Literature DB >> 19755629

Religious care required for Japanese terminally ill patients with cancer from the perspective of bereaved family members.

Takuya Okamoto1, Michiyo Ando, Tatsuya Morita, Kei Hirai, Ryo Kawamura, Miyashita Mitsunori, Kazuki Sato, Yasuo Shima.   

Abstract

The aim of this study was to explore the most suitable religious care for Japanese terminally ill patients with cancer based on the opinions of bereaved family members. A multicenter questionnaire survey on palliative care service was sent to 592 bereaved family members of patients with cancer who were admitted to palliative care units in Japan, and 430 responded by mail. In the section of the questionnaire about religious care, 382 responses were used for quantitative analysis, and 71 responses about religious care for qualitative analysis. In the current study, the 71 responses were grouped into families with and without a religion and were analyzed qualitatively. Families with a religion (N = 28) chose answers such as ''Instrumental care'' such as music or a religious event, ''Freedom of choice of kinds for religious care,'' ''Staff involvement of religious care,'' ''Meeting with a pastoral care workers,'' and ''Burden of offering a different kind of personal religion.'' In contrast, families without a religion (N = 44) chose answers such as ''Instrumental care,'' ''Freedom of choice whether patients receive religious care or not,'' ''Spiritual care,'' ''Not being able to accept religious care,'' and ''Burden of thinking about a religion and nuisance.'' These findings suggest that Japanese bereaved families with a religion generally regard religious care positively and prefer care through their own religion, whereas some families without a religion require religious care but some do not prefer it.

Entities:  

Mesh:

Year:  2009        PMID: 19755629     DOI: 10.1177/1049909109346562

Source DB:  PubMed          Journal:  Am J Hosp Palliat Care        ISSN: 1049-9091            Impact factor:   2.500


  1 in total

1.  Spiritual and emotional support of primary informal end-of-life caregivers in Nova Scotia.

Authors:  Leila Sloss; Beverley Lawson; Frederick I Burge
Journal:  J Palliat Care       Date:  2012       Impact factor: 2.250

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.