Dr. Ernest Moy
Ernest Moy is a medical officer in the Center for Quality Improvement and Patient Safety at the Agency for Healthcare Research and Quality (AHRQ). At AHRQ, his work has included directing the development of the annual National Healthcare Disparities Report and National Healthcare Quality Report and supporting AHRQ’s Excellence Centers for the Elimination of Ethnic/Racial Disparities and AHRQ’s Patient Safety Organization program. Prior to joining AHRQ, he was director of research and assistant vice president of the Center for the Assessment and Management of Change in Academic Medicine at the Association of American Medical Colleges, where he conducted research on the missions of academic medical centers and developed benchmarking tools to help these institutions improve performance.
Dr. Moy is a graduate of Harvard College and New York University School of Medicine. Following internal medicine residency, he was a general internal medicine fellow at Columbia University, a Robert Wood Johnson Health Care Finance fellow at Johns Hopkins University, and an assistant professor of medicine at University of Maryland School of Medicine.
Dr. Moy’s research interests include disparities in access and quality of care, particularly as they relate to academic medical centers, patient safety, and technology diffusion. He is chair of the Racial and Ethic Disparities Committee of the American Public Health Association’s Medical Care Section.

For individuals living with complex, often chronic conditions, and their families, palliative care can provide relief from symptoms, improve satisfaction and outcomes, and help address critical mental and spiritual needs during difficult times. Now more than ever, there is growing recognition of the importance of palliative care services for individuals with serious illness, such as advance care planning, pain and symptom management, care coordination, and team-based, multi-disciplinary support. These services can help patients and families cope with the symptoms and stressors of disease, better anticipate and avoid crises, and reduce unnecessary and/or unwanted care. While this model is grounded in evidence that demonstrates improved quality of life, better outcomes, and reduced cost for patients, only a fraction of individuals who could benefit from palliative care receive it. 























































































































































