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革兰氏阴性菌耐药性的出现:广谱β-内酰胺类药物使用的风险。

Emergence of resistance in gram-negative bacteria: a risk of broad-spectrum beta-lactam use.

作者信息

Dworzack D L

出版信息

Drug Intell Clin Pharm. 1986 Jul-Aug;20(7-8):562-7. doi: 10.1177/106002808602000711.

Abstract

A number of new beta-lactam antibiotics have been developed to overcome bacterial resistance to older agents. Such resistance usually is caused by plasmid-mediated, constituently produced beta-lactamases. Second- and third-generation cephalosporins, ureidopenicillins, acylamino penicillins, and monobactams generally are resistant to hydrolysis by these enzymes. However, inducible beta-lactamases may confer resistance to these antibiotics. This induction may occur spontaneously or in response to cefoxitin or other beta-lactam agents. The mechanisms by which inducible enzymes produce this resistance are reviewed and implications for the prophylactic and therapeutic use of newer beta-lactams are considered.

摘要

为克服细菌对旧有药物的耐药性,已研发出多种新型β-内酰胺类抗生素。此类耐药性通常由质粒介导、持续产生的β-内酰胺酶引起。第二代和第三代头孢菌素、脲基青霉素、酰氨基青霉素及单环β-内酰胺类抗生素通常对这些酶的水解具有抗性。然而,可诱导的β-内酰胺酶可能会使这些抗生素产生耐药性。这种诱导可能自发发生,也可能因头孢西丁或其他β-内酰胺类药物而引发。本文综述了可诱导酶产生这种耐药性的机制,并探讨了其对新型β-内酰胺类抗生素预防和治疗应用的影响。

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