Bowel colonization with vancomycin-resistant enterococci after antimicrobial therapy for intra-abdominal infections:

Mark J DiNubile1, Ian R Friedland, Christina Y Chan

  • 1Merck & Co., Inc., Whitehouse Station, NJ, USA. mark_dinubile@merck.com

Insights

Different antibiotic treatments for intra-abdominal infections showed similar rates of bowel colonization with vancomycin-resistant enterococci (VRE). This finding is crucial for understanding VRE spread and guiding antimicrobial stewardship in clinical practice.

Area of Science:

  • Infectious Diseases
  • Microbiology
  • Clinical Pharmacology

Background:

  • Intra-abdominal infections (IAIs) are common and require effective antimicrobial therapy.
  • The emergence of vancomycin-resistant enterococci (VRE) poses a significant challenge in healthcare settings.
  • Bowel colonization with VRE is a risk factor for VRE infections.

Purpose of the Study:

  • To evaluate the impact of different antimicrobial regimens on VRE bowel colonization.
  • To compare piperacillin-tazobactam, ceftriaxone/metronidazole, and ertapenem regarding VRE colonization.
  • To inform antimicrobial selection for IAIs to minimize VRE selection pressure.

Main Methods:

  • Two randomized open-label trials were conducted.
  • Patients with intra-abdominal infections were randomized to receive specific antimicrobial treatments.
  • VRE bowel colonization was assessed after treatment.

Main Results:

  • Overall rates of VRE bowel colonization were comparable across treatment groups.
  • Piperacillin-tazobactam, ceftriaxone/metronidazole, and ertapenem showed similar effects on VRE colonization.
  • No significant difference in VRE colonization frequency was observed between the regimens.

Conclusions:

  • The choice of antimicrobial regimen (piperacillin-tazobactam, ceftriaxone/metronidazole, or ertapenem) did not significantly alter the frequency of VRE bowel colonization in short-term studies.
  • These findings suggest that current common antimicrobial choices for IAIs may have a similar impact on VRE selection in the gut.
  • Further research may be needed to explore long-term effects and specific patient populations.

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