Department of Respiratory and Sleep Medicine, Hunter Medical Research Institute, Newcastle, NSW, Australia; Priority Research Centre for Healthy Lungs, The University of Newcastle, Newcastle, NSW, Australia; Woolcock Institute of Medical Research, Sydney, NSW, Australia.
Faculty of Medicine, The University of Queensland, Brisbane, QLD, Australia; Department of Thoracic Medicine, The Prince Charles Hospital, Brisbane, QLD, Australia.
Lancet. 2017 Aug 12;390(10095):659-668. doi: 10.1016/S0140-6736(17)31281-3. Epub 2017 Jul 4.
Exacerbations of asthma cause a substantial global illness burden. Adults with uncontrolled persistent asthma despite maintenance treatment require additional therapy. Since macrolide antibiotics can be used to treat persistent asthma, we aimed to assess the efficacy and safety of oral azithromycin as add-on therapy in patients with uncontrolled persistent asthma on medium-to-high dose inhaled corticosteroids plus a long-acting bronchodilator.
We did a randomised, double-blind, placebo controlled parallel group trial to determine whether oral azithromycin decreases the frequency of asthma exacerbations in adults (≥18 years) with symptomatic asthma despite current use of inhaled corticosteroid and long-acting bronchodilator, and who had no hearing impairment or abnormal prolongation of the corrected QT interval. Patients were randomly assigned (1:1) to receive azithromycin 500 mg or placebo three times per week for 48 weeks. Patients were centrally allocated using concealed random allocation from a computer-generated random numbers table with permuted blocks of 4 or 6 and stratification for centre and past smoking. Primary efficacy endpoints were the rate of total (severe and moderate) asthma exacerbations over 48 weeks and asthma quality of life. Data were analysed on an intention-to-treat basis. The trial is registered at the Australian and New Zealand Clinical Trials Registry (ANZCTR), number 12609000197235.
Between June 12, 2009, and Jan 31, 2015, 420 patients were randomly assigned (213 in the azithromycin group and 207 in the placebo group). Azithromycin reduced asthma exacerbations (1·07 per patient-year [95% CI 0·85-1·29]) compared with placebo (1·86 per patient-year [1·54-2·18]; incidence rate ratio [IRR] 0·59 [95% CI 0·47-0·74]; p<0·0001). The proportion of patients experiencing at least one asthma exacerbation was reduced by azithromycin treatment (127 [61%] patients in the placebo group vs 94 [44%] patients in the azithromycin group, p<0·0001). Azithromycin significantly improved asthma-related quality of life (adjusted mean difference, 0·36 [95% CI 0·21-0·52]; p=0·001). Diarrhoea was more common in azithromycin-treated patients (72 [34%] vs 39 [19%]; p=0·001).
Adults with persistent symptomatic asthma experience fewer asthma exacerbations and improved quality of life when treated with oral azithromycin for 48 weeks. Azithromycin might be a useful add-on therapy in persistent asthma.
National Health and Medical Research Council of Australia, John Hunter Hospital Charitable Trust.
哮喘加重会导致全球疾病负担的大幅增加。尽管接受了维持治疗,但仍存在哮喘控制不佳的持续性哮喘的成年人需要额外的治疗。由于大环内酯类抗生素可用于治疗持续性哮喘,我们旨在评估口服阿奇霉素作为附加疗法在中至高剂量吸入皮质类固醇加长效支气管扩张剂治疗的哮喘控制不佳的持续性哮喘患者中的疗效和安全性。
我们进行了一项随机、双盲、安慰剂对照的平行组试验,以确定口服阿奇霉素是否能降低有症状哮喘的成年人(≥18 岁)在使用吸入皮质类固醇和长效支气管扩张剂时哮喘加重的频率,这些患者没有听力损伤或校正 QT 间期异常延长。患者被随机分配(1:1)接受阿奇霉素 500mg 或安慰剂每周 3 次,共 48 周。患者使用计算机生成的随机数表进行中心随机分配,使用隐蔽随机分配,置换块大小为 4 或 6,分层因素为中心和既往吸烟。主要疗效终点是 48 周内总(严重和中度)哮喘加重的发生率和哮喘生活质量。数据按意向治疗进行分析。该试验在澳大利亚和新西兰临床试验注册处(ANZCTR)注册,编号为 12609000197235。
2009 年 6 月 12 日至 2015 年 1 月 31 日期间,共有 420 名患者被随机分配(阿奇霉素组 213 名,安慰剂组 207 名)。与安慰剂相比,阿奇霉素降低了哮喘加重的发生率(1.07 例/患者年[95%CI 0.85-1.29])(1.86 例/患者年[1.54-2.18];发病率比[IRR]0.59[95%CI 0.47-0.74];p<0.0001)。阿奇霉素治疗降低了至少一次哮喘加重的患者比例(安慰剂组 127[61%]例患者与阿奇霉素组 94[44%]例患者,p<0.0001)。阿奇霉素显著改善了哮喘相关的生活质量(调整平均差异,0.36[95%CI 0.21-0.52];p=0.001)。阿奇霉素治疗组腹泻更为常见(72[34%]例患者与 39[19%]例患者;p=0.001)。
对于持续存在症状性哮喘的成年人,口服阿奇霉素治疗 48 周可减少哮喘加重并改善生活质量。阿奇霉素可能是持续性哮喘的一种有用的附加治疗方法。
澳大利亚国家卫生和医学研究委员会,约翰亨特医院慈善信托基金。