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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 張媚(Mei Chang) | |
dc.contributor.author | Shu-Ya Chang | en |
dc.contributor.author | 張淑雅 | zh_TW |
dc.date.accessioned | 2021-06-13T05:50:04Z | - |
dc.date.available | 2006-08-02 | |
dc.date.copyright | 2006-08-02 | |
dc.date.issued | 2006 | |
dc.date.submitted | 2006-07-07 | |
dc.identifier.citation | 一、中文部分
行政院衛生署(2005)。衛生統計資訊網。http://www.doh.gov.tw/statistic/ index.htm。 朱秀珠、鄭綺(1999)。頭部外傷病患出院前後家屬照顧者壓力源及因應方式之探討。新台北護理期刊,1(1),39-47。 李怡娟(1997)。城鄉社區老人使用居家護理服務情形及其之預測因子探討。護理研究,5(2),127-136。 林家瑋、蔡宛真、邱文達、林天仁、江培業、林乾坤、陳俊甫、甘宜弘、蔡行瀚、蔡卓城(2004)。台灣地區外傷性顱內出血之研究。J Emerg Crit Care Med.,15(1),20-28。 林璟鈺、楊銘欽、劉紹興(2001)。勞保被保險人腦血管疾病之疾病成本分析。台灣衛誌,20(1),30-42。 林秀純、徐亞瑛(1998)。失能老人家庭照顧者之照顧回饋與負荷及相因素探討。長庚護理,9(2),1-11。 林梅香、顧乃瓶、劉仲冬、陳政友、林麗嬋(1996)。肝癌患者家屬主要照顧者的壓力、因應行為、健康狀況及其相關因素之探討。護理研究,4(2),171-185。 吳淑瓊、林惠生(1999)。台灣功能障礙老人家庭照護者的全國概況剖析。中華衛誌,18(1),44-53。 吳肖祺(1996)。出院準備服務之執行評價。行政院衛生署八十五年度慢性病病患出院準備服務北區成果觀摩會。 邱啟潤、許淑敏、吳淑如(2003)。居家照護病患之主要照顧者綜合性需求調查。醫護科技學刊,5(1),12-25。 胡綾真、陳美伶、陳明岐、林佳靜、林玲華(2001)。轉移性癌症病患之居家照顧者的照顧負荷極其影響因素。長庚護理,12(4),282-293。 酒小蕙(1999)。某醫學中心神經外科病房出院準備服務成果初探。長庚護理,10(4),1-7。 酒小蕙(1998)。以多元化方法探討脊髓損傷患者出院過渡期間家屬角色緊張與需求之變化。護理研究,6(6),513-525。 曾明月、徐亞瑛、史麗珠、陳獻宗(2001)。家人照顧者於失能老人出院過渡其期之需求、需求滿足變化探討。護理研究,9(3),311-321。 徐亞瑛(1999)。住院老人及其照顧者出院需求量表之發展。行政院衛生署八十八年度整合性醫藥衛生科技研究計畫-年度成果報告。 莊孟蓉、陳琮琳、郭雪敏、黃美智(2003)。燒傷病患及家屬出院前之擔心及訊息需要探討。公共衛生,15,399-407。 陳月枝、戴玉慈、楊清姿、王祖祺、鄭雅心(1995)。長期照護服務對象分類之探討。行政院衛生署八十四年度委託研究計畫。 張興春(1989)。張氏心理學辭典。台北市:東華。 張秉宜、李淑燕、洪佩珊、張玲華、卓妙如(2002)。Glasgow昏迷評估量表與反應程度量表知性效度評估。Taiwain Crit. Care Med.,4,17-27。 張玨(1993)。心理壓力調適與健康促進。健康教育,71,32-37。 張嘉秀(2003)。出院準備服務對脫離長期呼吸器依賴病患之主要照顧者的影響。國立台北護理學院長期照護研究所碩士論文,未發表,台北市。 葉莉莉、黃瑩雯、陳盈伶、陳淑桂(1998)。出院準備服務計畫評值表之建立。護理雜誌,45(6),71-80。 楊錦雀(1998)。巴金森氏患者之主要照顧者的護理指導方案之成效探討。國立台灣大學護理學研究所碩士論文,未發表,台北市。 劉宇平(2004)。臨床神經外科護理技術。載于陳真瑗、周守民(合著),神經外科專科護理(60-63頁)。台北市:合記。 潘依琳、田聖芳、張媚(1998)。居家臥床病人其主要照顧者之壓力源、因應行為與身心健康之探討。公共衛生,24(4),219-233。 鄭雪英(1997)。台北市植物人居家主要照顧者的社會支持、壓力與健康狀況之探討。國立陽明大學社區護理研究所碩士論文,未發表,台北市。 蔡宗學、莊坤洋、戴玉慈、曾淑芬、吳淑瓊(2004)。中風病人具身體功能障礙者出院準備服務之執行評估-病患角度。台灣公共衛生雜誌,23(2),235-248。 蔡淑美(2002)。智障兒母親之照顧者緊張、社會支持與憂鬱的相關性。國立高雄醫學大學護理研究所碩士論文,未發表,高雄市。 鍾月琴、黃正文(1999)。社區中風病人主要照顧者的需要。中台學報,11,29-55。 鍾嫈嫈、蔡正河、林擁章(1990)。居家完全臥床病人主要照顧者的壓力、心態及相關因素之探討。中華民國家庭醫學學會會刊,8,45-58。 鍾思嘉、龍長風(1984)。修訂情境與特質焦慮量表。中國測驗學會測驗學刊,31,27-36。 簡乃卉、徐亞瑛(2000)。住院失能老人之家庭照顧者出院需求的探討。護理研究,8(4),410-421。 戴臆珊(2003)。住院癌症病童照顧者之疲倦、焦慮、睡眠品質、健康狀態與疲倦之相關因素。國立成功大學護理研究所碩士論文,未發表,台南市。 戴玉慈、張丹蓉、羅美芳(1998)。台灣地區之出院準備服務-試行計畫成果分析。慈濟醫學,10,61-68。 戴玉慈、羅美芳(1996)。身體功能評估的概念與量表。護理雜誌,43(2),63-68。 羅淑芬、黃秀梨、姚開屏、劉雪娥(2001)。復健期病患照顧者壓力感受、社會支持及相關因素。台灣醫學,5(1),28-37。 Aday, L. A.(2000)。健康調查設計與執行(應純哲、翁慧卿編譯)。台北市:合記。(原著出版於1996)。 二、英文部分 Amaryll, P., Glynda, K., & Simon, C. (2000). Psychological Distress and Family Following Traumatic Brain Injury: Injury Individuals and Their Primary, Secondary, and Tertiary Carers. Journal of Head Trauma Rehabilitation, 15(3), 909-929. Anderson, M. A., & Helms, L. B. (1994). Quality improvement in discharge planning: an evaluation of factors in communication between health care providers. Journal of Nursing Care Quality, 8(2), 62-72. Artinian, N. T. (1991). Stress experience of spouses of patients having coronary artery bypass during hospitalization and 6 weeks after discharge. Heart Lung, 20(1),52-59. Beach et dl. (2005). Risk Factor for Potentially Harmful Information Caregiver Behavior. Journal of the American Geriatrics Society, 53, 255-261. Bedell, E. (2000). Anesthetic management of traumatic brain injury. Anesthesiology Clinics of North America, 20, 417-439. Bookwala, J., & Schulz, R. (1998). The role of neuroticism and mastery in spouse caregivers’ assessment of and response to a contextual stressor. The Journal of Gerontology, Serise B, Psychological Sciences Social Sciences, 53B, 155-164. CARF, The Rehabilitation Accreditation Commission (1996). Standards Manual and Interpretative Guidelines for Medical Rehabilitation. Tuscon, Arizona: CARF. Cameron, J. I., Franche, R., Cheung, A. M., & Stewart, D. E. (2002). Lifestyle interference and emotional distress in family caregivers of advanced cancer patients. Cancer, 94, 521-527. Carter, P. A., & Chang, B. L. (2000). Sleep and Depression in Cancer Caregivers. Cancer Nursing, 23(6), 410-415. Chien, C. P., & Cheng, T. A. (1985). Depression in Taiwan: Epidemiological survey utilizing. Seishin Shinkeigaku Zasshi-Psychiatria et Neurologia Japonica, 87(5), 335-338 Coppens, P. (1995). Subpopulations in close-head damage: preliminary result. Brain Injury, 9, 195-208. Clyburn, L., Stones, M., Hadjistavropoulos, T., & Tuokko, H. (2000). Predicting caregiver burden and depression in Alzheimer’s disease. The Journal of Gerontology, Serise B, Psychological Sciences Social Sciences, 55B, S2-13. Driscoll, A. (2000). Managing post-discharge care at home: an analysis of patients’ and their carers’ perceptions of information received during their stay in hospital. Journal of Advanced Nursing , 31(5),1165-1173. Diringer, M. N., & Edwards, D. F. (1997). Dose Modification of Innsbruck and the Glasgow Coma Scales Improve Their Ability to predict Functional Outcome?. Arch Neurology, 54(5), 606-611. Dutton, R. P., & McCunn M. (2003). Traumatic brain injury. Current Opinion in Critical Care, 9(6):503-509. Journal of Advanced Nursing , 32(2),318-326. Davies, N. (2000). Patient’s and carer’s perception of factors influencing recovery after cardiac surgery. Feuerstein, M., Labbe, E. E., & Kuczmierczyk, A. R. (1986). Health psychology: A psychobiological perspective (pp. 124-146). New York: Plenum Press. Ford, G. R., Goode, K. T., Barrett, J. J., Harrell, L. E., & Haley, W. E. (1997). Gender roles and caregiving stress: an examination of subjective appraisals of specific primary stressors in Alzheimer’s caregivers. Aging & Mental Health, 1(2), 158-165. Ghajar, J. (2000).Traumatic brain injury. Lancet, 356(9233), 923-929. Gitlin, L., Corcoran, M., Winter, L., Boyce, A., & Hauck, W. (2001). A randomized controlled triad of a home environmental intervention: Effect efficacy and upset in caregivers and on daily function of persons with dementia. Gerontologist, 41, 4-14. Greenberger, H., & Litwin, H. (2003). Can burden caregivers be effective facilitators of elder care-recipient health care?. Journal of Advanced Nursing , 41(4), 332-341. Goode, k. T., Haley, W. E., Roth, D. L., & Ford, G. R. (1998). Predicting Longitudinal Changes in Caregiver Physical and Mental Health: A Stress Process Model . Health Psychology , 17(2), 190-198. Hafseteinsdóttir, T.B., & Grypdonck, M. (1997). Being a stroke patient: a review of the literature. Journal of Advanced Nursing, 26, 580-588. Hall, K. M., Karzmark, P., Stevens, M., Englander, J., O’Hare, B., & Wright, J. (1994). Family Stressors in Traumatic Brain Injury: A Two-Year Follow-Up. Arch Phys Med Rehabil, 75, 876-884. Hemingway, S., & McAndrew, S. (1997). Acquired brain injury: identifying emotional and cognitive needs. Nursing Standard, 12(10), 40-46. Holmes, T. H., & Rahe, R.H. (1967). The social readjustment rating scale. Journal of Psychosomatic Research, 11, 213-218. Hunt, C. K. (2003). Concepts in Caregiver Research. Journal of Nursing Scholarship ,35(1), 27-32. Harrison, N., & Smith, B. (1990). Information wanted. Nursing Times, 86, 46-48. Jennett, B., Teasdale, G., Braakman, R., Minderhoud, J., & Knill-Jones, R. (1976). Predicting outcome in individual patients after severe head injury. The Lancet, 15, 1031-1034. Knight, B. G., Silverstein, M., McCallum, T. J., & Fox, L. S. (2000). A Sociocultural Stress and Coping Model for Mental Health Outcome Among African American Caregivers in Southern California. Journal of Gerontology: PSYCHOLOGICAL SCIENCES, 55B(3), 142-150. Lazarus, R. S., & Folkman, S. (1984). Stress, appraisal, and coping. New York: Springer. Lim, Jung-won., & Zebrack, B., (2004). Caring for family members with chronic physical illness: A critical review of caregiver literature . Health and Quality of Life Outcomes , 2(50), 1-9. Merriam-Webster Online Dictionary. (2005) . Stress. http://www.merriam-webster. com. Marsh, N. V., Kersel, D. A., Havill, J. H., & Sleigh, J. W. (2002). Caregiver Burden During the Year Following Severe Traumatic Brain Injury. Journal of Clinical and Experimental Neuropsychology , 24(4), 435-447. Morris, K. C. (2001). Psychological distress in carers of head injured individuals: the provision of written information. Brain Injury, 15(3), 239-254. Mu, P. F., Ma, F. C., Hwang, B., & Chao, Y. M. (2001). Family of Childdren With Cancer: The Impact on Anxiety Experienced by Fathers. Cancer Nursing, 25(1), 66-73. Mcdowell, I., & Newell, C. (1996). Measuring Health: A Guide to Rating Scale and Questionnaires (2en ed.). New York: Oxford University Press. Neuman, B. (1995). The Neuman System Model (3rd ed.). Norwalk: Appleton & Lange. Neundorfer, M. (1991). Coping and health outcomes in spouse caregivers of persons with dementia. Nursing Research, 40, 260-265. Nolan, M., Grant, K., & Ellis, N. (1990). Stress is in the eye of the beholder: Reconceptualizing the measurement of carer burden. Journal of Advanced Nursing ,15, 544-555. North, N., Cornbleet, M., Knowles, G., & Leonard R. (1992). Information giving in oncology: a preliminary study of tape recorder use. British Journal of Clinical Oncology , 31, 357-359. Pearlin, L., Mullan, J., Semple, S. & Skaff, M. (1990). Caregiving and the stress process: An overview of concepts and measures. The Gerontologist, 30, 583-594. Robinson, K., & Kaye, J. (1994). The relationship between spiritual perspective, social support, and depression in caregiving and noncaregiving wives. Scholarly Inquiry for Nursing Practice, 8, 375-396. Ruff, R. M., & Jurica, P. (1999). In search of a unified definition for mild traumatic brain injury. Brain Injury, 13(12), 943-952. Sansoni, J., Vellone, E., & Piras, G. (2004). Anxiety and depression in community-dwelling, Italian Alzheimer’s disease caregiver. International Journal of Nursing Practice, 10, 93-100. Scherbring, M. (2002). Effect of Caregiver Perception of Preparedness on Burden in an Oncology Population. Oncology Nursing, 29(6), E70-76. Sherwood, P., Given, B., Given, C., Schiffman, R., Murman, D., & Lovely, M. (2004). Caregiver of persons with a Brain tumor: a conceptual model. Nursing inquiry, 11(1), 43-53. Shyu, Yea-Ing. L. (2000a). Patterns of caregiving when family caregivers face competing needs. Journal of Advanced Nursing , 31(1), 35-43. Shyu, Yea-Ing. L. (2000b). The needs of family caregivers of frail elders during the transition from hospital to home: a Taiwanese sample. Journal of Advanced Nursing , 32(3), 537-543. Shin, F. J., & Huang, L. H. (1996). A multidimensional model of the antecedents of stress and coping appraisals: An approach to studying patients’ perceptions of post cardiac surgery pain and their coping strategies. Kaohsiung J Med Sci, 12, 202-215. Shah, S., Vanclay, F., & Cooper, B. (1989). Improving the sensitivity of the Barthel Index for stroke rehabilitation. Journal clinical Epidemiology, 42, 703-709. Sosin, D. M., Sniezek, J. E., & Thurman D.J. (1991). Incidence of mild and moderate brain injury in the United States. Brain Injury, 10, 47-54. Swift, T. L., & Wilson, S. L. (2001). Misconceptions about brain injury among the general public and non-expert health professional: an explorative study. Brain Injury, 15(2), 149-165. Teasdale, G., & Jennett, B. (1974). Assessment of coma and impaired consciousness. The Lancet, 13, 81-83. Vedhara, K., Shanks. N., Anderson, S., & Lightman. (2004). The role of stressors and psychosocial variables in the stress process: A study of chronic caregiver stress. Psychosomatic Medicine , 62, 374-385. Vitaliano, P. P., Russo, J., Young, H. M., Teri, L., & Maiuro, R. D. (1991). Predictors of burden in spouse caregivers of individuals with Alzheimer’s disease. Psychology and Aging, 6(3), 392-402. Wallhagen, M. I. (1992). Perceived control and adaptation in elder caregivers: development of an explanatory model. Int Aging Hum, 36, 219-237. Watanable, Y., Shiel, A., Asami, T., Taki, K., & Tabuchi. (2000). An evaluation of neurobehavioral problems as perceived by family members and level of family stress 1-3 years. Clinical Rehabilitation, 14, 172-177. Waters K., Allsopp, D., Davidson, I., & Dennis, A. (2001). Sources of support for older people after discharge from hospital: 10 years on. Journal of Advanced Nursing, 33(5), 575-582. Weaver, F. M., Perloff, L., & Water. (1998). Patients’ and Caregivers’ Transition from Hospital to Home: Needs and Recommendations. Home Health Care Services Quarterly, 17(3), 27-48. Wenzel, L.B., Glanz, K., & Lerman, C. (2002). Stress, Coping and Health Behavior. In Glanz, K., Rimer, B., & Lewis, F. (Eds), Health Behavior and Health Education: Theory, Research and Practice (pp. 210-239). San Francisco: Jossey-Bass. Wiles, R., Pain, H., Buckland, S., & McLellan, L. (1998). Providing appropriate information to patients and carers following a stroke. Journal of Advanced Nursing , 28(4), 794-801. Warren, M. L., Cberyl, J., Senegal, R., Parker, A., Kraus, J., & Hartgraves, D. (2004). An Interdisciplinary Approach to Transitioning Ventilator-dependent Patients to Home. Journal of Nursing Care Quality , 19(1), 67-73. Zarit, S., Reever, K., & Bach-Peterson, J. (1980). Relatives of the impaired elderly: Correlates of feelings of burden. The Gerontologist, 20, 649-655 | |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/33960 | - |
dc.description.abstract | 本研究為橫斷式描述性相關研究,研究目的在探討主要照顧者在腦部神經損傷病患出院前的壓力感受與情緒反應相關因素。以立意取樣方式,於北部某醫學中心神經內外科病房收集63位腦部神經損傷病患之主要照顧者,運用結構性問卷包含腦部損傷患者主要照顧者壓力感受問卷、流行病學憂鬱量表(CES-D)、情境焦慮量表(SAI)、病患與照顧者的基本資料表與照顧資源問卷,與照顧者面對面親自訪談進行收集資料。研究對象所照顧的腦部損傷病患疾病多以腦部梗塞為主,平均為65.38歲,男性,屬輕度腦部損傷,巴氏指數平均為13.33分;主要照顧者平均年齡為48.69歲,多數為女性、高中職學歷、已婚、為病人的配偶、與病患感情還不錯、自覺健康狀況普通、平均照顧時數為14.44小時。將所得資料進行描述性統計與推論性統計分析。研究結果如下:
一、照顧者於病患出院前自覺有輕度到中度的壓力感受、65.1%的人具有憂鬱傾向。 二、照顧者在病患出院前最擔心的前十項壓力事件順序為:「病況再次發生變化」、「害怕病人死亡」、「花費增加、支出增加」、「缺乏照顧人力」、「害怕病人跌倒」、「不會處理病人突發問題」、「不清楚病患未來狀況,無法做好後續照顧計畫的規劃」、「幫病人抽痰」、「就醫往返不方便或困難」、「害怕自己照顧能力不好」。再經文獻概念分析,將本研究照顧者壓力感受歸納為四個構面,依序為病況變化之醫療處置、經濟及資源不足、直接照顧困難及照顧病人對自己與家人的影響。 三、照顧者照顧時數越長、面對病人出院之準備度越差,以及護理人員提供出院前之護理指導完成率越低,則整體壓力感受越大。此三變項可解釋照顧者壓力感受10%的變異量。 四、病患意識狀況越差、出院時病患身上所具有的管路越多;照顧者教育程度越低者、對病患照顧技能純熟度越不熟練、無法找到照顧諮詢的人來解決照顧問題、護理人員提供出院前之護理指導完成率越低,與照顧者的整體壓力感受越大,照顧者越有憂鬱傾向。這些變項共可解釋照顧者憂鬱反應38.9%的變異量。其中,「照顧者的整體壓力感受」為最具預測力的變項。 五、病患發病前為家中主要經濟來源者;照顧者教育程度越低者、對病患照顧技能純熟度越不熟練、無法找到照顧諮詢的人來解決照顧問題、護理人員提供出院前之護理指導完成率越低,與照顧者的整體壓力感受越大,照顧者的焦慮反應越高。這些變項共可解釋照顧者焦慮反應42%的總變異量。而「照顧者的整體壓力感受」為最具預測力的變項。 故建議在未來臨床護理實務方面,瞭解此類病患出院前主要照顧者的壓力感受,規劃提供一系列完善的護理指導方案並提高護理指導完成率,使照顧者可以經由增強整體照顧能力,認識與瞭解相關社會資源的運用,降低其出院前的壓力感受,進而降低憂鬱與焦慮。 | zh_TW |
dc.description.abstract | This study uses a cross-sectional design with a descriptive correlation approach. The main purpose of this study is to investigate the primary caregiver’s stress perception and emotional response with brain damaged patients at pre-discharge. A purposive sample of 63 primary caregivers were face-to-face interviewed through structured questionnaires in a neurological and neurosurgical units at a medical center in northern Taiwan, including Questionnaire for Primary Caregiver’s Stress Perception, Center for Epidemiologic Studies Depression Scale (CES-D), State Anxiety Inventory (SAI), basic information about patient and caregiver, and Questionnaire for Caregiver’s Resource. Brain infarction is the most common disease among all brain damaged patients cared by these subjects. The mean age of patients is 65.38, male with mild brain damage, and the mean score of Barthel Index is 13.33. The mean age of primary caregivers is 48.69. Most of the caregivers were female, married, patient’s spouse, with high school background, having a good relationship with patients, ordinary health status on his/her own initiative, and the average care time is 14.44 hours. The results show:
1.The degree of primary caregiver’s stress perception before patient discharge was mild to moderate. 65.1% of them have tendency toward depression. 2.The top 10 stress events that the caregiver worried about are: “patient condition changes again”, “patient will dead after discharge”, “expenditure increase”, “short of caring manpower”, “fear of patient falling down”, “can’t handle the unexpected problems”, “unable to make a good plan because patient’s status is unclear in the future”, “suction for the patient”, “inconvenient or hard to go to hospital”, “inadequate care ability”. After that, we separate caregiver’s stress perception into 4 categories by using concept analysis, which are “medical treatment when patient’s status is changed”, “financial burden and short of resource”, “difficult to provide direct care”, and “the influence of caring patient upon caregiver and caregiver’s family members”. 3.The longer care time for caregiver, the less readiness for patient’s discharge, and the lower completion rate of nursing instruction from nursing staff before discharge, and the larger degree of stress perception would be. These 3 independent variables can explain 10% variance at the caregiver’s stress perception level. 4.The worse patient conscious level, the more tubes on patient at discharge; the lower level education for caregiver, the worse caregiver’s mastery in caring patient; fewer people can be found to counsel on solving caring problems, the lower completion rate of nursing instruction before discharge, the higher overall stress perception of caregiver, and the more tendency toward depression on caregiver. These independent variables can explain 38.9% variance in caregiver’s depression scale. Among them, the “caregiver’s stress perception level” is the strongest predictor. 5.These items will cause caregiver with higher degree of anxiety and can explain 42.0% variance of caregiver’s anxiety scale: “patient takes most responsibility for family income before being sick”, “lower education level of the caregiver”, “worse caregiver’s mastery”, “caregiver unable to find counselors to solve caring problems”, “low completion rate of receiving information and care training from nursing staff before discharge”, and “high caregiver’s stress perception level”. The “caregiver’s overall stress perception level” is the strongest predictor. In clinical nursing practice, this study recommends understanding the primary caregiver’s stress perception before patient discharge, providing a complete and better nursing plan to increase the completion rate of nursing instruction. These can help the caregiver to lessen his/her stress perception and further decrease his/her depression and anxiety through strengthening overall care ability and understanding how to utilize social resources. | en |
dc.description.provenance | Made available in DSpace on 2021-06-13T05:50:04Z (GMT). No. of bitstreams: 1 ntu-95-R91426008-1.pdf: 1868667 bytes, checksum: 7705e60845f82d0f6c2c6e8063322526 (MD5) Previous issue date: 2006 | en |
dc.description.tableofcontents | 致 謝 I
中文摘要 II 英文摘要 V 目錄 VII 圖表目錄 XII 第一章 緒論 第一節 研究背景與重要性 1 第二節 研究動機 4 第三節 研究目的 5 第二章 文獻查證 第一節 壓力理論 一、壓力定義 6 二、壓力理論 8 三、壓力源 10 第二節 腦部損傷病患照顧者出院前壓力感受與影響因素 一、照顧者出院前壓力感受 11 二、影響照顧者壓力感受之因素 (一)腦部損傷病患特性 14 (二)病患與主要照顧者之基本屬性 15 第三節 主要照顧者情緒反應與影響因素 16 第四節 主要照顧者照顧資源 18 第三章 研究方法 第一節 研究架構 21 第二節 名詞界定 23 第三節 研究假設 24 第四節 研究設計 25 第五節 研究對象 25 第六節 研究場所 26 第七節 研究工具 26 第八節 研究工具信效度檢定 31 第九節 資料收集過程 35 第十節 資料分析 36 第四章 研究結果 第一節 基本屬性 一、主要照顧者基本屬性 41 二、病患基本屬性 45 第二節 主要照顧者出院前壓力感受 49 第三節 主要照顧者情緒反應 一、主要照顧者憂鬱反應 52 二、主要照顧者焦慮反應 54 第四節 主要照顧者的照顧資源 一、照顧者照顧能力 56 二、家庭收入 58 三、出院後尋求照顧諮詢能力 58 四、護理人員提供照顧者出院前之護理指導 59 第五節 主要照顧者與病患基本屬性、照顧資源與壓力感受之關係 65 第六節 主要照顧者與病患基本屬性、照顧資源與情緒反應之關係 一、憂鬱反應 72 二、憂鬱反應之重要預測變項分析 76 三、焦慮反應 77 四、焦慮反應之重要預測變項分析 81 第五章 討論 第一節 主要照顧者出院前壓力感受 83 第二節 主要照顧者出院前壓力感受、病患及照顧者基本屬性與照顧者照顧資源之相關性 一、主要照顧者出院前壓力感受與病患及照顧者基本屬性之相關性 89 二、主要照顧者出院前壓力感受與照顧者照顧資源之相關性 91 第三節 主要照顧者情緒反應、病患及照顧者基本屬性、照顧者照顧資源和照顧者出院前壓力感受之相關性 一、主要照顧者情緒反應與病患及照顧者基本屬性之關係 92 二、主要照顧者情緒反應與照顧者照顧資源之關係 94 三、主要照顧者情緒反應與照顧者出院前壓力感受之關係 94 第四節 預測主要照顧者情緒反應的變項探討 95 第六章 結論與建議 第一節 結論 97 第二節 建議 99 第三節 研究限制 102 參考文獻 中文部分 104 英文部分 107 附錄 附錄一 內容效度之專家名單(依姓氏筆畫順序排列)113 附錄二 流行病學憂鬱量表(CES-D)使用同意書 114 附錄三 情境焦慮量表(Status Anxiety Inventory)使用同意書 115 附錄四 研究場所回函公文 116 附錄五 研究場所同意臨床試驗證明書 117 附錄六 研究同意書 118 附錄七 主要照顧者壓力感受問卷 119 附錄八 主要照顧者憂鬱量表 120 附錄九 主要照顧者焦慮量表 121 附錄十 病患基本資料 122 附錄十一 主要照顧者基本資料 123 附錄十二 照顧能力評估表 124 附錄十三 護理人員提供照顧者出院前之護理指導評估表 125 附錄十四 巴氏量表(Barthel Index)126 附錄十五 Glasgow Coma Scale(GCS)127 | |
dc.language.iso | zh-TW | |
dc.title | 腦部損傷病患照顧者出院前壓力感受與情緒反應探討 | zh_TW |
dc.title | An Exploration of Caregiver’s Stress Perception and Emotional Response with Brain Damaged Patients at Pre-discharge | en |
dc.type | Thesis | |
dc.date.schoolyear | 94-2 | |
dc.description.degree | 碩士 | |
dc.contributor.oralexamcommittee | 黃俊一,蔡欣玲 | |
dc.subject.keyword | 主要照顧者,腦部神經損傷病患,出院前壓力感受,情緒反應,憂鬱,焦慮, | zh_TW |
dc.subject.keyword | primary caregiver,brain damage patient,stress perception before discharge,emotional response,depression and anxiety, | en |
dc.relation.page | 127 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2006-07-07 | |
dc.contributor.author-college | 醫學院 | zh_TW |
dc.contributor.author-dept | 護理學研究所 | zh_TW |
顯示於系所單位: | 護理學系所 |
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