| Literature DB >> 31582005 |
Patrick R Heck1, Michelle N Meyer2.
Abstract
Compared to clinicians previously surveyed, primary care providers employed in a health system known for clinical genomics were more likely to have ordered or referred a patient for genetic testing, but had only modestly more genetics training and reported similarly low levels of comfort answering patient questions about genetic risk. Most supported population genomic screening, reported willingness to get screened themselves, and judged a hypothetical patient's decision to be screened favorably relative to a similar patient's decision to decline screening. Stakeholder perceptions of the ethical appropriateness of nudging at-risk patients to discuss testing with counselors were mixed.Entities:
Keywords: Ethics; Genetics; Genomics; Information avoidance; Nudge; Personalized medicine; Population screening; Whole exome sequencing
Mesh:
Year: 2019 PMID: 31582005 DOI: 10.1016/j.mcna.2019.08.004
Source DB: PubMed Journal: Med Clin North Am ISSN: 0025-7125 Impact factor: 5.456