posted on 2025-05-09, 18:33authored byJamie BryantJamie Bryant, Marcus Sellars, Amy Waller, Karen Detering, Craig Sinclair, Rasa Ruseckaite, Ben White, Linda Nolte
Objectives: To describe among individuals with dementia: (1) self-reported awareness of, and engagement in, advance care planning; (2) presence of advance care planning documentation in the health record and (3) concordance between self-reported completion of advance care planning and presence of documentation in the health record. Methods: An Australian prospective multicentre audit and cross-sectional survey. Individuals diagnosed with dementia who were able to speak English and were judged by a healthcare provider as having decision-making capacity were recruited from self-selected hospitals, residential aged care facilities and general practices across Australia. Results: Fifty-two people with dementia completed surveys and were included. Overall, 59.6% of participants had heard about advance care planning and 55.8% had discussed advance care planning with someone, most often a family member (48.1%). While 38.5% of participants had appointed a medical substitute decision maker, only 26.9% reported that they had written down their values and preferences for future care. Concordance between self-reported completion of advance care planning and presence of documentation in the health record was low (56.8%, κ=0.139; 57.7%, κ=0.053). Conclusion: Effective models that promote discussion, documentation and accessible storage of advance care planning documents for people with dementia are needed.
History
Journal title
BMJ Supportive and Palliative Care
Volume
12
Issue
3
Pagination
e464-e468
Publisher
BMJ Group
Language
en, English
College/Research Centre
College of Health, Medicine and Wellbeing
School
School of Medicine and Public Health
Rights statement
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