Literature DB >> 2179063

A critique of the caregiving literature.

B M Barer1, C L Johnson.   

Abstract

In this critical review of the recent caregiving literature, we identify several methodological problems. Specifically noted are the variable and often confusing definitions of the caregiver, the lack of specification of needs, overrepresentation of self-selected samples, and the absence of attention to the total support network. We conclude that future researchers should focus on the total support process in later life, rather than on a single caregiver, so that policy can best be designed to mesh the informal and formal support systems.

Mesh:

Year:  1990        PMID: 2179063     DOI: 10.1093/geront/30.1.26

Source DB:  PubMed          Journal:  Gerontologist        ISSN: 0016-9013


  10 in total

1.  Caring too much? Cultural lag in African Americans' perceptions of filial responsibilities.

Authors:  L Groger; P S Mayberry
Journal:  J Cross Cult Gerontol       Date:  2001-03

2.  Cross-survey differences in national estimates of numbers of caregivers of disabled older adults.

Authors:  Erin R Giovannetti; Jennifer L Wolff
Journal:  Milbank Q       Date:  2010-09       Impact factor: 4.911

3.  Limit of support and reaction to illness: An exploration of black elders' pathways to long-term care settings.

Authors:  L Groger
Journal:  J Cross Cult Gerontol       Date:  1994-10

4.  Informal care and caregiver's health.

Authors:  Young Kyung Do; Edward C Norton; Sally C Stearns; Courtney Harold Van Houtven
Journal:  Health Econ       Date:  2014-04-17       Impact factor: 3.046

5.  Elder Care, Multiple Role Involvement, and Well-Being Among Middle-Aged Men and Women in Japan.

Authors:  Saeko Kikuzawa
Journal:  J Cross Cult Gerontol       Date:  2015-12

Review 6.  Frailty in elderly people: an evolving concept.

Authors:  K Rockwood; R A Fox; P Stolee; D Robertson; B L Beattie
Journal:  CMAJ       Date:  1994-02-15       Impact factor: 8.262

7.  A randomized trial of mobile health support for heart failure patients and their informal caregivers: impacts on caregiver-reported outcomes.

Authors:  John D Piette; Dana Striplin; Nicolle Marinec; Jenny Chen; James E Aikens
Journal:  Med Care       Date:  2015-08       Impact factor: 2.983

8.  Defining the role of the caregiver in Alzheimer's disease treatment.

Authors:  Henry Brodaty; Alisa Green
Journal:  Drugs Aging       Date:  2002       Impact factor: 3.923

9.  Care inequality: care received according to gender, marital status, and socioeconomic status among Korean older adults with disability.

Authors:  Soong-Nang Jang; Ichiro Kawachi
Journal:  Int J Equity Health       Date:  2019-07-03

10.  Māori elders' perspectives of end-of-life family care: whānau carers as knowledge holders, weavers, and navigators.

Authors:  Mary Louisa Simpson; Kirstie McAllum; John Oetzel; Kay Berryman; Rangimahora Reddy
Journal:  Palliat Care Soc Pract       Date:  2022-09-08
  10 in total

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