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Article
Men as Caregivers at the End of Life
Journal of Palliative Medicine
  • Erik K. Fromme, Oregon Health & Science University
  • Linda L. Drach, Oregon Health & Science University
  • Susan W. Tolle, Oregon Health & Science University
  • Patricia Ebert, Oregon Health & Science University
  • Pamela Miller, Portland State University
  • Nancy Perrin, Oregon Health & Science University
  • Virginia P. Tilden, University of Nebraska Medical Center
Document Type
Article
Publication Date
12-1-2005
Subjects
  • Social workers -- United States -- Case studies,
  • Caregivers -- Case studies
Abstract

Background: Few studies have focused on men as caregivers at the end-of-life. The objective of this secondary data analysis was to examine the experiences of men involved in end-oflife caregiving, focusing on caregiver strain.

Methods: We used a random sample of Oregon death certificates to telephone survey family caregivers of Oregonians who had died 2 to 5 months earlier in private homes, nursing homes, and other community-based settings. Measurements included single-item indicators and embedded scales to measure caregiver strain and perceived decedent symptom distress. For the 25 husbands, sons, wives, and daughters who reported the highest levels of strain, we also analyzed caregivers' description of the decedent's last few days of life.

Results: The sample included 1384 caregiver interviews from a pool of 3048 death certificates. Men constituted 29% of the caregivers, including 15% sons, 9% husbands, and 5% others. In a linear regression model, male gender was a significant predictor of lower caregiver strain (p < 0.001). The strongest predictor of high end-of-life caregiver strain was the severity of the decedents' symptom distress. The qualitative analysis revealed that men used fewer words than women did to describe their experiences, and, despite subsequently reporting the highest levels of caregiving strain, only 15% of men spontaneously mentioned their own struggles.

Conclusions: As caregivers at the end of life, men are less common and less likely to report caregiver strain and decedent symptom distress. Health care professionals should actively ask men about these issues and listen carefully, as their responses may be brief and understated.

Description

This is the publisher's final pdf. Copyright (2005) Mary Ann Liebert Inc. http://www.liebertpub.com/

Persistent Identifier
http://archives.pdx.edu/ds/psu/14430
Citation Information
Fromme, E. K., Drach, L. L., Tolle, S. W., Ebert, P., Miller, P., Perrin, N., & Tilden, V. P. (2005). Men as caregivers at the end of life. Journal of palliative medicine, 8(6), 1167-1175.