Compensation of human variability in pulse oximetry

Abstract

The invention relates to a method of calibrating a pulse oximeter, in which the effects caused by tissue of a subject can be taken into account. A detector output signal is measured when living tissue of the subject is present between emitters and the detector in a sensor. Nominal calibration and nominal calibration characteristics are read from a memory, whereupon values for the same nominal characteristics for the sensor on living tissue of the subject are established using the detector output signal. Then, changes in the nominal calibration characteristics induced by the living tissue are calculated and a subject-specific calibration is formed by correcting the nominal calibration with the changes. Finally, the hemoglobin fractions are solved using the corrected nominal calibration. The invention also relates to a pulse oximeter having pre-stored data in a memory comprising data of initial characterization measurements, data of nominal characteristics describing calibration conditions under which a predetermined calibration of the apparatus has been applied, and data of nominal calibration and nominal calibration characteristics. An extinction coefficient compensation block is operatively connected to the first signal processing means and to the memory for reading data, said block comprising first calculation means adapted to correct the nominal characteristics of the sensor on living tissue of the subject. A transformation compensation block is operatively connected to the first signal processing means for receiving the DC signals and to the memory for reading data, said block comprising second calculation means adapted to correct the transformation values based on the changes in the DC signals induced by tissue of the subject. Alternatively, said data may be stored in the sensor part of the pulse oximeter.

Description

FIELD OF THE INVENTION [0001] The invention relates generally to pulse oximeters used to detect blood oxygenation. More specifically, the invention relates to a method for taking into account human variability in pulse oximeters. The invention further relates to a sensor allowing compensation for the inaccuracies caused by human variability, the sensor being an integral part of the pulse oximeter. BACKGROUND OF THE INVENTION [0002] Pulse oximetry is at present the standard of care for continuous monitoring of arterial oxygen saturation (SPO2). Pulse oximeters provide instantaneous in-vivo measurements of arterial oxygenation, and thereby an early warning of arterial hypoxemia, for example. [0003] A pulse oximeter comprises a computerized measuring unit and a probe attached to the patient, typically to a finger or ear lobe. The probe includes a light source for sending an optical signal through the tissue and a photo detector for receiving the signal after transmission through the ti...

AI Technical Summary

Benefits of technology

This approach significantly improves the accuracy of pulse oximeter readings by accounting for individual tissue variations, enhancing the precision of blood oxygenation measurements and reducing errors associated with human variability.

Problems solved by technology

Therefore, if these species of hemoglobin are present in higher concentrations than normal, a pulse oximeter may display erroneous data.

Secondly, intravenous dyes used for diagnostic purposes may cause considerable deviation in pulse oximeter readings.

However, the effect of these dyes is short-lived since the liver purifies blood efficiently.

Thirdly, coatings like nail polish may in practice impair the accuracy of a pulse oximeter, even though the absorption caused by them is constant, not pulsatile, and thus in theory it should not have an effect on the accuracy.

Fourthly, the optical signal may be degraded by both noise and motion artifacts.

One source of noise is the ambient light received by the photodetector.

As mentioned above, the accuracy of a pulse oximeter utilizing an average transformation is not necessarily sufficient, especially if analytes which are weak absorbers are to be measured or if two analytes absorb similarly, whereby it is difficult to distinguish the said analytes from each other.

This causes one drawback of the current pulse oximeters; they are incapable of taking this human variability into account.

However, in multi-wavelength applications in general, and especially if weak absorbers, such as COHb, are to be measured, the human variability represents a much more serious problem.

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