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Patient-level analysis of incident vancomycin-resistant enterococci colonization and antibiotic days of therapy
J A McKINNELL1, D F Kunz2, S A Moser3
1Infectious Disease Clinical Outcomes Research Unit (ID-CORE),Division of Infectious Disease,Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center,Torrance,CA,USA.
Abstract:
Vancomycin-resistant enterococci (VRE) infections are a public health threat associated with increased patient mortality and healthcare costs. Antibiotic usage, particularly cephalosporins, has been associated with VRE colonization and VRE bloodstream infections (VRE BSI). We examined the relationship between antimicrobial usage and incident VRE colonization at the individual patient level. Prospective, weekly surveillance was undertaken for incident VRE colonization defined by negative admission but positive surveillance swab in a medical intensive care unit over a 17-month period. Antimicrobial exposure was quantified as days of therapy (DOT)/1000 patient-days. Multiple logistic regression was used to analyse incident VRE colonization and antibiotic DOT, controlling for demographic and clinical covariates. Ninety-six percent (1398/1454) of admissions were swabbed within 24 h of intensive care unit (ICU) arrival and of the 380 patients in the ICU long enough for weekly surveillance, 83 (22%) developed incident VRE colonization. Incident colonization was associated in bivariate analysis with male gender, more previous hospital admissions, longer previous hospital stay, and use of cefepime/ceftazidime, fluconazole, azithromycin, and metronidazole (P < 0·05). After controlling for demographic and clinical covariates, metronidazole was the only antibiotic independently associated with incident VRE colonization (odds ratio 2·0, 95% confidence interval 1·2-3·3, P < 0·009). Our findings suggest that risk of incident VRE colonization differs between individual antibiotic agents and support the possibility that antimicrobial stewardship may impact VRE colonization and infection.
Insights
Metronidazole use, not other antibiotics, independently increased the risk of vancomycin-resistant enterococci (VRE) colonization in ICU patients. Antimicrobial stewardship may help reduce VRE colonization and infection rates.
Area of Science:
- Infectious Diseases
- Critical Care Medicine
- Clinical Pharmacy
Background:
- Vancomycin-resistant enterococci (VRE) infections pose a significant public health risk, leading to increased mortality and healthcare expenses.
- Previous studies suggest a link between antibiotic use, particularly cephalosporins, and VRE colonization and bloodstream infections (VRE BSI).
Purpose of the Study:
- To investigate the association between specific antimicrobial agents and the incidence of VRE colonization at the individual patient level within a medical intensive care unit (MICU).
Main Methods:
- Prospective, weekly surveillance for VRE colonization in MICU patients over 17 months.
- Quantification of antimicrobial exposure using days of therapy (DOT) per 1000 patient-days.
- Multivariable logistic regression analysis to identify independent predictors of VRE colonization, controlling for covariates.
Main Results:
- Of 380 eligible patients, 83 (22%) developed incident VRE colonization.
- Bivariate analysis showed associations with male gender, prior hospitalizations, and use of cefepime/ceftazidime, fluconazole, azithromycin, and metronidazole.
- Metronidazole was the sole antibiotic independently associated with incident VRE colonization (OR 2.0; 95% CI 1.2-3.3; P < 0.009) after adjusting for confounders.
Conclusions:
- The risk of developing VRE colonization varies among different antibiotic classes.
- Findings support the potential role of antimicrobial stewardship programs in mitigating VRE colonization and subsequent infections.
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