首页> 外文期刊>The lancet. Respiratory medicine. >Azithromycin maintenance treatment in patients with frequent exacerbations of chronic obstructive pulmonary disease (COLUMBUS): A randomised, double-blind, placebo-controlled trial
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Azithromycin maintenance treatment in patients with frequent exacerbations of chronic obstructive pulmonary disease (COLUMBUS): A randomised, double-blind, placebo-controlled trial

机译:阿奇霉素维持治疗对慢性阻塞性肺疾病频繁加重的患者(COLUMBUS):一项随机,双盲,安慰剂对照试验

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Background: Macrolide resistance is an increasing problem; there is therefore debate about when to implement maintenance treatment with macrolides in patients with chronic obstructive pulmonary disease (COPD). We aimed to investigate whether patients with COPD who had received treatment for three or more exacerbations in the previous year would have a decrease in exacerbation rate when maintenance treatment with azithromycin was added to standard care. Methods: We did a randomised, double-blind, placebo-controlled, single-centre trial in the Netherlands between May 19, 2010, and June 18, 2013. Patients (≥18 years) with a diagnosis of COPD who had received treatment for three or more exacerbations in the previous year were randomly assigned, via a computer-generated randomisation sequence with permuted block sizes of ten, to receive 500 mg azithromycin or placebo three times a week for 12 months. Randomisation was stratified by use of long-term, low-dose prednisolone (≤10 mg daily). Patients and investigators were masked to group allocation. The primary endpoint was rate of exacerbations of COPD in the year of treatment. Analysis was by intention to treat. This study is registered with ClinicalTrials.gov, number NCT00985244. Findings: We randomly assigned 92 patients to the azithromycin group (n=47) or the placebo group (n=45), of whom 41 (87%) versus 36 (80%) completed the study. We recorded 84 exacerbations in patients in the azithromycin group compared with 129 in those in the placebo group. The unadjusted exacerbation rate per patient per year was 1·94 (95% CI 1·50-2·52) for the azithromycin group and 3·22 (2·62-3·97) for the placebo group. After adjustment, azithromycin resulted in a significant reduction in the exacerbation rate versus placebo (0·58, 95% CI 0·42-0·79; p=0·001). Three (6%) patients in the azithromycin group reported serious adverse events compared with five (11%) in the placebo group. During follow-up, the most common adverse event was diarrhoea in the azithromycin group (nine [19%] patients vs one [2%] in the placebo group; p=0·015). Interpretation: Maintenance treatment with azithromycin significantly decreased the exacerbation rate compared with placebo and should therefore be considered for use in patients with COPD who have the frequent exacerbator phenotype and are refractory to standard care.
机译:背景:大环内酯的耐药性是一个日益严重的问题。因此,对于慢性阻塞性肺疾病(COPD)患者何时应使用大环内酯类维持治疗存在争议。我们的目的是调查在标准护理中加入阿奇霉素的维持治疗后,在过去一年中接受过3次或更多急性加重治疗的COPD患者的急性加重率是否降低。方法:我们在2010年5月19日至2013年6月18日之间在荷兰进行了一项随机,双盲,安慰剂对照,单中心试验。诊断为COPD的18岁以上患者接受了以下药物的治疗:通过计算机生成的随机序列,将前一年中的三个或更多急性发作随机分配,每个变异块大小为十个,每周12次,每周三次,接受500 mg阿奇霉素或安慰剂。使用长期,低剂量泼尼松龙(每天≤10mg)对随机分组进行分层。患者和研究者被掩盖到小组分配中。主要终点是治疗年份COPD的恶化率。分析是按意向进行的。该研究已在ClinicalTrials.gov上注册,编号为NCT00985244。结果:我们将92例患者随机分为阿奇霉素组(n = 47)或安慰剂组(n = 45),其中41名(87%)对36名(80%)完成了研究。我们记录了阿奇霉素组患者的84次加重,而安慰剂组为129次。阿奇霉素组每名患者每年未经调整的急性加重率为1·94(95%CI 1·50-2·52),安慰剂组为3·22(2·62-3·97)。调整后,阿奇霉素与安慰剂相比导致急性发作率显着降低(0·58,95%CI 0·42-0·79; p = 0·001)。阿奇霉素组三例(6%)报告严重不良事件,而安慰剂组五例(11%)。在随访期间,最常见的不良事件是阿奇霉素组的腹泻(安慰剂组中9名[19%]患者与1名[2%]; p = 0·015)。解释:与安慰剂相比,阿奇霉素维持治疗可显着降低加重率,因此应考虑用于加重表型频繁且标准治疗难治的COPD患者。

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