Documenti di Didattica
Documenti di Professioni
Documenti di Cultura
0614-905519G
Printed: 2014/11/04
Operator’s Manual
Central Monitor
CNS-6201
Keep this manual near the instrument or in the reach of the operator and refer to it whenever the operation is unclear.
This product stores personal patient information. Manage the information appropriately.
Patient names on the screen shots and recording examples in this manual are fictional and any resemblance to any
person living or dead is purely coincidental.
Copyright Notice
The entire contents of this manual are copyrighted by Nihon Kohden. All rights are reserved. No part of this document
may be reproduced, stored, or transmitted in any form or by any means (electronic, mechanical, photocopied, recorded,
or otherwise) without the prior written permission of Nihon Kohden.
Contents 1
8
Section 1 General.................................................................................... 1.1
Introduction....................................................................................................................... 1.3 9
Features.................................................................................................................. 1.4
Central Monitor Composition............................................................................................ 1.6 10
Network Composition Example......................................................................................... 1.7
Operation Restrictions Depending on Monitored Bed Type.................................... 1.8 11
Alarm Function............................................................................................. 1.8
Parameter, Personal and Other Setups........................................................ 1.8 12
Operation Restrictions Depending on Whether Data Is Stored in the Central
Monitor.................................................................................................................... 1.9
13
Dual Display Monitoring.................................................................................................. 1.10
14
Number of Patients on Each Display.................................................................... 1.10
Expand Individual Bed Screen........................................................................................ 1.11
15
Types of Screens and Windows...................................................................................... 1.12
Touch Keys, Keyboard, Mouse and Remote Controller Operation.................................. 1.15 16
Touch Keys Operation........................................................................................... 1.15
Keyboard Operation.............................................................................................. 1.15 17
Mouse Operation.................................................................................................. 1.15
Remote Control Operation.................................................................................... 1.16
Basic Operation.............................................................................................................. 1.17
Basic Operation on the All Beds Screen.............................................................. 1.17
Basic Operation on the Individual Bed Window.................................................... 1.18
Setting the Items................................................................................................... 1.18
Entering Letters and Numbers.............................................................................. 1.19
Using the Screen Keyboard........................................................................ 1.19
Using the Hard Keyboard........................................................................... 1.19
Using the Setting Bar................................................................................. 1.19
Caution Mark.................................................................................................................. 1.21
PU-621R Central Monitor Processing Unit........................................................... 1.21
WS-960P Recorder Unit....................................................................................... 1.21
Transport Function.......................................................................................................... 1.22
Patient Transfer..................................................................................................... 1.22
Review Data Transfer............................................................................................ 1.23
Review Data that can be Transferred.......................................................... 1.23
Precautions on Data Transfer..................................................................... 1.24
13
Section 4 Admitting and Discharging Patients.................................... 4.1
14
Admitting a Patient............................................................................................................ 4.2
Patient Information List........................................................................................... 4.5
15
Importing Patient Information from the Hospital Network....................................... 4.5
Entering Patient Information Using a Bar Code Reader......................................... 4.6
16
Replacing the Current Patient Information with Patient Information from
a Bar Code Reader...................................................................................... 4.7 17
Readmitting a Recently Discharged Patient........................................................... 4.9
Discharging a Patient...................................................................................................... 4.11
Pausing Monitoring of a Patient...................................................................................... 4.14
Pause Timer.......................................................................................................... 4.16
When the Bed Is Paused............................................................................ 4.17
Resume Monitoring.............................................................................................. 4.18
Transferring a Patient to a Different Bedside Monitor..................................................... 4.20
Transferred Data................................................................................................... 4.20
Patient Information and Settings................................................................ 4.20
Review Data............................................................................................... 4.20
Transfer Limitation................................................................................................ 4.21
Transferring a Patient............................................................................................ 4.22
Moving Data from One Monitor to a Different Monitor.................................................... 4.25
Exchanging Two Beds..................................................................................................... 4.29
Changing the Receiving Channel Number..................................................................... 4.32
Other.......................................................................................................... 8.11
Recording on the Individual Bed Window....................................................................... 8.12
Manual Recording................................................................................................ 8.12
Settings for Manual Recording................................................................... 8.12
Recording Example.................................................................................... 8.12
Individual Bed Window Printing............................................................................ 8.13
Other Recordings................................................................................................. 8.13
Performance............................................................................................... 17.6
LCD Display................................................................................................ 17.6
Environment............................................................................................... 17.6
Power Requirements.................................................................................. 17.6
Acoustic Energy (noise)............................................................................. 17.7
Mechanical Strength................................................................................... 17.7
Dimensions and Weight (approximate, without protrusion)........................ 17.7
Safety Standard.......................................................................................... 17.7
Electromagnetic Compatibility.................................................................... 17.8
Electromagnetic Emissions........................................................................ 17.9
Electromagnetic Immunity.......................................................................... 17.9
Recommended Separation Distances between Portable and Mobile RF
Communications Equipment.................................................................... 17.11
System Composition for EMC Test........................................................... 17.11
Restriction of Radio Equipment (European Union countries only)........... 17.12
European Community CE Notice............................................................. 17.12
Standard Accessories................................................................................................... 17.13
PU-621R Central Monitor Processing Unit......................................................... 17.13
Options and Consumables........................................................................................... 17.13
PU-621R Central Monitor Processing Unit......................................................... 17.13
LCD Display........................................................................................................ 17.14
WS-960P Recorder Unit..................................................................................... 17.14
General Requirements for Connecting Medical Electrical Systems.............................. 17.15
Please read these precautions thoroughly before attempting to operate the instrument.
1. To safely and effectively use the instrument, its operation must be fully understood.
3. Before Operation
(1) Check that the instrument is in perfect operating order.
(2) Check that the instrument is grounded properly.
(3) Check that all cords are connected properly.
(4) Pay extra attention when the instrument is combined with other instruments to avoid misdiagnosis or other
problems.
(5) All circuitry used for direct patient connection must be doubly checked.
(6) Check that battery level is acceptable and battery condition is good when using battery-operated models.
4. During Operation
(1) Both the instrument and the patient must receive continual, careful attention.
(2) Turn power off or remove electrodes and/or transducers when necessary to assure the patient’s safety.
(3) Avoid direct contact between the instrument housing and the patient.
6. The instrument must receive expert, professional attention for maintenance and repairs. When the instrument is
not functioning properly, it should be clearly marked to avoid operation while it is out of order.
9. When the instrument is used with an electrosurgical instrument, pay careful attention to the application and/or
location of electrodes and/or transducers to avoid possible burn to the patient.
10. When the instrument is used with a defibrillator, make sure that the instrument is protected against defibrillator
discharge. If not, remove patient cables and/or transducers from the instrument to avoid possible damage.
WARRANTY POLICY
Nihon Kohden Corporation (NKC) shall warrant its products against all defects in materials and workmanship for one year
from the date of delivery. However, consumable materials such as recording paper, ink, stylus and battery are excluded
from the warranty.
NKC or its authorized agents will repair or replace any products which prove to be defective during the warranty period,
provided these products are used as prescribed by the operating instructions given in the operator’s and service manuals.
No other party is authorized to make any warranty or assume liability for NKC’s products. NKC will not recognize any
other warranty, either implied or in writing. In addition, service, technical modification or any other product change
performed by someone other than NKC or its authorized agents without prior consent of NKC may be cause for voiding
this warranty.
Defective products or parts must be returned to NKC or its authorized agents, along with an explanation of the failure.
Shipping costs must be pre-paid.
This warranty does not apply to products that have been modified, disassembled, reinstalled or repaired without Nihon
Kohden approval or which have been subjected to neglect or accident, damage due to accident, fire, lightning, vandalism,
water or other casualty, improper installation or application, or on which the original identification marks have been
removed.
CAUTION
United States law restricts this product to sale by or on the order of a physician.
The following describes some common interference sources and remedial actions:
1. Strong electromagnetic interference from a nearby emitter source such as an authorized radio station
or cellular phone:
Install the equipment and/or system at another location. Keep the emitter source such as cellular phone
away from the equipment and/or system, or turn off the cellular phone.
2. Radio-frequency interference from other equipment through the AC power supply of the equipment
and/or system:
Identify the cause of this interference and if possible remove this interference source. If this is not
possible, use a different power supply.
4. Electromagnetic interference with any radio wave receiver such as radio or television:
If the equipment and/or system interferes with any radio wave receiver, locate the equipment and/or
system as far as possible from the radio wave receiver.
5. Interference of lightning:
When lightning occurs near the location where the equipment and/or system is installed, it may induce
an excessive voltage in the equipment and/or system. In such a case, disconnect the AC power cord
from the equipment and/or system and operate the equipment and/or system by battery power, or use
an uninterruptible power supply.
If the above suggested remedial actions do not solve the problem, consult your Nihon Kohden
representative for additional suggestions.
The CE mark is a protected conformity mark of the European Community. Products with the CE mark
comply with the requirements of the Medical Device Directive 93/42/EEC.
This equipment complies with EUROPEAN STANDARD EN-60601-1-2: 1993 which requires EN-55011,
class A. Class A EQUIPMENT is allowed in domestic establishments when used under the jurisdiction of
a health care professional.
NOTE about Waste Electrical and Electronic Equipment (WEEE) Directive 2002/96/EC
For the member states of the European Union only:
The purpose of WEEE directive 2002/96/EC is, as a first priority, the prevention of waste electrical and
electronic equipment (WEEE), and in addition, the reuse, recycling and other forms of recovery of such
wastes so as to reduce the disposal of waste.
Contact your Nihon Kohden representative for disposal.
• Austria
• Belgium
• Cyprus
• Czech Republic
• Denmark
• Estonia
• Finland
• France
• Germany
• Greece
• Hungary
• Iceland
• Ireland
• Italy
• Latvia
• Liechtenstein
• Lithuania
• Luxembourg
• Malta
• The Netherlands
• Norway
• Poland
• Portugal
• Slovakia
• Slovenia
• Spain
• Sweden
• Switzerland
• The U.K.
Notice:
• The available transmitter is different depending on the states. For details, contact your Nihon Kohden
representative.
• Refer to “Restriction of Radio Equipment (European Union countries only)” in the “Specifications”
section for more details.
• This device is also authorized for use in Norway in accordance with regulation No.1399 of 20
December 2000.
As this equipment complies with Class 1.7 (Receive-only radio equipment), “Alert Sign” is not displayed.
This equipment complies with International Standard IEC 60601-1-2: 2001 and Amendment 1: 2004 which
require CISPR11, Group 1, Class B. Class B EQUIPMENT is equipment suitable for use in domestic
establishments and in establishments directly connected to a low voltage power supply network which
supplies buildings used for domestic purposes.
WARNING
A warning alerts the user to possible injury or death associated with the use or misuse of the instrument.
CAUTION
A caution alerts the user to possible injury or problems with the instrument associated with its use or
misuse such as instrument malfunction, instrument failure, damage to the instrument, or damage to other
property.
NOTE
A note provides specific information, in the form of recommendations, prerequirements, alternative methods or
supplemental information.
On Screen
Print Settings
Printer disconnected
Calibrate touch key
Printer error
Alarm volume 1 to 3
Transmitter battery status*2
Alarm volume 4 to 6
Alarm volume 7
*1 On the All Beds Alarms window and Discharged Patients List window only.
*2 Only available for transmitters with a transmitter battery status display function and setting on the transmitter is
required. Refer to the transmitter operator’s manual.
USB0/USB1/USB2/USB3/USB4/
Attention, consult operator’s manual
USB5 connector
The CNS-6201 Central Monitor comes with the following manuals in addition to the Operator’s Manual.
Administrator’s Guide
Describes how to install the central monitor. It also explains about the password protected settings which only an
administrator can change.
Service Manual
Describes information on servicing the central monitor. Only qualified service personnel can service the central monitor.
Introduction........................................................................................................................................................... 1.3
Features..................................................................................................................................................... 1.4
Central Monitor Composition................................................................................................................................ 1.6
Network Composition Example............................................................................................................................ 1.7
Operation Restrictions Depending on Monitored Bed Type........................................................................ 1.8
Alarm Function................................................................................................................................. 1.8
Parameter, Personal and Other Setups........................................................................................... 1.8
Operation Restrictions Depending on Whether Data Is Stored in the Central Monitor............................... 1.9
Dual Display Monitoring...................................................................................................................................... 1.10
Number of Patients on Each Display........................................................................................................ 1.10
Expand Individual Bed Screen........................................................................................................................... 1.11
Types of Screens and Windows.......................................................................................................................... 1.12
Touch Keys, Keyboard, Mouse and Remote Controller Operation..................................................................... 1.15
Touch Keys Operation.............................................................................................................................. 1.15
Keyboard Operation................................................................................................................................. 1.15
Mouse Operation...................................................................................................................................... 1.15
Remote Control Operation....................................................................................................................... 1.16
Basic Operation.................................................................................................................................................. 1.17
Basic Operation on the All Beds Screen.................................................................................................. 1.17
Basic Operation on the Individual Bed Window........................................................................................ 1.18
Setting the Items...................................................................................................................................... 1.18
Entering Letters and Numbers................................................................................................................. 1.19
Using the Screen Keyboard........................................................................................................... 1.19
Using the Hard Keyboard............................................................................................................... 1.19
Using the Setting Bar..................................................................................................................... 1.19
Caution Mark...................................................................................................................................................... 1.21
PU-621R Central Monitor Processing Unit............................................................................................... 1.21
WS-960P Recorder Unit........................................................................................................................... 1.21
Transport Function.............................................................................................................................................. 1.22
Patient Transfer......................................................................................................................................... 1.22
Review Data Transfer............................................................................................................................... 1.23
Review Data that can be Transferred............................................................................................. 1.23
Precautions on Data Transfer......................................................................................................... 1.24
Important Safety Information.............................................................................................................................. 1.25
General..................................................................................................................................................... 1.25
CPU Reset............................................................................................................................................... 1.26
Installation................................................................................................................................................ 1.27
Network.................................................................................................................................................... 1.28
Turning the Power On or Off..................................................................................................................... 1.29
Transmitter................................................................................................................................................ 1.29
Admission, Discharge and Changing the Receiving Channel.................................................................. 1.30
Pause Monitoring..................................................................................................................................... 1.30
Changing Monitor..................................................................................................................................... 1.30
Introduction
WARNING
Do not diagnose a patient based only on data acquired by the central
monitor. Overall judgement must be performed by a physician who
understands the features, limitations and characteristics of the
central monitor and by reading the biomedical signals acquired by
other instruments.
NOTE
• Upgrade the central monitor processing unit and each optional unit
to the Nihon Kohden recommended software version. Only use the
specified configuration of units. If more than one CNS-6201 central
monitor is used in the same facility, make sure the central monitors
have the same software version. If CNS-6201 central monitors with
different software versions are used together, correct system operation
cannot be guaranteed.
• The Alarm CAP function is available on the following bedside monitors,
central monitors and multiple patient receivers.
- BSM-9101A software version 13-03 or later
- BSM-6000A series software version 04-01 or later
- CNS-9701A software version 01-95 or later
- CNS-6201 (PU-621R Op No. 21A) software version 02-10 or later
- ORG-9100A or ORG-9110A software version 03-06 or later
- ORG-9700A software version 03-06 or later
For details on Alarm CAP function, refer to manual for each instrument
of the above and Section 6-1 of the CNS-6201 Administrator’s Guide.
For the parameter settings, refer to Section 6-1 of the Administrator’s Guide.
The PU-621R Central Monitor Processing Unit can be installed horizontally
or vertically. This manual shows it in the horizontal position. Refer to the
“Attaching the Rubber Feet” in Section 1 of the Administrator’s Guide.
The option number (Op No.) is printed on the name plate of the unit.
For simplicity, the suffix A/K is omitted in this manual. There is no difference in
operation among models with different suffixes unless otherwise specified.
Features
Read the manuals for the bedside monitors, transmitters and multiple patient
receiver together with this manual.
• 32 patient monitoring
Up to 32 patients can be monitored with one display. (QP-627P 32 Patient
Software is required) For details, refer to Section 1.
• Remote control
When a YL-611P or YL-612P Alarm Indicator is connected to the PU-621R
Central Monitor Processing Unit, the central monitor can be operated with an
RY-910PA Remote Controller. For details, refer to Section 1.
• Review data 1
The past data of the selected patient can be displayed in various formats on the
review windows. Two review windows can be displayed on the same screen.
For details, refer to Section 9.
• Function keys
The All Beds screen and each monitored bed have functions keys. Central
monitor and other functions can be assigned to the function keys. For details,
refer to Administrator’s Guide.
YS-098P1/YS-098P2
YL-611P/YL-612P Alarm Indicator WS-960P Recorder Unit
Additional Alarm Indicator Unit
1
Network Composition Example
The central monitor shows data of any bed in the central monitor network. The
bedside monitor can show data of any bed in the network using the interbed
function.
The number of central monitors and bedside monitors that can be connected to
a central monitor network and the method of network communication depend
on the type of monitor used. For details, refer to the Network and System
Installation Guide.
Network group Central monitor Central monitor
e.g. ICU Example: CNS-9701 CNS-6201
CNS-9601
Printer
Transmitter
Interface
QI-910R
Transmitter
Multiple patient receiver Transmitter Bedside monitor Bedside monitor Bedside monitor
The models for the monitor, transmitter and multiple patient receiver
are the same as those for the ICU group.
WARNING WARNING
Install all network devices, including printer and Check the software version number of the central
hubs, outside the patient environment (IEC monitor before connecting it to the network.
60601-1-1). If they are installed inside the patient Different software versions have different
environment, the patient or operator may receive communication methods. More than one
electrical shock or injury. For installation, contact communication method in a network may cause
your Nihon Kohden representative. communication failure. For details, refer to the
Network and System Installation Guide.
Alarm Function
Alarm Function
Monitored Bed Type Temporarily
Temporarily Turning Alarm
Silence Priority
Suspend alarms On or Off
Alarms
Multiple patient receiver Setting on the central
Available Not available
with transmitter monitor
Not available.
The alarm priority at the
The alarm suspend
central monitor coincides
functions on the
with the alarm priority at the
transmitter or
BSM series bedside Temporarily silence bedside monitor.
bedside monitor
monitor any current alarms Not available
suspends all alarm
When all alarms The alarm priority settings
functions.
are set to OFF on at the bedside monitor are
the bedside monitor synchronized.
which has a all The alarm priority at the
alarms off function, central monitor does not
Not available. the alarm function is coincide with the alarm
BSM series bedside The alarm suspend OFF on the central priority at the bedside
Temporarily silence
monitor through key suspends all monitor. monitor.
all alarm functions
QI-910R interface alarms when there
is no alarm. The settings at the bedside
monitor and central monitor
are not synchronized.
Personal Setup
Monitored Bed Type
Alarm Settings Other Settings
BSM series bedside
The settings at the bedside
monitor Some of the setting items that can be set on
monitor and central monitor are
BSM series bedside the bedside monitor can also be set on the
synchronized. Changing one changes
monitor through central monitor.
the other.
QI-910R interface
Multiple patient receiver
Can be set on the central monitor.
with transmitter
NOTE
BSM in the table includes bedside monitors that receive or display data
from a transmitter connected to the patient.
* You can enter and edit patient data for an admitted bed whose data is not
saved in the central monitor. Changing a bed name or group operation cannot
be used.
Monitored bed
A monitored bed is a bed which is registered on the Monitor Setting window of
the System Setup and is continuously monitored at the central monitor.
The number of patients on each display is set on the [Monitor Setting] → [Screen
Composition] on the System Setup screen. Refer to “Screen Composition” in
Section 6-1 of the Administrator’s Guide.
The central monitor can monitor up to 32 patients with main and second display
together.
• When 16 patients are monitored on one display, 2 to 16 patients can be
monitored on the other display.
• When 32 patients are monitored on one display, only the Expand Individual
Bed screen can be displayed on the other display.
1
Expand Individual Bed Screen
When monitoring with dual displays, you can set one display to All Beds screen
and the other display to Expand Individual Bed screen.
Monitoring
All Beds Screen (Refer to Section 6) Individual Bed Window (Refer to Section 8)
Admit/Discharge Window (Refer to Section 4) All Beds Alarms Window (Refer to Section 7)
Alarm Setting Window (Refer to Section 5) Recording Window (Refer to Section 10)
Report Window (Refer to Section 10) Display Window (Refer to Section 6 and 8)
Parameter Setup Window (Refer to Section 12) System Setup Screen (Refer to Section 13)
1
Touch Keys, Keyboard, Mouse and Remote Controller
Operation
The operation of the central monitor is controlled through the touch keys, mouse,
keyboard and remote controller.
To operate, directly touch an area of the screen with your finger. When the key is
touched, there is a pip sound.
In this manual, directly touching the XX key on the screen with your finger is
referred to as “Touch [XX]”.
Example: Touch [Menu].
Keyboard Operation
From the keyboard, you can enter letters and numbers. When the ENTER key is
pressed, there is a pip sound.
In this manual, pressing the XX key on the keyboard is referred to as “Press the
XX key”.
Mouse Operation
Mouse input is also available throughout the screens. Click items and menus on
the screen to select them. This technique has basically the same effect on screen
operations as the touch keys operation.
Press the keys on the remote control to display or close a window. Move the
selection knob up, down, left or right to scroll the data or select a setting then
press the ENTER key to register the setting.
There is a pip sound when a key on the remote control is pressed or the selection
knob is moved to scroll the data.
NOTE
• Watch the monitor screen and check the operation when using the
remote control to avoid wrong operation.
• Make sure that the remote control is handled appropriately.
Transmitter
Point the transmitter to
the remote control sensor
on the alarm indicator
LED when operating the
Lights when the pointer on monitor with the remote
the screen is moved by the control.
selection knob. Blinks when a
key on the remote control is pressed.
Power button
POWER
Not available
Selection knob
Move this knob up, down,
left or right to move the cursor
MENU/HOME key or mouse pointer on the
SILENCE Enter key
Not available MENU/HOME ALARMS screen.
Registers the setting
selected on the screen.
SILENCE ALARMS
key
Customized keys
Not available
Not available
CHANNEL keys
DISPLAY
SELECT CHANNEL
Select the monitor when a
channel is assigned to
DISPLAY SELECT key the monitor.
Not available
Display
Displays the channel Battery cover
number and the display Contains two AAA
number. batteries.
Display number
Strap hole
Use a strap to prevent Channel number
dropping the remote control.
1
Basic Operation
Menu
Displays each window.
Menu
Same as the All Beds screen.
Displays the Individual Bed Window Menu Displays the Setup Menu.
where you can change the window to the Touch each item to change the
Individual Waveforms window, Individual window. Touch again to close
Numeric Vital Signs window or ECG 12 the Setup Menu.
Leads window. Touch again to close the
Individual Bed Window Menu.
2. Touch the desired key. Depending on the setting item, select or deselect
changes or setting window is displayed.
Touch [ON].
Setting bar
Touch the bar to change the settings.
1
Caution Mark
This section explains the caution mark on the instrument and indicates where
to find the information. Read the instructions to fully understand how to use the
instrument safely and appropriately.
CAUTION
While the central monitor is on, do not touch unused sockets or cables
connected to the sockets. Failure to follow this instruction may damage
the central monitor by static electricity and cause malfunction.
Transport Function
When the input unit is transported between bedside monitors and the transport
function is enabled on the bedside monitors, patient transfer and review data
transfer are done on the central monitor automatically.
WARNING
When using the transport function:
• Do not connect or disconnect the network cable from the bedside
monitors and central monitor.
• Do not perform the following operations on the bedside monitor
which is being monitored and whose data is saved by the central
monitor. Patient data may be mixed together or lost in the following
cases:
• Removing the input unit while the bedside monitor power is off.
• Using transport function and wireless LAN at the same time.
WARNING
When using the transport function, use 10 BASE-T/100 BASE-TX
switching hubs for the entire network. If you use another type of hub,
the network may intermittently lose connection and the patient
cannot be monitored on the central monitor.
Patient Transfer
When the transport function is enabled at the bedside monitors in the central
monitor network and the input unit is disconnected from the source bedside
monitor and connected to the destination bedside monitor, patient transfer is
automatically performed on the central monitor.
CAUTION
If there are too many patient transfers, old review data might not be
displayed on the central monitor.
CAUTION
Do not remove the input unit from the bedside monitor while the
central monitor is receiving data from the bedside monitor. The data
may be lost.
NOTE
• Only the data saved in the input unit can be transferred. Refer to the
bedside monitor operator’s manual.
• Alarm history data cannot be transferred.
Review Data
• The last 90 seconds of a full disclosure waveform which is sent from the
bedside monitor might not be displayed on the central monitor.
• The trendgraph data from the bedside monitor might not have the event
information.
• The full disclosure data from the bedside monitor does not have the
arrhythmia information. The waveforms might not be displayed with
arrhythmia color on the Full Disclosure window of the central monitor.
Other
• While data is being sent from a bedside monitor to the central monitor,
you cannot transfer a patient to or from that monitor, exchange the
monitoring beds or change the monitor.
• When the data of a bedside monitor which has “COMMUNICATION
LOSS” status is deleted on the central monitor and then that bedside
monitor is connected to the network, the data is sent to the central
monitor and part of the old review data for that bedside monitor may be
displayed on the central monitor.
• When you pause monitoring of a bed while data is being sent from the
bedside monitor to the central monitor, the data sending may stop.
• If you change the date and time while sending data from a bedside
monitor, the data sending may stop.
1
Important Safety Information
General
WARNING WARNING
Never use the central monitor in the presence of Never use the central monitor in a hyperbaric
any flammable anesthetic gas or high oxygen chamber. Failure to follow this warning
concentration oxygen atmosphere. Failure to may cause explosion or fire.
follow this warning may cause explosion or fire.
WARNING WARNING
Do not install or run any software not specified by Do not monitor the patients over the number of
Nihon Kohden in the central monitor. Nihon receivers in a multiple patient receiver (up to 8
Kohden does not warrant normal operation of the patients) by changing the channels. The patient’s
CNS-6201 system program if unspecified data will be mixed together. It can only monitor
software is installed or used. the patients who are set at the receiving channels
in the central monitor. You cannot know the
information if there is a sudden change in
condition of a patient who is not set in the central
monitor.
WARNING WARNING
After attaching electrodes, probes and sensors Do not diagnose a patient based only on data
on the patient and connecting cables to the acquired by the central monitor. Overall
bedside monitor and/or transmitter, check that judgement must be performed by a physician
there is no error messages and the waveforms who understands the features, limitations and
and numeric data are appropriately displayed on characteristics of the central monitor and by
the screen. If there is an error message, or reading the biomedical signals acquired by other
waveform or numeric data is not appropriate, instruments.
check the electrodes, probes and sensor
attachment, patient condition and settings on the
WARNING
bedside monitor and/or transmitter and remove
When monitoring with two displays, do not turn
the cause.
off either display. Some monitored beds cannot
be monitored.
WARNING
While the central monitor is on, do not connect
WARNING
any external devices such as USB memory.
Do not turn off the display to which the speaker
Nihon Kohden does not warrant the normal
cable is connected. The alarm sound cannot be
operation of the central monitor if an application
heard.
or software installation starts automatically.
CAUTION CAUTION
While the central monitor is on, do not touch If fluids are accidentally spilled into the central
unused sockets or cables connected to the sockets. monitor, take the central monitor out of service
Failure to follow this instruction may damage the and contact your Nihon Kohden representative.
central monitor by static electricity and cause The central monitor must be disassembled,
malfunction. cleaned, dried and tested for safety and function.
CAUTION
When receiving data from a transmitter
connected to the bedside monitor or a transmitter
which has a display, the measurement data and
waveforms may be different on the central
monitor depending on the detection setting and
display timing. Be aware of this when reading the
measurement data and waveforms.
CPU Reset
CAUTION
The central monitor CPU may be reset when
there is unit failure, considerable static electricity
or noise and monitoring stops for about
3 minutes. If this occurs, there is a 5-beep alarm
sound for 5 seconds. After the central monitor is
reset, check that it is working properly.
Installation 1
WARNING WARNING
Install the central monitor outside the patient Make sure that the speaker cable is connected to
environment (IEC 60601-1-1). If the central the display and main unit. Otherwise the alarm
monitor are installed inside the patient sound cannot be heard.
environment, the patient or operator may receive
electrical shock or injury. For installation, contact
your Nihon Kohden representative.
CAUTION CAUTION
Connect only the specified instrument to the When installing, connecting and assembling the
central monitor and follow the specified central monitor, only use specified instruments
procedure. Failure to follow this instruction may and parts and follow the specified procedure.
result in electrical shock or injury to the operator, Otherwise, the operator may receive electrical
and cause fire or instrument malfunction. shock or injury.
CAUTION CAUTION
Only use the provided power cord. Using other Keep the cable out of the way by running it along
power cords may result in electrical shock or the floor or wall. Otherwise people may trip over
injury to the operator. it, causing the instrument to fall and injure the
patient and operator.
CAUTION CAUTION
Before connecting or disconnecting instruments, Turn off the power of mobile phones, small
make sure that each instrument is turned off and wireless devices and other devices which
the power cord is disconnected from the AC produce strong electromagnetic interference
socket. Otherwise, the patient or operator may around a patient (except for devices allowed by
receive electrical shock or injury. the hospital administrator). Radio waves from
devices such as mobile phones or small wireless
devices may be mistaken as pulse waves and the
displayed data may be incorrect.
CAUTION CAUTION
Connect the power cord to an AC outlet which If the power is turned off while the central monitor
can supply sufficient AC current to the central is used, the hard disk may be damaged and data
monitor. The central monitor cannot function may be lost.
properly with low current. Also the breaker trips
and it causes electric power failure.
Network
WARNING WARNING
Connect the central monitor to the network as Install all network devices, including printer and
specified in the Network and System Installation hubs, outside the patient environment (IEC
Guide. Otherwise the patient and operator may 60601-1-1). If they are installed inside the patient
receive electrical shock or injury. To connect the environment, the patient or operator may receive
network, contact your Nihon Kohden electrical shock or injury. For installation, contact
representative. your Nihon Kohden representative.
WARNING WARNING
Do not use a damaged network cable. The patient Check the software version number of the central
or operator may receive electrical shock when the monitor before connecting it to the network.
damaged part is touched. Different software versions have different
communication methods. More than one
communication method in a network may cause
WARNING
communication failure. For details, refer to the
Do not diagnose a patient based on alarm
Network and System Installation Guide.
information of an instrument which can view the
data by setting [Extended Network] to [ON].
There is a time delay. Confirm the alarm
information on this central monitor.
CAUTION CAUTION
The network and system must be managed by The network must be managed by the network
the network or system administrator. Incorrect administrator. Make sure that each instrument in
settings may cause instrument or network failure. the network has a different IP address.
Otherwise, data communication cannot be
performed properly. When adding an instrument
to an already operating network, set the IP
address on the instrument before connecting the
instrument to the network.
CAUTION CAUTION
The system should be used in a closed network When the monitor is connected to a central
to prevent computer viruses and unexpected monitor network, set the Bed Name or CNS
software updates. Name and Group Name on the monitor.
Otherwise, the default settings are used for the
names and the bed may be incorrectly identified
on the central monitor.
CAUTION CAUTION
Follow the specified procedure to turn off the When the central monitor is first turned on and
central monitor. Otherwise, patient data will be periodically during operation, check that the red,
deleted and the storage device and data in the yellow, cyan and green alarm indicator lamps
storage device may be damaged. light and sound is generated.
Transmitter
WARNING
The following actions must be taken to properly
receive the transmitter signal of the correct
patient on the receiving instrument. Otherwise,
there may be signal loss or signals may mix
causing a serious accident, such as monitoring a
different patient.
• Assign a channel administrator in the hospital
and only he or she should manage channel
assignment.
• The channel administrator must manage the
channels in the facility so that there is no signal
interference.
• When the transmitter channel is changed,
the channel administrator must check that
the channel on the receiving monitor is also
changed and the signal is properly received.
• The channel administrator must replace the
channel number label on the transmitter with
the new one after changing the channel.
WARNING WARNING
Check that the channel number of the transmitter After admitting a patient at a bedside monitor,
corresponds to the receiving channel (the confirm that the patient is also admitted at the
channel displayed on the monitor screen). central monitor and that the central monitor starts
Otherwise, the central monitor monitors a monitoring the patient.
different patient.
CAUTION CAUTION
When admitting a new patient, first discharge the When you change the receiving channel to monitor
previous patient and delete all data of the a new patient, discharge the previous patient and
previous patient. Otherwise, the data of the admit a new patient. If you only change the channel
previous patient and new patient will be mixed and does not delete the previous patient data, the
data of the previous patient and new patient will be
together.
mixed together and it will cause misunderstanding
of the patient history.
CAUTION
When admitting a new patient, check that the
patient information is entered correctly.
Pause Monitoring
WARNING
When the bed is set to automatically resume
monitoring after pause, check that monitoring is
resumed at the central monitor when the pause
condition is ended. Monitoring might not resume
if there is network failure.
Changing Monitor
CAUTION CAUTION
Keep the current bedside monitor and the new If the monitoring bed is changed to a different
bedside monitor power on and connected to the monitor on a central monitor other than CNS-
network until the monitor is changed. Otherwise 6201, the monitoring bed does not change on this
the patient data is lost. After changing the central monitor. Register the bed again on this
monitor, confirm that the data and settings before central monitor. Otherwise, the patient data might
changing the monitor are displayed in the new not be displayed or data of a different patient may
monitor. be displayed on this central monitor.
CAUTION CAUTION
Keep the source bedside monitor and the When transferring a patient, confirm the
destination bedside monitor power on and destination bed you want to transfer by the
connected to the network until the patient transfer message on the screen. If you select the wrong
or bed exchange is complete. Otherwise the destination bed, the patient data of the source
patient transfer or bed exchange fails and the bed overwrites the patient data of the destination
data is lost. After transferring or exchanging the bed and the overwritten data cannot be
patient, confirm that the data before the patient recovered.
transfer or bed exchange can be displayed at the
destination bed.
CAUTION
After patient transfer, settings other than patient
information and alarm settings are returned to the
default settings. Change the settings if necessary.
Patient Transfer (When the destination bed’s data is saved on a central monitor other than CNS-6201)
CAUTION
If there are too many patient transfers, old review
data might not be displayed on the central
monitor.
Recorder Unit
CAUTION
Do not touch the thermal head inside the
recorder unit. The thermal head may be damaged
by static electricity or become dirty and cause
printing failure.
Remote Controller
WARNING
• Keep the batteries away from fire. They may
explode.
• Keep the batteries away from patients.
• Never short-circuit the + and – terminals on the
battery. It may cause overheating and fire.
• Do not damage, disassemble, drop or give
impact to the battery.
CAUTION
• Set the remote control channel on the monitor
to prevent the remote control from operating a
different monitor.
• When several monitors are installed close
together, check that the remote control
operates only the desired monitor. If the remote
control operates a different monitor, recheck the
channel setting.
Alarm 1
WARNING WARNING
When alarm is suspended at the transmitter, all When the [Communication Loss Alarm] is set to
alarms are turned off for that transmitter. Be [Only Message], there will be no communication
careful when you suspend the alarm. loss alarm. When it is set to [Only Message],
always pay careful attention to the
communication status.
WARNING WARNING
When admitting a new patient, confirm alarm When an alarm occurs:
settings. Also check the alarm settings during • Check the patient first and take necessary
monitoring and change the settings according to measure to ensure patient’s safety.
the patient condition. For a bed monitored • Remove the cause of the alarm.
through a multiple patient receiver, the alarm • Check the alarm settings on the central monitor
settings change to the [Alarm Master 1] settings and change the alarm settings if necessary.
in the following cases:
• When the bed is discharged
WARNING
• When you touch the [Delete Data] key on the
Do not diagnose a patient based on only the
Admit/Discharge window
alarm information of the central monitor. An alarm
• When you delete all data of the bed when the
may not be indicated due to alarm level or alarm
receiving channel is changed
on/off setting and critical changes on the patient
may be overlooked.
WARNING WARNING
A physician must be within the range where he/ If more than one medical equipment is used
she can hear the alarm sound of the central together in the same facility, make sure all
monitor while monitoring a patient on the central equipments have the same alarm default settings
monitor. If the physician cannot hear the alarm (alarm master). If the medical equipments have
sound, critical changes on the patient may be different alarm default settings and when
overlooked. initialized, the alarm settings differ with the other
equipments and alarm cannot be managed
appropriately in the facility. If using different alarm
default settings according to areas or wings in the
facility, manage the alarms appropriately.
CAUTION CAUTION
When the alarm limit is set to [OFF], there will be When the [Communication Loss Alarm] in the
no alarm for that limit. Be careful when you set [Single Sound] mode is silenced, an alarm for the
the alarm limit to [OFF]. same alarm condition does not occur again while
communication is still lost. In [Single Sound]
mode, always pay careful attention to the
CAUTION
communication status.
When the alarm is turned [OFF] for an
arrhythmia, there will be no alarm for that
arrhythmia type. There is no message or mark to
indicate that a certain arrhythmia alarm is turned
off. Therefore, be careful when you turn off an
arrhythmia alarm.
CAUTION CAUTION
When receiving bedside monitor data through a While the “SIGNAL LOSS” message is displayed,
ZB-800P, ZB-900P or ZS-900P transmitter, check parameters are not monitored and the alarms do
the alarm settings on the bedside monitor and not function. Check the transmitter and
central monitor. The alarm setting information of communication status and remove the cause.
the bedside monitor is not transmitted.
CAUTION CAUTION
When monitoring SpO2 only, arrhythmia and When monitoring SpO2 only, do not set upper/
asystole are not detected. The transmitter does lower limit alarms for PR and SpO2 to OFF on the
not monitor ECG if the electrode lead is not receiving monitor. Even when the lower limit
connected. Arrhythmia analysis, such as alarm is not set to OFF, PR and SpO2 alarms do
ASYSTOLE, V FIB or V TACHY, is not performed not occur if there is no pulse on a patient. In this
and arrhythmia alarms do not occur. Also, upper/ case, “---” is displayed for PR and SpO2 on the
lower limit alarms related to SpO2 do not occur transmitter display and a technical alarm such as
when the transmitter cannot detect pulse wave CANNOT DETECT PULSE or SpO2 CHECK
properly due to asystole. When ECG is needed to PROBE occurs on the receiving monitor.
be measured, monitor ECG.
CAUTION
When the “CONNECTOR OFF” message
appears on the screen, check that the connection
cords are connected to the sockets properly. The
patient cannot be monitored and the alarm does
not function while this message is displayed.
ECG Monitoring 1
WARNING WARNING
Turn the pacing pulse detection* to [ON] when Even when the pacing pulse detection is set to
monitoring a pacemaker patient. Otherwise the [ON], the pacemaker pulse can be overlooked or
pacemaker pulse is not rejected. However, even detected as QRS. You cannot confirm the
when the pacing pulse detection is set to [ON], pacemaker operation only from the detected
the pacemaker pulse might not be rejected. When pacemaker pulse.
the pacemaker pulse is not rejected, the
pacemaker pulse is detected as QRS and false
WARNING
heart rate may be indicated or critical arrhythmia
For arrhythmia monitoring, set [Arrhythmia
such as asystole may be overlooked. Keep
Analysis] on the ECG window to [ON]. Otherwise,
pacemaker patients under close observation.
there is no sound or indication for arrhythmia
* For the pacemaker pulse rejection capability, refer to the alarms (except for ASYSTOLE).
operator’s manual of the monitoring device.
CAUTION CAUTION
When the [ECG Measurement] is [OFF], ECG The central monitor does not perform ECG
alarms do not occur even if each ECG alarm item is analysis. Therefore, the QRS sync sound at the
set to [ON]. central monitor might not synchronize with the
patient’s actual QRS during pacing or when
complicated arrhythmias occur.
CAUTION CAUTION
If there is any doubt about the arrhythmia The QRS sound at the central monitor has a time
analysis, make the monitor relearn the patient’s delay of several seconds because of network
ECG and check that the dominant QRS is connection.
appropriate. Otherwise, an important arrhythmia
may be overlooked.
CAUTION CAUTION
• Although the ST algorithm has been tested When the full disclosure waveform is expanded in
for accuracy of the ST analysis result, the actual size, steep slopes such as QRS may be
significance of the ST level changes need to be distorted because it has been compressed then
determined only by a physician. expanded. When reading the expanded ECG
• The ECG from transmitters other than ZM waveforms, be aware of this distortion.
series is not processed by a 3.2 second
time constant filter. Therefore, the ST level
measurement of other transmitters is not
designed to be accurate enough for diagnosis.
Do not rely on this ST level measurement.
CAUTION CAUTION
When the “CHECK LEADS” message is When the “NOISE” or “CANNOT ANALYZE”
displayed, ECG is not monitored properly and the message is displayed, ECG data and alarm are
ECG alarm does not function. Check the not reliable. Remove the cause by checking the
electrode, electrode leads and connection cord, electrodes, electrode leads, patient’s body
and if necessary, replace with new ones. movement, EMG and peripheral instruments
grounding. Also check that no electric blanket is
used.
Respiration Measurement
CAUTION
When measuring respiration by impedance
method and [Impedance Respiration
Measurement] on the RESP window is set to
[OFF], respiration alarms do not occur even if
each respiration alarm item is set to [ON].
SpO2 Monitoring
CAUTION CAUTION
When the probe is attached on an appropriate The sensitivity of the pulse waveform measured
site with sufficient circulation and an error by a ZM-930P transmitter is automatically
message about probe attachment repeatedly changed inside the transmitter. When the
appears, the probe may be deteriorated. Replace sensitivity is changed, the waveform becomes flat
it with a new one. for about one second.
NIBP Measurement 1
WARNING
When performing long term measurement at
intervals less than 2.5 minutes, perform
measurements while observing the state of the
patient, blood vessels and limb to ensure
adequate circulation. Congestion may occur at
the measurement site. When performing periodic
measurement for a long time, periodically check
the circulation condition.
CAUTION
Before you remotely start and stop NIBP
measurement from the central monitor, confirm
the state of the patient at the bedside monitor.
Carefully start and stop NIBP measurement from
the central monitor.
Temperature Monitoring
CAUTION
The ZB-800P, ZB-900P and ZS-900P transmitters
can only transmit temperature data from 5 to
45°C (41 to 113°F). Be careful when reading the
value.
CO2 Monitoring
CAUTION CAUTION
When receiving CO2 data from a bedside monitor When the “CHECK SENSOR” message is
through a ZB-800P, ZB-900P or ZS-900P displayed, check the CO2 sensor kit and replace it
transmitter, if a measured value is out of the if necessary. CO2 cannot be monitored while the
range of the central monitor, only the maximum message is displayed.
value is displayed. Be careful when reading the
value.
Extended Units
WARNING WARNING
When using the Extended Units setting, the When using the Extended Units, before you
following parameter unit settings only affect the perform the patient transfer, make sure that all
individual bedside monitor, not on all monitors unit settings on the source and destination beds
connected to the network. The unit settings must are set to the same units. If the unit settings differ
be the same on all bedside monitors and central between the beds, the alarm settings may
monitors in the network. Otherwise, different change and cause incorrect measurement on the
measurement values and alarms will be destination bed.
displayed on different monitors depending on the
unit settings on each monitor.
• CO2 Unit
• Respiration Unit
• tcPO2/tcPCO2 Unit
WARNING WARNING
The CO2 Unit setting only affects the individual When using the Extended Units, before you
central monitor, not on all monitors connected to change a monitor for a patient, make sure that all
the network. The CO2 unit must be the same on unit settings on the source and destination
all bedside monitors and central monitors in the monitors are set to the same units. If the unit
network. Otherwise, different CO2 values and CO2 settings differ between the monitors, the alarm
alarms will be displayed on different monitors settings may change and cause incorrect
depending on the unit setting on each monitor. measurement on the destination monitor.
WARNING WARNING
The Respiration Unit setting only affects the The tcPO2/tcPCO2 Unit setting only affects the
individual central monitor, not on all monitors individual central monitor, not on all monitors
connected to the network. The respiration unit connected to the network. The tcPO2/tcPCO2 unit
must be the same on all bedside monitors and must be the same on all bedside monitors and
central monitors in the network. Otherwise, central monitors in the network. Otherwise,
different respiration values and respiration alarms different tcPO2/tcPCO2 values and tcPO2/tcPCO2
will be displayed on different monitors depending alarms will be displayed on different monitors
on the unit setting on each monitor. depending on the unit setting on each monitor.
CAUTION CAUTION
When using the Extended Units, you cannot set When using the Extended Units setting, do not
the following vital sign alarm limits and alarm connect the monitor which does not have
master settings on the central monitor. Extended Units setting.
• ETCO2
• FiCO2
• tcPO2/tcPCO2
Transport Function 1
WARNING WARNING
When using the transport function: When using the transport function, use 10
• Do not connect or disconnect the network cable BASE-T/100 BASE-TX switching hubs for the
from the bedside monitors and central monitor. entire network. If you use another type of hub, the
• Do not perform the following operations on the network may intermittently lose connection and
bedside monitor which is being monitored and the patient cannot be monitored on the central
whose data is saved by the central monitor. monitor.
Patient data may be mixed together or lost in
the following cases:
• Removing the input unit while the bedside
monitor power is off.
• Using transport function and wireless LAN at
the same time.
CAUTION
Do not remove the input unit from the bedside
monitor while the central monitor is receiving data
from the bedside monitor. The data may be lost.
Maintenance
CAUTION CAUTION
Before maintenance, cleaning or disinfection, turn Restart the central monitor once every three
the central monitor power off and disconnect the months. Otherwise operation becomes unstable
power cord from the AC socket. Failure to follow and monitoring may stop. While restarting,
this instruction may result in electrical shock and patients monitored by the central monitor must be
central monitor malfunction. monitored by alternate instruments such as
bedside monitors.
CAUTION CAUTION
During maintenance and servicing, patients Never disassemble or repair the central monitor.
monitored by the central monitor must be Disassembly and repair must be performed by
monitored by alternate instruments such as qualified service personnel. When there is any
bedside monitors. abnormality, contact your Nihon Kohden
representative.
CAUTION CAUTION
Do the regular inspection twice a year. Otherwise, Dispose of Nihon Kohden products according to
a decrease and loss in function will not be your local laws and your facility’s guidelines for
noticed and this results in incorrect monitoring. waste disposal. Otherwise, it may affect the
environment. If there is a possibility that the
product may have been contaminated with
infection, dispose of it as medical waste
according to your local laws and your facility’s
guidelines for medical waste. Otherwise, it may
cause infection.
This section explains the name of each component and its description.
YS-098P1/YS-098P2
YL-611P/YL-612P Alarm Indicator WS-960P Recorder Unit
Additional Alarm Indicator Unit
WARNING
While the central monitor is on, do not connect any external devices
such as USB memory. Nihon Kohden does not warrant the normal
operation of the central monitor if an application or software
installation starts automatically.
CAUTION
While the central monitor is on, do not touch unused sockets or cables
connected to the sockets. Failure to follow this instruction may damage
the central monitor by static electricity and cause malfunction.
Rear Panel
7 8 9 10
17 6 16 15 14 13 12 11
WARNING
Do not turn off the display to which the speaker cable is connected.
The alarm sound cannot be heard.
1 2
1 Alarm indicator
2 Additional Alarm Indicator Unit
The cable length depends on the Additional Alarm
Indicator Unit model.
YS-098P1: 2.5 m
YS-098P2: 5 m
4
2
3
6
11
POWER
1 7
2 MENU/HOME
SILENCE
ALARMS
8
DISPLAY 10
SELECT CHANNEL
3
Use the laser printer that Nihon Kohden recommends. Connect to the network
when you use the network printer. Refer to the printer manual together.
The recommended model may be changed without notice. Contact your Nihon
Kohden representative when you locally purchase a laser printer.
This section explains preparation such as loading recording paper, turning power
on or off before starting monitoring and check items.
Installation Conditions
Install the central monitor where the screen can be seen clearly and does not
reflect light.
WARNING
Install the central monitor outside the patient
environment (IEC 60601-1-1). If the central
monitor are installed inside the patient
environment, the patient or operator may receive
electrical shock or injury. For installation, contact
your Nihon Kohden representative.
CAUTION CAUTION
Do not install the monitor where it will be exposed Avoid exposing the monitor to direct sunlight.
to water or chemical solutions. Avoid direct Otherwise, the temperature rises and it causes
sprinkling, spray or moist air from the nebulizer or malfunction and shortens the life of the monitor.
humidifier. These cause malfunction and shorten
the life of the monitor.
CAUTION CAUTION
Make sure that there is enough space between Do not place blankets or cloth over the monitor. It
the monitor and the wall for adequate ventilation. may affect monitoring.
Otherwise the internal temperature of the monitor
rises, which leads to inaccurate operation and
CAUTION
shortens the monitor life.
Do not install the monitor in a dusty area.
• Leave more than 5 cm of space between the
wall and vent holes on the sides and rear
panels of the monitor. CAUTION
• When the monitor is surrounded, leave more Connect the power cord to an AC outlet which
than 10 cm of space above the monitor can supply sufficient AC current to the monitor.
for ventilation. Do not let the surrounding The monitor cannot function properly with low
temperature exceed 35°C (95°F) during current. Also the breaker trips and it causes
operation. electric power failure.
CAUTION CAUTION
When there is any problem with the monitor, turn Do not place cables in the way or where people
off the power immediately and disconnect the walk.
power cord from the AC outlet. Take the monitor
out of service and check for damage.
CAUTION CAUTION
Connect only the specified instrument to the Before connecting or disconnecting instruments,
central monitor and follow the specified make sure that each instrument is turned off and
procedure. Failure to follow this instruction may the power cord is disconnected from the AC
result in electrical shock or injury to the operator, socket. Otherwise, the patient or operator may
and cause fire or instrument malfunction. receive electrical shock or injury.
NOTE
Connection must be done by an authorized personnel in your hospital.
Standard Instruments
• PU-621R Central Monitor Processing Unit
• LCD display (Nihon Kohden specified display)
• YL-611P or YL-612P Alarm Indicator
• WS-960P Recorder Unit
• Keyboard
• Mouse
Optional Instruments
• LS2208 Bar code reader
• RY-910PA Remote Controller
• Laser printer (Nihon Kohden specified printer)
• Bedside monitor
The connection method and grounding method depends on the location where
the central monitor is installed and the types and installation locations of other
instruments.
NOTE
Connection must be done by authorized personnel in your hospital.
For network connection, refer to the Network and System Installation Guide
which is available from your Nihon Kohden representative.
The connection must comply with IEC 60601-1-1 “General Requirements for
Safety of Medical Electrical Equipment”. Refer to the “General Requirements
for Connecting Medical Electrical Systems” in Section 17.
WARNING
Connect the central monitor to the network as specified in the
Network and System Installation Guide. Otherwise the patient and
operator may receive electrical shock or injury. To connect the
network, contact your Nihon Kohden representative.
NOTE
System and network connection, hospital installation conditions, default
settings and system setup settings that meet the specifications must be
managed by authorized personnel and a system administrator in your
hospital.
For system and network connection and system setup settings for administrator,
refer to the Administrator’s Guide.
1. Installing the instruments and connecting the central monitor to the network.
Refer to the Administrator’s Guide.
6. Admitting patients.
Refer to “Admitting a Patient” in Section 4.
8. Start monitoring.
CAUTION
Avoid high humidity, high temperature, direct sunlight and direct
fluorescent light when storing recording paper. Otherwise the paper
may discolor. Store the recording paper in a dry, cool place.
CAUTION CAUTION
Clean the head surface with the provided head Do not touch the recording head with any hard
cleaner pen before loading new paper. After a object. If the head is tapped with a hard object, it
period of usage, paper dust may accumulate may crack and the heater element wire may
between the paper and the head surface so good short-circuit.
printing cannot be obtained.
NOTE
• Only use the specified recording paper, FQW50-2-100.
• Do not allow the paper to contact paste, adhesive agent, oil-based felt
pen tips or diazo process (ditto/spirit) copying paper. These discolor the
paper surface.
• Do not allow the paper to contact any materials containing vinyl
chloride, plastic eraser, adhesive tape, fluorescent felt tip pen, or
cinnabar seal ink because these discolor the recorded waveforms and
data.
• Do not apply strong pressure to the paper. Rubbing or scratching
discolors the paper surface.
1. Move the recorder release lever in the direction of the arrow (▲) to release
the lock.
CAUTION
Do not touch the thermal head inside the recorder unit. The
thermal head may be damaged by static electricity or become dirty
and cause printing failure.
NOTE
• Load the recording paper so that the detection mark of the paper
is on the right side.
• When the [Recording Start Position] is set to [From Mark] on the
Recording of the System Setup screen, feed the paper to the
Detection mark
mark position before starting the recording. Refer to “Recording”
in Section 6-1 of the Administrator’s Guide.
NOTE 3
• Watch the screen and check the operation when using the remote
control to avoid wrong operation.
• Make sure that the remote control is handled appropriately.
WARNING WARNING
• Keep the batteries away from fire. They may If the battery is damaged and the substance
explode. inside the battery contacts the eyes or skin, wash
• Keep the batteries away from patients. immediately and thoroughly with water and see a
• Never short-circuit the + and – terminals on the physician. Never rub your eyes, because you may
battery. It may cause overheating and fire. lose your eyesight.
• Do not damage, disassemble, drop or give
impact to the battery.
1. Remove the battery cover on the rear panel of the remote control as shown.
2. Insert two new AAA alkaline batteries into the remote control observing the
correct polarity.
NOTE
Insert the (–) end of the battery first and press it against the spring.
If you try to force the (+) end of the battery in first as shown, it will
deform the spring and damage the battery and remote controller.
Spring Spring
NOTE
• Remove the battery from the remote controller when not using it.
• Check with your local solid waste officials for details in your area for
recycling options or proper disposable.
• Take care not to drop or lose the remote controller.
The infrared light emitted from the remote control has wide directivity and it
may reflect off the ceiling and wall and operate other monitors.
The remote control channel sets on the remote controller setting. Refer to the
Administrator’s Guide.
CAUTION
• Set the remote control channel on the monitor to prevent the
remote control from operating a different monitor.
• When several monitors are installed close together, check that the
remote control operates only the desired monitor. If the remote
control operates a different monitor, recheck the channel setting.
2. Press the Main power switch on the rear panel of the central monitor
processing unit to “ ” side to supply the power.
3. Press the Power button on the front panel of the central monitor processing
unit to turn the power on. The alarm indicator and power LED on the central
monitor processing unit lights.
Lamp lit
Power button
Lamp lit
The central monitor starts and the All Beds screen is displayed.
CAUTION
When the central monitor is first turned on and periodically during
operation, check that the red, yellow, cyan and green alarm indicator
lamps light and sound is generated.
NOTE
• It takes a few minutes for the LCD screen to reach full brightness.
• The shadow of the previous screen may remain for a few minutes after
changing screens.
• There may be some dots on the LCD screen which are always on or
always off, but it does not affect monitoring. This is normal for all LCD
screens.
CAUTION
Follow the specified procedure to turn off the central monitor.
Otherwise, patient data will be deleted and the storage device and
data in the storage device may be damaged.
The power can be turned off by pressing and holding the Power button on the
PU-621R Central Monitor Processing Unit.
NOTE
Data before the patient transfer is saved in the source central monitor. To
observe the data before the patient transfer, keep the power of the source
central monitor on.
When [System Setup] is assigned to one of the all beds function keys,
the Information window of the System Setup screen can be displayed by
touching the function key. Refer to “Function Keys Setting” in Section 6-1
of the Administrator’s Guide to assign a function to the function key.
2. Keep touching [POWER OFF] for five seconds until the countdown ends to
turn the central monitor power off.
NOTE
The shaded settings need an administrator password to access. These
settings must be set by authorized personnel in your hospital.
WARNING
When admitting a new patient, confirm alarm settings. Also check
the alarm settings during monitoring and change the settings
according to the patient condition. For a bed monitored through a
multiple patient receiver, the alarm settings change to the [Alarm
Master 1] settings in the following cases:
• When the bed is discharged
• When you touch the [Delete Data] key on the Admit/Discharge
window
• When you delete all data of the bed when the receiving channel is
changed
1. Admit a patient.
When you monitor a patient through a multiple patient receiver, set the
receiving channel. Refer to “Admitting a Patient” in Section 4.
3. Set the Personal Setup, Parameter Setup and Other Setup such as Recording
Setting as needed.
Daily Check
Perform the following daily check before, during and after use of the instrument 3
and check that the instrument can be used normally and safely. If any problem is
detected, take the proper countermeasure according to the troubleshooting and
maintenance sections. If the instrument is suspected to be faulty as a result of
checking, attach an “Unusable” or “Repair request” label to the instrument and
contact your Nihon Kohden representative.
When there are not enough consumables, order the consumables from Nihon
Kohden.
Perform the regular inspection twice a year in addition to daily check. Check if
the instrument operates normally and change the parts which require periodic
replacement. For the regular inspection, refer to the Section 15 “Maintenance”.
section.
Appearance
• No scratches, damage or dirt on the monitor.
• No damage to the switch, lamps and displays.*
• No damage to the power cord.
• The monitor is not in a wet place.
* Do not use anything sharp to touch the LCD screen (touch keys), power
switches and other keys. Sharp objects may damage the instrument.
• The monitor is not too hot. The monitor does not give an electric shock when
touched.
• No error message is displayed on the screen.
• The time on the screen is correct.
• The low battery mark for the transmitter does not appear on the
transmitter LCD display or central monitor screen when using a multiple
patient receiver.
• The monitor does not affect surrounding equipment.
Basic Operations
• The screen display is normal. (No abnormal brightness, distortion or color)
• The touch keys function properly.
• The keyboard, mouse and remote controller operate properly.
• Following alarm functions properly.
- The red, yellow, cyan and green alarm indicator lamps light.
- Alarm sound can be heard.
- Alarm sound volume setting is appropriate.
• When the CALL button on the transmitter is pressed within the specified range
of the central monitor, a message appears on the central monitor screen when
using a multiple patient receiver.
• The transmitter signal is properly displayed on the central monitor when using
a multiple patient receiver.
• Paper feeding is correct. (No crawling or catching)
• There is no trouble in recording. (No faint recording)
• No error display and malfunction during operation.
• Other instruments on the system operate normally.
CAUTION
When the central monitor is first turned on and periodically during
operation, check that the red, yellow, cyan and green alarm indicator
lamps light and sound is generated.
NOTE
After turning the monitor on and when admitting a patient on the monitor,
make sure that the time displayed at the upper right of the screen is
correct. The central monitor clock function uses the clock of the PC.
When the date or time is changed during monitoring, the date and time of
all stored data is also changed and may not match the date and time on
the printout.
For the date and time setting, refer to the Administrator’s Guide.
Admitting a Patient
WARNING
After admitting a patient at a bedside monitor, confirm that the
patient is also admitted at the central monitor and that the central
monitor starts monitoring the patient.
CAUTION
When admitting a new patient, first discharge the previous patient
and delete all data of the previous patient. Otherwise, the data of the
previous patient and new patient will be mixed together.
CAUTION
When admitting a new patient, check that the patient information is
entered correctly.
CAUTION
At the start of ECG monitoring, check that the correct patient type is
set for QRS Detection Type on the following window.
• When using a multiple patient receiver: QRS Detection window of
the ECG window.
• When using a bedside monitor and transmitter: Home screen or
ECG window of the monitor.
If an inappropriate patient type is set, heart rate cannot be counted
accurately and noise or P waves may be counted as QRS and
cardiac arrest may be overlooked.
NOTE
Patients can only be admitted for monitored beds whose data is saved in
this central monitor.
The default alarm setting when admitting is Alarm Master 1 of the bedside
monitor or Alarm Master 1 of the central monitor if the bed is monitored through
an ORG-9100 multiple patient receiver.
You can also display the Admit/Discharge window by the following procedures.
• Touch [Admit/Discharge] on the Individual Bed window.
• Touch [ ] to display the Setup Menu. Touch [Admit Discharge] of [Personal
Setup].
• Touch [Admit/Discharge] individual function key if [Admit/Discharge] is
registered to an individual function key. For setting individual function keys,
refer to “Changing the All Beds Screen Display Settings” in Section 6.
2. Touch [Admit].
[Readmit]
Readmits a patient who
was discharged within the
past 120 hours.
When [Patient Attribute Input Device] is set to [Bar Code Reader], the bar
code reader window is displayed after [OK] is touched on the message
window. Refer to “Entering the Patient Information Using a Bar Code
Reader” later in this section.
[ ]
Touch to display the setting window of the
items that are set on the System Setup screen.
Touch [Keyboard] on the setting window to
display the keyboard entry window and enter
data.
[ ]
Touch to display the keyboard entry window.
Refer to “Using the Keyboard on the Screen”
in Section 1.
Item Description
Bed Name*1 Up to 10 alphanumeric characters
Group*1 Select from 10 groups and “None”.
Patient ID Up to 16 alphanumeric characters
Patient Name Up to 32 alphanumeric characters 4
Height*2 0.1 to 299.9 cm / 0 to 9 ft, 0.0 to 11.9 inch
Weight*2 0.1 to 449.9 kg / 0.1 to 654.9 lb
Automatically calculated when the height and weight are
BSA
entered.
Date of Birth YYYY-MM-DD
From 0 years 0 months to 127 years 11 months
Age*3 Automatically calculated when the date of birth is
entered. You can also enter the age manually.
Gender Male, Female, unknown
Blood Type A−, A+, B−, B+, AB−, AB+, O−, O+, unknown
Physician*1 Up to 20 alphanumeric characters
Up to 200 alphanumeric characters, up to 8 lines when
Diagnosis
inserting the line
Up to 64 alphanumeric characters, the line breaks can be
Note*4
entered.
*1 You can select from items registered at [Pre-registration] of the System Setup
screen.
*2 For the height and weight, you can change inch/cm and lb/kg at [System
Configuration] → [System] of the System Setup screen.
* When the bedside monitor in the network has day data, the day can be
3
synchronized.
*4 The note is displayed on the All Beds screen when [Monitor Setting] →
[Display Settings] → [All Beds Screen] → [Display Patient Name] of the
System Setup screen is set to [ON]. Even the [Display Patient Name] is set to
[ON]. The note is not displayed when 24 or 32 beds are displayed on the All
Beds screen.
This function is available when [Use QRY] of [QRY] on the [External Output]
→ [HL7] of the System Setup screen is set to [ON]. Refer to “External Output”
in Section 6-1 of the Administrator’s Guide.
To use [Synchronize with HIS Server] to import the information, enter the patient
ID on the Admit/Discharge window.
3. Touch [OK].
Data which is imported from the hospital network can be edited and added
manually.
Set [Patient Attribute Read Device] → [Patient Attribute Read Setting] of the
System Setup screen to [Bar Code Reader] beforehand.
To cancel while entering the patient information, touch [Cancel] to close the
window.
4. Read the bar code with the bar code reader. To cancel entering the
information, touch [Cancel].
5. Confirm that the scanned information is displayed on the Bar Code Reader
window and touch [Apply]. To cancel entering the information, touch
[Cancel].
The data entered from the bar code reader can be added or changed manually.
Set [Patient Attribute Read Device] → [Patient Attribute Read Setting] of the
System Setup screen to [Bar Code Reader] beforehand.
1. Touch the data area of the bed to change the patient information for. The
Individual Bed window is displayed. Touch [Admit/Discharge] to display the
Admit/Discharge window.
2. Touch [Bar Code Reader] on the Admit/Discharged window. The Bar Code
window is displayed.
1
3. Scan the bar code of the patient. The information from the bar code
overwrites the previous data. Other items are not changed.
4. Confirm that the scanned information is displayed on the Bar Code window
and touch [Apply]. To cancel changing the information, touch [Cancel].
The data entered from the bar code reader can be added or changed manually.
NOTE
4
• The readmitting function is only available when [System Configuration]
→ [System] → [Admit] → [Discharge Mode] of the System Setup screen
is set to [Discharge]. If [Discharge Mode] is set to [Delete Data], the
patient cannot be readmitted. Refer to “System Configuration Settings”
in Section 6-1 of the Administrator’s Guide.
• Data for up to 16 patients can be saved as patients who can be
readmitted. If more than 16 patients are discharged within 120 hours,
the oldest patient data is deleted.
When a patient is readmitted, alarm settings and stored wave settings of review
windows are the settings before the patient was discharged.
2. Touch [Readmit] to display the discharged patient list window. To close the
window, touch [ ].
1
2
Sort
On the PU-621R Op No. 21A, touch the sort
marks to sort the list.
• Discharge Time: Sort by date and time of
discharge.
• Patient ID: Sort by patient ID.
• Name: Sort by patient name.
3
5. After confirming the message, touch [OK]. The patient is readmitted and
monitoring starts.
Discharging a Patient
On the Discharged Patients List window, the past 120 hours of review windows
of discharged patients or patients whose data were deleted on this central monitor
can be displayed.
CAUTION
When admitting a new patient, first discharge the previous patient
and delete all data of the previous patient. Otherwise, the data of the
previous patient and new patient will be mixed together.
NOTE
This operation can only be performed for monitored beds whose data is
saved in this central monitor.
1. Touch the data area of the bed you are going to discharge a patient from to
display the Individual Bed window.
You can also display the Admit/Discharge window by the following procedures.
• Touch [ ] to display the Setup Menu. Touch [Admit Discharge] of [Personal
Setup].
• Touch [Admit/Discharge] individual function key if [Admit/Discharge] is
registered to an individual function key. For setting individual function keys,
refer to “Changing the All Beds Screen Display Settings” in Section 6.
4
When the [Discharge Mode] is
[Delete Data]
4
The message depends on the [Discharge Mode].
NOTE
For the PU-621R Central Monitor Processing Unit Op No. 21A, when
[Telemetry Setting Master] is set to [ON], settings for the ORG-9100
series Multiple Patient Receiver are initialized as set on the Telemetry
Settings Master window. For details on [Telemetry Setting Master],
refer to “Telemetry Setting Master” in Section 6-1 of the Administrator’s
Guide.
When the patient is temporarily away from the bed and no data from that bedside
monitor is sent to the central monitor, you can pause monitoring of the patient
without deleting the patient data and settings.
The pause function pauses the displaying of measurement values and alarm
function without losing patient information and settings. While monitoring is
paused, a pause reason is displayed beside the paused bed on the central monitor
screen. You can select the reason from preset customizable reasons.
With the pause timer function, the expected return time and pause timer can be
displayed and overtime past the expected return time is notified.
NOTE
The pause operation can only be done at the central monitor where the
bed’s data is saved.
1. Touch the data area of the bed for which you are going to pause monitoring.
You can also display the Admit/Discharge window by the following procedures.
• Touch [ ] to display the Setup Menu. Touch [Admit Discharge] of [Personal
Setup].
• Touch [Admit/Discharge] individual function key if [Admit/Discharge] is
registered to an individual function key. For setting individual function keys,
refer to “Changing the All Beds Screen Display Settings” in Section 6.
4
3. Touch [Pause] to display the Pause window.
5. Touch [Pause]. Monitoring pauses and the selected pause reason appears on
the screen.
Pause Timer
When setting [Pause Timer] → [System Configuration] → [System] → [Admit]
to [ON] on the System Setup screen and selecting the pause time, the expected
return time and pause timer are displayed on the screen. When [Pause Time Over
Time Notification Sound] of the System Setup is set to [ON], a notification sound
occurs after the expected return time elapsed. Refer to “System Configuration
Settings” in Section 6-1 of the Administrator’s Guide.
1. Touch the data area of the bed for which you are going to pause monitoring.
3 6. Touch [Pause]. Monitoring pauses and the pause reason, pause timer and
expected return time are displayed on the screen.
The pause reason and pause time can be registered on the Pre-registration
of the System Setup screen. Refer to “Pre-registration” in Section 6-1 of the
Administrator’s Guide.
6
Select the pause Select the pause
reason from the list. time.
NOTE
The pause time only appears on the central monitor. It does not appear
on the bedside monitor.
Pause time
Expected return time
Remaining time
When the time
elapses, overtime is
displayed in yellow.
[Reduce] [Extend]
When the pause time is set to [Free], [Free] is displayed Reduces the pause Extends the pause
for the pause time and the expected return time, remaining time 15 minutes by time 15 minutes by
time and pause timer are not displayed. The [Reduce] and every touch. every touch.
[Extend] keys are not available.
Resume Monitoring
WARNING
When the patient returns, resume monitoring. During pause, the
measurement data is not displayed and the alarm does not function.
1. Touch the pause reason key displayed on the patient’s bed. The Pause
window of the Admit/Discharge window is displayed.
Resume Setting
Monitoring of the bed automatically resumes at the central monitor when the
resume time is set at [Auto Resume After Pause] → [System Configuration] →
[System] → [Admit] of the System Setup screen and any one of the following
conditions is met at the paused bed:
• Heart rate is continuously monitored for the selected time.
• SpO2 is continuously monitored for the selected time.
• PR from the invasive blood pressure (ART, ART2, RAD, DORS, AO, FEM,
UA, LVP or P1 to 8) is continuously monitored for the selected time at the
bedside monitor or transmitter.
Monitoring of the bed automatically resumes at the central monitor when any
one of the following conditions are met at paused bed:
• NIBP is properly measured and the SYS, DIA or MAP value is displayed at the
bedside monitor or transmitter.
• ASYSTOLE is generated (HR becomes 0).
WARNING
When the bed is set to automatically resume monitoring after pause,
check that monitoring is resumed at the central monitor when the
pause condition is ended. Monitoring might not resume if there is
network failure.
4
NOTE
• When [Auto Resume After Pause] is set to [OFF], the monitoring does
not resume until the [Resume] is touch on the Admit/Discharge window.
• When a patient is paused from a transmitter which has a pause function
and the power of the transmitter is on, the monitoring does not resume
even when the time is set at [Auto Resume After Pause] on this central
monitor. In this case, the monitoring resumes by the [AUTO RESUME
AFTER PAUSE] setting of the transmitter. When [AUTO RESUME
AFTER PAUSE] is set to [OFF] on the transmitter, monitoring of the
transmitter does not resume even when the monitoring resumes.
CAUTION CAUTION
After patient transfer, settings other than patient Keep the source bedside monitor and the
information and alarm settings are returned to the destination bedside monitor power on and
default settings. Change the settings if necessary. connected to the network until the patient transfer
or bed exchange is complete. Otherwise the
patient transfer or bed exchange fails and the
data is lost. After transferring or exchanging the
patient, confirm that the data before the patient
transfer or bed exchange can be displayed at the
destination bed.
NOTE
The patient transfer can only be performed for monitored beds whose
data is saved in this central monitor.
Transferred Data
The following data can be transferred.
Review Data
• Trendgraph • ST recall data
• Tabular trend • Arrhythmia recall data
• Full disclosure waveform • ECG 12 lead analysis file
• Expanded waveform • Hemodynamics list data
• Event list • Alarm events
4.20 Operator’s Manual CNS-6201
4. ADMITTING/DISCHARGING PATIENTS
NOTE
• The data for ECG 12 lead analysis is moved if the transfer is two beds
in the same central monitor or between a CNS-6201, CNS-9601 and
CNS-9701 central monitor.
• The data for event list or alarm events are moved if the transfer is two
beds in the same central monitor or CNS-6201. Otherwise, no data will
be moved. 4
• Data before the patient transfer is saved in the source central monitor
and can be viewed as long as the power of the source central monitor
remains on.
• While a patient is being transferred between different central monitors,
up to one minute of full disclosure waveform and trend data may be lost.
Transfer Limitation
When the source bed and destination bed use the same central monitor or CNS-
6201, there is no limit to the number of times a patient can be transferred without
losing data.
When the destination bed’s data is saved on a central monitor other than CNS-
6201, there is limit to the number of times a patient can be transferred without
losing data.
CAUTION
If there are too many patient transfers, old review data might not be
displayed on the central monitor.
NOTE
When transferring a patient to a bed whose data is saved in a central
monitor other than CNS-6201, the number of transfer times with no data
loss depends on the destination central monitor.
Transferring a Patient
CAUTION
When transferring a patient, confirm the destination bed you want to
transfer by the message on the screen. If you select the wrong
destination bed, the patient data of the source bed overwrites the
patient data of the destination bed and the overwritten data cannot
be recovered.
1. Touch the data area of the source bed you want to transfer.
You can also display the Admit/Discharge window by the following procedures.
• Touch [ ] to display the Setup Menu. Touch [Admit Discharge] of [Personal
Setup].
• Touch [Admit/Discharge] individual function key if [Admit/Discharge] is
registered to an individual function key. For setting individual function keys,
refer to the Administrator’s Guide.
4
4. Select a destination group. The registered beds of the group are displayed.
Group
Touch the destination group from the list. 4
Destination Bed
The list of available beds which are
registered to the selected group are
displayed. Touch a destination bed. 5
Bed name
Patient name
IP address
6
7. Check the patient information (bed name, patient name, patient ID) of the
source and destination bed and touch [Yes].
NOTE
Before touching [Yes], check the source and destination with the
patient and bed name.
NOTE
For the PU-621R Central Monitor Processing Unit Op No. 21A, when
[Telemetry Setting Master] is set to [ON], settings for the ORG-9100
series Multiple Patient Receiver are initialized as set on the Telemetry
Settings Master window. For details on [Telemetry Setting Master],
refer to “Telemetry Setting Master” in Section 6-1 of the Administrator’s
Guide.
This procedure is only available for a bed whose data is saved in this central
monitor.
4
Do the following procedure when you change to a different monitor (bedside
monitor or multiple patient receiver) for a patient. The bed position for the
patient on the central monitor does not change. The monitoring data and settings
(e.g. waveform selection) for the bed are kept after the monitor is changed.
CAUTION
Keep the current bedside monitor and the new bedside monitor
power on and connected to the network until the monitor is changed.
Otherwise the patient data is lost. After changing the monitor,
confirm that the data and settings before changing the monitor are
displayed in the new monitor.
NOTE
• You cannot change the monitor for a bed whose data is saved in
another central monitor.
• On the PU-621R Central Monitor Processing Unit Op No. 21A, if
the alarm level of the following parameters is set to “CRISIS” on the
destination monitor, the upper and lower alarm limits settings on the
destination monitor have priority and the source monitor settings are
not applied to the destination monitor.
Parameters:
HR upper, HR lower, PR upper, PR lower, SpO2 upper, SpO2 lower,
SpO2-2 upper, SpO2-2 lower, ETCO2 upper, ETCO2 lower, RR upper,
RR lower, APNEA, arrhythmia alarms
1. Connect the new monitor to the central monitor network and turn the power
on.
2. On the central monitor, touch the data area of the bed you want to change the
monitor for.
You can also display the Admit/Discharge window by the following procedures.
• Touch [ ] to display the Setup Menu. Touch [Admit Discharge] of [Personal
Setup].
• Touch [Admit/Discharge] individual function key if [Admit/Discharge] is
registered to an individual function key. For setting individual function keys,
refer to “Changing the All Beds Screen Display Settings” in Section 6.
4
The current bed ID, patient name and IP
address of the monitor are displayed.
Group
Touch the destination group from the list. 5
Available Device
The list of available monitors which
are registered to the selected group are
displayed. Touch a destination monitor. 6
Bed name
Patient name
IP address
7
NOTE
Before touching [Yes], check the current and new monitor by the bed
ID and IP address.
NOTE
• After changing the monitor, check that the old monitor is no longer
monitored by other central monitors. This central monitor notifies
other central monitors that the old monitor is changed to a new
monitor and automatically updates the monitoring beds.
• For the PU-621R Central Monitor Processing Unit Op No. 21A,
when [Telemetry Setting Master] is set to [ON], settings for the
ORG-9100 series Multiple Patient Receiver are initialized as set on
the Telemetry Settings Master window. For details on [Telemetry
When the bed is monitored through an ORG-9100 series multiple patient receiver
before changing the monitors, the alarm settings return to the Alarm Master 1
settings after changing the monitors.
CAUTION
If the monitoring bed is changed to a different monitor on a central
monitor other than CNS-6201, the monitoring bed does not change
on this central monitor. Register the bed again on this central
monitor. Otherwise, the patient data might not be displayed or data of
a different patient may be displayed on this central monitor.
CAUTION
Keep the source bedside monitor and the destination bedside 4
monitor power on and connected to the network until the patient
transfer or bed exchange is complete. Otherwise the patient transfer
or bed exchange fails and the data is lost. After transferring or
exchanging the patient, confirm that the data before the patient
transfer or bed exchange can be displayed at the destination bed.
This procedure is only for two beds whose data is saved in this central monitor.
When exchanging the patient’s beds in the monitor network, all patient’s data can
also be exchanged.
NOTE
• You cannot exchange a monitored bed whose data is saved in another
central monitor.
• You cannot exchange a monitored bed when the bed is monitored
through a multiple patient receiver.
• Before exchanging the beds, remove the sensors from the patient. If the
beds are exchanged while monitoring, the data of the patients will be
mixed together and it will cause misunderstanding of the patient history.
• On the PU-621R Central Monitor Processing Unit Op No. 21A, if
the alarm level of the following parameters is set to “CRISIS” on the
destination bed, the upper and lower alarm limits settings on the
destination bed have priority and the source bed settings are not
applied to the destination bed.
Parameters:
HR upper, HR lower, PR upper, PR lower, SpO2 upper, SpO2 lower,
SpO2-2 upper, SpO2-2 lower, ETCO2 upper, ETCO2 lower, RR upper,
RR lower, APNEA, arrhythmia alarms
1. Remove the sensors from the patients whose beds are going to be exchanged.
2. On the central monitor, touch the data area of the bed you want to exchange.
You can also display the Admit/Discharge window by the following procedures.
• Touch [ ] to display the Setup Menu. Touch [Admit Discharge] of [Personal
Setup].
• Touch [Admit/Discharge] individual function key if [Admit/Discharge] is
registered to an individual function key. For setting individual function keys,
refer to “Changing the All Beds Screen Display Settings” in Section 6.
4
The current bed name, patient name and
IP address of the monitor are displayed.
Group
Touch the destination group from the list. 5
Available Beds
The list of available beds which are
registered to the selected group are
displayed. Touch a bed to exchange. 6
Bed name
Patient name
IP address
7
8. Check the patient information (bed name, patient name, patient ID) of the
current monitored bed and the bed to exchange and touch [Yes].
NOTE
Before touching [Yes], check the current monitored bed and the bed
to exchange with the patient and bed name.
NOTE
For the PU-621R Central Monitor Processing Unit Op No. 21A, when
[Telemetry Setting Master] is set to [ON], settings for the ORG-9100
series Multiple Patient Receiver are initialized as set on the Telemetry
Settings Master window. For details on [Telemetry Setting Master],
refer to “Telemetry Setting Master” in Section 6-1 of the Administrator’s
Guide.
10. After exchanging the beds, reattach the sensors to the patients.
Operator’s Manual CNS-6201 4.31
4. ADMITTING/DISCHARGING PATIENTS
Set the receiving channel number when monitoring starts or when changing the
transmitter.
WARNING
Check that the channel number of the transmitter corresponds to the
receiving channel (the channel displayed on the monitor screen).
Otherwise, the central monitor monitors a different patient.
CAUTION
When you change the receiving channel to monitor a new patient,
discharge the previous patient and admit a new patient. If you only
change the channel and does not delete the previous patient data,
the data of the previous patient and new patient will be mixed
together and it will cause misunderstanding of the patient history.
NOTE
• The receiving channel number is set at the moment you touch [Yes] or
[No] on the confirmation window.
• The receiving channel can be set only when receiving data from a
transmitter through a multiple patient receiver.
• This operation can only be performed for monitored beds whose data is
saved in this central monitor.
1. Touch the data area of the bed you want to set the channel for.
You can also display the Admit/Discharge window by the following procedures.
• Touch [ ] to display the Setup Menu. Touch [Admit Discharge] of [Personal
Setup].
• Touch [Admit/Discharge] individual function key if [Admit/Discharge] is
registered to an individual function key. For setting individual function keys,
refer to “Changing the All Beds Screen Display Settings” in Section 6.
4. Select the transmitter channel number from the registered list. You can also
enter the channel number from the screen keyboard.
[Keyboard]
Touch to display the keyboard.
i) Enter the numbers with keyboard.
ii) Touch [OK]. The window to confirm the change
appears.
i
i
ii
ii
NOTE
• You cannot set a channel number which is not included in the
connected multiple patient receiver.
• When [Prohibit Duplicate Channels] of the [System Configuration] in
the System Setup screen is set to [ON], you cannot select the same
channel with the monitoring (paused) beds. The channel number of
the discharged beds can be set. When entering the same number
When [Yes] is touched, the alarm settings change to the Alarm Master 1 settings.
CAUTION
When you change the receiving channel to monitor a new patient,
discharge the previous patient and admit a new patient. If you only
change the channel and does not delete the previous patient data,
the data of the previous patient and new patient will be mixed
together and it will cause misunderstanding of the patient history.
NOTE
Confirm that the correct channel number is displayed on the screen.
This section explains alarm type and level, central monitor operation when an
alarm occurs, temporary silencing and suspending alarms, alarm recording and
alarm settings.
Overview of Alarms
WARNING WARNING
A physician must be within the range where he/ Do not diagnose a patient based on only the
she can hear the alarm sound of the central alarm information of the central monitor. An alarm
monitor while monitoring a patient on the central may not be indicated due to alarm level or alarm
monitor. If the physician cannot hear the alarm on/off setting and critical changes on the patient
sound, critical changes on the patient may be may be overlooked.
overlooked.
WARNING WARNING
If more than one medical equipment is used When an alarm occurs:
together in the same facility, make sure all • Check the patient first and take necessary
equipments have the same alarm default settings measure to ensure patient’s safety.
(alarm master). If the medical equipments have • Remove the cause of the alarm.
different alarm default settings and when • Check the alarm settings on the central monitor
initialized, the alarm settings differ with the other and change the alarm settings if necessary.
equipments and alarm cannot be managed
appropriately in the facility. If using different alarm
default settings according to areas or wings in the
facility, manage the alarms appropriately.
WARNING
When admitting a new patient, confirm alarm
settings. Also check the alarm settings during
monitoring and change the settings according to
the patient condition. For a bed monitored
through a multiple patient receiver, the alarm
settings change to the [Alarm Master 1] settings
in the following cases:
• When the bed is discharged
• When you touch the [Delete Data] key on the
Admit/Discharge window
• When you delete all data of the bed when the
receiving channel is changed
Bedside monitor Multiple patient The table below shows which alarm functions are available on which
receiver
Transmitter instruments.
Monitor network
Central monitor
CNS-6201
Monitored Bed
Monitor Network
Central Monitor Transmitter through
Bedside Monitor Multiple Patient
Receiver
Alarm Functions
NOTE
For 8000 series bedside monitors, the central monitor generates an alarm
sound and indication and starts alarm recording according to the alarm
judgement on the bedside monitor.
Alarm Types
There are four alarm types.
Alarm Level
Alarms are divided into three alarm levels. The central monitor operation when
the alarm occurs and the priority when two or more alarms occur together depend
on the alarm level.
Level Description
Higher CRISIS Patient is in critical condition and the patient’s life may
be at risk. Immediate action must be taken. Electrodes
↑ or probe off, or incorrect lead or other cable connections
may also cause this alarm.
Priority WARNING Patient is in critical condition. Prompt action should be
taken. Electrodes or probe off, or incorrect lead or other
cable connections may also cause this alarm.
↓ ADVISORY Electrodes, probe, cuff, lead and other cable connections
or settings on the monitor are not appropriate for
Lower accurate measurement. Prompt action should be taken.
When the bed is monitored through the ORG-9100 and alarm escalation is ON,
the level of the vital sign and technical alarm can be automatically raised to the
next level when a set time elapses or SpO2 drops below a set level. For details,
refer to Section 6-1 of the Administrator’s Guide.
Alarm Indication
When an alarm occurs, the central monitor indicates the alarm as follows
according to the alarm level. The alarm level on the central monitor is the same
as the alarm level on the monitored bed. Refer to the Operator’s Manual of the
bedside monitor.
When monitoring a bed through a multiple patient receiver, the alarm level can
be changed. Refer to “ORG Setting” in Section 6-1 of the Administrator’s Guide.
The relation between alarm level and central monitor indication is as follows.
is the factory default setting.
*1 You can change the alarm sound, advisory alarm sound interval and advisory
alarm color on the Alarm window of the System Configuration window. Refer
to “System Configuration Settings” in Section 6-1 of the Administrator’s
Guide.
* Displayed on the All Beds screen and the data area only.
2
*3 Blinks in yellow or orange when WARNING is the highest priority of all the
alarms generated on the monitored bed. Lights in yellow or orange in other
alarms.
Arrhythmia Alarms
NOTE
A message is not displayed when:
• Alarm functions are set to OFF on the
bedside monitor. The frame of the waveform display Highlighted arrhythmia name in
• Alarm for the arrhythmia is set to OFF. is highlighted for CRISIS and the color for the alarm level
WARNING alarm levels.
When several alarms occur simultaneously,
some messages are not displayed depending Individual Bed window
on the alarm level. Refer to “Alarm
Highlighted arrhythmia name in the
Priority” in this section. color and place according to the level
Technical Alarms
Alarm Priority
Screen Message
When several alarms occur on the same monitored bed, a message is displayed
on different places according to the alarm level.
CRISIS level alarm message WARNING level alarm message ADVISORY level alarm message
When several alarms occur When several alarms occur When several alarms occur
simultaneously, the messages are simultaneously, the messages are simultaneously, the messages are
alternated. alternated. alternated.
When an alarm occurs, after checking the cause, silence the alarm sound and
stop the blinking of the alarm indicator.
NOTE
When the two types of the beds are selected as monitored bed and
Silence Alarms key is touched, alarms for each bed is silenced as
mentioned above.
At the central monitor, you can silence alarms at all the monitored beds which
are directly connected to the network. When you silence alarms at the central
monitor, they are also silenced at the bedside monitor. When you silence alarms
at the bedside monitor, they are also silenced at the central monitor.
On the Individual Bed window, the alarm silence mark and the remaining
minutes are also displayed.
NOTE
When the SpO2 probe is disconnected and a “Probe Off” alarm is
displayed, silence the alarm and stop monitoring to clear the display.
For the 8000 series beds, refer to At the central monitor, you can temporarily suspend all alarm functions of all the
Section 1. 8000 series monitored beds. During alarm suspend, there is no alarm sound, no
alarm message display and no alarm recording. When you suspend alarms at the
bedside monitor, they are also suspended at the central monitor.
To suspend all alarm functions of the 8000 series monitored beds, touch
[ ]. During alarm suspend, the alarm suspend mark with the remaining
minutes indication and the “Alarm Suspended” message are displayed in the
display area of the suspended beds.
On the Individual Bed window, the alarm silence mark and the remaining
minutes are also displayed.
WARNING
When alarm is suspended at the transmitter, all alarms are turned off
for that transmitter. Be careful when you suspend the alarm.
By pressing the alarm suspend key on the transmitter, you can suspend all alarms
before occurrence. This is useful to prevent unnecessary alarms during electrode
5
replacement or treatment. This function is only available for transmitters with a
SUSPEND key.
When the alarm suspend key on the transmitter is pressed, all alarm function for
the patient is suspended for two minutes. The “Alarms Suspended” message and
alarm suspend mark are displayed in the display area of the patient on the
All Beds screen, Individual Bed window and data area of each screen. It depends
on the transmitter settings.
Message Mark
NOTE
Displayed at the measurement value Display condition is different depending on the monitored bed.
All alarms off mark This mark is displayed when all alarms are turned off on the bedside
monitor.
Alarm suspend mark This mark is displayed when alarms are suspended on the bedside
monitor.
Alarm silence mark This mark is displayed when all alarms are temporarily silenced.
NOTE
The function is different depending on the monitored bed.
On the System Configuration window of the System Setup screen, you can
set whether or not the vital sign alarm off mark is displayed. Refer to “System
Configuration Settings” in Section 6-1 of the Administrator’s Guide.
NOTE
Some bedside monitor models allow you to set the conditions to display
the vital sign alarm off mark on the bedside monitor screen. The vital sign
alarm off mark is displayed on the central monitor depending on the setup
of the bedside monitor.
5.14 Operator’s Manual CNS-6201
5. ALARM FUNCTION
Alarm Recording
When a vital sign alarm or arrhythmia alarm occurs, waveforms on the All Beds
screen can be recorded automatically. The WS-960P Recorder Unit is used for
alarm recording.
NOTE 5
When all alarms are set to OFF on the bedside monitor, the alarm
recording for the bed is not performed.
The recording time can be set on the System Setup screen. For setting recording
time, refer to “Recording” in Section 6-1 of the Administrator’s Guide.
Recording Example
Refer to “Recorded/Printed Data” in Section 10.
Setting Alarms
NOTE
• Do not change alarm settings on the bedside monitor and the central
monitor simultaneously.
• For a bed monitored through an ORG-9100 series multiple patient
receiver, the alarm settings are saved even when the central monitor is
turned off. In the following cases, the alarm settings become the Alarm
Master 1 settings:
- When the bed is discharged
- When you touch the [Delete Data] key on the Admit/Discharge
window
- When you delete all data of the bed when the receiving channel is
changed
CAUTION
When the alarm limit is set to [OFF], there will be no alarm for that
limit. Be careful when you set the alarm limit to [OFF].
3. Touch [Alarm Limits] of the Personal Setup to display the Alarm Limits
window.
You can also display the Alarm Limits window by the following operation.
• Touch [Admit/Discharge] on the Individual Bed window to display the
Admit/Discharge window. Touch [Alarm Settings] → [Alarm Limits].
• Touch the [Alarm Limits] individual function key if Alarm Limits is
registered to an individual function key. For setting individual function
keys, refer to “Changing the All Beds Screen Display Settings” in Section
6.
4. Touch the parameter key to set the alarm limits. Set the alarm limits on the
Alarm Limits Setting window.
Upper/lower limit
Current value
Lower limit
Current lower value is
displayed.
AUTO
Current measurement value Touch to set the
For IBP parameter, touch parameter upper/lower
Trendgraph of past four hours Upper/lower limit slide bar
the SYS, DIA or MEAN key limit automatically.
is displayed. Touch the bars to set the value.
to change the alarm setting
windows. When set the limit to OFF, set the limit
to the maximum or minimum value and
touch the increase or decrease key.
Example: HR alarm setting window Setting Alarm Limits Automatically (Auto Alarm Setting)
The auto alarm setting is the function to calculate and set the upper and lower
limits automatically based on the patient’s current vital values. When [Auto] is
touched on the Alarm Setting window of the Alarm Limits window, the alarm
limits for the parameters are automatically set.
To open the Alarm Limits window, refer to “Manually Setting the Alarms” in this
section.
NOTE
The setting range depends on the bedside monitor. The central monitor
setting might not be applied to the bedside monitor. For the setting range
of the bedside monitor, refer to the Operator’s Manual of the bedside
monitor.
WARNING
For arrhythmia monitoring, set [Arrhythmia Analysis] on the ECG
window to [ON]. Otherwise, there is no sound or indication for
arrhythmia alarms (except for ASYSTOLE).
CAUTION
When the alarm is turned [OFF] for an arrhythmia, there will be no
alarm for that arrhythmia type. There is no message or mark to
indicate that a certain arrhythmia alarm is turned off. Therefore, be
careful when you turn off an arrhythmia alarm.
1. Touch the data area of the bed you are going to set alarms for. The Individual
Bed window for the bed is displayed.
You can also display the Arrhythmia Alarm window by the following operation.
• Touch [Admit/Discharge] on the Individual Bed window to display the Admit/
Discharge window. Touch [Alarm Settings] → [Arrhythmia Alarm].
• Touch the [Arrhythmia Alarm] individual function key if [Arrhythmia Alarm]
is registered to an individual function key. For setting individual function
keys, refer to “Changing the All Beds Screen Display Settings” in Section 6.
4. Set the arrhythmia alarm [ON] or [OFF] or set the detection condition. When
a detection condition is touched, the setting window is displayed. 5
Closes the
window.
Setting value
Depending on the bedside monitor setting, some items are not available.
Detection Condition
Item Alarm
Setting Range Step
ASYSTOLE 3 to 10 s 1
V FIB —
ON (fixed) 16 to 300 bpm* 1
1
V TACHY The value must be more than V BRADY value (bpm).
VPC RUN value (beats) to 9 beats*1 1
16 to 300 bpm
EXT TACHY The value must be the same or more than TACHYCARDIA value 1
(bpm).
15 to 299 bpm
EXT BRADY The value must be the same or less than BRADYCARDIA value 1
(bpm).
16 to 300 bpm*1
1
ON, OFF The value is synchronized with the V TACHY value (bpm).
VPC RUN
3 to 8 beats
1
The value must be the same or less than V TACHY value (beats).
15 to 299 bpm
V BRADY*1 1
The value must be less than the V TACHY value (bpm).
16 to 300 bpm 1
SV TACHY*1
3 to 9 beats 1
PAUSE*1 1.0 to 3.0 s 0.1
TACHYCARDIA*2
—
BRADYCARDIA*2
COUPLET
EARLY VPC
MULTIFORM
—
V RHYTHM*1 ON, OFF
BIGEMINY
TRIGEMINY*1
FREQ VPC 1 to 99 bpm 1
IRREGULAR RR*1
PROLONGED RR —
NO PACER PULSE*1 ON, OFF
PACER NON-
40 to 480 ms 4
CAPTURE*1
*1 For these items, alarm detection condition can be set when arrhythmia type for bedside monitor is set to “EXTENDED”.
*2 The settings are synchronized with the HR alarm limits settings. The values cannot be set on the Arrhythmia Alarm
setting window.
3. Touch [ST Alarm] of the Personal Setup to display the ST Alarm window.
You can also display the ST Alarm window by the following operation.
• Touch [Admit/Discharge] on the Individual Bed window to display the
Admit/Discharge window. Touch [Alarm Settings] → [ST Alarm].
• Touch [ST Alarm] individual function key if [ST Alarm] is registered to
an individual function key. For setting individual function keys, refer to
“Changing the All Beds Screen Display Settings” in Section 6.
4. Touch the parameter key for set the alarm limits. Set the alarm limits on the
Alarm Limits Setting window.
AUTO
Touch to automatically set the upper/lower
limit of all the measurable leads for the bed.
Upper/lower limit
Current value
Upper/
lower limit Upper limit
Current value is displayed.
Current
value Increase/Decrease keys
Increases or decreases the
value. Press and hold the
key to change the value
continuously.
Lower limit
Current value is displayed.
Auto
Current measurement value Touch to automatically
set the upper or lower
Trendgraph of past four hours Upper/lower limit slide bar
limit of the lead.
is displayed. Upper or lower Touch the bars to set the value.
limit is shown in the blue line
when changing the limit. When setting the limit to OFF, set the
limit to the maximum or minimum value
and touch the increase or decrease key.
Setting Range
Item Step Unit
Lower Limit Upper Limit
ST −2.00 to 1.99 −1.99 to 2.00 0.01 mV
ST alarm setting window Touch [Auto] on the ST alarm setting window to set the upper or lower limit of
the lead.
ST Alarm window Touch [Auto] on the ST Alarm window to set the upper or lower limit of all the
measurable leads for the bed.
1. Touch the data area of the bed you are going to set alarms for. The Individual
Bed window for the bed is displayed.
3. Touch [Alarm Limits] of the Personal Setup to display the Alarm Limits
window.
You can also display the Alarm Limits window by the following operation.
• Touch [Admit/Discharge] on the Individual Bed window to display the Admit/
Discharge window. Touch [Alarm Settings] → [Alarm Limits].
• Touch the [Alarm Limits] individual function key if [Alarm Limits] is
registered to an individual function key. For setting individual function keys,
refer to “Changing the All Beds Screen Display Settings” in Section 6.
5. Select the alarm master and alarm type and check the settings.
Touch to change the alarm
master.
Touch [ ] or [ ] to scroll
the window.
Example: When a bed monitored 6. After checking the settings, touch [Apply]. The confirmation window
through a multiple patient receiver
appears.
7. Touch [Yes]. The alarm limits, arrhythmia alarm and ST alarm master
settings are copied to the alarm settings. If the bed is monitored through an
ORG-9100 series multiple patient receiver, ECG analysis detection leads and
QRS detection type are also copied.
Adjust the alarm sound volume at the Sound Control window on the System
Setup. There are seven volume levels.
NOTE
• You cannot set the alarm sound volume to OFF.
• You cannot lower the alarm volume set at [Alarm Volume Limit] on
the [Alarm] of the System Configuration window. For [Alarm Volume
Limit], refer to “System Configuration Settings” in Section 6-1 of the
Administrator’s Guide.
1. Touch [Menu] on the left lower corner of the screen → [System Setup] to
display the Information window of the System Setup screen.
When [System Setup] is assigned to one of the all beds function keys,
the Information window of the System Setup screen can be displayed by
touching the function key. Refer to “Function Keys Setting” in Section 6-1
of the Administrator’s Guide to assign a function to the function key.
Alarm volume
(white) 5
Set on the System
Setup screen.
Alarm Notice
You can set the alarm notice function to display an alarm notice icon on the All
Beds screen, data area of the bed and Individual Bed window when a vital sign,
arrhythmia or technical alarm occurs on this central monitor.
NOTE
• To activate the alarm notice function, you need to set the notice mode
at [Alarm Notice Icon] on [System Configuration] → [Alarm] of the
System Setup screen. [ON] is the factory default setting. Refer to
“System Configuration Settings” in Section 6-1 of the Administrator’s
Guide.
• The alarm notice function is only available for beds whose data is saved
in this central monitor.
• When you use the alarm notice function and there are two or more
central monitors in the network, confirm that all central monitors in the
network have the same settings for [Alarm Notice Icon] on the [System
Configuration] → [Alarm] window of the System Setup screen. If some
central monitors activate the alarm notice function and others do not,
you might misjudge that there was no alarm for a bed by observing the
bed at a central monitor where the notice function is not activated.
• When 24 or 32 beds are monitored, the alarm notice icon is not
displayed on the data area for each bed of the Individual Bed window.
Touch the alarm notice icon to display the Event List window and check details
of the alarms. When the screen is changed, the alarm for the bed is silenced.
NOTE
The oldest file of the Event List is automatically deleted to create a new
file. If an alarm history file with an alarm notice icon is deleted before you
touch the icon, the icon remains on the screen.
5
Touch to sort the files by
presence of an alarm notice
icon.
Technical Icon
NOTE
To display the technical icons, [Technical Icon] of the [System
Configuration] → [Alarm] on the System Setup must be set to [ON].
The default setting is [OFF]. Refer to “System Configuration Settings” in
Section 6-1 of the Administrator’s Guide.
You can set the technical icon display function to display an ECG or SpO2
technical icon on the All Beds screen when the ECG or SpO2 technical status
become yellow or red.
When a technical icon is touched, the Alarm Events window of the bed and
action message for the icon are displayed.
The technical icon disappears when the technical status becomes green or [Yes]
is touched for the action message.
ECG technical icon
When the technical icon is touched,
the Alarm Event window of the bed is
displayed.
SpO2 technical
icon
Action message
When [Yes] is touched, the technical icon
and action message disappear. When [No]
is touched, the message disappears but the
icon is displayed continuously.
When the ECG and SpO2 measurement conditions become yellow or red at the
same time, only the ECG technical icon is displayed. When the icon is touched,
both ECG and SpO2 action messages are displayed.
You can check that the alarm indicator and alarm sound are functioning properly.
During an alarm occurrence, you cannot check the alarm function.
CAUTION 5
When the monitor is turned on, check that a single beep sounds and
the red, yellow, cyan and green alarm indicator lamps blink once.
This shows that the alarm is functioning properly.
1. Touch [Menu] on the left lower corner of the screen → [Alarm Check] to
display the Alarm Check window.
When [Alarm Check] is assigned to one of the all beds function keys, the
Alarm Check window can be displayed by touching the function key. Refer
to “Function Keys Setting” in Section 6-1 of the Administrator’s Guide to
assign a function to the function key.
Overview............................................................................................................................................................... 6.2
Displaying the All Beds Screen.................................................................................................................. 6.2
Description of All Beds Screen............................................................................................................................. 6.4
Monitored Group........................................................................................................................................ 6.5 6
Transmitter Battery Status Icon.................................................................................................................. 6.5
Changing the All Beds Screen Display Settings................................................................................................... 6.7
Displaying All Beds Screen Setup Window................................................................................................ 6.7
Setting the All Beds Screen Setup............................................................................................................. 6.8
Setting Items.............................................................................................................................................. 6.9
Wave Selection................................................................................................................................ 6.9
Numerical Selection....................................................................................................................... 6.10
Other.............................................................................................................................................. 6.11
Function Keys................................................................................................................................. 6.11
Setting Parameter Priority.................................................................................................................................. 6.12
Displaying the Parameter Priority Window............................................................................................... 6.12
Setting Parameter Priority........................................................................................................................ 6.13
Recording on the All Beds Screen...................................................................................................................... 6.14
Manual Recording.................................................................................................................................... 6.14
Settings for Manual Recording....................................................................................................... 6.14
Recording Example........................................................................................................................ 6.14
All Beds Recording................................................................................................................................... 6.14
Settings for All Beds Recording..................................................................................................... 6.15
Recording Example........................................................................................................................ 6.15
Other Recordings..................................................................................................................................... 6.15
On the All Beds screen, you can view waveforms and numeric data of all
monitored beds at the same time. This section explains how to display the All
Beds screen, screen description, display settings and recording on the All Beds
screen.
Overview
NOTE
Sometimes numeric data and messages disappear for a moment. This is
normal and occurs when the display is refreshed.
WARNING WARNING
Do not diagnose a patient based only on data After attaching electrodes, probes and sensors
acquired by the central monitor. Overall on the patient and connecting cables to the
judgement must be performed by a physician bedside monitor and/or transmitter, check that
who understands the features, limitations and there is no error messages and the waveforms
characteristics of the central monitor and by and numeric data are appropriately displayed on
reading the biomedical signals acquired by other the screen. If there is an error message, or
instruments. waveform or numeric data is not appropriate,
check the electrodes, probes and sensor
attachment, patient condition and settings on the
bedside monitor and/or transmitter and remove
the cause.
WARNING
A physician must be within the range where he/
she can hear the alarm sound of the central
monitor while monitoring a patient on the central
monitor. If the physician cannot hear the alarm
sound, critical changes on the patient may be
overlooked.
NOTE
When a screen other than the All Beds screen is displayed and there is
no key operation for a certain period, the screen automatically returns to
the All Beds screen. You can set the period at [Screen Timeout] on the
System Configuration window of the System Setup screen. The factory
default setting is set to five minutes.
Management
group color
NOTE: You can change the display type when Data area for each bed
monitoring more than one blood pressure When you touch inside the frame for a bed, the Individual Paused bed
waveform on [Display] → [BP Scale] of the Bed window for the touched bed is displayed. Refer to Section 4.
PRESS window (Refer to Section 12) or
[Other] → [BP Scale] of the Individual Bed
Screen Setup window (Refer to Section 8).
[ ]
Appears on a bed when an alarm occurs.
Touch to silence the alarm.
[ ]
Appears on a bed when an alarm occurs
if the [Alarm Notice Icon] is set to [ON].
Touch to display the Event List window.
Refer to Section 5.
Menu Messages about the All beds function key Date and time
Displays each screen. system are displayed. Changes the screen. The screen for the
function keys are set on the System Setup Icons
screen. Refer to the Administrator's Guide.
Monitored Group
On each bed of the All Beds screen, monitored group color is displayed
corresponding to the monitored group. The monitored group of each bed is set on
the [Admit/Discharge] window. A color for each group can be set on the [Pre-
registration] → [Group Color] window on the System Setup screen. Refer to
“Pre-registration” in Section 6-1 of the Administrator’s Guide.
The large change transmitter battery icon disappears in the following cases:
• When the central monitor receives a signal from the transmitter again.
• When the channel is changed.
• When the patient is admitted or discharged.
• When the central monitor power is turned on or off.
NOTE
The “Change Transmitter Battery” message/alarm and the change battery
icon might only be displayed for a short time depending on the battery.
When the message is displayed, change the battery immediately.
You can select whether or not to display the transmitter battery status icon in
[Monitor Setting] → [Display Settings] → [All Beds Screen] of the System
Setup screen. Refer to “Monitor Setting” in Section 6-1 of the Administrator’s
Guide.
Set the settings for the All Beds screen display for each bed on the All Beds
Screen Setup window of the Setup window.
The following settings can be set on the [Monitor Setting] → [Display Settings]
→ [All Beds Screen] of the System Setup screen.
• All Beds Numeric Area (Normal, Wide)
• All Beds Numeric Size (Normal, Large) 6
• Display Patient Name (ON, OFF)
• Large Patient Name (ON, OFF)
3. Touch [All Beds Screen Setup] of the Setup Menu to display the All Beds
Screen Setup window.
You can also display the All Beds Screen Setup window by the following
procedures.
• Touch [Admit/Discharge] on the individual window to display the [Admit/
Discharge] window. Touch [Display Settings] → [All Beds Screen Setup].
• Touch [All Beds Screen Setup] individual function key if [All Beds Screen
Setup] is registered to an individual function key. For setting individual
function keys, refer to “Changing the All Beds Screen Display Settings” in
Section 6.
Waveform
display order
Parameter of
the waveform
Sensitivity and
scale can be
changed by
touching the key.
Setting Items
Wave Selection
• Auto + 1 ECG:
The ECG waveform which is set to [Arrhythmia
Detection Lead 1] is displayed. Other waveforms are
selected automatically depending on the parameter
priority.
• Auto + 2 ECG:
The ECG waveforms which are set to [Arrhythmia
Detection Lead 1] and [Arrhythmia Detection Lead
2] are displayed. Other waveforms are selected
automatically depending on the parameter priority.
Display
order of the
waveforms
Sens/Scale Set for each waveform. Sets the sensitivity and scale of the displayed waveforms. The
sensitivity and scale setting is synchronized with the setting of
the Individual Bed Window Display Setting and each parameter
setting window.
Touch the Sens/Scale key to display the setting
window and set the sensitivity and scale.
Numerical Selection
The first parameter is displayed in larger size and the other parameters
are displayed in the remaining area in equal smaller size when the
[All Beds Numeric Size] is set to [Large]. However, on the All Beds
screen or when monitoring 24 or 32 beds, the first parameter cannot be
displayed in larger size.
Display
order of the
numeric value
NOTE
If the number of measured parameters is less than the selected
maximum number of parameters, the number of displayed
parameters decreases automatically.
Other
• Wide
All Beds Normal, Large Selects the size of the numeric data on the All Beds screen. 6
Numeric
• Normal
Size*
• Large
HR Display HR+VPC+ST, HR Only Selects the display format when the display order of HR is 1 on
Display of the Numerical Selection.
• HR+VPC+ST: VPC count and ST value are displayed together
with the heart rate.
• HR: HR only
* [All Beds Numeric Area] and [All Beds Numeric Size] settings cannot be used when monitoring 24 or 32 beds.
Function Keys
Set the parameter priority for each bed on the Parameter Priority window. The
parameter priority is synchronized with the Individual Bed window.
You can also display the Parameter Priority window by either of the following
procedures.
• Touch [Admit/Discharge] on the individual window to display the [Admit/
Discharge] window. Touch [Display Settings] → [Parameter Priority].
• Touch [Parameter Priority] of the individual function key if [Parameter
Priority] is registered to an individual function key. For setting of individual
function keys, refer to the Administrator’s Guide.
2. Touch the priority position to move the parameter to. The parameter which
was selected in step 1 moves to the priority which is selected in step 2.
Before After
Parameter
priority AO moves from priority
8 to 3
The parameters of
priority 3 to 7 is move to
priority 4 to 8.
Reset
Return the parameter priority to the default setting.
Manual Recording
Touch [ ] of the desired bed on the All Beds screen. The waveform of the
selected period and numeric data are printed on the WS-960P Recorder Unit.
Recording Example
NOTE
[Record All] key must be registered to an all beds function key on
the [Function Keys] setting of the System Setup screen. Refer to the
Administrator’s Guide.
Touch the [Record All] function key to start recording. To stop recording, touch
[Record All] again.
Set for each bed. The settings are same as the settings for manual recording.
Refer to “Settings for Manual Recording” in this section.
6
Recording Example
Other Recordings
On the All Beds screen, the following recordings are available with the WS-960P
Recorder Unit.
• Auto Recording
Periodic Recording: refer to “Periodic Recording” in Section 10.
Alarm Recording: refer to “Alarm Recording” in Section 5.
On the All Beds Alarms window, you can check the alarm events of several
patients on one window and check the upper and lower limits alarm settings.
This section explains how to display the window and change the display format,
window layout and recording on the window.
When [All Beds Alarm Events] or [All Beds Limits] is assigned to one of
the all beds function keys, the All Beds Alarms window can be displayed by
touching the function key. Refer to “Function Keys Setting” in Section 6-1 of the
Administrator’s Guide to assign a function to the function key.
Tabs
Change the display format of the All Beds Alarms window. Each group is set on the
Admit/Discharged window.
[Admitted Patient]: Displayed in the same format as the All beds screen.
[Group A to J]: Displays the group of beds set on the Admit/Discharged window.
Group name is set in [Pre-registration] → [Group Color]. Refer
to the Administrator’s Guide, Section 6-1.
[ ]
Changes the display type.
[ ]
In dual display composition, touch [ ] → [Change Disp.] to display the
setting window and select beds to be displayed on the window. In single
display composition, only the [Main and Second Display] is displayed.
[Main and Second Display]: Displays all registered beds on the central
monitor.
[Main Display]: Displays registered beds on the main display.
[Second Display]: Displays registered beds on the second display.
Displays the All Beds Displays each All Beds Alarms Returns to the All Beds screen.
screen. window.
The All Beds Alarm Events window displays up to 120 hours of alarm events for
the several patients on one window in the most recent 10,000 files.
NOTE
• The All Beds Alarm Events window is only available at the central
monitor where the bed’s data is saved.
• After 10,000 files are created for the patient, the oldest file of the patient
is automatically deleted when a new file is created.
Specified alarm events are displayed depending on the following display type.
• Vital Alarm Event
• Arrhythmia Alarm Event
• Technical Alarm Event
To change the display type, refer to the “Changing the Display Type” in this
section.
The All Beds Alarm Events window can be displayed by touching [All Beds
Alarm Events] on the bottom of the screen.
When [All Beds Alarm Events] is assigned to one of the all beds function keys,
the All Beds Alarm Events window can be displayed by touching the function
key. Refer to “Function Keys Setting” in Section 6-1 of the Administrator’s
Guide to assign a function to the function key.
Alarm event
Alarm Alarm Displays in color corresponding
Patient name and bed name Generated Recovered to its alarm level from alarm
generation to recovery.
Technical status
Display Item
Displays the judged
Displays specified alarm
technical status. Refer
events depending on the
to later in this section.
display type.
Tabs
Changes the display format of the All
Beds Alarms window.
7
Touching each bed area displays
the Individual Bed window (Alarm
Events window). Refer to Section 9.
[ ]
Changes the
display type.
*1 Typical labels of arterial pressure (ART, ART2, RAD, DORS, AO, and FEM)
*2 “COMMUNICATION LOSS” is displayed when the monitored bed is a
bedside monitor on the network.
For details about technical alarms, refer to “Error Messages” in Section 14.
The judgment is done in each ECG, SpO2 and Other category and the color of the
highest level is displayed.
On a All Beds Limits window, you can display the alarm limits for several
patients on one window.
Upper and lower limit settings are set on the Alarm Limits window. Refer to
“Setting Alarm Limits” in Section 5.
The All Beds Limits window can be displayed by touching the [All Beds Limits]
on the bottom of the All Beds Alarms window.
When [All Beds Limits] is assigned to one of the all beds function keys, the All
Beds Limits window can be displayed by touching the function key. Refer to
“Function Keys Setting” in Section 6-1 of the Administrator’s Guide to assign a
function to the function key.
Touching the each bed name
displays the All Beds Limits
window. Refer to “Displaying an
All Beds Alarms Window” in this Patient name and bed name Parameter
section. Displays the monitoring parameter or
parameter set on [Parameter Setup] →
[Parameter Selection] on the System Setup
screen.
Upper/lower limit
Tabs
Change the display format of the All
Beds Alarms window.
[ < ][ > ]
Scrolls the window left to right.
Display the window and touch [ ]. With the laser printer, you can print the
displayed window.
Overview............................................................................................................................................................... 8.2
Displaying the Individual Waveforms Window............................................................................................ 8.2
Displaying the Individual Numeric Vital Signs Window or ECG 12 Leads Window.................................... 8.3
Description of the Individual Bed Window............................................................................................................ 8.4
Individual Waveforms Window.................................................................................................................... 8.4
Individual Numeric Vital Signs Window...................................................................................................... 8.5
ECG 12 Leads Window.............................................................................................................................. 8.6
Changing the Individual Bed Window Display Settings........................................................................................ 8.7 8
Setting the Individual Bed Window Setup................................................................................................... 8.8
Setting Items.............................................................................................................................................. 8.9
Wave Selection................................................................................................................................ 8.9
Numerical Selection....................................................................................................................... 8.10
Other.............................................................................................................................................. 8.11
Recording on the Individual Bed Window........................................................................................................... 8.12
Manual Recording.................................................................................................................................... 8.12
Settings for Manual Recording....................................................................................................... 8.12
Recording Example........................................................................................................................ 8.12
Individual Bed Window Printing................................................................................................................ 8.13
Other Recordings..................................................................................................................................... 8.13
The Individual Bed window displays waveforms and numerical data of one
monitored bed. This section explains how to display the Individual Bed window
and change the display format, screen layout and recording on the window.
Overview
NOTE
Sometimes numeric data and messages disappear for a moment. This is
normal and occurs when the display is refreshed.
Displaying the Individual Numeric Vital Signs Window or ECG 12 Leads Window
1. Display the Individual Waveforms window.
Waveform
Sensitivity Touch the waveform to display
Message area Lead name the setting window to change the
[ ] QRS sync mark sensitivity and scale.
Messages are
Records displayed numeric
displayed.
data and waveforms. Numeric data
When a vital sign alarm occurs, the numeric data is highlighted. When an alarm occurs for
a parameter which is not displayed on the screen, the displayed parameter changes to the
Data area for each bed alarmed parameter and is highlighted. Upper and lower limits can be changed by touching the
When you touch inside the frame for a bed, numeric data and displaying the setting window.
the Individual Bed window for the touched
bed is displayed. The background of the
selected bed turns blue.
On the PU-621R Op No. 21A, the
background can be set to off. Refer to
“Selecting Bed Display” in Section 6-2 of
the Administrator’s Guide.
[ ]
Appears on a bed when an alarm occurs. Touch
to silence the alarm.
[ ]
Appears on a bed when an alarm occurs if
the [Alarm Notice Icon] is set to [ON]. Touch
to display the Event List window. Refer to
Section 5.
When a CRISIS or WARNING level
alarm occurs, the data display frame of the
alarming bed blinks or is highlighted. Refer
to Section 5.
Menu Date and time
Messages about system are Records or prints the displayed
Displays each screen
displayed. window. Icons
or window.
For the basic operation, refer to the “Basic Operation on the Individual Bed
Window” in Section 1.
[ ]
Appears on a bed when an alarm occurs
Receiving channel*
Patient name if the [Alarm Notice Icon] is set to [ON].
8
Touch to display the Event List window.
: Vital sign alarm limit off mark Refer to Section 5.
: Non-paced mark
Message area Note
On the Expand Individual Bed screen, Messages are displayed. Refer to Section 4.
the waveforms are displayed to the
right of the numeric data. Refer to the
“Expand Individual Bed Screen” in
Section 1.
Numeric data
When a vital sign alarm occurs, the numeric data is highlighted. Upper and lower
limits can be changed by touching the numeric data and displaying the setting
window. Refer to Section 5.
Menu
Records or prints the Date and time
Displays each screen. Message about the system are
displayed window.
displayed. Icons
For the basic operation, refer to the “Basic Operation on the Individual Bed
Window” in Section 1.
Receiving channel*
Patient name
Message area
Messages are displayed.
Waveform
Lead name Sensitivity Touch the waveform to display
QRS sync mark the setting window to change the
sensitivity and scale.
Numeric data
When a vital sign alarm occurs, the numeric data is highlighted. When an alarm occurs for
a parameter which is not displayed on the screen, the displayed parameter changes to the
alarmed parameter and is highlighted.
Menu
Records or prints the Date and time
Displays each screen. Message about the system are
displayed window.
displayed. Icons
For the basic operation, refer to the “Basic Operation on the Individual Bed
Window” in Section 1.
8.6 Operator’s Manual CNS-6201
8. INDIVIDUAL BED WINDOW
On the Individual Bed Screen Setup window of the Setup window, set the
settings for each Individual Bed window display.
1. Touch the desired bed on the All Beds screen to display Individual Bed
window.
3. Touch [Other Setup] → [Individual Bed Screen Setup] of the Setup Menu to
display the Individual Screen Setup window.
You can also display the Individual Screen Setup window by the following
procedures.
• Touch [Admit/Discharge] on the Individual Bed window to display the Admit/
Discharge window. Touch [Display Settings] → [Individual Bed Screen
Setup].
• Touch [Individual Bed Screen Setup] of the individual function keys if
[Individual Bed Screen Setup] is registered to an individual function key.
For setting individual function keys, refer to “Changing the All Beds Screen
Display Settings” in Section 6.
Operator’s Manual CNS-6201 8.7
8. INDIVIDUAL BED WINDOW
Waveform
display order
Parameter of
the waveform
Sensitivity and
scale can be
changed by
touching the key.
Setting Items
Wave Selection
• Auto + 1 ECG:
The ECG waveform which is set to [Arrhythmia 8
Detection Lead 1] is displayed. Other waveforms are
selected automatically depending on the parameter
priority.
• Auto + 2 ECG:
The ECG waveforms which are set to [Arrhythmia
Detection Lead 1] and [Arrhythmia Detection Lead
2] are displayed. Other waveforms are selected
automatically depending on the parameter priority.
Display
order of the
waveforms
Sens/Scale Set for each waveform. Sets the sensitivity and scale of the displayed waveforms. The
sensitivity and scale setting is synchronized with the setting of
the All Beds Screen Display Setting and each parameter setting
window.
Touch the Sens/Scale key to display the setting
window and set the sensitivity and scale.
Touch the Customize scale key to select a custom scale for the
waveform. The value of the custom scale is set on the Trend
window. Refer to the “Setting the Customized Scale” in Section
9.
Numerical Selection
VPC and ST are also displayed when the first parameter is HR.
Display
order of the
numeric value
Other
Manual Recording
Touch [ ] of the desired bed on the Individual Bed window. The waveform of
the selected period and numeric data are printed on the WS-960P Recorder Unit.
When the [ ] of the data area is touched, the waveform of the bed is recorded.
Recording Example
Refer to “Recorded/Printed Data” in Section 10.
8
Other Recordings
On the Individual Bed window, the following recordings are available with the
WS-960P Recorder Unit.
• Auto Recording
Periodic Recording: refer to “Periodic Recording” in Section 10.
Alarm Recording: refer to “Alarm Recording” in Section 5.
This section explains the review windows which can display past data of a
monitored bed.
The review window displays the vital sign data of one bed that is selected from
the monitored beds. There are eleven types of review windows. Two review
windows can be displayed together on the same window.
• Trend window
• Tabular Trend window
• Full Disclosure window 9
• Expanded Waveform window
• Event List window
• ST Recall window
• Arrhythmia Recall window
• SpO2 Trend window (Full size display only)
• ECG 12 Lead Analysis window (Full size display only)
• Hemodynamics List window
• Alarm Events window
For the Discharged Patients List window, refer to the “Discharged Patients List”
later in this section.
Review data of a discharged patient or a patient whose data was deleted can be
displayed within 120 hours after the patient is discharged or the data deletion.
If you want to check an event in the Event List window and the waveform of
the same time, select the event and change the window to Expanded Waveform
window. The expanded waveform for the time of the selected event is displayed
on the window. The time of the two review windows displayed on the same
window is also synchronized. In the review windows, various data such as
vital sign data at the time of the selected patient can be viewed by changing the
review window.
NOTE
If a new file is created when the maximum number of files has already
been reached, the oldest file is deleted. Data is automatically deleted
after the maximum 120 hours regardless of the number of files.
Review Window
Display Pattern
Upper Area Lower Area
Custom Review Tabular Trend Trend
Tabular Trend Tabular Trend Trend
Trend Trend Expanded Waveform
Trend Trend Alarm Events
Full Disclosure Full Disclosure Expanded Waveform
Arrhythmia Recall Arrhythmia Recall Full Disclosure
Event List Event List Expanded Waveform
Alarm Events Alarm Events Expanded Waveform
Full Disclosure Full Disclosure (Full size display)
ECG 12 Lead Analysis ECG 12 Lead Analysis (Full size display)
ST Recall ST Recall (Full size display)
Hemodynamics List Hemodynamics List (Full size display)
* The display pattern and pattern name for Custom Review can be changed.
Other display patterns cannot be changed.
1. Touch [ ] on the Individual Bed window and select the Custom Review
and display the review window.
The selected pattern is displayed on the upper right area of the review
window.
Display pattern name
2. Touch the display pattern name to display a keyboard and change it to the
desired name. The changed name is displayed on the upper right area of the
review window.
Registers a comment. Refer to later in this section. Displays the review window.
For the basic operation, refer to “Basic Operation on the Individual Bed
Window” in Section 1.
Registering Comments
You can register the comments on the review window which are common for all
the review windows. The registered comments are displayed on the event list.
Example: Tabular Trend window 1. Move the cursor to the data and time to register the comment on each review
window.
2 ii) Enter the date and time or comment and touch [ENTER].
iii
Delete
ii Deletes a registered comment.
Checking Comments
Example: Tabular Trend window Touch the comment icon [ ] on each review window and check the registered
comment.
Date and time of comment registry Comment
If several comments are displayed, Displays the registered comment.
select the date and time.
[ ]
Closes the window.
Edit
Displays the comment registry window and
allows editing or deleting the registered
comments.
Trend
The Trend window displays measured parameter values and events of the most
recent 120 hours as trendgraphs.
[ ]: Changes between split display and full size display.
[ ]: Changes to a different review window.
[ ]: Changes to a different Trend window (Trend 1 to 3 and Common
Scale).
Scale [ ]: Changes the trendgraph display format. Refer to “Changing the
Changes the scale. Refer to “Setting Display Format of the Trendgraph”.
the Scale of a Displayed Parameter”.
Parameter name
Comment icon Cursor
Changes the displayed
Synchronizes with other review windows. On
parameters. Refer to “Setting Displayed when a comment is entered.
Touch to check the comment. Refer to the upper part of the cursor, the date and time
the Displayed Parameters Measurement
“Checking Comments”. at the cursor is displayed. You can move the
and Events”. data at the cursor
cursor by touching directly on the cursor.
position.
Trendgraph
Time bar (Displayed time width)
Window name
Parameter
trendgraphs
Event trendgraphs
Changes the
displayed event.
Time axis (120 hours) Range before admission Range of displayed time width
The range before admission and the
range of the displayed time width and
the cursor are displayed on the time axis.
Registers a comment at the date and You can move the cursor by directly
time of the cursor position. Refer to touching the time axis. Cursor
“Registering Comments”.
Number of
Trend Window Number of Events
Parameters
Trend 1 and Trend 2 3 parameter 6 events
Trend 3 7 parameters 3 events
Common Scale 4 parameters 3 events
Example: Trend 3
7 parameters
9
3 events
4 parameters
3 events
When the Trend window is Common Scale, the layout is fixed to four parameters
and three events. For other layouts, the event can be changed to parameter. Refer
to “Setting the Displayed Parameters and Events”.
The display format of the trendgraph and cursor display label depends on the
parameter.
When the Trend window is Common Scale, the graph layout is fixed to AVE.
Setting
Parameter
Max-Min Ave
Parameters other Max Mean
than following:
• IBP parameters
• PAW, PAW Graph display
(EXT)
• NIBP (when
the display time Min
width is 8, 12,
24, 48, 96, or 120 Measurement
hours) data at the cursor Max, Min, Inst*1 Average, Inst*1
• VPC position
• APNEA (T)
Max Max
IBP parameters
(ART, ART2, RAD,
DORS, AO, FEM, Graph display
UA, UV, PAP,
CVP, RAP, RVP, Mean Mean
LAP, LVP, ICP, Min Min
ICP2 to ICP4, P1 Measurement
to P8, CNIBP) SYS (MAX), DIA SYS (MAX), DIA
data at the cursor
(MIN), MEAN (MIN), MEAN*2
position
Ppeak (Max) Ppeak (Mean)
Graph display
PAW, PAW(EXT)
PEEP (Min) PEEP (Mean)
Measurement
data at the cursor Ppeak/PEEP Ppeak/PEEP*2
position
Systolic
Graph display
VPC, APNEA (T)
Measurement
data at the cursor VPC or APNEA (T) value
position
IBP parameters, PAW and PAW (EXT) at the cursor position are displayed as
each average value.
The parameters can be set from the monitoring parameters and parameters set on
the [Parameter Setup] → [Parameter Selection] of the System Setup screen. For
the parameter settings, refer to Section 6-1 of the Administrator’s Guide.
iii) Touch [ ] to close the setting window after the setting is complete.
AUTO
The monitoring parameters are set according to the parameter
priority. The event trends are not displayed and all the parameter
trendgraphs are displayed.
iii
ii
i
Event name To deselect the event, touch [NONE] or touch the selected event again.
When deselecting all the selected events, iv) Touch [ ] to close the setting window after the setting is complete.
the [Parameter Setup] tab is available.
AUTO
The parameters which have the trend data are set
NOTE: When the display layout is Number of selected events according to the parameter priority. The event trends
[Common Scale], the [Parameter are not displayed and all the parameter trendgraphs are
Setup] tab is not available. displayed.
iv
ii
i iii
3. Enter the scale using the numeric key pad and touch [ENTER].
2
4. After entering the upper limit and lower limit scale, touch [OK] to close the
Customize Scale window.
Scale
Parameter Description Unit
Setting Range Default
0-100, 0-200, 0-300,
HR Heart rate bpm 0-200
Customize (Default: 0-200)
0-20, 0-50, 0-100,
VPC VPC rate count/min 0-20
Customize (Default: 0-20)
−0.20-0.20, −0.50-0.50,
ST mV −1.00-1.00, −2.00-2.00, −0.20-0.20
(I, II, III, aVR, aVL, Customize (Default: −0.20-0.20)
ST level
aVF, V1 to V6, V, MCL, −2.0-2.0, −5.0-5.0, −10.0-10.0,
ECG1, ECG2) mm −20.0-20.0, −2.0-2.0
Customize (Default: −2.0-2.0)
0-20, 0-50, 0-75, 0-100, 0-160,
mmHg 0-200, 0-300, 50-200, 0-200
ART, ART2, RAD,
Customize (Default: 0-200)
DORS, AO, FEM, LVP,
P1 to P8 0.0-3.0, 0.0-7.0, 0.0-10.0, 0.0-14.0,
kPa 0.0-22.0, 0.0-28.0, 0.0-40.0, 7.0-28.0, 0.0-28.0
Customize (Default: 0.0-28.0)
0-20, 0-50, 0-75, 0-100, 0-160,
mmHg 0-200, 0-300, 50-200, 0-100
Invasive blood Customize (Default: 0-100)
UA
pressure 0.0-3.0, 0.0-7.0, 0.0-10.0, 0.0-14.0
kPa 0.0-22.0, 0.0-28.0, 0.0-40.0, 7.0-28.0, 0.0-14.0
Customize (Default: 0.0-14.0 )
0-20, 0-50, 0-75, 0-100, 0-160,
mmHg 0-200, 0-300, 50-200, 0-50
UV, PAP, RAP, RVP,
Customize (Default: 0-50)
CVP, LAP, ICP, ICP2 to
0.0-3.0, 0.0-7.0, 0.0-10.0, 0.0-14.0,
ICP4
kPa 0.0-22.0, 0.0-28.0, 0.0-40.0, 7.0-28.0, 0.0-7.0
Customize (Default: 0.0-7.0)
0-100, 0-200, 0-300,
mmHg 0-200
Customize (Default: 0-200)
NIBP
0.0-16.0, 0.0-32.0, 0.0-40.0,
kPa 0.0-32.0
Customize (Default: 0.0-32.0)
Non-invasive blood 0-20, 0-50, 0-75, 0-100, 0-160,
pressure mmHg 0-200, 0-300, 50-200, 0-200
Customize (Default: 0-200)
CNIBP
0.0-3.0, 0.0-7.0, 0.0-10.0, 0.0-14.0,
kPa 0.0-22.0, 0.0-28.0, 0.0-40.0, 7.0-28.0, 0.0-28.0
Customize (Default: 0.0-28.0)
Spontaneous
RRspon (EXT)
respiration rate 0-50, 0-150,
count/min 0-50
RR, RR (IMP, THM, Customize (Default: 0-50)
Respiration rate
CO2, FLOW, EXT, GAS)
Apnea time
(Total time in one 0-60,
APNEA (T) s 0-60
data segment, in Customize (Default: 0-60)
seconds)
0-100, 50-100, 80-100,
SpO2, SpO2-2 80-100
Saturated oxygen Customize (Default: 80-100)
%
from pulse oximeter −5-5, −10-10, −20-20,
Delta SpO2 −5-5
−50-50, Customize (Default: −5-5)
Scale
Parameter Description Unit
Setting Range Default
Scale
Parameter Description Unit
Setting Range Default
MV, MV (EXT) Minute volume
0.0-6.0, 0.0-12.0, 0.0-30.0,
Spontaneous minute L/min 0.0-12.0
MVspon (EXT) Customize (Default: 0.0-12.0)
volume
0-500, 0-1000, 0-2000,
TV mL 0-1000
Customize (Default: 0-1000)
Tidal volume
0.0-0.5, 0.0-1.0, 0.0-2.0, 0.0-6.0,
TV (EXT) L 0.0-1.0
Customize (Default: 0.0-1.0)
Paw, Paw (EXT) Airway pressure
Mean airway
Pmean (EXT)
pressure cmH2O, 0-10, 0-20, 0-50, 0-100, 0-150,
0-50
Minimum airway hPa Customize (Default: 0-50 )
Pmin (EXT)
pressure
Pplat (EXT) Plateau pressure
mL/
0-50, 0-100, 0-200,
C (EXT) Compliance cmH2O, 0-100
Customize (Default: 0-100)
mL/hPa
cmH2O/L/ 0-6, 0-10, 0-20,
R (EXT) Airway resistance 0-10
S, hPa/L/S Customize (Default: 0-10)
N2O (E) (GAS), N2O (I) 0-80, 0-100, 50-100,
Nitrous oxide 0-80
(GAS) Customize (Default: 0-80)
HAL (E)(GAS),
HAL (I)(GAS), ISO
(E)(GAS), ISO (I)(GAS),
%
ENF (E)(GAS), 0.0-6.0, 0.0-10.0, 0.0-20.0,
Anesthetic gas 0.0-6.0
ENF (I)(GAS), Customize (Default: 0.0-6.0)
DES (E)(GAS),
DES (I)(GAS), SEV
(E)(GAS), SEV (I)(GAS)
0-100, 50-100,
BIS Bispectral index − 0-100
Customize (Default: 0-100)
SEF (EEG1), SEF Spectral edge 0.0-15.0, 0.0-30.0, 0.0-60.0,
Hz 0.0-60.0
(EEG2) frequency Customize (Default: 0.0-60.0)
0.00-0.10, 0.00-0.50, 0.00-1.00,
TP (EEG1), TP (EEG2) Total power nW 0.00-5.00, 0.00-10.00, 0.00-10.00
Customize (Default: 0.00-10.00)
aEEG (1 s) (EEG1),
aEEG (3 s) (EEG1), 0.0-10.0, 0.0-100.0, 0.0-1000.0, 0.0-
— μV 0.0-100.0
aEEG (1 s) (EEG2), 2000.0, Customize (Default: 0.0-100.0)
aEEG (3 s) (EEG2),
NOTE
• The event trend on the Trend window cannot be recorded.
• When two review windows are displayed on one window, both review
windows can be recorded.
NOTE
When two review windows are displayed on one window, both review
windows can be printed.
Tabular Trend
The Tabular Trend window displays measured parameter values of the most
recent 120 hours as a tabular trend. There are five tabular trend windows (Vital
Sign 1 to 4 and NIBP). Up to 255 parameters can be displayed for each window.
In the NIBP tabular trend window, the numeric values at the NIBP measurement
are listed.
Window name
Parameters
(8 files/display)
The parameters can be selected from the monitoring parameters and parameters
set on the [Parameter Setup] → [Parameter Selection]. For the parameter
settings, refer to Section 6-1 of the Administrator’s Guide.
Parameter name 2. Touch the parameter name to change. The setting window appears.
You can select monitoring labels and leads for PRESS, TEMP and ST.
For NIBP tabular trend, NIBP SYS, NIBP DIA and NIBP MAP are fixed
to display.
ii) Touch [ ] to close the setting window after the setting is complete.
AUTO
The monitoring parameters are set as the displaying
parameters according to the priority.
ii
NOTE
When a transmitter measures SpO2 at a finger that is used for NIBP
measurement, select “PR (SpO2)” to display the PR measured at the
transmitter on the NIBP tabular trend.
NOTE
When two review windows are displayed on one window, both review
windows can be recorded.
NOTE
When two review windows are displayed on one window, both review
windows can be printed.
Full Disclosure
The central monitor saves 120 hour full disclosure waveforms for up to 16
parameters for each bed. You can select the displayed full disclosure waveforms
from the stored parameters. You can register three Full Disclosure windows
(Single Wave, ECG 12 Lead and All Waves) and up to 16 parameters can be
displayed for each window.
When the full disclosure waveform is displayed on full screen, you can create
a recall file of any 8-second ECG and display the file on the arrhythmia recall
window. Refer to “Creating a Recall File of Desired ECG” later in this section.
CAUTION
When the full disclosure waveform is expanded in actual size, steep 9
slopes such as QRS may be distorted because it has been
compressed then expanded. When reading the expanded ECG
waveforms, be aware of this distortion.
Automatic scroll
Parameter name Scrolls one page every three seconds when the
Scale
Changes the displayed [ ] or [ ] is touched. If the [ ] touched to display
Changes the scale. Refer to “Setting
parameters. Refer to “Setting the latest data, the data is updated when acquiring data.
the Scale of a Displayed Parameter”.
the Displayed Waveforms”. Touch [ ] to stop scrolling. Scrolling can be stopped by
Date and time touching the window while scrolling.
Time at the top of the Display time length of the
Date and time cursor window
Window name
Comment icon
Displayed when
the comment is
entered. Touch to
check the comment.
Refer to “Checking
Comments”.
The parameters can be set from the monitoring parameters and parameters set on
the [Parameter Setup] → [Parameter Selection] of the System Setup screen. For
the parameter settings, refer to Section 6-1 of the Administrator’s Guide.
NOTE
This setting is only available at the central monitor where the bed’s data is
stored.
When [Auto] is touched, the measured waveforms are set to the stored
waveforms according to the parameter priority. For the parameter
priority, refer to Section 16. When a patient is admitted, up to 16
measured waveforms are set as the stored waveforms. If the stored
waveform settings are changed, the settings cannot be restored.
ii) Touch [ ] to close the setting window after the setting is complete.
1. Display the desired Full Disclosure window (Single Wave, ECG 12 Lead and
All Waves).
iii) Touch [ ] to close the setting window after the setting is complete.
iii
i
ii
NOTE
When the arrhythmia analysis is set to OFF, the display color cannot be
changed.
ON: Indicates the arrhythmia alarm occurrence on ECG waveform in the alarm
priority color.
OFF: ECG waveform display color does not change.
9
You can set whether to display the pacing mark [Above Wave] or [Overlap
Wave] on the [Monitor Setting] → [Display Settings] → [ECG Display] →
[Pacing Mark Position] of the System Setup screen. Refer to Section 6-1 of the
Administrator’s Guide.
i 1. Display the Full Disclosure window (Single Wave, ECG 12 Lead and All
Waves).
ii
ii) Select the scale.
iii) Touch [ ] to close the setting window after the setting is complete.
Customize Scale
When [Customize Scale] is touched, waveforms can be displayed on the
desired scale. The value of the customize scale is set on the Trend window.
The [Customize Scale] appears when the parameter waveform is a scale type
(except for FLOW, FLOW(EXT), VOL, EEG1 and EEG2). Refer to “Setting the
Customized Scale” in Trend section.
NOTE
When two review windows are displayed on one window, both review
windows can be printed.
[ ], [ ]
Scrolls the displayed waveform
1 second right or left.
ii
iii
iv
9
v) Touch [Create] to create a recall file. The ECG of the selected lead
displayed on the expanded waveform window is registered as an
arrhythmia recall file.
Touch [Cancel] to cancel creating a recall file and close the window.
[Lead]
Selected lead is displayed.
You can change the lead
by touching the key.
v
Expanded Waveform
You can expand the full disclosure waveforms (up to 16 parameters) stored in
the central monitor. Select the displayed waveforms of the parameter from the
stored waveforms of the parameter. You can register three Expanded Waveform
windows (Single Wave, ECG 12 Lead and All Waves). Up to 16 parameters* can
be displayed for each window.
CAUTION
When the full disclosure waveform is expanded in actual size, steep
slopes such as QRS may be distorted because it has been
compressed then expanded. When reading the expanded ECG
waveforms, be aware of this distortion.
Automatic scroll
Scale Scrolls one page every three seconds when [ ] or
Changes the scale. Refer Comment icon [ ] is touched. If [ ] is touched to display the latest
to “Setting the Scale of a Displayed when the comment is data, the data is updated when more data is acquired.
Displayed Parameter”. entered. Touch to check the comment. Touch [ ] to stop scrolling. Scrolling can be stopped by
Refer to “Checking Comments”. touching the window while scrolling.
Parameter name
Changes the displayed Date and time
parameters. Refer to “Setting at the top of the
the Displayed Waveforms”. Time waveform Sweep speed
Window name
Calibration waveform
Displays 1 mV of
calibration waveform on
the ECG leads.
Expanded waveform
Parameter waveforms which is set to the displayed waveform are displayed.
When the monitored bed is a multiple patient receiver and there is signal loss or [ ]: Changes between split display and full size
running out of the battery, triangle waveform is displayed. display.
Waveforms are not displayed in the following case. [ ]: Changes to a different review window.
• When the patient is temporarily discharged. [ ]: Changes to a different Expanded Waveform
• The time before admission is displayed. window (Single Wave, ECG 12 Lead and All
• Communication loss Waves).
• Displayed parameter is not monitored. [ ]: Change settings.
Caliper and divider measurements are available on the displayed waveforms
Refer to “Measuring a Waveform”.
The stored waveforms are set on the [ ] → [Stored Waves] on the Full
Disclosure window. Refer to the “Full Disclosure”.
9
According to the [Waveform Alarm Color] setting, the arrhythmia alarm
occurrence can be indicated on the ECG waveform with a alarm priority color.
Select the parameter from the stored waveforms set on the [ ] → [Stored
Waves] on the Full Disclosure window.
1. Display the Expanded Waveform window (Single Wave, ECG 12 Lead and
All Waves).
Parameter name You can display the setting window by touching the parameter name.
iii) Touch [ ] to close the setting window after the setting is complete.
iii
i
ii
You can set the waveform sweep speed for each Expanded Waveform window
(Single Wave, ECG 12 Lead and All Waves) when the expanded waveforms are
full size display.
NOTE
When the arrhythmia analysis is set to OFF, the display color cannot be
changed.
ON: Indicates the arrhythmia alarm occurrence on ECG waveform in the alarm
priority color.
OFF: ECG waveform display color does not change.
You can set whether to display the pacing mark [Above Wave] or [Overlap
Wave] on the [Monitor Setting] → [Display Settings] → [ECG Display] →
[Pacing Mark Position] of the System Setup screen. Refer to Section 6-1 of the
Administrator’s Guide. 9
Measuring a Waveform
You can measure an expanded waveform on the window with the calipers or
dividers.
Caliper Measurement
Measure the distance between any two points using calipers. When you register
the measurement data, the data is displayed in the event list. Measurement items
depend on the waveform of the parameter.
Use the optional mouse to measure the expanded waveform with the caliper
more precisely.
1. Display the Expanded Waveform window (Single Wave, ECG 12 Lead and
All Waves).
iii) To register the measurement results to the event list, touch [Entry]. Refer
to “Event List”.
NOTE
The line and measured values on the waveforms are temporary
information and are deleted when you exit the caliper
measurement mode.
If you change the measured waveform during caliper measurement, the line and
measured value on the waveform are deleted.
ii ii
Clear
Deletes all the measurement results.
iii
Divider Measurement
You can measure an expanded waveform with the dividers.
1. Display the Expanded Waveform window (Single Wave, ECG 12 Lead and
All Waves).
1. Display the Expanded Waveform window (Single Wave, ECG 12 Lead and
All Waves).
iii) Touch [ ] to close the setting window after the setting is complete.
iii
Customize Scale
When [Customize Scale] is touched, waveforms can be displayed on the
desired scale. The value of the customize scale is set on the Trend window.
ii
The [Customize Scale] appears when the parameter waveform is a scale type
(except for FLOW, FLOW(EXT), VOL, EEG1 and EEG2). Refer to “Setting the
Customized Scale” in Trend section.
NOTE
When two review windows are displayed on one window, both review
windows can be recorded.
9
NOTE
When two review windows are displayed on one window, both review
windows can be printed.
Event List
The Event List window displays the latest 120 hours of events on the monitored
beds. The most recent 10,000 files can be saved for each bed.
NOTE
• When the bed’s data is saved on a central monitor other than CNS-
6201, the data cannot be displayed on the Event List window.
• If a new file is created when the maximum number of files has already
been reached, the oldest file is deleted. Data is automatically deleted
after the maximum 120 hours regardless of the number of files.
• IBP (SYS/DIA/MEAN) technical alarms are treated as one file and
displayed on the Event List window as one file.
Event duration time* Level Displays the event Displays the contents of events.
Displays the duration time of the alarm. Displayed in case of types.
alarm.
NOTE
When two review windows are displayed on one window, both review
windows can be recorded.
NOTE
When two review windows are displayed on one window, both review
windows can be printed.
ST Recall
The ST Recall window displays ST recall files of up to 120 hours. ST recall files
are created every one minute and saved for each bed.
NOTE
If a new file is created when the maximum number of files has already
been reached, the oldest file is deleted.
CAUTION
• Although the ST algorithm has been tested for accuracy of the ST
analysis result, the significance of the ST level changes need to be
determined only by a physician.
• The ECG from transmitters other than ZM series is not processed 9
by a 3.2 second time constant filter. Therefore, the ST level
measurement of other transmitters is not designed to be accurate
enough for diagnosis. Do not rely on this ST level measurement.
Comment icon
Displayed when a comment is entered. Touch to check the
comment. Refer to “Checking Comments”.
Sensitivity
Changes the displayed sensitivity. Cursor Touch [ ] or [ ] to
Refer to “Setting the Sensitivity”. Synchronizes with other review scroll the list up and down.
Heart rate windows. Select the file on the window. Date and time
Lead name
Changes the displayed
lead. Refer to ”Setting
the Displayed Lead”.
ST value
ST recall waveform
Reference file
ST recall file registered as a
Check box
reference file is displayed. [ ]: Changes between split display and full size
Touch to check the file to record or print.
To register the reference file, display.
Touch again to deselect the file.
select the file to register and [ ]: Changes to a different review window.
touch [Reference]. [ ]: Touch [ ] → [Interval] to display the setting
window and set the display interval of the ST
recall file. (1, 5, 10, 30, 60 minutes)
Registers a comment to the file at the Time axis (120 hours) Range before admission Cursor
cursor. Refer to “Registering Comments”. Range before admission and the cursor
are displayed on the time axis. You can
move the cursor by directly touching the
time axis.
1. Touch the lead name on the ST Recall window to display the setting window.
Lead name
NOTE
When two review windows are displayed on one window, both review
windows can be recorded.
NOTE
When two review windows are displayed on one window, both review
windows can be printed.
Arrhythmia Recall
The Arrhythmia Recall window displays the list of arrhythmia recall files. The
arrhythmia recall files are created for the most recent 1,500 arrhythmias for each
bed.
[ ]
Touch to display the
setting window and set
Sort Sort
the displayed arrhythmia
Touch to sort the list. Touch to sort the list by
types. [ALL] selects or
• Date/Time: Sort by date and time of file check mark on or off.
deselects all files.
creation.
• Event: Sort by arrhythmia name.
QRS annotation
Cursor
Synchronizes with other
review windows. Select the
list on the window.
Comment icon
Displayed when a comment
is entered. Touch to check the
comment. Refer to “Checking
Comments”.
MANUAL arrhythmia recall files are created on the Full Disclosure Waveform
window. Refer to “Creating a Recall File of Desired ECG” in this section.
NOTE
• When [Arrhythmia Analysis] is set to [OFF] on the bedside monitor and
central monitor, arrhythmia recall files cannot be created.
• Arrhythmia recall files are created only when the arrhythmia which is set
on [Create Recall Waveform] are detected.
• If a new file is created when the maximum number of files has already
been reached, the oldest file is deleted. Data is automatically deleted
after the maximum 120 hours regardless of the number of files.
Classification Description
ASYSTOLE Asystole
V FIB Ventricular fibrillation
V TACHY Ventricular tachycardia
EXT TACHY Extreme tachycardia
EXT BRADY Extreme bradycardia
VPC RUN VPC short run
V BRADY* Ventricular bradycardia
SV TACHY* Supraventricular tachycardia
High ← Priority → Low
TACHYCARDIA Tachycardia
BRADYCARDIA Bradycardia
PAUSE* Pause
COUPLET VPC couplet (Paired VPCs)
EARLY VPC Early VPC
MULTIFORM Multi-form ECG
V RHYTHM* Ventricular rhythm
BIGEMINY Ventricular bigeminy
TRIGEMINY* Ventricular trigeminy
VPC Ventricular premature contraction
IRREGULAR RR* Irregular RR
PROLONGED RR Prolonged R-R interval
NO PACER PULSE* Oversensing
PACER NON-CAPTURE* Non-capture
Annotation Description
N Normal QRS complex
S Supraventricular contraction
V Ventricular premature contraction
A Abnormal beat
E Early VPC
P Paced QRS
QRS which cannot be analyzed because of noise, or
―
QRS which is currently being learned.
? QRS which cannot be judged.
NOTE
When two review windows are displayed on one window, both review
windows can be recorded.
NOTE
When two review windows are displayed on one window, both review
windows can be printed.
SpO2 Trend
The SpO2 Trend window displays the trend information of a selected period in
the most recent 120 hours. It shows trendgraphs and histograms of SpO2 values
including number and duration of SpO2 drops.
To display the SpO2 Trend window, display the Review window and touch [ ]
to select [SpO2 Trend].
Time bar
(Displayed
Window name time width)
Scale Threshold
You can touch to change the The threshold is automatically set according to
scale. Refer to “Setting the Scale the SpO2 value of the calm, resting state and
Trendgraph
of a Displayed Parameter”. the % decrease below the calm value. Refer to Measurement data at the
“Setting the SpO2 Trend Threshold”. cursor position
Parameter name
You can touch to change the
displayed parameters. Refer
to “Setting the Displayed
Parameters and Events”.
Event
trendgraphs
You can touch
to change the
displayed event.
Event
Events are displayed in the color corresponds to the alarm Number of events
priority. The width of event is from the alarm occurrence to
alarm end. [ ]: Changes to a different review window
Cursor [ ]: Changes to a different SpO2 Trend window
Synchronizes with other review windows. The date and time (SpO2 Trend 1 and 2)
at the cursor position is displayed above the cursor. You can [ ]: Changes the SpO2 trend display format and
move the cursor by touching directly on the cursor. threshold setting. Refer to “Changing the
Display Format of the SpO2 Trendgraph”.
Time axis (120 hours) Range before admission Range of displayed time width
Start Time The range before admission and the range of
The start time of the displayed range is the displayed time width and the cursor are
based on the end time and displayed time displayed on the time axis. You can move
width. The start time cannot be changed. the cursor by directly touching the time axis.
Cursor
Touch [Histogram] on SpO2 Trend window (SpO2 Trend 1 and 2) to display the
Histogram window.
Only SpO2 can be displayed as a histogram. The histogram can only be displayed
when the displayed parameter is set to SpO2.
Number of
SpO2 Trend Window Number of Events
Parameters
SpO2 Trend 1 3 parameters 5 events
SpO2 Trend 2 5 parameters 3 events
The display format of the trendgraph and cursor display label depends on the
parameter. For the display format for each parameter, refer to “Changing the
Display Format of the Trendgraph” in this section.
Threshold
The threshold is shown as a yellow line on the SpO2 trendgraph. The threshold is
automatically set according to the SpO2 value of the calm, resting state and the %
decrease below the calm value.
If “SpO2 fall” is set as the displayed event, the time when the threshold is lower
than the SpO2 value is displayed as the event. Also the number of times that the
threshold is lower than the SpO2 value is displayed. Refer to the “Setting the
Displayed Event” in this section.
Example: If you set Calm 96% and Fall 2%, then threshold is automatically set
to 94%.
Threshold
The parameters can be set from the monitoring parameters and parameters set on
the [Parameter Setup] → [Parameter Selection] of the System Setup screen. For
the parameter settings, refer to Section 6-1 of the Administrator’s Guide.
Parameter name
2. Touch the parameter name to display the setting window.
iii) Touch [ ] to close the setting window after the setting is complete.
AUTO
The monitoring parameters are set according to the
parameter priority. The event trends are not displayed
and all the parameter trendgraphs are displayed.
iii
i
ii
When deselecting all the selected events, iv) Touch [ ] to close the setting window after the setting is complete.
the [Parameter Setup] tab is available.
AUTO
The monitoring parameters are set according to the
parameter priority. The event trends are not displayed
and all the parameter trendgraphs are displayed.
Available number of events
iv
ii
iii
i 9
Clear All Events
Deselects all the settings in each event category of
Arrhythmia, Limit and Technical.
Scale
2. Set the scale of the displayed parameter.
i) Touch the parameter scale to be displayed on the SpO2 Trend window to
display the setting window.
i
ii) Select the scale.
ii
3. Enter the scale using the numeric key pad and touch [ENTER].
2
4. After entering the upper limit and lower limit scale, touch [OK] to close the
Customize Scale window.
The ECG 12 Lead Analysis window displays the results of ECG 12 lead analysis
performed at bedside monitors. Up to 200 files can be saved for each bed at the
central monitor.
The ECG 12 Lead Analysis window has the following analysis or comparison
windows.
• Analysis Wave (3 × 4)
• Analysis Wave (6 × 2)
• Analysis Wave (12 × 1)
• Averaged Wave (3 × 4)
• Analysis Wave Comparison
• Averaged Wave Comparison
9
The analysis report cannot be displayed on the following analysis or comparison
windows.
• Analysis Wave (12 × 1)
• Analysis Wave Comparison
• Averaged Wave Comparison
NOTE
• If a new file is created when the maximum number of files has already
been reached, the oldest file is deleted. Data is automatically deleted
after the maximum 120 hours regardless of the number of files.
• For details about the analysis and the clinical findings, refer to the
ECAPS 12C Program User’s Guide.
Analysis report
Displays an analysis
report at the cursor file.
Comment icon
Displayed when a comment
is entered. Touch to check the
comment. Refer to “Checking
Comments”.
Representative measurement
value of analysis
Reference file
The file registered as a
reference file is displayed.
Delete all the selected files (with a check mark). When the confirmation window Check box Cursor
is displayed after [Delete] is touched, touch [Yes] and delete the file. Touch to check the file to Synchronizes with other review
record or delete. windows. Select the file on the
NOTE: Files can be deleted on a central monitor where the bed’s data is Touch again to deselect window.
saved. [Delete] cannot be touched on the central monitor where the bed’s the file.
data is not saved.
Touch [ ] or [ ] to scroll
the list right and left.
Analysis waveform of the reference file Analysis waveform of the cursor file
Calibration waveform (1 mV) The setting window can be displayed by directly touching the calibration
waveform.
The setting window can be displayed by directly touching the rhythm waveform
on each analysis window.
Rhythm waveform
Caliper Measurement
Measure the distance between any two points using calipers. Caliper
measurement can be performed on the following windows.
• Analysis Wave (3 × 4)
• Analysis Wave (6 × 2)
• Analysis Wave (12 × 1)
• Averaged Wave (3 × 4)
Use the optional mouse to more precisely measure the analysis waveform and
average waveform with the caliper.
NOTE
The line and measured values on the waveforms are temporary
information and are deleted when you exit the caliper
measurement mode.
ii ii
Clear
Deletes all the measurement results.
If you change the lead during caliper measurement, the measured value, the
line and measured value on the waveform are deleted when you exit the caliper
measurement mode.
Divider Measurement
You can measure an analysis waveform with the dividers. Divider measurement
can be performed on the following analysis and comparison windows.
• Analysis Wave (3 × 4)
• Analysis Wave (6 × 2)
• Analysis Wave (12 × 1)
• Analysis Wave Comparison
Displays a divider. 9
(Defaults: 1,000 ms, HR: 60/min)
Hemodynamics List
Registers a comment
to the selected list.
Refer to “Registering
Comments”. Touch [ ] or [ ] to scroll the Touch [ ] or [ ] to scroll the
hemodynamics list right and left. hemodynamics list up and down.
Abbreviations
The following table shows the abbreviations, units and calculations of the
parameters used in the hemodynamics list. “---” is displayed when the
parameters is not measured.
NOTE
When two review windows are displayed on one window, both review
windows can be recorded.
Alarm Events
The Alarm Events window displays up to 10,000 files of alarm events for
one patient in the most recent 120 hours. You can register two Alarm Events
windows (Limit or Tech, Arrhy or Tech) and for each window, up to 12 events
can be displayed.
NOTE
If a new file is created when the maximum number of files has already
been reached, the oldest file is deleted. Data is automatically deleted
after the maximum 120 hours regardless of the number of files.
The Alarm Events window can be displayed by one of the following methods:
• touching the bed name on the All Beds Alarm Events window. Refer to “All
9
Beds Alarm Events Window” in Section 7.
• touching the technical icon on the All Beds screen. Refer to “Technical Icon”
in Section 5.
Window name
Event name 2. Touch the event name and display the setting window.
iii) Touch [ ] to close the setting window after the setting is complete.
Clear All Events
Touch to deselect all the selected events in the each
event categories [Arrhythmia], [Limit], [Technical].
iii
ii
When displaying the Limit or Tech window, the Arrhythmia tab is not available.
When displaying the Arrhy or Tech window, the Limit tab is not available.
Event List
The following table shows displayed events. When the displayed event is
changed, the event is displayed in the following display order in the table.
Default Settings*1
(Display Order)
Setting Item Displayed Alarm
Limit or Arrhy or
Tech Tech
Arrhythmia ASYSTOLE Each arrhythmia 1
V FIB alarm 2
V TACHY 3
EXT TACHY 4
EXT BRADY 5
VPC RUN 8
V BRADY
––
SV TACHY
TACHYCARDIA 6
BRADYCARDIA 7 9
PAUSE
COUPLET ––
EARLY VPC
MULTIFORM ––
V RHYTHM
BIGEMINY
TRIGEMINY
FREQ VPC 9
VPC
IRREGULAR RR
PROLONGED RR
NO PACER PULSE
PACER NON-CAPTURE
Limits HR Upper and lower 1
PR limit alarm of each 2
ST parameter ––
RR 7
APNEA (T) 8
NIBP 3
––
SpO2 5
ART*2 4
CVP
PAP
ICP ALL ––
TEMP ALL
O2
CO2 6
GAS ALL
BIS ––
EEG
Technical ECG Technical LEAD OFF alarm,
9 10
NOISE alarm
Default Settings*1
(Display Order)
Setting Item Displayed Alarm
Limit or Arrhy or
Tech Tech
Technical SpO2 Technical SpO2 technical
11 11
alarm*3
ART*2 + NIBP ART and NIBP
10
technical alarm*3
TEMP Technical TEMP technical
––
alarm*3
––
CO2 Technical CO2 technical
alarm*3
SIGNAL LOSS*4 SIGNAL LOSS
12*5 12*5
alarm*4
COMMUNICATION COMMUNICATION
12*6 12*6
LOSS LOSS
BATTERY BATTERY alarm*6 –– ––
*1 Default display order is different from the display order in the table.
*2 Typical labels of arterial pressure (ART, ART2, RAD, DORS, AO, and FEM)
*3 For details about technical alarms, refer to “Error Messages” in Section 14.
*4 For a bed monitored through an ORG-9100 series multiple patient receiver
*5 Default display order for a bed monitored through an ORG-9100 series multiple patient
receiver
* Default display order for a hardwired bedside monitor
6
NOTE
To display the technical icons, [Technical Icon] of the [System
Configuration] → [Alarm] on the System Setup screen must be set
to [ON]. The default setting is [OFF]. Refer to “System Configuration
Settings” in Section 6-1 of the Administrator’s Guide.
Action message
When [Yes] is touched, the technical icon and action message disappear. When
[No] is touched, the message disappear but the icon is displayed continuously.
When [Yes] is touched on the action message window, the past technical alarms
are cleared and the technical status becomes green.
NOTE
When two review windows are displayed on one window, both review
windows can be recorded.
The Discharged Patients List window displays the past 120 hours of review
windows of discharged patients or patients whose data were deleted on this
central monitor.
NOTE
If a new file is created when the maximum number of files has already
been reached, the oldest file is deleted. Data is automatically deleted
after the maximum 120 hours regardless of the number of files.
To display the Discharged Patients List window, set the [System Composition]
→ [System] → [Admit] → [Discharge Mode] of the System Setup screen to
[Discharge]. Refer to “System Composition” in Administrator’s Guide.
When [Discharged Patients List] is assigned to one of the all beds function
keys, the Discharged Patients List window can be displayed by touching
the function key. Refer to “Function Keys Setting” in Section 6-1 of the
Administrator’s Guide to assign a function to the function key.
Discharged
date and time Patient ID Patient name Physician
Sort
On the PU-621R Op No. 21A, touch the sort
marks to sort the list.
• Discharge Time: Sort by date and time of
discharge.
• Patient ID: Sort by patient ID.
• Patient name: Sort by patient name.
2. Touch the patient to display the review window. The Discharged Patients
List window is displayed in the display pattern of Custom Review. For the
operation of each review window, refer to each section.
Discharged time
Discharged time of the patient is
Discharged Patients List displayed.
Changes to the Discharged Patients List window.
Patient name Window title
Displays each
Records or prints the displayed window. review window.
The review window is displayed in the display pattern of Custom Review when
Admit/Discharge window is displayed from the Discharged Patients List window
by touching [Review]. For displaying the review window, “Displaying the
Review Window”.
Overview............................................................................................................................................................. 10.2
Types of Recording and Printing.............................................................................................................. 10.2
Recording....................................................................................................................................... 10.2
Printing........................................................................................................................................... 10.2
Description of Recording Modes.............................................................................................................. 10.3
Manual Recording.......................................................................................................................... 10.3
Waveform Printing.......................................................................................................................... 10.3
All Beds Alarm Management Printing............................................................................................ 10.3
Review Recording or Printing......................................................................................................... 10.4
Automatic Recording...................................................................................................................... 10.4
Remote Recording......................................................................................................................... 10.5
10
Recording Priority..................................................................................................................................... 10.6
Recorder Unit (WS-960P).............................................................................................................. 10.6
Printer............................................................................................................................................ 10.6
Recorded/Printed Data............................................................................................................................. 10.6
Manual Recording.............................................................................................................................................. 10.8
Manual Recording.................................................................................................................................... 10.8
Necessary Settings for Manual Recording..................................................................................... 10.8
Starting Manual Recording............................................................................................................ 10.8
Waveform Printing.............................................................................................................................................. 10.9
All Beds Alarm Management Printing................................................................................................................. 10.9
Review Recording and Printing.......................................................................................................................... 10.9
Automatic Recording........................................................................................................................................ 10.10
Periodic Recording................................................................................................................................. 10.10
Necessary Settings for Periodic Recording.................................................................................. 10.10
Clock Time Periodic Recording.............................................................................................................. 10.10
Necessary Settings for Clock Time Periodic Recording............................................................... 10.10
Alarm Recording.................................................................................................................................... 10.11
Remote Recording............................................................................................................................................ 10.12
Call Recording........................................................................................................................................ 10.12
Necessary Settings for Call Recording........................................................................................ 10.12
Changing Recording Settings........................................................................................................................... 10.13
Changing Settings on the [Recording] of the Setup Window.................................................................. 10.13
Overview of Reports......................................................................................................................................... 10.14
Report Settings................................................................................................................................................. 10.15
Report Setting on the Setup Window..................................................................................................... 10.15
Printing a Report.............................................................................................................................................. 10.17
Printing a Report in Manual Mode.......................................................................................................... 10.17
Printing a Report in Periodic Mode........................................................................................................ 10.17
Printing Example.................................................................................................................................... 10.18
This section explains the types of recording and procedure for recording, printing
and reports and settings of the recording and report.
Overview
Recording
Records the data with the WS-960P Recorder Unit that is connected to the
central monitor. The WS-960P Recorder Unit is an option. Touch [ ] to start
recording. It records on 50 mm width recording paper.
Printing
Prints the data on a printer in the network. Touch [ ] to start printing. It prints
on A4 size paper.
Manual Recording
Waveform Printing 10
Tabular Record [ ]
Displayed tabular trend Displayed data Tabular Trend window
trend Print [ ]
Automatic Recording
Automatic recording starts at the preset time if the preset conditions are met.
Remote Recording
Remote recording is performed when there is a recording request from a
transmitter.
NOTE
Remote recording is available only at the central monitor where the bed’s
data is saved.
Postponed Canceled
Stop Manual recording • Alarm recording Manual recording on each review window
Recording > (All beds recording) > • Periodic recording
• Call recording
• Manual recording (all beds recording) has the highest priority. If manual
recording starts during other recording, the other recording is canceled.
• During any type of recording, if an equal priority recording occurs, the second
recording is not performed; only the current recording is performed.
• When other recording is performed at the start of alarm, periodic or call
recording, the alarm, periodic or call recording starts after the other recording
stops.
• If a higher priority recording occurs, during call recording, alarm recording
and periodic recording, the current recording changes to standby and is
continued after the higher priority recording.
Printer
When printing with the printer there is no priority. All print requests are printed.
Recorded/Printed Data
WS-960P Recorder Unit
Numeric data when recording starts or file is
Recording date and created
Bed name Patient name
time or file creation
date and time
Manual Recording
Touch [ ] to record the monitoring numeric value and selected waveforms (up
to three channels) with the WS-960P Recorder Unit. When [Record All] is set
to an all beds function key, you can perform manual recording for all monitored
beds on the All Beds screen. Refer to “All Beds Recording” in Section 6.
Manual Recording
Manual recording is available on all screens and windows with the [ ] key.
Displayed numeric values and selected waveforms (up to three channels) are
recorded. For recording example, refer to “Recorded/Printed Data” in this
section.
Waveform Printing
You can print the waveform and numeric value displayed on the Individual Bed
window. For details, refer to “Individual Bed Window Printing” in Section 8.
You can print the displayed All Beds Alarm Management window. For details,
refer to “Printing on the All Beds Alarms Window” in Section 7.
10
You can record or print the displayed review window. For details, refer to the
following sections.
Review Refer to
Trend Recording the Trendgraph
Printing the Trendgraph
Tabular Trend Recording the Tabular Trend
Printing the Tabular Trend
Full Disclosure Printing the Full Disclosure Waveform
Expanded Waveform Recording the Expanded Waveform
Printing the Expanded Waveform
Event List Recording the Event List
Printing the Event List
ST Recall Recording the Waveform of ST Recall File
Printing the ST Recall Window
Arrhythmia Recall Recording the Waveform of an Arrhythmia Recall
File
Printing the Arrhythmia Recall Window
SpO2 Trend Printing the SpO2 trendgraph
ECG 12 Lead Analysis Printing the ECG 12 Lead Analysis Window
Hemodynamics List Printing the Hemodynamics List
Alarm Events Printing the Alarm Events Window
Automatic Recording
Recording starts automatically at the preset recording conditions. There are three
automatic recording modes: periodic recording, clock time periodic recording
and alarm recording. For recording examples, refer to “Recorded/Printed Data”
in this section.
Periodic Recording
The numeric values and selected waveforms of up to three channels are recorded
at the preset intervals with the WS-960P Recorder Unit. Recording stops when
[ ] of the recording bed is touched.
The recording sweep speed is the same as manual recording. Refer to “Necessary
Settings for Manual Recording” in this section.
The recording sweep speed is the same as manual recording. Refer to “Necessary
Settings for Manual Recording” in this section.
Alarm Recording
Refer to “Alarm Recording” in Section 5.
10
Remote Recording
NOTE
Remote recording is available only at the central monitor where the bed’s
data is saved.
Call Recording
This recording starts when there is a recording request from a transmitter. The
numeric values and selected waveforms of up to three channels are recorded with
the WS-960P Recorder Unit.
The recording sweep speed is the same as manual recording. Refer to “Necessary
Settings for Manual Recording” in this section.
To start recording, press the CALL button on the transmitter. The recorder
automatically stops after the preset recording time.
You can change recording settings on the [Recording] of the Setup window.
Overview of Reports
The central monitor can print review data for a patient as a report. Reports are
printed on a printer in the network. Report printing has manual and periodic
modes.
NOTE
The periodic mode is only for beds whose data is saved in this central
monitor. A bed whose data is not saved in this central monitor is fixed to
manual mode.
• Manual: You can print the past review data (already saved data) as a report.
• Periodic: Automatically prints the report at periodic intervals.
Report Settings
Before printing a report, set the report settings on the [Report] of the Setup
window.
For the settings, refer to “Report” in Section 6-1 of the Administrator’s Guide.
10
3. Touch [Other Setup] → [Report] of the Setup Menu. The Report window
opens.
When [Report] is assigned to one of the individual function keys, the Report
window can be displayed by touching the function key. For setting individual
function keys, refer to “Changing the All Beds Screen Display Settings” in
Section 6.
again.
Periodic Report Interval 1 hour, 2 hours, 4 hours, 8 Set the interval to print the report in auto mode.
mode hours, 12 hours, 24 hours
Print Start Time Enter the report printing Set the time to print the report first in auto mode. Touch
start time [Print Start Time] to display the input window and enter the
time.
You can set the print start time by touching the time axis.
Report Items Trend, Tabular Trend, Touch and select review items to print on the report.
Full Disclosure,
Expanded Waveform,
Arrhythmia Recall, ST
Recall, Hemodynamics
List, ECG 12 Lead
Analysis, Event List,
Alarm Events
Nurse Notes Up to 500 characters, Set the nurse notes to print on the report. Touch [ ] to
up to 11 lines when display the input window, then enter the notes.
inserting the line
Touch [Save] to register the input notes as a template. Touch
[Recall] to recall the registered notes.
Printing a Report
Check the settings to create a report. The Nurse Notes are not printed if the notes
are entered beforehand. In periodic mode, the report is automatically printed at
the set intervals. Refer to “Report Settings” in this section.
10
NOTE
If [Print] is not touched after setting the items, periodic printing cannot be
performed.
To stop printing, touch [Print Stop] or change the mode to manual mode.
Printing Example
11
This section explains how to display the Overview Bed window and recording
and printing on the window.
If you want to temporarily monitor a bed which is not a monitored bed on this
central monitor, you can monitor it on the Overview Bed window. The Overview
Bed window has almost the same display items as the monitored bed. You can
select one overview bed from up to 300 bedside monitors in the network.
NOTE
On the Overview Bed window, alarms are not displayed even if the
Individual Waveforms window is displayed. If you want to monitor the
alarms of the bed, set the bed as a monitored bed.
When [Overview] is assigned to one of the all beds function keys, the
Overview bed window can be displayed by touching the function key. Refer
to “Function Keys Setting” in Section 6-1 of the Administrator’s Guide to
assign a function to the function key.
The Individual Bed window of the overview bed is displayed. For the screen
operation, refer to each item.
Scrolls the list up and down
11
with [ ] and [ ] keys.
Group name Bed name Patient name Physician
Sort
On the PU-621R Op No. 21A, touch the sort
marks to sort the list.
• Group: Sort by group.
• Bed Name: Sort by bed name.
• Patient Name: Sort by patient name.
When the [Review] is touched on the Overview Bed window when the window
other than review window is displayed, the display pattern is “Custom Review”.
Refer to the “Displaying the Review Window” in Section 9.
NOTE
When the overview bed data is not saved in CNS-6201, event list and
alarm events data cannot be displayed.
NOTE
• Reports cannot be printed.
• All beds recording, automatic recording and remote recording cannot
be performed.
This section explains about each parameter settings for each bed.
On the Parameter Setup window, set the ECG, RESP, SpO2, NIBP, PRESS,
TEMP settings.
1. Touch the data area of the bed you want to set the settings for. The Individual
Bed window appears.
3. Touch a parameter key under Parameter Setup to display the setting window
for the parameter.
Example: ECG
You can also display the Parameter Setup windows by the following operation.
• On the Individual Bed window, touch the parameter you want to display the
setting window for.
• Touch the parameter individual function key if the parameter is registered
to an individual function key. For setting individual function keys, refer to
“Changing the All Beds Screen Display Settings” in Section 6.
12
ECG Settings
On the Setup Menu of the Individual Bed window, touch [ECG] to display the
ECG window.
1
The ECG window has six tabs. Touch the tab of the category name to switch to
another category.
• Main
• Arrhythmia Alarm
• ST Alarm
• Arrhythmia Analysis Setting
2 • ST Point
3
• Other
Main Settings
The upper half of the window shows the first ECG trace and measurement
information. You can also change the sensitivity or learn ECG. The lower half of
the window shows the upper and lower alarm limits of the HR (Heart Rate). You
can set the HR upper/lower limit.
ECG
ECG set at [Arrhythmia Detection Lead 1] is [Learn ECG]
displayed. You can change the sensitivity by Touch to relearn ECG. Refer to
touching the waveform. Section 12.
Sens/Scale window
Touch to change
sensitivity. The
sensitivity setting is
synchronized with All
Beds screen display and
Individual Bed window
setting.
Measurement information
For beds connected through an
ORG-9100 series multiple patient
receiver, the current ECG settings
(filter, analysis, QRS detection type
and pacing) are displayed.
Learning ECG
If there is any doubt about the arrhythmia analysis result, relearn the dominant
ECG. During ECG learning, the “LEARNING” message appears on the screen.
CAUTION
If there is any doubt about the arrhythmia analysis, make the monitor
relearn the patient’s ECG and check that the dominant QRS is
appropriate. Otherwise, an important arrhythmia may be overlooked.
NOTE
• When you touch [Learn ECG] at the central monitor, the command is
sent to the bedside monitor and the bedside monitor relearns ECG.
• Some bedside monitor models automatically relearn ECG whenever the
pattern of normal ECG changes.
Setting ST Alarms
Sets the ST alarms. Touch [ST Alarm] to change the window. The setting
procedure is the same as on the ST Alarm window of the Personal Setup. Refer
to Section 5.
WARNING
For arrhythmia monitoring, set [Arrhythmia Analysis] on the ECG
window to [ON]. Otherwise, there is no sound or indication for
arrhythmia alarms (except for ASYSTOLE).
NOTE
When arrhythmia analysis is set to OFF, the following operations for
arrhythmia analysis are not performed.
• Display of VPC count and ST measurement value
• Generating arrhythmia alarms
• Creating arrhythmia recall files
• Arrhythmia alarm recording
• Creating ST recall files
• Learning ECG waveform
Analysis Mode Single, Multi When [Arrhythmia Analysis] is set to [ON], you can set the analysis lead.
Touch Single (one lead analysis) or Multi (2 lead analysis).
NOTE
For PU-621R Op No. 21A, when the [Telemetry Setting Master] is
set to [ON], the Analysis Mode setting returns to the setting on the
Telemetry Setting Master window when discharging a bed or deleting
data.
Optimum Lead
NOTE
Follow the physician’s instructions for lead position when available.
12
It is generally considered that Lead II and Lead V1 are suitable for arrhythmia
monitoring and that Lead V4 and Lead V5 are suitable for myocardial
ischemia monitoring.
Some types of ECGs are difficult for automatic analysis, and heart rate or
arrhythmia detection level is not accurate for some patients. In these cases, use
the following procedure to find the appropriate lead for automatic analysis.
1. Measure the patient’s ECG with the standard 12 ECG leads using an ECG
instrument.
2. Select the optimum lead according to the following guidelines:
i) Select the lead with the highest QRS wave amplitude and least
difference in amplitude compared with a VPC or pacing pulse.
0.5 ≤ QRS1/QRS2 ≤ 2
ii) Select the lead with less than 0.2 mV amplitude of the P-wave.
P ≤ 0.2 mV
iii) Select the lead with a T-wave amplitude which is less than one-third
of the QRS wave.
T1 ≤ 1/3QRS1, T2 ≤ 1/3QRS2
QRS1
P T1 T2
QRS2
CAUTION
At the start of ECG monitoring, check that the correct patient type
is set for QRS Detection Type on the following window.
• When using a multiple patient receiver: QRS Detection window
of the ECG window.
• When using a bedside monitor and transmitter: Home screen or
ECG window of the monitor.
If an inappropriate patient type is set, heart rate cannot be
counted accurately and noise or P waves may be counted as
QRS and cardiac arrest may be overlooked.
NOTE
When [Adult] or [Neonate] is selected, QRS Detection Sensitivity
setting is not displayed.
The following table shows the difference of each QRS detection type.
NOTE
For PU-621R Op No. 21A, when the [Telemetry Setting Master] is set
to [ON], the Sensitivity setting returns to the setting on the Telemetry
Setting Master window when discharging a bed or deleting data.
ST Point Settings
This setting is only available for beds connected through an ORG-9100 series
multiple patient receiver.
Set the ST analysis point (ISO point and ST point). Based on the QRS wave
position (R point), set the time from the position as ISO (Isolation) point and ST
point. The ST value is measured according to the set value.
NOTE
For PU-621R Op No. 21A, when the [Telemetry Setting Master] is set to
[ON], the ISO point is fixed to 80 ms and ST point is fixed to 108 ms when
discharging a bed or deleting data.
Touch [ ▲ ] or [ ▼ ] to
set each value. One touch
increases or decreases the
value by 4 ms.
[Reset] [Apply]
Returns to the Set the setting value and
R default setting. apply to the ST analysis.
Other Settings
Sets the detailed settings for ECG. Touch [Other] to change the window.
WARNING
Turn the pacing pulse detection* to [ON] when
monitoring a pacemaker patient. Otherwise the
pacemaker pulse is not rejected. However, even when
the pacing pulse detection is set to [ON], the
pacemaker pulse might not be rejected. When the
pacemaker pulse is not rejected, the pacemaker pulse
is detected as QRS and false heart rate may be
indicated or critical arrhythmia such as asystole may
be overlooked. Keep pacemaker patients under close
observation.
WARNING
Even when the pacing pulse detection is set to [ON],
the pacemaker pulse can be overlooked or detected
as QRS. You cannot confirm the pacemaker operation
only from the detected pacemaker pulse.
NOTE
• When you monitor a premature baby or infant and the
monitor miscounts the narrow width QRS, set this to
[OFF].
• For PU-621R Op No. 21A, when the [Telemetry Setting
Master] is set to [ON], the Detection setting returns to
the setting on the Telemetry Setting Master window when
discharging a bed or deleting data.
Mark* ON, OFF Set whether or not to display pacing marks on the ECG
waveform. Touch [ON] or [OFF] in [Mark].
Hum Filter ON, OFF Set the hum filter on or off. Set to [ON] when there is a lot of AC
hum interference from the use of an electrosurgical unit or other
instrument. Touch [ON] or [OFF] in [Hum Filter].
NOTE
For PU-621R Op No. 21A, when the [Telemetry Setting
Master] is set to [ON], the Hum Filter setting returns to
the setting on the Telemetry Setting Master window when
discharging a bed or deleting data.
* If the pacing pulse is detected, pacing marks are indicated on waveform of the Main page of the ECG window if the
[Detection] and [Mark] in PACING are set to [OFF].
NOTE
For PU-621R Op No. 21A, when the [Telemetry Setting
Master] is set to [ON], the AUTO LEAD CHANGE setting
returns to the setting on the Telemetry Setting Master
window when discharging a bed or deleting data.
CAUTION
When the [ECG Measurement] is [OFF], ECG alarms
do not occur even if each ECG alarm item is set to
[ON].
NOTE
• This setting cannot be set to [OFF] while ECG is being
monitored.
• When [ECG Measurement] is set to [OFF] at the central
monitor when ECG monitoring starts at the monitoring
device (bedside monitor, transmitter, etc.), ECG
measurement automatically turns to [ON] at the central
monitor. If ECG does not appear on the screen in 10
seconds, manually turn it to [ON].
• After setting [ECG Measurement] to [ON], confirm that
ECG is displayed on the screen.
• When a transmitter which can set the ECG measurement
[ON] or [OFF] is used and the ECG measurement is 12
turned OFF at the transmitter, the ECG measurement
automatically turns OFF and cannot be set to ON.
• For PU-621R Op No. 21A, when the [Telemetry Setting
Master] is set to [ON], the ECG Measurement setting
returns to the setting on the Telemetry Setting Master
window when discharging a bed or deleting data.
NOTE
Chest Lead This setting only changes the lead name displayed on the
screen. It does not change the ECG lead measured at
transmitters or bedside monitors. This setting can only be
set when receiving from a transmitter without lead switching
function.
RESP Settings
On the Setup Menu of the Individual Bed window, touch [RESP] to display the
RESP window.
1
The RESP window has three tabs. Touch the tab of the category name to switch
to another category.
• Main
• Display Settings
• Other
2
3
Main Settings
The upper half of the window shows the respiration curve and measurement
information. You can change the sensitivity. Touch the respiration parameter tab
to change the window. The lower half of the window (RR tab only) shows the
upper and lower alarm limits of the RR (Respiration Rate). You can set the RR
upper/lower limit.
Respiration curve
Displays respiration waveform. You can change
the sensitivity by touching the waveform.
Sens/Scale window
Touch to change
sensitivity. The
sensitivity setting is
synchronized with All
Beds screen display and
Individual Bed window
setting.
Measurement information
Current RESP setting is
displayed.
Current respiration rate
Respiration rate
trendgraph of the
past four hours
Display Settings
Sets the RESP display settings. Touch [Display Settings] to change the window.
Other Settings
Sets other RESP settings. Touch [Other] to change the window.
12
The display sensitivity of respiration curve on the All Beds screen and Individual Bed
window is not synchronized with this respiration detection sensitivity setting.
NOTE
For PU-621R Op No. 21A, when the [Telemetry Setting Master] is set to [ON],
the Sensitivity setting returns to the setting on the Telemetry Setting Master
window when discharging a bed or deleting data.
NOTE
• Respiration settings are only available while measuring respiration.
• For PU-621R Op No. 21A, when the [Telemetry Setting Master] is set to
[ON], the Impedance Respiration Measurement setting returns to the setting
on the Telemetry Setting Master window when discharging a bed or deleting
data.
Set whether or not to use impedance method respiration measurement. Touch [ON] or
[OFF] to change the setting.
SpO2 Settings
On the Setup Menu of the Individual Bed window, touch [SpO2] to display the
SpO2 window.
1
The SpO2 window has one tab.
• Main
3
2
Main Settings
The upper half of the window shows the SpO2 or SpO2-2 waveform and
measurement information. You can change the sensitivity. Touch the SpO2 or
SpO2-2 tab to change the window. The lower half of the window shows the upper
and lower alarm limits of the SpO2 or SpO2-2. You can set the upper/lower limit.
12
SpO2 waveform
Displays the SpO2 or SpO2-2 waveform. You can change the
sensitivity by touching the waveform.
Sens/Scale window
Touch to change sensitivity.
The sensitivity setting is
synchronized with All Beds
screen display and Individual
Bed window setting.
Measurement information
Current SpO2 or SpO2-2
setting is displayed.
Current SpO2 value
NIBP Settings
On the Setup Menu of the Individual Bed window, touch [NIBP] to display the
NIBP window.
1
The NIBP window has one tab.
• Main
3 2
Main Settings
The upper half of the window shows the Measurement Interval, NIBP
Measurement START and STOP key, and Connected Cuff type. The lower half
of the window shows the upper and lower alarm limits of the NIBP. You can set
the upper/lower limit of SYS, DIA and MAP.
You can start or stop NIBP masurement by the touching the [NIBP Measurement]
individual function key if the [NIBP Measurement] is registered to an individual
function key. For setting individual function keys, refer to “Changing the All
Beds Screen Display Settings” in Section 6.
CAUTION
Before you remotely start and stop NIBP measurement from the
central monitor, confirm the state of the patient at the bedside monitor.
Carefully start and stop NIBP measurement from the central monitor.
Start measurement
Touch [START] to start NIBP measurement. A confirmation window is
displayed. Touch [YES] to start measurement.
Stop measurement
To stop measurement during NIBP measurement, touch [STOP]. For
When an interval is set, the interval measurement, only the current measurement stops.
measurement continues at the interval
until [Manual] is set. NOTE: When the bedside monitor is connected to the network
through QI-910R interface, you cannot stop the monitoring from the
central monitor. Stop monitoring on the bedside monitor.
Measurement Interval
Touch to change the
interval. 12
NIBP trendgraph of
the past four hours
NIBP alarm limits setting
The setting procedure is the same as on the Alarm Limits
window of the Personal Setup. Refer to Section 5.
Sets the measurement interval of the NIBP measurement. The connected cuff and
setting keys are displayed on the screen.
Manual: Perform single measurement. If the measurement finishes, the
individual bed window appears.
STAT: Continuously repeat measurements for 15 minutes.
(Specific interval): Intervals selectable at the bedside monitor appear in [Measurement
Interval]. Perform measurements at the selected interval.
When setting the measurement interval to 2.5 min or less, a confirmation message is
displayed. Check the message and touch [YES].
PRESS Settings
On the Setup Menu of the Individual Bed window, touch [PRESS] to display the
PRESS window.
1
The PRESS window has three tabs. Touch the tab of the category name to switch
to another category.
• Main
• Display Settings
• Other
3 2
Main Settings
The upper half of the window shows the blood pressure waveform of each blood
pressure label and measurement information. You can change the scale. The
lower half of the window shows the upper and lower alarm limits of each blood
pressure label. You can set the upper/lower limit.
12
Measurement information
Displays the current PRESS settings.
Blood pressure
trendgraph of the past
four hours
Display Settings
Sets the settings for PRESS label and display. Touch [Display Settings] to change
the window.
Touch the label name key. The label selection window opens. Touch
the desired label.
NOTE
For PU-621R Op No. 21A, when the [Telemetry Setting Master]
is set to [ON], the Label Name settings are fixed to P1, P2 and
P3 when discharging a bed or deleting data.
Display Pattern S/D/M, MEAN Select the display style for each label. Touch the key to change the
setting.
• S/D/M: systolic/diastolic/mean
• Mean
NOTE
For PU-621R Op No. 21A, when the [Telemetry Setting Master]
is set to [ON], the Display Pattern setting is fixed to S/D/M
when discharging a bed or deleting data.
BP Scale Separate, Set the scale display mode of the blood pressure waveform.
Common, High/ • Separate: Waveforms are displayed separately on
Low Pressure different scales.
• Common: Waveforms are displayed on the same scale.
• High/Low Pressure: Waveforms are separated into high and low
pressures.
12
Other Settings
This setting is only available for beds that are monitored through an ORG-9100
multiple patient receiver which accepts the arterial pressure detection sensitivity
setting.
NOTE
For PU-621R Op No. 21A, when the [Telemetry Setting Master]
is set to [ON], the Arterial Pressure Detection Sensitivity setting
returns to the setting on the Telemetry Setting Master window
when discharging a bed or deleting data.
TEMP Settings
On the Setup Menu of the Individual Bed window, touch [TEMP] to display the
TEMP window.
1
The TEMP window has two tabs. Touch the tab of the category name to switch to
another category.
• Main
• Display Settings
3 2
Main Settings
The upper and lower alarm limits of each temperature are displayed. You can set
the upper/lower limit.
Temperature trendgraph
of the past four hours
Display Settings
This setting is only available for a bed that is monitored through an ORG-9100
multiple patient receiver.
Sets the settings for TEMP label and ∆T calculation formula. Touch [Display
Settings] to change the window.
Touch the desired label name key. The label select window opens.
Touch the label to set.
NOTE
For PU-621R Op No. 21A, when the [Telemetry Setting Master]
is set to [ON], the Label Name setting is fixed to T1 and T2
when discharging a bed or deleting data.
Delta T T1 (label name) Select the calculation formula to display as ∆T.
- T2 (label name),
T2 (label name) - T1
NOTE
(label name)
For PU-621R Op No. 21A, when the [Telemetry Setting Master]
is set to [ON], the Delta T setting is fixed to T1 - T2 when
discharging a bed or deleting data.
13
On the System Setup screen, you can set settings that affect the system.
NOTE
The shaded settings need an administrator password to access. These
settings can only be entered or changed by authorized personnel.
When [System Setup] is assigned to one of the all beds function keys, the
Information window of the System Setup screen can be displayed by touching
the function key. Refer to “Function Keys Setting” in Section 6-1 of the
Administrator’s Guide to assign a function to the function key.
Tabs Password input column
Touch to display another When the password is entered, setting
window. Touch [ ] or [ ] to windows for the administrator are
scroll the tab right and left. available.
13
POWER OFF
Central monitor information Refer to “Turning the
Power Off” in Section 3.
Sound Control
Set alarm sound volume, sync sound on or off, sync sound pitch, sync sound bed
and sync sound volume.
There are two tabs of sound control settings. The windows can be changed by
touching the tab.
• Alarm
• Sync Sound
Alarm
Touch [Alarm] on the Sound Control window and set the alarm volume. Refer to
“Adjusting the Alarm Sound Volume” in Section 5.
Sync Sound
Touch [Sync Sound] tab on the Sound Control window and set the sync sound
setting.
CAUTION CAUTION
The central monitor does not perform ECG The QRS sound at the central monitor has a time
analysis. Therefore, the QRS sync sound at the delay of several seconds because of network
central monitor might not synchronize with the connection.
patient’s actual QRS during pacing or when
complicated arrhythmias occur.
This section explains troubleshooting when the central monitor does not operate
properly and error messages displayed on the screen.
Troubleshooting
Following is the list of causes and countermeasures for troubles. After the action,
check that the problem is solved and the central monitor operates properly. Then
restart monitoring.
NOTE
If the following countermeasures do not solve the problem, attach an
“Unusable” or “Repair request” label to the central monitor and contact
your Nihon Kohden representative.
System
CPU Reset
CAUTION
The central monitor CPU may be reset when there is unit failure,
considerable static electricity or noise and monitoring stops for about
3 minutes. If this occurs, there is a 5-beep alarm sound for 5
seconds. After the central monitor is reset, check that it is working
properly.
If the CPU is reset, settings and all patient data except for the data during the
CPU reset are backed up and monitoring can continue. There are no settings for
the CPU reset.
Network
Measurement Value
* The QRS detection sensitivity can be set when the QRS detection type is Child.
Alarm
Admitting or Discharging
14
Trend Window
ST Recall Window
14
Parameter Setup
Remote Control
Error Messages
Error messages are categorized into two types, messages sent from bedside
monitors/multiple patient receiver and messages generated at the central monitor.
Some messages displayed at the bedside monitor or multiple patient receiver are
not displayed or are different on the central monitor.
Parameter Message
* CHECK ELECTRODES
* CHANGE ELECTRODE
* NOISE
* CANNOT ANALYZE
— PACING
ECG — Arrhythmia Analysis Off
— SMALL QRS
— RHYTHM CHANGE
— LEARNING
— LOW mV
— HIGH mV
Parameter Message
* Module Failure
* Too Many Params
* Connector Off
* Probe Off
* Probe Broken
SpO2 — No Pulse
* Light Interfer.
— Pulse Search
* Check Probe Site
—/* M (Unstable Pulse)*1
— Small Pulse
Parameter Message
* Module Failure
* Too Many Params
RESP
* Connector Off
* Check Sensor
Parameter Message
* Module Failure
* Too Many Params
* Connector Off
* Safety Valve Open
* No Pulse
* Meas Time Out
* Check Cuff/Hose
NIBP
* Systolic Over
— Re-measuring
— Please Wait
— Small Pulse
— Zeroing
— Noise
* Check Interval Setting*2
Parameter Message
* Module Failure 14
* Too Many Params
* Check Label
* Connector Off
* Check Sensor
— Out of Range
PRESS
— Zero Imbalance
— Zero Unstable
— Zero Out of Range
— Zeroing Complete
* Catheter Disconnect*2
* Cannot Detect Pulse*2
Parameter Message
* Module Failure
* Too Many Params
TEMP * Check Label
* Connector Off
* Check Sensor
Parameter Message
* Module Failure
* Too Many Params
* Connector Off
* Check Sensor
CO2
* Adapter Error
(Mainstream)
* Unspecified Accuracy*2
* Out of Range*2
* Check CO2 Cell*2
* CO2 Cell Off*2
Parameter Message
* Module Failure
* Module Overheat
CO2
* Line Block
(Sidestream)
* Filter Line Off
* Replace Scrubber
Parameter Message
* Module Failure
* Too Many Params
* Connector Off
O2
* Check Sensor
— Cal?
— Calibrating
Parameter Message
* Module Failure
* Connector Off
FLOW/Paw * Check Sensor
* Change Sensor
— Calibrating
Parameter Message
* Unit Failure
* Connector Off
* Check Catheter
* Catheter Location
— CO<1.0L/min
— Signal Adapting
— Unstable Tb
CCO
* Check Waveform
* Unstable
* Highly Variable Pulse Rate
* Check Patient Information
* Zero Imbalance
* Zero Unstable
* Zeroing Complete
Parameter Message
* Module Failure
* Connector Off
PiCCO (EXT)
* Check Sensor
* Alarm
Parameter Message
* Unit Failure
GAS * Too Many Params
* Com Error
Parameter Message
* Module Failure
tcPO2/tcPCO2
* Connector Off
(EXT)
* Com Error
Parameter Message
* Module Failure
* Too Many Params
BIS
* Connector Off
* Com Error 14
Parameter Message
* Unit Failure
* Connector Off
* Check Sensor
CNIBP
— Pulse Search
— Sensor Expired
— Out of Range
Parameter Message
* Module Failure
* Too Many Params
EEG
* Connector Off
* Check Sensor
Parameter Message
* Connector Off
VENT (EXT)
* Alarm
Parameter Message
* Alarm
* esCCO Error
— Check ECG/SpO2
— Check ECG
— Check SpO2
esCCO
— Check CAL Parameter
— Collecting Data
— Ready for CAL
— CAL Complete
— CAL Error
Other
Duplicated” message. Multiple patient receiver might not detect channel duplication properly within 3 minutes
after turning on the multiple patient receiver.
*4 “Input Unit Disconnected” and “Receiving Data” are only displayed when the bedside monitor on which transport
function is set to on is connected.
* Displayed only when Available Alarm Types is set to All on the System Setup screen.
5
Printer
Other
ECG Monitoring
SpO2 Monitoring
* This applies only when data is being sent from a combination of a vital sensor (a monitor from A&D Co., Ltd.) and a
ZB-900P or ZS-900P transmitter.
NIBP Monitoring
CO2 Monitoring
Daily Check
1. Touch [Menu] on the left lower corner of the screen → [Touchkeys Setting]
and display the setting window. A confirmation window appears.
When [Touchkeys Setting] is assigned to one of the all beds function keys,
the [Touchkeys Setting] screen can be displayed by touching the function
key. Refer to “Function Keys Setting” in Section 6-1 of the Administrator’s
Guide to assign a function to the function key.
3. Touch the exact center of the mark. When the mark is correctly touched, the
mark appears in another place. The mark appears in three places.
When all three places are touched correctly, the screen changes.
CAUTION
Before maintenance, cleaning or disinfection, turn
the central monitor power off and disconnect the
power cord from the AC socket. Failure to follow
this instruction may result in electrical shock and
central monitor malfunction.
CAUTION CAUTION
This instrument is not waterproof. Be careful not If the instrument accidentally gets wet,
to let any liquid get inside the instrument. immediately stop using it and disconnect the
power cord from the AC outlet. Contact your
Nihon Kohden representative for inspection.
CAUTION
Do not use volatile liquid such as thinner or
benzine as these agents will melt or crack the
materials.
15
Wipe the panel with a soft cloth moistened with water, neutral soap or alcohol
(76.9 to 81.4 vol%) and wrung out. Wipe off moisture with a dry cloth or gauze
and thoroughly dry before use.
Check if the vent hole is dusty. Wipe the dust off with a cotton swab or vacuum it
with a cleaner.
Disinfecting
CAUTION CAUTION
Do not use volatile liquids such as thinner or This instrument is not waterproof. Be careful not
benzine as these agents will melt or crack the to let any liquid get inside the instrument.
materials.
CAUTION CAUTION
If you put spray on the instrument, wipe off the Do not sterilize. It deteriorates and damages the
instrument with a dry cloth after spraying. instrument surface and causes malfunction.
To disinfect, wipe the main unit with a soft cloth moistened with any of the
disinfectants listed below. Use the recommended concentration. Wipe off
moisture with a dry cloth or gauze and thoroughly dry before use.
LCD Display
Disable the touchkeys function before cleaning.
1. Touch [Menu] on the left lower corner of the screen → [Touchkeys Off] and
display the setting window.
When [Touchkeys Off] is assigned to one of the all beds function keys,
the [Touchkeys Off] can be displayed by touching the function key. Refer
to “Function Keys Setting” in Section 6-1 of the Administrator’s Guide to
assign a function to the function key.
3. Click the mouse, press any key on the keyboard or touch the icon which
appears during a touchkeys off to restore the touchkeys function. Or, wait for
120 seconds to restore the touchkeys function.
CAUTION
Do not touch the thermal head inside the recorder unit. The thermal
head may be damaged by static electricity or become dirty and
cause printing failure.
Panel
Clean the panel of the recorder unit in the same way as cleaning the PU-621R
Central Monitor Processing Unit. Refer to the “PU-621R Central Monitor
Processing Unit” section.
Thermal Head
To protect the thermal head from abrasion or damage and assure optimum
performance for a long time, clean the head surface of the recorder with the
thermal head cleaning pen (recorder unit accessory) after every 10 to 15 sets of
recording paper.
CAUTION
Be careful not to cut yourself with the paper cutter on the recorder.
2. Push down the magazine release lever and open the magazine.
15
3. Clean the black part of the thermal head with the thermal head cleaning pen.
Sensor
The paper sensor is located by the thermal head. Clean the sensor surface with a
dry cotton swab.
Network Printer
Refer to network printer manual.
Disposal
CAUTION
Dispose of Nihon Kohden products according to your local laws and
your facility’s guidelines for waste disposal. Otherwise, it may affect
the environment. If there is a possibility that the product may have
been contaminated with infection, dispose of it as medical waste
according to your local laws and your facility’s guidelines for medical
waste. Otherwise, it may cause infection.
15
Regular Inspection
CAUTION CAUTION
Software upgrade must only be done by qualified Do the regular inspection twice a year. Otherwise,
service personnel or a person with technical a decrease and loss in function will not be
knowledge. If upgrade is not done correctly, the noticed and this results in incorrect monitoring.
central monitor may freeze.
CAUTION CAUTION
During maintenance and servicing, patients Restart the central monitor once every three
monitored by the central monitor must be months. Otherwise operation becomes unstable
monitored by alternate instruments such as and monitoring may stop. While restarting,
bedside monitors. patients monitored by the central monitor must be
monitored by alternate instruments such as
bedside monitors.
CAUTION
Never disassemble or repair the central monitor.
Disassembly and repair must be performed by
qualified service personnel. When there is any
abnormality, contact your Nihon Kohden
representative.
15
Nihon Kohden Corporation (NKC) shall stock repair parts (parts necessary to
maintain the performance of the instrument) for a period of 5 years from the
date of delivery. In that period NKC or its authorized agents will repair the
instrument. This period may be shorter than 5 years if the board or part necessary
for the faulty section is not available.
This section explains the setting items, description and factory default settings on
this manual.
The Copy Bed Settings and Backup Settings columns mean as follows:
OK: The copy bed settings and backup settings are available.
NO: The copy bed settings and backup settings are not available.
–: The displayed setting is the setting maintained on the bed. So the copy
settings and backup settings are not available.
Setup
Admit/Discharge
Copy
Backup
Item Settings Bed
Settings
Settings
Bed Name Up to 10 alphanumeric characters –– ––
Monitored
Select from the 10 groups and “None”. OK OK
group
Patient ID Up to 16 alphanumeric characters
Patient Name Up to 32 alphanumeric characters
Height 0.1 to 299.9 cm / 0 to 9 ft, 0.0 to 11.9 inch
Weight 0.1 to 449.9 kg / 0.1 to 654.9 lb
Automatically calculated when the height and weight are
BSA
entered.
Date of Birth YYYY-MM-DD
Admit/Discharge From 0 years 0 months to 127 years 11 months
Automatically calculated when the date of birth is entered. –– ––
Age You can also enter the age manually. When the bedside
monitor in the network has day data, the day can be
synchronized.
Gender Male, Female, unknown
Blood Type A−, A+, B−, B+, AB−, AB+, O−, O+, unknown
Physician Up to 20 alphanumeric characters
Up to 200 alphanumeric characters, up to 8 lines when
Diagnosis
inserting the line
Note Up to 64 alphanumeric characters NO OK
Alarm
Copy
Backup
Item Settings Bed
Settings
Settings
Alarm Limits Refer to “Setting Alarm Limits” in Section 5.
Arrhythmia Alarm Refer to “Setting the Arrhythmia Alarm” in Section 5. –– ––
ST Alarm Refer to “Setting the ST Alarm” in Section 5.
Factory Copy
Backup
Item Settings Default Bed
Settings
Setting Settings
Auto, Auto + 1 ECG, Auto + 2 Auto + 1
Display Settings
ECG, Manual ECG
I, II, III,
aVR, aVL,
aVF, V1 to
ECG
6, V, MCL, ×1/4, ×1/2, ×3/4, ×1, ×3/2, ×2, ×4 ×1
ECG1,
ECG2
Trace1, Trace2
0-20, 0-50, 0-75, 0-100, 0-160,
0-200, 0-300, 50-200, Customize 0-200
ART, ART2, RAD,
scale (mmHg)
DORS, AO, FEM,
0.0-3.0, 0.0-7.0, 0.0-10.0, 0.0-14.0,
LVP, P1 to 8
0.0-22.0, 0.0-28.0, 0.0-40.0, 7.0- 0.0-28.0
28.0, Customize scale (kPa)
0-20, 0-50, 0-75, 0-100, 0-160,
0-200, 0-300, 50-200, Customize 0-50
UV, PAP, CVP,
scale (mmHg)
RAP, RVP, LAP,
0.0-3.0, 0.0-7.0, 0.0-10.0, 0.0-14.0,
All Beds Screen Setup
ICP, ICP2 to 4
0.0-22.0, 0.0-28.0, 0.0-40.0, 7.0- 0.0-7.0
16
28.0, Customize scale (kPa)
Sensitivity/Scale
Factory Copy
Backup
Item Settings Default Bed
Settings
Setting Settings
0-80, 0-100, 50-100, Customize
N2O (GAS) 0-80
scale (%)
Sensitivity/Scale 0.0-6.0, 0.0-10.0, 0.0-20.0,
GAS1, GAS2 0.0-6.0
Customize scale (%)
Wave
EEG1 (BIS) ×1/8, ×1/4, ×1/2, ×1, ×2, ×4, ×8 ×1
Selection
EXT1 to 4 ×1/8, ×1/4, ×1/2, ×1, ×2, ×4, ×8 ×1
10, 20, 30, 50, 70, 100, 150, 200,
EEG1, EEG2 300, 500, 750, 1000, 1500, 2000 100
(μV/cm)
Numerical
Display Settings Auto, Manual Auto
Selection
All Beds Numeric Area*1 Normal, Wide Normal
Other All Beds Numeric Size*1 Normal, Large Normal
HR Display HR+VPC+ST, HR Only HR+VPC+ST
• Screen Admit/
All Beds Screen Setup
Factory Copy
Backup
Item Settings Default Bed
Settings
Setting Settings
Auto, Auto + 1 ECG, Auto + 2 Auto + 2
Wave Selection Display Settings
Individual Bed Screen Setup
Parameter Priority
Copy
Backup
Item Settings Bed
Settings
Settings
Select from all the parameters which can be displayed
Parameter Priority OK OK
on this central monitor.
Recording
Factory Copy
Backup
Item Settings Default Bed
Settings
Setting Settings
First Wave,
Depends on
Record Wave Second Wave, Measured parameters
the bed
Third Wave
Alarm Limits
Recording
Recording
Alarm
Arrhythmia ON, OFF OFF OK OK
Recording
Record
Call Recording
OFF, Periodic Recording, Clock Time
Periodic Recording OFF
Periodic Recording
Recording Sweep Speed 25 mm/s, 50 mm/s 25 mm/s
Report
Factory Copy
Backup
Item Settings Default Bed
Settings
Setting Settings
Report Mode Manual, Periodic Manual OK OK
Saved Data Range Display only — —
Print Start Time Blank
Manual mode Free setting OK OK
Print End Time Blank
Print Range Display only — —
1 hour, 2 hours, 4 hours, 8 hours,
Report Interval 8 hours
12 hours, 24 hours OK OK
Report
Parameter Setup
Copy
Factory Backup
Item Settings Bed
Default Setting Settings
Settings
Refer to “Setting Alarm
Main HR alarm
Limits” in Section 5.
Refer to “Setting the
Arrhythmia Alarm Arrhythmia Alarm” in Section *1
5.
Refer to “Setting the ST
ST Alarm
Alarm” in Section 5.
Arrhythmia
ON, OFF ON*2
Analysis
Analysis
Single, Multi Multi*2
Mode
Arrhythmia
Analysis I, II, III, aVR, aVL, aVF, V1
Detection II*2 –– ––
to V6, V, MCL, ECG1, ECG2
Arrhythmia Lead 1
Analysis Arrhythmia I, II, III, aVR, aVL, aVF,
Setting Detection V1 to V6, V, MCL, ECG1, NONE*2
ECG
(EXT), RR (GAS)
×1/4, ×1/2, ×3/4, ×1, ×3/2,
Sensitivity ×1*2
×2, ×4
Other
Impedance Respiration
ON, OFF ON*2
Measurement
Refer to “Setting Alarm
SpO2
Copy
Factory Backup
Item Settings Bed
Default Setting Settings
Settings
Refer to “Setting Alarm
Main Alarm Limits *1
Limits” in Section 5.
Label that –– ––
Refer to “PRESS Settings” in
Label Label Name is currently
Section 12.
Name/ measured.*2
PRESS
Temperature
–– ––
Display Label Name Refer to “TEMP Settings” in that is currently
Settings Section 12. measured.*2
Delta T T1 − T2*2
*1 • For a bed being monitored through the ORG-9100 series, “Alarm Master 1” is set as the default. Any other bedside
monitor depends on the setup value on the bed side.
• For a bed being monitored through the ORG-9100 series, “Alarm Master 1” is set as the default when the following
operation is performed: Discharge, Delete data, or Delete data upon transmitter channel change. Any other bedside
monitor depends on the setup value on the bed side.
* Depends on the settings at the bedside monitor.
2
*3 QRS Detection Sensitivity can be set only when the QRS Detection Type is set to “Child”.
*4 Depends on the monitoring leads at the central monitor.
Review
Review Menu
Copy
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
Custom Review to
Displayed review pattern Custom Review
Hemodynamics List
Frame Name Up 16 alphanumeric characters Custom Review
Trend, Tabular Trend, Full
Upper Disclosure, Expanded Waveform, Tabular Trend OK OK
Custom
Displayed Review Event List, ST Recall, Arrhythmia
Review
Window Recall, SpO2 Trend, ECG 12 Lead
Lower Analysis, Hemodynamics List, Trend
Alarm Events
Fixed display
Displayed Review
Displayed Pattern
Window
Frame Name Tabular Upper Tabular Trend
Trend Lower Trend
Upper Trend
Trend
Lower Expanded Waveform
Tabular Trend to Hemodynamics List
Upper Trend
Trend
Lower Alarm Events
Full Upper Full Disclosure
Disclosure Lower Expanded Waveform
Arrhythmia Upper Arrhythmia Recall
Recall Lower Full Disclosure –– ––
Upper Event List
Event List
Lower Expanded Waveform
Alarm Upper Alarm Events
Displayed Review Window
Events Lower Expanded Waveform 16
Full Disclosure (Full size
Full Disclosure
display)
ECG 12 Lead Analysis
ECG 12 Lead Analysis
(Full size display)
ST Recall (Full size
ST Recall
display)
Hemodynamics List (Full
Hemodynamics List
size display)
Trend
Copy
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
Trend 1, Trend 2, Trend 3,
Displayed trendgraph Trend 1 NO NO
Common Scale
Displayed
Trendgraph: 3 parameters
parameters and –– ––
Event trendgraph: 6 events
events
Monitoring
Select from the monitoring
parameters when
parameters and parameters set on
the screen is
[Parameter Selection] of System
Trend Parameter displayed at the
Setup screen.
Setting start of monitoring
Excluding the parameters which
and the parameter
cannot be displayed on this central
of the top 3
monitor.
priority.
ASYSTOLE, V FIB, V TACHY,
EXT TACHY, EXT BRADY, VPC
RUN, V BRADY, SV TACHY,
PAUSE, TACHYCARDIA,
BRADYCARDIA, COUPLET, ASYSTOLE,
Trend
NON-CAPTURE
HR, PR, ST, RR, APNEA, NIBP,
SpO2, ART (ART2, RAD, DORS,
Limit AO, FEM), CVP, PAP, ICP ALL, NONE
TEMP ALL, O2, CO2, GAS ALL,
BIS, EEG
ECG Technical, SpO2 Technical,
ART+NIBP, TEMP Technical,
ECG Technical,
Technical CO2 Technical, SIGNAL LOSS
SIGNAL LOSS
(COMMUNICATION LOSS
(wired)), BATTERY
Scale Setting Refer to Section 9.
Display
MAX - MIN, AVE MAX - MIN
Setting
Copy
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
Displayed
Trendgraph: 7 parameters
parameters and –– ––
Event trendgraph: 3 events
events
Monitoring
parameters when
the screen is
Trend Parameter displayed at the
Setting start of monitoring
and the parameter
Trend 3 Same as Trend 1 of the top 7
priority.
ASYSTOLE, OK OK
Arrhythmia V FIB,
Event
V TACHY
Limit NONE
Technical NONE
Scale Setting Refer to Section 9.
Display
MAX-MIN, AVE MAX-MIN
Setting
Trend
Displayed
Trendgraph: 4 parameters
parameters and –– ––
Event trendgraph: 3 events
events
Monitoring
parameters when
the screen is
Trend Parameter displayed at the
Setting start of monitoring
Common and the parameter
Scale of the top 4
Same as Trend 1
priority.
ASYSTOLE, OK OK
Arrhythmia V FIB, 16
Event
V TACHY
Limit NONE
Technical NONE
Scale Setting Refer to Section 9.
1 hour, 2 hours, 4 hours, 8 hours,
Displayed time width 12 hours, 24 hours, 48 hours, 8 hours
96 hours, 120 hours
Tabular Trend
Copy
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
Vital Sign 1, Vital Sign 2, Vital
Displayed tabular trend Vital Sign 1 NO NO
Sign 3, Vital Sign 4, NIBP
Select from the monitoring
parameters and parameters set on Monitoring
[Parameter Selection] of System parameters when
Trend Parameter
Setup screen. the screen is
Vital Sign 1 Setting
Excluding the parameters which displayed at the
to 4
cannot be displayed on this central start of monitoring.
monitor.
Tabular Trend
Full Disclosure
Copy
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
Displayed expanded Single Wave, ECG 12 Lead, Single Wave NO NO
waveform All Waves
Parameters which
were monitored at
Stored Waveform Setting Select from the monitoring the time of patient
1-16 (common setting for parameters which can be admission and the
each window) displayed on this central monitor. OK OK
parameters with the
top 16 priority.
Sensitivity/Scale
Same as the All Beds Screen Setup.
Setting
Displayed Select from the parameters that 1: TRACE 1
NO NO
Wave 1 to 16 have the waveform data. 2 to 16: NONE
Single Wave
Waveform
ON, OFF OFF
Alarm Color
Display
ON, OFF ON OK OK
Pacing Mark
Sensitivity/Scale
Same as the All Beds Screen Setup.
Setting
Full Disclosure
1: I 2: II
3: III 4: aVR
5: aVL 6: aVF
Displayed Select from the parameters that
7: V1 8: V2 NO NO
ECG 12 Wave 1 to 16 have the waveform data.
9: V3 10: V4
Lead
11: V5 12: V6
13 to 16: NONE
Waveform
ON, OFF OFF
Alarm Color
Display
ON, OFF ON OK OK
Pacing Mark
16
Sensitivity/Scale
Same as the All Beds Screen Setup.
Setting
16 monitoring
Displayed Select from the parameters that parameters
NO NO
Wave 1 to 16 have the waveform data. according to the
All Waves
priority
Waveform
ON, OFF OFF
Alarm Color
Display OK OK
ON, OFF ON
Pacing Mark
Interval 10 s, 20 s, 30 s, 60 s, 90 s 60 s
Expanded Waveform
Copy
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
Displayed expanded Single Wave, ECG 12 Lead,
All Stored Waves NO NO
waveform All Waves
Sensitivity/Scale
Same as the All Beds Screen Setup OK OK
Setting
Displayed Select from the parameters that 1: TRACE 1
NO NO
Wave 1 to 16 have the waveform data. 2 to 16 : NONE
Single Wave Sweep Speed* 6.25 mm/s, 25 mm/s, 50 mm/s 25 mm/s
Waveform
ON, OFF OFF
Alarm Color
Display OK OK
ON, OFF ON
Pacing Mark
Sensitivity/Scale
Same as the All Beds Screen Setup
Setting
1: I 2: II
3: III 4: aVR
Expanded Waveform
5: aVL 6: aVF
Displayed Select from the parameters that
7: V1 8: V2 NO NO
Wave 1 to 16 have the waveform data.
ECG 12 9: V3 10: V4
Lead 11: V5 12: V6
13 to 16: NONE
Sweep Speed* 6.25 mm/s, 25 mm/s, 50 mm/s 25 mm/s
Waveform
ON, OFF OFF
Alarm Color
Display OK OK
ON, OFF ON
Pacing Mark
Sensitivity/Scale
Same as the All Beds Screen Setup
Setting
16 monitoring
Displayed Select from the parameters that parameters
NO NO
Wave 1 to 16 have the waveform data. according to the
All Waves priority
Sweep Speed* 6.25 mm/s, 25 mm/s, 50 mm/s 25 mm/s
Waveform
ON, OFF OFF
Alarm Color
OK OK
Display
ON, OFF ON
Pacing Mark
Display Zoom × 1, × 2, × 4 ×1
* The sweep speed can be set when the window is displayed in full size.
Event List
Copy
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
Event Arrhythmia, Limit, Technical,
Displayed event ALL OK OK
List System, Comment, Caliper, ALL
ST Recall
Copy
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
I, II, III, aVR, aVL, aVF, V1 to 6, I, II, III, aVR, aVL,
Displayed lead
V, MCL, ECG1, ECG2 aVF, V1 to 6
ST Recall
Arrhythmia Recall
Copy
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
SpO2 Trend
Copy
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
NON-CAPTURE OK OK
V TACHY,
HR, PR, ST, RR, APNEA, NIBP,
V BRADY
SpO2, ART (ART2, RAD, DORS,
Limit AO, FEM), CVP, PAP, ICP ALL,
TEMP ALL, O2, CO2, GAS ALL,
SpO2 Trend
Copy
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
Analysis Wave (3 rows × 4
column), Analysis Wave (6 rows
ECG 12 Lead Analysis
Alarm Events
Copy
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
Copy 16
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
Display Setting Admitted Patient, Group A to J*1 Admitted Patient
All Beds Alarm Events
*1 Group name is displayed as set in [Pre-registration] → [Group Color] of the System Setup screen.
*2 Only available when monitoring with dual displays.
System Setup
Sound Control
Copy
Factory Default Backup
Item Settings Bed
Setting Settings
Settings
Alarm Alarm Volume 1, 2, 3, 4, 5, 6, 7 3
Sync Sound ON, OFF OFF
Sound Control
OK
Sync Sound
High, Low High
Pitch NO
Sync Sound
Sync Sound Bed Current Bed, Selected Bed Current Bed NO
Sync Sound
1, 2, 3, 4, 5, 6, 7 3 OK
Volume
Specifications..................................................................................................................................................... 17.2
Function.................................................................................................................................................... 17.2
Display........................................................................................................................................... 17.2
Full Disclosure Window.................................................................................................................. 17.3
Arrhythmia Recall Window............................................................................................................. 17.3
ST Recall Window.......................................................................................................................... 17.3
Trend Window................................................................................................................................. 17.3
Hemodynamics List Window.......................................................................................................... 17.3
ECG 12 Lead Analysis Window..................................................................................................... 17.4
Report Window............................................................................................................................... 17.4
Overview Bed Window................................................................................................................... 17.4
Alarm.............................................................................................................................................. 17.4
Recording....................................................................................................................................... 17.4
Printing........................................................................................................................................... 17.5
Operation....................................................................................................................................... 17.5
Sound and Light Output................................................................................................................. 17.5
Data Output.................................................................................................................................... 17.5
Network.......................................................................................................................................... 17.5
System Settings............................................................................................................................. 17.5
Saving Data.................................................................................................................................... 17.5
Performance................................................................................................................................... 17.6
LCD Display................................................................................................................................... 17.6
Environment................................................................................................................................... 17.6
Power Requirements...................................................................................................................... 17.6
Acoustic Energy (noise)................................................................................................................. 17.7 17
Mechanical Strength...................................................................................................................... 17.7
Dimensions and Weight (approximate, without protrusion)............................................................ 17.7
Safety Standard............................................................................................................................. 17.7
Electromagnetic Compatibility........................................................................................................ 17.8
Electromagnetic Emissions............................................................................................................ 17.9
Electromagnetic Immunity.............................................................................................................. 17.9
Recommended Separation Distances between Portable and Mobile RF Communications
Equipment.................................................................................................................................... 17.11
System Composition for EMC Test............................................................................................... 17.11
Restriction of Radio Equipment (European Union countries only)............................................... 17.12
European Community CE Notice................................................................................................. 17.12
Standard Accessories...................................................................................................................................... 17.13
PU-621R Central Monitor Processing Unit............................................................................................. 17.13
Options and Consumables............................................................................................................................... 17.13
PU-621R Central Monitor Processing Unit............................................................................................. 17.13
LCD Display........................................................................................................................................... 17.14
WS-960P Recorder Unit......................................................................................................................... 17.14
General Requirements for Connecting Medical Electrical Systems................................................................. 17.15
Specifications
Function
Display
All Beds screen
Number of patients: Up to 32 patients
Number of waveform traces: More than 1 trace/patient (Up to 16 patients)
Sweep speed: 6.25, 25, 50 mm/s (when 24 inch LCD display is used)
Waveform selection: Maximum 16 traces/auto
Waveform display: ECG, IBP, respiration wave, EEG, ETCO2, external input, pulse wave (SpO2),
FLOW/Paw, others depends on the connected bedside monitor or transmitter
Number of numeric data: More than 3 parameters/patient (less than 3 parameters are also available)
Numerical selection: Up to 17 parameters/auto
Numeric data display: Heart rate, VPC rate, respiration rate, pulse rate, IBP (systolic, diastolic, mean),
NIBP (systolic, diastolic, MAP), temperature, ΔT, blood temperature, ETCO2,
tcPO2, tcPCO2, SpO2, ST level, O2, CO, CCO, PiCCO, ventilator, anesthetic gas,
BIS, others depends on the connected bedside monitor or transmitter
Numeric data display size: Numeric data display size depends on the parameters
Waveform and numeric data display color: 32 colors
Alarm indication: Displays for each bed. Frame of alarmed bed lights or blinks*, highlighted
message for arrhythmia (when arrhythmia is detected)*, highlighted numeric
data (when vital signs alarms are generated)*, alarm sound* (Volume can be
adjusted.* Minimum volume is more than 45 dB. Minimum volume can be set
by the administrator.), alarm indicator lights
* Essential performance in EMC standard
Alarm silence: Displays alarm silence mark or silence mark with remaining minutes.
Alarm can be silence for each patient.
Recording: Alarm recording, manual recording, all beds recording
Alarm recording starts when an alarm is generated even which screen is
displayed.
Sync sound: Displays QRS sync mark at the selected patient data display area. Sync sound is
generated from the speaker (volume can be adjusted). Sync sound is generated
even which screen is displayed. Alarm indicator lights.
Alarm silence: Displays alarm silence mark or silence mark with remaining minutes.
Alarm can be silence for each bed.
Patient settings: Patient information can be entered when admitting or discharging the patient.
Receiving channel number can be set when using the multiple patient receiver.
Alarm settings can be changed.
Recording: 10 seconds of waveforms (on the network printer), manual recording
ST Recall Window
Display formats: ST file display, comparison display
Number of recall files: Up to 120 hours/bed
ST recall file recording: Recorder, network printer 17
Trend Window
Display formats: Trendgraph, tabular trend
Display times: Up to 120 hours/bed
Zoom in display: 1, 2, 4, 8, 12, 24, 48, 96 or 120 hours
Display interval: 1, 2, 5, 10, 15, 30, 60 minutes at NIBP measurement
Parameters: Depends on the connected bedside monitor
Trend recording: Network printer
Tabular trend recording: Network printer
NIBP trend recording: Network printer
Report Window
Printing: Network printer
Printing type: Manual, periodic
Printing items: Bed name, patient information, comment, tabular trend, trendgraph, full
disclosure waveform, expanded waveform, event list, arrhythmia
recall, ST recall, hemodynamics list, ECG 12 lead analysis, alarm event
Printing settings: Interval, printing start time, printing end time
Alarm
Alarm indication: Frame of alarmed bed lights or blinks*, highlighted message*, highlighted
numeric data*, alarm sound* and alarm indicator
* Essential performance in EMC standard
Alarm type: Arrhythmia, vital signs, technical
Setting method: Default setting applies unless the setting is changed. Settings can be changed on
the Alarm Master window. A group of alarm items can be set all together to one
group of preset setting.
Alarm silence: Alarm silence key is available on each screen.
Alarm On/Off: Available on each bed
Alarm setting range: Depends on the connected bedside monitor
Alarm history: Displayed by event list
Alarm volume: 45 to 85 dB (A) (Requirement of IEC 60601-2-49: 2001) (at 1 m in front of
central monitor) Crisis ≥ Warning ≥ Advisory
Alarm delay time
Delay between alarm occurrence on the central monitor and output of the alarm signal from a device that generates
alarm in the network: ≤4s
Recording
Record unit: WS-960P Recorder Unit
Record type: Manual recording, automatic alarm recording, periodic recording, remote
recording
Recorded items: Patient information, 3 traces of waveforms, waveform information, measurement
data, date and time, recording type and paper speed
Record color: Monochrome
Printing
Print device: Network printer
Print type: Manual recording or periodic recording
Printed items: Patient information, up to 16 traces of waveforms, waveform information,
measurement data, date and time, print type, paper speed
Print color: Monochrome, color
Operation
Touch panel (touch panel/LCD display with speaker), keyboard (option) and
mouse (option)
Data Output
Available through network
Network
This central monitor has a LS-NET interface and connect to other LS-NET
communication devices and display patient data. Through the LS-NET interface,
data can be output. The communication method complies with the Ethernet
standard.
System Settings
Information: Displays the version and password window.
Environment: Settings for the system such as unit settings. 17
Bed composition: Select the bed to be monitored always or only displays waveform.
ORG: Settings for the ORG-9100 series multiple patient receiver.
Recorder: Settings for recording.
Mouse: Setting the available range of network mouse.
Parameters: Selecting parameters.
Name registration: Editing the group name.
Waveform color: Setting for waveform display color.
Alarm master: Registering or changing the alarm master.
Function keys: Assigning functions to function keys.
Alarm volume: Setting for the alarm volume.
QRS sync sound: Setting for the QRS sync sound.
Touch panel: Calibrating the touch panel.
Date & Time: Setting for the date and time.
Maintenance: Displays the Maintenance window.
Saving Data
When monitoring a bedside monitor with several central monitors, the data is saved in the one central monitor and other
central monitor refer the data from the central monitor.
Performance
Display type: 24 inch LCD
Resolution (Maximum): 1920 × 1200 dots
Sweep speed: 6.25, 25, 50 mm/s
Memory: More than 1 GB
Processor: Core2Duo 2.2 GHz or better
Bulit-in display interface (compatible with WUXGA)
Built-in USB interface
Built-in sound interface
Built-in network interface
Large-capacity HDD: More than 250 GB
3-ch Recorder (option)
Recording paper: 50 mm width
Paper speed: 25, 50 mm/s
Number of channels: 3
Network printer
Paper size: A4, letter
USB I/F: Touch panel, mouse, bar code reader, USB-serial conversion cable
COM I/F: Alarm indicator, 3-ch recorder
PS/2 I/F: Keyboard
OS: Windows XP Embedded
Keyboard, mouse and bar code reader: Available as an option
LCD Display
LCD display: Local purchase
Environment
Operating environment
Temperature: 10 to 40°C (50 to 104°F)
Humidity: 30 to 85%
30 to 80% (PU-621R)
(10 to 40°C, noncondensing)
Atmospheric pressure: 700 to 1060 hPa
Transport and storage environment
Temperature: –20 to +65°C (–4 to +149°F)
–20 to +60°C (PU-621R) (–4 to +140°F)
–15 to +55°C (recording paper) (5 to 131°F)
Humidity: 10 to 95%
10 to 90% (noncondensing) (PU-621R)
Atmospheric pressure: 700 to 1060 hPa
Power Requirements
Line voltage: AC 100 to 240 V
Line frequency: 50, 60 Hz
Power consumption: 180 VA
Rated current: 4.8 to 1.9 A
Mechanical Strength
STATIONARY type
Safety Standard
Safety standard: IEC 60601-1-1: 2000
IEC 60950-1: 2005*1
IEC 60601-1: 1988*2
IEC 60601-1 Amendment 1: 1991*2
IEC 60601-1 Amendment 2: 1995*2
IEC 60601-1-2: 2001
IEC 60601-1-2 Amendment 1: 2004
IEC 60601-1-4: 1996
IEC-60601-1-4 Amendment 1: 1999
IEC 60601-1-6: 2004
IEC 60601-1-8: 2006
CAN/CSA C22.2 No.60950-1-07*3
CAN/CSA C22.2 No.601-1 M90: 1990*4
CAN/CSA C22.2 No.601-1 1S1-94: 1994*4
CAN/CSA C22.2 No.601-1B-98*4
CAN/CSA C22.2 No.60601-1-1-02 (R2006)*5
UL 60601-1 (1st edition)*5
*1 IEC 60950-1: 2005 applies to the following items.
17
• PU-621R Central Monitor Processing Unit (Op No. 21K)
• YL-611P/YL-612P Alarm Indicator
• YS-098P1/YS-098P2 Additional Alarm Indicator Unit
• YS-097P5/YS-097P6 VL Cable Set (Main)
• YS-097P8/YS-097P9 VL Cable Set (Second)
*2 IEC 60601-1: 1988, IEC 60601-1 Amendment 1: 1991 and IEC 60601-1
Amendment 2: 1995 applies to the following items.
• WS-960P Recorder Unit
• SC-611R WS-960P Power Supply
*3 CAN/CSA C22.2 No.60950-1-07 applies to the following items.
• PU-621R Central Monitor Processing Unit (manufactured by PFU
LIMITED, Op No. 21A)
• YL-611P/YL-612P Alarm Indicator
• YS-098P1/YS-098P2 Additional Alarm Indicator Unit
• YS-097P5/YS-097P6 VL Cable Set (Main)
• YS-097P8/YS-097P9 VL Cable Set (Second)
*4 CAN/CSA C22.2 No.601-1 M90: 1990, CAN/CSA C22.2 No.601-1 1S1-94:
1994 and CAN/CSA C22.2 No.601-1B-98 applies to the following items.
• WS-960P Recorder Unit
Operator’s Manual CNS-6201 17.7
17. REFERENCE
Electromagnetic Compatibility
IEC 60601-1-2: 2001
IEC 60601-1-2 Amendment 1: 2004
Electromagnetic Emissions
This Model CNS-6201 is intended for use in the electromagnetic environment specified below.
The customer or the user of the CNS-6201 should assure that it is used in such an environment.
Electromagnetic Immunity
This Model CNS-6201 is intended for use in the electromagnetic environment specified below.
The customer or the user of the CNS-6201 should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
Electrostatic discharge ±6 kV contact ±6 kV contact Floors should be wood, concrete or ceramic
(ESD) ±8 kV air ±8 kV air tiles. If floors are covered with synthetic
IEC 61000-4-2 material, the relative humidity should be at least
30%.
Electrical fast ±2 kV for power ±2 kV for power Mains power quality should be that of a typical
transient/ burst supply lines supply lines commercial or hospital environment.
IEC 61000-4-4 ±1 kV for input/output ±1 kV for input/output
lines lines
Surge ±1 kV differential ±1 kV differential Mains power quality should be that of a typical
IEC 61000-4-5 mode mode commercial or hospital environment.
±2 kV common mode ±2 kV common mode
Voltage dips, short <5% UT (>95% dip in <5% UT (>95% dip in Mains power quality should be that of a typical
interruptions and UT) for 0.5 cycles UT) for 0.5 cycles commercial or hospital environment.
voltage variations on If the user of the CNS-6201 requires continued
power supply input 40% UT (60% dip in 40% UT (60% dip in operation during power mains interruptions, it 17
lines UT) for 5 cycles UT) for 5 cycles is recommended that the CNS-6201 be powered
IEC 61000-4-11 from an uninterruptible power supply or a
70% UT (30% dip in 70% UT (30% dip in battery.
UT) for 25 cycles UT) for 25 cycles
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
*1 Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile
radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy.
To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be
considered. If the measured field strength in the location in which the CNS-6201 is used exceeds the applicable RF
compliance level above, the CNS-6201 should be observed to verify normal operation. If abnormal performance is
observed, additional measures may be necessary, such as re-orienting or relocating the CNS-6201.
*2 Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
Standard Accessories
NOTE
Use only Nihon Kohden specified parts and accessories to assure
maximum performance from your instrument.
Name Qty
Microsoft Windows license agreement 1
Recovery CD 1
Ferrite core 1
Operator’s manual 1
Administrator’s guide 1
Service manual 1
NOTE
• Use only Nihon Kohden specified options and consumables to assure
maximum performance from your instrument.
• When ordering the following items, specify the supply code. When the
17
supply code is not provided with the item, specify the model or code
number.
LCD Display
Name Qty
Power supply adapter 1
Power cord UL 1
Power cord N 1
When more than one electrical instrument is used, there may be electrical potential difference between the instruments.
Potential difference between instruments may cause current to flow to the patient connected to the instruments, resulting
in electrical shock. Therefore, electrical instruments must be appropriately installed as specified in IEC 60601-1-1: 2000
Second edition.
The following is an extract from IEC 60601-1-1 “Medical electrical equipment Part 1-1: General requirements for safety”,
For details, refer to IEC 60601-1-1 and consult with a biomedical engineer.
KEY TO TABLE
• Additional protective earth: If necessary, provide additional protective earthing, which is permanently connected (see also
58.201).
NOTE: Equipment modification may be required.
• Separating transformer: If necessary, limit the ENCLOSURE LEAKAGE CURRENT, by using an additional separating
transformer according to annex EEE.
NOTE 1: No equipment modification is required.
NOTE 2: A separating transformer is a transformer with one or more input winding(s) separated from the output
winding(s) by at least basic insulation [IEC 60989].
• SEPARATION DEVICE: If necessary, apply SEPARATION DEVICE.
• IEC 60601: MEDICAL ELECTRICAL EQUIPMENT in compliance with IEC 60601.
• IEC XXXXX: Non-medical equipment in compliance with relevant IEC safety standards.
Contact information is accurate as of April 2014. Visit www.nihonkohden.com for the latest information.
The model and serial number of your instrument are identified on the rear or bottom of the unit.
Write the model and serial number in the spaces provided below. Whenever you call your representative concerning
this instrument, mention these two pieces of information for quick and accurate service.
Your Representative