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For the Record: Protecting Electronic Health Information (1997)

Chapter: Appendix B Individuals Who Briefed the Study Committee

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Suggested Citation:"Appendix B Individuals Who Briefed the Study Committee." National Research Council. 1997. For the Record: Protecting Electronic Health Information. Washington, DC: The National Academies Press. doi: 10.17226/5595.
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Appendix B Individuals Who Briefed the Study Committee

Joshua S. Auerbach, IBM T.J. Watson Research Center

Kit Bakke, Group Health Cooperative of Puget Sound

Glenda Barnes, Cylink Corporation

Paul Billings, Veterans Administration, Palo Alto Health Care Center

William R. Braithwaite, U.S. Department of Health and Human Services

Patricia L. Branum, Merck-Medco Inc.

A.G. Breitenstein, JRI Health Associates

Jean Chenowith, HCIA Inc.

James S. Corbett, Medical Information Bureau Inc.

Neil Day, Medical Information Bureau Inc.

Donald E. Detmer, University of Virginia

Gary Dickinson, Health Data Sciences Corporation

John P. Fanning, U.S. Department of Health and Human Services

Hansjürgen Garstka, Berlin Data Commission

Janlori Goldman, Center for Democracy and Technology

Donald Haines, American Civil Liberties Union

Isaac S. Kohane, Children's Hospital, Boston

Terry S. Latanich, Merck-Medco Inc.

John Lauer, Health Data Sciences Corporation

Donald A. Lindberg, National Library of Medicine

William H. Murray, Deloitte and Touche, LLP

Gary S. Persinger, Pharmaceutical Research and Manufacturers of America

Marc Rotenberg, Electronic Privacy Information Center

H. Jeffrey Smith, Georgetown University

Burt Tregub, Cylink Corporation

Daniel C. Walden, Merck-Medco Inc.

Suggested Citation:"Appendix B Individuals Who Briefed the Study Committee." National Research Council. 1997. For the Record: Protecting Electronic Health Information. Washington, DC: The National Academies Press. doi: 10.17226/5595.
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When you visit the doctor, information about you may be recorded in an office computer. Your tests may be sent to a laboratory or consulting physician. Relevant information may be transmitted to your health insurer or pharmacy. Your data may be collected by the state government or by an organization that accredits health care or studies medical costs. By making information more readily available to those who need it, greater use of computerized health information can help improve the quality of health care and reduce its costs. Yet health care organizations must find ways to ensure that electronic health information is not improperly divulged. Patient privacy has been an issue since the oath of Hippocrates first called on physicians to "keep silence" on patient matters, and with highly sensitive data--genetic information, HIV test results, psychiatric records--entering patient records, concerns over privacy and security are growing.

For the Record responds to the health care industry's need for greater guidance in protecting health information that increasingly flows through the national information infrastructure--from patient to provider, payer, analyst, employer, government agency, medical product manufacturer, and beyond. This book makes practical detailed recommendations for technical and organizational solutions and national-level initiatives.

For the Record describes two major types of privacy and security concerns that stem from the availability of health information in electronic form: the increased potential for inappropriate release of information held by individual organizations (whether by those with access to computerized records or those who break into them) and systemic concerns derived from open and widespread sharing of data among various parties.

The committee reports on the technological and organizational aspects of security management, including basic principles of security; the effectiveness of technologies for user authentication, access control, and encryption; obstacles and incentives in the adoption of new technologies; and mechanisms for training, monitoring, and enforcement.

For the Record reviews the growing interest in electronic medical records; the increasing value of health information to providers, payers, researchers, and administrators; and the current legal and regulatory environment for protecting health data. This information is of immediate interest to policymakers, health policy researchers, patient advocates, professionals in health data management, and other stakeholders.

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