:
• ECG LEADS OFF
ECG/ARRH ALARM OFF (yellow only, no red INOP)
• CUFF OVERPRESS
• CUFF NOT DEFLATED
• OCCLUSION
• TELE DISCONNECT.
• Replace TeleBatt
All monitors in a unit should have the same severity configured for these INOPs. Alarms are indicated after the alarm delay time. This is made up of the system delay time plus the
trigger delay time for the individual measurement. See the specifications section for details.
If more than one alarm is active, the alarm messages are shown in the alarm status area in succession. An arrow symbol next to the alarm message informs you that more than one message is active.
** HR HIGH
39
4Alarms Visual Alarm Indicators
The monitor sounds an audible indicator for the highest priority alarm. If more than one alarm condition is active in the same measurement, the monitor announces the most severe. Your monitor may be configured to increase alarm indicator volume automatically during the time when the alarm is not acknowledged.

Visual Alarm Indicators

WARNING • No alarms are available on the MP5 when connected to a host monitor. Alarms become active again
as soon as the MP5 is disconnected from the host monitor.
• Alarm fields and other visual alarm indicators are disabled on the MP5 when connected to a host monitor. The only visual alarm indication is provided by the alarm lamps, which are controlled by the host monitor. No Alarm Display is shown in the field for red alarms, Companion
Mode is shown in the yellow alarms field, and the INOPs field is blacked out.
Companion Mode
Alarm message: An alarm message text appears in the alarm status area at the top of the screen indicating the source of the alarm. If more than one measurement is in an alarm condition, the message changes every two seconds, and has an arrow ( ) at the side. The background color of the alarm message matches the alarm priority: red for red alarms, yellow for yellow alarms, light blue for standard INOPs, red for red INOPs and yellow for yellow INOPs. The asterisk symbols (*) beside the alarm message match the alarm priority: *** for red alarms, ** for yellow alarms, * for short yellow alarms. Standard INOPs do not have a symbol, red and yellow INOPs have exclamation marks beside the alarm message: !!! for red INOPs and !! for yellow INOPs.
Depending on how your monitor is configured, it may display alarm limit violation messages
• in text form, for example “**SpO
• in numeric form, for example “**SpO deviation from the alarm limit, and the second number shows the currently set limit.
Flashing numeric: The numeric of the measurement in alarm flashes.
Bright alarm limits: If the alarm was triggered by an alarm limit violation, the corresponding alarm
limit on the monitor screen is shown more brightly if Show AlarmLimits is enabled and there is sufficient room on the screen.
LOW” or
2
94<96”, where the first number shows the maximum
2
No Alarm Display
40
Alarm lamp: A lamp on the monitor’s front panel flashes. The alarm lamp is divided into two
sections. The right one flashes for a patient alarm, except for short yellow alarms where the lamp will light for approximately six seconds. The color is yellow or red corresponding to the highest priority patient alarm currently present. The left one lights continuously for a light blue INOP and flashes for yellow or red INOPs as follows:
Audible Alarm Indicators 4Alarms
INOP Lamp Color
Yellow 1.0 seconds 1.0 seconds Red 0.25 seconds 0.25 seconds
If only patient alarms are present, and no INOPs, the patient alarms will use both left and right sections to flash (for red and yellow alarms) or light for approximately six seconds (for short yellow alarms). If only INOPs are present, and no patient alarms, red and yellow INOPs will use both left and right sections to flash but light blue INOPs will always light continuously in the left section only.
Nurse call systems: If configured to do so, red, yellow and light blue alarms are indicated on any device connected to the nurse call relay.
Modulation (how long the lamp is on or off while flashing)
On Off

Audible Alarm Indicators

The audible alarm indicators configured for your monitor depend on which alarm standard applies in your hospital. Audible alarm indicator patterns are repeated until you acknowledge the alarm by switching it off or pausing it, or until the alarm condition ceases (if audible alarm indication is set to non-latching).
WARNING • Do not rely exclusively on the audible alarm system for patient monitoring. Adjustment of alarm
volume to a low level or off during patient monitoring may result in patient danger. Remember that the most reliable method of patient monitoring combines close personal surveillance with correct operation of monitoring equipment.
• No alarms are available on the MP5 when connected to a host monitor (Companion Mode is indicated). Alarms become active again as soon as the MP5 is disconnected from the host monitor.
• When connected to a host monitor (Companion Mode is indicated), no alarm tones are available on the MP5.

Alarm Tone Configuration

The audible alarm indicators of your monitor are configurable. In the monitor’s Configuration Mode, you can:
• increase the alarm volume of unacknowledged alarms at regular intervals
• change the interval between alarm sounds (ISO/IEC Standard alarms only)
• change the base volume of the red and yellow alarm tones and the INOP tones
• change the alarm sound to suit the different alarm standards valid in different countries.
Traditional Audible Alarms (HP/Agilent/Philips/Carenet)
• Red alarms and red INOPs: A high pitched sound is repeated once a second.
• Two-star yellow alarms and yellow INOPs: A lower pitched sound is repeated every two seconds.
41
4Alarms Audible Alarm Indicators
• One-star yellow alarms (short yellow alarms): The audible indicator is the same as for yellow alarms, but of shorter duration.
• Standard INOPs: an INOP tone is repeated every two seconds.
ISO/IEC Standard Audible Alarms
• Red alarms and red INOPs: A high pitched tone is repeated five times, followed by a configurable pause.
• Two-star yellow alarms and yellow INOPs: A lower pitched tone is repeated three times, followed by a configurable pause.
• One-star yellow alarms (short yellow alarms): The audible indicator is the same as for yellow alarms, but of shorter duration.
• Standard INOPs: a lower pitched tone is repeated twice, followed by a pause.

Changing the Alarm Tone Volume

The alarm volume symbol at the top right of the monitor screen gives you an
indication of the current volume. To change the volume, select the volume symbol and then select the required volume from the pop-up selection.
If you want to see a numerical indication of the current alarm volume on a scale
from zero to 10, or change the setting, select the Alarm Volume SmartKey. The volume scale pops up. The current setting is indented. To change the setting, select the required number on the scale. Any settings that are inactive (“grayed out”) have been disabled in the monitor’s Configuration Mode.
When the alarm volume is set to zero (off), the alarm volume symbol reflects this. If you switch the alarm volume off, you will not get any audible indication of alarm conditions.
There is no alarm volume indication on the MP5 screen when the MP5 is connected to a host monitor (Companion Mode is indicated).

Minimum Volume for No Central Monitoring INOP

If your monitor is connected to an Information Center, and the connection is interrupted, the INOP message No Central Monit. will appear within 30 seconds, accompanied by an INOP tone. To help ensure that this INOP, and any other active alarm, is not overlooked, the INOP and alarm tones may be configured to have a minimum volume. In this case, INOP and alarm tones will sound even if the monitor alarm volume is set to zero.

Minimum Volume for Severe Yellow or Red INOPs

Severe yellow or red INOPs require action to ensure the well-being of the patient. Therefore the minimum volume for the INOP tone is set to at least alarm volume 8, irrespective of the current alarm volume setting. The INOP tone will sound even if the monitor alarm volume is set to zero.
Alarm
Volume
42
The severe INOPs for which this applies are:
Cuff Not Deflated (configurable to yellow or red)
Acknowledging Alarms 4Alarms
NBP Cuff Overpress (configurable to yellow or red)

Power Loss Tone

When power is lost - no power is available from the power cable or from a battery - a buzzer will sound, if so configured. The tone can be silenced by pressing the On/Off power switch.

Acknowledging Alarms

To acknowledge all active alarms and INOPs, select the Silence permanent key. This switches off the audible alarm indicators and alarm lamps.
Silence
A check mark beside the alarm message indicates that the alarm has been acknowledged. If the monitor is configured to re-alarm, a dashed check mark will be shown.
If the condition that triggered the alarm is still present after the alarm has been acknowledged, the alarm message stays on the screen with a check mark symbol beside it, except for NBP alarms. When an NBP alarm is acknowledged the alarm message disappears.
If the alarm condition is no longer present, all alarm indicators stop and the alarm is reset. Switching off the alarms for the measurement in alarm, or switching off the measurement itself, also
stops alarm indication.

Acknowledging Disconnect INOPs

Acknowledging an INOP that results from a disconnected transducer switches off the associated measurement. The only exception is ECG/Resp: acknowledging a disconnect INOP for ECG leads does not switch off the ECG and Resp measurements. Acknowledging a disconnect INOP at the Information Center switches off the audible INOP indicator but does not switch off the measurement.

Alarm Reminder (ReAlarm)

If Alarm Reminder is configured on for your monitor, you will get an audible reminder of alarm conditions that remain active after you have acknowledged the alarm. This reminder may take the form of a repetition of the alarm tone for a limited time, or an unlimited repetition of the alarm tone (this is the same as a new alarm). Alarm reminder is not available for standard, light blue INOPs but for yellow and red INOPs.
In Configuration Mode, you can set the interval between silencing the alarm and sounding the reminder tone to one, two, or three minutes.
APNEA
The alarm reminder behavior at the Information Center is different to that at the monitor. Refer to the Information Center Instructions for Use for further information.
43
4Alarms Pausing or Switching Off Alarms

Pausing or Switching Off Alarms

If you want to temporarily prevent alarms from sounding, for example while you are moving a patient, you can pause alarms. Depending on your monitor configuration, alarms are paused for one, two, or three minutes, or infinitely.
To view the alarm pause setting chosen for your unit,
1 Select Main Setup -> Alarms -> Alarm Settings
2 Check the Alarms Off setting.
This setting can only be changed in Configuration Mode.

To Pause All Alarms

Select the Pause Alarms permanent key. If your monitor is configured to
infinite pause time, the permanent key is labelled Alarms Off, and selecting it switches alarms off.
Depending on the configuration, you may need to select Confirm to complete the change.
Pause
Alarms

To Switch All Alarms Off

You can only switch alarms off permanently if your monitor is configured to allow infinite alarms pause and the permanent key is labelled Alarms Off.
Select the Alarms Off permanent key.
Depending on the configuration, you may need to select Confirm to complete the change.
Pausing alarms infinitely is the same as switching them off.

To Switch Individual Measurement Alarms On or Off

1 Select the measurement numeric to enter its setup menu.
2 Select Alarms to toggle between On and Off.
The alarms off symbol is shown beside the measurement numeric.

While Alarms are Paused or Off

• The red Alarms Paused lamp on the monitor front panel is lit.
In the alarm field, the monitor displays the message
ALARMS PAUSED or ALARMS OFF, together with the alarms paused symbol and the remaining pause time in minutes and seconds, or alarms off symbol.
ALARMS PAUSED 1:28
Alarms
Off
44
Alarm Limits 4Alarms
• No alarms are sounded and no alarm messages are shown.
• INOP messages are shown but no INOP tones are sounded.
The only exceptions are the INOPs CUFF NOT DEFLATED, CUFF OVERPRESS and INOPs relating to empty, missing and malfunctioning batteries.
These INOPs switch the alarms on, and the INOP tones are sounded, even if alarms are paused or off. You need to remove the INOP condition first before you can switch the alarm tones off again.
• The nurse call relay is not active.
If a NO SENSOR or NO TRANSDUCER INOP is present and alarms are paused or switched off, the measurement in question is switched off.
ALARMS OFF

Restarting Paused Alarms

To manually switch on alarm indication again after a pause, select the permanent key
PAUSE ALARMS (or ALARMS OFF) again.
Alarm indication starts again automatically after the pause period expires. If the monitor is configured to stay paused infinitely, you must select ALARMS OFF again to restart alarm indication.

Resetting Arrhythmia Alarm Timeouts

To reset the arrhythmia alarm timeout period, select the ALARMS OFF or PAUSE ALARMS
permanent key and then reselect it.

Extending the Alarm Pause Time

If your monitor has extended alarm pause enabled, you can extend the alarm pause time. Use this to prevent alarms being indicated, for example, while you are washing a patient or carrying out a procedure. Only extend the alarm pause time when you are sure that clinical personnel are available to monitor the patient’s condition closely.
To extend the alarm pause time to five or 10 minutes,
1 Select one of the alarm fields. This calls up the Alarm Messages window.
2 Select either the pop-up key Pause Al. 5 min or the pop-up key Pause Al. 10 min.
Each time you select one of these pop-up keys, the Alarm Pause Time is reset to five (or 10) minutes.

Alarm Limits

The alarm limits you set determine the conditions that trigger yellow and red limit alarms. For some measurements (for example, SpO to 100 switches the high alarm off. In these cases, the alarms off symbol is not displayed.
), where the value ranges from 100 to 0, setting the high alarm limit
2
WARNING Be aware that the monitors in your care area may each have different alarm settings, to suit different
patients. Always check that the alarm settings are appropriate for your patient before you start monitoring.
45
4Alarms Alarm Limits

Viewing Individual Alarm Limits

HR
120
85
You can usually see the alarm limits set for each measurement next to the measurement numeric on the main screen.
50
If your monitor is not configured to show the alarm limits next to the numeric,
Alarm limits
you can see them in the appropriate measurement setup menu. Select the measurement numeric to enter the menu and check the limits.

Viewing All Alarm Limits

The Alarm Limits overview window lists the currently set alarm limits for all measurements. If an Apnea alarm delay time is set, this is also shown. The ALARMS OFF symbol is shown beside the measurement label of any measurement whose alarm switched off.
To open the Alarm Limits window, either select any alarm field to open the Alarm
Messages window, then select the Alarm Limits pop-up key, or select the Alarm Limits SmartKey, if configured.
ST-V4
Alarm Limits
ST-V5
ST-V6
SpO
2
Pulse (SpO2)
NBPs
ABPs
PAPd
awRR
Apnea Time
1
3
Off
sec
2
46
Alarm Limits 4Alarms
1 2 3
Measurement labels, with alarms off symbol where appropriate
Current alarm limits
Graphic view of current yellow and red alarm limits and currently monitored measurement value.
Off indicates the measurement is switched off
Select Show ST Limits to expand the list of ST leads and view the currently set alarm limits.
Selecting Hide ST Limits hides the list again.
You can use the pop-up keys that open with the Alarm Limits window to perform common tasks:
All Al. On/All Al. Off, – All Lim. Narrow/All Lim. Wide to set narrow or wide alarm AutoLimits for all
measurements.
Print Limits/Record Limits to print a list of all current alarm limit settings on a
connected printer or recorder.
These pop-up keys are not available in the window for changing individual alarm limits which you access by selecting the measurement label in the Alarm Limits window.

Changing Alarm Limits

To change individual measurement alarm limits using the measurement’s Setup Menu,
1 In the measurement’s setup menu, select the alarm limit you want to change. This calls up a list of
available values for the alarm limit.
2 Select a value from the list to adjust the alarm limit.
Alternatively, you can use the keys in the measurement Change Limits window, which you access by selecting the measurement label in the Alarm Limits window.
47
4Alarms Alarm Limits
1
2
HR
3
4
Alarms On/Off
5
6
7
8
9
1 2 3 4 5 6 7 8 9 10
10
Parameter label
High red alarm (view only)
High yellow alarm field. Select to open a pop-up list of high alarm limits
Alarms On/Off key - select to toggle between alarms on or off
Preview Alarm AutoLimits for a measurement before applying
Select to apply wide AutoLimits
Select to apply narrow AutoLimits
Low yellow alarm field. Select to open a pop-up list of low alarm limits
Low red alarm (view only)
Graphic view of alarm limits with currently measured value
To change alarm limits,
1 Enter the Alarm Limits window.
2 To set the high alarm limit, select the high yellow alarm field to open a pop-up list of high alarm
limits. Select a limit from the list. Repeat to set the low yellow alarm field.
If you set the yellow alarm limit outside the red alarm limit, the monitor will automatically set the red alarm to the yellow alarm limit.
48
When an ST measurement is in the Change Limits window there are also two pop-up keys available labeled All ST Narrow/All ST Wide. With these keys you can set Auto Limits for all ST Leads.
Alarm Limits 4Alarms

About Automatic Alarm Limits (AutoLimits)

The monitor can automatically set alarm limits suited to your individual patient, using the Automatic Alarm Limits function. This tells the monitor to adapt the alarm limits of selected measurements to the measured vital signs within a defined safe limit. The monitor calculates safe AutoLimits for each patient based on the measured values from the last 12 seconds.
The wide and narrow limits have a fixed relationship to the measured value within the non­pathological range. Outside of this range, no auto limits are calculated. To set values outside of the non-pathological range, limits must be changed manually, based on the clinician’s judgement about the specific patient.
1
2
3
4
1 Wide alarm limits 2 Narrow alarm limits 3Alarm Limits 4 Measurement value
2 1
Limits Narrow sets limits close to the currently measured values for situations where it is critical for you to be informed about small changes in your patient’s vital signs.
Limits Wide sets limits further away from the currently measured values for situations where small changes are not so critical.
Use the keys in the Change Limits window to apply AutoLimits for individual measurements.
These keys are not available if AutoLimits have been disabled for the measurement in the monitor’s Configuration Mode.
AutoLimits are not available for all measurements. The list of measurements for which AutoLimits can be used is defined in the monitor’s Configuration mode.
Use the Change Limits window to check AutoLimits before you apply them to ensure that they are appropriate for your individual patient and their clinical condition. Once applied, AutoLimits are shown on the monitor screen just like manually-set alarm limits. If the AutoLimits are not appropriate for your patient, you must set alarm limits manually. The limits remain unchanged until you set them again or change them manually.

Documenting Alarm Limits

The alarm limits pop-up keys appear with the Alarm Limits and Change Limits windows.
Select the Print Limits pop-up key to print an overview of all alarm limits on a connected
printer.
49
4Alarms Reviewing Alarms
Select the Record Limits pop-up key to send a recording of the alarm limits to a recorder.

Reviewing Alarms

You can see which alarms and INOPs are currently active in the respective alarms and INOPs fields at the top of the screen.
To see the currently active alarms and INOPs listed in one place, select any of the alarm status areas on the monitor screen. The Alarm Messages window pops up.
All alarms and INOPs are erased from the Review Alarms window when you discharge a patient, or if you change to Demonstration Mode.

Alarm Messages Window

The Alarm Messages window shows all the currently active alarms and INOPs sorted by priority, beginning at the top with the most recent. INOPs are shown on the left hand side and patient alarms are shown on the right hand side. Any active red alarms are shown first, followed by yellow alarms. Acknowledged alarms or INOPs are shown with the check mark symbol.
The Alarm Messages window pop-up keys appear when the window is opened. If alarm pause extension is disabled, the pause pop-up keys are inactive (“grayed-out”). Selecting the Review
Alarms pop-up key opens the Review Alarms window.
Alarm Messages
Resp LEADS OFF
LL LEAD OFF
Alarm Limits
If you do not immediately understand an INOP or alarm message, refer to its help text.
•In the Alarm Messages window, select the INOP message. This calls up a help window with an explanation of the INOP message and, where appropriate, a suggested solution for the problem.
• If the alarm or INOP was generated in a device other than the monitor (for instance, in an MMS or FMS), this source is specified at the end of the help text (Source: FMS).
Review Alarms
** awRR LOW
Pause Al. 5 Min.
Pause Al. 10 Min.

Review Alarms Window

50
Reviewing Alarms 4Alarms
The Review Alarms window contains a list of the most recent alarms and INOPs with date and time information.
Review Alarms
5 Apr 16:55:18 *** Apnea
5 Apr 16:55:18 ** ABPs HIGH (120 >95) 5 Apr 16:55:18 Alarms On 5 Apr 16:45:15 ** SpO 5 Apr 16:44:57 Alarms Off 5 Apr 16:44:46 ** awRR LOW (14<15) 5 Apr 16:44:39 ** SpO 5 Apr 16:44:28 ** ABPs HIGH (120>95)
NON-PULSAT.
2
LOW (95<99)
2
If configured to do so, each alarm is shown with the alarm limit active when the alarm was triggered and the maximum value measured beyond this limit. The Review Alarms window also shows when the monitor was switched on (after being switched off for longer than 1 minute) and any changes made to the Alarms On/Off, Standby, Silence or ECG source.
No entries are made in the Review Alarms window of the MP5 while it is connected to a host monitor, except the time when the MP5 was connected to the host (Companion Entered), and when it was disconnected (Companion Left). Alarms can be reviewed on the host monitor.
When you select an item from the list, you can get additional information about that item. If you select a high or low limit alarm in the list, the Graphical Trends window will open to provide further data. If you select an alarm resulting from an event alarm notification, the Event Episode window for that event will open. If you select an alert other than a high or low alarm, a help text window opens with more information. This is the same as the help text window that opens in the Alarm Messages window. Some items in the list are simply log items not related to a patient alert as such (for example, Alarms On or Alarms Off). You cannot see any further information if you select one of these items. When you close these windows you will return to the Review Alarms window.
The information in the Review Alarms window is deleted when a patient is discharged, and when you leave Demonstration Mode.
The Review Alarms window pop-up keys appear when the window is opened. If alarm pause extension is disabled, the pause pop-up keys are inactive. Selecting the Active Alarms pop-up key opens the Alarm Messages window.
Alarm Limits
Active Alarms
Pause Al. 5 Min.
Pause Al. 10 Min.
51
4Alarms Latching Alarms

Latching Alarms

The alarm latching setting for your monitor defines how the alarm indicators behave when you do not acknowledge them. When alarms are set to non-latching, their indicators end when the alarm condition ends. Switching alarm latching on means that visual and/or audible alarm indications are still displayed or announced by the monitor after the alarm condition ends. The indication lasts until you acknowledge the alarm.

Viewing the Alarm Latching Settings

To see the alarm latching setting for your monitor
1 In the monitor’s Main Setup menu, select Alarms.
2 Select Alarm Settings, and see the Visual Latching and Audible Latching
settings.
This setting can only be changed in Configuration Mode. You should be aware of the settings chosen for your unit. There are three possible choices each for visual and audible latching, Red, Red and Yellow, and Off. These choices can be combined to give the following settings:
Visual Latching
Audible latching
R = red alarms, Y = yellow alarms

Alarm Latching Behavior

Red and Yellow Measurement Alarms
Alarm has not been acknowledged.
Alarm has been acknowledged.
All INOPs are non-latching. See “Yellow Arrhythmia Alarms” on page 122 for information on one-star yellow alarms latching behavior.
Alarm condition still present.
Alarm condition no longer present.
Alarm condition still present.
Alarm condition no longer present.
R&Y R&Y R&Y RROff R&Y ROffROffOff
Non-latching alarms
Alarm tone on. Alarm lamp on. Alarm message. Flashing numerics.
All audible and visual alarm indicators automatically stop.
Alarm tone off. Alarm lamp off. Alarm message. Flashing numerics. Audible alarm reminder (if configured).
Audible and visual alarm indicators automatically stop.
Visual and audible latching
Alarm tone on. Alarm lamp on. Alarm message. Flashing numerics.
Visual latching, audible non-latching
Alarm message. Flashing numerics. Audible alarm indicators automatically stop.

Te s t i n g A l a r m s

When you switch the monitor on, a selftest is started. You must check that the alarms lamps light, one after the other, and that you hear a single tone. This indicates that the visible and audible alarm indicators are functioning correctly. For further testing of individual measurement alarms, perform the measurement on yourself (for example SpO that appropriate alarm behavior is observed.
52
or CO2) or use a simulator. Adjust alarm limits and check
2
Alarm Behavior at On/Off 4Alarms

Alarm Behavior at On/Off

When you switch alarms on, the settings defined in the currently active Profile are used.
If the monitor is switched off for longer than one minute and then switched on again, or after a loss of power lasting longer than one minute, or when a patient is discharged, the monitor can be configured to restore either the alarm settings from the monitor's configured default Profile, or the most recently used alarm settings. After any of these situations, you should check that the alarm settings are appropriate for your patient, and if necessary, select the correct Profile and patient category.
If power is lost for less than one minute, the alarm settings prior to the power loss are restored.

Alarm Recordings

You can set up your monitor so that it automatically triggers alarm recordings at the Information Center, or if configured, to a printer as a realtime report.
1 Press the Main Setup SmartKey.
2 Select Alarms from the Main Setup menu.
3 Select Alarm Recording from the Alarms menu to open the Alarm Recordings menu.
4 Select a measurement from those listed for which you want to change the alarm condition that
triggers an alarm recording. This opens a pop-up list.
5 For the desired measurement(s), choose the alarm condition to trigger an alarm recording:
Red Only: an alarm recording will automatically be triggered when the measurement enters a red alarm condition.
Red&Yell: both yellow and red alarms will trigger an alarm recording. Off: disables automatic alarm recording.
Refer to the chapter “Recording” for details of how to set up a recording.
53
4Alarms Alarm Recordings
54

5Patient Alarms and INOPs

This chapter lists patient alarms and technical alarms (INOPs) alphabetically, irrespective of their priority. INOPs start on page 61. All alarms and INOPs are listed here; the ones which can appear on your monitor will depend on the model and the individual options.
For information on alarms and INOPs from the gas module refer to your Gas Module Instructions for Use.

Patient Alarm Messages

The measurement labels and abbreviations for pressure, temperature, SpO2, and anesthetic agent alarms are explained in the individual chapters.
Some alarms may be shown at the Information Center in shortened form, when transferred through IntelliVue Instrument Telemetry. These shortened alarm texts are included in the list and identified with the note “at Information Center”.
5
Note that yellow arrhythmia alarms may be shown with one or with two stars, depending on your monitor configuration and the Information Center revision you are using.
Refer to your IntelliBridge Device Driver Instructions for Use for patient alarms from connected external devices.
Refer to your Gas Module Instructions for Use for patient alarms and INOPs from the gas module.
Alarm Message From Condition Indication
*/**AFIB ECG/
Arrhythmia
***APNEA or ***APNEA mm:ss sec
or
***APNEA >10min
***ASYSTOLE ECG No QRS detected for a period greater
**awRR HIGH CO2, Resp,
**awRR LOW CO2, Resp,
, Resp,
CO
2
Spirometry
AGM
AGM
Atrial fibrillation waveform detected yellow alarm lamp, short
yellow audible alarm.
Respiration has stopped for longer than the preset apnea time. “mm:ss” denotes the Apnea duration in minutes and seconds.
than the asystole threshold (in the absence of Vfib or chaotic ECG).
The airway respiration rate has exceeded the high alarm limit.
The airway respiration rate has dropped below the low alarm limit.
numeric flashes, red alarm lamp, alarm tone.
numeric flashes, red alarm lamp, alarm tone.
numeric flashes and high limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and low limit is highlighted, yellow alarm lamp, alarm tone.
55
5 Patient Alarms and INOPs Patient Alarm Messages
Alarm Message From Condition Indication
**BIS HIGH BIS The Bispectral Index value has
exceeded the high alarm limit.
**BIS LOW BIS The Bispectral Index value has dropped
below the low alarm limit.
***BRADY/P xxx<yyy
or ***BRADY xxx<yyy
**CCO/CCI HIGH CCO Continuous Cardiac Output or CC
**CCO/CCI LOW CCO Continuous Cardiac Output or CC
**CPP HIGH CPP The CPP value has exceeded the high
**CPP LOW CPP The CPP value has fallen below the low
***DESAT or ***DESAT xxx<yyy
**etCO2 HIGH CO2, Resp,
**etCO2 LOW CO2, Resp,
**etO2 HIGH O2, AGM The end tidal O2 high alarm limit has
**etO2 LOW O2, AGM The end tidal O2 value has fallen below
*/**/*** EVENT:<GRP>
*/**/*** EVENT
at Information center
***EXTREME BRADY ECG The bradycardia limit has been
***EXTREME TACHY ECG The tachycardia limit has been
Press, SpO2The heart rate from the Pulse signal has
fallen below the bradycardia limit. xxx denotes the lowest measured value; yyy is the bradycardia limit.
Index is above the high alarm limit.
Index is below the low alarm limit.
alarm limit.
alarm limit.
SpO
2
AGM
AGM
Event surveillance
Event surveillance
The SpO2 value has fallen below the desaturation alarm limit. xxx denotes the lowest measured value, and yyy is the desaturation limit.
The end tidal CO2 high alarm limit has been exceeded.
The end tidal CO2 value has fallen below the low alarm limit.
been exceeded.
the low alarm limit.
An event has occurred and the event notification is configured to alarm. <GRP> is the event group
An event has occurred and the event notification is configured to alarm. Check on the monitor for more details on event group.
exceeded.
exceeded.
numeric flashes and high limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and low limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and alarm limit is highlighted, red alarm lamp, alarm tone.
numeric flashes and high alarm limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and low alarm limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and high limit is highlighted, yellow alarm lamp, alarm tone
numeric flashes and low limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes, red alarm lamp, alarm tone.
numeric flashes and high limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and low limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and high limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes, and low limit is highlighted, yellow alarm lamp, alarm tone.
event group name flashes, yellow or red alarm lamp and alarm tone
(on monitor) event group name flashes, yellow or red alarm lamp and alarm tone
numeric flashes and alarm limit is highlighted, red alarm lamp, alarm tone.
numeric flashes and alarm limit is highlighted, red alarm lamp, alarm tone.
56
Patient Alarm Messages 5 Patient Alarms and INOPs
Alarm Message From Condition Indication
**HR HIGH ECG The heart rate high alarm limit has
been exceeded.
**HR LOW ECG The heart rate has fallen below the low
alarm limit.
*/**IRREGULAR HR ECG/
Arrhythmia
*/**MISSED BEAT ECG/
Arrhythmia
*/**MULTIFORM PVCs ECG/
Arrhythmia
**NBP HIGH NBP The measured NBP value is above the
**NBP LOW NBP The measured NBP value is below the
*/**NON-SUSTAIN VT ECG/
Arrhythmia
*/**PACER NOT CAPT ECG/
Arrhythmia (paced patients only)
*/**PACER NT PACING ECG/
Arrhythmia (paced patients only)
*/**PAIR PVCs ECG/
Arrhythmia
*/**PAUSE ECG/
Arrhythmia
Consistently irregular heart rhythm. numeric flashes, yellow alarm
No beat detected for 1.75*R-R interval, or if HR>120bpm no beat detected for one second (non-paced patients only).
Two differently shaped Vs detected, each occurring at least twice within the last 300 beats and at least once within the last 60 beats.
high alarm limit. s, d, or m after the label indicates whether the systolic, diastolic or mean pressure has crossed the limit.
low alarm limit. s, d, or m after the label indicates whether the systolic, diastolic or mean pressure has crossed the limit.
A run of Vs having a ventricular HR>V-Tach HR limit, but lasting for less than the V-Tach Run limit has been detected.
A missed beat with a pace pulse was detected.
A missed beat without a pace pulse was detected.
A non-ventricular contraction, followed by two ventricular contractions, followed by a non-ventricular contraction has been detected.
No beat detected for a period greater than the pause threshold.
numeric flashes and high limit is highlighted, yellow alarm lamp, alarm tone. If configured to short yellow, the sound switches off after 5 seconds if Arrhythmia is On.
numeric flashes and low limit is highlighted, yellow alarm lamp, alarm tone. If configured to short yellow, the sound switches off after 5 seconds if Arrhythmia is On.
lamp, short yellow audible alarm.
numeric flashes, yellow alarm lamp, short yellow audible alarm.
numeric flashes, yellow alarm lamp, short yellow audible alarm.
numeric flashes and high limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and low limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes, yellow alarm lamp, short yellow audible alarm.
numeric flashes, yellow alarm lamp, short yellow audible alarm.
numeric flashes, yellow alarm lamp, short yellow audible alarm.
numeric flashes, yellow alarm lamp, short yellow audible alarm.
numeric flashes, yellow alarm lamp, short yellow audible alarm.
57
5 Patient Alarms and INOPs Patient Alarm Messages
Alarm Message From Condition Indication
***<Pressure> DISCONNECT
***<Pressure> HIGH PRESS The measured pressure value is above
**<Pressure> HIGH PRESS The measured pressure value is above
***<Pressure> LOW PRESS The measured pressure value is below
**<Pressure> LOW PRESS The measured pressure value is below
**Pulse HIGH PRESS
**Pulse LOW PRESS
*/**PVCs/min HIGH ECG/
**QTc HIGH ECG/QT QTc value has exceeded the QTc high
**QTc HIGH ECG/QT QTc value has exceeded the QTc
*/**R-ON-T PVCs ECG/
**RR HIGH RESP The respiration rate has exceeded the
PRESS The pressure is non-pulsatile and the
mean pressure is continuously less than 10mmHg (1.3kPa). This alarm occurs only with arterial pressures (P, ABP, ART, Ao, BAP, FAP, PAP, UAP, P1, P2, P3, P4).
the extreme high alarm limit. s, d, or m after the label indicates whether the systolic, diastolic or mean pressure has crossed the limit.
the high alarm limit. s, d, or m after the label indicates whether the systolic, diastolic or mean pressure has crossed the limit.
the extreme low alarm limit. s, d, or m after the label indicates whether the systolic, diastolic or mean pressure has crossed the limit.
the low alarm limit. s, d, or m after the label indicates whether the systolic, diastolic or mean pressure has crossed the limit.
The pulse rate has exceeded the high
SpO
2
alarm limit.
The pulse rate has dropped below the
SpO
2
low alarm limit.
More premature ventricular
Arrhythmia
contractions have been detected in a minute than the limit.
limit for more than 5 minutes
high limit for more than 5 minutes
For HR <100, a PVC with R-R interval
Arrhythmia
< 1/3 the average interval followed by a compensatory pause of 1.25 x average R-R interval or two such Vs without compensatory pause occurring within 5 minutes of each other. (When HR >100, 1/3 R-R interval is too short for detection.).
high alarm limit.
numeric flashes, red alarm lamp, alarm tone.
numeric flashes, high limit is highlighted, red alarm lamp, alarm tone.
numeric flashes, high limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and low limit is highlighted, red alarm lamp, alarm tone.
numeric flashes and low limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and high limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and low limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes, yellow alarm lamp, short yellow audible alarm.
numeric flashes, yellow alarm lamp, alarm tone.
numeric flashes, yellow alarm lamp, alarm tone.
numeric flashes, yellow alarm lamp, short yellow audible alarm.
numeric flashes and high limit is highlighted, yellow alarm lamp, alarm tone.
58
Patient Alarm Messages 5 Patient Alarms and INOPs
Alarm Message From Condition Indication
**RR LOW RESP The respiration rate has dropped below
the low alarm limit.
*/**RUN PVCs HIGH ECG/
Arrhythmia
A run of PVCs greater than 2 was detected.
**<SO2 label> HIGH SvO2/SO2The the measured intravascular oxygen
saturation has exceeded the high limit.
**<SO2 label> LOW SvO2/SO2The measured intravascular oxygen
saturation has fallen below the low limit.
**<SpO2 label> HIGH SpO
2
The arterial oxygen saturation has exceeded the high alarm limit.
**<SpO2 label> LOW SpO
2
The arterial oxygen saturation has fallen below the low alarm limit.
**ST<n> HIGH ECG/ST The ST elevation in lead <n> is higher
than the limit.
**ST<n> LOW ECG/ST The ST depression in lead <n> is lower
than the limit.
**ST MULTI <n>,<n> ECG/ST The ST depression or elevation is
outside of the limit in two or more leads <n> and <n>
**ST MULTI
at Information Center
ECG/ST The ST depression or elevation is
outside of the limit in two or more leads. Check on the monitor for more details about which leads are affected.
*/**SVT ECG/
Arrhythmia
A run of supraventricular beats greater than the SVT run limit has been detected and the HR has exceeded the SVT HR limit.
***TACHY/P xxx>yyy or ***TACHY xxx>yyy
Press, SpO2The heart rate from the Pulse signal has
exceeded the tachycardia limit. xxx denotes the highest measured value; yyy is the tachycardia limit.
**Tblood HIGH C.O. The blood temperature value has
exceeded the high alarm limit.
**Tblood LOW C.O. The blood temperature value has fallen
below the low alarm limit.
**tcpO2 HIGH/ **tcpCO2 HIGH
**tcpO2 LOW/ **tcpCO
LOW
2
tcGas The tcpO2 or tcpCO2 value has
exceeded the high alarm limit.
tcGas The tcpO
or tcpCO2 value has fallen
2
below the low alarm limit.
numeric flashes and low limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes, yellow alarm lamp, short yellow audible alarm.
numeric flashes and high alarm limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and low alarm limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and high limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and low limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and high alarm limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and low alarm limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes, yellow alarm lamp, alarm tone
(on monitor) numeric flashes, yellow alarm lamp, alarm tone
numeric flashes, yellow alarm lamp, alarm tone.
numeric flashes, alarm limit is highlighted, red alarm lamp, alarm tone.
numeric flashes, high alarm limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes, low alarm limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes, high alarm limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes, low alarm limit is highlighted, yellow alarm lamp, alarm tone.
59
5 Patient Alarms and INOPs Patient Alarm Messages
Alarm Message From Condition Indication
*/**/***TELE ALARM Telemetry This is a generic alarm from the
telemetry system. The specific alarm cause is indicated in the alarm message in the Telemetry Data Window.
**<Temperature label> HIGH
**<Temperature label> LOW
*/**VENT BIGEMINY ECG/
***VENT FIB/TACH ECG A fibrillatory waveform for 4
*/**VENT RHYTHM ECG/
*/**VENT TRIGEMINY ECG/
***VTACH ECG,
**/***VueLink ALARM
at Information Center
TEMP The temperature has exceeded the high
alarm limit.
TEMP The temperature has fallen below the
low alarm limit.
A dominant rhythm of N, V, N, V (N =
Arrhythmia
Arrhythmia
Arrhythmia
Arrhythmia
VueLink A yellow (**) or red (***) patient alarm
supraventricular beat, V = ventricular beat) was detected.
consecutive seconds was detected.
A dominant rhythm of adjacent Vs > vent rhythm limit and ventricular HR < VTach HR limit was detected.
A dominant rhythm of N, N, V, N, N, V (N = supraventricular beat, V = ventricular beat) was detected.
Ventricular tachycardia has been detected (Consecutive PVCs exceed V­Tach Run limit and HR exceeds V-Tach HR limit).
is present on the VueLink module. Check the monitor display for more detailed alarm information.
yellow or red alarm lamp and alarm tone
numeric flashes and high limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes and low limit is highlighted, yellow alarm lamp, alarm tone.
numeric flashes, yellow alarm lamp, short yellow audible alarm.
numeric flashes, red alarm lamp, alarm tone.
numeric flashes, yellow alarm lamp, short yellow audible alarm.
numeric flashes, yellow alarm lamp, short yellow audible alarm.
numeric flashes, red alarm lamp, alarm tone.
(on monitor) yellow or red alarm lamp, alarm tone
60
Technical Alarm Messages (INOPs) 5 Patient Alarms and INOPs

Technical Alarm Messages (INOPs)

If an INOP interrupts monitoring and alarm detection, the measurement numeric will be replaced by -?-. If an INOP may lead to unreliable measurement values, a ? appears next to the numeric.
The measurement labels and abbreviations for pressure, temperature and SpO
INOP messages are
2
explained in the individual chapters.
INOP Message, Indication Source What to do
ABP INOPS PRESS See <Pressure label> INOPS (under Pressure).
ALL ECG ALARMS OFF ECG/
Arrhythmia
Ao INOPS PRESS See <Pressure label> INOPS (under Pressure).
ART INOPS PRESS See <Pressure label> INOPS (under Pressure).
AWF CHANGE SCALE Spirometry Airway flow signal exceeds range of selected scale. Adjust scale
AWP CHANGE SCALE Spirometry Airway pressure signal exceeds range of selected scale. Adjust
AWV CHANGE SCALE Spirometry Airway volume signal exceeds range of selected scale. Adjust
Bad Serverlink
INOP tone
BAP INOPS PRESS See <Pressure label> INOPS (under Pressure).
BATT EMPTY
INOP tone, battery LED flashes During this INOP, alarms cannot be paused or switched off.
BATT INCOMPAT
INOP tone
BATT LOW
INOP tone
BATT MALFUNCTION
INOP tone, battery LED flashes During this INOP, alarms cannot be paused or switched off unless the monitor is connected to mains power.
BATTERIES EMPTY or BATT 1/ BATT 2 EMPTY
INOP tone, battery LED flashes During this INOP, alarms cannot be paused or switched off.
Monitor 1) An MMS with an incompatible software revision is
Battery The estimated remaining battery-powered operating time is less
Battery The battery cannot be used with this monitor. Replace with the
Battery The estimated battery-powered operating time remaining is less
Battery The monitor cannot determine the battery status. If this INOP
Batteries The estimated remaining battery-powered operating time of
All ECG alarms have been switched off, or the HR alarm source is not ECG. To resume ECG alarm generation, switch ECG alarms on or select ECG as the alarms source.
to display complete wave.
scale to display complete wave
scale to display complete wave.
connected to the monitor. This combination does not allow monitoring, OR
2) You cannot use this combination of monitor, MMS and cable. Switch off the monitor and contact your service personnel.
than 10 minutes. Replace the battery immediately.
If the condition persists and the monitor is not connected to mains power, this INOP is re-issued two minutes after you acknowledge it.
correct battery
than 20 minutes.
persists, replace the faulty battery. If the condition persists and the monitor is not connected to mains power, this INOP is re­issued two minutes after you acknowledge it.
Place the battery in a different monitor or in a battery charger. If the same INOP is shown, contact your service personnel.
the indicated battery or batteries is less than 10 minutes. Replace the batteries immediately.
If the condition persists and the monitor is not connected to mains power, this INOP is re-issued two minutes after you acknowledge it.
(M4607A).
61
5 Patient Alarms and INOPs Technical Alarm Messages (INOPs)
INOP Message, Indication Source What to do
BATTERIES INCOMP or BATT 1/ BATT 2 INCOMPAT
INOP tone
BATTERIES LOW or BATT 1/ BATT 2 LOW
INOP tone
BATTERIES MALFUNC. or BATT 1/BATT 2/ BATTERY MALFUNCT.
INOP tone, battery LED flashes During this INOP, alarms cannot be paused or switched off unless the monitor is connected to mains power.
BATTERY LOW T Telemetry The battery in the Telemetry device is low and must be
BATT 1/BATT 2 MISSING
INOP tone. During this INOP, alarms cannot be paused or switched off.
BIS CABLE INCOMPAT
INOP tone.
BIS CABLE USAGE
INOP tone.
BIS DSC DISCONN
INOP tone
BIS DSC INCOMPT
INOP tone
BIS DSC MALFUNC BIS Electrocautery used during self-test OR malfunction in the
BIS DSC UPDATE
INOP tone
BIS ELECTR. DISC
INOP tone.
BIS ENGINE DISCONN
INOP tone
Batteries The indicated battery or batteries cannot be used with this
monitor. Replace with the correct battery or batteries as specified in this book.
Batteries The estimated battery-powered operating time remaining is less
than 20 minutes.
Batteries The monitor cannot determine the battery status. If this INOP
persists, replace the faulty battery or batteries. If the condition persists and the monitor is not connected to mains power, this INOP is re-issued two minutes after you acknowledge it.
Place the batteries in a different monitor or in a battery charger. If the same INOP is shown, contact your service personnel.
replaced soon.
Batteries The monitor requires two batteries but can detect only one
battery. Insert the missing battery immediately.
BIS The semi-reusable sensor cable connected is unknown or not
supported by your software revision. Replace it with a Philips­supported sensor cable.
BIS The semi-reusable sensor cable has exceeded the maximum
number of uses. Replace the cable.
BIS DSC is not properly connected OR either DSC or BIS engine
may be faulty. Make sure that the DSC is properly connected to the BIS Engine. If INOP persists, replace DSC with a known good one of the same type. If INOP persists replace BIS engine. Silencing this INOP switches the measurement off.
BIS DSC is not supported by the BIS engine or new DSC
connected to an old BIS engine. A software upgrade may be required. Contact your service personnel.
DSC hardware. Make sure not to use electrocautery during the self-test procedure. Disconnect and reconnect the DSC to the BIS engine. If the INOP persists, replace the DSC or contact your service personnel.
BIS DSC update currently being carried out. This INOP will
disappear when the DSC update is finished. Do not disconnect the DSC during the update. No action is needed.
BIS One or more electrodes are not connected to the semi-reusable
sensor cable. Check all electrode connections.
BIS BIS engine not connected OR Module Cable defective.
Make sure that the Module Cable is properly connected. If INOP persists, replace the Module Cable. Silencing this INOP switches the measurement off.
62
Technical Alarm Messages (INOPs) 5 Patient Alarms and INOPs
INOP Message, Indication Source What to do
BIS ENGINE INCOMPT
INOP tone
BIS ENGINE MALFUNC
INOP tone
BIS EQUIP MALF
INOP tone
BIS HIGH IMPEDANCE
INOP tone may sound
BIS IMPEDANCE CHCK
INOP tone may sound
BIS BIS engine software is not supported. A software upgrade may
be required. Contact your service personnel. MP20/30 - BIS engine not supported.
BIS Malfunction in the BIS engine hardware. Disconnect and
reconnect the BIS engine. If the INOP persists, replace BIS engine.
BIS There is a malfunction in the BIS hardware. Unplug and replug
the BIS module. If the INOP persists, contact your service personnel.
BIS Impedance of one or more electrode(s) is above the valid range,
most often caused by bad skin preparation. Check the sensor montage and press the electrode pads firmly. If this INOP persists, replace the sensor(s) in question using correct skin preparation. If INOP persists, contact your service personnel.
BIS The Cyclic Impedance check is running. It will stop
automatically if all impedances are within the valid range. If any electrodes do not pass the impedance test, check the sensor montage and press the electrode pads firmly. To manually stop the Cyclic Impedance Check, select
Cyclic Check off in the Setup BIS menu.
BIS ISOELECTRC EEG BIS No discernible EEG activity is detected for longer than one
minute. Check the patient. Check that the electrodes are properly connected.
BIS LEAD OFF
INOP tone may sound
BIS OVERCURRENT
INOP tone
BIS SENSOR DISCONN
INOP tone
BIS SENSOR INCOMPT
INOP tone
BIS One or more electrodes have no skin contact and therefore
impedances cannot be measured. Check the sensor montage and press the electrode pads firmly. If this INOP persists, replace the sensor(s) in question, using correct skin preparation.
BIS Unplug and replug the BIS module or, f or the MP20/MP30,
disconnect and reconnect the BISx from the Interface board. If the INOP persists, contact your service personnel.
BIS The sensor is not properly connected to the patient interface
cable (PIC) and/or the PIC is not properly connected to the DSC or BISx, or the sensor or PIC or DSC or BISx may be faulty. Check all the connections. Disconnect and reconnect the sensor, PIC, DSC, BISx. If the INOP persists, replace the sensor. If the INOP persists, replace PIC. If INOP persists, contact your service personnel. Silencing this INOP switches the measurement off.
BIS Unsupported sensor connected or sensor type unknown or not
supported by your software revision. Replace the sensor, using only Philips supported sensors.
63
5 Patient Alarms and INOPs Technical Alarm Messages (INOPs)
INOP Message, Indication Source What to do
BIS SENSOR MALFUNC
INOP tone
BIS SENSOR USAGE
INOP tone
BIS SQI < 15% (INOP tone)
OR
BIS SQI < 50% (no INOP tone)
BIS UNPLUGGED
INOP tone
BISx DISCONNECTED
INOP tone
BISx INCOMPATIBLE
INOP tone
BISx MALFUNCTION
INOP tone
CANNOT ANALYZE ECG ECG/
CANNOT ANALYZE QT QT The QT algorithm cannot generate a valid QT value for more
CANNOT ANALYZE ST ST The ST algorithm cannot generate a valid ST value. Possible
BIS Malfunction in the sensor hardware, most often caused by
liquids permeating into the connectors OR patient interface cable (PIC) or DSC or BISx may be faulty. Replace the sensor. Manually initiate a Cyclic Impedance Check. Make sure all electrodes pass the test. Make sure that the both sides of the PIC connector (between PIC and sensor) are dry. If you are not sure that the connector is dry, replace the PIC until it has dried. If this INOP persists, contact your service personnel.
BIS Excessive sensor usage. Replace sensor.
A Cyclic Impedance Check will start automatically.
BIS If the signal quality is below 50%, BIS numerics cannot be
reliably derived. If the signal quality is below 15%, no BIS numerics can be derived. This may occur as a result of artifacts such as those generated from motion or the presence of electrocautery devices. Make sure the sensor is properly attached to the patient. Manually initiate a Cyclic Impedance Check. Make sure all electrodes pass the test. Make sure the patient is completely relaxed (even small motions of the facial muscles affect the signal quality).
BIS Plug in the BIS module. Silencing this INOP switches off the
measurement.
BIS The BISx is not connected to the BIS module or the BIS
interface board. Silencing this INOP switches the measurement off.
BIS The BISx software is not compatible with the BIS module or
with the MP20/MP30 monitor software. A software upgrade may be required. Contact your service personnel.
BIS The BISx is faulty. Disconnect and reconnect it to the module
or BIS interface board. If the INOP persists, replace the BISx. MP20/MP30 - Malfunction on interface board. If the INOP persists, contact your service personnel.
The arrhythmia algorithm cannot reliably analyze the ECG
Arrhythmia
data. Check the ECG signal quality of the selected primary and secondary leads. If necessary, improve lead position or reduce patient motion. If you have arrhythmia analysis on, and you are not getting a reliable HR because the signal is below a minimum amplitude, unstable, or contains artifact, and you have tried to improve the system performance by choosing another lead and changing electrodes, you should consider turning arrhythmia analysis off.
than 10 minutes, or 1 minute in the initial phase.
causes are large variations in the measured ST values for consecutive beats, or ventricular paced beats. Review the ECG signal quality and the ST measurement points. If the patient has a ventricular pacemaker, ST analysis is not possible.
64
Technical Alarm Messages (INOPs) 5 Patient Alarms and INOPs
INOP Message, Indication Source What to do
CCI NO BSA
CCI numeric unavailable INOP tone
CCO BAD PRESS SIGN
numeric is replaced by -?­INOP tone
CCO NO <Pressure label>
numeric is replaced by -?­INOP tone may sound
CCO NO CALIBRATION
numeric is replaced by -?-
CCO NO PRESS
at Information Center
CCO NOT SUPPORTED
numeric is replaced by -?­INOP tone
CCO/CCI OVERRANGE
numeric is replaced by -?­INOP tone
CCO <Pressure label> INVALID
numeric is replaced by -?­INOP tone may sound
CCO PRESS INVALID
at Information Center
CCO PRESS OVERRANG
numeric is replaced by -?­INOP tone
CCO PULSE OVERRANG
numeric is replaced by -?­INOP tone
CCO/Tbl NO TRANSD
Numeric is replaced by -?­INOP tone
CCO RECALIBRATE
numeric is replaced by -?-
C.O. CCI cannot be calculated because the patient's body surface
area is unknown. Enter the patient weight and height to provide the BSA for CCI calculation.
C.O. The arterial pressure wave can currently not be used for pulse
contour calculation for CCO or CCI measurement. Possible causes are air bubbles in the tubing or a physiological condition, for example severe arrhythmia.
C.O. CCO/CCI cannot be calculated. Make sure that the pressure
chosen in the Setup CCO menu under CCO From matches the pressure measured with the arterial catheter for CCO measurement. A pressure from an external device cannot be used. Select another pressure label, either ABP, Ao, ART, B AP, FA P, o r U A P.
C.O. The CCO measurement is currently not calibrated.
C.O. CCO/CCI cannot be calculated. Make sure that the pressure
chosen in the Setup CCO menu under CCO From matches the pressure measured with the arterial catheter for CCO measurement. A pressure from an external device cannot be used. Select another pressure label, either ABP, Ao, ART, B AP, FA P, o r U A P.
C.O. A catheter for transpulmonary C.O. measurements has been
unplugged and replaced with a Right Heart C.O. catheter, or the measurement mode has been changed manually. Silencing this INOP switches the measurement off.
C.O. The measured CCO or CCI value is not within the specified
range for CCO/CCI measurement.
C.O. The arterial pressure selected for pulse contour calculation for
CCO is available but currently invalid. Make sure the pressure transducer is connected and the zero calibration is valid.
C.O. The arterial pressure selected for pulse contour calculation for
CCO is available but currently invalid. Make sure the pressure transducer is connected and the zero calibration is valid.
C.O. The mean value of the arterial pressure values used for pulse
contour calculation for CCO is below 0 mmHg or above 300 mmHg.
C.O. The pulse rate of the pressure used for pulse contour
calculation for CCO is below 30 bpm or above 240 bpm.
C.O. No transducer attached to the module or catheter
disconnected.
C.O. The most recent CCO or CCI calibration was made over 8
hours ago or the arterial pressure measurement used for CCO calculation has been zeroed after the CCO calibration was performed. You should recalibrate CCO or CCI with transpulmonary C.O. measurements at least every 8 hours or when the hemodynamic condition of the patient has changed. The pressure measurement must be zeroed before a CCO calibration.
65
5 Patient Alarms and INOPs Technical Alarm Messages (INOPs)
INOP Message, Indication Source What to do
CENTRAL:TELE ONLY
INOP tone
Charge BATT1/BATT2 now
INOP tone
CHARGER MALFUNC
INOP tone, battery LED may flash
Check Alarm Lamps
INOP tone.
CHECK BATT TEMP
INOP tone
Check DrugSettings
INOP tone
Check ECG Settings
INOP tone
!!CHECK ECG SOURCE
INOP tone
Check Flex Texts
INOP tone
CheckInternVoltage
at Information Center
Check Keyboard
INOP tone
Check Main Board 2
INOP tone.
Check Monitor Func
INOP tone.
Check Monitor Temp
INOP tone
Check Mouse Device
INOP tone.
Check MSL Voltage
INOP tone
Monitor System connectivity via telemetry device is limited (No alarms,
only local numerics) when in companion mode and host monitor does not have system connectivity. Only telemetry device parameters can be displayed at central station.
Batteries Battery must be charged. Connect the monitor to mains power
or exchange the battery.
Batteries There is a problem with the battery charger in the monitor.
Connect the monitor to mains power and contact your service personnel.
Monitor Perform a visual check of the alarm lamp to establish whether
there is a problem. Contact your service personnel to check the internal connections to the alarm lamps.
Battery The temperature of one or both batteries is too high. Check
that ventilation openings (if applicable) are not blocked and monitor is not exposed to heat.
Monitor There was a problem loading the drug settings. Check that the
settings are complete and correct.
Telemetry Synchronization of ECG settings between the monitor and
Information Center has failed. Check that the ECG settings in use are appropriate.
Monitor The telemetry device and the monitor both have valid ECG
signals. Unpair the telemetry device and the monitor if they are no longer used for the same patient.
Monitor Check the names of the monitor menus, for example the labels
for screens, profiles, event or trend group names, before you resume monitoring. If they are unexpected, there may be a problem with the monitor software. Contact your service personnel.
Monitor Potential problem with alarm lamps, display or interfaces
detected. Contact your service personnel. This INOP will appear on the monitor as Check Monitor Func.
Monitor Perform a visual and functional check of the keyboard. Contact
your service personnel.
Monitor There is a problem with the second main board in the monitor.
Contact your service personnel.
Monitor Potential problem with alarm lamps, display or interfaces
detected. Contact your service personnel. This INOP may appear on the Information Center as
CheckInternVoltage.
Monitor The temperature inside the monitor is too high. Check that the
monitor ventilation is not obstructed. If the situation continues, contact your service personnel.
Monitor Perform a visual and functional check of the mouse input
device. Contact your service personnel.
Monitor/ Multi­Measuremt Module
There is a problem with the voltage of the Measurement Link (MSL). Contact your service personnel.
66
Technical Alarm Messages (INOPs) 5 Patient Alarms and INOPs
INOP Message, Indication Source What to do
Check Network Conf
INOP tone
Check Nurse Relay
INOP tone
!!Check Pairing
INOP tone
Check Screen Res
INOP tone
Monitor The monitor is receiving network topology information from
more than one source, e.g. the Database Server and an Application Server. Contact your service personnel.
Monitor There is a problem with the connection to the nurse relay.
Contact your service personnel.
Monitor There is a problem with device pairing. Check that the monitor
and telemetry device are correctly paired.
Monitor The Screen you have selected uses a resolution which is not
supported by the display. The monitor will show a generic Screen instead until you select a different Screen.
Contact your service personnel if you want the Screen deleted from the Profile(s) to avoid this in future.
Check Settings
INOP tone
Monitor If this INOP appears, check the monitor and patient settings
before you resume monitoring. If the settings are unexpected, there may be a problem with the monitor software. Contact your service personnel.
Check SpeedPoint
INOP tone.
Check Touch Input
INOP tone
Check Waves
INOP tone
Monitor Perform a visual and functional check of the SpeedPoint input
device. Contact your service personnel.
Monitor Perform a visual and functional check of the touch input
device. Contact your service personnel.
Monitor The options purchased with this monitor may not support the
number of waves required to show the selected Screen, so some waves or high resolution trends are missing from the Screen. Select a different Screen with fewer waves.
Contact your service personnel if you want the Screen deleted from the Profile(s) to avoid this in future.
CHK ECG Sync Cable
INOP tone
Monitor The ECG Sync is detecting an invalid signal, or the ECG Sync
cable is disconnected.
Chk IndepDsp Cable Monitor The monitor cannot communicate with the D80 Intelligent
Display. Check the MSL coupling cable. The end with the grey connector must be connected to the Intelligent Display.
CHK MSL Connection
INOP tone
Chk SpO2T Settings
INOP tone
Monitor Check that the MSL connector or cable are properly
connected. Check the cable and connector for damage.
Telemetry Synchronization of SpO2T settings between the monitor and
Information Center has failed. Check that the SpO
T settings
2
in use are appropriate.
C LEAD OFF
HR Numeric is replaced by -?- for 10 seconds. INOP tone.
ECG The C electrode (AAMI: V electrode) has become detached
from the patient or the lead set has been changed. Reattach the electrode or select
New Lead Setup in the Setup ECG
menu to confirm the new lead set.
CO2 AUTO ZERO
Numeric is replaced by a -?­if the Autozero lasts >15 sec, INOP tone sounds.
CO2 CAL MODE
CO
numeric displays current CO2
2
value for accuracy check
CO2 CAL RUNNING
CO
CO
CO
2
The automatic zero calibration is in progress. This typically takes 10 seconds. During this time the CO
values may not be
2
updated, or they may be replaced by -?-. Wait until the zero calibration is complete to resume monitoring.
2
Currently no calibration is running. Accuracy can be checked by placing the transducer on the two cells of the calstick and starting calibration. To start monitoring, leave Cal. Mode.
2
Wait until calibration is finished.
Numeric is replaced by a -?-
67
5 Patient Alarms and INOPs Technical Alarm Messages (INOPs)
INOP Message, Indication Source What to do
CO2 CHANGE SCALE CO
CO2 CHK ADAPTER
CO Numeric is replaced by a -?­INOP tone.
CO2 CHECK CAL
CO Numeric is replaced by a -?­INOP tone.
CO2 DEACTIVATED
CO INOP tone.
C.O. DEACTIVATED
C.O. The Cardiac Output measurement label in the measurement INOP tone.
C.O. EQUIP MALF
C.O. There is a problem with the C.O. hardware. Contact your Numeric is replaced by a -?­INOP tone.
CO2 EQUIP MALF
CO Numeric is replaced by -?­INOP tone.
CO2 FAILED CAL
CO Numeric is replaced by -?­INOP tone.
CO2 NO SENSOR
CO Numeric is replaced by -?­INOP tone.
CO2 NO TRANSDUC
CO Numeric is replaced by -?­INOP tone.
CO2 NO TUBING
CO Numeric is replaced by -?­INOP tone.
(!!/!!!)CO2 OCCLUSION
CO Numeric is replaced by a -?­INOP tone.
CO2 OVERRANGE
CO Numeric is replaced by -?­INOP tone.
CO2 PUMP OFF
CO Numeric is replaced by a -?-.
2
The CO2 wave is clipped. Select a more appropriate wave scale to display the whole wave.
2
Check that the sensor is connected to the airway adapter, clean the airway adapter, if necessary. Perform a zero calibration. If the INOP persists, contact your service personnel.
2
The CO2 value is outside the measurement range. Perform an accuracy check for both calstick cells and, if necessary, recalibrate the transducer.
2
The CO2 measurement label in the measurement device has been deactivated by deactivating the label in the Measurement Selection window. The measurement automatically disappears from the display. To switch the measurement on again, reactivate the measurement label in the Measurement Selection window.
device has been deactivated by deactivating the label in the Measurement Selection window. The measurement automatically disappears from the display. To switch the measurement on again, reactivate the measurement label in the Measurement Selection window.
service personnel.
2
The Measurement Extension is faulty. Unplug and replug the Multi-Measurement Module with Extension. If you are using the mainstream method, unplug and replug the transducer or try another transducer. If the INOP persists, contact your service personnel.
2
Make sure that the Cal cell was changed between CAL1 and CAL2. Repeat the calibration. If the INOP reappears, try another transducer. If the INOP persists, contact your service personnel.
2
2
There is no CO2 sensor connected. If you silence this INOP
measurement will be switched off.
the CO
2
There is no CO2 transducer connected. If you replace the transducer, the new transducer must be calibrated. If you silence this INOP the CO
2
Either the sample line is disconnected, or an incorrect line is
measurement will be switched off.
2
attached. Check the connection. If necessary, connect another sample line (Use only the approved accessories). If you silence this INOP, the measurement will be switched off.
2
The sample line or exhaust tube is blocked. Check the tubing, then disconnect and reconnect the sample line. If the INOP persists, connect a new sample line.
2
The CO2 value is higher than the measurement range. If you suspect a false high value, contact your service personnel.
2
The pump has been switched off for fifteen minutes. To switch it on again, select Pump On in the Setup CO
menu.
2
68
Technical Alarm Messages (INOPs) 5 Patient Alarms and INOPs
INOP Message, Indication Source What to do
CO2 PURGING
Numeric is replaced by a -?­INOP tone.
CO
2
The Filterline is being purged to remove an occlusion in the line or airway adapter. If the occlusion is removed, the INOP will disappear. If not, the INOP
CO2 OCCLUSION is
displayed.
CO2 SENS. WARMUP
Numeric is displayed with a -?­Microstream CO
: INOP tone.
2
CO
2
Wait until the sensor reaches operating temperature and the INOP disappears.
Mainstream CO2: no INOP tone
C.O. UNPLUGGED
numeric is replaced by -?-
C.O. Plug in the C.O. module. Silencing this INOP switches off the
measurement.
INOP tone.
CO2 UPDATE FW
Numeric is replaced by a -?-
CO
2
The software in the Measurement Extension does not match the software in the MMS. Contact your service personnel.
INOP tone.
CO2 WAIT CAL2
Numeric is replaced by a -?-
CO
2
Calibration on the first calstick cell is complete. Place the transducer on the other calstick cell and start the CAL2 calibration cycle.
CO2 ZERO FAILED
Numeric is replaced by a -?­INOP tone.
CO
2
An error occurred during the last zero calibration. Check the airway adapter and clean, if necessary. Perform another zero calibration. If the INOP persists, contact your service personnel.
CO2 ZERO REQU’D
Numeric is replaced by a -?-
CO
2
Perform zero calibration for the CO2 sensor. If the INOP persists, contact your service personnel.
INOP tone
CO2 ZERO RUNNING CO
CPP CHK SOURCES
CPP Not all measurements or values required to perform the Numeric is replaced by a -?-
CPP CHK UNITS
CPP The monitor has detected a conflict in the units used for this Numeric is replaced by a -?-
!!/!!!CUFF NOT DEFLAT
NBP Remove the cuff from the patient. Make sure that the tubing is
Numeric is displayed with a -?­Severe yellow/red INOP tone.
During this INOP, alarms cannot be paused or switched off.
2
Wait until zero calibration is finished.
calculation are available. Check the measurement sources.
calculation. Check the unit settings.
not kinked or twisted and that the correct patient category is selected. Try repeating the measurement. You can silence the INOP, but the INOP message remains visible until the next NBP measurement is started or the
Stop All SmartKey is selected.
[Adult or pediatric patients: The NBP cuff pressure has exceeded 15mmHg (2kPa) for more than 3 minutes. Neonatal patients: The NBP cuff pressure has exceeded 5mmHg (0.7kPa) for more than 90 seconds.]
!!/!!!CUFF OVERPRESS
Numeric displayed with -?- ;
Severe yellow/red INOP tone.
During this INOP, alarms cannot be paused or switched off.
NBP The NBP cuff pressure exceeds the overpressure safety limits.
Remove the cuff from the patient. Make sure that the tubing is not kinked or twisted and that the correct patient category is selected. Try restarting the measurement. You can silence this INOP, but the INOP message remains visible until the next measurement is started or the
All
SmartKey is selected.
CVP INOPS PRESS See <Pressure label> INOPS (under Pressure).
DEVICE CHECK SETUP
INOP tone.
IntelliBridge Device identification completed, but communication could
not be established due to timeout.
IntelliBridge INOP abbreviations may differ slightly depending on the device category.
Stop
69
5 Patient Alarms and INOPs Technical Alarm Messages (INOPs)
INOP Message, Indication Source What to do
DEVICE CHECK CONF.
INOP tone.
DEVICE DEMO DATA
INOP tone
DEVICE REAL DATA
INOP tone
<Device> UNPLUGGED
INOP tone.
DEVICE UNSUPPORTED
INOP tone.
<EC10/EC40> EQUIP MALF
INOP tone.
ECG/ARRH ALARM OFF
!!ECG/AR ALARM OFF
ECG EQUIP MALF
Numeric is displayed with a -?­INOP tone.
ECG EQUIP MALF T
Numeric is displayed with a -?­INOP tone.
(!!/!!!)<ECG LEAD> LEAD OFF
Numeric is displayed with a -?­INOP tone.
ECG EL. NOISY <ECG LEAD> ECG The ECG signal from the named ECG electrodes [RA, LA, LL,
(!!/!!!)ECG LEADS OFF ECG Check that all of the required ECG leads are attached, and that
IntelliBridge Device identification completed, but communication could
not be established due to error.
IntelliBridge INOP abbreviations may differ slightly depending on the device category.
IntelliBridge The device connected to the IntelliBridge module reports demo
data but the monitor is not in DEMO mode.
IntelliBridge The monitor is in DEMO mode but the device connected to
the IntelliBridge module reports data that are not flagged as demo data.
IntelliBridge The IntelliBridge module has been unplugged from the rack, or
the whole rack has been disconnected. Silencing this INOP switches off the measurement.
IntelliBridge INOP abbreviations may differ slightly depending on the device category.
IntelliBridge Device identification completed, but no appropriate device
driver installed.
IntelliBridge INOP abbreviations may differ slightly depending on the device category.
IntelliBridge Malfunction in the IntelliBridge module. If this message
appears repeatedly, the module must be replaced. Contact your service personnel.
ECG All ECG alarms have been switched off, or the HR alarm
source is not ECG. To resume ECG alarm generation, switch ECG alarms on or select ECG as the alarm source.
ECG Contact your service personnel.
The ECG hardware is faulty.
Monitor Contact your service personnel.
The ECG in the Telemetry device is faulty.
ECG Not all the required leads for ECG monitoring are connected.
Check the ECG connections and make sure that the electrode indicated by <ECG lead> [RA, LA, LL, RL, V or C] electrodes is attached. In EASI mode, all 5 electrodes must be connected.
RL, V (or C)] is noisy. Check the ECG connections and make sure that the electrode indicated is attached.
none of the electrodes have been displaced.
70
ECG NOISY SIGNAL
INOP tone.
EcgOut EQUIP MALF
INOP tone
EEG EQUIP MALF
INOP tone
ECG The ECG signal is too noisy. Check that the electrodes are
properly placed and have not dried out. Remove any possible sources of signal noise (such as power cords) from the area around the cable and the patient. The ECG signal may be saturated or overloaded.
ECG Check that the ECG out cable is securely connected. Contact
your service personnel.
EEG The EEG hardware is faulty. Contact your service personnel.
Technical Alarm Messages (INOPs) 5 Patient Alarms and INOPs
INOP Message, Indication Source What to do
EEG IMPEDANCE HIGH or EEG1 and/or EEG2 IMPED. HIGH
EEG<X> LEAD OFF <n>
[X = channel, n = electrode]
EEG<X> LEAD OFF
[X = channel] at Information Center
EEG<X> LEADS OFF
[X = channel]
EEG LINE NOISE
EEG 1 or 2 LINE NOISE
EEG MUSCLE NOISE
EEG 1 or 2 MUSCLE NOISE
EEG NO TRANSDUCER
INOP tone
EEG UNPLUGGED
INOP tone
EEG OVERRANGE, or
EEG<X> OVERRANGE
FAP INOPS PRESS See <Pressure label> INOPS (under Pressure).
FMS UNPLUGGED
INOP tone.
FMS UNSUPPORTED
INOP tone.
IC1/IC2 INOPS PRESS See <Pressure label> INOPS (under Pressure).
ICP INOPs PRESS See <Pressure label> INOPS (under Pressure).
Indep.Dsp Malfunc. Display A problem has occurred with the second main display. Contact
Indep.Dsp NotSupp. Display The monitor does not support a second main display. The
!!INSERT BATTERY
Severe yellow INOP tone.
During this INOP, alarms cannot be paused or switched off.
Intell.Dsp Malf.
INOP tone
EEG The signal electrode in one or both channels exceeds the user-
selected impedance limit, or the impedance of a single electrode exceeds the limit. Check the impedance. If the impedance is too high, reconnect the electrodes according to the EEG monitoring setup guidelines. If the INOP persists, contact your service personnel.
EEG Reconnect specified electrode.
EEG One or more electrodes are not connected. Check in the EEG
Impedance/Montage
electrode(s) are affected and reconnect the electrodes.
EEG Two or more electrodes are not connected. Check in the EEG
Impedance/Montage
affected and reconnect the electrodes.
EEG Excessive line noise has been detected in either channel EEG1
or EEG2, or in both EEG channels. Keep all cables together and away from metallic bodies, other cables & radiated fields.
EEG Too much power above 30 Hz has been detected in channel
EEG1 or EEG2, or both. Check the Electrode-to-Skin Impedance and reposition the electrode away from possible muscle activity, if necessary.
EEG The trunk cable is disconnected from the EEG plug-in module.
Reconnect the trunk cable. Silencing this INOP switches the measurement off.
EEG Plug in module. Silencing this INOP switches off the
measurement.
EEG Input signal is too high in one or both channels. This is usually
caused by interfering signals such as line noise or electro­surgery. X denotes the EEG channel.
FMS Make sure that the Flexible Module Rack is connected to the
monitor. All FMS measurements are off while the FMS is unplugged.
FMS The Flexible Module Rack is not supported by your monitor.
Contact your service personnel.
your service personnel.
monitor software is incompatible. Contact your service personnel.
Battery X2/MP2 only: There is no battery in the battery compartment.
You cannot operate the monitor on AC mains while the battery compartment is open (not sealed with a battery). Load a battery immediately.
Display There is a problem with the Intelligent Display. Check the
MSL coupling cable then contact your service personnel.
window on the monitor which
window which electrodes are
71
5 Patient Alarms and INOPs Technical Alarm Messages (INOPs)
INOP Message, Indication Source What to do
Intell.Dsp Missing Display The monitor has lost contact with the connected Intelligent
Display. Contact your service personnel.
Intell.Dsp Unsupp. Display The monitor does not support the connected Intelligent
Display. The monitor software is incompatible.
Internal.Comm.Malf
INOP tone
INVALID LEADSET Telemetry
LA LEAD OFF
Numeric is replaced by -?- for 10 seconds; INOP tone.
LAP INOPs PRESS See <Pressure label> INOPS (under Pressure).
LEADSET UNPLUGGED Telemetry The leadset has been unplugged from the telemetry device.
LL LEAD OFF
Numeric is replaced by -?- for 10 seconds; INOP tone.
MCC Reversed
INOP tone
MCC Unsupported
INOP tone
Meas. DEACTIVATED An X2 or MP5 has been connected to a host monitor
MEASSRV UNSUPPORTD
INOP tone
MMS Ext. EQUIP MALF
INOP tone
MMS Ext. UNPLUGGED
INOP tone
MMS Ext. Unpowered
INOP tone
MMSExt.Unsupported
INOP tone
MMS UNPLUGGED INOP tone.
MMS UNSUPPORTED INOP tone.
!!/!!!MORE BED ALARMS
At Information Center
Monitor There is a problem with I2C Bus communication in the
monitor. Contact your service personnel.
ECG The LA electrode has become detached from the patient or the
lead set has been changed. Reattach the electrode or select New
Lead Setup
new lead set.
ECG The LL electrode has become detached from the patient or the
lead set has been changed. Reattach the electrode or select New
Lead Setup
new lead set.
Monitor The MSL coupling cable is reversed. Connect the end with the
grey connector to the Intelligent Display.
Monitor An MSL coupling cable has been connected to a device which
does not support MSL coupling.
(companion mode) and all derived measurements have been deactivated and/or measurements with a label conflict. The measurements can only be reactivated by disconnecting the measurement device from the host monitor.
MMS The Multi-Measurement module is not supported by the
monitor. Contact your service personnel.
MMS
Extension
MMS
Extension
MMS
Extension
MMS
Extension
MMS Make sure that the Multi-Measurement Module is connected
MMS The Multi-measurement Module is not supported by your
Monitor The monitor is associated with a telemetry device and is
Loss of communication between the Multi-Measurement Module and the MMS extension. Contact your service personnel.
The MMS extension has been disconnected from the Multi­Measurement Module.
The MMS extension cannot operate while the Multi­Measurement Module is running on battery power.
The MMS extensions not supported by your monitor. Contact your service personnel.
to the monitor. All MMS measurements are off while the MMS is unplugged.
monitor. Contact your service personnel.
sending data to the Information Center via the telemetry device. There are currently more alarms at the bedside than can be transmitted to the Information Center.
in the Setup ECG menu to confirm the
in the Setup ECG menu to confirm the
72
Technical Alarm Messages (INOPs) 5 Patient Alarms and INOPs
INOP Message, Indication Source What to do
MSL Power High Monitor The power consumption of the devices connected to the
Measurement Link (MSL) cable is too high. If this situation continues, the MSL will be switched off. Contact your service personnel.
MSL Power Off
INOP tone.
MSL Power Overload
INOP tone.
NBP Deactivated
INOP tone.
NBP EQUIP MALF
Numeric is replaced by -?­INOP tone.
NBP INTERRUPTED
Numeric is replaced by -?­INOP tone.
NBP MEASURE FAILED
Numeric may be displayed with a -?­INOP tone.
No Central Monit.
INOP tone
!!/!!! NO DEVICE DATA
NO DEVICE DATA
NO ECG AT CENTRAL Monitor The ECG measured with the monitor ECG is not being sent to
NO ECG SOURCE Telemetry A telemetry device is paired with the monitor but the
Monitor The power consumption of the devices connected to the
Measurement Link (MSL) cable was too high for too long and the MSL has been switched off. Contact your service personnel.
Monitor The power consumption of the devices connected to the
Measurement Link (MSL) cable is much too high or there has been a short circuit. The MSL has been switched off. Contact your service personnel.
NBP The NBP measurement label in the measurement device has
been deactivated by deactivating the label in the Measurement Selection window. The measurement automatically disappears from the display. To switch the measurement on again, reactivate the measurement label in the Measurement Selection window.
NBP Remove the cuff from the patient. The NBP hardware is faulty.
Contact your service personnel. You can silence this INOP, but the INOP message remains visible until the next measurement is started or the
All
SmartKey is selected.
NBP Check the tubing and cuff for leakages or kinks. Check that
you are using the correct cuff size and placement, and that the correct patient category is selected. Try restarting the measurement. If the INOP occurs repeatedly, contact your service personnel. You can silence this INOP, but the INOP message remains visible until the next measurement is started or the
All
SmartKey is selected. This INOP arises when the measurement needed longer than the maximum time for inflation, deflation or the total measurement.
NBP Check that you are using the correct cuff size and placement,
and that the correct patient category is selected. Try restarting the measurement. You can silence this INOP, but the INOP message remains visible until the next measurement is started or the
All
SmartKey is selected. Check the condition and suitability of the patient for NBP monitoring. Use another cuff to continue measuring.
Monitor There is a problem with the communication to the network.
Central monitoring is currently not possible (no patient alarms or information). Check the connection. Contact your service personnel.
IntelliBridge Communication with connected device has been lost.
the Information Center via the telemetry device.
Information Center is not detecting a valid ECG signal from either of them.
Stop
Stop
Stop
73
5 Patient Alarms and INOPs Technical Alarm Messages (INOPs)
INOP Message, Indication Source What to do
NO PPV FROM MeasSrv
at Information Center
NO PPV FROM <Device> MMS or
OUT OF AREA Telemetry The telemetry device has left the access point coverage area.
P/P1/P2/P3/P4 INOPS PRESS See <Pressure label> INOPS (under Pressure).
PAP INOPS PRESS See <Pressure label> INOPS (under Pressure).
PPV BAD <Pressure Label> SIGNAL
PPV BAD SIGNAL
at Information Center
PPV CHK SOURCES PPV The arterial pressure source selected for PPV is unplugged or
<Pressure label> ARTIFACT
Numeric questionable
<Pressure label> DEACTIVATED
INOP tone
<Pressure label> EQUIP MALF
Numeric is replaced by -?­INOP tone.
<Pressure label> NO TRANSDUCER
Numeric is replaced by -?­INOP tone.
<Pressure label> NOISY SIGNAL
Pulse numeric is replaced by -?­INOP tone.
<Pressure label> NON­PULSATILE
Pulse numeric is replaced by -?­INOP tone.
<Pressure label> OVERRANGE
Numeric is replaced by -?­INOP tone.
<Pressure label> REDUCE SIZE
MMS or FMS
FMS
PPV The arterial pressure source selected for PPV is not providing a
PPV The arterial pressure source selected for PPV is not providing a
PRESS A non-physiological event is detected (for example, a flush or
PRESS A Pressure measurement label in the measurement device or
PRESS Contact your service personnel.
PRESS Make sure that the pressure transducer is connected to the
PRESS This INOP can only arise when a pressure is selected as the
PRESS This INOP can only arise when a pressure is selected as the
PRESS Make sure that the measurement has been properly prepared
PRESS Increase the scale for the pressure wave.
The measurement device does not supply a beat-to-beat arterial pressure value. Contact your service personnel.
The measurement device does not supply a beat-to-beat arterial pressure value. Contact your service personnel.
pulsatile signal.
pulsatile signal.
switched off. When this INOP has displayed for 1 minute PPV will be switched off.
blood sample). A resulting high limit alarm will be suppressed.
extension has been deactivated, either by connecting a Temp transducer in the shared Press/Temp socket, or by deactivating the label in the Measurement Selection window.
The measurement automatically disappears from the display.
To switch the measurement on again, either reconnect a Pressure transducer or reactivate the measurement label in the Measurement Selection window.
The pressure hardware is faulty.
measurement device or module. If you silence this INOP, the measurement will be switched off.
pulse source. It occurs when the pulse detector finds a pulse rate above 350bpm. This is usually caused by movement artifact or electrical interference.
pulse source. It occurs when the pulse rate being measured is less than 25 beats per minute or the amplitude is less than three mmHg. Check the catheter and connections to the patient.
and zeroed, and that the transducer is level with the heart. If this INOP persists, try another transducer. Possible causes are a measured pressure outside the allowed pressure range, or a broken wire to the transducer.
74
Technical Alarm Messages (INOPs) 5 Patient Alarms and INOPs
INOP Message, Indication Source What to do
<Pressure label> UNPLUGGED
INOP tone.
<Pressure label> ZERO+CHECK CAL
Numeric is replaced by -?-
<pTemp label> CHECK PROBE
Numeric is replaced by -?­INOP tone.
<pTemp label> DEACTIVATED
INOP tone.
<pTemp label> EQUIP MALF
Numeric is replaced by -?­INOP tone.
<pTemp label> INCOMPAT. Predictive
<pTemp label> MEAS FAILED
Numeric is replaced by -?­INOP tone.
<pTemp label> NO PROBE
Numeric is replaced by -?­INOP tone.
<pTemp label> OVERRANGE
Numeric is replaced by -?­INOP tone.
<pTemp label> PROBE MALF
Numeric is replaced by -?­INOP tone.
pTaxil INOPS Predictive
pToral INOPS Predictive
pTrect INOPS Predictive
(!!)PW:Action Required Protocol
PW:Check Settings Protocol
PW in conflict Protocol
PRESS A Pressure measurement label has been deactivated, either by
PRESS Perform a zero and check the calibration of the transducer.
Predictive Te m p
Predictive Te m p
Predictive Te m p
Te m p
Predictive Te m p
Predictive Te m p
Predictive Te m p
Predictive Te m p
Te m p
Te m p
Te m p
Watc h
Watc h
Watc h
unplugging a module, or by deactivating the label in the Measurement Selection window.
The measurement automatically disappears from the display.
To switch the measurement on again, either replug the module or reactivate the measurement label in the Measurement Selection window.
Check that the probe holder is correctly installed and that a compatible probe is in use. If the INOP does not clear, remove the probe from the holder then replace it. If the INOP still does not clear, disconnect and reconnect the probe.
The Predictive temperature has been deactivated.
The Predictive Temperature hardware is defective. Contact your service personnel.
The Predictive Temperature version is not supported by the monitor.
The ambient temperature is outside the specified range (10 to 40°C /50 to 104°F). Bring the temperature into range to continue monitoring. If the INOP does not clear, disconnect and reconnect the probe.
Connect a probe to the Predictive temperature unit.
The temperature at the measurement site is out of range. Check that the probe is correctly located. If the INOP does not clear, disconnect and reconnect the probe.
The connected probe may be defective. Disconnect and reconnect the probe. If the INOP does not clear, try another probe.
See <pTemp label> INOPS
See <pTemp label> INOPS
See <pTemp label> INOPS
The protocol currently running requires a user response. Check which pop-up window is displayed and provide the appropriate response.
Contact your service personnel. Settings could not be loaded or interpreted correctly
There is a patient information mismatch which has not yet been resolved (>15 minutes).
75
5 Patient Alarms and INOPs Technical Alarm Messages (INOPs)
INOP Message, Indication Source What to do
RA LEAD OFF
Numeric is replaced by -?­INOP tone.
ECG The RA electrode has become detached from the patient or the
lead set has been changed. Reattach the electrode or select
Lead Setup
in the Setup ECG menu to confirm the
new lead set.
RAP INOPS PRESS See <Pressure label> INOPS (under Pressure).
Rem.Alarmdev.Malf
INOP tone
Rem. Display Malf. Remote
Monitor There is a problem with the connection to the remote alert
device. Contact your service personnel to check the remote alert device and its connections.
There is a problem with an input device at the remote display.
display
Perform a visual and functional check of all input devices. Contact your service personnel.
!!/!!! REPLACE BATTERY T
Severe yellow/red INOP tone.
Telemetry The battery in the telemetry device is almost empty and must
be replaced.
During this INOP, alarms cannot be paused or switched off.
RESP EQUIP MALF
RESP Contact your service personnel. The RESP hardware is faulty. Numeric is replaced by -?­INOP tone.
RESP ERRATIC
Numeric is replaced by -?-
RESP The monitor has detected too many artifacts in the measured
Resp signal. Check that the RA and LL electrodes are correctly attached and have not dried out.
RESP LEADS OFF
Numeric is replaced by -?-
RESP Not all the required leads for Resp monitoring are attached.
Make sure that the RA and LL leads are attached.
INOP tone.
RL LEAD OFF
Numeric is replaced by -?- for 10 seconds; INOP tone.
ECG The RL electrode has become detached from the patient or the
lead set has been changed. Reattach the electrode or select New
Lead Setup
in the Setup ECG menu to confirm the
new lead set.
Settings Malfunc.
INOP tone.
<SO2 Label> CAL FAILED
Numeric is replaced by -?­INOP tone.
<SO2 Label> CAL MODE
Numeric is replaced by -?­INOP tone.
<SO2 Label>CAL REQUIRED
Numeric is replaced by -?-
Monitor The monitor cannot use the predefined settings for
monitoring. Contact your service personnel.
SO
2
The calibration failed. Check the catheter-to-Optical-Module connection. Manually restart the calibration. Try another catheter and Optical Module. If the catheter is already inserted, perform an in-vivo calibration.
SO
2
Pre-insertion calibration is complete, but the catheter tip is still inside the optical reference. The catheter is now ready for insertion.
SO
2
There is no valid calibration data in the Optical Module. Perform either a pre-insertion or an in-vivo calibration.
INOP tone.
<SO2 Label> CANNOT MEAS
Numeric is replaced by -?­INOP tone.
<SO2 Label>CONFIG ERROR
Numeric is replaced by -?­INOP tone.
<SO2 Label> CONN OPTMOD
Numeric is replaced by -?-
SO
SO
SO
2
2
2
The signal is out of the normal range, and no oxygen saturation can be derived. Perform an in-vivo calibration. If the INOP persists, try another Optical Module and catheter.
The Optical Module has been configured to SaO2 Mode. Use Change to Venous in the setup menu to reconfigure to venous saturation mode.
The Optical Module was disconnected during data storage. Reconnect the Optical Module for at least 20 seconds.
INOP tone.
New
76
Technical Alarm Messages (INOPs) 5 Patient Alarms and INOPs
INOP Message, Indication Source What to do
<SO2 Label> EQUIP MALF
Numeric displays -?-. INOP tone
SO2 INCOMPATIBLE
INOP tone
<SO2 Label> IN-VIVO CAL SO
SO
SO
2
The SO2/SvO2 Module or Optical Module is faulty. Unplug and replug the Optical Module and SO
/SvO2 module.
2
Exchange the modules. If the INOP persists, contact your service personnel.
2
The SO2 Module or Optical Module is not supported. Contact your service personnel.
2
The in-vivo calibration is not yet complete. Lab values must be stored to the Optical Module to complete the calibration. Either continue with the next steps of the current calibration or recall the previous calibration.
<SO2 Label>LIGHT INTENS
Numeric is replaced by -?­INOP tone.
SO
2
The intensity changed considerably since the last light intensity calibration. This may indicate that the catheter tip is positioned against a blood vessel wall or that there is low blood flow. Reposition the catheter (and perform a Light Intensity Calibration).
<SO2 Label> LOW LIGHT
SO
Numeric is replaced by -?­INOP tone.
<SO2 Label> NO OPTMOD
SO
Numeric is replaced by -?­INOP tone.
<SO2 Label> OPTMOD MALF SO
2
2
2
The optical signal levels are too low. Check that the catheter is either in the optical reference or inserted into the patient. Check the catheter-to-Optical Module connection. If INOP persists, try another catheter and Optical Module.
Connect the Optical Module. If the INOP persists, try another Optical Module. Silencing this INOP switches the measurement off.
The Optical Module memory is faulty, and calibration data cannot be stored for transport or during power failure. If this capability is needed, use another Optical Module.
<SO2 Label> PRE-INS CAL
Numeric displays -?­INOP tone
<SO2 Label> UNPLUGGED
Numeric displays -?-. INOP tone
SO2 UPGRADE
INOP tone
<SO2 Label> WARMUP
Numeric is displayed with ?
SO
SO
SO
SO
2
The pre-insertion calibration is running. This typically takes one minute. During this time alarms are switched off. Wait until the calibration is complete.
2
Measurement switched on and SO2/SvO2 module unplugged from the rack.
2
The SO2 module is currently in upgrade mode.
Monitoring is not possible in this mode.
2
The Optical Module has not yet reached the operating temperature. Wait a few minutes until warm-up is finished.
SOME ECG ALRMS OFF Arrhythmia This message appears (if configured to do so) when the on/off
settings of the yellow arrhythmia alarms differ from the current Profile.
Speaker Malfunct.
INOP tone
Monitor Contact your service personnel to check the speaker and the
connection to the speaker.
SPIRO MALFUNCTION Spirometry Module failure detected. Contact your service personnel.
SPIRO INCOMPATIBLE Spirometry Module revision not compatible with the host monitor
software revision. Contact your service personnel.
SPIRO UPGRADE Spirometry The module is running a firmware upgrade. Wait until upgrade
is completed before resuming monitoring.
SPIRO CANNOT MEAS Spirometry Measurement is at its limit, e.g. ambient pressure out of range.
77
5 Patient Alarms and INOPs Technical Alarm Messages (INOPs)
INOP Message, Indication Source What to do
SPIRO PURGE FAILED Spirometry The purge operation could not be completed successfully.
Check for kinked sensor tubings, hard occlusions and make sure that the pump is running and all valves are switching.
SPIRO UNKN. SENSOR Spirometry An unknown sensor ID code was detected. Use only the sensors
listed in the Accessories chapter.
SPIRO ALARMS SUPPR Spirometry Alarming is suppressed for the spirometry module.
SPIRO PURGING Spirometry A purge operation is in progress - no data update on the screen.
Wait until purge is complete.
SPIRO NO SENSOR Spirometry No sensor detected. Make sure the correct sensor is attached to
the breathing circuit.
SPIRO NO BREATH Spirometry No breath was detected for more than 25 seconds. Breath
derived numerics are not available.
SPIRO GAS COMPENS? Spirometry Gas compensation is set to “gas analyzer” but not all gases
necessary for compensation are measured by a gas monitor. Some of the fall-back values provided by the user are used. Measurement accuracy might be reduced.
SPIRO PATIENT CAT. Spirometry Mismatch of patient size configured in the host monitor and
sensor type plugged into the module. Check the instructions on selecting the correct sensor in the Spirometry chapter.
SpO
CHK SOURCES
2
Numeric is replaced by -?-
SpO
CHK UNITS
2
Numeric is replaced by -?-
<SpO2 label> DEACTIVATED
INOP tone
<SpO2 label> EQUIP MALF
Numeric is replaced by -?­INOP tone.
<SpO2 label> ERRATIC
Numeric is replaced by -?­INOP tone.
<SpO2 label> EXTD. UPDATE
Label is displayed with a -?­(questionable numeric)
<SpO2 label> INTERFERNCE
Numeric is replaced by -?­INOP tone.
<SpO2 label> LOW PERF
Label is displayed with a -?­(questionable numeric)
<SpO2 label> NOISY SIGN.
Numeric is replaced by -?­INOP tone.
SpO
2
Difference
SpO
2
Difference
SpO
2
SpO
2
SpO
2
SpO
2
SpO
2
SpO
2
SpO
2
Not all measurements or values required to perform the calculation are available. Check measurement sources.
The monitor has detected a conflict in the units used for this calculation. Check the unit settings.
The SpO2 measurement label in the measurement device has been deactivated by deactivating the label in the Measurement Selection window. The measurement automatically disappears from the display. To switch the measurement on again, reactivate the measurement label in the Measurement Selection window.
The MMS or module is faulty. Unplug and replug the MMS or module. If the INOP persists, contact your service personnel.
Check the sensor placement. Try another adapter cable and sensor. If the INOP persists, contact your service personnel.
The update period of displayed values is extended due to an NBP measurement on the same limb or an excessively noisy signal.
There is too much interference, caused by a high level of ambient light and/or electrical interference. Cover the sensor to minimize ambient light. If the INOP persists, make sure that the sensor cable is not damaged or positioned too close to power cables.
Accuracy may be compromised due to very low perfusion. Stimulate circulation at sensor site. If INOP persists, change the measurement site.
Excessive patient movement or electrical interference is causing irregular pulse patterns. Try to reduce patient movement or to relieve the cable strain on the sensor.
78
Technical Alarm Messages (INOPs) 5 Patient Alarms and INOPs
INOP Message, Indication Source What to do
<SpO2 label> NON-PULSAT.
Numeric is replaced by -?­INOP tone.
SpO
2
Check the perfusion at measurement site. If necessary, stimulate circulation or change measurement site. If the INOP is due to NBP measurement on the same limb, wait until the NBP measurement is finished.
<SpO2 label> NO SENSOR
Numeric is replaced by -?­INOP tone.
<SpO2 LABEL> POOR SIGNAL
Label is displayed with a -?-
SpO
SpO
2
Make sure the SpO2 sensor is connected. If the INOP persists, try another adapter cable and sensor. If you silence this INOP, the measurement will be switched off.
2
The signal condition of the SpO2 measurement is poor and measurement accuracy may be compromised.
(questionable numeric)
<SpO2 LABEL> PULSE?
Numeric is replaced by -?-
SpO
2
The detectable pulsations of the SpO2 signal are outside the specified pulse rate range.
INOP tone
<SpO2 LABEL> SEARCHING
Numeric unavailable
<SpO2 label> SENSOR MALF
Numeric is replaced by -?­INOP tone.
<SpO2 LABEL> SENSOR OFF
Numeric is replaced by -?­INOP tone
<SpO2 LABEL> UNKN.SENSOR
Numeric is replaced by a -?-
<SpO2 LABEL> UNPLUGGED
Numeric is replaced by -?­INOP tone
SpO
SpO
SpO
SpO
SpO
2
SpO2 is analyzing the patient signal to derive Pulse, SpO2 and Perf values. Please wait until the search analysis is complete.
2
The SpO2 sensor or adapter cable is faulty. Try another adapter cable and sensor. If the INOP persists, contact your service personnel.
2
The SpO2 sensor is not properly applied to the patient. Apply the sensor following the instructions supplied by the manufacturer.
2
The connected sensor or adapter cable is not supported by the SpO2 measurement. Use only specified sensors and cables.
2
An SpO2 measurement label has been deactivated, either by unplugging a module, or by deactivating the label in the Measurement Selection window.
The measurement automatically disappears from the display.
To switch the measurement on again, either replug the module or reactivate the measurement label in the Measurement Selection window.
<SpO2 LABEL> UPGRADE
Label is displayed with a -?-, numeric is
SpO
2
The SpO2 measurement is currently in UPGRADE mode. Monitoring is not possible in this mode.
unavailable
Sp - vO2 CHK SOURCES
Numeric is replaced by -?-
Sp - vO2 CHK UNITS
Numeric is replaced by -?-
SRR INTERFERENCE
INOP tone
SRR INVALID CHAN
INOP tone
Sp - vO2Not all measurements or values required to perform the
calculation are available. Check measurement sources.
Sp - vO2The monitor has detected a conflict in the units used for this
calculation. Check the unit settings.
Monitor The short range radio connection has interference from
another device. Try using another channel.
Monitor The channel configuration of the Short Range Radio is invalid.
Check channel and channel mask configuration.
SRR MALFUNCTION Malfunction in the short range radio device. If the INOP
persists contact your service personnel.
SVR/SVRI CHK SOURCES
Numeric is replaced by -?-
SVR/SVRI CHK UNITS
Numeric is replaced by -?-
SVR/SVRI Not all measurements or values required to perform the
calculation are available. Check measurement sources.
SVR/SVRI The monitor has detected a conflict in the units used for this
calculation. Check the unit settings.
79
5 Patient Alarms and INOPs Technical Alarm Messages (INOPs)
INOP Message, Indication Source What to do
SVR/SVRI SET CVP USED
Numeric is replaced by -?-
T/T1/T2/T3/T4 INOPs TEMP See <Temp label> INOPs (under Temp)
TAAP DISABLED
INOP tone
Tamb INOPs TEMP See <Temp label> INOPs (under Temp)
Tart INOPs TEMP See <Temp label> INOPs (under Temp)
Tblood NO TRANSDUC
Numeric is replaced by -?­INOP tone
Tblood OVERRANGE
Numeric is replaced by -?-
Tcereb INOPS TEMP See <Temp label> INOPs (under Temp)
Tcore INOPs TEMP See <Temp label> INOPs (under Temp).
tcpO2 (or tcpCO2 or tcGas) CAL FAILED
Numeric is replaced by -?­INOP tone.
tcpO2 (or tcpCO2 or tcGas) CAL REQUIRD
Numeric is replaced by -?­INOP tone.
tcpO2 (or tcpCO2 or tcGas) CAL RUNNING
Numeric displays first -?- , then numeric is displayed with a ?
tcpO2 (or tcpCO2 or tcGas) CHECK TIME
tcpO2 (or tcpCO2 or tcGas) CHANGE SITE
If Heat Switch Off is configured to Yes, numeric is replaced by -?­INOP tone.
tcpO2 (or tcpCO2 or tcGas) EQUIP MALF
Numeric is replaced by -?­INOP tone.
tcpO2 (or tcpCO2 or tcGas) NO TRANSDUC
Numeric is replaced by -?­INOP tone.
tcpO2 (or tcpCO2 or tcGas) STABILIZING
Numeric is displayed with a ?
SVR/SVRI A CVP value is required for this calculation, but is not
currently being measured. The monitor is using the CVP value preset in the
Monitor The currently selected telemetry configuration on the monitor
does not allow connection of telemetry devices to the monitor.
C.O. No transducer attached to the module or catheter
disconnected.
C.O. Tblood out of range 17°C - 43°C.
tcGas A calibration failed. Check the calibration unit, gas pressure,
and tubing connections, then restart the calibration. If the calibration has failed more than once, remembrane the transducer and restart the calibration. If this INOP persists, contact your service personnel.
tcGas Calibration is required before applying the transducer to the
patient. Insert a membraned transducer into the calibration chamber on the module, connect the calibration unit to the calibration chamber, open the gas valve and start the calibration. If this INOP occurs during a calibration, there may be a module or transducer malfunction: contact your service personnel.
tcGas Wait until the tcpO2/tcpCO2 calibration is finished.
tcGas Site Timer due to time out in 15 minutes or less.
tcGas Site Timer has timed out. Change the application site to avoid
skin burns. To reset the Site Timer, either calibrate and change the measurement site, or change the measurement site and reset the Site Timer manually by selecting the appropriate site time from the
tcGas There is a malfunction in the transducer or module. Connect
another transducer. If this INOP persists, contact your service personnel.
tcGas No transducer is connected to the tcpO2/tcpCO2 module.
Silencing the alarm switches off the measurement.
tcGas The transducer has not yet reached the selected temperature
and/or skin hyperemization is not yet finished. This INOP will disappear within three minutes.
Setup SVR menu.
Setup TCGas menu.
80
Technical Alarm Messages (INOPs) 5 Patient Alarms and INOPs
INOP Message, Indication Source What to do
tcpO2 (or tcpCO2 or tcGas) UNPLUGGED
Numeric is replaced by -?­INOP tone.
TELE CONFIG UNSUPP
INOP tone
!!/!!!TELE DISCONNECT
INOP tone
TELE EQUIP MALF
INOP tone
TELE INCOMPATIBLE Monitor SRR-enabled telemetry device is not supported by this central
!!/!!! TELE INOP
Severe yellow/red INOP tone.
Tele Sync Unsupp.
INOP tone
TELE UNSUPPORTED
INOP tone
<Temp> CHK SOURCES
Numeric is replaced by -?-
<Temp> CHK UNITS
Numeric is replaced by -?-
<Temp label> DEACTIVATED
INOP tone
<Temp label> EQUIP MALF
Numeric is replaced by -?­INOP tone.
<Temp label> NO TRANSDUCER
Numeric is replaced by -?­INOP tone.
tcGas The measurement is switched on but the module is unplugged.
The measurement automatically disappears from the display. Silencing this INOP switches off the measurement.
Monitor Telemetry device not supported (companion mode)
Telemetry Telemetry transceiver was disconnected or short range radio
link was lost. For cable connections; check Telemetry interface, cable connection and setup. For short range radio connections: if the telemetry transceiver has not moved out-of-range, check for interference sources close to the monitor (bluetooth devices, DECT phones, cellular phones, microwaves, etc.) If this INOP persists, ask your service personnel to survey the interference sources.
Monitor The telemetry device has a malfunction. Disconnect and
reconnect the telemetry device. If the INOP reappears, replace the telemetry device.
software revision. Please check configuration.
Telemetry Check for further details at the Information Center or in the
Telemetry Data window on the monitor.
Telemetry The MMS in use does not support synchronization of ECG
and SpO after a telemetry device has been paired. Use an MMS with revision E.0 or above.
Monitor This telemetry device is not supported for direct connection to
the monitor.
TEMP
Difference
TEMP
Difference
TEMP A Temp measurement label in the measurement device has
TEMP Contact your service personnel.
TEMP Make sure the TEMP probe is connected to the MMS or
Not all measurements or values required to perform the calculation are available. Check measurement sources.
The monitor has detected a conflict in the units used for this calculation. Check the unit settings.
been deactivated, either by connecting a Pressure transducer in the shared Press/Temp socket, or by deactivating the label in the Measurement Selection window.
The measurement automatically disappears from the display.
To switch the measurement on again, either reconnect a Temp transducer or reactivate the measurement label in the Measurement Selection window.
The temperature hardware is faulty.
module. If you silence this INOP, the measurement will be switched off.
settings between the monitor and central station
2
81
5 Patient Alarms and INOPs Technical Alarm Messages (INOPs)
INOP Message, Indication Source What to do
<Temp label> UNPLUGGED
INOP tone
<Temp label> OVERRANGE
Numeric is replaced by -?­INOP tone.
Tesoph INOPS TEMP See <Temp label> INOPs (under Temp).
TEXT UPLOAD FAILED
INOP tone
TimeExpired:<timer label> INOP tone
Tnaso INOPS TEMP See <Temp label> INOPs (under Temp).
Trect INOPS TEMP See <Temp label> INOPs (under Temp).
Tskin INOPS TEMP See <Temp label> INOPs (under Temp).
Ttymp INOPS TEMP See <Temp label> INOPs (under Temp)
Tven INOPS TEMP See <Temp label> INOPs (under Temp).
Tvesic INOPS TEMP See <Temp label> INOPs (under Temp)
UAP INOPS PRESS See <Pressure label> INOPS (under Pressure).
Unsupported LAN
INOP tone
User I/F Malfunct. INOP tone.
UVP INOPS PRESS See <Pressure label> INOPS (under Pressure).
V LEAD OFF
Numeric is replaced by -?- for 10 seconds; INOP tone.
<VueLink option> CHK CABLE
INOP tone.
<VueLink option> CHK CONF.
INOP tone.
TEMP A Temp measurement label has been deactivated, either by
unplugging a module, or by deactivating the label in the Measurement Selection window.
The measurement automatically disappears from the display.
To switch the measurement on again, either replug the module or reactivate the measurement label in the Measurement Selection window.
TEMP Try changing the application site of the transducer.
[The temperature is less than -1
IntelliBridge Incoming text from the IntelliBridge modules exceeds the
maximum limit. Try unplugging one of the IntelliBridge modules. If the INOP occurs repeatedly contact your service personnel; a software upgrade may be necessary.
Monitor The time has expired for the timer indicated in the INOP text.
Clearing the timer clears the INOP.
Monitor There is a problem with the communication to the network
and central monitoring is currently not possible. Check the connection. If the INOP persists, switch off the monitor and contact your service personnel.
Monitor Perform a visual and functional check of all the monitor input
devices. Contact your service personnel.
ECG The V electrode (IEC: C electrode) has become detached from
the patient or the lead set has been changed. Reattach the electrode or select menu to confirm the new lead set.
VueLink No cable or the wrong cable connected to the VueLink module,
or incorrect device selected. Silencing this INOP switches the measurement off. VueLink INOP abbreviations may differ slightly depending on the device category.
VueLink The wrong external device has been selected on the VueLink
module, or the external device has not been correctly setup, or the wrong cable has been used to connect the device to the VueLink module. VueLink INOP abbreviations may differ slightly depending on the device category.
New Lead Setup in the Setup ECG
C, or greater than 45C.]
82
Technical Alarm Messages (INOPs) 5 Patient Alarms and INOPs
INOP Message, Indication Source What to do
<VueLink option> CHECK SETUP
INOP tone.
VueLnk EQUIP MALF
INOP tone.
VueLnk NO CONFIG
INOP tone.
VueLnk UNPLUGGED
INOP tone.
VueLink No information was received from the external device. The
device may be switched off or disconnected. VueLink INOP abbreviations may differ slightly depending on the device category.
VueLink Malfunction in the VueLink module. If this message appears
repeatedly, the module must be replaced. Contact your service personnel. VueLink INOP abbreviations may differ slightly depending on the device category.
VueLink The VueLink module has not been configured during
installation. The installation process should be completed by either your biomedical engineering department or the Philips service engineer. VueLink INOP abbreviations may differ slightly depending on the device category.
VueLink The VueLink module has been unplugged from the rack, or the
whole rack has been disconnected. The measurement automatically disappears from the display. Silencing this INOP switches off the measurement. VueLink INOP abbreviations may differ slightly depending on the device category.
83
5 Patient Alarms and INOPs Technical Alarm Messages (INOPs)
84
Use the Patient Demographics window and its associated pop-up keys to admit, discharge, and transfer (ADT) patients.
All patient demographic and ADT information is shared between the patient monitor and the Information Center, for example, patients admitted to the monitor are automatically admitted to a connected Information Center.
Note that when the MP5 is connected to a host monitor, its ability to admit or discharge a patient is disabled, and the host monitor controls patient demographic and ADT information.

Admitting a Patient

The monitor displays physiological data and stores it in the trends as soon as a patient is connected. This lets you monitor a patient who is not yet admitted. It is however important to admit patients properly so that you can identify your patient on recordings, reports, and networked devices.
6

6Managing Patients

During admission you enter data that the monitor needs for safe and accurate operation. For example, the patient category setting determines the algorithm the monitor uses to process and calculate some measurements, the safety limits that apply for some measurements, and the alarm limit ranges.
NOTE It is strongly recommended that the same patient data fields be configured to be mandatory at the
monitor and the Information Center.
To admit a patient,
1 Select the patient name field or select the Admit/Dischrge SmartKey to open the
Patient Demographics window.
85
6 Managing Patients Admitting a Patient
Patient Demographics
Last Name First Name Middle Name Lifetime Id Encounter Id Patient Cat. Paced
Adult
No Height Weight BSA (D) DOB Age Gender Notes (1): Notes (2):
Clear any previous patient data by selecting the Dischrge Patient or End Case pop-up
2
key and then Confirm. If you do not discharge the previous patient, you will not be able to distinguish data from the
previous and current patients, for example, in the trend database.
3 Select Admit Patient.
4 Enter the patient information: select each field and use the on-screen keyboard or choose from the
pop-up list of alternatives to input information. – Last Name: Enter the patient’s last name (family name), for example Smith.First Name: Enter the patient’s first name, for example Joseph.Middle Name (if configured to appear): Enter the patient’s middle name. – Lifetime Id, Encounter Id: Whether these fields appear and how they are labelled can
be configured for your hospital. One or both fields may be displayed and the labels may read:
MRN, Case Id, Visit Id, etc. Enter the appropriate data for the fields displayed. – Patient Cat: Choose the patient category, either Adult, Pediatric, or Neonatal. – Paced: Choose Yes or No (You must use “Yes” if your patient has a pacemaker). – Height: Enter the patient’s height. – Weight: Enter the patient’s weight. – BSA: The monitor calculates the body surface area automatically. – Date Of Birth: Enter the patient’s date of birth. Enter this in the form dd/mm/yyyy. – Age: The monitor calculates the patient age automatically. – Gender: Choose Male or Female. – Notes: Enter any extra information about the patient or treatment.
86
5 Select Confirm. The patient status changes to admitted.
Quick Admitting a Patient 6 Managing Patients

Patient Category and Paced Status

The patient category setting determines the algorithm the monitor uses to process and calculate some measurements, the safety limits that apply for some measurements, and the alarm limit ranges.
The paced setting determines whether the monitor shows pacemaker pulses or not. When Paced is set to No, pace pulses are filtered and therefore do not show in the ECG wave.
WARNING Patient Category and Paced status will always contain a value, regardless of whether the
patient is fully admitted or not. If you do not specify settings for these fields, the monitor uses the default settings from the current profile, which might not be correct for your patient.
Patient category Changing the patient category may change the arrhythmia and NBP alarm limits. Always check alarm limits to make sure that they are appropriate for your patient.
Paced status For paced patients, you must set Paced to Yes. If it is incorrectly set to No, the monitor could mistake a pace pulse for a QRS and fail to alarm during asystole.

Admitting a Centrally-Monitored Patient

You can admit a patient at either the bedside or the Information Center. When you admit a patient, the patient’s name appears on the bedside monitor and the Information Center.
If you do not fill in all patient information required by the Information Center, the Information Center may reject the admission. Complete all the required fields and try again to admit the patient.

Quick Admitting a Patient

Use Quick Admit only if you do not have the time or information to fully admit a patient. Complete the rest of the patient demographic details later.
1 Select the Quick Admit SmartKey.
2 Enter the required data (ID fields or Last Name depending on configuration) with the keyboard.
3 Select Enter.
4 In the confirmation window, select Confirm to discharge the previous patient (if confirmation is
configured).
5 Check that patient category and paced status are correct for the new patient.
If the monitor is connected to an Information Center and only the ID field is entered, the patient name is set to - - - at the Information Center. Complete the rest of the demographic details as soon as possible to fully identify the patient on the network, on the monitor and on printed reports. To complete the details, select Admit Patient again and complete all required fields.

Editing Patient Information

To edit the patient information after a patient has been admitted, select the patient name field on the Main Screen to open the Patient Demographics window, and make the required changes.
87
6 Managing Patients Discharging a Patient

Discharging a Patient

WARNING Always perform a discharge before starting monitoring for a new patient, even if your previous patient
was not admitted. Failure to do so can lead to data being attributed to the wrong patient.
A discharge:
– clears the information in the Patient Demographics window – erases all patient data (such as trend, event, and calculation data) from the monitor and
Information Center. This ensures that data from a previous patient are not mixed with data from
the new patient. – resets patient category and paced settings to the settings defined in the default Profile – resets all monitor and measurement settings as well as the active Screen to the settings defined in
the default Profile – discharges the patient from the Information Center.
When a patient is discharged from the monitor or from an Information Center, all patient data is deleted. Make sure that you have printed out any required reports before discharging. Check that a functioning central printer is available before you use End Case.
To discharge a patient,
1 Select the patient name field or select the Admit/Dischrge SmartKey to open the
Patient Demographics window and associated pop-up keys.
2 Select the pop-up key for either:
End Case - to print any configured end case reports or vital signs recording, discharge the
patient and clear the patient database, then enter standby mode. If an End Case SmartKey is
configured for your monitor, you can also select this instead and then confirm.
To see which end case reports are set up for your monitor, select Main Setup -> Reports ->
Auto Reports. For each auto report, if End Case Report is set to On, this report will be printed when you select End Case. See the section on AutoReports for information on setting up end case reports.
Dischrge Patient - to discharge the patient without printing any reports.

New Patient Check

The monitor can be configured to ask you in certain situations:
• after a specified power-off period
• after a specified standby period
• when no basic vitals (HR, RR, Pulse, SpO
whether a new patient is now being monitored. The pop-up window is entitled Is this a new Patient?. The monitor offers a Yes key to discharge the previous patient and begin monitoring a new patient and a No key to continue monitoring with the current patient data and settings.
, NBP) have been measured for a specified period
2
88
The time periods for the three conditions can be configured independently.
Transferring Patients 6 Managing Patients

Transferring Patients

To save you from having to enter the same patient data multiple times and enable patient transfer without loss of data, patient demographic information is shared between patient monitors and Information Centers.

Transferring a Centrally-Monitored Patient using IIT

Scenario: A centrally-monitored patient is moved with the MP5 to another monitoring location on the same Information Center database server without interrupting the collection of patient trend information. The MP5 has an IntelliVue Instrument Telemetry interface (IIT), is connected to a host monitor and is declared as a “telemetry device” at the Information Center.
NOTE The Transfer key is not available while the MP5 is connected to a host monitor (Companion
Mode is indicated).
1 Remove the MP5 from the host monitor.
2 Move the patient using the MP5 as the transport monitor.
3 At the new location, just before connecting the MP5 to the new host monitor:
– open the Patient Demographics window. – select the Transfer pop-up key. – wait until the transfer has completed.
4 Connect the MP5 to the new host monitor. The monitor detects a patient mismatch and a window
will open showing your patient’s data and asking Complete transfer of this patient?.
5 Select Yes to complete the transfer. This re-admits the patient from the transfer list to the new
monitor. This will upload the patient demographics, and, if configured, the measurement settings and trend data stored in the MP5 to the receiving monitor.
Verify that the settings for patient category and paced mode are correct.

Transferring a Centrally-Monitored Patient with the Monitor

Scenario: A centrally-monitored patient is moved with the monitor to another monitoring location on the same Information Center database server without interrupting the collection of patient trend information.
1 Select the patient name field or select the Admit/Dischrge SmartKey to open the
Patient Demographics window, then select the Transfer pop-up key. If the patient is
not admitted or not monitored by an Information Center, the Transfer key is inactive (“grayed-out”).
This step preserves the patient’s demographic data during the transfer.
2 At the new location, connect the monitor to the network (only needed for wired networks). If the
monitor detects a patient mismatch, a window will open showing your patient’s data and asking Complete transfer of this patient?.
3 Select Yes to complete the transfer.
4 Verify that the settings for patient category and paced mode are correct.
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6 Managing Patients Transferring Patients
If you accidentally transfer a patient, use Re-Admit to restore this patient’s data to the Information Center. If you are not connected to the network, select Clear Transfer to leave transfer mode. The patient data remains in the monitor.

Data Exchange Between Information Centers

You can transfer demographic data and trend data from one IIC to another by selecting Transfer on the patient monitor. Trend data is not shared between Information Centers and monitors.

Resolving Patient Information Mismatch

When you connect together devices which store patient demographic data, for example:
• an MMS and a monitor,
• an X2 or MP5 and a host monitor,
• a monitor and an Information Center,
the system compares patient category, paced status, and unique patient identification in order to synchronize this information. If configured to do so, the monitor indicates a mismatch if the information is not identical.
WARNING 1 When a monitor is connected to an Information Center by the wireless IntelliVue Instrument
Telemetry interface, the patient data will automatically be merged in the case of a transfer. This means there is no patient discharge at the monitor and settings and trend data will be retained. You will see a message on the monitor and the Patient Demographics window will automatically appear so that you can check the data and change it if necessary.
2 It is important to resolve the mismatches as soon as they are identified. Failure to do so could result
in using incorrect/confusing data to make clinical decisions. Certain settings, for example Paced and Patient Category, may not match between the Information Center and the monitor. If the Paced status is set incorrectly, the system could mistake a pace pulse for a QRS and fail to alarm in the case of asystole. It is important that the Patient Category is set correctly so the ECG can be analyzed correctly and initial arrhythmia alarm limits set. In the case where an MP5 or X2 with an IntelliVue Instrument Telemetry interface is declared as a “telemetry device” at the Information Center and is connected to a host monitor, it is important to resolve an existing mismatch between the monitor and the Information Center before disconnecting the MP5/X2. Failure to do so discharges the MP5/X2 and synchronizes the demographics and settings to the Information Center.

Manually Resolving Patient Mismatch

The patient mismatch is indicated by question marks (???) beside the questionable fields in the Monitor Info Line and in the Select Patient window. The monitor displays a message such as Different patients in Central and Monitor.
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The Select Patient window automatically opens so you can decide which patient data to use. You do not have to resolve the mismatch immediately, but the indicators remain until you do.
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