期刊
EUROPEAN JOURNAL OF HUMAN GENETICS
卷 31, 期 8, 页码 945-952出版社
SPRINGERNATURE
DOI: 10.1038/s41431-022-01179-7
关键词
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Genetic information can provide clinical benefits to families of palliative patients, but integrating genetics into mainstream medicine has not prioritized palliative populations. This study explores the views and experiences of genetic health professionals in addressing genetics with palliative patients. The findings reveal challenges and misunderstandings regarding the value of genetic information in palliative care, highlighting the need for improved service leadership and awareness of the familial benefits of palliative genetic testing.
Genetic information can provide clinical benefits to families of palliative patients. However, integration of genetics into mainstream medicine has not focused on palliative populations. We explored the views and experiences of genetic health professionals in addressing genetics with palliative patients, and their families. We conducted an interpretive descriptive qualitative study with genetic counsellors and clinical geneticists using interviews and focus groups. Findings were generated using reflexive thematic analysis. Three themes were identified: (1) Focusing on the benefit to the family, (2) The discomfort of addressing genetics near end-of-life and (3) It's always on the back-burner: Challenges to getting genetics on the palliative care agenda. Participants discussed the familial benefit of genetics in palliative care alongside the challenges when patients are near end-of-life. They perceived genetics as low priority for palliative care due to misunderstandings related to the value of genetic information. Acknowledging the challenges in the palliative care context, genetic health professionals want improved service leadership and awareness of the familial benefits of palliative genetic testing. Strong leadership to support genetic health professionals in addressing these barriers is needed for the benefits of genetic information to be realised.
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