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The safety of formoterol among patients with asthma using inhaled corticosteroids. Systematic review and meta?analysis

机译:吸入皮质类固醇对哮喘患者中福莫特罗的安全性。系统评价和荟萃分析

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Introduction. It has been postulated that inhaled long acting β?agonists (LABAs) when used as monotherapy in asthma may increase the incidence of asthma related deaths, intubations and hospitalizations, but concomitant use of inhaled corticosteroids (ICS) may modify this effect. Objectives. To assess the safety of formoterol in patients with asthma using ICS. Patients and methods. We conducted a systematic review and meta?analysis of parallel group, blinded, randomized controlled trials with at least 12 weeks of treatment examining the impact of twice a day formoterol on asthma?related and total morbidity and mortality in patients concurrently using ICS. Our main analysis considering impact of LABAs (salmeterol and formoterol) has already been published. In this report we present detailed information from studies investigating use of twice daily formoterol among patients receiving ICS. Results. The search yielded 16 relevant studies included in this analysis. Among over 10,000 participants (5,996 taking formoterol with over 4,000 patient?years observation in formoterol groups) there were 2 asthma?related deaths (both in formoterol groups) and no asthma?related non?fatal intubations. The risk of asthma?related hospitalizations (odds ratio [OR] 0.59, 95% CI 0.37–0.93) and asthma?related serious adverse events (mostly hospitalizations) [OR 0.58, 95%0.37–0.91] were significantly lower in patients on formoterol and ICS compared to patients on ICS alone. The OR for total mortality was 1.22, 95% CI 0.38–3.90, reflecting 7 deaths in formoterol groups and 3 deaths in control groups respectively. Conclusions. In patients with asthma using inhaled corticosteroids formoterol decreased the risk of asthma?related hospitalizations. There were too few asthma?related deaths and intubations to establish formoterol’s relative impact on these outcomes.
机译:介绍。据推测,吸入性长效β受体激动剂(LABAs)在哮喘中作为单一疗法使用时,可能会增加与哮喘相关的死亡,插管和住院的发生率,但同时使用吸入性糖皮质激素(ICS)可能会改变这种效果。目标。使用ICS评估福莫特罗在哮喘患者中的安全性。患者和方法。我们对平行组,盲法,随机对照试验进行了系统的回顾和荟萃分析,该试验至少进行了12周的治疗,研究了每天两次福莫特罗对同时使用ICS的患者与哮喘相关的总发病率和死亡率的影响。考虑到LABA(沙美特罗和福莫特罗)的影响,我们的主要分析已经发表。在本报告中,我们提供了来自研究的详细信息,这些研究调查了接受ICS的患者中每日两次福莫特罗的使用。结果。搜索产生了16项相关研究,包括在此分析中。在10,000多名参与者中(5,996名服用了福莫特罗,在福莫特罗组中观察了4,000多年的患者),有2例与哮喘相关的死亡(均在福莫特罗组中),没有与哮喘相关的非致命性插管。服用福莫特罗的患者与哮喘有关的住院风险(几率[OR] 0.59,95%CI 0.37–0.93)和与哮喘有关的严重不良事件(多数为住院)[OR 0.58,95%0.37–0.91]明显降低与仅使用ICS的患者相比。总死亡率的OR为1.22,95%CI为0.38–3.90,分别反映了福莫特罗组7例死亡和对照组3例死亡。结论。在哮喘患者中,使用吸入糖皮质激素福莫特罗降低了哮喘相关住院的风险。与哮喘相关的死亡和插管术很少,因此无法确定福莫特罗对这些结果的相对影响。

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