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Biomedical Research and Regulation Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: No defined compartments |
ShEx statement for clinicalusedefinition
PREFIX fhir: <http://hl7.org/fhir/> PREFIX fhirvs: <http://hl7.org/fhir/ValueSet/> PREFIX xsd: <http://www.w3.org/2001/XMLSchema#> PREFIX rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> IMPORT <code.shex> IMPORT <Range.shex> IMPORT <Group.shex> IMPORT <string.shex> IMPORT <Device.shex> IMPORT <markdown.shex> IMPORT <canonical.shex> IMPORT <Reference.shex> IMPORT <Substance.shex> IMPORT <Identifier.shex> IMPORT <Expression.shex> IMPORT <Medication.shex> IMPORT <DomainResource.shex> IMPORT <PlanDefinition.shex> IMPORT <CodeableConcept.shex> IMPORT <BackboneElement.shex> IMPORT <NutritionProduct.shex> IMPORT <DeviceDefinition.shex> IMPORT <CodeableReference.shex> IMPORT <ActivityDefinition.shex> IMPORT <ObservationDefinition.shex> IMPORT <MedicinalProductDefinition.shex> IMPORT <BiologicallyDerivedProduct.shex> start=@<ClinicalUseDefinition> AND {fhir:nodeRole [fhir:treeRoot]} # A single issue - either an indication, contraindication, interaction or an undesirable effect for a medicinal product, medication, device or procedure <ClinicalUseDefinition> EXTENDS @<DomainResource> CLOSED { a [fhir:ClinicalUseDefinition]?;fhir:nodeRole [fhir:treeRoot]?; fhir:identifier @<OneOrMore_Identifier>?; # Business identifier for this issue fhir:type @<code> AND {fhir:v @fhirvs:clinical-use-definition-type}; # indication | contraindication | # interaction | undesirable-effect | # warning fhir:category @<OneOrMore_CodeableConcept>?; # A categorisation of the issue, # primarily for dividing warnings # into subject heading areas such as # "Pregnancy", "Overdose" fhir:subject @<OneOrMore_Reference_ActivityDefinition_OR_BiologicallyDerivedProduct_OR_Device_OR_DeviceDefinition_OR_Medication_OR_MedicinalProductDefinition_OR_NutritionProduct_OR_PlanDefinition_OR_Substance>?; # The medication, product, # substance, device, procedure etc. # for which this is an indication, # contraindication, interaction, # undesirable effect, or warning fhir:status @<CodeableConcept>?; # Whether this is a current issue or # one that has been retired etc fhir:contraindication @<ClinicalUseDefinition.contraindication>?; # Specifics for when this is a # contraindication fhir:indication @<ClinicalUseDefinition.indication>?; # Specifics for when this is an # indication fhir:interaction @<ClinicalUseDefinition.interaction>?; # Specifics for when this is an # interaction fhir:population @<OneOrMore_Reference_Group>?; # The population group to which this # applies fhir:library @<OneOrMore_canonical>?; # Logic used by the clinical use # definition fhir:undesirableEffect @<ClinicalUseDefinition.undesirableEffect>?; # A possible negative outcome from # the use of this treatment fhir:warning @<ClinicalUseDefinition.warning>?; # Critical environmental, health or # physical risks or hazards. For # example 'Do not operate heavy # machinery', 'May cause drowsiness' } # Specifics for when this is a contraindication <ClinicalUseDefinition.contraindication> EXTENDS @<BackboneElement> CLOSED { fhir:diseaseSymptomProcedure @<CodeableReference>?; # The situation that is being # documented as contraindicating # against this item fhir:diseaseStatus @<CodeableReference>?; # The status of the disease or # symptom for the contraindication fhir:comorbidity @<OneOrMore_CodeableReference>?; # A comorbidity (concurrent # condition) or coinfection fhir:indication @<OneOrMore_Reference_ClinicalUseDefinition>?; # The indication which this is a # contraidication for fhir:applicability @<Expression>?; # An expression that returns true or # false, indicating whether the # indication is applicable or not, # after having applied its other # elements fhir:otherTherapy @<OneOrMore_ClinicalUseDefinition.contraindication.otherTherapy>?; # Information about use of the # product in relation to other # therapies described as part of the # contraindication } # Information about use of the product in relation to other therapies described as part of the contraindication <ClinicalUseDefinition.contraindication.otherTherapy> EXTENDS @<BackboneElement> CLOSED { fhir:relationshipType @<CodeableConcept>; # The type of relationship between # the product # indication/contraindication and # another therapy fhir:treatment @<CodeableReference>; # Reference to a specific # medication, substance etc. as part # of an indication or # contraindication } # Specifics for when this is an interaction <ClinicalUseDefinition.interaction> EXTENDS @<BackboneElement> CLOSED { fhir:interactant @<OneOrMore_ClinicalUseDefinition.interaction.interactant>?; # The specific medication, product, # food etc. or laboratory test that # interacts fhir:type @<CodeableConcept>?; # The type of the interaction e.g. # drug-drug interaction, drug-lab # test interaction fhir:effect @<CodeableReference>?; # The effect of the interaction, for # example "reduced gastric # absorption of primary medication" fhir:incidence @<CodeableConcept>?; # The incidence of the interaction, # e.g. theoretical, observed fhir:management @<OneOrMore_CodeableConcept>?; # Actions for managing the # interaction } # Critical environmental, health or physical risks or hazards. For example 'Do not operate heavy machinery', 'May cause drowsiness' <ClinicalUseDefinition.warning> EXTENDS @<BackboneElement> CLOSED { fhir:description @<markdown>?; # A textual definition of this # warning, with formatting fhir:code @<CodeableConcept>?; # A coded or unformatted textual # definition of this warning } # Specifics for when this is an indication <ClinicalUseDefinition.indication> EXTENDS @<BackboneElement> CLOSED { fhir:diseaseSymptomProcedure @<CodeableReference>?; # The situation that is being # documented as an indicaton for # this item fhir:diseaseStatus @<CodeableReference>?; # The status of the disease or # symptom for the indication fhir:comorbidity @<OneOrMore_CodeableReference>?; # A comorbidity or coinfection as # part of the indication fhir:intendedEffect @<CodeableReference>?; # The intended effect, aim or # strategy to be achieved fhir:duration @<Range> OR @<string> ?; # Timing or duration information fhir:undesirableEffect @<OneOrMore_Reference_ClinicalUseDefinition>?; # An unwanted side effect or # negative outcome of the subject of # this resource when being used for # this indication fhir:applicability @<Expression>?; # An expression that returns true or # false, indicating whether the # indication is applicable or not, # after having applied its other # elements fhir:otherTherapy @<OneOrMore_ClinicalUseDefinition.contraindication.otherTherapy>?; # The use of the medicinal product # in relation to other therapies # described as part of the # indication } # The specific medication, product, food etc. or laboratory test that interacts <ClinicalUseDefinition.interaction.interactant> EXTENDS @<BackboneElement> CLOSED { fhir:item (@<Reference> AND {fhir:link @<MedicinalProductDefinition> OR @<Medication> OR @<Substance> OR @<NutritionProduct> OR @<BiologicallyDerivedProduct> OR @<ObservationDefinition> }) OR @<CodeableConcept> ; # The specific medication, product, # food etc. or laboratory test that # interacts } # A possible negative outcome from the use of this treatment <ClinicalUseDefinition.undesirableEffect> EXTENDS @<BackboneElement> CLOSED { fhir:symptomConditionEffect @<CodeableReference>?; # The situation in which the # undesirable effect may manifest fhir:classification @<CodeableConcept>?; # High level classification of the # effect fhir:frequencyOfOccurrence @<CodeableConcept>?; # How often the effect is seen } #---------------------- Cardinality Types (OneOrMore) ------------------- <OneOrMore_Identifier> CLOSED { rdf:first @<Identifier> ; rdf:rest [rdf:nil] OR @<OneOrMore_Identifier> } <OneOrMore_CodeableConcept> CLOSED { rdf:first @<CodeableConcept> ; rdf:rest [rdf:nil] OR @<OneOrMore_CodeableConcept> } <OneOrMore_Reference_ActivityDefinition_OR_BiologicallyDerivedProduct_OR_Device_OR_DeviceDefinition_OR_Medication_OR_MedicinalProductDefinition_OR_NutritionProduct_OR_PlanDefinition_OR_Substance> CLOSED { rdf:first @<Reference> AND {fhir:link @<ActivityDefinition> OR @<BiologicallyDerivedProduct> OR @<Device> OR @<DeviceDefinition> OR @<Medication> OR @<MedicinalProductDefinition> OR @<NutritionProduct> OR @<PlanDefinition> OR @<Substance> } ; rdf:rest [rdf:nil] OR @<OneOrMore_Reference_ActivityDefinition_OR_BiologicallyDerivedProduct_OR_Device_OR_DeviceDefinition_OR_Medication_OR_MedicinalProductDefinition_OR_NutritionProduct_OR_PlanDefinition_OR_Substance> } <OneOrMore_Reference_Group> CLOSED { rdf:first @<Reference> AND {fhir:link @<Group> } ; rdf:rest [rdf:nil] OR @<OneOrMore_Reference_Group> } <OneOrMore_canonical> CLOSED { rdf:first @<canonical> ; rdf:rest [rdf:nil] OR @<OneOrMore_canonical> } <OneOrMore_CodeableReference> CLOSED { rdf:first @<CodeableReference> ; rdf:rest [rdf:nil] OR @<OneOrMore_CodeableReference> } <OneOrMore_Reference_ClinicalUseDefinition> CLOSED { rdf:first @<Reference> AND {fhir:link @<ClinicalUseDefinition> } ; rdf:rest [rdf:nil] OR @<OneOrMore_Reference_ClinicalUseDefinition> } <OneOrMore_ClinicalUseDefinition.contraindication.otherTherapy> CLOSED { rdf:first @<ClinicalUseDefinition.contraindication.otherTherapy> ; rdf:rest [rdf:nil] OR @<OneOrMore_ClinicalUseDefinition.contraindication.otherTherapy> } <OneOrMore_ClinicalUseDefinition.interaction.interactant> CLOSED { rdf:first @<ClinicalUseDefinition.interaction.interactant> ; rdf:rest [rdf:nil] OR @<OneOrMore_ClinicalUseDefinition.interaction.interactant> } #---------------------- Value Sets ------------------------ # Overall defining type of this clinical use definition. fhirvs:clinical-use-definition-type ["indication" "contraindication" "interaction" "undesirable-effect" "warning"]
Usage note: every effort has been made to ensure that the ShEx files are correct and useful, but they are not a normative part of the specification.
FHIR ®© HL7.org 2011+. FHIR R6 hl7.fhir.core#6.0.0-ballot2 generated on Wed, Nov 6, 2024 22:16+0000.
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