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第五章 研究討論與結論

第五節 研究結論

本研究以淡水馬偕紀念醫院

100

名癌症第三或第四期別病人之家屬作為研究 多項,探討其善終觀念。善終觀念包括善終概念以及臨終照護兩部分,研究更以 不同的分析方法瞭解不同背景變項的家屬對其善終觀念之差異性,以及觀念間之 相關和差異。本研究為「韓、日、臺三國對善終感受之比較」研究案中臺灣癌症 病人的家屬的部分,問卷以韓國主辦方參考

Miyashita

等人

(2007)

Morita

等人

(2006)

Sanjo

等人

(2007)

的日本善終研究中所使用的短版善終概念問卷

(Good

Death Inventory)

和臨終照護問卷為測量工具。

本研究為臺灣少有以癌症病人的家屬作為研究對象的善終觀念研究,研究結 果初步分析出癌症病人的家屬認為重要的善終概念,以及對於臨終照顧的選擇和 看法。研究結果發現,癌症病人的家屬在眾多善種屬性中,免於身體的疼痛、不 造成家人的負擔、自然的死亡、保持愉快的心情和對於醫師的信任為最重要,但 他們較希望能自己決定自己的醫療抉擇、不希望有無效和無謂的治療和不希望猝

出直接的對比,但研究中家屬們的臨終地點和死亡地點偏好、預後告知的偏好方 式和善終概念的重要性比較,可作為未來研究的基礎,往後可朝更多不同的方向 進一步研究。

研究結果可供生死相關教育者和醫療相關人士有初步參考,建議未來可朝此 方向繼續進行研究,更深入瞭解此族群的善終觀念和其重要性。經翻譯的短版善 終概念問卷獲良好的信度,未來可繼續使用此問卷為臨床測量工具,讓醫療相關 人員更瞭解病人、家屬或其他相關人士的善終概念,配合著臨終照顧的選項,以 在與病人和家庭討論時協助做出更適合的醫療決定和滿足個別不同的需求。

參考文獻

一、中文文獻

林子涵(2017)。末期病人的善終觀點(未出版之碩士論文)。國立臺北護理健 康大學,臺北市。

[Lin, T. H. (2017). The terminally ill’s perspectives on good death. (Unpublished master thesis). The National Taipei University of Nursing and Health

Science, Taipei.]

林美伶、葉莉莉、陳清惠(

2009

)。影響病人參與醫療決策之論述。護理雜誌,

56(3)

83-87

[Lin, M. L., Yeh, L., & Chen, C. H. (2009). Patient involvement in medical decision making. The Journal of Nursing, 56(3), 83-87.]

財團法人中華民國(臺灣)安寧照顧基金會(

2017

11

14

日)。現有合約 醫院。取自

http://www.hospice.org.tw/2009/chinese/hospital.php

陳亭儒、胡文郁(2011)。善終之概念分析。長庚護理,

22(1),45-52。

[Chen, T. R., & Hu, W. Y. (2011). Concept analysis of good dying. Chang Gung Nursing, 22(1), 45-52.]

陳亭儒、胡文郁、程邵儀、邱泰源(

2013

)。善終評量之反思。安寧療護,

18 (1)

76-88

doi:10.6537/TJHPC.2013.18(1).7

[Chen, T. R., Hu, W. Y., Cheng, S. Y., & Chiu, T. Y. (2013). Reflection on measurement of good death. Taiwan Journal of Hospice Palliative Care, 18(1), 76-88. doi:10.6537/TJHPC.2013.18(1).7]

陳錫琦、陳淑香(

2007

)。生命教育課程建構

以善終為取向。醫護科技學刊,

9(2)

154-168

doi:10.6563/TJHS.2007.9(2).7

[Chen, S. C., & Chen, S. H. (2007). A life education curriculum from a ‘good death’prespective. The Journal of Health Science, 9(2), 154-168.

doi:10.6563/TJHS.2007.9(2).7]

張珠玲、胡庭禎(2008)。護理系學生對「善終」觀念的分析。弘光學報,

52

113-221。doi:10.6615/HAR.200804.52.11

[Chang, C. L.,& Hu, T. C. (2008). The analysis of the conception of ‘serene death’for

part-time nursing students.Hungkuang Academic Review,52,113-121.

張麗卿(2016)。病人自主權利法-善終的抉擇。東海大學法學研究,

50

1-47。

[Zhang, L. Q. (2016). Patient autonomy act- choice of good death. Tunghai University Law Study, 50, 1-47.]

曾韻如、邱泰源、胡文郁、程邵儀、姚建安、陳慶餘(

2005

)。老年癌末病人善 終之評估。安寧療護雜誌,

10(1)

13-23

doi:10.6537/TJHPC.2005.10(1).2 [Tseng, Y. J., Chiu, T. Y., Hu, W. Y., Cheng, S. Y., Yao, C. A., & Chen, C. Y. (2005).

Good death assessment of geriatric patients with termnal cancers. Taiwan Journal of Hospice Palliative Care, 10(1), 13-23. doi:10.6537/TJHPC.2005.10(1).2]

曾麗華(

2013

)。失親家屬的哀傷與接受安寧緩和療護病人善終之探討(未出版 之碩士論文)。輔英科技大學,高雄市。

[Tseng, L. H. (2013). The bereaved family member’s grief and the hospice palliative care patients’ good death from familie’s perspective

.

(Unpublished master thesis).

Fooyin Univerisity, Kaohsiung.]

趙可式(1997)。臺灣癌症期末病患對善終意義的體認。安寧療護雜誌,

5

51-61。

[Chao, C. S. (1997). The meaning of good dying for terminally ill cancer patients in Taiwan. The Journal of Nursing, 5, 51-61.]

熊誼芳、賴允亮、蘇韋如(

2014

)。邁向安寧緩和醫療的新一頁。生命教育研究,

6(2)

99-118

[Hsiung, Y., Lai, Y. L., & Su, W. J. (2014). The next era of palliative care in Taiwan:

A look at where we have been and where we may go. Journal of Life Education, 6(2), 99-118.]

羅耀明(

2011

)。克服善終障礙-我國高齡者之善終教育現況與因應策略。安寧 療護雜誌,

16(3)

361-370

doi:10.6537/TJHPC.2011.16(3).7

[Lo, Y. M. (2011). Conquering the good death barriers-the current good death education for the elderly and coping strategies in Taiwan. Taiwan Journal of Hospice Palliative Care, 16(3), 361-370.]

蘇完女、林秀珍(2011)。從意義建構觀點談喪親者的哀傷調適歷程。諮商與輔 導,

294

,46-51。

[Su, W. N., & Lin, X. Z. (2011). The grieving adjustment process of the bereaved from the view of meaning reconstruction. Counseling & Guidance, 294, 46-51. ]

謝麗鳳、林佳靜、賴裕和、鄒宗山(

1998

)。癌症家屬對止痛劑的擔心與病人疼

痛控制的相關性。護理研究,

6(4)

327-337

[Hsieh, L. F., Lin, C. C., Lai, Y. H., & Tsou, T. S. (1998). The relationship of the caregiver’s concerns about using analgesics to the patient’s cancer pain management. The Journal of Nursing, 6(4), 327-337.]

二、外文文獻

Akechi, T., Miyashita, M., Morita, T., Okuyama, T., Skamoto, M., Sagawa. R., &

Uchitomi, Y. (2012). Good death in elderly adults with cancer in Japan cased on perspectives of the general population. Journal of American Geriatrics Society, 60, 271-276. doi:10.1111/j.1532-5415.2012.03895.x

Ando, M., Somchi, S., Miyashita, M., & Jamjan, L. (2016). The perception for good death of community dwelling Japenese and Thailand respondents. Asian/Pacific Island Nursing Journal, 1(3), 91-96. doi:10.9741/23736658.1042

Chan, W. C. H., & Epstein, I. (2012). Researching ‘good death’ in a Hong Kong palliative care program: A clinical data-mining study. OMEGA, 64(3), 203-222. doi: 10.2190/OM.64.3.b

Cheng, S. Y., Hu, W. Y., Chen, C. Y., & Chiu, T. Y. (2012). Factors afffecting the improvement of quality of dying of terminally ill patients with cancer through palliative care: A ten-year experience. Journal of Palliative Medicine, 15(8), 854-862. doi:10.1089/jpm.2012.0033

Chiu, T. Y., Hu, W. Y., Chuang, R. B., & Chen, C. Y. (2002). Nutrition and hydration for terminal cancer patients in Taiwan. Support Care Cancer, 10, 630-636.

doi:10.1007/s00520-002-0397-5

Chiu, T. Y., Hu, W. Y.,Lue, B. H., Yao, C A., Chen, C. Y., & Wakai, S. (2004).

Dyspnea and its correlates in Taiwanese patients with terminal cancer. Journal of Pain and Sympton Management, 28(2), 123-132.

doi:10.1016/j.jpainsymman.2003.11.009

Chochinov, H. M. (2006). Dying, dignity, and new horizons in palliative end-of-life care. CA Cancer J Clin, 56, 84-103.

Choi, J. E., Miyashita, M., Hirai, K., Sato, K., Morita, T., Tsuneto, S., & Shima, Y.

(2010). Preference of place for end-of-life cancer care and death among bereaved Japanese families who experienced home hospice care and death of a loved one.

Support Care Caner, 18, 1445-1453. doi:10.1007/s00520-009-0767-3

Choi, K. S., Chae, Y. M., Lee, C. G., Lee , S. W., Heo, D. S., . . . Yun, Y. H. (2005).

Factors influencing preference for place of terminal care and of death among cancer patients and their families in Korea. Support Care Cancer, 13,

565-572. doi:10.1007/s00520-005-0809-4

Chung, T. K., French, P., & Chan, S. (1999). Patient-related barriers to cancer pain management in a palliative care setting in Hong Kong. Cancer Nursing, 22(3), 196-203.

Depaola, S. J., Griffin, M., Young, J. R., & Neimeyer, R. A. (2010). Death anxiety and attitudes toward the elderly among older adults: The role of gender and ethnicity. Death Studies, 27(4), 335-354. doi:10.1080/07481180302904

Emanuel, E. J., & Emanuel, L. L. (1998). The promise of a good death. The Lancet, 351, 21-29.

Fried, T. R., van Doorn, C., O’Leary, J. R., Tinetti, M. E., & Drickamer, M. A. (1995).

Older person’s preferences for site of termianl care. Annual International Medicine, 131, 109-112.

Glass, A. P., Chen, L. K., Hwang, E., Ono, Y., & Nahapetyan, L. (2010). A cross-cultural comparison of hospice development in Japan, South Korea, and Taiwan. Journal of Cross Cultural Gerontology, 25, 1-19.

doi:10.1007/s10823-009-9108-8

Goldsteen, M., Houtepen, R., Proot, I. M., Abu-Saad, H. H., Spreeuwenbery, C., &

Widdershoven, G. (2005). What is a good death? Terminally ill patients dealing with normative expectations around death and dying. Patient Education and Counseling, 64, 378-386. doi:10.1016/j.pec.2006.04.008

Good, M. D., Gadmer, N. M., Ruopp, P., Lakoma, M. L., Sullivan, A. M.,

Redinbaugh, E., . . . Block, S. D. (2004). Narratives nuances on good and bad deaths: Internist’s tales from high-technology work places. Social Science &

Medicine, 58, 939-953. doi:10.1016/j.socscimed.2003.10.043

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. Palliative Medicine, 18, 460-467. doi:10.1191/0269216304pm889oa

Granda-Cameron, C., & Houldin, A. (2012). Concept analysis of good death in

terminally ill patients. American Journal of Hospice & Palliative Medicine, 29(8),

632-639. doi: 10.1177/1049909111434976

Hattori, K., McCubbi, M. A., & Ishida, D. N. (2006). Concept analysis of good death in the Japanese community. Journal of Nursing Scholarship, 38(2), 165-170.

Hagerty, R. G., Butow, P. N., Ellis, P. A., Lobb, E. A., Pendlebury, S. Leighl, N., . . . Tattersall, M. H. N. (2004). Cancer patient preferences for communication of prognosis in the metastic setting. Journal of Clinical Oncology, 22(9),

1721-1730.doi:10.1200/JCO.2004.04.095

Hart, B., Sainsbury, P., & Short, S. (1998). Whose dying? A sociological critique of the ‘good death’. Mortality, 3(1), 65-77. doi:10.1080/713685884

Higginson, I., Wade, A., & McCarthy, M. (1990). Palliative care: Views of patients and their families. BMJ, 301, 277-281.

Hirai, K., Miyashita, M., Morita, T., Sanjo, M., & Uchitomi, Y. (2006). Good death in Japanese cancer care: A qualitative study. Journal of Pain and Symptom

Management, 31(2), 140-147. doi:10.1016/j.jpainsymman.2005.06.012 Ho, A. H. Y., Leung, P. P. Y., Tse, D. M. W., Pang, S. M. C., Chochinov, H. M.,

Neimeyer, R. A., & Chan, C. L. W. (2013). Dignity amidst liminality: Healing within suffering among Chinese Terminal cancer patients. Death Studies, 37(10), 963-970. doi:10.1080/07481187.2012.703078

Hsu, M. T., & Kahn, D. L. (2003). Adaptation as meaning construction: a cultural analysis of spousal death in Taiwanese women. OMEGA, 47(2), 169-186.

Huang, H., Liu, H., Zeng, T., & Pu, X. (2015). Preference of Chinese general public and healthcare providers for a good death. Nursing Ethics, 22(2), 217-227.

doi:10.1177/0969733014524760

Kastbom, L., Milberg, A., & Karlsson, M. (2016). A good death from the perspective of palliative cancer patients. Support Care Cancer, 25, 933-939. doi:

10.1007/s00520-016-3483-9

Kehl, K. A. (2006). Moving toward peace: An analysis of the concept of a good death.

American.Journal of Hospice & Palliative Medicine, 23(4), 277-286.

Kristjanson, L. J., McPhee, I., Pickstock, S., Wilson, D., Oldman, L., & Martin, K.

(2001). Palliative care nurses’ perceptions of good and bad deaths and care expectations: a qualitative analysis. International Journal of Palliative Nursing, 7(3), 129-139.

Lamont, E. B., & Christakis, N. A. (2001). Prognostic disclosure to patients with

cancer near the end of life. Annual of Internal Medicine, 134(12), 1096-1105.

Lee, G. L., Woo, I. M. H., & Goh, C. (2011). Understanding the concept of a ‘good death’ among bereaved family caregivers of cancer patients in Singapore.

Palliative and Supportive Care, 11, 37-46. doi:10.1017/S1478951511000691 Leichtentritt, R. D., & Rettig, K. D. (2000). The good death: Reaching an inductive

understanding. Omega, 41(3), 221-248.

Leung K. K., Liu, W. J., Cheng, S. Y., Chiu, T. Y., & Chen, C. Y. (2009). What do laypersons condifer as a good death. Support Care Cancer, 17, 691-699. doi:

10.1007/s00520-008-0530-1

Lin, C. C. (2000). Barriers to the analgesics management of cancer pain: A comparison of attitudes of Taiwanese patients and their family caregivers.

International Association for the Study of Pain, 88, 7-14.

Leung, K. K., Tsai, J. S., Cheng, S. Y., Liu, W. J., Chiu, T. Y., Wu, C. H., & Chen, C.

Y. (2010). Can a good death and quality of life be achieved for patients with t erminal cancer in a palliative care unit? Journal of Palliative Medicine, 13(12), 1433-1438. doi:10.1089/jpm.2010.0240

Lin, C. C., & Ward, E. W. (1995). Patient-related barriers to cancer pain management in Taiwan. Cancer Nursing, 18(1), 16-22.

Lloyd, L., White, K., & Sutton, E. (2011). Researching the end-of-life in old age:

Cultural, ethical and methodological issues. Ageing & Society, 31, 386-407.

doi:10.1017/S0144686X10000966

Lo, Y. T., Chen, R. Y., Wang, C. N., & Chen, Y. S. (2011). Discrepant effect of age on hospice utilization by cancer patients in Taiwan: Hospital versus home care services. Palliative Medicine, 25(6), 766-767. doi: 10.1177/0269216311421836 Long, S. O. (2001). Negotiating the ‘good death’: Japanese ambivalence about new

ways to die. Ethnology, 40(4), 271-289.

Luijkx, K. G., & Schols, J. M. G. A. (2011). Perceptions of terminally ill patients and family members regarding home and hospice as places of care at the end of life.

European Journal of Cancer Care, 20, 577-584. doi:

10.1111/j.1365-2354.2010.01228.x

Mak, J. M. H., & Clinton, M. (1999). Promoting a good death: An agenda for outcome research - a review of the literature. Nursing Ethics, 6(2), 97-106.

Malhotra, C., Chan, A., Do, Y. K., Malhotra, R., & Goh, C. (2012). Good end-of-life

care: Perspectives of middle-aged and older Singaporeans. Journal of Pain and

Symptom Management, 44(2), 252-263. doi:10.1016/j.jpainsymman.2011.09.007

Masson, J. D. (2002). Non-professional perceptions of ‘good death’: a study of the views of hospice care patients and relatives of deceased hospice care patients.

Mortality, 7(2), 191-209. doi:10.1080/13576270220136294 McLanhlan, J. R. (1999). A good death. Tahoma West, 3(1), 59-64.

Min, D., & Cho, E. (2017). Concept analysis of good death in the Korean community.

Journal of Korean Gerontology Nursing, 19(1), 28-38.

doi:10.17079/jkgn.2017.19.1.28

McNamara, B. (2004). Good enough death: autonomy and choice in Australian palliative care. Social Science & Medicine, 58, 929-938.

doi:10.1016/j.socscimed.2003.10.042

McNamara, B., Waddell, C., & Colvi,M. (1995). Threats to the good death: the cultural context of stress and coping among hospice nurses. Sociology of Health

& Illness, 17(2), 222-244.

Miyashita, M., Kawakami, S., Kato, D., Yamashita, H., Igaki, H., Nakano, K., . . . Nakagawa, K. (2015). The importance of good death components among cancer patients, the general population, oncologists, and oncology nurses in Japan:

Patients prefer “fight against cancer”. Support Care Cancer, 23, 103-110. doi:

10.1007/s00520-014-2323-z

Miyashita, M., Morita, T., Sato. K., Hirai, K., Shima, Y., & Uchitomi, Y. (2008).

Good death inventory: A measure for evaluating good death from the bereaved family member’s perspective. Journal of Pain and Symptom Management, 35(5), 486-498. doi:10.1016/j.jpainsymman.2007.07.009

Miyashita, M., Sanjo, M., Morita, T., Hirai, K., & Uchitomi, Y. (2007). Good death in cancer care: A nationwide quantitative study. Annals of Oncology, 18, 1090-1097.

doi:10.1093/annonc/mdm068

Morita, T., Miyashita, M., Shibagaki. M., Hirai, K., Ashiya, T., Ishihara, T., . . . Uchitomi, Y. (2006). Knowledge and beliefs about end-of-life care and the effects of specialized palliative care: A population-based survey in Japan.

Journal of Pain and Symptom Management, 31(4), 306-315.

doi:10.1016/j.jpainsymman.2005.09.004

Morita, T., Oyama, Y., Suh, S. Y., Koh, S. J., Kim, H. S., Chiu, T. Y., . . .Tsuneto, S.

(2015). Palliative care physicians’ attitudes toward patient autonomy and a

good death in east Asian countries. Journal of Pain and Symptom Management,

National Cancer Institute. (December, 2017). What is cancer? Retrieved from https://www.cancer.gov/about-cancer/understanding/what-is-cancer

Payne, S. A., Evans, A. L., & Hiller, R. (1996). Perceptions of a ‘good’ death: A comparative study of the views of hospice staff and patients. Palliative Medicine, 10, 307-312.

Prigerson, H. G., Cherlin, E., Chen, J. H., Kasl, S. V., Hurzeler, R., & Bradley, E. H.

(2003). The stressful caregiving adult reactions to experiences of dying (SCARED) scale: A measre for assessing caregiver exposure to distress in terminal care. American Journal of Geriatric Psychiatry, 11(3), 309-319.

Samerchua, W., Nantachaipan, P., & Sittisonbut, S. (2016). Good death as perceived by cancer survivor. International Journal of Evidence-Based Healthcare, 14, S27.

Shin, D. W., Choi, J. E., Miyashita, M., Choi, J. Y., Kand, J., Baik, Y. J., . . . Lee, H.

S. (1011). Measuring comprehensive outcomes in palliative care: validation of the Korean version of the good death inventory.Journal of Pain and Symptom Management, 42(4), 632-642.doi:10.1016/j.jpainsymman.2010.12.012

Sanjo, M., Miyashita, M., Morita, T., Hirai, K., Kawa, M., Akechi, T., & Uchitomi, Y.

(2007). Preferences regarding end-of-life cancer care and associations with good-death concepts: A populations-based survey in Japan. Annals of Oncology, 18, 1539-1547. doi:10.1093/annonc/mdm199

Shinjo, T., Morita, T., Hirai, K., Miyashita, M., Shimizu, M., Tsuneto, S., & Shima, Y.

Why people accept opioids: Role of general attitudes toward drugs, experience as a bereaved toward drugs, experience as a bereaved family, information from medical professionals, and personal beliefs regarding a good death. Journal of Pain and Symptom Management, 49(1), 49-54.

doi:10.1016/j.jpainsymman.2014.04.015

Singer, P. A., Martin, D. K., & Kelner, M. (1999). Quality end-of-life care: Patients’

perspectives. Journal of American Medical Association, 281(2), 163-168.

Steinhauser, K. E., Christakis, N. A., Clipp, E. C., McNeilly, M., Grambow, S., Parker, J., & Tulsky, J. A. (2001). Preparing for the end of life: Preferences of patients, families, physicians, and other care providers. Journal of Pain and Symptom Management, 22(3), 727-737.

Steinhauser, K. E., Christakis, N. A., Clipp, E. C., McNeilly, M., McIntyre, L., &

Tulsky, J. A. (2000). Factors considered important at the end of life by patients,

family, physicians, and other careproviders. Journal of American Medical Association, 284(19), 2476-22482.

Steinhauser, K. E., Clipp, E. C., McNeilly, M., Christakis, N. A., McIntyre, L. M., &

Tulsky J. A. (2000). In search of a good death: observations of patients, families and providers. Annals of Internal Medicine, 132(10), 825-832. doi:

10.7326/0003-4819-132-10-200005160-00011

Stewart, A. L., Teno, J., Patrick, D. L., Lynn, J. (1999). The concept of quality of life of dying persons in the context of health care. Journal of Pain Symptom

Management, 17, 93-108.

Tang, S. T. (2000). Meanings of dying at home for Chinese patients in Taiwan with terminal cancer. Cancer Nursing, 23(5), 367-370.

Tang, S. T. (2003). When death is imminent: where terminally ill patients with cancer prefer to die and why. Cancer Nursing, 26, 245-251.

Tang, S. T., Liu, T. W., Chow, J. M., Chiu, C. F., Hsieh, R. K., Chen, C. H., . . . Feng, W. L. (2014). Associations between accurate prognostic understanding and end-of-life care preferences and its correlates among Taiwanese terminally ill cancer patients surveyed in 2011-2012. Psycho-Oncology, 23, 780-787.

doi:10.1002/pon.3482

Vig, E. K., & Pearlman, R. A. (2004). Good and bad dying from the perspective of terminally ill men. Arch Intern Med., 164, 977-981.

Ward, S. E., Goldberg, N., Miller-McCauley, V., Mueller, C., Nolan, A., Pawlik-Plank, D., . . . Weissman, D. E. (1993). Patient-related barriers to management of cancer pain. Pain, 52, 319-324.

Yao, C., Hu, W., Lai, Y., Cheng, S., Chen, C.,& Chiu, T. (2007). Does dying at home influence the good death of terminal cancer patients. Journal of Pan and

Symptom Management, 34(5), 479-504. doi:10.1016/j.jpainsymman.2007.01.004 Yun, Y. H., Kwon, Y. C., Lee, M. Y., Lee, W. J. , Jung, K. H., Do, Y. R., . . . Park, S.

Y. (2010). Experiences and attitudes of patients with terminal cancer and their family caregivers toward the disclosure of terminal illness. Journal of Clinical Oncology, 28(11), 1950-1957. doi:10.1200/JCO.2009.22.9658

Yun, Y. H., Lee, C. G., Kim, S. Y., Lee, S. W., Heo, D. S., Kim, J. S., . . . You, C. H.

(2004). The attitudes of cancer patients and their families toward the disclosure

of terminal illness. Journal of Clinical Oncology, 22(2), 307-314. doi:

附錄一

附錄二 家屬問卷

韓、日、臺三國對善終觀念之比較 家屬

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韓國目前對安寧療護進行關於死亡的意義和辨識癌症患者對於善終的看法,進行 相關的研究和調查。這項調查將瞭解韓國、臺灣和日本三國的臨床醫師、患者和 家屬對善終看法之差異。最後,這調查將確保對臨終關懷服務中的所有患者及家 屬提供良好的安寧療護及臨終關懷。

19

歲以上的成年人方能參與調查。這一項調查是瞭解您的意見且對您沒有傷害,

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參與者姓名:

日期:

______,______,2017

計畫主持人:方俊凱(馬偕紀念醫院

/

安寧療護教育示範中心

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主任)

聯絡方式:

02-28094661*3138

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