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This project provided input to inform the development of nine proposed Stage 3 MU objectives focused on patient engagement, interoperability, and care coordination.
This project created recommendations for the development of a health information technology enabled tool to support transitions of care for those with sickle cell disease.
Develops a patient Master Visit Registry (MVR), addressing the need for better information sharing among clinical organizations and enhancing their ability to give patients continuous high-quality care when they change providers. The MVR will expand upon an existing patient record-keeping system, while improving local handling and exchange of records.
Developed approaches to share data on patient clinical and diagnostic information across systems and created an implementation plan for systems integration.