Safety of formoterol in patients with asthma: Combined analysis of data from double-blind, randomized controlled trials

被引:34
作者
Nelson, Harold [1 ]
Bonuccelli, Catherine [2 ]
Radner, Finn [3 ]
Ottosson, Anders [3 ]
Carroll, Kevin J. [4 ]
Andersson, Tomas L. G. [3 ]
LaForce, Craig [5 ]
机构
[1] Natl Jewish Hlth, Dept Med, Denver, CO 80206 USA
[2] AstraZeneca LP, Wilmington, DE USA
[3] AstraZeneca, Lund, Sweden
[4] AstraZeneca, Macclesfield, Cheshire, England
[5] Univ N Carolina, Sch Med, Chapel Hill, NC USA
关键词
Asthma; formoterol; inhaled corticosteroid; long-acting beta(2)-adrenergic agonist; safety; serious adverse events; METERED-DOSE INHALER; ACTING BETA-AGONISTS; PERSISTENT ASTHMA; REPORTED OUTCOMES; SINGLE INHALER; BUDESONIDE; ADULTS; BUDESONIDE/FORMOTEROL; EFFICACY; MODERATE;
D O I
10.1016/j.jaci.2009.11.036
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Concerns exist that regular long-acting beta(2)-adrenergic agonist (LABA) therapy may increase the risk of serious asthma-related events. Objective: To assess risks of formoterol-containing versus non-LABA treatment by using a large asthma database. Methods: This analysis included all blind, parallel-arm, randomized, active-controlled and/or placebo-controlled AstraZeneca-sponsored asthma studies with formoterol-containing and non-LABA comparator arms. Serious adverse events were assessed for inclusion in all-cause death, asthma-related death, asthma-related intubation, and asthma-related hospitalization categories by using blind adjudication. Data were combined across trials; relative risk (RR) was assessed by using Mantel-Haenszel methods. Results: Data were from 13,542 formoterol-randomized and 9968 non-LABA patients 4 years or older (42 trials), of whom 93% and 89%, respectively, received inhaled corticosteroid as part of randomized treatment or allowed medication. Incidence of all-cause death was low (n = 3 and n = 4, respectively), with numerically lower all-cause deaths/1000 patient-treatment years in the formoterol-treated group (0.53) versus the non-LABA group (0.82) (RR, 0.64; 95% confidence interval [CI], 0.14-2.92). No asthma-related deaths and 1 asthma-related intubation (formoterol-treated group) occurred. Asthma-related hospitalizations/1000 patient-treatment years were lower numerically in the formoterol-treated group (12.1) versus the non-LABA group (16.4) (RR, 0.73; 95% CI, 0.54-1.01), with fewer study discontinuations in the formoterol-treated group (12.7% vs 15.4%, respectively; RR, 0.79; 95% CI, 0.74-0.85). Relative to non-LABA, increasing daily formoterol dose (>= 4.5, 9, 18, 36 mu g) did not increase the rate or incidence of asthma-related hospitalization. Conclusion: No evidence of increased risk of asthma-related hospitalization, no asthma-related deaths, and a low incidence of all-cause death and asthma-related intubation were seen with formoterol-containing versus non-LABA treatment. (J Allergy Clin Immunol 2010;125:390-6.)
引用
收藏
页码:390 / 396
页数:7
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