Fukuda Denshi DynaScope 7000 Series, Руководство по обслуживанию

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Precautions about the DS-7000
D A N G E R
Be cautious when connecting to other device.
Danger such as electric shock may result to the patient and operator.
W A R N I N G
The DS-7000 is not a life-support equipment.
The DS-7000 is not intended for use during patient transport outside a
healthcare facility, and is not considered as mobile or portable equipment.
The DS-7000 is not intended for use with flammable anesthetic agents.
Do not connect unit or cable not authorized by Fukuda Denshi to any I/O
connector. If done so by mistake, the DS-7000 cannot deliver its maximum
performance and the connected units may be damaged, resulting in a
safety hazard.
If the DS-7000 is used under an environment not fulfilling the specified
condition, not only that the equipment cannot deliver its maximum
performance, the equipment may be damaged and safety cannot be
ensured.
Use only the accompanying 3-way AC power cable. Use of other cables
may result in electric shock to the patient and the operator.
The power cable must be connected to hospital grade outlet.
When using multiple ME equipment simultaneously, perform equipotential
grounding to prevent potential difference between the equipment. Even a
small potential difference may result in electric shock to the patient and the
operator.
Make sure to set the patient classification and pacemaker usage. These
settings influence the precision of the QRS detection and NIBP
measurement. Make sure the correct selection is made.
The pacemaker usage selection influences the precision of the QRS
detection and arrhythmia analysis. Make sure the correct selection is made.
If the QRS pace pulse mask function is set to OFF , 10ms or 20ms ,
a decrease in heart rate may not generate HR or ASYSTOLE alarms by
erroneously detecting pacemaker pulse as QRS. Set this function to
OFF , 10ms or 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 attachment site will rise 2to
3
°
C due to the sensor heat which may result in burn injury.
For the following case, accurate measurement 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
Be cautious when setting the "SpO
2
Averaging" duration as the SpO
2
alarm
is based on the displayed SpO
2
value which is averaged from the duration
set in "SpO
2
Averaging". The alarm occurrence time will be affected or may
not occur for the transient value of SpO
2
depending on the set duration.
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 monitoring multigas concentration, use the specified water trap.
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