The 21st Century Cures Act and electronic health records one year later: will patients see the benefits?
Author(s) -
Carolyn T. Lye,
Howard P. Forman,
Jodi G. Daniel,
Harlan M. Krumholz
Publication year - 2018
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/ocy065
Subject(s) - interoperability , health information exchange , health information technology , certification , health records , incentive , business , internet privacy , protected health information , public relations , information exchange , electronic health record , medicine , health care , health information , health policy , nursing , political science , computer science , public health , hrhis , law , world wide web , telecommunications , microeconomics , economics
While federal regulation provides patients the right to access their electronic health records and promotes increased use of health information technology, patient access to electronic health records remains limited. The 21st Century Cures Act, signed into law over a year ago, has important provisions that could significantly improve access and availability of health data. Specifically, the provisions call for partnerships among health information exchange networks, educational and research initiatives, and health information technology certification requirements that encourage interoperability. The article reviews the potential benefits and concerns regarding implementation of these provisions, particularly the difficulty of aligning incentives and requirements for data sharing and the question of whether currently proposed rules and guidance will support the goal of improved patient access and health information exchange. Researchers, clinicians, and patients have the power to advocate for improved patient access and interoperability as policy development and implementation of the 21st Century Cures Act continues.
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