ID

41612

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, 16:48 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 Recovery Phase data. Please note that only cases with known outcome are collected at LEOSS! At Day, your patient has entered the Recovery Phase of disease. All questions below ask you to aggregate over the whole known course of recovery. Criteria of the Recovery Phase: Improvement by at least one phase, i.e. Critical to Complicated or Complicated to Uncomplicated Defervescence Uncomplicated asymptomatic patients enter recovery phase after 14 days of observation without disease progression No further progression or re-hospitalization If a text field can't be filled out, note 'ND' (for not determined).

Link

https://leoss.net

Keywords

  1. 11/27/20 11/27/20 -
  2. 6/28/21 6/28/21 -
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

Recovery Phase

  1. StudyEvent: ODM
    1. Recovery Phase
Not recovered symptoms / sequelae: Respiratory symptoms
Description

Not recovered symptoms / sequelae: Respiratory symptoms

Alias
UMLS CUI-1
C0243088
UMLS CUI-2
C1709277
UMLS CUI-3
C1457887
UMLS CUI-4
C0037090
Cough
Description

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

Data type

integer

Alias
UMLS CUI [1]
C0010200
Shortness of breath
Description

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

Data type

integer

Alias
UMLS CUI [1]
C0013404
Need for oxygen supplementation
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C0686904
UMLS CUI [1,2]
C0919655
Not recovered symptoms / sequelae: Cardiovascular symptoms
Description

Not recovered symptoms / sequelae: Cardiovascular symptoms

Alias
UMLS CUI-1
C0243088
UMLS CUI-2
C1709277
UMLS CUI-3
C1457887
UMLS CUI-4
C0476270
Congestive heart failure
Description

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

Data type

integer

Alias
UMLS CUI [1]
C0018802
Arrhythmia
Description

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

Data type

integer

Alias
UMLS CUI [1]
C0003811
Not recovered symptoms / sequelae: Neurological symptoms
Description

Not recovered symptoms / sequelae: Neurological symptoms

Alias
UMLS CUI-1
C0243088
UMLS CUI-2
C1709277
UMLS CUI-3
C1457887
UMLS CUI-4
C0235031
Headache
Description

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

Data type

integer

Alias
UMLS CUI [1]
C0018681
Neurologic deficits
Description

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

Data type

integer

Alias
UMLS CUI [1]
C0521654
Severe cognitive impairment
Description

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

Data type

integer

Alias
UMLS CUI [1]
C3554639
Not recovered symptoms / sequelae: Further findings
Description

Not recovered symptoms / sequelae: Further findings

Alias
UMLS CUI-1
C0243088
UMLS CUI-2
C1709277
UMLS CUI-3
C1457887
UMLS CUI-4
C0243095
UMLS CUI-5
C0205394
Muscle aches
Description

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

Data type

integer

Alias
UMLS CUI [1]
C0231528
Mild fatigue
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C0015672
UMLS CUI [1,2]
C2945599
Severe fatigue
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C0015672
UMLS CUI [1,2]
C0205082
Kidney failure
Description

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

Data type

integer

Alias
UMLS CUI [1]
C0035078
Other
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C0243088
UMLS CUI [2,1]
C0205394
UMLS CUI [2,2]
C1709277
UMLS CUI [2,3]
C1457887
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]
C0205394
UMLS CUI [1,2]
C0243088
UMLS CUI [1,3]
C1521902
UMLS CUI [2,1]
C0205394
UMLS CUI [2,2]
C1709277
UMLS CUI [2,3]
C1457887
UMLS CUI [2,4]
C1521902
None
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C0549184
UMLS CUI [1,2]
C0243088
UMLS CUI [2,1]
C0549184
UMLS CUI [2,2]
C1709277
UMLS CUI [2,3]
C1457887
Unknown
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C0439673
UMLS CUI [1,2]
C0243088
UMLS CUI [2,1]
C0439673
UMLS CUI [2,2]
C1709277
UMLS CUI [2,3]
C1457887
Chest CT results:
Description

Chest CT results:

Alias
UMLS CUI-1
C0202823
UMLS CUI-2
C1274040
Air trapping
Description

Note: This question is critical for the further course of the questionnaire. Most recent results from all CTs during this phase of disease.

Data type

integer

Alias
UMLS CUI [1,1]
C0231819
UMLS CUI [1,2]
C0202823
Areas of consolidation
Description

Note: This question is critical for the further course of the questionnaire. Most recent results from all CTs during this phase of disease.

Data type

integer

Alias
UMLS CUI [1,1]
C0521530
UMLS CUI [1,2]
C0202823
Bronchiolitis
Description

Note: This question is critical for the further course of the questionnaire. Most recent results from all CTs during this phase of disease.

Data type

integer

Alias
UMLS CUI [1,1]
C0006271
UMLS CUI [1,2]
C0202823
Crazy paving pattern
Description

Note: This question is critical for the further course of the questionnaire. Most recent results from all CTs during this phase of disease.

Data type

integer

Alias
UMLS CUI [1]
C4476749
Ground glass opacities
Description

Note: This question is critical for the further course of the questionnaire. Most recent results from all CTs during this phase of disease.

Data type

integer

Alias
UMLS CUI [1,1]
C3827002
UMLS CUI [1,2]
C0202823
Interlobular septal thickening
Description

Note: This question is critical for the further course of the questionnaire. Most recent results from all CTs during this phase of disease.

Data type

integer

Alias
UMLS CUI [1]
C4280727
Nodulary lesions
Description

Note: This question is critical for the further course of the questionnaire. Most recent results from all CTs during this phase of disease.

Data type

integer

Alias
UMLS CUI [1,1]
C1518345
UMLS CUI [1,2]
C0202823
Pleural effusion
Description

Note: This question is critical for the further course of the questionnaire. Most recent results from all CTs during this phase of disease.

Data type

integer

Alias
UMLS CUI [1,1]
C0032227
UMLS CUI [1,2]
C0202823
Other relevant CT results
Description

Note: This question is critical for the further course of the questionnaire. Most recent results from all CTs during this phase of disease.

Data type

integer

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C1274040
UMLS CUI [1,3]
C2347946
UMLS CUI [1,4]
C0202823
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. Most recent results from all CTs during this phase of disease.

Data type

text

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C1274040
UMLS CUI [1,3]
C2347946
UMLS CUI [1,4]
C1521902
UMLS CUI [1,5]
C0202823
Normal CT
Description

Note: This question is critical for the further course of the questionnaire. Most recent results from all CTs during this phase of disease.

Data type

integer

Alias
UMLS CUI [1,1]
C0205307
UMLS CUI [1,2]
C0202823
Not done
Description

Note: This question is critical for the further course of the questionnaire. Most recent results from all CTs during this phase of disease.

Data type

integer

Alias
UMLS CUI [1,1]
C1272696
UMLS CUI [1,2]
C0202823
Vital signs and respiratory parameters
Description

Vital signs and respiratory parameters

Alias
UMLS CUI-1
C0518766
UMLS CUI-2
C0035237
UMLS CUI-3
C0549193
Worst during recovery phase: Systolic BP
Description

Note: This question is critical for the further course of the questionnaire. Worst means farthest from normal range.

Data type

integer

Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Worst during recovery phase: Diastolic BP
Description

Note: This question is critical for the further course of the questionnaire. Worst means farthest from normal range.

Data type

integer

Alias
UMLS CUI [1,1]
C0428883
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Worst during recovery phase: Pulse
Description

Note: This question is critical for the further course of the questionnaire. Worst means farthest from normal range.

Data type

integer

Alias
UMLS CUI [1,1]
C0232117
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Worst during recovery phase: SO2
Description

Note: This question is critical for the further course of the questionnaire. Worst means farthest from normal range.

Data type

integer

Alias
UMLS CUI [1,1]
C0523807
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Worst during recovery phase: paO2
Description

Note: This question is critical for the further course of the questionnaire. Worst means farthest from normal range.

Data type

integer

Alias
UMLS CUI [1,1]
C0202155
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Worst during recovery phase: paCO2
Description

Note: This question is critical for the further course of the questionnaire. Worst means farthest from normal range.

Data type

integer

Alias
UMLS CUI [1,1]
C1822070
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Worst during recovery phase: Temperature
Description

Note: This question is critical for the further course of the questionnaire. Worst means farthest from normal range.

Data type

integer

Alias
UMLS CUI [1,1]
C0039476
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Worst during recovery phase: Respiratory rate / minute
Description

Note: This question is critical for the further course of the questionnaire. Worst means farthest from normal range.

Data type

integer

Alias
UMLS CUI [1,1]
C0231832
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Worst during recovery phase: Glasgow Coma scale
Description

Note: This question is critical for the further course of the questionnaire. Worst means farthest from normal range.

Data type

integer

Alias
UMLS CUI [1,1]
C0017594
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Super-Infections
Description

Super-Infections

Alias
UMLS CUI-1
C0038826
Proven bacterial infection:
Description

Note: This question is critical for the further course of the questionnaire. Pleaase fill in the site and respecitve patogen if available.

Data type

integer

Alias
UMLS CUI [1,1]
C0004623
UMLS CUI [1,2]
C0456369
Proven bacterial infection, please specify:
Description

Note: This question is critical for the further course of the questionnaire. Pleaase fill in the site and respecitve patogen if available.

Data type

text

Alias
UMLS CUI [1,1]
C0004623
UMLS CUI [1,2]
C0456369
UMLS CUI [1,3]
C1521902
Probable or suspected bacterial infection:
Description

Note: This question is critical for the further course of the questionnaire. Pleaase fill in the site and respecitve patogen if available.

Data type

integer

Alias
UMLS CUI [1,1]
C0004623
UMLS CUI [1,2]
C0332147
Probable or suspected bacterial infection, please specify:
Description

Note: This question is critical for the further course of the questionnaire. Pleaase fill in the site and respecitve patogen if available.

Data type

text

Alias
UMLS CUI [1,1]
C0004623
UMLS CUI [1,2]
C0332147
UMLS CUI [1,3]
C1521902
Proven fungal infection:
Description

Note: This question is critical for the further course of the questionnaire. Pleaase fill in the site and respecitve patogen if available.

Data type

integer

Alias
UMLS CUI [1,1]
C0026946
UMLS CUI [1,2]
C0456369
Proven fungal infection, please specify:
Description

Note: This question is critical for the further course of the questionnaire. Pleaase fill in the site and respecitve patogen if available.

Data type

text

Alias
UMLS CUI [1,1]
C0026946
UMLS CUI [1,2]
C0456369
UMLS CUI [1,3]
C1521902
Probable or suspected fungal infection:
Description

Note: This question is critical for the further course of the questionnaire. Pleaase fill in the site and respecitve patogen if available.

Data type

integer

Alias
UMLS CUI [1,1]
C0026946
UMLS CUI [1,2]
C0332147
Probable or suspected fungal infection, please specify:
Description

Note: This question is critical for the further course of the questionnaire. Pleaase fill in the site and respecitve patogen if available.

Data type

text

Alias
UMLS CUI [1,1]
C0026946
UMLS CUI [1,2]
C0332147
UMLS CUI [1,3]
C1521902
None
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C0549184
UMLS CUI [1,2]
C0038826
Unknown
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C0439673
UMLS CUI [1,2]
C0038826
Antibacterial treatment: Betalactams
Description

Antibacterial treatment: Betalactams

Alias
UMLS CUI-1
C0279516
UMLS CUI-2
C0087111
UMLS CUI-3
C0282215
Penicillins/ aminopenicilins
Description

Note: This question is critical for the further course of the questionnaire. Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Data type

integer

Alias
UMLS CUI [1]
C0030842
UMLS CUI [2]
C0304324
Cephalosporins I-III
Description

Note: This question is critical for the further course of the questionnaire. Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Data type

integer

Alias
UMLS CUI [1]
C0304317
UMLS CUI [2]
C0304319
UMLS CUI [3]
C0304320
Carbapenems (meropenem, imipenem, ertapenem, doripenem)
Description

Note: This question is critical for the further course of the questionnaire. Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Data type

integer

Alias
UMLS CUI [1]
C0006968
UMLS CUI [2]
C0066005
UMLS CUI [3]
C0020933
UMLS CUI [4]
C1120106
UMLS CUI [5]
C0389169
Piperacillin/tazobactam
Description

Note: This question is critical for the further course of the questionnaire. Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Data type

integer

Alias
UMLS CUI [1]
C0250480
New betalactams for multi-resistent bacteria (ceftazidime/avibactam, ceftolozane/tazobactam, cefiderocol)
Description

Note: This question is critical for the further course of the questionnaire. Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Data type

integer

Alias
UMLS CUI [1,1]
C0205314
UMLS CUI [1,2]
C0282215
UMLS CUI [1,3]
C3826980
UMLS CUI [2]
C3656596
UMLS CUI [3]
C3656593
UMLS CUI [4]
C4548369
Antibacterial treatment: Macrolides
Description

Antibacterial treatment: Macrolides

Alias
UMLS CUI-1
C0279516
UMLS CUI-2
C0087111
UMLS CUI-3
C0003240
Azithromycin
Description

Note: This question is critical for the further course of the questionnaire. Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Data type

integer

Alias
UMLS CUI [1]
C0052796
Other macrolide (erythromycin, clarithromycin, roxithromycin)
Description

Note: This question is critical for the further course of the questionnaire. Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Data type

integer

Alias
UMLS CUI [1,1]
C0003240
UMLS CUI [1,2]
C0205394
UMLS CUI [2]
C0014806
UMLS CUI [3]
C0055856
UMLS CUI [4]
C0035891
Antibacterial treatment: Other antibacterial treatment
Description

Antibacterial treatment: Other antibacterial treatment

Alias
UMLS CUI-1
C0279516
UMLS CUI-2
C0087111
UMLS CUI-3
C0205394
Glycopeptides (vancomycin, teicoplanin)
Description

Note: This question is critical for the further course of the questionnaire. Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Data type

integer

Alias
UMLS CUI [1]
C0017953
UMLS CUI [2]
C0042313
UMLS CUI [3]
C0145106
Other gram-positive active drugs for multiresistant bacteria (e.g. linezolid, daptomycin)
Description

Note: This question is critical for the further course of the questionnaire. Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Data type

integer

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C00032332
UMLS CUI [1,3]
C0018154
UMLS CUI [1,4]
C3826980
UMLS CUI [2]
C0663241
UMLS CUI [3]
C0057144
Fluorochinolones (ciprofloxacin, moxifloxacin, levofloxacin)
Description

Note: This question is critical for the further course of the questionnaire. Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Data type

integer

Alias
UMLS CUI [1]
C0034428
UMLS CUI [2]
C0008809
UMLS CUI [3]
C0536495
UMLS CUI [4]
C0282386
Other
Description

Note: This question is critical for the further course of the questionnaire. Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Data type

integer

Alias
UMLS CUI [1,1]
C0279516
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C0205394
If Other, please specify
Description

Note: This question is critical for the further course of the questionnaire. Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Data type

integer

Alias
UMLS CUI [1,1]
C0279516
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C1521902
Severity of multiple sclerosis after COVID-19 infection:
Description

Severity of multiple sclerosis after COVID-19 infection:

Alias
UMLS CUI-1
C0026769
UMLS CUI-2
C0439793
UMLS CUI-3
C0687676
UMLS CUI-4
C5203670
Severity of multiple sclerosis after COVID-19 infection:
Description

RC_MS_severity

Data type

integer

Alias
UMLS CUI [1,1]
C0026769
UMLS CUI [1,2]
C0439793
UMLS CUI [1,3]
C0687676
UMLS CUI [1,4]
C5203670
Pulmonary function test in recovery phase (Spirometry):
Description

Pulmonary function test in recovery phase (Spirometry):

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C0024119
UMLS CUI-4
C0037981
Pulmonary function test in recovery phase (Spirometry):
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0024119
UMLS CUI [2]
C0037981
Deterioration of the prior chronic pulmonary disease
Description

Deterioration of the prior chronic pulmonary disease

Alias
UMLS CUI-1
C0746102
UMLS CUI-2
C2347662
UMLS CUI-3
C0868945
Change in medication
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C2169461
UMLS CUI [1,2]
C0746102
UMLS CUI [1,3]
C2347662
UMLS CUI [1,4]
C0868945
Continuous use of oxygen therapy
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C0184633
UMLS CUI [1,2]
C0549178
UMLS CUI [1,3]
C0746102
UMLS CUI [1,4]
C2347662
UMLS CUI [1,5]
C0868945
Other
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C0746102
UMLS CUI [1,3]
C2347662
UMLS CUI [1,4]
C0868945
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]
C0205394
UMLS CUI [1,2]
C0746102
UMLS CUI [1,3]
C2347662
UMLS CUI [1,4]
C0868945
UMLS CUI [1,5]
C1521902
No deterioration
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C0549184
UMLS CUI [1,2]
C0746102
UMLS CUI [1,3]
C2347662
UMLS CUI [1,4]
C0868945
Unknown
Description

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

Data type

integer

Alias
UMLS CUI [1,1]
C0439673
UMLS CUI [1,2]
C0746102
UMLS CUI [1,3]
C2347662
UMLS CUI [1,4]
C0868945
Is data entry for this section finished?
Description

Is data entry for this section finished?

Alias
UMLS CUI-1
C4684556
UMLS CUI-2
C1828479
UMLS CUI-3
C0205197
Is data entry for this section finished?
Description

BL_Completed

Data type

integer

Alias
UMLS CUI [1,1]
C4684556
UMLS CUI [1,2]
C1828479
UMLS CUI [1,3]
C0205197

Similar models

Recovery Phase

  1. StudyEvent: ODM
    1. Recovery Phase
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Not recovered symptoms / sequelae: Respiratory symptoms
C0243088 (UMLS CUI-1)
C1709277 (UMLS CUI-2)
C1457887 (UMLS CUI-3)
C0037090 (UMLS CUI-4)
Item
Cough
integer
C0010200 (UMLS CUI [1])
Code List
Cough
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Shortness of breath
integer
C0013404 (UMLS CUI [1])
Code List
Shortness of breath
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Need for oxygen supplementation
integer
C0686904 (UMLS CUI [1,1])
C0919655 (UMLS CUI [1,2])
Code List
Need for oxygen supplementation
CL Item
not quoted (0)
CL Item
quoted (1)
Item Group
Not recovered symptoms / sequelae: Cardiovascular symptoms
C0243088 (UMLS CUI-1)
C1709277 (UMLS CUI-2)
C1457887 (UMLS CUI-3)
C0476270 (UMLS CUI-4)
Item
Congestive heart failure
integer
C0018802 (UMLS CUI [1])
Code List
Congestive heart failure
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Arrhythmia
integer
C0003811 (UMLS CUI [1])
Code List
Arrhythmia
CL Item
not quoted (0)
CL Item
quoted (1)
Item Group
Not recovered symptoms / sequelae: Neurological symptoms
C0243088 (UMLS CUI-1)
C1709277 (UMLS CUI-2)
C1457887 (UMLS CUI-3)
C0235031 (UMLS CUI-4)
Item
Headache
integer
C0018681 (UMLS CUI [1])
Code List
Headache
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Neurologic deficits
integer
C0521654 (UMLS CUI [1])
Code List
Neurologic deficits
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Severe cognitive impairment
integer
C3554639 (UMLS CUI [1])
Code List
Severe cognitive impairment
CL Item
not quoted (0)
CL Item
quoted (1)
Item Group
Not recovered symptoms / sequelae: Further findings
C0243088 (UMLS CUI-1)
C1709277 (UMLS CUI-2)
C1457887 (UMLS CUI-3)
C0243095 (UMLS CUI-4)
C0205394 (UMLS CUI-5)
Item
Muscle aches
integer
C0231528 (UMLS CUI [1])
Code List
Muscle aches
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Mild fatigue
integer
C0015672 (UMLS CUI [1,1])
C2945599 (UMLS CUI [1,2])
Code List
Mild fatigue
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Severe fatigue
integer
C0015672 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Code List
Severe fatigue
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Kidney failure
integer
C0035078 (UMLS CUI [1])
Code List
Kidney failure
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Other
integer
C0205394 (UMLS CUI [1,1])
C0243088 (UMLS CUI [1,2])
C0205394 (UMLS CUI [2,1])
C1709277 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
CL Item
not quoted (0)
CL Item
quoted (1)
Other not recovered symptoms / sequelae
Item
If Other, please specify
text
C0205394 (UMLS CUI [1,1])
C0243088 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
C0205394 (UMLS CUI [2,1])
C1709277 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
C1521902 (UMLS CUI [2,4])
Item
None
integer
C0549184 (UMLS CUI [1,1])
C0243088 (UMLS CUI [1,2])
C0549184 (UMLS CUI [2,1])
C1709277 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Unknown
integer
C0439673 (UMLS CUI [1,1])
C0243088 (UMLS CUI [1,2])
C0439673 (UMLS CUI [2,1])
C1709277 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
CL Item
not quoted (0)
CL Item
quoted (1)
Item Group
Chest CT results:
C0202823 (UMLS CUI-1)
C1274040 (UMLS CUI-2)
Item
Air trapping
integer
C0231819 (UMLS CUI [1,1])
C0202823 (UMLS CUI [1,2])
Code List
Air trapping
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Areas of consolidation
integer
C0521530 (UMLS CUI [1,1])
C0202823 (UMLS CUI [1,2])
Code List
Areas of consolidation
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Bronchiolitis
integer
C0006271 (UMLS CUI [1,1])
C0202823 (UMLS CUI [1,2])
Code List
Bronchiolitis
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Crazy paving pattern
integer
C4476749 (UMLS CUI [1])
Code List
Crazy paving pattern
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Ground glass opacities
integer
C3827002 (UMLS CUI [1,1])
C0202823 (UMLS CUI [1,2])
Code List
Ground glass opacities
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Interlobular septal thickening
integer
C4280727 (UMLS CUI [1])
Code List
Interlobular septal thickening
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Nodulary lesions
integer
C1518345 (UMLS CUI [1,1])
C0202823 (UMLS CUI [1,2])
Code List
Nodulary lesions
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Pleural effusion
integer
C0032227 (UMLS CUI [1,1])
C0202823 (UMLS CUI [1,2])
Code List
Pleural effusion
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Other relevant CT results
integer
C0205394 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C2347946 (UMLS CUI [1,3])
C0202823 (UMLS CUI [1,4])
CL Item
not quoted (0)
CL Item
quoted (1)
Other relevant chest CT results - specify
Item
If Other relevant CT results, please specify (short description: no copy & paste)
text
C0205394 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C2347946 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C0202823 (UMLS CUI [1,5])
Item
Normal CT
integer
C0205307 (UMLS CUI [1,1])
C0202823 (UMLS CUI [1,2])
Code List
Normal CT
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Not done
integer
C1272696 (UMLS CUI [1,1])
C0202823 (UMLS CUI [1,2])
Code List
Not done
CL Item
not quoted (0)
CL Item
quoted (1)
Item Group
Vital signs and respiratory parameters
C0518766 (UMLS CUI-1)
C0035237 (UMLS CUI-2)
C0549193 (UMLS CUI-3)
Item
Worst during recovery phase: Systolic BP
integer
C0871470 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
Code List
Worst during recovery phase: 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
> 179 mmHg (7)
CL Item
Not done (8)
CL Item
Unknown (9)
Item
Worst during recovery phase: Diastolic BP
integer
C0428883 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
Code List
Worst during recovery phase: 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
Unknown (7)
CL Item
Unknown (7)
Item
Worst during recovery phase: Pulse
integer
C0232117 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
Code List
Worst during recovery phase: 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
Worst during recovery phase: SO2
integer
C0523807 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
Code List
Worst during recovery phase: 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
Worst during recovery phase: paO2
integer
C0202155 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
Code List
Worst during recovery phase: 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
Worst during recovery phase: paCO2
integer
C1822070 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
Code List
Worst during recovery phase: 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
Worst during recovery phase: Temperature
integer
C0039476 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
Code List
Worst during recovery phase: 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
Worst during recovery phase: Respiratory rate / minute
integer
C0231832 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
Code List
Worst during recovery phase: 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
Worst during recovery phase: Glasgow Coma scale
integer
C0017594 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
Code List
Worst during recovery phase: 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
Super-Infections
C0038826 (UMLS CUI-1)
Item
Proven bacterial infection:
integer
C0004623 (UMLS CUI [1,1])
C0456369 (UMLS CUI [1,2])
Code List
Proven bacterial infection:
CL Item
not quoted (0)
CL Item
quoted (1)
Proven bacterial infection, specify
Item
Proven bacterial infection, please specify:
text
C0004623 (UMLS CUI [1,1])
C0456369 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
Item
Probable or suspected bacterial infection:
integer
C0004623 (UMLS CUI [1,1])
C0332147 (UMLS CUI [1,2])
Code List
Probable or suspected bacterial infection:
CL Item
not quoted (0)
CL Item
quoted (1)
Probable or suspected bacterial infection, specify
Item
Probable or suspected bacterial infection, please specify:
text
C0004623 (UMLS CUI [1,1])
C0332147 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
Item
Proven fungal infection:
integer
C0026946 (UMLS CUI [1,1])
C0456369 (UMLS CUI [1,2])
Code List
Proven fungal infection:
CL Item
not quoted (0)
CL Item
quoted (1)
Proven fungal infection, specify
Item
Proven fungal infection, please specify:
text
C0026946 (UMLS CUI [1,1])
C0456369 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
Item
Probable or suspected fungal infection:
integer
C0026946 (UMLS CUI [1,1])
C0332147 (UMLS CUI [1,2])
Code List
Probable or suspected fungal infection:
CL Item
not quoted (0)
CL Item
quoted (1)
Probable or suspected fungal infection, specify
Item
Probable or suspected fungal infection, please specify:
text
C0026946 (UMLS CUI [1,1])
C0332147 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
Item
None
integer
C0549184 (UMLS CUI [1,1])
C0038826 (UMLS CUI [1,2])
Code List
None
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Unknown
integer
C0439673 (UMLS CUI [1,1])
C0038826 (UMLS CUI [1,2])
Code List
Unknown
CL Item
not quoted (0)
CL Item
quoted (1)
Item Group
Antibacterial treatment: Betalactams
C0279516 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
C0282215 (UMLS CUI-3)
Item
Penicillins/ aminopenicilins
integer
C0030842 (UMLS CUI [1])
C0304324 (UMLS CUI [2])
Code List
Penicillins/ aminopenicilins
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Cephalosporins I-III
integer
C0304317 (UMLS CUI [1])
C0304319 (UMLS CUI [2])
C0304320 (UMLS CUI [3])
Code List
Cephalosporins I-III
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Carbapenems (meropenem, imipenem, ertapenem, doripenem)
integer
C0006968 (UMLS CUI [1])
C0066005 (UMLS CUI [2])
C0020933 (UMLS CUI [3])
C1120106 (UMLS CUI [4])
C0389169 (UMLS CUI [5])
Code List
Carbapenems (meropenem, imipenem, ertapenem, doripenem)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Piperacillin/tazobactam
integer
C0250480 (UMLS CUI [1])
Code List
Piperacillin/tazobactam
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
New betalactams for multi-resistent bacteria (ceftazidime/avibactam, ceftolozane/tazobactam, cefiderocol)
integer
C0205314 (UMLS CUI [1,1])
C0282215 (UMLS CUI [1,2])
C3826980 (UMLS CUI [1,3])
C3656596 (UMLS CUI [2])
C3656593 (UMLS CUI [3])
C4548369 (UMLS CUI [4])
Code List
New betalactams for multi-resistent bacteria (ceftazidime/avibactam, ceftolozane/tazobactam, cefiderocol)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Antibacterial treatment: Macrolides
C0279516 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
C0003240 (UMLS CUI-3)
Item
Azithromycin
integer
C0052796 (UMLS CUI [1])
Code List
Azithromycin
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other macrolide (erythromycin, clarithromycin, roxithromycin)
integer
C0003240 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0014806 (UMLS CUI [2])
C0055856 (UMLS CUI [3])
C0035891 (UMLS CUI [4])
Code List
Other macrolide (erythromycin, clarithromycin, roxithromycin)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Antibacterial treatment: Other antibacterial treatment
C0279516 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
C0205394 (UMLS CUI-3)
Item
Glycopeptides (vancomycin, teicoplanin)
integer
C0017953 (UMLS CUI [1])
C0042313 (UMLS CUI [2])
C0145106 (UMLS CUI [3])
Code List
Glycopeptides (vancomycin, teicoplanin)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other gram-positive active drugs for multiresistant bacteria (e.g. linezolid, daptomycin)
integer
C0205394 (UMLS CUI [1,1])
C00032332 (UMLS CUI [1,2])
C0018154 (UMLS CUI [1,3])
C3826980 (UMLS CUI [1,4])
C0663241 (UMLS CUI [2])
C0057144 (UMLS CUI [3])
Code List
Other gram-positive active drugs for multiresistant bacteria (e.g. linezolid, daptomycin)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Fluorochinolones (ciprofloxacin, moxifloxacin, levofloxacin)
integer
C0034428 (UMLS CUI [1])
C0008809 (UMLS CUI [2])
C0536495 (UMLS CUI [3])
C0282386 (UMLS CUI [4])
Code List
Fluorochinolones (ciprofloxacin, moxifloxacin, levofloxacin)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other
integer
C0279516 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
If Other, please specify
integer
C0279516 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
Code List
If Other, please specify
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Severity of multiple sclerosis after COVID-19 infection:
C0026769 (UMLS CUI-1)
C0439793 (UMLS CUI-2)
C0687676 (UMLS CUI-3)
C5203670 (UMLS CUI-4)
Item
Severity of multiple sclerosis after COVID-19 infection:
integer
C0026769 (UMLS CUI [1,1])
C0439793 (UMLS CUI [1,2])
C0687676 (UMLS CUI [1,3])
C5203670 (UMLS CUI [1,4])
Code List
Severity of multiple sclerosis after COVID-19 infection:
CL Item
Walking distance unrestricted (1)
CL Item
500 meters without walking aid (2)
CL Item
Use of a walking aid (3)
CL Item
Wheelchair (4)
CL Item
Bedridden (5)
CL Item
Unknown (6)
CL Item
Not applicable (7)
Item Group
Pulmonary function test in recovery phase (Spirometry):
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0024119 (UMLS CUI-3)
C0037981 (UMLS CUI-4)
Item
Pulmonary function test in recovery phase (Spirometry):
integer
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0024119 (UMLS CUI [1,3])
C0037981 (UMLS CUI [2])
Code List
Pulmonary function test in recovery phase (Spirometry):
CL Item
FEV1 > 80 % (1)
CL Item
FEV1 60 - 80 % (2)
CL Item
FEV1 40 - 59 % (3)
CL Item
FEV1 <40% (4)
CL Item
Not done (5)
CL Item
Unknown (6)
Item Group
Deterioration of the prior chronic pulmonary disease
C0746102 (UMLS CUI-1)
C2347662 (UMLS CUI-2)
C0868945 (UMLS CUI-3)
Item
Change in medication
integer
C2169461 (UMLS CUI [1,1])
C0746102 (UMLS CUI [1,2])
C2347662 (UMLS CUI [1,3])
C0868945 (UMLS CUI [1,4])
Code List
Change in medication
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Continuous use of oxygen therapy
integer
C0184633 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])
C0746102 (UMLS CUI [1,3])
C2347662 (UMLS CUI [1,4])
C0868945 (UMLS CUI [1,5])
Code List
Continuous use of oxygen therapy
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Other
integer
C0205394 (UMLS CUI [1,1])
C0746102 (UMLS CUI [1,2])
C2347662 (UMLS CUI [1,3])
C0868945 (UMLS CUI [1,4])
CL Item
not quoted (0)
CL Item
quoted (1)
Other deterioration of prior chronic pulmonary disease - specify
Item
If Other, please specify
text
C0205394 (UMLS CUI [1,1])
C0746102 (UMLS CUI [1,2])
C2347662 (UMLS CUI [1,3])
C0868945 (UMLS CUI [1,4])
C1521902 (UMLS CUI [1,5])
Item
No deterioration
integer
C0549184 (UMLS CUI [1,1])
C0746102 (UMLS CUI [1,2])
C2347662 (UMLS CUI [1,3])
C0868945 (UMLS CUI [1,4])
CL Item
not quoted (0)
CL Item
quoted (1)
Item
Unknown
integer
C0439673 (UMLS CUI [1,1])
C0746102 (UMLS CUI [1,2])
C2347662 (UMLS CUI [1,3])
C0868945 (UMLS CUI [1,4])
CL Item
not quoted (0)
CL Item
quoted (1)
Item Group
Is data entry for this section finished?
C4684556 (UMLS CUI-1)
C1828479 (UMLS CUI-2)
C0205197 (UMLS CUI-3)
Item
Is data entry for this section finished?
integer
C4684556 (UMLS CUI [1,1])
C1828479 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
Code List
Is data entry for this section finished?
CL Item
Yes (1)
CL Item
No (2)

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