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Instructions for use – Infinity Acute Care System – Monitoring Applications VG6.n
273
SpO2 and pulse rate with Nellcor OxiMax MCable
SpO2 precautions
Interfering substances: Carboxyhemoglobin may
erroneously increase measurement values. The
level of increase is approximately equal to the
amount of carboxyhemoglobin present. Dyes, or
any substance containing dyes that change arterial
pigmentation may cause erroneous measurement
values.
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WARNING
High oxygen levels may predispose a
premature baby to retinopathy of prematurity.
If this is a consideration do NOT set the high
alarm limit to 100%, which is equivalent to
switching the alarm off. Transcutaneous SpO2
monitoring is recommended for premature
babies receiving supplemental oxygen.
WARNING
An SpO2 sensor should not be used as an
apnea monitor.
WARNING
Use only
Nellcor-
and Dräger-specified
sensors. Other sensors may not provide
adequate protection against defibrillation and
may put the patient at risk.
WARNING
An SpO2 sensor should be considered an
early warning device. If a trend towards
patient hypoxemia is observed, blood
samples should be analyzed by laboratory
instruments to completely understand the
condition of the patient.
WARNING
The pulsations from an intra-aortic balloon
support can elevate the pulse rate. Verify the
pulse rate of the patient against the heart rate.
WARNING
To reduce the hazard of burns during surgery,
keep the sensor or transducer and their
associated cables away from the surgical site,
the electro-surgical unit return electrode, and
earth ground.
WARNING
Inspect the application site every two to three
hours to ensure skin quality and correct
optical alignment. If the skin quality changes,
move the sensor to another site. Change the
application site at least every four hours.
WARNING
Patient injury can occur if the oximeter is
applied wrong or if it is subject to excessive
pressure over a prolonged interval.
CAUTION
Do not immerse the sensor or patient cable in any
liquid. Moisture may present a safety risk.
NOTE
An SpO2 sensor can be used during defibrillation,
but the readings may be inaccurate for up to
20 seconds.
NOTE
Possession or purchase of this device does not
convey any express or implied license to use the
device with unauthorized consumable products
which would, alone, or in combination with this
device, fall within the scope of one or more of the
patents relating to this device and/or consumable
products. For a list of approved sensors, see the
Instructions for use
Infinity Acute Care System
–
Accessories
.