Literature DB >> 22287248

Anonymization of longitudinal electronic medical records.

Acar Tamersoy1, Grigorios Loukides, Mehmet Ercan Nergiz, Yucel Saygin, Bradley Malin.   

Abstract

Electronic medical record (EMR) systems have enabled healthcare providers to collect detailed patient information from the primary care domain. At the same time, longitudinal data from EMRs are increasingly combined with biorepositories to generate personalized clinical decision support protocols. Emerging policies encourage investigators to disseminate such data in a deidentified form for reuse and collaboration, but organizations are hesitant to do so because they fear such actions will jeopardize patient privacy. In particular, there are concerns that residual demographic and clinical features could be exploited for reidentification purposes. Various approaches have been developed to anonymize clinical data, but they neglect temporal information and are, thus, insufficient for emerging biomedical research paradigms. This paper proposes a novel approach to share patient-specific longitudinal data that offers robust privacy guarantees, while preserving data utility for many biomedical investigations. Our approach aggregates temporal and diagnostic information using heuristics inspired from sequence alignment and clustering methods. We demonstrate that the proposed approach can generate anonymized data that permit effective biomedical analysis using several patient cohorts derived from the EMR system of the Vanderbilt University Medical Center.

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Year:  2012        PMID: 22287248      PMCID: PMC3779068          DOI: 10.1109/TITB.2012.2185850

Source DB:  PubMed          Journal:  IEEE Trans Inf Technol Biomed        ISSN: 1089-7771


  28 in total

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3.  A globally optimal k-anonymity method for the de-identification of health data.

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Journal:  J Am Med Inform Assoc       Date:  2009-06-30       Impact factor: 4.497

4.  The disclosure of diagnosis codes can breach research participants' privacy.

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5.  Anonymization of administrative billing codes with repeated diagnoses through censoring.

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6.  Myocardial infarction and the validation of physician billing and hospitalization data using electronic medical records.

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Review 8.  Adopting electronic medical records in primary care: lessons learned from health information systems implementation experience in seven countries.

Authors:  D A Ludwick; John Doucette
Journal:  Int J Med Inform       Date:  2008-07-21       Impact factor: 4.046

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10.  Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip.

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  6 in total

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2.  Reducing patient re-identification risk for laboratory results within research datasets.

Authors:  Ravi V Atreya; Joshua C Smith; Allison B McCoy; Bradley Malin; Randolph A Miller
Journal:  J Am Med Inform Assoc       Date:  2012-07-21       Impact factor: 4.497

3.  Getting personal: understanding how genetic variation affects clinical outcomes in patients with tetralogy of Fallot.

Authors:  Mark W Russell; Nicole S Wilder
Journal:  Pediatr Res       Date:  2012-10       Impact factor: 3.756

4.  Privacy Policy and Technology in Biomedical Data Science.

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Journal:  Annu Rev Biomed Data Sci       Date:  2018-07

5.  Secondary use of clinical data: the Vanderbilt approach.

Authors:  Ioana Danciu; James D Cowan; Melissa Basford; Xiaoming Wang; Alexander Saip; Susan Osgood; Jana Shirey-Rice; Jacqueline Kirby; Paul A Harris
Journal:  J Biomed Inform       Date:  2014-02-14       Impact factor: 6.317

Review 6.  Use and Understanding of Anonymization and De-Identification in the Biomedical Literature: Scoping Review.

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Journal:  J Med Internet Res       Date:  2019-05-31       Impact factor: 5.428

  6 in total

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