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The project team developed a technical brief on the current literature around core functionalities for pediatric electronic health records to describe current practice and to provide a framework for future research.
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.
This project developed a secure Web-based electronic health record for children with special health care needs called the Tennessee Child Health Profile.
Developed a detailed plan for the implementation and support of informatics tools in regional health centers including the creation of informatics tools to manage institutional surgical care information, creation of a multi-institutional partnership to manage both the informatics and surgical quality improvement programs, and the development of an economic model related to the business and safety benefits.
Developed a database that includes diagnoses, health records, and educational information on children with special health care needs, with emphasis on children with genetic conditions and developmental disabilities. This information was made available to physicians via a secure Web-based system.
Developed approaches to share data on patient clinical and diagnostic information across systems and created an implementation plan for systems integration.
In this project, the MidSouth eHealth Alliance implemented and evaluated a regional data-sharing and interoperability service for health care entities in the Greater Memphis area.