DIGIOXI PO-930 Gebruikershandleiding - Pagina 15

Blader online of download pdf Gebruikershandleiding voor {categorie_naam} DIGIOXI PO-930. DIGIOXI PO-930 19 pagina's. Pulse oximeter monitor

SpO

Monitoring

Until the patient cable is connected and the probe is placed in patient, the message SENSOR OFF is displayed

in screen.

In normal operation, the monitor displays SpO

alarm limits.

Reposition the probe at least once every 18-20 hours to allow the patient's skin to respire.

Loss of pulse signal can occur if:

- The sensor is to tight.

- There is excessive illumination (e.g., a surgical or bilirubin lamp or direct sunlight).

- The sensor is placed on an extremity with a blood pressure cuff, arterial catheter or intravascular line.

- The patient experiences shock, hypertension, severe vasoconstriction, severe anemia, hypothermia,

arterial occlusion to the sensor, or cardiac arrest.

Inaccurate measurements may be caused by:

- Incorrect application of dysfunctional hemoglobin's, such as carboxyhemoglobin or methemoglobin.

- Significant, levels of indocyanine green, ethylene blue or other intravascular dyes.

- 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 pulsation's.

- Electrosurgical interference.

- Placement of the sensor on an extremity that has a blood pressure cuff, arterial catheter or intravascular

line.

Do not attach a probe to the same limb with a blood pressure cuff. The data received will not be valid

when the cuff is inflated. Attach the probe to the limb opposite the site used for the blood pressure cuff.

The amplitude of the PLETHYSMOGRAM waveform is automatically adjusted in screen.

Operators Manual Pulse Oximeter Monitor DIGIOXI "PO-930"

and Pulse Rate values, a bar graph indicating pulse height and

Digicare Biomedical Technology Inc.