Author: Publisher: DIANE Publishing
ISBN: 1428922997
Category :
Languages : en
Pages : 153
Book Description
Federal government information technology : electronic record systems and individual privacy.
Author: Publisher: DIANE Publishing
ISBN: 1428922997
Category :
Languages : en
Pages : 153
Book Description
Federal Government Information Technology
Author: United States. Congress. Office of Technology AssessmentPublisher: Washington, D.C. : Congress of the United States, Office of Technology Assessment
ISBN:
Category : Administrative agencies
Languages : en
Pages : 168
Book Description
Federal Government Information Technology
Author: United States. Congress. Office of Technology AssessmentPublisher:
ISBN:
Category : Administrative agencies
Languages : en
Pages : 152
Book Description
Federal Government Information Technology
Author: Federal Government Information Technology
Author: Gordon Press PublishersPublisher:
ISBN: 9780849050183
Category :
Languages : en
Pages :
Book Description
For the Record
Author: National Research CouncilPublisher: National Academies Press
ISBN: 0309056977
Category : Medical
Languages : en
Pages : 287
Book Description
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 dataâ€"genetic information, HIV test results, psychiatric recordsâ€"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 infrastructureâ€"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.
Computers and Privacy
Author: United States. General Accounting OfficePublisher:
ISBN:
Category : Computers
Languages : en
Pages : 72
Book Description
Computers and Privacy
Author: Registries for Evaluating Patient Outcomes
Author: Agency for Healthcare Research and Quality/AHRQPublisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 396
Book Description
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.
Federal government information technology : electronic surveillance and civil liberties.
Author: UNITED STATES. CONGRESS. OFFICE OF TECHNOLOGY ASSESSMENT.Publisher: DIANE Publishing
ISBN: 142892339X
Category :
Languages : en
Pages : 74
Book Description