Conceptualization of a good end-of-life experience with dementia in Japan: a qualitative study.


Journal

International psychogeriatrics
ISSN: 1741-203X
Titre abrégé: Int Psychogeriatr
Pays: England
ID NLM: 9007918

Informations de publication

Date de publication:
02 2020
Historique:
pubmed: 29 8 2019
medline: 26 3 2021
entrez: 29 8 2019
Statut: ppublish

Résumé

To conceptualize a "good end of life" for people with dementia from the perspectives of bereaved family caregivers in Japan. A qualitative study using in-depth, semi-structured interviews focused on the family caregivers' perceptions of their loved one's experiences. Family caregivers who had lost their relatives with dementia more than six months previously were recruited using maximum variation sampling by cultural subpopulation. A thematic analysis was conducted. From 30 interviews held, four main themes emerged. A good end of life for people with dementia means experiencing a "Peaceful Death" while "Maintaining Personhood" at a "Preferred Place" allowing for feelings of "Life Satisfaction." A "Preferred Place" emerged as a basic requirement to achieving a good end of life according to the three other themes, in particular, "Maintaining Personhood." However, the interviewees experienced difficulties in ensuring that their loved ones stayed at a "Preferred Place." Despite different cultural backgrounds, perceptions of a good end of life with dementia were remarkably similar between Japan and Western countries. However, recent societal changes in family structures and long-term care access in Japan may explain the theme of a comfortable place taking a central position. We suggest that these themes be considered and translated into care goals. They could supplement established end-of-life care goals for quality of life in dementia, which aim to maximize functioning and increase comfort. Ethics Committee of the Graduate School and Faculty of Medicine, Kyoto University (R0808-2).

Identifiants

pubmed: 31455444
pii: S1041610219001017
doi: 10.1017/S1041610219001017
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

255-265

Auteurs

Mayumi Nishimura (M)

Department of Health Informatics, School of Public Health, Kyoto University, Kyoto, Japan.

Ayako Kohno (A)

Department of Health Informatics, School of Public Health, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Jenny T van der Steen (JT)

Department of Public Health and Primary Care, Leiden University Medical Center, Leiden, The Netherlands.
Department of Primary and Community Care, Radboud University Medical Center, Nijmegen, The Netherlands.

Toru Naganuma (T)

Center for Innovative Research for Communities and Clinical Excellence (CiRC LE) Fukushima Medical University, Fukushima, Japan.

Takeo Nakayama (T)

Department of Health Informatics, School of Public Health, Kyoto University, Kyoto, Japan.
Department of Health Informatics, School of Public Health, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

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