HL7 Version 3 offers a semantically robust method for healthcare interoperability but has been criticized as overly complex to implement. This paper reviews initiatives to simplify HL7 Version 3 messaging and presents a novel approach based on semantic mapping. Based on user-defined definitions, precise transforms between simple and full messages are automatically generated. Systems can be interfaced with the simple messages and achieve interoperability with full Version 3 messages through the transforms. This reduces the costs of HL7 interfacing and will encourage better uptake of HL7 Version 3 and CDA.
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Stud Health Technol Inform
November 2024
Medical University of Vienna, Center for Medical Data Science, Institute of Artificial Intelligence, Spitalgasse 23, 1090 Vienna, Austria.
The Arden Syntax is a language designed for the encoding of medical knowledge into clinical decision support systems. Its evolution is overseen by Health Level 7. A significant enhancement in its new version 3.
View Article and Find Full Text PDFJMIR Med Inform
October 2024
IT Center for Clinical Research, University of Luebeck, Luebeck, Germany.
Stud Health Technol Inform
August 2024
Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Core Facility Digital Medicine and Interoperability, Charitéplatz 1, 10117 Berlin, Germany.
This work presents the Fast Healthcare Interoperability Resources (FHIR®) specification of the NFDI4Health Metadata schema based on FHIR Version 4: We created 16 profiles to facilitate the integration of clinical, epidemiological, and public health study data. Despite challenges arising from the extensive MDS as well as missing concepts in semantic standards, it marks a significant advance in applying information technology standards to health research.
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August 2024
Core Facility Digital Medicine and Interoperability, Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Germany.
The National Research Data Infrastructure for Personal Health Data (NFDI4Health) uses Local Data Hubs (LDHs) to manage locally research studies, documents and sensitive personal data to support controlled data sharing. While research data management (RDM) systems facilitate the storage and preparation of data and metadata as well as organizational access, they often lack support for interoperability standards of the application domain. To support the exchange with external registries of research studies, we chose 17 attributes to characterize the most relevant aspects of clinical trials (in the following named "metadata profile").
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August 2024
German Childhood Cancer Registry, IMBEI, University Medical Center Mainz, Germany.
Innovation in cancer therapy has increased childhood cancer survival rates. However, survivors are still at risk of developing late effects. In the digital transformation of the health sector, the Survivorship Passport (SurPass) can support long-term follow-up care plans.
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