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Clinical Trials/NCT00431483
NCT00431483
Completed
Not Applicable

Clinical and Economic Impact of Interventions by a Clinical Pharmacist on Antibiotic Use on Surgical Wards

Ludwig-Maximilians - University of Munich1 site in 1 country779 target enrollmentFebruary 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bacterial Infections
Sponsor
Ludwig-Maximilians - University of Munich
Enrollment
779
Locations
1
Primary Endpoint
overall duration of antibiotic therapy during study period
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The purpose of this study is to establish the impact of a pharmacist's recommendations regarding choice, dosing and duration of antibiotic therapy on quality and cost of antibiotic treatment on surgical wards.

Detailed Description

Inappropriate or incorrect use of antibacterials exerts selection pressure on pathogens potentiating emergence of resistance, puts patients at risk for unnecessary adverse drug reactions and potentially prolongs the length of stay in hospital thus increasing healthcare costs. In an effort to improve the quality of antibiotic drug therapy on surgical wards of a large university hospital, specific consulting by a clinical pharmacist was established. The objective of this study is to assess the impact of pharmaceutical consulting on the quality and costs of antibiotic use in surgical wards. Comparison: Within a control period the current pattern of antibiotic use is monitored. During the intervention period, the impact of the interventions made by the clinical pharmacist on antibiotic use is examined. One ward serves as a parallel control group; no intervention is being made on this ward throughout this study.

Registry
clinicaltrials.gov
Start Date
February 2007
End Date
February 2008
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Alexandra Weber

Pharmacist

Ludwig-Maximilians - University of Munich

Eligibility Criteria

Inclusion Criteria

  • female and male patients receiving antibiotics for a proven or suspected infection on designated surgical wards

Exclusion Criteria

  • patients under 18
  • patients unable or unwilling to consent to their data being evaluated
  • patients receiving antibiotics perioperatively as prophylaxis
  • patients receiving antibiotics for less than 48hrs

Outcomes

Primary Outcomes

overall duration of antibiotic therapy during study period

Time Frame: Feb 2008

Secondary Outcomes

  • iv to oral switch(Feb 2008)
  • compliance of treatment with hospital formulary for antibiotic therapy(Feb 2008)
  • cost of antibiotic therapy(Feb 2008)
  • number and duration of therapy with antibiotics with redundant spectra(Feb 2008)

Study Sites (1)

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