Foundation
This
page
is
part
of
the
FHIR
Specification
(v4.0.1:
R4
(v5.0.0-draft-final:
Final
QA
Preview
for
R5
-
Mixed
Normative
and
STU
see
ballot
notes
)
in
it's
permanent
home
(it
will
always
be
available
at
this
URL).
).
The
current
version
which
supercedes
this
version
is
5.0.0
.
For
a
full
list
of
available
versions,
see
the
Directory
of
published
versions
.
Page
versions:
R5
R4B
R4
R3
|
|
Maturity Level : N/A | Standards Status : Informative |
Compartments
:
|
This
is
the
narrative
for
the
resource.
See
also
the
XML
,
JSON
or
Turtle
Raw
ShEx
format.
This
example
conforms
to
the
profile
GraphDefinition
.
Generated
Narrative
with
Details
id
:
example
url
:
http://h7.org/fhir/GraphDefinition/example
name
:
Document
Generation
Template
status
:
draft
date
:
04/08/2015
publisher
:
FHIR
Project
contact
:
type
:
List
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#>Compartments -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 <Substance.shex> IMPORT <Condition.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 <MedicationStatement.shex> IMPORT <FamilyMemberHistory.shex> IMPORT <QuestionnaireResponse.shex> IMPORT <MedicationAdministration.shex> IMPORT <BiologicallyDerivedProduct.shex>Usestart=@<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]?;Codefhir: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 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: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 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 # have increased the probability or # severity of the adverse event fhir:preventiveAction @<OneOrMore_AdverseEvent.preventiveAction>?; # 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:note @<OneOrMore_Annotation>?; # Comment on 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 # caused the adverse event fhir:causality @<AdverseEvent.suspectEntity.causality>?; # Information on the possible cause # of the 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 }Rule# 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 # event or the potential adverse # 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 } # 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 } # 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 # possible cause of the 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 }requirement#---------------------- Cardinality Types (OneOrMore) -------------------Patient<OneOrMore_Identifier> CLOSED { rdf:first @<Identifier> ; rdf:rest [rdf:nil] OR @<OneOrMore_Identifier> }identical<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> }Links<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_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"]
Usage
note:
every
effort
has
been
made
to
ensure
that
the
examples
ShEx
files
are
correct
and
useful,
but
they
are
not
a
normative
part
of
the
specification.
FHIR
®©
HL7.org
2011+.
FHIR
Release
4
(Technical
Correction
#1)
(v4.0.1)
R5
hl7.fhir.core#5.0.0-draft-final
generated
on
Fri,
Nov
Wed,
Mar
1,
2019
09:35+1100.
QA
Page
2023
23:06+1100.
Links:
Search
|
Version
History
|
Table
of
Contents
|
Credits
Glossary
|
QA
|
Compare
to
R3
R4B
|
Compare
to
R5
Draft
|
|
Propose
a
change