The Children's Research Institute
Center for Pediatric Biomedical Informatics
The Center for Pediatric Biomedical Informatics was organized in 2006 as a multidisciplinary group comprised of faculty and staff with informatics background, and an interest and/or vision to optimally develop and use the electronic health medical record to both understand and improve the quality of healthcare delivery and research in children. The Center’s primary goals are to utilize novel information technology, computer science, and knowledge management methods to: deliver safer and more effective care; increase the efficiency of care delivery; improve disease prevention; increase the effectiveness of translational research; improve knowledge access and technology-enhanced education; and enhance regulatory compliance.
To address these goals, the Center’s primary objective is to derive meaningful data from electronic health records in support of organizational functions including: Clinical Effectiveness; Performance Improvement; Quality Improvement; Risk Reduction; Regulatory Compliance; Patient Satisfaction, Safety, and Evidence Based Care Delivery. Other Center objectives include:
- Development of metrics to assess quality and variance in care delivery at Children’s National
- Provision of a home for the Clinical Decision Support and Reporting Group
- Provision of an academic and administrative home for faculty from each Center with interest in informatics quality and research
- Improvement in system access and education for patients, families, and community physicians
- Analysis of population trends
- Automated surveillance for adverse events
- Optimization of the computer-user interface
- Dissemination of knowledge through presentations and publications
Since the Center’s inception in 2006, center members have been active at regional, national, and international levels in information technology and informatics meetings and workshops, with multiple presentations and peer-reviewed publications.