Related Experiment Videos
Developing drug use evaluation criteria for parenteral fluoroquinolones
D R Guay1, T R Covington, V L Alexander
1College of Pharmacy, University of Minnesota, Minneapolis.
Pharmacotherapy
|March 1, 1993
Summary
Drug Use Evaluation (DUE) is essential for optimizing pharmacotherapy. This study proposes specific DUE criteria for parenteral fluoroquinolones to ensure safe and cost-effective antimicrobial use.
Area of Science:
- Pharmaceutical Care
- Antimicrobial Stewardship
- Drug Use Evaluation
Background:
- Optimal pharmacotherapy requires identifying, resolving, and preventing drug-related problems.
- Drug Use Evaluation (DUE) is a key tool for achieving optimal pharmacotherapy.
- Fluoroquinolone antimicrobials are frequently used, costly, and associated with high-risk populations, making them suitable for DUE.
Purpose of the Study:
- To establish evidence-based Drug Use Evaluation (DUE) criteria for parenteral fluoroquinolones.
- To guide the appropriate and cost-effective use of intravenous fluoroquinolones.
- To address the lack of published DUE criteria for parenteral fluoroquinolones.
Main Methods:
- Review of Joint Commission criteria for targeting drugs for DUE.
- Analysis of fluoroquinolone characteristics (cost, risk, usage patterns).
- Development of suggested DUE criteria for parenteral fluoroquinolone use.
Main Results:
- Fluoroquinolones meet criteria for DUE due to high-risk populations, cost, potential for inappropriate use, and frequent prescription.
- Suggested DUE criteria include specific patient populations (e.g., GI malabsorption), severe infections, aminoglycoside replacement, targeting resistant pathogens, and therapeutic use only.
- No prior published DUE criteria for parenteral fluoroquinolones were identified.
Conclusions:
- The DUE process is critical for ensuring safe, effective, appropriate, and economical drug therapy.
- Implementing DUE criteria for parenteral fluoroquinolones can enhance antimicrobial stewardship.
- DUE serves as an effective mechanism for evaluating new agents and educating clinicians post-marketing.