Literature DB >> 21169618

Never too old for anonymity: a statistical standard for demographic data sharing via the HIPAA Privacy Rule.

Bradley Malin1, Kathleen Benitez, Daniel Masys.   

Abstract

OBJECTIVE: Healthcare organizations must de-identify patient records before sharing data. Many organizations rely on the Safe Harbor Standard of the HIPAA Privacy Rule, which enumerates 18 identifiers that must be suppressed (eg, ages over 89). An alternative model in the Privacy Rule, known as the Statistical Standard, can facilitate the sharing of more detailed data, but is rarely applied because of a lack of published methodologies. The authors propose an intuitive approach to de-identifying patient demographics in accordance with the Statistical Standard.
DESIGN: The authors conduct an analysis of the demographics of patient cohorts in five medical centers developed for the NIH-sponsored Electronic Medical Records and Genomics network, with respect to the US census. They report the re-identification risk of patient demographics disclosed according to the Safe Harbor policy and the relative risk rate for sharing such information via alternative policies. MEASUREMENTS: The re-identification risk of Safe Harbor demographics ranged from 0.01% to 0.19%. The findings show alternative de-identification models can be created with risks no greater than Safe Harbor. The authors illustrate that the disclosure of patient ages over the age of 89 is possible when other features are reduced in granularity. LIMITATIONS: The de-identification approach described in this paper was evaluated with demographic data only and should be evaluated with other potential identifiers.
CONCLUSION: Alternative de-identification policies to the Safe Harbor model can be derived for patient demographics to enable the disclosure of values that were previously suppressed. The method is generalizable to any environment in which population statistics are available.

Entities:  

Mesh:

Year:  2011        PMID: 21169618      PMCID: PMC3005867          DOI: 10.1136/jamia.2010.004622

Source DB:  PubMed          Journal:  J Am Med Inform Assoc        ISSN: 1067-5027            Impact factor:   4.497


  23 in total

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8.  Beyond Safe Harbor: Automatic Discovery of Health Information De-identification Policy Alternatives.

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  27 in total

1.  Ethical and practical challenges of sharing data from genome-wide association studies: the eMERGE Consortium experience.

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2.  iDASH: integrating data for analysis, anonymization, and sharing.

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3.  Data governance requirements for distributed clinical research networks: triangulating perspectives of diverse stakeholders.

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4.  R-U policy frontiers for health data de-identification.

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8.  SHARE: system design and case studies for statistical health information release.

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Review 9.  A review of the role of electronic health record in genomic research.

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10.  Examining Data Repository Guidelines for Qualitative Data Sharing.

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