ID

41615

Description

Study Title: LEOSS: Lean European Open Survey on SARS-CoV-2 Infected Patients https://leoss.net Study Indication: COVID-19 Date: 14.10.2020, 16:54 Published with permission by Prof. Dr. med. J.-J. Vehreschild. LEOSS is mandated by the ESCMID Emerging Infections Task Force (EITaF) and supported by the German Infectious Disease Society. It aims at a better understanding of the implications of the new virus on patients by systematically documenting patient data across Europe (Text adapted from leoss.net). For more information please visit the official website. This document is for baseline information. A related document "Baseline II" documents further baseline information related to baseline timepoint and to disease periods. Baseline / diagnosis is defined as the day the sample of the first positive SARS-CoV-2 result was taken. Please note that only cases with known outcome are collected! If a text field can't be filled out, note 'ND' (for not determined).

Link

https://leoss.net

Keywords

Versions (4)
  1. 11/12/20 11/12/20 -
  2. 11/27/20 11/27/20 -
  3. 4/19/21 4/19/21 -
  4. 6/24/21 6/24/21 - Sarah Riepenhausen
Copyright Holder

LEOSS

Uploaded on

November 27, 2020

DOI

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License

Creative Commons BY 4.0
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LEOSS: Lean European Open Survey on SARS-CoV-2 Infected Patients

English

Baseline I

1 forms  
  1. StudyEvent: ODM
    1. Baseline I
Demography
Description

Demography

Alias
UMLS CUI-1
C0011298
Age at diagnosis
Description

Note: This question is critical for the further course of the questionnaire.

Data type

integer

Alias
UMLS CUI [1]
C1828181
Gender
Description

Note: This question is critical for the further course of the questionnaire.

Data type

integer

Alias
UMLS CUI [1]
C0079399
Ethnicity
Description

Note: This question is critical for the further course of the questionnaire.

Data type

integer

Alias
UMLS CUI [1]
C0015031
Country of residence
Description

ISO Alpha-3 code (e.g. Germany= DEU, Iceland= ISL, Spain= ESP) Note: This question is critical for the further course of the questionnaire.

Data type

text

Alias
UMLS CUI [1]
C1562954
Diagnosis information
Description

Diagnosis information

Alias
UMLS CUI-1
C0011900
Country of diagnosis
Description

ISO Alpha-3 code (e.g. Germany= DEU, Iceland= ISL, Spain= ESP) Note: This question is critical for the further course of the questionnaire.

Data type

text

Alias
UMLS CUI [1,1]
C0454664
UMLS CUI [1,2]
C0011900
UMLS CUI [1,3]
C5203676
ZIP code area
Description

Please enter the first 3-digits of the zip code of the place of residence

Data type

text

Alias
UMLS CUI [1,1]
C1514254
UMLS CUI [1,2]
C0682130
Reason for consultation / admission: COVID-19 or treatment for other medical conditions
Description

Note: This question is critical for the further course of the questionnaire. Please fill in ICD-10 code

Data type

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0009818
UMLS CUI [2,1]
C0392360
UMLS CUI [2,2]
C0809949
UMLS CUI [3]
C5203670
UMLS CUI [4,1]
C0012634
UMLS CUI [4,2]
C0205394
UMLS CUI [4,3]
C0087111
UMLS CUI [5]
C2598420
Coded DRG:
Description

Note: This question is critical for the further course of the questionnaire. Please note that a DRG has the structure: LetterNumberNumberLetter (e.g. A11A). Please do not provide the ICD10 here.

Data type

text

Alias
UMLS CUI [1]
C0011928
Day of admission to hospital in reference to first SARS-CoV-2-detection (day 0)
Description

e.g. if admission has been before the detection, the day is negative. If there has been no admission to hospital, note ND. For additional information and examples regarding the timeline, you can find more information at https://leoss.net/wp-content/uploads/2020/06/Support_LEOSS_Phases.pdf

Data type

text

Alias
UMLS CUI [1,1]
C0806429
UMLS CUI [1,2]
C1272706
UMLS CUI [1,3]
C5203676
UMLS CUI [1,4]
C1511790
How did the patient come to the health care facility ?
Description

Note: This question is critical for the further course of the questionnaire. Facility as the place where the first positive PCR swab was taken. In case of transfer from another hospital, plase indicate the respective means of transport (e.g. transport patient ambulance)

Data type

integer

Alias
UMLS CUI [1,1]
C3263562
UMLS CUI [1,2]
C0018704
UMLS CUI [2,1]
C0150390
UMLS CUI [2,2]
C0018704
How did the patient come to the health care facility ? If Other, please specify
Description

Note: This question is critical for the further course of the questionnaire. Facility as the place where the first positive PCR swab was taken. In case of transfer from another hospital, plase indicate the respective means of transport (e.g. transport patient ambulance)

Data type

text

Alias
UMLS CUI [1,1]
C3263562
UMLS CUI [1,2]
C0018704
UMLS CUI [1,3]
C3845569
UMLS CUI [2,1]
C0150390
UMLS CUI [2,2]
C0018704
UMLS CUI [2,3]
C3845569
Where did the patient stay before SARS-CoV-2 detection?
Description

Note: This question is critical for the further course of the questionnaire.

Data type

integer

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0450429
UMLS CUI [1,3]
C0332152
UMLS CUI [1,4]
C5203676
UMLS CUI [1,5]
C1511790
Where did the patient stay before SARS-CoV-2 detection? If Other, please specify
Description

Note: This question is critical for the further course of the questionnaire.

Data type

text

Alias
UMLS CUI [1,1]
C0450429
UMLS CUI [1,2]
C0332152
UMLS CUI [1,3]
C5203676
UMLS CUI [1,4]
C1511790
UMLS CUI [1,5]
C3845569
Where did the patient stay after the follow-up period?
Description

Note: This question is critical for the further course of the questionnaire. In case of inpatient treatment indicate where was the patient discharged to. In case of outpatient treatment indicate where the patient was staying at the last contact.

Data type

integer

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0450429
UMLS CUI [1,3]
C0687676
UMLS CUI [1,4]
C1522577
Where did the patient stay after the follow-up period? If Other, please specify
Description

Note: This question is critical for the further course of the questionnaire. In case of inpatient treatment indicate where was the patient discharged to. In case of outpatient treatment indicate where the patient was staying at the last contact.

Data type

text

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0450429
UMLS CUI [1,3]
C0687676
UMLS CUI [1,4]
C1522577
UMLS CUI [1,5]
C3845569
Did the patient come through the emergency room?
Description

ER means a unit with possible emergency care in case of acute illnesses and injuries, including admission station and in some cases monitoring station and/or ICU.

Data type

integer

Alias
UMLS CUI [1,1]
C3263562
UMLS CUI [1,2]
C4291935
Month of first diagnosis
Description

Note: This question is critical for the further course of the questionnaire.

Data type

integer

Alias
UMLS CUI [1,1]
C0439231
UMLS CUI [1,2]
C0205265
UMLS CUI [1,3]
C0011900
UMLS CUI [1,4]
C5203676
Assumed days between contracting infection and diagnosis
Description

Assumed days between contracting infection and diagnosis

Alias
UMLS CUI-1
C5203676
UMLS CUI-2
C3483764
UMLS CUI-3
C2316983
UMLS CUI-4
C1272706
Assumed days between contracting infection and diagnosis:
Description

Note: This question is critical for the further course of the questionnaire. Please keep our definition of diagnosis in mind: diagnosis is defined as the day the sample of the first positive SARS-CoV-2 result was taken.

Data type

integer

Alias
UMLS CUI [1,1]
C5203676
UMLS CUI [1,2]
C3483764
UMLS CUI [1,3]
C2316983
UMLS CUI [1,4]
C1272706
First known contact with infected person, days before diagnosis:
Description

Note: This question is critical for the further course of the questionnaire. Please keep our definition of diagnosis in mind: diagnosis is defined as the day the sample of the first positive SARS-CoV-2 result was taken.

Data type

text

Measurement units
  • days
Alias
UMLS CUI [1,1]
C0205435
UMLS CUI [1,2]
C0332158
UMLS CUI [1,3]
C5203676
UMLS CUI [1,4]
C2316983
UMLS CUI [1,5]
C1272706
UMLS CUI [1,6]
C1521902
days
Disease phases at baseline and during follow-up
Description

Disease phases at baseline and during follow-up

Alias
UMLS CUI-1
C0920316
UMLS CUI-2
C0699749
UMLS CUI-3
C1522577
UMLS CUI-4
C1442488
Phase at diagnosis
Description

Note: This question is critical for the further course of the questionnaire. Please keep our definition of diagnosis in mind. For additional information and examples regarding the LEOSS phases, see https://leoss.net/wp-content/uploads/2020/06/Support_LEOSS_Phases.pdf. Uncomplicated Phase: Asymtomatic OR Symptoms of upper respiratory tract infection Nausea, emesis, diarrhea Fever Complicated Phase: Need for new oxygen supplementation Clinically meaningful increase of prior oxygen home therapy paO2 at room air < 70 mmHg SO2 at room air < 90 % AST or ALT > 5x ULN New cardiac arrhythmia New pericardial effusion > 1 cm New heart failure with pulmonary edema, congestive hepatopathy or peripheral edema Critical Phase: Need for catecholamines Life-threatening cardiac arrhythmia Need for unplanned mechanical ventilation (invasive or non-invasive) Prolongation (> 24 h) of planned mechanical ventilation Liver failure with Quick < 50 % / INR > 3.5 qSOFA >= 2 Acute renal failure in need of dialysis Recovery Phase: Improvement by one degree of severity according to this scheme or discharge from hospital AND Defervescence AND No further progression or re-hospitalization

Data type

integer

Alias
UMLS CUI [1,1]
C0521117
UMLS CUI [1,2]
C5203676
UMLS CUI [1,3]
C0011900
Note all phases the patient went through within the follow-up period. Uncomplicated phase, start day:
Description

Note: This question is critical for the further course of the questionnaire. Please keep our definition of diagnosis in mind and provide days from DIAGNOSIS (day 0) until the START of each phase. If e.g. uncomplicated pase started before diagnosis, use negative days. Note that ambulatory treatment implies an uncomplicated phase. Recovery does not necessarily mean the absence of all symptoms, but an improvement according to the delivered criteria. If recovery phase is defined by discharge, the start of recovery phase is equal to the date of discharge. Recovery phase in outpatient settings can be achieved by uncomplicated patients after 14 days of observation without disease progression. For additional information and examples regarding the LEOSS phases, see https://leoss.net/wp-content/uploads/2020/06/Support_LEOSS_Phases.pdf

Data type

boolean

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0443334
UMLS CUI [1,3]
C0205390
Note all phases the patient went through within the follow-up period. Uncomplicated phase, start day, specify:
Description

Note: This question is critical for the further course of the questionnaire. Please keep our definition of diagnosis in mind and provide days from DIAGNOSIS (day 0) until the START of each phase. If e.g. uncomplicated pase started before diagnosis, use negative days. Note that ambulatory treatment implies an uncomplicated phase. Recovery does not necessarily mean the absence of all symptoms, but an improvement according to the delivered criteria. If recovery phase is defined by discharge, the start of recovery phase is equal to the date of discharge. Recovery phase in outpatient settings can be achieved by uncomplicated patients after 14 days of observation without disease progression. For additional information and examples regarding the LEOSS phases, see https://leoss.net/wp-content/uploads/2020/06/Support_LEOSS_Phases.pdf

Data type

text

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0443334
UMLS CUI [1,3]
C0205390
UMLS CUI [1,4]
C1521902
Note all phases the patient went through within the follow-up period. Complicated phase, start day:
Description

Note: This question is critical for the further course of the questionnaire. Please keep our definition of diagnosis in mind and provide days from DIAGNOSIS (day 0) until the START of each phase. If e.g. uncomplicated pase started before diagnosis, use negative days. Note that ambulatory treatment implies an uncomplicated phase. Recovery does not necessarily mean the absence of all symptoms, but an improvement according to the delivered criteria. If recovery phase is defined by discharge, the start of recovery phase is equal to the date of discharge. Recovery phase in outpatient settings can be achieved by uncomplicated patients after 14 days of observation without disease progression. For additional information and examples regarding the LEOSS phases, see https://leoss.net/wp-content/uploads/2020/06/Support_LEOSS_Phases.pdf

Data type

boolean

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0231242
UMLS CUI [1,3]
C0205390
Note all phases the patient went through within the follow-up period. Complicated phase, start day, specify:
Description

Note: This question is critical for the further course of the questionnaire. Please keep our definition of diagnosis in mind and provide days from DIAGNOSIS (day 0) until the START of each phase. If e.g. uncomplicated pase started before diagnosis, use negative days. Note that ambulatory treatment implies an uncomplicated phase. Recovery does not necessarily mean the absence of all symptoms, but an improvement according to the delivered criteria. If recovery phase is defined by discharge, the start of recovery phase is equal to the date of discharge. Recovery phase in outpatient settings can be achieved by uncomplicated patients after 14 days of observation without disease progression. For additional information and examples regarding the LEOSS phases, see https://leoss.net/wp-content/uploads/2020/06/Support_LEOSS_Phases.pdf

Data type

text

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0231242
UMLS CUI [1,3]
C0205390
UMLS CUI [1,4]
C1521902
Note all phases the patient went through within the follow-up period. Critical phase, start day:
Description

Note: This question is critical for the further course of the questionnaire. Please keep our definition of diagnosis in mind and provide days from DIAGNOSIS (day 0) until the START of each phase. If e.g. uncomplicated pase started before diagnosis, use negative days. Note that ambulatory treatment implies an uncomplicated phase. Recovery does not necessarily mean the absence of all symptoms, but an improvement according to the delivered criteria. If recovery phase is defined by discharge, the start of recovery phase is equal to the date of discharge. Recovery phase in outpatient settings can be achieved by uncomplicated patients after 14 days of observation without disease progression. For additional information and examples regarding the LEOSS phases, see https://leoss.net/wp-content/uploads/2020/06/Support_LEOSS_Phases.pdf

Data type

boolean

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C1511545
UMLS CUI [1,3]
C0205390
Note all phases the patient went through within the follow-up period. Critical phase, start day, specify:
Description

Note: This question is critical for the further course of the questionnaire. Please keep our definition of diagnosis in mind and provide days from DIAGNOSIS (day 0) until the START of each phase. If e.g. uncomplicated pase started before diagnosis, use negative days. Note that ambulatory treatment implies an uncomplicated phase. Recovery does not necessarily mean the absence of all symptoms, but an improvement according to the delivered criteria. If recovery phase is defined by discharge, the start of recovery phase is equal to the date of discharge. Recovery phase in outpatient settings can be achieved by uncomplicated patients after 14 days of observation without disease progression. For additional information and examples regarding the LEOSS phases, see https://leoss.net/wp-content/uploads/2020/06/Support_LEOSS_Phases.pdf

Data type

text

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C1511545
UMLS CUI [1,3]
C0205390
UMLS CUI [1,4]
C1521902
Note all phases the patient went through within the follow-up period. Recovery phase, start day:
Description

Note: This question is critical for the further course of the questionnaire. Please keep our definition of diagnosis in mind and provide days from DIAGNOSIS (day 0) until the START of each phase. If e.g. uncomplicated pase started before diagnosis, use negative days. Note that ambulatory treatment implies an uncomplicated phase. Recovery does not necessarily mean the absence of all symptoms, but an improvement according to the delivered criteria. If recovery phase is defined by discharge, the start of recovery phase is equal to the date of discharge. Recovery phase in outpatient settings can be achieved by uncomplicated patients after 14 days of observation without disease progression. For additional information and examples regarding the LEOSS phases, see https://leoss.net/wp-content/uploads/2020/06/Support_LEOSS_Phases.pdf

Data type

boolean

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C2004454
UMLS CUI [1,3]
C0205390
Note all phases the patient went through within the follow-up period. Recovery phase, start day, specify:
Description

Note: This question is critical for the further course of the questionnaire. Please keep our definition of diagnosis in mind and provide days from DIAGNOSIS (day 0) until the START of each phase. If e.g. uncomplicated pase started before diagnosis, use negative days. Note that ambulatory treatment implies an uncomplicated phase. Recovery does not necessarily mean the absence of all symptoms, but an improvement according to the delivered criteria. If recovery phase is defined by discharge, the start of recovery phase is equal to the date of discharge. Recovery phase in outpatient settings can be achieved by uncomplicated patients after 14 days of observation without disease progression. For additional information and examples regarding the LEOSS phases, see https://leoss.net/wp-content/uploads/2020/06/Support_LEOSS_Phases.pdf

Data type

text

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C2004454
UMLS CUI [1,3]
C0205390
UMLS CUI [1,4]
C1521902
Duration (days) of...
Description

Duration (days) of...

Alias
UMLS CUI-1
C0449238
Overall inpatient stay:
Description

Note: This question is critical for the further course of the questionnaire. Overall inpatient stay is the entire period from first admission (days before SARS-CoV-2 testing included) to final discharge including any short outpatient stay with re-hospitalization in between. If the respective health care option has not been applied, please indicate 0.

Data type

text

Measurement units
  • days
Alias
UMLS CUI [1]
C0420496
days
Intensive care unit (ICU) stay:
Description

Note: This question is critical for the further course of the questionnaire. Overall inpatient stay is the entire period from first admission (days before SARS-CoV-2 testing included) to final discharge including any short outpatient stay with re-hospitalization in between. If the respective health care option has not been applied, please indicate 0.

Data type

text

Measurement units
  • days
Alias
UMLS CUI [1,1]
C0085559
UMLS CUI [1,2]
C0023303
days
Intermediate care unit (IMCU) stay:
Description

Note: This question is critical for the further course of the questionnaire. Overall inpatient stay is the entire period from first admission (days before SARS-CoV-2 testing included) to final discharge including any short outpatient stay with re-hospitalization in between. If the respective health care option has not been applied, please indicate 0.

Data type

text

Measurement units
  • days
Alias
UMLS CUI [1,1]
C0021767
UMLS CUI [1,2]
C0023303
days
Mechanical ventilation
Description

Note: This question is critical for the further course of the questionnaire. Overall inpatient stay is the entire period from first admission (days before SARS-CoV-2 testing included) to final discharge including any short outpatient stay with re-hospitalization in between. If the respective health care option has not been applied, please indicate 0.

Data type

text

Measurement units
  • days
Alias
UMLS CUI [1,1]
C0199470
UMLS CUI [1,2]
C0449238
days
ECMO support:
Description

Note: This question is critical for the further course of the questionnaire. Overall inpatient stay is the entire period from first admission (days before SARS-CoV-2 testing included) to final discharge including any short outpatient stay with re-hospitalization in between. If the respective health care option has not been applied, please indicate 0.

Data type

text

Measurement units
  • days
Alias
UMLS CUI [1,1]
C0015357
UMLS CUI [1,2]
C0023303
days
Days of follow-up since the day the sample of the first positive SARS-CoV-2 result was taken
Description

Days of follow-up since the day the sample of the first positive SARS-CoV-2 result was taken

Alias
UMLS CUI-1
C1522577
UMLS CUI-2
C0449238
UMLS CUI-3
C0011900
UMLS CUI-4
C5203676
Days of follow-up since the day the sample of the first positive SARS-CoV-2 result was taken
Description

Note: This question is critical for the further course of the questionnaire. Follow-up is meant in the context of the current COVID-19 treatment but does not include long-term follow-ups (e.g. for clinical studies). In case of inpatient settings end of follow-up is identical to discharge. In case of outpatient settings end of follow-up is identical to the last contact in the context of the current SARS-CoV-2 infection. In case of patient's death end of follow-up is identical to the day of death. For additional information and examples regarding the LEOSS phases and timeline, see https://leoss.net/wp-content/uploads/2020/06/Support_LEOSS_Phases.pdf

Data type

text

Alias
UMLS CUI [1,1]
C1522577
UMLS CUI [1,2]
C0449238
UMLS CUI [1,3]
C0011900
UMLS CUI [1,4]
C5203676
Last known status
Description

Last known status

Alias
UMLS CUI-1
C0699749
UMLS CUI-2
C0011008
UMLS CUI-3
C1517741
Last known status:
Description

Uncomplicated asympotmatic patients enter recovery phase after 14 days of observation without disease progression. Please indicate a last known status according to your information (e.g. in case of discharge, last documented status at dischage).

Data type

integer

Alias
UMLS CUI [1,1]
C0699749
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C1517741
If Dead from other causes, please specify
Description

Uncomplicated asympotmatic patients enter recovery phase after 14 days of observation without disease progression. Please indicate a last known status according to your information (e.g. in case of discharge, last documented status at dischage).

Data type

text

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0205394
UMLS CUI [1,3]
C1521902
Was limitation of therapy discussed at any time during the SARS-CoV-2 infection?
Description

Was limitation of therapy discussed at any time during the SARS-CoV-2 infection?

Alias
UMLS CUI-1
C0557061
UMLS CUI-2
C0449295
UMLS CUI-3
C0087111
UMLS CUI-4
C0347984
UMLS CUI-5
C5203676
Was limitation of therapy discussed at any time during the SARS-CoV-2 infection?
Description

Limitation of therapy discussed during SARS-CoV-2 infection

Data type

integer

Alias
UMLS CUI [1,1]
C0557061
UMLS CUI [1,2]
C0449295
UMLS CUI [1,3]
C0087111
UMLS CUI [1,4]
C0347984
UMLS CUI [1,5]
C5203676
Did the patient receive specialist palliative care during the SARS-CoV-2 infection?
Description

Did the patient receive specialist palliative care during the SARS-CoV-2 infection?

Alias
UMLS CUI-1
C5203676
UMLS CUI-2
C0030231
Did the patient receive specialist palliative care during the SARS-CoV-2 infection?
Description

Specialist palliative care includes PCU (palliative care unit), PCHT (palliative care hospital team), palliative home care team, inpatient hospice. Please do also keep current patients in mind receiving palliative care at any point.

Data type

integer

Alias
UMLS CUI [1,1]
C5203676
UMLS CUI [1,2]
C0030231
Did the patient suffer from a life limiting disease with a prognosis of less than one year to live before first positive testing of SARS-CoV-2?
Description

Did the patient suffer from a life limiting disease with a prognosis of less than one year to live before first positive testing of SARS-CoV-2?

Alias
UMLS CUI-1
C0012634
UMLS CUI-2
C0439801
UMLS CUI-3
C0023671
UMLS CUI-4
C0332152
UMLS CUI-5
C5203676
UMLS CUI-6
C0039593
UMLS CUI-7
C1446409
Did the patient suffer from a life limiting disease with a prognosis of less than one year to live before first positive testing of SARS-CoV-2?
Description

Disease limiting life expectancy before positive SARS-CoV-2 testing

Data type

integer

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0023671
UMLS CUI [1,4]
C0332152
UMLS CUI [1,5]
C5203676
UMLS CUI [1,6]
C0039593
UMLS CUI [1,7]
C1446409
Comorbidities, Central nervous system / Neurological disesases
Description

Comorbidities, Central nervous system / Neurological disesases

Alias
UMLS CUI-1
C0009488
UMLS CUI-2
C0007682
UMLS CUI-3
C0027765
Hemiplegia
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0018991
Dementia
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0497327
Cerebrovascular disease, stroke, TIA
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0007820
UMLS CUI [2]
C0038454
UMLS CUI [3]
C0007787
Motoneuron disease (e.g. amyotrophic lateral sclerosis, spinal muscular atrophy)
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1,1]
C0026609
UMLS CUI [1,2]
C0012634
UMLS CUI [2]
C0002736
UMLS CUI [3]
C0026847
Movement disorder (e.g. Parkinson's disease, Dystonia, Ataxia, Tremor)
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0026650
UMLS CUI [2]
C0030567
UMLS CUI [3]
C0013421
UMLS CUI [4]
C0004134
UMLS CUI [5]
C0040822
Multiple sclerosis
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0026769
Myasthenia gravis
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0026896
Neuromyelitis optica spectrum disorder (NMOSD)
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0027873
Other neurological autoimmune diseases
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1,1]
C0004364
UMLS CUI [1,2]
C0027765
UMLS CUI [1,3]
C0205394
Other prior neurological disease
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1,1]
C2015799
UMLS CUI [1,2]
C0332152
UMLS CUI [1,3]
C5203670
Comorbidities, Cardiovascular diseases
Description

Comorbidities, Cardiovascular diseases

Alias
UMLS CUI-1
C0009488
UMLS CUI-2
C0728936
Myocardial infarction
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0027051
Aortic stenosis
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0003507
AV block
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0004245
Carotid arterial disease
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0007273
Chronic heart failure
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0264716
Peripheral vascular disease
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0085096
Hypertension
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0020538
Atrial fibrillation
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0004238
Coronary artery disease
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C1956346
Other cardiovascular disease
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1,1]
C0007222
UMLS CUI [1,2]
C0205394
Comorbidities, Pulmonary diseases
Description

Comorbidities, Pulmonary diseases

Alias
UMLS CUI-1
C0009488
UMLS CUI-2
C0024115
COPD
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0024117
Asthma
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0004096
Other chronic pulmonary diseases
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1,1]
C0746102
UMLS CUI [1,2]
C0205394
Comorbidities, Hematological / oncological diseases
Description

Comorbidities, Hematological / oncological diseases

Alias
UMLS CUI-1
C0009488
UMLS CUI-2
C0018939
UMLS CUI-3
C0442867
Leukemia
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0023418
Lymphoma
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0024299
Solid tumor
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0280100
Solid tumor, metastasized
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1,1]
C0280100
UMLS CUI [1,2]
C0027627
Stem cell transplantation
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C1504389
Other hematological disease
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1,1]
C0018939
UMLS CUI [1,2]
C0205394
Comorbidities, Rheumatological diseases
Description

Comorbidities, Rheumatological diseases

Alias
UMLS CUI-1
C0419922
UMLS CUI-2
C0035435
Rheumatic disease (e.g. rheumatoid arthritis, vasculitis, spondyloarthritis, psoriatic arthritis)
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0035435
UMLS CUI [2]
C0003873
UMLS CUI [3]
C0042384
UMLS CUI [4]
C0949690
UMLS CUI [5]
C0003872
Connective tissue disease (e.g. systemic lupus erythematosus, dermatomyositis, Sjögren's syndrome)
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0009782
UMLS CUI [2]
C0409974
UMLS CUI [3]
C0011633
UMLS CUI [4]
C1527336
Comorbidities, Allergology
Description

Comorbidities, Allergology

Alias
UMLS CUI-1
C0009488
UMLS CUI-2
C0020517
Pollen sensitization
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0740919
Dust mite senzitization
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0339808
Other sensitization
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0205394
Comorbidities, Other internal disorders
Description

Comorbidities, Other internal disorders

Alias
UMLS CUI-1
C0009488
UMLS CUI-2
C0205394
UMLS CUI-3
C0012634
UMLS CUI-4
C0205102
Peptic ulcer disease
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0030920
Chronic liver disease
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0341439
Liver cirrhosis
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0023890
Diabetes, no end-organ damage
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1,1]
C0011849
UMLS CUI [1,2]
C0743496
UMLS CUI [1,3]
C0332197
Diabetes, with end-organ damage
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1,1]
C0011849
UMLS CUI [1,2]
C0743496
Chronic kidney disease
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C1561643
On dialysis
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0011946
Comorbidities, Other conditions
Description

Comorbidities, Other conditions

Alias
UMLS CUI-1
C0009488
UMLS CUI-2
C0205394
Organ transplantation
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0029216
HIV/AIDS
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0019693
UMLS CUI [2]
C0001175
Traumatic injury (e.g. head, chest, abdominal and skeletal injuries)
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C3263723
UMLS CUI [2]
C0018674
UMLS CUI [3]
C0039980
UMLS CUI [4]
C0848377
UMLS CUI [5]
C0597457
Burn
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0006434
Alcohol abuse
Description

Comorbidities that existed before the positive testing for SARS-CoV-2 Unknown means that there is no access to the patient history

Data type

integer

Alias
UMLS CUI [1]
C0085762
Prior heart failure at diagnosis
Description

Prior heart failure at diagnosis

Alias
UMLS CUI-1
C0018801
UMLS CUI-2
C0332152
UMLS CUI-3
C5203676
Prior heart failure at diagnosis
Description

Note: This question is critical for the further course of the questionnaire.

Data type

integer

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0262926
UMLS CUI [1,3]
C0332152
UMLS CUI [1,4]
C5203676
Stage of heart failure at diagnosis (NYHA classification)
Description

Stage of heart failure at diagnosis (NYHA classification)

Alias
UMLS CUI-1
C1275491
Stage of heart failure at diagnosis (NYHA classification)
Description

Note: This question is critical for the further course of the questionnaire.

Data type

integer

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1306673
UMLS CUI [1,3]
C5203676
UMLS CUI [1,4]
C0011900
UMLS CUI [2]
C1275491
Body-Mass-Index (BMI)
Description

Body-Mass-Index (BMI)

Alias
UMLS CUI-1
C1305855
Body-Mass-Index (BMI)
Description

BMI = (weight in kilogram) / (height in meters)^2

Data type

integer

Alias
UMLS CUI [1]
C1305855
Smoking status
Description

Smoking status

Alias
UMLS CUI-1
C1519386
Smoking status
Description

Smoking in this context refers to regular cigarettes (no e-cigarettes) Note: This question is critical for the further course of the questionnaire.

Data type

integer

Alias
UMLS CUI [1]
C1519386
Use of e-cigarettes and / or vaporizer?
Description

Use of e-cigarettes and / or vaporizer?

Alias
UMLS CUI-1
C3849993
UMLS CUI-2
C4083280
Use of e-cigarettes and / or vaporizer?
Description

Use of e-cigarettes and / or vaporizer?

Data type

integer

Alias
UMLS CUI [1]
C3849993
UMLS CUI [2]
C4083280
Treatments received
Description

Treatments received

Alias
UMLS CUI-1
C0087111
ACE inhibitors (e.g. enalapril, captopril, most drugs ending on -pril)
Description

Following drugs were taken at the time of diagnosis

Data type

integer

Alias
UMLS CUI [1]
C0003015
UMLS CUI [2]
C0006938
UMLS CUI [3]
C0014025
AT-1 inhibitors (e.g. candesartan, losartan, most drugs ending on -sartan)
Description

Following drugs were taken at the time of diagnosis

Data type

integer

Alias
UMLS CUI [1]
C0521942
UMLS CUI [2]
C0717550
UMLS CUI [3]
C0126174
Statines (e.g. atorvastatin, pravastatin, most drugs ending on -statin)
Description

Following drugs were taken at the time of diagnosis

Data type

integer

Alias
UMLS CUI [1]
C0360714
UMLS CUI [2]
C0286651
UMLS CUI [3]
C0085542
Ibuprofen
Description

Following drugs were taken at the time of diagnosis

Data type

integer

Alias
UMLS CUI [1]
C0020740
Vitamin D
Description

Following drugs were taken at the time of diagnosis

Data type

integer

Alias
UMLS CUI [1]
C0420176
Immunosuppressive medication in the past 3 months?
Description

Immunosuppressive medication in the past 3 months?

Alias
UMLS CUI-1
C0021081
UMLS CUI-2
C0332185
Immunosuppressive medication in the past 3 months?
Description

Consider drugs for treatment of cancer, rheumatological/inflammatory diseases, chronic inflammatory bowel disease, multiple sclerosis etc.

Data type

integer

Alias
UMLS CUI [1,1]
C0021081
UMLS CUI [1,2]
C0332185
Known colonisation with multi-resistant pathogens
Description

Known colonisation with multi-resistant pathogens

Alias
UMLS CUI-1
C3826980
UMLS CUI-2
C2747813
MRSA (Methicillin-resistant St. aureus)
Description

Please do only indicate colonization, super / coinfections are addressed in further questions.

Data type

integer

Alias
UMLS CUI [1,1]
C1265292
UMLS CUI [1,2]
C2747813
VRE (Vancomycin-resistant Enterococci)
Description

Please do only indicate colonization, super / coinfections are addressed in further questions.

Data type

integer

Alias
UMLS CUI [1,1]
C1265175
UMLS CUI [1,2]
C2747813
3rd generation cephalosporin-resistant enterobacteriacae (3GCREB)
Description

Please do only indicate colonization, super / coinfections are addressed in further questions.

Data type

integer

Alias
UMLS CUI [1,1]
C0014346
UMLS CUI [1,2]
C0304320
UMLS CUI [1,3]
C0013203
UMLS CUI [1,4]
C2747813
Other
Description

Please do only indicate colonization, super / coinfections are addressed in further questions.

Data type

integer

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C2747813
Other, please specify
Description

Please do only indicate colonization, super / coinfections are addressed in further questions.

Data type

text

Alias
UMLS CUI [1,1]
C3845569
UMLS CUI [1,2]
C2747813
Complications at baseline: Thrombotic and thromboembolic manifestations
Description

Complications at baseline: Thrombotic and thromboembolic manifestations

Alias
UMLS CUI-1
C0009566
UMLS CUI-2
C1442488
UMLS CUI-3
C0040053
UMLS CUI-4
C0040038
Abdominal thrombosis/thromboembolism (venous or arterial)
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0151942
UMLS CUI [2,2]
C0000726
UMLS CUI [3,1]
C0042487
UMLS CUI [3,2]
C0000726
UMLS CUI [4,1]
C3544094
UMLS CUI [4,2]
C0000726
UMLS CUI [5,1]
C1861172
UMLS CUI [5,2]
C0000726
Myocardial infarction
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0027051
Venous thrombosis, e.g. deep leg vein thrombosis
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0042487
UMLS CUI [3]
C0149871
Pulmonary embolism
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0034065
Microangiopathies and microthromboses
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C2717961
UMLS CUI [3]
C3686869
Complications at baseline: Neurological
Description

Complications at baseline: Neurological

Alias
UMLS CUI-1
C0235029
UMLS CUI-2
C1442488
Intracerebral bleeding
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C2937358
Ischemic Stroke
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0948008
Meningitis / Encephalitis
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0497299
Critical Illness Myopathy (CIM)
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0010340
UMLS CUI [2,2]
C0026848
Critical Illness Polyneuropathy (CIP)
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0010340
UMLS CUI [2,2]
C0152025
Seizure
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0036572
Complications at baseline: Other severe organ damage
Description

Complications at baseline: Other severe organ damage

Alias
UMLS CUI-1
C0009566
UMLS CUI-2
C1442488
UMLS CUI-3
C0178784
UMLS CUI-4
C1883709
UMLS CUI-5
C0205082
UMLS CUI-6
C0205394
Acute renal failure
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0022660
Severe liver failure
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0085605
UMLS CUI [2,2]
C0205082
Congestive heart failure
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0018802
Complications at baseline: Other
Description

Complications at baseline: Other

Alias
UMLS CUI-1
C0009566
UMLS CUI-2
C1442488
UMLS CUI-3
C0205394
Life threatening cardiac arrhythmia
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0003811
UMLS CUI [2,2]
C2826244
Myocarditis
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0027059
Vasculitis
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0042384
Gastrointestinal bleeding
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0017181
Endotracheal bleeding
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0019080
UMLS CUI [2,2]
C0599554
Other, please specify
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0009566
UMLS CUI [2,2]
C0205394
Other, please specify
Description

Please indicate the complications on the day when the swab of the first positive testing for SARS-CoV-2 was taken.

Data type

text

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0009566
UMLS CUI [2,2]
C3845569
Symptoms: Please click all symptoms which occurred in the respective clinical phase
Description

Symptoms: Please click all symptoms which occurred in the respective clinical phase

Alias
UMLS CUI-1
C1457887
Baseline (BL): None / asymptomatic
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C1298908
UMLS CUI [2,2]
C0037088
UMLS CUI [3]
C0231221
Baseline (BL): Runny nose
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C1260880
Baseline (BL): Sore throat
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0242429
Baseline (BL): Dry cough
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0850149
Baseline (BL): Productive cough
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0239134
Baseline (BL): Wheezing
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0043144
Baseline (BL): Dyspnoe
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0013404
Baseline (BL): Palpitations
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0030252
Baseline (BL): Diarrhea
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0011991
Baseline (BL): Nausea / Emesis
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0027497
UMLS CUI [3]
C0042963
Baseline (BL): Muscle aches
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0231528
Baseline (BL): Muscle weakness
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0151786
Baseline (BL): Fever
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0015967
Baseline (BL): Delirium
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0011206
Baseline (BL): Excessive tiredness
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0442802
Baseline (BL): Headache
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0018681
Baseline (BL): Meningism
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0025287
Baseline (BL): Smell disorder
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0553757
Baseline (BL): Taste disorder
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0549590
Baseline (BL): Other neurological symptoms
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0235031
UMLS CUI [2,2]
C0205394
Baseline (BL): Red eye
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0015392
UMLS CUI [2,2]
C0332575
Uncomplicated (UC): None / asymptomatic
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2,1]
C1298908
UMLS CUI [2,2]
C0037088
UMLS CUI [3]
C0231221
Uncomplicated (UC): Runny nose
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C1260880
Uncomplicated (UC): Sore throat
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0242429
Uncomplicated (UC): Dry cough
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0850149
Uncomplicated (UC): Productive cough
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0239134
Uncomplicated (UC): Wheezing
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0043144
Uncomplicated (UC): Dyspnoe
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0013404
Uncomplicated (UC): Palpitations
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0030252
Uncomplicated (UC): Diarrhea
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0011991
Uncomplicated (UC): Nausea / Emesis
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0027497
UMLS CUI [3]
C0042963
Uncomplicated (UC): Muscle aches
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0231528
Uncomplicated (UC): Muscle weakness
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0151786
Uncomplicated (UC): Fever
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0015967
Uncomplicated (UC): Delirium
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0011206
Uncomplicated (UC): Excessive tiredness
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0442802
Uncomplicated (UC): Headache
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0018681
Uncomplicated (UC): Meningism
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0025287
Uncomplicated (UC): Smell disorder
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0553757
Uncomplicated (UC): Taste disorder
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0549590
Uncomplicated (UC): Other neurological symptoms
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2,1]
C0235031
UMLS CUI [2,2]
C0205394
Uncomplicated (UC): Red eye
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0443334
UMLS CUI [1,2]
C0205390
UMLS CUI [2,1]
C0015392
UMLS CUI [2,2]
C0332575
Complicated (CO): None / asymptomatic
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2,1]
C1298908
UMLS CUI [2,2]
C0037088
UMLS CUI [3]
C0231221
Complicated (CO): Runny nose
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C1260880
Complicated (CO): Sore throat
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0242429
Complicated (CO): Dry cough
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0850149
Complicated (CO): Productive cough
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0239134
Complicated (CO): Wheezing
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0043144
Complicated (CO): Dyspnoe
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0013404
Complicated (CO): Palpitations
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0030252
Complicated (CO): Diarrhea
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0011991
Complicated (CO): Nausea / Emesis
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0027497
UMLS CUI [3]
C0042963
Complicated (CO): Muscle aches
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0231528
Complicated (CO): Muscle weakness
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0151786
Complicated (CO): Fever
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0015967
Complicated (CO): Delirium
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0011206
Complicated (CO): Excessive tiredness
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0442802
Complicated (CO): Headache
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0018681
Complicated (CO): Meningism
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0025287
Complicated (CO): Smell disorder
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0553757
Complicated (CO): Taste disorder
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0549590
Complicated (CO): Other neurological symptoms
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2,1]
C0235031
UMLS CUI [2,2]
C0205394
Complicated (CO): Red eye
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C0231242
UMLS CUI [1,2]
C0205390
UMLS CUI [2,1]
C0015392
UMLS CUI [2,2]
C0332575
Critical (CR): None / asymptomatic
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2,1]
C1298908
UMLS CUI [2,2]
C0037088
UMLS CUI [3]
C0231221
Critical (CR): Runny nose
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C1260880
Critical (CR): Sore throat
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0242429
Critical (CR): Dry cough
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0850149
Critical (CR): Productive cough
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0239134
Critical (CR): Wheezing
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0043144
Critical (CR): Dyspnoe
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0013404
Critical (CR): Palpitations
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0030252
Critical (CR): Diarrhea
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0011991
Critical (CR): Nausea / Emesis
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0027497
UMLS CUI [3]
C0042963
Critical (CR): Muscle aches
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0231528
Critical (CR): Muscle weakness
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0151786
Critical (CR): Fever
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0015967
Critical (CR): Delirium
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0011206
Critical (CR): Excessive tiredness
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0442802
Critical (CR): Headache
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0018681
Critical (CR): Meningism
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0025287
Critical (CR): Smell disorder
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0553757
Critical (CR): Taste disorder
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2]
C0549590
Critical (CR): Other neurological symptoms
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2,1]
C0235031
UMLS CUI [2,2]
C0205394
Critical (CR): Red eye
Description

Order of symptoms: upper-, lower respiratory, cardiac, gastrointestinal, musculoskeletal, systemic, neurological, other.

Data type

integer

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0205390
UMLS CUI [2,1]
C0015392
UMLS CUI [2,2]
C0332575
Vital signs and respiratory parameters
Description

Vital signs and respiratory parameters

Alias
UMLS CUI-1
C0518766
UMLS CUI-2
C0521346
UMLS CUI-3
C0549193
Systolic BP
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate values determined closest to the first positive PCR. If values were not determined within the first 48 hours, report as "Not done". You will have the opportunity to document further values later.

Data type

integer

Alias
UMLS CUI [1,1]
C1442488
UMLS CUI [1,2]
C0871470
Diastolic BP
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate values determined closest to the first positive PCR. If values were not determined within the first 48 hours, report as "Not done". You will have the opportunity to document further values later.

Data type

integer

Alias
UMLS CUI [1,1]
C1442488
UMLS CUI [1,2]
C0428883
Pulse
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate values determined closest to the first positive PCR. If values were not determined within the first 48 hours, report as "Not done". You will have the opportunity to document further values later.

Data type

integer

Alias
UMLS CUI [1,1]
C1442488
UMLS CUI [1,2]
C0232117
SO2
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate values determined closest to the first positive PCR. If values were not determined within the first 48 hours, report as "Not done". You will have the opportunity to document further values later.

Data type

integer

Alias
UMLS CUI [1,1]
C1442488
UMLS CUI [1,2]
C0523807
paO2
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate values determined closest to the first positive PCR. If values were not determined within the first 48 hours, report as "Not done". You will have the opportunity to document further values later.

Data type

integer

Alias
UMLS CUI [1,1]
C1442488
UMLS CUI [1,2]
C0391840
paCO2
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate values determined closest to the first positive PCR. If values were not determined within the first 48 hours, report as "Not done". You will have the opportunity to document further values later.

Data type

integer

Alias
UMLS CUI [1,1]
C1442488
UMLS CUI [1,2]
C1822070
Temperature
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate values determined closest to the first positive PCR. If values were not determined within the first 48 hours, report as "Not done". You will have the opportunity to document further values later.

Data type

integer

Alias
UMLS CUI [1,1]
C1442488
UMLS CUI [1,2]
C0005903
Respiratory rate / minute
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate values determined closest to the first positive PCR. If values were not determined within the first 48 hours, report as "Not done". You will have the opportunity to document further values later.

Data type

integer

Alias
UMLS CUI [1,1]
C1442488
UMLS CUI [1,2]
C0231832
Glasgow Coma Scale
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate values determined closest to the first positive PCR. If values were not determined within the first 48 hours, report as "Not done". You will have the opportunity to document further values later.

Data type

integer

Alias
UMLS CUI [1,1]
C1442488
UMLS CUI [1,2]
C1271007
Heart function: Ejection fraction (EF) at SARS-CoV-2 detection
Description

Heart function: Ejection fraction (EF) at SARS-CoV-2 detection

Alias
UMLS CUI-1
C0232164
UMLS CUI-2
C0013516
UMLS CUI-3
C0232174
UMLS CUI-4
C1511790
UMLS CUI-5
C5203676
Heart function: Ejection fraction (EF) at SARS-CoV-2 detection
Description

Note: This question is critical for the further course of the questionnaire. Baseline Echo results. If values were not determined within the first 48 hours, report as "not done".

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0232164
UMLS CUI [2,2]
C0013516
UMLS CUI [3,1]
C0232174
UMLS CUI [3,2]
C1511790
UMLS CUI [3,3]
C5203676
Chest CT results at SARS-CoV-2 detection
Description

Chest CT results at SARS-CoV-2 detection

Alias
UMLS CUI-1
C1442488
UMLS CUI-2
C0202823
UMLS CUI-3
C1274040
UMLS CUI-4
C5203676
UMLS CUI-5
C1511790
Air trapping
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0231819
Areas of consolidation
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0521530
UMLS CUI [2,2]
C0205146
Bronchioloitis
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0006271
Crazy paving pattern
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C4476749
Ground glass opacities
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C3827002
Interlobular septal thickening
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C4280727
Nodulary lesions
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C1518345
Pleural effusion
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2]
C0032227
Chest x-ray results
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0039985
UMLS CUI [2,2]
C1274040
If Chest x-ray results, please specify (short description: no copy & paste)
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

text

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0039985
UMLS CUI [2,2]
C1274040
UMLS CUI [2,3]
C1521902
Other relevant CT results
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0040405
UMLS CUI [2,2]
C1274040
UMLS CUI [2,3]
C2826293
UMLS CUI [2,4]
C0205394
If Other relevant CT results, please specify (short description: no copy & paste)
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

text

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0040405
UMLS CUI [2,2]
C1274040
UMLS CUI [2,3]
C2826293
UMLS CUI [2,4]
C0205394
UMLS CUI [2,5]
C1521902
Normal CT
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0040405
UMLS CUI [2,2]
C0205307
Not done
Description

Note: This question is critical for the further course of the questionnaire. Baseline Please indicate the results of the CT / x-ray closest to the first positive PCR. If CT / x-ray was not done within the first 48 hours, report as "not done". You will have the opportunity to document further results later.

Data type

integer

Alias
UMLS CUI [1]
C1442488
UMLS CUI [2,1]
C0040405
UMLS CUI [2,2]
C1272696
Has a cardiovascular magnetic resonance imaging (CMR) been performed in any clinical phase?
Description

Has a cardiovascular magnetic resonance imaging (CMR) been performed in any clinical phase?

Alias
UMLS CUI-1
C3873775
UMLS CUI-2
C0205390
UMLS CUI-3
C0205210
UMLS CUI-4
C1552551
Has a cardiovascular magnetic resonance imaging (CMR) been performed in any clinical phase?
Description

If you have the opportunity to fill out a specific Sub-eCRF in consultation with a CMR specialist, please contact crf@leoss.net to get access.

Data type

integer

Alias
UMLS CUI [1,1]
C3873775
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0205210
UMLS CUI [1,4]
C1552551
Has neurological diagnostic taken place in the various phases?
Description

Has neurological diagnostic taken place in the various phases?

Alias
UMLS CUI-1
C0852602
UMLS CUI-2
C0205390
Baseline
Description

E.g. cCT, cMRI, EEG, Electrophysiology

Data type

integer

Alias
UMLS CUI [1,1]
C0852602
UMLS CUI [1,2]
C1442488
Uncomplicated phase
Description

E.g. cCT, cMRI, EEG, Electrophysiology

Data type

integer

Alias
UMLS CUI [1,1]
C0852602
UMLS CUI [1,2]
C0443334
UMLS CUI [1,3]
C0205390
Complicated phase
Description

E.g. cCT, cMRI, EEG, Electrophysiology

Data type

integer

Alias
UMLS CUI [1,1]
C0852602
UMLS CUI [1,2]
C0231242
UMLS CUI [1,3]
C0205390
Critical phase
Description

E.g. cCT, cMRI, EEG, Electrophysiology

Data type

integer

Alias
UMLS CUI [1,1]
C0852602
UMLS CUI [1,2]
C1511545
UMLS CUI [1,3]
C0205390
Was complementary and/or integrative medicine (CIM) used in any phase?
Description

Was complementary and/or integrative medicine (CIM) used in any phase?

Alias
UMLS CUI-1
C4053461
UMLS CUI-2
C0205390
UMLS CUI-3
C1552551
Was complementary and/or integrative medicine (CIM) used in any phase?
Description

E.g. Naturopathy, wraps and pads, Phytotherapy

Data type

integer

Alias
UMLS CUI [1]
C4053461
Has the patient signed a general agreement to share data for scientific purposes?
Description

Has the patient signed a general agreement to share data for scientific purposes?

Alias
UMLS CUI-1
C0680240
UMLS CUI-2
C0035168
UMLS CUI-3
C2713450
Yes, to share data
Description

Yes, to share data

Data type

integer

Alias
UMLS CUI [1,1]
C0680240
UMLS CUI [1,2]
C0035168
Yes, to share biomaterial samples
Description

Yes, to share biomaterial samples

Data type

integer

Alias
UMLS CUI [1,1]
C0680240
UMLS CUI [1,2]
C2347026
UMLS CUI [1,3]
C0457083
No
Description

No

Data type

integer

Alias
UMLS CUI [1]
C1298908
Unknown
Description

Unknown

Data type

integer

Alias
UMLS CUI [1]
C0439673
Is biomaterial of this patient available for research proposes?
Description

Is biomaterial of this patient available for research proposes?

Alias
UMLS CUI-1
C2347026
UMLS CUI-2
C0470187
UMLS CUI-3
C0035168
Serum
Description

Serum

Data type

integer

Alias
UMLS CUI [1]
C0229671
Blood
Description

Blood

Data type

integer

Alias
UMLS CUI [1]
C0005767
Cells
Description

Cells

Data type

integer

Alias
UMLS CUI [1]
C0007634
Stool
Description

Stool

Data type

integer

Alias
UMLS CUI [1]
C0015733
Cerebrospinal fluid
Description

Cerebrospinal fluid

Data type

integer

Alias
UMLS CUI [1]
C0007806
Other
Description

Other

Data type

integer

Alias
UMLS CUI [1]
C0205394
If Other, please specify:
Description

Other, specify

Data type

text

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C1521902
None
Description

None

Data type

integer

Alias
UMLS CUI [1]
C0549184
Unknown
Description

Unknown

Data type

integer

Alias
UMLS CUI [1]
C0439673
Did the patient participate in an interventional clinical trial?
Description

Did the patient participate in an interventional clinical trial?

Alias
UMLS CUI-1
C2348568
UMLS CUI-2
C3274035
Did the patient participate in an interventional clinical trial?
Description

Note: This question is critical for the further course of the questionnaire.

Data type

integer

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C3274035
If Yes, please name the trial
Description

Note: This question is critical for the further course of the questionnaire.

Data type

text

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C3274035
UMLS CUI [1,3]
C1521902
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Similar models

Baseline I

1 forms
  1. StudyEvent: ODM
    1. Baseline I
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Demography
C0011298 (UMLS CUI-1)
Item
Age at diagnosis
integer
C1828181 (UMLS CUI [1])
Age at diagnosis
Code List
Age at diagnosis
CL Item
<1 years (1)
CL Item
1-3 years (2)
CL Item
4 - 8 years (3)
CL Item
9 - 14 years (4)
CL Item
15 - 17 years (5)
CL Item
18 - 25 years (6)
CL Item
26 - 35 years (7)
CL Item
36 - 45 years (8)
CL Item
46 - 55 years (9)
CL Item
56 - 65 years (10)
CL Item
66 - 75 years (11)
CL Item
76 - 85 years (12)
CL Item
>85 years (13)
Item
Gender
integer
C0079399 (UMLS CUI [1])
Gender
Code List
Gender
CL Item
Male (1)
CL Item
Female (2)
CL Item
Diverse (3)
CL Item
Not specified (4)
Item
Ethnicity
integer
C0015031 (UMLS CUI [1])
Ethnicity
Code List
Ethnicity
CL Item
African & African American (1)
CL Item
American (2)
CL Item
Asian & Pacific Islander (3)
CL Item
Caucasian (4)
CL Item
Hispanic or Latino (5)
CL Item
Unknown (6)
Item
Country of residence
text
C1562954 (UMLS CUI [1])
BL_Residence
Code List
Country of residence
CL Item
Aruba (ABW)
CL Item
Afghanistan (AFG)
CL Item
Angola (AGO)
CL Item
Anguilla (AIA)
CL Item
Åland Islands (ALA)
CL Item
Albania (ALB)
CL Item
Andorra (AND)
CL Item
United Arab Emirates (ARE)
CL Item
Argentina (ARG)
CL Item
Armenia (ARM)
CL Item
American Samoa (ASM)
CL Item
Antarctica (ATA)
CL Item
French Southern Territories (ATF)
CL Item
Antigua and Barbuda (ATG)
CL Item
Australia (AUS)
CL Item
Austria (AUT)
CL Item
Azerbaijan (AZE)
CL Item
Burundi (BDI)
CL Item
Belgium (BEL)
CL Item
Benin (BEN)
CL Item
Bonaire, Sint Eustatius and Saba (BES)
CL Item
Burkina Faso (BFA)
CL Item
Bangladesh (BGD)
CL Item
Bulgaria (BGR)
CL Item
Bahrain (BHR)
CL Item
Bahamas (BHS)
CL Item
Bosnia and Herzegovina (BIH)
CL Item
Saint Barthélemy (BLM)
CL Item
Belarus (BLR)
CL Item
Belize (BLZ)
CL Item
Bermuda (BMU)
CL Item
Bolivia, Plurinational State of (BOL)
CL Item
Brazil (BRA)
CL Item
Barbados (BRB)
CL Item
Brunei Darussalam (BRN)
CL Item
Bhutan (BTN)
CL Item
Bouvet Island (BVT)
CL Item
Botswana (BWA)
CL Item
Central African Republic (CAF)
CL Item
Canada (CAN)
CL Item
Cocos, Keeling Islands (CCK)
CL Item
Switzerland (CHE)
CL Item
Chile (CHL)
CL Item
China (CHN)
CL Item
Côte d'Ivoire (CIV)
CL Item
Cameroon (CMR)
CL Item
Congo, Democratic Republic of the (COD)
CL Item
Congo (COG)
CL Item
Cook Islands (COK)
CL Item
Colombia (COL)
CL Item
Comoros (COM)
CL Item
Cabo Verde (CPV)
CL Item
Costa Rica (CRI)
CL Item
Cuba (CUB)
CL Item
Curaçao (CUW)
CL Item
Christmas Island (CXR)
CL Item
Cayman Islands (CYM)
CL Item
Cyprus (CYP)
CL Item
Czechia (CZE)
CL Item
Germany (DEU)
CL Item
Djibouti (DJI)
CL Item
Dominica (DMA)
CL Item
Denmark (DNK)
CL Item
Dominican Republic (DOM)
CL Item
Algeria (DZA)
CL Item
Ecuador (ECU)
CL Item
Egypt (EGY)
CL Item
Eritrea (ERI)
CL Item
Western Sahara (ESH)
CL Item
Spain (ESP)
CL Item
Estonia (EST)
CL Item
Ethiopia (ETH)
CL Item
Finland (FIN)
CL Item
Fiji (FJI)
CL Item
Falkland Islands, Malvinas (FLK)
CL Item
France (FRA)
CL Item
Faroe Islands (FRO)
CL Item
Micronesia, Federated States of (FSM)
CL Item
Gabon (GAB)
CL Item
United Kingdom of Great Britain and Northern Ireland (GBR)
CL Item
Georgia (GEO)
CL Item
Guernsey (GGY)
CL Item
Ghana (GHA)
CL Item
Gibraltar (GIB)
CL Item
Guinea (GIN)
CL Item
Guadeloupe (GLP)
CL Item
Gambia (GMB)
CL Item
Guinea-Bissau (GNB)
CL Item
Equatorial Guinea (GNQ)
CL Item
Greece (GRC)
CL Item
Grenada (GRD)
CL Item
Greenland (GRL)
CL Item
Guatemala (GTM)
CL Item
French Guiana (GUF)
CL Item
Guam (GUM)
CL Item
Guyana (GUY)
CL Item
Hong Kong (HKG)
CL Item
Heard Island and McDonald Islands (HMD)
CL Item
Honduras (HND)
CL Item
Croatia (HRV)
CL Item
Haiti (HTI)
CL Item
Hungary (HUN)
CL Item
Indonesia (IDN)
CL Item
Isle of Man (IMN)
CL Item
India (IND)
CL Item
British Indian Ocean Territory (IOT)
CL Item
Ireland (IRL)
CL Item
Iran, Islamic Republic of (IRN)
CL Item
Iraq (IRQ)
CL Item
Iceland (ISL)
CL Item
Israel (ISR)
CL Item
Italy (ITA)
CL Item
Jamaica (JAM)
CL Item
Jersey (JEY)
CL Item
Jordan (JOR)
CL Item
Japan (JPN)
CL Item
Kazakhstan (KAZ)
CL Item
Kenya (KEN)
CL Item
Kyrgyzstan (KGZ)
CL Item
Cambodia (KHM)
CL Item
Kiribati (KIR)
CL Item
Saint Kitts and Nevis (KNA)
CL Item
Korea, Republic of (KOR)
CL Item
Kuwait (KWT)
CL Item
Lao People's Democratic Republic (LAO)
CL Item
Lebanon (LBN)
CL Item
Liberia (LBR)
CL Item
Libya (LBY)
CL Item
Saint Lucia (LCA)
CL Item
Liechtenstein (LIE)
CL Item
Sri Lanka (LKA)
CL Item
Lesotho (LSO)
CL Item
Lithuania (LTU)
CL Item
Luxembourg (LUX)
CL Item
Latvia (LVA)
CL Item
Macao (MAC)
CL Item
Saint Martin, French part (MAF)
CL Item
Morocco (MAR)
CL Item
Monaco (MCO)
CL Item
Moldova, Republic of (MDA)
CL Item
Madagascar (MDG)
CL Item
Maldives (MDV)
CL Item
Mexico (MEX)
CL Item
Marshall Islands (MHL)
CL Item
North Macedonia (MKD)
CL Item
Mali (MLI)
CL Item
Malta (MLT)
CL Item
Myanmar (MMR)
CL Item
Montenegro (MNE)
CL Item
Mongolia (MNG)
CL Item
Northern Mariana Islands (MNP)
CL Item
Mozambique (MOZ)
CL Item
Mauritania (MRT)
CL Item
Montserrat (MSR)
CL Item
Martinique (MTQ)
CL Item
Mauritius (MUS)
CL Item
Malawi (MWI)
CL Item
Malaysia (MYS)
CL Item
Mayotte (MYT)
CL Item
Namibia (NAM)
CL Item
New Caledonia (NCL)
CL Item
Niger (NER)
CL Item
Norfolk Island (NFK)
CL Item
Nigeria (NGA)
CL Item
Nicaragua (NIC)
CL Item
Niue (NIU)
CL Item
Netherlands (NLD)
CL Item
Norway (NOR)
CL Item
Nepal (NPL)
CL Item
Nauru (NRU)
CL Item
New Zealand (NZL)
CL Item
Oman (OMN)
CL Item
Pakistan (PAK)
CL Item
Panama (PAN)
CL Item
Pitcairn (PCN)
CL Item
Peru (PER)
CL Item
Philippines (PHL)
CL Item
Palau (PLW)
CL Item
Papua New Guinea (PNG)
CL Item
Poland (POL)
CL Item
Puerto Rico (PRI)
CL Item
Korea, Democratic People's Republic of (PRK)
CL Item
Portugal (PRT)
CL Item
Paraguay (PRY)
CL Item
Palestine, State of (PSE)
CL Item
French Polynesia (PYF)
CL Item
Qatar (QAT)
CL Item
Réunion (REU)
CL Item
Romania (ROU)
CL Item
Russian Federation (RUS)
CL Item
Rwanda (RWA)
CL Item
Saudi Arabia (SAU)
CL Item
Sudan (SDN)
CL Item
Senegal (SEN)
CL Item
Singapore (SGP)
CL Item
South Georgia and the South Sandwich Islands (SGS)
CL Item
Saint Helena, Ascension and Tristan da Cunha (SHN)
CL Item
Svalbard and Jan Mayen (SJM)
CL Item
Solomon Islands (SLB)
CL Item
Sierra Leone (SLE)
CL Item
El Salvador (SLV)
CL Item
San Marino (SMR)
CL Item
Somalia (SOM)
CL Item
Saint Pierre and Miquelon (SPM)
CL Item
Serbia (SRB)
CL Item
South Sudan (SSD)
CL Item
Sao Tome and Principe (STP)
CL Item
Suriname (SUR)
CL Item
Slovakia (SVK)
CL Item
Slovenia (SVN)
CL Item
Sweden (SWE)
CL Item
Eswatini (SWZ)
CL Item
Sint Maarten, Dutch part (SXM)
CL Item
Seychelles (SYC)
CL Item
Syrian Arab Republic (SYR)
CL Item
Turks and Caicos Islands (TCA)
CL Item
Chad (TCD)
CL Item
Togo (TGO)
CL Item
Thailand (THA)
CL Item
Tajikistan (TJK)
CL Item
Tokelau (TKL)
CL Item
Turkmenistan (TKM)
CL Item
Timor-Leste (TLS)
CL Item
Tonga (TON)
CL Item
Trinidad and Tobago (TTO)
CL Item
Tunisia (TUN)
CL Item
Turkey (TUR)
CL Item
Tuvalu (TUV)
CL Item
Taiwan, Province of China (TWN)
CL Item
Tanzania, United Republic of (TZA)
CL Item
Uganda (UGA)
CL Item
Ukraine (UKR)
CL Item
United States Minor Outlying Islands (UMI)
CL Item
Uruguay (URY)
CL Item
United States of America (USA)
CL Item
Uzbekistan (UZB)
CL Item
Holy See (VAT)
CL Item
Saint Vincent and the Grenadines (VCT)
CL Item
Venezuela, Bolivarian Republic of (VEN)
CL Item
Virgin Islands, British (VGB)
CL Item
Virgin Islands, U.S. (VIR)
CL Item
Viet Nam (VNM)
CL Item
Vanuatu (VUT)
CL Item
Wallis and Futuna (WLF)
CL Item
Samoa (WSM)
CL Item
Yemen (YEM)
CL Item
South Africa (ZAF)
CL Item
Zambia (ZMB)
CL Item
Zimbabwe (ZWE)
Item Group
Diagnosis information
C0011900 (UMLS CUI-1)
Item
Country of diagnosis
text
C0454664 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
C5203676 (UMLS CUI [1,3])
BL_CountryDiagnosis
Code List
Country of diagnosis
CL Item
Aruba (ABW)
CL Item
Afghanistan (AFG)
CL Item
Angola (AGO)
CL Item
Anguilla (AIA)
CL Item
Åland Islands (ALA)
CL Item
Albania (ALB)
CL Item
Andorra (AND)
CL Item
United Arab Emirates (ARE)
CL Item
Argentina (ARG)
CL Item
Armenia (ARM)
CL Item
American Samoa (ASM)
CL Item
Antarctica (ATA)
CL Item
French Southern Territories (ATF)
CL Item
Antigua and Barbuda (ATG)
CL Item
Australia (AUS)
CL Item
Austria (AUT)
CL Item
Azerbaijan (AZE)
CL Item
Burundi (BDI)
CL Item
Belgium (BEL)
CL Item
Benin (BEN)
CL Item
Bonaire, Sint Eustatius and Saba (BES)
CL Item
Burkina Faso (BFA)
CL Item
Bangladesh (BGD)
CL Item
Bulgaria (BGR)
CL Item
Bahrain (BHR)
CL Item
Bahamas (BHS)
CL Item
Bosnia and Herzegovina (BIH)
CL Item
Saint Barthélemy (BLM)
CL Item
Belarus (BLR)
CL Item
Belize (BLZ)
CL Item
Bermuda (BMU)
CL Item
Bolivia, Plurinational State of (BOL)
CL Item
Brazil (BRA)
CL Item
Barbados (BRB)
CL Item
Brunei Darussalam (BRN)
CL Item
Bhutan (BTN)
CL Item
Bouvet Island (BVT)
CL Item
Botswana (BWA)
CL Item
Central African Republic (CAF)
CL Item
Canada (CAN)
CL Item
Cocos, Keeling Islands (CCK)
CL Item
Switzerland (CHE)
CL Item
Chile (CHL)
CL Item
China (CHN)
CL Item
Côte d'Ivoire (CIV)
CL Item
Cameroon (CMR)
CL Item
Congo, Democratic Republic of the (COD)
CL Item
Congo (COG)
CL Item
Cook Islands (COK)
CL Item
Colombia (COL)
CL Item
Comoros (COM)
CL Item
Cabo Verde (CPV)
CL Item
Costa Rica (CRI)
CL Item
Cuba (CUB)
CL Item
Curaçao (CUW)
CL Item
Christmas Island (CXR)
CL Item
Cayman Islands (CYM)
CL Item
Cyprus (CYP)
CL Item
Czechia (CZE)
CL Item
Germany (DEU)
CL Item
Djibouti (DJI)
CL Item
Dominica (DMA)
CL Item
Denmark (DNK)
CL Item
Dominican Republic (DOM)
CL Item
Algeria (DZA)
CL Item
Ecuador (ECU)
CL Item
Egypt (EGY)
CL Item
Eritrea (ERI)
CL Item
Western Sahara (ESH)
CL Item
Spain (ESP)
CL Item
Estonia (EST)
CL Item
Ethiopia (ETH)
CL Item
Finland (FIN)
CL Item
Fiji (FJI)
CL Item
Falkland Islands, Malvinas (FLK)
CL Item
France (FRA)
CL Item
Faroe Islands (FRO)
CL Item
Micronesia, Federated States of (FSM)
CL Item
Gabon (GAB)
CL Item
United Kingdom of Great Britain and Northern Ireland (GBR)
CL Item
Georgia (GEO)
CL Item
Guernsey (GGY)
CL Item
Ghana (GHA)
CL Item
Gibraltar (GIB)
CL Item
Guinea (GIN)
CL Item
Guadeloupe (GLP)
CL Item
Gambia (GMB)
CL Item
Guinea-Bissau (GNB)
CL Item
Equatorial Guinea (GNQ)
CL Item
Greece (GRC)
CL Item
Grenada (GRD)
CL Item
Greenland (GRL)
CL Item
Guatemala (GTM)
CL Item
French Guiana (GUF)
CL Item
Guam (GUM)
CL Item
Guyana (GUY)
CL Item
Hong Kong (HKG)
CL Item
Heard Island and McDonald Islands (HMD)
CL Item
Honduras (HND)
CL Item
Croatia (HRV)
CL Item
Haiti (HTI)
CL Item
Hungary (HUN)
CL Item
Indonesia (IDN)
CL Item
Isle of Man (IMN)
CL Item
India (IND)
CL Item
British Indian Ocean Territory (IOT)
CL Item
Ireland (IRL)
CL Item
Iran, Islamic Republic of (IRN)
CL Item
Iraq (IRQ)
CL Item
Iceland (ISL)
CL Item
Israel (ISR)
CL Item
Italy (ITA)
CL Item
Jamaica (JAM)
CL Item
Jersey (JEY)
CL Item
Jordan (JOR)
CL Item
Japan (JPN)
CL Item
Kazakhstan (KAZ)
CL Item
Kenya (KEN)
CL Item
Kyrgyzstan (KGZ)
CL Item
Cambodia (KHM)
CL Item
Kiribati (KIR)
CL Item
Saint Kitts and Nevis (KNA)
CL Item
Korea, Republic of (KOR)
CL Item
Kuwait (KWT)
CL Item
Lao People's Democratic Republic (LAO)
CL Item
Lebanon (LBN)
CL Item
Liberia (LBR)
CL Item
Libya (LBY)
CL Item
Saint Lucia (LCA)
CL Item
Liechtenstein (LIE)
CL Item
Sri Lanka (LKA)
CL Item
Lesotho (LSO)
CL Item
Lithuania (LTU)
CL Item
Luxembourg (LUX)
CL Item
Latvia (LVA)
CL Item
Macao (MAC)
CL Item
Saint Martin, French part (MAF)
CL Item
Morocco (MAR)
CL Item
Monaco (MCO)
CL Item
Moldova, Republic of (MDA)
CL Item
Madagascar (MDG)
CL Item
Maldives (MDV)
CL Item
Mexico (MEX)
CL Item
Marshall Islands (MHL)
CL Item
North Macedonia (MKD)
CL Item
Mali (MLI)
CL Item
Malta (MLT)
CL Item
Myanmar (MMR)
CL Item
Montenegro (MNE)
CL Item
Mongolia (MNG)
CL Item
Northern Mariana Islands (MNP)
CL Item
Mozambique (MOZ)
CL Item
Mauritania (MRT)
CL Item
Montserrat (MSR)
CL Item
Martinique (MTQ)
CL Item
Mauritius (MUS)
CL Item
Malawi (MWI)
CL Item
Malaysia (MYS)
CL Item
Mayotte (MYT)
CL Item
Namibia (NAM)
CL Item
New Caledonia (NCL)
CL Item
Niger (NER)
CL Item
Norfolk Island (NFK)
CL Item
Nigeria (NGA)
CL Item
Nicaragua (NIC)
CL Item
Niue (NIU)
CL Item
Netherlands (NLD)
CL Item
Norway (NOR)
CL Item
Nepal (NPL)
CL Item
Nauru (NRU)
CL Item
New Zealand (NZL)
CL Item
Oman (OMN)
CL Item
Pakistan (PAK)
CL Item
Panama (PAN)
CL Item
Pitcairn (PCN)
CL Item
Peru (PER)
CL Item
Philippines (PHL)
CL Item
Palau (PLW)
CL Item
Papua New Guinea (PNG)
CL Item
Poland (POL)
CL Item
Puerto Rico (PRI)
CL Item
Korea, Democratic People's Republic of (PRK)
CL Item
Portugal (PRT)
CL Item
Paraguay (PRY)
CL Item
Palestine, State of (PSE)
CL Item
French Polynesia (PYF)
CL Item
Qatar (QAT)
CL Item
Réunion (REU)
CL Item
Romania (ROU)
CL Item
Russian Federation (RUS)
CL Item
Rwanda (RWA)
CL Item
Saudi Arabia (SAU)
CL Item
Sudan (SDN)
CL Item
Senegal (SEN)
CL Item
Singapore (SGP)
CL Item
South Georgia and the South Sandwich Islands (SGS)
CL Item
Saint Helena, Ascension and Tristan da Cunha (SHN)
CL Item
Svalbard and Jan Mayen (SJM)
CL Item
Solomon Islands (SLB)
CL Item
Sierra Leone (SLE)
CL Item
El Salvador (SLV)
CL Item
San Marino (SMR)
CL Item
Somalia (SOM)
CL Item
Saint Pierre and Miquelon (SPM)
CL Item
Serbia (SRB)
CL Item
South Sudan (SSD)
CL Item
Sao Tome and Principe (STP)
CL Item
Suriname (SUR)
CL Item
Slovakia (SVK)
CL Item
Slovenia (SVN)
CL Item
Sweden (SWE)
CL Item
Eswatini (SWZ)
CL Item
Sint Maarten, Dutch part (SXM)
CL Item
Seychelles (SYC)
CL Item
Syrian Arab Republic (SYR)
CL Item
Turks and Caicos Islands (TCA)
CL Item
Chad (TCD)
CL Item
Togo (TGO)
CL Item
Thailand (THA)
CL Item
Tajikistan (TJK)
CL Item
Tokelau (TKL)
CL Item
Turkmenistan (TKM)
CL Item
Timor-Leste (TLS)
CL Item
Tonga (TON)
CL Item
Trinidad and Tobago (TTO)
CL Item
Tunisia (TUN)
CL Item
Turkey (TUR)
CL Item
Tuvalu (TUV)
CL Item
Taiwan, Province of China (TWN)
CL Item
Tanzania, United Republic of (TZA)
CL Item
Uganda (UGA)
CL Item
Ukraine (UKR)
CL Item
United States Minor Outlying Islands (UMI)
CL Item
Uruguay (URY)
CL Item
United States of America (USA)
CL Item
Uzbekistan (UZB)
CL Item
Holy See (VAT)
CL Item
Saint Vincent and the Grenadines (VCT)
CL Item
Venezuela, Bolivarian Republic of (VEN)
CL Item
Virgin Islands, British (VGB)
CL Item
Virgin Islands, U.S. (VIR)
CL Item
Viet Nam (VNM)
CL Item
Vanuatu (VUT)
CL Item
Wallis and Futuna (WLF)
CL Item
Samoa (WSM)
CL Item
Yemen (YEM)
CL Item
South Africa (ZAF)
CL Item
Zambia (ZMB)
CL Item
Zimbabwe (ZWE)
Place of residence ZIP code
Item
ZIP code area
text
C1514254 (UMLS CUI [1,1])
C0682130 (UMLS CUI [1,2])
Reason for consultation / admission: COVID-19 or treatment for other medical conditions; ICD-10 code
Item
Reason for consultation / admission: COVID-19 or treatment for other medical conditions
text
C0392360 (UMLS CUI [1,1])
C0009818 (UMLS CUI [1,2])
C0392360 (UMLS CUI [2,1])
C0809949 (UMLS CUI [2,2])
C5203670 (UMLS CUI [3])
C0012634 (UMLS CUI [4,1])
C0205394 (UMLS CUI [4,2])
C0087111 (UMLS CUI [4,3])
C2598420 (UMLS CUI [5])
Coded DRG:
Item
Coded DRG:
text
C0011928 (UMLS CUI [1])
Interval between hospital admission date and SARS-CoV-2-detection
Item
Day of admission to hospital in reference to first SARS-CoV-2-detection (day 0)
text
C0806429 (UMLS CUI [1,1])
C1272706 (UMLS CUI [1,2])
C5203676 (UMLS CUI [1,3])
C1511790 (UMLS CUI [1,4])
Item
How did the patient come to the health care facility ?
integer
C3263562 (UMLS CUI [1,1])
C0018704 (UMLS CUI [1,2])
C0150390 (UMLS CUI [2,1])
C0018704 (UMLS CUI [2,2])
How did the patient come to the health care facility ?
Code List
How did the patient come to the health care facility ?
CL Item
By himself/herself (by foot, by car) (1)
CL Item
By taxi or patient transport ambulance (2)
CL Item
By emergency ambulance (3)
CL Item
By air-bound transport (4)
CL Item
By intra-hospital patient transfer (5)
CL Item
By intensive care transport (6)
CL Item
Other, please specify (7)
CL Item
Unknown (8)
Patient arrival/transport to health care facility: Other, please specify
Item
How did the patient come to the health care facility ? If Other, please specify
text
C3263562 (UMLS CUI [1,1])
C0018704 (UMLS CUI [1,2])
C3845569 (UMLS CUI [1,3])
C0150390 (UMLS CUI [2,1])
C0018704 (UMLS CUI [2,2])
C3845569 (UMLS CUI [2,3])
Item
Where did the patient stay before SARS-CoV-2 detection?
integer
C0030705 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C5203676 (UMLS CUI [1,4])
C1511790 (UMLS CUI [1,5])
Where did the patient stay before SARS-CoV-2 detection?
Code List
Where did the patient stay before SARS-CoV-2 detection?
CL Item
At home (1)
CL Item
Homelessness (2)
CL Item
Clinic/hospital (3)
CL Item
Nursing home (4)
CL Item
Rehabilitation facility (5)
CL Item
Refugee accomodation (6)
CL Item
Other, please specify (7)
CL Item
Unknown (8)
Place of stay before SARS-CoV-2 detection: Other, please specify
Item
Where did the patient stay before SARS-CoV-2 detection? If Other, please specify
text
C0450429 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
C5203676 (UMLS CUI [1,3])
C1511790 (UMLS CUI [1,4])
C3845569 (UMLS CUI [1,5])
Item
Where did the patient stay after the follow-up period?
integer
C0030705 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
C0687676 (UMLS CUI [1,3])
C1522577 (UMLS CUI [1,4])
Where did the patient stay after the follow-up period?
Code List
Where did the patient stay after the follow-up period?
CL Item
At home (1)
CL Item
Homelessness (2)
CL Item
Clinic/hospital (3)
CL Item
Nursing home (4)
CL Item
Rehabilitation facility (5)
CL Item
Refugee accomodation (6)
CL Item
Patient died (7)
CL Item
Other, please specify (8)
CL Item
Unknown (9)
Patient place of stay after the follow-up period: Other, please specify
Item
Where did the patient stay after the follow-up period? If Other, please specify
text
C0030705 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
C0687676 (UMLS CUI [1,3])
C1522577 (UMLS CUI [1,4])
C3845569 (UMLS CUI [1,5])
Item
Did the patient come through the emergency room?
integer
C3263562 (UMLS CUI [1,1])
C4291935 (UMLS CUI [1,2])
Did the patient come through the emergency room?
Code List
Did the patient come through the emergency room?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Month of first diagnosis
integer
C0439231 (UMLS CUI [1,1])
C0205265 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,3])
C5203676 (UMLS CUI [1,4])
Month of first diagnosis
Code List
Month of first diagnosis
CL Item
1_2020 (1)
CL Item
2_2020 (2)
CL Item
3_2020 (3)
CL Item
4_2020 (4)
CL Item
5_2020 (5)
CL Item
6_2020 (6)
CL Item
7_2020 (7)
CL Item
8_2020 (8)
CL Item
9_2020 (9)
CL Item
10_2020 (10)
CL Item
11_2020 (11)
CL Item
12_2020 (12)
CL Item
Unknown (13)
Item Group
Assumed days between contracting infection and diagnosis
C5203676 (UMLS CUI-1)
C3483764 (UMLS CUI-2)
C2316983 (UMLS CUI-3)
C1272706 (UMLS CUI-4)
Item
Assumed days between contracting infection and diagnosis:
integer
C5203676 (UMLS CUI [1,1])
C3483764 (UMLS CUI [1,2])
C2316983 (UMLS CUI [1,3])
C1272706 (UMLS CUI [1,4])
first contact with infection, days before diagnosis
Code List
Assumed days between contracting infection and diagnosis:
CL Item
Unknown (1)
CL Item
First known contact with infected person, days before diagnosis: (6)
first contact with infection, days before diagnosis, count of entities
Item
First known contact with infected person, days before diagnosis:
text
C0205435 (UMLS CUI [1,1])
C0332158 (UMLS CUI [1,2])
C5203676 (UMLS CUI [1,3])
C2316983 (UMLS CUI [1,4])
C1272706 (UMLS CUI [1,5])
C1521902 (UMLS CUI [1,6])
Item Group
Disease phases at baseline and during follow-up
C0920316 (UMLS CUI-1)
C0699749 (UMLS CUI-2)
C1522577 (UMLS CUI-3)
C1442488 (UMLS CUI-4)
Item
Phase at diagnosis
integer
C0521117 (UMLS CUI [1,1])
C5203676 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,3])
Severity of illness at diagnosis
Code List
Phase at diagnosis
CL Item
Uncomplicated phase (1)
CL Item
Complicated phase (2)
CL Item
Critical phase (3)
CL Item
Recovery phase (4)
CL Item
Dead (5)
CL Item
Unknown (6)
Uncomplicated phase, start day
Item
Note all phases the patient went through within the follow-up period. Uncomplicated phase, start day:
boolean
C0808070 (UMLS CUI [1,1])
C0443334 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
Uncomplicated phase, start day - specify
Item
Note all phases the patient went through within the follow-up period. Uncomplicated phase, start day, specify:
text
C0808070 (UMLS CUI [1,1])
C0443334 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
Complicated phase, start day
Item
Note all phases the patient went through within the follow-up period. Complicated phase, start day:
boolean
C0808070 (UMLS CUI [1,1])
C0231242 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
Complicated phase, start day - specify
Item
Note all phases the patient went through within the follow-up period. Complicated phase, start day, specify:
text
C0808070 (UMLS CUI [1,1])
C0231242 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
Critical phase, start day
Item
Note all phases the patient went through within the follow-up period. Critical phase, start day:
boolean
C0808070 (UMLS CUI [1,1])
C1511545 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
Critical phase, start day - specify
Item
Note all phases the patient went through within the follow-up period. Critical phase, start day, specify:
text
C0808070 (UMLS CUI [1,1])
C1511545 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
Recovery phase, start day
Item
Note all phases the patient went through within the follow-up period. Recovery phase, start day:
boolean
C0808070 (UMLS CUI [1,1])
C2004454 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
Recovery phase, start day - specify
Item
Note all phases the patient went through within the follow-up period. Recovery phase, start day, specify:
text
C0808070 (UMLS CUI [1,1])
C2004454 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
Item Group
Duration (days) of...
C0449238 (UMLS CUI-1)
Overall inpatient stay
Item
Overall inpatient stay:
text
C0420496 (UMLS CUI [1])
Intensive care unit stay
Item
Intensive care unit (ICU) stay:
text
C0085559 (UMLS CUI [1,1])
C0023303 (UMLS CUI [1,2])
Intermediate care unit stay
Item
Intermediate care unit (IMCU) stay:
text
C0021767 (UMLS CUI [1,1])
C0023303 (UMLS CUI [1,2])
Mechanical ventilation
Item
Mechanical ventilation
text
C0199470 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
ECMO support
Item
ECMO support:
text
C0015357 (UMLS CUI [1,1])
C0023303 (UMLS CUI [1,2])
Item Group
Days of follow-up since the day the sample of the first positive SARS-CoV-2 result was taken
C1522577 (UMLS CUI-1)
C0449238 (UMLS CUI-2)
C0011900 (UMLS CUI-3)
C5203676 (UMLS CUI-4)
BL_FollowUp
Item
Days of follow-up since the day the sample of the first positive SARS-CoV-2 result was taken
text
C1522577 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,3])
C5203676 (UMLS CUI [1,4])
Item Group
Last known status
C0699749 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
C1517741 (UMLS CUI-3)
Item
Last known status:
integer
C0699749 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,3])
BL_Status_2020-03-20
Code List
Last known status:
CL Item
Not recovered (means recovery phase not achieved) (1)
CL Item
Recovered (at least recovery phase achieved or better) (2)
CL Item
Dead from COVID-19 (3)
CL Item
Dead from other causes, please specify (4)
Dead from other causes, specify
Item
If Dead from other causes, please specify
text
C0007465 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
Item Group
Was limitation of therapy discussed at any time during the SARS-CoV-2 infection?
C0557061 (UMLS CUI-1)
C0449295 (UMLS CUI-2)
C0087111 (UMLS CUI-3)
C0347984 (UMLS CUI-4)
C5203676 (UMLS CUI-5)
Item
Was limitation of therapy discussed at any time during the SARS-CoV-2 infection?
integer
C0557061 (UMLS CUI [1,1])
C0449295 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C0347984 (UMLS CUI [1,4])
C5203676 (UMLS CUI [1,5])
Was limitation of therapy discussed at any time during the SARS-CoV-2 infection?
Code List
Was limitation of therapy discussed at any time during the SARS-CoV-2 infection?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Did the patient receive specialist palliative care during the SARS-CoV-2 infection?
C5203676 (UMLS CUI-1)
C0030231 (UMLS CUI-2)
Item
Did the patient receive specialist palliative care during the SARS-CoV-2 infection?
integer
C5203676 (UMLS CUI [1,1])
C0030231 (UMLS CUI [1,2])
Did the patient receive specialist palliative care during the SARS-CoV-2 infection?
Code List
Did the patient receive specialist palliative care during the SARS-CoV-2 infection?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Did the patient suffer from a life limiting disease with a prognosis of less than one year to live before first positive testing of SARS-CoV-2?
C0012634 (UMLS CUI-1)
C0439801 (UMLS CUI-2)
C0023671 (UMLS CUI-3)
C0332152 (UMLS CUI-4)
C5203676 (UMLS CUI-5)
C0039593 (UMLS CUI-6)
C1446409 (UMLS CUI-7)
Item
Did the patient suffer from a life limiting disease with a prognosis of less than one year to live before first positive testing of SARS-CoV-2?
integer
C0012634 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0023671 (UMLS CUI [1,3])
C0332152 (UMLS CUI [1,4])
C5203676 (UMLS CUI [1,5])
C0039593 (UMLS CUI [1,6])
C1446409 (UMLS CUI [1,7])
Did the patient suffer from a life limiting disease with a prognosis of less than one year to live before first positive testing of SARS-CoV-2?
Code List
Did the patient suffer from a life limiting disease with a prognosis of less than one year to live before first positive testing of SARS-CoV-2?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Comorbidities, Central nervous system / Neurological disesases
C0009488 (UMLS CUI-1)
C0007682 (UMLS CUI-2)
C0027765 (UMLS CUI-3)
Item
Hemiplegia
integer
C0018991 (UMLS CUI [1])
Hemiplegia
Code List
Hemiplegia
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Dementia
integer
C0497327 (UMLS CUI [1])
Dementia
Code List
Dementia
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Cerebrovascular disease, stroke, TIA
integer
C0007820 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0007787 (UMLS CUI [3])
Cerebrovascular disease, stroke, TIA
Code List
Cerebrovascular disease, stroke, TIA
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Motoneuron disease (e.g. amyotrophic lateral sclerosis, spinal muscular atrophy)
integer
C0026609 (UMLS CUI [1,1])
C0012634 (UMLS CUI [1,2])
C0002736 (UMLS CUI [2])
C0026847 (UMLS CUI [3])
Motoneuron disease (e.g. amyotrophic lateral sclerosis, spinal muscular atrophy)
Code List
Motoneuron disease (e.g. amyotrophic lateral sclerosis, spinal muscular atrophy)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Movement disorder (e.g. Parkinson's disease, Dystonia, Ataxia, Tremor)
integer
C0026650 (UMLS CUI [1])
C0030567 (UMLS CUI [2])
C0013421 (UMLS CUI [3])
C0004134 (UMLS CUI [4])
C0040822 (UMLS CUI [5])
Movement disorder (e.g. Parkinson's disease, Dystonia, Ataxia, Tremor)
Code List
Movement disorder (e.g. Parkinson's disease, Dystonia, Ataxia, Tremor)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Multiple sclerosis
integer
C0026769 (UMLS CUI [1])
Multiple Sclerosis
Code List
Multiple sclerosis
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Myasthenia gravis
integer
C0026896 (UMLS CUI [1])
Myasthenia
Code List
Myasthenia gravis
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Neuromyelitis optica spectrum disorder (NMOSD)
integer
C0027873 (UMLS CUI [1])
Neuromyelitis optica spectrum disorder (NMOSD)
Code List
Neuromyelitis optica spectrum disorder (NMOSD)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other neurological autoimmune diseases
integer
C0004364 (UMLS CUI [1,1])
C0027765 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
Other neurological autoimmune diseases
Code List
Other neurological autoimmune diseases
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other prior neurological disease
integer
C2015799 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
C5203670 (UMLS CUI [1,3])
Other prior neurological diagnosis
Code List
Other prior neurological disease
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Comorbidities, Cardiovascular diseases
C0009488 (UMLS CUI-1)
C0728936 (UMLS CUI-2)
Item
Myocardial infarction
integer
C0027051 (UMLS CUI [1])
Myocardial infarction
Code List
Myocardial infarction
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Aortic stenosis
integer
C0003507 (UMLS CUI [1])
Aortic stenosis
Code List
Aortic stenosis
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
AV block
integer
C0004245 (UMLS CUI [1])
AV block
Code List
AV block
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Carotid arterial disease
integer
C0007273 (UMLS CUI [1])
Carotid arterial disease
Code List
Carotid arterial disease
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Chronic heart failure
integer
C0264716 (UMLS CUI [1])
Chronic heart failure
Code List
Chronic heart failure
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Peripheral vascular disease
integer
C0085096 (UMLS CUI [1])
Peripheral vascular disease
Code List
Peripheral vascular disease
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Hypertension
integer
C0020538 (UMLS CUI [1])
Hypertension
Code List
Hypertension
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Atrial fibrillation
integer
C0004238 (UMLS CUI [1])
Atrial fibrillation
Code List
Atrial fibrillation
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Coronary artery disease
integer
C1956346 (UMLS CUI [1])
Coronary artery disease
Code List
Coronary artery disease
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other cardiovascular disease
integer
C0007222 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Coronary artery disease
Code List
Other cardiovascular disease
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Comorbidities, Pulmonary diseases
C0009488 (UMLS CUI-1)
C0024115 (UMLS CUI-2)
Item
COPD
integer
C0024117 (UMLS CUI [1])
COPD
Code List
COPD
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Asthma
integer
C0004096 (UMLS CUI [1])
Asthma
Code List
Asthma
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other chronic pulmonary diseases
integer
C0746102 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Other chronic pulmonary disease
Code List
Other chronic pulmonary diseases
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Comorbidities, Hematological / oncological diseases
C0009488 (UMLS CUI-1)
C0018939 (UMLS CUI-2)
C0442867 (UMLS CUI-3)
Item
Leukemia
integer
C0023418 (UMLS CUI [1])
Leukemia
Code List
Leukemia
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Lymphoma
integer
C0024299 (UMLS CUI [1])
Lymphoma
Code List
Lymphoma
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Solid tumor
integer
C0280100 (UMLS CUI [1])
Solid tumor
Code List
Solid tumor
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Solid tumor, metastasized
integer
C0280100 (UMLS CUI [1,1])
C0027627 (UMLS CUI [1,2])
Solid tumor, metastasized
Code List
Solid tumor, metastasized
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Stem cell transplantation
integer
C1504389 (UMLS CUI [1])
Stem cell transplantation
Code List
Stem cell transplantation
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other hematological disease
integer
C0018939 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Stem cell transplantation
Code List
Other hematological disease
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Comorbidities, Rheumatological diseases
C0419922 (UMLS CUI-1)
C0035435 (UMLS CUI-2)
Item
Rheumatic disease (e.g. rheumatoid arthritis, vasculitis, spondyloarthritis, psoriatic arthritis)
integer
C0035435 (UMLS CUI [1])
C0003873 (UMLS CUI [2])
C0042384 (UMLS CUI [3])
C0949690 (UMLS CUI [4])
C0003872 (UMLS CUI [5])
Rheumatic disease (e.g. rheumatoid arthritis, vasculitis, spondyloarthritis, psoriatic arthritis)
Code List
Rheumatic disease (e.g. rheumatoid arthritis, vasculitis, spondyloarthritis, psoriatic arthritis)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Connective tissue disease (e.g. systemic lupus erythematosus, dermatomyositis, Sjögren's syndrome)
integer
C0009782 (UMLS CUI [1])
C0409974 (UMLS CUI [2])
C0011633 (UMLS CUI [3])
C1527336 (UMLS CUI [4])
Connective tissue disease (e.g. systemic lupus erythematosus, dermatomyositis, Sjögren's syndrome)
Code List
Connective tissue disease (e.g. systemic lupus erythematosus, dermatomyositis, Sjögren's syndrome)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Comorbidities, Allergology
C0009488 (UMLS CUI-1)
C0020517 (UMLS CUI-2)
Item
Pollen sensitization
integer
C0740919 (UMLS CUI [1])
Pollen sensitization
Code List
Pollen sensitization
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Dust mite senzitization
integer
C0339808 (UMLS CUI [1])
Dust mite senzitization
Code List
Dust mite senzitization
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other sensitization
integer
C0020517 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Other senzitization
Code List
Other sensitization
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Comorbidities, Other internal disorders
C0009488 (UMLS CUI-1)
C0205394 (UMLS CUI-2)
C0012634 (UMLS CUI-3)
C0205102 (UMLS CUI-4)
Item
Peptic ulcer disease
integer
C0030920 (UMLS CUI [1])
Peptic ulcer disease
Code List
Peptic ulcer disease
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Chronic liver disease
integer
C0341439 (UMLS CUI [1])
Chronic liver disease
Code List
Chronic liver disease
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Liver cirrhosis
integer
C0023890 (UMLS CUI [1])
Liver cirrhosis
Code List
Liver cirrhosis
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Diabetes, no end-organ damage
integer
C0011849 (UMLS CUI [1,1])
C0743496 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Diabetes, no end-organ damage
Code List
Diabetes, no end-organ damage
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Diabetes, with end-organ damage
integer
C0011849 (UMLS CUI [1,1])
C0743496 (UMLS CUI [1,2])
Diabetes, with end-organ damage
Code List
Diabetes, with end-organ damage
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Chronic kidney disease
integer
C1561643 (UMLS CUI [1])
Chronic kidney disease
Code List
Chronic kidney disease
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
On dialysis
integer
C0011946 (UMLS CUI [1])
On dialysis
Code List
On dialysis
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Comorbidities, Other conditions
C0009488 (UMLS CUI-1)
C0205394 (UMLS CUI-2)
Item
Organ transplantation
integer
C0029216 (UMLS CUI [1])
Organ transplantation
Code List
Organ transplantation
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
HIV/AIDS
integer
C0019693 (UMLS CUI [1])
C0001175 (UMLS CUI [2])
HIV/AIDS
Code List
HIV/AIDS
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Traumatic injury (e.g. head, chest, abdominal and skeletal injuries)
integer
C3263723 (UMLS CUI [1])
C0018674 (UMLS CUI [2])
C0039980 (UMLS CUI [3])
C0848377 (UMLS CUI [4])
C0597457 (UMLS CUI [5])
Traumatic injury (e.g. head, chest, abdominal and skeletal injuries)
Code List
Traumatic injury (e.g. head, chest, abdominal and skeletal injuries)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Burn
integer
C0006434 (UMLS CUI [1])
Burn
Code List
Burn
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Alcohol abuse
integer
C0085762 (UMLS CUI [1])
Alcohol abuse
Code List
Alcohol abuse
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Prior heart failure at diagnosis
C0018801 (UMLS CUI-1)
C0332152 (UMLS CUI-2)
C5203676 (UMLS CUI-3)
Item
Prior heart failure at diagnosis
integer
C0018801 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C5203676 (UMLS CUI [1,4])
BL_HeartFailure
Code List
Prior heart failure at diagnosis
CL Item
< 1 year (1)
CL Item
1 - 5 years (2)
CL Item
> 5 years (3)
CL Item
None (4)
CL Item
Unknown (5)
Item Group
Stage of heart failure at diagnosis (NYHA classification)
C1275491 (UMLS CUI-1)
Item
Stage of heart failure at diagnosis (NYHA classification)
integer
C0018801 (UMLS CUI [1,1])
C1306673 (UMLS CUI [1,2])
C5203676 (UMLS CUI [1,3])
C0011900 (UMLS CUI [1,4])
C1275491 (UMLS CUI [2])
Stage of heart failure at diagnosis (NYHA classification)
Code List
Stage of heart failure at diagnosis (NYHA classification)
CL Item
NYHA I: No symptoms and no limitation in ordinary physical activity, e.g. shortness of breath when walking, climbing stairs etc. (1)
CL Item
NYHA II: Mild symptoms (mild shortness of breath and/or angina) and slight limitation during ordinary activity (2)
CL Item
NYHA III: Marked limitation in activity due to symptoms, even during less-than-ordinary activity, e.g. walking short distances (20-100 m). Comfortable only at rest. (3)
CL Item
NYHA IV: Severe limitations. Experiences symptoms even while at rest. Mostly bedbound patients. (4)
CL Item
None (5)
CL Item
Unknown (6)
Item Group
Body-Mass-Index (BMI)
C1305855 (UMLS CUI-1)
Item
Body-Mass-Index (BMI)
integer
C1305855 (UMLS CUI [1])
BL_BMI_2020-03-28
Code List
Body-Mass-Index (BMI)
CL Item
< 18,5 kg/m2 (1)
CL Item
18,5 - 24,9 kg/m2 (2)
CL Item
25 - 29,9 kg/m2 (3)
CL Item
30 - 34,9 kg/m2 (4)
CL Item
> 34,9 km/m2 (5)
CL Item
Unknown (6)
Item Group
Smoking status
C1519386 (UMLS CUI-1)
Item
Smoking status
integer
C1519386 (UMLS CUI [1])
BL_Smoking
Code List
Smoking status
CL Item
1-10 pack years (1)
CL Item
11-20 pack years (2)
CL Item
>21 pack years (3)
CL Item
Smoker, unknown pack years (4)
CL Item
Nonsmoker (5)
CL Item
Former smoker (6)
CL Item
Unknown (7)
Item Group
Use of e-cigarettes and / or vaporizer?
C3849993 (UMLS CUI-1)
C4083280 (UMLS CUI-2)
Item
Use of e-cigarettes and / or vaporizer?
integer
C3849993 (UMLS CUI [1])
C4083280 (UMLS CUI [2])
Use of e-cigarettes and / or vaporizer?
Code List
Use of e-cigarettes and / or vaporizer?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Treatments received
C0087111 (UMLS CUI-1)
Item
ACE inhibitors (e.g. enalapril, captopril, most drugs ending on -pril)
integer
C0003015 (UMLS CUI [1])
C0006938 (UMLS CUI [2])
C0014025 (UMLS CUI [3])
ACE inhibitors (e.g. elanapril, captopril, most drugs ending on -pril)
Code List
ACE inhibitors (e.g. enalapril, captopril, most drugs ending on -pril)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
AT-1 inhibitors (e.g. candesartan, losartan, most drugs ending on -sartan)
integer
C0521942 (UMLS CUI [1])
C0717550 (UMLS CUI [2])
C0126174 (UMLS CUI [3])
AT-I inhibitors (e.g. candesartan, losartan, most drugs ending on -sartan)
Code List
AT-1 inhibitors (e.g. candesartan, losartan, most drugs ending on -sartan)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Statines (e.g. atorvastatin, pravastatin, most drugs ending on -statin)
integer
C0360714 (UMLS CUI [1])
C0286651 (UMLS CUI [2])
C0085542 (UMLS CUI [3])
Statines (e.g. atorvastatin, pravastatin, most drugs ending on -statin)
Code List
Statines (e.g. atorvastatin, pravastatin, most drugs ending on -statin)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Ibuprofen
integer
C0020740 (UMLS CUI [1])
Ibuprofen
Code List
Ibuprofen
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Vitamin D
integer
C0420176 (UMLS CUI [1])
Vitamin D
Code List
Vitamin D
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Immunosuppressive medication in the past 3 months?
C0021081 (UMLS CUI-1)
C0332185 (UMLS CUI-2)
Item
Immunosuppressive medication in the past 3 months?
integer
C0021081 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
BL_Immunosuppressiva
Code List
Immunosuppressive medication in the past 3 months?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Known colonisation with multi-resistant pathogens
C3826980 (UMLS CUI-1)
C2747813 (UMLS CUI-2)
Item
MRSA (Methicillin-resistant St. aureus)
integer
C1265292 (UMLS CUI [1,1])
C2747813 (UMLS CUI [1,2])
MRSA (Methicillin-resistant St. aureus)
Code List
MRSA (Methicillin-resistant St. aureus)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not done (3)
CL Item
Unknown (4)
Item
VRE (Vancomycin-resistant Enterococci)
integer
C1265175 (UMLS CUI [1,1])
C2747813 (UMLS CUI [1,2])
MRSA (Methicillin-resistant St. aureus)
Code List
VRE (Vancomycin-resistant Enterococci)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not done (3)
CL Item
Unknown (4)
Item
3rd generation cephalosporin-resistant enterobacteriacae (3GCREB)
integer
C0014346 (UMLS CUI [1,1])
C0304320 (UMLS CUI [1,2])
C0013203 (UMLS CUI [1,3])
C2747813 (UMLS CUI [1,4])
MRSA (Methicillin-resistant St. aureus)
Code List
3rd generation cephalosporin-resistant enterobacteriacae (3GCREB)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not done (3)
CL Item
Unknown (4)
Item
Other
integer
C0205394 (UMLS CUI [1,1])
C2747813 (UMLS CUI [1,2])
MRSA (Methicillin-resistant St. aureus)
Code List
Other
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not done (3)
CL Item
Unknown (4)
Other, specify
Item
Other, please specify
text
C3845569 (UMLS CUI [1,1])
C2747813 (UMLS CUI [1,2])
Item Group
Complications at baseline: Thrombotic and thromboembolic manifestations
C0009566 (UMLS CUI-1)
C1442488 (UMLS CUI-2)
C0040053 (UMLS CUI-3)
C0040038 (UMLS CUI-4)
Item
Abdominal thrombosis/thromboembolism (venous or arterial)
integer
C1442488 (UMLS CUI [1])
C0151942 (UMLS CUI [2,1])
C0000726 (UMLS CUI [2,2])
C0042487 (UMLS CUI [3,1])
C0000726 (UMLS CUI [3,2])
C3544094 (UMLS CUI [4,1])
C0000726 (UMLS CUI [4,2])
C1861172 (UMLS CUI [5,1])
C0000726 (UMLS CUI [5,2])
Abdominal thrombosis/thromboembolism (venous or arterial)
Code List
Abdominal thrombosis/thromboembolism (venous or arterial)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Myocardial infarction
integer
C1442488 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
Abdominal thrombosis/thromboembolism (venous or arterial)
Code List
Myocardial infarction
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Venous thrombosis, e.g. deep leg vein thrombosis
integer
C1442488 (UMLS CUI [1])
C0042487 (UMLS CUI [2])
C0149871 (UMLS CUI [3])
Abdominal thrombosis/thromboembolism (venous or arterial)
Code List
Venous thrombosis, e.g. deep leg vein thrombosis
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Pulmonary embolism
integer
C1442488 (UMLS CUI [1])
C0034065 (UMLS CUI [2])
Abdominal thrombosis/thromboembolism (venous or arterial)
Code List
Pulmonary embolism
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Microangiopathies and microthromboses
integer
C1442488 (UMLS CUI [1])
C2717961 (UMLS CUI [2])
C3686869 (UMLS CUI [3])
Abdominal thrombosis/thromboembolism (venous or arterial)
Code List
Microangiopathies and microthromboses
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Complications at baseline: Neurological
C0235029 (UMLS CUI-1)
C1442488 (UMLS CUI-2)
Item
Intracerebral bleeding
integer
C1442488 (UMLS CUI [1])
C2937358 (UMLS CUI [2])
Intracerebral bleeding
Code List
Intracerebral bleeding
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Ischemic Stroke
integer
C1442488 (UMLS CUI [1])
C0948008 (UMLS CUI [2])
Intracerebral bleeding
Code List
Ischemic Stroke
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Meningitis / Encephalitis
integer
C1442488 (UMLS CUI [1])
C0497299 (UMLS CUI [2])
Intracerebral bleeding
Code List
Meningitis / Encephalitis
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical Illness Myopathy (CIM)
integer
C1442488 (UMLS CUI [1])
C0010340 (UMLS CUI [2,1])
C0026848 (UMLS CUI [2,2])
Intracerebral bleeding
Code List
Critical Illness Myopathy (CIM)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical Illness Polyneuropathy (CIP)
integer
C1442488 (UMLS CUI [1])
C0010340 (UMLS CUI [2,1])
C0152025 (UMLS CUI [2,2])
Intracerebral bleeding
Code List
Critical Illness Polyneuropathy (CIP)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Seizure
integer
C1442488 (UMLS CUI [1])
C0036572 (UMLS CUI [2])
Intracerebral bleeding
Code List
Seizure
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Complications at baseline: Other severe organ damage
C0009566 (UMLS CUI-1)
C1442488 (UMLS CUI-2)
C0178784 (UMLS CUI-3)
C1883709 (UMLS CUI-4)
C0205082 (UMLS CUI-5)
C0205394 (UMLS CUI-6)
Item
Acute renal failure
integer
C1442488 (UMLS CUI [1])
C0022660 (UMLS CUI [2])
Acute renal failure
Code List
Acute renal failure
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Severe liver failure
integer
C1442488 (UMLS CUI [1])
C0085605 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Acute renal failure
Code List
Severe liver failure
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Congestive heart failure
integer
C1442488 (UMLS CUI [1])
C0018802 (UMLS CUI [2])
Acute renal failure
Code List
Congestive heart failure
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Complications at baseline: Other
C0009566 (UMLS CUI-1)
C1442488 (UMLS CUI-2)
C0205394 (UMLS CUI-3)
Item
Life threatening cardiac arrhythmia
integer
C1442488 (UMLS CUI [1])
C0003811 (UMLS CUI [2,1])
C2826244 (UMLS CUI [2,2])
Life threatening cardiac arrhythmia
Code List
Life threatening cardiac arrhythmia
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Myocarditis
integer
C1442488 (UMLS CUI [1])
C0027059 (UMLS CUI [2])
Life threatening cardiac arrhythmia
Code List
Myocarditis
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Vasculitis
integer
C1442488 (UMLS CUI [1])
C0042384 (UMLS CUI [2])
Life threatening cardiac arrhythmia
Code List
Vasculitis
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Gastrointestinal bleeding
integer
C1442488 (UMLS CUI [1])
C0017181 (UMLS CUI [2])
Life threatening cardiac arrhythmia
Code List
Gastrointestinal bleeding
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Endotracheal bleeding
integer
C1442488 (UMLS CUI [1])
C0019080 (UMLS CUI [2,1])
C0599554 (UMLS CUI [2,2])
Life threatening cardiac arrhythmia
Code List
Endotracheal bleeding
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other, please specify
integer
C1442488 (UMLS CUI [1])
C0009566 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
Life threatening cardiac arrhythmia
Code List
Other, please specify
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other, please specify
text
C1442488 (UMLS CUI [1])
C0009566 (UMLS CUI [2,1])
C3845569 (UMLS CUI [2,2])
Life threatening cardiac arrhythmia
Code List
Other, please specify
Item Group
Symptoms: Please click all symptoms which occurred in the respective clinical phase
C1457887 (UMLS CUI-1)
Item
Baseline (BL): None / asymptomatic
integer
C1442488 (UMLS CUI [1])
C1298908 (UMLS CUI [2,1])
C0037088 (UMLS CUI [2,2])
C0231221 (UMLS CUI [3])
Y/N/U
Code List
Baseline (BL): None / asymptomatic
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Runny nose
integer
C1442488 (UMLS CUI [1])
C1260880 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Runny nose
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Sore throat
integer
C1442488 (UMLS CUI [1])
C0242429 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Sore throat
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Dry cough
integer
C1442488 (UMLS CUI [1])
C0850149 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Dry cough
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Productive cough
integer
C1442488 (UMLS CUI [1])
C0239134 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Productive cough
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Wheezing
integer
C1442488 (UMLS CUI [1])
C0043144 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Wheezing
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Dyspnoe
integer
C1442488 (UMLS CUI [1])
C0013404 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Dyspnoe
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Palpitations
integer
C1442488 (UMLS CUI [1])
C0030252 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Palpitations
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Diarrhea
integer
C1442488 (UMLS CUI [1])
C0011991 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Diarrhea
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Nausea / Emesis
integer
C1442488 (UMLS CUI [1])
C0027497 (UMLS CUI [2])
C0042963 (UMLS CUI [3])
Y/N/U
Code List
Baseline (BL): Nausea / Emesis
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Muscle aches
integer
C1442488 (UMLS CUI [1])
C0231528 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Muscle aches
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Muscle weakness
integer
C1442488 (UMLS CUI [1])
C0151786 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Muscle weakness
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Fever
integer
C1442488 (UMLS CUI [1])
C0015967 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Fever
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Delirium
integer
C1442488 (UMLS CUI [1])
C0011206 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Delirium
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Excessive tiredness
integer
C1442488 (UMLS CUI [1])
C0442802 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Excessive tiredness
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Headache
integer
C1442488 (UMLS CUI [1])
C0018681 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Headache
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Meningism
integer
C1442488 (UMLS CUI [1])
C0025287 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Meningism
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Smell disorder
integer
C1442488 (UMLS CUI [1])
C0553757 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Smell disorder
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Taste disorder
integer
C1442488 (UMLS CUI [1])
C0549590 (UMLS CUI [2])
Y/N/U
Code List
Baseline (BL): Taste disorder
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Other neurological symptoms
integer
C1442488 (UMLS CUI [1])
C0235031 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
Y/N/U
Code List
Baseline (BL): Other neurological symptoms
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Baseline (BL): Red eye
integer
C1442488 (UMLS CUI [1])
C0015392 (UMLS CUI [2,1])
C0332575 (UMLS CUI [2,2])
Y/N/U
Code List
Baseline (BL): Red eye
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): None / asymptomatic
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1298908 (UMLS CUI [2,1])
C0037088 (UMLS CUI [2,2])
C0231221 (UMLS CUI [3])
Y/N/U
Code List
Uncomplicated (UC): None / asymptomatic
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Runny nose
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1260880 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Runny nose
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Sore throat
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0242429 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Sore throat
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Dry cough
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0850149 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Dry cough
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Productive cough
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0239134 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Productive cough
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Wheezing
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0043144 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Wheezing
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Dyspnoe
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0013404 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Dyspnoe
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Palpitations
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0030252 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Palpitations
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Diarrhea
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0011991 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Diarrhea
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Nausea / Emesis
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0027497 (UMLS CUI [2])
C0042963 (UMLS CUI [3])
Y/N/U
Code List
Uncomplicated (UC): Nausea / Emesis
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Muscle aches
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0231528 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Muscle aches
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Muscle weakness
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0151786 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Muscle weakness
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Fever
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0015967 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Fever
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Delirium
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0011206 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Delirium
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Excessive tiredness
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0442802 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Excessive tiredness
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Headache
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0018681 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Headache
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Meningism
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0025287 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Meningism
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Smell disorder
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0553757 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Smell disorder
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Taste disorder
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0549590 (UMLS CUI [2])
Y/N/U
Code List
Uncomplicated (UC): Taste disorder
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Other neurological symptoms
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0235031 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
Y/N/U
Code List
Uncomplicated (UC): Other neurological symptoms
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated (UC): Red eye
integer
C0443334 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0015392 (UMLS CUI [2,1])
C0332575 (UMLS CUI [2,2])
Y/N/U
Code List
Uncomplicated (UC): Red eye
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): None / asymptomatic
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1298908 (UMLS CUI [2,1])
C0037088 (UMLS CUI [2,2])
C0231221 (UMLS CUI [3])
Y/N/U
Code List
Complicated (CO): None / asymptomatic
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Runny nose
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1260880 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Runny nose
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Sore throat
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0242429 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Sore throat
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Dry cough
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0850149 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Dry cough
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Productive cough
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0239134 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Productive cough
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Wheezing
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0043144 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Wheezing
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Dyspnoe
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0013404 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Dyspnoe
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Palpitations
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0030252 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Palpitations
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Diarrhea
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0011991 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Diarrhea
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Nausea / Emesis
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0027497 (UMLS CUI [2])
C0042963 (UMLS CUI [3])
Y/N/U
Code List
Complicated (CO): Nausea / Emesis
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Muscle aches
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0231528 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Muscle aches
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Muscle weakness
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0151786 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Muscle weakness
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Fever
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0015967 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Fever
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Delirium
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0011206 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Delirium
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Excessive tiredness
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0442802 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Excessive tiredness
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Headache
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0018681 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Headache
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Meningism
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0025287 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Meningism
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Smell disorder
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0553757 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Smell disorder
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Taste disorder
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0549590 (UMLS CUI [2])
Y/N/U
Code List
Complicated (CO): Taste disorder
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Other neurological symptoms
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0235031 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
Y/N/U
Code List
Complicated (CO): Other neurological symptoms
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated (CO): Red eye
integer
C0231242 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0015392 (UMLS CUI [2,1])
C0332575 (UMLS CUI [2,2])
Y/N/U
Code List
Complicated (CO): Red eye
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): None / asymptomatic
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1298908 (UMLS CUI [2,1])
C0037088 (UMLS CUI [2,2])
C0231221 (UMLS CUI [3])
Y/N/U
Code List
Critical (CR): None / asymptomatic
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Runny nose
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1260880 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Runny nose
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Sore throat
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0242429 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Sore throat
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Dry cough
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0850149 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Dry cough
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Productive cough
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0239134 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Productive cough
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Wheezing
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0043144 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Wheezing
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Dyspnoe
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0013404 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Dyspnoe
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Palpitations
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0030252 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Palpitations
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Diarrhea
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0011991 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Diarrhea
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Nausea / Emesis
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0027497 (UMLS CUI [2])
C0042963 (UMLS CUI [3])
Y/N/U
Code List
Critical (CR): Nausea / Emesis
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Muscle aches
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0231528 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Muscle aches
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Muscle weakness
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0151786 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Muscle weakness
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Fever
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0015967 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Fever
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Delirium
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0011206 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Delirium
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Excessive tiredness
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0442802 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Excessive tiredness
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Headache
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0018681 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Headache
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Meningism
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0025287 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Meningism
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Smell disorder
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0553757 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Smell disorder
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Taste disorder
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0549590 (UMLS CUI [2])
Y/N/U
Code List
Critical (CR): Taste disorder
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Other neurological symptoms
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0235031 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
Y/N/U
Code List
Critical (CR): Other neurological symptoms
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical (CR): Red eye
integer
C1511545 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0015392 (UMLS CUI [2,1])
C0332575 (UMLS CUI [2,2])
Y/N/U
Code List
Critical (CR): Red eye
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Vital signs and respiratory parameters
C0518766 (UMLS CUI-1)
C0521346 (UMLS CUI-2)
C0549193 (UMLS CUI-3)
Item
Systolic BP
integer
C1442488 (UMLS CUI [1,1])
C0871470 (UMLS CUI [1,2])
Baseline (Systolic BP) 18692
Code List
Systolic BP
CL Item
< 80 mmHg (1)
CL Item
80 - 99 mmHg (2)
CL Item
100 - 119 mmHg (3)
CL Item
120 - 139 mmHg (4)
CL Item
140 - 159 mmHg (5)
CL Item
160 - 179 mmHg (6)
CL Item
> 180 mmHg (7)
CL Item
Not done (8)
CL Item
Unknown (9)
Item
Diastolic BP
integer
C1442488 (UMLS CUI [1,1])
C0428883 (UMLS CUI [1,2])
Baseline (Diastolic BP) 18693
Code List
Diastolic BP
CL Item
< 40 mmHg (1)
CL Item
40 - 59 mmHg (2)
CL Item
60 - 89 mmHg (3)
CL Item
90 - 109 mmHg (4)
CL Item
110 - 119 mmHg (5)
CL Item
> 119 mmHg (6)
CL Item
Not done (7)
CL Item
Unknown (8)
Item
Pulse
integer
C1442488 (UMLS CUI [1,1])
C0232117 (UMLS CUI [1,2])
Baseline (Pulse) 18694
Code List
Pulse
CL Item
< 45 bpm (1)
CL Item
45 - 59 bpm (2)
CL Item
60 - 89 bpm (3)
CL Item
90 - 119 bpm (4)
CL Item
> 119 bpm (5)
CL Item
Not done (6)
CL Item
Unknown (7)
Item
SO2
integer
C1442488 (UMLS CUI [1,1])
C0523807 (UMLS CUI [1,2])
Baseline (SO2) 18696
Code List
SO2
CL Item
< 60% (1)
CL Item
60 - 69% (2)
CL Item
70 - 79% (3)
CL Item
80 - 89% (4)
CL Item
90 - 95% (5)
CL Item
96 - 100% (6)
CL Item
Not done (7)
CL Item
Unknown (8)
Item
paO2
integer
C1442488 (UMLS CUI [1,1])
C0391840 (UMLS CUI [1,2])
Baseline (paO2) 18698
Code List
paO2
CL Item
< 50 mmHg (< 6.66 kPa) (1)
CL Item
50 - 59 mmHg (6.67 - 7.86 kPa) (2)
CL Item
60 - 69 mmHg (7.87 - 9.2 kPa) (3)
CL Item
70 - 79 mmHg (9.21 - 10.53 kPa) (4)
CL Item
> 79 mmHg (> 10.53 kPa) (5)
CL Item
Not done (6)
CL Item
Unknown (7)
Item
paCO2
integer
C1442488 (UMLS CUI [1,1])
C1822070 (UMLS CUI [1,2])
Baseline (paCO2) 18697
Code List
paCO2
CL Item
< 30 mmHg (< 4 kPa) (1)
CL Item
30 - 38 mmHg (4 - 5.06 kPa) (2)
CL Item
39 - 45 mmHg (5.07 - 5.99 kPa) (3)
CL Item
46 - 55 mmHg (6 - 7.33 kPa) (4)
CL Item
> 55 mmHg (> 7.33 kPa) (5)
CL Item
Not done (6)
CL Item
Unknown (7)
Item
Temperature
integer
C1442488 (UMLS CUI [1,1])
C0005903 (UMLS CUI [1,2])
Baseline (Temperature) 18695
Code List
Temperature
CL Item
< 35.1°C (< 95.2°F) (1)
CL Item
35.1 - 37.2°C (95.2 - 99.0°F) (2)
CL Item
37.3 - 37.9°C (99.1 - 100.2°F) (3)
CL Item
38 - 38.9°C (100.4 - 102.0°F) (4)
CL Item
39 - 39.9°C (102.1 - 103.8°F) (5)
CL Item
> 39.9°C (>103.8 °F) (6)
CL Item
Not done (7)
CL Item
Unknown (8)
Item
Respiratory rate / minute
integer
C1442488 (UMLS CUI [1,1])
C0231832 (UMLS CUI [1,2])
Baseline (Respiratory rate / minute) 18699
Code List
Respiratory rate / minute
CL Item
< 16 (1)
CL Item
16-21 (2)
CL Item
22-29 (3)
CL Item
> 29 (4)
CL Item
Not done (5)
CL Item
Unknown (6)
Item
Glasgow Coma Scale
integer
C1442488 (UMLS CUI [1,1])
C1271007 (UMLS CUI [1,2])
Baseline (GCS)
Code List
Glasgow Coma Scale
CL Item
15 (1)
CL Item
13 - 14 (2)
CL Item
9 - 12 (3)
CL Item
3 - 8 (4)
CL Item
Not done (5)
CL Item
Unknown (6)
Item Group
Heart function: Ejection fraction (EF) at SARS-CoV-2 detection
C0232164 (UMLS CUI-1)
C0013516 (UMLS CUI-2)
C0232174 (UMLS CUI-3)
C1511790 (UMLS CUI-4)
C5203676 (UMLS CUI-5)
Item
Heart function: Ejection fraction (EF) at SARS-CoV-2 detection
integer
C1442488 (UMLS CUI [1])
C0232164 (UMLS CUI [2,1])
C0013516 (UMLS CUI [2,2])
C0232174 (UMLS CUI [3,1])
C1511790 (UMLS CUI [3,2])
C5203676 (UMLS CUI [3,3])
BL_EjectionFraction
Code List
Heart function: Ejection fraction (EF) at SARS-CoV-2 detection
CL Item
<20% (1)
CL Item
20 - 30% (2)
CL Item
31 - 40% (3)
CL Item
41 - 55% (4)
CL Item
>55% (5)
CL Item
Not done (6)
CL Item
Unknown (7)
Item Group
Chest CT results at SARS-CoV-2 detection
C1442488 (UMLS CUI-1)
C0202823 (UMLS CUI-2)
C1274040 (UMLS CUI-3)
C5203676 (UMLS CUI-4)
C1511790 (UMLS CUI-5)
Item
Air trapping
integer
C1442488 (UMLS CUI [1])
C0231819 (UMLS CUI [2])
Air trapping
Code List
Air trapping
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Areas of consolidation
integer
C1442488 (UMLS CUI [1])
C0521530 (UMLS CUI [2,1])
C0205146 (UMLS CUI [2,2])
Areas of consolidation
Code List
Areas of consolidation
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Bronchioloitis
integer
C1442488 (UMLS CUI [1])
C0006271 (UMLS CUI [2])
Bronchiolitis
Code List
Bronchioloitis
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Crazy paving pattern
integer
C1442488 (UMLS CUI [1])
C4476749 (UMLS CUI [2])
Bronchiolitis
Code List
Crazy paving pattern
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Ground glass opacities
integer
C1442488 (UMLS CUI [1])
C3827002 (UMLS CUI [2])
Bronchiolitis
Code List
Ground glass opacities
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Interlobular septal thickening
integer
C1442488 (UMLS CUI [1])
C4280727 (UMLS CUI [2])
Bronchiolitis
Code List
Interlobular septal thickening
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Nodulary lesions
integer
C1442488 (UMLS CUI [1])
C1518345 (UMLS CUI [2])
Bronchiolitis
Code List
Nodulary lesions
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Pleural effusion
integer
C1442488 (UMLS CUI [1])
C0032227 (UMLS CUI [2])
Bronchiolitis
Code List
Pleural effusion
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Chest x-ray results
integer
C1442488 (UMLS CUI [1])
C0039985 (UMLS CUI [2,1])
C1274040 (UMLS CUI [2,2])
Bronchiolitis
Code List
Chest x-ray results
CL Item
not quoted (0)
CL Item
quoted (1)
Baseline: Chest x-ray results, specify
Item
If Chest x-ray results, please specify (short description: no copy & paste)
text
C1442488 (UMLS CUI [1])
C0039985 (UMLS CUI [2,1])
C1274040 (UMLS CUI [2,2])
C1521902 (UMLS CUI [2,3])
Item
Other relevant CT results
integer
C1442488 (UMLS CUI [1])
C0040405 (UMLS CUI [2,1])
C1274040 (UMLS CUI [2,2])
C2826293 (UMLS CUI [2,3])
C0205394 (UMLS CUI [2,4])
Other relevant CT results
Code List
Other relevant CT results
CL Item
not quoted (0)
CL Item
quoted (1)
Baseline: Other relevant CT results, specify
Item
If Other relevant CT results, please specify (short description: no copy & paste)
text
C1442488 (UMLS CUI [1])
C0040405 (UMLS CUI [2,1])
C1274040 (UMLS CUI [2,2])
C2826293 (UMLS CUI [2,3])
C0205394 (UMLS CUI [2,4])
C1521902 (UMLS CUI [2,5])
Item
Normal CT
integer
C1442488 (UMLS CUI [1])
C0040405 (UMLS CUI [2,1])
C0205307 (UMLS CUI [2,2])
Normal CT
Code List
Normal CT
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Not done
integer
C1442488 (UMLS CUI [1])
C0040405 (UMLS CUI [2,1])
C1272696 (UMLS CUI [2,2])
Normal CT
Code List
Not done
CL Item
not quoted (0)
CL Item
quoted (1)
Item Group
Has a cardiovascular magnetic resonance imaging (CMR) been performed in any clinical phase?
C3873775 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0205210 (UMLS CUI-3)
C1552551 (UMLS CUI-4)
Item
Has a cardiovascular magnetic resonance imaging (CMR) been performed in any clinical phase?
integer
C3873775 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,3])
C1552551 (UMLS CUI [1,4])
Has a cardiovascular magnetic resonance imaging (CMR) been performed in any clinical phase?
Code List
Has a cardiovascular magnetic resonance imaging (CMR) been performed in any clinical phase?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Has neurological diagnostic taken place in the various phases?
C0852602 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
Item
Baseline
integer
C0852602 (UMLS CUI [1,1])
C1442488 (UMLS CUI [1,2])
Baseline
Code List
Baseline
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Uncomplicated phase
integer
C0852602 (UMLS CUI [1,1])
C0443334 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
Baseline
Code List
Uncomplicated phase
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Complicated phase
integer
C0852602 (UMLS CUI [1,1])
C0231242 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
Baseline
Code List
Complicated phase
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Critical phase
integer
C0852602 (UMLS CUI [1,1])
C1511545 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
Baseline
Code List
Critical phase
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Was complementary and/or integrative medicine (CIM) used in any phase?
C4053461 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C1552551 (UMLS CUI-3)
Item
Was complementary and/or integrative medicine (CIM) used in any phase?
integer
C4053461 (UMLS CUI [1])
Was complementary and/or integrative medicine (CIM) used in any phase?
Code List
Was complementary and/or integrative medicine (CIM) used in any phase?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Has the patient signed a general agreement to share data for scientific purposes?
C0680240 (UMLS CUI-1)
C0035168 (UMLS CUI-2)
C2713450 (UMLS CUI-3)
Item
Yes, to share data
integer
C0680240 (UMLS CUI [1,1])
C0035168 (UMLS CUI [1,2])
Yes, to share data
Code List
Yes, to share data
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Yes, to share biomaterial samples
integer
C0680240 (UMLS CUI [1,1])
C2347026 (UMLS CUI [1,2])
C0457083 (UMLS CUI [1,3])
Yes, to share biomaterial samples
Code List
Yes, to share biomaterial samples
CL Item
not quoted (0)
CL Item
quoted (1)
Item
No
integer
C1298908 (UMLS CUI [1])
No
Code List
No
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Unknown
integer
C0439673 (UMLS CUI [1])
Unknown
Code List
Unknown
CL Item
not quoted (0)
CL Item
quoted (1)
Item Group
Is biomaterial of this patient available for research proposes?
C2347026 (UMLS CUI-1)
C0470187 (UMLS CUI-2)
C0035168 (UMLS CUI-3)
Item
Serum
integer
C0229671 (UMLS CUI [1])
Serum
Code List
Serum
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Blood
integer
C0005767 (UMLS CUI [1])
Blood
Code List
Blood
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Cells
integer
C0007634 (UMLS CUI [1])
Cells
Code List
Cells
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Stool
integer
C0015733 (UMLS CUI [1])
Stool
Code List
Stool
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Cerebrospinal fluid
integer
C0007806 (UMLS CUI [1])
Stool
Code List
Cerebrospinal fluid
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Other
integer
C0205394 (UMLS CUI [1])
Other
Code List
Other
CL Item
not quoted (0)
CL Item
quoted (1)
Other, specify
Item
If Other, please specify:
text
C0205394 (UMLS CUI [1,1])
C1521902 (UMLS CUI [1,2])
Item
None
integer
C0549184 (UMLS CUI [1])
None
Code List
None
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Unknown
integer
C0439673 (UMLS CUI [1])
Unknown
Code List
Unknown
CL Item
not quoted (0)
CL Item
quoted (1)
Item Group
Did the patient participate in an interventional clinical trial?
C2348568 (UMLS CUI-1)
C3274035 (UMLS CUI-2)
Item
Did the patient participate in an interventional clinical trial?
integer
C2348568 (UMLS CUI [1,1])
C3274035 (UMLS CUI [1,2])
Did the patient participate in an interventional clinical trial?
Code List
Did the patient participate in an interventional clinical trial?
CL Item
Yes, please name the trial (1)
CL Item
No (2)
CL Item
Unknown (3)
If Yes, please name the trial
Item
If Yes, please name the trial
text
C2348568 (UMLS CUI [1,1])
C3274035 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
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