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Patient-led data sharing for clinical bioinformatics research: USCDI and beyond
Author(s) -
William J. Gordon,
Daniel Gottlieb,
David Kreda,
Joshua C. Mandel,
Kenneth D. Mandl,
Isaac S. Kohane
Publication year - 2021
Publication title -
journal of the american medical informatics association
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.614
H-Index - 150
eISSN - 1527-974X
pISSN - 1067-5027
DOI - 10.1093/jamia/ocab133
Subject(s) - interoperability , data sharing , context (archaeology) , computer science , value proposition , process (computing) , data science , value (mathematics) , health information exchange , knowledge management , world wide web , business , health care , medicine , health information , political science , marketing , biology , pathology , alternative medicine , operating system , paleontology , law , machine learning
The 21st Century Cures Act, passed in 2016, and the Final Rules it called for create a roadmap for enabling patient access to their electronic health information. The set of data to be made available, as determined by the Office of the National Coordinator for Health IT through the US Core Data for Interoperability expansion process, will impact the value creation of this improved data liquidity. In this commentary, we look at the potential for significant value creation from USCDI in the context of clinical bioinformatics research and advocate for the research community's involvement in the USCDI process to propel this value creation forward. We also describe 1 mechanism-using existing required APIs for full data export capabilities-that could pragmatically enable this value creation at minimal additional technical lift beyond the current regulatory requirements.

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