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Planning for Serious Illness amongst Community-Dwelling Older Adults

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  • Donna Goodridge

Abstract

Older adults have long been encouraged to maintain their autonomy by expressing their wishes for health care before they become too ill to meaningfully participate in decision making. This study explored the manner in which community-dwelling adults aged 55 and older plan for serious illness. An online survey was conducted within the province of Saskatchewan, Canada, with 283 adults ranging in age from 55 to 88 years. Planning for future medical care was important for the majority (78.4%) of respondents, although only 25.4% possessed a written advance care plan and 41.5% had designated a substitute decision maker. Sixty percent of respondents reported conversations about their treatment wishes; nearly half had discussed unacceptable states of health. Associations between key predictor variables and planning behaviors (discussions about treatment wishes or unacceptable states of health; designation of a substitute decision maker; preparation of a written advance care plan) were assessed using binary logistic regression. After controlling for all predictor variables, self-reported knowledge about advance care planning was the key variable significantly associated with all four planning behaviors. The efforts of nurses to educate older adults regarding the process of advance care planning can play an important role in enhancing autonomy.

Suggested Citation

  • Donna Goodridge, 2013. "Planning for Serious Illness amongst Community-Dwelling Older Adults," Nursing Research and Practice, Hindawi, vol. 2013, pages 1-7, April.
  • Handle: RePEc:hin:jnlnrp:427917
    DOI: 10.1155/2013/427917
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    1. Kellehear, Allan, 1984. "Are we a 'death-denying' society? A sociological review," Social Science & Medicine, Elsevier, vol. 18(9), pages 713-721, January.
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