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The goal of this project is to generate a systematic and replicable process for transforming evidence-based research findings, including findings from patient-centered outcomes research, into shareable clinical decision support (CDS) standards and a publicly available CDS prototype.
This report was created to address the nationally significant challenge of developing comprehensive clinical datasets, collected in real world environments and accessible in real time, to support clinical research and to address public health concerns.
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.