FHIR IG analytics| Package | hl7.fhir.us.icsr-ae-reporting |
| Resource Type | Composition |
| Id | Composition-TransfusionExample.json |
| FHIR Version | R4 |
No resources found
No resources found
Note: links and images are rebased to the (stated) source
Generated Narrative: Composition
Resource Composition "TransfusionExample"
Profile: ICSR Composition
AdditionalDocumentInformation
url
availableFlagvalue: false
ExpeditedReport
url
localCriteriaFlagvalue: false
url
localCriteriaReportTypevalue: Non-Expedited AE (unknown#2)
FirstSenderType: Other (unknown#2)
CombinationProductReport: false
FirstReceiveDate: 2021-01-05
MostRecentDate: 2021-01-05
CaseIdentifier: id: BEST_beafb541-3eab-eb9e-1bf1-5fa477d56e77
identifier: id: BEST_beafb541-3eab-eb9e-1bf1-5fa477d56e77
status: final
type: Adverse event note (LOINC#85893-6)
category: Spontaneous report (unknown#1)
date: 2021-01-05
author: PractitionerRole/BESTAuthorRole
title: ICSR Submission
{
"resourceType": "Composition",
"id": "TransfusionExample",
"meta": {
"profile": [
"http://hl7.org/fhir/us/icsr-ae-reporting/StructureDefinition/icsr-composition"
]
},
"text": {
"status": "extensions",
"div": "<!-- snip (see above) -->"
},
"extension": [
{
"extension": [
{
"url": "availableFlag",
"valueBoolean": false
}
],
"url": "http://hl7.org/fhir/us/icsr-ae-reporting/StructureDefinition/icsr-ext-additionaldocumentinformation"
},
{
"extension": [
{
"url": "localCriteriaFlag",
"valueBoolean": false
},
{
"url": "localCriteriaReportType",
"valueCodeableConcept": {
"coding": [
{
"system": "urn:oid:2.16.840.1.113883.3.989.2.1.1.1003",
"code": "2",
"display": "Non-Expedited AE"
}
]
}
}
],
"url": "http://hl7.org/fhir/us/icsr-ae-reporting/StructureDefinition/icsr-ext-expeditedreport"
},
{
"url": "http://hl7.org/fhir/us/icsr-ae-reporting/StructureDefinition/icsr-ext-firstsendertype",
"valueCodeableConcept": {
"coding": [
{
"system": "urn:oid:2.16.840.1.113883.3.989.2.1.1.3",
"code": "2",
"display": "Other"
}
]
}
},
{
"url": "http://hl7.org/fhir/us/icsr-ae-reporting/StructureDefinition/icsr-ext-combinationproductreport",
"valueBoolean": false
},
{
"url": "http://hl7.org/fhir/us/icsr-ae-reporting/StructureDefinition/icsr-ext-firstreceivedate",
"valueDateTime": "2021-01-05"
},
{
"url": "http://hl7.org/fhir/us/icsr-ae-reporting/StructureDefinition/icsr-ext-mostrecentdate",
"valueDateTime": "2021-01-05"
},
{
"url": "http://hl7.org/fhir/us/icsr-ae-reporting/StructureDefinition/icsr-ext-caseidentifier",
"valueIdentifier": {
"system": "urn:oid:2.16.840.1.113883.3.989.2.1.3.2",
"value": "BEST_beafb541-3eab-eb9e-1bf1-5fa477d56e77"
}
}
],
"identifier": {
"system": "urn:oid:2.16.840.1.113883.3.989.2.1.3.1",
"value": "BEST_beafb541-3eab-eb9e-1bf1-5fa477d56e77"
},
"status": "final",
"type": {
"coding": [
{
"system": "http://loinc.org",
"code": "85893-6",
"display": "Adverse event note"
}
]
},
"category": [
{
"coding": [
{
"system": "urn:oid:2.16.840.1.113883.3.989.2.1.1.2",
"code": "1",
"display": "Spontaneous report"
}
]
}
],
"subject": {
"reference": "Patient/BESTPatient"
},
"date": "2021-01-05",
"author": [
{
"extension": [
{
"url": "http://hl7.org/fhir/us/icsr-ae-reporting/StructureDefinition/icsr-ext-authorprimarysource",
"valueBoolean": true
}
],
"reference": "PractitionerRole/BESTAuthorRole"
}
],
"title": "ICSR Submission",
"section": [
{
"title": "Reaction/Event",
"code": {
"coding": [
{
"system": "http://hl7.org/fhir/us/icsr-ae-reporting/CodeSystem/ICSRSectionCodeCS",
"code": "ReactionEvent"
}
]
},
"text": {
"status": "generated",
"div": "<div xmlns=\"http://www.w3.org/1999/xhtml\">Allergic transfusion reaction</div>"
},
"entry": [
{
"reference": "AdverseEvent/TransfusionExampleEvent"
}
]
},
{
"title": "Drug Information",
"code": {
"coding": [
{
"system": "http://hl7.org/fhir/us/icsr-ae-reporting/CodeSystem/ICSRSectionCodeCS",
"code": "DrugInformation"
}
]
},
"text": {
"status": "generated",
"div": "<div xmlns=\"http://www.w3.org/1999/xhtml\">Description code for blood products: E7003, Blood group and type: N/A Blood processing type: Apheresis PLATELETS|ACD-A>PAS-C/XX/20-24C|ResLeu:&lt;5E6|2nd container</div>"
},
"entry": [
{
"reference": "Procedure/TransfusionExampleTransfusion"
},
{
"reference": "MedicationAdministration/TransfusionEpinephrine"
},
{
"reference": "MedicationAdministration/TransfusionDiphenhydramine"
}
]
},
{
"title": "Case Summary Narrative",
"code": {
"coding": [
{
"system": "http://hl7.org/fhir/us/icsr-ae-reporting/CodeSystem/ICSRSectionCodeCS",
"code": "CaseSummaryNarrative"
}
]
},
"text": {
"status": "generated",
"div": "<div xmlns=\"http://www.w3.org/1999/xhtml\">Header: FDA CBER BEST Automated AE Reporting Prototype Case BEST Detection Phenotype Algorithm: Phenotype link: rules-cd BEST Certainty: Definite BEST Severity: Non-Severe BEST Imputability: Probable Form Type: 3500 Contact Method: Email Adverse Event: 1 Center to which the case is being routed to: CBER Whether the case is being sent to DQRS: false Whether the report is related to drugs or food/cosmetics: 1 Whether the blood report is of type Transfusion or Collection: 2 Patient Race Code: 2f, Blood group of patient: N/A, Onset location for reaction: MedStar Location Description code for blood products: N/A, Blood group and type: N/A Blood processing type: N/A Product available for evaluation: 2 Volume of transfusion: NI NHSN Workup: NI Preliminary investigation results: Developed rash &#38; stridor following transfusion prbc for anemia. Tx with benadryl &#38; epinephrine &#38; sx improved., Adverse Event Type Imputability: Blood Transfusion - Certainty: Definite; Notes: 1. notes, Eval+Plan Note, For admission to Hosp with Dx Anemia. Transfuse PRBC now., Date 20020109; 2. notes, Eval+Plan Note, Patient has developed a new maculopapular rash following transfusion. Will give Benadryl 25 mg., Date 20020109; 3. notes, Eval+Plan Note, New onset Stridor following transfusion. Will give Epinephrine .5mg, and do transfusion Rxn workup, Date 20020109; 4. notes, Eval+Plan Note, RN note - Administered Benadryl 25mg IV for skin sx. After 30 min pt. reports some improvement in skin symptoms, Date 20020109 Labs, Vitals, and Tests: 1. labs, Diastolic Blood Pressure, 75.918 mm[Hg], Date 20020109; 2. labs, Systolic Blood Pressure, 123.08 mm[Hg], Date 20020109; 3. labs, Physical findings of Skin, generalized rash, Date 20020109; 4. labs, Respiratory status finding, Stridor, Date 20020109; Illness at Time of Vaccination: 1. illness, Problem, Anemia, Date 20020109;</div>"
}
},
{
"title": "Patient Information",
"code": {
"coding": [
{
"system": "http://hl7.org/fhir/us/icsr-ae-reporting/CodeSystem/ICSRSectionCodeCS",
"code": "PatientInformation"
}
]
},
"entry": [
{
"reference": "Observation/BESTPatientAgeGroup"
}
]
},
{
"title": "Relevant Medical History",
"code": {
"coding": [
{
"system": "http://hl7.org/fhir/us/icsr-ae-reporting/CodeSystem/ICSRSectionCodeCS",
"code": "RelevantMedicalHistory"
}
]
},
"text": {
"status": "generated",
"div": "<div xmlns=\"http://www.w3.org/1999/xhtml\">NI</div>"
}
}
]
}