Advances in genetic research have allowed us to develop testing, treatment, and prevention strategies based upon patients’ unique genetic characteristics, medical history, and environment. But what happens when patients whose ancestry or ethnicity was not represented in the research dataset are seeking care? This can lead to deepening and concerning health inequities. In this episode, we’ll discuss these health equity concerns in genetic databases and their impact on underrepresented and mixed populations.
- Provider:American Medical Association
- Activity Link: https://edhub.ama-assn.org/science-medicine-public-health/audio-player/18860881
- Start Date: 2024-03-19 05:00:00
- End Date: 2024-03-19 05:00:00
- Credit Details: AMA PRA Category 1 Credit™️: 0.5 hours
- MOC Credit Details: ABS - 0.5 Point; Credit Type(s): Accredited CME (ABS)
ABPATH - 0.5 Point; Credit Type(s): Lifelong Learning (ABPATH)
ABIM - 0.5 Point; Credit Type(s): Medical Knowledge (ABIM)
ABP - 0.5 Point; Credit Type(s): Lifelong Learning and Self-Assessment (ABP)
ABOHNS - 0.5 Point; Credit Type(s): Self-Assessment (ABOHNS) - Commercial Support: No
- Activity Type: Enduring Material
- CME Finder Type: Online Learning
- Fee to Participate: No, it's free
- Measured Outcome: Learner Competence, Learner Knowledge
- Provider Ship: Directly Provided
- Registration: Open to all
- Specialty: All Practice Areas (e.g. ethics), General Otolaryngology, General Pediatrics, General Surgery, Internal Medicine
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