參考文獻
一、英文文獻
Aranda SK and Hayman-White K(2001). Home caregivers of the person with advanced cancer. An Australian perspective. Cancer Nursing,24(4),300-7.
Blank JJ,Clark L, Longman AJ & Atwood JR.( 1989).Perceived home-care needs of cancer patients and their caregivers. Cancer Nursing,12(2),78-84.
Bridge M,Roughton DI,Lewis S, et al. Using caregivers-as-proxies to retrospectively assess and measure quality of dying of palliative care clients. Ameri J of Hospi and Pallia Care.2002,19(3):193-9
Bridge M,Roughton DI,Lewis S, et al.( 2002). Using caregivers-as-proxies to ret-rospectively assess and measure quality of dying of palliative care clients. Ameri J of Hospi and Pallia Care,19(3),193-9.
Bullinger M, Schmidt S, Petersen C, Grp D(2002). Assessing quality of life of children with chronic health conditions and disabilities: a European approach. International Journal of Rehabilitation Research , 25,197-206.
Carter PA(2000), Chang BL. Sleep and depression in cancer caregivers. Cancer Nursing , 23(6) 410-415.
Cohen SR& Mount BM(1992). Quality of life in terminal illness:defining and measuring subjective well-being in the dying. J Palliative care,8(3),40-5.
Garfinkel, L. Cancer statistics and trends. In H. Arthur, D.Fink, & G. Murphy (Eds.)(1991). American cancer textbook of clinical oncology. Atlant: The American Cancer Society.
Laizner AM,Shegda Yost LM, Barg FK et al(1993).Needs of family caregivers of persons with cancer:a review. Semin Oncol Nurs,9,114-20.
Lewis FM(1986). The impact of cancer on the family:a critical analysis of the research literature. Patient education and counseling,269-89
McMillan SC(1996). Quality of life of primary caregivers of hospice patients with cancer. Cancer Pract ,4,191-198.
McMillan SC,Mahon M(1994). The impact of hospice services on the quality of life of primary caregivers.Oncology Nursing forum, 21(7),1189-95.
Meier DE(2011). Increased access to palliative care and hospice services: opportunities to improve value in health care.Milbank Q,89(3),343-80.
Northouse LL, Wortman CB(1990). Models of Helping and Coping in Cancer Care.Patient Education and Counseling ,15, 49-64.
Northouse LL, Wortman CB. Models of Helping and Coping in Cancer Care. Patient Education and Counseling 1990; 15: 49-64
Schacter S(1990).Quality of life for families in the management of home care patients with advanced cancer.J of ferontology,45(5),181-91.
Schott-Baer D(1993). Dependent care,caregiver burden, and self-care agency of spouse caregivers. Cancer Nurs,16,230-6.
Seamark DA,Williams S,Hall M et al. (1994).Dying from cancer in community hospitals or a hospice,closest lay carers’ perceptions. Pallia Medi,8,39-44.
Seamark DA,Williams S,Hall M et al.Dying from cancer in community hospitals or a hospice,closest lay carers’ perceptions. Pallia Medi.1994,8:39-44
Toseland RW,Blanchard CG,McCallion P(1995). A problemsolving intervention for caregivers of cancer patients.Soc Sci Med,40,517-28.
Weitzner MA(2000), Haley WE,Chen H.The family caregiver of older cancer patient. Hematology/Oncology clinics of North America,14(1),269-81.
Weitzner MA,McMillan SC(1998).The caregiver quality of life index- cancer (CQQLC) scale:development and validation of an instrument to measure quality of life of the family caregiver of patients of cancer. Quality of life researc,8,55-63.
Weitzner MA,McMillan SC, Jacobsen PB(1997). Family caregiver quality of life:differences betweens curative and palliative cancer treatment settings.J of pain and symptom management,17(6),418-28.
Weitzner MA,McMillan SC, Jacobsen PB. Family caregiver quality of life:differences betweens curative and palliative cancer treatment settings.J of pain and symptom management.1999,17(6):418-28
WHO Expert Committee.Cancer pain relief and palliative care(1990). Technical report series, no 804. Geneva,World Health Organization.
Young-Graham K,Longman AJ(1987). Quality of life and persons with melanoma:preliminary model testing. Cancer Nurs,10(6),338-46.
Yulia CD, Shuchter S, Hutchin S, Strause L, Burns K, Zisook S(2000). The psy-chological and physical health of hospice caregivers. Annals of clinical psy-chiatry ,12(1),19-27.
二、中文文獻
何怡儒(2002)。癌患家屬照顧經驗中壓力之探討。南華大學生死學研究所碩士論文，嘉義市。何怡儒：癌患家屬照顧經驗中壓力之探討。南華大學生死學研究所碩士論文2002
李淑真、劉雪娥、蔡培葵、賴裕和(2003)。接受安寧住院療護期間主要照顧者生活品質的變化。安寧療護雜誌 ，8(3)， 259-269。李淑真、劉雪娥、蔡培葵、賴裕和：接受安寧住院療護期間主要照顧者生活品質的變化。安寧療護雜誌 2003;8(3) 259-269。姚建安、邱泰源、陳慶餘、吳英璋、林瑞雄(2003)。緩和醫療住院病患主要家屬照顧者的訊息需求與滿意度的研究。安寧療護，8(3)，270-282。姚建安、邱泰源、陳慶餘、吳英璋、林瑞雄：緩和醫療住院病人主要家屬照顧者的訊息需求與滿意度的研究。安寧療護2003;8(3):270-282。姚開屏(2001)。台灣簡明版世界衛生組織生活品質問卷之發展及使用手冊（第一修定版）。台灣大學世界衛生組織生活品質問卷台灣版問卷發展小組。
姚開屏(2005)。台灣版世界衛生組織生活品質問卷之發展及使用手冊。台灣大學世界衛生組織生活品質問卷台灣版發展小組。
洪淑惠(2007)。癌末病患主要家屬照顧者照顧負荷影響因素之探討。高雄醫學大學醫學研究所碩士論文，高雄市。胡文郁(1998)。淺談癌末病患之生活品質評估。安寧療護雜誌，10，3-10。胡綾真、陳美伶、陳明歧、林佳靜、林玲華(2001)。轉移性癌症病患之居家主要照顧負荷及其影響因素。長庚護理，12(4)，282-292。
范聖育(2002)。家庭功能與安寧療護主要照顧者生活品質的相關性探討。國立成功大學行為醫學研究所碩士論文，台南市。范聖育：家庭功能與安寧療護主要照顧者生活品質的相關性探討。國立成功大學行為醫學研究所碩士論文2002。
張苙雲(1998)。醫療社會學的探索（第一版）。醫療與社會。
張苙雲：醫療與社會：醫療社會學的探索（第一版）。1998
陳玉葉、陳桂敏(2007)。癌末病患居家照顧工作量及困難度與照顧壓力負荷之相關性探討。安寧療護，12(2)，143-155。陳惠津：居家癌病家屬照顧者之需要狀況及其相關因素之探討。國立陽明醫學大學社區護理研究所碩士論文1996。陳惠津：居家癌病家屬照顧者之需要狀況及其相關因素之探討。國立陽明醫學大學社區護理研究所碩士論文1996。陳麗如、邱啟潤、高金盆(2005)。居家照護病患主要照顧者人格韌性、健康狀況與生活品質相關性探討。長期照護雜誌，10(1)，53-67。
楊美玲(1999)。居家安寧療護家屬主要照顧者照顧經驗及需要之探討。台北醫學院護理學研究所碩士論文，台北市。
楊美玲：居家安寧療護家屬主要照顧者照顧經驗及需要之探討。台北醫學院護理學研究所碩士論文1999。
衛生福利部統計處：死因統計表http://www.mohw.gov.tw/cht/DOS/Statistic.aspx?f_list_no=312&fod_list_no=1601
鍾佳真：安寧療護病患主要照顧者的居家照顧需要及其相關因素之探討。國立陽明醫學大學社區護理研究所碩士論文1998。
鍾佳真：安寧療護病患主要照顧者的居家照顧需要及其相關因素之探討。國立陽明醫學大學社區護理研究所碩士論文1998。