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Validation and enhancement of a computable medication indication resource (MEDI) using a large practice-based dataset
Wei-Qi Wei1, Jonathan D Mosley2, Lisa Bastarache1
1Department of Biomedical Informatics, Vanderbilt University, Nashville, TN.
The MEDI resource accurately links medications to indications, covering 97.3% of real-world drug data. This computable tool enhances clinical informatics and electronic health record research by providing medication-indication prevalence.
Area of Science:
- Clinical Informatics
- Pharmacovigilance
- Health Services Research
Background:
- Accurate medication-indication linkage is crucial for clinical practice and research.
- Existing resources lack comprehensive, computable medication-indication data.
- The MEDI (Medication-Indication) resource was developed to address this gap.
Purpose of the Study:
- To evaluate the medication coverage of the MEDI resource using real-world clinical data.
- To calculate the prevalence of indications for each medication within a large patient cohort.
- To assess the clinical utility of MEDI for informatics and phenotype recognition.
Main Methods:
- Extracted medication and diagnosis data for 1.3 million individuals from Vanderbilt University Medical Center.
- Assessed MEDI's coverage of recorded medications and mapped indications to ICD-9 codes.
- Conducted manual physician review for four example medications to validate indications and prevalence estimates.
Main Results:
- MEDI demonstrated high medication coverage, linking 97.3% of medications found in electronic health records.
- A 'high precision subset' of MEDI covered 93.8% of recorded medications.
- Manual review confirmed MEDI's accuracy in identifying indications and estimating medication prevalence.
Conclusions:
- MEDI provides comprehensive and accurate medication-indication linkage, essential for clinical informatics.
- The inclusion of indication prevalence data enhances MEDI's clinical usability.
- MEDI is a valuable tool for electronic health record-based research, aiding in phenotype recognition.
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