Pulse oximetry estimates arterial oxygen saturation noninvasively from wavelength-dependent optical signals that vary with the arterial pulse. A typical sensor combines red and infrared light-emitting diodes with a photodetector. The pulsatile component helps distinguish changing arterial blood contribution from relatively steady tissue and blood contributions; it is not a direct measurement of arterial oxygen partial pressure.
A primary instrument-design note implements 660 nm and 940 nm illumination, a shared photodetector and alternating channel acquisition. It separates pulsatile and steady components before estimating saturation.[ref]
Pulse Oximeter Fundamentals and Design by Santiago Lopez. Sections 2.2 and 3.1.2, printed pp. 3–5 and 7, optical channels and acquisition
These wavelengths and electronics describe that implementation rather than every possible sensor.Writing pulsatile and steady signal magnitudes as AC and DC, a common normalized optical quantity isFor original channel values AC, DC, AC and DC, this ratio is 0.5. Halving both red-channel magnitudes leaves the ratio unchanged. This illustrates intensity normalization; it does not determine a saturation without a validated relation between and saturation.
That relation is experimentally checked against an independent reference. The FDA's technical guidance describes comparing oximeter readings with simultaneous co-oximetry of arterial samples during controlled inspired-oxygen changes in volunteers, and reporting an accuracy statistic.[ref]
Pulse Oximeters: Premarket Notification Submissions by the FDA. Clinical Performance, SpO2 Accuracy: reference arterial sampling, inspired mixtures and paired readings
Such comparisons test the whole sensor–algorithm measurement chain, rather than only the arithmetic of a two-channel ratio.One summary is the root mean square differenceFor invented paired errors percentage points, percentage points even though mean error is zero. A small mean bias does not guarantee small individual errors.
Motion, weak pulsatile signals and additional absorbing hemoglobin species can invalidate assumptions behind a simple estimate. Pulse oximetry does not measure pH, carbon-dioxide tension or hemoglobin concentration. A stable displayed percentage therefore cannot establish every aspect of ventilation, oxygen content or gas exchange.
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