首页> 美国卫生研究院文献>Oxford Open >1581. Comparative In Vitro Activity of Ceftolozane/tazobactam and Comparator Agents Against Enterobacteriaceae and Pseudomonas Aeruginosa Clinical Isolates in Colombia
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1581. Comparative In Vitro Activity of Ceftolozane/tazobactam and Comparator Agents Against Enterobacteriaceae and Pseudomonas Aeruginosa Clinical Isolates in Colombia

机译:1581.头孢洛赞/他唑巴坦和比较剂对肠杆菌科和铜绿假单胞菌临床分离株的体外比较活性

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摘要

BackgroundMultidrug-resistant Enterobacteriaceae (Ent) and Pseudomonas aeruginosa (Pae) are involved in a considerable number of healthcare-associated infections, thus representing a therapeutic challenge. Ceftolozane–tazobactam (C/T) is a combination of a novel cephalosporin with a known β-lactamase inhibitor. Ceftolozane has high affinity for penicillin-binding proteins, improved outer membrane permeability, increased stability against efflux and enhanced stability against chromosomal AmpC β-lactamases compared with other β-lactam antibiotics. This agent is not active against carbapenemases. We evaluated the in vitro activity of C/T against clinical isolates of Ent and Pae collected from 2016- 2017 and compared it to the activity of broad-spectrum antimicrobial agents.
机译:背景技术耐多药肠杆菌科(Ent)和铜绿假单胞菌(Pae)参与了大量与医疗保健相关的感染,因此代表了治疗挑战。头孢唑烷-他唑巴坦(C / T)是新型头孢菌素与已知的β-内酰胺酶抑制剂的组合。与其他β-内酰胺类抗生素相比,头孢唑烷对青霉素结合蛋白具有高亲和力,改善了外膜通透性,增加了对外排的稳定性,增强了对染色体AmpCβ-内酰胺酶的稳定性。该药物对碳青霉烯酶没有活性。我们评估了C / T对2016-2017年收集的Ent和Pae临床分离株的体外活性,并将其与广谱抗菌剂的活性进行了比较。

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