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阿奇霉素与青霉素V治疗儿童急性链球菌性咽炎和扁桃体炎的多中心评估

Multicentre evaluation of azithromycin and penicillin V in the treatment of acute streptococcal pharyngitis and tonsillitis in children.

作者信息

Hamill J

机构信息

Pasley Road Health Centre, Leicester, UK.

出版信息

J Antimicrob Chemother. 1993 Jun;31 Suppl E:89-94. doi: 10.1093/jac/31.suppl_e.89.

Abstract

Of 96 children (aged 2-12 years) with either acute pharyngitis or acute tonsillitis, 49 received a single daily dose of azithromycin 10 mg/kg (maximum 500 mg) for three days, and 47 received penicillin V at a dose of 125 mg or 250 mg qid (depending on body weight) for ten days. Clinical assessments and laboratory safety tests were performed during and after therapy. Before enrollment, all patients were screened for group A beta-haemolytic streptococci (GABHS) with a rapid test, and a throat swab was taken for confirmatory culture. The presence of GABHS at baseline was confirmed in 41 azithromycin- and 44 penicillin V-treated patients. Cure or improvement was seen in 98% and 100% of azithromycin- and penicillin V-treated patients, respectively. At day 11, bacterial eradication was achieved in 39/41 (95%) azithromycin-treated patients, 38 (93%) of whom were considered clinically cured, while one patient (2%) relapsed. In the penicillin V group, 42/44 (95%) had GABHS eradicated, with 41 (93%) clinically cured and three patients (7%) improved. The remaining two patients in each group were clinically cured despite persistence of Streptococcus pyogenes. At follow-up evaluation (day 30), re-occurrence was observed in 5/37 (14%) and 3/40 (8%) of azithromycin- and penicillin V-treated patients, respectively; all patients were asymptomatic. Both drugs were well-tolerated with only two patients in the azithromycin group complaining of side effects. Treatment related laboratory test abnormalities were observed in 6/47 (13%) and 4/45 (9%) azithromycin- and penicillin V-treated patients, respectively, but none was judged to be clinically significant.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在96名患有急性咽炎或急性扁桃体炎的儿童(年龄2至12岁)中,49名儿童连续三天每日单次服用10毫克/千克阿奇霉素(最大剂量500毫克),47名儿童每日四次服用125毫克或250毫克青霉素V(取决于体重),疗程为十天。在治疗期间及之后进行了临床评估和实验室安全性测试。入组前,所有患者均通过快速检测筛查A组β溶血性链球菌(GABHS),并采集咽拭子进行确诊培养。在41名接受阿奇霉素治疗和44名接受青霉素V治疗的患者中,基线时均确诊存在GABHS。阿奇霉素治疗组和青霉素V治疗组分别有98%和100%的患者治愈或病情改善。在第11天,41名接受阿奇霉素治疗的患者中有39名(95%)实现细菌清除,其中38名(93%)被认为临床治愈,1名患者(2%)复发。在青霉素V组中,44名患者中有42名(95%)GABHS被清除,41名(93%)临床治愈,3名患者(7%)病情改善。每组其余两名患者尽管化脓性链球菌持续存在,但临床治愈。在随访评估(第30天)时,阿奇霉素治疗组和青霉素V治疗组分别有5/37(14%)和3/40(8%)的患者复发;所有患者均无症状。两种药物耐受性良好,阿奇霉素组只有两名患者抱怨有副作用。阿奇霉素治疗组和青霉素V治疗组分别有6/47(13%)和4/45(9%)的患者出现与治疗相关的实验室检查异常,但均未被判定具有临床意义。(摘要截选至250词)

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