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Barnes, Jonathan; Paterson-Brown, Lucy – Journal of Education and Training Studies, 2017
Introduction: Malawi is one of the world's poorest countries with very limited healthcare spending and a lack of post-graduate training for healthcare workers, including in critical illness management. Critical illness simulation courses have been shown to be an effective training tool and form a key part of training for healthcare professionals…
Descriptors: Foreign Countries, Medical Services, Patient Education, Simulation
Mullet, Etienne; Sorum, Paul C.; Teysseire, Nathalie; Nann, Stephanie; Martinez, Guadalupe Elizabeth Morales; Ahmed, Ramadan; Kamble, Shanmukh; Olivari, Cecilia; Sastre, Maria Teresa Munoz – Psicologica: International Journal of Methodology and Experimental Psychology, 2012
We present, in a synthetic way, some of the main findings from five studies that were conducted in the field of empirical bioethics, using the Functional Measurement framework. These studies were about (a) the rationing of rare treatments, (b) adolescents' abortions, (c) end-of-life decision-making regarding damaged neonates, (d) end-of-life…
Descriptors: Biology, Ethics, Decision Making, Personal Autonomy
Olokor, Christiana O. – ICHPER-SD Journal of Research, 2011
The purpose of this study was to analyze the attitudes of terminally ill patients toward death and dying. Four hospitals in Nigeria were randomly selected: University College Hospital, Ibadan; University of Benin Teaching Hospital, Benin City; the Lagos University Teaching Hospital, Lagos; and Igbinedion Specialist Hospital, Okada, Benin City.…
Descriptors: Hospitals, Terminal Illness, Interviews, Patients
Neff, John M. – Exceptional Parent, 2009
The arrival of summer signals a season of endless days of swimming, fishing, summer camps, and other outdoor activities. For children with chronic or terminal illnesses, it can be difficult to participate in many of these activities as well as challenging for parents to find summer camps that not only engage their children, but also offer the…
Descriptors: Medical Services, Recreational Activities, Summer Programs, Chronic Illness
Schmid, Bettina; Allen, Rebecca S.; Haley, Philip P.; DeCoster, Jamie – Gerontologist, 2010
Purpose: We examined race/ethnicity and cultural context within hypothetical end-of-life medical decision scenarios and its influence on patient-proxy agreement. Design and Methods: Family dyads consisting of an older adult and 1 family member, typically an adult child, responded to questions regarding the older adult's preferences for…
Descriptors: First Aid, Race, Research Methodology, Older Adults
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
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

Connelly, R. J. – Omega: Journal of Death and Dying, 1990
Presents sentiment argument, distinguishing artificial feeding from medical treatments which may be discontinued when there is little hope of recovery. Describes probable origins of feelings about food and drink and shows that such feelings cannot be transferred without distortion to the hospital world. Argues that authentic sentiment seems to…
Descriptors: Death, Diseases, Ethics, Food

Stephens, Ronald L.; Grady, Rosemary – Omega: Journal of Death and Dying, 1992
Notes that, in survey of 50 cancer patients offered living wills, 6 individuals declined to sign advance directives. Contains detailed evaluation of each of six cases. Discusses potential value of living wills in context of other, newer forms of advance directives, such as durable power of attorney for health care, and more detailed living will…
Descriptors: Cancer, Death, Decision Making, Individual Power

Farrugia, David – Counseling and Values, 1993
Explores issues related to "right to die." Makes case for counselors to assist clients and families with concerns related to refusal or withdrawal of medical treatment in cases of terminal illness or in cases where quality of life is severely impaired such as permanent comatose state. Presents historical, ethical, and legal perspectives.…
Descriptors: Counselor Role, Death, Ethics, Euthanasia

Foytack, Jane; West, Daniel J. – Omega: Journal of Death and Dying, 1994
Discusses, in context of physician-patient relationship, workable model on advance directives for physicians to use with patients along with appropriate guidelines. Examines variables involved in establishment of guidelines for use by physician in office and inpatient settings. Identifies key management and clinical factors for initiating and…
Descriptors: Death, Guidelines, Medical Services, Physician Patient Relationship

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

Whitney, Simon N.; Brown, Byron W.; Brody, Howard; Alcser, Kirsten H.; Bachman, Jerald G.; Greely, Henry T. – Journal of General Internal Medicine, 2001
Ascertained the views of physicians and physician leaders toward legalization of physician-assisted suicide. Results indicated members of AMA House of Delegates strongly oppose physician-assisted suicide, but rank-and-file physicians show no consensus either for or against its legalization. Although the debate is adversarial, most physicians are…
Descriptors: Attitude Measures, Beliefs, Bioethics, Death