Abstract
Purpose
Patients’ knowledge, beliefs, or concerns about opioids, palliative care, and homecare can be potential barriers to providing quality palliative care. The primary aim of this study was to clarify knowledge about opioids, beliefs about palliative care, and concerns about homecare in advanced cancer patients.
Methods
An anonymous questionnaire was sent to 1,619 outpatients with advanced cancer at 25 hospitals in four different regions of Japan. The respondents were asked to report their knowledge about opioids, beliefs about palliative care, and concerns about homecare, in addition to the levels of their sense of security regarding receiving cancer care in the region.
Results
A total of 925 responses were received. In total, 28% believed that opioids are addictive and/or shorten life; 52% believed that palliative care is only for terminally ill patients; 75% agreed that being taken care of at home puts a heavy burden on the family; and 61% agreed that home-visit services cannot respond to sudden changes in a patient’s condition. Levels of patients’ sense of security were significantly higher in those who agreed that “opioids can relieve most pain caused by cancer” “palliative care relieves pain and distress”, “palliative care is provided along with chemotherapy and/or radiation therapy”, and “pain can be alleviated as effectively through home-visit services as it can at the hospital”, and those who disagreed with the statements that “home-visit services cannot respond to sudden changes in a patient’s condition” and “being taken care of at home puts a burden on the family”.
Conclusions
Advanced cancer patients frequently had incorrect knowledge about opioids, a belief that palliative care is only for terminally ill patients, and concerns about homecare, especially the family burden and responses to sudden changes. Providing appropriate information about the safety of opioids, the availability of palliative care during the entire course of the disease, and realistic information about homecare is of marked importance to promote patients’ sense of security.
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References
Yabroff KR, Mandelblatt JS, Ingham J (2004) The quality of medical care at the end-of-life in the USA: existing barriers and examples of process and outcome measures. Palliat Med 18:202–216
Morita T, Miyashita M, Shibagaki M et al (2006) Knowledge and beliefs about end-of-life care and the effects of specialized palliative care: a population-based survey in Japan. J Pain Symptom Manag 31:306–316
Jacobsen R, Møldrup C, Christrup L, Sjøgren P (2009) Patient-related barriers to cancer pain management: a systematic exploratory review. Scand J Caring Sci 23:190–208
Ward SE, Goldberg N, McCauley VM et al (1993) Patient-related barriers to management of cancer pain. Pain 52:319–329
Weiss SC, Emanuel LL, Fairclough DL, Emanuel EJ (2001) Understanding the experience of pain in terminally ill patients. Lancet 357:1311–1315
Yates PM, Edwards HE, Nash RE et al (2002) Barriers to effective cancer pain management: a survey of hospitalized cancer patients in Australia. J Pain Symptom Manag 23:393–405
Morita T, Tsunoda J, Inoue S, Chihara S (2000) Concerns of Japanese hospice inpatients about morphine therapy as a factor in pain management: a pilot study. J Palliat Care 16(4):54–58
Morita T, Akechi T, Ikenaga M et al (2005) Late referrals to specialized palliative care service in Japan. J Clin Oncol 23:2637–2644
Fadul N, Elsayem A, Palmer JL et al (2009) Supportive versus palliative care: what’s in a name?: a survey of medical oncologists and midlevel providers at a comprehensive cancer center. Cancer 115:2013–2021
Miyashita M, Hirai K, Morita T, Sanjo M, Uchitomi Y (2008) Barriers to referral to inpatient palliative care units in Japan: a qualitative survey with content analysis. Support Care Cancer 16:217–222
Sanjo M, Miyashita M, Morita T et al (2008) Perceptions of specialized inpatient palliative care: a population-based survey in Japan. J Pain Symptom Manag 35:275–282
Morita T, Miyashita M, Tsuneto S, Sato K, Shima Y (2009) Late referrals to palliative care units in Japan: nationwide follow-up survey and effects of palliative care team involvement after the Cancer Control Act. J Pain Symptom Manag 38:191–196
Gomes B, Higginson IJ (2006) Factors influencing death at home in terminally ill patients with cancer: systematic review. Br Med J 332:515–521
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
Ministry of Health, Labor, and Welfare. Place of end-of-life care. http://www.mhlw.go.jp/shingi/2004/07/s0723-8d8.html. Accessed 8 March, 2011 (In Japanese)
Fukui S, Fukui N, Kawagoe H (2004) Predictors of place of death for Japanese patients with advanced-stage malignant disease in homecare settings: a nationwide survey. Cancer 101:421–429
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
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
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
Funk L, Allan D, Stajduhar K (2009) Palliative family caregivers’ accounts of health care experiences: the importance of “security.”. Palliat Support Care 7:435–447
Milberg A, Strang P (2000) Met and unmet needs in hospital-based homecare: qualitative evaluation through open-ended questions. Palliat Med 14:533–534
Milberg A, Strang P, Carlsson M, Börjesson S (2003) Advanced palliative homecare: next-of-kin’s perspective. J Palliat Med 6:749–756
Igarashi A, Miyashita M, Morita T, et al. (2011) A scale for measuring feelings of support and security about cancer care in a region of Japan: a potential new endpoint of palliative care. J Pain Symptom Manag (in press)
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
Uki J, Mendoza T, Cleeland CS, Nakamura Y, Takeda F (1998) A brief cancer pain assessment tool in Japanese: the utility of the Japanese Brief Pain Inventory–BPI-J. J Pain Symptom Manag 16:364–373
Morita T, Hirai K, Sakaguchi Y, Maeyama E, Tsuneto S, Shima Y (2004) Measuring the quality of structure and process in end-of-life care from the bereaved family perspective. J Pain Symptom Manag 27:492–501
Miyashita M, Morita T, Hirai K (2008) Evaluation of end-of-life cancer care from the perspective of bereaved family members: the Japanese experience. J Clin Oncol 26:3845–3852
Morita T, Miyashita M, Tsuneto S, Shima Y (2008) Palliative care in Japan: shifting from the stage of disease to the intensity of suffering. J Pain Symptom Manag 36:e6–e7
Tang ST (2003) When death is imminent: where terminally ill patients with cancer prefer to die and why. Cancer Nurs 26:245–251
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
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
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 Manag 40:224–234
Acknowledgments
We gratefully thank all staff of the participating institutions. This study was funded by the Third Term Comprehensive Control Research for Cancer Health and Labour Sciences Research Grant.
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Akiyama, M., Takebayashi, T., Morita, T. et al. Knowledge, beliefs, and concerns about opioids, palliative care, and homecare of advanced cancer patients: a nationwide survey in Japan. Support Care Cancer 20, 923–931 (2012). https://doi.org/10.1007/s00520-011-1161-5
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DOI: https://doi.org/10.1007/s00520-011-1161-5