Multinight Prevalence, Variability, and Diagnostic Misclassification of Obstructive Sleep Apnea

被引:116
作者
Lechat, Bastien [1 ,2 ]
Naik, Ganesh [1 ,2 ]
Reynolds, Amy [1 ,2 ]
Aishah, Atqiya [1 ,2 ,3 ]
Scott, Hannah [1 ,2 ]
Loffler, Kelly A. [1 ,2 ]
Vakulin, Andrew [1 ,2 ]
Escourrou, Pierre [4 ]
McEvoy, R. Doug [1 ,2 ]
Adams, Robert J. [1 ,2 ]
Catcheside, Peter G. [1 ,2 ]
Eckert, Danny J. [1 ,2 ]
机构
[1] Flinders Univ S Australia, Coll Med & Publ Hlth, Adelaide Inst Sleep Hlth, Adelaide, SA, Australia
[2] Flinders Univ S Australia, Coll Med & Publ Hlth, Flinders Hlth & Med Res Inst Sleep Hlth, Adelaide, SA, Australia
[3] Univ New South Wales, Sch Med Sci, Sydney, NSW, Australia
[4] Ctr Interdisciplinaire Sommeil, Paris, France
基金
英国医学研究理事会;
关键词
sleep-disordered breathing; misdiagnosis; wearables; polysomnography; TO-NIGHT VARIABILITY; POPULATION; SEVERITY; RISK;
D O I
10.1164/rccm.202107-1761OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Recent studies suggest that obstructive sleep apnea (OSA) severity can vary markedly from night to night, which may have important implications for diagnosis and management. Objectives: This study aimed to assess OSA prevalence from multinight in-home recordings and the impact of night-to-night variability in OSA severity on diagnostic classification in a large, global, nonrandomly selected community sample from a consumer database of people that purchased a novel, validated, under-mattress sleep analyzer. Methods: A total of 67,278 individuals aged between 18 and 90 years underwent in-home nightly monitoring over an average of approximately 170 nights per participant between July 2020 and March 2021. OSA was defined as a nightly mean apnea-hypopnea index (AHI) of more than 15 events/h. Outcomes were multinight global prevalence and likelihood of OSA misclassification from a single night's AHI value. Measurements and Main Results: More than 11.6 million nights of data were collected and analyzed. OSA global prevalence was 22.6% (95% confidence interval, 20.9-24.3%). The likelihood of misdiagnosis in people with OSA based on a single night ranged between approximately 20% and 50%. Misdiagnosis error rates decreased with increased monitoring nights (e.g., 1-night F1-score = 0.77 vs. 0.94 for 14 nights) and remained stable after 14 nights of monitoring. Conclusions: Multinight in-home monitoring using novel, noninvasive under-mattress sensor technology indicates a global prevalence of moderate to severe OSA of approximately 20%, and that approximately 20% of people diagnosed with a single-night study may be misclassified. These findings highlight the need to consider night-to-night variation in OSA diagnosis and management.
引用
收藏
页码:563 / 569
页数:7
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