Spacelabs Healthcare 76A91341-1400 91341-09 User Manual 2 of 3

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Date Submitted	2003-10-28 00:00:00
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Document Title	Users Manual 2 of 3
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To Initiate ECG monitoring:
Select a transmitter.
Note its channel number.
Attach lead wires to transmitter.
Attach lead wires to electrodes.
Apply electrodes to patient.
Install a transmitter battery.
Close the transmitter case
“manure-A
ECG
Contents
Overview ...............
Setting Up ECG Monitoring .
Display Detail ...........
Monitoring Faced ECG Patients .
Restoring Delault Settings. .
Changing the Display Resolution.
Selecting Options lor Lead Display . .
ECG Alarm Message summary ........................
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Overview
Digital telemetry ECG monitoring provides continuous monitoring ot
electrocardiographic signals in order to detect abnormal cardiac rhythms,
including life-threatening arrhythmias such as asystole, ventricular fibrillation, and
ventricular tachycardia.
Setting Up ECG Monitoring
To set up ECG monitoring, plug each lead wrre into the transmitter, connect each
to an electrode, and then attach the leads to the patient. Match the lead wire color
to the color-coded connectors on the top 01 the transmitter case. Refer to the ECG
chapter in the UCN Operations Manualtcr details regarding electrode application,
Telemetry patients are commonly ambulatory and require optimal skin preparation
and lead application to minimize motion anitact. After the electrodes and lead
wires have been attached, it is important to tape a loop at lead wire close to the
electrode to minimize stress or pulling on the electrode itsell. This is called stress-
looping.
ECG monitoring begins when the telemetry receiver module detects a signal sent
by a telemetry transmitter. The telemetry transmitter sends a signal as soon as its
battery is installed.
ECG telemetry reception requires the lollowing minimum conditions:
- The telemetry receiver module must be connected to an Ultraview or PCMS
monitor. either directly or through a module housing, with the power ON and a
Spacelabs Medical diversity antenna connected.
- ECG electrodes must be properly attached to the patient; and lead wires
must be properly attached to the transmitter.
- The transmitter battery must be lunctional.
- The telemetry receiver module must be tuned to the telemetry transmitters
lrequency (channel number).
———_—_fi—
071-0774-00 Rev. A
2-1
Ultraview D g tat Telemetry
0-‘
5 WA
All system connections must be made by Space/abs Medical
personnel only.
Leakage currents are not affected by the high level output.
The patient is electrically isolated from the patient monitor by
the HF link.
HNING:
Operating television receivers or other CRT displays near
the transmitter (within 2 to 3 feet), or operation of some
pacemaker programmers may suppress the ECG
waveform, preventing OHS detection and rate counting. An
erroneous asystole alarm may result.
Signals resulting from devices such as Automatic
Implantable Cardiac Defibrillators (AICD) may momentarily
blank the ECG trace rather than display an out—of-rango
signal. In such cases, it may not be apparent that the AICD
has signaled and the condition of the patient should be
checked. In all Instances of AICD signaling, the bedside or
central will redisplay the ECG waveform within 5 seconds.
ECG monitoring in telemetry is identical to hardwired ECG monitoring. Refer to
lhe ECG. Arrhythmia, and STAnalysis chapters 01 the UCN Operations Manual
for detailed descriptions of configurations, displays, and controls. A brief overview
cl ECG monitoring lollows.
Electrodes
For ECG tracing with telemetry, use silver/silver—chloride electrodes or their
equivatent. Always connect all the electrodes required tor a particular lead,
Missing electrodes may result in the loss of ECG tracing. Refer to the ECG
chapter in the UCN Operations Manual lor inlormation on placing the electrodes.
Some electrodes may be subiect to large offset potentials
WARNING:
& - Use only Spacelabs Medical recommended electrodes.
due to polarization. Recovery time after application of
defibrillator pulses may be especially compromised.
Squeeze bulb electrodes, commonly used for diagnostic
ECG recording, may be particularly vulnerable to this
effect.
2 2 0710774410 Rev. A
ECG
CAUTION:
- Visually inspect each lead wire for obvious damage and
replace them as needed.
0 Only use patient cables and lead wires specified by
Spacelabs Medical. other cables and lead wires may
degrade performance and may damage the monitor during
delibrillation. Non-Spacelabe Medical cables and lead
wires may also change the required input impedance and
DC oilsel voltage, affecting monitor performance.
- Do not use stainless steel electrodes.
- Do not allow conductive parts of electrodes and
connectors, including the reierence electrode, to contact
other conductive parts, including the ground.
- Poor cable dressing or Improper electrode preparation
may cause Ilne isolation monitor transients to resemble
actual cardiac waveiorms and inhibit heart rate alarms.
Reler to the ECG chapter of the UCN Operafions Manual for
details on proper electrode preparation and application.
071-0774-00 Rev. A 23
Ultravrew D tal Telemetry
Full Screen 0k
CentraVBedside
95669000009
Display Detail
Signal detection is indicated on your monitor when an ECG signal appears next to
the ECG parameter key in the zone assigned to receive the transmitted telemetry
channel. The transmitters channel number is always identilied above the
waveform, to the Ielt of the ECG keyu
K II MON PACED/a
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70 \‘i:
VI
31m
..
é £44
00m
Vl/“VVWVWVV
HFl=70 A=3 ll CHAN22M ‘
1P®
00m
NIBP=120/68(94) tome Spoz=se% 10:20
Split Screen Central BED “1 DAN'ELS'R
HR=70 VI
VVVWMMIV
BED 01 DANIELS,R
00m
Figure 2-1: Display Detail
ECG trace for first lead
Telemetry channel number
ECG key for first lead
OHS indicator (flashes once per detected beat)
ECG lead designator
Display resolution (monitor or extended)
Paced operation indication (pacemaker detection is enabled)
Abnormals per minule alarm Iimit'
ST segment level for first lead "
Abnormals in a row alarm limit’
ECG rate alarm limits; split screen oentrals display a bell symbol when alarms
are enabled; bedsides display the rate alarm limits (120/40)
24
0710774470 FIGV, A
ECG
Abnormals per minute counter '
Current heart rate
ECG lead designator for second lead
ST segment level for second lead"
ECG key for second lead
966666
NIBP measurements: systolic/diastolic (mean) at hourszminutes; SpOz
measurement at hourszminutes (91343 only; hhzmm not seen on continuous
Spoz). Depending on the patient monitor‘s display size, the title “NIBP” may
not appear.
Spoz SensorWatch bar: shaded area (waveform index) expands up
proportionally to signal strength; horizontal line is minimum signal leveL
Waveform Index (WFI) is used for displaying signal strength in SensorWatch.
Q Large size bell indicates ECG alarms enabled.
@ Equal sign becomes a bell when Sp02 alarms enabled.
Equal sign becomes a bell when NIBP alarms enabled.
' Only appears with the MultiView l or II option in the adult mode with Arrhythmia
detection enabled.
"" Only appears in adult mode with the ST segment analysis option.
Monitoring Paced ECG Patients
——_
To monitor paced when“: When monitoring pacemaker patients, use the paced feature to automatically
1 Touch ECG. enhance pacemaker spikes for display and eliminate them from the heart rate
2 Touch SETUP. counter. The last VES/NO setting of the paced feature you select is retained as
3 Select PACED YES. the default.
If the intenral between the pacemaker pulse and the OHS complex is greater than
150 milliseconds, the beat is considered to have originated in the atria and is not
classified as a paced beat.
To prevent pacemaker pulses from being counted as actual beats, specialized
circuitry removes the pacemaker pulses from the ECG signal and replaces them
with pacemaker flags.
' - The optimal leads for monitoring paced patients may vary. In
telemetry monitoring, pacemaker spikes are detected on lead ll.
. ll‘ pacemaker spikes are not detected, change the electrode
position.
071-0774-00 Fiev. A 2-5
Ultraview Digital Telemetry
To restore default settings:
1 Touch ECG.
2 Touch SETUP.
3 Touch RESTORE SETTINGS.
4 Select YES.
To change the display resolution:
1 Touch ECG.
2 Touch SETUP.
3 Select MONITOR or
EXTENDED.
pacemaker rate during occurrences of cardiac arrest or
some arrhythmias. Do not rely entirer upon ECG rate
alarms. Keep pacemaker patients under close surveillance.
WARNING:
E - ECG detection circuitry may continue to count the
0 The system may insert pacemaker flags into the ECG
signal in response to signals that are not pacemaker
pulses. Therefore, il you use a Spacelabs Medical monitor
to observe pacemaker performance, you must take into
account all possible sources of pacemaker flags.
- Use the pacemaker manufacturer's performance analyzer
as the primary means of evaluating pacemaker operation.
Restoring Default Settings
With the Module Configuration Manager leature, you can restore all delault
settings, User-configurable options are listed in the Module Configuration
Manager chapter of the UCN Operations Manual.
' - RESTORE SETTINGS changes the user—configurable options
. for ALL parameters in the module.
- This feature is not available for remote views.
Changing the Display Resolution
The MONITOR/EXTENDED key determines the display resolution of the two ECG
traces. whether or not both traces are currently displayed on the monitort
Table 1: Display Resolution
Key Display Resolution
Monitor (0.5 — 30 Hz)
Extended (0,05 — 30 Hz)
' - Changing the display resolution does not change the waveform
bandwidth used to analyze the ECG signals for the arrhythmia
. and ST segment level.
The lactovy default setting for display resolution is monitor mode,
2—6
071-0774-00 Rev. A
Ultraview D tat Telemetry
Hl RATE ALARM
Displayed during high rate alarms tor either 10 seconds or the duration 01 the
alarm.
IN LEARN
Displayed when the software is in learn mode.
CHAN 1 & 2 LEADS OFF
Displayed when lead failures preclude ECG monitoring in both ECG channels 1
and 2, The message is displayed in the wavelorm zone tor the first ECG channel.
An alarm tone sounds it the module has completed its initial period ol learning and
ECG processing has not been suspended,
CHAN 1 LEADS OFF
Displayed when a lead failure occurs on ECG channel 1 when automatic lead
switching is disabled.
CHAN 2 LEADS OFF
Displayed when a lead failure occurs on ECG channel 2. The message is
displayed in the wavetorm zone tor both ECG channels 1 and 2.
L0 RATE ALARM
Displayed during low rate alarms tor either 10 seconds or the duration 01 the
alarm.
NEW DOMINANT
Displayed for 1 minute when a switch to a different dominant ECG morphology
occurs.
NOlSY SIGNAL
Displayed in ECG channel 1 when the ECG software suspends processing on
either channel because at excessive noise on the ECG signal. Alter 10 seconds in
this condition, an alarm tone sounds it ECG alarms are enabled and alarm tones
have not been turned OFF or suspended. This message is displayed tor the
duration of the noisy signal condition plus approximately three seconds. The
patient may be moving excessively. Secure the lead wires to the patient.
- Check the electrodes for good skin adhesion.
- Check lead wires at the transmitter tor contact.
RUN ALARM
Displayed whenever a RUN 01 three or more beats is detected and the ADM lN
ROW limit is set lower than or equal to the number at beats in the run. This
message is displayed for either 10 seconds or the duration ol the alarm.
V FIB
Displayed whenever ventricular fibrillation is detected, This message is displayed
tor either 10 seconds or the duration at the alarm.
2-10 071-0774-00 Rev. A
Sp02 (91343 only)
Contents
Overview .....................................
Setting Up Sp02 Monitoring .
Ensuring Accurate Monitoring .
Setting or Adjusting Alarm Limits. .
Setting Sp02 Data Averaging Period and Sampling interval ,
Viewing Pulse Rate ................ .
Sp02 with Inna-Aortic Balloon Pumps .
Using Sp02 with Neonates . . . .
Sp02 Alarm Message summary
Sp02 Troubleshooting Guide , .
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Oven/lew
Pulse oximetry enables you to noninvasively monitor a patient‘s hemoglobin
oxygen saturation either continuously or opisodically. The oximetry sensor
contains two light emitting diodes (LEDs) that transmit speciiic wavelengths
(approximately 660 and 940 nanometers) of light that are received by a
photodetector.
Oxygen saturated blood absorbs light differently than unsaturated blood. Thus,
the amount oi light absorbed by the blood can be used to calculate the ratio oi
oxygenated hemoglobin to total hemoglobin in arterial blood. This ratio is
displayed as percent Sp02. Normal values range irom 95 to 100%.
WARNING:
b ' A pulse oximeter should NOTbe used as an apnea monitor.
- A pulse oxlmeter should be considered an earty warning
device. II a trend towards patient deoxygenation is
indicated, blood samples should be analyzed by a
laboratory co—oximeter.
your own default settings [or characteristics such as alarm
limits, alarm priority, and display configuration. Refer to the
Module Configuration Manager chapter in the UCN Operations
Manual for further details.
' - With the Module Configuration Manager feature, you can define
- Blood oxygen saturation monitoring must be performed in
conjunction with ECG monitoring. The ECG lead wires of the
91343 must be connected to the patient in order to perform
ECG and blood oxygen saturation monitoring.
071-0774-00 Rev, A 3-1
Ultraview D gihl Telemetry
To set up Spo, monitoring:
wmflm
Open the battery cover and
remove the battery.
Confirm that the DIP switches 1
through 8 are in the correct
setting (switch 7 must be set to
ON for neonatal use and to OFF
for adult use).
Reinstall the battery and close
the battery cover.
Connect the Sp02 adapter
Cable (P/N 700-0014-00) to the
transmitter.
Attach the sensor to the patient
and connect the sensor cable to
the SpOQ adapter cable.
Initiate ECG monitoring.
Touch ECG.
Touch CHANNEL FORMAT.
Select Sp02 ON.
Setting Up Sp02 Monitoring
The 91343 digital telemetry Mufti-parameter transmitter uses Spacelabs Medical
sensors as well as those from other manufacturers. Refer to Accessories on page
1-13 for information concerning specific sensors.
CAUTION:
- Use only patient sensors specified by Spacelabs Medical.
Using sensors other than those specified may degrade
performance and damage the transmitter during
deflbrillatlon.
0 Check the sensor site frequently. Do not allow the sensor
on one site for a prolonged time, especially when
9 neonates. Refer to the sensor manufacturer's
- Never attach an Spo, sensor on a limb being monitored
with a blood pressure cuff or a limb with restricted blood
flow.
- A poorly applied sensor may give Inaccurate saturation
values.
- Choose a site with sufficient perfusion to ensure accurate
oxlmetry values.
All sensors require an adapter cable between the sensor and the transmitter.
Because the adaptor cable is reusable, do not discard t| when you have finished
using a disposable oximetry sensor. Disconnect the sensor cable from the adapter
cable before discarding the sensor.
To connect the Spoz adapter cable to the transmitter, align the cable with the
notch on the front of the transmitter connector, and push the cable straight down
into the transmitter. To remove the cable. press the latch release on the bottom of
the cable, and pull the cable straight out.
CAUTION:
E - Never twist the cable.
MEEGD
Figure 3-1: SpOz Adapter Cable to Transmitter
To enable Spoz monitoring in the 91343 digital telemetry mum-parameter
transmitter. choose an averaging interval of 4, a, or 16, seconds by setting DIP
switches 1 and 2 as explained in Setting 5502 Data Averaging Period and
Sampling Interval on page 3-6.
071-0774-00 Rev. A
Sp02 (91343 only)
CHECK XX cum 22"
sec WA verorw ZONE _
“a now 5
oh SpOQ=985$ 10 22 W 78 130
BED NAME PATIENT NAME ‘U
' xxvvv PACED
Amto
(Dom
Figure 3-2: Display Zone — Full Screen
Hn=xxx Azxx LEAD
CHAN 2241 ‘
ECG WA VEFOHM ZONE
sack/9m 10 22
7-2 Jane Doe
Figure 3-3: Display Zone — Split Screen
0 Current Spoz value (percent) and episodic time oi reading. (Time is not
displayed when using continuous mode 01 operation.)
9 The bell indicates that alarms are enabled (equal sign turns to a small bell
when SpOZ alarms are enabled).
a SensorWatch bar:
Shaded area (wavelorm index. WFl) expands up proportionally to signal
strength; horizontal line is minimum signal level.
No shading (lowest wavelorm index) corresponds to no detected signal
strength or a faulty sensor.
' - When the battery voltage in the 91345 falls below 5.5 volts, the
. Spog value is displayed as 77? and the sensor watch bar is
Empty-
Ensuring Accurate Monitoring
Each sensor requires site specific application procedures. and the lollowing
general points will aid oximetry monitoring success.
- Choose a site that provides proper alignment ot the LEDs and receiving
photodetector,
- Reduce light interference when monitoring under bright light by using a light
block over the sensor.
- Select a site that has unrestricted blood flow and can remain as immobile as
possible to reduce or eliminate movement artilact.
- Do not restrict blood flow when securing a sensor with tape.
- Do not select a site near potential electrical interterence (e.g., electrical
cords).
0 The SensorWatch bar should be above the minimum signal level.
[171-0774-00 Rev. A 3-3
Ultraview Digital Telemetry
To set or adjust Spa; alarms:
Touch ECG.
Touch ALARM LIMITS.
Touch SPOZ ALARM LIMITS.
Select SpOZ ALARMS ON.
Select H|=, LO=, ALM DELAY,
and MSG ALARM DELAY.
Use arrow keys to adjust.
mbflN-l
3-4
Setting or Adjusting Alarm Limits
Pulse oximetry alarm limits and delays are based either on factory default limits or
user-defined limits. The factory detault settings lor alarm limits are 100% for high
and 85% for low. For alarm delays. the lactory delault settings are 15 seconds for
alarm limit delay and 20 seconds for message alarm delay. Reler to the Alarms
chapter in the UCN Operations Manualior details concerning UCN alarm
operation.
When Spoz alarms are enabled, a bell symbol will be displayed between the
‘Spoi label and the SpOz measured saturation value. When any SpOz alarm is
detected. the displayed parameter value (item 1 in Figure 3-2 and Figure 3-3 on
page 3-3) will blink yellow it the alarm priority is Low or Medium. and will blink red
if the alarm priority is High. This is done independently 0! any other ECG or NIBP
alarm indications.
When Spoz alarms are enabled and the Spoz high limit is exceeded, the Spoz
High=Xxx key will blink in the color of the highest priority alarm present. when the
SpOg low limit is exceeded, the SpOz Low=XXX key will blink in the color at the
highest priority alarm present. Refer to Directory 0! Keys - UCW and Ultraview
17GOon page 1-1.
Flefer to the Module Configuration Manager chapter of the UCN Operations
Manuailor Sp02 parameter tables that list available user settings and factory
delaults lor this parameter.
' - The following ECG alarm messages lake priority over other
. ECG and Spoz alarm messages for display, other ECG and
Spoz alarm messages can be adjusted in priority by using the
Module Configuration Manager.
LEADS OFF
NOIS V SIGNAL
ECG ALAFIMS SUSPENDED
ALM DELAY Key
This key sets the number at seconds the system will wait before it reports that an
alarm limit has been violated. When this leature is OFF, the key label will read
"ALM DELAY OFF". When it is on, the label will read “ALM DELAV xx", where "xx“
is the value, in seconds, ol the delay.
To set the delay time:
1. Touch ALM DELAY xx (or ALM DELAY OFF),
2. Touch the up and down arrow keys until the value is set as desired. Possible
settings are OFF, 5, to, 15, 20. 25, or 30 seconds.
' - it you press the down arrow key after the lowest value has been
0 reached, the following message will appear on the prompt line:
Minimum alarm delay time has been reached.
- if you press the up arrow key after the highest value has been
reached, the following message will appear on the prompt line:
Maximum alarm delay time has been reached.
[77141774410 Rev, A
Spoz (91343 only)
MSG ALM DELAY Key
This key sets the number oi seconds the system will wait belore it issues an alarm
lone after any of the lollowing messages:
' SpOz UNAVAILABLE
- SpOz FAULTY SENSOR
0 SpOz SENSOR DISCONNECTED
0 Sp02 SENSOR OFF PATIENT
0 Sp02 lNSUFFlCIENT SIGNAL
- SpOz AMBIENT LIGHT INTF.
° SpOz NOISY SIGNAL
When this feature is OFF. the key label will read “MSG ALM DELAY OFF'C When
it is ON, the label will read “MSG ALM DELAV xx" Where “xf is the value, in
seconds, at the delay.
To set the message delay lime:
1. Touch MSG ALM DELAY xx (or MSG ALM DELAY OFF),
2. Touch the up and down arrow keys until the value is set as desired. Possible
settings are OFF, 10, 20, 30, 40. 50, or 60 seconds.
' - If you press the down arrow key alter the lowest value has been
. reached, the following message will appear on the prompt line:
Minimum message alan-n delay time has been reached,
v ll you press the up arrow key alter the highest value has been
reached, the following message will appear on the prompt line:
Maximum message alarm delay time has been reached.
071-0774-00 Flev. A 3 5
Ultraview Dl
To set spo, data averaging
period and sampling interval, set
transmitter DIP switches 1
through 4 to correct
configuration
tal Telemetry
Setting Sp02 Data Averaging Period and
Sampling Interval
SpOz data averaging is used to smooth the oximetry saturation value by
averaging the patient input values over 4. 5. or 16 seconds. This selection is made
by setting the DIP switches 1 and 2 beneath the battery compartment in the 91343
digital telemetry multi-parameter transmitter. The default value is 5 seconds,
Refer to Figure 3-4 on page 3-6.
' 0 Setting both DIP switches 1 and 2 to ON disables Spoe data
transmission.
- To enable SpOz, remove the battery set the selected interval,
and re-install the battery.
- Disabling Spoz operation in the 91543 transmitter lengthens
battery lile.
pens or pencils to configure the DIP switches since they
may cause contamination. Avoid using sharp cutting
instruments which may cause physical damage.
CAUTION:
g - Use care when configuring the DIP switches. Avoid using
Table 1: DIP Switch 1 and 2 Settings
DIP Switch 1 DIP S ' h 2 Effect
OFF OFF 4 seconds averaging enabled
OFF ON E! seconds averaging enabled (default)
ON OFF 16 seconds averaging enabled
ON 1 ON Disable srnoz operation
The current setting of the Spoz averaging period may be displayed by pressing
the ECG CHANNEL FORMAT key and enabling SpOz.
enable enable enable enable
NIBP IAEP Neonate Serviceuse
5 7
1 2 3 4 8
I ON
I I I I I I I OFF
0 avera in $130 reading disable disable enable enable
Sp fuelled g g "flew NIBP IABP Adult normal
operation
Flgure 3-4: DIP Switch Setting in Battery Compartment
The sampling interval selection enables you to determine how often an SpOg
measurement will be taken. Loss lrequent Spoz readings can extend the usable
life of the battery. (Refer to the Ultraview Digital Telemetry Products data sheet.
P/N 061-0501-xx, for more information on battery service lite.) This selection is
made by setting DIP switches 3 and 4 beneath the battery compartment. The
default setting is in continuous.
071-0774-00 Rev. A
_“
To display heart rate from Sp02
sensor:
Touch ECG.
Touch SETUP.
Touch RATE SOURCE.
Select Sp02 ON.
Select Sp02 as rate source.
“fl
To use with balloon pump:
1 Set transmitter DIP switch 6 to
ON.
utbth-e
___
To view the current setting of the
IABP DIP switch:
1 Touch ECG.
2 Touch CHANNEL FORMAT.
3 Select Sp02 ON.
Sp02 (91343 only)
intervals. clinical practice or medical iudgement should be
used in selecting continuous or episodic Sp02 monitoring
made for each specific patient.
CAUTION:
Q - No Sp02 monitoring occurl between episodic sampling
Table 2: DIP Switch 3 and 4 Settings
DIP Switch 3 DIP Switch 4 Effect
OFF OFF Continuous sampling (default)
OFF ON 2 minute sampling interval
ON OFF 5 minute sampling interval
ON ON 30 minute sampling interval
CAUTION:
9 - DIP switch 8 must remaln OFF for normal operation.
Viewing Pulse Rate
In normal operations, the heart rate for display is obtained directly lrom the
acquired ECG leads or an alternate rate source. Sp02 can be used as the
alternate source, if it is set for continuous measurement. When it is set for
episodic measurement. Sp02 cannot be used as an alternate rate source.
Sp02 with Intra-Aortic Balloon Pumps
Enabling the intra-aonic balloon pump (IABP) feature informs the Sp02 software
that an IABP is in use. The 91343 must differentiate between this arterial
pulsations and those produced by the IABP. With the IABP feature enabled. the
transmitter excludes the IABP-generated pulsations from the calculation for Sp02.
The IABP teature also may be uselul with patients experiencing irregular heart
rhythms. Enabling the IABP feature permits the transmitter to reject irregular
pulses, providing a more accurate Sp02 measurement.
' a
When the IABP feature is enabled, the pulse rate obtained from
Sp02 may not match the heart rate obtained from ECG.
- In cases of excessive patient motion or artifact, the accuracy of
the Sp02 measurement may be compromised when the IABP
feature is enabled,
0 When the IABP operation is selected, the Sp02 status key in
the Channel Format menu indicates iABP.
_—__—______—__————-
37
071-0774-00 Rev. A
———_——_
Ultraview Digital Telemetry
3-8
Using Sp02 with Neonates
Enabling neonatal operation, by setting transmitter DIP switch 7. changes the
sensor detection operation in the transmitter. improving the signal quality tor
neonatal patients. This switch must be set ON lor neonatal use and set OFF for
adult use. When the neonate operation is selected the SpOz status key in the
Channel Format menu indicates NEO.
Sp02 Alarm Message Summary
WARNING:
- Error messages indicate a problem or condition that may
affect accurate monitoring values. Do not ignore these
messages. Correct any fault before contlnulng.
' - When any Spoz alarm message is displayed, the saturation
. value is immediately changed to 77? and an alarm is triggered.
ll your module has been configured for an alarm using the
Module Configuration Manager the parameter display will blink
yellow for Low and Medium priority alarms, and will blink red for
High priority alarms. An alarm will begin alter the message
alarm delay time has elapsed, (Reler to the Module
Configuration Manager chapter ol the UCN Operations
Manual).
Sp02 SENSOR DISCONNECTED
Displayed when the transmitter does not detect either an adapter cable or a
sensor connected to an adapter cable. it the message persists and the adapter
cable is secure, replace the adapter cable. The alarm will stop after approximately
10 seconds. On remote view. there may be no audible alarm on the remote
mainlrame before the local alarm stops.
Sp02 FAULTY SENSOR
The 91343 Spoz processor has detected a detective sensor that will require
replacement. The SensorWaich bar can be used to confirm absence ol sensor
output.
Sp02 UNAVAILABLE
Displayed when the LED and/or photcdiode have tailed. Replace the sensor
and/or SDOZ adapter cable.
SpOZ AMBIENT LIGHT INTF.
Displayed when:
- The sensor is receiving external light interlerence lrom a bright light source
near the sensor. Shield the sensor from the external light source. If the
condition persists lor more than 30 seconds. 77? will replace the data
display.
- The sensor photodiode and LEDs are misaligned on flexible sensors allowing
light to enter. Realign the sensor photooiode with LEDs,
- It a message appears with linger clip. replace the sensor.
07147774470 Rev. A
Sp02 (91343 only)
$902 INSUFFICIENT SIGNAL
Displayed when:
- Insufficient signal tor proper operation.
- Poor sensor application or site. Correctly re-apply or reposition to a more
perfused site. message the site, or apply a new sensor.
Sp02 NOISY SIGNAL
Displayed when:
0 The sensor signal is disturbed by motion or other interlerence. Eliminate
sensor movement. The message disappears when a value is obtained.
- The sensor is placed adjacent to power oords or other electrically noisy
devices. Move the noisy device or move the sensor to another site.
SpOZ SENSOR OFF PATIENT
Displayed when:
- The transmitter is unable to detect a valid sensor input signal. Check the
patient tor proper sensor placement.This alarm is only available when the
SpOz sensor is a reusable, linger-clip type.
' - This message is not available with disposable SPOQ sensors or
. non—clip type sensors.
- Tissue between the LED and photodiode is too transmissive. Il sensor
placement seems correct and the message persists. try a sensor site with a
thicker tissue bed.
' - Adapter cables and sensors are ordered separately through the
. Space/abs Medical Supplies Products Catalog.
071—0774-00 Flsv. A
3—9
Sp02 Troubleshooting Guide
Clinical Situation Possible Cause
Solution
No sipo2 label is
displayed
I sipo2 is not enabled at the 91343.
I Sp02 is not enabled at the 90478
receiver.
I Be sure transmitter DIP switch 1 and 2
are set correctly.
I Be sure transmitter DIP switch 8 is
OFF.
5p02 value displays ?’?? I Sensor not connected to patient.
I Adapter cable not connected to module
properly.
I Sensor not connected to adapter cable.
I Excessive patient motion.
I Transmitter is in the initialization phase
(the first 15 seconds after sensor
application).
I Low battery indicator constantly
illuminated.
I Re—aitach sensor.
I Correctly connect the adapter cable.
I Correctly connect the sensor.
I Urge patient to remain still while
reading is in progress.
I Wait uniii initialization is complete.
I Call qualified service person.
Insuliicient signal or
noisy signal
I Sensor placement not optimum.
I Sensor placed below blood pressure
cu".
I Move sensor to a site with better
periusion.
I Align LED with sensor photodetector.
I Move sensor to an alternate limb.
Intermittent or complete I Depleted battery.
failure to operate
I Low battery light constantly illuminated.
I Replace battery.
I Call qualified service person.
Factors that cause
significant variances in
Presence ol dysfunctional hemoglobins
(COHD, MetHh).
sensor accuracy
Presence of intravascular dyes
(indocyamine green, methylene blue)
depending on their concentration in the
blood stream.
I High ambient light level.
I Electrosurgical interlerence.
I Patient is significantly anemic (Hb less
than 5 gm/dl) or patient has received
large amounts of IV solutions.
I Follow hospital procedure tor
determining oxygenation in these
patients.
I Follow hospital procedure tor
determining oxygenation in these
patients.
I Fleduce light levels near patient: wrap
sensor with light blocking material.
I Ultravlew digital telemetry is contra-
indicated for electrosurgical use.
I Follow hospital procedure tor
determining oxygenation in these
patients.
3-10
071-0774-00 Flev. A
Sp02 Troubleshooting Guide (continued)
Clinical Situation Possible Cause Solution
No Spo2 alarms are I ECG "Leads Otf' condition exists, I Fie-attach ECG lead wires to patient and
displayed I Higher priority alarm condition is resume ECG monitoring to clear
present. pending ECG alarms.
I Clear current alarm condition and/or
reprioritize Sp02 alarms of interest in the
Module Configuration Manager.
I When silo2 alarms are set ON, all Sp02
alarm conditions will cause the
parameter value (or ??'.7) to blink
according to the alarm priority set by
using the Module Configuration
Manager.
071-0774-00 FIEV. A 3-11

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