Literature DB >> 26484426

Gender Differences in Caregiving at End of Life: Implications for Hospice Teams.

Karla T Washington1, Kenneth C Pike2, George Demiris3,4, Debra Parker Oliver1, David L Albright5, Alexandria M Lewis6.   

Abstract

BACKGROUND: Researchers have identified important gender differences in the experience of caring for a family member or friend living with advanced disease; however, trends suggest that these differences may be diminishing over time in response to changing gender roles. In addition, while many studies have found caregiving experiences and outcomes to be poorer among female caregivers, noteworthy exceptions exist.
OBJECTIVE: The primary aim of this exploratory study was to determine how, if at all, current day caregiving at end of life varies by gender.
METHODS: We conducted a secondary analysis of data from a multisite randomized controlled trial of a family caregiving intervention performed between 2010 and 2014. We compared female and male hospice family caregivers on baseline variables using χ(2) tests for association of categorical variables and t-tests for continuous variables. Our sample included 289 family caregivers of individuals receiving services from one of two hospice agencies located in the northwestern United States. Demographic data and other categorical variables of interest were provided via caregiver self-report using an instrument created specifically for this study. Reaction to caregiving and caregiving burden were measured using the Caregiver Reaction Assessment (CRA).
RESULTS: As it related to caregiving, females had significantly lower self-esteem and more negative impact on their schedule, health, and family support than males. No gender differences were detected with regard to the impact of caregiving on individuals' finances.
CONCLUSIONS: Despite changing social expectations, pronounced gender differences persist in caregiving at the end of life.

Mesh:

Year:  2015        PMID: 26484426      PMCID: PMC4677542          DOI: 10.1089/jpm.2015.0214

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  18 in total

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Authors:  C Nijboer; M Triemstra; R Tempelaar; R Sanderman; G A van den Bos
Journal:  Soc Sci Med       Date:  1999-05       Impact factor: 4.634

3.  The caregiver reaction assessment (CRA) for caregivers to persons with chronic physical and mental impairments.

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4.  Caregiving and the stress process: an overview of concepts and their measures.

Authors:  L I Pearlin; J T Mullan; S J Semple; M M Skaff
Journal:  Gerontologist       Date:  1990-10

Review 5.  Part 1: Home-based family caregiving at the end of life: a comprehensive review of published quantitative research (1998-2008).

Authors:  Ki Stajduhar; L Funk; C Toye; Ge Grande; S Aoun; Cj Todd
Journal:  Palliat Med       Date:  2010-06-18       Impact factor: 4.762

6.  Gender differences in caregiver stressors, social resources, and health: an updated meta-analysis.

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Journal:  J Gerontol B Psychol Sci Soc Sci       Date:  2006-01       Impact factor: 4.077

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Authors:  Debra Parker Oliver; Marlys Peck
Journal:  J Soc Work End Life Palliat Care       Date:  2006

8.  Problem solving interventions: an opportunity for hospice social workers to better meet caregiver needs.

Authors:  Debra Parker Oliver; Karla Washington; George Demiris; Elaine Wittenberg-Lyles; Hannah Novak
Journal:  J Soc Work End Life Palliat Care       Date:  2012

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