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溴化阿地溴铵可改善中重度 COPD 患者的运动耐力和肺过度充气。

Aclidinium bromide improves exercise endurance and lung hyperinflation in patients with moderate to severe COPD.

机构信息

Centre de recherche, Institut Universitaire de cardiologie et de pneumologie de Québec, Université Laval, 2725 Chemin Sainte-Foy, Québec G1V 4G5, Canada.

出版信息

Respir Med. 2011 Apr;105(4):580-7. doi: 10.1016/j.rmed.2010.11.019. Epub 2010 Dec 22.

Abstract

BACKGROUND

Static and dynamic lung hyperinflation are associated with exercise impairment and poor outcomes in COPD patients. Aclidinium bromide is a novel, long-acting inhaled muscarinic antagonist currently in development for COPD treatment.

METHODS

Patients with moderate to severe COPD (N = 181) were randomized to once-daily aclidinium 200 μg or placebo for 6 weeks. Constant work rate cycling exercises at 75% of peak work rate were performed at baseline, Day 1, Week 3, and Week 6. The primary efficacy measure was change in exercise endurance time (ET) from baseline to Week 6. Secondary outcomes included changes in trough forced expiratory volume in 1 s (FEV(1)), inspiratory capacity (IC), IC/total lung capacity (TLC), and functional residual capacity (FRC) from baseline to Day 1, Week 3, and Week 6. Borg dyspnea scores during exercise, locus of symptom limitation, and safety measures were assessed.

RESULTS

Aclidinium significantly improved ET on Day 1 (P = 0.0002), and improvements were sustained through Week 3 (P = 0.0007) and Week 6 (P = 0.0042) vs placebo. Compared with placebo, aclidinium improved trough FEV(1), IC, and IC/TLC at Weeks 3 and 6 (P < 0.05 for all). Exertional dyspnea scores at isotime were reduced on Day 1, Week 3, and Week 6 for aclidinium vs placebo (P < 0.05). Furthermore, the likelihood of stopping exercise due to breathing discomfort was lower in the aclidinium group at study end (P = 0.0208) compared with placebo. No differences in safety outcomes were reported between treatments.

CONCLUSIONS

Aclidinium significantly increased exercise tolerance, improved airflow obstruction and lung hyperinflation, and was safe and well tolerated. REGISTRATION OF TRIAL: This trial was registered with ClinicalTrials.gov (NCT00500318) under the name "A Study of Exercise Endurance and Lung Hyperinflation in Patients with Moderate to Severe COPD".

摘要

背景

静态和动态肺过度充气与 COPD 患者的运动能力受损和预后不良相关。阿地溴铵是一种新型长效吸入性毒蕈碱拮抗剂,目前正在开发用于 COPD 的治疗。

方法

181 例中重度 COPD 患者随机分为每日一次阿地溴铵 200μg 或安慰剂治疗 6 周。在基线、第 1 天、第 3 周和第 6 周进行恒定工作率踏车运动,运动强度为峰值工作率的 75%。主要疗效指标为从基线到第 6 周的运动耐力时间(ET)变化。次要终点包括从基线到第 1 天、第 3 周和第 6 周的谷值用力呼气 1 秒量(FEV1)、吸气量(IC)、IC/总肺容量(TLC)和功能残气量(FRC)的变化。运动时的 Borg 呼吸困难评分、症状限制的部位和安全性措施也进行了评估。

结果

阿地溴铵显著改善了第 1 天的 ET(P = 0.0002),并在第 3 周(P = 0.0007)和第 6 周(P = 0.0042)持续改善,优于安慰剂。与安慰剂相比,阿地溴铵在第 3 周和第 6 周时改善了谷值 FEV1、IC 和 IC/TLC(P < 0.05)。与安慰剂相比,在第 1 天、第 3 周和第 6 周时,阿地溴铵治疗组的等时用力呼气呼吸困难评分降低(P < 0.05)。此外,与安慰剂相比,在研究结束时,阿地溴铵组因呼吸不适而停止运动的可能性更低(P = 0.0208)。两种治疗方法的安全性结果无差异。

结论

阿地溴铵显著提高了运动耐量,改善了气流阻塞和肺过度充气,且安全耐受良好。试验注册:这项试验在 ClinicalTrials.gov 注册(NCT00500318),名称为“阿地溴铵治疗中重度 COPD 患者运动耐力和肺过度充气的研究”。

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