McLinn S E
Scottsdale Pediatric Center, AZ.
Pediatr Infect Dis J. 1987 Oct;6(10):997-1001. doi: 10.1097/00006454-198710000-00042.
Cefixime, a new third generation cephalosporin antibiotic for oral use, was evaluated for safety and efficacy in the treatment of children with acute otitis media with effusion. Fifteen United States clinical investigators participated in the multicenter clinical trial. One hundred twenty children were randomly assigned to a 10-day course of either cefixime, 8 mg/kg, given daily (qd) (60 patients) or amoxicillin, 40 mg/kg/day, administered in three divided doses (60 patients). Tympanocentesis was performed on each patient before therapy was initiated. Pathogens were isolated from a middle ear aspirate in 88% of the cases. Of the specimens from which pathogens were cultured, 33% yielded Haemophilus sp., 41% Streptococcus pneumoniae and 6% Branhamella catarrhalis. Of the 120 patients, 64 (30 cefixime and 34 amoxicillin) were evaluable for assessment of efficacy. Favorable clinical responses (cure or improvement) were obtained in 93% of cefixime-treated patients and in 94% of amoxicillin-treated patients. Overall, bacteriologic eradication rates (as determined by clinical criteria) were 94 and 95%, respectively. Clinical failure or relapse was documented in 2 of 30 (7%) patients treated with cefixime and in 2 of 34 (6%) patients treated with amoxicillin. Gastrointestinal disturbance and rash were significantly more common in children treated with cefixime (22 and 15%, respectively) than in those taking amoxicillin (8 and 2%, respectively), but in only one case was it necessary to discontinue medication because of these adverse effects (rash). Results of this study demonstrate that cefixime given once daily is as safe and effective as amoxicillin in the treatment of acute otitis media with effusion in children and has the possible advantage of less frequent dosing.
头孢克肟是一种新型口服第三代头孢菌素抗生素,对其治疗儿童急性分泌性中耳炎的安全性和有效性进行了评估。15名美国临床研究人员参与了这项多中心临床试验。120名儿童被随机分配接受为期10天的治疗,其中60名患者每日服用一次头孢克肟,剂量为8mg/kg;另外60名患者每日服用三次阿莫西林,剂量为40mg/kg/天。在开始治疗前,对每位患者进行了鼓膜穿刺术。88%的病例中耳吸出物中分离出了病原体。在培养出病原体的标本中,33%为嗜血杆菌属,41%为肺炎链球菌,6%为卡他布兰汉菌。120名患者中,64名(30名服用头孢克肟和34名服用阿莫西林)可评估疗效。服用头孢克肟治疗的患者中有93%获得了良好的临床反应(治愈或改善),服用阿莫西林治疗的患者中有94%获得了良好的临床反应。总体而言,细菌学根除率(根据临床标准确定)分别为94%和95%。服用头孢克肟治疗的30名患者中有2名(7%)出现临床失败或复发,服用阿莫西林治疗的34名患者中有2名(6%)出现临床失败或复发。服用头孢克肟治疗的儿童出现胃肠道不适和皮疹的情况(分别为22%和15%)明显比服用阿莫西林的儿童(分别为8%和2%)更常见,但只有1例因这些不良反应(皮疹)而停药。这项研究的结果表明,每日服用一次头孢克肟在治疗儿童急性分泌性中耳炎方面与阿莫西林一样安全有效,并且可能具有给药频率较低的优势。