TEMPLATE Symptome LEOSS (Symptome LEOSS)

TEMPLATE IDSymptome LEOSS
ConceptSymptome LEOSS
DescriptionZur Repräsentation der Symptome der Erkrankung aus dem LEOSS-Datensatz für COVID-19 Patienten.
UseZur Repräsentation der Symptome für das COVID-19 Projekt.
MisuseNicht zur Repräsentation alle Symptome verwenden.
PurposeZur Repräsentation der Symptome der Erkrankung aus dem LEOSS-Datensatz für COVID-19 Patienten.
References
AuthorsName: Sarah Ballout; Organisation: MHH-Hannover; Email: ballout.sarah@mh-hannover.de
Other Details LanguageName: Sarah Ballout; Organisation: MHH-Hannover; Email: ballout.sarah@mh-hannover.de
Other Details (Language Independent)
  • MetaDataSet:Sample Set : Template metadata sample set
KeywordsSymptome; Erkrankung; Krankheitsanzeichen
Language useden
Citeable Identifier1246.169.785
Root archetype idopenEHR-EHR-COMPOSITION.report.v1
ReportReport: Document to communicate information to others, commonly in response to a request from another party.
Other Context
Bericht NameBericht Name: Identification information about the report.
  • Symptome LEOSS
StatusStatus: The status of the entire report. Note: This is not the status of any of the report components.
SymptomsSymptoms: A generic section header which should be renamed in a template to suit a specific clinical context.
Symptom/KrankheitsanzeichenSymptom/Krankheitsanzeichen: An individual- or self-reported questionnaire screening for symptoms and signs.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
Runny NoseRunny Nose: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Runny Nose
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
Sore throatSore throat: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Sore throat
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
Dry coughDry cough: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Dry cough
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
Productive coughProductive cough: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Productive cough
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
WheezingWheezing: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Wheezing
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
DyspnoeDyspnoe: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Dyspnoe
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
Feeling of breathlessnessFeeling of breathlessness: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Feeling of breathlessness
How you feel of breathlessness?How you feel of breathlessness?: Free text.
AnswerAnswer: Free text.
  • None
  • Mild
  • Moderate
  • Severe
  • Unknown
PalpitationsPalpitations: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Palpitations
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
Nausea / emesisNausea / emesis: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Nausea / emesis
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
DiarrheaDiarrhea: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Diarrhea
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
Muscle achesMuscle aches: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Muscle aches
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
Muscle weaknessMuscle weakness: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Muscle weakness
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
FeverFever: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Fever
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
DeliriumDelirium: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Delirium
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
Excessive tirednessExcessive tiredness: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Excessive tiredness
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
HeadacheHeadache: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Headache
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
MeningismMeningism: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Meningism
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
Smell disordersSmell disorders: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Smell disorders
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
Taste disorderTaste disorder: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Taste disorder
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
Other neurological symptomsOther neurological symptoms: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Other neurological symptoms
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
Red eyeRed eye: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Red eye
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
AsymptomaticAsymptomatic: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Asymptomatic
Presence?Presence?: Presence of the symptom or sign.
  • Present 
  • Absent 
  • Unknown 
Cardiovascular ComplicationsCardiovascular Complications: A generic section header which should be renamed in a template to suit a specific clinical context.
Symptom/sign screening questionnaireSymptom/sign screening questionnaire: An individual- or self-reported questionnaire screening for symptoms and signs.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
Specific symptom/signSpecific symptom/sign: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Cardiac arrhytmia
Cardiac arrhytmiaCardiac arrhytmia: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Cardiac arrhytmia
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Life threatening arrhytmiaLife threatening arrhytmia: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Life threatening arrhytmia
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Myocardial ischemia, acute coronary syndromeMyocardial ischemia, acute coronary syndrome: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Myocardial ischemia, acute coronary syndrome
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
CommentComment: Additional narrative about the symptom or sign not captured in other fields.
MyocarditisMyocarditis: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Myocarditis
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
(Congestive) heart failure(Congestive) heart failure: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • (Congestive) heart failure
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Pericardial effusionPericardial effusion: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Pericardial effusion
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
CommentComment: Additional narrative about the symptom or sign not captured in other fields.
Any bleedingAny bleeding: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Any bleeding
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
CommentComment: Additional narrative about the symptom or sign not captured in other fields.
Respiratory ComplicationsRespiratory Complications: A generic section header which should be renamed in a template to suit a specific clinical context.
Symptom/sign screening questionnaireSymptom/sign screening questionnaire: An individual- or self-reported questionnaire screening for symptoms and signs.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
Specific symptom/signSpecific symptom/sign: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Respiratory Complications
Need for oxygen supplementationNeed for oxygen supplementation: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Need for oxygen supplementation
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Clinical indication for intubationClinical indication for intubation: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Clinical indication for intubation
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Re-intubationRe-intubation: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Re-intubation
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
CommentComment: Additional narrative about the symptom or sign not captured in other fields.
ECMOECMO: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • ECMO
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
CommentComment: Additional narrative about the symptom or sign not captured in other fields.
Renal complicationsRenal complications: A generic section header which should be renamed in a template to suit a specific clinical context.
Symptom/sign screening questionnaireSymptom/sign screening questionnaire: An individual- or self-reported questionnaire screening for symptoms and signs.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
Specific symptom/signSpecific symptom/sign: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Renal complications
Acute kidney injury (KDIGO)Acute kidney injury (KDIGO): Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Acute kidney injury (KDIGO)
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
StadiumStadium: Simple body site where the symptom or sign was reported.
Occurrences of this data element are set to 0..* to allow multiple body sites to be separated out in a template if desired. This allows for representation of clinical scenarios where a symptom or sign needs to be recorded in multiple locations or identifying both the originating and distal site in pain radiation, but where all of the other attributes such as impact and duration are identical. If the requirements for recording the body site are determined at run-time by the application or require more complex modelling such as relative locations then use the CLUSTER.anatomical_location or CLUSTER.relative_location within the Detailed anatomical location' SLOT in this archetype. If the anatomical location is included in the Symptom name via precoordinated codes, this data element becomes redundant. If the anatomical location is recorded using the 'Structured body site' SLOT, then use of this data element is not allowed - record only the simple 'Body site' OR 'Structured body site', but not both.
  • Stage I
  • Stage II
  • Stage III
  • None
  • Unknown
New renal failure with need for dialysisNew renal failure with need for dialysis: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • New renal failure with need for dialysis
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Not recovered kidney failureNot recovered kidney failure: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Not recovered kidney failure
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Thrombotic and thrombembolic complicationsThrombotic and thrombembolic complications: A generic section header which should be renamed in a template to suit a specific clinical context.
Symptom/sign screening questionnaireSymptom/sign screening questionnaire: An individual- or self-reported questionnaire screening for symptoms and signs.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
Specific symptom/signSpecific symptom/sign: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Thrombotic and thrombembolic complications
Abdominal thrombosisAbdominal thrombosis: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Abdominal thrombosis
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Arterial thrombosisArterial thrombosis: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Arterial thrombosis
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Microangiopathy, -thrombosisMicroangiopathy, -thrombosis: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Microangiopathy, -thrombosis
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Venous thrombosis, pulmonary thrombembolismVenous thrombosis, pulmonary thrombembolism: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Venous thrombosis, pulmonary thrombembolism
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Neurological complicationsNeurological complications: A generic section header which should be renamed in a template to suit a specific clinical context.
Symptom/sign screening questionnaireSymptom/sign screening questionnaire: An individual- or self-reported questionnaire screening for symptoms and signs.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
Specific symptom/signSpecific symptom/sign: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Neurological complications
Intracerebral bleedingIntracerebral bleeding: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Intracerebral bleeding
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Ischemic strokeIschemic stroke: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Ischemic stroke
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Cause of strokeCause of stroke: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Cause of stroke
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
TOAST-ClassificationTOAST-Classification: Simple body site where the symptom or sign was reported.
Occurrences of this data element are set to 0..* to allow multiple body sites to be separated out in a template if desired. This allows for representation of clinical scenarios where a symptom or sign needs to be recorded in multiple locations or identifying both the originating and distal site in pain radiation, but where all of the other attributes such as impact and duration are identical. If the requirements for recording the body site are determined at run-time by the application or require more complex modelling such as relative locations then use the CLUSTER.anatomical_location or CLUSTER.relative_location within the Detailed anatomical location' SLOT in this archetype. If the anatomical location is included in the Symptom name via precoordinated codes, this data element becomes redundant. If the anatomical location is recorded using the 'Structured body site' SLOT, then use of this data element is not allowed - record only the simple 'Body site' OR 'Structured body site', but not both.
  • Cardioembolic
  • Large-ateryatherosclerosis
  • Small artery occlusion
  • Other causes
  • Undefined
Stroke score NIHSSStroke score NIHSS: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Stroke score NIHSS
Number of Stroke score NIHSSNumber of Stroke score NIHSS: The number of times this symptom or sign has previously occurred.
>=0
Meningitis/EncephalitisMeningitis/Encephalitis: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Meningitis/Encephalitis
Nil significantNil significant: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
MyositisMyositis: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Myositis
Nil significantNil significant: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
SeizureSeizure: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Seizure
Nil significantNil significant: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Neurological sequelaeNeurological sequelae: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Neurological sequelae
Nil significantNil significant: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Severe cognitive impairmentSevere cognitive impairment: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Severe cognitive impairment
Nil significantNil significant: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Further complicationsFurther complications: A generic section header which should be renamed in a template to suit a specific clinical context.
Symptom/sign screening questionnaireSymptom/sign screening questionnaire: An individual- or self-reported questionnaire screening for symptoms and signs.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
Specific symptom/signSpecific symptom/sign: Grouping of data elements related to screening for a single symptom or sign.
Symptom or sign nameSymptom or sign name: Name of the symptom or sign being screened.
  • Further complications
VasculitisVasculitis: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Vasculitis
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Septic shockSeptic shock: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Septic shock
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
qSOFA >= 2qSOFA >= 2: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • qSOFA >= 2
Vorhanden?Vorhanden?: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
TOAST-ClassificationTOAST-Classification: Simple body site where the symptom or sign was reported.
Occurrences of this data element are set to 0..* to allow multiple body sites to be separated out in a template if desired. This allows for representation of clinical scenarios where a symptom or sign needs to be recorded in multiple locations or identifying both the originating and distal site in pain radiation, but where all of the other attributes such as impact and duration are identical. If the requirements for recording the body site are determined at run-time by the application or require more complex modelling such as relative locations then use the CLUSTER.anatomical_location or CLUSTER.relative_location within the Detailed anatomical location' SLOT in this archetype. If the anatomical location is included in the Symptom name via precoordinated codes, this data element becomes redundant. If the anatomical location is recorded using the 'Structured body site' SLOT, then use of this data element is not allowed - record only the simple 'Body site' OR 'Structured body site', but not both.
  • Cardioembolic
  • Large-ateryatherosclerosis
  • Small artery occlusion
  • Other causes
  • Undefined
Other complications, specifyOther complications, specify: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Other complications, specify
Nil significantNil significant: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
KommentarKommentar: Simple body site where the symptom or sign was reported.
Occurrences of this data element are set to 0..* to allow multiple body sites to be separated out in a template if desired. This allows for representation of clinical scenarios where a symptom or sign needs to be recorded in multiple locations or identifying both the originating and distal site in pain radiation, but where all of the other attributes such as impact and duration are identical. If the requirements for recording the body site are determined at run-time by the application or require more complex modelling such as relative locations then use the CLUSTER.anatomical_location or CLUSTER.relative_location within the Detailed anatomical location' SLOT in this archetype. If the anatomical location is included in the Symptom name via precoordinated codes, this data element becomes redundant. If the anatomical location is recorded using the 'Structured body site' SLOT, then use of this data element is not allowed - record only the simple 'Body site' OR 'Structured body site', but not both.
Number of Stroke score NIHSSNumber of Stroke score NIHSS: The number of times this symptom or sign has previously occurred.
>=0
Severe fatigueSevere fatigue: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Severe fatigue
Nil significantNil significant: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Other sequelaeOther sequelae: Reported observation of a physical or mental disturbance in an individual.
Symptom/Sign nameSymptom/Sign name: The name of the reported symptom or sign.
Symptom name should be coded with a terminology, where possible.
  • Other sequelae
Nil significantNil significant: The identified symptom or sign was reported as not being present to any significant degree.
Record as True if the subject of care has reported the symptom as not significant. For example: if the individual has never experienced the symptom it is appropriate to record 'nil significant'; or if the individual commonly experiences the symptom, in some circumstances it may be considered appropriate to record 'nil significant' if the individual has experienced no deviation from their 'normal' baseline.
Vital signsVital signs: A group of observations that are recorded at the same time and record the blood pressure, pulse, temperature and other readings.
Blood pressureBlood pressure: The local measurement of arterial blood pressure which is a surrogate for arterial pressure in the systemic circulation.
Most commonly, use of the term 'blood pressure' refers to measurement of brachial artery pressure in the upper arm.
DataData: History Structural node.
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
SystolicSystolic: Peak systemic arterial blood pressure - measured in systolic or contraction phase of the heart cycle.
0..1000 mmHg
DiastolicDiastolic: Minimum systemic arterial blood pressure - measured in the diastolic or relaxation phase of the heart cycle.
0..1000 mmHg
ProtocolProtocol: List structure.
Systolic pressure formulaSystolic pressure formula: Formula used to calculate the systolic pressure from from mean arterial pressure (if recorded in data).
  • < 80mmHg
  • 80-119 mmHg
  • 120-139 mmHg
  • 140-179 mmHg
  • >= 180 mmHg
  • not done
  • unknown
Diastolic pressure formulaDiastolic pressure formula: Formula used to calculate the diastolic pressure from mean arterial pressure (if recorded in data).
  • < 40 mmHg
  • 41-60 mmHg
  • 61-89 mmHg
  • 90-110 mmHg
  • > 110 mmHg
  • not done
  • unknown
Pulse/Heart beatPulse/Heart beat: The rate and associated attributes for a pulse or heart beat.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
RateRate: The rate of the pulse or heart beat, measured in beats per minute.
0..1000 /min
RhythmRhythm: Specific conclusion about the rhythm of the pulse or heartbeat, drawn from a combination of the heart rate, pattern and other characteristics observed on examination.
  • < 45 bpm
  • 46-59 bpm
  • 60-89 bpm
  • 90-119 bpm
  • >= 120 bpm
  • not done
  • unknown
Pulse oximetryPulse oximetry: Blood oxygen and related measurements, measured by pulse oximetry or pulse CO-oximetry.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
Oxygen saturationOxygen saturation: The saturation of oxygen in the peripheral blood, measured via pulse oximetry.
SpO₂ is defined as the percentage of oxyhaemoglobin (HbO₂) to the total concentration of haemoglobin (HbO₂ + deoxyhaemoglobin) in peripheral blood.
  • Percent
SpOCSpOC: The oxygen content of the peripheral blood, calculated based on pulse oximetry and pulse CO-oximetry.
>=0 ml/dl
InterpretationInterpretation: Single word, phrase or brief description which represents the clinical meaning and significance of the measurements.
Coding with a terminology is preferred, if possible. For example, normal oxygen saturation or hypoxaemia.
  • <60 %
  • 60-69 %
  • 70-79%
  • 80-89%
  • 90-95%
  • 96-100%
  • not done
  • unknown
Body temperatureBody temperature: A measurement of the body temperature, which is a surrogate for the core body temperature of the individual.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
TemperatureTemperature: The measured temperature.
0..100; 30..200
Units:
  • °C
  • °F
Klinische BeschreibungKlinische Beschreibung: Additional comment about the body temperature measurement not captured in other fields.
  • < 35.0°C
  • 35.1 - 37.2°C
  • 37.3 - 37.9°C
  • 38.0 - 38.9°C
  • 39.0 - 39.9°C
  • >= 40°C
  • not done
  • unknown
Protocol
Location of measurementLocation of measurement: Simple description about the site of measurement.
  •  Coded Text
    • Rectum 
    • Axilla 
    • Ear canal 
    • Forehead 
    • Mouth 
    • Nasopharynx 
    • Urinary bladder 
    • Intravascular 
    • Skin 
    • Vagina 
    • Oesophagus 
    • Inguinal skin crease 
    • Temple 
  •  Text
RespirationRespiration: The characteristics of spontaneous breathing by an individual.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
RateRate: The frequency of spontaneous breathing.
0..200 /min
Clinical descriptionClinical description: A narrative description about the spontaneous breathing of the individual.
For example: noting respiratory distress, use of accessory muscles or intermittent apnoea; noting characteristics such as stridor, sighing, grunting, groaning, gasping. Conducting a full respiratory examination, then some of these findings might be more appropriately recorded as part of examination findings.
  • <= 16
  • 16-21
  • 22-29
  • >=30
  • not done
  • unknown
BlutgasanalyseBlutgasanalyse: The result, including findings and the laboratory's interpretation, of an investigation performed on specimens collected from an individual or related to that individual.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
BlutgasanalyseBlutgasanalyse: Name of the laboratory investigation performed on the specimen(s).
A test result may be for a single analyte, or a group of items, including panel tests. It is strongly recommended that 'Test name' be coded with a terminology, for example LOINC or SNOMED CT. For example: 'Glucose', 'Urea and Electrolytes', 'Swab', 'Cortisol (am)', 'Potassium in perspiration' or 'Melanoma histopathology'. The name may sometimes include specimen type and patient state, for example 'Fasting blood glucose' or include other information, as 'Potassium (PNA blood gas)'.
SauerstoffpartialdruckSauerstoffpartialdruck: The result of a laboratory test for a single analyte value.
Analyte nameAnalyte name: The name of the analyte result.
The value for this element is normally supplied in a specialisation, in a template or at run-time to reflect the actual analyte. For example: 'Serum sodium', 'Haemoglobin'. Coding with an external terminology is strongly recommended, such as LOINC, NPU, SNOMED CT, or local lab terminologies.
Optional[{fhir_mapping=Observation.code, hl7v2_mapping=OBX.3}]
  • PaO2
Analyte resultAnalyte result: The value of the analyte result.
For example '7.3 mmol/l', 'Raised'. The 'Any' data type will need to be constrained to an appropriate data type in a specialisation, a template or at run-time to reflect the actual analyte result. The Quantity data type has reference model attributes that include flags for normal/abnormal, reference ranges and approximations - see https://specifications.openehr.org/releases/RM/latest/data_types.html#_dv_quantity_class for more details.
Optional[{fhir_mapping=Observation.value[x], hl7v2_mapping=OBX.2, OBX.5, OBX.6, OBX.7, OBX.8}]
  • < 50 mmHg (<6.66)
  • 50 - 59 mmHg (6.66 - 7.86)
  • 60 - 69 mmHg (7.87 - 9.2)
  • 70 - 79 mmHg (9.21 - 10.53)
  • >= 80 mmHg (>10.53)
  • not done
  • unknown
Arterieller KohlendioxidpartialdruckArterieller Kohlendioxidpartialdruck: The result of a laboratory test for a single analyte value.
Analyte nameAnalyte name: The name of the analyte result.
The value for this element is normally supplied in a specialisation, in a template or at run-time to reflect the actual analyte. For example: 'Serum sodium', 'Haemoglobin'. Coding with an external terminology is strongly recommended, such as LOINC, NPU, SNOMED CT, or local lab terminologies.
Optional[{fhir_mapping=Observation.code, hl7v2_mapping=OBX.3}]
  • PaCO2
Analyte resultAnalyte result: The value of the analyte result.
For example '7.3 mmol/l', 'Raised'. The 'Any' data type will need to be constrained to an appropriate data type in a specialisation, a template or at run-time to reflect the actual analyte result. The Quantity data type has reference model attributes that include flags for normal/abnormal, reference ranges and approximations - see https://specifications.openehr.org/releases/RM/latest/data_types.html#_dv_quantity_class for more details.
Optional[{fhir_mapping=Observation.value[x], hl7v2_mapping=OBX.2, OBX.5, OBX.6, OBX.7, OBX.8}]
  • < 30 mmHg (<4)
  • 30 - 38 mmHg (4 - 5.06)
  • 39 - 45 mmHg (5.07 - 5.99)
  • 46 - 55 mmHg (6 - 7.33)
  • > 55 mmHg (>7.33)
  • not done
  • unknown
Further diagnosticsFurther diagnostics: A generic section header which should be renamed in a template to suit a specific clinical context.
Glasgow Coma Scale (GCS)Glasgow Coma Scale (GCS): Fifteen point scale used to assess impairment of consciousness in response to defined stimuli.
More correctly known as the Modified Glasgow coma scale.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
Best eye response (E)Best eye response (E): Best response of eyes to test stimulus.
Most commonly, the score for eye response will be selected from one of the ordinal values, however if a response cannot be tested, for example if the subject of care cannot physically open their eyes due to other injuries, then the "Not Applicable" null flavour should be recorded.
  • 1: None 
  • 2: To pressure 
  • 3: To sound 
  • 4: Spontaneous 
Best verbal response (V)Best verbal response (V): Best verbal response to test stimulus.
Most commonly, the score for verbal response will be selected from one of the ordinal values, however if a response cannot be tested, for example if the subject of care is intubated, then the "Not Applicable" null flavour should be recorded.
  • 1: None 
  • 2: Sounds 
  • 3: Words 
  • 4: Confused 
  • 5: Orientated 
Best motor response (M)Best motor response (M): Best motor response to test stimulus.
Most commonly, the score for motor response will be selected from one of the ordinal values, however if a response cannot be tested, for example if the subject of care cannot move their limbs due to injury or paralysis, then the "Not Applicable" null flavour should be recorded.
  • 1: None 
  • 2: Extension 
  • 3: Abnormal flexion 
  • 4: Normal flexion 
  • 5: Localising 
  • 6: Obeys commands 
Total scoreTotal score: The sum of the ordinal scores recorded for each of the three component responses.
The Total Score may be derived as the sum of the three response data elements and, if so, should be validated by the clinical information system against the individual scores entered by the clinician to ensure there is no conflict or inconsistency. Do not report a total score when one or more components are not testable because the score will be artificially low - in this situation record the EVM profile.
3..15
SOFA scoreSOFA score: The SOFA score represents a score which is used in medicine for the assessment of patients in intensive care units. It is used to assess the degree of organ dysfunction and helps to determine the mortality risk of a patient. SOFA stands for Sequential Organ Failure Assessment.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
RespirationRespiration: The respiratory activity as PaO2/FiO2 ratio in mmHg to evaluate lung function.
  • 1: < 400 
  • 2: < 300 
  • 3: < 200 and artificial respiration 
  • 4: < 100 and artificial respiration 
Central nervous systemCentral nervous system: The evaluation of the CNS with Glasgow Coma Score.
  • 1: 13-14 
  • 2: 10-12 
  • 3: 6-9 
  • 4: <6 
Cardiovascular SystemCardiovascular System: Mean arterial pressure (MAP) or administration of vasopressors.
  • 1: MAP < 70 mmHg 
  • 2: Dopamine ≤ 5 µg/kg/min or Dobutamine (regardless of dosage) 
  • 3: Dopamine > 5 µg/kg/min or adrenaline ≤ 0,1 µg/kg/min oder noradrenaline ≤ 0,1 µg/kg/min 
  • 4: Dopamine > 15 µg/kg/min oder adrenaline > 0,1 µg/kg/min or noradrenaline > 0,1 µg/kg/min 
Liver functionLiver function: The bilirubin value in milligrams per deciliter [mg/dl].
  • 1: 1,2 -1,9 mg/dl 
  • 2: 2,0 - 5,9 mg/dl 
  • 3: 6,0 - 11,9 mg/dl 
  • 4: >12,0 mg/dl 
Blood clottingBlood clotting: The platelet count per microliter [10³/µl].
  • 1: < 150 
  • 2: < 100 
  • 3: < 50 
  • 4: < 20 
Renal functionRenal function: The creatinine value in milligrams per deciliter [mg/dl].
  • 1: 1,2 - 1,9 mg/dl 
  • 2: 2,0 - 3,4 mg/dl 
  • 3: 3,5 - 4,9 mg/dl 
  • 4: > 5 mg/dl 
Total scoreTotal score: Sum of points assigned for each of the component parameters.
6..24
Neurological diagnosticNeurological diagnostic: A screening questionnaire about screening, investigative, diagnostic, curative, therapeutic, evaluative or palliative procedures which may have been performed.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
Screening purposeScreening purpose: The reason for overall screening.
For example: screening for post-operative infection.
Any performed?Any performed?: Were any procedures performed?
  • Performed/carried out 
  • Not performed/carried out 
Imaging examination resultImaging examination result: Record the findings and interpretation of an imaging examination performed.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
Test nameTest name: The name of the imaging examination or procedure performed.
Coding with a terminology, potentially a pre-coordinated term specifying both modality and anatomical location, is desirable where possible. Possible candidate terminologies: LOINC, SNOMED CT or RadLex.
BefundeBefunde: Description of clinical information available at the time of interpretation of results.
This may include a link to the clinical information provided in the original examination request. If other sources of clinical information have been used, this should be clearly stated using this data element.
  • Air trapping
  • Areas of consolidation
  • Bronchitits
  • Crazy caving pattern
  • Ground glass opacities
  • Interlobular septal thickening
  • Nodulary lesions
  • Pleural effusion
Other relevant resultsOther relevant results: Narrative description of the clinical findings.
  • Normal CT
  • Not done
CommentComment: Additional narrative about the examination not captured in other fields.
For example: a note that the film was given to the patient.