Literature DB >> 16218162

Preferences for place of care and place of death among informal caregivers of the terminally ill.

Kevin Brazil1, Doris Howell, Michel Bedard, Paul Krueger, Christine Heidebrecht.   

Abstract

OBJECTIVES: (1) To determine informal caregivers perceptions about place of care and place of death; and (2) to identify variables associated with a home death among terminally ill individuals who received in-home support services in a publicly funded home care system. PARTICIPANTS AND
DESIGN: A total of 216 informal caregivers participated in a bereavement interview. Data collection included care recipient and informal caregiver characteristics, the use of and satisfaction with community services, and preferences about place of death.
RESULTS: Most caregivers reported that they and the care recipient had a preferred place of death (77 and 68%, respectively) with over 63% reporting home as the preferred place of death. Caregivers had a greater preference for an institutional death (14%) than care recipients (4.7%). While 30% of care recipients did not die in their preferred location, most caregivers (92%) felt, in retrospect, that where the care recipient died was the appropriate place of death. Most caregivers reported being satisfied with the care that was provided. The odds of dying at home were greater when the care recipient stated a preference for place of death (OR: 2.92; 95% CI: 1.25, 6.85), and the family physician made home visits during the care recipients last month of life (Univariate odds ratios (OR): 4.42; 95% CI: 1.46, 13.36). DISCUSSION: The ethic of self-control and choice for the care recipient must be balanced with consideration for the well being of the informal caregiver and responsiveness of the community service system.

Entities:  

Mesh:

Year:  2005        PMID: 16218162     DOI: 10.1191/0269216305pm1050oa

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  47 in total

1.  Health Care for People Approaching the End of Life: An Evidentiary Framework.

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Journal:  Ont Health Technol Assess Ser       Date:  2014-12-01

2.  Preferred place of care and place of death of the general public and cancer patients in Japan.

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3.  A place to die: The case for paediatric inpatient hospices.

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Journal:  Paediatr Child Health       Date:  2008-05       Impact factor: 2.253

4.  The family physician's perceived role in preventing and guiding hospital admissions at the end of life: a focus group study.

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Journal:  Ann Fam Med       Date:  2014 Sep-Oct       Impact factor: 5.166

5.  Which hospice patients with cancer are able to die in the setting of their choice? Results of a retrospective cohort study.

Authors:  Neha Jeurkar; Sue Farrington; Teresa R Craig; Julie Slattery; Joan K Harrold; Betty Oldanie; Joan M Teno; David J Casarett
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6.  Temporal association between home nursing and hospital costs at end of life in three provinces.

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Review 7.  [Palliative care : Challenges in the intensive care unit].

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8.  Why are some patients in treatment for advanced cancer reluctant to consult their GP?

Authors:  Birgit Aabom; Per Pfeiffer
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9.  Where do you want to spend your last days of life? Low concordance between preferred and actual site of death among hospitalized adults.

Authors:  Stacy Fischer; Sung-Joon Min; Lilia Cervantes; Jean Kutner
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10.  Visioning for secondary palliative care service hubs in rural communities: a qualitative case study from British Columbia's interior.

Authors:  Valorie A Crooks; Heather Castleden; Nadine Schuurman; Neil Hanlon
Journal:  BMC Palliat Care       Date:  2009-10-09       Impact factor: 3.234

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