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肠球菌对甲氧苄啶-磺胺甲恶唑的体内外敏感性。一个陷阱。

In vivo v in vitro susceptibility of enterococcus to trimethoprim-sulfamethoxazole. A pitfall.

作者信息

Goodhart G L

出版信息

JAMA. 1984 Nov 16;252(19):2748-9.

PMID:6333522
Abstract

Two patients with uncomplicated enterococcal urinary tract infections were treated with trimethoprim-sulfamethoxazole based on in vitro susceptibilities. Bacteremia developed in both patients and they recovered only after the cessation of trimethoprim-sulfamethoxazole administration and institution of therapy with penicillin G potassium or vancomycin hydrochloride plus streptomycin sulfate. Although the enterococcus may appear susceptible to trimethoprim-sulfamethoxazole in vitro, it escapes the antifolate activity of the drug in vivo by its unique ability to incorporate preformed exogenous folates. The practice by clinical microbiology laboratories of reporting the susceptibilities of the enterococcus to drugs other than the penicillins or vancomycin is misleading and potentially dangerous.

摘要

两名患有单纯性肠球菌尿路感染的患者根据体外药敏试验结果接受了甲氧苄啶-磺胺甲恶唑治疗。两名患者均发生了菌血症,仅在停用甲氧苄啶-磺胺甲恶唑并开始使用青霉素G钾或盐酸万古霉素加硫酸链霉素治疗后才康复。尽管肠球菌在体外可能对甲氧苄啶-磺胺甲恶唑敏感,但它凭借摄取预先形成的外源性叶酸的独特能力在体内逃避了该药物的抗叶酸活性。临床微生物学实验室报告肠球菌对青霉素或万古霉素以外其他药物的药敏情况的做法具有误导性且可能存在危险。

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