Provider Training

ACCREDITATION INFORMATION

CEI is accredited by the Accreditation Council for Pharmacy Education (ACPE) as a provider of continuing pharmacy education (CPE). The following course is approved for 8.0 contact hour of CPE credit (.8 CEUs). The ACPE Universal Activity Number for this activity is: 0107-0000-20-352-H01-P (pharmacists).

Available: December 21, 2020
Expiration Date: December 21, 2023

ON DEMAND: CEImpact is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Obtain CPE credit by completing the course, followed by the exam and evaluation (if applicable). Once successfully completed, your course will appear in your Completed Courses tab. Access your CPE statement of credit at www.MyCPEMonitor.net.

To obtain 8.0 contact hours of CPE credit for completing this course, CEImpact provides you with two (2) opportunities to complete the exam. The learner will not receive CPE credit after two failed attempts.

TARGET AUDIENCE

• Pharmacists

ACPE ACTIVITY TYPE

Knowledge-based

ACTIVITY FEE

There is a fee of $299 associated with this activity.

SYSTEM REQUIREMENTS

The course is designed to work with any current web browser. If you have any technical difficulties, please contact CEimpact at: team@ceimpact.com.

FACULTY

D. Max Smith, PharmD, BCPS
Clinical Pharmacogenomics Specialist
MedStar Health

David Kisor, BS, PharmD, FCP
Professor and Director
Manchester University Pharmacogenomics

Behnaz Sarrami, MS, PharmD
Director of Consulting
Missouri Pharmacogenomics Consulting LLC

John A Galdo, PharmD, MBA, BCPS, BCGP
CEimpact
Ross Bridge Pharmacy

D. Max Smith, David Kisor and Jake Galdo report no actual or potential conflicts of interest in relation to this continuing pharmacy education course.

Behnaz Sarrami is a Consultant for Missouri Pharmacogenomics Consulting, LLC.

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