Background
The draft roadmap, titled "Connecting Health and Care for the Nation: A Shared Nationwide Interoperability Roadmap Draft Version 1.0," aims to achieve basic electronic health data interoperability by 2017.
It outlines short- and long-term goals for the next 10 years, with 2017 set as the deadline by which "a majority of individuals and providers across the care continuum" should be able "to send, receive, find and use a common set of electronic clinical information."
Interoperability Roadmap Public Comments
ONC requested public commentary on it's program for health information interoperability.
ONC accepted public comments on Connecting Health and Care for the Nation: A Shared Nationwide Interoperability Roadmap Draft Version 1.0. The comment period ended on April 3, 2015.
The draft Roadmap proposes critical actions that need to be taken by both private and public stakeholders to advance the nation towards a more connected, interoperable health IT infrastructure and was drafted by ONC based on input from private and public stakeholders. The draft Roadmap outlines the critical actions for different stakeholder groups necessary to help achieve an interoperable health IT ecosystem.
Selected commentary:
C.Krinkie
Radiological Association of North America
Joel White
Executive Director
Health IT Now
Karen Boruff
Project Manager
California Association of Health Information Exchanges
Andrew Schlafly
General Counsel
Association of American Physicians & Surgeons
Stephen Beller
President/CEO
National Health Data Systems, inc
Peter N. Kaufman, MD
Chief Medical Officer
DrFirst, Inc
Steven Kelmar
Executive Vice President, Corporate Affairs
Aetna, Inc.
William Rich, MD
Medical Director, Health Policy & President Elect
American Academy of Ophthalmology
American Congress of Gynecology and Obstetrics
Jamie Ferguson
VP, Health IT Strategy & Policy
Kaiser Permanente
Selected comment
iHealthBeat Summary
Several comments are in regard to lack of incentives for HIT developers.
I am very opposed to this. It proposes to repeal federal law that allows state legislatures to enact true medical privacy laws for citizens. It views patient data as public property rather than personal property. It has uses of data that many patients will not accept.