Department of Endocrinology and Diabetes, Yokohama City University Medical Center, Yokohama, Japan.
Oku Medical Clinic, Shimmori, Japan.
J Sleep Res. 2022 Dec;31(6):e13682. doi: 10.1111/jsr.13682. Epub 2022 Jul 6.
This study aimed to evaluate the diagnostic accuracy of home sleep apnea testing using peripheral arterial tonometry for sleep apnea as an alternative to polysomnography. We conducted a systematic review and meta-analysis of observational studies, randomized controlled trials, and diagnostic case-control studies examining the diagnostic accuracy of peripheral arterial tonometry by searching the CENTRAL, MEDLINE, EMBASE, ICTRP and ClinicalTrials.gov databases on 5 October 2021. We assessed the risk of bias of the included studies using the Quality Assessment of Diagnostic Accuracy Studies-2 tool. A bivariate random-effects model was generated to derive the summary point estimates of sensitivity and specificity with 95% confidence intervals at different apnea-hypopnea index cutoffs. This meta-analysis included 13 studies (1227 participants, median prevalence of sleep apnea with apnea-hypopnea index ≥ 5 events per hr: 85%). The risk of bias in the included studies was low to moderate. The pooled sensitivity and specificity estimates were 96% (95% confidence interval: 93%-97%) and 44% (95% confidence interval: 32%-56%) at apnea-hypopnea index ≥ 5 events per hr, 88% (85%-91%) and 74% (63%-83%) at apnea-hypopnea index ≧ 15 events per hr, and 80% (66%-89%) and 90% (83%-95%) at apnea-hypopnea index ≧ 30 events per hr, respectively. Peripheral arterial tonometry resulted in a significant number of false negatives and false positives at any apnea-hypopnea index cutoff when applied to the median prevalence setting of the included studies. The inadequate sensitivity and specificity of peripheral arterial tonometry render it an unsuitable alternative to polysomnography for detecting sleep apnea for apnea-hypopnea index ≧ 5, 15 and 30 events per hr.
本研究旨在评估使用外周动脉张力测定法进行家庭睡眠呼吸暂停测试作为替代多导睡眠图进行睡眠呼吸暂停诊断的准确性。我们通过检索 CENTRAL、MEDLINE、EMBASE、ICTRP 和 ClinicalTrials.gov 数据库,于 2021 年 10 月 5 日对观察性研究、随机对照试验和诊断病例对照研究进行了系统评价和荟萃分析,以检查外周动脉张力测定法的诊断准确性。我们使用诊断准确性研究质量评估-2 工具评估了纳入研究的偏倚风险。生成了双变量随机效应模型,以在不同的呼吸暂停-低通气指数截止值下得出敏感性和特异性的汇总点估计值及其 95%置信区间。本荟萃分析纳入了 13 项研究(1227 名参与者,呼吸暂停-低通气指数≥5 次/小时的睡眠呼吸暂停中位数患病率:85%)。纳入研究的偏倚风险为低至中度。呼吸暂停-低通气指数≥5 次/小时时,汇总的敏感性和特异性估计值分别为 96%(95%置信区间:93%-97%)和 44%(95%置信区间:32%-56%),呼吸暂停-低通气指数≥15 次/小时时分别为 88%(85%-91%)和 74%(63%-83%),呼吸暂停-低通气指数≥30 次/小时时分别为 80%(66%-89%)和 90%(83%-95%)。在任何呼吸暂停-低通气指数截止值下,外周动脉张力测定法应用于纳入研究的中位数患病率设置时,会导致大量假阴性和假阳性结果。外周动脉张力测定法的敏感性和特异性不足,使其不适合替代多导睡眠图用于检测呼吸暂停-低通气指数≥5、15 和 30 次/小时的睡眠呼吸暂停。