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Showing 76 to 90 of 96 results Save | Export
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Welch, Lisa C.; Miller, Susan C.; Martin, Edward W.; Nanda, Aman – Gerontologist, 2008
Purpose: Given concerns about end-of-life care for many nursing home (NH) residents, this study sought to understand factors influencing hospice referral or nonreferral as well as timing of referral. Design and Methods: We conducted semistructured interviews with personnel from seven participating NHs and two hospices. We interviewed NH directors…
Descriptors: Nurses, Nursing Homes, Referral, Hospices (Terminal Care)
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Temkin-Greener, Helena; Zheng, Nan; Norton, Sally A.; Quill, Timothy; Ladwig, Susan; Veazie, Peter – Gerontologist, 2009
Purpose: The objectives of this study were to develop measures of end-of-life (EOL) care processes in nursing homes and to validate the instrument for measuring them. Design and Methods: A survey of directors of nursing was conducted in 608 eligible nursing homes in New York State. Responses were obtained from 313 (51.5% response rate) facilities.…
Descriptors: Nurses, Construct Validity, Nursing, Quality Control
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Stein, Gary L.; Sherman, Patricia A.; Bullock, Karen – Educational Gerontology, 2009
An educational program was developed to train practitioners to provide care for patients and families that are responsive to cultural concerns. The aim was to increase knowledge and improve attitudes toward providing culturally proficient and culturally sensitive care for patients and families facing life-threatening illnesses. The program…
Descriptors: Nursing Education, Patients, Program Effectiveness, Program Evaluation
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Csikai, Ellen L.; Herrin, Charlotte; Tang, Maggie; Church, Wesley T., II – Child Welfare, 2008
A mailed survey of child welfare workers in one southern state assessed various aspects of encounters with end-of-life situations in practice. Findings revealed that child deaths, children with life-threatening or life-limiting illnesses, and parental deaths were most commonly encountered and that coworkers were relied on for support. Many had no…
Descriptors: Child Abuse, Child Welfare, Welfare Services, Caseworkers
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Winter, Laraine; Parker, Barbara; Schneider, Melissa – Death Studies, 2007
Deciding for or against a life-prolonging treatment represents a choice between prolonged life and death. When the death alternative is not described, individuals must supply their own assumptions. How do people imagine the experience of dying? The authors asked 40 elderly people open-ended questions about dying without 4 common life-prolonging…
Descriptors: Psychological Patterns, Patients, Terminal Illness, Death
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Munn, Jean C.; Dobbs, Debra; Meier, Andrea; Williams, Christianna S.; Biola, Holly; Zimmerman, Sheryl – Gerontologist, 2008
Purpose: We designed this study to examine the end-of-life (EOL) experience in long-term care (LTC) based on input from key stakeholders. Design and Methods: The study consisted of 10 homogeneous focus groups drawn from a purposive sample of LTC residents (2 groups; total n = 11), family caregivers (2 groups; total n = 19), paraprofessional staff…
Descriptors: Grounded Theory, Proximity, Residential Care, Hospices (Terminal Care)
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Keranen, Lisa – Quarterly Journal of Speech, 2007
"Code status" is a prominent feature of end-of-life discussions in U.S. hospitals. This essay analyzes how the rhetoric of code status articulates the terms of end-of-life decision-making in one hospital's "Patient" Preferences Worksheet. The Worksheet signifies the abandonment of the technological fix as the preferred…
Descriptors: Worksheets, Rhetoric, Patients, Personal Autonomy
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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
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Dewar, Belinda; Sharp, Cathy – Educational Action Research, 2006
This article discusses the use of action learning as a structured and deliberate learning process to support practitioners to implement change in an action research project. It discusses both action learning and action research before describing the context of the study. The article then goes on to discuss how the process of action learning…
Descriptors: Action Research, Experiential Learning, Nursing, Terminal Illness
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Washington, Karla T.; Bickel-Swenson, Denise; Stephens, Nathan – Health & Social Work, 2008
The present review was undertaken to explore recent evidence in the professional literature pertaining to use of hospice services by African Americans. The article addresses the research methods that have been used to study African American hospice use, obstacles to African American participation in hospice that have been identified, and…
Descriptors: Hospices (Terminal Care), African Americans, African American Community, Research Methodology
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Waldrop, Deborah P. – Health & Social Work, 2007
Caregivers experience multiple losses during the downhill trajectory of a loved one's terminal illness. Using mixed methods, this two-stage study explored caregiver grief during a terminal illness and after the care recipient's death. Caregiver grief was a state of heightened responsiveness during end-stage care: anxiety, hostility, depression,…
Descriptors: Social Environment, Caregivers, Terminal Illness, Sleep
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Friedman, Sandra L.; Choueiri, Roula; Gilmore, Dana – Journal of Policy and Practice in Intellectual Disabilities, 2008
Staff carers in pediatric skilled nursing facilities (PSNF) deal directly with dying residents, and are on the forefront of communication with families. These providers have expressed misunderstandings regarding the meaning of resuscitation status and redirection of care. This descriptive study evaluated perceptions and understanding of end of…
Descriptors: Developmental Disabilities, Death, Patients, Health Facilities
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Black, Kathy – Death Studies, 2007
The study surveyed 135 health care professionals (74 nurses, 32 physicians, and 29 social workers) to examine their personal death attitudes and experiences in relation to their reported advance directive communication practice behavior. Negative correlations were found between collaborating with other health care professionals regarding the…
Descriptors: Physicians, Terminal Illness, Social Work, Health Services
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Olden, Megan; Rosenfeld, Barry; Pessin, Hayley; Breitbart, William – Assessment, 2009
Depression at the end of life is a common mental health issue with serious implications for quality of life and decision making. This study investigated the reliability and validity of one of the most frequently used measures of depression, the Hamilton Depression Rating Scale (HAM-D) in 422 patients with terminal cancer admitted to a palliative…
Descriptors: Quality of Life, Validity, Suicide, Rating Scales
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Bigelow, Terry Patrick; Ried, C. A. – English Journal, 2006
The first part of this article recounts the experiences of a language arts teacher, Terry Patrick Bigelow, and his former student, Cynthia (Noyes) Ried, who suffers from Fahr's Syndrome, a neurodegenerative congenital disease that forms calcium deposits deep inside the brain. It is irreversible, inoperable, and incurable. In the first part of the…
Descriptors: Poetry, Middle Schools, Middle School Teachers, Language Arts
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