Comparison of clarithromycin suspension and amoxycillin syrup for the treatment of children with pharyngitis and/or tonsillitis.

N L Kearsley, A Campbell, A A Sanderson, R D Weir, M K Kamdar, S J Coles
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Abstract

Twenty-three general practices in the UK randomised 229 paediatric patients (aged 1-12 years, body weight > 8 kg) with clinical evidence suggestive of streptococcal tonsillitis and/or pharyngitis in this physician-blind study. Patients received either clarithromycin suspension (7.5 mg/kg twice daily) or amoxycillin syrup (125 mg/kg three times daily body weight < 25 kg, or 250 mg/kg three times daily body weight 25 kg) for 7 days and were followed up 3-8 days post treatment and 21-28 days later. Clinical and microbiological assessments were made at each visit. A total of 189 patients (98 on clarithromycin and 91 on amoxycillin) were clinically evaluable. At the post-treatment visit, clinical success rates were high and comparable: 98% on clarithromycin and 97% on amoxycillin. Streptococcus pyogenes was eradicated in 88% of clarithromycin patients and 86% of amoxycillin patients. Both treatments were well tolerated. In conclusion, clarithromycin suspension was as safe and at least as effective as amoxycillin syrup for the treatment of pharyngitis and/or tonsillitis in children, and would be a suitable alternative therapy.

克拉霉素混悬液与阿莫西林糖浆治疗儿童咽炎和/或扁桃体炎的比较。
在这项医生盲法研究中,英国23家全科医院随机选取229例临床证据提示链球菌扁桃体炎和/或咽炎的儿童患者(年龄1-12岁,体重> 8kg)。患者接受克拉霉素混悬液(7.5 mg/kg每日2次)或阿莫西林糖浆(125 mg/kg每日3次体重< 25 kg,或250 mg/kg每日3次体重25 kg)治疗7天,治疗后3-8天和21-28天随访。在每次访问时进行临床和微生物学评估。共有189例患者(克拉霉素组98例,阿莫西林组91例)具有临床可评价性。在治疗后的随访中,临床成功率很高且具有可比性:克拉霉素组为98%,阿莫西林组为97%。88%的克拉霉素患者和86%的阿莫西林患者的化脓性链球菌被根除。两种治疗方法均耐受良好。综上所述,克拉霉素混悬液与阿莫西林糖浆治疗儿童咽炎和/或扁桃体炎一样安全,至少同样有效,是一种合适的替代治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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