Perplexed by PGx? Exploring the impact of pharmacogenomic results on medical management, disclosures and patient behavior

Author:

Waldman Larissa12,Shuman Cheryl12,Cohn Iris3,Kaiser Amy2,Chitayat David14,Wasim Syed5,Hazell Allison6

Affiliation:

1. Department of Genetic Counselling, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

2. Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada

3. Division of Clinical Pharmacology & Toxicology, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

4. Prenatal Diagnosis & Medical Genetics Program, Department of Obstetrics & Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada

5. Fred A Litwin Family Centre in Genetic Medicine, University Health Network & Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada

6. Medcan Health Management, Inc., Toronto, Ontario, Canada

Abstract

Pharmacogenomic (PGx) tests represent significant advances in precision medicine. Our aim was to explore perceptions following the return of PGx results, medication management, and disclosure to providers. We surveyed clients who had PGx testing and conducted a chart review of PGx results. Respectively, 84% and 94% of participants found pre- and post-test genetic counseling helpful. There was a significant difference in disclosure, while 6% disclosed results to a pharmacist, 50% disclosed to a physician. Qualitative analysis identified three themes: 1) psychological response; 2) perceived utility; 3) experiences with disclosure. Our study supports the provision of genetic counseling for a non-disease related genetic test. Benefits of PGx testing can be optimized by the collaboration of physicians, pharmacists, genetic counselors and patients.

Publisher

Future Medicine Ltd

Subject

Pharmacology,Genetics,Molecular Medicine

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