Abstract
The changing context of palliative care over the last decade highlights the importance of recent research on home-based family caregiving at the end of life. This article reports on a comprehensive review of quantitative research (1998-2008) in this area, utilizing a systematic approach targeting studies on family caregivers, home settings, and an identified palliative phase of care (n = 129). Methodological challenges were identified, including: small, non-random, convenience samples; reliance on descriptive and bivariate analyses; and a dearth of longitudinal research. Robust evidence regarding causal relationships between predictor variables and carer outcomes is lacking. Findings suggest the need for knowledge regarding: family caregiving for patients with non-malignant terminal conditions; whether needs and outcomes differ between family caregivers at the end of life and comparison groups; and caregiver outcomes in bereavement. Clear definitions of family caregiving, end of life, and needs are required as well as greater application and testing of theoretical and conceptual explanations. © 2010 The Author(s).
Original language | English |
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Pages (from-to) | 573-593 |
Number of pages | 20 |
Journal | Palliative Medicine |
Volume | 24 |
Issue number | 6 |
DOIs | |
Publication status | Published - Sept 2010 |
Keywords
- caregivers
- home care services
- palliative care
- review
- terminally ill