Omron m24-7 Benutzerhandbuch
17
Note:
Note: It is recommended that the cuff be applied as tightly as acceptable for the
patient. A too loose cuff will cause much longer blood pressure measurement
times and possibly aborted measurements. With an overly loose cuff, the
monitor must pump to tighten the cuff on the arm and then it must reach the
pressure necessary for measurement. This causes considerable inconvenience
for the patient and results in less data for evaluation. If the patient removes
the cuff for a period during the monitoring session, it should be re-applied
with appropriate tightness, with help from another person, if necessary. Should
blood pressure measurements cause blood shots, torpidity or pain in the hand
after an individual measurement, the cuff should be removed from the arm and
disconnected from the monitor. Such occurrence should be reported to the
physician at once after the monitoring session.
patient. A too loose cuff will cause much longer blood pressure measurement
times and possibly aborted measurements. With an overly loose cuff, the
monitor must pump to tighten the cuff on the arm and then it must reach the
pressure necessary for measurement. This causes considerable inconvenience
for the patient and results in less data for evaluation. If the patient removes
the cuff for a period during the monitoring session, it should be re-applied
with appropriate tightness, with help from another person, if necessary. Should
blood pressure measurements cause blood shots, torpidity or pain in the hand
after an individual measurement, the cuff should be removed from the arm and
disconnected from the monitor. Such occurrence should be reported to the
physician at once after the monitoring session.
OMRON M24/7 recognizes and functions with three different cuff sizes. Please
set the appropriate cuff size to be used during the programming of the device.
Attention: inappropriate setting of the cuff size may lead to device malfunctioning,
which is inconvenient for the patient and may lead to an unsuccessful measurement.
set the appropriate cuff size to be used during the programming of the device.
Attention: inappropriate setting of the cuff size may lead to device malfunctioning,
which is inconvenient for the patient and may lead to an unsuccessful measurement.
Name
Bladder
dimensions
Sleeve
dimensions
Arm circumference
range*
Small cuff (child)
9 x 18 cm
11 x 32 cm
under 24 cm
Normal cuff
12 x 25 cm
15 x 56 cm
24-32 cm
Large cuff
15 x 33 cm
17 x 77 cm
32-42 cm
* When properly applied, the end of the sleeve (the one closer to the tube) should
fall in the indicated range.
fall in the indicated range.
The cuff is the component which, by de nition of the relevant standard, is
protected against a de brillator discharge.
protected against a de brillator discharge.
Caution!
Substitution of a cuff different from that supplied might result in measurement
error and/or in certain cases cause damage to the main monitor unit.
error and/or in certain cases cause damage to the main monitor unit.
3. Care and Maintenance
3.1. Handling Errors and Problems
Below you can nd a list of potential error code displays, their meaning and a
description of the error code.
description of the error code.
Unsuccessful measurements
E 1 aborted measurement
the measurement timeout is over, the
measurement had to be aborted (the
patient was moving)
measurement had to be aborted (the
patient was moving)
E 2 (Off) manually interrupted
the measurement was stopped by pressing
a button (the display differs from others:
“OFF” on the LCD)
a button (the display differs from others:
“OFF” on the LCD)
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