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Search found 35 items
This research will further scale clinical decision support aimed at preventing the prescription of inappropriate medications to older adults upon discharge from the emergency department.
This research’s goal is to show that interoperability, including adoption of regional health information exchanges, improves mortality rates and care efficiency at the population and patient levels.
This study will evaluate the effectiveness of patient photographs displayed in electronic health record systems for preventing wrong-patient errors.
The purpose of this research was to investigate the relationships between electronic health record adoption and usability, work environment, and patient and nurse outcomes.
This project will develop and validate new measures needed for automatically identifying violations of the “Five Rights of Medication Safety”: right patient, right dose, right medication, right route, and right frequency.
The investigators used a mixed-methods approach to incorporate quantitative and qualitative research in developing and validating a health IT adaptation survey.
This project enhanced the Children’s Electronic Health Record Format (Format) by identifying a high priority set of 47 functional requirements from the initial larger set, and creating a list of 16 recommended uses of the Format along with implementation notes.
This project evaluated the feasibility of two Stage 3 Meaningful Use Care Coordination measures and provided feedback to policymakers and providers for their improvement.
This project evaluated select Stage 3 Meaningful Use criteria in the Patient and Family Engagement, Care Coordination, and Interoperability domains and developed recommendations to improve them and increase their value to hospitals and practices implementing them.
This project assessed and made recommendations about draft Stage 3 Meaningful Use objectives in the areas of care coordination and patient and family engagement.