Publication: Empiric Therapy With Carbapenem-Sparing Regimens for Bloodstream Infections due to Extended-Spectrum β-Lactamase-Producing Enterobacteriaceae: Results From the INCREMENT Cohort.
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Identifiers
Date
2017-07-13
Authors
Palacios-Baena, Zaira Raquel
Gutierrez-Gutierrez, Belen
Calbo, Esther
Almirante, Benito
Viale, Pierluigi
Oliver, Antonio
Pintado, Vicente
Gasch, Oriol
Martinez-Martinez, Luis
Pitout, Johann
Advisors
Journal Title
Journal ISSN
Volume Title
Publisher
Oxford University Press
Abstract
There is little information about the efficacy of active alternative drugs to carbapenems except β-lactam/β-lactamase inhibitors for the treatment of bloodstream infections (BSIs) due to extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E). The objective of this study was to assess the outcomes of patients with BSI due to ESBL-E who received empiric therapy with such drugs (other active drugs [OADs]) or carbapenems. A multinational retrospective cohort study of patients with BSI due to ESBL-E who received empiric treatment with OADs or carbapenems was performed. Cox regression including a propensity score for receiving OADs was performed to analyze 30-day all-cause mortality as main outcome. Clinical failure and length of stay were also analyzed. Overall, 335 patients were included; 249 received empiric carbapenems and 86 OADs. The most frequent OADs were aminoglycosides (43 patients) and fluoroquinolones (20 patients). Empiric therapy with OADs was not associated with mortality (hazard ratio [HR], 0.75; 95% confidence interval [CI], .38-1.48) in the Cox regression analysis. Propensity score-matched pairs, subgroups, and sensitivity analyses did not show different trends; specifically, the adjusted HR for aminoglycosides was 1.05 (95% CI, .51-2.16). OADs were neither associated with 14-day clinical failure (adjusted odds ratio, 0.62; 95% CI, .29-1.36) nor length of hospital stay. We were unable to show that empiric treatment with OAD was associated with a worse outcome compared with carbapenems. This information allows more options to be considered for empiric therapy, at least for some patients, depending on local susceptibility patterns of ESBL-E.
Description
MeSH Terms
Anti-bacterial agents
Bacteremia
Carbapenems
Enterobacteriaceae
Enterobacteriaceae infections
Female
Humans
Kaplan-Meier estimate
Male
Middle aged
Retrospective studies
beta-Lactam resistance
beta-Lactamases
Bacteremia
Carbapenems
Enterobacteriaceae
Enterobacteriaceae infections
Female
Humans
Kaplan-Meier estimate
Male
Middle aged
Retrospective studies
beta-Lactam resistance
beta-Lactamases
DeCS Terms
Antibacterianos
Carbapenémicos
Estimación de Kaplan-Meier
Infecciones por Enterobacteriaceae
Resistencia betalactámica
Carbapenémicos
Estimación de Kaplan-Meier
Infecciones por Enterobacteriaceae
Resistencia betalactámica
CIE Terms
Keywords
Aminoglycosides, Antimicrobial resistance, Bloodstream infections, Extended-spectrum β-lactamase–producing Enterobacteriaceae, Therapy
Citation
Palacios-Baena ZR, Gutiérrez-Gutiérrez B, Calbo E, Almirante B, Viale P, Oliver A, et al. Empiric Therapy With Carbapenem-Sparing Regimens for Bloodstream Infections due to Extended-Spectrum β-Lactamase-Producing Enterobacteriaceae: Results From the INCREMENT Cohort. Clin Infect Dis. 2017 Oct 30;65(10):1615-1623