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克拉霉素与硬脂酸红霉素治疗社区获得性肺炎的安全性和疗效对比研究。

A comparative safety and efficacy study of clarithromycin and erythromycin stearate in community-acquired pneumonia.

作者信息

Anderson G, Esmonde T S, Coles S, Macklin J, Carnegie C

机构信息

Newport Chest Clinic, Gwent, UK.

出版信息

J Antimicrob Chemother. 1991 Feb;27 Suppl A:117-24. doi: 10.1093/jac/27.suppl_a.117.

Abstract

The efficacy and tolerance of clarithromycin and erythromycin stearate in the treatment of community-acquired pneumonia were compared in a multicentre, double-blind randomized trial. Two hundred and eight adult patients were randomized to receive either clarithromycin 250 mg 12-hourly (96 patients) or erythromycin stearate 500 mg 6-hourly (112 patients), each for 14 days. One hundred and eight patients were evaluable for efficacy, 64 receiving clarithromycin and 44 erythromycin stearate. There was no significant difference between the two groups in terms of clinical cure (52% for clarithromycin, 40% for erythromycin) or clinical success (clinical cure and improvement; 89% for clarithromycin, 98% for erythromycin stearate), or radiological response (90% for both groups). An intention-to-treat analysis, including all patients entering the study revealed significant differences in favour of clarithromycin. The clinical cure rate after two weeks of treatment was 45% in those who received clarithromycin compared with 25% in the erythromycin stearate group (P = 0.003), whilst improvement in cough was observed in 97% and 80% of patients receiving clarithromycin and erythromycin stearate, respectively (P = 0.07). Adverse effects, mainly gastrointestinal, caused discontinuation of treatment in 4% (4/96) patients in the clarithromycin group in comparison with 19% (21/112) treated with erythromycin stearate (P less than 0.01). These results demonstrate that clarithromycin twice daily is at least as effective as four times daily erythromycin stearate for the treatment of community-acquired pneumonia and is better tolerated.

摘要

在一项多中心、双盲随机试验中,比较了克拉霉素和硬脂酸红霉素治疗社区获得性肺炎的疗效和耐受性。208例成年患者被随机分为两组,一组每12小时接受250mg克拉霉素治疗(96例患者),另一组每6小时接受500mg硬脂酸红霉素治疗(112例患者),疗程均为14天。108例患者可进行疗效评估,其中64例接受克拉霉素治疗,44例接受硬脂酸红霉素治疗。两组在临床治愈率(克拉霉素组为52%,硬脂酸红霉素组为40%)、临床有效率(临床治愈和改善;克拉霉素组为89%,硬脂酸红霉素组为98%)或影像学反应(两组均为90%)方面无显著差异。意向性分析,包括所有进入研究的患者,结果显示克拉霉素组有显著优势。治疗两周后的临床治愈率,克拉霉素组为45%,而硬脂酸红霉素组为25%(P = 0.003),同时,接受克拉霉素和硬脂酸红霉素治疗的患者中,咳嗽改善的比例分别为97%和80%(P = 0.07)。不良反应主要为胃肠道反应,克拉霉素组4%(4/96)的患者因不良反应停药,而硬脂酸红霉素组为19%(21/112)(P<0.01)。这些结果表明,每日两次服用克拉霉素治疗社区获得性肺炎的疗效至少与每日四次服用硬脂酸红霉素相当,且耐受性更好。

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