Disney F A, Dillon H, Blumer J L, Dudding B A, McLinn S E, Nelson D B, Selbst S M
Department of Pediatrics, Elmwood Pediatric Group, Rochester, NY.
Am J Dis Child. 1992 Nov;146(11):1324-7. doi: 10.1001/archpedi.1992.02160230082024.
To determine whether cephalexin or penicillin is more effective in the treatment of group A beta-hemolytic streptococcal tonsillopharyngitis in children.
Randomized, double-blind, crossover study conducted from 1981 to 1984.
Seven pediatric practices in the United States, including private offices and pediatric clinics.
Of the 654 patients, 525 children and adolescents with clinical evidence of tonsillitis or pharyngitis and throat cultures positive for group A beta-hemolytic streptococcal infection were evaluable. Eighty percent of patients completed the study; none were withdrawn because of adverse reaction.
Children and adolescents who had acute illness suggestive of group A beta-hemolytic streptococcal infection were enrolled in the study. Treatment was continued if the throat culture was positive for group A beta-hemolytic streptococcal infection.
Four doses of cephalexin and penicillin (27 mg/kg per day) were prescribed to be taken on an empty stomach for 10 days.
MEASUREMENTS/MAIN RESULTS: Symptomatic clinical failure occurred in 8% of penicillin-treated patients and in 3% of cephalexin-treated patients. Bacteriologic failure rates were 11% in the penicillin treatment group and 7% in the cephalexin treatment group. The combined treatment failure rate of clinical relapse plus asymptomatic bacteriologic failure was 19% in the penicillin treatment group and 10% in the cephalexin treatment group. Paired antistreptolysin-O titer increased significantly in 62.3% of penicillin-treated patients and in 64.2% of cephalexin-treated patients. Similarly, anti-DNase B titers rose 52.2% in penicillin-treated patients and 52.4% in cephalexin-treated patients.
Cephalexin is a more effective drug than penicillin in the treatment of group A beta-hemolytic streptococcal throat infection in children.
确定头孢氨苄或青霉素在治疗儿童A组β溶血性链球菌扁桃体咽炎方面哪种更有效。
1981年至1984年进行的随机、双盲、交叉研究。
美国的七家儿科医疗机构,包括私人诊所和儿科门诊。
654例患者中,525例患有扁桃体炎或咽炎临床证据且咽拭子培养A组β溶血性链球菌感染呈阳性的儿童和青少年可进行评估。80%的患者完成了研究;无人因不良反应退出。
患有提示A组β溶血性链球菌感染的急性疾病的儿童和青少年纳入研究。如果咽拭子培养A组β溶血性链球菌感染呈阳性,则继续治疗。
开具四剂头孢氨苄和青霉素(每日27mg/kg),空腹服用10天。
测量指标/主要结果:青霉素治疗组有8%的患者出现有症状的临床治疗失败,头孢氨苄治疗组为3%。青霉素治疗组的细菌学失败率为11%,头孢氨苄治疗组为7%。青霉素治疗组临床复发加无症状细菌学失败的联合治疗失败率为19%,头孢氨苄治疗组为10%。青霉素治疗组62.3%的患者抗链球菌溶血素-O滴度显著升高,头孢氨苄治疗组为64.2%。同样,青霉素治疗组抗脱氧核糖核酸酶B滴度升高52.2%,头孢氨苄治疗组为52.4%。
在治疗儿童A组β溶血性链球菌咽喉感染方面,头孢氨苄比青霉素更有效。