Infections due to carbapenemase-producing bacteria, clinical burden, and impact of screening strategies on outcome.

Adequate antibiotic therapy Bactérie productrice de carbapénémases Carbapenem resistance Carbapenemase-producing bacteria Dépistage rectal Enterobacteriaceae Entérobactéries Rectal screening Résistance aux carbapénèmes Traitement antibiotique approprié

Journal

Medecine et maladies infectieuses
ISSN: 1769-6690
Titre abrégé: Med Mal Infect
Pays: France
ID NLM: 0311416

Informations de publication

Date de publication:
Nov 2020
Historique:
received: 07 06 2019
revised: 27 09 2019
accepted: 23 12 2019
pubmed: 10 2 2020
medline: 29 10 2021
entrez: 10 2 2020
Statut: ppublish

Résumé

To characterize the risk factors, impact of screening, and clinical burden of colonization and/or infection by carbapenemase-producing bacteria (CPB) in hospitalized patients. Retrospective study in a tertiary care hospital between 2008 and 2016. Among 88 included patients, 41% were colonized, 59% developed an infection, and 69% of all cases were hospital-acquired. Risk factors for CPB contamination included recent invasive medical device (94% of patients), antibiotic therapy (82%), travel abroad (17%), and hospitalization (>50%) with 80% of all patients with underlying chronic condition. Intestinal carriage represented 89% of all colonization cases and 50% of infections were located in the urinary tract. The recent use of mechanical ventilation devices was significantly more observed in infected patients than colonized patients. The most frequent CPB was Klebsiella pneumoniae and the most frequent carbapenemase was OXA-48. Overall mortality rate was 19%. Prevalence of CPB detection in intensive care units (ICU) based on systematical rectal screen swab upon admission remained <0.5%. The infected/colonized ratio (CPB colonization cases evolving into an infection) was 23%. The time between CPB infection diagnosis and start of appropriate antimicrobial therapy increased from 1 day in previously screened patients with positive CPB to 4 days in patients with previous negative or absent screening. Our results emphasize the importance of CPB screening in all ICU patients and in at-risk patients hospitalized in other units, to allow earlier adequate antibiotic therapy in case of infection which occurred in 23% of the colonized patients.

Identifiants

pubmed: 32035722
pii: S0399-077X(20)30024-X
doi: 10.1016/j.medmal.2019.12.011
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Bacterial Proteins 0
beta-Lactamases EC 3.5.2.6
carbapenemase EC 3.5.2.6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

658-664

Informations de copyright

Copyright © 2020 Elsevier Masson SAS. All rights reserved.

Auteurs

Louise Abramowicz (L)

Infectious Diseases Department, Saint-Pierre University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Michèle Gerard (M)

Infection Prevention and Control team, Saint-Pierre University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Delphine Martiny (D)

Department of Microbiology, Laboratoire Hospitalier Universitaire de Bruxelles-Universitair Laboratorium Brussel (LHUB-ULB), Brussels, Belgium; Faculté de Médecine et Pharmacie, Université de Mons (UMONS), Mons, Belgium.

Marc Delforge (M)

Infectious Diseases Department, Saint-Pierre University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Stéphane De Wit (S)

Infectious Diseases Department, Saint-Pierre University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Deborah Konopnicki (D)

Infectious Diseases Department, Saint-Pierre University Hospital, Université Libre de Bruxelles, Brussels, Belgium. Electronic address: deborah_konopnicki@stpierre-bru.be.

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Classifications MeSH