Fukuda Denshi Dynascope 8000 Series, Руководство по обслуживанию

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Safety Precautions for Using the Equipment

Carefully route cables to reduce the possibility of patient entanglement and strangulation.

When lifting this equipment, hold it by the handle or the bottom part of the main unit.

When using this equipment, the operator should stay in a distance close enough to recognize an alarm sound.
Do not move too far away from the equipment where an alarm sound cannot be recognized.
Warnings about the monitoring

The patient classification selection influences the precision of the QRS detection and NIBP measurement.
Make sure the proper selection is made.

The pacemaker usage setting influences the precision of the QRS detection and arrhythmia analysis. Make sure
the correct selection is made.

If the QRS pace mask function is set to [OFF], [10ms]/[20ms], the pace pulse may be erroneously detected as
a QRS complex and HR alarm or asystole alarm may not generate due to incorrect HR (counting pace pulse as
QRS complex). Select [OFF], [10ms]/[20ms] only if you are sure that pacing failure will not occur, or when
the patient can be constantly monitored.

When measuring the SpO
2
of patient with high fever or peripheral circulatory insufficiency, check the sensor
attachment periodically and change the attachment site. The temperature of the attachment site will rise due to
the sensor heat which may result in burn injury.

For the following case, accurate measurement of SpO
2
may not be possible.

Patient with excessive abnormal hemoglobin (COHb, MetHb)

Patient with the pigment injected to the blood

Patient receiving CPR treatment

When a sensor is applied to a limb with NIBP cuff, arterial catheter, or intracatheter

When measuring at site with venous pulse

Patient with body motion

Patient with small pulse

When a patient is receiving a photodynamic therapy, measuring SpO
2
on a same site for a long duration may
cause blisters from the irradiation light of the SpO
2
sensor. Make sure to periodically change the sensor
attachment site.

Before the measurement, make sure the patient classification (Adult/Child/Neonate) is properly selected.
Otherwise, correct measurement cannot be performed, and congestion or other injury may result.

When the system alarm is suspended, all the alarm will be suspended even if the parameter alarm is set to [ON].
Also, the alarms will not be stored as recall events.

If the upper/lower alarm limit of the parameter is set to [OFF], or arrhythmia alarm is set to [OFF], alarm will
not function even if the individual alarm is set to [ON]. Pay attention when setting them [OFF].

Objective and constant arrhythmia detection is possible through the fixed algorithm incorporated in this
monitor. However, excessive waveform morphology change, motion artifact, or the inability to determine the
waveform pattern may cause an error, or fail to make adequate detection. Therefore, physicians should make
final decisions using manual printing, alarm printing and recall waveform for evaluation.

The RR/APNEA alarm will not be generated unless the numeric data box corresponded to the selected RR/
APNEA alarm source is displayed.Make sure to display the numeric data box for the RR/APNEA alarm source.

When selecting [0] for "Volume" or [Timer] for "Display" for the Night Mode, pay attention not to miss any
important alarm by simultaneously monitoring the patient on central monitor or other monitors.

When the alarm sound is suspended, the alarm sound will not generate for the fixed amount of time. Pay
attention not to miss any important alarm by simultaneously monitoring the patient on central monitor or other
monitors.

If the safety of the patient cannot be ensured, do not suspend the alarm or decrease the alarm volume.
WARNING