{
 "id": "vgl-fhir-openehr-omop",
 "url": "/vgl-fhir-openehr-omop/",
 "md_url": "/vgl-fhir-openehr-omop.md",
 "json_url": "/vgl-fhir-openehr-omop.json",
 "claims_url": "/vgl-fhir-openehr-omop/beweringen/",
 "type": {
  "code": "Topic",
  "label": "Overzicht of dossier"
 },
 "schema_type": "Thing",
 "title": "FHIR, openEHR en OMOP: vergelijking",
 "aliases": [
  "FHIR vs openEHR vs OMOP",
  "FHIR, openEHR en OMOP CDM",
  "uitwisseling vs persistentie vs analyse"
 ],
 "names": {
  "nl": "FHIR, openEHR en OMOP: vergelijking",
  "fr": "FHIR, openEHR et OMOP : comparaison",
  "en": "FHIR, openEHR and OMOP compared",
  "de": null
 },
 "jurisdiction": [
  {
   "code": "internationaal",
   "label": "Internationaal"
  },
  {
   "code": "eu",
   "label": "Europese Unie"
  },
  {
   "code": "belgie",
   "label": "België (federaal/interfederaal)"
  }
 ],
 "themes": [
  {
   "code": "architectuur-en-infrastructuur",
   "label": "Architectuur en infrastructuur"
  },
  {
   "code": "terminologie",
   "label": "Terminologie en codering"
  },
  {
   "code": "secundair-gebruik",
   "label": "Secundair datagebruik en registers"
  }
 ],
 "lifecycle": {
  "code": "onbekend",
  "label": "onbekend"
 },
 "lifecycle_note_html": "Niet van toepassing (vergelijkingspagina); de status per standaard staat in de tabel en op de eigen pagina's. Mappings FHIR→OMOP (HL7-IG v1.0.0, Informative) en openEHR↔FHIR (IG in ontwikkeling, onderzoeksprototypes) verschillen sterk in maturiteit.",
 "version": null,
 "vendor": null,
 "sectors": [],
 "homologations": [],
 "summary_text": "FHIR, openEHR en OMOP CDM dienen verschillende doelen: FHIR voor uitwisseling, openEHR voor klinische modellering en persistentie in het EPD, OMOP CDM voor longitudinale analyse en secundair gebruik. Bronnen (HL7 Vulcan FHIR-to-OMOP IG, JMIR 2023/2025) noemen ze complementair. SNOMED CT en LOINC vormen de gedeelde semantische laag. Transformaties zijn niet verliesvrij. De EHDS-verordening laat de Commissie tegen 26 maart 2027 de technische specificaties van een uitwisselingsformaat (EEHRxF) vastleggen; de uitwisselingsverplichtingen gelden gefaseerd vanaf 26 maart 2029 en 2031. België pleit voor één FHIR-standaard per berichttype; of de uitvoeringshandelingen FHIR normatief voorschrijven, is nog open. Voor openEHR en OMOP werd geen EHDS-verplichting gevonden; OMOP was in de HealthData@EU-pilot een optie.",
 "summary_html": "<p>FHIR, openEHR en OMOP CDM dienen verschillende doelen: FHIR voor uitwisseling, openEHR voor klinische modellering en persistentie in het EPD, OMOP CDM voor longitudinale analyse en secundair gebruik. Bronnen (HL7 Vulcan FHIR-to-OMOP IG, JMIR 2023/2025) noemen ze complementair. SNOMED CT en LOINC vormen de gedeelde semantische laag. Transformaties zijn niet verliesvrij. De EHDS-verordening laat de Commissie tegen 26 maart 2027 de technische specificaties van een uitwisselingsformaat (EEHRxF) vastleggen; de uitwisselingsverplichtingen gelden gefaseerd vanaf 26 maart 2029 en 2031. België pleit voor één FHIR-standaard per berichttype; of de uitvoeringshandelingen FHIR normatief voorschrijven, is nog open. Voor openEHR en OMOP werd geen EHDS-verplichting gevonden; OMOP was in de HealthData@EU-pilot een optie.</p>",
 "last_verified": "2026-09-26",
 "verification_outdated": false,
 "sections": [
  {
   "id": "vraag-of-patroon",
   "title": "Vraag of patroon",
   "kind": "tekst",
   "html": "<p>Welke rol spelen <a href=\"/fhir/\">HL7 FHIR</a>, openEHR en <a href=\"/omop-cdm/\">OMOP CDM</a> naast elkaar, en wat moet een Vlaams ziekenhuis ervan\nkennen in het licht van de <a href=\"/ehds/\">EHDS (European Health Data Space)</a>? Als kader gebruikt deze pagina de drie datadomeinen van de HL7 FHIR-to-OMOP IG:\nklinische zorg en administratie, data-uitwisseling en longitudinale analyse<sup class=\"cite\" id=\"t-CLM-cfdf8dac\" data-claims=\"CLM-cfdf8dac\"><a class=\"cite-ref\" href=\"#bron-1\" aria-label=\"Bron 1\">[1]</a></sup>. Die IG ziet FHIR en OMOP\nals complementair, niet als concurrenten<sup class=\"cite\" id=\"t-CLM-2dc7d72b\" data-claims=\"CLM-2dc7d72b\"><a class=\"cite-ref\" href=\"#bron-1\" aria-label=\"Bron 1\">[1]</a></sup>. Een expertpanel komt tot dezelfde conclusie voor openEHR,\nISO 13606 en FHIR: elk is nuttig voor een eigen doel en ze zijn samen inzetbaar<sup class=\"cite\" id=\"t-CLM-3ccf652d\" data-claims=\"CLM-3ccf652d\"><a class=\"cite-ref\" href=\"#bron-2\" aria-label=\"Bron 2\">[2]</a></sup>.</p>"
  },
  {
   "id": "vergelijking",
   "title": "Vergelijking",
   "kind": "tekst",
   "html": "<table>\n<thead>\n<tr>\n<th>Dimensie</th>\n<th>HL7 FHIR</th>\n<th>openEHR</th>\n<th>OMOP CDM (OHDSI)</th>\n</tr>\n</thead>\n<tbody>\n<tr>\n<td>Doel</td>\n<td>Elektronische uitwisseling van zorginformatie<sup class=\"cite\" id=\"t-CLM-20ccab31\" data-claims=\"CLM-20ccab31\"><a class=\"cite-ref\" href=\"#bron-3\" aria-label=\"Bron 3\">[3]</a></sup>; domein data-uitwisseling (REST-API, resources)<sup class=\"cite\" id=\"t-CLM-6c1c8ed6\" data-claims=\"CLM-6c1c8ed6\"><a class=\"cite-ref\" href=\"#bron-1\" aria-label=\"Bron 1\">[1]</a></sup></td>\n<td>Scheiden van technische opslag en klinische betekenis, zodat systemen evolueren zonder dataverlies<sup class=\"cite\" id=\"t-CLM-75e965e1\" data-claims=\"CLM-75e965e1\"><a class=\"cite-ref\" href=\"#bron-4\" aria-label=\"Bron 4\">[4]</a></sup>; volledig platformmodel voor registratie, persistentie en querying<sup class=\"cite\" id=\"t-CLM-a5de0448\" data-claims=\"CLM-a5de0448\"><a class=\"cite-ref\" href=\"#bron-2\" aria-label=\"Bron 2\">[2]</a></sup></td>\n<td>Structuur en inhoud van observationele data standaardiseren voor analyse<sup class=\"cite\" id=\"t-CLM-0d763233\" data-claims=\"CLM-0d763233\"><a class=\"cite-ref\" href=\"#bron-5\" aria-label=\"Bron 5\">[5]</a></sup>; domein longitudinale analyse<sup class=\"cite\" id=\"t-CLM-e6250916\" data-claims=\"CLM-e6250916\"><a class=\"cite-ref\" href=\"#bron-1\" aria-label=\"Bron 1\">[1]</a></sup></td>\n</tr>\n<tr>\n<td>Beheer</td>\n<td>HL7 International; in België is HL7 Belgium de affiliate<sup class=\"cite\" id=\"t-CLM-6070feb3\" data-claims=\"CLM-6070feb3\"><a class=\"cite-ref\" href=\"#bron-6\" aria-label=\"Bron 6\">[6]</a></sup>, werken HL7 Belgium-werkgroepen FHIR-profielen uit<sup class=\"cite\" id=\"t-CLM-cef569f6\" data-claims=\"CLM-cef569f6\"><a class=\"cite-ref\" href=\"#bron-7\" aria-label=\"Bron 7\">[7]</a></sup> en publiceert het eHealth-platform FHIR-profielen<sup class=\"cite\" id=\"t-CLM-43dc8f12\" data-claims=\"CLM-43dc8f12\"><a class=\"cite-ref\" href=\"#bron-8\" aria-label=\"Bron 8\">[8]</a></sup></td>\n<td>openEHR International (operationeel, sinds 2019), IP bij de openEHR Foundation<sup class=\"cite\" id=\"t-CLM-f455020e\" data-claims=\"CLM-f455020e\"><a class=\"cite-ref\" href=\"#bron-9\" aria-label=\"Bron 9\">[9]</a></sup>; specificaties CC-BY-ND<sup class=\"cite\" id=\"t-CLM-c6ad972d\" data-claims=\"CLM-c6ad972d\"><a class=\"cite-ref\" href=\"#bron-9\" aria-label=\"Bron 9\">[9]</a></sup></td>\n<td>OHDSI CDM Working Group<sup class=\"cite\" id=\"t-CLM-8016d826\" data-claims=\"CLM-8016d826\"><a class=\"cite-ref\" href=\"#bron-5\" aria-label=\"Bron 5\">[5]</a></sup></td>\n</tr>\n<tr>\n<td>Granulariteit</td>\n<td>De resource is de basisbouwsteen<sup class=\"cite\" id=\"t-CLM-d3f779a6\" data-claims=\"CLM-d3f779a6\"><a class=\"cite-ref\" href=\"#bron-3\" aria-label=\"Bron 3\">[3]</a></sup></td>\n<td>Stabiel referentiemodel met archetypes en templates als domeinniveau<sup class=\"cite\" id=\"t-CLM-5472e46b\" data-claims=\"CLM-5472e46b\"><a class=\"cite-ref\" href=\"#bron-10\" aria-label=\"Bron 10\">[10]</a></sup>; templates vormen volledige Compositions (bv. ontslagbrief)<sup class=\"cite\" id=\"t-CLM-f3a32110\" data-claims=\"CLM-f3a32110\"><a class=\"cite-ref\" href=\"#bron-10\" aria-label=\"Bron 10\">[10]</a></sup></td>\n<td>Persoonsgericht: alle klinische event-tabellen hangen aan PERSON<sup class=\"cite\" id=\"t-CLM-b378c72d\" data-claims=\"CLM-b378c72d\"><a class=\"cite-ref\" href=\"#bron-11\" aria-label=\"Bron 11\">[11]</a></sup></td>\n</tr>\n<tr>\n<td>Querying</td>\n<td>REST-API is een van de mogelijkheden<sup class=\"cite\" data-claims=\"CLM-6c1c8ed6\"><a class=\"cite-ref\" href=\"#bron-1\" aria-label=\"Bron 1\">[1]</a></sup>, maar REST is niet vereist om resources te gebruiken<sup class=\"cite\" id=\"t-CLM-22b16816\" data-claims=\"CLM-22b16816\"><a class=\"cite-ref\" href=\"#bron-3\" aria-label=\"Bron 3\">[3]</a></sup></td>\n<td>AQL<sup class=\"cite\" id=\"t-CLM-8025c8fd\" data-claims=\"CLM-8025c8fd\"><a class=\"cite-ref\" href=\"#bron-10\" aria-label=\"Bron 10\">[10]</a></sup></td>\n<td>Relationeel model, realiseerbaar in elke relationele database (bv. SQL-databanken)<sup class=\"cite\" id=\"t-CLM-5eaebd11\" data-claims=\"CLM-5eaebd11\"><a class=\"cite-ref\" href=\"#bron-11\" aria-label=\"Bron 11\">[11]</a></sup>; geen aparte querytaal in de bronnen gevonden</td>\n</tr>\n<tr>\n<td>Maturiteit en versie</td>\n<td>R5 (5.0.0) is de huidige versie<sup class=\"cite\" id=\"t-CLM-9566eb8c\" data-claims=\"CLM-9566eb8c\"><a class=\"cite-ref\" href=\"#bron-12\" aria-label=\"Bron 12\">[12]</a></sup>; R4 (4.0.1) mengt normatieve en STU-inhoud<sup class=\"cite\" id=\"t-CLM-1badcbfb\" data-claims=\"CLM-1badcbfb\"><a class=\"cite-ref\" href=\"#bron-13\" aria-label=\"Bron 13\">[13]</a></sup></td>\n<td>Architecture Overview BASE 1.2.0, status STABLE<sup class=\"cite\" id=\"t-CLM-f00aa165\" data-claims=\"CLM-f00aa165\"><a class=\"cite-ref\" href=\"#bron-10\" aria-label=\"Bron 10\">[10]</a></sup></td>\n<td>v5.5<sup class=\"cite\" data-claims=\"CLM-8016d826\"><a class=\"cite-ref\" href=\"#bron-5\" aria-label=\"Bron 5\">[5]</a></sup>, enkel optionele toevoegingen t.o.v. v5.4<sup class=\"cite\" id=\"t-CLM-ac400acb\" data-claims=\"CLM-ac400acb\"><a class=\"cite-ref\" href=\"#bron-14\" aria-label=\"Bron 14\">[14]</a></sup></td>\n</tr>\n<tr>\n<td>Rol van terminologie</td>\n<td>Terminologiemodule met CodeSystem, ValueSet, ConceptMap<sup class=\"cite\" id=\"t-CLM-81841f02\" data-claims=\"CLM-81841f02\"><a class=\"cite-ref\" href=\"#bron-15\" aria-label=\"Bron 15\">[15]</a></sup>; elk codesysteem een URL (bv. LOINC, SNOMED)<sup class=\"cite\" id=\"t-CLM-89c84b92\" data-claims=\"CLM-89c84b92\"><a class=\"cite-ref\" href=\"#bron-16\" aria-label=\"Bron 16\">[16]</a></sup></td>\n<td>Archetypes en templates als semantische toegangspoort naar terminologieën<sup class=\"cite\" id=\"t-CLM-19680c4c\" data-claims=\"CLM-19680c4c\"><a class=\"cite-ref\" href=\"#bron-10\" aria-label=\"Bron 10\">[10]</a></sup></td>\n<td>Standardized Vocabularies centraal<sup class=\"cite\" id=\"t-CLM-5068e15a\" data-claims=\"CLM-5068e15a\"><a class=\"cite-ref\" href=\"#bron-5\" aria-label=\"Bron 5\">[5]</a></sup>; één Standard Concept per event, bij aandoeningen SNOMED<sup class=\"cite\" id=\"t-CLM-8b25e1f2\" data-claims=\"CLM-8b25e1f2\"><a class=\"cite-ref\" href=\"#bron-17\" aria-label=\"Bron 17\">[17]</a></sup></td>\n</tr>\n<tr>\n<td>Belgisch gebruik</td>\n<td>Voorkeursstandaard voor nieuwe stromen (sinds het Actieplan e-Gezondheid 2019-2021)<sup class=\"cite\" id=\"t-CLM-a8067de8\" data-claims=\"CLM-a8067de8\"><a class=\"cite-ref\" href=\"#bron-18\" aria-label=\"Bron 18\">[18]</a></sup>; <a href=\"/be-fhir-igs/\">Belgische IG's</a> op R4<sup class=\"cite\" id=\"t-CLM-4c97a5a4\" data-claims=\"CLM-4c97a5a4\"><a class=\"cite-ref\" href=\"#bron-19\" aria-label=\"Bron 19\">[19]</a></sup></td>\n<td>Niet gevonden (gap; betekent niet dat het niet bestaat)</td>\n<td>Belgische OHDSI-node uit de EHDEN-gemeenschap<sup class=\"cite\" id=\"t-CLM-ba340bd5\" data-claims=\"CLM-ba340bd5\"><a class=\"cite-ref\" href=\"#bron-20\" aria-label=\"Bron 20\">[20]</a></sup>; 14 Belgische EHDEN-datapartners<sup class=\"cite\" id=\"t-CLM-23727b49\" data-claims=\"CLM-23727b49\"><a class=\"cite-ref\" href=\"#bron-21\" aria-label=\"Bron 21\">[21]</a></sup></td>\n</tr>\n</tbody>\n</table>\n<p>Volgens een JMIR-artikel (2025) gebruiken FHIR en OMOP dezelfde internationale terminologieën, en past OMOP beter bij\nanalyse dan bij operationele uitwisseling<sup class=\"cite\" id=\"t-CLM-85e934d1\" data-claims=\"CLM-85e934d1\"><a class=\"cite-ref\" href=\"#bron-22\" aria-label=\"Bron 22\">[22]</a></sup>. In de Belgische FHIR-profielen is <a href=\"/snomed-ct/\">SNOMED CT</a> de\nvoorkeurscodering<sup class=\"cite\" id=\"t-CLM-530b635f\" data-claims=\"CLM-530b635f\"><a class=\"cite-ref\" href=\"#bron-23\" aria-label=\"Bron 23\">[23]</a></sup>, en in de Belgische Lab-IG (v1.0.0, trial use) moeten de meeste gangbare\nlabometingen in <a href=\"/loinc/\">LOINC</a> volgens de FOD-subset gecodeerd worden<sup class=\"cite\" id=\"t-CLM-e0e48933\" data-claims=\"CLM-e0e48933\"><a class=\"cite-ref\" href=\"#bron-24\" aria-label=\"Bron 24\">[24]</a></sup>. De registratieclassificatie <a href=\"/icd-10-be/\">ICD-10-BE</a> valt buiten deze drie modellen; in OMOP worden ICD-codes als\nbroncodes op SNOMED-standaardconcepten gemapt<sup class=\"cite\" id=\"t-CLM-71837b87\" data-claims=\"CLM-8b25e1f2 CLM-71837b87\"><a class=\"cite-ref\" href=\"#bron-17\" aria-label=\"Bron 17\">[17]</a></sup>.</p>"
  },
  {
   "id": "mappings-en-informatieverlies",
   "title": "Mappings en informatieverlies",
   "kind": "tekst",
   "html": "<ul>\n<li><strong>FHIR → OMOP</strong>: de HL7 Vulcan FHIR-to-OMOP IG v1.0.0 (Informative, FHIR R5) behandelt enkel die richting, voor een\n  IPA-kern plus Encounter en Procedure (US Core), met CDM v5.4 als doel<sup class=\"cite\" id=\"t-CLM-77f1c57f\" data-claims=\"CLM-77f1c57f\"><a class=\"cite-ref\" href=\"#bron-1\" aria-label=\"Bron 1\">[1]</a></sup>. Een 2.0.0-ballot staat als\n  continuous build online (ontwerp)<sup class=\"cite\" id=\"t-CLM-2eb05c91\" data-claims=\"CLM-2eb05c91\"><a class=\"cite-ref\" href=\"#bron-25\" aria-label=\"Bron 25\">[25]</a></sup>. De IG stelt dat de transformatie niet verliesvrij kan zijn en\n  onderscheidt fideliteits-, informatie-, relatie- en accuraatheidsverlies<sup class=\"cite\" id=\"t-CLM-cd749309\" data-claims=\"CLM-cd749309\"><a class=\"cite-ref\" href=\"#bron-1\" aria-label=\"Bron 1\">[1]</a></sup>.</li>\n<li><strong>openEHR ↔ FHIR</strong>: een implementatiegids die openEHR-datatypes op FHIR-datatypes mapt, is in ontwikkeling (R5; op\n  GitHub in de organisatie openehr-fhir, geconfigureerd als HL7 FHIR IG met publisher HL7 FHIR Infrastructure; een\n  formele HL7-publicatie werd niet vastgesteld)<sup class=\"cite\" id=\"t-CLM-4d28e36b\" data-claims=\"CLM-4d28e36b\"><a class=\"cite-ref\" href=\"#bron-26\" aria-label=\"Bron 26\">[26]</a></sup>. FHIRconnect is een onderzoeksvoorstel (preprint 2025) dat 24 archetypes naar 15 FHIR-profielen mapte\n<sup class=\"cite\" id=\"t-CLM-dc514fc0\" data-claims=\"CLM-dc514fc0\"><a class=\"cite-ref\" href=\"#bron-27\" aria-label=\"Bron 27\">[27]</a></sup>.</li>\n<li><strong>openEHR ↔ OMOP</strong>: geen officiële mappingstandaard gevonden (gap).</li>\n</ul>"
  },
  {
   "id": "wat-de-ehds-wel-en-niet-verplicht",
   "title": "Wat de EHDS wel en niet verplicht",
   "kind": "tekst",
   "html": "<ul>\n<li><strong>Toepassingsdata</strong>: de verordening is van toepassing vanaf 26 maart 2027<sup class=\"cite\" id=\"t-CLM-96d3720e\" data-claims=\"CLM-96d3720e\"><a class=\"cite-ref\" href=\"#bron-28\" aria-label=\"Bron 28\">[28]</a></sup>. De bepalingen over\n  registratie en uitwisseling (art. 3-15) gelden vanaf 26 maart 2029 voor patiëntsamenvatting, e-voorschrift en\n  e-aflevering, en vanaf 26 maart 2031 voor beeldvorming, testresultaten en ontslagverslagen\n<span class=\"cite-anchor\" id=\"t-CLM-c01f0160\"></span><sup class=\"cite\" id=\"t-CLM-14501017\" data-claims=\"CLM-14501017 CLM-c01f0160\"><a class=\"cite-ref\" href=\"#bron-28\" aria-label=\"Bron 28\">[28]</a></sup>. Hoofdstuk IV (secundair gebruik) geldt vanaf 26 maart 2029<sup class=\"cite\" id=\"t-CLM-943c06f1\" data-claims=\"CLM-943c06f1\"><a class=\"cite-ref\" href=\"#bron-28\" aria-label=\"Bron 28\">[28]</a></sup>, met\n  enkele categorieën van art. 51(1) pas vanaf 26 maart 2031<sup class=\"cite\" id=\"t-CLM-4a614894\" data-claims=\"CLM-4a614894\"><a class=\"cite-ref\" href=\"#bron-28\" aria-label=\"Bron 28\">[28]</a></sup>.</li>\n<li><strong>Wel (met die toepassingsdata)</strong>: de Commissie legt tegen 26 maart 2027 de technische specificaties van het\n  <a href=\"/eehrxf/\">EEHRxF</a> vast<sup class=\"cite\" id=\"t-CLM-14a07bfc\" data-claims=\"CLM-14a07bfc\"><a class=\"cite-ref\" href=\"#bron-28\" aria-label=\"Bron 28\">[28]</a></sup>; zorgverleners zullen prioritaire gegevens in een EPD-systeem moeten registreren\n<sup class=\"cite\" id=\"t-CLM-08580fc7\" data-claims=\"CLM-08580fc7\"><a class=\"cite-ref\" href=\"#bron-28\" aria-label=\"Bron 28\">[28]</a></sup>; gegevenshouders zullen onder meer EPD-gegevens beschikbaar moeten stellen voor secundair gebruik\n<sup class=\"cite\" id=\"t-CLM-eb2f08a7\" data-claims=\"CLM-eb2f08a7\"><a class=\"cite-ref\" href=\"#bron-28\" aria-label=\"Bron 28\">[28]</a></sup>.</li>\n<li><strong>FHIR-richting</strong>: HL7 Europe publiceerde Base- en Core-FHIR-IG's ter ondersteuning van de EHDS<sup class=\"cite\" id=\"t-CLM-c6b73f2f\" data-claims=\"CLM-c6b73f2f\"><a class=\"cite-ref\" href=\"#bron-29\" aria-label=\"Bron 29\">[29]</a></sup>;\n  België pleit voor één Europese FHIR-standaard per berichttype<sup class=\"cite\" id=\"t-CLM-c444a1e8\" data-claims=\"CLM-c444a1e8\"><a class=\"cite-ref\" href=\"#bron-30\" aria-label=\"Bron 30\">[30]</a></sup>. Dit is een Belgisch standpunt, geen\n  EU-besluit.</li>\n<li><strong>Niet (gevonden)</strong>: een expertpanel stelde eind 2023, over het toenmalige EHDS-voorstel, dat de EHDS geen concrete\n  standaarden regelt<sup class=\"cite\" id=\"t-CLM-2906b45d\" data-claims=\"CLM-2906b45d\"><a class=\"cite-ref\" href=\"#bron-2\" aria-label=\"Bron 2\">[2]</a></sup>; de definitieve verordening delegeert de technische specificaties van het EEHRxF\n  wel naar uitvoeringshandelingen<sup class=\"cite\" data-claims=\"CLM-14a07bfc\"><a class=\"cite-ref\" href=\"#bron-28\" aria-label=\"Bron 28\">[28]</a></sup>, die concrete standaarden kunnen bevatten (interpretatie). OMOP was in\n  de <a href=\"/healthdata-at-eu/\">HealthData@EU-pilot</a> een optie, geen verplichting<sup class=\"cite\" id=\"t-CLM-c4f61547\" data-claims=\"CLM-c4f61547\"><a class=\"cite-ref\" href=\"#bron-31\" aria-label=\"Bron 31\">[31]</a></sup>; een academisch raamwerk\n  noemt OMOP als standaard, maar dat is een voorstel<sup class=\"cite\" id=\"t-CLM-f8e9a39f\" data-claims=\"CLM-f8e9a39f\"><a class=\"cite-ref\" href=\"#bron-22\" aria-label=\"Bron 22\">[22]</a></sup>. Voor openEHR werd geen EHDS-verwijzing gevonden\n  (gap).</li>\n</ul>"
  },
  {
   "id": "conclusie",
   "title": "Conclusie",
   "kind": "tekst",
   "html": "<p>Bevindingen: de drie standaarden zijn volgens de geraadpleegde bronnen complementair<sup class=\"cite\" data-claims=\"CLM-2dc7d72b CLM-3ccf652d\"><a class=\"cite-ref\" href=\"#bron-1\" aria-label=\"Bron 1\">[1]</a><a class=\"cite-ref\" href=\"#bron-2\" aria-label=\"Bron 2\">[2]</a></sup> en\nmappings verliezen informatie<sup class=\"cite\" data-claims=\"CLM-cd749309\"><a class=\"cite-ref\" href=\"#bron-1\" aria-label=\"Bron 1\">[1]</a></sup>. Van de drie modellen raakt enkel het uitwisselingsformaat (EEHRxF) aan\neen EU-verplichting<sup class=\"cite\" data-claims=\"CLM-14a07bfc\"><a class=\"cite-ref\" href=\"#bron-28\" aria-label=\"Bron 28\">[28]</a></sup>; voor openEHR en OMOP werd geen EHDS-verplichting gevonden (gap)\n<sup class=\"cite\" data-claims=\"CLM-c4f61547\"><a class=\"cite-ref\" href=\"#bron-31\" aria-label=\"Bron 31\">[31]</a></sup>. De EHDS bevat daarnaast verplichtingen die los van deze modellen staan, zoals registratie in een\nEPD-systeem en terbeschikkingstelling voor secundair gebruik (vanaf 2029/2031, zie hierboven).</p>\n<p class=\"aanbeveling\"><strong>Aanbeveling</strong>: behandel FHIR (Belgische en EU-profielen) als de verwachte buitenkant van het EPD voor uitwisseling,\nen volg de EEHRxF-uitvoeringshandelingen op om te zien of FHIR normatief wordt voorgeschreven. Codeer zo veel\nmogelijk aan de bron in SNOMED CT en LOINC (dat verlaagt de kosten van elke latere FHIR-, openEHR- of OMOP-omzetting),\nen beschouw OMOP als optionele onderzoekskopie en openEHR als architectuurkeuze die een eigen businesscase vraagt.\nHoud brondata altijd bij als referentie, omdat een OMOP-kopie per definitie verlies bevat.</p>"
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  {
   "id": "CLM-14501017",
   "statement": "De artikelen 3 tot 15 (waaronder de registratieplicht van art. 13 en het EEHRxF van art. 15) gelden vanaf 26 maart 2029 voor patiëntsamenvatting, e-voorschrift en e-aflevering en voor EPD-systemen die de fabrikant voor die categorieën bestemt; voor beeldvorming, testresultaten en ontslagverslagen vanaf 26 maart 2031.",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "art. 105, derde alinea, punt (a)",
   "as_of": "2026-09-26",
   "source": {
    "id": "SRC-af26b6d770",
    "title": "Regulation (EU) 2025/327 of the European Parliament and of the Council of 11 February 2025 on the European Health Data Space and amending Directive 2011/24/EU and Regulation (EU) 2024/2847",
    "publisher": "Europees Parlement en Raad van de EU (EUR-Lex)",
    "url": "https://eur-lex.europa.eu/eli/reg/2025/327/oj/eng",
    "published": "2025-03-05"
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-c01f0160",
   "statement": "Voor de tweede groep prioritaire categorieën (art. 14(1) d-f: medische beeldvorming met verslagen, testresultaten incl. labo, ontslagverslagen) gelden die bepalingen vanaf 26 maart 2031.",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "artikel 105, derde alinea, punt (b)",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-af26b6d770",
    "title": "Regulation (EU) 2025/327 of the European Parliament and of the Council of 11 February 2025 on the European Health Data Space and amending Directive 2011/24/EU and Regulation (EU) 2024/2847",
    "publisher": "Europees Parlement en Raad van de EU (EUR-Lex)",
    "url": "https://eur-lex.europa.eu/eli/reg/2025/327/oj/eng",
    "published": "2025-03-05"
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-943c06f1",
   "statement": "Hoofdstuk IV (secundair gebruik) is van toepassing vanaf 26 maart 2029, met enkele bepalingen (o.a. art. 75(1) over HealthData@EU-contactpunten) al vanaf 26 maart 2027.",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "artikel 105",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-af26b6d770",
    "title": "Regulation (EU) 2025/327 of the European Parliament and of the Council of 11 February 2025 on the European Health Data Space and amending Directive 2011/24/EU and Regulation (EU) 2024/2847",
    "publisher": "Europees Parlement en Raad van de EU (EUR-Lex)",
    "url": "https://eur-lex.europa.eu/eli/reg/2025/327/oj/eng",
    "published": "2025-03-05"
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-4a614894",
   "statement": "Volgens de verordening is art. 75(5) (aansluiting van derde landen/internationale organisaties op HealthData@EU) pas van toepassing vanaf 26 maart 2035.",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "art. 105, zesde alinea",
   "as_of": "2026-09-26",
   "source": {
    "id": "SRC-af26b6d770",
    "title": "Regulation (EU) 2025/327 of the European Parliament and of the Council of 11 February 2025 on the European Health Data Space and amending Directive 2011/24/EU and Regulation (EU) 2024/2847",
    "publisher": "Europees Parlement en Raad van de EU (EUR-Lex)",
    "url": "https://eur-lex.europa.eu/eli/reg/2025/327/oj/eng",
    "published": "2025-03-05"
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-14a07bfc",
   "statement": "Tegen 26 maart 2027 moet de Commissie via uitvoeringshandelingen de technische specificaties voor de prioritaire categorieën vastleggen die samen het Europees uitwisselingsformaat voor EPD's (EEHRxF) vormen.",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "artikel 15(1)",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-af26b6d770",
    "title": "Regulation (EU) 2025/327 of the European Parliament and of the Council of 11 February 2025 on the European Health Data Space and amending Directive 2011/24/EU and Regulation (EU) 2024/2847",
    "publisher": "Europees Parlement en Raad van de EU (EUR-Lex)",
    "url": "https://eur-lex.europa.eu/eli/reg/2025/327/oj/eng",
    "published": "2025-03-05"
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-08580fc7",
   "statement": "Zorgverleners moeten de gegevens die (deels) onder de prioritaire categorieën vallen elektronisch registreren in een EPD-systeem.",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "artikel 13(1)",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-af26b6d770",
    "title": "Regulation (EU) 2025/327 of the European Parliament and of the Council of 11 February 2025 on the European Health Data Space and amending Directive 2011/24/EU and Regulation (EU) 2024/2847",
    "publisher": "Europees Parlement en Raad van de EU (EUR-Lex)",
    "url": "https://eur-lex.europa.eu/eli/reg/2025/327/oj/eng",
    "published": "2025-03-05"
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-eb2f08a7",
   "statement": "Gegevenshouders (waaronder ziekenhuizen, tenzij vrijgesteld) moeten minimaal bepaalde categorieën beschikbaar stellen voor secundair gebruik, te beginnen met elektronische gezondheidsgegevens uit EPD's.",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "artikel 51(1)(a)",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-af26b6d770",
    "title": "Regulation (EU) 2025/327 of the European Parliament and of the Council of 11 February 2025 on the European Health Data Space and amending Directive 2011/24/EU and Regulation (EU) 2024/2847",
    "publisher": "Europees Parlement en Raad van de EU (EUR-Lex)",
    "url": "https://eur-lex.europa.eu/eli/reg/2025/327/oj/eng",
    "published": "2025-03-05"
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-c6b73f2f",
   "statement": "HL7 Europe publiceerde in het najaar van 2025 Base- en Core-FHIR-IG's (STU, R4 en R5) en een Extensions-pakket ter ondersteuning van de EHDS; de uitvoeringshandelingen over het EEHRxF worden begin 2027 verwacht.",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "alinea's 1 en 5",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-f046cd4082",
    "title": "New HL7 Europe FHIR Implementation Guides to support the European Health Data Space",
    "publisher": "HL7 International (HL7 News)",
    "url": "https://hl7news.hl7.org/2026/01/02/new-hl7-europe-fhir-implementation-guides-to-support-the-european-health-data-space/",
    "published": "2026-01-02"
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-c444a1e8",
   "statement": "België pleit voor één unieke Europese technische FHIR-standaard per berichttype (patiëntsamenvatting, e-voorschrift, e-aflevering, beeldvorming, testresultaten, ontslagverslagen).",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "sectie 'Organisatie in België'",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-41ee539e0b",
    "title": "EHDS (European Health Data Space) - De Europese Verordening betreffende de Europese ruimte voor gezondheidsgegevens",
    "publisher": "eHealth-platform",
    "url": "https://www.ehealth.fgov.be/nl/page/ehds-european-health-data-space-de-europese-verordening-betreffende-de-europese-ruimte-voor-gezondheidsgegevens",
    "published": null
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-2906b45d",
   "statement": "Volgens een expertpanel (JMIR Med Inform, 2023) streeft de EHDS harmonisatie en hergebruik na zonder de concrete te gebruiken standaarden te regelen.",
   "kind": "research-finding",
   "kind_label": "onderzoeksbevinding",
   "locator": "sectie Discussion/Conclusions",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-b22ee5ef19",
    "title": "Can OpenEHR, ISO 13606, and HL7 FHIR Work Together? An Agnostic Approach for the Selection and Application of Electronic Health Record Standards to the Next-Generation Health Data Spaces",
    "publisher": "JMIR Medical Informatics (Pedrera-Jiménez et al.)",
    "url": "https://pmc.ncbi.nlm.nih.gov/articles/PMC10784985/",
    "published": "2023-12-28"
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-c4f61547",
   "statement": "In de EMA-use case van de pilot gebruikte DARWIN EU de OMOP CDM; andere knooppunten mochten kiezen tussen analyse op brondata of conversie naar OMOP. OMOP was dus een optie in de pilot, geen verplichting.",
   "kind": "research-finding",
   "kind_label": "onderzoeksbevinding",
   "locator": "sectie 'Summary of the EMA use case'",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-b280053090",
    "title": "The European Health Data Space in communicable diseases surveillance and monitoring of medicines and vaccines: achievements of a pilot project examining the user journey",
    "publisher": "European Journal of Public Health",
    "url": "https://pmc.ncbi.nlm.nih.gov/articles/PMC12420905/",
    "published": "2025"
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-f8e9a39f",
   "statement": "Een interoperabiliteitsraamwerk voor EHDS-secundair gebruik (JMIR 2025) noemt OMOP CDM als standaard voor semantische interoperabiliteit (academisch voorstel, geen EU-besluit).",
   "kind": "research-finding",
   "kind_label": "onderzoeksbevinding",
   "locator": "sectie Results, semantische laag",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-55ef771c33",
    "title": "Interoperability Framework of the European Health Data Space for the Secondary Use of Data: Interactive European Interoperability Framework-Based Standards Compliance Toolkit for AI-Driven Projects",
    "publisher": "Journal of Medical Internet Research",
    "url": "https://pmc.ncbi.nlm.nih.gov/articles/PMC12059490/",
    "published": "2025"
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-57376d36",
   "statement": "België kiest ervoor de velden van de Europese berichttypes ook te gebruiken in de Belgische caresets; een grensoverschrijdend bericht wordt zo dicht mogelijk bij de bron aangemaakt, bij informatie in het EPD door het EPD-softwarepakket.",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "sectie 'Organisatie in België'",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-41ee539e0b",
    "title": "EHDS (European Health Data Space) - De Europese Verordening betreffende de Europese ruimte voor gezondheidsgegevens",
    "publisher": "eHealth-platform",
    "url": "https://www.ehealth.fgov.be/nl/page/ehds-european-health-data-space-de-europese-verordening-betreffende-de-europese-ruimte-voor-gezondheidsgegevens",
    "published": null
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-ac8d824b",
   "statement": "Implementers van de Belgische core-clinical FHIR-specificaties moeten over een SNOMED CT Affiliate-licentie beschikken.",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "sectie IP statements",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-854e8cb270",
    "title": "HL7 Belgium FHIR IG - core-clinical profiles: Home",
    "publisher": "eHealth-platform / HL7 Belgium",
    "url": "https://www.ehealth.fgov.be/standards/fhir/core-clinical/en/index.html",
    "published": null
   },
   "citaat": null,
   "in_text": true,
   "on_page": true
  },
  {
   "id": "CLM-0537aba1",
   "statement": "Voor primair gebruik legt de EHDS geen persistentiemodel op, alleen het uitwisselingsformaat (EEHRxF) voor de prioritaire categorieën, en België vraagt daarvoor één FHIR-standaard. Voor een Belgisch ziekenhuis is FHIR (EU-/BE-profielen met SNOMED CT/LOINC) daarom de directe verplichting. openEHR en OMOP zijn architectuurkeuzes en worden niet door de EHDS opgelegd.",
   "kind": "interpretation",
   "kind_label": "interpretatie",
   "locator": "synthese van eehrxf-01/02, ehds-12/13/15, ehds-16",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-af26b6d770",
    "title": "Regulation (EU) 2025/327 of the European Parliament and of the Council of 11 February 2025 on the European Health Data Space and amending Directive 2011/24/EU and Regulation (EU) 2024/2847",
    "publisher": "Europees Parlement en Raad van de EU (EUR-Lex)",
    "url": "https://eur-lex.europa.eu/eli/reg/2025/327/oj/eng",
    "published": "2025-03-05"
   },
   "citaat": null,
   "in_text": false,
   "on_page": false
  },
  {
   "id": "CLM-1e57ae00",
   "statement": "Synthese: FHIR is een uitwisselingsstandaard (API/berichten, EEHRxF-richting), openEHR een standaard voor klinische modellering en persistentie in het EPD, OMOP CDM een analysemodel voor secundair gebruik; SNOMED CT en LOINC zijn de gedeelde semantische laag die in alle drie wordt gebruikt (FHIR via CodeSystem/ValueSet-binding, openEHR via terminologiebinding in archetypes, OMOP als Standard Concepts). Ze zijn complementair: een ziekenhuis kan intern openEHR of een leveranciersmodel gebruiken, extern FHIR aanbieden en een OMOP-kopie voeden voor onderzoek.",
   "kind": "interpretation",
   "kind_label": "interpretatie",
   "locator": "synthese van vgl-01..10, openehr-03/06, omop-cdm-07, fhir-03/04",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-4762fc1944",
    "title": "Vulcan FHIR to OMOP FHIR Implementation Guide",
    "publisher": "HL7 International / Biomedical Research and Regulation",
    "url": "https://hl7.org/fhir/uv/omop/en/index.html",
    "published": null
   },
   "citaat": null,
   "in_text": false,
   "on_page": false
  },
  {
   "id": "CLM-9933480b",
   "statement": "Onder de EHDS wordt deelname aan MyHealth@EU, dat vroeger vrijwillig was, verplicht voor de lidstaten.",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "overweging 33",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-af26b6d770",
    "title": "Regulation (EU) 2025/327 of the European Parliament and of the Council of 11 February 2025 on the European Health Data Space and amending Directive 2011/24/EU and Regulation (EU) 2024/2847",
    "publisher": "Europees Parlement en Raad van de EU (EUR-Lex)",
    "url": "https://eur-lex.europa.eu/eli/reg/2025/327/oj/eng",
    "published": "2025-03-05"
   },
   "citaat": null,
   "in_text": false,
   "on_page": true
  },
  {
   "id": "CLM-23e1f00b",
   "statement": "HealthData@EU is de grensoverschrijdende infrastructuur voor secundair gebruik; nationale contactpunten voor secundair gebruik en de Union health data access service moeten erop aansluiten.",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "artikel 75(3)",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-af26b6d770",
    "title": "Regulation (EU) 2025/327 of the European Parliament and of the Council of 11 February 2025 on the European Health Data Space and amending Directive 2011/24/EU and Regulation (EU) 2024/2847",
    "publisher": "Europees Parlement en Raad van de EU (EUR-Lex)",
    "url": "https://eur-lex.europa.eu/eli/reg/2025/327/oj/eng",
    "published": "2025-03-05"
   },
   "citaat": null,
   "in_text": false,
   "on_page": true
  },
  {
   "id": "CLM-1a78183e",
   "statement": "Elke lidstaat wijst één nationaal contactpunt voor digitale gezondheid aan en meldt het tegen 26 maart 2027 aan de Commissie; de uitwisseling via MyHealth@EU steunt op het EEHRxF.",
   "kind": "fact",
   "kind_label": "feit",
   "locator": "artikel 23(2) (aanwijzing en melding tegen 26 maart 2027; zie CLM-4fda078c); citaat uit artikel 23(3) (uitwisseling op basis van het EEHRxF)",
   "as_of": "2026-09-25",
   "source": {
    "id": "SRC-af26b6d770",
    "title": "Regulation (EU) 2025/327 of the European Parliament and of the Council of 11 February 2025 on the European Health Data Space and amending Directive 2011/24/EU and Regulation (EU) 2024/2847",
    "publisher": "Europees Parlement en Raad van de EU (EUR-Lex)",
    "url": "https://eur-lex.europa.eu/eli/reg/2025/327/oj/eng",
    "published": "2025-03-05"
   },
   "citaat": null,
   "in_text": false,
   "on_page": true
  }
 ],
 "diagrams": [
  {
   "id": "fhir-openehr-omop-terminologie",
   "kind": "lagen",
   "title": "FHIR, openEHR, OMOP en terminologieën: conceptueel model",
   "alt": "Drie lagen: de Europese laag (EHDS, EEHRxF, MyHealth@EU, HealthData@EU), de modellen voor uitwisseling, klinische modellering en analyse (HL7 FHIR, Belgische FHIR-IG's, openEHR, OMOP CDM) en de semantische laag (SNOMED CT, LOINC, ICD-10-BE), met veertien genummerde verbanden.",
   "note": "Toont de verhouding tussen standaarden volgens de bronnen; geen ziekenhuisarchitectuur en geen bewezen operationele koppelingen. Gestippeld = ontwerp, voorstel of standpunt.",
   "layers": [
    {
     "title": "Europese laag",
     "subtitle": "EHDS",
     "nodes": [
      {
       "id": "ehds",
       "label": "EHDS",
       "sublabel": "Verordening (EU) 2025/327",
       "type": {
        "code": "LegalAct",
        "label": "Wettekst of verordening"
       },
       "url": "/ehds/",
       "title": "EHDS (Verordening (EU) 2025/327)"
      },
      {
       "id": "eehrxf",
       "label": "EEHRxF",
       "sublabel": "Europees uitwisselingsformaat",
       "type": {
        "code": "Specification",
        "label": "Standaard of specificatie"
       },
       "url": "/eehrxf/",
       "title": "EEHRxF (Europees uitwisselingsformaat)"
      },
      {
       "id": "mh",
       "label": "MyHealth@EU",
       "sublabel": "BE-NCPeH: eHealth-platform",
       "type": {
        "code": "Platform",
        "label": "Platform of dienst"
       },
       "url": "/myhealth-at-eu/",
       "title": "MyHealth@EU (BE-NCPeH: eHealth-platform)"
      },
      {
       "id": "hd",
       "label": "HealthData@EU",
       "sublabel": "BE: Health Data Agency",
       "type": {
        "code": "Platform",
        "label": "Platform of dienst"
       },
       "url": "/healthdata-at-eu/",
       "title": "HealthData@EU (BE: Health Data Agency)"
      }
     ]
    },
    {
     "title": "Modellen",
     "subtitle": "uitwisseling · klinische modellering · analyse",
     "nodes": [
      {
       "id": "fhir",
       "label": "HL7 FHIR",
       "sublabel": "uitwisseling",
       "type": {
        "code": "Specification",
        "label": "Standaard of specificatie"
       },
       "url": "/fhir/",
       "title": "HL7 FHIR (uitwisseling)"
      },
      {
       "id": "beig",
       "label": "Belgische FHIR-IG's",
       "sublabel": "R4 4.0.1",
       "type": {
        "code": "Specification",
        "label": "Standaard of specificatie"
       },
       "url": "/be-fhir-igs/",
       "title": "Belgische FHIR-IG's (R4 4.0.1)"
      },
      {
       "id": "oehr",
       "label": "openEHR",
       "sublabel": "klinische modellering, archetypes",
       "type": null,
       "url": null,
       "title": "openEHR (klinische modellering, archetypes)"
      },
      {
       "id": "omop",
       "label": "OMOP CDM v5.5",
       "sublabel": "analyse en onderzoek",
       "type": {
        "code": "Specification",
        "label": "Standaard of specificatie"
       },
       "url": "/omop-cdm/",
       "title": "OMOP CDM v5.5 (analyse en onderzoek)"
      }
     ]
    },
    {
     "title": "Semantische laag",
     "subtitle": "terminologie en classificatie",
     "nodes": [
      {
       "id": "snomed",
       "label": "SNOMED CT",
       "sublabel": "Belgian Edition",
       "type": {
        "code": "Terminology",
        "label": "Terminologie of classificatie"
       },
       "url": "/snomed-ct/",
       "title": "SNOMED CT (Belgian Edition)"
      },
      {
       "id": "loinc",
       "label": "LOINC",
       "sublabel": "Belgische subset",
       "type": {
        "code": "Terminology",
        "label": "Terminologie of classificatie"
       },
       "url": "/loinc/",
       "title": "LOINC (Belgische subset)"
      },
      {
       "id": "icd",
       "label": "ICD-10-BE",
       "sublabel": null,
       "type": {
        "code": "Terminology",
        "label": "Terminologie of classificatie"
       },
       "url": "/icd-10-be/",
       "title": "ICD-10-BE"
      }
     ]
    }
   ],
   "participants": [],
   "edges": [
    {
     "n": "1",
     "source": "ehds",
     "target": "eehrxf",
     "text": "EHDS: de Commissie legt de EEHRxF-specificaties vast (tegen 26/3/2027)",
     "status": "established",
     "reply": false,
     "claims": [
      "CLM-14a07bfc"
     ],
     "refs": [
      28
     ]
    },
    {
     "n": "2",
     "source": "ehds",
     "target": "mh",
     "text": "EHDS: deelname aan MyHealth@EU verplicht voor lidstaten",
     "status": "established",
     "reply": false,
     "claims": [
      "CLM-9933480b"
     ],
     "refs": [
      28
     ]
    },
    {
     "n": "3",
     "source": "ehds",
     "target": "hd",
     "text": "EHDS: secundair gebruik via HealthData@EU; OMOP enkel een optie in de pilot",
     "status": "established",
     "reply": false,
     "claims": [
      "CLM-23e1f00b",
      "CLM-c4f61547"
     ],
     "refs": [
      28,
      31
     ]
    },
    {
     "n": "4",
     "source": "mh",
     "target": "eehrxf",
     "text": "MyHealth@EU-uitwisseling steunt op EEHRxF",
     "status": "established",
     "reply": false,
     "claims": [
      "CLM-1a78183e"
     ],
     "refs": [
      28
     ]
    },
    {
     "n": "5",
     "source": "eehrxf",
     "target": "fhir",
     "text": "HL7 Europe Base/Core-IG's (STU); uitvoeringshandelingen verwacht begin 2027",
     "status": "hypothesis",
     "reply": false,
     "claims": [
      "CLM-c6b73f2f"
     ],
     "refs": [
      29
     ]
    },
    {
     "n": "6",
     "source": "beig",
     "target": "fhir",
     "text": "Belgische IG's profileren FHIR R4 (geen R5)",
     "status": "established",
     "reply": false,
     "claims": [
      "CLM-4c97a5a4"
     ],
     "refs": [
      19
     ]
    },
    {
     "n": "7",
     "source": "beig",
     "target": "eehrxf",
     "text": "EU-velden ook in Belgische CareSets (Belgisch standpunt)",
     "status": "hypothesis",
     "reply": false,
     "claims": [
      "CLM-57376d36"
     ],
     "refs": [
      30
     ]
    },
    {
     "n": "8",
     "source": "beig",
     "target": "snomed",
     "text": "SNOMED CT als voorkeurscodering in Belgische IG's",
     "status": "established",
     "reply": false,
     "claims": [
      "CLM-530b635f"
     ],
     "refs": [
      23
     ]
    },
    {
     "n": "9",
     "source": "beig",
     "target": "loinc",
     "text": "BE Lab-IG: LOINC verplicht (FOD-subset)",
     "status": "established",
     "reply": false,
     "claims": [
      "CLM-e0e48933"
     ],
     "refs": [
      24
     ]
    },
    {
     "n": "10",
     "source": "oehr",
     "target": "snomed",
     "text": "openEHR: terminologiebinding via archetypes (SNOMED CT als voorbeeld is een interpretatie)",
     "status": "established",
     "reply": false,
     "claims": [
      "CLM-19680c4c"
     ],
     "refs": [
      10
     ]
    },
    {
     "n": "11",
     "source": "oehr",
     "target": "fhir",
     "text": "Een openEHR↔FHIR-IG voor datatype-mapping is in ontwikkeling",
     "status": "hypothesis",
     "reply": false,
     "claims": [
      "CLM-4d28e36b"
     ],
     "refs": [
      26
     ]
    },
    {
     "n": "12",
     "source": "fhir",
     "target": "omop",
     "text": "HL7 Vulcan FHIR-to-OMOP IG v1.0.0 (Informative; CDM v5.4); niet verliesvrij",
     "status": "established",
     "reply": false,
     "claims": [
      "CLM-77f1c57f",
      "CLM-cd749309"
     ],
     "refs": [
      1
     ]
    },
    {
     "n": "13",
     "source": "omop",
     "target": "snomed",
     "text": "OMOP: SNOMED CT als standaardconcept voor aandoeningen",
     "status": "established",
     "reply": false,
     "claims": [
      "CLM-8b25e1f2"
     ],
     "refs": [
      17
     ]
    },
    {
     "n": "14",
     "source": "icd",
     "target": "omop",
     "text": "ICD als broncode, gemapt op een standaardconcept (ICD-10-BE specifiek is een interpretatie)",
     "status": "established",
     "reply": false,
     "claims": [
      "CLM-8b25e1f2",
      "CLM-71837b87"
     ],
     "refs": [
      17
     ]
    }
   ],
   "footer": null
  }
 ],
 "facets": {
  "type": [
   "Topic"
  ],
  "jurisdiction": [
   "internationaal",
   "eu",
   "belgie"
  ],
  "theme": [
   "architectuur-en-infrastructuur",
   "terminologie",
   "secundair-gebruik"
  ],
  "lifecycle": [
   "onbekend"
  ],
  "section": [
   "terminologie",
   "europa"
  ]
 },
 "search_terms": [
  "FHIR, openEHR en OMOP: vergelijking",
  "FHIR vs openEHR vs OMOP",
  "FHIR, openEHR en OMOP CDM",
  "uitwisseling vs persistentie vs analyse",
  "FHIR, openEHR et OMOP : comparaison",
  "FHIR, openEHR and OMOP compared"
 ],
 "release_id": "2026.10.05-1",
 "license": "CC BY 4.0"
}
