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Pulse oximetry: fundamentals and technology update

Oxygen saturation in the arterial blood (SaO(2)) provides information on the adequacy of respiratory function. SaO(2) can be assessed noninvasively by pulse oximetry, which is based on photoplethysmographic pulses in two wavelengths, generally in the red and infrared regions. The calibration of the...

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Autores principales: Nitzan, Meir, Romem, Ayal, Koppel, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099100/
https://www.ncbi.nlm.nih.gov/pubmed/25031547
http://dx.doi.org/10.2147/MDER.S47319
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author Nitzan, Meir
Romem, Ayal
Koppel, Robert
author_facet Nitzan, Meir
Romem, Ayal
Koppel, Robert
author_sort Nitzan, Meir
collection PubMed
description Oxygen saturation in the arterial blood (SaO(2)) provides information on the adequacy of respiratory function. SaO(2) can be assessed noninvasively by pulse oximetry, which is based on photoplethysmographic pulses in two wavelengths, generally in the red and infrared regions. The calibration of the measured photoplethysmographic signals is performed empirically for each type of commercial pulse-oximeter sensor, utilizing in vitro measurement of SaO(2) in extracted arterial blood by means of co-oximetry. Due to the discrepancy between the measurement of SaO(2) by pulse oximetry and the invasive technique, the former is denoted as SpO(2). Manufacturers of pulse oximeters generally claim an accuracy of 2%, evaluated by the standard deviation (SD) of the differences between SpO(2) and SaO(2), measured simultaneously in healthy subjects. However, an SD of 2% reflects an expected error of 4% (two SDs) or more in 5% of the examinations, which is in accordance with an error of 3%–4%, reported in clinical studies. This level of accuracy is sufficient for the detection of a significant decline in respiratory function in patients, and pulse oximetry has been accepted as a reliable technique for that purpose. The accuracy of SpO(2) measurement is insufficient in several situations, such as critically ill patients receiving supplemental oxygen, and can be hazardous if it leads to elevated values of oxygen partial pressure in blood. In particular, preterm newborns are vulnerable to retinopathy of prematurity induced by high oxygen concentration in the blood. The low accuracy of SpO(2) measurement in critically ill patients and newborns can be attributed to the empirical calibration process, which is performed on healthy volunteers. Other limitations of pulse oximetry include the presence of dyshemoglobins, which has been addressed by multiwavelength pulse oximetry, as well as low perfusion and motion artifacts that are partially rectified by sophisticated algorithms and also by reflection pulse oximetry.
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spelling pubmed-40991002014-07-16 Pulse oximetry: fundamentals and technology update Nitzan, Meir Romem, Ayal Koppel, Robert Med Devices (Auckl) Review Oxygen saturation in the arterial blood (SaO(2)) provides information on the adequacy of respiratory function. SaO(2) can be assessed noninvasively by pulse oximetry, which is based on photoplethysmographic pulses in two wavelengths, generally in the red and infrared regions. The calibration of the measured photoplethysmographic signals is performed empirically for each type of commercial pulse-oximeter sensor, utilizing in vitro measurement of SaO(2) in extracted arterial blood by means of co-oximetry. Due to the discrepancy between the measurement of SaO(2) by pulse oximetry and the invasive technique, the former is denoted as SpO(2). Manufacturers of pulse oximeters generally claim an accuracy of 2%, evaluated by the standard deviation (SD) of the differences between SpO(2) and SaO(2), measured simultaneously in healthy subjects. However, an SD of 2% reflects an expected error of 4% (two SDs) or more in 5% of the examinations, which is in accordance with an error of 3%–4%, reported in clinical studies. This level of accuracy is sufficient for the detection of a significant decline in respiratory function in patients, and pulse oximetry has been accepted as a reliable technique for that purpose. The accuracy of SpO(2) measurement is insufficient in several situations, such as critically ill patients receiving supplemental oxygen, and can be hazardous if it leads to elevated values of oxygen partial pressure in blood. In particular, preterm newborns are vulnerable to retinopathy of prematurity induced by high oxygen concentration in the blood. The low accuracy of SpO(2) measurement in critically ill patients and newborns can be attributed to the empirical calibration process, which is performed on healthy volunteers. Other limitations of pulse oximetry include the presence of dyshemoglobins, which has been addressed by multiwavelength pulse oximetry, as well as low perfusion and motion artifacts that are partially rectified by sophisticated algorithms and also by reflection pulse oximetry. Dove Medical Press 2014-07-08 /pmc/articles/PMC4099100/ /pubmed/25031547 http://dx.doi.org/10.2147/MDER.S47319 Text en © 2014 Nitzan et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Nitzan, Meir
Romem, Ayal
Koppel, Robert
Pulse oximetry: fundamentals and technology update
title Pulse oximetry: fundamentals and technology update
title_full Pulse oximetry: fundamentals and technology update
title_fullStr Pulse oximetry: fundamentals and technology update
title_full_unstemmed Pulse oximetry: fundamentals and technology update
title_short Pulse oximetry: fundamentals and technology update
title_sort pulse oximetry: fundamentals and technology update
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099100/
https://www.ncbi.nlm.nih.gov/pubmed/25031547
http://dx.doi.org/10.2147/MDER.S47319
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