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Author : United States. Congress. Office of Technology Assessment
Publisher : Washington, D.C. : Congress of the United States, Office of Technology Assessment
Page : 168 pages
File Size : 42,5 Mb
Release : 1986
Category : Administrative agencies
ISBN : UOM:39015015394995
Author : Gordon Press Publishers
Publisher : Unknown
Page : 128 pages
File Size : 54,5 Mb
Release : 1991-10
Category : Electronic
ISBN : 0849050189
Author : Anonim
Publisher : DIANE Publishing
Page : 153 pages
File Size : 55,8 Mb
Release : 2024-06-05
Category : Electronic
ISBN : 9781428922990
Author : Anonim
Publisher : Unknown
Page : 164 pages
File Size : 40,5 Mb
Release : 1986
Category : Administrative agencies
ISBN : UIUC:30112026099488
Author : Anonim
Publisher : Unknown
Page : 202 pages
File Size : 43,6 Mb
Release : 1986
Category : Administrative agencies
ISBN : UCR:31210024830042
Author : Anonim
Publisher : DIANE Publishing
Page : 195 pages
File Size : 46,5 Mb
Release : 2024-06-05
Category : Electronic
ISBN : 9781428923003
Author : United States. General Accounting Office
Publisher : Unknown
Page : 72 pages
File Size : 53,5 Mb
Release : 1990
Category : Computers
ISBN : SRLF:D0007729882
Author : Anonim
Publisher : Unknown
Page : 72 pages
File Size : 53,6 Mb
Release : 1990
Category : Computers
ISBN : NWU:35556020257689
Author : Committee on Maintaining Privacy and Security in Health Care Applications of the National Information Infrastructure,Commission on Physical Sciences, Mathematics, and Applications,Computer Science and Telecommunications Board,Division on Engineering and Physical Sciences,National Research Council
Publisher : National Academies Press
Page : 287 pages
File Size : 50,9 Mb
Release : 1997-06-23
Category : Medical
ISBN : 9780309524254
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.
Author : United States. Congress. House. Committee on Ways and Means
Publisher : Unknown
Page : 116 pages
File Size : 43,6 Mb
Release : 1986
Category : Budget
ISBN : UCR:31210024924654
Author : United States. Congress. Office of Technology Assessment
Publisher : Unknown
Page : 48 pages
File Size : 53,6 Mb
Release : 1990
Category : Government publications
ISBN : MINN:31951D002703184
Author : United States. Congress. Senate. Committee on Homeland Security and Governmental Affairs. Subcommittee on Oversight of Government Management, the Federal Workforce, and the District of Columbia
Publisher : Unknown
Page : 196 pages
File Size : 54,7 Mb
Release : 2007
Category : Business & Economics
ISBN : PSU:000061500242
Author : Agency for Healthcare Research and Quality/AHRQ
Publisher : Government Printing Office
Page : 396 pages
File Size : 46,7 Mb
Release : 2014-04-01
Category : Medical
ISBN : 9781587634338
This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.
Author : DIANE Publishing Company
Publisher : DIANE Publishing
Page : 253 pages
File Size : 55,7 Mb
Release : 1994-12
Category : Electronic
ISBN : 9780788114014
Author : United States. Congress. Office of Technology Assessment
Publisher : Unknown
Page : 92 pages
File Size : 48,8 Mb
Release : 1987
Category : Technological innovations
ISBN : PURD:32754073523072