Literature DB >> 18996981

Defining distinct caregiver subpopulations by intensity of end-of-life care provided.

A Abernethy1, C Burns, J Wheeler, D Currow.   

Abstract

Interventions designed to assist informal caregivers who serve individuals at or near the end of life have predominantly focused on caregiving spouses. Can we define other caregiver subpopulations--by intensity of care provided--so as to enable better a) identification of caregiver needs and b) targeting of support to caregivers? The Health Omnibus Survey, an annual face-to-face survey in South Australia, collects health-related data from a representative sample of 4400 households. Piloted questions included in the 2001-2005 Health Omnibus surveys addressed death of a loved one, caregiving provided, impact of caregiving and caregiver characteristics. Of 18,224 respondents, 5302 reported a loved one's death due to terminal illness in the previous 5 years. In all, 502 (10%) provided daily care [5-7 days/week], 619 (12%) provided intermittent care [2-4 days/week] and 425 (8%) provided rare care. Active (daily plus intermittent) caregivers, compared with non-active (rare) caregivers, were more often women (63% vs 50%; P < 0.0001). Daily caregivers were distinguishable from intermittent; daily caregivers were more often widowed (95% vs 7%; P < 0.0001) and >or=60 years (80% vs 64%; P < 0.0001); intermittent caregivers were more commonly children/parents (35%), other relatives (33%), or friends (26%; P < 0.0001) and were better educated, more active in paid work and wealthier. Financial burden, experience at time of death, ability to move on after the death and need for grief support also differed by intensity of caregiving. Caregiver subpopulations can be defined according to intensity of caregiving with distinct demographic features helping to distinguish them.

Entities:  

Mesh:

Year:  2008        PMID: 18996981     DOI: 10.1177/0269216308098793

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  8 in total

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4.  Caregivers' perceived adequacy of support in end-stage lung disease: results of a population survey.

Authors:  David C Currow; Morag Farquhar; Alicia M Ward; Gregory B Crawford; Amy P Abernethy
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5.  Psychological morbidity and general health among family caregivers during end-of-life cancer care: A retrospective census survey.

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Journal:  Palliat Med       Date:  2018-08-21       Impact factor: 4.762

6.  Response to: Investigating the neurobehavioral symptoms of neuronopathic Hunter syndrome.

Authors:  J B Eisengart; K E King; E Shapiro; C B Whitley; J Muenzer
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7.  The Changing Tides of Caregiving During the COVID-19 Pandemic: How Decreasing and Increasing Care Provision Relates to Caregiver Well-Being.

Authors:  Amanda Leggett; Hyun Jung Koo; Bona Park; HwaJung Choi
Journal:  J Gerontol B Psychol Sci Soc Sci       Date:  2022-05-20       Impact factor: 4.942

8.  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 in total

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