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Bitmos sat801+ - Alarms; 8.1 In General; 8.2 Alarm filter

Bitmos sat801+
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sat801+ Pulse Oximeter
Alarms
52
8 Alarms
8.1 In General
As a monitoring system the unit has been equipped audio and optical signals for a multiple
number of alarm situations. Alarms are activated:
When deviations from pre-set value limits occur
In problem situations during technical monitoring
Internal unit malfunctions
WARNING! Danger with incorrectly entered alarm limits!
Before each use test the unit on a patient to see if the configured alarm limits are
patient appropriate.
If the accuracy of the displayed values is questioned, check the patient’s vital
parameters first using a different method. Then check the functionality of the unit.
Inaccurate measurements can be caused by:
Incorrect sensor connection or incorrectly selected Masimo-sensor
A significant inclusion of dysfunctional hemoglobin (e.g. (carboxyhemoglobin or
methemoglobin)
Intravascular dyes such as indocyanine green or methylene blue are present in the blood
stream
Excessive light intrusion, such as operating lamps (especially xenon light sources), bilirubin
lamps, fluorescent lights, infrared heat sources or direct sun light (excessive light intrusion
can be avoided with a dark or transparent sensor shade)
Excessive movement of the patient
Venous blood pulse
Connection of the sensors is to a body part already connected to a blood pressure cup, an
arterial catheter, or an intravenous line.
Loss of pulse signal can occur under the following conditions:
The sensor is attached too tightly.
There is excessive illumination from light sources such as operation or bilirubin lamps or
sunlight.
An inflated blood pressure cuff is attached on the same extremity as the sensor.
The patient suffers from low blood pressure, serious vascular constriction and/or
anemia or hypothermia.
There is an arterial occlusion proximal to the sensor.
The patient suffered from shock or heart failure.
The fingernail is polished.
8.2 Alarm filter
CAUTION!
Changing the alarm filter settings is a serious intervention in the device functions
and must never be done without first consulting the doctor in charge of the
treatment!

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