Evaluation of the activity of cefepime/enmetazobactam against Enterobacterales bacteria collected in Europe from 2019 to 2021, including third-generation cephalosporin-resistant isolates.

ESBL Enterobacterales enmetazobactam

Journal

Journal of global antimicrobial resistance
ISSN: 2213-7173
Titre abrégé: J Glob Antimicrob Resist
Pays: Netherlands
ID NLM: 101622459

Informations de publication

Date de publication:
07 May 2024
Historique:
received: 13 12 2023
revised: 05 04 2024
accepted: 19 04 2024
medline: 10 5 2024
pubmed: 10 5 2024
entrez: 9 5 2024
Statut: aheadofprint

Résumé

This study was performed to investigate the activity of the novel ß-lactam/ß-lactamase inhibitor combination cefepime/enmetazobactam, against recently circulating Enterobacterales isolates from Europe in 2019 to 2021. A total of 2,627 isolates were collected and antimicrobial susceptibility determined according to EUCAST guidelines. Isolates with phenotypic resistance to ceftriaxone and ceftazidime (but susceptible to meropenem), and isolates non-susceptible to meropenem were screened for the presence of ß-lactamases. Overall, susceptibility to third-generation cephalosporins was 77%, and 97.3% were susceptible to meropenem. Cefepime/enmetazobactam susceptibility was 97.9% (72% of these isolates were Klebsiella pneumoniae from Italy), compared to 80.0% susceptibility to piperacillin/tazobactam and 99.4% to ceftazidime/avibactam. A total of 320 isolates (12.2%) were resistant to third-generation cephalosporins but susceptible to meropenem and virtually all (96.3%) carried an ESBL with or without an AmpC and these were all susceptible to cefepime/enmetazobactam. Most meropenem-non-susceptible isolates carried a KPC (68%) which were not inhibited by cefepime/enmetazobactam but were inhibited by ceftazidime/avibactam. Most meropenem-non-susceptible isolates carrying OXA-48 (9/12 isolates) were susceptible to cefepime/enmetazobactam. Cefepime/enmetazobactam was highly active against Enterobacterales isolates, especially those resistant to third-generation cephalosporins. These data suggest that cefepime/enmetazobactam could be used as a carbapenem sparing agent to replace piperacillin/tazobactam.

Identifiants

pubmed: 38723712
pii: S2213-7165(24)00086-9
doi: 10.1016/j.jgar.2024.04.014
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Competing interests AB was a paid consultant for Allecra Therapeutics GmbH during this study; MA, ASH and IM are paid consultants for Advanz Pharma UK; SH and NK are employees of IHMA Europe Sàrl; ND and JQ are employees of Advanz Pharma UK

Auteurs

Ian Morrissey (I)

Antimicrobial Focus, Sawbridgeworth, UK. Electronic address: ian@antimicrobialfocus.com.

Stephen Hawser (S)

IHMA Europe Sàrl, Monthey, Switzerland.

Nimmi Kothari (N)

IHMA Europe Sàrl, Monthey, Switzerland.

Nathalie Dunkel (N)

Advanz Pharma UK, London, United Kingdom.

Juan Quevedo (J)

Advanz Pharma UK, London, United Kingdom.

Adam Belley (A)

Allecra Therapeutics SAS, Saint-Louis, France.

Anne Santerre Henriksen (AS)

Maxel Consulting, Jyllinge, Denmark.

Marie Attwood (M)

Bristol Centre for Antimicrobial Research & Evaluation (BCARE), Bristol, UK.

Classifications MeSH