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Azithromycin for bronchial asthma in adults: An effectiveness trial

机译:阿奇霉素治疗成人支气管哮喘的有效性试验

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Background: Macrolides have antimicrobial and anti-inflammatory properties that may be useful in the treatment of chronic asthma. Methods: We performed a randomized, placebo-controlled, double-blinded effectiveness trial of 12 weekly doses of adjunctive azithromycin, with follow-up to 1 year after randomization, in adults with persistent asthma. Measurements included overall asthma symptoms, asthma quality of life (AQL), and asthma control. Eligible subjects who declined to participate in randomization were offered enrollment into a parallel open-label (OL) azithromycin treatment arm. Results: Of 304 adult asthma patients screened, 97 (32%) were enrolled: 38 were randomized to azithromycin, 37 were randomized to placebo, and 22 opted in as OL subjects. OL subjects had higher rates of severe persistent asthma compared with randomized subjects (32% vs 8%, respectively; P=.012). At 1 year, compared with the placebo arm, subjects randomized to azithromycin were more likely to have an AQL score ≥1 unit increase compared with baseline, but this difference was not statistically significant (36% vs 21% for placebo; P=.335). Compared with placebo, OL subjects had significant improvements in overall asthma symptoms from baseline (P=.0196), AQL (P=.0006), and asthma control (P=.0148). Conclusions: Adults with asthma who were randomized to azithromycin did not show statistically significant improvement in asthma outcomes, although the study was underpowered to detect clinical improvement in 15% (number needed to treat = 7). Adults with severe persistent asthma who elected OL treatment documented clinical improvements in asthma symptoms, AQL, and asthma control that persisted after completion of OL azithromycin (number needed to treat = 2).
机译:背景:大环内酯类药物具有抗微生物和抗炎特性,可用于治疗慢性哮喘。方法:我们对患有持续性哮喘的成人进行了一项随机,安慰剂对照,双盲有效性试验,该试验为每周12剂辅助阿奇霉素,随访至随机化后1年。测量包括总体哮喘症状,哮喘生活质量(AQL)和哮喘控制。拒绝参加随机试验的合格受试者被纳入平行开放标签(OL)阿奇霉素治疗组。结果:在304例成人哮喘患者中,有97例(32%)入组:阿奇霉素随机分组38例,安慰剂随机分组37例,其中22例为OL受试者。与随机受试者相比,OL受试者的严重持续性哮喘发生率更高(分别为32%和8%; P = .012)。与安慰剂组相比,与安慰剂组相比,在1年时,与基线相比,阿奇霉素组的AQL评分更有可能增加≥1个单位,但这一差异没有统计学意义(36%vs安慰剂为21%; P = .335 )。与安慰剂相比,OL受试者的总体哮喘症状较基线(P = .0196),AQL(P = .0006)和哮喘控制(P = .0148)有显着改善。结论:随机接受阿奇霉素治疗的成人哮喘患者的哮喘结局没有统计学上的显着改善,尽管这项研究不足以检测出15%的临床改善(需要治疗的人数= 7)。选择OL治疗的患有严重持续性哮喘的成年人,其哮喘症状,AQL和哮喘控制的临床改善在OL阿奇霉素完成后仍持续存在(需要治疗的人数= 2)。

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