Department of Respiratory Medicine, Middlemore Hospital, Counties Manukau District Health Board, Auckland, New Zealand.
Lancet. 2012 Aug 18;380(9842):660-7. doi: 10.1016/S0140-6736(12)60953-2.
Azithromycin is a macrolide antibiotic with anti-inflammatory and immunomodulatory properties. We tested the hypothesis that azithromycin would decrease the frequency of exacerbations, increase lung function, and improve health-related quality of life in patients with non-cystic fibrosis bronchiectasis.
We undertook a randomised, double-blind, placebo-controlled trial at three centres in New Zealand. Between Feb 12, 2008, and Oct 15, 2009, we enrolled patients who were 18 years or older, had had at least one pulmonary exacerbation requiring antibiotic treatment in the past year, and had a diagnosis of bronchiectasis defined by high-resolution CT scan. We randomly assigned patients to receive 500 mg azithromycin or placebo three times a week for 6 months in a 1:1 ratio, with a permuted block size of six and sequential assignment stratified by centre. Participants, research assistants, and investigators were masked to treatment allocation. The coprimary endpoints were rate of event-based exacerbations in the 6-month treatment period, change in forced expiratory volume in 1 s (FEV(1)) before bronchodilation, and change in total score on St George's respiratory questionnaire (SGRQ). Analyses were by intention to treat. This study is registered with the Australian New Zealand Clinical Trials Registry, number ACTRN12607000641493.
71 patients were in the azithromycin group and 70 in the placebo group. The rate of event-based exacerbations was 0·59 per patient in the azithromycin group and 1·57 per patient in the placebo group in the 6-month treatment period (rate ratio 0·38, 95% CI 0·26-0·54; p<0·0001). Prebronchodilator FEV(1) did not change from baseline in the azithromycin group and decreased by 0·04 L in the placebo group, but the difference was not significant (0·04 L, 95% CI -0·03 to 0·12; p=0·251). Additionally, change in SGRQ total score did not differ between the azithromycin (-5·17 units) and placebo groups (-1·92 units; difference -3·25, 95% CI -7·21 to 0·72; p=0·108).
Azithromycin is a new option for prevention of exacerbations in patients with non-cystic fibrosis bronchiectasis with a history of at least one exacerbation in the past year.
Health Research Council of New Zealand and Auckland District Health Board Charitable Trust.
阿奇霉素是一种具有抗炎和免疫调节特性的大环内酯类抗生素。我们检验了一个假设,即阿奇霉素可以减少非囊性纤维化支气管扩张症患者的恶化频率,增加肺功能,并改善与健康相关的生活质量。
我们在新西兰的三个中心进行了一项随机、双盲、安慰剂对照试验。在 2008 年 2 月 12 日至 2009 年 10 月 15 日期间,我们招募了年龄在 18 岁或以上的患者,这些患者在过去一年中至少有一次需要抗生素治疗的肺部恶化,并且通过高分辨率 CT 扫描诊断为支气管扩张症。我们将患者随机分配接受每周三次 500 毫克阿奇霉素或安慰剂治疗,比例为 1:1,使用大小为 6 的置换块和按中心分层的连续分配。参与者、研究助理和研究人员对治疗分配进行了掩蔽。主要终点是 6 个月治疗期间基于事件的恶化率、支气管扩张前用力呼气量(FEV(1))的变化以及圣乔治呼吸问卷(SGRQ)总评分的变化。分析采用意向治疗。这项研究在澳大利亚和新西兰临床试验注册中心注册,编号为 ACTRN12607000641493。
阿奇霉素组有 71 名患者,安慰剂组有 70 名患者。在 6 个月的治疗期间,阿奇霉素组的基于事件的恶化率为 0.59 例/患者,安慰剂组为 1.57 例/患者(发生率比为 0.38,95%CI 0.26-0.54;p<0.0001)。阿奇霉素组的支气管扩张前 FEV(1)与基线相比没有变化,安慰剂组下降了 0.04 L,但差异无统计学意义(0.04 L,95%CI -0.03 至 0.12;p=0.251)。此外,阿奇霉素组(-5.17 单位)和安慰剂组(-1.92 单位)的 SGRQ 总评分变化也没有差异(差异-3.25,95%CI -7.21 至 0.72;p=0.108)。
阿奇霉素是一种治疗非囊性纤维化支气管扩张症患者的新方法,这些患者在过去一年中至少有一次恶化。
新西兰健康研究理事会和奥克兰地区卫生委员会慈善信托基金。