FHIR IG analytics

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Source1

{
  "resourceType": "Observation",
  "id": "mii-exa-onko-studienteilnahme-prob",
  "meta": {
    "profile": [
      "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/StructureDefinition/mii-pr-onko-studienteilnahme|2026.0.2"
    ]
  },
  "code": {
    "coding": [
      {
        "code": "709491003",
        "system": "http://snomed.info/sct",
        "display": "Enrollment in clinical trial (procedure)"
      }
    ]
  },
  "status": "final",
  "subject": {
    "reference": "Patient/example"
  },
  "focus": [
    {
      "reference": "Condition/primaertumor-example"
    },
    {
      "reference": "ResearchStudy/mii-exa-onko-studie-prob"
    }
  ],
  "valueCodeableConcept": {
    "coding": [
      {
        "code": "J",
        "system": "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/CodeSystem/mii-cs-onko-studienteilnahme",
        "display": "Ja"
      }
    ],
    "text": "Patientin wurde in PRO-B Studie eingeschlossen"
  },
  "effectiveDateTime": "2021-06-20",
  "note": [
    {
      "text": "Patientin mit metastasiertem Mammakarzinom in PRO-B Studie randomisiert. Teilnahme am alarm-basierten PROMs-Monitoring zur Erfassung von Symptomen und Nebenwirkungen."
    }
  ]
}