| Package | package.teste |
| Type | StructureDefinition |
| Id | Id |
| FHIR Version | R4B |
| Source | https://simplifier.net/resolve?scope=package.teste@1.0.7-draft&canonical=https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/AdverseEventPTCore |
| Url | https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/AdverseEventPTCore |
| Version | 1.0.0 |
| Status | draft |
| Date | 2024-02-09T14:29:46.6406318+00:00 |
| Name | AdverseEventPTCore |
| Experimental | False |
| Description | O recurso AdverseEvent caracteriza de forma abrangente um evento adverso ou qualquer alteração do estado do utente, estando este associado a efeitos indesejados que poderão requerer monitorização, tratamento, hospitalização ou resultar na morte do utente. Exemplos de eventos adversos incluem a administração incorreta de um medicamento ou dose de um medicamento que causa uma reação adversa, o uso de um dispositivo implantado que causa uma infecção, entre outros. O recurso AdverseEvent PT Core corresponde a uma normalização nacional do recurso AdverseEvent. |
| Type | AdverseEvent |
| Kind | resource |
No resources found
FHIR
{
"resourceType" : "StructureDefinition",
"id" : "AdverseEventPTCore",
"url" : "https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/AdverseEventPTCore",
"version" : "1.0.0",
"name" : "AdverseEventPTCore",
"status" : "draft",
"date" : "2024-02-09T14:29:46.6406318+00:00",
"publisher" : "SPMS",
"contact" : [
{
"name" : "Interoperabilidade Semântica",
"telecom" : [
{
"system" : "url",
"value" : "https://www.spms.min-saude.pt"
}
]
}
],
"description" : "O recurso AdverseEvent caracteriza de forma abrangente um evento adverso ou qualquer alteração do estado do utente, estando este associado a efeitos indesejados que poderão requerer monitorização, tratamento, hospitalização ou resultar na morte do utente. Exemplos de eventos adversos incluem a administração incorreta de um medicamento ou dose de um medicamento que causa uma reação adversa, o uso de um dispositivo implantado que causa uma infecção, entre outros. O recurso AdverseEvent PT Core corresponde a uma normalização nacional do recurso AdverseEvent.",
"fhirVersion" : "4.3.0",
"kind" : "resource",
"abstract" : false,
"type" : "AdverseEvent",
"baseDefinition" : "http://hl7.org/fhir/StructureDefinition/AdverseEvent",
"derivation" : "constraint",
"differential" : {
"element" : [
{
"id" : "AdverseEvent.id",
"path" : "AdverseEvent.id",
"min" : 1
},
{
"id" : "AdverseEvent.extension:supportingInfoPTExtension",
"path" : "AdverseEvent.extension",
"sliceName" : "supportingInfoPTExtension",
"type" : [
{
"code" : "Extension",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/SupportingInfoPTExtension"
]
}
]
},
{
"id" : "AdverseEvent.extension:preventiveActionPTExtension",
"path" : "AdverseEvent.extension",
"sliceName" : "preventiveActionPTExtension",
"type" : [
{
"code" : "Extension",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/PreventiveActionPTExtension"
]
}
]
},
{
"id" : "AdverseEvent.extension:mitigatingActionPTExtension",
"path" : "AdverseEvent.extension",
"sliceName" : "mitigatingActionPTExtension",
"type" : [
{
"code" : "Extension",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/MitigatingActionPTExtension"
]
}
]
},
{
"id" : "AdverseEvent.extension:causeOccurrencePTExtension",
"path" : "AdverseEvent.extension",
"sliceName" : "causeOccurrencePTExtension",
"type" : [
{
"code" : "Extension",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/CauseOccurrencePTExtension"
]
}
]
},
{
"id" : "AdverseEvent.extension:effectOccurrencePTExtension",
"path" : "AdverseEvent.extension",
"sliceName" : "effectOccurrencePTExtension",
"type" : [
{
"code" : "Extension",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/EffectOccurrencePTExtension"
]
}
]
},
{
"id" : "AdverseEvent.extension:notePTExtension",
"path" : "AdverseEvent.extension",
"sliceName" : "notePTExtension",
"type" : [
{
"code" : "Extension",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/NotePTExtension"
]
}
]
},
{
"id" : "AdverseEvent.identifier",
"path" : "AdverseEvent.identifier",
"type" : [
{
"code" : "Identifier",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/IdentifierPTCore"
]
}
]
},
{
"id" : "AdverseEvent.identifier.type.coding.id",
"path" : "AdverseEvent.identifier.type.coding.id",
"comment" : "."
},
{
"id" : "AdverseEvent.actuality",
"path" : "AdverseEvent.actuality",
"definition" : "Identifica se o evento efetivamente ocorreu ou se apenas existia potencial para acontecer."
},
{
"id" : "AdverseEvent.category",
"path" : "AdverseEvent.category",
"definition" : "Identifica a categoria de evento adverso.",
"type" : [
{
"code" : "CodeableConcept",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/CodeableConceptPTCore"
]
}
]
},
{
"id" : "AdverseEvent.event",
"path" : "AdverseEvent.event",
"definition" : "Define o tipo especÃfico de evento adversos. Os tipos de eventos adversos estão disponÃveis no catálogo CPARA, Value Set Adverse Event.",
"comment" : "Value Set Name: Adverse Event",
"type" : [
{
"code" : "CodeableConcept",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/CodeableConceptPTCore"
]
}
],
"binding" : {
"strength" : "required",
"valueSet" : "https://www.ctc.min-saude.pt/catalogos/alergias-e-outras-reacoes-adversas/"
}
},
{
"id" : "AdverseEvent.event.coding",
"path" : "AdverseEvent.event.coding",
"min" : 1
},
{
"id" : "AdverseEvent.subject",
"path" : "AdverseEvent.subject",
"definition" : "Identifica quem foi impactado pelo evento adverso.",
"type" : [
{
"code" : "Reference",
"targetProfile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/PatientPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/PractitionerPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/RelatedPersonPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/GroupPTCore"
]
}
]
},
{
"id" : "AdverseEvent.encounter",
"path" : "AdverseEvent.encounter",
"definition" : "Identifica o episódio associado à ocorrência do evento adverso..",
"type" : [
{
"code" : "Reference",
"targetProfile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/EncounterPTCore"
]
}
]
},
{
"id" : "AdverseEvent.encounter.identifier",
"path" : "AdverseEvent.encounter.identifier",
"short" : "An identifier intended for computation",
"definition" : "An identifier - identifies some entity uniquely and unambiguously. Typically this is used for business identifiers."
},
{
"id" : "AdverseEvent.date",
"path" : "AdverseEvent.date",
"definition" : "Identifica quando é que o evento ocorreu. \r\nUma data ou data parcial ou data e hora, sendo o formato definido pela ISO8601.\r\nSe a hora e minutos forem especificados, descrição da time zone (UTC) DEVE ser preenchida.\r\nOs segundos devem ser fornecidos devido a restrições de tipo de esquema, mas podem ser preenchidos com zero. O horário \"24:00\" não é permitido. Formatos possÃveis:\r\n ano\r\n ano e mês\r\n ano, mês e dia\r\n <YYYY-MM-DDThh:mm:ss+zz:zz> - ano, mês, dia , hora, minutos , segundos e time zone",
"max" : "0"
},
{
"id" : "AdverseEvent.detected",
"path" : "AdverseEvent.detected",
"definition" : "Identifica quando é que o evento foi detetado. \r\nUma data ou data parcial ou data e hora, sendo o formato definido pela ISO8601.\r\nSe a hora e minutos forem especificados, descrição da time zone (UTC) DEVE ser preenchida.\r\nOs segundos devem ser fornecidos devido a restrições de tipo de esquema, mas podem ser preenchidos com zero. O horário \"24:00\" não é permitido. Formatos possÃveis:\r\n ano\r\n ano e mês\r\n ano, mês e dia\r\n <YYYY-MM-DDThh:mm:ss+zz:zz> - ano, mês, dia , hora, minutos , segundos e time zone"
},
{
"id" : "AdverseEvent.recordedDate",
"path" : "AdverseEvent.recordedDate",
"definition" : "Identifica quando é que o evento foi registado. \r\nUma data ou data parcial ou data e hora, sendo o formato definido pela ISO8601.\r\nSe a hora e minutos forem especificados, descrição da time zone (UTC) DEVE ser preenchida.\r\nOs segundos devem ser fornecidos devido a restrições de tipo de esquema, mas podem ser preenchidos com zero. O horário \"24:00\" não é permitido. Formatos possÃveis:\r\n ano\r\n ano e mês\r\n ano, mês e dia\r\n <YYYY-MM-DDThh:mm:ss+zz:zz> - ano, mês, dia , hora, minutos , segundos e time zone"
},
{
"id" : "AdverseEvent.resultingCondition",
"path" : "AdverseEvent.resultingCondition",
"definition" : "Identifica informações sobre a reação que ocorreu como resultado da exposição a uma substância.",
"type" : [
{
"code" : "Reference",
"targetProfile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/ConditionPTCore"
]
}
]
},
{
"id" : "AdverseEvent.location",
"path" : "AdverseEvent.location",
"definition" : "Identifica o local onde o evento ocorreu.",
"type" : [
{
"code" : "Reference",
"targetProfile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/LocationPTCore"
]
}
]
},
{
"id" : "AdverseEvent.seriousness",
"path" : "AdverseEvent.seriousness",
"definition" : "Avalia a seriedade do evento adverso Os tipos de seriedade estão disponÃveis no catálogo CPARA, Value Set Adverse Event Seriousness.",
"comment" : "Value Set Name: Adverse Event Seriousness",
"type" : [
{
"code" : "CodeableConcept",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/CodeableConceptPTCore"
]
}
],
"binding" : {
"strength" : "required",
"valueSet" : "https://www.ctc.min-saude.pt/catalogos/alergias-e-outras-reacoes-adversas/"
}
},
{
"id" : "AdverseEvent.seriousness.coding",
"path" : "AdverseEvent.seriousness.coding",
"min" : 1
},
{
"id" : "AdverseEvent.seriousness.coding.system",
"path" : "AdverseEvent.seriousness.coding.system",
"fixedUri" : "urn:oid:2.16.620.1.101.10.4.1.7"
},
{
"id" : "AdverseEvent.severity",
"path" : "AdverseEvent.severity",
"type" : [
{
"code" : "CodeableConcept",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/CodeableConceptPTCore"
]
}
]
},
{
"id" : "AdverseEvent.outcome",
"path" : "AdverseEvent.outcome",
"comment" : "Value Set Name: Adverse Event Outcome",
"type" : [
{
"code" : "CodeableConcept",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/CodeableConceptPTCore"
]
}
],
"binding" : {
"strength" : "required",
"valueSet" : "https://www.ctc.min-saude.pt/catalogos/alergias-e-outras-reacoes-adversas/"
}
},
{
"id" : "AdverseEvent.recorder",
"path" : "AdverseEvent.recorder",
"definition" : "Identifica quem registou o evento adverso. Pode ser o utente, pessoa relacionada com o utente ou um profissional.",
"type" : [
{
"code" : "Reference",
"targetProfile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/PatientPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/PractitionarPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/PractitionerRolePTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/RelatedPersonPTCore"
]
}
]
},
{
"id" : "AdverseEvent.contributor",
"path" : "AdverseEvent.contributor",
"definition" : "Partes que podem ter contribuÃdo com informações para descrição do evento adverso.",
"type" : [
{
"code" : "Reference",
"targetProfile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/PractitionerPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/PractitionerRolePTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/DevicePTCore"
]
}
]
},
{
"id" : "AdverseEvent.suspectEntity",
"path" : "AdverseEvent.suspectEntity",
"definition" : "Identifica a entidade suspeita de ter causado o evento adverso."
},
{
"id" : "AdverseEvent.suspectEntity.instance",
"path" : "AdverseEvent.suspectEntity.instance",
"definition" : "Referencia a entidade suspeita de ter causado o evento adverso.",
"type" : [
{
"code" : "Reference",
"targetProfile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/ImmunizationPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/ProcedurePTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/SubstancePTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/MedicationPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/MedicationAdministrationPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/MedicationStatementPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/DevicePTCore"
]
}
]
},
{
"id" : "AdverseEvent.suspectEntity.causality",
"path" : "AdverseEvent.suspectEntity.causality",
"definition" : "Apresenta informação relativa à possÃvel causa do evento adverso."
},
{
"id" : "AdverseEvent.suspectEntity.causality.assessment",
"path" : "AdverseEvent.suspectEntity.causality.assessment",
"definition" : "Os termos que caracterizam a causalidade estão disponÃveis no catálogo CPARA, Value Set Adverse Event Causality.",
"comment" : "Value Set Name: Adverse Event Causality",
"type" : [
{
"code" : "CodeableConcept",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/CodeableConceptPTCore"
]
}
],
"binding" : {
"strength" : "example",
"valueSet" : "https://www.ctc.min-saude.pt/catalogos/alergias-e-outras-reacoes-adversas"
}
},
{
"id" : "AdverseEvent.suspectEntity.causality.assessment.coding",
"path" : "AdverseEvent.suspectEntity.causality.assessment.coding",
"min" : 1
},
{
"id" : "AdverseEvent.suspectEntity.causality.assessment.coding.system",
"path" : "AdverseEvent.suspectEntity.causality.assessment.coding.system",
"fixedUri" : "urn:oid:2.16.620.1.101.10.4.1.8"
},
{
"id" : "AdverseEvent.suspectEntity.causality.productRelatedness",
"path" : "AdverseEvent.suspectEntity.causality.productRelatedness",
"definition" : "Indicar em texto livre o produto relacionado com a causalidade."
},
{
"id" : "AdverseEvent.suspectEntity.causality.author",
"path" : "AdverseEvent.suspectEntity.causality.author",
"definition" : "Autor da informação da possÃvel causa do evento adverso.",
"type" : [
{
"code" : "Reference",
"targetProfile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/PractitionerPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/PractitionerRolePTCore"
]
}
]
},
{
"id" : "AdverseEvent.suspectEntity.causality.method",
"path" : "AdverseEvent.suspectEntity.causality.method",
"type" : [
{
"code" : "CodeableConcept",
"profile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/CodeableConceptPTCore"
]
}
]
},
{
"id" : "AdverseEvent.subjectMedicalHistory",
"path" : "AdverseEvent.subjectMedicalHistory",
"definition" : "Histórico clÃnico.",
"type" : [
{
"code" : "Reference",
"targetProfile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/ConditionPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/ObservationPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/AllergyIntolerancePTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/FamilyMemberHistoryPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/ImmunizationPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/ProcedurePTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/MediaPTCore",
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/DocumentReferencePTCore"
]
}
]
},
{
"id" : "AdverseEvent.referenceDocument",
"path" : "AdverseEvent.referenceDocument",
"definition" : "Identifica documentos relacionados com o evento.",
"type" : [
{
"code" : "Reference",
"targetProfile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/DocumentReferencePTCore"
]
}
]
},
{
"id" : "AdverseEvent.study",
"path" : "AdverseEvent.study",
"definition" : "Identificar estudos relacionados com o evento.",
"type" : [
{
"code" : "Reference",
"targetProfile" : [
"https://spms.min-saude.pt/fhir-r4B/iop/StructureDefinition/ResearchStudyPTCore"
]
}
]
}
]
},
"text" : {
}
}
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