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

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...

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Veröffentlicht in:Infection control and hospital epidemiology 2019-04, Vol.40 (4), p.408-413
Hauptverfasser: Emmanuel Martinez, Aurélien, Widmer, Andreas, Frei, Reno, Pargger, Hans, Tuchscherer, Daniel, Marsch, Stephan, Egli, Adrian, Tschudin-Sutter, Sarah
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container_issue 4
container_start_page 408
container_title Infection control and hospital epidemiology
container_volume 40
creator Emmanuel Martinez, Aurélien
Widmer, Andreas
Frei, Reno
Pargger, Hans
Tuchscherer, Daniel
Marsch, Stephan
Egli, Adrian
Tschudin-Sutter, Sarah
description 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.
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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). 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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 &gt;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.</abstract><cop>United States</cop><pub>Cambridge University Press</pub><pmid>30786948</pmid><doi>10.1017/ice.2019.5</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-9709-0644</orcidid></addata></record>
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subjects Aged
Aged, 80 and over
Antibiotics
Bacteria
beta-Lactamases
Bone marrow
Carbapenems - therapeutic use
Carrier State - microbiology
Chronic obstructive pulmonary disease
Colonization
Comorbidity
Enterobacteriaceae Infections - drug therapy
Enterobacteriaceae Infections - epidemiology
Female
Gram-negative bacteria
Hematology
Hospitalization
Hospitals
Humans
Intensive care
Intensive Care Units
Male
Middle Aged
Multidrug resistant organisms
Nursing
Patient safety
Proportional Hazards Models
Prospective Studies
Rectum - microbiology
Risk Factors
Sepsis
Software
Spectrum analysis
Staphylococcus infections
Stem cell transplantation
Switzerland - epidemiology
Treatment Outcome
title ESBL-colonization at ICU admission: impact on subsequent infection, carbapenem-consumption, and outcome
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