Daniel R R
Pfizer Central Research, Sandwich, Kent, UK.
J Antimicrob Chemother. 1993 Jun;31 Suppl E:65-71. doi: 10.1093/jac/31.suppl_e.65.
An open randomized trial was conducted in 159 children (aged 1 to 8 years) with acute otitis media to compare the clinical efficacy of azithromycin (n = 105) and co-amoxiclav (n = 54). Azithromycin (10 mg/kg/day) was administered as a single dose for three days and co-amoxiclav was given tid for ten days at a dosage according to the manufacturer's instructions for the country. Of 103 evaluable azithromycin patients on day 3 to 5 after the start of therapy, 31 (30%) were considered cured, 67 (65%) improved and five (5%) failed compared with eight (15%) cured, 45 (83%) improved and one (2%) failed among the 54 evaluable co-amoxiclav treated patients. There was a higher number of azithromycin patients with complete resolution of symptoms at this first visit (P = 0.056). By day 10 to 12, clinical equivalence between the two treatment groups was observed with clinical cure in 86 (88%), improvement in 11 (11%) and failure in one (1%) of the 98 azithromycin patients, and in the 54 patients treated with co-amoxiclav, clinical cure was observed in 45 (83%), and improvement in nine (17%) patients. Both drugs were well tolerated and treatment related side-effects were reported in 8/105 (8%) azithromycin and 2/54 (4%) co-amoxiclav patients. In the azithromycin treatment group, these were predominantly mild to moderate gastrointestinal effects, whilst in the co-amoxiclav treatment group, both reports were of mild erythematous rash. One patient from each treatment group was withdrawn due to side-effects (azithromycin--diarrhoea and vomiting; co-amoxiclav--erythematous pruritic rash).(ABSTRACT TRUNCATED AT 250 WORDS)
对159名1至8岁的急性中耳炎儿童进行了一项开放性随机试验,以比较阿奇霉素(n = 105)和阿莫西林克拉维酸(n = 54)的临床疗效。阿奇霉素(10 mg/kg/天)单剂量给药三天,阿莫西林克拉维酸按照该国制造商的说明分三次每日给药十天。在治疗开始后第3至5天,103名可评估的阿奇霉素患者中,31名(30%)被认为治愈,67名(65%)病情改善,5名(5%)治疗失败;而在54名可评估的接受阿莫西林克拉维酸治疗的患者中,8名(15%)治愈,45名(83%)病情改善,1名(2%)治疗失败。首次就诊时,阿奇霉素组症状完全缓解的患者数量更多(P = 0.056)。到第10至12天,观察到两个治疗组之间临床疗效相当,98名阿奇霉素患者中86名(88%)临床治愈,11名(11%)病情改善,1名(1%)治疗失败;在54名接受阿莫西林克拉维酸治疗的患者中,45名(83%)临床治愈,9名(17%)病情改善。两种药物耐受性均良好,阿奇霉素组8/105(8%)、阿莫西林克拉维酸组2/54(4%)的患者报告有与治疗相关的副作用。在阿奇霉素治疗组中,主要是轻度至中度胃肠道反应,而在阿莫西林克拉维酸治疗组中,两份报告均为轻度红斑疹。每个治疗组各有一名患者因副作用退出治疗(阿奇霉素组——腹泻和呕吐;阿莫西林克拉维酸组——红斑瘙痒疹)。(摘要截断于250字)