Abstract

BackgroundThe emergence of vancomycin-resistant Staphylococcus aureus (VRSA) has become a global concern for public health. The proximity of vancomycin-resistant enterococcus (VRE) and methicillin-resistant S. aureus (MRSA) is considered to be one of the foremost risk factors for the development of VRSA. This study aimed to determine the incidence, risk factors, and clinical outcomes of intestinal co-colonization with VRE and MRSA.MethodsA case–control study was conducted in 52-bed intensive care units (ICUs) of a university-affiliated hospital from September 2012 to October 2017. Active surveillance using rectal cultures for VRE were conducted at ICU admission and on a weekly basis. Weekly surveillance cultures for detection of rectal MRSA were also conducted in patients with VRE carriage. Patients with intestinal co-colonization of VRE and MRSA were compared with randomly selected control patients with VRE colonization alone (1:1). Vancomycin minimum inhibitory concentrations (MICs) for MRSA isolates were determined by the Etest.ResultsOf the 4679 consecutive patients, 195 cases and 924 controls were detected. The median monthly incidence and duration of intestinal co-colonization with VRE and MRSA were 2.3/1000 patient-days and 7 days, respectively. The frequency of both MRSA infections and mortality attributable to MRSA were higher in the case group than in the control group: 56.9% vs. 44.1% (P = 0.011) and 8.2% vs. 1.0% (P = 0.002), respectively. Independent risk factors for intestinal co-colonization were enteral tube feeding (odds ratio [OR], 2.09; 95% confidence interval [CI] 1.32–3.32), metabolic diseases (OR, 1.75; 95% CI 1.05–2.93), male gender (OR, 1.62; 95% CI 1.06–2.50), and Charlson comorbidity index < 3 (OR, 3.61; 95% CI 1.88–6.94). All MRSA isolates from case patients were susceptible to vancomycin (MIC ≤ 2 mg/L).ConclusionsOur study indicates that intestinal co-colonization of VRE and MRSA occurs commonly among patients in the ICU with MRSA endemicity, which might be associated with poor clinical outcomes.

Highlights

  • The emergence of vancomycin-resistant Staphylococcus aureus (VRSA) has become a global concern for public health

  • Epidemiology of intestinal co‐colonization with vancomycin-resistant enterococcus (VRE) and methicillin-resistant S. aureus (MRSA) From September 2012 to October 2017, surveillance cultures for rectal VRE were obtained from 4679 patients and disclosed 5410 VRE-positive samples (37.2%) out of 14,548 rectal swabs from intensive care unit (ICU) patients; this accounted for 1273 patients

  • In active surveillance using a nasal swab for MRSA, there was a significant difference in the frequency of MRSA nasal carriage between the case group and control group (16.4% vs. 0, P < 0.001)

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Summary

Introduction

The emergence of vancomycin-resistant Staphylococcus aureus (VRSA) has become a global concern for public health. The proximity of vancomycin-resistant enterococcus (VRE) and methicillin-resistant S. aureus (MRSA) is considered to be one of the foremost risk factors for the development of VRSA. Methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococcus (VRE) have been endemic in hospital settings throughout the world. Vancomycin minimum inhibitory concentration (MIC) creep for MRSA isolates, probably associated with poorer clinical outcomes, has become a major worldwide concern [3, 4]. Inconsistent information about the MIC creep phenomenon and conflicting results have been noted [5, 6], the emergence of vancomycin-intermediate S. aureus (VISA) since 1997 and vancomycin-resistant S. aureus (VRSA) since 2002 has become a global challenge [7, 8]

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