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Title: | Advance care planning participation by people with dementia: a cross-sectional survey and medical record audit. | Austin Authors: | Bryant, Jamie;Sellars, Marcus ;Waller, Amy;Detering, Karen M ;Sinclair, Craig;Ruseckaite, Rasa;White, Ben;Nolte, Linda | Affiliation: | Health Behaviour Research Collaborative,School of Medicine and Public Health, The University of Newcastle, Callaghan, New South Wales, Australia School of Medicine and Public Health, University of Newcastle, Callaghan, New South Wales, Australia Centre of Excellence in Population Ageing Research, University of New South Wales, Sydney, New South Wales, Australia Neuroscience Research Australia, Randwick, New South Wales, Australia Australian Centre for Health Law Research, Queensland University of Technology, Brisbane, Queensland, Australia Department of Epidemiology and Preventive Medicine, Monash University, Clayton, Victoria, Australia Health Behaviour Research Collaborative,School of Medicine and Public Health, The University of Newcastle, Callaghan, New South Wales, Australia School of Medicine and Public Health, Health Behaviour Research Collaborative, The University of Newcastle, Callaghan, New South Wales, Australia Advance Care Planning |
Issue Date: | 3-Mar-2021 | Date: | 2021 | Publication information: | BMJ Supportive & Palliative Care 2021; online first: 3 March | Abstract: | 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. 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. 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). Effective models that promote discussion, documentation and accessible storage of advance care planning documents for people with dementia are needed. | URI: | https://ahro.austin.org.au/austinjspui/handle/1/26004 | DOI: | 10.1136/bmjspcare-2020-002550 | ORCID: | 0000-0001-9378-5852 0000-0002-8299-0313 0000-0003-3365-939X |
Journal: | BMJ supportive & palliative care | PubMed URL: | 33658249 | Type: | Journal Article | Subjects: | quality of life terminal care |
Appears in Collections: | Journal articles |
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