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This research will estimate the cost-effectiveness of pharmacogenomics clinical decision support alerts and create a tool that provides estimates of the value of developing and implementing them.
This project will redesign approaches for collecting and using allergy information with the goal of improving healthcare quality and safety, including completeness and accuracy of allergy data.
The project sought to create a generalizable system to facilitate detection and clinician reporting of vaccine adverse events and found that it is possible to automatically detect adverse events in defined ways, and to electronically report them.
This project demonstrated the ability of an interoperable health information exchange and an electronic health record to provide useful quality and safety measures for the vulnerable populations served by two community health center clinics.
In this project, a clinical decision support tool was developed for Otitis Media, and then studied in a cluster randomized controlled trial to evaluate its impact on the quality of care of Otitis Media.
This project evaluated the Pharmaceutical Safety Tracking (PhaST) system, which monitors medication safety in children and adolescents who are taking antidepressants.
The project team successfully developed and implemented an automated system for measuring the rate of adverse drug events in pediatric patients.
Implemented an integrated electronic patient medical record, electronic medication administration record, computerized physician order entry (CPOE), and clinical decision support software that is accessible at all participating facilities which include an acute care hospital, home health care agency, ambulatory clinics, a rehab facility, and to the patient/resident from home.