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The overall goal of the research is to advance the integration and use of patient-generated digital health data in ambulatory care settings.
This research will create patient-centered, interoperable, shareable clinical decision support tools that will support providers and patients in making patient-centered decisions about management of hypertension.
This project will develop a series of standards for electronic health records to ensure adequate and accurate data communication for care team members in the intensive care environment.
The research team identified key information needs for clinicians providing and coordinating care for patients with complex medical, social, and economic needs, and developed and tested design principles for electronic health record systems to support social determinants of health data capture and clinical decision support.
This project conducted a large scale systematic review to synthesize existing evidence on health information exchange use and effectiveness.
This project evaluated the impact of an integrated care coordination information system (ICCIS) on the outcomes and satisfaction of patients with chronic and complex illnesses.
This project refined a set of asthma care quality measures and developed and validated the use of an automated method using natural language processing to utilize the measures.
This project investigated the feasibility and impact of novel approaches to clinician decision support in multidisciplinary ambulatory care, emphasizing high-risk transitions of care.
This project was designed to evaluate and improve the quality of screening and diagnostic colonoscopies in ambulatory care settings. Defined quality measures for colonoscopy were used in individual quality report cards with 15 measures created.