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莫西沙星五日疗法与克拉霉素七日疗法治疗慢性支气管炎急性加重的比较。

Five day moxifloxacin therapy compared with 7 day clarithromycin therapy for the treatment of acute exacerbations of chronic bronchitis.

作者信息

Wilson R, Kubin R, Ballin I, Deppermann K M, Bassaris H P, Leophonte P, Schreurs A J, Torres A, Sommerauer B

机构信息

Royal Brompton Hospital and Imperial College of Science, Technology and Medicine, National Heart and Lung Institute, London, UK.

出版信息

J Antimicrob Chemother. 1999 Oct;44(4):501-13. doi: 10.1093/jac/44.4.501.

Abstract

In this multinational, randomized, double-blind study, the efficacy and safety of a 5 day course of moxifloxacin 400 mg orally od was compared with that of a 7 day course of clarithromycin 500 mg orally bd. in 750 patients with acute exacerbations of chronic bronchitis, characterized by at least two of the symptoms: sputum purulence, increased sputum volume or increased dyspnoea. Seven days after the end of therapy, clinical cure was achieved for 89% (287 of 322) of efficacy-evaluable patients in the moxifloxacin group and 88% (289 of 327) of patients in the clarithromycin group (95% CI, -3.9%, 5.8%). At follow-up (21-28 days post-treatment), the continued clinical cure rates were 89% (256 of 287) for moxifloxacin and 89% (257 of 289) for clarithromycin. A total of 342 pathogenic bacteria were isolated from the sputum of 287 patients. The most common pathogens were Haemophilus influenzae (37%), Streptococcus pneumoniae (31%) and Moraxella catarrhalis (18%). Seven days post-treatment, a successful bacteriological response was obtained for 77% (89 of 115) of patients in the moxifloxacin group and 62% (71 of 114) of patients in the clarithromycin group, indicating superiority of moxifloxacin (95% CI, 3.6%, 26.9%). Both treatments were well tolerated with few adverse events. This study demonstrated that for the treatment of acute exacerbations of chronic bronchitis a 5 day course of moxifloxacin 400 mg od was clinically equivalent and bacteriologically superior to a 7 day course of clarithromycin 500 mg bd.

摘要

在这项跨国、随机、双盲研究中,将口服莫西沙星400mg每日一次、疗程5天的疗效和安全性,与口服克拉霉素500mg每日两次、疗程7天的疗效和安全性进行了比较。研究对象为750例慢性支气管炎急性加重患者,其特征为至少出现以下两种症状:痰液脓性、痰量增加或呼吸困难加重。治疗结束7天后,莫西沙星组89%(322例中的287例)可评估疗效的患者实现了临床治愈,克拉霉素组为88%(327例中的289例)(95%置信区间,-3.9%,5.8%)。在随访期(治疗后21 - 28天),莫西沙星的持续临床治愈率为89%(287例中的256例),克拉霉素为89%(289例中的257例)。共从287例患者的痰液中分离出342株病原菌。最常见的病原菌为流感嗜血杆菌(37%)、肺炎链球菌(31%)和卡他莫拉菌(18%)。治疗后7天,莫西沙星组77%(115例中的89例)患者获得了成功的细菌学反应,克拉霉素组为62%(114例中的71例),表明莫西沙星具有优越性(95%置信区间,3.6%,26.9%)。两种治疗的耐受性均良好,不良事件较少。本研究表明,对于慢性支气管炎急性加重的治疗,口服莫西沙星400mg每日一次、疗程5天在临床疗效上与口服克拉霉素500mg每日两次、疗程7天相当,但在细菌学方面更具优势。

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