Stanford University School of Medicine, Stanford, CA, USA.
Am J Med. 2010 Apr;123(4):322-8.e2. doi: 10.1016/j.amjmed.2009.07.035. Epub 2010 Feb 20.
It is unclear whether long-acting beta-agonists with concomitant inhaled corticosteroids increase asthma-related intubations and deaths. We pooled data on long-acting beta-agonists with variable and concomitant inhaled corticosteroids to evaluate the risk for catastrophic asthma events.
We conducted searches of electronic databases, the US Food and Drug Administration website, clinical-trials registries, and selected references through December 2008. We analyzed randomized controlled trials in patients with asthma, which lasted at least 3 months, evaluated long-acting beta-agonists compared with placebo or long-acting beta-agonists with inhaled corticosteroids compared with corticosteroids alone, and included at least 1 catastrophic event, defined as asthma-related intubation or death.
In pooled trial data that included 36,588 participants, long-acting beta-agonists increased catastrophic events 2-fold (Peto odds ratio [OR] 2.10; 95% confidence interval [CI], 1.37-3.22). Statistically significant increases were seen for long-acting beta-agonists with variable corticosteroids compared with placebo (OR 1.83; 95% CI, 1.14-2.95) and for concomitant treatment with corticosteroids compared with corticosteroids alone (OR 3.65; 95% CI, 1.39-9.55). Similar increases in risk were seen for variable and concomitant corticosteroid use, salmeterol and formoterol, and children and adults. When the analysis was restricted to trials with controlled corticosteroid use, given as part of the study intervention, concomitant treatment still increased catastrophic events compared with corticosteroids alone (OR 8.19; 95% CI, 1.10-61.18).
Long-acting beta-agonists increase the risk for asthma-related intubations and deaths, even when used in a controlled fashion with concomitant inhaled corticosteroids.
目前尚不清楚是否同时使用长效β-激动剂和吸入皮质类固醇会增加哮喘相关的插管和死亡。我们汇集了长效β-激动剂和不同剂量及合用吸入皮质类固醇的数据,以评估灾难性哮喘事件的风险。
我们对电子数据库、美国食品和药物管理局网站、临床试验注册处进行了检索,并通过 2008 年 12 月查阅了选定的参考文献。我们分析了持续至少 3 个月的、接受哮喘治疗的患者的随机对照试验,评价长效β-激动剂与安慰剂相比、与吸入皮质类固醇合用的长效β-激动剂与单独使用皮质类固醇相比的疗效,且试验至少包括 1 例灾难性事件,即哮喘相关的插管或死亡。
在纳入 36588 名患者的汇总试验数据中,长效β-激动剂使灾难性事件增加了 2 倍(Peto 比值比[OR]2.10;95%置信区间[CI],1.37-3.22)。与安慰剂相比,长效β-激动剂联合不同剂量皮质类固醇治疗(OR 1.83;95%CI,1.14-2.95)和联合皮质类固醇治疗(OR 3.65;95%CI,1.39-9.55)的风险显著增加。不同剂量皮质类固醇和联合皮质类固醇治疗、沙美特罗和福莫特罗、儿童和成人的风险增加情况相似。当分析仅限于试验中使用作为研究干预一部分的受控皮质类固醇时,与单独使用皮质类固醇相比,联合治疗仍会增加灾难性事件(OR 8.19;95%CI,1.10-61.18)。
即使以受控方式联合吸入皮质类固醇使用,长效β-激动剂也会增加哮喘相关插管和死亡的风险。