ESBL-colonization at ICU admission: impact on subsequent infection, carbapenem-consumption, and outcome.


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
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

Pagination

408-413

Auteurs

Aurélien Emmanuel Martinez (A)

Division of Infectious Diseases and Hospital Epidemiology,University Hospital Basel,Basel,Switzerland.

Andreas Widmer (A)

Division of Infectious Diseases and Hospital Epidemiology,University Hospital Basel,Basel,Switzerland.

Reno Frei (R)

Division of Infectious Diseases and Hospital Epidemiology,University Hospital Basel,Basel,Switzerland.

Hans Pargger (H)

Department of Anesthesiology, Operative Intensive Care, Preclinical Emergency Medicine and Pain Management,University Hospital Basel,Basel,Switzerland.

Daniel Tuchscherer (D)

Department of Anesthesiology, Operative Intensive Care, Preclinical Emergency Medicine and Pain Management,University Hospital Basel,Basel,Switzerland.

Stephan Marsch (S)

Department of Intensive Care Medicine,University Hospital of Basel,Basel,Switzerland.

Adrian Egli (A)

Clinical Microbiology,University Hospital Basel,Basel,Switzerland.

Sarah Tschudin-Sutter (S)

Division of Infectious Diseases and Hospital Epidemiology,University Hospital Basel,Basel,Switzerland.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH