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. 2013 Oct 5:13:114.
doi: 10.1186/1472-6947-13-114.

Evaluating the risk of patient re-identification from adverse drug event reports

Affiliations

Evaluating the risk of patient re-identification from adverse drug event reports

Khaled El Emam et al. BMC Med Inform Decis Mak. .

Abstract

Background: Our objective was to develop a model for measuring re-identification risk that more closely mimics the behaviour of an adversary by accounting for repeated attempts at matching and verification of matches, and apply it to evaluate the risk of re-identification for Canada's post-marketing adverse drug event database (ADE).Re-identification is only demonstrably plausible for deaths in ADE. A matching experiment between ADE records and virtual obituaries constructed from Statistics Canada vital statistics was simulated. A new re-identification risk is considered, it assumes that after gathering all the potential matches for a patient record (all records in the obituaries that are potential matches for an ADE record), an adversary tries to verify these potential matches. Two adversary scenarios were considered: (a) a mildly motivated adversary who will stop after one verification attempt, and (b) a highly motivated adversary who will attempt to verify all the potential matches and is only limited by practical or financial considerations.

Methods: The mean percentage of records in ADE that had a high probability of being re-identified was computed.

Results: Under scenario (a), the risk of re-identification from disclosing the province, age at death, gender, and exact date of the report is quite high, but the removal of province brings down the risk significantly. By only generalizing the date of reporting to month and year and including all other variables, the risk is always low. All ADE records have a high risk of re-identification under scenario (b), but the plausibility of that scenario is limited because of the financial and practical deterrent even for highly motivated adversaries.

Conclusions: It is possible to disclose Canada's adverse drug event database while ensuring that plausible re-identification risks are acceptably low. Our new re-identification risk model is suitable for such risk assessments.

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Figures

Figure 1
Figure 1
Example to illustrate how the percentage of ADE records at risk are computed from the matched equivalence classes. In this example we assume there are only two quasi-identifying attributes: age at death and gender.
Figure 2
Figure 2
Plot showing how the re-identification risk, R j , varies with the number of attempts ( M ) and the probability of being able to verify a match ( p ).
Figure 3
Figure 3
An example illustrating how province is assigned to the ADE dataset from the virtual obituary file.
Figure 4
Figure 4
The relationship between M, p, and k.

References

    1. El Emam K. Guide to the de-identification of personal health information. Auerbach: CRC Press; 2013.
    1. Canadian Newspaper Association. National Freedom of Information Audit. 2007. [Online]. Available: http://www.newspaperscanada.ca/public-affairs/freedom-information.
    1. El Emam K, Jonker E, Arbuckle L, Malin B. A systematic review of re-identification attacks on health data. PLoS ONE. 2011;13(12):e28071. doi: 10.1371/journal.pone.0028071. - DOI - PMC - PubMed
    1. Health Canada. Canada Vigilance Adverse Reaction Online Database. 2013. [Online]. Available: http://www.hc-sc.gc.ca/dhp-mps/medeff/databasdon/index-eng.php.
    1. Health Canada. Canada Vigilance Program. 2009. [Online]. Available: http://hc-sc.gc.ca/dhp-mps/medeff/vigilance-eng.php.

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