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[大环内酯类抗生素阿奇霉素在儿科患者中的临床研究]

[Clinical study of a macrolide antibiotic, azithromycin, in pediatric patients].

作者信息

Kobayashi Y, Kino M, Higashino H, Takaya J, Harada Y, Kawamura Y, Kawasaki H, Nagao Y

机构信息

Department of Pediatrics, Kansai Medical University.

出版信息

Jpn J Antibiot. 1996 Nov;49(11):1004-12.

PMID:8988412
Abstract

Azithromycin (AZM), 10% fine granules or 100 mg capsules, were given orally to 27 children with various pediatric infections. The results of the study are shown below. 1. Pharmacokinetic investigation. We studied plasma and urinary concentrations after 100 mg AZM capsules were given. One patient received 8.3 mg/kg of AZM once a day for 3 days, and AZM concentration in plasma was 0.033 microgram/ml 48 hours after the final dosing. Doses of 8.3 and 12.5 mg/kg body weight of AZM were respectively given to two patients once daily for 3 days. As a result, AZM concentrations in urine during a period between 96 and 120 hours post-dosing were 1.67 and 4.53 micrograms/ml, respectively, and urinary excretion rate in 120 hours after the first dosing was 10.54% in the patient that was given 12.5 mg/kg. 2. Clinical investigation. Clinical efficacies were examined in 24 patients. Excellent results were obtained in 7 patients, good results in 14 patients, hence the clinical efficacy rate was 87.5%. Bacteriologically, Haemophilus influenzae strains isolates from 2 patients were eradicated in 1 and decreased in the other. Safety was evaluated in 26 patients. An adverse reaction was observed in 1 patient (urticaria). Abnormal laboratory test results were observed in 2 patients, decreased WBC in 1 and elevation of eosinophils in the other. The above results suggest that AZM is a useful oral antibiotic for pediatric patients with infection with susceptible organisms.

摘要

对27名患有各种儿科感染的儿童口服给予阿奇霉素(AZM),剂型为10%细颗粒或100毫克胶囊。研究结果如下。1. 药代动力学研究。我们研究了给予100毫克AZM胶囊后的血浆和尿液浓度。一名患者每天一次接受8.3毫克/千克的AZM,共给药3天,末次给药后48小时血浆中AZM浓度为0.033微克/毫升。分别给予两名患者每天一次8.3毫克/千克和12.5毫克/千克体重的AZM,共给药3天。结果,给药后96至120小时期间尿液中AZM浓度分别为1.67微克/毫升和4.53微克/毫升,给予12.5毫克/千克的患者首次给药后120小时的尿排泄率为10.54%。2. 临床研究。对24名患者的临床疗效进行了检查。7名患者获得优异结果,14名患者获得良好结果,因此临床有效率为87.5%。从细菌学角度看,2名患者分离出的流感嗜血杆菌菌株,1例被根除,另1例数量减少。对26名患者进行了安全性评估。1名患者出现不良反应(荨麻疹)。2名患者观察到实验室检查结果异常,1名白细胞减少,另1名嗜酸性粒细胞升高。上述结果表明,AZM对于感染易感病原体的儿科患者是一种有用的口服抗生素。

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