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长效β2受体激动剂与长效毒蕈碱拮抗剂用于稳定期慢性阻塞性肺疾病患者的疗效比较:一项随机对照试验的系统评价和荟萃分析

Long-acting beta2-agonists versus long-acting muscarinic antagonists in patients with stable COPD: A systematic review and meta-analysis of randomized controlled trials.

作者信息

Chen Wang-Chun, Huang Chi-Hsien, Sheu Chau-Chyun, Chong Inn-Wen, Chu Kuo-An, Chen Yung-Che, Tsai Jong-Rung, Lee Cheng-Hung, Wei Yu-Feng

机构信息

Department of Pharmacy, E-Da Hospital, I-Shou University, Kaohsiung, Taiwan.

Department of Family Medicine, E-Da Hospital, I-Shou University, Kaohsiung, Taiwan.

出版信息

Respirology. 2017 Oct;22(7):1313-1319. doi: 10.1111/resp.13100. Epub 2017 Jun 27.

Abstract

Several long-acting bronchodilators have been developed and are widely used as first-line treatment in patients with stable chronic obstructive pulmonary disease (COPD). However, the initial choice of therapy is still uncertain. The aim of this study was to examine the clinical efficacy and safety of long-acting muscarinic antagonist (LAMA) and long-acting beta2-agonist (LABA) in patients with stable COPD. We searched several databases and manufacturers' websites to identify relevant randomized clinical trials for meta-analysis. Outcomes of interest were trough forced expiratory volume in 1 s (FEV ), acute exacerbations, transitional dyspnoea index (TDI) score, St George's Respiratory Questionnaire (SGRQ) score and adverse events. Sixteen trials with a total of 22 872 patients were included in this study. Compared with LABA, LAMA were associated with a greater reduction in acute exacerbations (OR: 0.84, 95% CI: 0.74-0.94, P = 0.003) and fewer adverse events (OR: 0.92, 95% CI: 0.86-0.97, P = 0.005). There were no significant differences in trough FEV , TDI and SGRQ scores. In patients with stable COPD, LAMA were associated with a greater reduction in acute exacerbations and fewer adverse effects compared with LABA.

摘要

几种长效支气管扩张剂已被研发出来,并广泛用作稳定期慢性阻塞性肺疾病(COPD)患者的一线治疗药物。然而,初始治疗的选择仍不明确。本研究的目的是探讨长效毒蕈碱拮抗剂(LAMA)和长效β2受体激动剂(LABA)在稳定期COPD患者中的临床疗效和安全性。我们检索了多个数据库和制造商网站,以确定相关的随机临床试验进行荟萃分析。感兴趣的结局指标为1秒用力呼气容积(FEV₁)谷值、急性加重次数、过渡性呼吸困难指数(TDI)评分、圣乔治呼吸问卷(SGRQ)评分及不良事件。本研究纳入了16项试验,共22872例患者。与LABA相比,LAMA与急性加重次数的显著减少相关(比值比:0.84,95%置信区间:0.74 - 0.94,P = 0.003),且不良事件较少(比值比:0.92,95%置信区间:0.86 - 0.97,P = 0.005)。FEV₁谷值、TDI和SGRQ评分无显著差异。在稳定期COPD患者中,与LABA相比,LAMA与急性加重次数的更大幅度减少及更少的不良反应相关。

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