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持续气道正压通气与标准治疗用于治疗轻度阻塞性睡眠呼吸暂停的疗效对比(MERGE):一项多中心、随机对照试验。

Continuous positive airway pressure versus standard care for the treatment of people with mild obstructive sleep apnoea (MERGE): a multicentre, randomised controlled trial.

机构信息

Department of Medicine, University of Sydney, Sydney, Australia; ResMed Science Center, ResMed Ltd, Sydney, Australia.

National Heart and Lung Institute, Imperial College London, London, UK; Royal Brompton and Harefield NHS Foundation Trust, London, UK.

出版信息

Lancet Respir Med. 2020 Apr;8(4):349-358. doi: 10.1016/S2213-2600(19)30402-3. Epub 2019 Dec 2.

Abstract

BACKGROUND

The evidence base for the treatment of mild obstructive sleep apnoea is limited and definitions of disease severity vary. The MERGE trial investigated the clinical effectiveness of continuous positive airway pressure in patients with mild obstructive sleep apnoea.

METHODS

MERGE, a multicentre, parallel, randomised controlled trial enrolled patients (≥18 years to ≤80 years) with mild obstructive sleep apnoea (apnoea-hypopnoea index [AHI] ≥5 to ≤15 events per h using either AASM 2007 or AASM 2012 scoring criteria) from 11 UK sleep centres. Participants were assigned (1:1) to either 3 months of continuous positive airway pressure plus standard care (sleep counselling), or standard care alone, by computer-generated randomisation; neither participants nor researchers were blinded. The primary outcome was a change in the score on the Short Form-36 questionnaire vitality scale in the intention-to-treat population of patients with mild obstructive sleep apnoea diagnosed using the American Academy of Sleep Medicine 2012 scoring criteria. The study is registered with ClinicalTrials.gov, NCT02699463.

FINDINGS

Between Nov 28, 2016 and Feb 12, 2019, 301 patients were recruited and randomised. 233 had mild obstructive sleep apnoea using AASM 2012 criteria and were included in the intention-to-treat analysis: 115 were allocated to receive continuous positive airway pressure and 118 to receive standard care. 209 (90%) of these participants completed the trial. The vitality score significantly increased with a treatment effect of a mean of 10·0 points (95% CI 7·2-12·8; p<0·0001) after 3 months of continuous positive airway pressure, compared with standard care alone (9·2 points [6·8 to 11·6] vs -0·8 points [-3·2 to 1·5]). Using the ANCOVA last-observation-carried-forward analysis, a more conservative estimate, the vitality score also significantly increased with a treatment effect of a mean of 7·5 points (95% CI 5·3 to 9·6; p<0·0001) after 3 months of continuous positive airway pressure, compared with standard care alone (7·5 points [6·0 to 9·0] vs 0·0 points [-1·5 to 1·5]). Three serious adverse events occurred (one allocated to the continuous positive airway pressure group) and all were unrelated to the intervention.

INTERPRETATION

3 months of treatment with continuous positive airway pressure improved the quality of life in patients with mild obstructive sleep apnoea. These results highlight the need for health-care professionals and providers to consider treatment for patients with mild obstructive sleep apnoea.

FUNDING

ResMed Ltd.

摘要

背景

轻度阻塞性睡眠呼吸暂停治疗的证据基础有限,疾病严重程度的定义也有所不同。MERGE 试验研究了持续气道正压通气在轻度阻塞性睡眠呼吸暂停患者中的临床疗效。

方法

MERGE 是一项多中心、平行、随机对照试验,招募了来自英国 11 个睡眠中心的轻度阻塞性睡眠呼吸暂停(使用 AASM 2007 或 AASM 2012 评分标准,AHI≥5 至≤15 次/小时)的患者(年龄≥18 岁至≤80 岁)。参与者按 1:1 被分配到持续气道正压通气加标准护理(睡眠咨询)或单独标准护理组,采用计算机生成的随机分组;参与者和研究人员均未设盲。主要结局是使用美国睡眠医学学会 2012 评分标准诊断的轻度阻塞性睡眠呼吸暂停患者的简明 36 健康调查量表活力评分在意向治疗人群中的变化。该研究在 ClinicalTrials.gov 注册,NCT02699463。

结果

2016 年 11 月 28 日至 2019 年 2 月 12 日期间,共招募了 301 名患者并进行了随机分组。233 名患者根据 AASM 2012 标准诊断为轻度阻塞性睡眠呼吸暂停,并纳入意向治疗分析:115 名患者被分配接受持续气道正压通气,118 名患者接受标准护理。其中 209 名(90%)参与者完成了试验。与单独标准护理相比,持续气道正压通气治疗 3 个月后,活力评分显著提高,平均提高 10.0 分(95%CI7.2-12.8;p<0.0001)(9.2 分[6.8-11.6] vs -0.8 分[-3.2-1.5])。使用更保守的最后观察值结转分析(ANCOVA),持续气道正压通气治疗 3 个月后,活力评分也显著提高,平均提高 7.5 分(95%CI5.3-9.6;p<0.0001),与单独标准护理相比(7.5 分[6.0-9.0] vs 0.0 分[-1.5-1.5])。发生了 3 例严重不良事件(1 例分配到持续气道正压通气组),均与干预无关。

结论

持续气道正压通气治疗 3 个月可改善轻度阻塞性睡眠呼吸暂停患者的生活质量。这些结果强调了医疗保健专业人员和提供者需要考虑为轻度阻塞性睡眠呼吸暂停患者提供治疗。

资金来源

瑞思迈有限公司。

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