Introduction Cautions
viii 0070-10-0699-02 Accutorr V Operating Instructions
CAUTION: When equipped with DPM SpO
2
, use only DPM oxygen
sensors and cables. Use of other oxygen sensors may cause
improper oximeter performance.
CAUTION: Excessive ambient light may cause inaccurate SpO
2
measurements. Cover the sensor with opaque materials.
CAUTION: Inaccurate readings may be caused by incorrect sensor
application or use; significant levels of dysfunctional
hemoglobins (i.e. carbohemoglobins or methemoglobin); or
intra-vascular dyes such as indocyanine green or methylene
blue; exposure to excessive illumination, such as surgical
lamps (especially ones with a Xenon light source), bilirubin
lamps, fluorescent lights, infrared heating lamps, or direct
sunlight; excessive patient movement; venous pulsations;
electro-surgical interference; and placement of a sensor on
an extremity that has a blood pressure cuff, arterial
catheter, or intra-vascular line.
CAUTION: Route cables neatly. Ensure cables, hoses, and wires are
kept away from patient’s neck to avoid strangulation. Keep
floors and walkways free of cables to reduce risk to
hospital personnel, patients, and visitors. If the sensor or
patient cable is damaged in any way, discontinue use
immediately.
CAUTION: When cleaning sensors, do not use excessive amounts of
liquid. Wipe the sensor surface with a soft cloth, dampened
with the cleaning solution. To prevent damage, do not soak
or immerse the sensor in any liquid solution. DO NOT
ATTEMPT TO STERILIZE.
CAUTION: Prolonged and continuous monitoring may increase the risk
of skin erosion and pressure necrosis at the site of the
sensor. Check the SpO
2
sensor site frequently to ensure
proper positioning, alignment, and skin integrity at least
every eight (8) hours; with the Adult and Pediatric re-usable
finger sensor, check every four (4) hours; for neonates and
patients of poor perfusion or with skin sensitive to light,
check every 2 - 3 hours; more frequent examinations may
be required for different patients. Change the sensor site if
signs of circulatory compromise occur. Ensure proper
adhesion, skin integrity, and proper alignment. Exercise
extreme caution with poorly perfused patients. When
sensors are not frequently monitored, skin erosion and
pressure necrosis can occur. Assess the site every two (2)
hours with poorly perfused patients and neonates.
CAUTION: Recharge the Lithium ion battery while in the unit at room
temperature. If using the Accutorr V in a hot environment,
the Lithium ion battery may not charge when the unit is
connected to the AC mains.
CAUTION: Remove the battery if the Accutorr V is not likely to be used
for an extended period of time.
CAUTION: The Communications Connectors on the Accutorr V are only
for use with IEC 60601-1-1 compliant equipment.
CAUTION: Never place fluids on top of this monitor. If fluid spills on the
unit, wipe clean immediately and refer the unit to qualified
service personnel.
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