The needs of terminally ill cancer patients versus those of caregivers for information regarding prognosis and end‐of‐life issues
暂无分享,去创建一个
Phyllis N Butow | P. Butow | M. Tattersall | J. Clayton | Martin H N Tattersall | Josephine M Clayton
[1] I. Maddocks. Palliative care in the 21st century , 2003, Medical Journal of Australia.
[2] D. Schrijvers. Oxford Textbook of Palliative Medicine, 3rd edition , 2004 .
[3] Tringali Ca. The needs of family members of cancer patients. , 1986 .
[4] P. Strang,et al. Receiving Bad News: Experiences of Family Members , 2001, Journal of palliative care.
[5] P. Butow,et al. Attitudes and information needs of Chinese migrant cancer patients and their relatives. , 1999, Australian and New Zealand journal of medicine.
[6] P. Butow,et al. Communicating prognosis to patients with metastatic disease: what do they really want to know? , 2002, Supportive Care in Cancer.
[7] P. Butow,et al. Communicating in a multicultural society II: Greek community attitudes towards cancer in Australia , 2002, Internal medicine journal.
[8] P Maguire,et al. Communicate with cancer patients: 2. Handling uncertainty, collusion, and denial. , 1988, BMJ.
[9] P. Butow,et al. The dynamics of change: cancer patients' preferences for information, involvement and support. , 1997, Annals of oncology : official journal of the European Society for Medical Oncology.
[10] M. Fitch. How Much Should I Say to Whom? , 1994, Journal of palliative care.
[11] N. Britten,et al. Respecting the autonomy of cancer patients when talking with their families: qualitative analysis of semistructured interviews with patients , 1996, BMJ.
[12] N. Christakis,et al. The health impact of health care on families: a matched cohort study of hospice use by decedents and mortality outcomes in surviving, widowed spouses. , 2003, Social science & medicine.
[13] W H Isbister,et al. Qualitative research in health care , 2000, BMJ : British Medical Journal.
[14] G. Freyer,et al. Quality of final care for terminal cancer patients in a comprehensive cancer centre from the point of view of patients' families , 1996, Supportive Care in Cancer.
[15] S. O’Keeffe,et al. Telling the truth about cancer: views of elderly patients and their relatives. , 2000, Irish medical journal.
[16] D. Parker,et al. Communication and Information Needs of Care-Givers of Adult Family Members at Diagnosis and during Treatment of Terminal Cancer , 2000 .
[17] K. White,et al. Empowerment through information: supporting rural families of oncology patients in palliative care. , 2000, The Australian journal of rural health.
[18] C. Tringali. The needs of family members of cancer patients. , 1986, Oncology nursing forum.
[19] E. Bruera,et al. Ethical decision-making on communication in palliative cancer care: a personalist approach , 2001, Supportive Care in Cancer.
[20] B. Freedman. Offering truth. One ethical approach to the uninformed cancer patient. , 1993, Archives of internal medicine.
[21] J. Hansford,et al. Death from cancer at home: the carers' perspective. , 1993, BMJ.
[22] K. Hess,et al. Revisiting the Truth-Telling Debate: A Study of Disclosure Practices at a Major Cancer Center , 2000, The Journal of Clinical Ethics.
[23] C. Newell. Qualitative Research Methods: A Health Focus , 2000 .