医学
狼牙棒
持续气道正压
气道正压
体质指数
慢性阻塞性肺病
心力衰竭
心脏病学
冲程(发动机)
队列研究
前瞻性队列研究
内科学
阻塞性睡眠呼吸暂停
心肌梗塞
传统PCI
机械工程
工程类
作者
Miguel Divo,Miguel Ángel Martínez‐García,Mónica González,Francisco Campos‐Rodríguez,Patrícia Lloberes,Marta Marín‐Oto,Marta Forner,David Sánz-Rubio,D Nieto,Bartolomé R. Celli,José M. Marı́n
出处
期刊:The European respiratory journal
[European Respiratory Society]
日期:2025-08-21
卷期号:66 (5): 2500519-2500519
被引量:1
标识
DOI:10.1183/13993003.00519-2025
摘要
Background Evidence regarding the efficacy of positive airway pressure (PAP) therapy in reducing the risk of non-fatal major cardiovascular events (NF-MACE) and mortality in patients with obstructive sleep apnoea (OSA) remains controversial. This study aims to quantify the impact of PAP therapy on these risks and develop a predictive risk estimator. Methods We conducted a multicentre, observational, prospective study involving 5358 individuals diagnosed with OSA, with a median (interquartile range (IQR)) follow-up of 14 (10–15) years. We derived and validated a risk estimator of NF-MACE (including myocardial infarction, stroke, revascularisation procedures and congestive heart failure) and all-cause mortality, incorporating PAP adherence alongside clinical and sleep-related data. Results The cohort had mean± sd age 55±11 years, body mass index 32.0±5.4 kg·m −2 and apnoea–hypopnoea index (AHI) 35±22 events·h −1 ; 26% were females and 1467 (37%) were PAP adherent. Over the follow-up period, 754 participants experienced NF-MACE, while 858 deaths were recorded. Significant predictors included prior cardiovascular events, non-high-density lipoprotein cholesterol ≥200 mg·dL −1 , COPD diagnosis, AHI >30 events·h −1 and age >60 years. PAP adherence was protective (OR 0.46, 95% CI 0.38–0.56) and the absolute risk reduction varied depending on the baseline risk (median (IQR) 16% (12–18%)). The risk estimator yielded an area under the receiver operating characteristic curve of 0.75 and a Brier score of 0.17, with 64% sensitivity and 75% specificity. Conclusions PAP therapy is associated with long-term risk reduction of NF-MACE and mortality in OSA patients, while the developed risk estimator enhances clinical decision making regarding therapy initiation.
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