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Validation of peripheral arterial tonometry as tool for sleep assessment in chronic obstructive pulmonary disease

Obstructive sleep apnea (OSA) worsens outcomes in Chronic Obstructive Pulmonary Disease (COPD), and reduced sleep quality is common in these patients. Thus, objective sleep monitoring is needed, but polysomnography (PSG) is cumbersome and costly. The WatchPAT determines sleep by a pre-programmed alg...

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Autores principales: Holmedahl, Nils Henrik, Fjeldstad, Odd-Magne, Engan, Harald, Saxvig, Ingvild West, Grønli, Janne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6920446/
https://www.ncbi.nlm.nih.gov/pubmed/31852958
http://dx.doi.org/10.1038/s41598-019-55958-2
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author Holmedahl, Nils Henrik
Fjeldstad, Odd-Magne
Engan, Harald
Saxvig, Ingvild West
Grønli, Janne
author_facet Holmedahl, Nils Henrik
Fjeldstad, Odd-Magne
Engan, Harald
Saxvig, Ingvild West
Grønli, Janne
author_sort Holmedahl, Nils Henrik
collection PubMed
description Obstructive sleep apnea (OSA) worsens outcomes in Chronic Obstructive Pulmonary Disease (COPD), and reduced sleep quality is common in these patients. Thus, objective sleep monitoring is needed, but polysomnography (PSG) is cumbersome and costly. The WatchPAT determines sleep by a pre-programmed algorithm and has demonstrated moderate agreement with PSG in detecting sleep stages in normal subjects and in OSA patients. Here, we validated WatchPAT against PSG in COPD patients, hypothesizing agreement in line with previous OSA studies. 16 COPD patients (7 men, mean age 61 years), underwent simultaneous overnight recordings with PSG and WatchPAT. Accuracy in wake and sleep staging, and concordance regarding total sleep time (TST), sleep efficiency (SE), and apnea hypopnea index (AHI) was calculated. Compared to the best fit PSG score, WatchPAT obtained 93% sensitivity (WatchPAT = sleep when PSG = sleep), 52% specificity (WatchPAT = wake when PSG = wake), 86% positive and 71% negative predictive value, Cohen’s Kappa (κ) = 0.496. Overall agreement between WatchPat and PSG in detecting all sleep stages was 63%, κ = 0.418. The mean(standard deviation) differences in TST, SE and AHI was 25(61) minutes (p = 0.119), 5(15) % (p = 0.166), and 1(5) (p = 0.536), respectively. We conclude that in COPD-patients, WatchPAT detects sleep stages in moderate to fair agreement with PSG, and AHI correlates well.
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spelling pubmed-69204462019-12-20 Validation of peripheral arterial tonometry as tool for sleep assessment in chronic obstructive pulmonary disease Holmedahl, Nils Henrik Fjeldstad, Odd-Magne Engan, Harald Saxvig, Ingvild West Grønli, Janne Sci Rep Article Obstructive sleep apnea (OSA) worsens outcomes in Chronic Obstructive Pulmonary Disease (COPD), and reduced sleep quality is common in these patients. Thus, objective sleep monitoring is needed, but polysomnography (PSG) is cumbersome and costly. The WatchPAT determines sleep by a pre-programmed algorithm and has demonstrated moderate agreement with PSG in detecting sleep stages in normal subjects and in OSA patients. Here, we validated WatchPAT against PSG in COPD patients, hypothesizing agreement in line with previous OSA studies. 16 COPD patients (7 men, mean age 61 years), underwent simultaneous overnight recordings with PSG and WatchPAT. Accuracy in wake and sleep staging, and concordance regarding total sleep time (TST), sleep efficiency (SE), and apnea hypopnea index (AHI) was calculated. Compared to the best fit PSG score, WatchPAT obtained 93% sensitivity (WatchPAT = sleep when PSG = sleep), 52% specificity (WatchPAT = wake when PSG = wake), 86% positive and 71% negative predictive value, Cohen’s Kappa (κ) = 0.496. Overall agreement between WatchPat and PSG in detecting all sleep stages was 63%, κ = 0.418. The mean(standard deviation) differences in TST, SE and AHI was 25(61) minutes (p = 0.119), 5(15) % (p = 0.166), and 1(5) (p = 0.536), respectively. We conclude that in COPD-patients, WatchPAT detects sleep stages in moderate to fair agreement with PSG, and AHI correlates well. Nature Publishing Group UK 2019-12-18 /pmc/articles/PMC6920446/ /pubmed/31852958 http://dx.doi.org/10.1038/s41598-019-55958-2 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Holmedahl, Nils Henrik
Fjeldstad, Odd-Magne
Engan, Harald
Saxvig, Ingvild West
Grønli, Janne
Validation of peripheral arterial tonometry as tool for sleep assessment in chronic obstructive pulmonary disease
title Validation of peripheral arterial tonometry as tool for sleep assessment in chronic obstructive pulmonary disease
title_full Validation of peripheral arterial tonometry as tool for sleep assessment in chronic obstructive pulmonary disease
title_fullStr Validation of peripheral arterial tonometry as tool for sleep assessment in chronic obstructive pulmonary disease
title_full_unstemmed Validation of peripheral arterial tonometry as tool for sleep assessment in chronic obstructive pulmonary disease
title_short Validation of peripheral arterial tonometry as tool for sleep assessment in chronic obstructive pulmonary disease
title_sort validation of peripheral arterial tonometry as tool for sleep assessment in chronic obstructive pulmonary disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6920446/
https://www.ncbi.nlm.nih.gov/pubmed/31852958
http://dx.doi.org/10.1038/s41598-019-55958-2
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