Literature DB >> 24381039

Understanding the dementia diagnosis: the impact on the caregiving experience.

Laura A Stokes1, Helen Combes, Graham Stokes.   

Abstract

OBJECTIVES: There is a paucity of research surrounding disclosure from the perspective of caring partners, therefore this research explores how caring partners understand and make sense of diagnostic information.
METHOD: Semi-structured interviews were conducted with 10 spouses of people with dementia. Interviews aimed to elicit participants' understanding of dementia and the way that information was used to make sense of dementia. Interviewee accounts were analysed using interpretative phenomenological analysis.
RESULTS: Four main themes emerged: lack of information; personal understanding and implications for adjustment; societal understanding and persistent stigma; and lack of partnership working.
CONCLUSIONS: The analysis indicated a lack of information and continued support following a diagnosis. In the absence of information and support, caring partners described difficulty understanding and adjusting to behavioural, physical and psychological changes in their partner. A greater understanding of the condition was beneficial in terms of adjustment and emotional responses to a partner.

Entities:  

Keywords:  carers; dementia diagnosis; experience; qualitative

Mesh:

Year:  2012        PMID: 24381039     DOI: 10.1177/1471301212447157

Source DB:  PubMed          Journal:  Dementia (London)        ISSN: 1471-3012


  8 in total

1.  A human factors and ergonomics approach to conceptualizing care work among caregivers of people with dementia.

Authors:  Nicole E Werner; Rachel A Rutkowski; Richard J Holden; Siddarth Ponnala; Andrea Gilmore-Bykovskyi
Journal:  Appl Ergon       Date:  2022-06-08       Impact factor: 3.940

2.  A process-based approach to exploring the information behavior of informal caregivers of people living with dementia.

Authors:  Rachel A Rutkowski; Siddarth Ponnala; Laura Younan; Dustin T Weiler; Andrea Gilmore Bykovskyi; Nicole E Werner
Journal:  Int J Med Inform       Date:  2020-11-12       Impact factor: 4.046

3.  How do factors of sociodemographic, health literacy and dementia experience influence carers' knowledge of dementia?

Authors:  Sophie Crawley; Kirsten Moore; Victoria Vickerstaff; Emily Fisher; Claudia Cooper; Elizabeth L Sampson
Journal:  Dementia (London)       Date:  2022-03-02

4.  In the Information Age, do dementia caregivers get the information they need? Semi-structured interviews to determine informal caregivers' education needs, barriers, and preferences.

Authors:  Kendra Peterson; Howard Hahn; Amber J Lee; Catherine A Madison; Alireza Atri
Journal:  BMC Geriatr       Date:  2016-09-23       Impact factor: 3.921

5.  Association Between Family Caregiver Burden and Affiliate Stigma in the Families of People with Dementia.

Authors:  Jian-An Su; Chih-Cheng Chang
Journal:  Int J Environ Res Public Health       Date:  2020-04-17       Impact factor: 3.390

Review 6.  Becoming a Family Caregiver to a Person With Dementia: A Literature Review on the Needs of Family Caregivers.

Authors:  Vibeke Østergaard Steenfeldt; Lars Christian Aagerup; Anna Holm Jacobsen; Ulla Skjødt
Journal:  SAGE Open Nurs       Date:  2021-07-22

7.  That mr. Alzheimer… you never know what he's up to, but what about me? A discourse analysis of how Swedish spouse caregivers can make their subject positions understandable and meaningful.

Authors:  Annica Lövenmark; Martina Summer Meranius; Lena Marmstål Hammar
Journal:  Int J Qual Stud Health Well-being       Date:  2018-12

8.  Perspectives of caregivers and volunteers on Stepping Stones for people with dementia.

Authors:  Areum Han; Diane Brown
Journal:  Hong Kong J Occup Ther       Date:  2018-11-14       Impact factor: 0.917

  8 in total

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