Fukuda Denshi DS-8200, Руководство по обслуживанию

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W A R N I N G
z 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 system alarm is set to
[ON]. Pay attention when setting them [OFF].
z 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 recording, alarm
recording and recall waveform for evaluation.
z The RR/APNEA alarm will not be generated unless the parameter key
(Numeric Data Box) corresponded to the selected RR/APNEA source is
displayed. Make sure to display the parameter key (Numeric Data Box) for the
RR/APNEA source.
z 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.
z 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.
Warnings about the CO
2
Monitoring (HPD-800/HPD-810, HCP-800/HCP-810)
z For HPD-800/HPD-810 with Capnostat 5;
y Use only the specified airway adapter manufactured by Respironics
Novametrix, LLC. Refer to the section on "Optional Accessories" for list of
specified airway adapters.
These accessories may be purchased from Fukuda Denshi or any
authorized Respironics Novametrix, LLC distributor.
y Always consider the circumference of the intubation tube when using the
airway adapter. If inappropriate airway adapter is used for a patient with low
ventilation, CO
2
may mix in to the inspired air resulting in incorrect
measurement, or apnea detection may become difficult.
z For HCP-800/HCP-810;
y When using a sampling line for intubated patients with a closed suction
system, do not place the airway adapter between the suction catheter and
endotracheal tube. This is to ensure that the airway adapter does not
interfere with the functioning of the suction catheter.
y Loose or damaged connections of the sampling line may compromise
ventilation or cause an inaccurate measurement of respiratory gases.
Securely connect all components and check connections for leaks
according to standard clinical procedures.
y Do not cut or remove any part of the sampling line. Cutting the sample line
could lead to erroneous readings.
y If too much moisture enters the sampling line (i.e., from ambient humidity or
breathing of unusually humid air), the message "Check Sample Line" will
appear in the message area. Replace the sampling line once the "Check
Sample Line" message appears.
y
Carefully route the sampling line to reduce the possibility of patient
entanglement or strangulation.
y Do not lift the HCP-800/HCP-810 by the sampling line, as the sampling line
could disconnect from the equipment, causing the equipment to fall on the
patient.
y CO
2
readings and respiratory rate can be affected by sensor application
errors, certain ambient environmental conditions, and certain patient
conditions.
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