Session Information
2009 Midyear Clinical Meeting
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From Research to Clinical Practice: Evidence-Based Pharmacogenomic Recommendations
Track: Educational Sessions (CE)
Program Code: 252-L04
Date: Tuesday, December 8, 2009
Time: 4:00 PM to 5:00 PM EST
Location: Palazzo M, Level 5
MEETING PLANNING ASSOCIATE:   Click the plus sign to see more detailed information about each speaker.
 Grace Kuo, PharmD, MPH, Associate Professor of Clinical Pharmacy, Skaggs School of Pharmacy and Pharmaceutical Sciences; and Associate Professor of Family and Preventive Medicine, School of Medicine, University of California, San Diego
PRESENTER(S):   Click the plus sign to see more detailed information about each speaker.
 Grace Kuo, PharmD, MPH, Associate Professor of Clinical Pharmacy, Skaggs School of Pharmacy and Pharmaceutical Sciences; and Associate Professor of Family and Preventive Medicine, School of Medicine, University of California, San Diego
 Joseph Ma, PharmD, Assistant Professor, University of California, San Diego, Skaggs School of Pharmacy & Pharmaceutical Sciences
Description
Planned in cooperation with the ASHP Section of Clinical Specialists and Scientists Taskforce on Science
ACPE Activity #204-000-09-252-L04P
1.0 Contact Hour / Knowledge-based
Educational Content: Level 2
Moderator: Grace M. Kuo, PharmD, MPH, Associate Professor of Clinical Pharmacy, Skaggs School of Pharmacy and Pharmaceutical Sciences; and Associate Professor of Family and Preventive Medicine, School of Medicine, University of California, San Diego, La Jolla

4:00 p.m. – 4:05 p.m.
Announcements and Introduction

4:05 p.m. – 4:30 p.m.
Pharmacogenomic Recommendations in Therapeutic Areas
Joseph D. Ma, PharmD, Assistant Professor, University of California, San Diego, Skaggs School of Pharmacy & Pharmaceutical Sciences, San Diego

4:30 p.m. – 4:50 p.m.
Pharmacogenomic Recommendations in Therapeutic Areas
Grace M. Kuo

4:50 p.m. – 5:00 p.m.
Questions, Answers, and Discussion

Learning Objectives:

LEARNER OUTCOMES:
  • Compare the risks and benefits of pharmacogenomic testing for a medication based upon primary literature evidence.
  • For each therapeutic area, identify the pharmacogenomic testing that is available to determine therapeutic or toxic outcomes for a medication.
  • Identify key therapeutic areas in which pharmacogenomic testing can be applied in the clinical setting.
  • Summarize the recommendations for pharmacogenomic testing based upon recommendations from the Evaluation of Genomic Applications in Practice and Prevention (EGAPP), other agencies (e.g. FDA), and published literature.
  • Using patient case scenarios, formulate a plan for pharmacogenomic testing based upon available scientific evidence, ethical issues, and feasibility.


Audio Synchronized to PowerPoint
(Code: 252-L04)
Attendee:Free
  
This session is a part of:
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