Literature DB >> 28276143

Experiences and needs of spouses of persons with young-onset frontotemporal lobe dementia during the progression of the disease.

Aud Johannessen1, Anne-Sofie Helvik1,2,3, Knut Engedal1, Kirsten Thorsen1,4.   

Abstract

BACKGROUND: Two of the most common types of young-onset dementia (<65 years old) are Alzheimer's disease and frontotemporal lobe dementia (FTLD). A limited amount of research that focuses on the needs of spouses of persons with young-onset FTLD (yo-FTLD) has been published. Thus, we have carried out a study aiming to examine the spouses of yo-FTLD experiences and needs for assistance in daily life.
METHOD: Qualitative interviews with 16 informants (aged 51-69 years; nine wives, six husbands and one male cohabitant) were conducted in 2014 and 2015. The data were analysed by reformulated and modified method of Grounded Theory.
FINDINGS: From the interviews, three main themes with subthemes emerged: The first main theme that appeared is sneaking signs at the early stage of dementia. It covers two subthemes: incomprehensible early signs and lack of self-insight. The second main theme that appeared is other relations, and it covers three subthemes: the torment, interference with work and vanishing social relations. The third main theme: needs for assistance through all stages of dementia, are described under three subthemes: Relief of the diagnosis, support at home and the path to the nursing home.
CONCLUSION: The interviews showed that spouses and the whole family of yo-FTLD need interdisciplinary, individualised and specialised support throughout the progression of the disorder. Furthermore, there is a need for more knowledge about yo-FTLD among health personnel, including general practitioners. IT-solutions can contribute to developing such services and support to the entire family.
© 2017 Nordic College of Caring Science.

Entities:  

Keywords:  coping; early-onset dementia; experiences; frontotemporal lobe dementia; need; partners; qualitative study; services; support

Mesh:

Year:  2017        PMID: 28276143     DOI: 10.1111/scs.12397

Source DB:  PubMed          Journal:  Scand J Caring Sci        ISSN: 0283-9318


  16 in total

1.  Relationship Turmoil and Emotional Empathy in Frontotemporal Dementia.

Authors:  Akitoshi Takeda; Virginia E Sturm; Katherine P Rankin; Robin Ketelle; Bruce L Miller; David C Perry
Journal:  Alzheimer Dis Assoc Disord       Date:  2019 Jul-Sep       Impact factor: 2.703

2.  In It Together: A Qualitative Meta-Synthesis of Common and Unique Psychosocial Stressors and Adaptive Coping Strategies of Persons With Young-Onset Dementia and Their Caregivers.

Authors:  Sarah Bannon; Mira Reichman; Paula Popok; Juliana Wagner; Melissa Gates; Simrit Uppal; Lisa LeFeber; Bonnie Wong; Bradford C Dickerson; Ana-Maria Vranceanu
Journal:  Gerontologist       Date:  2022-02-09

3.  Time from Symptom Debut to Dementia Assessment by the Specialist Healthcare Service in Norway.

Authors:  Anne-Sofie Helvik; Knut Engedal; Jūratė Šaltytė Benth; Geir Selbæk
Journal:  Dement Geriatr Cogn Dis Extra       Date:  2018-03-27

4.  "To be, or not to be": experiencing deterioration among people with young-onset dementia living alone.

Authors:  Aud Johannessen; Knut Engedal; Per Kristian Haugen; Marcia Cristina Nascimento Dourado; Kirsten Thorsen
Journal:  Int J Qual Stud Health Well-being       Date:  2018-12

5.  How Children of Parents With Dementia Can Make Their Subject Positions Understandable and Meaningful.

Authors:  Annica Lövenmark
Journal:  Qual Health Res       Date:  2019-09-18

6.  Sex and gender differences in caregiving burden experienced by family caregivers of persons with dementia: A systematic review.

Authors:  Chen Xiong; Melissa Biscardi; Arlene Astell; Emily Nalder; Jill I Cameron; Alex Mihailidis; Angela Colantonio
Journal:  PLoS One       Date:  2020-04-20       Impact factor: 3.240

7.  Metaphors for the Meaning of Caring for a Spouse with Dementia.

Authors:  Kirsten Thorsen; Aud Johannessen
Journal:  J Multidiscip Healthc       Date:  2021-01-29

8.  The value of "us"-Expressions of togetherness in couples where one spouse has dementia.

Authors:  Anna Swall; Christine Williams; Lena Marmstål Hammar
Journal:  Int J Older People Nurs       Date:  2019-12-30       Impact factor: 2.115

9.  Awareness of dementia and coping to preserve quality of life: a five-year longitudinal narrative study.

Authors:  Kirsten Thorsen; Marcia C N Dourado; Aud Johannessen
Journal:  Int J Qual Stud Health Well-being       Date:  2020-12

10.  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
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