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心力衰竭合并睡眠呼吸暂停的自动辅助通气:一项随机对照试验。

Auto-servoventilation in heart failure with sleep apnoea: a randomised controlled trial.

机构信息

Division of Respirology, University Hospital Regensburg, Regensburg.

出版信息

Eur Respir J. 2013 Nov;42(5):1244-54. doi: 10.1183/09031936.00083312. Epub 2012 Dec 6.

DOI:10.1183/09031936.00083312
PMID:23222879
Abstract

We tested the hypotheses that in patients with congestive heart failure (CHF) and sleep disordered breathing (SDB) auto-servoventilation (ASV) improves cardiac function and quality of life. Between March 2007 and September 2009, patients with stable CHF (left ventricular ejection fraction (LVEF) ≤ 40%) and SDB (apnoea/hypopnoea index ≥ 20 events · h(-1)) were randomised to receive either ASV (BiPAP ASV (Philips Respironics, Murrysville, PA, USA), n=37) and optimal medical management, or optimal medical management alone (n=35). Outcomes were assessed at baseline and 12 weeks. The apnoea/hypopnoea index assessed with polysomnography scored in one core laboratory was significantly more reduced in the ASV group (-39 ± 16 versus -1 ± 13 events · h(-1); p<0.001) with an average use of 4.5 ± 3.0 h · day(-1). Both groups showed similar improvements of the primary end-point LVEF (+3.4 ± 5 versus +3.5 ± 6%; p=0.915) assessed with echocardiography. In the ASV group, reduction of N-terminal pro-brain natriuretic peptide (NT-proBNP) was significantly greater (-360 ± 569 versus +135 ± 625 ng · mL(-1); p=0.010). No differences were observed between the groups in subjective quality of life. In patients with CHF and SDB, ASV reduced NT-proBNP levels, but improvement of LVEF or quality of life was not greater than in the control group. The data support that such patients can be randomised in large-scale, long-term trials of positive airway pressure therapy versus control to determine effects on cardiovascular outcome.

摘要

我们检验了以下假设,即对于充血性心力衰竭(CHF)和睡眠呼吸紊乱(SDB)患者,自动伺服通气(ASV)可改善心功能和生活质量。2007 年 3 月至 2009 年 9 月,我们对稳定的 CHF(左心室射血分数(LVEF)≤40%)和 SDB(呼吸暂停/低通气指数(apnoea/hypopnoea index,AHI)≥20 次·h(-1))患者进行了随机分组,分别接受 ASV(双水平气道正压通气 ASV(Philips Respironics,Murrysville,PA,美国),n=37)和最佳药物治疗(n=35)。在基线和 12 周时评估结局。多导睡眠图评估的 AHI 在一个核心实验室评分显著降低,ASV 组减少了(-39±16 比-1±13 次·h(-1)),平均使用时间为 4.5±3.0 小时·天(-1)。两组患者的主要终点 LVEF(超声心动图评估)均有相似的改善(+3.4±5 比+3.5±6%;p=0.915)。ASV 组的 N 端脑利钠肽前体(N-terminal pro-brain natriuretic peptide,NT-proBNP)降低更显著(-360±569 比+135±625 ng·mL(-1)),p=0.010)。两组患者的生活质量主观评分无差异。在 CHF 和 SDB 患者中,ASV 降低了 NT-proBNP 水平,但 LVEF 或生活质量的改善并不优于对照组。该数据支持将此类患者随机分组纳入大规模、长期的气道正压治疗与对照组的试验,以确定对心血管结局的影响。

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