Table 5.
Topic | Hours | Sample Active Learning Exercise(s) |
---|---|---|
Fundamentals of human genetics and pharmacogenomics | 2–4 |
|
Advanced concepts in pharmacogenomics (e.g., haplotypes, genome-wide approaches) | 1–2 | |
Genomic basis of disease and “omics” (i.e., genomics, proteomics, metabolomics) | 1–2 | |
Direct-to-consumer-based genotyping | 1–2 | |
Use of pharmacogenomic databases (e.g., PharmGKB) | 2 |
|
Commercially available genotyping tests: ordering, sample collection and processing, interpreting and evaluating results | 2 |
|
Types of clinical pharmacogenomics evidence and guidelines | 1–2 |
|
Interpretation of the clinical pharmacogenomics literature | 1–2 | |
Pharmacogenomics in the drug development and FDA approval process (e.g., ivacaftor) | 1–2 |
|
Genetics and Clinical Pharmacology (i.e., drug metabolism, transport, PK, PD) | 3–4 |
|
Oncology: germline (e.g., thiopurines) and somatic (e.g., trastuzumab) | 3–5 | |
Drug-induced hypersensitivity reactions (i.e., abacavir, carbamazepine, phenytoin, allopurinol) | 2–3 | |
Infectious diseases (i.e., voriconazole, pegylated interferon) | 1–2 | |
Pain, neurology, psychiatry (i.e., codeine, phenytoin, tricyclic antidepressants, SSRIs) | 2–4 | |
Cardiology (e.g., clopidogrel, warfarin, statins) | 2–4 | |
Transplant (e.g., tacrolimus) | 1–2 | |
Controversial evidence (e.g., tamoxifen) | 1 | |
Ethical, social, and economic implications | 1–2 |
|
Clinical implementation (e.g., clinical decision support tools) | 2–3 |
|
Communicating pharmacogenomics information and recommendations | 1–2 |
|
Sample activities and assignments based upon authors’ experiences at the University of Florida (K.W.W.), University of Colorado (C.L.A.), Manchester University (D.F.K.), and University of Pittsburgh (P.E.E.).