
Forum.
References
AldersonP, Goodey C. Theories of consent. BMJ 1998;317:1313-15.
Bratjman S. The impact on the family of terminal restlessness and its management. Palliative Medicine 2003;17(5):454-60.
Bridson J, Hammond C, Leach A, Chester MR. Making consent patient centred. BMJ 2003;327:1159-61
British Medical Association. Medical Ethics today. The BMA’s Handbook of ethics and law. 2 nd Ed. BMA, London 2004.
Chan KS, Sham MMK, Tse DMW, Thorsen AB. Palliative medicine in malignant respiratory diseases. In Doyle D, Hanks G, Cherny N and Calman K. Oxford Textbook of Palliative Medicine 2004. 3 rd Ed. Oxford University Press, Oxford.
Chater S, Viola R, Paterson J, Jarvis V. Palliat Med 1998;12:255-269).
Cherny NI, Portenoy RK. Sedation in the management of refractory symptoms: guidelines for evaluation and treatment. J Pall Care 1994; 10(2):31-38
Chiu TY, Hu WY, Lue BH, Cheng SY, Chen CY. Sedation for refractory symptoms of terminal cancer patients in Taiwan. J Pain Symptom Manage 2001;21:467-472
Fainsinger RL, Nunez-Olarte JM, Demoissac DM. The cultural differences in perceived value of disclosure and cognition: Spain and Canada. J Pall Care 2003;19(1):43-48
Gatellari M, Butow PN, Tattersall MHN. Sharing decisions in cancer care. Soc Sci and Med 2001;52:1865-1878
Gillon R. Philosophical medical ethics. 1985. John Wiley & Sons. Chichester UK.
General Medical Council. Seeking patients’ consent: the ethical considerations. London: GMC, 1998
Harris J. Consent and end of life decisions. J Med Ethics 2003;29:10-15.
Hawryluck LA, Harvey WRC, Lemieux-Charles L, Singer PA. Consensus guidelines on analgesia and sedation in dying intensive care unit patients. BMC Medical Ethics 2002;3:3
Lewin SA, Skea ZC, Entwistle V, Zwarenstein M, Dick J. Interventions for providers to promote a patient centred approach in clinical consultations (Cochrane Review). In: The Cochrane Library, Issue 4, 2001. Oxford: Update Software.
Marks P. The evolution of the doctrine of consent. Clin Med 2003;3:45-47.
Mayberry MK, Mayberry JF. Consent with understanding: a movement towards informed decisions. Clin Med JRCPL 2002;2:523-6.
Morita T, Inoue S, Chihara S. Sedation for symptom control in Japan: The importance of intermittent use and communication with family members. J Pain Symptom Manage 1996;12:32-38
Morita T, Tsunoda J, Inoue S, Chihara S. Do hospice clinicians sedate patients intending to hasten death? J Pall Care 1999;15(3):20-23
Morita T, Hirai K, Akechi T, Uchitomi Y. Similarity and difference among standard medical care, palliative sedation therapy and euthanasia: A multidimensional scaling analysis on physicians and the general populations’ opinions. J Pain Symptom Manage 2003:25:357-362.
Muller-Busch HC, Andres I, Jehser T. Sedation in palliative care – a critical analysis of 7 years experience. BMC Palliative Care 2003,2:2 (www.biomedcentral.com/1472-684X/2/2
Murtagh F, Thorns A. The evaluation of using an ethics history with hospice in-patients. Poster presentation, EAPC Conference, The Hague, 2003.
Quill TE, Lo B, Brock DW. Palliative options of last resort. A comparison of voluntary stopping eating and drinking, terminal sedation, physician assisted suicide and voluntary active euthanasia. JAMA 1997; 278(23):2099-2104
Randall F, Downie R. Truth-telling and consent. In Doyle D, Hanks G, Cherny N and Calman K. Oxford Textbook of Palliative Medicine 2004. 3 rd Ed. Oxford University Press, Oxford.
Say RE, Thomson R. The importance of patient preferences in treatment decisions – challenges for doctors. BMJ 2003;327:542-5).
Steinhauser KE, Christakis NA, Clipp EC, McNeilly M, McIntyre L, Tulsky JA. Factors considered important at the end of life by patients, family, physicians and other care providers. JAMA 2000;284:2476-2482
Tschann JM, Kaufman SR, Micco GP. Family involvement in end of life hospital care. J Am Geriatrics Sc 2003; 51(6):835-840.
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