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Genetics in palliative care: too much to ask?
Chris Jacobs1, Stephanie White2, Jane Phillips3
1Senior Lecturer, Genetic Counselling, University of Technology Sydney (UTS) Ultimo, NSW Australia.
International Journal of Palliative Nursing
|May 23, 2019
Summary
Palliative care patients with inherited conditions may miss opportunities to save DNA samples. Storing DNA aids relatives in genetic risk assessment and preventative measures for inherited diseases.
Area of Science:
- Genetics and Genomics
- Palliative Care Medicine
Background:
- Individuals with inherited conditions receiving palliative care may not consider the future implications of genetic information for their families.
- Advances in genetic and genomic testing necessitate better communication regarding family history and potential genetic risks within palliative care settings.
Purpose of the Study:
- To emphasize the critical importance of discussing genetics and genomics with patients undergoing palliative care.
- To inform palliative care professionals about the benefits of genetic sample storage for families.
- To highlight the role of palliative care in facilitating genetic risk assessment and management for relatives.
Main Methods:
- This article is a review and discussion piece, synthesizing current understanding and best practices.
- It focuses on the communication aspects between healthcare professionals, patients, and their families regarding genetic information.
Main Results:
- Failure to discuss genetic and genomic implications can lead to missed opportunities for vital family health information.
- Palliative care professionals are increasingly likely to encounter discussions about inherited conditions and genetic testing.
Conclusions:
- Integrating discussions about genetic and genomic issues into palliative care is essential.
- Proactive communication can empower families with information for genetic risk assessment, surveillance, and risk-reducing strategies.
- Palliative care settings represent a crucial, yet often overlooked, point for addressing familial genetic health concerns.
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