Wijesinghe M, Weatherall M, Perrin K, Harwood M, Beasley R
Medical Research Institute of New Zealand, Wellington, New Zealand.
Eur Respir J. 2009 Oct;34(4):803-11. doi: 10.1183/09031936.00159708.
There is concern long-acting beta-agonist (LABA) drugs may increase the risk of asthma mortality. We undertook a systematic review which included the AstraZeneca Formoterol Clinical Trial Safety Database and Novartis Food and Drug Administration Formoterol Briefing Document. Randomised controlled clinical trials of duration > or = 4 weeks that compared formoterol with a non-LABA comparator treatment in asthma were included in a meta-analysis of the risk of all-cause mortality and asthma death. Simple contingency tables, Peto's one-step method and a Bayesian analysis were used. There were 42 deaths (nine from asthma) recorded in 62 studies with 49,327 subjects. The simple contingency table odds ratio for risk of all-cause mortality with formoterol was 1.1 (95% CI 0.6-2.2) and for asthma death was 2.7 (95% CI 0.5-26.7). Analyses by the other methods using both "as randomised" and "as exposed" classifications of treatment gave similar risk estimates with wide confidence and credible intervals. We conclude that there was insufficient power to determine whether formoterol increases the risk of mortality. However, the point estimates of a 2.0- to 3.2-fold increased risk of asthma death are not reassuring and add weight to evidence that LABA use in certain circumstances may increase the risk of asthma mortality.
人们担心长效β-激动剂(LABA)药物可能会增加哮喘死亡率。我们进行了一项系统评价,其中包括阿斯利康福莫特罗临床试验安全数据库和诺华食品药品监督管理局福莫特罗情况说明书。在一项关于全因死亡率和哮喘死亡风险的荟萃分析中,纳入了持续时间≥4周、将福莫特罗与非LABA对照治疗在哮喘中进行比较的随机对照临床试验。使用了简单列联表、佩托一步法和贝叶斯分析。在涉及49327名受试者的62项研究中记录了42例死亡(9例死于哮喘)。福莫特罗全因死亡率风险的简单列联表优势比为1.1(95%可信区间0.6 - 2.2),哮喘死亡的优势比为2.7(95%可信区间0.5 - 26.7)。使用“随机分组”和“暴露”两种治疗分类方法进行的其他分析得出了类似的风险估计值,但置信区间和可信区间较宽。我们得出结论,没有足够的能力来确定福莫特罗是否会增加死亡风险。然而,哮喘死亡风险增加2.0至3.2倍的点估计值并不令人放心,这进一步证明了在某些情况下使用LABA可能会增加哮喘死亡率。