Surrogatedecision makers' understanding of dementia patients' prior wishes for end-of-life care

Betty S. Black, Linda A. Fogarty, Hilary Phillips, Thomas Finucane, David J. Loreck, Alva Baker, David M. Blass, Peter V. Rabins

Research output: Contribution to journalArticlepeer-review

Abstract

Objectives: This study examines how surrogate decision makers for dementia patients developed an understanding of patient preferences about end-of-life (EOL) care and patient wishes. Methods: Semistructured interviews were conducted with 34 surrogate decision makers for hospice-eligible nursing home patients with dementia. The data were content analyzed. Results: Most surrogates reported that patients had previously completed an advance directive (59%), discussed preferences for EOL care (56%), or done both (38%). Catalysts for and barriers to completing an advance directive or having EOL care discussions included factors that were both intrinsic and extrinsic to the patient. The most commonly reported wish for EOL care was to not be kept alive by "machines" or "extraordinary measures." Discussion: Health care providers may be able to assist patients and families by normalizing discussions of dying, encouraging advance care planning, helping them identify goals for EOL care, and providing information to support treatment decisions consistent with patients' wishes.

Original languageEnglish (US)
Pages (from-to)627-650
Number of pages24
JournalJournal of Aging and Health
Volume21
Issue number4
DOIs
StatePublished - Jun 2009

Keywords

  • Advance care planning
  • Advance directives
  • Advanced dementia
  • Nursing home patients
  • Treatment preferences

ASJC Scopus subject areas

  • Health(social science)
  • Sociology and Political Science
  • Life-span and Life-course Studies

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