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茚达特罗对 COPD 患者运动耐力和肺过度充气的影响。

Effect of indacaterol on exercise endurance and lung hyperinflation in COPD.

机构信息

Queen's University and Kingston General Hospital, Kingston, Ontario K7L 2V7, Canada.

出版信息

Respir Med. 2011 Jul;105(7):1030-6. doi: 10.1016/j.rmed.2011.03.014. Epub 2011 Apr 16.

Abstract

BACKGROUND

Indacaterol is a novel, inhaled, once-daily ultra long-acting β(2)-agonist (ultra-LABA) for the treatment of COPD. This study investigated the effect of indacaterol on exercise endurance, and on lung hyperinflation during exercise and at rest in patients with moderate-to-severe COPD.

METHODS

In this double-blind, placebo-controlled, two-period crossover study (3-week treatment, 3-week washout between treatments), patients were randomized to receive indacaterol 300 μg once-daily or matching placebo. The primary efficacy variable was exercise endurance time after 3 weeks of treatment, measured through constant-load cycle ergometry testing performed at 75% of the peak work rate in a screening incremental exercise test.

RESULTS

Of 90 patients randomized (mean age: 62.8 years; post-bronchodilator FEV(1): 61.2% predicted and FEV(1)/FVC: 51.6%), 74 completed the study. Pre-treatment exercise tolerance averaged 459 s. Improvement in exercise endurance time was higher with indacaterol 300 μg than with placebo both after the first dose (treatment difference: 101 s; p < 0.001) and after 3 weeks (treatment difference: 111 s; p = 0.011). In addition, indacaterol increased end-exercise inspiratory capacity (IC) versus placebo after 3 weeks (0.28 L, p = 0.002). Significant improvements were also observed in resting IC (0.17 L, p = 0.001), FEV(1) (0.25 L, p < 0.001) and FVC (0.26 L, p < 0.001) with indacaterol compared with placebo at 75 min post-dose after 3 weeks.

CONCLUSION

In conclusion, indacaterol treatment improved the ability of patients with COPD to exercise. In addition, the improvements observed in resting and end-exercise IC indicate reductions in lung hyperinflation after 3 weeks treatment (ClinicalTrials.gov registration number: NCT00620022).

摘要

背景

茚达特罗是一种新型、每日一次吸入的长效β2-激动剂(ultra-LABA),用于治疗 COPD。本研究旨在探讨茚达特罗对 COPD 患者运动耐力的影响,以及对运动中和运动后静息时的肺过度充气的影响。

方法

这是一项双盲、安慰剂对照、两周期交叉研究(3 周治疗,治疗之间 3 周洗脱期),患者被随机分配接受茚达特罗 300μg 每日一次或匹配安慰剂。主要疗效变量是经过 3 周治疗后,在筛选递增运动试验中以 75%的峰值做功率进行的恒负荷循环测功机测试后的运动耐力时间。

结果

90 例随机患者(平均年龄:62.8 岁;支气管扩张剂后 FEV1:61.2%预测值和 FEV1/FVC:51.6%)中,74 例完成了研究。治疗前运动耐量平均为 459 秒。与安慰剂相比,茚达特罗 300μg 在第一次给药后(治疗差异:101 秒;p<0.001)和 3 周后(治疗差异:111 秒;p=0.011)均提高了运动耐力时间。此外,与安慰剂相比,茚达特罗在 3 周后增加了运动终末吸气量(IC)(0.28L,p=0.002)。与安慰剂相比,在 3 周后 75 分钟时,茚达特罗还显著改善了静息 IC(0.17L,p=0.001)、FEV1(0.25L,p<0.001)和 FVC(0.26L,p<0.001)。

结论

总之,茚达特罗治疗改善了 COPD 患者的运动能力。此外,静息和运动终末 IC 的改善表明,经过 3 周治疗后,肺过度充气减少(临床试验注册编号:NCT00620022)。

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