Methods Inf Med 2011; 50(04): 326-336
DOI: 10.3414/ME10-01-0075
Original Articles
Schattauer GmbH

A Model-driven Privacy Compliance Decision Support for Medical Data Sharing in Europe

Boussi H. Rahmouni
1   Bristol Institute of Technology, University of the West of England, Bristol, UK
,
T. Solomonides
1   Bristol Institute of Technology, University of the West of England, Bristol, UK
,
Casassa M. Mont
2   HP Labs, Bristol, UK
,
S. Shiu
2   HP Labs, Bristol, UK
,
M. Rahmouni
2   HP Labs, Bristol, UK
› Institutsangaben
Weitere Informationen

Publikationsverlauf

received: 17. Oktober 2010

accepted: 07. März 2011

Publikationsdatum:
18. Januar 2018 (online)

Summary

Objectives: Clinical practitioners and medical researchers often have to share health data with other colleagues across Europe. Privacy compliance in this context is very important but challenging. Automated privacy guidelines are a practical way of increasing users’ awareness of privacy obligations and help eliminating unintentional breaches of privacy. In this paper we present an ontology-plus-rules based approach to privacy decision support for the sharing of patient data across European platforms.

Methods: We use ontologies to model the required domain and context information about data sharing and privacy requirements. In addition, we use a set of Semantic Web Rule Language rules to reason about legal privacy requirements that are applicable to a specific context of data disclosure. We make the complete set invocable through the use of a semantic web application acting as an interactive privacy guideline system can then invoke the full model in order to provide decision support.

Results: When asked, the system will generate privacy reports applicable to a specific case of data disclosure described by the user. Also reports showing guidelines per Member State may be obtained.

Conclusion: The advantage of this approach lies in the expressiveness and extensibility of the modelling and inference languages adopted and the ability they confer to reason with complex requirements interpreted from high level regulations. However, the system cannot at this stage fully simulate the role of an ethics committee or review board.