Drehobl Margaret A, De Salvo Maria C, Lewis Drew E, Breen Jeanne D
Scripps Clinic-Clinical Research, San Diego, CA, USA.
Chest. 2005 Oct;128(4):2230-7. doi: 10.1378/chest.128.4.2230.
Community-acquired pneumonia (CAP) is a major cause of morbidity and mortality worldwide. The inability or failure of many subjects to adhere to standard antibiotic regimens, which may last up to 10 days, results in suboptimal antibiotic treatment. Treatment with a single-dose antibiotic regimen may improve compliance with prescribed therapy. A novel microsphere formulation of azithromycin provides a single-dose regimen while maintaining tolerability.
To compare the efficacy and safety of a single 2.0-g dose of azithromycin microspheres to that of an extended-release formulation of clarithromycin (1.0 g/d for 7 days) for the treatment of adults with mild-to-moderate CAP.
A phase III, multinational, multicenter, randomized, double-blind, double-dummy study, comparing single-dose azithromycin microspheres to extended-release clarithromycin, both administered orally.
Subjects with mild-to-moderate CAP (Fine class I and II) were included. The primary end point was clinical response at the test-of-cure (TOC) visit (days 14 to 21) in the clinical per protocol (CPP) population. The bacteriologic response at the TOC visit was assessed in subjects with a baseline pathogen.
A total of 501 subjects were randomized, and 499 were treated. Clinical cure rates at the TOC visit in the CPP population were 92.6% (187 of 202 subjects) for azithromycin microspheres and 94.7% (198 of 209 subjects) for extended-release clarithromycin. Overall pathogen eradication rates were 91.8% (123 of 134 subjects) for azithromycin microspheres and 90.5% (153 of 169 subjects) for extended-release clarithromycin. Both agents were well tolerated. The incidence of treatment-related adverse events was 26.3% with azithromycin microspheres and 24.6% with extended-release clarithromycin. Most adverse events were mild to moderate in severity.
A single 2.0-g dose of azithromycin microspheres was as effective and well tolerated as a 7-day course of extended-release clarithromycin in the treatment of adults with mild-to-moderate CAP.
社区获得性肺炎(CAP)是全球发病和死亡的主要原因。许多患者无法或未能坚持长达10天的标准抗生素治疗方案,导致抗生素治疗效果欠佳。单剂量抗生素治疗方案可能会提高患者对规定治疗的依从性。一种新型阿奇霉素微球制剂可提供单剂量治疗方案,同时保持耐受性。
比较单剂量2.0克阿奇霉素微球与克拉霉素缓释制剂(1.0克/天,共7天)治疗轻至中度CAP成人患者的疗效和安全性。
一项III期、多国、多中心、随机、双盲、双模拟研究,比较口服单剂量阿奇霉素微球与克拉霉素缓释制剂。
纳入轻至中度CAP(费氏I级和II级)患者。主要终点是临床符合方案(CPP)人群在治疗结束检查(TOC)访视(第14至21天)时的临床反应。对有基线病原体的患者在TOC访视时评估细菌学反应。
共501例患者随机分组,499例接受治疗。CPP人群中,阿奇霉素微球组在TOC访视时的临床治愈率为92.6%(202例患者中的187例),克拉霉素缓释制剂组为94.7%(209例患者中的198例)。总体病原体清除率,阿奇霉素微球组为91.8%(134例患者中的123例),克拉霉素缓释制剂组为90.5%(169例患者中的153例)。两种药物耐受性均良好。阿奇霉素微球治疗相关不良事件发生率为26.3%,克拉霉素缓释制剂为24.6%。大多数不良事件为轻至中度。
单剂量2.0克阿奇霉素微球在治疗轻至中度CAP成人患者时,疗效与7天疗程的克拉霉素缓释制剂相当,且耐受性良好。