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Subject Areas on Research
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"It Is Like Heart Failure. It Is Chronic … and It Will Kill You": A Qualitative Analysis of Burnout Among Hospice and Palliative Care Clinicians.
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A Cohort Study of Patient-Reported Outcomes and Healthcare Utilization in Acute Myeloid Leukemia Patients Receiving Active Cancer Therapy in the Last Six Months of Life.
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A Review of Race and Ethnicity in Hospice and Palliative Medicine Research: Representation Matters.
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A Systems Approach to Improving Care for All Bereaved Families.
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A prospective cohort study assessing aggressive interventions at the end-of-life among patients with solid metastatic cancer.
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Accountable and Transparent Palliative Quality Measures Will Improve Care.
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Addressing Palliative Care Clinician Burnout in Organizations: A Workforce Necessity, an Ethical Imperative.
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Adherence to Measuring What Matters Measures Using Point-of-Care Data Collection Across Diverse Clinical Settings.
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Advance Care Planning Claims and Health Care Utilization Among Seriously Ill Patients Near the End of Life.
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Advance directives and end-of-life care preferences among adults in Wuhan, China: a cross-sectional study.
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Advanced imaging and hospice use in end-of-life cancer care.
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African Americans With Advanced Heart Failure Are More Likely to Die in a Health Care Facility Than at Home or in Hospice: An Analysis From the PAL-HF Trial.
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Amyotrophic lateral sclerosis care and research in the United States during the COVID-19 pandemic: Challenges and opportunities.
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Antidepressant medication use in palliative care.
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Are Hospice Admission Practices Associated With Hospice Enrollment for Older African Americans and Whites?
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Are Trends in Hospitalization Prior to Hospice Use Associated With Hospice Episode Characteristics?
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Are supportive care-based treatment strategies preferable to standard chemotherapy in recurrent cervical cancer?
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Association Between Delivery System Structure and Intensity of End-of-Life Cancer Care.
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Association of hospice patients' income and care level with place of death.
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Barriers to Hospice Care in Trauma Patients: The Disparities in End-of-Life Care.
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Better Together: The Palliative Care Research Cooperative Group as a Model for Increasing Equity in the Science of Hospice and Palliative Care.
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Characterization of Death in Infants With Neonatal Seizures.
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Characterization of Death in Neonatal Encephalopathy in the Hypothermia Era.
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Characterizing the Hospice and Palliative Care Workforce in the U.S.: Clinician Demographics and Professional Responsibilities.
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Complexities of defibrillator deactivation.
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Concerns underlying treatment preferences of advanced cancer patients with children.
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Continuing Non-Invasive Ventilation During Amyotrophic Lateral Sclerosis-Related Hospice Care Is Medically, Administratively, and Financially Feasible.
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Cross Country Comparison of Expert Assessments of the Quality of Death and Dying 2021.
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Cultivating Cultural Competence: How Are Hospice Staff Being Educated to Engage Racially and Ethnically Diverse Patients?
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Cutaneous Metastasis of a Mucoepidermoid Carcinoma of the Pancreas: First Reported Case.
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Death service ratio: a measure of hospice utilization and cost impact.
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Delivery of Community-Based Palliative Care: Findings from a Time and Motion Study.
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Dementia assessment and management.
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Depression and Health Care Utilization at End of Life Among Older Adults With Advanced Non-Small-Cell Lung Cancer.
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Developing the evidence base for palliative care: formation of the Palliative Care Research Cooperative and its first trial.
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Differences Between For-profit and Non-profit Hospice Agencies in the US Medicare Population.
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Disparities in Asians' Hospice Utilization and Location of Death.
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Do Live Discharge Rates Increase as Hospices Approach Their Medicare Aggregate Payment Caps?
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EMPOWER: an intervention to address barriers to pain management in hospice.
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Early supportive medication use and end-of-life care among Medicare beneficiaries with advanced breast cancer.
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End-of-life Heart Failure Care in the United States.
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End-of-life care quality outcomes among Medicare beneficiaries with hematologic malignancies.
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Enhancing awareness of hospice through physician assisted living: public health perspectives.
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Establishing a regional, multisite database for quality improvement and service planning in community-based palliative care and hospice.
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Ethnic differences in the place of death of elderly hospice enrollees.
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Evaluating the Contribution of Patient-Provider Communication and Cancer Diagnosis to Racial Disparities in End-of-Life Care Among Medicare Beneficiaries.
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Evaluating the Feasibility and Acceptability of a Telehealth Program in a Rural Palliative Care Population: TapCloud for Palliative Care.
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Evolution in measuring the quality of dying.
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Factors Associated with Health Care Utilization at the End of Life for Patients with Acute Myeloid Leukemia.
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Findings of Sequential Pilot Trials of Aliviado Dementia Care to Inform an Embedded Pragmatic Clinical Trial.
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Hospice Care Preferences and Its Associated Factors among Community-Dwelling Residents in China.
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Hospice Care for Heart Failure: Challenges Faced by Hospice Staff in a Predominantly Rural Setting.
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Hospice Employees' Perceptions of Their Work Environment: A Focus Group Perspective.
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Hospice Use Among Patients With Cancer: Trends, Barriers, and Future Directions.
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Hospice education about people with AIDS as terminally ill patients: coping with a new epidemic of death.
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Hospice. Care when there is no cure.
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How Medicine Has Changed the End of Life for Patients With Cardiovascular Disease.
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Identifying Core Domains to Assess the "Quality of Death": A Scoping Review.
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Identifying high-risk surgical patients: A study of older adults whose code status changed to Do-Not-Resuscitate.
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Impact of Early Palliative Care on End-of-Life Outcomes in Hematologic Malignancies.
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Impact of a Formal Advance Care Planning Program on End-of-Life Care for Patients With Heart Failure: Results From a Randomized Controlled Trial.
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In the clinic. Palliative care.
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Incorporating palliative radiotherapy education into hospice and palliative medicine fellowship training: a feasibility study.
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Information Framing Reduces Initial Negative Attitudes in Cancer Patients' Decisions About Hospice Care.
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Instability in End-of-Life Care Preference Among Heart Failure Patients: Secondary Analysis of a Randomized Controlled Trial in Singapore.
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Integrating palliative care information and hospice referral in medicaid primary care.
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Integrating the biopsychosocial model into quality measures in palliative care: a case for improving the hospice item set.
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Introduction to a New Special Series for the Journal of Pain and Symptom Management-Science in Action: Evidence and Opportunities for Palliative Care Across Diverse Populations and Care Settings.
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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.
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Is a home-care network necessary to access the Medicare hospice benefit?
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Is there no place like home? Caregivers recall reasons for and experience upon transfer from home hospice to inpatient facilities.
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It Is Time to Discuss Dying.
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Letter to the Editor Regarding "Prevalence and Predictors of Burnout Among Hospice and Palliative Care Professionals".
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Maintaining the Momentum of Measuring What Matters: Overcoming Hurdles To Develop Electronic Clinical Quality Measures.
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Medicare Shared Savings ACOs and Hospice Care for Ischemic Stroke Patients.
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Medicare as insurance innovator: the case of hospice.
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Meeting Basic Needs: Social Supports and Services Provided by Hospice.
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Methodological Research Priorities in Palliative Care and Hospice Quality Measurement.
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Multidimensional Pain Inventory-Screening Chinese version (MPI-sC): psychometric testing in terminal cancer patients in Taiwan.
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NCCN Guidelines Insights: Palliative Care, Version 2.2017.
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National Trends in End-of-Life Care for Veterans With Advanced Cancer in the Veterans Health Administration: 2009 to 2016.
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National Trends in Hospice Facility Deaths in the United States, 2003-2017.
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Palliative and hospice care in gynecologic cancer: a review.
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Physician Decision-Making in the Setting of Advanced Illness: An Examination of Patient Disposition and Physician Religiousness.
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Policy Changes Key To Promoting Sustainability And Growth Of The Specialty Palliative Care Workforce.
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Predicting Length of Hospice Stay: An Application of Quantile Regression.
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Prevalence and Predictors of Burnout Among Hospice and Palliative Care Clinicians in the U.S.
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Provision of spiritual support to patients with advanced cancer by religious communities and associations with medical care at the end of life.
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Quality Improvement Pearls for the Palliative Care and Hospice Professional.
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Race and residence: intercounty variation in black-white differences in hospice use.
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Racial differences in hospice revocation to pursue aggressive care.
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Racial differences in location before hospice enrollment and association with hospice length of stay.
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Racial differences in self-reported exposure to information about hospice care.
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Racism in Palliative Care Research: We Still have a Ways to Go.
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Refining a checklist for reporting patient populations and service characteristics in hospice and palliative care research.
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Resource Use in the Last Year of Life Among Patients Who Died With Versus of Prostate Cancer.
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Review of Religious Variables in Advance Care Planning for End-of-Life Care: Consideration of Faith as a New Construct.
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Significant Morbidity and Mortality Among Hospitalized End-Stage Liver Disease Patients in Medicare.
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Standardization and Scaling of a Community-Based Palliative Care Model.
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Symptom burden of haematological malignancies as death approaches in a community palliative care service: a retrospective cohort study of a consecutive case series.
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Targeted investment improves access to hospice and palliative care.
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The Act of Hospice: Understanding a Family's Perception of Palliative Care--When You're Family.
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The Compliance of End-of-Life Care Preferences Among Older Adults and Its Facilitators and Barriers: A Scoping Review.
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The Implementation of Measuring What Matters in Research and Practice: Series Commentary.
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The Quality Improvement Environment: Results of the 2016 AAHPM/HPNA Membership Needs Assessment Survey.
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The benefits of expanded physician assistant practice in hospice and palliative medicine.
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The need for a Serious Illness Digital Ecosystem (SIDE) to improve outcomes for patients receiving palliative and hospice care.
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Top Ten Tips Palliative Care Clinicians Should Know About Bereavement and Grief.
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Top Ten Tips Palliative Care Clinicians Should Know About Caring for Serious Illness in Pregnancy.
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Top Ten Tips Palliative Care Clinicians Should Know About End-Stage Liver Disease.
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Top Ten Tips Palliative Care Clinicians Should Know About Spirituality in Serious Illness.
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Top Ten Tips for Palliative Care Clinicians Caring for Heart Failure Patients.
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Tracking Patients in Community-Based Palliative Care through the Centers for Medicare & Medicaid Services Healthcare Innovation Project.
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Transfusion dependence, use of hospice services, and quality of end-of-life care in leukemia.
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Trends and Characteristics of Medicare Hospice Beneficiaries in the USA.
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Trends in Hospice Discharge and Relative Outcomes Among Medicare Patients in the Get With The Guidelines-Heart Failure Registry.
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Trends in Place of Death for Individuals With Cardiovascular Disease in the United States.
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US Physicians Overwhelmingly Endorse Hospice as the Better Option for Most Patients at the End of Life.
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Update in Hospice and Palliative Care.
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Update in hospice and palliative care.
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Use of Hospital Referral Regions in Evaluating End-of-Life Care.
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Utilization of Hospice Services in a Population of Patients With Huntington's Disease.
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Utilization of hospice and predicted mortality risk among older patients hospitalized with heart failure: findings from GWTG-HF.
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What explains racial differences in the use of advance directives and attitudes toward hospice care?
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What is a Good Death? A Choice Experiment on Care Indicators for Patients at End of Life.
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What is different about patients with hematologic malignancies? A retrospective cohort study of cancer patients referred to a hospice research network.
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What length of hospice use maximizes reduction in medical expenditures near death in the US Medicare program?
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Where Children Die: Obstacles to Quality End-of-Life Care.
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Who is coordinating pediatric concurrent hospice care?
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Will Changes to Medicare Payment Rates Alter Hospice's Cost-Saving Ability?
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Keywords of People
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Bolar, Erica,
Consulting Associate in the School of Nursing,
School of Nursing
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Curtis, Lesley H.,
Professor in Population Health Sciences,
Medicine, General Internal Medicine
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LeBlanc, Thomas William,
Associate Professor of Medicine,
Duke Cancer Institute