Big Bad Data: Law, Public Health, and Biomedical Databases
Abstract
The accelerating adoption of electronic health record (HER) systems will have profound impacts on clinical care. It will also have far-reaching implications for public health research and surveillance, which in turn could lead to changes in public policy, statutes, and regulations. The public health benefits of HER use can be significant. However, researchers and analysts who rely on HER data must proceed with caution and understand the potential limitations of EHRs.
Much has been written about the risk of HER privacy breaches. This paper focuses on a different set of concerns, those relating to data quality. HER data can be erroneous, miscoded, fragmented, and incomplete. In addition, if causation is at issue, analysts must grapple with the complexities of causal inference. Public health findings can be tainted by the problems of selection bias, confounding bias, and measurement bias. These and other obstacles can easily lead to invalid conclusions and unsound public health policies.
The paper will highlight the public health uses of EHRs. It will also probe the shortcomings of HER information and the challenges of collecting and analyzing it. Finally, we outline several regulatory and other interventions to address data analysis difficulties.
Keywords
electronic health records, public health, biomedical databases, health care informatics, clinical care, public health emergencies, causal inference, data infrastructure, data integrity, interoperability, data collection, data storage, data analysis
Publication Date
2013
Document Type
Article
Place of Original Publication
Journal of Law, Medicine and Ethics
Publication Information
41 Journal of Law, Medicine and Ethics 56 (Supp. S1 2013)
Repository Citation
Hoffman, Sharona and Podgurski, Andy, "Big Bad Data: Law, Public Health, and Biomedical Databases" (2013). Faculty Publications. 1046.
https://scholarlycommons.law.case.edu/faculty_publications/1046
