r5/resource_types/clinical/summary/summary
library
Classes
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AdverseEvent
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AdverseEvent An event (i.e. any change to current patient status) that
may be related to unintended effects on a patient or research participant.
The unintended effects may require additional monitoring, treatment,
hospitalization, or may result in death. The AdverseEvent resource also
extends to potential or avoided events that could have had such effects.
There are two major domains where the AdverseEvent resource is expected to
be used. One is in clinical care reported adverse events and the other is
in reporting adverse events in clinical research trial management.
Adverse events can be reported by healthcare providers, patients,
caregivers or by medical products manufacturers. Given the differences
between these two concepts, we recommend consulting the domain specific
implementation guides when implementing the AdverseEvent Resource. The
implementation guides include specific extensions, value sets and
constraints.
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AdverseEventCausality
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AdverseEventCausality An event (i.e. any change to current patient
status) that may be related to unintended effects on a patient or research
participant. The unintended effects may require additional monitoring,
treatment, hospitalization, or may result in death. The AdverseEvent
resource also extends to potential or avoided events that could have had
such effects. There are two major domains where the AdverseEvent resource
is expected to be used. One is in clinical care reported adverse events
and the other is in reporting adverse events in clinical research trial
management. Adverse events can be reported by healthcare providers,
patients, caregivers or by medical products manufacturers. Given the
differences between these two concepts, we recommend consulting the domain
specific implementation guides when implementing the AdverseEvent
Resource. The implementation guides include specific extensions, value
sets and constraints.
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AdverseEventContributingFactor
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AdverseEventContributingFactor An event (i.e. any change to current
patient status) that may be related to unintended effects on a patient or
research participant. The unintended effects may require additional
monitoring, treatment, hospitalization, or may result in death. The
AdverseEvent resource also extends to potential or avoided events that
could have had such effects. There are two major domains where the
AdverseEvent resource is expected to be used. One is in clinical care
reported adverse events and the other is in reporting adverse events in
clinical research trial management. Adverse events can be reported by
healthcare providers, patients, caregivers or by medical products
manufacturers. Given the differences between these two concepts, we
recommend consulting the domain specific implementation guides when
implementing the AdverseEvent Resource. The implementation guides include
specific extensions, value sets and constraints.
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AdverseEventMitigatingAction
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AdverseEventMitigatingAction An event (i.e. any change to current patient
status) that may be related to unintended effects on a patient or research
participant. The unintended effects may require additional monitoring,
treatment, hospitalization, or may result in death. The AdverseEvent
resource also extends to potential or avoided events that could have had
such effects. There are two major domains where the AdverseEvent resource
is expected to be used. One is in clinical care reported adverse events
and the other is in reporting adverse events in clinical research trial
management. Adverse events can be reported by healthcare providers,
patients, caregivers or by medical products manufacturers. Given the
differences between these two concepts, we recommend consulting the domain
specific implementation guides when implementing the AdverseEvent
Resource. The implementation guides include specific extensions, value
sets and constraints.
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AdverseEventParticipant
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AdverseEventParticipant An event (i.e. any change to current patient
status) that may be related to unintended effects on a patient or research
participant. The unintended effects may require additional monitoring,
treatment, hospitalization, or may result in death. The AdverseEvent
resource also extends to potential or avoided events that could have had
such effects. There are two major domains where the AdverseEvent resource
is expected to be used. One is in clinical care reported adverse events
and the other is in reporting adverse events in clinical research trial
management. Adverse events can be reported by healthcare providers,
patients, caregivers or by medical products manufacturers. Given the
differences between these two concepts, we recommend consulting the domain
specific implementation guides when implementing the AdverseEvent
Resource. The implementation guides include specific extensions, value
sets and constraints.
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AdverseEventPreventiveAction
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AdverseEventPreventiveAction An event (i.e. any change to current patient
status) that may be related to unintended effects on a patient or research
participant. The unintended effects may require additional monitoring,
treatment, hospitalization, or may result in death. The AdverseEvent
resource also extends to potential or avoided events that could have had
such effects. There are two major domains where the AdverseEvent resource
is expected to be used. One is in clinical care reported adverse events
and the other is in reporting adverse events in clinical research trial
management. Adverse events can be reported by healthcare providers,
patients, caregivers or by medical products manufacturers. Given the
differences between these two concepts, we recommend consulting the domain
specific implementation guides when implementing the AdverseEvent
Resource. The implementation guides include specific extensions, value
sets and constraints.
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AdverseEventSupportingInfo
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AdverseEventSupportingInfo An event (i.e. any change to current patient
status) that may be related to unintended effects on a patient or research
participant. The unintended effects may require additional monitoring,
treatment, hospitalization, or may result in death. The AdverseEvent
resource also extends to potential or avoided events that could have had
such effects. There are two major domains where the AdverseEvent resource
is expected to be used. One is in clinical care reported adverse events
and the other is in reporting adverse events in clinical research trial
management. Adverse events can be reported by healthcare providers,
patients, caregivers or by medical products manufacturers. Given the
differences between these two concepts, we recommend consulting the domain
specific implementation guides when implementing the AdverseEvent
Resource. The implementation guides include specific extensions, value
sets and constraints.
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AdverseEventSuspectEntity
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AdverseEventSuspectEntity An event (i.e. any change to current patient
status) that may be related to unintended effects on a patient or research
participant. The unintended effects may require additional monitoring,
treatment, hospitalization, or may result in death. The AdverseEvent
resource also extends to potential or avoided events that could have had
such effects. There are two major domains where the AdverseEvent resource
is expected to be used. One is in clinical care reported adverse events
and the other is in reporting adverse events in clinical research trial
management. Adverse events can be reported by healthcare providers,
patients, caregivers or by medical products manufacturers. Given the
differences between these two concepts, we recommend consulting the domain
specific implementation guides when implementing the AdverseEvent
Resource. The implementation guides include specific extensions, value
sets and constraints.
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AllergyIntolerance
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AllergyIntolerance Risk of harmful or undesirable physiological response
which is specific to an individual and associated with exposure to a
substance.
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AllergyIntoleranceParticipant
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AllergyIntoleranceParticipant Risk of harmful or undesirable
physiological response which is specific to an individual and associated
with exposure to a substance.
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AllergyIntoleranceReaction
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AllergyIntoleranceReaction Risk of harmful or undesirable physiological
response which is specific to an individual and associated with exposure
to a substance.
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ClinicalImpression
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ClinicalImpression A record of a clinical assessment performed to
determine what problem(s) may affect the patient and before planning the
treatments or management strategies that are best to manage a patient's
condition. Assessments are often 1:1 with a clinical consultation /
encounter, but this varies greatly depending on the clinical workflow.
This resource is called "ClinicalImpression" rather than
"ClinicalAssessment" to avoid confusion with the recording of assessment
tools such as Apgar score.
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ClinicalImpressionFinding
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ClinicalImpressionFinding A record of a clinical assessment performed to
determine what problem(s) may affect the patient and before planning the
treatments or management strategies that are best to manage a patient's
condition. Assessments are often 1:1 with a clinical consultation /
encounter, but this varies greatly depending on the clinical workflow.
This resource is called "ClinicalImpression" rather than
"ClinicalAssessment" to avoid confusion with the recording of assessment
tools such as Apgar score.
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Condition
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Condition A clinical condition, problem, diagnosis, or other event,
situation, issue, or clinical concept that has risen to a level of concern.
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ConditionParticipant
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ConditionParticipant A clinical condition, problem, diagnosis, or other
event, situation, issue, or clinical concept that has risen to a level of
concern.
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ConditionStage
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ConditionStage A clinical condition, problem, diagnosis, or other event,
situation, issue, or clinical concept that has risen to a level of concern.
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DetectedIssue
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DetectedIssue Indicates an actual or potential clinical issue with or
between one or more active or proposed clinical actions for a patient;
e.g. Drug-drug interaction, Ineffective treatment frequency,
Procedure-condition conflict, gaps in care, etc.
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DetectedIssueEvidence
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DetectedIssueEvidence Indicates an actual or potential clinical issue
with or between one or more active or proposed clinical actions for a
patient; e.g. Drug-drug interaction, Ineffective treatment frequency,
Procedure-condition conflict, gaps in care, etc.
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DetectedIssueMitigation
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DetectedIssueMitigation Indicates an actual or potential clinical issue
with or between one or more active or proposed clinical actions for a
patient; e.g. Drug-drug interaction, Ineffective treatment frequency,
Procedure-condition conflict, gaps in care, etc.
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FamilyMemberHistory
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FamilyMemberHistory Significant health conditions for a person related to
the patient relevant in the context of care for the patient.
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FamilyMemberHistoryCondition
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FamilyMemberHistoryCondition Significant health conditions for a person
related to the patient relevant in the context of care for the patient.
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FamilyMemberHistoryParticipant
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FamilyMemberHistoryParticipant Significant health conditions for a person
related to the patient relevant in the context of care for the patient.
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FamilyMemberHistoryProcedure
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FamilyMemberHistoryProcedure Significant health conditions for a person
related to the patient relevant in the context of care for the patient.
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Procedure
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Procedure An action that is or was performed on or for a patient,
practitioner, device, organization, or location. For example, this can be
a physical intervention on a patient like an operation, or less invasive
like long term services, counseling, or hypnotherapy. This can be a
quality or safety inspection for a location, organization, or device.
This can be an accreditation procedure on a practitioner for licensing.
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ProcedureFocalDevice
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ProcedureFocalDevice An action that is or was performed on or for a
patient, practitioner, device, organization, or location. For example,
this can be a physical intervention on a patient like an operation, or
less invasive like long term services, counseling, or hypnotherapy. This
can be a quality or safety inspection for a location, organization, or
device. This can be an accreditation procedure on a practitioner for
licensing.
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ProcedurePerformer
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ProcedurePerformer An action that is or was performed on or for a
patient, practitioner, device, organization, or location. For example,
this can be a physical intervention on a patient like an operation, or
less invasive like long term services, counseling, or hypnotherapy. This
can be a quality or safety inspection for a location, organization, or
device. This can be an accreditation procedure on a practitioner for
licensing.