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Mortality associated with tiotropium mist inhaler in patients with chronic obstructive pulmonary disease: systematic review and meta-analysis of randomised controlled trials

机译:慢性阻塞性肺疾病患者噻托溴铵雾剂吸入器的死亡率:随机对照试验的系统评价和荟萃分析

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摘要

>Objective To systematically review the risk of mortality associated with long term use of tiotropium delivered using a mist inhaler for symptomatic improvement in chronic obstructive pulmonary disease.>Data sources Medline, Embase, the pharmaceutical company clinical trials register, the US Food and Drug Administration website, and ClinicalTrials.gov for randomised controlled trials from inception to July 2010.>Study selection Trials were selected for inclusion if they were parallel group randomised controlled trials of tiotropium solution using a mist inhaler (Respimat Soft Mist Inhaler, Boehringer Ingelheim) versus placebo for chronic obstructive pulmonary disease; the treatment duration was more than 30 days, and they reported data on mortality. Relative risks of all cause mortality were estimated using a fixed effect meta-analysis, and heterogeneity was assessed with the I2 statistic.>Results Five randomised controlled trials were eligible for inclusion. Tiotropium mist inhaler was associated with a significantly increased risk of mortality (90/3686 v 47/2836; relative risk 1.52, 95% confidence interval, 1.06 to 2.16; P=0.02; I2=0%). Both 10 µg (2.15, 1.03 to 4.51; P=0.04; I2=9%) and 5 µg (1.46, 1.01 to 2.10; P=0.04; I2=0%) doses of tiotropium mist inhaler were associated with an increased risk of mortality. The overall estimates were not substantially changed by sensitivity analysis of the fixed effect analysis of the five trials combined using the random effects model (1.45, 1.02 to 2.07; P=0.04), limiting the analysis to three trials of one year’s duration each (1.50, 1.05 to 2.15), or the inclusion of additional data on tiotropium mist inhaler from another investigational drug programme (1.42, 1.01 to 2.00). The number needed to treat for a year with the 5 µg dose to see one additional death was estimated to be 124 (95% confidence interval 52 to 5682) based on the average control event rate from the long term trials.>Conclusions This meta-analysis explains safety concerns by regulatory agencies and indicates a 52% increased risk of mortality associated with tiotropium mist inhaler in patients with chronic obstructive pulmonary disease.
机译:>目的系统地审查与长期使用雾化吸入器递送的噻托溴铵有关的症状,以改善慢性阻塞性肺疾病的死亡率。>数据来源,Medline,Embase,制药公司临床试验注册,美国食品和药物管理局网站和ClinicalTrials.gov进行从开始到2010年7月的随机对照试验。>研究选择如果是平行组随机对照试验,则选择包括在内的试验。使用雾化吸入器(Respimat Soft Mist吸入器,勃林格殷格翰公司)与安慰剂治疗噻托溴铵溶液对慢性阻塞性肺疾病的作用;治疗持续时间超过30天,他们报告了死亡率数据。使用固定效应荟萃分析评估所有原因死亡的相对风险,并使用I 2 统计量评估异质性。>结果有5项随机对照试验符合纳入条件。噻托溴铵雾吸入器与死亡风险显着增加相关(90/3686 v 47/2836;相对风险1.52,95%置信区间,1.06至2.16; P = 0.02; I 2 = 0% )。 10 µg(2.15,1.03至4.51; P = 0.04; I 2 = 9%)和5 µg(1.46,1.01至2.10; P = 0.04; I 2 = 0%剂量的噻托铵雾吸入器与死亡风险增加相关。通过使用随机效应模型对五项试验的固定效应分析进行敏感性分析(1.45,1.02至2.07; P = 0.04),总体估计值并未发生实质性变化,将分析限制在三项试验中,每种试验的期限均为一年(1.50) ,1.05至2.15),或包含来自其他研究药物计划的噻托铵雾化吸入器的其他数据(1.42,1.01至2.00)。根据长期试验的平均对照事件发生率,用5 µg剂量治疗一年即可看到另一例死亡的人数估计为124(95%置信区间52至5682)。>结论< / strong>这项荟萃分析解释了监管机构对安全性的担忧,并指出,慢性阻塞性肺疾病患者与噻托溴铵雾剂吸入器相关的死亡率上升了52%。

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