Pvm2700 Ag e
Pvm2700 Ag e
Pvm2700 Ag e
Bedside Monitor
PVM-2701/PVM-2703
0614-904404E
In order to use this product safely and fully understand all its functions, make sure to read this manual before using the
product.
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 and operate 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.
If you have any comments or suggestions on this manual, please contact us at: www.nihonkohden.com
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.
Trademark
The mark printed on the SD card that is used in this instrument is a trademark. The company name and model name are
trademarks and registered trademarks of each company.
Contents 1
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.
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.
WARNING
The bioelectric impedance measurement sensor of a minute ventilation rate-adaptive implantable
pacemaker may be affected by cardiac monitoring and diagnostic equipment which is connected to the
same patient. If this occurs, the pacemaker may pace at its maximum rate and give incorrect data to the
monitor or diagnostic equipment. If this occurs, disconnect the monitor or diagnostic equipment from the
patient or change the setting on the pacemaker by referring to the pacemaker’s manual. For more details,
contact your pacemaker representative or Nihon Kohden representative.
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.
Related Documentation
The PVM-2701 and PVM-2703 Bedside Monitor comes with the following manuals in addition to the Operator’s Manual.
Administrator’s Guide
Describes how to install the bedside monitor. It also explains about the password protected settings on the SYSTEM
SETUP window and SYSTEM CONFIGURATION screen which only an administrator can change.
User’s Guide
Gives supplemental information on the operation of the bedside monitor.
Describes the features and settings of the monitoring parameters.
Service Manual
Describes information on servicing the bedside monitor. Only qualified service personnel can service the bedside monitor.
This section describes installation conditions, connecting cables and power cords
and check items for this bedside monitor.
Installation Conditions
Note the following points for the installation location of your bedside monitor.
WARNING
• Do not install the monitor above the patient.
• Only use the specified tools or equipment when installing the
monitor. Failure to follow this warning may result in the monitor or
unit falling and injuring the patient.
CAUTION
Only use the specified cart or equipment for installing the monitor
and instruments. Using non-specified equipment may result in the
instruments falling and causing injury.
CAUTION
When not using the specified cart, carefully set the monitor to
prevent it from falling off or tipping over.
• Install the monitor where you can see the monitor screen clearly.
• Install the monitor on a strong shelf or dedicated cart (option). Secure the
monitor to the shelf to prevent it from falling.
• When moving a cart with a monitor, avoid collision. Strong impact may
damage the monitor.
• The monitor is not intended to be used in an ambulance. The monitor might
not function properly in a moving vehicle.
• The display screen is made of glass. Strong impact may damage it.
• Avoid locations where the monitor is sprinkled with liquid. Avoid direct
sprinkling, spray or moist air from a nebulizer or a humidifier.
• Avoid exposing the monitor to direct sunlight.
• Make sure that there is at least 5 cm of space between the monitor and the wall 1
for adequate ventilation. When the monitor is surrounded on all sides, make
sure that there is about 10 cm of space above the monitor for ventilation so that
the operating temperature does not exceed 40°C (104°F).
10 cm
5 cm Rear
5 cm 5 cm 5 cm 5 cm
Side
• Do not cover the monitor with a blanket or cloth. It may affect monitoring.
• Do not install the monitor in a dusty area.
• Connect the power cord to an AC outlet which can supply enough AC current
to the monitor. The monitor cannot function properly with low current.
• When there is any problem on the monitor, turn off the power immediately and
disconnect the power cord from the AC outlet. Take the monitor out of service
and check for damage.
The optional DH-270P adapter is required to mount the monitor on the KC-013P
cart.
The optional DI-270P adapter is required to mount the monitor on the KC-600P
cart.
CAUTION
Only use the specified cart or equipment for installing the monitor
and instruments. Using non-specified equipment may result in the
instruments falling and causing injury.
CAUTION
When not using the specified cart, carefully set the monitor to
prevent it from falling off or tipping over.
1
Installation Flowchart
2. Prepare the battery pack and recorder. Refer to the “Installing the Optional
Units to the Monitor” in this section.
4. Check or change any initial settings on the SYSTEM SETUP window. These
settings are password protected settings which only an administrator can
change. Refer to Section 3 in this guide.
6. Enter the name of the new patient. Refer to “Entering Patient Name” in
Section 3 of the User’s Guide.
7. Check or change all alarm items for the patient. Alarm settings return to the
default settings 30 minutes after the monitor is turned off. Refer to Section 5
of the User’s Guide.
10. Prepare electrodes, cuffs, probes, etc. for monitoring individual parameters
and check or change the settings for each parameter. Refer to Sections 9 to
15 in the User’s Guide.
WARNING WARNING
Connect only the specified instrument to the When several medical instruments are used
monitor and follow the specified procedure. Failure together, ground all instruments to the same one-
to follow this warning may result in electrical shock point ground. Any potential difference between
or injury to the patient and operator, and cause fire instruments may cause electrical shock to the
or instrument malfunction. patient and operator.
NOTE
• For details on connecting an external instrument to the monitor, contact
your Nihon Kohden representative.
• Leakage current may increase when interconnecting many medical
instruments to the monitor.
Medically-used room
Non-medically used room
Patient Environment Outside the Patient Environment
Interface Transmitter
QI-201P ZS-900PG/PK
Hyper isolation
transformer Central monitor
Bedside Interface QW-100Y (IEC xxx complied)
monitor QI-202P (HIT-100)
PVM-2701
PVM-2703
External
instruments
External (IEC 60601-1 complied)
instruments
Recorder (IEC 60601-1 complied)
module
WS-201P
Connection Overview 1
The following is the connection overview of PVM-2701/2703 bedside monitor.
Bedside Monitor
To a wall outlet
To a wall ground
terminal
Serial communication
Hyper isolation
QI-202P Interface transformer
QW-100Y
(HIT-100)
Network
NOTE
発売 日本光電工業株式会社
データ送信中
製造 日本光電富岡株式会社
monitor. Turn off the monitor, connect the transmitter and turn on the
monitor.
• During transmitting the data with ZS-900PG/PK to a receiver such as
QI-201P cardiac telemetry system or central monitor, using electrical surgical
Interface unit causes the data not to be transmitted by the noise from the
electrical surgical unit and “SIGNAL LOSS” to be displayed on the
screen of the receiver.
When the transmitter is connected to the monitor, turn the monitor power on and
check that the LED on the transmitter lights in green. Also check that the channel
number displayed in the upper part of the screen is correct.
Channel number and patient type are displayed alternately.
CAUTION CAUTION
When using a ZS-900PG/PK transmitter, the The ZS-900PG/PK transmitter can only transmit
measurement value on the telemetry system and temperature data from 5 to 45°C (41 to 113°F).
transmission side monitor may be different due to Be careful when reading the value.
timing delay of the display.
CAUTION CAUTION
When the ZS-900PG/PK transmitter is attached When transmitting CO2 data through a ZS-900P
to the bedside monitor, check the alarm, transmitter to a receiving monitor, if the
arrhythmia and monitoring settings on the central transmitted CO2 data is out of the range of the
monitor or telemetry system. The transmitter does receiving monitor, the maximum value of the
not transmit the alarm, arrhythmia and monitoring receiving monitor is displayed instead. Be careful
setting information. when reading the value.
NOTE
• Before connecting the transmitter, turn off the monitor power.
• The CE mark does not apply to the ZS-900PK transmitter.
Battery cover
NOTE
Be careful not to scratch the monitor screen.
2. Remove the battery cover by removing the screw at the bottom of the
Battery cover monitor, pressing the tab on the battery cover and sliding the cover off.
Screw
3. Connect the battery cable of the battery pack to the battery connector in the
label
battery pack holder of the monitor.
Step 4
4. Insert the battery pack into the battery pack holder with the on the label
pointing down.
Battery
cable
Step 3
5. Attach the battery cover and fasten the cover to the monitor with the screw
Battery cover and put the monitor in the upright position.
Screw
NOTE
Be careful not to scratch the monitor screen.
2. Remove the battery cover by removing the screw at the bottom of the
Battery cover monitor, pressing the tab on the battery cover and sliding the cover off.
Screw
Step 3 3. Take out the battery from the battery pack holder. 1
Step 4
Screw
1. Press the [Power] switch on the front panel while pressing the [CHECK] key
on the right side panel until the DIAGNOSTIC CHECK screen is displayed.
2. Touch the MANUAL CHECK key to display the MANUAL CHECK screen.
5. Touch YES to start the reset operation. During the reset operation, the
battery charge display lamp turns off. This takes about one minute.
6. When the reset operation ends, the battery charge lamp lights and the battery
is automatically charged until it is fully charged.
Charging takes about 12 hours when monitoring a patient and about 2.5
hours when not monitoring a patient. Charging time may be longer at high
temperatures.
3. Use the monitor only with battery power until the monitor automatically
turns off. When the monitor automatically turns off, the battery information
is automatically updated.
NOTE
Do not connect the AC power cord to the monitor while updating the
battery information.
1
Connecting the External Instruments to the Monitor
Connect the YS-100P6 serial cable to the external instrument and the serial
socket on the QI-202P interface.
NOTE
Do not connect or remove the YS-100P6 serial cable while the monitor
power is on. The monitor might not function properly.
To external instrument
YS-100P6 serial cable
General
The monitor can operate on either battery or AC power.
When the power cord is plugged into an AC outlet and the power switch on the
front panel is turned on, the monitor operates on AC power.
When a battery pack is installed and the power cord is disconnected or there is a
sudden power failure, the monitor automatically switches to battery power.
The battery pack is charged when the power cord is plugged into an AC outlet
and the AC current is supplied to the monitor. The battery is also charged during
monitoring.
The monitor can operate for about 3 hours with a new fully charged battery pack
when:
• Used in normal temperature.
• Optional recorder is not installed.
• No alarm occurs.
• Only monitoring ECG.
• <POWER SAVING MODE> on the SYSTEM SETUP window is set to ON.
• NIBP is not measured.
NOTE
Operate the monitor on battery power if you cannot confirm the grounding
or wiring in your facility.
WARNING
Only use the provided power cord. Using other power cords may
result in electrical shock or injury to the patient and operator.
Connect the provided power cord to the AC SOURCE socket on the rear panel of
the monitor and plug the cord into a 3-prong AC outlet.
When AC power is supplied to the monitor, the AC power lamp on the front
panel lights.
AC power lamp is
turned on.
NOTE 1
If the AC power lamp does not light, check the power cord connection.
WARNING
When several medical instruments are used together, ground all
instruments to the same one-point ground. Any potential difference
between instruments may cause electrical shock to the patient and
operator.
When more than one electrical instrument is used, there may be electrical
potential difference between the instruments. The potential difference between
the instruments may cause current to flow to the patient connected to the
instruments, resulting in electrical shock.
Wall ground terminal
Always perform equipotential grounding when required. It is often required in
the ICU room, CCU room, cardiac catheterization room and X-ray room. Consult
with a biomedical engineer to determine if it is required.
WARNING WARNING
Install all network devices, including printer and Check the software version number of the
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.
WARNING WARNING
Connect the monitor to network as specified. In a network where this monitor is connected,
Otherwise the patient and operator may receive connect only the specified instruments.
electrical shock or injury. To connect the network, Unspecified instruments may cause electrical
contact your Nihon Kohden representative. shock or injury to the patient and operator or
cause instrument malfunction, instrument stop, or
data loss.
WARNING
Do not use a damaged network cable. The patient
or operator may receive electrical shock when the
damaged part is touched.
CAUTION CAUTION
When the monitor is connected to a central The network must be managed by the network
monitor network, set the Bed Name (Bed ID) and administrator. Make sure that each monitor in the
Group Name on the monitor. Otherwise, the network has a different IP address. Otherwise, data
default settings are used for the bed name and communication cannot be performed properly.
group name and the bed may be incorrectly When adding a monitor to an already operating
identified on the central monitor. network, set the IP address on the monitor before
connecting the monitor to the network.
NOTE
When “EXTENDED” is selected for arrhythmia type and the bedside
monitor is connected to a central monitor network that has old
software so that “EXTENDED” arrhythmias cannot be monitored, the
“COMMUNICATION LOSS” message appears for the bedside monitor
and the bedside monitor cannot be monitored on the central monitor.
Connect the monitor to the network with the specified LAN cable. Connect
the QW-100Y (HIT-100) hyper isolation transformer between the monitor and
network.
NOTE
• The time on this monitor is automatically adjusted to match the time of
the network as long as the monitor is connected to the network. The
date and time on all monitors in the network are set to the same setting.
• When a CNS-9601K or CNS-9701J/K central monitor is used, check
that the software version of the central monitor is as follows:
CNS-9601K: version 01-06 or later
CNS-9701J/K: version 01-75 or later
Ferrite core
LAN cable
To network
YS-100P7 network
connection cable
CAUTION
Do not turn the monitor off when the system check screen is displayed.
Otherwise the saved data may be damaged or deleted. If the monitor is
turned off during system check, delete all data because the data is not
reliable.
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.
Press the [Power] switch on the front panel to turn the power on. The power
lamp and the AC power lamp light and self check starts. When the check is
complete, the home screen appears.
If the power lamp does not light, check the power cord connection.
CAUTION
When the monitor is turned on, check that one “bong” sounds and
the red, yellow, cyan and green alarm indicator lamps blink once to
show that the alarm functions properly.
When the monitor power is turned on, alarms are suspended while the monitor is 1
waiting for the electrodes and probe to be attached to the patient. The monitoring
starts when the connection cord is connected to the socket on the monitor and the
electrodes or probe are attached to the patient. The alarm activates when one of
the following occurs:
• at least one parameter is measured and a value is displayed (when AUTO is
selected for <ALARM ACTIVATION DELAY> on the ALARM window of
the SYSTEM SETUP window)
• ECG or SpO2 is continuously monitored for the selected time (when 1 min, 2
min or 3 min is selected for <ALARM ACTIVATION DELAY>)
• NIBP is measured (when 1 min, 2 min or 3 min is selected for <ALARM
ACTIVATION DELAY>)
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. When the date or time is changed during monitoring, the date and
time of all stored data is also changed and might not match the date and
time on the printout.
1
Calibrating the Touch Screen
Calibrate the touch screen when the pressed position and the activated position
do not match.
2. Press the [Power] switch on the front panel while pressing the [CHECK] key
on the right side panel until the DIAGNOSTIC CHECK screen is displayed.
4. Touch the @ mark at the upper left corner of the screen for 2 seconds. When
the mark is correctly touched, another mark appears in the lower right corner
of the screen. Touch the mark for 2 seconds.
Overview............................................................................................................................................................... 2.2
Setting Items on the SYSTEM CONFIGURATION Screen........................................................................ 2.2
Displaying the SYSTEM CONFIGURATION Screen.................................................................................. 2.3
Closing the SYSTEM CONFIGURATION Screen...................................................................................... 2.5
UNITS Window..................................................................................................................................................... 2.6
CHANGE PASSWORD Window........................................................................................................................... 2.7
OTHER Window................................................................................................................................................... 2.8
LANGUAGE Window.......................................................................................................................................... 2.10
OPTIONS Window.............................................................................................................................................. 2.10
Initializing the Monitor......................................................................................................................................... 2.11
NETWORK Window............................................................................................................................................ 2.13
IP ADDRESS/PROTOCOL Page............................................................................................................. 2.14
LS-NET Page........................................................................................................................................... 2.14
HL7 Page................................................................................................................................................. 2.15
PC Window......................................................................................................................................................... 2.17
Overview
You can check the contents of the SYSTEM CONFIGURATION screen settings
on the CONFIGURATION page of the SYSTEM SETUP window so that the
monitor power does not need to be turned off and monitoring is not interrupted.
Refer to Section 3 of this guide.
This section also explains how to initialize the monitor. This procedure returns
all settings to the factory default settings and deletes all stored data in memory.
PC window
CAUTION
This procedure interrupts all monitoring. Only change these settings
before or after monitoring.
2. Press and hold the [CHECK] key on the right side panel and press the
[Power] switch on the front panel until the DIAGNOSTIC CHECK screen is
displayed.
3. Touch the SYSTEM CONFIG key. The dialog box to enter the password
appears.
4. Enter the password with the number keys and touch the ENT key. The
SYSTEM CONFIGURATION screen appears.
UNITS Window
Select the unit for each parameter. CO2 unit is only available for PVM-2703.
1. Enter the current password in the <OLD PASSWORD> box using the
number keys on the screen. The default password is “1234”.
2. Touch the ENT key. The “PLEASE ENTER NEW PASSWORD” message
appears.
3. Enter the new password in the <NEW PASSWORD> box using the number
keys on the screen.
OTHER Window
Parameters
TYPE 8: ECG, RESP, SpO2, NIBP, IBP and TEMP
TYPE A: ECG, RESP, SpO2, NIBP, IBP, TEMP, CO2 and error message for
NIBP*, “–” for NIBP*
* Only for compatible receivers, monitors and telemetry systems.
This setting must be the same on all monitors in the same network. Otherwise
data communication problems may occur.
SIMULATION MODE
When this item is checked, the monitor enters SIMULATION MODE and when
it returns to the home screen, simulated waveforms and numeric values appear 2
on the screen. These can be used for demonstration of the monitor. You can select
CO2 or PRESS as the displayed parameter for PVM-2703.
SIMULATION MODE is turned off when the power is turned off.
DATE FORMAT
Select the date format from YYYY-MM-DD, DD-MM-YYYY, or MM-DD-
YYYY.
LANGUAGE Window
You can check the selected language in the LANGUAGE column of the
DIAGNOSTIC CHECK screen.
OPTIONS Window
Use the following procedure to initialize the monitor. Initializing the monitor
sets all settings to the factory default settings. The factory default settings of the
SYSTEM CONFIGURATION screen and SYSTEM SETUP window are listed
in “Factory Default Settings” in Section 4 of this guide. Other default settings are
listed in the operator’s manual.
CAUTION
All patient data, stored data and error history are deleted and all
settings return to the factory default settings.
2. Press the [Power] switch on the front panel while pressing the [CHECK] key
on the right side panel until the DIAGNOSTIC CHECK screen is displayed.
3. Touch the INITIALIZE key. The dialog box to enter the password appears.
4. Enter the password with the number keys and touch the ENT key. The
confirmation dialog box appears.
NETWORK Window
2
The network window is only available when the QI-202P interface is installed.
Set the network settings when the bedside monitor is connected to a central
monitor network.
CAUTION
When the monitor is connected to a central monitor network, set the
Bed Name (Bed ID) and Group Name on the monitor. Otherwise, the
default settings are used for the bed name and group name and the
bed may be incorrectly identified on the central monitor.
CAUTION
The network must be managed by the network administrator. Make
sure that each monitor in the network has a different IP address.
Otherwise, data communication cannot be performed properly. When
adding a monitor to an already operating network, set the IP address
on the monitor before connecting the monitor to the network.
IP ADDRESS/PROTOCOL Page
IP ADDRESS SETUP: AUTO, MANUAL
When set to AUTO, the IP address and subnet mask are set automatically.
When set to MANUAL, touch the EDIT key to set the IP address, subnet mask
and default gateway.
Do not assign all zeros or all ones for the subnet mask.
Select HL7 when connecting to the hospital network (HIS). When HL7 is
selected, the bedside monitor cannot communicate with the devices on the
monitor network.
LS-NET Page
When the PROTOCOL setting on the IP ADDRESS/PROTOCOL page is set
to LS-NET, assign a group name for the bedside monitor. When the monitor
has acquired the information of the network to which it is connected, the group
names assigned by the central monitor appear. Select the group name from this
list for the bedside monitor. For details, refer to the central monitor operator’s
manual.
HL7 Page
When the PROTOCOL setting on the IP ADDRESS/PROTOCOL page is set to
HL7, touch the HL7 tab on the NETWORK window and set the settings.
2
2. Change the setting. When the number keys or keyboard is used to enter the
setting, touch the ENT key to close the window.
Setting Range
Setting Item Description
( : Default)
ORU USE ORU ON, OFF Selects whether or not to output the ORU (current
numeric) data.
ORU PORT 1024 to 65535 (Default: 7998) Sets the port number to use for ORU data output.
No.
ORU 1 min, 5 min, 10 min, 30 min, 1 h Sets the interval to output the ORU data. Touch the
SAMPLING ORU SAMPLING key and select the time.
ORF USE ORF ON, OFF Selects whether or not to output the ORF (old
numeric) data. Up to the latest 120 hours of old
data can be output.
ORF PORT No. 1024 to 65535 (Default: 9004) Sets the port number to use for ORF data output.
QRY USE QRY ON, OFF Selects whether or not to request patient
information.
HIS SERVER Set depending on the hospital Sets the IP address of the HIS server.
IP ADDRESS network. (Default: 0.0.0.0)
HIS SERVER 1024 to 65535 (Default: 7997) Sets the port number that is used by HIS server for
PORT No. receiving patient information.
ADT USE ADT ON, OFF Selects whether or not to output the admit and
ADT 1024 to 65535 (Default: 9005) discharge, patient information update and presence
MONITORING check information.
PORT No.
• ADT MONITORING PORT No.
ADT PATIENT 1024 to 65535 (Default: 9006)
Sets the port number for admitting or discharging
INFO PORT
a patient from an external system.
No.
PATIENT LIST 1024 to 65535 (Default: 9007) • ADT PATIENT INFO PORT No.
PORT No. Sets the port number for entering the patient
information including patient ID from an
external system.
NOTE
A bedside monitor does not give any notification if a receiver in the
hospital network cannot receive data or response from the bedside
monitor. Set the receiver to give notification of a problem when it cannot
receive signals.
PC Window
2
BAUD RATE
Set the baud rate of the serial communication.
PARITY
Set the communication error detection method.
WORD LENGTH
Set the word length of the communication data.
STOP BIT
Set the stop bit of the serial communication.
Overview............................................................................................................................................................... 3.3
Setting Items on the SYSTEM SETUP Window......................................................................................... 3.3
Displaying the SYSTEM SETUP Window.................................................................................................. 3.8
Closing the SYSTEM SETUP Window....................................................................................................... 3.9
SYSTEM Window............................................................................................................................................... 3.10
INFO Page............................................................................................................................................... 3.10
CONFIGURATION Page.......................................................................................................................... 3.10
HL7 Page................................................................................................................................................. 3.11
MAINTENANCE Page.............................................................................................................................. 3.11
BATTERY Tab................................................................................................................................. 3.11
LOAD/SAVE SETTINGS Tab......................................................................................................... 3.12
SYSTEM CONFIGURATION Tab................................................................................................... 3.12
DISPLAY Window............................................................................................................................................... 3.13
GENERAL Page....................................................................................................................................... 3.13
LAYOUT Page.......................................................................................................................................... 3.15
VOLUME Page......................................................................................................................................... 3.17
INTERBED Page...................................................................................................................................... 3.18
BED ID Window.................................................................................................................................................. 3.19
PARAMETERS Window...................................................................................................................................... 3.20
ECG Page................................................................................................................................................ 3.20
MAIN Tab........................................................................................................................................ 3.20
V-LEADS Tab................................................................................................................................. 3.22
ARRHYTH Page....................................................................................................................................... 3.23
NIBP Page................................................................................................................................................ 3.24
MAIN Tab........................................................................................................................................ 3.24
INTERVAL Tab............................................................................................................................... 3.25
VENOUS PUNCTURE Tab............................................................................................................ 3.26
STAT Tab........................................................................................................................................ 3.26
SIM Tab.......................................................................................................................................... 3.27
OTHER PARAM Page.............................................................................................................................. 3.28
SpO2 Page................................................................................................................................................ 3.29
ALARM Window.................................................................................................................................................. 3.30
SILENCE/SUSPEND Page...................................................................................................................... 3.30
DISPLAY/SOUND Page........................................................................................................................... 3.32
ALARM PRIORITY Page.......................................................................................................................... 3.33
ARRHYTH PRIORITY Page..................................................................................................................... 3.37
TECHNICAL PRIORITY Page.................................................................................................................. 3.38
SLEEP Page............................................................................................................................................ 3.39
NETWORK Page...................................................................................................................................... 3.41
COLOR Window................................................................................................................................................. 3.42
BASIC PARAM Page................................................................................................................................ 3.42
RECORD Window.............................................................................................................................................. 3.43
RECORDER Page................................................................................................................................... 3.43
Overview
This section explains how to change settings on the SYSTEM SETUP window. 3
The SYSTEM SETUP window can only be accessed with a password.
Changing the settings on the SYSTEM SETUP window does not interrupt
monitoring, but it is recommended to check and change them before monitoring
a patient because these settings involve basic measurement conditions.
SYSTEM – MAINTENANCE – LOAD/SAVE SETTINGS tab SYSTEM – MAINTENANCE – SYSTEM CONFIG tab
* The HL7 tab appears only when the QI-202P interface is installed in the monitor and PROTOCOL is set to HL7 on the
NETWORK – IP ADDRESS/PROTOCOL page of the SYSTEM CONFIGURATION screen.
KEYS window
1. Touch the Menu key on the screen to display the MENU window.
3. Enter the password with the number keys and touch the ENT key. The
SYSTEM SETUP window appears. (The default password is “1234”.)
SYSTEM Window
INFO Page
The INFO page shows the software version and language of the monitor. The
page also lists the options installed in the monitor.
CONFIGURATION Page
The CONFIGURATION page shows the settings on the SYSTEM
CONFIGURATION screen of the DIAGNOSTIC CHECK screen. You can check
the contents of the settings without restarting the monitor.
NOTE
The settings on the CHANGE PASSWORD window are not displayed.
HL7 Page
The HL7 tab appears only when the QI-202P interface is installed in the monitor
and PROTOCOL is set to HL7 on the NETWORK – IP ADDRESS/PROTOCOL
page of the SYSTEM CONFIGURATION screen.
3
You can check the HL7 settings on this page without restarting the monitor.
MAINTENANCE Page
The MAINTENANCE page has three tabs.
BATTERY Tab
The BATTERY tab shows the status of the battery pack.
To refresh the
battery information,
touch this key.
DISPLAY Window
GENERAL Page
NOTE
When the QI-202P interface is installed, only SCREEN KEYBOARD is
available.
When a patient was not discharged at the monitor power off and
<SHOW ADMIT CONFIRMATION WINDOW> is set to off, if the
monitor is turned on more than 30 minutes after turning the power
off, the message appears indicating that the patient data is deleted
at the power off and the settings are initialized. If the monitor is
turned on within 30 minutes after turning the power off, the patient
data and settings at the power off are kept and monitoring continues
when the same conditions as the alarm function resuming after
suspending alarms are met.
When <ADMIT MODE> is set to MANUAL and the patient was discharged
before turning the power off, the “DISCHARGED” message and the
STANDBY window appear instead of the ADMIT CONFIRMATION
window.
Off: The ADMIT CONFIRMATION window does not appear when the monitor
is turned on.
When the monitor is turned on after the monitor has been off for 30 minutes
or more, the message appears indicating that the patient data at the power
off is deleted and the settings are initialized.
When the monitor is turned on within 30 minutes after the power was turned
off, the patient data and settings at the power off are kept and monitoring
resumes when the same conditions as the alarm function resuming after
suspending alarms are met.
On Off
LAYOUT Page
LEFT SIDE:
The numeric
values are
displayed at the
left side of the
home screen.
LARGE BOTTOM:
The numeric
values are
displayed at the
bottom of the
home screen.
The values at the
bottom of the
screen are large.
VOLUME Page
NIBP COMPLETION
Set the volume for the NIBP measurement completion sound. The NIBP
measurement completion sound is enabled when <COMPLETION SOUND>
is set to NK1 or NK2. When <COMPLETION SOUND> is set to Off, there
is no sound. The NIBP completion sound can be set on the NIBP page of the
PARAMETERS window.
KEY CLICK
Set the volume for the click sound when a key on the screen is touched. When set
to minimum, there is no click sound.
INTERBED ALARM
Set the volume for the interbed alarm sound. The interbed alarm sound is enabled
when <INTERBED ALARMS TO DISPLAY> on the INTERBED page of the
SYSTEM SETUP window is set to ALL, CRISIS AND WARNING, or CRISIS.
When it is set to NONE, there is no sound.
NOTE
This setting is only available when the QI-202P interface is installed in the
monitor.
INTERBED Page
When alarms occur at several interbed beds at the same time, the alarms are
displayed on this bedside monitor one after the other.
NOTE
When ALL, CRISIS AND WARNING, or CRISIS is selected, the alarm
sounds near the patient. If the sound indication is unwanted, select
NONE.
BED ID Window
2. Touch the desired letters and numbers to enter the bed ID.
PARAMETERS Window
The PARAMETERS window has five pages: ECG, ARRHYTH, NIBP, OTHER
PARAM and SpO2.
You can set the settings for ECG on the ECG page and ARRYTH page, the
settings for NIBP on the NIBP page, the settings for SpO2 on the SpO2 page, and
the settings for respiration and IBP on the OTHER PARAM page.
ECG Page
MAIN Tab
NOTE
• When “EXTENDED” is selected for arrhythmia type and the bedside
monitor is connected to a central monitor network that has old
software so that “EXTENDED” arrhythmias cannot be monitored, the
“COMMUNICATION LOSS” message appears for the bedside monitor
and the bedside monitor cannot be monitored on the central monitor.
• When the ARRHYTHMIA TYPE is changed from “STANDARD” to
“EXTENDED”, the settings for “STANDARD” are used. However, the
settings may be changed automatically depending on the setting. Check
the arrhythmia alarm settings after changing the ARRHYTHMIA TYPE.
WARNING
For arrhythmia monitoring, set <ARRHYTHMIA ANALYSIS> on the
ECG page of the PARAMETERS window on the SYSTEM SETUP
window to ON. Otherwise, there is no sound or indication for
arrhythmia alarms (except for ASYSTOLE).
When the monitor is initialized, or turned off for more than 30 minutes
when <SHOW ADMIT CONFIRMATION WINDOW> is set to Off, the
ARRHYTHMIA ANALYSIS setting on the MASTER window of the SYSTEM
SETUP window is applied.
The pacing marks appear only when the PACING DETECT setting is set to On
on the ECG window.
V-LEADS Tab
Select the leads for Ca/Va and Cb/Vb by touching the keys for the leads.
The selected lead are displayed on the ECG1 LEAD/SENSITIVITY and ECG2
LEAD/SENSITIVITY pages on the ECG window.
ARRHYTH Page
WARNING
For arrhythmia monitoring, set <ARRHYTHMIA ANALYSIS> on the
ECG page of the PARAMETERS window on the SYSTEM SETUP 3
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.
You can display the ARRHYTH page by touching the SETUP key on the
ARRHYTH ALARMS window of the ECG window or ARRHYTH ALARMS
tab of the Menu window.
Set arrhythmia alarm ON or OFF by touching the ON/OFF key beside each
arrhythmia type. ASYSTOLE, VF and VT are fixed to ON. The setting changes
to the master setting when the monitor is initialized or turned off for more than
30 minutes.
Set the threshold for each arrhythmia by touching the arrow keys beside the
value.
For detailed settings for each arrhythmia, refer to “Factory Default Settings
– SYSTEM SETUP Window” in Section 4.
NIBP Page
MAIN Tab
NOTE
When 24 h is selected, the NIBP data is hidden 24 hours after
measurement even when DIM is selected for <OLD DATA DISPLAY>.
Example
When you start periodic measurement at 12:03 at 5 min interval, measurement is
performed at:
CLOCK: 12:03, 12:05, 12:10, 12:15 ...
PERIOD: 12:03, 12:08, 12:13 ... 3
INTERVAL Tab
NIBP INTERVALS
Select the NIBP measurement mode to be displayed on the NIBP
MEASUREMENT INTERVALS window which appears on the screen when
the NIBP Interval key on the home screen or MEASUREMENT INTERVAL
key on the NIBP window is touched. For the NIBP window and NIBP
MEASUREMENT INTERVALS window, refer to Section 13 of the User’s
Guide.
NOTE
When the SIM mode is selected, you cannot change the NIBP intervals or
start or stop NIBP measurement from the central monitor.
Slider
1. Select the patient type by touching the ADULT, CHILD or NEONATE key.
2. Touch and drag the slider to select the cuff pressure. Use the or key to
adjust setting.
STAT Tab
The STAT mode is for measuring blood pressure during induction of general
anesthesia. There are two stages. In <STAGE 1>, repetitive measurement
is performed at the interval set for <INTERVAL> for the period set for
<OPERATING TIME>. After stage 1 finishes, periodic measurement starts at the
interval set for <STAGE 2>. 3
Setting Items
STAGE 1 INTERVAL: STAT/1 min*
STAGE 1 OPERATING TIME: 5 min/10 min
STAGE 2 INTERVAL: MANUAL/1 min/2 min/2.5 min/5 min/
10 min/15 min/30 min
* 1 minute interval measurement reduces burden on the patient.
SIM Tab
The SIM mode is for measuring blood pressure during infusion of local
anesthesia such as spinal anesthesia (also called lumbar anesthesia or
subarachnoid block) and epidural anesthesia. There are two stages. In <STAGE
1>, repetitive measurement is performed at the interval set for <INTERVAL>
for the period set for <OPERATING TIME>. After stage 1 finishes, periodic
measurement starts at the interval set for <STAGE 2>.
Setting Items
STAGE 1 INTERVAL: 1 min/2 min/2.5 min
STAGE 1 OPERATING TIME: 5 min/10 min/15 min
STAGE 2 INTERVAL: 2 min/2.5 min/5 min
NOTE
When this item is set to On and the timing of the respiration and heart
beat coincide, respiration rate might not be counted. If this occurs, set this
item to Off or check the patient’s respiration by observing the patient’s
chest movement or the respiration waveform on the screen.
SpO2 Page
ALARM Window
SILENCE/SUSPEND Page
WARNING
During alarm suspension (“ALARMS SUSPENDED” or “ALL
ALARMS OFF” message displayed), all alarms are turned off. Be
careful when you suspend the alarm.
SUSPEND ALARMS
DISPLAY/SOUND Page
ALARM SOUND
CRISIS WARNING ADVISORY
TYPE setting
IEC standard (ceg-gC) IEC standard (ceg) IEC standard (ec every
IEC
20 or 120 seconds)
Continuous pip sound Continuous bing bong Single beep every 20
NK1
sound or 120 seconds
Continuous ping sound Continuous ding ding Single beep every 20
NK2
sound or 120 seconds
Select the alarm level and alarm indicator color for each parameter. The color
combination depends on the <ALARM PRIORITY COLOR> setting on the
DISPLAY/SOUND page.
CRISIS: The parameter data is highlighted with a sound selected at
<ALARM SOUND TYPE> and red lamp blinks.
WARNING: The parameter data is highlighted with a sound selected at
<ALARM SOUND TYPE> and yellow or orange (color selected
at <ALARM PRIORITY COLOR>) lamp blinks.
ADVISORY: The parameter data is highlighted with a sound selected at
<ALARM SOUND TYPE> every 20 or 120 seconds (interval
selected at <ADVISORY ALARM SOUND INTERVAL>)
and cyan or yellow (color selected at <ALARM PRIORITY
COLOR>) lamp lights.
<Example>
APNEA alarm level: WARNING
Escalation setting: AFTER ELAPSED TIME: ON, TIME UNTIL ESCALATION: 30 s, PRIORITY: CRISIS
30 seconds
1. Touch the key in the ESCALATION column for APNEA. The APNEA
ESCALATION window opens.
CRISIS level
Time
• When the AFTER VALUE DROP is ON and the SpO2 value drops below a
set level (3, 5 or 10% below the lower alarm limit) for a selected duration, the
alarm escalates to the CRISIS level.
Time
1. Touch the key in the ESCALATION column for SpO2. The SpO2
ESCALATION window opens.
2. Select ON for AFTER ELAPSED TIME and/or AFTER VALUE DROP. The
TIME UNTIL ESCALATION, VALUE DROP and DELAY TIME setting
become available.
<Example>
SpO2 DELAY TIME: 10 s
10 seconds
Time
1. Touch the DELAY TIME key. The SpO2 DELAY TIME window appears.
3. Touch the close button ( ) to close the SpO2 DELAY TIME window.
Select the alarm level and alarm indicator color for each arrhythmia type. The
color combination depends on the <ALARM PRIORITY COLOR> setting on
the DISPLAY/SOUND page.
CRISIS: The parameter data is highlighted with a sound selected at
<ALARM SOUND TYPE> and red blinking lamp.
WARNING: The parameter data is highlighted with a sound selected at
<ALARM SOUND TYPE> and yellow or orange (color selected
at <ALARM PRIORITY COLOR>) blinking lamp.
ADVISORY: The parameter data is highlighted with a sound selected at
<ALARM SOUND TYPE> every 20 or 120 seconds (interval
selected at <ADVISORY ALARM SOUND INTERVAL>)
and cyan or yellow (color selected at <ALARM PRIORITY
COLOR>) lamp lit.
Select the alarm level and alarm indicator color for the three technical alarms.
The color combination depends on the <ALARM PRIORITY COLOR> setting
on the DISPLAY/SOUND page.
WARNING: The parameter data is highlighted with a sound selected at
<ALARM SOUND TYPE> and yellow or orange (color selected
at <ALARM PRIORITY COLOR>) blinking lamp.
ADVISORY: The parameter data is highlighted with a sound selected at
<ALARM SOUND TYPE> every 20 or 120 seconds (interval
selected at <ADVISORY ALARM SOUND INTERVAL>)
and cyan or yellow (color selected at <ALARM PRIORITY
COLOR>) lamp lit.
Alarm Escalation
For CHECK ELECTRODES, CANNOT ANALYZE and CHECK PROBE
alarms, an alarm escalation is available. When the setting is ON and no action
is taken on an alarm for a selected duration, the alarm escalates to the selected
level.
5 minutes
CHECK ELECTRODES
ALARM ADVISORY WARNING
SLEEP Page
NOTE
• This SLEEP page is displayed when a QI-201P or QI-202P interface is
installed in the bedside monitor.
• The sleep mode is only available when the ZS-900PG/PK transmitter is
attached to the bedside monitor or the bedside monitor is connected to
the central monitor network.
WARNING
When the <EXIT SLEEP MODE ON CRISIS ALARM> check box
on the ALARM page of the SYSTEM SETUP window is OFF, the
bedside monitor alarm cannot be seen or heard on the bedside
monitor during sleep mode. In this case, monitor the bedside
monitor alarms on the central monitor or telemetry system.
Otherwise, the bedside monitor alarms may be overlooked.
On: When a crisis alarm occurs during sleep mode, the sleep mode is exited
and the home screen appears. When an alarm other than crisis occurs, sleep
mode continues.
Off: The sleep mode continues even when a crisis alarm occurs.
1. Touch the EDIT key in the <SLEEP MODE WILL END AT> box.
NETWORK Page
The network page is only available when the QI-202P interface is installed.
NOTE
• When <COMMUNICATION LOSS NOTIFICATION> is set to OFF, there
is no COMMUNICATION LOSS alarm. When it is set to OFF, always
pay careful attention to the communication status.
• When <COMMUNICATION LOSS NOTIFICATION> is set to NO
SOUND, an alarm for the same alarm condition does not occur again
while communication is still lost. While it is in NO SOUND, always pay
careful attention to the communication status.
• When checking the monitoring conditions of the receiving monitors in
the network, check it on each receiving monitor.
RE-ALARM: When the Silence Alarms key is pressed, the alarm sounds again
at every alarm silence interval (which is set on the SILENCE/
SUSPEND page of the SYSTEM SETUP screen) until the
alarm condition is resolved. The screen message continues to be
displayed.
NO SOUND: When the Silence Alarms key is pressed, there is no sound again.
The screen message continues to be displayed.
OFF: No sound or screen message even when the LAN cable is
disconnected.
COLOR Window
2. Touch the parameter key to change the color. The COLOR TABLE window
appears.
The PRESS, PRESS-PR and PPV/SPV are only available for PVM-2703.
3. Select the desired color for the parameter on the COLOR TABLE window.
RECORD Window
RECORDER Page
When CONTINUOUS is selected, the recording starts when the Record key
on the screen is touched and stops when the Record key on the screen is
touched again.
For details on periodic recording, also refer to Section 7 of the User’s Guide.
Arrow keys
Example
When you start periodic recording at 12:03 at 5 min interval, recording is
performed at:
CLOCK: 12:05, 12:10, 12:15 ...
PERIOD: 12:08, 12:13, 12:18 ...
PRINTER Page
IP ADDRESS
Set the IP address of the network printer.
2. Use the number keys on the screen to enter the IP address of the network
printer.
PRINTER NAME
Enter the printer name. Up to 16 alphanumeric characters can be entered.
Normally, use the default setting “lp”. If data cannot be printed, change the
setting to the printer name specified in the printer manual. If the printing still
cannot be performed, contact your Nihon Kohden representative.
2. Use the alphanumeric keys on the screen to enter the printer name of the
network printer.
HOSPITAL
You can print the hospital or institution name at the top of the printing paper. Up
to 32 alphanumeric characters can be entered.
2. Use the alphanumeric keys on the screen to enter the hospital name of the
network printer.
After changing the settings on the printer, turn the printer power off and on so
that the IP address is recognized by the printer.
MASTER Window
For fast and easy alarm setup, a group of alarm items can be set all together
at one time. This is called an alarm master. For example, there may be typical
alarm settings at your hospital, or you may have certain alarm settings for certain
patients. Set the master for each patient type.
Even when alarms are set by an alarm master, individual alarm settings in the
alarm master can still be changed on the ALARM LIMITS or the alarm setting in
each parameter setup window.
If the monitor is turned off for more than 30 minutes when <SHOW ADMIT
CONFIRMATION WINDOW> is set to Off, the changed individual alarms
return to the alarm master settings.
WARNING
If more than one medical equipment is used together in the same
facility, make sure all equipments have the same alarm default
settings (alarm master). If the medical equipments have different
alarm default settings and when 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.
Select the master setting of the PATIENT TYPE. The PATIENT TYPE setting
on the ADMIT DISCHARGE window returns to this master setting when the
monitor is turned off for more than 30 minutes* or the patient data is deleted.
MAIN ALARMS, PRESS 1 ALARMS, PRESS 2 ALARMS, and PRESS 3 ALARMS Pages
Set the upper and lower limits for master alarm settings.
PVM-2703 only
1. To set alarm limits, select the parameter in the MAIN ALARMS, PRESS 1
ALARMS, PRESS 2 ALARMS, or PRESS 3 ALARMS tab. A window with
alarm limits and setting bar for the selected parameter appears.
Upper limit
slider
Selected
parameter
Upper limit
Setting
bar
Lower limit
Lower limit slider
2. Touch and drag the sliders to the desired level on the setting bar.
You can also adjust the settings with the or key. When you touch the
or key, the value increases or decreases in steps of 1. When you touch
and hold the or key, the value increases or decreases until you stop
holding the key.
If the upper limit is set to a value above the maximum, the upper limit alarm
is set to OFF. If the lower limit is set to a value below the minimum, the
lower limit alarm is set to OFF.
ARRHYTH Pages
ARRHYTHMIA ANALYSIS
Select the ARRHYTHMIA ANALYSIS master setting. The arrhythmia analysis
is turned on or off on the ECG page of the PARAMETER window but the setting
returns to this master setting when the monitor is turned off for more than 30
minutes* or the patient data is deleted.
Arrhythmia Alarms
Set the master alarm settings for arrhythmias. When EXTENDED is selected for
the <ARRHYTHMIA TYPE> on the ECG page of the PARAMETERS window
in the SYSTEM SETUP window, there are two tabs for arrhythmia alarms master
settings.
ARRHYTH 1 tab when ARRHYTHMIA TYPE is ARRHYTH 2 tab when ARRHYTHMIA TYPE is
EXTENDED EXTENDED
NIBP Page
INTERVAL MASTER: MANUAL, STAT, SIM, 1, 2, 2.5, 5, 10, 15, 30 min,
1, 2, 4 or 8 h
Select the initial NIBP measurement mode after the monitor is turned off for 30
minutes or more, or the patient data is deleted. 3
You can also use the alarm master function on the ALARM LIMITS page of the
MENU window.
2. Touch the ALARM MASTER key. The alarm master settings are applied,
and the “APPLY SETTINGS FROM MASTER?” message and the ALARM
MASTER key become gray.
KEYS Window
NOTE
• The SUSPEND ALARMS, SUSPEND MONITORING and SLEEP key
is only available when the ALARM INACTIVATION on the SILENCE/
SUSPEND page of the ALARM window is set to SUSPEND ALARMS.
• The SLEEP key is only available when the QI-201P or QI-202P
interface is installed in the monitor.
• The INTERBED and PRINT WAVE key is only available when the
QI-202P interface is installed in the monitor.
• PRESS ZERO CAL key is only available for PVM-2703.
Function keys
A function or window can be assigned to one of three function keys on the upper
left corner of the screen so you can easily access the function or window just by
touching the function key.
4
Factory Default Settings....................................................................................................................................... 4.2
SYSTEM CONFIGURATION Screen......................................................................................................... 4.2
SYSTEM SETUP Window.......................................................................................................................... 4.4
Connector Pin Assignment................................................................................................................................. 4.14
ZS Socket (When QI-201P Interface is Installed)..................................................................................... 4.14
Network Socket (When QI-202P Interface is Installed)............................................................................ 4.14
Serial Socket (When QI-202P Interface is Installed)................................................................................ 4.14
OK: The setting remains in memory even when the power is turned off.
30 min: When <SHOW ADMIT CONFIRMATION WINDOW> in the
SYSTEM SETUP window is set to Off, the setting remains in memory
for at least 30 minutes after turning power off. After 30 minutes, the
setting changes back to the default setting. When the <SHOW ADMIT
CONFIRMATION WINDOW> in the SYSTEM SETUP window is set
to On, you can select whether saving or initializing the settings.
–: The setting returns to the default setting when the power is turned off.
PORT No.
USE ADT ON, OFF OFF
ADT
MONITORING 1024 to 65535 9005
OK
PORT No.
HL7 ADT
ADT PATIENT
1024 to 65535 9006
INFO PORT No.
PATIENT LIST
1024 to 65535 9007
PORT No.
HL7 VERSION — (Display only) 2.4
CHARACTER
— (Display only) ASCII
SET
MSH SEGMENT
SENDING
NIHON KOHDEN
APPLICATION
RECEIVING
CLIENT APP
APPLICATION
Up to 32 characters
SENDING
NIHON KOHDEN
FACILITY
RECEIVING CLIENT
FACILITY FACILITY
BAUD RATE 9600, 19200, 38400 9600
PARITY NONE, EVEN, ODD NONE
PC*
WORD LENGTH 7 bits, 8 bits 8 bits
STOP BIT 1, 2 1
* Only available when the QI-202P interface is installed.
Window MAINTE- Page Setting Item Setting Range Default Setting Backup
NANCE RUN SYSTEM
SYSTEM
SYSTEM CONFIGURATION AT NEXT On, Off Off –
CONFIG
POWER ON
SCREEN KEYBOARD, SCREEN
PATIENT NAME ENTRY
FREEHAND KEYBOARD
ADMIT MODE AUTO, MANUAL AUTO
POWER SAVING MODE On, Off On
GENERAL SHOW ADMIT
On, Off Off
CONFIRMATION WINDOW
SHOW OPERATION KEY
On, Off On
LABELS
DISPLAY
PUNCTURE
VENOUS
70 mmHg
ADULT: 20 to 120 mmHg
CHILD:
TARGET CUFF PRESSURE CHILD: 20 to 80 mmHg
50 mmHg
NEONATE: 20 to 50 mmHg
NEONATE:
40 mmHg 4
STAGE 1
STAT, 1 min STAT
INTERVAL
NIBP
STAGE 1 OPERATING TIME 5 min, 10 min 5 min
STAT
PARAMETERS
RECORD PAGE,
REVIEW RECORD PAGE
RECORD ALL
RECORD ON CENTRAL
— —
MONITOR*5
TREND TABLE RECORD
NORMAL, LARGE NORMAL
FONT
PAPER SIZE A4, LETTER A4
0 to 255. 0 to 255. 0 to 255.
IP ADDRESS 0.0.0.0
PRINTER*2 0 to 255
PRINTER NAME — lp
HOSPITAL — —
* Available only when the QI-201P interface is installed, or the QI-202P interface is installed and PROTOCOL is set to
1
Window Page Setting Item Setting Range Step Default Setting Backup
PATIENT TYPE ADULT, CHILD, NEONATE — ADULT 30 min
ADULT: 140
Upper OFF, 16 to 300 beats/min*1 CHILD: 170
NEONATE: 200
HR/PR 1
ADULT: 50
Lower OFF, 15 to 299 beats/min*2 CHILD: 75
NEONATE: 100
4
VPC Upper OFF, 1 to 99 beats/min 1 OFF
ST-I, ST-II, ST-III, OFF, –1.99 to 2.00 mV 0.01
Upper OFF
ST-aVR, ST-aVL, OFF, –19.9 to 20.0 mm 0.1
ST-aVF, ST-V1 to OFF, –2.00 to 1.99 mV 0.01
ST-V6 Lower OFF
OFF, –20.0 to 19.9 mm 0.1
ADULT, CHILD:
OFF
Upper OFF, 51 to 100%SpO2
NEONATE:
95%SpO2
SpO2 1
ADULT, CHILD:
90%SpO2
Lower OFF, 50 to 99%SpO2
NEONATE:
85%SpO2
Upper OFF, 2 to 150 counts/min
RR 2 OFF
Lower OFF, 0 to 148 counts/min
APNEA Upper OFF, 5 to 40 s 5 20 s
ADULT: 38.0
MASTER
Window Page Setting Item Setting Range Step Default Setting Backup
OFF, 2 to 99 mmHg 1
Upper OFF
OFF, 0.6 to 13.0 kPa 0.1
CO2 (E)*
OFF, 1 to 98 mmHg 1
Lower OFF
OFF, 0.5 to 12.9 kPa 0.1
MAIN ADULT,
ALARMS OFF, 1 to 99 mmHg 1 NEONATE: OFF
CHILD: 3
CO2 (I)* Upper
ADULT,
OFF, 0.1 to 13.0 kPa 0.1 NEONATE: OFF
CHILD: 0.4
OFF, –48 to 300 mmHg 2
Upper OFF
OFF, –6.0 to 40.0 kPa 0.5
ADULT:
80 mmHg
ART-SYS*, CHILD:
OFF, –50 to 298 mmHg 2
RAD-SYS*, 66 mmHg
AO-SYS*, NEONATE:
FEM-SYS* Lower
50 mmHg
ADULT: 10.5 kPa
CHILD: 9.0 kPa
OFF, –6.5 to 39.5 kPa 0.5
NEONATE:
6.5 kPa
ADULT: OFF
CHILD:
OFF, –48 to 300 mmHg 2
200 mmHg
Upper NEONATE: OFF
MASTER
ADULT: OFF
OFF, –6.0 to 40.0 kPa 0.5 CHILD: 26.5 kPa OK
NEONATE: OFF
PRESS 1 ADULT:
ALARMS*, DORS-SYS* 80 mmHg
CHILD:
OFF, –50 to 298 mmHg 2
PRESS 2 66 mmHg
ALARMS*, NEONATE:
Lower 50 mmHg
PRESS 3 ADULT: 10.5 kPa
ALARMS* CHILD: 9.0 kPa
OFF, –6.5 to 39.5 kPa 0.5
NEONATE:
6.5 kPa
ART-DIA*, OFF, –48 to 300 mmHg 2
RAD-DIA*, Upper OFF
OFF, –6.0 to 40.0 kPa 0.5
DORS-DIA*,
AO-DIA*, OFF, –50 to 298 mmHg 2
Lower OFF
FEM-DIA* OFF, –6.5 to 39.5 kPa 0.5
OFF, –48 to 300 mmHg 2
Upper OFF
OFF, –6.0 to 40.0 kPa 0.5
ADULT:
60 mmHg
ART-MEAN*, CHILD:
OFF, –50 to 298 mmHg 2
RAD-MEAN*, 46 mmHg
AO-MEAN*, NEONATE:
FEM-MEAN* Lower
30 mmHg
ADULT: 8.0 kPa
CHILD: 6.0 kPa
OFF, –6.5 to 39.5 kPa 0.5
NEONATE:
4.0 kPa
* Only available for PVM-2703.
4.10 Administrator’s Guide PVM-2700
4. REFERENCE
Window Page Setting Item Setting Range Step Default Setting Backup
ADULT: OFF
CHILD:
OFF, –48 to 300 mmHg 2
186 mmHg
Upper NEONATE: OFF
ADULT: OFF
OFF, –6.0 to 40.0 kPa 0.5 CHILD: 25.0 kPa
NEONATE: OFF 4
ADULT:
DORS-MEAN* 60 mmHg
CHILD:
OFF, –50 to 298 mmHg 2
46 mmHg
NEONATE:
Lower
30 mmHg
ADULT: 8.0 kPa
CHILD: 6.0 kPa
PRESS 1 OFF, –6.5 to 39.5 kPa 0.5
NEONATE:
ALARMS*, 4.0 kPa
MASTER
Window Page Setting Item Setting Range Step Default Setting Backup
ARRHYTHMIA
ON, OFF — ON
ANALYSIS
ADULT, CHILD:
ON fixed
ASYSTOLE 5s
3 to 10 s 1
NEONATE: 3 s
VF ON fixed — ON
ON fixed — ON
ADULT, CHILD:
VT 16 to 300 bpm* 1 100
NEONATE: 140
Value set in VPC RUN to 9 beats* 1 6
ON, OFF — OFF
ADULT: 160
EXT TACHY*
HR upper limit to 300 (bpm) 1 CHILD: 190
NEONATE: 220
ON, OFF — OFF
ADULT: 40
EXT BRADY*
15 to HR lower limit (bpm) 1 CHILD: 60
NEONATE: 80
ADULT: ON
ON, OFF — CHILD,
NEONATE: OFF
VPC RUN ADULT, CHILD:
16 to 300 bpm 1 100
MASTER
Window Page Setting Item Setting Range Step Default Setting Backup
IRREGULAR
ON, OFF — OFF
RR*1
PROLONGED
ON, OFF — OFF
RR*1
ARRHYTH
MASTER
NO PACER
ON, OFF — OFF
PULSE*1
4
PACER NON- ON, OFF — OFF
CAPTURE*1 40 to 480 ms 4 400
MANUAL, STAT, SIM, 1 min,
NIBP INTERVAL 2 min, 2.5 min, 5 min, 10 min, — MANUAL
15 min, 30 min, 1 h, 2 h, 4 h, 8 h OK
FREEZE, ALL ALARMS OFF*2,
SUSPEND ALARMS*3, SUSPEND
MONITORING*3, SLEEP*3*4, PRESS 1: TREND
ZERO CAL*5, TOUCHKEYS OFF, MENU, TABLE
LARGE NUMERICS, DISCHARGE, 2: LARGE
KEYS FUNCTION KEYS
GUIDE, INTERBED*6, VENOUS NUMERICS
PUNCTURE*7, TREND TABLE, NIBP 3: ALARM
TABLE, TREND GRAPH, RECALL, HISTORY
FULL DISC, ALARM HISTORY, PRINT
WAVE*8, NONE
*1 Available only when <EXTENDED> is selected for arrhythmia type on the ECG page of the SYSTEM SETUP
window.
*2 Available only when ALL ALARMS OFF is set to On on the ALARM – SILENCE/SUSPEND page on the SYSTEM
SETUP window.
*3 Available only when ALL ALARMS OFF is set to Off on the ALARM – SILENCE/SUSPEND page on the SYSTEM
SETUP window.
*4 Available only when the QI-201P interface is installed, or QI-202P interface is installed and PROTOCOL is set to LS-
NET on the NETWORK – IP ADDRESS/PROTOCOL page of the SYSTEM CONFIGURATION screen.
*5 Only available for PVM-2703.
*6 Available only when the QI-202P interface is installed and PROTOCOL is set to LS-NET on the NETWORK – IP
ADDRESS/PROTOCOL page of the SYSTEM CONFIGURATION screen.
*7 Available only when VENOUS PUNCTURE is set to On on the PARAMETER – NIBP – VENOUS PUNCTURE page
on the SYSTEM SETUP window.
*8 Available only when the QI-202P interface is installed.
Sales
USA Asia
NIHON KOHDEN AMERICA, INC. SHANGHAI KOHDEN MEDICAL ELECTRONIC
90 Icon Street, Foothill Ranch, CA 92610, USA INSTRUMENT CORPORATION
Phone +1 (949) 580-1555 7th Floor, Dawning Centre Tower A No.500
Fax +1 (949) 580-1550 Hongbaoshi Road, Changning District
Shanghai 201103, China
Europe Phone +86 (21) 6270-0909
Fax +86 (21) 6270-9700
European Representative
NIHON KOHDEN EUROPE GmbH Beijing Branch
Room 1701, East Ocean Centre
Raiffeisenstrasse 10
No. 24A JianGuoMenWai Street, Beijing, 100004
D-61191 Rosbach v.d.H., Germany
Phone 010-6515-5750
Phone +49 6003 827-0 Fax 010-6515-5758
Fax +49 6003 827-599
Guangzhou Branch
NIHON KOHDEN ITALIA S.r.l. Room 2514, Yian Plaza
Via Fratelli Bronzetti 28 No. 33 Jian She Liu Ma Road, Guangzhou, 510060
I-24124 Bergamo, Italy Phone 020-8363-3737
Phone +39 035 219 543 Fax 020-8363-3807
Fax +39 035 232 546
NIHON KOHDEN SINGAPORE PTE LTD
NIHON KOHDEN FRANCE SARL 1 Maritime Square, #10-34 (Lobby C), Harbour Front Centre
8, rue Francois Delage, 94230 Cachan, France Singapore 099253
Phone +33 1 49 08 05 50 Phone +65 6376-2210
Fax +33 1 49 08 93 32 Fax +65 6376-2264
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
PRINTED IN JAPAN