Literature DB >> 21227632

Palliative caregivers who would not take on the caring role again.

David C Currow1, Catherine Burns, Meera Agar, Jane Phillips, Nikki McCaffrey, Amy P Abernethy.   

Abstract

CONTEXT: Health and social services rely heavily on family and friends for caregiving at the end of life.
OBJECTIVES: This study sought to determine the prevalence and factors associated with an unwillingness to take on the caregiving role again by interviewing former caregivers of palliative care patients.
METHODS: The setting for this study was South Australia, with a population of 1.6 million people (7% of the Australian population) and used the South Australian Health Omnibus, an annual, face-to-face, cross-sectional, whole-of-population, multistage, systematic area sampling survey, which seeks a minimum of 3000 respondents each year statewide. One interview was conducted per household with the person over the age of 15 who most recently had a birthday. Using two years of data (n=8377; 65.4% participation rate), comparisons between those who definitely would care again and those who would not was undertaken.
RESULTS: One in 10 people across the community provided hands-on care for someone close to them dying an expected death in the five years before being interviewed. One in 13 (7.4%) former caregivers indicated that they would not provide such care again irrespective of time since the person's death and despite no reported differences identified in unmet needs between those who would and would not care again. A further one in six (16.5%) would only "probably care again." The regression model identified that increasing age lessens the willingness to care again (odds ratio [OR] 3.94; 95% confidence interval [CI] 1.56, 9.95) and so does lower levels of education (OR 0.413; 95% CI 0.18, 0.96) controlling for spousal relationship.
CONCLUSION: These data suggest that assessment of willingness to care needs to be considered by clinical teams, especially in the elderly. Despite most active caregivers being willing to provide care again, a proportion would not.
Copyright © 2011 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2011        PMID: 21227632     DOI: 10.1016/j.jpainsymman.2010.06.017

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


  9 in total

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Authors:  Ruth McConigley; Tania Shelby-James; David C Currow
Journal:  Health Expect       Date:  2013-08-19       Impact factor: 3.377

Review 2.  Physical, psychosocial, relationship, and economic burden of caring for people with cancer: a review.

Authors:  Afaf Girgis; Sylvie Lambert; Claire Johnson; Amy Waller; David Currow
Journal:  J Oncol Pract       Date:  2012-12-04       Impact factor: 3.840

3.  Measuring caregiver outcomes in palliative care: a construct validation study of two instruments for use in economic evaluations.

Authors:  Renske Hoefman; Hareth Al-Janabi; Nikki McCaffrey; David Currow; Julie Ratcliffe
Journal:  Qual Life Res       Date:  2014-11-08       Impact factor: 4.147

4.  Self-Reporting by Unsafe Drivers Is, with Education, More Effective than Mandatory Reporting by Doctors.

Authors:  Nathan J Elgar; Adrian J Esterman; Nick A Antic; Brian J Smith
Journal:  J Clin Sleep Med       Date:  2016-03       Impact factor: 4.062

5.  Better informing decision making with multiple outcomes cost-effectiveness analysis under uncertainty in cost-disutility space.

Authors:  Nikki McCaffrey; Meera Agar; Janeane Harlum; Jonathon Karnon; David Currow; Simon Eckermann
Journal:  PLoS One       Date:  2015-03-09       Impact factor: 3.240

6.  Health-related quality of life measured using the EQ-5D-5L: South Australian population norms.

Authors:  Nikki McCaffrey; Billingsley Kaambwa; David C Currow; Julie Ratcliffe
Journal:  Health Qual Life Outcomes       Date:  2016-09-20       Impact factor: 3.186

7.  Family Caregivers Who Would Be Unwilling to Provide Care at the End of Life Again: Findings from the Health Survey for England Population Survey.

Authors:  Miriam J Johnson; Victoria Allgar; Una Macleod; Annie Jones; Steven Oliver; David Currow
Journal:  PLoS One       Date:  2016-01-25       Impact factor: 3.240

8.  Protocol for a systematic review of preference-based instruments for measuring care-related outcomes and their suitability for the palliative care setting.

Authors:  Nikki McCaffrey; Hareth Al-Janabi; David Currow; Renske Hoefman; Julie Ratcliffe
Journal:  BMJ Open       Date:  2016-09-12       Impact factor: 2.692

9.  The contributions of family care-givers at end of life: A national post-bereavement census survey of cancer carers' hours of care and expenditures.

Authors:  Christine Rowland; Barbara Hanratty; Mark Pilling; Bernard van den Berg; Gunn Grande
Journal:  Palliat Med       Date:  2017-02-01       Impact factor: 4.762

  9 in total

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