Key result
Prospective genotyping for CYP2C19 variants linked to point-of-care decision support was successfully implemented in approximately 3,000 patients over one year.
Prospective genotyping for CYP2C19 variants can be successfully integrated into the EMR with point-of-care decision support to guide personalized antiplatelet therapy.
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Demonstrates feasibility of EMR-integrated CYP2C19 genotyping with point-of-care support; leaves open impact on clinical outcomes.
The promise of "personalized medicine" guided by an understanding of each individual's genome has been fostered by increasingly powerful and economical methods to acquire clinically relevant information. We describe the operational implementation of prospective genotyping linked to an advanced clinical decision-support system to guide individualized health care in a large academic health center. This approach to personalized medicine entails engagement between patient and health-care provider, identification of relevant genetic variations for implementation, assay reliability, point-of-care decision support, and necessary institutional investments. In one year, approximately 3,000 patients, most of whom were scheduled for cardiac catheterization, were genotyped on a multiplexed platform that included genotyping for CYP2C19 variants that modulate response to the widely used antiplatelet drug clopidogrel. These data are deposited into the electronic medical record (EMR), and point-of-care decision support is deployed when clopidogrel is prescribed for those with variant genotypes. The establishment of programs such as this is a first step toward implementing and evaluating strategies for personalized medicine.
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Pulley et al. (2012) studied Patients scheduled for cardiac catheterization (n=3,000). Prospective genotyping and clinical decision-support system was evaluated. Prospective genotyping for CYP2C19 variants linked to point-of-care decision support was successfully implemented in approximately 3,000 patients over one year.
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