| TEMPLATE ID | Symptome LEOSS |
|---|---|
| Concept | Symptome LEOSS |
| Description | Zur Repräsentation der Symptome der Erkrankung aus dem LEOSS-Datensatz für COVID-19 Patienten. |
| Use | Zur Repräsentation der Symptome für das COVID-19 Projekt. |
| Misuse | Nicht zur Repräsentation alle Symptome verwenden. |
| Purpose | Zur Repräsentation der Symptome der Erkrankung aus dem LEOSS-Datensatz für COVID-19 Patienten. |
| References | |
| Authors | Name: Sarah Ballout; Organisation: MHH-Hannover; Email: ballout.sarah@mh-hannover.de |
| Other Details Language | Name: Sarah Ballout; Organisation: MHH-Hannover; Email: ballout.sarah@mh-hannover.de |
| Other Details (Language Independent) |
|
| Keywords | Symptome; Erkrankung; Krankheitsanzeichen |
| Language used | en |
| Citeable Identifier | 1246.169.785 |
| Root archetype id | openEHR-EHR-COMPOSITION.report.v1 |
| Report | Report: Document to communicate information to others, commonly in response to a request from another party. |
| Other Context | |
| Bericht Name | Bericht Name: Identification information about the report.
|
| Status | Status: The status of the entire report. Note: This is not the status of any of the report components. |
| Symptoms | Symptoms: A generic section header which should be renamed in a template to suit a specific clinical context. |
| Symptom/Krankheitsanzeichen | Symptom/Krankheitsanzeichen: An individual- or self-reported questionnaire screening for symptoms and signs. |
| Data | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Runny Nose | Runny Nose: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Sore throat | Sore throat: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Dry cough | Dry cough: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Productive cough | Productive cough: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Wheezing | Wheezing: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Dyspnoe | Dyspnoe: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Feeling of breathlessness | Feeling of breathlessness: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| How you feel of breathlessness? | How you feel of breathlessness?: Free text. |
| Answer | Answer: Free text.
|
| Palpitations | Palpitations: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Nausea / emesis | Nausea / emesis: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Diarrhea | Diarrhea: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Muscle aches | Muscle aches: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Muscle weakness | Muscle weakness: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Fever | Fever: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Delirium | Delirium: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Excessive tiredness | Excessive tiredness: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Headache | Headache: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Meningism | Meningism: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Smell disorders | Smell disorders: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Taste disorder | Taste disorder: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Other neurological symptoms | Other neurological symptoms: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Red eye | Red eye: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Asymptomatic | Asymptomatic: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Presence? | Presence?: Presence of the symptom or sign.
|
| Cardiovascular Complications | Cardiovascular Complications: A generic section header which should be renamed in a template to suit a specific clinical context. |
| Symptom/sign screening questionnaire | Symptom/sign screening questionnaire: An individual- or self-reported questionnaire screening for symptoms and signs. |
| Data | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Specific symptom/sign | Specific symptom/sign: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Cardiac arrhytmia | Cardiac arrhytmia: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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 arrhytmia | Life threatening arrhytmia: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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 syndrome | Myocardial ischemia, acute coronary syndrome: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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. |
| Comment | Comment: Additional narrative about the symptom or sign not captured in other fields. |
| Myocarditis | Myocarditis: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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 name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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 effusion | Pericardial effusion: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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. |
| Comment | Comment: Additional narrative about the symptom or sign not captured in other fields. |
| Any bleeding | Any bleeding: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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. |
| Comment | Comment: Additional narrative about the symptom or sign not captured in other fields. |
| Respiratory Complications | Respiratory Complications: A generic section header which should be renamed in a template to suit a specific clinical context. |
| Symptom/sign screening questionnaire | Symptom/sign screening questionnaire: An individual- or self-reported questionnaire screening for symptoms and signs. |
| Data | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Specific symptom/sign | Specific symptom/sign: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Need for oxygen supplementation | Need for oxygen supplementation: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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 intubation | Clinical indication for intubation: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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-intubation | Re-intubation: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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. |
| Comment | Comment: Additional narrative about the symptom or sign not captured in other fields. |
| ECMO | ECMO: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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. |
| Comment | Comment: Additional narrative about the symptom or sign not captured in other fields. |
| Renal complications | Renal complications: A generic section header which should be renamed in a template to suit a specific clinical context. |
| Symptom/sign screening questionnaire | Symptom/sign screening questionnaire: An individual- or self-reported questionnaire screening for symptoms and signs. |
| Data | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Specific symptom/sign | Specific symptom/sign: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Acute kidney injury (KDIGO) | Acute kidney injury (KDIGO): Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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. |
| Stadium | Stadium: 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.
|
| New renal failure with need for dialysis | New renal failure with need for dialysis: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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 failure | Not recovered kidney failure: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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 complications | Thrombotic and thrombembolic complications: A generic section header which should be renamed in a template to suit a specific clinical context. |
| Symptom/sign screening questionnaire | Symptom/sign screening questionnaire: An individual- or self-reported questionnaire screening for symptoms and signs. |
| Data | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Specific symptom/sign | Specific symptom/sign: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Abdominal thrombosis | Abdominal thrombosis: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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 thrombosis | Arterial thrombosis: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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, -thrombosis | Microangiopathy, -thrombosis: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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 thrombembolism | Venous thrombosis, pulmonary thrombembolism: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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 complications | Neurological complications: A generic section header which should be renamed in a template to suit a specific clinical context. |
| Symptom/sign screening questionnaire | Symptom/sign screening questionnaire: An individual- or self-reported questionnaire screening for symptoms and signs. |
| Data | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Specific symptom/sign | Specific symptom/sign: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
|
| Intracerebral bleeding | Intracerebral bleeding: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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 stroke | Ischemic stroke: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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 stroke | Cause of stroke: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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-Classification | TOAST-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.
|
| Stroke score NIHSS | Stroke score NIHSS: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| Number of Stroke score NIHSS | Number of Stroke score NIHSS: The number of times this symptom or sign has previously occurred. >=0 |
| Meningitis/Encephalitis | Meningitis/Encephalitis: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| Nil significant | Nil 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. |
| Myositis | Myositis: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| Nil significant | Nil 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. |
| Seizure | Seizure: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| Nil significant | Nil 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 sequelae | Neurological sequelae: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| Nil significant | Nil 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 impairment | Severe cognitive impairment: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| Nil significant | Nil 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 complications | Further complications: A generic section header which should be renamed in a template to suit a specific clinical context. |
| Symptom/sign screening questionnaire | Symptom/sign screening questionnaire: An individual- or self-reported questionnaire screening for symptoms and signs. |
| Data | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Specific symptom/sign | Specific symptom/sign: Grouping of data elements related to screening for a single symptom or sign. |
| Symptom or sign name | Symptom or sign name: Name of the symptom or sign being screened.
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| Vasculitis | Vasculitis: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
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| 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 shock | Septic shock: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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 >= 2 | qSOFA >= 2: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| 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-Classification | TOAST-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.
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| Other complications, specify | Other complications, specify: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
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| Nil significant | Nil 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. |
| Kommentar | Kommentar: 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 NIHSS | Number of Stroke score NIHSS: The number of times this symptom or sign has previously occurred. >=0 |
| Severe fatigue | Severe fatigue: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| Nil significant | Nil 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 sequelae | Other sequelae: Reported observation of a physical or mental disturbance in an individual. |
| Symptom/Sign name | Symptom/Sign name: The name of the reported symptom or sign. Symptom name should be coded with a terminology, where possible.
|
| Nil significant | Nil 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 signs | Vital signs: A group of observations that are recorded at the same time and record the blood pressure, pulse, temperature and other readings. |
| Blood pressure | Blood 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. |
| Data | Data: History Structural node. |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Systolic | Systolic: Peak systemic arterial blood pressure - measured in systolic or contraction phase of the heart cycle. 0..1000 mmHg |
| Diastolic | Diastolic: Minimum systemic arterial blood pressure - measured in the diastolic or relaxation phase of the heart cycle. 0..1000 mmHg |
| Protocol | Protocol: List structure. |
| Systolic pressure formula | Systolic pressure formula: Formula used to calculate the systolic pressure from from mean arterial pressure (if recorded in data).
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| Diastolic pressure formula | Diastolic pressure formula: Formula used to calculate the diastolic pressure from mean arterial pressure (if recorded in data).
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| Pulse/Heart beat | Pulse/Heart beat: The rate and associated attributes for a pulse or heart beat. |
| Data | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Rate | Rate: The rate of the pulse or heart beat, measured in beats per minute. 0..1000 /min |
| Rhythm | Rhythm: 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.
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| Pulse oximetry | Pulse oximetry: Blood oxygen and related measurements, measured by pulse oximetry or pulse CO-oximetry. |
| Data | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Oxygen saturation | Oxygen 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.
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| SpOC | SpOC: The oxygen content of the peripheral blood, calculated based on pulse oximetry and pulse CO-oximetry. >=0 ml/dl |
| Interpretation | Interpretation: 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.
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| Body temperature | Body temperature: A measurement of the body temperature, which is a surrogate for the core body temperature of the individual. |
| Data | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Temperature | Temperature: The measured temperature. 0..100; 30..200 Units:
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| Klinische Beschreibung | Klinische Beschreibung: Additional comment about the body temperature measurement not captured in other fields.
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| Protocol | |
| Location of measurement | Location of measurement: Simple description about the site of measurement.
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| Respiration | Respiration: The characteristics of spontaneous breathing by an individual. |
| Data | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Rate | Rate: The frequency of spontaneous breathing. 0..200 /min |
| Clinical description | Clinical 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.
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| Blutgasanalyse | Blutgasanalyse: 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 event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Blutgasanalyse | Blutgasanalyse: 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)'. |
| Sauerstoffpartialdruck | Sauerstoffpartialdruck: The result of a laboratory test for a single analyte value. |
| Analyte name | Analyte 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}]
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| Analyte result | Analyte 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}]
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| Arterieller Kohlendioxidpartialdruck | Arterieller Kohlendioxidpartialdruck: The result of a laboratory test for a single analyte value. |
| Analyte name | Analyte 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}]
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| Analyte result | Analyte 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}]
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| Further diagnostics | Further 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 event | Any 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.
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| 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.
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| 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.
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| Total score | Total 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 score | SOFA 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 event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Respiration | Respiration: The respiratory activity as PaO2/FiO2 ratio in mmHg to evaluate lung function.
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| Central nervous system | Central nervous system: The evaluation of the CNS with Glasgow Coma Score.
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| Cardiovascular System | Cardiovascular System: Mean arterial pressure (MAP) or administration of vasopressors.
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| Liver function | Liver function: The bilirubin value in milligrams per deciliter [mg/dl].
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| Blood clotting | Blood clotting: The platelet count per microliter [10³/µl].
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| Renal function | Renal function: The creatinine value in milligrams per deciliter [mg/dl].
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| Total score | Total score: Sum of points assigned for each of the component parameters. 6..24 |
| Neurological diagnostic | Neurological diagnostic: A screening questionnaire about screening, investigative, diagnostic, curative, therapeutic, evaluative or palliative procedures which may have been performed. |
| Data | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Screening purpose | Screening purpose: The reason for overall screening. For example: screening for post-operative infection. |
| Any performed? | Any performed?: Were any procedures performed?
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| Imaging examination result | Imaging examination result: Record the findings and interpretation of an imaging examination performed. |
| Data | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| Data | |
| Test name | Test 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. |
| Befunde | Befunde: 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.
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| Other relevant results | Other relevant results: Narrative description of the clinical findings.
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| Comment | Comment: Additional narrative about the examination not captured in other fields. For example: a note that the film was given to the patient. |