Møte 32 i FHIR fagforum
- Dato: 2025-10-22
- Klokkeslett: 1300-1500
- 66 personer innom møtet virtuelt (3 i møterom på Helsedirektoratet)
FHIR fagforum (FFF) er et åpent forum om bruk og implementering av HL7 FHIR i Norge. FFF er åpent for alle.
Agenda: EHDS on FHIR
- Welcome, Thomas og Info from HL7 Norway Øyvind, 10 min
- EHDS and Xt-EHR work in Norway, 20 min, Morten Bakken og Kerstin Engelhardt (Helsedirektoratet)
- EEHRxF FHIR profiling in the EU, 30 min, Giorgio Cangioli (HL7 Europe)
- Profiling of EEHRxF format in Norway, 30 min, Linn Brandt (Helsedirektoratet)
- EHDS – 20 år for sent i Norsk helsetjeneste?, 30 min, Eirik Nikolai Arnesen (Legeforeningen)
Presentations
- FHIR fagforum intro
- EHDS and Xt-EHR work in Norway
- EEHRxF FHIR profiling in the EU
- Profiling of EEHRxF format in Norway
- EHDS – 20 år for sent i Norsk helsetjeneste?
Info from HL7 Norge
- HL7 Norge og Hackathon - registrere deg nå
- WGM deltakelse Køln desember
EHDS and Xt-EHR work in Norway
- EHDS
- History from 2008- 2027
- Cross border healthcare directive legal basis for patient mobility.
- eHDSI infrastructure 2015
- Commission release the implementing acts.
- EU4Health primary use of health data XtEHR project
- Norwegian directorate of healht are appointed as expert organization
- Participate on behalf of Norway in the XtEHR work.
- Extended comunication to the stakeholders in Norway
- Organizing feedback throug stakeholder involvment process.
- EEHRxF (or The format)
- Prioritized categories: patient summary, HDR etc.
- Choice of technical standards for EEHRxF
- recommend HL7 FHIR as recommended standard for interoperability
- Use cases in EEHRxF
- download
- transmit for portability
- exhange cross border
- Harmonized interoperability component
- Projects for developing the format
- Logical models vs XtEHR FHIR technical IG’s
- Guideline level are released from the commission.
- HL7 Europe draft the implementation profiles
- EURIDICE - HL7 and IHE profiles
EEHRxF FHIR profiling in the EU
- Started presenting lab report IG 18 months ago…
- Focus on the FHIR IG’s developed by HL7 Europe for EHDS
- The European “Format”
- Prioritized categories
- The format will be formally defined by European Commission in the implementing act
- Based on the artefacts available today how can we defined these artifacts
- European wide FHIR IG’s
- EEHRxF as of today, as defined by the FHIR IG’s published.
- FHIR IG ecosystem
- FHIR IG for all the prioritized categories
- Latest releases of the IG’s
- Content of the guides
- Extension package
- common extensions for use in the other IG’s
- Base og core profiles
- Base and core profiles of HL7 Europe
- base loosely defined
- Core - essential constraints that can be reused across profiles.
- Align with IPS.
- Base and core profiles of HL7 Europe
- Lab report already v1.1
- Balancing different requirements
- Balance requirements from many countries
- Medication Prescription and dispense
- R4, R5, and pharmacy
- EHDS logical models input have to be taken into account.
- Situations adressed
- multi item prescription
- indication
- additional health info
- etc.
- Prescription is not documents, but always structured
- Hospital Discharge report
- HDR R4 IG
- Flexible section structure
- Flat structure as reusable section library
- Sections can be organized flat or nested
- Key principles
- Few required sections
- open slicing
- sub sections allowed
- to achieve
- local adapt
- standardized content model
- consistency
- Section entry optional
- strongly recommend to use structured data.
- Imaging study report
- informal cooperation effort with HL7 int, IHE Europe and IHE int.
- Multi version guide both R4 and R5
- Imaging study
- Umaging workflow
- imaging generated
- result DICOM imaging study
- Stored in PACS
- Radiologist reads the Imaging study
- Typically stored in EHR/PACS
- Imating manifest information required to access imaging study
- imaging report - holds the imaging report (data from RIS)
- Imaging report use the same principles as lab report
- individual resources, but available as a bundle
- IHE radiology profile
- Result of EUDICIE coop
- Umaging workflow
- Patient summary
- IPS 2.0 based
- FHIR IGs overview
- You can join in the coop effort to make the HL7 Europe IG work.
- Schedule for bi weekly meetings in HL7 Europe
- Please contact HL7 europe og europe channel on zulip
- WGM in Køln in Desember
Profiling of EEHRxF format in Norway
- EHDS regulation is not specifically on FHIR, what technology and standards to use is decided in the implementing acts.
- We do know that MyHealth@EU have chosen all new work to be FHIR
- Joint action work propose FHIR profiles
- We use FHIR for interoperability in Norway and Europe already
- EEHRxF will support multiple use-cases
- National use cases that needs to support the national infrastructure and implementation?
- National additions to the EU format
- Will HL7 Norway have a role in developing implementable IG’s for use in Norway
- Government functions to be established
- Digital HEalth Authority
- Rights and obligations to be implemented
- ensure that exchange is possible
- Marked surveillance authority
- supervise EHR vendors to implement according to regulation
- Digital HEalth Authority
- Directorate of Health
- Will get some new tasks conceringn DHA and MSA
- The directorate do not publish fhir Profiles
- HL7 Norway
- HL7 Norway publish FHIR profiles
- official representative in the international standardization of HL7
- non profit and no employees
- NHN
- Do publish some FHIR profiles
- responsible for NCP in Norway (technical)
- Other actors like vendors, Health regions etc.
- Collaboration model for international standards
- Goverment
- National vs implemented IGs in Norway
- no-basis - will it need some alignment in EEHRxF?
- Should it be
- Who will maintain the norwegian/EEHRxF framework
- no-basis - will it need some alignment in EEHRxF?
Q: coop IHE and HL7 A: Have to consider IHE for testing and alignment.
Q: How to sell products in Norway and europe A:
Q: What level of norwegian profileing should we aim at A: Not really anchored in the healthcre organization - do we need to develop a new way to exchange the data we already do with norwegian messages today.
A: How to transition from what we have today into the future and with the EHDS and XtEHRF implemented.
A: The european level does not define everything relevant to all norwegian use-cases. We do need some norwegian guides.
EHDS – 20 år for sent i Norsk helsetjeneste?
- Devils advocate high level perspectives from the clinicians in Norway
- Medical practice is built by the clinicians
- EHDS will have huge impact on clinicians in Norway
- Pan-european interoperability idea is not new.
- The concept is supported by clinicians
- Will it improve healthcare processes and patient outcomes?
- Are there any benefits for Norwegian healthcare sector
- clinicans burden (documentation)
- Primary use at Myhealth@EU
- Secondary use
- WG’s that work on the technical standards and guidelines
- Work going on in Norway
- GAP analysis economical and admin consequences
- GAP analysis and socioeconomical analysis of the EHDS impact
- The Clinicians in Norway have worked with Helsedirektoratet in EHDS work
- EHR system is the doctor’s most importan tool
- Reduce the number of structured data elements
- They disturb the clinicians way of thinking and working
- Want avoid componants strictly for secondary use.
- The EHDS regulation
- Will be expensive
- Prescriptions in Norway are mostly electronic total 69 millions prescriptions eacy year
- Just a little more time pr. prescriptions would lead to a lot of extra work for the clinicians to cater for a few european prescriptions
- Patient medication list work in progress for 7-8 years
- In denmark they estimated cost for development to 1 billion euros
- Lack of personell
- Digitalization might save time and money if you do it correctly and cater for clinicans needs.
- Usability of norwegian EHR’s
- Corrolation between burnout of clinicans and workloads, usability has to be good in the tools the clinicians use the most like EHR’s
- Clinicians do not need standards that interferes with the clinicians work that makes that work more time consuming.
- Documentation work is increasing in some cases
- Interoperability and the EIF
- EHDS is a lot about technical standards
- The hard part is practical interoperability, organizational interoperability
- Is it relevant to try to align the processes in all of europe?
- Concerned about going directly into technical specification without considering the process differences.
Comment: the eHDS standardization will disrupt some work processess A: Flexibility to different workflows.
Clinicians involvement Two books about medical records and clinical informatics worth reading:
- Bjørn Bentz on how to write medical records
- Petter Hurlen about clinical informatics