Hostname: page-component-cd9895bd7-lnqnp Total loading time: 0 Render date: 2024-12-26T06:38:25.680Z Has data issue: false hasContentIssue false
  • English
  • Français

The dying patient: The right to know versus the duty to be aware

Published online by Cambridge University Press:  13 November 2008

Shlomit Pery  and
Simon Wein
Shlomit Pery*
Affiliation:
Department of Psycho-oncology, The Davidoff Center, Rabin Medical Center, Petach Tikvah, Israel
Simon Wein
Affiliation:
Pain and Palliative Care Service, The Davidoff Center, Rabin Medical Center, Petach Tikvah, Israel
*
Address correspondence and reprint requests to: Shlomit Pery, Department of Psycho-oncology, The Davidoff Center, Rabin Medical Center, Petach Tikvah, 49100, Israel. E-mail: perys@clalit.org.il
Get access Rights & Permissions [Opens in a new window]

Extract

Should terminal patients know about their impending deaths? How much should they know? How do we determine “should”?

Type
Essay/Personal Reflections
Information
Palliative & Supportive Care , Volume 6 , Issue 4 , December 2008 , pp. 397 - 401
Copyright
Copyright © Cambridge University Press 2008

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Brody, B. (1988). Life and Death Decision-Making. New York: Oxford University Press.Google Scholar
Burns, C., Broom, D.H., Smith, W., et al. (2007). Fluctuating awareness of treatment goals among patients and their caregivers: A longitudinal study of a dynamic process. Supportive Care in Cancer, 15, 187–196.CrossRefGoogle ScholarPubMed
Camus, A. (1978). The Myth of Sisyphus, Afikim Book. Tel Aviv: Am Oved.Google Scholar
Chochinov, H.M., Tataryn, D.J., Wilson, K.G., et al. (2000). Prognostic awareness and the terminally ill. Psychosomatics, 41, 500–504.CrossRefGoogle ScholarPubMed
Christakis, N.A. & Iwashyna, T.J. (2003). The health impact of health care on families: A matched control cohort study of hospice use by decedents and mortality outcomes in surviving widowed spouses. Social Science in Medicine, 57, 465–475.CrossRefGoogle Scholar
Christakis, A.N. & Lemont, E.B. (2000). Extent and determinant of error in doctors' prognosis in terminally-ill patients: Prospective cohort study. British Medical Journal, 320, 469–473.CrossRefGoogle ScholarPubMed
Emanuel, L., Bennett, K. & Richardson, V.E. (2007). The dying role. Journal of Palliative Medicine, 10, 159–168.CrossRefGoogle ScholarPubMed
Epicurus. (2007). Letter to Menoeceus, translated by Robert Drew Hicks. Retreived from ebooks.adelaide.edu.au/e/epicurus/menoeceus.Google Scholar
Fried, T.R., Bradley, E.H. & O'Leary, J. (2006). Changes in prognostic awareness among seriously ill older persons and their caregivers. Journal of Palliative Medicine, 9, 61–69.CrossRefGoogle ScholarPubMed
Glaser, B.G. & Strauss, A.L. (1965). Awareness of Dying. Chicago: Aldine.Google Scholar
Hebert, R.S., Dang, Q. & Schulz, R. (2006 a). Preparedness for death of loved one and mental health in bereaved caregivers of dementia patients: Findings from the REACH study. Journal of Palliative Medicine, 9, 683–693.CrossRefGoogle ScholarPubMed
Hebert, R.S., Prigerson, H.G. & Schulz, R. (2006 b). Preparing caregivers for death of a loved one: A theoretical framework and suggestions for future research. Journal of Palliative Medicine, 9, 1164–1171.CrossRefGoogle Scholar
John, W. & Riley, J.R. (1983). Dying and the meaning of death: Sociological inquiries. Annual Review of Sociology, 9, 191–216.Google Scholar
Kubler-Ross, E. (1969). On Death and Dying. London: Collier-Macmillan Ltd.Google Scholar
Lamont, E.B. & Christakis, N.A. (2001). Prognostic disclosure to patients with cancer near the end of life. Annals of Internal Medicine, 134, 1096–1105.CrossRefGoogle ScholarPubMed
Parsons, T. & Renee, C.F. (1952). Illness, therapy and the modern urban American family. Journal of Social Issues, 14, 31–44.CrossRefGoogle Scholar
Patient Rights Act. 5756 Sefer HaChukkim: 327, 1996.Google Scholar
Ray, A., Block, S.D. & Friedlander, R.J. (2006). Peaceful awareness in patients with advanced cancer. Journal of Palliative Medicine, 9, 1359–1368.CrossRefGoogle ScholarPubMed
Spinoza, B. (2003). Ethics. Tel Aviv: Hakibbutz Hameuchad.Google Scholar
Steinberg, A. & Sprung, C.L. (2006). The dying patient: New Israeli legislation. Intensive Care Medicine, 32, 1234–1237.CrossRefGoogle ScholarPubMed
Tong, R. (1998). The ethics of care: A feminist virtue of care for healthcare practitioners. Journal of Medicine and Philosophy, 23, 131–152.CrossRefGoogle Scholar
Weeks, J.C., Cook, E.F., O'Day, S.J., et al. (1998). Relationship between cancer patients' predictions of prognosis and their treatment preferences. JAMA, 279, 1709–1714.CrossRefGoogle ScholarPubMed
Weisman, A. (1972). On Dying and Denying. New York: Behavioral Publications.Google Scholar
Weisman, A. (1989). Denial, coping and cancer. In Denial: A Clarification of Concepts and Research, Edelstein, E.L., Nathanson, D.L. & Stone, A.M. (eds.). New York: Plenum Press.Google Scholar
Wenger, N.S., Golan, O., Shalev, C., et al. (2002). Hospital ethics committees in Israel: Structure, function and heterogeneity in the setting of statutory ethics committees. Journal of Medical Ethics, 28, 177–182.CrossRefGoogle ScholarPubMed
Zimmermann, C. (2004). Denial of impending death: A discourse analysis of the palliative care literature. Social Science & Medicine, 59, 1769–1780.CrossRefGoogle Scholar
Zimmermann, C. (2007). Death denial: Obstacle or instrument for palliative care? An analysis of clinical literature. Sociology of Health & Illness, 29, 297–314.CrossRefGoogle ScholarPubMed