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Learning Objectives

Sep 26, 2019

At the completion of this activity, pharmacists will be able to:

  1. Describe the pharmacists’ role in pharmacogenomics
  2. Discuss the state of pharmacogenetic implementations across the industry
  3. Recognize basic mechanisms of the expression of genetic information as traits
  4. Describe the major types of genetic variation (poor, normal, or ultrarapid metabolizer)
  5. Compare and contrast different types of genetic tests and application
  6. Provide specific examples that establish the relationship between altered drug disposition and polymorphic cytochrome P450 enzymes
  7. Describe how polymorphic genetic variation can be utilized to predict an individual’s response to drug therapy
  8. Detail ethical, legal, and regulatory concerns surrounding pharmacogenetic testing
  9. Review regulatory activity, especially FDA guidance and rulemaking impacting pharmacogenomics
  10. Describe the potential limitations of pharmacogenomic testing
  11. Discuss legal considerations of PGx and broader genetic testing (GINA, consent, HIPAA, etc.)
  12. Describe the role of various pharmacogenetic resources available to support clinical application
  13. Discuss strategies to identify whether a drug-gene pair is ready for clinical use
  14. Recognize the value that pharmacogenetics can bring to patient care
  15. Develop a pharmacotherapy regimen based on patient characteristics
  16. Apply guidelines and other evidence to patient cases across multiple medical specialties and subspecialties (e.g., behavioral health, cardiology, oncology, pain management)
  17. Identify variations in genetic response among racial or ethnic groups
  18. Apply guidelines and other evidence to patient cases across multiple medical specialties and 30 subspecialties (e.g., behavioral health, cardiology, oncology, pain management)
  19. Identify variations in genetic response among racial or ethnic groups
  20. Describe the roles and responsibilities of clinical laboratories
  21. Establish criteria for selecting a PGx laboratory
  22. Compare and contrast PGx lab testing vs Direct-to-Consumer genetic testing
  23. Detail the key components required in a pharmacogenomic test for clinical practice
  24. Describe utilization of PGx in terms relevant for healthcare providers and payors
  25. Utilize clinical decision support tools to inform therapeutic recommendations
  26. Apply evidence-based literature to therapy recommendations
  27. Create strategies to develop and deliver pharmacogenetic recommendations to prescribers
  28. Describe the applicability of pharmacogenomics for patients
  29. Counsel a patient on their test results