Acquisition of extended-spectrum cephalosporin-resistant Gram-negative bacteria: epidemiology and risk factors in a 6-year cohort of 507 severe trauma patients.

AmpC beta-lactamase Antimicrobial resistance Extended-spectrum beta-lactamase Extended-spectrum cephalosporin-resistant Gram-negative bacteria Trauma ICU

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:
12 2022
Historique:
received: 11 09 2022
revised: 05 10 2022
accepted: 09 10 2022
pubmed: 6 11 2022
medline: 21 12 2022
entrez: 5 11 2022
Statut: ppublish

Résumé

Severe trauma patients are at higher risk of infection and often exposed to antibiotics, which could favor acquisition of antimicrobial resistance. In this study, we aimed to assess prevalence, acquisition, and factors associated with acquisition of extended-spectrum cephalosporin-resistant Gram-negative bacteria (ESCR-GNB) in severe trauma patients. We conducted a retrospective monocentric cohort study in a French level one Regional Trauma Centre between 01 January 2010and 31 December 2015. Patients admitted for ≥ 7 days, with an Injury Severity Score ≥ 15, and ≥ 1 microbiological sample were included in the analysis. Prevalence and acquisition rate of ESCR-GNB were determined then, factors associated with ESCR-GNB acquisition were assessed using a Cox model. Of 1873 patients admitted during the study period, 507 were included (median Injury Severity Score = 29 [22-34] and median intensive care unit length of stay = 16 days [10-28]). Most of them (450; 89%) had an antimicrobial therapy. Prevalence of ESCR-GNB increased from 13% to 33% during intensive care unit stay, bringing the ESCR-GNB acquisition rate to 29%. Acquisition of ESCR-GNB was mainly related to AmpC beta-lactamase Enterobacterales and was independently associated with mechanical ventilation needs (hazard ratio [HR] = 6.39; 95% confidence interval [CI] [1.51-27.17]; P = 0.01), renal replacement therapy needs (HR = 2.44; 95% CI [1.24-4.79]; P = 0.01), exposure to cephalosporins (HR = 1.06; 95% CI [1.01-1.12]; P = 0.02), and/or combination therapy with non-beta-lactam antibiotics such as vancomycin, linezolid, clindamycin, or metronidazole (HR = 1.03; 95% CI [1.01-1.06]; P = 0.02). Acquisition of ESCR-GNB was prevalent in severe trauma patients. Our results suggest selecting antibiotics with caution, particularly in the most severely ill.

Identifiants

pubmed: 36334873
pii: S2213-7165(22)00235-1
doi: 10.1016/j.jgar.2022.10.005
pii:
doi:

Substances chimiques

Cephalosporins 0
Anti-Bacterial Agents 0
Monobactams 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

363-370

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Competing interests The authors report there are no competing interests to declare.

Auteurs

Romaric Larcher (R)

Trauma Critical Care Unit, Montpellier University Hospital, Montpellier, France; OcciTRAUMA Network, Regional Network of Medical Organization and Management for Severe Trauma in Occitanie, France; Department of Infectious and Tropical Diseases, Nimes University Hospital, Nimes, France; PhyMedExp, INSERM (French Institute of Health and Medical Research), CNRS (French National Centre for Scientific Research), University of Montpellier, Montpellier, France. Electronic address: r-larcher@outlook.fr.

Camille Maury (C)

Trauma Critical Care Unit, Montpellier University Hospital, Montpellier, France; OcciTRAUMA Network, Regional Network of Medical Organization and Management for Severe Trauma in Occitanie, France.

Guillaume Faivre (G)

Trauma Critical Care Unit, Montpellier University Hospital, Montpellier, France; OcciTRAUMA Network, Regional Network of Medical Organization and Management for Severe Trauma in Occitanie, France.

Geoffrey Dagod (G)

Trauma Critical Care Unit, Montpellier University Hospital, Montpellier, France; OcciTRAUMA Network, Regional Network of Medical Organization and Management for Severe Trauma in Occitanie, France.

Yann Dumont (Y)

Bacteriology Laboratory, Bacteriology-Virology Department, Montpellier University Hospital, Montpellier, France.

Vincent Le Moing (V)

Department of Infectious and Tropical Diseases, Montpellier University Hospital, Montpellier, France; TransVIHMI, IRD (Research and Development Institute), CNRS (French National Centre for Scientific Research), University of Montpellier, Montpellier, France.

Maxime Villiet (M)

Clinical Pharmacy Department, Montpellier University Hospital, Montpellier, France.

Xavier Capdevila (X)

Trauma Critical Care Unit, Montpellier University Hospital, Montpellier, France; OcciTRAUMA Network, Regional Network of Medical Organization and Management for Severe Trauma in Occitanie, France; Institute for Neurosciences of Montpellier (INM), INSERM (French Institute of Health and Medical Research), CNRS (French National Centre for Scientific Research), University of Montpellier, Montpellier, France.

Jonathan Charbit (J)

Trauma Critical Care Unit, Montpellier University Hospital, Montpellier, France; OcciTRAUMA Network, Regional Network of Medical Organization and Management for Severe Trauma in Occitanie, France.

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Classifications MeSH