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dc.creatorGostin, Lawrence O.en
dc.creatorTurek-Brezina, Joanen
dc.creatorPowers, Madisonen
dc.creatorKozloff, Reneen
dc.creatorFaden, Ruthen
dc.creatorSteinauer, Dennis D.en
dc.date.accessioned2015-05-05T18:48:44Zen
dc.date.available2015-05-05T18:48:44Zen
dc.date.created1993-11-24en
dc.date.issued1993-11-24en
dc.identifier10.1001/jama.270.20.2487en
dc.identifier.bibliographicCitationJAMA. 1993 Nov 24; 270(20): 2487-2493.en
dc.identifier.issn0098-7484en
dc.identifier.urihttp://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.urihttp://dx.doi.org/10.1001/jama.270.20.2487en
dc.identifier.urihttp://hdl.handle.net/10822/743149en
dc.description.abstractA 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.formatArticleen
dc.languageenen
dc.sourceBRL:KIE/42367en
dc.subjectAutonomyen
dc.subjectComputersen
dc.subjectConfidentialityen
dc.subjectConsenten
dc.subjectDecision Makingen
dc.subjectDisclosureen
dc.subjectData Banksen
dc.subjectFederal Governmenten
dc.subjectGoalsen
dc.subjectGovernmenten
dc.subjectGovernment Regulationen
dc.subjectHealthen
dc.subjectHealth Careen
dc.subjectHealth Care Deliveryen
dc.subjectInformation Disseminationen
dc.subjectInformed Consenten
dc.subjectKnowledgeen
dc.subjectLegal Aspectsen
dc.subjectMoral Policyen
dc.subjectNatureen
dc.subjectPatient Careen
dc.subjectPatientsen
dc.subjectPrivacyen
dc.subjectProfessional Patient Relationshipen
dc.subjectPublic Healthen
dc.subjectRecordsen
dc.subjectRegulationen
dc.subjectResearchen
dc.subjectRightsen
dc.subjectStandardsen
dc.subjectState Governmenten
dc.titlePrivacy and Security of Personal Information in a New Health Care Systemen
dc.provenanceDigital 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.provenanceDigital 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


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