Challenges and strategies among family care partners of community‐dwelling persons with dementia nearing end of life

Author:

McDarby Meghan1ORCID,Russell David23,King Lori3,Kozlov Elissa4,Luth Elizabeth A.5ORCID

Affiliation:

1. Department of Psychiatry and Behavioral Sciences Memorial Sloan Kettering Cancer Center New York New York USA

2. Department of Sociology Appalachian State University Boone North Carolina USA

3. Center for Home Care Policy & Research VNS Health New York New York USA

4. Department of Health Behavior, Society and Policy Rutgers School of Public Health Piscataway New Jersey USA

5. Institute for Health, Health Care Policy, and Aging Research and Department of Family Medicine and Community Health Rutgers University Piscataway New Jersey USA

Abstract

AbstractBackgroundA growing number of persons living with dementia (PLwD) die at home with hospice care. However, there is limited information describing the needs of dying, community‐dwelling persons with dementia and their family care partners (FCPs). Understanding the range of challenges faced by these FCPs is requisite to developing resources and refining support infrastructure. The current study identifies caregiving challenges unique to this population and strategies FCPs use to address those challenges.MethodsSemi‐structured interviews were conducted with 40 current or recently bereaved FCPs of home hospice patients living with dementia, recruited from geriatrics clinics and a hospice agency in the New York metropolitan area. A thematic analysis guided by deductive and inductive approaches was used to code interview transcripts, identify broader conceptual categories, and search for themes.ResultsThree themes were identified related to challenges faced by FCPs: (1) managing emotions and reacting to behaviors associated with advanced dementia; (2) lack of knowledge and adequate information related to dementia: disease progression and caregiving skills; and (3) maintaining FCP well‐being: self‐care and caregiver burden. Three themes were identified that describe strategies FCPs of PLwD employ to cope with end‐of‐life caregiving demands: (1) accepting help from professional caregivers and hospice support services; (2) getting knowledge and information about dementia; and (3) pragmatic approaches and acceptance of signs and symptoms of disease progression.ConclusionsFCPs of PLwD near the end of life (EOL) face caregiving challenges unique to dementia and dying. While FCPs are resourceful in identifying novel strategies for managing burden and caregiving responsibilities, our results point to gaps in the current support infrastructure for this population at the EOL. Findings also identify areas of need for care partners navigating end‐of‐life issues.

Funder

NIH Clinical Center

Publisher

Wiley

Subject

Geriatrics and Gerontology

Reference32 articles.

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3. Change in End-of-Life Care for Medicare Beneficiaries

4. National Hospice and Palliative Care Organization. NHPCO Facts and Figures 2021 Edition. NHPCO; 2021. Accessed February 23 2022.file:///C:/Users/Elizabeth%20Luth/Downloads/NHPCO-Facts-Figures-2021%20(1).pdf.

5. Trends and Factors Associated with Place of Death for Individuals with Dementia in the United States

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