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The Health Insurance Portability and Accountability Act Privacy Rule

A Practical Guide for Researchers

Bibliographic Data

ID9102174
AuthorsPatrick P Gunn (Cooley (United States), corresponding author), Allen M Fremont, Allen Fremont (RAND Corporation), Melissa Bottrell, Melissa M Bottrell (RAND Corporation), Lisa R Shugarman (RAND Corporation), Jolene Galegher (RAND Corporation), Tora K Bikson (RAND Corporation), Tora Bikson
Year2004
Volume42
Issue4
Pages321-327
Publication date2004-04-01
Peer ReviewedYes
Open AccessNo
TypeARTICLE
VenueMedical Care (JOURNAL)
Journal identifiersISSN: 0025-7079 • E-ISSN: 1537-1948
PublisherOvid Technologies (Wolters Kluwer Health) (PUBLISHER)
DOI10.1097/01.mlr.0000119578.94846.f2
PMID15076808
OpenAlexW2063129336
LanguageEN
Citations received1
References cited5

BACKGROUND: The Health Insurance Portability and Accountability Act (HIPAA) Privacy Rule, intended to address potential threats to patient privacy posed by the computerization and standardization of medical records, provides a new floor level of federal protection for health information in all 50 states. In most cases, compliance with the Privacy Rule was required as of April 2003. Yet considerable confusion and concern remain about the Privacy Rule and the specific changes it requires in the way healthcare providers, health plans, and others use, maintain, and disclose health information. Researchers worry that the Privacy Rule could hinder their access to health information needed to conduct their research. OBJECTIVES: In this article, we explain how the final version of the Privacy Rule governs disclosure of health information, assess implications of the Privacy Rule for research, and offer practical suggestions for researchers who require access to health information. CONCLUSION: The Privacy Rule is fundamentally changing the way that healthcare providers, health plans, and others use, maintain, and disclose health information and the steps that researchers must take to obtain health data. The Privacy Rule requires researchers who seek access to identifiable health information to obtain written authorization from subjects, or, alternatively, to demonstrate that their research protocols meet certain Privacy Rule requirements that permit access without written authorization. To ensure continued access to data, researchers will need to work more closely than before with healthcare providers, health plans, and other institutions that generate and maintain health information

Business · Common Rule · Computer security · Confidentiality · Health care · Health Insurance Portability and Accountability Act · HRHIS · Information privacy · Informed consent · Internet privacy · Political science · Privacy by Design · Privacy law · Privacy policy · Protected health information · Computer Science · Digital Imaging in Medicine · Electronic Health Records Systems · Ethics in Clinical Research · Law · Medicine · Health Policy

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    Open Access•Yu-Ting Yeh, Min-Hui Hsu et al.•International Journal of…•2014

  • "Exempt" Research after the Privacy Rule

    Mark Barnes, Katherine E Gallin•IRB Ethics and Human Research•2003

Unique citing works1
Citations per year0,08
Citation span2014 - 2014 (1)
Citation velocityhistorical
Highly citedNo
Citation typesNeutral: 1

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Open DOISci-Hub
Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae