Study Evaluating Vancomycin-Resistant Enterococci in a Hematology Unit

Overview

To determine the impact of the restriction of the third and forth generation cephalosporins on the reduction of intestinal colonization or infection with vancomycin-resistant enterococci (VRE) in a surgical intensive care unit (SICU)

Full Title of Study: “Effects on the Emergence and Transmission of Vancomycin-Resistant Enterococci After Changes in Antibiotic Use in a Hematology Unit.”

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective

Interventions

  • Drug: Piperacillin/tazobactam and other β-lactam/β-lactamase

Participating in This Clinical Trial

Inclusion Criteria

  • All patients admitted to or transferred to the SICU. – Eligible patients will be patients of either sex, 18 years of age or older who are admitted or transferred to the SICU. – Provide written informed consent Exclusion Criteria:

  • Patients who have hypersensitivity to penicillin, cephalosporins or beta-lactamase inhibitors. – Females who are pregnant and breast feeding – Any underlying conditions or non-infectious diseases that will be ultimately fatal within 48 hours. – Those who have already been participating other clinical study related with antibiotics.

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Wyeth is now a wholly owned subsidiary of Pfizer
  • Overall Official(s)
    • Medical Monitor, Study Director, Wyeth is now a wholly owned subsidiary of Pfizer

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