H041 Experiences and perceptions of affected individuals, families, caregivers and healthcare professionals regarding end-of-life planning in Huntington’s disease: a narrative synthesis
<h3>Background</h3> Huntington’s disease (HD) is a rare neurological condition characterised by progressive decline affecting movement, speech, swallow and cognition, and often requiring long-term care. Due to the complex needs that may emerge, those affected are encouraged to consider end-of-life (EOL) planning early on to mitigate future challenges. Initial evidence shows that undertaking planning discussions around this subject encounter various barriers; those with HD are disinclined to address such questions, and healthcare professionals (HCPs) can be reluctant to engage in these distressing conversations. <h3>Aims</h3> To provide an up-to-date synthesis of evidence regarding EOL planning discussions among people affected by HD and HCPs considering these conversations. <h3>Methods</h3> We undertook systematic searches of six databases, seeking peer-reviewed articles addressing the research question. After screening, nine articles were identified, and a narrative synthesis undertaken to develop key themes. <h3>Results</h3> Preliminary synthesis shows polarisation between patients and HCPs. Gene-carrying individuals express a need for control while families feel ‘in the dark’, and HCPs are unwilling to undertake these conversations without initiation from the patient. Discussions that do occur appear more focused on process than broader holistic care. <h3>Conclusions</h3> EOL planning in HD remains inconsistently implemented, and often process-focused, with a need for more holistic and patient-centred discussions. Further research is necessary to explore opinions and experiences among HD families, and to support HCPs to successfully lead on introducing these broader discussions. Additionally, much of the literature addressed euthanasia rather than natural death, which may have influenced the findings, and highlights a need for ongoing research.
Authors
- Christopher Williams (ORCID: https://orcid.org/0000-0001-6036-5157)
- Catherine Lyon
- Sarah Gunn
Institutions
- University of Leicester (GB)
- Huntington's Disease Association (GB)
Publication Details
- Published
- 2024-09-01
- DOI
- https://doi.org/10.1136/jnnp-2024-ehdn.271
- Primary Topic
- Genetic Neurodegenerative Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00