Part Number M8105-9001C
Printed in Germany 09/08
4512 610 29031
*M8105-9001C*
M8105-9001C
1Table Of Contents
1 Installation1
Installation Checklist1
Unpacking and Checking the Shipment2
Mounting the Monitor3
Connecting the Monitor to AC Mains3
Checking Out The Monitor3
Loading Paper4
Operating the Monitor5
Setting the Date and Time6
Checking Country-Specific Default Settings6
Handing Over the Monitor6
2 Basic Operation9
Introducing the Monitor9
Operating and Navigating13
Operating Modes19
Understanding Screens20
Using the XDS Remote Display (not MP5T)21
Using the Visitor Screen21
Understanding Profiles22
Understanding Settings24
Adjusting a Measurement Wave25
Freezing Waves26
Using Labels27
Entering Measurements Manually29
Changing Monitor Settings29
Checking Your Monitor Revision30
Getting Started30
Disconnecting from Power32
Networked Monitoring32
Using the MP5 with a Host Monitor33
3 What’s New?35
What’s New in Release G.0?35
What’s New in Release F.0?36
4 Alarms39
Visual Alarm Indicators40
Audible Alarm Indicators41
Acknowledging Alarms 43
Pausing or Switching Off Alarms44
Alarm Limits45
Reviewing Alarms50
i
Latching Alarms52
Testing Alarms52
Alarm Behavior at On/Off53
Alarm Recordings53
Admitting a Patient85
Quick Admitting a Patient87
Editing Patient Information87
Discharging a Patient88
Transferring Patients89
Care Groups92
7 ECG, Arrhythmia, ST and QT Monitoring99
Skin Preparation for Electrode Placement99
Connecting ECG Cables99
Selecting the Primary and Secondary ECG Leads100
Checking Paced Status100
Understanding the ECG Display100
Monitoring Paced Patients101
Changing the Size of the ECG Wave103
Changing the Volume of the QRS Tone103
Changing the ECG Filter Settings104
Selecting Positions of Va and Vb Chest Leads (for 6-lead placement)104
Choosing EASI or Standard Lead Placement105
About ECG Leads105
ECG Lead Fallback106
ECG Lead Placements106
Capture 12-Lead110
EASI ECG Lead Placement111
ECG and Arrhythmia Alarm Overview 112
Using ECG Alarms113
ECG Safety Information114
About Arrhythmia Monitoring115
Switching Arrhythmia Analysis On and Off116
Choosing an ECG Lead for Arrhythmia Monitoring116
Understanding the Arrhythmia Display117
Arrhythmia Relearning120
Arrhythmia Alarms121
About ST Monitoring127
Switching ST On and Off127
Understanding the ST Display128
ii
Updating ST Baseline Snippets129
Recording ST Segments130
About the ST Measurement Points130
ST Alarms132
Viewing ST Maps133
About QT/QTc Interval Monitoring137
QT Alarms140
Switching QT Monitoring On and Off141
8 Monitoring Pulse Rate143
Entering the Setup Pulse Menu143
System Pulse Source 143
Switching Pulse On and Off144
Using Pulse Alarms144
9 Monitoring Respiration Rate (Resp)147
Lead Placement for Monitoring Resp147
Understanding the Resp Display148
Changing Resp Detection Modes148
Changing the Size of the Respiration Wave149
Changing the Speed of the Respiration Wave150
Using Resp Alarms150
Changing the Apnea Alarm Delay150
Resp Safety Information150
10 Monitoring SpO
SpO2 Sensors153
Applying the Sensor153
Connecting SpO2 Cables154
Measuring SpO
SpO2 Signal Quality Indicator (Fast SpO2 only)155
Assessing a Suspicious SpO2 Reading155
Changing the Averaging Time156
Setting the Measurement Mode156
Understanding SpO2 Alarms156
Pleth Wave157
Perfusion Numeric158
Perfusion Change Indicator158
Setting SpO2/Pleth as Pulse Source158
Setting Up Tone Modulation158
Setting the QRS Volume159
2
2
154
11 Monitoring NBP161
Introducing the Oscillometric NBP Measurement161
Preparing to Measure NBP162
Starting and Stopping Measurements164
153
iii
Enabling Automatic Mode and Setting Repetition Time165
Enabling Sequence Mode and Setting Up The Sequence165
Choosing the NBP Alarm Source166
Switching Pulse from NBP On/Off166
Assisting Venous Puncture167
Calibrating NBP167
12 Measuring Predictive Temperature169
Making a Temperature Measurement169
13 Monitoring Temperature173
Making a Temp Measurement173
Calculating Temp Difference174
14 Monitoring Invasive Pressure175
Setting up the Pressure Measurement175
Zeroing the Pressure Transducer176
Adjusting the Calibration Factor178
Displaying a Mean Pressure Value Only178
Changing the Pressure Wave Scale 178
Optimizing the Waveform179
Using the Wave Cursor179
Non-Physiological Artifact Suppression179
Choosing the Pressure Alarm Source179
Calibrating Reusable Transducer CPJ840J6181
Calculating Cerebral Perfusion182
Calculating Pulse Pressure Variation182
15 Monitoring Carbon Dioxide 185
Using the CO2 Measurement186
Measuring Microstream CO
Setting up all CO2 Measurements190
2
189
16 Assigning Two Devices to One Patient195
How Can You Combine Devices?195
Functions Available When the Telemetry Data Window is Displayed199
Functions Available For Devices Connected Via SRR200
General Telemetry-related Functions201
Use Models With Telemetry202
17 Enhancing Telemetry Monitoring with the Monitor205
18 Tre nd s207
Viewing Trends207
Setting Up Trends210
Documenting Trends213
Starting and Stopping Recordings237
Overview of Recording Types238
All ECG Waves Recordings239
Creating and Changing Recordings Templates239
Changing ECG Wave Gain240
Recording Priorities241
Sample Recording Strip241
Reloading Paper243
Recorder Status Messages243
23 Printing Patient Reports245
Starting Report Printouts245
Stopping Reports Printouts246
Setting Up Reports246
Setting Up Individual Print Jobs248
Checking Printer Settings249
Printing a Test Report249
Switching Printers On Or Off for Reports249
Dashed Lines on Reports249
Unavailable Printer: Re-routing Reports249
Checking Report Status and Printing Manually250
Printer Status Messages251
Sample Report Printouts252
v
24 Using the Drug Calculator257
Accessing the Drug Calculator257
Performing Drug Calculations258
Charting Infusion Progress260
Using the Titration Table260
Documenting Drug Calculations260
25 Using the Timer261
Viewing the Timer261
Timer Setup Pop-up Keys261
Setting Up Timers262
Displaying a Timer On The Main Screen263
Displaying A Clock On The Main Screen264
26 Laboratory Data265
Viewing Received Data265
27 Care and Cleaning267
General Points267
Cleaning the Monitor268
Disinfecting the Monitor268
Sterilizing the Monitor268
Cleaning, Sterilizing and Disinfecting Monitoring Accessories269
Cleaning and Disinfecting the Predictive Temperature Accessories269
Cleaning Batteries and the Battery Compartment269
28 Using Batteries271
Battery Power Indicators271
Checking Battery Charge274
Replacing a Battery274
Optimizing Battery Performance274
Battery Safety Information275
29 Maintenance and Troubleshooting277
Inspecting the Equipment and Accessories277
Inspecting the Cables and Cords277
Maintenance Task and Test Schedule278
Troubleshooting279
Disposing of the Monitor279
Disposing of Empty Calibration Gas Cylinders279
Temperature Accessories291
Predictive Temperature Accessories291
Mainstream CO2 Accessories292
Sidestream CO2 Accessories292
Microstream CO2 Accessories292
Recorder Accessories293
Cable for Direct Connection of a Telemetry Device294
Battery Accessories294
31 Installation and Specifications295
Intended Use295
Manufacturer’s Information296
Symbols296
Installation Safety Information298
Altitude Setting300
Monitor Safety Specifications300
EMC And Radio Regulatory Compliance301
Out-Of-Hospital Transport - Standards Compliance302
Monitor Performance Specifications304
M4605A Battery Specifications308
Measurement Specifications309
Safety and Performance Tests321
32 Default Settings Appendix327
Country-Specific Default Settings327
Alarm and Measurement Default Settings333
Alarm Default Settings333
ECG, Arrhythmia, ST and QT Default Settings334
Pulse Default Settings337
Respiration Default Settings337
SpO2 Default Settings338
NBP Default Settings339
Temperature Default Settings339
Predictive Temperature Default Settings340
Invasive Pressure Default Settings340
CO2 Default Settings342
vii
viii
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.
1
• 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.
StepTa s kCheck Box
1Perform initial inspection of delivery, unpack and check the shipment (see
“Unpacking and Checking the Shipment” on page 2)
2Mount the monitor as appropriate for your installation (see “Mounting the
Monitor” on page 3)
3Connect the monitor to AC mains using the supplied power cord (see
“Connecting the Monitor to AC Mains” on page 3)
4Perform Visual, Power On and Functional test blocks (see “Checking Out
The Monitor” on page 3)
5Perform Safety Tests, if required by local laws and regulations (see “Checking
Out The Monitor” on page 3)
6Load paper into the recorder, if present (see “Loading Paper” on page 4)❏
when Task
Done
❏
❏
❏
❏
❏
1
1 InstallationUnpacking and Checking the Shipment
StepTa s kCheck Box
when Task
Done
7Check/set the time and date (see “Setting the Date and Time” on page 6)❏
8Check that the country-specific default settings are appropriate (see
“Checking Country-Specific Default Settings” on page 6)
9Perform 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 SuppliesComments
Monitor with options as ordered1
ECG accessoriesoptional
NBP accessories1
SpO2 accessoriesoptional
Pressure accessoriesoptional
Temperature accessoriesoptional
Predictive Temperature accessoriesoptional
CO2 Accessoriesoptional
Recorder paper optional
Powercord1
Telemetry Interface cableoptional
Measurement Link (MSL) cable optional
Instructions for Use1
Quick Guide1
Documentation CD-ROM (includes Service Guide and Instructions
for Use)
Claims for Damage
If the shipping cartons are damaged, contact the carrier.
1
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 Monitor1 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
VisualInspect the monitor, measurement accessories and cables for any damage.
Are they free of damage?
Power OnPower 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 TestAfter 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 InstallationLoading 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.
SystemPerform 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
1Use the latch on the right side of the recorder door to pull the door open.
2Remove the empty core.
3Insert 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.
4With at least one inch of paper extending beyond the edge of the door,
swing the recorder door up and push it firmly closed.
5To 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 Monitor1 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.
3Touch again to select an item on the menu and
work through the menu activities.
2Touch 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.
4You can touch numerics, waves and any
item on the screen, to get you to the
corresponding menu.
5If 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 InstallationSetting the Date and Time
Setting the Date and Time
To set the date and time:
1Select the Date, Time screen element from the monitor’s info line to enter the Date, Time
menu.
2Select, 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.
3Select 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.
WARNINGBefore 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:
1In the Main Setup menu, select Operating Modes.
2Select 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
6
Handing Over the Monitor1 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.
7
1 InstallationHanding 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
9
2 Basic OperationIntroducing 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:
NBP33
Predictive Temperature33
Te m p e r at u r e3
Invasive Pressure3
Carbon Dioxide3
Direct Telemetry Connection33
ECG Output signal3
LAN networking capability3
WLAN networking capability3
Short range radio interface3
IntelliVue Instrument Telemetry networking capability3
Severe Sepsis Screening3
OxyCRG high resolution trend3
Neonatal event review3
Integrated recorder33
Drug Calculator33
Gas monitor support3
Connection to a host monitor (companion mode) 3
Connection to an external display3
Nurse call capability3
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 OperationIntroducing the Monitor
MP5/MP5T Major Parts and Keys
1
3
4
5
2
US measurement connectors
Pressure
and Temp
Noninvasive
Pressure
SpO
1Color-coded alarm lamps
2Alarms off lamp
3Measurement connectors (see
below)
4Predictive Temperature Unit
5ECG out (not MP5T and MP5
options without ECG)
6On/Standby Switch
7Indicator 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
1234
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 Navigating2 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, JohnAdult
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
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 lineOther 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
1514
Delayed
Record
Vitals
Trend
Default
Profile
End Case
Main
Setup
1312
hrs
Main
Screen
11
13
2 Basic OperationOperating and Navigating
Monitor information lineOther 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
1Select the title of the window and keep your finger on the title.
2Move your finger on the Touchscreen to move the window.
3Take 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.
14
Operating and Navigating2 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 wavesquick 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
15
2 Basic OperationOperating 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 waveaccess 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
16
access Vital Signs recording key
access Select Waves recording key
set wide automatic alarm limitsset narrow automatic alarm limits
switch CO
pump offaccess neonatal event review
2
review vital signs trendreview graph trend
access the calculatoraccess the Drug Calculator
gas analyzer - exit standby modesuppress zero for all gas measurements
Operating and Navigating2 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 placementaccess patient reports
new lead setupmanual data entry
access ProtocolWatchstart/stop car seat assessment record
open the histogram windowopen 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 OperationOperating 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
18
Operating Modes2 Basic Operation
Operating Modes
When you switch the monitor on, it starts up in monitoring mode. To change to a different mode:
1Select the Main Setup menu.
2Select 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 OperationUnderstanding 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
1To switch to a different Screen, select the monitor info line and then Change
Screen in the Setup Menu, or select the Change Screen SmartKey.
2Choose 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,
1Select the element you want to change.
2From 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,
1Select the monitor info line to open the Setup menu
2Select Change Screen
3Select 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 OperationUnderstanding 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 Profiles2 Basic Operation
WARNINGIf 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 OperationUnderstanding Settings
Swapping a Complete Profile
1Select the monitor info line and then Profiles in the Setup menu, or select the
Profiles SmartKey.
2In the Profiles menu, select Profile.
3Chose a profile from the pop-up list.
4Confirm your selection.
Swapping a Settings Block
1Select the monitor info line and then Profiles in the Setup menu, or select the
Profiles SmartKey.
2In the Profiles menu, select DisplayorMeasmnt. Settings or
Monitor Settings to call up a list of the settings blocks in each category.
3Choose a settings block from the pop-up list.
4Confirm 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 Wave2 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.
1Enter the measurement’s setup menu and select the measurement.
2Select 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,
1Select Main Setup -> User Interface
2Select Global Speed or RespiratorySpeed, as required
3Select a value from the list of available speeds.
25
2 Basic OperationFreezing Waves
Changing Wave Speed for a Channel
To change the wave speed of an individual wave channel,
1Enter the Wave menu for a measurement by selecting its wave.
2Select Change Speed.
3To 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,
1Enter the Wave menu for the measurement by selecting the wave on the screen.
2Select Freeze Wave.
The realtime wave is replaced with the frozen wave.
Freezing All Waves
To freeze all waves on the screen,
1Select the Freeze Waves SmartKey.
All realtime waves are replaced with frozen waves.
Measuring Frozen Waves
To measure a frozen wave,
1Select the frozen wave.
This automatically positions the vertical cursor. The cursor can be repositioned by touching the
required point on the wave, or
2Use 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 Labels2 Basic Operation
To change the wave speed:
1Select the frozen wave.
2Select Change Speed.
3Select a speed from the list.
Updating The Frozen Wave
To update the wave, that is freeze the current wave:
1Select the frozen wave.
2Select Freeze Again.
Releasing Frozen Waves
To release frozen waves,
1Select a frozen wave.
2Select 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),
1Enter the Wave menu of the measurement.
2Select Label.
3Choose 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 OperationUsing 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.
WARNINGWhen 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,
1Select the measurement selection key or select Main Setup -> Measurement Selection
to display the Measurement Selection window.
2Select the measurement to be deactivated.
3Select 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 Manually2 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,
1Select the Enter Values SmartKey or select Main Setup -> Enter MeasValues
2Select the measurement you want to enter values for. The Edit <Measurement> window will
open.
3If the measurement is switched off, switch it on by selecting the label.
4Select Value and enter the value.
5Select Date/Time to enter the date and time for the value. The default is always the current date
and time.
6For compound labels, for example ABPs, ABPd and ABPm, select the Format field to select
whether all values are required or a single value.
7Select 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,
1Select the Enter Values SmartKey or select Main Setup -> Enter MeasValues
2Select the measurement you want to switch on or off.
3Select 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 OperationChecking Your Monitor Revision
Adjusting the Screen Brightness
1Select the Brightness SmartKey.
2Select 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,
1In the Main Setup menu, select User Interface
2Select 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.
1Select the Date, Time screen element from the monitor’s info line to enter the Date, Time
menu.
2Select, 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.
3Select Store Date, Time to change the date and time.
Checking Your Monitor Revision
1Select Main Setup -> Revision to open the Monitor Revision menu.
2From 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
WARNINGIf 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.
1Before you start to make measurements, carry out the following checks on the monitor.
– Check for any mechanical damage.
30
Getting Started2 Basic Operation
– Check all the external cables, plug-ins and accessories.
2Plug 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.
3Check 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
1Decide which measurements you want to make.
2Connect the required patient cables and sensors. The connectors are color-coded to the patient
cables and sensors for easy identification.
WARNINGWhen 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,
1Admit your patient to the monitor.
2Check 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.
3Refer to the appropriate measurement section for details of how to perform the measurements you
require.
31
2 Basic OperationDisconnecting from Power
WARNINGDuring 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)
WARNINGDo 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 Monitor2 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 OperationUsing 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
4AlarmsVisual 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:
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)
OnOff
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
4AlarmsAudible 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 Alarms4Alarms
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
4AlarmsPausing 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,
1Select Main Setup -> Alarms -> Alarm Settings
2Check 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
1Select the measurement numeric to enter its setup menu.
2Select 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 Limits4Alarms
• 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,
1Select one of the alarm fields. This calls up the Alarm Messages window.
2Select 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
4AlarmsAlarm 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 Limits4Alarms
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,
1In 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.
2Select 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
4AlarmsAlarm 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,
1Enter the Alarm Limits window.
2To 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 Limits4Alarms
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
1Wide alarm limits
2Narrow alarm limits
3Alarm Limits
4Measurement 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
4AlarmsReviewing 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 Alarms4Alarms
The Review Alarms window contains a list of the most recent alarms and INOPs with date and
time information.
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
4AlarmsLatching 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
1In the monitor’s Main Setup menu, select Alarms.
2Select 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&YR&YR&YRROff
R&YROffROffOff
Non-latching
alarms
Alarm tone on. Alarm lamp on. Alarm message. Flashing numerics.
All audible and visual
alarm indicators
automatically stop.
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/Off4Alarms
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.
1Press the Main Setup SmartKey.
2Select Alarms from the Main Setup menu.
3Select Alarm Recording from the Alarms menu to open the Alarm Recordings menu.
4Select 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.
5For 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
4AlarmsAlarm 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 MessageFromConditionIndication
*/**AFIBECG/
Arrhythmia
***APNEA or
***APNEA mm:ss sec
or
***APNEA >10min
***ASYSTOLEECGNo QRS detected for a period greater
**awRR HIGHCO2, Resp,
**awRR LOWCO2, Resp,
, Resp,
CO
2
Spirometry
AGM
AGM
Atrial fibrillation waveform detectedyellow 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 INOPsPatient Alarm Messages
Alarm MessageFromConditionIndication
**BIS HIGHBISThe Bispectral Index value has
exceeded the high alarm limit.
**BIS LOWBISThe Bispectral Index value has dropped
below the low alarm limit.
***BRADY/P xxx<yyy
or
***BRADY xxx<yyy
**CCO/CCI HIGHCCOContinuous Cardiac Output or CC
**CCO/CCI LOWCCOContinuous Cardiac Output or CC
**CPP HIGHCPPThe CPP value has exceeded the high
**CPP LOWCPPThe CPP value has fallen below the low
***DESAT or
***DESAT xxx<yyy
**etCO2 HIGHCO2, Resp,
**etCO2 LOWCO2, Resp,
**etO2 HIGHO2, AGMThe end tidal O2 high alarm limit has
**etO2 LOWO2, AGMThe end tidal O2 value has fallen below
*/**/***
EVENT:<GRP>
*/**/*** EVENT
at Information center
***EXTREME BRADYECGThe bradycardia limit has been
***EXTREME TACHYECGThe 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 Messages5 Patient Alarms and INOPs
Alarm MessageFromConditionIndication
**HR HIGHECGThe heart rate high alarm limit has
been exceeded.
**HR LOWECGThe heart rate has fallen below the low
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 INOPsPatient Alarm Messages
Alarm MessageFromConditionIndication
***<Pressure>
DISCONNECT
***<Pressure> HIGHPRESSThe measured pressure value is above
**<Pressure> HIGHPRESSThe measured pressure value is above
***<Pressure> LOWPRESSThe measured pressure value is below
**<Pressure> LOWPRESSThe measured pressure value is below
**Pulse HIGHPRESS
**Pulse LOWPRESS
*/**PVCs/min HIGHECG/
**QTc HIGHECG/QTQTc value has exceeded the QTc high
**QTc HIGHECG/QTQTc value has exceeded the QTc
*/**R-ON-T PVCs ECG/
**RR HIGHRESPThe respiration rate has exceeded the
PRESSThe 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 Messages5 Patient Alarms and INOPs
Alarm MessageFromConditionIndication
**RR LOWRESP The respiration rate has dropped below
the low alarm limit.
*/**RUN PVCs HIGHECG/
Arrhythmia
A run of PVCs greater than 2 was
detected.
**<SO2 label> HIGHSvO2/SO2The the measured intravascular oxygen
*/**/***TELE ALARMTelemetryThis 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 BIGEMINYECG/
***VENT FIB/TACHECGA fibrillatory waveform for 4
*/**VENT RHYTHMECG/
*/**VENT TRIGEMINYECG/
***VTACHECG,
**/***VueLink ALARM
at Information Center
TEMPThe temperature has exceeded the high
alarm limit.
TEMPThe temperature has fallen below the
low alarm limit.
A dominant rhythm of N, V, N, V (N =
Arrhythmia
Arrhythmia
Arrhythmia
Arrhythmia
VueLinkA 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 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.
Monitor1) An MMS with an incompatible software revision is
BatteryThe estimated remaining battery-powered operating time is less
BatteryThe battery cannot be used with this monitor. Replace with the
BatteryThe estimated battery-powered operating time remaining is less
BatteryThe monitor cannot determine the battery status. If this INOP
BatteriesThe 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 INOPsTechnical Alarm Messages (INOPs)
INOP Message, IndicationSourceWhat 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 TTelemetryThe 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 MALFUNCBISElectrocautery used during self-test OR malfunction in the
BIS DSC UPDATE
INOP tone
BIS ELECTR. DISC
INOP tone.
BIS ENGINE DISCONN
INOP tone
BatteriesThe indicated battery or batteries cannot be used with this
monitor. Replace with the correct battery or batteries as
specified in this book.
BatteriesThe estimated battery-powered operating time remaining is less
than 20 minutes.
BatteriesThe 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.
BatteriesThe monitor requires two batteries but can detect only one
battery. Insert the missing battery immediately.
BISThe semi-reusable sensor cable connected is unknown or not
supported by your software revision. Replace it with a Philipssupported sensor cable.
BISThe semi-reusable sensor cable has exceeded the maximum
number of uses. Replace the cable.
BISDSC 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.
BISDSC 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.
BISDSC 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.
BISOne or more electrodes are not connected to the semi-reusable
sensor cable. Check all electrode connections.
BISBIS 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, IndicationSourceWhat 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
BISBIS engine software is not supported. A software upgrade may
be required. Contact your service personnel.
MP20/30 - BIS engine not supported.
BISMalfunction in the BIS engine hardware. Disconnect and
reconnect the BIS engine. If the INOP persists, replace BIS
engine.
BISThere is a malfunction in the BIS hardware. Unplug and replug
the BIS module. If the INOP persists, contact your service
personnel.
BISImpedance 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.
BISThe 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 EEGBISNo 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
BISOne 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.
BISUnplug 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.
BISThe 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.
BISUnsupported 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 INOPsTechnical Alarm Messages (INOPs)
INOP Message, IndicationSourceWhat 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 ECGECG/
CANNOT ANALYZE QTQTThe QT algorithm cannot generate a valid QT value for more
CANNOT ANALYZE STSTThe ST algorithm cannot generate a valid ST value. Possible
BISMalfunction 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.
BISExcessive sensor usage. Replace sensor.
A Cyclic Impedance Check will start automatically.
BISIf 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).
BISPlug in the BIS module. Silencing this INOP switches off the
measurement.
BISThe BISx is not connected to the BIS module or the BIS
interface board. Silencing this INOP switches the measurement
off.
BISThe 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.
BISThe 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, IndicationSourceWhat 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 INOPsTechnical Alarm Messages (INOPs)
INOP Message, IndicationSourceWhat 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
MonitorSystem 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.
BatteriesBattery must be charged. Connect the monitor to mains power
or exchange the battery.
BatteriesThere is a problem with the battery charger in the monitor.
Connect the monitor to mains power and contact your service
personnel.
MonitorPerform 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.
BatteryThe 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.
MonitorThere was a problem loading the drug settings. Check that the
settings are complete and correct.
TelemetrySynchronization of ECG settings between the monitor and
Information Center has failed. Check that the ECG settings in
use are appropriate.
MonitorThe 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.
MonitorCheck 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.
MonitorPotential problem with alarm lamps, display or interfaces
detected. Contact your service personnel. This INOP will
appear on the monitor as Check Monitor Func.
MonitorPerform a visual and functional check of the keyboard. Contact
your service personnel.
MonitorThere is a problem with the second main board in the monitor.
Contact your service personnel.
MonitorPotential problem with alarm lamps, display or interfaces
detected. Contact your service personnel. This INOP may
appear on the Information Center as
CheckInternVoltage.
MonitorThe temperature inside the monitor is too high. Check that the
monitor ventilation is not obstructed. If the situation
continues, contact your service personnel.
MonitorPerform 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, IndicationSourceWhat to do
Check Network Conf
INOP tone
Check Nurse Relay
INOP tone
!!Check Pairing
INOP tone
Check Screen Res
INOP tone
MonitorThe monitor is receiving network topology information from
more than one source, e.g. the Database Server and an
Application Server. Contact your service personnel.
MonitorThere is a problem with the connection to the nurse relay.
Contact your service personnel.
MonitorThere is a problem with device pairing. Check that the monitor
and telemetry device are correctly paired.
MonitorThe 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
MonitorIf 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
MonitorPerform a visual and functional check of the SpeedPoint input
device. Contact your service personnel.
MonitorPerform a visual and functional check of the touch input
device. Contact your service personnel.
MonitorThe 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
MonitorThe ECG Sync is detecting an invalid signal, or the ECG Sync
cable is disconnected.
Chk IndepDsp CableMonitorThe 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
MonitorCheck that the MSL connector or cable are properly
connected. Check the cable and connector for damage.
TelemetrySynchronization 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.
ECGThe 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 INOPsTechnical Alarm Messages (INOPs)
INOP Message, IndicationSourceWhat to do
CO2 CHANGE SCALECO
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, IndicationSourceWhat 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 RUNNINGCO
CPP CHK SOURCES
CPPNot all measurements or values required to perform the
Numeric is replaced by a -?-
CPP CHK UNITS
CPPThe monitor has detected a conflict in the units used for this
Numeric is replaced by a -?-
!!/!!!CUFF NOT DEFLAT
NBPRemove 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.
NBPThe 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
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 INOPsTechnical Alarm Messages (INOPs)
INOP Message, IndicationSourceWhat 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>ECGThe ECG signal from the named ECG electrodes [RA, LA, LL,
(!!/!!!)ECG LEADS OFFECGCheck 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.
ECGAll 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.
ECGContact your service personnel.
The ECG hardware is faulty.
MonitorContact your service personnel.
The ECG in the Telemetry device is faulty.
ECGNot 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
ECGThe 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.
ECGCheck that the ECG out cable is securely connected. Contact
your service personnel.
EEGThe EEG hardware is faulty. Contact your service personnel.
Technical Alarm Messages (INOPs)5 Patient Alarms and INOPs
INOP Message, IndicationSourceWhat to do
EEG IMPEDANCE HIGH or
EEG1 and/or EEG2 IMPED. HIGH
Indep.Dsp Malfunc.DisplayA problem has occurred with the second main display. Contact
Indep.Dsp NotSupp.DisplayThe 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
EEGThe 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.
EEGReconnect specified electrode.
EEGOne or more electrodes are not connected. Check in the EEG
Impedance/Montage
electrode(s) are affected and reconnect the electrodes.
EEGTwo or more electrodes are not connected. Check in the EEG
Impedance/Montage
affected and reconnect the electrodes.
EEGExcessive 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.
EEGToo 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.
EEGThe 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.
EEGInput 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.
FMSMake sure that the Flexible Module Rack is connected to the
monitor. All FMS measurements are off while the FMS is
unplugged.
FMSThe Flexible Module Rack is not supported by your monitor.
Contact your service personnel.
your service personnel.
monitor software is incompatible. Contact your service
personnel.
BatteryX2/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.
DisplayThere 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 INOPsTechnical Alarm Messages (INOPs)
INOP Message, IndicationSourceWhat to do
Intell.Dsp MissingDisplayThe monitor has lost contact with the connected Intelligent
Display. Contact your service personnel.
Intell.Dsp Unsupp.DisplayThe monitor does not support the connected Intelligent
Display. The monitor software is incompatible.
Internal.Comm.Malf
INOP tone
INVALID LEADSETTelemetry
LA LEAD OFF
Numeric is replaced by -?- for 10
seconds; INOP tone.
LAP INOPsPRESSSee <Pressure label> INOPS (under Pressure).
LEADSET UNPLUGGEDTelemetryThe 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. DEACTIVATEDAn 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
MonitorThere is a problem with I2C Bus communication in the
monitor. Contact your service personnel.
ECGThe 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.
ECGThe 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.
MonitorThe MSL coupling cable is reversed. Connect the end with the
grey connector to the Intelligent Display.
MonitorAn 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.
MMSThe Multi-Measurement module is not supported by the
monitor. Contact your service personnel.
MMS
Extension
MMS
Extension
MMS
Extension
MMS
Extension
MMSMake sure that the Multi-Measurement Module is connected
MMSThe Multi-measurement Module is not supported by your
MonitorThe 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, IndicationSourceWhat to do
MSL Power HighMonitorThe 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 CENTRALMonitorThe ECG measured with the monitor ECG is not being sent to
NO ECG SOURCETelemetryA telemetry device is paired with the monitor but the
MonitorThe 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.
MonitorThe 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.
NBPThe 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.
NBPRemove 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.
NBPCheck 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.
NBPCheck 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.
MonitorThere 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 INOPsTechnical Alarm Messages (INOPs)
INOP Message, IndicationSourceWhat to do
NO PPV FROM MeasSrv
at Information Center
NO PPV FROM <Device>MMS or
OUT OF AREATelemetryThe telemetry device has left the access point coverage area.
PAP INOPSPRESSSee <Pressure label> INOPS (under Pressure).
PPV BAD <Pressure Label>
SIGNAL
PPV BAD SIGNAL
at Information Center
PPV CHK SOURCESPPVThe 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
PPVThe arterial pressure source selected for PPV is not providing a
PPVThe arterial pressure source selected for PPV is not providing a
PRESSA non-physiological event is detected (for example, a flush or
PRESSA Pressure measurement label in the measurement device or
PRESSContact your service personnel.
PRESSMake sure that the pressure transducer is connected to the
PRESSThis INOP can only arise when a pressure is selected as the
PRESSThis INOP can only arise when a pressure is selected as the
PRESSMake sure that the measurement has been properly prepared
PRESSIncrease 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, IndicationSourceWhat 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 INOPSPredictive
pToral INOPSPredictive
pTrect INOPSPredictive
(!!)PW:Action RequiredProtocol
PW:Check SettingsProtocol
PW in conflictProtocol
PRESSA Pressure measurement label has been deactivated, either by
PRESSPerform 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 INOPsTechnical Alarm Messages (INOPs)
INOP Message, IndicationSourceWhat to do
RA LEAD OFF
Numeric is replaced by -?INOP tone.
ECGThe RA electrode has become detached from the patient or the
lead set has been changed. Reattach the electrode or select
MonitorThere 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.
TelemetryThe 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
RESPContact your service personnel. The RESP hardware is faulty.
Numeric is replaced by -?INOP tone.
RESP ERRATIC
Numeric is replaced by -?-
RESPThe 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 -?-
RESPNot 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.
ECGThe 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 -?-
MonitorThe 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, IndicationSourceWhat to do
<SO2 Label> EQUIP MALF
Numeric displays -?-.
INOP tone
SO2 INCOMPATIBLE
INOP tone
<SO2 Label> IN-VIVO CALSO
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 MALFSO
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 OFFArrhythmia 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
MonitorContact your service personnel to check the speaker and the
connection to the speaker.
SPIRO MALFUNCTIONSpirometry Module failure detected. Contact your service personnel.
SPIRO INCOMPATIBLESpirometry Module revision not compatible with the host monitor
software revision. Contact your service personnel.
SPIRO UPGRADESpirometry The module is running a firmware upgrade. Wait until upgrade
is completed before resuming monitoring.
SPIRO CANNOT MEASSpirometry Measurement is at its limit, e.g. ambient pressure out of range.
77
5 Patient Alarms and INOPsTechnical Alarm Messages (INOPs)
INOP Message, IndicationSourceWhat to do
SPIRO PURGE FAILEDSpirometry 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. SENSORSpirometry An unknown sensor ID code was detected. Use only the sensors
listed in the Accessories chapter.
SPIRO ALARMS SUPPRSpirometry Alarming is suppressed for the spirometry module.
SPIRO PURGINGSpirometry A purge operation is in progress - no data update on the screen.
Wait until purge is complete.
SPIRO NO SENSORSpirometry No sensor detected. Make sure the correct sensor is attached to
the breathing circuit.
SPIRO NO BREATHSpirometry 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, IndicationSourceWhat 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.
MonitorThe short range radio connection has interference from
another device. Try using another channel.
MonitorThe channel configuration of the Short Range Radio is invalid.
Check channel and channel mask configuration.
SRR MALFUNCTIONMalfunction 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 INOPsTechnical Alarm Messages (INOPs)
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
MonitorThe 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.
tcGasA 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.
tcGasCalibration 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.
tcGasWait until the tcpO2/tcpCO2 calibration is finished.
tcGasSite Timer due to time out in 15 minutes or less.
tcGasSite 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
tcGasThere is a malfunction in the transducer or module. Connect
another transducer. If this INOP persists, contact your service
personnel.
tcGasNo transducer is connected to the tcpO2/tcpCO2 module.
Silencing the alarm switches off the measurement.
tcGasThe 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, IndicationSourceWhat 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 INCOMPATIBLEMonitorSRR-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.
tcGasThe measurement is switched on but the module is unplugged.
The measurement automatically disappears from the display.
Silencing this INOP switches off the measurement.
MonitorTelemetry device not supported (companion mode)
TelemetryTelemetry 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.
MonitorThe telemetry device has a malfunction. Disconnect and
reconnect the telemetry device. If the INOP reappears, replace
the telemetry device.
software revision. Please check configuration.
TelemetryCheck for further details at the Information Center or in the
Telemetry Data window on the monitor.
TelemetryThe 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.
MonitorThis telemetry device is not supported for direct connection to
the monitor.
TEMP
Difference
TEMP
Difference
TEMPA Temp measurement label in the measurement device has
TEMPContact your service personnel.
TEMPMake 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 INOPsTechnical Alarm Messages (INOPs)
Numeric is replaced by -?- for 10
seconds; INOP tone.
<VueLink option> CHK
CABLE
INOP tone.
<VueLink option> CHK
CONF.
INOP tone.
TEMPA 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.
TEMPTry 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.
MonitorThe time has expired for the timer indicated in the INOP text.
Clearing the timer clears the INOP.
MonitorThere 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.
MonitorPerform a visual and functional check of all the monitor input
devices. Contact your service personnel.
ECGThe 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.
VueLinkNo 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.
VueLinkThe 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, IndicationSourceWhat to do
<VueLink option> CHECK
SETUP
INOP tone.
VueLnk EQUIP MALF
INOP tone.
VueLnk NO CONFIG
INOP tone.
VueLnk UNPLUGGED
INOP tone.
VueLinkNo 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.
VueLinkMalfunction 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.
VueLinkThe 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.
VueLinkThe 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 INOPsTechnical 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,
1Select the patient name field or select the Admit/Dischrge SmartKey to open the
Patient Demographics window.
85
6 Managing PatientsAdmitting 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.
3Select Admit Patient.
4Enter 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
5Select Confirm. The patient status changes to admitted.
Quick Admitting a Patient6 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.
WARNINGPatient 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.
1Select the Quick Admit SmartKey.
2Enter the required data (ID fields or Last Name depending on configuration) with the keyboard.
3Select Enter.
4In the confirmation window, select Confirm to discharge the previous patient (if confirmation is
configured).
5Check 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 PatientsDischarging a Patient
Discharging a Patient
WARNINGAlways 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,
1Select the patient name field or select the Admit/Dischrge SmartKey to open the
Patient Demographics window and associated pop-up keys.
2Select 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 Patients6 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).
1Remove the MP5 from the host monitor.
2Move the patient using the MP5 as the transport monitor.
3At 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.
4Connect 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?.
5Select 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.
1Select 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.
2At 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?.
3Select Yes to complete the transfer.
4Verify that the settings for patient category and paced mode are correct.
89
6 Managing PatientsTransferring 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 1When 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.
2It 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.
90
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.
Loading...
+ hidden pages
You need points to download manuals.
1 point = 1 manual.
You can buy points or you can get point for every manual you upload.