Report on the use of automated personal data bases and information systems in the USA and the social implications thereof, with particular reference to the question of confidentiality - comments on the effects of computer-based records maintenance, the legal aspects of data collecting and research systems, the use of the social security number as a universal identifier, etc., and includes recommendations regarding draft legislation. Annotated bibliography pp. 298 to 330.

Excerpt from A Policy Analysis of Citizen Rights Issues in Health Data Systems The study had three objectives. First, it would describe the pre-computer base line of record - keeping practices and citizen - rights rules in the various sectors of American health care. Second, it would describe how computers were being used and identify the effects they were having on the content and uses of health records. Finally, the study would analyze public debates over computer uses and citizen rights in the health field, note parallel developments in other democratic nations, and identify those principles of good practice and possible policy actions that would best assure the observance of citizen rights in health-data practices, especially in automated data systems. About the Publisher Forgotten Books publishes hundreds of thousands of rare and classic books. Find more at www.forgottenbooks.com This book is a reproduction of an important historical work. Forgotten Books uses state-of-the-art technology to digitally reconstruct the work, preserving the original format whilst repairing imperfections present in the aged copy. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in our edition. We do, however, repair the vast majority of imperfections successfully; any imperfections that remain are intentionally left to preserve the state of such historical works.

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.

This edition provides practical advice & guidance in managing information technology. Topics include preparing an organization for emerging technologies, maintaining confidentiality & security, & managing the impact of technology on organizational change.