ESBL-colonization at ICU admission: impact on subsequent infection, carbapenem-consumption, and outcome.
Aged
Aged, 80 and over
Carbapenems
/ therapeutic use
Carrier State
/ microbiology
Enterobacteriaceae Infections
/ drug therapy
Female
Humans
Intensive Care Units
Male
Middle Aged
Proportional Hazards Models
Prospective Studies
Rectum
/ microbiology
Risk Factors
Switzerland
/ epidemiology
Treatment Outcome
beta-Lactamases
Journal
Infection control and hospital epidemiology
ISSN: 1559-6834
Titre abrégé: Infect Control Hosp Epidemiol
Pays: United States
ID NLM: 8804099
Informations de publication
Date de publication:
04 2019
04 2019
Historique:
pubmed:
23
2
2019
medline:
10
3
2020
entrez:
22
2
2019
Statut:
ppublish
Résumé
To determine whether colonization with extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-PE) predicts the risk for subsequent infection and impacts carbapenem-consumption and outcome in intensive care unit (ICU) patients. Prospective cohort study. The 2 ICUs in the University Hospital Basel in Switzerland. All patients admitted to the 2 ICUs providing mechanical ventilation and an expected ICU stay >48 hours. Patients were routinely screened for ESBL-PE carriage by rectal swab on admission. Competing risk regression analyses were applied to calculate hazard ratios (HRs) for infection with ESBL-PE and mortality. Length of hospital stay, length of ICU stay, and duration of carbapenem exposure were compared using the Mann-Whitney U test. Among 302 patients, 24 (8.0%) were colonized with ESBL-PE on ICU admission. Infections with ESBL-PE occurred in 4 patients, of whom 3 (75%) were identified as ESBL-PE colonized on admission. ESBL-PE colonization on admission was associated with subsequent ESBL-PE infection (hazard ratio [HR], 25.52; 95% confidence interval [CI], 2.40-271.41; P = .007) and exposure to carbapenems (HR, 2.42; 95% CI, 1.01-5.79; P = .047), whereas duration of carbapenem exposure did not differ in relation to ESBL-PE colonization (median, 7 days [IQR, 3-8 days] vs median, 6 days [IQR 3-9 days]; P = 0.983). Patients colonized with ESBL-PE were not at increased risk for death overall (HR, 1.00; 95% CI, 0.44-2.30; P = .993) or death attributable to infection (HR, 1.20; 95% CI, 0.28-5.11; P = .808). Screening strategies for detection of ESBL-PE colonization on ICU admission may allow the identification of patients at highest risk for ESBL-PE infection and the correct allocation of empiric carbapenem treatment.
Identifiants
pubmed: 30786948
pii: S0899823X19000059
doi: 10.1017/ice.2019.5
doi:
Substances chimiques
Carbapenems
0
beta-Lactamases
EC 3.5.2.6
Types de publication
Comparative Study
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM