The Legality of Collecting and Disclosing Patient Race and Ethnicity Data

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dc.contributor.authorRosenbaum, Saraen
dc.contributor.authorBurke, Tayloren
dc.contributor.authorNath, Sonia W.en
dc.contributor.authorThomas, Danaen
dc.contributor.authorSantos, Jenniferen
dc.coverage.spatialUnited Statesen
dc.date.accessioned2010-03-31T15:51:13Z
dc.date.accessioned2024-07-23T20:50:27Z
dc.date.available2010-03-31T15:51:13Z
dc.date.available2024-07-23T20:50:27Z
dc.date.issued2006-06-22en
dc.description.abstractExamines the legal liability of collecting and reporting race and ethnicity data as part of healthcare quality improvement. Recommends establishing government guidelines to encourage the development of better practices for delivering quality health care.en
dc.description.relatedorganizationsGeorge Washington University. School of Public Health and Health Servicesen
dc.identifier.citationhttp://www.rwjf.org/files/publications/other/RaceEthnicDisparitiesData06222006.pdfen
dc.identifier.otherfdc26400001en
dc.identifier.urihttps://hdl.handle.net/10244/527
dc.language.isoen_USen
dc.publisherRobert Wood Johnson Foundationen
dc.publisher.fundingsourcesRobert Wood Johnson Foundationen
dc.subjectHealthen
dc.subjectSocial Science, Ethnic Studiesen
dc.titleThe Legality of Collecting and Disclosing Patient Race and Ethnicity Dataen
dc.typeResearch Reportsen
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