Evidence map›Paper›PMID 33658249›Full record

ArticleBMJ supportive & palliative care2021

Advance care planning participation by people with dementia: a cross-sectional survey and medical record audit.

Jamie Bryant, Marcus Sellars, Amy Waller, Karen Detering, Craig Sinclair, Rasa Ruseckaite, Ben White, Linda Nolte

Abstract read
In one paragraph

Article in BMJ supportive & palliative care, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Observational
  4. Public awareness of legal decision-making capacity and planning instruments in dementia: implications for health care practitioners.Psychiatry, psychology, and law : an interdisciplinary journal of the Australian and New Zealand Association of Psychiatry, Psychology and Law · 2023
    Article
  5. Observational
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jamie BryantHealth Behaviour Research Collaborative,School of Medicine and Public Health, The University of Newcastle, Callaghan, New South Wales, Australia jamie.bryant@newcastle.edu.au.ORCID http://orcid.org/0000-0001-9378-5852
Marcus SellarsAdvance Care Planning Australia, Austin Health, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0002-8299-0313
Amy WallerHealth Behaviour Research Collaborative,School of Medicine and Public Health, The University of Newcastle, Callaghan, New South Wales, Australia.
Karen DeteringAdvance Care Planning Australia, Austin Health, Melbourne, Victoria, Australia.
Craig SinclairCentre of Excellence in Population Ageing Research, University of New South Wales, Sydney, New South Wales, Australia.
Rasa RuseckaiteDepartment of Epidemiology and Preventive Medicine, Monash University, Clayton, Victoria, Australia.
Ben WhiteAustralian Centre for Health Law Research, Queensland University of Technology, Brisbane, Queensland, Australia.ORCID http://orcid.org/0000-0003-3365-939X
Linda NolteAdvance Care Planning Australia, Austin Health, Melbourne, Victoria, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo 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.

methodsAn 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.

resultsFifty-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

conclusionEffective models that promote discussion, documentation and accessible storage of advance care planning documents for people with dementia are needed.

Indexed as

quality of lifeterminal care

Identifiers

PMID33658249
PMCPMC9380490

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.