Literature DB >> 10388247

Family caregiver quality of life: differences between curative and palliative cancer treatment settings.

M A Weitzner1, S C McMillan, P B Jacobsen.   

Abstract

To compare the impact of cancer caregiving in curative and palliative settings on family caregiver quality of life (QOL), 267 family caregivers of cancer patients receiving curative treatment were compared to 134 family caregivers of cancer patients receiving palliative treatment through hospice. Both groups completed a demographic profile in addition to two self-report QOL questionnaires. Patient performance status and disease site were also recorded. Family caregivers of patients receiving palliative care had significantly lower QOL scores and lower scores on physical health. Hierarchical multiple regressions showed that after accounting for patient performance status, treatment status accounted for no additional significant variability in QOL scores. After accounting for caregiver level of education, treatment status accounted for no additional significant variability in physical health. These results suggest that the lower QOL scores of caregivers in the palliative setting are a reflection of the patients' poorer performance status. The lower physical health scores of caregivers in the palliative setting appear to be a reflection of their lower educational level. Additional research is needed to evaluate the influence of specific demands of caregiving and emotional distress of the caregiver on caregiver QOL.

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Year:  1999        PMID: 10388247     DOI: 10.1016/s0885-3924(99)00014-7

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  74 in total

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Review 4.  Physical, psychosocial, relationship, and economic burden of caring for people with cancer: a review.

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6.  Social support needs: discordance between home hospice nurses and former family caregivers.

Authors:  Maija Reblin; Kristin G Cloyes; Joan Carpenter; Patricia H Berry; Margaret F Clayton; Lee Ellington
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7.  Psychological distress and quality of life of palliative cancer patients and their caring relatives during home care.

Authors:  Heide Götze; Elmar Brähler; Lutz Gansera; Nina Polze; Norbert Köhler
Journal:  Support Care Cancer       Date:  2014-05-09       Impact factor: 3.603

8.  Assessing the Reliability and Validity of a Brief Measure of Caregiver Quality of Life.

Authors:  Debra Parker Oliver; Robin L Kruse; Jamie Smith; Karla Washington; George Demiris
Journal:  J Pain Symptom Manage       Date:  2019-07-31       Impact factor: 3.612

9.  Family Relationships and Psychosocial Dysfunction Among Family Caregivers of Patients With Advanced Cancer.

Authors:  Kathrine G Nissen; Kelly Trevino; Theis Lange; Holly G Prigerson
Journal:  J Pain Symptom Manage       Date:  2016-08-09       Impact factor: 3.612

10.  The Caregiver Quality of Life Cystic Fibrosis (CQOLCF) scale: modification and validation of an instrument to measure quality of life in cystic fibrosis family caregivers.

Authors:  Whitney Boling; David M Macrina; John P Clancy
Journal:  Qual Life Res       Date:  2003-12       Impact factor: 4.147

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