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Identifying high-risk medications and error types in Danish patient safety database using disproportionality analysis
Olga Tchijevitch1, Søren F Birkeland1,2,3, Søren B Bogh1
1Research Unit OPEN, Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
Disproportionality analysis (DPA) can help screen medication errors (MEs) in healthcare safety reports. This study found DPA feasible for identifying high-risk drug associations with MEs in the Danish Patient Safety Database.
Area of Science:
- Healthcare safety
- Pharmacovigilance
- Medication error analysis
Background:
- Medication error (ME) surveillance in Denmark uses the national Danish Patient Safety Database (DPSD).
- Current analysis methods like case reviews and descriptive statistics have limitations, including underreporting and large data volumes.
- Disproportionality analysis (DPA), a tool for adverse drug reaction signal detection, has limited evidence for ME analysis in safety reporting systems.
Purpose of the Study:
- To assess the feasibility of using Disproportionality Analysis (DPA) for analyzing harmful medication errors (MEs).
- To evaluate DPA's potential as a supplementary tool for ME surveillance in healthcare safety reporting.
Main Methods:
- Utilized proportional reporting ratios (PRR) to detect disproportionality signals.
- Analyzed harmful medication errors reported to the Danish Patient Safety Database (DPSD) between 2014 and 2018.
Main Results:
- Successfully identified associations between high-risk medications (e.g., anticoagulants, opioids, insulins) and various medication error types and stages.
- Demonstrated the identification of well-known high-risk drug classes through DPA.
Conclusions:
- Disproportionality analysis (DPA) shows feasibility for screening medication errors in safety reporting systems.
- DPA can serve as an additional tool to identify priority areas for further investigation of medication errors.
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