行政院衛生署(2012) •中華民國一百年台灣地區死因統計結果摘要•摘自http://www.doh.gov.tw/statistic/data/死因摘要/100年/97.htm
行政院衛生署(2000).安寧療護疼痛處置參考指引。
史麗珠、李絳桃、徐亞瑛、高淑芬、徐麗華、陳美伶 (2000).護理研究法.台北:桂冠。
李淑婷、謝臥龍、邱啟潤(2001).衛生所護理師角色功能之探討--德爾菲研究.護理研究9(3),269-278。林玉娟(1997).癌症疼痛評估.護理新象7(4) ,753-773。林玲華、陳景彦、劉嘉逸、陳美伶(2002).癌症住院病人憂鬱狀態的盛行率及預測因素.台灣醫學6(4) ,535-545。
邱浩政 (2003).量化研究及統計分析.台北:五南。
邱淑芬、蔡欣玲(1996).德爾菲預測術-一種專家預測的護理研究方法.護理研究4(1),92-98。徐麗琴、林佳靜、賴裕和、陳美伶(2002).腫瘤護理人員對癌痛之評估及處置與相關因素探討.新台北護理期刊4(2),29-38。梁淑媛、林佳靜、陳品玲、劉淑娟(2000).癌症病人及其家屬對癌痛及其影響感受之比較.新臺北護理期刊2(2) ,17-28。高美玲、葉美玲 (1999).結構方程式的應用—驗證性的因素分析.護理研究7(6),594-606。陳佩英、史麗珠、王正旭、賴裕和、張獻崑、陳美伶(1999).疼痛對癌症病人焦慮與憂鬱之影響.台灣醫學3(4),373-382。黃安年、孫維仁、胡新實、簡志誠、洪至仁、葉宏軒、關暟麗、梁子安(2007).末期疾病疼痛治療學.新文京開發。
曾翠華、林佳靜 (2008).癌症疼痛.護理雜誌 55(2),16-21。蔡琇文、賴裕和、陳美伶、陳主智(2000).癌症疼痛生理感覺特質與疾病不確定感之探討.護理研究8(1),59-70。蔡麗雲、顧乃平、張澤芸、賴裕和 (2001).癌痛病人焦慮憂鬱及其相關因素之探討.新台北護理期刊3(1),23-33。盧皆成(1996) .研究工具之信度與效度於李選編著.護理研究與應用(273-288) .台北.華杏。
盧美秀、林佳靜、林秋芬、廖美南、張丹蓉(1999).發展專科護理師角色之可行性--德爾菲研究.護理研究7(4),347-362。謝臥龍(1997).優良國中教師特質之德爾菲分析.教育研究資訊5(3),14-28。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。Bonica, J. J. (1985). Treatment of cancer pain: Current status and further need. In H. L. Filds, R. Dubner, & R. Cervero (Eds.), Proceedings of the Fourth World Congress on Pain (pp.589-616.) New York: Raven Press.
Brown, C. G., McGuire, D. B., Beck, S. L., Peterson, D. E., & Mooney, K. H. (2007). Visual graphical analysis-A technique to investigate symptoms trajectories over time. Nursing Research, 56(3), 195-201.
Bryman, A., & Cramer, D. (1997). Quantitative data Analysis with SPSS for Windows. London: Routledge.
Byren, B. M. (1994) Structural equation modeling with EQS and EQS/Windows. Newbury Parek, CA: Sage.
Chiu, T. Y. (1997). Pain control in terminal cancer patients. Formosan Journal of Medicine, 1(3), 198-208.
Closs, S. J., & Briggs, M. (2002). Patients’ verbal descriptions of pain and discomfort following orthopedics surgery. International Journal of Nuring Studies, 39(3),563-572.
DeVellis, R. F., (1991). Scale development: Theory and applications. Newbury Park, CA: Sage.
Elliott, B. A., Elliott, T. E., Murray, D. M., Braun, B. L., & Johnsone, K. M. (1996). Patient and family members: The role of knowledge and attitudes in cancer pain. Journal of Pain and Symptom Management, 12(4), 209-220.
Escalante, A., Lichtenstein, M. J., Rios, N., & Hazuda, H. P. (1996). Measuring chronic rheumatic pain in Mexican americans: cross-cultural adaptation of the McGill Pain Questionnaire. Journal Clinical Epidemiol ,49(12), 1389-1399.
Ger, L. P., Ho, S.T., Wong, J. J., & Cherng, C. H. (1998). The prevalence and severity of cancer pain: A study of newly-diagnosed cancer patients in Taiwan. Journal of Pain and Symptom Management, 15(2), 285-259.
Hansen, G. R., & Streltzer, J. (2005). The psychology of pain. Emergency Medicine Clinics of North America. 23, 339-348.
Hasegawa, M., Hattori, S., Ishizaki, K., Suzuki, S., & Goto, F. (1996). The McGill Pain Questionnaire, Japanese version, reconsidered: Confirming the reliability and validity. Pain Research Management 1(4), 233-237.
Hasson, F., Keeney, S., & McKenna, H. (2000). Research guidelines for the Delphi survey technique. Journal of Advanced Nursing, 32(4), 1008-1015.
Holmes, S., & Eburn, E. (1989). Patients and nurses’ perceptions of symptom distress in cancer. Journal of Advanced Nursing, 14(2), 840-846.
Jensen, M., P. (2003). The Validity and Reliability of Pain Measures in Adults With Cancer. The Journal of Pain, 2(1), 2-21.
Joreskog, K., & Sorbom, D. (1993). LISREL 8: Structural equation modeling with the SIMPLIS common language. Hillsdale, NJ:Lawrence Erlbaum Associates Publlishers.
Klepac, R. K., Dowling, J., & Hauge, G. (1981). Sensivity of the McGill pain questionnaire to intensity and quality of laboratory pain. Pain, 10(2), 199-207.
Madison, J. L., & Wilkie, D. J. (1995). Family members’ perceptions of cancer pain. Nursing Clinics of North America, 30(4), 625-645.
McMillan, S. C., & Moody, L. E. (2003). Hospice patient and caregiver congruence in reporting patients’ symptoms intensity. Cancer Nursing, 26(2), 113-118.
Melazck, R. (1975). The McGill Pain Questionnaire: Major properties and scoring methods. Pain, 1, 277-299.
Miaskowski, C., Zimmer, E. F., Barrett, K. M., Dibble, S. L., & Wallhagen, M. (1997). Differences in patients’ and family caregivers’ perceptions of the pain experience influence patient and caregiver outcomes. Pain, 72, 217-226.
Mystakidou, K., Parpa, E., Tsilika, E., Kalaidopoulou, O., Georgaki, S., Galanos, A., & Vlahos, L. (2002). Greek McGill pain questionnaire: Validation and utility in cancer patients. Journal of Pain and Symptoms Management, 24(4), 379-387.
Oksuz, E., Malhan, S., & Tulunay, F. C., (2000). Turkish McGill Pain Questionnaire: Reliability and validation.
Turk, D, C.& Melzack, R., (1992). Handbook of pain assessment. Guilford press. New York: London.
Vallerand, A. H., Templin, T., Hasenau, S. M., & Doucet, C. R. (2007). Factors that affect functional status in patients with cancer-related pain. Pain, 132(3), 82-90.
Vanderah, T. W (2007). Pathophysiology of pain. Medical Clinics of North Americ, 91(1), 1-12.