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Circulation ; 133(14): 1410-8, 2016 Apr 05.
Article in English | MEDLINE | ID: mdl-27045129

ABSTRACT

The National Heart, Lung, and Blood Institute convened a working group in January 2015 to explore issues related to an integrated data network for congenital heart disease research. The overall goal was to develop a common vision for how the rapidly increasing volumes of data captured across numerous sources can be managed, integrated, and analyzed to improve care and outcomes. This report summarizes the current landscape of congenital heart disease data, data integration methodologies used across other fields, key considerations for data integration models in congenital heart disease, and the short- and long-term vision and recommendations made by the working group.


Subject(s)
Biomedical Research/organization & administration , Data Mining , Databases, Factual , Health Information Systems/organization & administration , Heart Defects, Congenital , Clinical Trials as Topic , Data Collection , Data Curation , Electronic Health Records , Health Information Systems/economics , Heart Defects, Congenital/epidemiology , Humans , Medical Informatics , Medical Record Linkage , National Heart, Lung, and Blood Institute (U.S.) , Registries , United States/epidemiology
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