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Implementation of Pharmacogenomic Clinical Decision Support for Health Systems: A Cost-Utility Analysis

We constructed a cost-effectiveness model to assess the clinical and economic value of a CDS alert program that provides pharmacogenomic (PGx) testing results, compared to no alert program in acute coronary syndrome (ACS) and atrial fibrillation (AF), from a health system perspective. We defaulted t...

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Detalles Bibliográficos
Autores principales: Jiang, Shangqing, Mathias, Patrick C., Hendrix, Nathaniel, Shirts, Brian H., Tarczy-Hornoch, Peter, Veenstra, David, Malone, Daniel, Devine, Beth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156556/
https://www.ncbi.nlm.nih.gov/pubmed/35365779
http://dx.doi.org/10.1038/s41397-022-00275-7
Descripción
Sumario:We constructed a cost-effectiveness model to assess the clinical and economic value of a CDS alert program that provides pharmacogenomic (PGx) testing results, compared to no alert program in acute coronary syndrome (ACS) and atrial fibrillation (AF), from a health system perspective. We defaulted that 20% of 500 000 health-system members between the ages of 55 and 65 received PGx testing for CYP2C19 (ACS-clopidogrel) and CYP2C9, CYP4F2 and VKORC1 (AF-warfarin) annually. Clinical events, costs, and quality-adjusted life years (QALYs) were calculated over 20 years with an annual discount rate of 3%. In total, 3 169 alerts would be fired. The CDS alert program would help avoid 16 major clinical events and 6 deaths for ACS; and 2 clinical events and 0.9 deaths for AF. The incremental cost-effectiveness ratio was $39 477/QALY. A PGx-CDS alert program was cost-effective, under a willingness-to-pay threshold of $100 000/QALY gained, compared to no alert program.