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題名 以壓力模式探討癌症末期病人於醫療決定之主觀經驗
Exploring the medical decision-making experience in advanced cancer patients - Using the stress model approach作者 盛心毓
Sheng, Hsin-Yu貢獻者 吳治勳
盛心毓
Sheng, Hsin-Yu關鍵詞 癌症末期病人
醫療決定
壓力模式
主題分析
Advanced cancer patients
Medical decision-making
Stress model
Thematic analysis日期 2022 上傳時間 1-Aug-2022 18:11:00 (UTC+8) 摘要 緒論:在心理腫瘤學相關研究中,可以發現癌症末期病人的醫療決定不僅是與疾病或醫療訊息的認識有關,亦與病人的主觀因素有所關聯,如:認知思考歷程、身心調適。唯過往針對癌症末期病人的醫療決定相關的研究,較多是探討醫療決定之結果而非心理歷程,較難以瞭解癌症末期病人是「如何」做選擇。因此本研究欲以癌症末期病人為研究對象,透過健康心理學之壓力模式為基礎,以瞭解病人在疾病末期與醫療相關之壓力源、壓力評估、及因應等心理歷程,並藉此探索癌末病人於醫療決定上之重要議題。研究方法:以半結構式訪談方法進行訪談,並以壓力模式作為訪談大綱設計指引,訪談大綱包含以下項目:疾病與治療背景、疾病之相關變化與轉折、治療效果之變化與醫療方式的選擇、關於安寧緩和醫療的認識與想法、家人/重要他人的想法及其他治療/改善身體狀況經驗。結果:共訪談16位癌症末期病人,以主題分析方法進行資料分析後,以病人資料為基礎,歸納出二大類共7個主題。第一類為癌症末期病人的疾病與治療經驗,包含(1)罹癌是充滿受苦的經驗,包含生理、心理與社會層面之苦痛、(2)面對生命有限性的述說方式等2個主題。第二類為癌症末期病人的治療選擇與考量,包含(3)避免身心痛苦、(4)因為治不好被迫做出決定、(5)想要活著、(6)社會性的因素影響、(7)資源上的考量等5個主題。本研究另初探受訪者對於安寧緩和醫療的認識,依照受訪者回應可分為「不清楚」、「偏向正向的認知」、「偏向負向的認知」等三個類型。討論:結果顯示,癌症末期病人的壓力源不僅是疾病本身,而是包含生理、心理及社會層面之痛苦,且彼此會交互影響。同一位受訪者的決定可能經常是矛盾或衝突的,例如有時候會希望能繼續治療,但有時則否。由心理歷程來看,發現病人經常會以「放棄治療」的說法形容安寧緩和醫療,這樣現象可能是與其面臨因應失敗的現狀有關。若癌症末期病人以治癒為因應目標時,醫療人員依循醫療系統常規轉介安寧緩和醫療服務,可能使病人認為醫療人員是放棄他們。病人在面臨因應失敗的情況下,常伴隨無奈、絕望、失落等負向情緒,再成為新的壓力源,此時對於病人來說更需要的是情緒上的調適,但結果顯示病人常常採取逃避情緒的因應方式,如:迴避死亡相關刺激,且他們經常沒有資源處理負向情緒。綜合前述,臨床人員可以生理-心理-社會層面的整體性角度來理解癌症末期病人的受苦經驗,除關心癌症末期病人醫療決定之結果外,可陪伴瞭解其在醫療決定的心理歷程,並留意病人的情緒反應,更有助於病人面對癌症末期的壓力調適。
Background: Through psycho-oncology related studies, it seems that the medical decisions made by advanced cancer patients are not only associated with the knowledge of the disease or medical information, but also the patients’ cognitive thinking process or psychological adjustment. However, past studies mainly focused on the outcome of medical decision-making rather than the process itself. Accordingly, this study aimed to explore the patients’ psychological processes from the medical decision-making experience with stress model in health psychology.Method: Semi-structured interview was adopted to explore the disease and medical decision-making experience. The outline was based on stress model and includes following items: disease and treatment background; related changes of disease and treatment effects, and influences on the choice of medical methods; personal thoughts of palliative care; treatment opinions of family members or significant others; other experience in treating/improving physical conditions.Result: On the basis of bottom-up thematic analysis, data from 16 participants showed 2 categories of 7 themes. The first category is disease and treatment experience: (1) the experiences included biological, psychological, and social suffer, (2) narratives about limitation of life. The second category is the considerations in medical decision-making: (3) reliving physical and psychological pain, (4) being forced to make decisions, (5) wanting to live, (6) social factors, and (7) limited-resources. In addition, this study explored patients’ understanding of palliative care, participants showed 3 types of response: feedback of not-sure, positive and negative comments.Discussion: The results show that the stressors of advanced cancer patients are not only disease itself, but include physical, psychological, social distress, and the interaction of them. The same person may encounter conflicting choices, such as he/she sometimes hopes to receive treatments but sometimes doesn’t. When understanding patients’ medical decision through their psychological process, it can be found that patients often describes palliative care as "give up", and the phenomenon may be related to the failure of coping outcome. The referrals to palliative care services under professional custom may let patients feel being abandoned by medical personnel if patients hold the coping goal to cure themselves. Faced with the failure of coping, there would be negative emotions like helplessness, despair, or loss accompanying by, which may then become a new stressor. As a result, emotional adjustment is more needed for patients. But patients often use emotion avoidance coping, such as: avoiding death-related stimuli. Also, they often lack resources to cope the negative emotion. In conclusion, medical personnel could understand the suffering experience of advanced cancer patients from a bio-psycho-social holistic perspective. 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Adaptive and maladaptive coping. In Handbook of coping: Theory, research, applications. (pp. 505-531). Oxford, England: John Wiley & Sons. 描述 碩士
國立政治大學
心理學系
107752004資料來源 http://thesis.lib.nccu.edu.tw/record/#G0107752004 資料類型 thesis dc.contributor.advisor 吳治勳 zh_TW dc.contributor.author (Authors) 盛心毓 zh_TW dc.contributor.author (Authors) Sheng, Hsin-Yu en_US dc.creator (作者) 盛心毓 zh_TW dc.creator (作者) Sheng, Hsin-Yu en_US dc.date (日期) 2022 en_US dc.date.accessioned 1-Aug-2022 18:11:00 (UTC+8) - dc.date.available 1-Aug-2022 18:11:00 (UTC+8) - dc.date.issued (上傳時間) 1-Aug-2022 18:11:00 (UTC+8) - dc.identifier (Other Identifiers) G0107752004 en_US dc.identifier.uri (URI) http://nccur.lib.nccu.edu.tw/handle/140.119/141172 - dc.description (描述) 碩士 zh_TW dc.description (描述) 國立政治大學 zh_TW dc.description (描述) 心理學系 zh_TW dc.description (描述) 107752004 zh_TW dc.description.abstract (摘要) 緒論:在心理腫瘤學相關研究中,可以發現癌症末期病人的醫療決定不僅是與疾病或醫療訊息的認識有關,亦與病人的主觀因素有所關聯,如:認知思考歷程、身心調適。唯過往針對癌症末期病人的醫療決定相關的研究,較多是探討醫療決定之結果而非心理歷程,較難以瞭解癌症末期病人是「如何」做選擇。因此本研究欲以癌症末期病人為研究對象,透過健康心理學之壓力模式為基礎,以瞭解病人在疾病末期與醫療相關之壓力源、壓力評估、及因應等心理歷程,並藉此探索癌末病人於醫療決定上之重要議題。研究方法:以半結構式訪談方法進行訪談,並以壓力模式作為訪談大綱設計指引,訪談大綱包含以下項目:疾病與治療背景、疾病之相關變化與轉折、治療效果之變化與醫療方式的選擇、關於安寧緩和醫療的認識與想法、家人/重要他人的想法及其他治療/改善身體狀況經驗。結果:共訪談16位癌症末期病人,以主題分析方法進行資料分析後,以病人資料為基礎,歸納出二大類共7個主題。第一類為癌症末期病人的疾病與治療經驗,包含(1)罹癌是充滿受苦的經驗,包含生理、心理與社會層面之苦痛、(2)面對生命有限性的述說方式等2個主題。第二類為癌症末期病人的治療選擇與考量,包含(3)避免身心痛苦、(4)因為治不好被迫做出決定、(5)想要活著、(6)社會性的因素影響、(7)資源上的考量等5個主題。本研究另初探受訪者對於安寧緩和醫療的認識,依照受訪者回應可分為「不清楚」、「偏向正向的認知」、「偏向負向的認知」等三個類型。討論:結果顯示,癌症末期病人的壓力源不僅是疾病本身,而是包含生理、心理及社會層面之痛苦,且彼此會交互影響。同一位受訪者的決定可能經常是矛盾或衝突的,例如有時候會希望能繼續治療,但有時則否。由心理歷程來看,發現病人經常會以「放棄治療」的說法形容安寧緩和醫療,這樣現象可能是與其面臨因應失敗的現狀有關。若癌症末期病人以治癒為因應目標時,醫療人員依循醫療系統常規轉介安寧緩和醫療服務,可能使病人認為醫療人員是放棄他們。病人在面臨因應失敗的情況下,常伴隨無奈、絕望、失落等負向情緒,再成為新的壓力源,此時對於病人來說更需要的是情緒上的調適,但結果顯示病人常常採取逃避情緒的因應方式,如:迴避死亡相關刺激,且他們經常沒有資源處理負向情緒。綜合前述,臨床人員可以生理-心理-社會層面的整體性角度來理解癌症末期病人的受苦經驗,除關心癌症末期病人醫療決定之結果外,可陪伴瞭解其在醫療決定的心理歷程,並留意病人的情緒反應,更有助於病人面對癌症末期的壓力調適。 zh_TW dc.description.abstract (摘要) Background: Through psycho-oncology related studies, it seems that the medical decisions made by advanced cancer patients are not only associated with the knowledge of the disease or medical information, but also the patients’ cognitive thinking process or psychological adjustment. However, past studies mainly focused on the outcome of medical decision-making rather than the process itself. Accordingly, this study aimed to explore the patients’ psychological processes from the medical decision-making experience with stress model in health psychology.Method: Semi-structured interview was adopted to explore the disease and medical decision-making experience. The outline was based on stress model and includes following items: disease and treatment background; related changes of disease and treatment effects, and influences on the choice of medical methods; personal thoughts of palliative care; treatment opinions of family members or significant others; other experience in treating/improving physical conditions.Result: On the basis of bottom-up thematic analysis, data from 16 participants showed 2 categories of 7 themes. The first category is disease and treatment experience: (1) the experiences included biological, psychological, and social suffer, (2) narratives about limitation of life. The second category is the considerations in medical decision-making: (3) reliving physical and psychological pain, (4) being forced to make decisions, (5) wanting to live, (6) social factors, and (7) limited-resources. In addition, this study explored patients’ understanding of palliative care, participants showed 3 types of response: feedback of not-sure, positive and negative comments.Discussion: The results show that the stressors of advanced cancer patients are not only disease itself, but include physical, psychological, social distress, and the interaction of them. The same person may encounter conflicting choices, such as he/she sometimes hopes to receive treatments but sometimes doesn’t. When understanding patients’ medical decision through their psychological process, it can be found that patients often describes palliative care as "give up", and the phenomenon may be related to the failure of coping outcome. The referrals to palliative care services under professional custom may let patients feel being abandoned by medical personnel if patients hold the coping goal to cure themselves. Faced with the failure of coping, there would be negative emotions like helplessness, despair, or loss accompanying by, which may then become a new stressor. As a result, emotional adjustment is more needed for patients. But patients often use emotion avoidance coping, such as: avoiding death-related stimuli. Also, they often lack resources to cope the negative emotion. In conclusion, medical personnel could understand the suffering experience of advanced cancer patients from a bio-psycho-social holistic perspective. In addition to the outcome of medical decisions, it is worth paying more attention to advanced cancer patients’ psychological process and emotion response, which may be more helpful for patients’ adjustment under the related stress of advanced cancer. en_US dc.description.tableofcontents 摘要 ivAbstract vi目次 viii表次 x圖次 xi第一章 緒論 1第一節 研究動機 1第二節 文獻回顧 4一、癌症末期病人醫療決定議題 4二、關於癌症末期病人的心理調適與醫療決定 16三、醫療決定與壓力模式 18第三節 研究目的 21第二章 研究方法 22第一節 研究參與者 22第二節 研究程序 23第三節 訪談大綱 24第四節 資料分析方法 27第三章 結果 29第一節 癌症末期病人的疾病與治療經驗 33一、罹癌是充滿受苦的經驗 33二、面對生命有限性的述說方式 42第二節 癌症末期病人的治療選擇與考量 53一、避免身心(繼續)痛苦或追求身心的平穩 53二、因為治不好被迫做出決定 60三、想要活著 65四、社會性的因素影響 69五、資源上的考量 76第三節 安寧緩和醫療相關主題 78一、安寧緩和醫療對受訪者而言是什麼 78第四章 討論 80第一節 以壓力模式看見癌症末期病人的心理歷程 80一、癌症末期病人的壓力來源與認知評估 83二、透過壓力互動歷程了解對癌症末期病人而言進入安寧緩和醫療場域可能是種放棄或被放棄 85三、癌症末期病人的因應方式 88四、小結 89第二節 由心理歷程探討臨床應用 91一、應以整體性的角度來理解受苦經驗 91二、實際受苦經驗的多樣性與專屬於自己的受苦經驗 91三、應試著理解選擇的過程而非僅重視結果 93四、研究臨床貢獻 94第三節 研究限制與未來研究方向 96一、研究限制 96二、未來研究方向 97參考文獻 98 zh_TW dc.format.extent 3016726 bytes - dc.format.mimetype application/pdf - dc.source.uri (資料來源) http://thesis.lib.nccu.edu.tw/record/#G0107752004 en_US dc.subject (關鍵詞) 癌症末期病人 zh_TW dc.subject (關鍵詞) 醫療決定 zh_TW dc.subject (關鍵詞) 壓力模式 zh_TW dc.subject (關鍵詞) 主題分析 zh_TW dc.subject (關鍵詞) Advanced cancer patients en_US dc.subject (關鍵詞) Medical decision-making en_US dc.subject (關鍵詞) Stress model en_US dc.subject (關鍵詞) Thematic analysis en_US dc.title (題名) 以壓力模式探討癌症末期病人於醫療決定之主觀經驗 zh_TW dc.title (題名) Exploring the medical decision-making experience in advanced cancer patients - Using the stress model approach en_US dc.type (資料類型) thesis en_US dc.relation.reference (參考文獻) 中文部分安寧緩和醫療條例(條文修正日期:民國 110 年 01 月 20 日)。取自:https://law.moj.gov.tw/LawClass/LawAll.aspx?pcode=L0020066吳欣烜、鄭逸如、張琦郁、楊于婷、吳治勳、林耀盛、陳勇仁(2020)。〈「一切都已經安排好了,不用擔心。」解析與了解照顧者的理智化因應〉。《安寧療護雜誌》,24(1),47-58。doi:10.6537/tjhpc.202003_24(1).04林耀盛、邱子芸(2015)。〈臨終處境的陪伴轉化:癌末病患及其照顧者心理經驗與存在現象探究〉。《中華心理衛生學刊》,28(2),189-219。 doi:10.30074/fjmh.201506_28(2).0002高綺吟、胡文郁、邱泰源(2012)。〈癌症病人末期病情告知與心理情緒之相關性研究〉。《安寧療護雜誌》,17(3),288-299。 doi:10.6537/tjhpc.2012.17(3).4陳怡伶、黃博浩、陳怡安、陳姍婷、蔡兆勳、黃獻樑(2021)。〈神經外科病人的安寧療護〉。《台灣家庭醫學雜誌》,31(1),5-12。doi:10.3966/168232812021033101002黃建勳、胡文郁、姚建安、邱泰源、呂碧鴻、陳慶餘(2006)。〈安寧緩和醫療之初次照會〉。《台灣醫學》,10(6),667-674。doi:10.6320/fjm.2006.10(6).01蔡兆勳、黃怡超、邱泰源(2008)。〈輔助與替代醫療的現況與挑戰〉。《台灣醫學》,12(2),171-177。doi:10.6320/fjm.2008.12(2).05鄭逸如、呂碧鴻(1997)。〈癌症末期患者心理層面的照顧〉。《台灣醫學》,1(2),209-213。doi:10.6320/fjm.1997.1(2).10衛生福利部中央健康保險署(2017):安寧療護(住院、居家、共照及社區)網路查詢服務。取自:https://www.nhi.gov.tw/Content_List.aspx?n=46505DE49DF0AA0B&topn=0B69A546F5DF84DC衛生福利部國民健康署(2020):中華民國 107 年癌症登記報告。取自:https://www.hpa.gov.tw/Pages/Detail.aspx?nodeid=269&pid=13498衛生福利部(2021)。109年國人死因統計結果分析。取自: https://www.mohw.gov.tw/dl-71446-e142a47c-14b3-4cef-8d80-f8e5747e8eb2.html衛生福利部(2021)。安寧療護。取自:https://www.hpa.gov.tw/Pages/List.aspx?nodeid=210英文部分American Cancer Society. 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