Author:
Collins Vicki L.,Marchaim Dror,Pogue Jason M.,Moshos Judy,Bheemreddy Suchitha,Sunkara Bharath,Shallal Alex,Chugh Neelu,Eiseler Sara,Bhargava Pragati,Blunden Christopher,Lephart Paul R.,Memon Babar Irfan,Hayakawa Kayoko,Abreu-Lanfranco Odaliz,Chopra Teena,Munoz-Price L. Silvia,Carmeli Yehuda,Kaye Keith S.
Abstract
ABSTRACTErtapenem is active against extended-spectrum-β-lactamase (ESBL)-producingEnterobacteriaceaeorganisms but inactive againstPseudomonas aeruginosaandAcinetobacter baumannii. Due to a lack of therapeutic data for ertapenem in the treatment of ESBL bloodstream infections (BSIs), group 2 carbapenems (e.g., imipenem or meropenem) are often preferred for treatment of ESBL-producingEnterobacteriaceae, although their antipseudomonal activity is unnecessary. From 2005 to 2010, 261 patients with ESBL BSIs were analyzed. Outcomes were equivalent between patients treated with ertapenem and those treated with group 2 carbapenems (mortality rates of 6% and 18%, respectively;P= 0.18).
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
52 articles.
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