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Efficacy and Tolerability of Eight Antimicrobial Regimens in the Outpatient Treatment of Exacerbations of Chronic Obstructive Pulmonary Disease

机译:八种抗菌药物在门诊治疗慢性阻塞性肺疾病加重中的疗效和耐受性

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BACKGROUND: Bacterial infections are considered as the most important cause of exacerbations in patients with chronic obstructive pulmonary disease. AIM: To compare the efficacy and tolerability of eight antibiotics empirically administered for outpatient treatment of exacerbations of COPD. METHODS: We performed an observational study including 343 COPD patients with probable bacterial exacerbation (Group A and Group B COPD patients) managed in an outpatient setting. Eight antibiotic regimens each used 10 days were evaluated: amoxicillin/clavulonic acid, doxycycline, cefuroxime, cefixime, clarithromycin, roxithromycin, ciprofloxacin, and moxifloxacin. All patients were followed up for 30 days, with an intermediate visits at 5, 7 and 10 days at which the duration of symptoms and the side-effects of the drug were evaluated. RESULTS: The clinical success rate varied from 69.8% with doxycycline to 80.9% with moxifloxacin. The mean time to relief of symptoms varied from 5.6 days with moxifloxacin to 6.3 days with amoxicillin/clavulonic acid. Significant increase of the post-treatment FEV1 value was registered in all treatment groups. Relapse within the first 20 days was registered in the group receiving doxycycline, clarithromycin, and ciprofloxacin. The prevalence of the adverse events was low varying from 6.7% with cefuroxime to 11.3% with ciprofloxacin. CONCLUSION: Our findings suggest high clinical success rate and high safety of all studied regimens.
机译:背景:细菌感染被认为是慢性阻塞性肺疾病加重的最重要原因。目的:比较经验性使用八种抗生素在门诊治疗COPD急性加重中的疗效和耐受性。方法:我们进行了一项观察性研究,包括在门诊就诊的343例COPD可能伴有细菌急性发作的患者(A组和B组COPD患者)。评估了八个抗生素方案,每个方案均使用10天:阿莫西林/克拉维酸,强力霉素,头孢呋辛,头孢克肟,克拉霉素,罗红霉素,环丙沙星和莫西沙星。所有患者均接受了30天的随访,在第5、7和10天进行了中间访视,评估了症状的持续时间和药物的副作用。结果:临床成功率从强力霉素的69.8%到莫西沙星的80.9%不等。缓解症状的平均时间从莫西沙星的5.6天到阿莫西林/克拉维酸的6.3天不等。所有治疗组的治疗后FEV1值均显着增加。在接受强力霉素,克拉霉素和环丙沙星治疗的组中,前20天内出现了复发。不良事件的发生率低,从头孢呋辛的6.7%到环丙沙星的11.3%不等。结论:我们的发现表明,所有研究方案均具有较高的临床成功率和较高的安全性。

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