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Giving Patients a Role in Data Exchange

“A pilot program at the University of Texas at Austin seeks to find the right processes for enabling patients to track who requests and receives their protected health information.
The pilot, being done under the umbrella of the Office of the National Coordinator for Health Information Technology, is designed to add transparency to the process of exchanging patient data. Providers have repositories within their electronic health records systems that can include signed patient consent directives for the use of their information, and the directives can be reviewed to determine what information to send.”

Article
Joseph Goedert, Health Data Management, 10 July 2013

11 July 2013 | Categories: News, RA News, Record Access | Country: United States | EHR: EHR, EHR USA | Tag(s): Access, Consent, Data Exchange, Health Information Exchange, Patient
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