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研究生:吳宜芳
研究生(外文):Yi-Fung Wu
論文名稱:探討加護病房家屬對疾病末期病人醫療決策行為意向及其影響因素
論文名稱(外文):The factors influenced the behavior intention of medical decision and targeting on the families with terminal patients at intensive care units(ICU)
指導教授:胡文郁胡文郁引用關係
指導教授(外文):Wen-Yu Hu
學位類別:碩士
校院名稱:國立臺灣大學
系所名稱:護理學研究所
學門:醫藥衛生學門
學類:護理學類
論文種類:學術論文
論文出版年:2005
畢業學年度:93
語文別:中文
論文頁數:168
中文關鍵詞:疾病末期加護病房行為意向醫療決策生活品質
外文關鍵詞:terminal stageintensive care unit(ICU)the behavior intentionmedical decisionquality of fife
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本研究旨在探討加護病房家屬對疾病末期病人醫療決策行為意向及其影響因素,採立意取樣,使用結構式問卷。訪談60位北部某醫學中心內外科加護病房之疾病末期病患家屬。將所收集之資料,以SPSS11.0版進行統計分析。重要結果為:(1)85%家屬同意讓疾病末期病人在加護病房內接受緩和性治療。(2)僅25%家屬聽過安寧緩和醫療條例。(3)91.7%家屬認為醫師第一個應告知家屬疾病末期病人之病情。(4)加護病房家屬對疾病末期病人之「真相告知態度」、「末期醫療處置態度」及「末期醫療決策行為意向」均較正向。(5)加護病房家屬認為病人之生活品質為4.58分,且五成認為病人未達善終。(6)「家屬對病人生活品質看法」之重要預測因子為「簽署DNR同意書」及「有看過他人CPR且有被影響」。(7)「末期醫療決策行為意向」之重要預測因子為「真相告知態度」及「末期醫療處置態度」。(8)「家屬對適切性醫療滿意度」之重要預測因子為「病人住ICU起始日至家屬受訪日」及「病人存活時間」。(9)「病人善終與否」之重要預測因子為「家屬對適切性醫療滿意度」及「病人存活時間」。(10)「有無簽屬DNR同意書」之重要預測因子為「家屬與病人關係」及「醫療決策行為意向」。研究結果讓醫護人員瞭解加護病房家屬,在做末期醫療決策行為時之重要預測因子。以利提供適當之護理措施、減少醫療資源之浪費,並藉著病情真相告知,間接促進病人善終之達成。
The aim of this study was to investigate the factors influenced the behavior intention of medical decision and targeting on the families with terminal patients at intensive care units(ICU).A purposive sampling method was used in.60 families.This data was analyzed by the software of SPSS11.0 version.
The important findings are: (1) When the patients are at the terminal stage of their diseases, 85% of their families are willing to have hospice care at ICU. (2) The Regulations of Hospice Care are known by only 25% of the families. (3) When the patients are at the terminal stage of their diseases,91.7% of their families consider themselves as the first ones to be informed by the doctors. (4) The family of the patients at ICU have a positive attitude toward “truth telling”, “the treatment for terminal stage”, and “terminal medical decision making”. (5) The family of the patients at ICU think the patients’ life quality score was 4.58 in average, and half of them feel that the patients do not have good dying. (6) “DNR agreement” and “having seen CPR to others and having been influenced” are significant predictors to “how the patients’ family think about patients’ life quality”. (7) Regarding to the attitudes of patients’ families, “attitudes toward truth telling” and “the treatment for terminal stage” are significant predictors to “attitudes towards terminal decision making”. (8) “The time interval from the first day of ICU admission to the day of interview” and “patients’ survival time” are significant predictors to “the family’s satisfaction of appropriate medical care”. (9) “The family’s satisfaction of appropriate medical care” and “patients’ survival time” are significant predictors to “ the familiy’s opinion of the patient’s good dying”. (10) “The family - patient relationship” and “attitudes toward terminal decision making” are significant predictors to “DNR agreement”.The results of this study can help medical professionals understand the factors and significant predictors of the terminal decision making by the family of the patients at ICU. It may facilitate us to implement appropriate nursing strategies for terminal patients at ICU and to reduce the medical cost. “Truth telling” is helpful for patients’ good dying.
中文摘要 III
Abstract V
目錄 VII
圖表目錄 X
第壹章 緒論 1
第一節 研究動機 1
第二節 研究目的 4
第三節 研究架構 5
第四節 名詞界定 7
第貳章 文獻查證 10
第一節 疾病末期及心肺復甦術的定義 10
第二節 加護病房家屬與醫護人員末期照護之倫理困境 13
第三節 醫療決策之概念 20
第四節 加護病房病患家屬對疾病末期病人醫療處置之影響因素 24
第五節 末期病人之生活品質及善終 29
第六節 適切性醫療滿意度 32
第參章 研究方法 34
第一節 研究設計 34
第二節 研究對象及場所 34
第三節 研究工具 35
第四節 研究工具信效度檢定 38
第五節 資料收集步驟 44
第六節 倫理關注 46
第七節 資料分析方法 47
第肆章 研究結果 49
第一節 基本資料 49
第二節 真相告知態度、末期醫療處置態度及末期醫療決策行為之意向 57
第三節 疾病末期病人之生活品質 72
第四節 家屬對適切性醫療與病人善終的滿意度 74
第五節 生活品質及簽署DNR同意書與其影響因素之關係 76
第六節 滿意度及善終與其影響因素之關係 83
第七節 簽署DNR同意書及善終之重要預測因子 90
第伍章 討論 92
第一節 國內外真相告知態度之比較 92
第二節 簽署DNR同意書及其影響因素之比較 93
第三節 加護病房病人生活品質及存活時間之比較 95
第四節 適切性醫療滿意度及善終之影響因素比較 96
第陸章 結論與未來研究之建議 98
第一節 結論 98
第二節 護理應用及建議 101
第三節 研究限制 103
中文部分 104
英文部分 107
毛家舲、張鈺(民85)。倫理困境與倫理決策過程。護理雜誌。43(1),40-45。
伊瑪紐 (Emanuel, Ezekiel)( 民88)。臨終之醫療倫理(柳麗珍譯)。台北市:五南。(原著出版年:1957年)。
吳研因等 (民83)。辭淵。北京:警官教育。
呂佩佩 (民92)。站在生死線上∼癌症病患與家屬面對急救的困境。未發表碩士論文,台灣:長庚大學護理學研究所。
易煥德、廖堃圻、林國正 (民84)。如何和病家商討放棄心肺復甦術。國防醫學,21 (5),427-428
夏明華與王清芳 (民88)。最新版國語大辭典。台北板橋。匯豐文化。
胡文郁、邱泰源、呂碧鴻、陳慶餘、謝長堯、陳月枝(民90)。醫護人員對「安寧緩和醫療條例」之教育需求。醫學教育,5(1),21-29。
許麗齡 (民88)。護理倫理─病人的自主性。護理雜誌,46 (4),57-61。
程邵儀、邱泰源、胡文郁、郭斐然、王浴、周玲玲等(民85)。癌症末期善終之初步研究。中華家醫誌, 6(2),83-91。
郭正典(民91)。治療的限制與撤除。台灣急重症醫學,4,310-317。
郭淑芬(2004)。從癌症病人及家屬觀點探討病情告知之經驗。未發表碩士論文,台灣:台灣大學護理學研究所。
陳文鍾(民89)。心肺復甦術。台灣醫學,4(2),138-142。
陳敏峻、姜安波、黃湘萍、蘇連瓔(民86)。癌症末期病人照護的倫理議題。台灣醫界,40 (10),10-14。
陳民虹、蔡甫昌 (民85)。臨終病人之照護─醫病關係倫理。基層醫學。11 (3),54-58。
陳榮基(民85)。衛生署推動安寧療護核可DNR措施。安寧照顧基金會會訊,23,14-5。
陳榮基(民88)。拒絕心肺復甦術的法源探討。醫學法事季刊。7(1),6-8。
陳敏鋑、姜安波、黃湘萍、蘇連瓔 (民87)。癌症末期病人照護的倫理問題。台灣醫界,40(10)。
馮雅芳(2003)。加護病房醫護人員對疾病末期病人醫療決策行為意向及其影響因素之研究。未發表碩士論文,台灣:台灣大學護理學研究所。
鄒海月、王守容、何裕芬(民88)。癌症末期病患對家屬不急救之態度及期相關因素之探討。榮總護理,16(4),344-356。
楊克平(民88)。論緩和醫療之意義及變化史。榮總護理,16(4),357-363。
趙可式(民85)。臨終病人照護的倫理與法律問題。護理雜誌,43(1),24-28。
鄭少珍(2004)。醫護人員於癌末病情告知之行為意向與照顧困擾之探討。未發表碩士論文,台灣:台灣大學護理學研究所。

英文部分
Asai, A. M., Y. Tanabe, N. Kurihara, M. & Fuhara, S. (1998). Advance directives and other medical decisions concerning the end of life in cancer patient in Tapan. European Journal of Cancer, 34(10), 1582-1586.
Baggs, J. G. Schmit, M. H. (1995). Intensive decision about level of aggressiveness. Research in Nursing & Health, 18, 345-355.
Belec, R. H. (1992). Quality of life: Perceptions of long-term survivors of bone marrow transplantation. Oncology of Nursing Forum, 19(1),31-37.
Bihl, M. A., Ferrans, C. E. & Powers, M. J.(1998). Comparing stressors and quality of life of dialysis patients. American Nephrology Nursing Association Journal,15(1),27-37.
Blackhall, L. J., Frank, G., Murphy, S. &Michel, V. (2001). Bioethics in a different tongue: The case of turth-telling. Journal oh Urban Health:Bulletin of the New York Academy of Medicine, 78(1), 59-71.
Blatt, L.(1999). Working with families in reaching end-of-life Decisions. Clinical Nurse Specialist, 13(5).
Blatt, L. (1997). Spouses experience in the do not resuscitate decision making process. Unpublished Masters thesis, Yale University , New Haven, CT.
Brennan, T. A. (1988). Incompetent patients with limited care in the absence of family consent. Ann Intern Med, 109, 819-825.
Cook, D. (2001). Patient autonomy versus parentalism. Critical Care Medical, 29(2), 24-25.
Cohen, L.M., Reiter, G.S., Poppel, D.M. & Germain, M.J. (2001) Palliative care for non-cancer patient(PP1003-112).. IN addington-Hall, J. M. & Higginson, I. J.,. New York: Oxford.
Cox DE.(1993). Letter to the editor. N Engl J Med.328:1201.
Curtis, J. R. P., D. L., Shannon, S. E., Treece, P., engelberg, R., & Rubenfeld, G. (2001). The family conference as a focus to improve communication about end-of-life in the intensive care unit: Opportunities for improvement. Critical Care Medical, 29(2), 26-33.
Danis, M., Feferman, D., Fins, J. J., Fox, E., Kastenbaum, B., Lanken, P.N., et al., (1999). Incorporating palliative care into critical care education: Principles, challenges, and opportunities. Critical Care Medical, 27(9), 2005-2031.
Darean K. H., Graeme M. R., Christopher J. O., Peter M. D., & Deborah J. C.(2003). Dying in the ICU;perspectives of family members. Chest, 124(1), 392-397.
Ellen R.(1994). Family Dynamic in end-of-life treatment decisions. General Hospital Psychiarty.16, 251-258.
Elwyn, T. S., Fetter, M. D., Sasaki, H., & Tsuda, T., (2002). Responsiblity and cancer disclosure in Japan. Social Science & Medicine, 54, 281-293.
Faber-Langendoen, K., & Lanken, P., (2000). Dying patients in the intensive care unit: Forgoing treatment, maintaining care. Annals of Internal Medicine., 133(11), 886-893.
Fallowfield, L. J., Jenkin, V. A., & Beveridge, H. A., (2002). Truth may hurt but decdit hurt more: Communication in palliative care. Palliative Medicine., 16, 297-303.
Forrest Lang, M. D., & Timothy Quill, M. D., (2004). Making Decision with Families at the End of Life. American Family Physician, 70(4), 719-722.
Gattellari, M. V., K. J., Buttow, P. N., & Tattersall, M. (2002). When the treatment goal is not care: Are cancer patients equipped to make informed decisions. Journal of Clinical Oncology, 20(2), 503-513.
Goodlin, S. J., Zhong, Z., Lynn, J., Teno, J., M. Fago, J. P., Desbiens, N. et al., (1999). Factor associated with use of cardiopulmonary resuscitation in seriously ill hospitalized adults. The Journal of American Medical Association, 284(24), 2333-2339.
Gove, P., &Babcock, M.W., (1986) Webster''s third new international dictionary of the English language, unabridged. Springfield, Mass. : Merriam-Webster.
Heyland, D. K., Hopman, W., Coo, H., Tranmer, J. & McColl, M. (2000). Long-term health-realted quality of life in survivors of sepsis. Short Form 36: A valid and reliable measure of health-related quality of life. Critical Care Medicine. 28(11), 3599-3605.
Hack,C. E. & Zeerleder, S. (2001). The endothelium in sepsis: Source of and a target for inflammation. Critical Care Medicine. 29(7), 21-29.
Hanrahan, P., Luchins, D. J. & Murphy, K. (2001). Palliative care for non-cancer patient (PP114-125.).IN Addington-Hall, J. & Higginson, I. J. , New York:Oxford.
Heneghan, M. A. & Graphy, J. G. (2001). Palliative care for non-cancer patient. (PP82-87). IN Addington-Hall, J. & Higginson, I. J. , New York: Oxford.
Hinkka, H., Kosun, E., Metsanoia, R., Lammi, U-K. KelloKumpu-Lehtinene, P. (2002). Factor affecting physician decisions to forgo life-sustaining treatment in terminal care. Journal of Medicine Ethics, 28, 109-114.
Jacob, D. (1998). Family members’ experience with decision making for incompetent patients in the ICU: a qualitative study. Am J Critical Care, 7, 30-36.
Jeanne, M. T.(2003). Family involvement in end-of-life hospital care. Journal of American Geriatrics Society, 51(6), 835-840.
Jezewski, M. A. F. D. S. (1998). The meaning of DNR status: Oncology nurses exoeriences with patients and families. Cancer Nursing, 21(3), 212-221.
John, B., & Angela, N.(1998). Do-not-resuscitate: an ethical dilemma for the decision-maker. British Journal of Nursing, 7(9), 543-549.
Jonsen, A. R., Siegler, M. & Winslade, W. J. (1998). New York: McGraw-Hill.
Kinzbrunner, B. M.(2002). IN Kinzbrunner, B. M. & Weinreb, N. J. & Policzer, J. S., End of Life Care. (PP29-46). New York: McGraw-Hill.
Leonard, K. M. E., S. S. Mctavish, J. Cumming, C. E. & Cumming, D. C. (1995). Prolong cancer death: A family affair. Cancer Nursing, 18(3), 222-227.
Lynn, M. R. (1986). Determination and quantification of content Validity. Nursing Research, 35, 382-385.
Millar, D.(1996). The Cambridge dictionary of scientists. England : Cambridge University.
Marshall, J. C., Cook, D. J., Christou, N. V. Bernard, G. R., Sprung, C. L. & Sibbald, W. J. (1995) Multiple Organ Dysfunction Score: A reliable descriptor of a complex clinical outcome. Critical Care Medicine, 23(10), 1638-1652.
Mary, A. J., Yvonne S., Colleen M., & Ellen B.(1993). Consenting to DNR: critical care nurses’ Interactions with patients and family members. American Journal of Critical Care, 2(4), 302-308.
Mary, A. J.(1994). Do-not-resuscitate status: conflict and culture brokering in critical care unit. HEART & LUNG, 23(6),458-465.
Matteson, P. & Hawkins, J. W. (1990). Concept analysis of decision making. Nursing Forum, 25(2), 4-10.
Mclean, R. T., J. Mazer, C. D. & Szalai J. P. (200). Death in two Canada intensive care unit: Institutional difference and changes over time. Critical Care medicine, 28(1), 100-103.
Norton, S. A. & Bowers, B. J. (2001). Working toward consensus:providers strategies to shift patients from curative to palliative treatmentchoices. Research in Nursing & Health. 24, 258-269.
Niskanen, M., Ruokonen, E., Takala, J., Rissanen, P. & Kari, A. (1999). Quality of life after prolonged intensive care. Critical Care Medicine, 27(6), 1132-1139.
Payton, R. J.(1979). Information control and autonomy. Nursing Clinics of North American, 14(1), 23-33.
Payne S. A., Langley-Evans A., Hillier R. (1996). Perceptions of a ''good'' death: A comparative study of the views of hospice staff and patients. Palliative Medicine, 10(4), 307-312.
Price, P. J. & Kish, S. K. (2001). End of life decision in cancer care. Critical Care Clinics, 17(3), 805-811.
Reckling, J. B. (1992). Deciding whether to withhold or withdraw life sustaining treatment. Unpublished doctoral dissertation. Kansas City, University of Kansas.
Robert, J. B. D., Elkins, T., Larson, D. (1997). Factor influencing view of patients with gynecologic cancer about end of life decisions. American Journal of Obstetrics Gynecology, 176(1), 166-172.
Prendergast, T. & Raffin, T. (1996). Variation in DNR rates: The onus is on physicans. Chest, 110(5), 1141-1142.
Rogers, A. (2001). Palliative care for non-cancer patient. (PP11-16).IN Addington-Hall, J. M. & Higginson, I. J., New York: Oxford.
Ruhnke, G. W., Wilson, S. R., Akamatsu, T., Kinoue, T., Takashima, Y., Goldstein, M. K. (2000). Ethics in cardiopulmonary medicine: Ethical decision making and patient autonomy: A comparison of physician and patient in Janpan and United States. CHEST, 118, 1172-1182.
Sainio, C., Eriksso, E. & Lauri, S. (2001). Patient participation in decision making about care. Cancer Nursing, 24(3), 172-179.
Seo, M., Tamura, K. Shijo, H., Morioka, E., Ikegame, C., & Hirasako, K. (2000). Telling the diagnosis to cancer pations in Japan: attitude and perception of patients, physicians and nurse. Palliative Medicine, 14, 105-110.
Stern, S. G. & Orlowski, J. P. (1992). DNR or CPR-the choice is ours. Critical Care Medicine, 20(9), 1263-1272.
Susanna, E. B., Denise, P., Patricia, L. M., & Paul, D. C.(1986). Do-not-resuscitate orders for critical ill patients in the Hospital; How are they used and what is their impact?. JAMA, 256(2), 233-237.
Swigart V. (1994). A study of family decision making about life support using the grounded theory method. Unpublished doctoral dissertation, Pittsburgh, PA, University of Pittsburgh.
Tang, S. T. (2000). Meanings of dying at home for Chinese patients in Taiwan with terminal cancer. Cancer Nursing, 23(5), 367-369.
Tilden, V., Tolle, S., Garland, M. (1995). Decisions about life sustaining treatment: impact of physicians behaviors on the family. Arch Inter Med, 155, 633-638.
Torian, L., Davidson, E., & Fillit, H.(1992). Decisions for and against resuscitation in an acute geriatric medicine unit serving the frail elderly. Arch Inter Med, 152, 561-565.
Vincent, J. L.(2001). Cultural differences in end-of-life care. Critical Care Medicine, 29(2), 52-55.
Ventres, W., Nichter, M., Reed R, et al. (1992). Do not resuscitate discussions: a qualitative analysis. Fam Pract Res J ,12, 157-169.
Weissman, D. E., Black, S. D., Blank, L., Cain, J., Cassen, N., Danoff, D., et al., (1999). Recommendations for incorporation palliative care education into the acute care hospital setting. Academic medicine, 74(8), 871-877.
Wiens, A. G. (1993). Patient autonomy in care: A theoretical framework for nursing. Journal of Professional Nursing, 9(2), 95-103.
William, V., Mark N., Richard R., & Richard F.(1992). Do-not-resuscitations: a qualitative analysis. Family Practice Research Journal, 12(2), 157-168.
Yeung, E. W., Fredch, F. P., & Leung, A. O. S. (1999). The impact of hospice inpatient care on the quality of lift of patients terminal ill with cancer. Cancer Nursing, 22(5), 350-357.
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