Abstract

The assessment of oxygen saturation in arterial blood by pulse oximetry (SpO2) is based on the different light absorption spectra for oxygenated and deoxygenated hemoglobin and the analysis of photoplethysmographic (PPG) signals acquired at two wavelengths. Commercial pulse oximeters use two wavelengths in the red and infrared regions which have different pathlengths and the relationship between the PPG-derived parameters and oxygen saturation in arterial blood is determined by means of an empirical calibration. This calibration results in an inherent error, and pulse oximetry thus has an error of about 4%, which is too high for some clinical problems. We present calibration-free pulse oximetry for measurement of SpO2, based on PPG pulses of two nearby wavelengths in the infrared. By neglecting the difference between the path-lengths of the two nearby wavelengths, SpO2 can be derived from the PPG parameters with no need for calibration. In the current study we used three laser diodes of wavelengths 780, 785 and 808 nm, with narrow spectral line-width. SaO2 was calculated by using each pair of PPG signals selected from the three wavelengths. In measurements on healthy subjects, SpO2 values, obtained by the 780–808 nm wavelength pair were found to be in the normal range. The measurement of SpO2 by two nearby wavelengths in the infrared with narrow line-width enables the assessment of SpO2 without calibration.

Highlights

  • Is based on the different light absorption spectra for oxygenated and deoxygenated hemoglobin and the analysis of photoplethysmographic (PPG) signals acquired at two wavelengths

  • Oxygen saturation in the blood is the ratio of oxygenated hemoglobin concentration to total hemoglobin concentration in the blood, and its value in the arterial blood, SaO2, is of great clinical and physiological significance since it reflects the adequacy of oxygen delivery and respiratory function

  • For each pair of wavelengths, the parameter R was calculated from the corresponding signals (using Equation (5)) and SaO2 was calculated using Equation (4), by making use of the corresponding values of the extinction coefficient from Table 1

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Summary

Introduction

Is based on the different light absorption spectra for oxygenated and deoxygenated hemoglobin and the analysis of photoplethysmographic (PPG) signals acquired at two wavelengths. Commercial pulse oximeters use two wavelengths in the red and infrared regions which have different pathlengths and the relationship between the PPG-derived parameters and oxygen saturation in arterial blood is determined by means of an empirical calibration. This calibration results in an inherent error, and pulse oximetry has an error of about 4%, which is too high for some clinical problems. We present calibration-free pulse oximetry for measurement of SpO2, based on PPG pulses of two nearby wavelengths in the infrared. The measurement of SpO2 by two nearby wavelengths in the infrared with narrow line-width enables the assessment of SpO2 without calibration. Normal values of SaO2 are 94%–98% at sea level but the values may decline somewhat beyond the age of 70 years [1]

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