Literature DB >> 18713199

Dying with dementia: the views of family caregivers about quality of life.

Cherry Russell1, Heather Middleton, Chris Shanley.   

Abstract

OBJECTIVE: To document the views of family caregivers of persons with dementia about quality of life for their relative during the late and terminal stages of the disease, as part of an exploratory study of best quality care and support.
METHODS: Fifteen former caregivers (five wives, five husbands, two sons, three daughters) participated in in-depth semistructured interviews.
RESULTS: Participants identified three main sets of indicators of quality of life: the physical body, the physical and social environment and treatment with respect and dignity. The constructs 'quality of life' and 'quality of care' tended to be conflated in the experience of caregivers. An important role for caregivers was to interpret and represent the subjective experience of the person with dementia.
CONCLUSION: Quality of life needs to be understood from multiple perspectives. Caregivers' views are a central part of this understanding and should be used to inform future research and service development.

Entities:  

Mesh:

Year:  2008        PMID: 18713199     DOI: 10.1111/j.1741-6612.2008.00282.x

Source DB:  PubMed          Journal:  Australas J Ageing        ISSN: 1440-6381            Impact factor:   2.111


  6 in total

1.  Improving patients' quality of life at the end of life: comment on "factors important to patients' quality of life at the end of life".

Authors:  Alan B Zonderman; Michele K Evans
Journal:  Arch Intern Med       Date:  2012-08-13

2.  A Literature Review on Care at the End-of-Life in the Emergency Department.

Authors:  Roberto Forero; Geoff McDonnell; Blanca Gallego; Sally McCarthy; Mohammed Mohsin; Chris Shanley; Frank Formby; Ken Hillman
Journal:  Emerg Med Int       Date:  2012-03-06       Impact factor: 1.112

3.  Perspectives of people with dementia and carers on advance care planning and end-of-life care: A systematic review and thematic synthesis of qualitative studies.

Authors:  Marcus Sellars; Olivia Chung; Linda Nolte; Allison Tong; Dimity Pond; Deirdre Fetherstonhaugh; Fran McInerney; Craig Sinclair; Karen M Detering
Journal:  Palliat Med       Date:  2018-11-08       Impact factor: 4.762

Review 4.  Understanding the Needs of Australian Carers of Adults Receiving Palliative Care in the Home: A Systematic Review of the Literature.

Authors:  Elizabeth M Miller; Joanne E Porter
Journal:  SAGE Open Nurs       Date:  2021-02-24

Review 5.  Social networks, social capital and end-of-life care for people with dementia: a realist review.

Authors:  Joseph M Sawyer; Libby Sallnow; Nuriye Kupeli; Patrick Stone; Elizabeth L Sampson
Journal:  BMJ Open       Date:  2019-12-09       Impact factor: 2.692

Review 6.  Dignifying and undignifying aspects of care for people with dementia: a narrative review.

Authors:  Wendy van der Geugten; Anne Goossensen
Journal:  Scand J Caring Sci       Date:  2019-11-21
  6 in total

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