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头孢噻肟治疗革兰氏阳性病原体引起感染的概述。

An overview of cefotaxime therapy in infections caused by gram-positive pathogens.

作者信息

Iannini P B

出版信息

Infection. 1985;13 Suppl 1:S3-6. doi: 10.1007/BF01644208.

Abstract

The in vitro activity of cefotaxime and other third-generation cephalosporins against gram-positive pathogens is generally considered to be less than that of earlier cephalosporins, such as cefazolin. A review of pooled pre-release data collected by numerous investigators and supplied by Hoechst-Roussel made it possible to evaluate the clinical and bacteriologic efficacy of cefotaxime in more than 900 infections caused by gram-positive organisms. The most commonly isolated pre-treatment organisms were Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pneumoniae, and other streptococcal species. The overall clinical efficacy rate was 95% and the bacteriologic eradication rate was 94.5%. Side-effects were limited to rash in two, diarrhea in one and fever in one. Pain at the administration site was reported by four patients. Comparative studies with cefazolin against S. aureus showed no statistically significant differences in efficacy. The highest failure rates were seen in enterococcal urinary tract infections, as predicted by in vitro sensitivity tests. Cefotaxime appears to be a safe, effective antibiotic for the therapy of infections caused by gram-positive pathogens.

摘要

头孢噻肟及其他第三代头孢菌素对革兰氏阳性病原体的体外活性通常被认为低于早期头孢菌素,如头孢唑林。对众多研究者收集并由赫斯特-罗素公司提供的汇总预发布数据进行回顾,使得评估头孢噻肟在900多例由革兰氏阳性菌引起的感染中的临床和细菌学疗效成为可能。治疗前最常分离出的病原体是金黄色葡萄球菌、表皮葡萄球菌、肺炎链球菌及其他链球菌属。总体临床有效率为95%,细菌清除率为94.5%。副作用局限于2例皮疹、1例腹泻和1例发热。4例患者报告了给药部位疼痛。与头孢唑林针对金黄色葡萄球菌的对照研究显示,疗效无统计学显著差异。正如体外敏感性试验所预测的,肠球菌尿路感染的失败率最高。头孢噻肟似乎是治疗革兰氏阳性病原体引起的感染的一种安全、有效的抗生素。

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