1. Hou SY, Ke CL, Su YC, Lung FW, Huang CJ. Exploring the burden of the primary family caregivers of schizophrenia patients in Taiwan. Psychiatry and Clinical Neurosciences 62: 508– 514, 2008.
2. Lowyck B, De Hert M, Peeters E, Wampers M, Gilis P, Peuskens J. A study of the family burden of 150 family members of schizophrenic patients. European Psychiatry 19: 395–401, 2004.
3. Perlick D, Clarkin JF, Sirey J, Raue P, Greenfield S, Struening E, Rosenheck R. Burden experienced by care-givers of persons with bipolar affective disorder. The British Journal of Psychiatry 175:56–62, 1999.
4. Sugiyama T, Tamiya N, Watanabe T, et al. Association of care recipients’ care‐need level with family caregiver participation in health check‐ups in Japan. Geriatrics and Gerontology International 18: 26-32, 2018.
5. Onwumere J, Zhou Z, Kuipers E. Informal caregiving relationships in psychosis: reviewing the impact of patient violence on caregivers. Frontiers in Psychology. 2018. Available from: https://doi.org/10.3389/fpsyg.2018.01530 (access date: 2020 September 16)
6. Velligan DI, Brain C, Bouérat Duvold L, Agid O. Caregiver burdens associated with treatment- resistant schizophrenia: a quantitative caregiver survey of experiences, attitudes, and perceptions. Frontiers in Psychiatry 10: 584, 2019. Available from:https://doi.org/10.3389/fpsyt.2019.00584 (access date: 2020 September 16)
7. Gater A, Rofail D, Tolley C, et al. "Sometimes it's difficult to have a normal life": Results from a qualitative study exploring caregiver burden in schizophrenia. Schizophrenia Research and Treatment. Available from: http://dx.doi.org/10.1155/2014/368215 (access date: 2020 September 25)
8. Visiting Nursing system in Japan. Available from: https://www.jvnf.or.jp/homon/homevisit_nursing_service.html (access date: 2016 Aug 27)
9. Home-visit Nursing Service. Available from: https://www.jvnf.or.jp/homon/english/hns2014.pdf (access date: 2016 Aug 27)
10. Rose G, Segesten K. Someone who cares--patients' experiences concerning health examinations. Scandinavian Journal of Caring Sciences 9(2):105–112, 1995.
11. Takahashi Y, Okamoto R, Ichimori A, et al. How attendance of a health guidance program relates to health checkup results and medical service data among specific medical checkup examinees after three years. Journal of Wellness and Health Care 43(1): 55‒64, 2019.
12. Hansen JO, Buus N. Living with a depressed person in Denmark: A qualitative study. International Journal of Social Psychiatry 59: 401–406, 2013.
13. González-Bono E, de Andrés-Garcia S, Romero-Martínez Á, et al. Cardiovascular response to psychosocial repeated stress in caregivers of offspring with schizophrenia. Spanish Journal of Psychology 16: e3:1–11, 2013.
14. Vadher S, Desai R, Panchal B, et al. Understanding resilience factors among caregivers of people with Alzheimer's disease in Spain. Psychology Research and Behavior Management 13: 1011– 1025, 2020.
15. McKibbin CL, Ancoli-Israel S, Dimsdale J, et al. Sleep in spousal caregivers of people with Alzheimer's disease. Sleep 28(10): 1245–1250, 2005.
16. Aas, I.M. Guidelines for rating Global Assessment of Functioning (GAF). Ann Gen Psychiatry 10, 2 (2011). Available from: https://doi.org/10.1186/1744-859X-10-2 (access date: 2020 Jan 12)
17. Van Wijngaarden B, Maarten K, Martin K, et.al. Caring for people with depression or with schizophrenia: Are the consequences different? Psychiatry Research 169(1): 62–69, 2009.
18. Lobban F, Postlethwaite A, Glentworth D, et al. A systematic review of randomised controlled trials of interventions reporting outcomes for relatives of people with psychosis. Clinical Psychology Review 33: 372–82, 2013.
19. Chadda RK. Caring for the family caregivers of persons with mental illness. Indian Journal of Psychiatry 56(3): 221–227, 2014.
20. Arai Y, Kudo K, Hosokawa T, Washio M, Miura H, Hisamichi S. Reliability and validity of the Japanese version of the Zarit Caregiver Burden interview. Psychiatry and Clinical Neurosciences 51(5): 281–287, 1997.
21. Bédard M, Molloy DW, Squire L, Dubois S, Lever JA, O'Donnell M. The Zarit Burden Interview: A new short version and screening version. Gerontologist 41: 652–657, 2001.
22. Hébert R, Bravo G, Préville M. Reliability, validity and reference values of the Zarit Burden Interview for assessing informal caregivers of community‐dwelling older persons with dementia. Canadian Journal of Aging 19: 494–507, 2000.
23. Kumamoto K, Arai Y. Validation of 'personal strain' and 'role strain': subscales of the short version of the Japanese version of the Zarit Burden Interview (J-ZBI_8). Psychiatry and Clinical Neurosciences 58(6):606-10 (2004).
24. Fukuhara S, Suzukamo Y. Manual of SF-8 Japanese version: Institute for Health Outcomes & Process Evaluation Research, Kyoto, 2004.
25. Liu Z, Heffernan C, Tan J. Caregiver burden: A concept analysis. International Journal of Nursing Sciences 7: 438–445, 2020.
26. Chen FP, Greenberg JS. A positive aspect of caregiving: The influence of social support on caregiving gains for family members of relatives with schizophrenia. Community Mental Health Journal 40: 423–435, 2004.
27. World Health Organization. Constitution. Available from: https://www.who.int/about/who-we-are/constitution (access date: 2019 May 4)
28. Ehsan N, Johar N, Saleem T, Khan MA, Ghauri S. Negative repercussions of caregiving burden: Poor psychological well-being and depression. Pakistan Journal of Medical Sciences 34(6): 1452– 1456, 2018.
29. Marutani T, Chhim S, Nishio A, et al. Quality of life and its social determinants for patients with schizophrenia and family caregivers in Cambodia. PLOS ONE. Available from: https://doi.org/10.1371/journal.pone.0229643 (access date: 2020 December 24)
30. Bipeta R, Yerramilli SSRR, Pillutla SV. Perceived stigma in remitted psychiatric patients and their caregivers and its association with self-esteem, quality of life, and caregiver depression. East Asian Archives of Psychiatry 30: 101–107, 2020.
論文の公開元へ
