dc.creator | Gostin, Lawrence O. | en |
dc.creator | Turek-Brezina, Joan | en |
dc.creator | Powers, Madison | en |
dc.creator | Kozloff, Rene | en |
dc.creator | Faden, Ruth | en |
dc.creator | Steinauer, Dennis D. | en |
dc.date.accessioned | 2015-05-05T18:48:44Z | en |
dc.date.available | 2015-05-05T18:48:44Z | en |
dc.date.created | 1993-11-24 | en |
dc.date.issued | 1993-11-24 | en |
dc.identifier | 10.1001/jama.270.20.2487 | en |
dc.identifier.bibliographicCitation | JAMA. 1993 Nov 24; 270(20): 2487-2493. | en |
dc.identifier.issn | 0098-7484 | en |
dc.identifier.uri | http://worldcatlibraries.org/registry/gateway?version=1.0&url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&atitle=Privacy+and+Security+of+Personal+Information+in+a+New+Health+Care+system&title=JAMA.++&volume=270&issue=20&pages=2487-2493&date=1993&au=Gostin,+Lawrence+O. | en |
dc.identifier.uri | http://dx.doi.org/10.1001/jama.270.20.2487 | en |
dc.identifier.uri | http://hdl.handle.net/10822/743149 | en |
dc.description.abstract | A complex health care information infrastructure will exist under a
reformed health care system as proposed in the American Health Security Act of
1993. The success of the new system will depend in part on the accuracy,
correctness, and trustworthiness of the information and the privacy rights of
individuals to control the disclosure of personal information. All
participants in the new system (consumers and patients, health plans, health
alliances, and a national health board) will need access to high-quality
information for informed decision making. At the same time, everyone must have
confidence that information of a private nature is adequately
protected....This article examines the privacy and security goals for the
collection, storage, and use of health care information in a new health care
system and the means to attain those goals. The goals are to ensure (1) the
integrity of health care data so that information is accurate, complete, and
trustworthy -- the integrity of information is critical to quality patient
care, assessment of services, research, and public health; (2) the
availability of health data so that authorized persons who need the
information for legitimate health purposes have ready access to the data -- if
clinical information is not readily available to health care providers, the
best interests of patients may be significantly compromised; and (3) the
privacy of patients so that they can be assured that personal information
remains private and will not be disclosed without their knowledge and
permission. | en |
dc.format | Article | en |
dc.language | en | en |
dc.source | BRL:KIE/42367 | en |
dc.subject | Autonomy | en |
dc.subject | Computers | en |
dc.subject | Confidentiality | en |
dc.subject | Consent | en |
dc.subject | Decision Making | en |
dc.subject | Disclosure | en |
dc.subject | Data Banks | en |
dc.subject | Federal Government | en |
dc.subject | Goals | en |
dc.subject | Government | en |
dc.subject | Government Regulation | en |
dc.subject | Health | en |
dc.subject | Health Care | en |
dc.subject | Health Care Delivery | en |
dc.subject | Information Dissemination | en |
dc.subject | Informed Consent | en |
dc.subject | Knowledge | en |
dc.subject | Legal Aspects | en |
dc.subject | Moral Policy | en |
dc.subject | Nature | en |
dc.subject | Patient Care | en |
dc.subject | Patients | en |
dc.subject | Privacy | en |
dc.subject | Professional Patient Relationship | en |
dc.subject | Public Health | en |
dc.subject | Records | en |
dc.subject | Regulation | en |
dc.subject | Research | en |
dc.subject | Rights | en |
dc.subject | Standards | en |
dc.subject | State Government | en |
dc.title | Privacy and Security of Personal Information in a New Health Care System | en |
dc.provenance | Digital citation created by the National Reference Center for Bioethics Literature at Georgetown University for the BIOETHICSLINE database, part of the Kennedy Institute of Ethics' Bioethics Information Retrieval Project funded by the United States National Library of Medicine. | en |
dc.provenance | Digital citation migrated from OpenText LiveLink Discovery Server database named NBIO hosted by the Bioethics Research Library to the DSpace collection BioethicsLine hosted by Georgetown University. | en |