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Reglin, Gary; Bradley, Johnetta – College Student Journal, 2021
Problem was few African Americans in rural southwest Georgia took advantage of hospice care. Primary purpose was to determine beliefs of hospice nonphysician medical care providers relative to referring African American patients for hospice care. Secondary purpose was to identify cultural and other factors hindering some African American families…
Descriptors: African Americans, Rural Areas, Hospices (Terminal Care), Medical Services
Kritz, Gabriela W. – ProQuest LLC, 2019
Purpose: The purpose of this preliminary, pre-post, interventional project was to (1) explore the pervasiveness of compassion fatigue & (2) promote self-care activities & evaluate the effectiveness of compassion fatigue education on reducing hospice nursing staffs' compassion fatigue symptoms in a single hospice care unit. Background and…
Descriptors: Intervention, Health Services, Medical Services, Nurses
Smith, Maureen A.; Seplaki, Christopher; Biagtan, Mark; DuPreez, Amanda; Cleary, James – Gerontologist, 2008
Purpose: Although caregivers desire specific information about hospice programs, there is little descriptive information available. We characterized agencies that provide formal or informal hospice care in the United States according to four types of services considered important by caregivers: medications and treatments; rehabilitative care;…
Descriptors: Hospices (Terminal Care), Medical Services, Caregivers, Drug Therapy
Waldrop, Deborah P.; Rinfrette, Elaine S. – Death Studies, 2009
Hospice care is available for 6 months before death but the length of use varies widely, suggesting that there are different perspectives on the appropriate timing for this transition. This qualitative study explored hospice professionals' views on the appropriate timing for and communication about hospice. Ethnography of team meetings informed…
Descriptors: Hospices (Terminal Care), Allied Health Personnel, Physicians, Attitudes
Wilson, Donna M.; Birch, Stephen; Sheps, Sam; Thomas, Roger; Justice, Christopher; MacLeod, Rod – Canadian Journal on Aging, 2008
The vast majority of the 220,000 Canadians who die each year, principally of old age and progressive ill health, do not have access to specialized hospice or palliative care. Hospice and palliative care programs are unevenly distributed across Canada, with existing programs limited in capacity and services varying considerably across programs.…
Descriptors: Hospices (Terminal Care), Terminal Illness, Older Adults, Foreign Countries

Reese, Dona J.; Raymer, Mary – Social Work, 2004
In a struggle to balance fiscal realities with hospice philosophy, some hospices have attempted to cut costs by reducing social work involvement. This cross-sectional survey of 66 hospices found, however, increased social work involvement was significantly associated with lower hospice costs. Additional benefits included better team functioning,…
Descriptors: Medical Services, Costs, Hospices (Terminal Care), Social Work

Death Studies, 1993
Notes that International Work Group on Death, Dying, and Bereavement recognizes wide variation of attitudes, beliefs, and behaviors pertaining to childhood death, dying, and bereavement. Statement identifies set of assumptions which can serve as guidelines, across cultures, in care of children with terminal illness and their families. (Author/NB)
Descriptors: Bereavement, Children, Death, Foreign Countries

Miller, Pamela J.; Mike, Paula B. – Death Studies, 1995
The political and social development of the Medicare Hospice Benefit combines humanitarian and cost-saving strategies. Although it mainstreamed care of the terminally ill and provided multiple services, four major constraints of the benefit package are identified and explored. It is important that we analyze this policy before we devise new ways…
Descriptors: Death, Federal Aid, Hospices (Terminal Care), Medical Care Evaluation

Wetle, Terrie; Shield, Renee; Teno, Joan; Miller, Susan C.; Welch, Lisa – Gerontologist, 2005
Purpose: The purpose of this study is to expand knowledge regarding end-of-life care received in nursing homes through the use of narrative interviews with family members close to the decedents. Design and Methods: We conducted follow-up qualitative interviews with 54 respondents who had participated in an earlier national survey of 1,578…
Descriptors: Family Attitudes, Nursing Homes, Hospices (Terminal Care), Older Adults

Reese, Dona J.; Sontag, Mary-Ann – Health & Social Work, 2001
Despite the holistic approach inherent in the hospice philosophy, social work may be viewed as ancillary to medicine. Social work, in turn, may lack sensitivity about other professions' expertise and values and therefore be unprepared to collaborate across cultural boundaries between professions. This article outlines the barriers and proposes…
Descriptors: Cooperation, Death, Hospices (Terminal Care), Interdisciplinary Approach
Current Research Findings on End-of-Life Decision Making among Racially or Ethnically Diverse Groups

Kwak, Jung; Haley, William E. – Gerontologist, 2005
Purpose: We reviewed the research literature on racial or ethnic diversity and end-of-life decision making in order to identify key findings and provide recommendations for future research. Design and Methods: We identified 33 empirical studies in which race or ethnicity was investigated as either a variable predicting treatment preferences or…
Descriptors: Race, Values, Minority Groups, Acculturation
Van Vorst, Rebecca F.; Crane, Lori A.; Barton, Phoebe Lindsey; Kutner, Jean S.; Kallail, K. James; Westfall, John M. – Journal of Rural Health, 2006
Context: Barriers to providing optimal palliative care in rural communities are not well understood. Purpose: To identify health care personnel's perceptions of the care provided to dying patients in rural Kansas and Colorado and to identify barriers to providing optimal care. Methods: An anonymous self-administered survey was sent to health care…
Descriptors: Patients, Hospices (Terminal Care), Rural Areas, Health Personnel
Congress of the U.S., Washington, DC. House Committee on Energy and Commerce. – 1987
This document presents the text of the Congressional hearing called to discuss the provision of health care services to people with Acquired Immune Deficiency Syndrome (AIDS) outside of hospitals, including home health care, hospice care, nursing home care, personal care and counseling, and other support services for patients and their families.…
Descriptors: Acquired Immune Deficiency Syndrome, Health Insurance, Health Needs, Hearings

Parker-Oliver, Debra; Bronstein, Laura R.; Kurzejeski, Lori – Health & Social Work, 2005
Although social work participation on interdisciplinary teams is long-standing, little research has been done to examine its effectiveness. This study used the Index of Interdisciplinary Collaboration to explore relationships between selected variables and teamwork in the hospice setting. The findings indicate that hospice social workers report a…
Descriptors: Cooperation, Hospices (Terminal Care), Social Work, Medical Services

Logue, Barbara J. – Omega: Journal of Death and Dying, 1994
Examines feasibility of palliative approach for all patients, showing reasonable people may refuse even the most exemplary care for themselves or an incompetent relative. Medical realities and alleviation of pointless suffering necessitate that policymakers consider other options, including "active" euthanasia, consistent with patient…
Descriptors: Death, Euthanasia, Health Personnel, Hospices (Terminal Care)
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