Integrating Maternal and Child Health Data Systems
What happens when state health programs use separate data systems to serve the same population, such as mothers and children? State policymakers know that when those data systems do not “talk” to one another, states may waste resources on duplicative data entry and system maintenance; providers and state agencies may struggle to access information important to the health of mothers and children; and care may be uncoordinated or otherwise compromised.
Some states are tackling the data integration challenge head-on. In spring 2015, NASHP, in partnership with the Iowa Child and Family Policy Center, asked state officials in Illinois, New Jersey, Rhode Island, and Utah–and a state contractor in Connecticut—to share their experiences integrating maternal and child health data systems.
- Blog post: Four Tips from States on Integrating Maternal and Child Health Data Systems
- Final report: Integrating Maternal and Child Health Data Systems



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. 























































































































































