Family support for hospice caregivers

Author:

Patterson Lisa B.1,Dorfman Lorraine T.2

Affiliation:

1. Hospice of Dubuque, Dubuque, Iowa

2. School of Social Work and Aging Studies Program, University of Iowa, Iowa City, Iowa

Abstract

This qualitative study investigated family supports for primary care-givers of hospice patients, as perceived by both the primary caregiver and other family members involved in patient care. Family support was conceptualized in terms of (1) who offers support; (2) types of support; (3) frequency of support; (4) family communication; and (5) change in family relationship during the caregiving process. Twenty-four interviews were conducted with 10 primary caregivers and six family members identified by the caregiver as the person they could most call on for help. Interviews were conducted shortly after admission to hospice and approximately two months after the death of the hospice patient. Primary caregivers and other family members involved in care agreed that the primary caregiver provided most care. They also agreed that family members provided instrumental and emotional support, the frequency of assistance was appropriate, and families had grown closer since learning of the terminal illness. There was less agreement regarding family communication during the caregiving process. Implications for interventions with families of hospice patients are discussed.

Publisher

SAGE Publications

Subject

General Medicine

Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The Communicative Ecology of End of Life Care;The Handbook of Applied Communication Research;2020-04-17

2. “One Size Doesn’t Fit All”—Partners in Hospice Care, an Individualized Approach to Bereavement Intervention;OMEGA - Journal of Death and Dying;2015-03-09

3. Caregiving for Older Latinos at End of Life;American Journal of Hospice and Palliative Medicine®;2012-05-25

4. The Caregiving Journey for Family Members of Relatives With Cancer;Clinical Journal of Oncology Nursing;2010-09-29

5. Part 2: Home-based family caregiving at the end of life: a comprehensive review of published qualitative research (1998-2008);Palliative Medicine;2010-06-24

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