Howard J B, Howard J E
Am J Dis Child. 1978 Nov;132(11):1085-7. doi: 10.1001/archpedi.1978.02120360041005.
A total of 118 children between 6 months and 10 years of age with acute urinary tract infection were treated in a random; double-blind manner with 12 mg/kg/day of trimethoprim-sulfamethoxazole (61 patients) or 50 mg/kg/day of sulfamethoxazole (57 patients) for ten days. Mean trimethoprim and sulfamethoxazole susceptibilities of Escherichia coli isolated from these patients were 1.2 and 0.6 microgram/ml, respectively. Mean serum concentrations of trimethoprim and sulfamethoxazole were 1.8 and 62 microgram/ml, respectively, one hour after the dose. Of the children who completed the ten days of prescribed medication, clinical and bacteriological cure was confirmed immediately after treatment for all but one patient in each group. Most patients in each treatment group with recurrent infections had underlying urological abnormalities. Severe hematological, renal, or hepatic toxicity requiring interruption of treatment was not encountered. No advantage of trimethoprim-sulfamethoxazole over sulfamethoxazole alone for acute urinary tract infection was demonstrated.
118名6个月至10岁的急性尿路感染儿童被随机、双盲地分为两组,一组每天服用12mg/kg的甲氧苄啶-磺胺甲恶唑(共61例),另一组每天服用50mg/kg的磺胺甲恶唑(共57例),疗程均为10天。从这些患者中分离出的大肠杆菌对甲氧苄啶和磺胺甲恶唑的平均药敏浓度分别为1.2微克/毫升和0.6微克/毫升。服药1小时后,甲氧苄啶和磺胺甲恶唑的平均血清浓度分别为1.8微克/毫升和62微克/毫升。在完成规定疗程的患儿中,除每组各有1例患者外,其余患儿在治疗后均立即得到临床及细菌学治愈的确认。每个治疗组中大多数反复感染的患者都有潜在的泌尿系统异常。未出现需要中断治疗的严重血液学、肾脏或肝脏毒性。未证明甲氧苄啶-磺胺甲恶唑比单用磺胺甲恶唑治疗急性尿路感染更具优势。