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Medical Records Confidentiality In The Modern Delivery Of Health Care
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Author :United States. Congress. House. Committee on Commerce. Subcommittee on Health and the Environment Publisher : ISBN 13 : Total Pages :128 pages Book Rating :4.0/5 ( download)
Book Synopsis Medical Records Confidentiality in the Modern Delivery of Health Care by : United States. Congress. House. Committee on Commerce. Subcommittee on Health and the Environment
Download or read book Medical Records Confidentiality in the Modern Delivery of Health Care written by United States. Congress. House. Committee on Commerce. Subcommittee on Health and the Environment and published by . This book was released on 1999 with total page 128 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Medical Records Confidentiality in the Modern Delivery of Health Care by : Michael Fleming
Download or read book Medical Records Confidentiality in the Modern Delivery of Health Care written by Michael Fleming and published by . This book was released on 2000-08 with total page 121 pages. Available in PDF, EPUB and Kindle. Book excerpt: Witnesses: Bob Amdur, Dartmouth Med. School; Dawn Gencarelli, Harvard Pilgrim Health Care; Margaret Hamburg, Assist. Sec. for Planning & Eval., Dept. of HHS; Lana Skirboll, Assoc. Dir. for Science Policy, NIH; John Eisenberg, Agency for Health Care Policy & Res.; Steven Jacobsen, Mayo Fdn.; Chris Koyanagi, Consumer Coalition for Health Privacy; Daniel Krinsky, Ritzman Pharmacies; Terry Latanich, Merck-Medco; Roberta Meyer, Amer. Council of Life Insur.; Abbey Meyers, Nat. Org. of Rare Disorders; Mark O'Keefe, Comm. of Insur., Montana; David Stump, Genentech Fellow; Fran Visco, Nat. Breast Cancer Coalition; & Kepa Zubeldia, Envoy Corp.
Author :Agency for Healthcare Research and Quality/AHRQ Publisher :Government Printing Office ISBN 13 :1587634333 Total Pages :396 pages Book Rating :4.5/5 (876 download)
Book Synopsis Registries for Evaluating Patient Outcomes by : Agency for Healthcare Research and Quality/AHRQ
Download or read book Registries for Evaluating Patient Outcomes written by Agency for Healthcare Research and Quality/AHRQ and published by Government Printing Office. This book was released on 2014-04-01 with total page 396 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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 :Committee on Improving the Patient Record Publisher :National Academies Press ISBN 13 :030957885X Total Pages :257 pages Book Rating :4.3/5 (95 download)
Book Synopsis The Computer-Based Patient Record by : Committee on Improving the Patient Record
Download or read book The Computer-Based Patient Record written by Committee on Improving the Patient Record and published by National Academies Press. This book was released on 1997-10-28 with total page 257 pages. Available in PDF, EPUB and Kindle. Book excerpt: Most industries have plunged into data automation, but health care organizations have lagged in moving patients' medical records from paper to computers. In its first edition, this book presented a blueprint for introducing the computer-based patient record (CPR). The revised edition adds new information to the original book. One section describes recent developments, including the creation of a computer-based patient record institute. An international chapter highlights what is new in this still-emerging technology. An expert committee explores the potential of machine-readable CPRs to improve diagnostic and care decisions, provide a database for policymaking, and much more, addressing these key questions: Who uses patient records? What technology is available and what further research is necessary to meet users' needs? What should government, medical organizations, and others do to make the transition to CPRs? The volume also explores such issues as privacy and confidentiality, costs, the need for training, legal barriers to CPRs, and other key topics.
Book Synopsis Beyond the HIPAA Privacy Rule by : Institute of Medicine
Download or read book Beyond the HIPAA Privacy Rule written by Institute of Medicine and published by National Academies Press. This book was released on 2009-03-24 with total page 334 pages. Available in PDF, EPUB and Kindle. Book excerpt: In the realm of health care, privacy protections are needed to preserve patients' dignity and prevent possible harms. Ten years ago, to address these concerns as well as set guidelines for ethical health research, Congress called for a set of federal standards now known as the HIPAA Privacy Rule. In its 2009 report, Beyond the HIPAA Privacy Rule: Enhancing Privacy, Improving Health Through Research, the Institute of Medicine's Committee on Health Research and the Privacy of Health Information concludes that the HIPAA Privacy Rule does not protect privacy as well as it should, and that it impedes important health research.
Book Synopsis Ethics and Information Technology by : James G. Anderson
Download or read book Ethics and Information Technology written by James G. Anderson and published by Springer Science & Business Media. This book was released on 2007-05-28 with total page 216 pages. Available in PDF, EPUB and Kindle. Book excerpt: This series is directed to health care professionals who are leading the tra- formation of health care by using information and knowledge. Launched in 1988 as Computers in Health Care, the series offers a broad range of titles: some addressed to specific professions such as nursing, medicine, and health administration; others to special areas of practice such as trauma and radi- ogy. Still other books in the series focus on interdisciplinary issues, such as the computer-based patient record, electronic health records, and networked health care systems. Renamed Health Informatics in 1998 to reflect the rapid evolution in the discipline now known as health informatics, the series will continue to add titles that contribute to the evolution of the field. In the series, eminent - perts, serving as editors or authors, offer their accounts of innovations in health informatics. Increasingly, these accounts go beyond hardware and so- ware to address the role of information in influencing the transformation of healthcare delivery systems around the world. The series also increasingly focuses on “peopleware” and the organizational, behavioral, and societal changes that accompany the diffusion of information technology in health services environments.
Book Synopsis Medical Privacy Regulation by : United States. General Accounting Office
Download or read book Medical Privacy Regulation written by United States. General Accounting Office and published by . This book was released on 2001 with total page 20 pages. Available in PDF, EPUB and Kindle. Book excerpt: Although there is a strong consensus supporting the protection of patient confidentiality, views differ as to the best ways in practice to achieve that goal. Pressures are increasing from insurers, providers, and researchers to draw on medical records to study treatment outcomes and monitor expenditures, activities that are becoming increasingly common as medical records are computerized and large databases compiled. In recognition of these trends, the Health Insurance Portability and Accountability Act of 1996 called for the development of comprehensive privacy standards that would establish rights for patients with respect to their medical records and define the conditions for using and disclosing personally identifiable health information. 1 On December 28, 2000, the Department of Health and Human Services (HHS) issued the final regulation on privacy, and it is now under review by the Congress and the new Secretary of HHS. 2.
Author :United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions Publisher : ISBN 13 : Total Pages :140 pages Book Rating :4.F/5 ( download)
Book Synopsis Medical Records Confidentiality in a Changing Health Care Environment by : United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions
Download or read book Medical Records Confidentiality in a Changing Health Care Environment written by United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions and published by . This book was released on 1999 with total page 140 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Privacy and Health Care by : James M. Humber
Download or read book Privacy and Health Care written by James M. Humber and published by Springer Science & Business Media. This book was released on 2001-04-20 with total page 194 pages. Available in PDF, EPUB and Kindle. Book excerpt: Western societies generally recognize both a legal and a moral right to privacy. However, at the present time there is no settled opin ion in the United States regarding how these rights should relate to medical information. On the one hand, virtually everyone agrees that one' s medical records should not be open to just any interested person' s inspection. On the other hand, most also agree that some sacrifices in medical privacy are necessary for scientific advancement, public health protection, and other social goals. However, what limits should be set upon those sacrifices, and how those limits should be determined, have long been issues of debate. In recent years this debate has intensified. There are a variety ofreasons for this; to mention only three: (1) Over the years the US health care delivery system has become increasingly complex, and with this complexity there has come a need for more and more people to have access to patients' medical records. With each transference of information, breaches in confidentiality become more likely. (2) Medical costs have risen at an alarming rate. This makes health insurance a virtual necessity for adequate medical care, and people worry that they will be denied employment and/or medical cov erage if certain sorts of medical information are not kept strictly confi dential. (3) Finally, many medical records are now kept in computer files, and the impossibility of guaranteeing confidentiality for files of this sort is a constant worry.
Book Synopsis Medical Records and the Law by : William H. Roach
Download or read book Medical Records and the Law written by William H. Roach and published by Aspen Publishers. This book was released on 1998 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Third Edition of this highly successful textbook addresses the issues associated with managed care and advances in computer technology that have occurred since the last edition. New legal issues arise when information is integrated and widely available in different electronic formats to a growing number of players in the health care delivery system. The legal issues surrounding technological advances in computer-based patient records, electronic links between patients and providers, telemedicine, community-wide information systems, and access to patient record information are addressed. The implications of new Federal regulation of the confidentiality of health care information, an overview and discussion of state and Federal regulation of managed care, provisions governing electronic payment claims contained in the Health Insurance Portability and Accountability Act and their impact on the transmission of other forms of health care information will all be features of the third edition of Medical Records and the Law. An Instructor's manual is available.
Book Synopsis Health Data in the Information Age by : Institute of Medicine
Download or read book Health Data in the Information Age written by Institute of Medicine and published by National Academies Press. This book was released on 1994-01-01 with total page 272 pages. Available in PDF, EPUB and Kindle. Book excerpt: Regional health care databases are being established around the country with the goal of providing timely and useful information to policymakers, physicians, and patients. But their emergence is raising important and sometimes controversial questions about the collection, quality, and appropriate use of health care data. Based on experience with databases now in operation and in development, Health Data in the Information Age provides a clear set of guidelines and principles for exploiting the potential benefits of aggregated health dataâ€"without jeopardizing confidentiality. A panel of experts identifies characteristics of emerging health database organizations (HDOs). The committee explores how HDOs can maintain the quality of their data, what policies and practices they should adopt, how they can prepare for linkages with computer-based patient records, and how diverse groups from researchers to health care administrators might use aggregated data. Health Data in the Information Age offers frank analysis and guidelines that will be invaluable to anyone interested in the operation of health care databases.
Book Synopsis Medical Records and the Law by : William H. Roach Jr.
Download or read book Medical Records and the Law written by William H. Roach Jr. and published by Jones & Bartlett Publishers. This book was released on 2006-04-18 with total page 613 pages. Available in PDF, EPUB and Kindle. Book excerpt: Published in conjunction with the American Health Information Management Association (AHIMA), Medical Records and the Law is the ideal text for programs in HIM as well as a valuable reference for health and legal professionals. The Fourth Edition features an expanded discussion of state laws affecting the use and disclosure of health information and the substantial changes brought about by HIPAA and the growth of electronic health record systems. It also discusses the highly complex interplay of federal and state laws as well as the challenging area of how patient information may be used in connection with medical research involving human subjects.
Book Synopsis Medical Records Privacy by : Bernice Steinhardt
Download or read book Medical Records Privacy written by Bernice Steinhardt and published by . This book was released on 1999 with total page 14 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author :United States. Congress. House. Committee on Ways and Means. Subcommittee on Health Publisher : ISBN 13 : Total Pages :186 pages Book Rating :4.F/5 ( download)
Book Synopsis Confidentiality of Patient Records by : United States. Congress. House. Committee on Ways and Means. Subcommittee on Health
Download or read book Confidentiality of Patient Records written by United States. Congress. House. Committee on Ways and Means. Subcommittee on Health and published by . This book was released on 2001 with total page 186 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author :United States. Congress. House. Committee on Oversight and Government Reform. Subcommittee on Information Policy, Census, and National Archives Publisher : ISBN 13 : Total Pages :118 pages Book Rating :4.F/5 ( download)
Book Synopsis Protecting Patient Privacy in Healthcare Information Systems by : United States. Congress. House. Committee on Oversight and Government Reform. Subcommittee on Information Policy, Census, and National Archives
Download or read book Protecting Patient Privacy in Healthcare Information Systems written by United States. Congress. House. Committee on Oversight and Government Reform. Subcommittee on Information Policy, Census, and National Archives and published by . This book was released on 2008 with total page 118 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author :United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions Publisher : ISBN 13 : Total Pages :72 pages Book Rating :4.0/5 (6 download)
Book Synopsis Privacy Under a Microscope by : United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions
Download or read book Privacy Under a Microscope written by United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions and published by . This book was released on 1999 with total page 72 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis For the Record by : National Research Council
Download or read book For the Record written by National Research Council and published by National Academies Press. This book was released on 1997-07-09 with total page 287 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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.
