All Stories

  1. Feeling groovy? The present and future of psychedelic research in palliative care
  2. Healing relationships between patients from visible minority groups and their clinicians in palliative care: Protocol for an interpretive description study
  3. Controlled Trials of “Palliative Care”—Where Do We Go from Here?
  4. Providing Palliative Care for Sexual and Gender Minority Individuals: A Qualitative Interview Study of Physicians’ Attitudes and Experiences
  5. E-Learning to Fill Gaps in Serious Illness Communication Education: A Missing Piece or an Unfinished Puzzle?
  6. Because You Matter: Betty Ferrell's Contributions to Inter-Professionalism in Palliative Care
  7. Home-based psilocybin-assisted therapy for a patient with advanced cancer: A case report
  8. Integrating Health Equity in the ASCO Guideline Agenda: Recommendations From Members of the Palliative Care Expert Panel
  9. Palliative Care for Patients With Cancer: ASCO Guideline Clinical Insights
  10. Reprogramming Healthcare: Leveraging AI to Strengthen Doctor-Patient Relationships
  11. Implementing the Serious Illness Care Program in Safety Net Health Systems: A Qualitative Study
  12. Opportunities for Expanding the Integration of Palliative Care in Oncology Care
  13. Palliative Care for Patients With Cancer: ASCO Guideline Update
  14. Donating One’s Body to HIV Cure Research Through Canadian Medical Assistance in Dying: A Case Study
  15. Acceptability of psilocybin‐assisted group therapy in patients with cancer and major depressive disorder: Qualitative analysis
  16. Lessons Learned About System-Level Improvement in Serious Illness Communication: A Qualitative Study of Serious Illness Care Program Implementation in Five Health Systems
  17. Disruption as an opportunity or threat: A qualitative analysis of factors influencing the attitudes of experts in serious illness care toward psychedelic-assisted therapies
  18. Acceptability of a Serious Illness Conversation Guide to Black Americans: Results from a focus group and oncology pilot study
  19. Psychedelic-Assisted Therapies in Patients With Serious Illness: Opportunities and Challenges
  20. Toward a basic science of communication in serious illness
  21. Leading from the Heart
  22. Reply to “Empathic communication: The premise of inclusive care for historically excluded populations”
  23. Identification of Digital Health Priorities for Palliative Care Research: Modified Delphi Study
  24. A Framework for Anti-Racist Publication in Palliative Care: Structures, Processes, and Outcomes
  25. Letter to the Editor: Author Response to Reader's Comments to Fitzgerald Jones et al., Top Ten Tips Palliative Care Clinicians Should Know About Delivering Antiracist Care to Black Americans (DOI: 10.1089/jpm.2021.0502)
  26. Environmental Considerations for Effective Telehealth Encounters: A Narrative Review and Implications for Best Practice
  27. Top Ten Tips Palliative Care Clinicians Should Know About Delivering Antiracist Care to Black Americans
  28. Discussing prognosis and what matters most for people with serious illness
  29. “ I think that she would have wanted. . .” : Qualitative interviews with bereaved caregivers reveal complexity in measuring goal-concordant care at the end of life
  30. Virtual environments to study emotional responses to clinical communication: A scoping review
  31. Mapping an Agenda for Psychedelic-Assisted Therapy Research in Patients with Serious Illness
  32. When treatment algorithms fail: A response to the development of a nomogram to determine the frequency of elevated risk for non-medical opioid use in cancer patients
  33. Physician empathy according to physicians: A multi-specialty qualitative analysis
  34. What is empathy? Oncology patient perspectives on empathic clinician behaviors
  35. “I was not able to keep myself away from tending to her immediate needs”: Primary Care Physicians’ Perspectives of Serious Illness Conversations at Community Health Centers
  36. Identification of Digital Health Priorities for Palliative Care Research: Modified Delphi Study (Preprint)
  37. Technology in Palliative Care (TIP): the identification of digital priorities for palliative care research using a modified Delphi method
  38. What is clinical empathy? Perspectives of community members, university students, cancer patients, and physicians
  39. Asian American Medicare Beneficiaries Disproportionately Receive Invasive Mechanical Ventilation When Hospitalized at the End-of-Life
  40. Reflections on Goal-Concordant Care: A Christmas Story
  41. Communication Tools to Support Advance Care Planning and Hospital Care During the COVID-19 Pandemic: A Design Process
  42. Adherence and Concordance between Serious Illness Care Planning Conversations and Oncology Clinician Documentation among Patients with Advanced Cancer
  43. Serious Illness Conversations With Outpatient Oncology Clinicians: Understanding the Patient Experience
  44. Toward Culturally Tailored Advance Care Planning for the Chinese Diaspora: An Integrative Systematic Review
  45. Measuring Goal-Concordant Care: Results and Reflections From Secondary Analysis of a Trial to Improve Serious Illness Communication
  46. Defining the Roles and Research Priorities for Psychedelic-Assisted Therapies in Patients with Serious Illness: Expert Clinicians' and Investigators' Perspectives
  47. Effect of the Serious Illness Care Program on Health Care Utilization at the End of Life for Patients with Cancer
  48. Implementing Serious Illness Communication Processes in Primary Care: A Qualitative Study
  49. “Find Out What They Lack, Try to Provide”: A Qualitative Investigation of Palliative Care Services Adapted to Local Need in a Low-Resource Setting
  50. Patient and clinician experience of a serious illness conversation guide in oncology: A descriptive analysis
  51. A Time-to-Death Analysis of Older Adults after Emergency Department Intubation
  52. Training Clinicians in Serious Illness Communication Using a Structured Guide: Evaluation of a Training Program in Three Health Systems
  53. Quality Measurement of Serious Illness Communication: Recommendations for Health Systems Based on Findings from a Symposium of National Experts
  54. Communication Skills
  55. Communication Strategies for Sharing Prognostic Information With Patients
  56. Factors That Impact Family Perception of Goal-Concordant Care at the End of Life
  57. A Qualitative Study of Serious Illness Conversations in Patients with Advanced Cancer
  58. Interprofessional Work in Serious Illness Communication in Primary Care: A Qualitative Study
  59. The Cambia Sojourns Scholars Leadership Program: Projects and Reflections on Leadership in Palliative Care
  60. Serious illness care Programme UK: assessing the ‘face validity’, applicability and relevance of the serious illness conversation guide for use within the UK health care setting
  61. Effect of the Serious Illness Care Program in Outpatient Oncology
  62. Evaluating an Intervention to Improve Communication Between Oncology Clinicians and Patients With Life-Limiting Cancer
  63. Differences by Race, Religiosity, and Mental Health in Preferences for Life-Prolonging Treatment Among Medicare Beneficiaries
  64. End-of-Life Care for Seriously Ill International Patients at a Global Destination Medical Center
  65. From Barriers to Assets: Rethinking factors impacting advance care planning for African Americans
  66. Achieving Goal-Concordant Care: A Conceptual Model and Approach to Measuring Serious Illness Communication and Its Impact
  67. Seeking and Accepting: U.S. Clergy Theological and Moral Perspectives Informing Decision Making at the End of Life
  68. How Community Clergy Provide Spiritual Care: Toward a Conceptual Framework for Clergy End-of-Life Education
  69. Factors Impacting Advance Care Planning among African Americans: Results of a Systematic Integrated Review
  70. Finding the Right Words at the Right Time — High-Value Advance Care Planning
  71. Meaning and Methadone
  72. Resident Physician Interactions with Surrogate Decision-Makers: The Resident Experience