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Clinical Trials/NCT01358916
NCT01358916
Completed
Not Applicable

Improvement of Antibiotic Prescription in Outpatient Care: a Cluster-randomised Intervention Study Using a Sentinel Surveillance Network of Physicians

University of Bern1 site in 1 country140 target enrollmentNovember 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Respiratory Tract Infections
Sponsor
University of Bern
Enrollment
140
Locations
1
Primary Endpoint
Percentage of prescriptions of penicillin for respiratory tract infections
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

Antimicrobial resistance has become a world-wide problem and antibiotic consumption is a major driving force for the development of resistance. Thus optimization of antibiotic prescription and reduction of unnecessary antimicrobial treatment are essential in the prevention and reduction of antimicrobial resistance rates.

The goal of this study is the improvement of antibiotic prescription in outpatient care. The study will take place within a Swiss-wide sentinel surveillance network of physicians. The participating physicians will be randomised in a control and intervention group. The intervention group will receive therapeutic guidelines for the treatment of upper and lower respiratory tract infections and lower urinary tract infection as well as regular feed-backs on the prescription pattern of the sentinel physicians during the past months. Sentinel physicians will collect information about each antibiotic prescription, its indication and characteristics of the patient.

Our hypothesis is that the prescription pattern in the intervention group will be optimised and unnecessary antibiotic therapy will be reduced compared to the control group.

Detailed Description

Background Antimicrobial resistance has become a world-wide problem and antibiotic consumption is a major driving force for the development of resistance. Thus optimization of antibiotic prescription and reduction of unnecessary antimicrobial treatment are essential in the prevention and reduction of antimicrobial resistance rates. The goal of this study is the qualitative and quantitative improvement of antibiotic prescription in outpatient care. The study will take place within a Swiss-wide sentinel surveillance network consisting of general practitioners, pediatricians and physicians specialized in internal medicine. The participating physicians will be randomised in a control and intervention group. The intervention group will receive therapeutic guidelines for the treatment of upper and lower respiratory tract infections and lower urinary tract infections. Furthermore, regular feed-backs on the prescription pattern of the sentinel physicians in the last months will be provided. Information about each antibiotic prescription, its indication and the characteristics of the patients will be collected by the sentinel physicians. The standardized reporting of antibiotic prescription by sentinel physicians has been carried out in Switzerland since 2006. Our hypothesis is that the intervention will affect the antibiotic prescription pattern and that the investigators will observe an optimization of antibiotic prescription and a decrease in the number of antibiotic prescriptions. Objective Primary goals: * Increase of the percentage of penicillin prescriptions for upper and lower respiratory tract infections * Increase of the percentage of TMP/SMX prescriptions for lower urinary tract infections in adults Secondary goal: * Decrease of the percentage of quinolone prescriptions for COPD exacerbations in adults * Decrease of the number of antibiotic prescriptions for sinusitis and other upper respiratory tract infections Methods Prospective cluster-randomised intervention study. The intervention is the mailing of treatment guidelines for upper and lower respiratory tract infections and lower urinary tract infections as well as regular feed-backs on the antibiotic prescription patterns of the sentinel physicians during the past months.

Registry
clinicaltrials.gov
Start Date
November 2010
End Date
December 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with respiratory tract infections or urinary tract infections
  • Exclusion Criteria
  • Patients with chronic disease requiring regular antibiotic treatment

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Percentage of prescriptions of penicillin for respiratory tract infections

Time Frame: Two years

Percentage of prescriptions of TMP/SMX for lower urinary tract infections in adults

Time Frame: Two years

Secondary Outcomes

  • Percentage of prescriptions of quinolone for COPD exacerbations in adults(Two years)
  • Percentage of antibiotic prescriptions for the indications "sinusitis" and "other upper respiratory tract infections"(Two years)

Study Sites (1)

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