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舒他西林细粒剂在儿科患者中的临床评价

[Clinical evaluation of sultamicillin fine granules in pediatric patients].

作者信息

Ito S, Mayumi M, Mikawa H

机构信息

Department of Pediatrics, School of Medicine, Kyoto University.

出版信息

Jpn J Antibiot. 1988 Dec;41(12):1914-22.

PMID:3249364
Abstract

The clinical efficacy and the safety of sultamicillin (SBTPC) fine granules, which is a semisynthetic beta-lactam antibiotic for oral use with ester linked ampicillin (ABPC) and sulbactam (SBT), a beta-lactamase inhibitor, in a ratio of 1:1, were evaluated in 31 patients with ages from 6 months old to 10 years and 4 months old with various bacterial infections. The results obtained are summarized as follows. 1. In a pharmacokinetic study with a dose level of 10 mg/kg SBTPC, serum levels reached a peak in 1 hour after oral administration, with peak levels of 3.94 micrograms/ml for ABPC and 4.08 micrograms/ml for SBT. Half-lives of ABPC and SBT were 64.8 minutes and 63.6 minutes, respectively. The urinary excretion of ABPC over 6 hours was 66.2% and that of SBT was 60.4%. 2. SBTPC fine granules were administered orally to 1 patient with bronchitis, 9 patients with bronchopneumonia, 7 patients with tonsillitis, 4 patients with scarlet fever, 1 patient each with pharyngitis, otitis media, purulent parotitis, and urinary tract infection and 6 patients with skin and soft tissue infections at daily dosage levels of 26.1-31.6 mg/kg divided into 3 or 4. Clinical evaluations of these 31 patients were as follows, excellent: 20 patients, good: 10 patients, poor: 1 patient. The efficacy rate was 96.8%. 3. Diarrhea was observed in a patient with otitis media on the fifth day of SBTPC administration. No other clinical adverse reaction was observed in any of the remaining 30 patients. No abnormal laboratory data was found in any of 23 patients who were subjected to laboratory examinations for safety.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

舒他西林(SBTPC)细颗粒是一种半合成β-内酰胺类口服抗生素,由酯基连接的氨苄西林(ABPC)和β-内酰胺酶抑制剂舒巴坦(SBT)按1:1比例组成。对31例年龄在6个月至10岁4个月之间的各种细菌感染患者进行了舒他西林细颗粒临床疗效和安全性评估。结果总结如下:1. 在剂量水平为10mg/kg SBTPC的药代动力学研究中,口服给药后1小时血清水平达到峰值,ABPC峰值水平为3.94μg/ml,SBT为4.08μg/ml。ABPC和SBT的半衰期分别为64.8分钟和63.6分钟。6小时内ABPC的尿排泄率为66.2%,SBT为60.4%。2. 对1例支气管炎、9例支气管肺炎、7例扁桃体炎、4例猩红热、1例咽炎、1例中耳炎、1例化脓性腮腺炎、1例尿路感染患者以及6例皮肤和软组织感染患者口服SBTPC细颗粒,日剂量为26.1 - 31.6mg/kg,分3或4次服用。这31例患者的临床评估如下:优:20例,良:10例,差:1例。有效率为96.8%。3. 在服用SBTPC第5天,1例中耳炎患者出现腹泻。其余30例患者未观察到其他临床不良反应。23例接受安全性实验室检查的患者未发现异常实验室数据。(摘要截选至250字)

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