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Non-intravenous, carbapenem-sparing antibiotics for the treatment of bacteremia due to ESBL or AMP-C β-lactamase: A propensity score study

Authors :
Ribera A
Sanz X
Ayestarán A
Ortega L
Pigrau C
Montserrat Sierra
Nuria Fernández-Hidalgo
Yolanda Meije
Martínez-Montauti J
Jesús Rodríguez-Baño
Clemente M
Loureiro-Amigo J
Morales-Cartagena A
Publication Year :
2018
Publisher :
Cold Spring Harbor Laboratory, 2018.

Abstract

Introduction Carbapenems are considered the treatment of choice for extended-spectrum β-lactamase (ESBL) or Amp-C β-lactamase-producing Enterobacteriaceae bacteremia. Data on the effectiveness of non-intravenous carbapenem-sparing antibiotic options are limited. Objective To compare the 30 day-mortality and clinical failures associated with the use of carbapenems vs an alternative non-intravenous antibiotic for the definitive treatment of ESBL/Amp-C positive Enterobacteriaceae bacteremia. Methods This is a 12-year retrospective study (2004 – 2015) including all patients with bacteremia due to ESBL/Amp-C-producing Enterobacteriaceae. Given the lack of randomization of the initial therapies, a propensity score for receiving carbapenems was calculated. Results There were 1115 patients with a first episode of bacteremia due to E. coli or K. pneumoniae, of which 123 were ESBL/Amp C-positive (11%). There were 101 eligible patients: 59 in the carbapenem group and 42 in the alternative treatment group (cotrimoxazole 59.5%, quinolones 21.4%). The most frequent sources of infection were urinary (63%) and biliary (15%). Compared to the carbapenem group, patients treated with the alternative regimen had a shorter hospital stay (median [IQR]: 7 days [5-10] vs 12 days [9-18], p Conclusion Alternative non-IV carbapenem-sparing antibiotics could have a role in the definitive treatment of ESBL/Amp-C-positive Enterobacteriaceae bloodstream infections, allowing a reduction in carbapenem use. The use of cotrimoxazole in this setting has shown favourable results. ESBL: Extended-spectrum β-lactamase Amp-C: Amp-C β-lactamase BL/BLIs: β-lactam/β-lactamase inhibitor combinations IV: Intravenous TMP-SMX: Trimethoprim-Sulfamethoxazole Some of the data contained in this article were presented at the 55th Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC) and at the 28th International Congress of Chemotherapy Meeting (ICC), San Diego, USA, 2015.

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....d3c80c00f13eb3a40fd9033464631a7a