Hospice Care
-
Subject Areas on Research
- "It Is Like Heart Failure. It Is Chronic … and It Will Kill You": A Qualitative Analysis of Burnout Among Hospice and Palliative Care Clinicians.
- A Systems Approach to Improving Care for All Bereaved Families.
- Addressing Palliative Care Clinician Burnout in Organizations: A Workforce Necessity, an Ethical Imperative.
- Adherence to Measuring What Matters Measures Using Point-of-Care Data Collection Across Diverse Clinical Settings.
- Advanced imaging and hospice use in end-of-life cancer care.
- Adverse events in hospice and palliative care: a pilot study to determine feasibility of collection and baseline rates.
- An international initiative to create a collaborative for pharmacovigilance in hospice and palliative care clinical practice.
- Antidepressant medication use in palliative care.
- Are Hospice Admission Practices Associated With Hospice Enrollment for Older African Americans and Whites?
- Are supportive care-based treatment strategies preferable to standard chemotherapy in recurrent cervical cancer?
- Association of hospice patients' income and care level with place of death.
- Barriers to Hospice Care in Trauma Patients: The Disparities in End-of-Life Care.
- Caregiver characteristics and bereavement needs: Findings from a population study.
- Caring at the end of life: do cancer caregivers differ from other caregivers?
- Characterization of Death in Neonatal Encephalopathy in the Hypothermia Era.
- Characterizing the Hospice and Palliative Care Workforce in the U.S.: Clinician Demographics and Professional Responsibilities.
- Complexities of defibrillator deactivation.
- Concerns underlying treatment preferences of advanced cancer patients with children.
- Cutaneous Metastasis of a Mucoepidermoid Carcinoma of the Pancreas: First Reported Case.
- Death service ratio: a measure of hospice utilization and cost impact.
- Delivery of Community-Based Palliative Care: Findings from a Time and Motion Study.
- Dementia assessment and management.
- Development of a health information technology-based data system in community-based hospice and palliative care.
- EMPOWER: an intervention to address barriers to pain management in hospice.
- Early supportive medication use and end-of-life care among Medicare beneficiaries with advanced breast cancer.
- Editorial: death to the fiefdoms.
- End-of-life Heart Failure Care in the United States.
- Establishing a regional, multisite database for quality improvement and service planning in community-based palliative care and hospice.
- Ethnic differences in the place of death of elderly hospice enrollees.
- Evolution in measuring the quality of dying.
- Five years' time and the next five things for the list of choosing wisely.
- Hospice education about people with AIDS as terminally ill patients: coping with a new epidemic of death.
- Hospice. Care when there is no cure.
- Hospices' preparation and practices for quality measurement.
- How Medicine Has Changed the End of Life for Patients With Cardiovascular Disease.
- In the clinic. Palliative care.
- Integrating palliative care information and hospice referral in medicaid primary care.
- Integrating the biopsychosocial model into quality measures in palliative care: a case for improving the hospice item set.
- Integration of palliative care practices into the ongoing care of children with cancer: individualized care planning and coordination.
- Is Risk-Standardized In-Hospital Stroke Mortality an Adequate Proxy for Risk-Standardized 30-Day Stroke Mortality Data? Findings From Get With The Guidelines-Stroke.
- Is a home-care network necessary to access the Medicare hospice benefit?
- Is there no place like home? Caregivers recall reasons for and experience upon transfer from home hospice to inpatient facilities.
- Measuring the net benefits of hospice and palliative care: a composite measure for multiple audiences-palliative net benefit.
- Medicare as insurance innovator: the case of hospice.
- Meeting Basic Needs: Social Supports and Services Provided by Hospice.
- Methodological Research Priorities in Palliative Care and Hospice Quality Measurement.
- NCCN Guidelines Insights: Palliative Care, Version 2.2017.
- Not published, not indexed: issues in generating and finding hospice and palliative care literature.
- Palliative and hospice care in gynecologic cancer: a review.
- Pc-facs.
- Prevalence and Predictors of Burnout Among Hospice and Palliative Care Clinicians in the U.S.
- Provision of spiritual support to patients with advanced cancer by religious communities and associations with medical care at the end of life.
- Quality Improvement Pearls for the Palliative Care and Hospice Professional.
- Race and residence: intercounty variation in black-white differences in hospice use.
- Racial differences in hospice revocation to pursue aggressive care.
- Racial differences in location before hospice enrollment and association with hospice length of stay.
- Racial differences in self-reported exposure to information about hospice care.
- Racially Associated Disparities in Hospice and Palliative Care Access: Acknowledging the Facts While Addressing the Opportunities to Improve.
- Refining a checklist for reporting patient populations and service characteristics in hospice and palliative care research.
- Repurposing Medications for Hospice/Palliative Care Symptom Control Is No Longer Sufficient: A Manifesto for Change.
- Resource Use in the Last Year of Life Among Patients Who Died With Versus of Prostate Cancer.
- Significant Morbidity and Mortality Among Hospitalized End-Stage Liver Disease Patients in Medicare.
- Standardization and Scaling of a Community-Based Palliative Care Model.
- Symptom burden of haematological malignancies as death approaches in a community palliative care service: a retrospective cohort study of a consecutive case series.
- Targeted investment improves access to hospice and palliative care.
- The Act of Hospice: Understanding a Family's Perception of Palliative Care--When You're Family.
- The Implementation of Measuring What Matters in Research and Practice: Series Commentary.
- The Quality Improvement Environment: Results of the 2016 AAHPM/HPNA Membership Needs Assessment Survey.
- Tracking Patients in Community-Based Palliative Care through the Centers for Medicare & Medicaid Services Healthcare Innovation Project.
- US Physicians Overwhelmingly Endorse Hospice as the Better Option for Most Patients at the End of Life.
- Update in Hospice and Palliative Care.
- Update in hospice and palliative care.
- Utilization of hospice and predicted mortality risk among older patients hospitalized with heart failure: findings from GWTG-HF.
- What explains racial differences in the use of advance directives and attitudes toward hospice care?
- What is different about patients with hematologic malignancies? A retrospective cohort study of cancer patients referred to a hospice research network.
- What length of hospice use maximizes reduction in medical expenditures near death in the US Medicare program?
- Where Children Die: Obstacles to Quality End-of-Life Care.
-
Keywords of People
- Curtis, Lesley H., Professor in Population Health Sciences, Medicine, General Internal Medicine
- LeBlanc, Thomas William, Associate Professor of Medicine, Duke Cancer Institute
- Webb, Jason Allen, Assistant Professor of Medicine, Medicine, General Internal Medicine