Prevalence and predictors of MRSA, ESBL, and VRE colonization in the ambulatory IBD population

J Crohns Colitis. 2012 Aug;6(7):743-9. doi: 10.1016/j.crohns.2011.12.005. Epub 2012 Jan 9.

Abstract

Background and aims: Inflammatory bowel disease (IBD) patients may be at increased risk of acquiring antibiotic-resistant organisms (ARO). We sought to determine the prevalence of colonization of methicillin-resistant Staphylococcus aureus (MRSA), Enterobacteriaceae containing extended spectrum beta-lactamases (ESBL), and vancomycin-resistant enterococi (VRE) among ambulatory IBD patients.

Methods: We recruited consecutive IBD patients from clinics (n=306) and 3 groups of non-IBD controls from our colon cancer screening program (n=67), the family medicine clinic (n=190); and the emergency department (n=428) from the same medical center in Toronto. We obtained nasal and rectal swabs for MRSA, ESBL, and VRE and ascertained risk factors for colonization.

Results: Compared to non-IBD controls, IBD patients had similar prevalence of colonization with MRSA (1.5% vs. 1.6%), VRE (0% vs. 0%), and ESBL (9.0 vs. 11.1%). Antibiotic use in the prior 3 months was a risk factor for MRSA (OR, 3.07; 95% CI: 1.10-8.54), particularly metronidazole. Moreover, gastric acid suppression was associated with increased risk of MRSA colonization (adjusted OR, 7.12; 95% CI: 1.07-47.4). Predictive risk factors for ESBL included hospitalization in the past 12 months (OR, 2.04, 95% CI: 1.05-3.95); treatment with antibiotics it the past 3 months (OR, 2.66; 95% CI: 1.37-5.18), particularly prior treatment with vancomycin or cephalosporins.

Conclusions: Ambulatory IBD patients have similar prevalence of MRSA, ESBL and VRE compared to non-IBD controls. This finding suggests that the increased MRSA and VRE prevalence observed in hospitalized IBD patients is acquired in-hospital rather than in the outpatient setting.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Ambulatory Care
  • Anti-Bacterial Agents / adverse effects*
  • Anti-Bacterial Agents / pharmacology
  • Carrier State / epidemiology
  • Carrier State / microbiology*
  • Cephalosporins / therapeutic use
  • Enterobacteriaceae Infections / epidemiology
  • Enterobacteriaceae* / enzymology
  • Enterococcus* / drug effects
  • Female
  • Histamine H2 Antagonists / therapeutic use
  • Hospitalization
  • Humans
  • Inflammatory Bowel Diseases / microbiology*
  • Logistic Models
  • Male
  • Methicillin-Resistant Staphylococcus aureus*
  • Metronidazole / therapeutic use
  • Middle Aged
  • Nose / microbiology
  • Prevalence
  • Proton Pump Inhibitors / therapeutic use
  • Rectum / microbiology
  • Risk Factors
  • Staphylococcal Infections / epidemiology
  • Vancomycin / pharmacology
  • Vancomycin / therapeutic use
  • Vancomycin Resistance
  • Young Adult
  • beta-Lactamases / biosynthesis

Substances

  • Anti-Bacterial Agents
  • Cephalosporins
  • Histamine H2 Antagonists
  • Proton Pump Inhibitors
  • Metronidazole
  • Vancomycin
  • beta-Lactamases