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The emerging threat of acquired carbapenemases in Gram-negative bacteria.

机译:革兰氏阴性细菌中获得性碳青霉烯酶的新威胁。

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Since their introduction into clinical practice, carbapenems have been among the most powerful antibiotics for treating serious infections caused by Gram-negative nosocomial pathogens, including Enterobactericeae, Pseudomonas aeruginosa and Acinetobacter baumannii [I]. Remarkable stability towards most beta-lactamases, including the extended-spectrum beta-lacta-mases (ESBLs), is one of the features accounting for the unprecedented broad spectrum of activity exhibited by carbapenems. Therefore, the emergence of beta-lactamases with carbapenem-hydrolyzing activity (carbapenemases)-which can confer resistance to carbapenems in major Gram-negative pathogens-is of major clinical concern. This concern is further reinforced by the awareness that carbapenems are the most effective agents for treatment of serious infections caused by ESBL-producing Enterobacteria-ceae [2,3], which are undergoing a massive increase both in hospitals and in community settings [4].
机译:自从进入临床以来,碳青霉烯类抗生素一直是治疗由革兰氏阴性医院病原体(包括肠杆菌,铜绿假单胞菌和鲍曼不动杆菌)引起的严重感染的最有效的抗生素之一。对大多数β-内酰胺酶(包括广谱β-内酯物质(ESBLs))具有显着的稳定性,这是碳青霉烯类药物具有前所未有的广谱活性的特征之一。因此,具有碳青霉烯水解活性的β-内酰胺酶的出现(卡巴碳烯酶)(可赋予革兰氏阴性主要病原体对碳青霉烯的抗性)是临床上需要关注的问题。碳青霉烯类是治疗由产ESBL的肠杆菌-大肠埃希菌引起的严重感染的最有效药物,这一认识进一步增强了这种担忧[2,3],医院和社区环境中,碳青霉烯类药物都在大量增加[4]。 。

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