Report

Dying in America: Improving Quality and Honoring Individual Preferences Near the End of Life


Released:

Report at a Glance

  • The Conversation (HTML)
  • Introductory Slides (HTML)
  • Organizational Commitment Statements (HTML)
  • Report Brief (PDF, HTML)
  • Stakeholder Webinar Recording (HTML)
  • Stakeholder Webinar Slides (HTML)
  • Key Findings and Recommendations (PDF)
  • Core Components of Quality End-of-Life Care (PDF)
  • Infographic (PDF)
  • Palliative Care Graphic (PDF, HTML)
  • Palliative Care Graphic (Spanish) (PDF, HTML)
  • Palliative Care Graphic (Portuguese) (PDF, HTML)

Previous Events: 

National Action Conference: Policies and Payment Systems to Improve End-of-Life Care - March 20, 2015 (Visit the meeting page)

Dying in America: IOM Recommendations and Next Steps for Stakeholders (Access the Archived Webinar | Download  PPT Slides)



For patients and their loved ones, no care decisions are more profound than those made near the end of life. For the millions of Americans who work in or with the health care sector—including clinicians, clergy, caregivers, and support staff—providing high-quality care for people who are nearing the end of life is a matter of professional commitment and responsibility. Health sys­tem managers, payers, and policy makers, likewise, have a responsibility to ensure that end-of-life care is compassionate, affordable, sustainable, and of the best quality possible. 

A substantial body of evidence shows that broad improvements to end-of-life care are within reach. In Dying in America, a consensus report from the Institute of Medicine (IOM), a committee of experts finds that improving the quality and availability of medical and social services for patients and their families could not only enhance quality of life through the end of life, but may also contribute to a more sustainable care system.

Actions Taken as a Result of this Report