Cho Eun Yeong, Kim Se Yong, Kim Min-Ji, Kim Seonwoo, Park Dong Ah, Yoo Kwang Ha, Park Yong Bum, Hwang Yong Il, Rhee Chin Kook, Jung Ji Ye, Lee Hyun, Park Hye Yun
Division of Pulmonary and Critical Care Medicine, Department of Medicine, Samsung Medical Center, Sungkyunkwan University of Medicine, Seoul, South Korea.
Statistics and Data Center, Research Institute for Future Medicine, Samsung Medical Center, Seoul, South Korea.
J Thorac Dis. 2018 Dec;10(12):6522-6530. doi: 10.21037/jtd.2018.11.50.
A single long-acting bronchodilator, ultra-long acting muscarinic antagonist (ultra-LAMA) or ultra-long acting β-agonist (ultra-LABA) is preferred for the initial treatment of patients with chronic obstructive pulmonary disease (COPD); however, there are few head-to-head comparative studies between the two. Here, a meta-analysis of randomized controlled trials was performed to compare the clinical efficacy between ultra-LABA and ultra-LAMA in patients with moderate-to-severe COPD.
MEDLINE, EMBASE, and the Cochrane Central Register of Controlled Trials were searched (to March 1, 2017) to identify all published randomized controlled trials.
Of the 12,906 articles found by searching the databases, we obtained data from 10,591 patients with COPD (LABA, n=5,058; LAMA, n=5,533) in seven published studies. Our results showed that COPD exacerbation were significantly lower in patients taking ultra-LAMA than those taking ultra-LABA (odds ratio =0.857, P=0.0008). However, no significant differences were observed between ultra-LAMA and ultra-LABA patients regarding improvement in trough forced expiratory volume in 1 s, the transitional dyspnea index, or St. George's Respiratory Questionnaire score.
This study suggests that COPD exacerbation occurred less often in patients taking an ultra-LAMA than in those taking an ultra-LABA with similar efficacy of lung function and quality of life.
对于慢性阻塞性肺疾病(COPD)患者的初始治疗,首选单一长效支气管扩张剂,即超长效毒蕈碱拮抗剂(ultra-LAMA)或超长效β受体激动剂(ultra-LABA);然而,两者之间的直接对比研究较少。在此,我们进行了一项随机对照试验的荟萃分析,以比较超长效β受体激动剂和超长效毒蕈碱拮抗剂在中重度COPD患者中的临床疗效。
检索MEDLINE、EMBASE和Cochrane对照试验中央注册库(截至2017年3月1日),以识别所有已发表的随机对照试验。
通过检索数据库找到12906篇文章,我们从7项已发表研究中的10591例COPD患者(长效β受体激动剂组,n = 5058;长效毒蕈碱拮抗剂组,n = 5533)获取了数据。我们的结果显示,服用超长效毒蕈碱拮抗剂的患者COPD急性加重显著低于服用超长效β受体激动剂的患者(比值比 = 0.857,P = 0.0008)。然而,在1秒用力呼气容积谷值改善、过渡性呼吸困难指数或圣乔治呼吸问卷评分方面,超长效毒蕈碱拮抗剂组和超长效β受体激动剂组患者之间未观察到显著差异。
本研究表明,服用超长效毒蕈碱拮抗剂的COPD患者急性加重发生率低于服用超长效β受体激动剂的患者,且肺功能和生活质量疗效相似。