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Preferred place of care and place of death of the general public and cancer patients in Japan

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Abstract

Dying at a favorite place is one of the important determinants for terminally ill cancer patients. The primary aim was to clarify (1) differences in preferred place of care and place of death among the general public across four areas across Japan and (2) preferred place of care and place of death among community-representative cancer patients. A cross-sectional mail survey was conducted on 8,000 randomly selected general population. We examined preferred place of care and place of death using two vignettes and obtained a total of 3,984 (50%) responses. For the pain scenario, approximately 50% of the general public throughout four areas chose home as their preferred place of care; and for the dependent-without-pain scenario, about 40% chose home as preferred place of care. In cancer patients, for both scenarios, approximately 40% chose home as the preferred place of care, and they were significantly less likely to choose home. The most preferred combination of place of care and place of death was home hospice for both groups. Although there were statistically significant differences in preferred place of care and place of death among the four regions, the absolute difference was less than 8%. Independent determinants of choosing home as place of care included concern about family burden and being unable to adequately respond to sudden changes out of working hours. In conclusion, establishing more accessible home and hospice service is strongly required through arranging regional resources to reduce family burden, alleviating patient-perceived burdens, and improving 24-h support at home.

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References

  1. Steinhauser KE, Christakis NA, Clipp EC, McNeilly M, McIntyre L, Tulsky JA (2000) Factors considered important at the end of life by patients, family, physicians, and other care providers. JAMA 284:2476–2482

    Article  PubMed  CAS  Google Scholar 

  2. Miyashita M, Sanjo M, Morita T, Hirai K, Uchitomi Y (2007) Good death in cancer care: a nationwide quantitative study. Ann Oncol 18:1090–1097

    Article  PubMed  CAS  Google Scholar 

  3. Detering KM, Hancock AD, Reade MC, Silvester W (2010) The impact of advance care planning on end of life care in elderly patients: randomized controlled trial. BMJ 340:c1345

    Article  PubMed  Google Scholar 

  4. Wood J, Storey L, Clark D (2007) Preferred place of care: an analysis of the ‘first 100’ patient assessments. Palliat Med 21:449–450

    Article  PubMed  Google Scholar 

  5. Meeussen K, Van de Block L, Bossuyt N et al (2009) GPs’ awareness of patients’ preference for place of death. Br J Gen Pract 59:665–670

    Article  PubMed  Google Scholar 

  6. Higginson IJ, Sen-Gupta GJ (2000) Place of care in advanced cancer: a qualitative systematic literature review of patient preferences. J Palliat Med 3:287–300

    Article  PubMed  CAS  Google Scholar 

  7. Sanjo M, Miyashita M, Morita T et al (2007) Preferences regarding end-of-life cancer care and associations with good-death concepts: a population-based survey in Japan. Ann Oncol 18:1539–1547

    Article  PubMed  CAS  Google Scholar 

  8. Ministry of Health, Labor, and Welfare. Available at http://www.mhlw.go.jp/shingi/2004/07/s0723-8d8.html. (In Japanese)

  9. Gomes B, Higginson IJ (2006) Factors influencing death at home in terminally ill patients with cancer: systematic review. BMJ 332:515–521

    Article  PubMed  Google Scholar 

  10. Fukui S, Fukui N, Kawagoe H (2004) Predictors of place of death for Japanese patients with advanced-stage malignant disease in home care settings: a nationwide survey. Cancer 101:421–429

    Article  PubMed  Google Scholar 

  11. Foreman LM, Hunt RW, Luke CG, Roder DM (2006) Factors predictive of preferred place of death in the general population of South Australia. Palliat Med 20:447–453

    Article  PubMed  Google Scholar 

  12. Choi KS, Chae YM, Lee CG et al (2005) Factors influencing preferences for place of terminal care and of death among cancer patients and their families in Korea. Support Care Cancer 13:565–572

    Article  PubMed  Google Scholar 

  13. Brazil K, Howell D, Bedard M, Krueger P, Heidebrecht C (2005) Preferences for place of care and place of death among informal caregivers of the terminally ill. Palliat Med 19:492–499

    Article  PubMed  Google Scholar 

  14. Yamasaki M, Ebihara S, Freeman S et al (2008) Sex differences in the preference for place of death in community-dwelling elderly people in Japan. J Am Geriatr Soc 56:376

    Article  PubMed  Google Scholar 

  15. Morita T, Akechi T, Ikenaga M et al (2005) Late referrals to specialized palliative care service in Japan. J Clin Oncol 23:2637–2644

    Article  PubMed  Google Scholar 

  16. Yamagishi A, Morita T, Miyashita M et al (2008) Palliative care in Japan: current status and a nationwide challenge to improve palliative care by the Cancer Control Act and the Outreach Palliative Care Trial of Integrated Regional Model (OPTIM) study. Am J Hosp Palliat Care 25:412–418

    PubMed  Google Scholar 

  17. Agar M, Currow DC, Shelby-James TM, Plummer J, Sanderson C, Abernethy AP (2008) Preference for place of care and place of death in palliative care: are these different questions? Palliat Med 22:787–795

    Article  PubMed  CAS  Google Scholar 

  18. Munday D, Petrova M, Dale J (2009) Exploring preferences for place of death with terminally ill patients: qualitative study of experiences of general practitioners and community nurses in England. BMJ 338:b2391

    Article  Google Scholar 

  19. Butow PN, Maclean M, Dunn SM, Tattersall MHN, Boyer MJ (1997) The dynamics of change: cancer patients’ preferences for information, involvement and support. Ann Oncol 8:857–863

    Article  PubMed  CAS  Google Scholar 

  20. Thomas C, Morris SM, Clark D (2004) Place of death: preferences among cancer patients and their careers. Soc Sci Med 58:2431–2444

    Article  PubMed  CAS  Google Scholar 

  21. McPherson CJ, Wilson KG, Murray MA (2007) Feeling like a burden: exploring the perspectives of patients at the end of life. Soc Sci Med 64:417–427

    Article  PubMed  Google Scholar 

  22. Akazawa T, Akechi T, Morita T et al (2010) Self-perceived burden in terminally ill cancer patients: a categorization of care strategies based on bereaved family members’ perspectives. J Pain Symptom Manage 40(2):224–234

    Article  PubMed  Google Scholar 

  23. Tang ST (2003) When death is imminent: where terminally ill patients with cancer prefer to die and why. Cancer Nurs 26:245–251

    Article  PubMed  Google Scholar 

  24. Gott M, Seymour J, Bellamy G, Clark D, Ahmedzai S (2004) Older people’s views about home as a place of care at the end of life. Palliat Med 18:460–467

    Article  PubMed  Google Scholar 

  25. Grunfeld E, Coyle D, Whelan T et al (2004) Family caregiver burden: results of a longitudinal study of breast cancer patients and their principal caregivers. CMAJ 170:1795–1801

    Article  PubMed  Google Scholar 

  26. Shaw C, McNamara R, Abrams K et al (2009) Systematic review of respite care in the frail elderly. Health Technol Assess 13:1–224, iii

    PubMed  CAS  Google Scholar 

  27. Bee PE, Barnes P, Luker KA (2008) A systematic review of informal caregivers’ needs in providing home-based end-of-life care to people with cancer. J Clin Nurs 18:1379–1393

    Article  Google Scholar 

  28. Docherty A, Owens A, Asadi-Lari M, Petchey R, Jacky W, Carter YH (2008) Knowledge and information needs of informal caregivers in palliative care: a qualitative systematic review. Palliat Med 22:153–171

    Article  PubMed  Google Scholar 

  29. Harding R, Higginson IJ (2003) What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness. Palliat Med 17:63–74

    Article  PubMed  CAS  Google Scholar 

  30. Sato K, Miyashita M, Morita T, Suzuki M (2009) The long-term effect of a population-based educational intervention focusing on end-of-life home care, life-prolongation treatment, and knowledge about palliative care. J Palliat Care 25:206–212

    PubMed  Google Scholar 

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Correspondence to Akemi Yamagishi.

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Yamagishi, A., Morita, T., Miyashita, M. et al. Preferred place of care and place of death of the general public and cancer patients in Japan. Support Care Cancer 20, 2575–2582 (2012). https://doi.org/10.1007/s00520-011-1373-8

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  • DOI: https://doi.org/10.1007/s00520-011-1373-8

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