阻塞性睡眠呼吸暂停是心房颤动的危险因素:一项荟萃分析。

Journal of sleep disorders & therapy Pub Date : 2018-01-01 Epub Date: 2018-02-12 DOI:10.4172/2167-0277.1000282
Irini Youssef, Haroon Kamran, Mena Yacoub, Nirav Patel, Clive Goulbourne, Shweta Kumar, Jesse Kane, Haley Hoffner, Moro Salifu, Samy I McFarlane
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引用次数: 59

摘要

目的:进行一项meta分析,评估阻塞性睡眠呼吸暂停(OSA)与心房颤动(AF)风险之间的关系。方法:采用关键词“心房颤动”、“阻塞性睡眠呼吸暂停”、“睡眠呼吸障碍(SDB)”检索PUBMED、Medline、Cochrane Library。所有受试者均确诊为OSA/SDB。然后,我们比较了房颤的发生与无房颤的发生。分析使用综合荟萃分析包V3 (Biostat,美国)完成。结果:共生成579条结果。根据不相关的摘要、标题、研究设计与所述结果不一致或无法获得全文,删除了重复的记录,并排除了372条记录。对符合纳入标准的12项研究进行全文综述;其中2篇文章由于未证实的OSA诊断方式最终被删除,1篇文章也基于与其他研究不一致的对照组而被删除。因此,共纳入9项研究(n= 19837)。样本量从n=160例到n=6841例不等。与对照组相比,OSA/SDB组发生房颤的风险更高(OR;2.120, c.i.: 1.845-2.436, z;10.598 p:结论:OSA/SDB与房颤密切相关,证实OSA/SDB人群是房颤发展的高危人群。需要前瞻性研究来确定OSA/SDB治疗对房颤的预防作用,房颤是一种日益严重的健康负担,后果严重。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Obstructive Sleep Apnea as a Risk Factor for Atrial Fibrillation: A Meta-Analysis.

Obstructive Sleep Apnea as a Risk Factor for Atrial Fibrillation: A Meta-Analysis.

Obstructive Sleep Apnea as a Risk Factor for Atrial Fibrillation: A Meta-Analysis.

Objectives: To conducted a meta-analysis assessing the relationship between Obstructive Sleep Apnea (OSA) and the risk of Atrial Fibrillation (AF).

Methods: We searched PUBMED, Medline, and Cochrane Library using the keywords "atrial fibrillation", "obstructive sleep apnea" and "sleep disordered breathing (SDB)". All subjects included had established diagnosis of OSA/SDB. We then compared the occurrence of AF versus no AF. Analysis done with Comprehensive Meta-Analysis package V3 (Biostat, USA).

Results: A total of 579 results were generated. Duplicates were removed and 372 records were excluded based on irrelevant abstracts, titles, study design not consistent with the stated outcome, or full-text unavailable. Twelve studies meeting the inclusion criteria were reviewed in full-text; 2 of these articles were eventually removed due to unconfirmed OSA diagnostic modality, and one was also removed based on a control group inconsistent with the other studies. Therefore, a total of 9 studies were included (n=19,837). Sample sizes ranged from n=160 patients to n=6841 patients. The risk of AF was found to be higher among OSA/SDB versus control group (OR; 2.120, C.I: 1.845-2.436, Z; 10.598 p: <0.001). The heterogeneity observed for the pooled analysis was Q-value; 22.487 df (Q); 8 P-value; 0.004, I-squared; 64.424 Tau2; 0.098, suggesting appropriate study selection and moderate heterogeneity.

Conclusion: OSA/SDB is strongly associated with AFib confirming the notion that OSA/SDB populations are high risk for development of AF. Prospective studies are needed to ascertain the effect of the treatment of OSA/SDB for the prevention of AF, a growing health burden with serious consequences.

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