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Oregon hospice nurses and social workers' assessment of physician progress in palliative care over the past 5 years

Published online by Cambridge University Press:  26 February 2004

ELIZABETH R. GOY
Affiliation:
Department of Veterans Affairs, Portland, Oregon Department of Psychiatry, Oregon Health & Science University, Portland, Oregon
ANN JACKSON
Affiliation:
The Oregon Hospice Association, Portland, Oregon
THERESA A. HARVATH
Affiliation:
The School of Nursing, Oregon Health & Science University, Portland, Oregon
LOIS L. MILLER
Affiliation:
The School of Nursing, Oregon Health & Science University, Portland, Oregon
MOLLY A. DELORIT
Affiliation:
Department of Veterans Affairs, Portland, Oregon
LINDA GANZINI
Affiliation:
Department of Veterans Affairs, Portland, Oregon Department of Psychiatry, Oregon Health & Science University, Portland, Oregon

Abstract

Background: The 1997 enactment of the Oregon Death with Dignity Act intensified interest in improving physician education and skills in caring for patients at the end of life.

Objective: To obtain hospice nurse and social workers' collateral ratings of efforts made by Oregon physicians to improve their palliative care skills over the previous 5 years.

Design: A descriptive survey of nurses and social workers from all 50 Oregon outpatient hospice agencies.

Measurement and Results: Oregon hospice nurse (N = 185) and social worker (N = 52) respondents, who had worked in hospice for at least 5 years, rated changes they observed over the past 5 years in physicians' approach to caring for their hospice clients. Six characteristics, including willingness to refer patients to hospice, willingness to prescribe sufficient pain medications, knowledge about using pain medications in hospice patients, interest in caring for hospice patients, competence in caring for hospice patients, and fearfulness of prescribing sufficient opioid medications were evaluated. Positive changes were endorsed by the majority of respondents on all but the scale measuring fearfulness of prescribing opioid medications; on the latter, 47% of nurses rated doctors as less fearful, whereas 53% rated them as about the same or more fearful than they were 5 years earlier.

Conclusions: Most respondents rated Oregon physicians as showing improvements in knowledge and willingness to refer and care for hospice patients.

Type
Research Article
Copyright
© 2003 Cambridge University Press

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References

REFERENCES

Drane, J.F. (1995). Physician assisted suicide & voluntary active euthanasia: Social ethics and the role of hospice. The American Journal of Hospice & Palliative Care, 12, 311.Google Scholar
Faber-Langendoen, K. (1998). Death by request: Assisted suicide and the oncologist. Cancer, 82, 3541.Google Scholar
Foley, K.M. (1997). Competent care for the dying instead of physician-assisted suicide. The New England Journal of Medicine, 336, 5458.Google Scholar
Ganzini, L., Harvath, T.A., Jackson, & A., et al. (2002). Experiences of Oregon nurses and social workers with hospice patients who requested assistance with suicide. New England Journal of Medicine, 347, 582588.Google Scholar
Ganzini, L., Nelson, H.D., Lee, & M.A., et al. (2001). Oregon physicians' attitudes about and experiences with end-of-life care since passage of the Oregon Death with Dignity Act. Journal of the American Medical Association, 285, 23632369.CrossRefGoogle Scholar
Ganzini, L., Nelson, H.D., Schmidt, & T.A., et al. (2000). Physicians' experiences with the Oregon Death with Dignity Act. New England Journal of Medicine, 342, 557563.Google Scholar
Hendin, H., Foley, K., & White, M. (1998). Physician-assisted suicide: Reflections on Oregon's first case. Issues in Law and Medicine, 14, 243270.Google Scholar
Last Acts. (2002). Means to a better end: A report on dying in America today. www.lastacts.org/files/misc/meansfull.pdf. Washington, D.C.
Lee, M.A. & Tolle, S.W. (1996). Oregon's assisted suicide vote: The silver lining. Annals of Internal Medicine, 124, 267269.Google Scholar
Sobel, R.M. & Layton, A.J. (1997). Physician assisted suicide: Compassionate care or brave new world? Archives of Internal Medicine, 157, 16381640.Google Scholar
Tolle, S.W. & Tilden, V.P. (2002). Changing end-of-life planning: The Oregon experience. Journal of Palliative Medicine, 5, 311317.Google Scholar
Tolle, S.W., Tilden, V.P., Rosenfeld, & A.G., et al. (2000). Family reports of barriers to optimal care of the dying. Nurse Researcher, 49, 310317.Google Scholar