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Women have unique information needs during their pregnancies, ranging from medical questions about pregnancy to logistical concerns about hospital policies. This project is designed to understand these needs, the contexts in which they occur, and the resources used.
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 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.