Adverseevent.shex

ShEx statement for adverseevent

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 <Group.shex>
IMPORT <Period.shex>
IMPORT <Timing.shex>

IMPORT <Device.shex>
IMPORT <Patient.shex>
IMPORT <boolean.shex>
IMPORT <dateTime.shex>
IMPORT <Location.shex>
IMPORT <CareTeam.shex>
IMPORT <Reference.shex>
IMPORT <Encounter.shex>
IMPORT <Procedure.shex>

IMPORT <Condition.shex>
IMPORT <Substance.shex>

IMPORT <Identifier.shex>
IMPORT <Annotation.shex>
IMPORT <Medication.shex>

IMPORT <Observation.shex>
IMPORT <DeviceUsage.shex>

IMPORT <Practitioner.shex>
IMPORT <Immunization.shex>

IMPORT <Organization.shex>
IMPORT <RelatedPerson.shex>
IMPORT <ResearchStudy.shex>
IMPORT <DomainResource.shex>
IMPORT <CodeableConcept.shex>
IMPORT <ResearchSubject.shex>

IMPORT <BackboneElement.shex>
IMPORT <PractitionerRole.shex>
IMPORT <DocumentReference.shex>
IMPORT <MedicationRequest.shex>
IMPORT <AllergyIntolerance.shex>
IMPORT <FamilyMemberHistory.shex>
IMPORT <MedicationStatement.shex>
IMPORT <QuestionnaireResponse.shex>
IMPORT <MedicationAdministration.shex>
IMPORT <BiologicallyDerivedProduct.shex>

IMPORT <CodeableReference.shex>

start=@<AdverseEvent> AND {fhir:nodeRole [fhir:treeRoot]}
# An event that may be related to unintended effects on a patient or research participant
<AdverseEvent> EXTENDS @<DomainResource> CLOSED {   
    a [fhir:AdverseEvent]?;
    fhir:nodeRole [fhir:treeRoot]?;
    fhir:identifier @<OneOrMore_Identifier>?;  # Business identifier for the event
    fhir:status @<code> AND
    	{fhir:v @fhirvs:adverse-event-status};  # in-progress | completed | 
                                            # entered-in-error | unknown 
    fhir:actuality @<code> AND
    	{fhir:v @fhirvs:adverse-event-actuality};  # actual | potential
    fhir:category @<OneOrMore_CodeableConcept>?;  # wrong-patient | procedure-mishap | 
                                            # medication-mishap | device | 
                                            # unsafe-physical-environment | 
                                            # hospital-aquired-infection | 
                                            # wrong-body-site 
    fhir:code @<CodeableConcept>?;          # Event or incident that occurred or 
                                            # was averted 
    fhir:subject @<Reference> AND {fhir:link 
    			@<Group> OR 
    			@<Patient> OR 
    			@<Practitioner> OR 
    			@<RelatedPerson> OR 
    			@<ResearchSubject> ? };  # Subject impacted by event

    			@<RelatedPerson> ? };  # Subject impacted by event

    fhir:encounter @<Reference> AND {fhir:link 
    			@<Encounter> ? }?;  # The Encounter associated with the 
                                            # start of the AdverseEvent 
    fhir:occurrence @<dateTime>  OR 
    			@<Period>  OR 
    			@<Timing>  ?;  # When the event occurred

    fhir:cause @<dateTime>  OR 
    			@<Period>  ?;  # When the cause of the AdverseEvent 
                                            # occurred 
    fhir:effect @<dateTime>  OR 
    			@<Period>  ?;  # When the effect of the 
                                            # AdverseEvent occurred 

    fhir:detected @<dateTime>?;             # When the event was detected
    fhir:recordedDate @<dateTime>?;         # When the event was recorded
    fhir:resultingEffect @<OneOrMore_Reference_Condition_OR_Observation>?;  # Effect on the subject due to this 
                                            # event 
    fhir:location @<Reference> AND {fhir:link 
    			@<Location> ? }?;  # Location where adverse event 
                                            # occurred 
    fhir:seriousness @<CodeableConcept>?;   # Seriousness or gravity of the event
    fhir:outcome @<OneOrMore_CodeableConcept>?;  # Type of outcome from the adverse 
                                            # event 
    fhir:recorder @<Reference> AND {fhir:link 
    			@<Patient> OR 
    			@<Practitioner> OR 
    			@<PractitionerRole> OR 
    			@<RelatedPerson> OR 
    			@<ResearchSubject> ? }?;  # Who recorded the adverse event

    			@<RelatedPerson> ? }?;  # Who recorded the adverse event

    fhir:participant @<OneOrMore_AdverseEvent.participant>?;  # Who was involved in the adverse 
                                            # event or the potential adverse 
                                            # event and what they did 
    fhir:study @<OneOrMore_Reference_ResearchStudy>?;  # Research study that the subject is 
                                            # enrolled in 
    fhir:expectedInResearchStudy @<boolean>?;  # Considered likely or probable or 
                                            # anticipated in the research study 
    fhir:suspectEntity @<OneOrMore_AdverseEvent.suspectEntity>?;  # The suspected agent causing the 
                                            # adverse event 
    fhir:contributingFactor @<OneOrMore_AdverseEvent.contributingFactor>?;  # Contributing factors suspected to 

    fhir:contributingFactor @<OneOrMore_CodeableReference>?;  # Contributing factors suspected to 

                                            # have increased the probability or 
                                            # severity of the adverse event 
    fhir:preventiveAction @<OneOrMore_AdverseEvent.preventiveAction>?;  # Preventive actions that 

    fhir:preventiveAction @<OneOrMore_CodeableReference>?;  # Preventive actions that 

                                            # contributed to avoiding the 
                                            # adverse event 
    fhir:mitigatingAction @<OneOrMore_AdverseEvent.mitigatingAction>?;  # Ameliorating actions taken after 
                                            # the adverse event occured in order 
                                            # to reduce the extent of harm 
    fhir:supportingInfo @<OneOrMore_AdverseEvent.supportingInfo>?;  # Supporting information relevant to 
                                            # the event 

    fhir:mitigatingAction @<OneOrMore_CodeableReference>?;  # Ameliorating actions taken after 
                                            # the adverse event occurred in 
                                            # order to reduce the extent of harm 
    fhir:supportingInfo @<OneOrMore_CodeableReference>?;  # Subject medical history or 
                                            # document relevant to this adverse 
                                            # event 

    fhir:note @<OneOrMore_Annotation>?;     # Comment on adverse event
}  
# Information on the possible cause of the event
<AdverseEvent.suspectEntity.causality> EXTENDS @<BackboneElement> CLOSED {   
    fhir:assessmentMethod @<CodeableConcept>?;  # Method of evaluating the 
                                            # relatedness of the suspected 
                                            # entity to the event 
    fhir:entityRelatedness @<CodeableConcept>?;  # Result of the assessment regarding 
                                            # the relatedness of the suspected 
                                            # entity to the event 
    fhir:author @<Reference> AND {fhir:link 
    			@<Patient> OR 
    			@<Practitioner> OR 
    			@<PractitionerRole> OR 
    			@<RelatedPerson> OR 
    			@<ResearchSubject> ? }?;  # Author of the information on the 

    			@<RelatedPerson> ? }?;  # Author of the information on the 

                                            # possible cause of the event 
}  
# Preventive actions that contributed to avoiding the adverse event
<AdverseEvent.preventiveAction> EXTENDS @<BackboneElement> CLOSED {   
    fhir:item (@<Reference>  AND {fhir:link @<Immunization> OR 
    			 @<Procedure> OR 
    			 @<DocumentReference> OR 
    			 @<MedicationAdministration> OR 
    			 @<MedicationRequest> })  OR 
    			@<CodeableConcept>  ;  # Action that contributed to 
                                            # avoiding the adverse event 
}  
# Ameliorating actions taken after the adverse event occured in order to reduce the extent of harm
<AdverseEvent.mitigatingAction> EXTENDS @<BackboneElement> CLOSED {   
    fhir:item (@<Reference>  AND {fhir:link @<Procedure> OR 
    			 @<DocumentReference> OR 
    			 @<MedicationAdministration> OR 
    			 @<MedicationRequest> })  OR 
    			@<CodeableConcept>  ;  # Ameliorating action taken after 
                                            # the adverse event occured in order 
                                            # to reduce the extent of harm 
}  

# Who was involved in the adverse event or the potential adverse event and what they did
<AdverseEvent.participant> EXTENDS @<BackboneElement> CLOSED {   
    fhir:function @<CodeableConcept>?;      # Type of involvement
    fhir:actor @<Reference> AND {fhir:link 
    			@<CareTeam> OR 
    			@<Device> OR 
    			@<Organization> OR 
    			@<Patient> OR 
    			@<Practitioner> OR 
    			@<PractitionerRole> OR 
    			@<RelatedPerson> OR 
    			@<ResearchSubject> ? };  # Who was involved in the adverse 

    			@<RelatedPerson> ? };  # Who was involved in the adverse 

                                            # event or the potential adverse 
                                            # event 
}  
# Contributing factors suspected to have increased the probability or severity of the adverse event
<AdverseEvent.contributingFactor> EXTENDS @<BackboneElement> CLOSED {   
    fhir:item (@<Reference>  AND {fhir:link @<Condition> OR 
    			 @<Observation> OR 
    			 @<AllergyIntolerance> OR 
    			 @<FamilyMemberHistory> OR 
    			 @<Immunization> OR 
    			 @<Procedure> OR 
    			 @<Device> OR 
    			 @<DeviceUsage> OR 
    			 @<DocumentReference> OR 
    			 @<MedicationAdministration> OR 
    			 @<MedicationStatement> })  OR 
    			@<CodeableConcept>  ;  # Item suspected to have increased 
                                            # the probability or severity of the 
                                            # adverse event 
}  
# Supporting information relevant to the event
<AdverseEvent.supportingInfo> EXTENDS @<BackboneElement> CLOSED {   
    fhir:item (@<Reference>  AND {fhir:link @<Condition> OR 
    			 @<Observation> OR 
    			 @<AllergyIntolerance> OR 
    			 @<FamilyMemberHistory> OR 
    			 @<Immunization> OR 
    			 @<Procedure> OR 
    			 @<DocumentReference> OR 
    			 @<MedicationAdministration> OR 
    			 @<MedicationStatement> OR 
    			 @<QuestionnaireResponse> })  OR 
    			@<CodeableConcept>  ;  # Subject medical history or 
                                            # document relevant to this adverse 
                                            # event 
}  

# The suspected agent causing the adverse event
<AdverseEvent.suspectEntity> EXTENDS @<BackboneElement> CLOSED {   
    fhir:instance @<CodeableConcept>  OR 
    			(@<Reference>  AND {fhir:link @<Immunization> OR 
    			 @<Procedure> OR 
    			 @<Substance> OR 
    			 @<Medication> OR 
    			 @<MedicationAdministration> OR 
    			 @<MedicationStatement> OR 
    			 @<Device> OR 
    			 @<BiologicallyDerivedProduct> OR 
    			 @<ResearchStudy> })  ;  # Refers to the specific entity that 

    fhir:instance @<CodeableReference>;     # Refers to the specific entity that 

                                            # caused the adverse event 
    fhir:causality @<AdverseEvent.suspectEntity.causality>?;  # Information on the possible cause 
                                            # of the event 
}  
#---------------------- 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_Condition_OR_Observation> CLOSED {
    rdf:first @<Reference> AND {fhir:link 
			@<Condition> OR 
			@<Observation> } ;
    rdf:rest [rdf:nil] OR @<OneOrMore_Reference_Condition_OR_Observation> 
}
<OneOrMore_AdverseEvent.participant> CLOSED {
    rdf:first @<AdverseEvent.participant>  ;
    rdf:rest [rdf:nil] OR @<OneOrMore_AdverseEvent.participant> 
}
<OneOrMore_Reference_ResearchStudy> CLOSED {
    rdf:first @<Reference> AND {fhir:link 
			@<ResearchStudy> } ;
    rdf:rest [rdf:nil] OR @<OneOrMore_Reference_ResearchStudy> 
}
<OneOrMore_AdverseEvent.suspectEntity> CLOSED {
    rdf:first @<AdverseEvent.suspectEntity>  ;
    rdf:rest [rdf:nil] OR @<OneOrMore_AdverseEvent.suspectEntity> 
}
<OneOrMore_AdverseEvent.contributingFactor> CLOSED {
    rdf:first @<AdverseEvent.contributingFactor>  ;
    rdf:rest [rdf:nil] OR @<OneOrMore_AdverseEvent.contributingFactor> 
}
<OneOrMore_AdverseEvent.preventiveAction> CLOSED {
    rdf:first @<AdverseEvent.preventiveAction>  ;
    rdf:rest [rdf:nil] OR @<OneOrMore_AdverseEvent.preventiveAction> 
}
<OneOrMore_AdverseEvent.mitigatingAction> CLOSED {
    rdf:first @<AdverseEvent.mitigatingAction>  ;
    rdf:rest [rdf:nil] OR @<OneOrMore_AdverseEvent.mitigatingAction> 
}
<OneOrMore_AdverseEvent.supportingInfo> CLOSED {
    rdf:first @<AdverseEvent.supportingInfo>  ;
    rdf:rest [rdf:nil] OR @<OneOrMore_AdverseEvent.supportingInfo> 

<OneOrMore_CodeableReference> CLOSED {
    rdf:first @<CodeableReference>  ;
    rdf:rest [rdf:nil] OR @<OneOrMore_CodeableReference> 

}
<OneOrMore_Annotation> CLOSED {
    rdf:first @<Annotation>  ;
    rdf:rest [rdf:nil] OR @<OneOrMore_Annotation> 
}
#---------------------- Value Sets ------------------------
# Overall nature of the adverse event, e.g. real or potential.
fhirvs:adverse-event-actuality ["actual" "potential"]
# Codes identifying the lifecycle stage of an adverse event.
fhirvs:adverse-event-status ["in-progress" "completed" "entered-in-error" "unknown"]