Sharing Information Across Physical and Behavioral Health – Debunking Myths, Developing Strategies
Date: August 6, 2015
Time: 2:30-4:00pm EDT
Integrating physical and mental health services requires that personal health information is shared appropriately across various settings in order to promote care coordination and better outcomes. In their efforts to support physical and mental health integration, state policymakers can sometimes face barriers to this flow of information due to federal and state laws, provider culture, technical roadblocks, and other factors. This webinar provides a brief overview by Karla Lopez from the Legal Action Center of the federal statutory framework, specifically in the context of integrating physical and behavioral health care. Presentations by state policymakers from New York and North Carolina highlight successful tools and strategies used by these states to support integrated care, including the development of standardized forms and tools, engaging behavioral health providers in using health IT, and working with diverse stakeholders to identify issues and solutions to state-specific problems.
| 5 min | Welcome & Introductions Call Moderator: Kitty Purington, Program Director, National Academy for State Health Policy (NASHP) |
| 15 | Overview: Karla Lopez, JD Legal Action Center |
| 15 | Amelia MahanDirector, Behavioral Health Integration Community Care of North Carolina |
| 15 | Greg AllenDirector, Division of Program Development and Management Office of Health Insurance Programs, New York State Department of Health |
| 25 | Q&A |
Supported by the Commonwealth Fund


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. 























































































































































