| Literature DB >> 22290982 |
Vicki L Collins1, Dror Marchaim, Jason M Pogue, Judy Moshos, Suchitha Bheemreddy, Bharath Sunkara, Alex Shallal, Neelu Chugh, Sara Eiseler, Pragati Bhargava, Christopher Blunden, Paul R Lephart, Babar Irfan Memon, Kayoko Hayakawa, Odaliz Abreu-Lanfranco, Teena Chopra, L Silvia Munoz-Price, Yehuda Carmeli, Keith S Kaye.
Abstract
Ertapenem is active against extended-spectrum-β-lactamase (ESBL)-producing Enterobacteriaceae organisms but inactive against Pseudomonas aeruginosa and Acinetobacter 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-producing Enterobacteriaceae, 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).Entities:
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Year: 2012 PMID: 22290982 PMCID: PMC3318320 DOI: 10.1128/AAC.05913-11
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191