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End-of-life decisions in individuals dying with dementia in Belgium.

Tijdschriftbijdrage - Tijdschriftartikel

OBJECTIVES: To describe the prevalence and characteristics of end-of-life decisions in individuals dying with dementia in Belgium. DESIGN: Retrospective mail survey. SETTING: Brussels and Flanders, Belgium. PARTICIPANTS: Physicians certifying a large random sample of deaths (n = 8,627). MEASUREMENTS: End-of-life decision-making in individuals dying with dementia (n = 361) was compared through bivariate and multivariable analyses with decision-making in individuals dying from cancer (n = 1,276) as reference group. RESULTS: Response rate was 54.7%. The intense pain and symptoms of individuals with dementia was alleviated less often than those of individuals with cancer (odds ratio (OR) = 0.50, P < .001), and individuals with dementia were more likely to have life-prolonging treatment withheld or withdrawn (OR = 1.40, P = .048). Five individuals with dementia (1.3%) requested euthanasia but did not receive it; 60 (4.7%) individuals with cancer who requested euthanasia received it, and 48 (3.8%) who requested it did not (OR = 0.04, P = .047). Individuals with dementia rarely had capacity to participate in decision-making, which more often involved their families than in individuals with cancer (OR = 1.99, P = .009). Little prospect of improvement (59.7%), pointless life prolongation (54.5%), poor quality of life (46.2%), and prevention of further suffering (37.6%) were important reasons for end-of-life decisions in individuals with dementia. CONCLUSION: End-of-life decision-making in individuals dying with dementia differs from that in individuals with cancer, more often involving forgoing of life-prolonging treatment and less often involving intensifying pain and symptom treatment. Considerations typically involve the prospects of the individual with dementia as opposed to the severity of their present situation. Optimal processes of advance care planning may address the burdensome decision falling to physicians and family regarding when to allow the individual to die.
Tijdschrift: J Am Geriatrics Soc
ISSN: 0002-8614
Issue: 2
Volume: 63
Pagina's: 290-296
Jaar van publicatie:2015
Trefwoorden:End-of-Life decisions, dementia, palliative care, advance care planning
  • WoS Id: 000349893300010
  • ORCID: /0000-0001-6277-072X/work/76555438
  • ORCID: /0000-0002-7224-9476/work/61725550
  • Scopus Id: 84923311489
  • DOI: https://doi.org/10.1111/jgs.13255
  • VABB Id: c:vabb:395974
Toegankelijkheid:Open