Family perspectives on end-of-life care at the last place of care.

By J. Teno, B. Clarridge, Virginia Casey, Lisa C. Welch, T. Wetle, R. Shield, V. Mor. Journal of the American Medical Association (JAMA), 2004

1,535 citations recorded by the source corpus.

Subfields: General Health Professions, Public Health, Environmental and Occupational Health, Radiological and Ultrasound Technology

View Paper: https://www.semanticscholar.org/paper/928ed0c4bddd77db687a1d882158bcc7ba746171

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Citations in the corpus

Associations between end-of-life discussions, patient mental health, medical care near death, and caregiver bereavement adjustment (2008, neutral): “The bereavement literature has begun to explore the associations between patients’ place of death, the receipt of hospice care, and caregivers’ subsequent risk for psychiatric disorders.(17,39,40) Recent studies have shown that communication interventions in the intensive care unit can reduce psycho”
Cost savings associated with US hospital palliative care consultation programs. (2008, background): “Hospital palliative care consultation programs have been associated with reductions in symptoms and higher family satisfaction with overall care, and greater emotional support as compared with usual care.(2,6,28,29) Although others have postulated that palliative care programs could substantially re”
Change in End-of-Life Care for Medicare Beneficiaries (2013, background): “One study found poorer quality of care in the institutional setting compared with care at home, especially with hospice services.(7) The place of care and site of”
Delivering High-Quality Cancer Care: Charting a New Course for a System in Crisis (2014, background): “The benefits of hospice care have been well documented in terms of improved quality of life, reductions in symptom distress, better outcomes for family caregivers, and patient and family satisfaction with care (Black et al., 2011; Shepperd et al., 2011; Teno et al., 2004; Wright et al., 2010).”
RELIEVING PAIN IN AMERICA: A BLUEPRINT FOR TRANSFORMING PREVENTION, CARE, EDUCATION, AND RESEARCH (2012, background): “Surveys of family members of people who have recently died find a wide range of satisfaction with pain management, associated with the place of care (Teno et al., 2004).”
Heterogeneity and changes in preferences for dying at home: a systematic review (2013, background): “Debates about the institutionalization of death and the fact that most people die in hospital have happened within and between countries since the beginning of the hospice movement [1-3].”
Evidence for Improving Palliative Care at the End of Life A Systematic Review (2008, background): “One national survey defined whether patients, caregivers, and providers have similar concerns (15), and an afterdeath survey evaluated whether health care achieves these ends (20).”
Place of death: correlations with quality of life of patients with cancer and predictors of bereaved caregivers' mental health. (2010, background): “In a retrospective, crosssectional study of bereaved family members, patients who died at home with hospice services had fewer unmet needs at the EOL.14 Others have questioned the importance of dying at home, suggesting that physicians may romanticize the experience.45 This study provides evidence t”