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口服头孢菌素对青霉素、阿莫西林或红霉素不敏感的肺炎链球菌儿科分离株的体外活性。

In vitro activity of oral cephalosporins against pediatric isolates of Streptococcus pneumoniae non-susceptible to penicillin, amoxicillin or erythromycin.

作者信息

Fenoll A, Giménez M J, Robledo O, Aguilar L, Tarragó D, Granizo J J, Gimeno M, Coronel P

机构信息

Spanish National Reference Pneumococcal Laboratory, Instituto de Salud Carlos III, Madrid, Spain.

出版信息

J Chemother. 2008 Apr;20(2):175-9. doi: 10.1179/joc.2008.20.2.175.

Abstract

The aim of this study was to evaluate the effects of penicillin, amoxicillin or erythromycin resistance on the in vitro activity of oral cephalosporins against Streptococcus pneumoniae pediatric isolates. A total of 282 pediatric isolates received during 2005 in the Spanish Reference Pneumococcal Laboratory were tested by agar dilution: 104 strains were penicillin-susceptible, 72 intermediate, and 106 resistant. Serotypes 9 and 14 were the most troublesome with <10% susceptibility to oral cephalosporins. Cefditoren exhibited the highest intrinsic activity against penicillin/amoxicillin-resistant pneumococci, with MIC(90s )of 0.5 microg/ml, followed by cefotaxime (2 microg/ml), cefpodoxime (4 microg/ml), cefuroxime (16 microg/ml), and cefaclor/cefixime (>or= 32 microg/ml), with 0% susceptibility to cefaclor, cefuroxime and cefpodoxime. Cefditoren 0.5 microg/ml inhibited 95.3%, 95.5%, and 98.6% of penicillin-, amoxicillin-, and erythromycin-resistant isolates, respectively. Susceptibility to oral cephalosporins shifted from >90% in penicillin-susceptible isolates to approximately 38% for cefuroxime/cefpodoxime and approximately 7% for cefaclor in penicillin-intermediate, and to 0% in resistant isolates. Despite the different in vitro activity of oral cephalosporins, full resistance to penicillin or amoxicillin implied lack of susceptibility to all oral cephalosporins with defined CLSI breakpoints, rendering them inadequate as empirical treatment in countries with a high prevalence of penicillin resistance.

摘要

本研究旨在评估青霉素、阿莫西林或红霉素耐药性对口服头孢菌素针对肺炎链球菌儿科分离株的体外活性的影响。2005年西班牙参考肺炎球菌实验室收到的总共282株儿科分离株通过琼脂稀释法进行检测:104株对青霉素敏感,72株中介,106株耐药。9型和14型血清型最为棘手,对口服头孢菌素的敏感性低于10%。头孢妥仑对青霉素/阿莫西林耐药的肺炎球菌表现出最高的固有活性,MIC(90s)为0.5微克/毫升,其次是头孢噻肟(2微克/毫升)、头孢泊肟(4微克/毫升)、头孢呋辛(16微克/毫升)以及头孢克洛/头孢克肟(≥32微克/毫升),头孢克洛、头孢呋辛和头孢泊肟的敏感性为0%。0.5微克/毫升的头孢妥仑分别抑制了95.3%、95.5%和98.6%的青霉素、阿莫西林和红霉素耐药分离株。口服头孢菌素的敏感性从青霉素敏感分离株中的>90%,转变为青霉素中介分离株中头孢呋辛/头孢泊肟约为38%、头孢克洛约为7%,而在耐药分离株中为0%。尽管口服头孢菌素的体外活性不同,但对青霉素或阿莫西林的完全耐药意味着对所有具有明确CLSI断点的口服头孢菌素均不敏感,这使得它们在青霉素耐药率高的国家作为经验性治疗并不充分。

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