Pulse oximetry is a non-invasive method used widely in clinical settings to monitor a patient's oxygenation status. By using light transmission through a vascular bed—most commonly a fingertip or earlobe—the device provides a real-time estimate of the percentage of hemoglobin saturated with oxygen. While it is a rapid and painless tool, understanding the underlying physics and the physiological principles behind it is essential for accurate clinical interpretation.
The Physics of Light Absorption
The fundamental principle behind pulse oximetry is spectrophotometry, which is the measurement of how much light a substance absorbs at specific wavelengths. In the context of blood, we are interested in how hemoglobin (the protein in red blood cells that carries oxygen) absorbs light.
Hemoglobin exists in different states, primarily:
- Oxygenated Hemoglobin (): Hemoglobin that is bound to oxygen.
- Deoxygenated Hemoglobin (): Hemoglobin that has released its oxygen.
These two forms have distinct absorption spectra. To differentiate between them, a pulse oximeter emits two specific wavelengths of light through the tissue:
- Red Light (~660 nm): Deoxygenated hemoglobin () absorbs more light at this wavelength.
- Infrared Light (~940 nm): Oxygenated hemoglobin () absorbs more light at this wavelength.
By calculating the ratio of the absorption of these two wavelengths, the device can estimate the oxygen saturation level.
Distinguishing Arterial Blood from Tissue
A significant challenge in measuring blood oxygen is that light does not just pass through arterial blood; it also passes through skin, bone, muscle, and venous blood. If the device measured all light absorption, it would be measuring the "total" absorption of everything in the finger, which would not accurately reflect arterial oxygenation.
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