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SMART-REFERRAL

Context-Aware Patient Record Summaries for Cross-Provider Referral Care
Targeted call
ITEA 4
Proposal deadline
2 November 2026
Target number of partners
10–15
Proposal coordinator
Replika PRO, Slovenia
Contact us
Irena Mesarič, project manager
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Challenge

When a patient is referred to a specialist clinic, the receiving physician typically gets almost no information — just the referral slip and a short note explaining why the patient was sent. Electronic health records often contain only a few sentences of usable history: past analyses, examinations, treatments and laboratory results are scattered across providers, locked in non-interoperable systems, or never digitised at all.

The consequences are repeated tests, missed clinically relevant history, slower and lower-quality clinical decisions, and unnecessary cost. The problem is equally acute in Slovenia, the Netherlands and most other European health systems, because the root cause is not missing digitalisation but the missing intelligent selection, structuring and transfer of data that already exists.

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Solution

The project will build a privacy-preserving platform that generates a structured, context-aware summary of the patient's health record at the moment of referral. Instead of transferring the full history, the platform intelligently selects and organises what is relevant to the reason for referral: completed analyses and examinations, past treatments, relevant laboratory results and trends, and tests that would be pointless to repeat.

An AI document-understanding module converts handwritten and non-digitised records into usable data. The core summarisation and transfer logic is shared across the consortium, while each partner adapts the solution to its national health system — making the project modular and resilient by design, with GDPR-compliant exchange and transparent access control as first-class requirements.

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Main activities

The consortium will develop a context-aware summarisation engine that ranks record content by relevance to the referral reason, together with multi-source health data collection and structuring for the receiving system based on HL7 FHIR and IHE interoperability. Trend highlighting, clinical alerts and duplicate-test prevention will surface what matters — for example flagging repeated laboratory visits in the past two months. An AI module for reading handwritten and non-digitised medical records will recover otherwise inaccessible history. Secure, GDPR-compliant health-data exchange with transparent access control will be designed in from the start, and national-system adaptation modules will be built per partner country. Referral-pathway pilots will run in Slovenia and the Netherlands, integrated with multidisciplinary council workflows.

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Consortium status
  • Open Line Vitaly d.o.o. — Industrial coordinator (project coordinator)
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Partners sought
  • Clinical pilot site — Provide the real referral pathways, clinical requirements, access to representative workflows and validation environments. They define what information is clinically relevant for different referral reasons, test the summaries, assess usability and quantify reduction of repeated tests or missing information. At least one clinical pilot partner is needed in Slovenia and one in the Netherlands, preferably covering both referring and receiving-care perspectives.
  • Interoperability partner — Develops the health-data collection, structuring and exchange layer using HL7 FHIR, IHE profiles and connections to national or provider-level systems. Handles integration with EHRs, referral systems, laboratory systems and receiving-clinic workflows. This partner is essential because the core problem is not only AI summarisation but safe transfer of structured data across fragmented systems.
  • AI provider — Builds the context-aware summarisation, relevance ranking, trend detection and duplicate-test prevention logic. Also develops or adapts document-understanding components for handwritten, scanned and non-digitised medical records. This role should bring strong NLP, medical AI, OCR/document AI and clinical-data modelling expertise.
  • Research organisation — Provides methodological support for clinical informatics, evaluation design, explainability, privacy-preserving AI and evidence generation. Helps define validation metrics such as summary relevance, clinician time saved, avoided duplicate tests, data completeness and safety of recommendations. This role strengthens credibility but should remain applied and closely linked to pilots, not purely academic.
  • Security partner — Ensures GDPR-compliant data exchange, access control, auditability, consent or legal-basis handling, and secure deployment across national settings. This role can be a separate partner if the consortium lacks in-house expertise, or covered by the industrial coordinator/interoperability partner if they have proven health-data security capabilities. It is particularly important because cross-provider referral summaries involve sensitive health data and trust is central to adoption.
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