Abstract

BackgroundThe aim of the German Medical Informatics Initiative is to establish a national infrastructure for integrating and sharing health data. To this, Data Integration Centers are set up at university medical centers, which address data harmonization, information security and data protection. To capture patient consent, a common informed consent template has been developed. It consists of different modules addressing permissions for using data and biosamples. On the technical level, a common digital representation of information from signed consent templates is needed. As the partners in the initiative are free to adopt different solutions for managing consent information (e.g. IHE BPPC or HL7 FHIR Consent Resources), we had to develop an interoperability layer.MethodsFirst, we compiled an overview of data items required to reflect the information from the MII consent template as well as patient preferences and derived permissions. Next, we created entity-relationship diagrams to formally describe the conceptual data model underlying relevant items. We then compared this data model to conceptual models describing representations of consent information using different interoperability standards. We used the result of this comparison to derive an interoperable representation that can be mapped to common standards.ResultsThe digital representation needs to capture the following information: (1) version of the consent, (2) consent status for each module, and (3) period of validity of the status. We found that there is no generally accepted solution to represent status information in a manner interoperable with all relevant standards. Hence, we developed a pragmatic solution, comprising codes which describe combinations of modules with a basic set of status labels. We propose to maintain these codes in a public registry called ART-DECOR. We present concrete technical implementations of our approach using HL7 FHIR and IHE BPPC which are also compatible with the open-source consent management software gICS.ConclusionsThe proposed digital representation is (1) generic enough to capture relevant information from a wide range of consent documents and data use regulations and (2) interoperable with common technical standards. We plan to extend our model to include more fine-grained status codes and rules for automated access control.

Highlights

  • The aim of the German Medical Informatics Initiative is to establish a national infrastructure for integrating and sharing health data

  • The German Medical Informatics Initiative (MII) is a largescale, long-term strategic funding program by the German Federal Ministry of Education and Research to establish a nationwide infrastructure for the re-use and sharing of health data to improve health care and research [1, 2]

  • Data elements The result of our analysis showed that in order to be able to derive permissions and restrictions regarding the use of data on the basis of the MII Informed Consent Template, the digital representation should be able to capture at least the following data elements:

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Summary

Introduction

The aim of the German Medical Informatics Initiative is to establish a national infrastructure for integrating and sharing health data. The German Medical Informatics Initiative (MII) is a largescale, long-term strategic funding program by the German Federal Ministry of Education and Research to establish a nationwide infrastructure for the re-use and sharing of health data to improve health care and research [1, 2]. For this purpose, Data Integration Centers (DICs) are being set up at academic medical centers, which harmonize and integrate data on the local level and support processes for interinstitutional data sharing. This work is carried out in close cooperation with both the WG biobanking of the permanent Working Party of the German Medical Ethics Committees [10] and the WG Science of the federal data protection representatives

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