Division of Pulmonary, Critical Care and Environmental Medicine, University of Missouri, School of Medicine, Columbia, USA.
School of Social and Community Medicine, University of Bristol, Bristol, UK.
Thorax. 2016 Jan;71(1):15-25. doi: 10.1136/thoraxjnl-2014-206732. Epub 2015 Oct 21.
The place of long-acting β agonist/long-acting muscarinic antagonist (LABA/LAMA) combinations in stable patients with COPD is not well defined. The purpose of this study was to systematically review the efficacy and safety of LABA/LAMA combinations.
Several databases and manufacturers' websites were searched for relevant clinical trials. Randomised control trials, at least 12 weeks duration, comparing a LABA/LAMA combination with placebo and/or monotherapy were included. The data were pooled using a network as well as a traditional direct comparison meta-analysis.
Twenty-three trials with a total of 27 172 patients were included in the analysis. LABA/LAMA combinations were associated with a greater improvement in lung function, St. George's Respiratory Questionnaire (SGRQ) score, and Transitional Dyspnoea Index (TDI) than monotherapies. LABA/LAMA combinations were associated with a significantly greater proportion of SGRQ and TDI responders than monotherapies (OR 1.23 (95% credible interval (CrI) 1.06-1.39), OR 1.34 (95% CrI 1.19-1.50) versus LABAs and OR 1.24 (95% CrI 1.11-1.36), OR 1.31 (95% CrI 1.18-1.46) versus LAMAs, respectively) and fewer moderate-to-severe exacerbations compared with LABAs (HR 0.82 (95% CrI 0.73-0.93)), but not when compared with LAMAs (HR 0.92 (95% CrI 0.84-1.00)). There were no statistically significant differences associated with LABA/LAMA combinations compared with monotherapies in safety outcomes as well as in severe exacerbations.
The combination therapy was the most effective strategy in improving lung function, quality of life, symptom scores and moderate-to-severe exacerbation rates, and had similar effects on safety outcomes and severe exacerbations as compared with monotherapies.
长效β激动剂/长效抗胆碱能药物(LABA/LAMA)联合制剂在稳定期 COPD 患者中的地位尚未明确。本研究旨在系统评价 LABA/LAMA 联合制剂的疗效和安全性。
检索多个数据库和制造商网站,以获取相关的临床试验。纳入比较 LABA/LAMA 联合制剂与安慰剂和/或单药治疗、至少持续 12 周的随机对照试验。采用网络荟萃分析和传统直接比较荟萃分析对数据进行合并。
纳入分析的共有 23 项试验,共计 27172 例患者。与单药治疗相比,LABA/LAMA 联合制剂可更显著地改善肺功能、圣乔治呼吸问卷(SGRQ)评分和过渡性呼吸困难指数(TDI)。LABA/LAMA 联合制剂在 SGRQ 和 TDI 应答者比例方面也显著高于单药治疗(比值比 1.23(95%可信区间 1.06-1.39),比值比 1.34(95%可信区间 1.19-1.50)优于 LABA,比值比 1.24(95%可信区间 1.11-1.36),比值比 1.31(95%可信区间 1.18-1.46)优于 LAMA),且与 LABA 相比,中重度恶化事件的发生风险降低(风险比 0.82(95%可信区间 0.73-0.93)),但与 LAMA 相比无统计学差异(风险比 0.92(95%可信区间 0.84-1.00))。与单药治疗相比,LABA/LAMA 联合制剂在安全性结局和重度恶化事件方面无统计学差异。
与单药治疗相比,联合治疗是改善肺功能、生活质量、症状评分和中重度恶化事件发生率的最有效策略,且在安全性结局和重度恶化事件方面与单药治疗的效果相似。