Quality of dying in nursing home residents dying with dementia: does advanced care planning matter? A nationwide postmortem study

PLoS One. 2014 Mar 10;9(3):e91130. doi: 10.1371/journal.pone.0091130. eCollection 2014.

Abstract

Background: Advance care planning is considered a central component of good quality palliative care and especially relevant for people who lose the capacity to make decisions at the end of life, which is the case for many nursing home residents with dementia. We set out to investigate to what extent (1) advance care planning in the form of written advance patient directives and verbal communication with patient and/or relatives about future care and (2) the existence of written advance general practitioner orders are related to the quality of dying of nursing home residents with dementia.

Methods: Cross-sectional study of deaths (2010) using random cluster-sampling. Representative sample of nursing homes in Flanders, Belgium. Deaths of residents with dementia in a three-month period were reported; for each the nurse most involved in care, GP and closest relative completed structured questionnaires.

Findings: We identified 101 deaths of residents with dementia in 69 nursing homes (58% response rate). A written advance patient directive was present for 17.5%, GP-orders for 56.7%. Controlling for socio-demographic/clinical characteristics in multivariate regression analyses, chances of having a higher mean rating of emotional well-being (less fear and anxiety) on the Comfort Assessment in Dying with Dementia scale were three times higher with a written advance patient directive and more specifically when having a do-not-resuscitate order (AOR 3.45; CI,1.1-11) than for those without either (AOR 2.99; CI,1.1-8.3). We found no association between verbal communication or having a GP order and quality of dying.

Conclusion: For nursing home residents with dementia there is a strong association between having a written advance directive and quality of dying. Where wishes are written, relatives report lower levels of emotional distress at the end of life. These results underpin the importance of advance care planning for people with dementia and beginning this process as early as possible.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Advance Care Planning / statistics & numerical data*
  • Aged, 80 and over
  • Autopsy
  • Belgium / epidemiology
  • Death*
  • Dementia / mortality*
  • Female
  • Humans
  • Male
  • Nursing Homes / statistics & numerical data*

Grants and funding

This study is supported by a grant from Vrije Universiteit Brussel (GOA HW, VUB 2007) and is part of the Dying Well with Dementia study. L. Van den Block is a postdoctoral research fellow of the Research Foundation-Flanders (FWO). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.