State Data Approaches to Neonatal Abstinence Syndrome
Thursday September 16, 10-11am ET
Between 2010 and 2017, the rate of Neonatal Abstinence Syndrome (NAS) diagnoses across states increased by 82%, indicating an increased need for policies that support substance use disorder (SUD) treatment and early intervention for pregnant and parenting individuals. Rates of NAS are also disproportionately high in babies born to people who are uninsured or covered by Medicaid; those babies diagnosed with NAS born to Medicaid-covered parents spend more time in the hospital and cost more than NAS babies born to privately-insured parents. While states are obliged under CAPTA/CARA to report instances of NAS, the legislation did not standardize a definition of NAS or data reporting processes, creating challenges for states.
This webinar explores two unique state approaches to data NAS data collection, analysis, and cross-agency data linkage, and how states leverage these data to inform better policy and improve health outcomes for both parents and infants.
Speakers:
Ohio:
- Susan Ford, MSN, RN, Quality Improvement Consultants Coordinator, Ohio Perinatal Quality Collaborative
- Jennifer Terry, MHA, Project Manager, James M. Anderson Center for Health Systems Excellence, Cincinnati Children’s Hospital
Kentucky:
- Connie White, MD, Senior Deputy Commissioner for the Kentucky Department of Public Health
- Henrietta Bada, MD, MPH, Director, Division of Maternal and Child Health, Kentucky Department of Public Health



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. 























































































































































