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Journal of Psychosocial Oncology Volume 1, 1983 - Issue 1
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Cancer Patient Visitor Programs

Hospice

History and Implications of the New Legislation

Barrie R. Cassileth PhD Director, Division of Human Resources Research, University of Pennsylvania Cancer Center
&
Judy A. Donovan RN, MS Nurse Coordinator, Palliative Care Program, University of Pennsylvania
Pages 59-69 | Published online: 18 Oct 2008

Citations (9)

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Read on this site (3)

Susan D. Decker & Eva Young. (1991) Self-Perceived Needs of Primary Caregivers of Home-Hospice Clients. Journal of Community Health Nursing 8:3, pages 147-154.
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DavidF. Cella, SuzanneM. Mahon & MarileeI. Donovan. (1990) Cancer Recurrence as a Traumatic Event. Behavioral Medicine 16:1, pages 15-22.
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Lenora Finn Paradis & Wayne M. Usui. (1987) Hospice Volunteers: The Impact of Personality Characteristics on Retention and Job Performance. The Hospice Journal 3:1, pages 3-30.
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Articles from other publishers (6)

Ora Gilbar. (1999) Gender as a predictor of burden and psychological distress of elderly husbands and wives of cancer patients. Psycho-Oncology 8:4, pages 287-294.
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David M. Dush. (2019) High–Tech, Aggressive Palliative Care: In the Service of Quality of Life. Journal of Palliative Care 9:1, pages 37-41.
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Karolynn Siegel, Victoria H. Raveis, Peter Houts & Vincent Mor. (1991) Caregiver burden and unmet patient needs. Cancer 68:5, pages 1131-1140.
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Inge B. Corless. (1995) Settings for Terminal Care. OMEGA - Journal of Death and Dying 18:4, pages 319-340.
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Sandra Jacoby Klein. 1986. Issues in Supportive Care of Cancer Patients. Issues in Supportive Care of Cancer Patients 173 188 .
Lenora FinnparadisScott Cummings. (2016) Examining the caring function of hospices. American Journal of Hospice Care 2:3, pages 20-26.
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