16:00 Uhr
Patientensicherheit: eine kritische Überprüfung von Herstellerangaben zum Hämolyse-Index
17:15 Uhr
P-08-03/FV-05:
AI in smart laboratory processes - medical values and smartLIS
D. Pechermeyer (Hamburg, DE)
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Autor:innen:
D. Pechermeyer (Hamburg, DE)
J. Kirchhoff (Karlsruhe, DE)
Introduction / Objectives
The power of modern laboratory medicine allows a wide range of analytes and measurements. In the short time available, it is not always possible for the sender to exhaust the complete diagnostic potential and also to consider new, innovative analytes. The focus is on targeted and personalized diagnostics for patients.
We want to show how networking of controlled requisition/CDS in the laboratory order system with processing in the laboratory system and guided validation in the practice can function, where added value is created and content can be managed.
The special feature here is the connection of an AI system with the process in the LIS.
The following 3 areas should be covered:
- Initial request: supporting the physician in selecting correct parameters in an intuitive interface.
- Reporting in the laboratory: support of the laboratory physician in the reporting of findings
- Reporting at the physician's site: information and possibilities for targeted reflex testing
Change management in the laboratory and at the sender will also be addressed.
Results
Using the example of different areas such as endocrinology, coagulation and infectiology, it will be shown how on the one hand
- Medical guidelines
- Requirement in accordance with guidelines
- Formal principles (EBM rules)
can be taken into account in the request, thus preventing or avoiding inquiries and incorrect requests, and on the other hand how the laboratory physician can be supported in the validation of the results.
Discussion and conclusion
For a sustainable implementation, international standards and interfaces such as FHIR and LOINC were used. This is supported by a modern software architecture, but also by a cooperative approach / mindset among all project participants. The presentation will also critically examine and discuss the medical device requirements.