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Cross-cultural conceptualization of a good end of life with dementia: a qualitative study

  • Mayumi Nishimura
  • , Karen Harrison Dening
  • , Elizabeth L. Sampson
  • , Edison Iglesias de Oliveira Vidal
  • , Wilson Correia de Abreu
  • , Sharon Kaasalainen
  • , Yvonne Eisenmann
  • , Laura Dempsey
  • , Kirsten J. Moore
  • , Nathan Davies
  • , Sascha R. Bolt
  • , Judith M.M. Meijers
  • , Natashe Lemos Dekker
  • , Mitsunori Miyashita
  • , Miharu Nakanishi
  • , Takeo Nakayama
  • , Jenny T. van der Steen
  • Kyoto University School of Public Health
  • Dementia UK
  • University College London
  • São Paulo State University
  • University of Porto
  • McMaster University, Faculty of Health Sciences
  • University Hospital of Cologne
  • Royal Melbourne Hospital
  • Maastricht University Medical Centre
  • Zuyderland Medical Center
  • Leiden University
  • Tohoku University Graduate School of Medicine
  • Leiden University Medical Center
  • Radboud University Medical Center

Research output: Contribution to journalArticlepeer-review

21 Citations (Scopus)

Abstract

Background: Research on the nature of a “good death” has mostly focused on dying with cancer and other life-limiting diseases, but less so on dementia. Conceptualizing common cross-cultural themes regarding a good end of life in dementia will enable developing international care models. Methods: We combined published qualitative studies about end of life with dementia, focus group and individual interviews with the researchers, and video-conferencing and continuous email discussions. The interviews were audio-recorded and transcribed verbatim. The data were analyzed thematically, and the researchers developed common themes referring to their original studies. Results: Fourteen qualitative researchers representing 14 cross-cultural studies covering qualitative data of 121 people with dementia and 292 family caregivers. The researchers and data were from eight countries UK, The Netherlands, Japan, Portugal, Germany, Canada, Brazil, and Ireland. Three focus groups, five individual interviews, and video-conferencing were conducted and feedback on multiple iterations was gained by 190 emails between May 2019 and April 2020 until consensus was achieved. Nine cross-culturally common themes emerged from the discussions and shared interpretation of the data of persons with dementia and family caregivers. Three represent basic needs: “Pain and Symptoms Controlled,” “Being Provided Basic Care,” and “A Place like Home.” Other themes were “Having Preferences Met,” “Receiving Respect as a Person,” “Care for Caregivers,” “Identity Being Preserved,” “Being Connected,” and “Satisfaction with Life and Spiritual Well-being.” “Care for Caregivers” showed the greatest difference in emphasis across cultures. Good relationships were essential in all themes. Conclusions: The common cross-cultural themes comprise a framework underpinned by value placed on personhood and dignity, emphasizing that interdependency through relationships is essential to promote a good end of life with dementia. These themes and valuing the importance of relationships as central to connecting the themes could support care planning and further development of a dementia palliative care model. Trial registration: The Graduate School and Faculty of Medicine Kyoto University (R1924–1).

Original languageEnglish
Article number106
JournalBMC Palliative Care
Volume21
Issue number1
DOIs
Publication statusPublished - Dec 2022

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Culture
  • Dementia
  • Palliative care

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