Journal
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY
Volume 59, Issue 8, Pages 1531-1536Publisher
WILEY-BLACKWELL
DOI: 10.1111/j.1532-5415.2011.03505.x
Keywords
hospice; quality of care; dying
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Funding
- National Institute of Aging [R01AG024265]
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OBJECTIVES: To examine the effectiveness of hospice services for persons dying from dementia from the perspective of bereaved family members. DESIGN: Mortality follow-back survey. SETTING: Death certificates were drawn from five states (AL, FL, TX, MA, and MN). PARTICIPANTS: Bereaved family members listed as the next of kin on death certificates when dementia was listed as the cause of death. MEASUREMENTS: Ratings of the quality of end-of-life care, perceptions of unmet needs, and opportunities to improve end-of-life care. Two questions were also asked about the peacefulness of dying and quality of dying. RESULTS: Of 538 respondents, 260 (48.3%) received hospice services. Family members of decedents who received hospice services reported fewer unmet needs and concerns with quality of care (adjusted odds ratio (AOR) = 0.49, 95% confidence interval (CI) = 0.33-0.74) and a higher rating of the quality of care (AOR = 2.0, 95% CI = 1.53-2.72). They also noted better quality of dying than those without hospice services. CONCLUSION: Bereaved family members of people with dementia who received hospice reported higher perceptions of the quality of care and quality of dying. J Am Geriatr Soc 59:1531-1536, 2011.
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