Geographical variation in therapy for bloodstream infections due to multidrug-resistant enterobacteriaceae: a post hoc analysis of the INCREMENT study
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Harris, Patrick N.A.; Pezzani, M. Diletta; Gutiérrez Gutiérrez, Belén; Viale, Pierluigi; Hsueh, Po-Ren; Ruiz Garbajosa, Patricia; Venditti, Mario; Tumbarello, Mario; Navarro Francisco, Carolina; Calbo, Esther; Akova, Murat; Giamarellou, Helen; Oliver, Antonio; Almirante, Benito; Gasch, Oriol; Martínez Martínez, Luis
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2017Derechos
© 2017, Elsevier. Licensed under the Creative Commons Reconocimiento-NoComercial-SinObraDerivada
Publicado en
Int J Antimicrob Agents. 2017 Nov;50(5):664-672
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Elsevier
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Palabras clave
Extended-spectrum beta-lactamase
Carbapenemase
Carbapenems
Beta-lactam/beta-lactamase inhibitors
Escherichia coli
Klebsiella pneumoniae
Resumen/Abstract
We aimed to describe regional differences in therapy for bloodstream infection (BSI) caused by extended-spectrum ?-lactamase-producing Enterobacteriaceae (ESBL-E) or carbapenemase-producing Enterobacteriaceae (CPE). 1,482 patients in 12 countries were included from an observational study of BSI caused by ESBL-E or CPE. Multivariate logistic regression was used to calculate adjusted odds ratios (aORs) for the influence of country of recruitment on empirical use of ?-lactam/?-lactamase inhibitors (BLBLI) or carbapenems, targeted use of BLBLI for ESBL-E and use of targeted combination therapy for CPE. The use of BLBLI for empirical therapy was least likely in sites from Israel (aOR 0.34, 95% CI 0.14-0.81), Greece (aOR 0.49, 95% CI 0.26-0.94) and Canada (aOR 0.31, 95% CI 0.11-0.88) but more likely in Italy (aOR 1.58, 95% CI 1.11-2.2) and Turkey (aOR 2.09, 95% CI 1.14-3.81), compared to Spain as a reference. Empirical carbapenems were more likely to be used in sites from Taiwan (aOR 1.73, 95% CI 1.03-2.92) and USA (aOR 1.89; 95% CI 1.05-3.39), and less likely in Italy (aOR 0.44, 95% CI 0.28-0.69) and Canada (aOR 0.10, 95% CI 0.01-0.74). Targeted BLBLI for ESBL-E was more likely in sites from Italy. Treatment at sites within Israel, Taiwan, Turkey and Brazil was associated with less combination therapy for CPE. Although this study does not provide precise data on the relative prevalence of ESBL-E or CPE, significant variation in therapy exists across countries even after adjustment for patient factors. A better understanding of what influences therapeutic choices for these infections will aid antimicrobial stewardship efforts.
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