EClinicalMedicine | 2019

Feasibility of Single Channel Oximetry for Mass Screening of Obstructive Sleep Apnea

 
 
 
 
 
 
 
 

Abstract


Background The growing awareness for the high prevalence of obstructive sleep apnea (OSA) coupled with the dramatic proportion of undiagnosed individuals motivates the elaboration of a simple but accurate screening test. This study assesses, for the first time, the performance of oximetry combined with demographic information as a screening tool for identifying OSA in a representative (i.e. non-referred) population sample. Methods A polysomnography (PSG) clinical database of 887 individuals from a representative population sample of São Paulo s city (Brazil) was used. Using features derived from the oxygen saturation signal during sleep periods and demographic information, a logistic regression model (termed OxyDOSA) was trained to distinguish between non-OSA and OSA individuals (mild, moderate, and severe). The OxyDOSA model performance was assessed against the PSG-based diagnosis of OSA (AASM 2017) and compared to the NoSAS and STOP-BANG questionnaires. Findings The OxyDOSA model had mean AUROC\u202f=\u202f0.94\u202f±\u202f0.02, Se\u202f=\u202f0.87\u202f±\u202f0.04 and Sp\u202f=\u202f0.85\u202f±\u202f0.03. In particular, it did not miss any of the 75 severe OSA individuals. In comparison, the NoSAS questionnaire had AUROC\u202f=\u202f0.83\u202f±\u202f0.03, and missed 23/75 severe OSA individuals. The STOP-BANG had AUROC\u202f=\u202f0.77\u202f±\u202f0.04 and missed 14/75 severe OSA individuals. Interpretation We provide strong evidence on a representative population sample that oximetry biomarkers combined with few demographic information, the OxyDOSA model, is an effective screening tool for OSA. Our results suggest that sleep questionnaires should be used with caution for OSA screening as they fail to identify many moderate and even some severe cases. The OxyDOSA model will need to be further validated on data recorded using overnight portable oximetry.

Volume 11
Pages 81 - 88
DOI 10.1016/j.eclinm.2019.05.015
Language English
Journal EClinicalMedicine

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