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Scand J Caring Sci. 2017 Dec;31(4):779-788. doi: 10.1111/scs.12397. Epub 2017 Mar 9.

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

Author information

1
Vestfold Hospital Trust, Norwegian National Advisory Unit on Ageing and Health, Tønsberg, Norway.
2
Department of Public Health and General Practice, Faculty of Medicine, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
3
St. Olav's University Hospital, Trondheim, Norway.
4
Norwegian Social Research (NOVA), University College of Oslo and Akershus, Oslo, Norway.

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.

KEYWORDS:

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

PMID:
28276143
DOI:
10.1111/scs.12397
[Indexed for MEDLINE]

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