FHIR IG analytics| Package | de.medizininformatikinitiative.kerndatensatz.seltene |
| Resource Type | ClinicalImpression |
| Id | ClinicalImpression-clinical-impression-erstvorstellung.json |
| FHIR Version | R4 |
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{
"resourceType": "ClinicalImpression",
"id": "clinical-impression-erstvorstellung",
"meta": {
"profile": [
"https://www.medizininformatik-initiative.de/fhir/ext/modul-seltene/StructureDefinition/mii-pr-seltene-clinical-impression|2026.0.0"
]
},
"status": "completed",
"subject": {
"reference": "Patient/patient-sma-001"
},
"encounter": {
"reference": "Encounter/encounter-ambulant-001"
},
"effectiveDateTime": "2024-07-22",
"date": "2024-07-22",
"problem": [
{
"reference": "Condition/condition-sma-suspected"
}
],
"investigation": [
{
"code": {
"text": "Familienanamnese"
},
"item": [
{
"reference": "FamilyMemberHistory/family-history-001"
}
]
},
{
"code": {
"text": "Labordiagnostik"
},
"item": [
{
"reference": "Observation/observation-troponin-001"
}
]
}
],
"summary": "Neugeborenes mit V.a. SMA aus Neugeborenenscreening. Familienanamnese zeigt unklare Muskelerkrankung der Urgroßmutter. Troponin T bereits erhöht (92 ng/l).",
"finding": [
{
"itemReference": {
"reference": "Condition/condition-sma-clinical"
}
},
{
"itemReference": {
"reference": "Condition/condition-sma-genetic"
}
},
{
"itemCodeableConcept": {
"coding": [
{
"system": "http://snomed.info/sct",
"code": "1363512008",
"display": "Troponin above reference range"
}
]
},
"itemReference": {
"reference": "Observation/observation-troponin-001"
}
}
],
"prognosisCodeableConcept": [
{
"coding": [
{
"system": "http://snomed.info/sct",
"code": "67334001",
"display": "Guarded prognosis"
}
]
}
],
"note": [
{
"text": "Klinische Untersuchung gemäß SMA-Diagnoseprotokoll. Blutentnahme für Genetik veranlasst."
},
{
"text": "Klinisches Bild vereinbar mit SMA Typ 1. Molekulargenetische Bestätigung ausstehend. Eltern über Therapieoptionen informiert."
}
]
}