請用此 Handle URI 來引用此文件：
http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/42348完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 賴裕和 | |
| dc.contributor.author | Shiuan - Chen Chiou | en |
| dc.contributor.author | 邱萱宸 | zh_TW |
| dc.date.accessioned | 2021-06-15T01:12:27Z | - |
| dc.date.available | 2010-07-07 | |
| dc.date.copyright | 2009-09-15 | |
| dc.date.issued | 2009 | |
| dc.date.submitted | 2009-07-30 | |
| dc.identifier.citation | 王麗香 (2001)．急診留觀區病患、照顧者及護理人員評估病患需求之差異及相關因素探討．未發表的碩士論文，桃園：長庚大學護理學研究所。
朱立寧 (2002) ．癌患配偶照顧者之生活品質及其相關因素．未發表的碩士論文，桃園：長庚大學護理學研究所。 行政院衛生署 (2008，10月15日) ．中華民國九十七年衛生統計系列與死因統計．衛生署統計資訊網，取自6月28日，2009，http://www.doh.gov.tw/statistic/data/衛生統計叢書2/94/上冊/目錄.htm. 何青蓉 (1995)．需求評估概念的澄清與分析．成人教育，23，41-46。 吳麗彬、顧乃平 (1994)．肝癌病人家屬的需要．護理研究，2 (2)，180-190。 李龍騰、陳建仁、索任、陸坤泰、林瑞雄 (1997) ．肺結核與肺癌：病例對照研究．台灣醫學，1 (2)，176-184。 李姿瑩 (1999) ．花蓮地區精神分裂病患主要照顧者需求及其相關因素探討．未發表的碩士論文．桃園：長庚大學護理學研究所。 林淑英 (2002)．急診室病患照顧者與護理人員自覺需求重要性之比較與獲得程度分析．未發表的碩士論文．桃園：長庚大學護理學研究所。 邱麗珠（1999）．內科重症病房病人家屬需求及其影響因素探討．未發表的碩士論文，台中：中山醫學院護理學研究所。 胡綾真 (1999)．居家照顧癌症轉移病患之主要照顧者的照顧負荷、憂鬱與生活品質之探討．已發表的碩士論文，桃園：長庚大學護理學研究所。 姚建安 (2002)．緩和醫療住院癌末病人主要照顧者的需求重要行性與滿意度的初探性研究．未發表的碩士論文，台北：台灣大學護理學研究所。 唐家駿 (2002)．肺癌概論及預後．呼吸胸腔保健季刊，16，3-8。 孫秀卿 (1999)．男性肝癌病患接受經導管肝動脈栓塞治療期間疲倦型態及其相關因素之探討．已發表的碩士論文，台北：台北醫學大學護理學研究所。 高淑芳、盧孳豔、葉淑惠、劉雪娥 (1999)．探討家庭功能、社會支持與社區殘病老人照顧者負荷之關係．護理研究，7 (2)，172-181。 許町子、杜異珍 (1997)．癌症病患和家屬對安寧照顧需求之探討．榮總護理，14 (1)，11-22。 許朝添 (2002) ．病理學．台北:藝軒。 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．慈濟醫學，15 (6)，399-407。 郭淑娥 (2000) ．長期依賴呼吸器病患與家屬之需求及其滿意度探討．未發表的碩士論文，桃園：長庚大學護理學研究所。 陳惠津 (1996) ．居家癌病家屬照顧者之需要狀況及其相關因素之探討．未發表的碩士論文，台北：陽明大學護理學研究所。 陳惠津、李怡娟、吳肖琪 (1998)．影響居家癌病患者家庭照顧者需要因素之研究．中華公共衛生雜誌，17 (5)，412-422。 陳佩英、史麗珠、王正旭、賴裕和、獻崑、陳美伶 (1999) ．疼痛對癌症病患焦慮與憂鬱之影響．台灣醫學，3 (4)，373-381。 陳秀娟、陳美伶 (2004)．癌症病患家屬照顧者照顧工作之探討．長庚護理，15 (3)，258-269。 陳美琴 (2005) ．主要照顧者對病患加護治療期之照護需求與壓力感探討，未發表的碩士論文，台中：中山醫學大學護理學研究所。 張基晟、陳焜結、楊宗穎、林聖皓、徐國軒 (2009) ．年齡增加在非小細胞肺癌使用Gefitinib治療是個預測因子．中華民國癌症醫學會雜誌，24 (6)，362-371。 國家衛生研究院 (2004) ．肺癌臨床指引．台北:台灣癌症臨床研究合作組織。 曾雅涓 (2006) ．急診重症病人家屬與護理人員對家屬需求重要性及滿足程度認知之差異．未發表的碩士論文，台北：台灣大學護理學研究所。 楊嘉玲 (2000) ．癌患照顧者需求Q-sort量表發展與測試．未發表的碩士論文，桃園：長庚大學護理學研究所。 劉長安、蘇婉麗 (1998)．某醫學中心住院患者家屬對醫院的需求及其滿意度之探討．護理雜誌，45 (2)，47-58。 劉會平 (2004) ．肺癌診斷與治療．腫瘤護理雜誌，4 (2)．25-34。 蔡佩真 (1999)．死亡壓力下的家庭溝通．安寧療護雜誌，12，26-31。 鄭秀容 (2004) ．居家失智老人家屬照顧者照顧負荷及照顧需求，未發表的碩士論文，台中：中山醫學大學護理學研究所。 鍾家真 (1998) ．安寧療護病患主要照顧者的照顧需要及其相關因素之探討．未發表的碩士論文，台北：陽明大學護理學研究所。 戴金英、唐秀治 (2006) ．影響癌末病人主要照顧家屬正向與負向照顧經驗之因素探討．新台北護理期刊，8 (1) ，17-31。 鍾若男 (2002) ．住院氣管造口病患家屬需求及其影響因素探討．未發表的碩士論文．台北：國立台北護理學院。 羅靜心 (1990) ．住院癌症病患家庭的社會資源及其因應策略之探討．未發表的碩士論文．台中：東海大學社會工作研究所。 Aranda, S.K., & Hayman-White, K. (2001). Home caregivers of the person with advanced cancer: an Australian perspective. Cancer Nursing, 24 (2), 300-307. Bach, P. B., Niewoehner, D. E., & Black, W. C. (2003). Screening for lung cancer: The guidelines. Chest, 123(1), 83-88. Baghi, M., Wagenblast, J., Hambeck, M., Radeloff, A., Gstoettner, W., Scherzed, A., et al. (2007). Demands on caring relatives of head and neck cancer patients. Laryngoscope, 117, 712-716. Bakas, T., Lewis, R.R., & Parsons, J.E. (2001). Caregiving tasks among family caregivers of patients with lung cancer. Oncology Nursing Forum, 28 (5), 847-854. Beaver, K., & Witham, G. (2007). Information needs of the informal carers of women treated for breast cancer. European Journal of Oncology Nursing, 11, 16-25. Blank, J. J., Clark, L., Longman, A. J., & Atwood, J. R. (1989). Perceived home care needs of cancer patients and their caregivers. Cancer Nursing, 12 (2), 78-84. Bonevki, B., Sanson-Fisher, R., Girgis, A., Burton, L., Cook, P., & Boyes, A. (2000). Evaluation of an instrument to assess the needs of patients with cancer. Cancer, 88 (1), 217-225. Bradshaw, W.H., Borus, J.F., O'Neill, P.H., & MacLennan, B.W. (1972). Mental health consultants in an educational charrette. Psychiatry, 35 (4), 317-35. Bradzil, K., Thabane, L., Foster, G., & Bedard, M. (2009). Gender differences among Canadian caregivers at the end of life. Health and Social Care in the Community, 17 (2), 159-166. Brewin, C. R. (1987). Principles and practice of measuring need in the long-term mentally ill: The MRC needs for care assessment. Psychological Medicine, 17, 971-981. Buchanan, D., Milroy, R., Baker, L., Thompson, A.M., & Levack, P.A. (2009). Perceptions of anxiety in lung cancer patients and their support network [published online ahead of print April 07, 2009]. Supportive Care in Cancer. 2009. doi: 10.1007/s00520-009-0626-2. Butt, Z., Rosenbloom, S.K., Abernethy, A.P., Beaumont, J.L., Paul, D., Hamptom, D., et al. (2008). Fatigue is the most important symptom for advanced cancer patients who have had chemotherapy. Journal of National Comprehension Cancer Network, 6 (5), 448-455. Carlsen, K., Jensen, A.B., Jacobsen, E., Krasnik, M., & Johansen, C. (2005). Psychosocial aspects of lung cancer. Lung Cancer, 47, 293-300. Cersosimo, R. J. (2004). Gefitinib: a new antineoplastic for advanced non-small-cell lung cancer. American journal of health-system pharmacy, 61 (9), 889-898. Cheung, W.Y., Le, L.W., & Zimmermann, C. (2009). Symptom clusters in patients with advanced cancers [published online ahead of print January 30, 2009]. Supportive Care in Cancer. 2009. doi: 10.1007/s00520-009-0577-7. Christ, G., & Siegel, K. (1990). Monitoring quality of life needs of cancer patients. Cancer, 65 (3 suppl), 760-765. Cleary, M., Freeman, A., Hunt, G.E., & Walter, G. (2005). What patients and carers want to know: an exploration of information and resource needs in adult mental health services? Australian and New Zealand Journal of Psychiatry, 39, 507-513. Cohen, J., & Cohen, P. (1983). Applied multiple regression/correlation analysis for the behavioral sciences, (2nd ed.). Hillsdale, N.J.: Lawrence Erlbaum Associates. Cooley, M.E., Short, T.H., & Moriarty, H.J. (2002). Patterns of symptom distress in adults receiving treatment for lung cancer. Journal of Palliative Care, 18,150-159. Dahlberg, L., Demack, S., & Bambra, C. (2007). Age and gender of informal carers: a population-based study in the UK. Health and Social Care in the Community, 15, 439-445. Derdiarian, A. (1987). Informational needs of recently diagnosed cancer patients. A theoretical framework. Part I. Cancer Nursing, 10 (2), 107-115. de Jong, N., Candel, M.J., Schouten, H.C., Abu-Saad, H.H., & Courtens, A.M. (2004). Prevalence and course of fatigue in breast cancer patients receiving adjuvant chemotherapy. Annals of Oncology, 15, 896-905. Dubenske, L.L., Wen, K., Gustafson, D.H., Guarnaccia, C.A., Cleary, J.F., Dinaure, S.K., et al. (2008). Caregivers’ differing needs across key experiences of the advanced cancer disease trajectory. Palliative and Supportive Care, 6, 265-272. Emanuel, E. J., Fairclough, D. L., Slutsman, J., Alpert, H., Baldwin, D., & Emanuel, L. L. (1999). Assistance from family members, friends, paid caregivers, and volunteers in the care of terminally ill patients. New England Journal Medicine, 341 (13), 956-963. Endacott, R. (1997). Clarifying the concept of need: A comparison of two approaches to concept analysis. Journal of Advance Nursing, 25, 471-476. Feinberg, L.F. (2008). Caregiver assessment. The American Journal of Nursing, 108 (9 Suppl), 38-39. Fox, S.H. & Lyon, D.E. (2006). Symptom clusters and quality of life in survivors of lung cancer. Oncology Nursing Forum, 33 (5), 931-936. Fukui, S. (2004). Information needs and the related variables of Japanese family caregivers of terminally ill cancer patients. Nursing and Health Sciences, 6, 29-36. Gaston-Johansson, F., Lachica, E.M., Fall-Dickson, J.M., & Kennedy, M.J. (2004). Psychological distress, fatigue, burden of care, and quality of life in primary caregivers of patients with breast cancer undergoing autologous bone marrow transplantation. Oncology Nursing Forum, 31 (6), 1161-1169. Given, B.A., Given, C.W., & Kozachik, S. (2001). Family support in advanced cancer. A Cancer Journal for Clinicians, 51 (4), 213-231. Given, B., Wyatt, G., Given, C., Sherwood, P., Gift, A., DeVoss, D., et al. (2004). Burden and depression among caregivers of patients with cancer at the end of life. Oncology Nursing Forum, 31 (6), 1105-1117. Given, B., Sherwood, P.R. (2006). Family care for the older patient with cancer. Seminars in Oncology Nursing, 22 (1), 43–50. Given, B., Sherwood, P.R., & Given, C.W. (2008). What knowledge and skills do caregivers needs? The American Journal of Nursing, 108 (9 Suppl), 28-34. Glajchen, M. (2004). The emerging role and needs of family caregivers in cancer care. Journal of Support Oncology, 2 (2), 144-155. Goldstein, N. E., Concato, J., Fried, T. R., Kasl, S. V., Johnson-Hurzeler, R., & Bradley, E. H. (2004). Factors associated with caregiver burden among caregivers of terminally ill patients with cancer. Journal of Palliative Care, 20 (1), 38-43. Gray, G., Adler, D., Fleming, C., & Brescia, F. (1988). A clinical data base for advanced cancer patients. Implication for nursing. Cancer Nursing, 11 (2), 77-83. Harrington, V., Lackey, N. R., & Gates, M. F. (1996). Needs of caregivers if clinic and hospice cancer patients. Cancer Nursing, 19 (2), 118-125. Hays, J.C. (1986). Patient’s symptoms and family coping: predictors of hospice utilization patterns. Cancer Nursing, 9 (6), 317-325. Hileman, J. W., & Lackey, N. R. (1990). Self-identified needs of patients with cancer at home and their home caregivers: a descriptive study. Oncology Nursing Forum, 17 (6), 907-913. Hileman, J.W., Lackey, N.R., & Hassanein, R.S. (1992). Identifying the needs of home caregivers of patients with cancer. Oncology Nursing Forum, 19 (5), 771-777. Hinds, C. (1985). The needs of families who care for patients at home: are we meeting them. Journal of Advanced Nursing, 10, 575-581. Hoffman, A.J., Given, B.A., von Eye, A., Gift, A.G. & Given, C.W. (2007). Relationship among pain, fatigue, insomnia, and gender in persons with lung cancer. Oncology Nursing Forum, 34 (4), 785-792. Hopwood, P., & Stephens, R.J. (2000). Depression in patients with lung cancer: prevalence and risk factors derived from quality-of-life data. Journal of Clinical Oncology, 18 (4), 893-903. Hudson, P.L., Aranda, S., & Kristjanson, L.J. (2004). Meeting the supportive needs of family caregivers in palliative care: challenges for health professionals. Journal of Palliative Medicine, 7 (1), 19-25. Ihde, D., Souhami, B., Comis, R., Gregor, A., Hansen, H., Johnson, B., et al. (1997). Small cell lung cancer. Lung Cancer, 17 (1), 19-21. Iwamoto, R. (2000). Lung cancer. In B. M. Nevidjon, & K. W. Sowers (Eds.), A nurse’s guide to cancer care (pp. 44-61). Philadelphia: Lippincatt. Janda, M., Steginga, S., Dunn, J., Langbecker, D., Walker, D., & Eakin, E. (2008). Unmet supportive care needs and interest in services among patients with a brain tumor and their carers. Patient Education and Counseling, 71, 251-258. Jansen, C., Halliburton, P., Dibble, S., & Dodd, M.J. (1993). Family problems during cancer chemotherapy. Oncology Nursing Forum, 20 (4), 689-694. Kolakowsky-Hayner, S.A., Miner, K.D., & Kreutzer, J.S. (2001). Long-term life quality and family needs after traumatic brain injury. Journal of Head Trauma Rehabilitation, 16 (4), 374-385. Krishnasamy, M., Wilkle, E., & Haviland, J. (2001). Lung cancer health care needs assessment: patients’ and informal carers’ responses to a national mail questionnaire survey. Palliative Medicine, 15 (3), 213-217. Kurtz, M. E., Kurtz, J.C., Stommel, M., Given, C.W., & Given, B. (2002). Predictors of depressive symptomatology of geriatric patients with colorectal cancer: a longitudinal view. Supportive Care in Cancer, 10 (6), 494-501. Laizner, A.M., Yost, L.M., Barg, F.K., & McCorkle, R. (1993). Needs of family caregivers of persons with cancer: a review. Seminars in Oncology Nursing, 9 (2), 114-120. Leavitt, M.B. (1984). Nursing and family-focused care. The Nursing Clinics of North America, 19 (1), 83-87. Lee, Y.H., Tasi, Y.F., Lai, Y.H., & Tasi, C.M. (2008). Fatigue experience and coping strategies in Taiwanese lung cancer patients receiving chemotherapy. Journal of Clinical Nursing, 17 (7), 876-883. Leske, J.S. (1986). Need of relatives of critically ill patients: A follow-up. Heart & Lung, 20 (3), 236-244. Longman, A.J., Atwood, J.R., & Blank-Sherman, J., (1992). Care needs of home-based cancer patients and their caregivers: Quantitative findings. Cancer Nursing, 15, 180-190. Longman, A.J., Atwood, J.R., Sherman, J.B., Benedict, J., & Shang, T.C. (1992). Care needs of home-based cancer patients and their caregivers. Cancer Nursing, 15 (3), 182-190. Maslow, A.H. (1954). The instinctoid nature of basic needs. Journal of Personality, 22 (3), 326-347. Matthews, B.A., Baker, F., & Spillers, R.L. (2004). Oncology professionals and patient requests for cancer support services. Supportive Care in Cancer, 12 (10), 731-738. McCorkle, R., Benoliel, J.Q., Donaldson, G., Georgiadou, F., Moinpour, C., & Goodell, B. (1989). A randomized clinical trial of home nursing care for lung cancer patients. Cancer, 64 (6), 1375-1382. McIlfatrick, S. (2006). Assessing palliative care needs: views of patients, informal carers and healthcare professionals. Journal of Advanced Nursing, 57 (1), 77-86. Mirtchell, S.A., Beck, S.L., Hoods, L.W., Moore, K., & Tanner, E.R. (2007). Putting Evidence Into Practices: Evidence-based interventions for fatigue during and following cancer and its treatment. Clinical Journal of Oncology Nursing, 11 (1), 99-113. Molter, N.C. (1979). Needs of relatives of critically ill patients: a descriptive study. Heart & Lung, 8 (2), 332-339. Montaxeri, A., Milroy, R., Hole, D., McEwen, J., & Gillis, C.R. (1998). Anxiety and depression in patients with lung cancer before and after diagnosis: finding from a population in Glasgow, Scotland. Journal of Epidemiol Community Health, 52, 203-204. Murtonen, I., Kuisma, M., Paunonen, M., Lehti, K., Koivula, M., & White, M. (1998). Family dynamics of families with cancer in Finland. Cancer Nursing, 21 (4), 252-258. Nijboer, C., Tempelaar, R., Sanderman, R., Triemstra, M., Spruijt, R.J., & van den Bos, G.A. (1998). Cancer and caregiving: the impact on the caregiver's health. Psychooncology, 7 (1), 3-13. Nijboer, C., Triemstra, M., Tempelaar, R., Sanderman, R., & van den Bos, G.A. (1999). Determinants of caregiving experiences and mental health of partners of cancer patients. Cancer, 86 (4), 577-588. Northouse, L. (2005). Helping families of patients with cancer. Oncology Nursing Forum, 32 (4), 743-750. Oberst, M.T., Thomas, S.E., Gass, K.A., & Ward, S.E. (1988). Caregiving demands and appraisal of stress among family caregivers. Cancer Nursing, 12 (4), 209-215. Oh, E.G.. (2004). Symptom experience in Korean adults with lung cancer. Journal of Pain and Symptom Management, 28 (2), 133-139. Payne, J.K. (2002). The trajectory of fatigue in adult patients with breast and ovarian cancer receiving chemotherapy. Oncology Nursing Forum, 29, 1334-1340. Pinqurt, M., & Sorensen, S. (2003). Differences of between caregivers and noncaregivers in psychology health and physical health: a meta-analysis. Psychology and Aging, 18 (2), 250-267. Porter, L.S., Keefe, F.J., Garst, J., McBride, C.M., & Baucom, D. (2007). Self-efficacy for managing pain, symptoms, and function in patients with lung cancer and their informal caregivers: associations with symptoms and distress. Pain, 137 (2), 306-315. Reed, D.G. (1986). Religious among terminally ill and health adults. Research in Nursing and Health, 9 (1), 35-41. Richardson, A., Plant, H., Moore, S., Medina, J., Cornwall, A., & Ream, E. (2007). Developing supportive care for family members of people with lung cancer: a feasibility study. Suppotivet Care in Cancer, 15, 1259-1269. Rivera, M. P., Detterbeck, F., & Mehta, A. C. (2003). Diagnosis of lung cancer: The guild lines. Chest, 123 (1), 129S-136S. Rolland, J.S. (2005). Cancer and the family: an integrative model. Cancer, 104 (11 Suppl), 2584-2595. Roth, A.J. & Massie, M.J. (2007). Anxiety and its management in advanced cancer. Current Opinion Support Palliative Care, 1, 50-56. Sales, E., Schulz, R., & Biegel, D. (1991). Psychosocial impact of the phase of cancer on the family: an update review. Journal of Psychosocial Oncology, 9, 1-8. Schott-Bear, D. (1993). Dependent care, caregiver burden, and self-care agency of spouse caregivers. Cancer Nursing, 16 (3), 230-236. Schulz, R., & Beach, S.R. (1993). Caregiving as a risk factor for mortality: The caregiver health effects study. The Journal of the American Medical Association, 282, 2215-2219. Schulz, R., & Sherwood, P.R. (2008). Physical and mental health effects of family caregiving, The American Journal of Nursing, 108 (9 Suppl), 23-27. Schumacher, K.L. (1996). Reconceptualizing family caregiving: family-based illness care during chemotherapy. Research in Nursing & Health, 19 (4), 261-271. Siegel, K., Raveis, V.H., Houts, P., & Mor, V. (1991). Caregiver burden and unmet patient needs. Cancer, 68 (5), 131-140. Silverira, J. M., & Winstead-Fry, P. (1997). The needs of patients with cancer and their caregiver in rural areas. Oncology Nursing Forum, 24 (1), 71-76. Smith, T.D., White, M.T., O'connor, L.J., Salinas, T.K., Lucas, J.A., & Bowar-Ferres, S., et al. (2002). Nursing Care Quality Initiative (NCQI) for hospitalized elders and their families: a demonstration and quality improvement model of nursing care. Applied Nursing Research, 15 (1), 48-50. Stasi, R., Abriani, L., Beccaglia, P., Terzoli, E., & Amadori, S. (2003). Cancer-related fatigue: evolving concepts in evaluation and treatment. Cancer, 98, 1786-1801. Stone, P., Richardson, A., Ream, E., Smith, A.G., Kerr, D.J., & Kearney, N. (2000). Cancer-related fatigue: inevitable, unimportant and untreatable? Result of a multi-centre patient survey. Cancer Fatigue Forum. Annals of Oncology, 11, 971-975. Taylor, E.J. (2003). Spiritual needs of patients with cancer and family caregivers. Cancer Nursing, 26 (4), 260-266. Taylor, E.J., & Mamier, I. (2005). Spiritual care nursing: what cancer patients and family caregivers want? Journal of Advanced Nursing, 49 (3), 260-267. Tishelman, C., Degner, L.F., Rudman, A., Bertilsson, K., Bond, R., Broberger, E., & et al. (2005). Symptoms in patients with lung carcinoma: distinguishing distress from intensity. Cancer, 104 (9), 2013-2021. Van Exel , J., De Graaf, G., & Brouwer, W. (2008). Give me a break! Informal caregivers attitudes toward respite care. Health Policy, 83, 73-87. Vitaliano, P.P., Zhang, J., & Scanlan, J.M. (2003). Is caregiving hazardous to one’s physical health? A meta-analysis. Psychological Bulletin, 129 (6), 946-972. Wackerbarth, S.B., & Johnson, M.S. (2002). Essential information and support needs of family caregivers. Patient Education and Counseling, 47, 95-100. Wang, X.S., Fairclough, D.L., Liao, Z., Komaki, R., Chang, J.Y., Mobley, G..M. & et al. (2006). Longitudinal study of the relationship between chemoradiation therapy for non-small-cell lung cancer and patient symptom. Journal of Clinical Oncology, 24 (27), 4485-4491. Wang, S.Y. Tasi, C.M. Chen, B.C. Lin, C.H. & Lin, C.C. (2008). Symptom clusters and relationships to symptom interference with daily life in Taiwanese lung cancer patient. Journal of Pain Symptom Management, 35 (3), 258-266. Weitzner, M. A., Jacobsen, P. B., Wagner, J.H., Friedland, J., & Cox, C. (1999). The Caregiver Quality of Life-Cancer (CQOLC) scale: development and validation of an instrument to measure quality of life of the family caregiver of patients with cancer. Quality of Life Research, 8, 55-63. Woods, N.F., Lewis, F.M., & Ellison, E.S. (1989). Living with cancer: family experience. Cancer Nursing, 12 (1), 28-33. Yedidia, M.J. & Tiedemann, A. (2008). How do family caregivers describe their needs for professional help? The American Journal of Nursing, 108 (9 Suppl), 35-37. Yeh, L.L., Hwu, H.G., Chen, C.H., Chen, C.H. & Wu, C.C. (2008). Factors related to perceived needs of primary caregivers of patients with schizophrenia. Journal of the Formosan Medical Association, 107 (8), 644-652. Young, R.F., & Kahana, E. (1987). Specifying caregiver outcome: Gender and relationship aspects of caregiving strain. The Gerontologist, 29 (5), 660-667. | |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/42348 | - |
| dc.description.abstract | 本研究目的為探討肺癌病患主要照顧者的照護需求及其相關因素。研究設計採橫斷性、描述相關性研究法，以立意取樣針對北部某醫學中心100對肺癌患者與其主要照顧者為研究對象；而為探討照顧者照護需求是否與病人有關，本研究使用Karnofsky身體功能狀態、症狀嚴重度、醫院焦慮憂鬱量表與基本資料表來評估肺癌病患；照顧者照護需求部分則使用「支持性照護需求量表-照顧者44 (SCNS-P&C 44)」，此量表共分為七層面次量表，訊息需求、法律/經濟需求、心理/情緒需求、健康照護專業人員/健康照護需求、日常生活需求、溝通/人際關係需求與其他需求。研究結果顯示主要照顧者未滿足需求部分，前十項未滿足之需求中，以健康照護專業人員/健康照護層面需求為最多，共包含五項 (37%~50%)，二項屬於心理/情緒層面需求 (45%~58%)，二項與法律/經濟層面 (43%~52%) 有關，另三項屬於訊息需求層面 (40%~45%)。病患無職業、年齡較大、身體功能較差、焦慮程度較高、症狀較嚴重及年齡較大的女性、沒有結婚且受教育年數較少之主要照顧者有較多的照護需求。本研究有助於臨床醫護人員對於肺癌主要照顧者照護需求有更深入的了解，並提供未來臨床照護與研究方面的參考依據。 | zh_TW |
| dc.description.abstract | The purpose of the study was to identify the care needs and related factors in primary caregivers of lung cancer. A cross-sectional, correlational study was conducted. One hundred pairs of eligible patients and caregivers were recruited from the pulmonary outpatient clinics in a medical center in Taiwan by convenience sampling. A set of questionnaires was used to assess patients’ needs, including the Karnofsky’s Performance Status Index, Symptom Severity Scale (SSS), and Hospital Anxiety and Depression Scale (HADS) and Background Information Form; the caregivers’ care needs was evaluated using the Supportive Care Need Survey-Partners & Caregivers 44 (SCNS-P&C 44), the Supportive Care Need Survey-Partners & Caregivers 44 (SCNS-P&C 44) include the seven domains, information needs• health care professional/health care service needs• daily needs• coummnication / interpersonal needs• Legal/Financial Needs• psychological/emotional needs and other needs.The results indicated that : (1) primary caregivers’ reported top ten unmet needs with the five items in the “health care professional/health care service needs” domain (37%~50%), two items were in “psychological/emotional needs” domain (45%~58%), two items were in “legal/financial needs” domain (43%~52%) and three items in “information needs” domain (40%~45%). Patients without work, older age, lower performance status, higher anxiety, symptom severity, female caregivers’ with older age, unmarried and less education level that their primary caregivers had more likely care needs. In conclusion, our data provides more information about care needs by primary caregivers in lung cancer for further clinical care and related studies. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-15T01:12:27Z (GMT). No. of bitstreams: 1 ntu-98-R96426018-1.pdf: 401636 bytes, checksum: 4ef2b99bc1b1462d72cb421d632d0131 (MD5) Previous issue date: 2009 | en |
| dc.description.tableofcontents | 口試委員審定書
致謝............................................................................................................................Ⅱ 中文摘要....................................................................................................................Ⅲ 英文摘要....................................................................................................................Ⅳ 目錄............................................................................................................................Ⅴ 表目錄.......................................................................................................................Ⅵ 圖目錄.......................................................................................................................Ⅵ 第一章 緒論...........................................................................................................1 第一節 研究背景與動機.........................................................................1 第二節 研究目的.....................................................................................4. 第二章 文獻查證...................................................................................................5 第一節 肺癌.............................................................................................5 第二節 照顧者需求概念.........................................................................8 第三節 癌症照顧者需求的相關研究...................................................10 第四節 影響照顧者需求之相關因素...................................................15 第三章 研究方法.................................................................................................18 第一節 研究設計...................................................................................18 第二節 研究假設...................................................................................19 第三節 研究場所及對象.......................................................................20 第四節 研究架構...................................................................................21. 第五節 名詞解釋...................................................................................22 第六節 研究工具...................................................................................23 第七節 資料收集及資料分析...............................................................26 第八節 倫理考量...................................................................................28 第四章 研究結果.................................................................................................29 第一節 肺癌病患及主要照顧者之基本資料與疾病特徵分析...........29 第二節 肺癌病患心理狀態與症狀嚴重度狀況...................................36 第三節 主要照顧者照護需求情形.......................................................39 第四節 肺癌病患及主要照顧者之基本資料與疾病特徵與照護需 求的相關...................................................................................43 第五節 肺癌病患之症狀嚴重度與心理狀態及照顧者需求的相關.......51 第六節 照顧者照護需求預測變項...........................................................53. 第五章 討論.........................................................................................................56 第一節 肺癌病患症狀嚴重度及心理狀態程度...................................56 第二節 主要照顧者照護需求情況.......................................................58 第三節 影響主要照顧者照護需求之相關因素...................................60 第六章 結論與建議.............................................................................................63 參考文獻...................................................................................................................65 表目錄 表一 推論統計方式.......................................................................................27 表二 肺癌病患人口學特質...........................................................................31 表三 肺癌病患疾病特徵...............................................................................33 表四 照顧者人口學特徵與照顧型態...........................................................34 表五 肺癌病患心理狀態...............................................................................37 表六 肺癌病患症狀嚴重度一覽表...............................................................38 表七 肺癌照顧者照護需求得分情形...........................................................40 表八 肺癌照顧者未滿足照護需求得分情形...............................................41 表九 肺癌照顧者照護需求與病患人口學及疾病特徵之相關性...............44 表十 肺癌照顧者照護需求與人口學及照顧型態之相關性.......................48. 表十一 照顧者照護需求及肺癌病患症狀嚴重度與心理狀態之相關性分析 ...........................................................................................................52 表十二 照顧者照顧需求預測變項...............................................................55 圖目錄 圖一 研究架構...............................................................................................21 | |
| dc.language.iso | zh-TW | |
| dc.subject | 照護需求 | zh_TW |
| dc.subject | 肺癌 | zh_TW |
| dc.subject | 主要照顧者 | zh_TW |
| dc.subject | lung cancer | en |
| dc.subject | care needs | en |
| dc.subject | primary caregiver | en |
| dc.title | 肺癌病患主要照顧者照護需求及其相關因素探討 | zh_TW |
| dc.title | Care Needs and Its Correlates in Primary Caregivers of Lung Cancer Patients | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 97-2 | |
| dc.description.degree | 碩士 | |
| dc.contributor.coadvisor | 余忠仁,孫秀卿 | |
| dc.contributor.oralexamcommittee | #VALUE! | |
| dc.subject.keyword | 肺癌,主要照顧者,照護需求, | zh_TW |
| dc.subject.keyword | lung cancer,primary caregiver,care needs, | en |
| dc.relation.page | 77 | |
| dc.rights.note | 有償授權 | |
| dc.date.accepted | 2009-07-30 | |
| 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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