
APPENDIX A: PRINCIPLES OF OPERATION
Oximetry Overview
OXIMETRY OVERVIEW
Pulse oximetry is based on two principles: that oxyhemoglobin
and deoxyhemoglobin differ in their absorption of red and
infrared light (i.e., spectrophotometry), and that the volume of
arterial blood in tissue (and hence, light absorption by that blood)
changes during the pulse (i.e., plethysmography). A pulse
oximeter determines SpO
2 by passing red and infrared light into
an arteriolar bed and measuring changes in light absorption
during the pulsatile cycle. Red and infrared low-voltage light-
emitting diodes (LEDs) in the oximetry sensor serve as light
sources; a photodiode serves as the photo detector.
Because oxyhemoglobin and deoxyhemoglobin differ in light
absorption, the amount of red and infrared light absorbed by
blood is related to hemoglobin oxygen saturation. To identify the
oxygen saturation of arterial hemoglobin, the monitor uses the
pulsatile nature of arterial flow. During systole, a new pulse of
arterial blood enters the vascular bed, and blood volume and light
absorption increase. During diastole, blood volume and light
absorption reach their lowest point. The monitor bases its SpO
2
measurements on the difference between maximum and minimum
absorption (i.e., measurements at systole and diastole). By doing
so, it focuses on light absorption by pulsatile arterial blood,
eliminating the effects of nonpulsatile absorbers such as tissue,
bone, and venous blood.
Automatic Calibration
Because light absorption by hemoglobin is wavelength dependent
and because the mean wavelength of LEDs varies, an oximeter
must know the mean wavelength of the sensor’s red LED to
accurately measure SpO
2. During manufacturing, the mean
wavelength of the red LED is encoded in a resistor in the sensor.
During monitoring, the instrument’s software reads this resistor
and selects coefficients that are appropriate for the wavelength of
that sensor’s red LED; these coefficients are then used to
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