Looking for a checklist of common-sense steps federal regulators should take to ensure the privacy and security of patient information? Look no further.
In Cincinnati, one of the nation's oldest health information exchanges studies the best way to give patients control over their data. Meanwhile, in Washington state, pilot projects test the health record bank approach.
A privacy and security "tiger team" will continue to meet this fall to draft recommendations on a number of issues related to the exchange of patient records.
Kevin Johnson, SANS instructor and security expert, on what you need to know about Stuxnet, Twitter worms and other new threats to organizations and privacy.
The Markle Foundation's "blue button" concept for enabling patients to download their records from a secure website is suitable for a wide variety of healthcare organizations, says Josh Lemieux, the foundation's director of personal health technology.
Detailed patient consent recommendations that a privacy and security "tiger team" recently completed are just a starting point toward giving patients far more control over their healthcare information, the co-chair of the team acknowledges.
The United States should look to the European Union for examples of how to successfully protect the privacy of patient information, the co-author of a new report on electronic health records says.
Patients have inadequate control over who can access their healthcare information, but existing technologies can solve the problem, says consumer advocate Deborah Peel, M.D.
Responding to market demand is ISACA, the non-profit security organization, which launched the Certified in Risk and Information Systems Control certification for IT risk professionals early this year.
To ensure patient privacy, healthcare organizations need to adopt clear-cut social media policies and educate staff about how to comply, says Jonathan Teich, M.D., assistant professor of medicine at Harvard University.
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