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茚达特罗对中重度 COPD 患者肺过度充气的急性影响:与噻托溴铵的比较。

Acute effects of indacaterol on lung hyperinflation in moderate COPD: a comparison with tiotropium.

机构信息

Unità Operativa Complessa di Pneumologia, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.

出版信息

Respir Med. 2012 Jan;106(1):84-90. doi: 10.1016/j.rmed.2011.09.006. Epub 2011 Oct 27.

Abstract

BACKGROUND

Evidence has been provided that high-dose indacaterol (300 μg) can reduce lung hyperinflation in moderate-to-severe chronic obstructive pulmonary disease (COPD).

AIM

To study whether low-dose indacaterol (150 μg) also reduces lung hyperinflation in comparison with the recommended dose of tiotropium (18 μg) in moderate COPD.

METHODS

This was a multicenter, randomized, blinded, 3-period cross-over, placebo-controlled study. Spirometry and lung volumes were measured before and 30, 60, 120, 180 and 240 min after the administration of single-doses of indacaterol, tiotropium, or placebo. The primary end-point was the change in peak inspiratory capacity (IC). The area under the 4-h curve (AUC(0-4)) for IC, 1-s forced expiratory volume (FEV(1)) and forced vital capacity (FVC) were secondary variables.

RESULTS

49 patients completed the study. On average, peak IC and AUC(0-4) for IC were significantly greater after indacaterol than placebo by 177 mL (p = 0.007) and 142 mL (p = 0.001), respectively. Differences in peak IC and AUC(0-4) for IC between tiotropium and placebo were 120 mL (p = 0.07) and 85 mL (p = 0.052), respectively. Differences between indacaterol and tiotropium were statistically insignificant. Peak IC increased by >20% in 12 patients with indacaterol and 9 with tiotropium (p = 0.001), and by >30% in 8 patients with indacaterol and 3 with tiotropium (p = 0.001). The effects of indacaterol and tiotropium on FEV(1) and FVC were statistically significant vs placebo.

CONCLUSIONS

Low-dose indacaterol has a bronchodilator effect that is similar to the recommended dose of tiotropium, but it is slightly superior in reducing lung hyperinflation.

TRIAL REGISTRATION

ClinicalTrials.gov number: NCT00999908.

摘要

背景

有证据表明,高剂量茚达特罗(300μg)可减少中重度慢性阻塞性肺疾病(COPD)患者的肺过度充气。

目的

研究与推荐剂量噻托溴铵(18μg)相比,低剂量茚达特罗(150μg)是否也能减少中重度 COPD 患者的肺过度充气。

方法

这是一项多中心、随机、双盲、三周期交叉、安慰剂对照研究。在给予单剂量茚达特罗、噻托溴铵或安慰剂前、后 30、60、120、180 和 240 分钟测量患者的肺活量和肺容积。主要终点为峰吸气流速(IC)的变化。IC 的 4 小时曲线下面积(AUC(0-4))、1 秒用力呼气量(FEV(1))和用力肺活量(FVC)为次要变量。

结果

49 例患者完成了研究。平均而言,与安慰剂相比,茚达特罗后 IC 的峰值和 AUC(0-4)分别显著增加了 177ml(p=0.007)和 142ml(p=0.001)。与安慰剂相比,噻托溴铵后 IC 的峰值和 AUC(0-4)分别增加了 120ml(p=0.07)和 85ml(p=0.052)。茚达特罗与噻托溴铵之间的差异无统计学意义。12 例患者使用茚达特罗后 IC 增加>20%,9 例患者使用噻托溴铵后 IC 增加>20%(p=0.001),8 例患者使用茚达特罗后 IC 增加>30%,3 例患者使用噻托溴铵后 IC 增加>30%(p=0.001)。与安慰剂相比,茚达特罗和噻托溴铵对 FEV(1)和 FVC 的作用均有统计学意义。

结论

低剂量茚达特罗具有与推荐剂量噻托溴铵相似的支气管扩张作用,但在减少肺过度充气方面略胜一筹。

试验注册

ClinicalTrials.gov 编号:NCT00999908。

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