ID

42367

Descripción

Study Title: LEOSS: Lean European Open Survey on SARS-CoV-2 Infected Patients https://leoss.net Study Indication: COVID-19 Date: 19.03.2021 Published with permission by Prof. Dr. med. J.-J. Vehreschild. LEOSS, a multi-center cohort study, has been created to get more in-depth knowledge about the epidemiology and clinical course of patients infected with SARS-CoV-2. Initiated by the ESCMID Emerging Infections Task Force (EITaF) and the German Infectious Disease Society, and supported by all German Centers for Health Research (DZG), LEOSS has developed into an international network of contributors. Via an integrative research approach with anonymous recruitment and collection of routine data in an open science context, LEOSS is building a uniform clinical dataset and providing real-time analyses. For more information feel free to explore https://leoss.net/. This document is for data aggregated in the recovery phase. If a text field can't be filled out, note 'ND'. Criteria of the Recovery Phase: Improvement by at least one phase, i.e. Critical to Complicated or Complicated to Uncomplicated Defervescence Remember: Uncomplicated asymptomatic patients enter recovery phase after 14 days of observation without disease progression No further progression or re-hospitalization

Link

https://leoss.net

Palabras clave

  1. 27/11/20 27/11/20 -
  2. 28/6/21 28/6/21 -
Titular de derechos de autor

LEOSS

Subido en

28 de junio de 2021

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

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
Recovery phase: Respiratory findings
Descripción

Recovery phase: Respiratory findings

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C0035237
UMLS CUI-4
C0243095
Cough
Descripción

RC (Cough)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0010200
Shortness of breath
Descripción

RC (Shortness of breath)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0013404
Need for oxygen supplementation
Descripción

RC (Need for oxygen supplementation)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0686904
UMLS CUI [1,4]
C0919655
Recovery phase: Cardiovascular findings
Descripción

Recovery phase: Cardiovascular findings

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C0007226
UMLS CUI-4
C0243095
Congestive heart failure
Descripción

RC (Congestive heart failure)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0018802
Arrhythmia
Descripción

RC (Arrhythmia)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0003811
Recovery phase: Neurological findings
Descripción

Recovery phase: Neurological findings

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C0235031
UMLS CUI-4
C0243095
Headache
Descripción

RC (Headache)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0018681
Neurologic deficits
Descripción

RC (Neurologic deficits)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0521654
Severe cognitive impairment
Descripción

RC (Severe cognitive impairment)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C3554639
Recovery phase: Further findings
Descripción

Recovery phase: Further findings

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C0243095
UMLS CUI-4
C0205394
Muscle aches
Descripción

RC (Muscle aches)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0231528
Mild fatigue
Descripción

RC (Mild fatigue)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0015672
UMLS CUI [1,4]
C2945599
Severe fatigue
Descripción

RC (Severe fatigue)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0015672
UMLS CUI [1,4]
C0205082
Kidney failure
Descripción

RC (Kidney failure)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0035078
Other not recovered symptoms / sequelae
Descripción

RC (Other not recovered symptoms / sequelae)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C0243088
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0205394
UMLS CUI [2,4]
C1709277
UMLS CUI [2,5]
C1457887
Indicate other not recovered symptoms / sequelae
Descripción

CR (indicate other not recovered symptoms / sequelae)

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C0243088
UMLS CUI [1,5]
C1521902
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0205394
UMLS CUI [2,4]
C1709277
UMLS CUI [2,5]
C1457887
UMLS CUI [2,6]
C1521902
None
Descripción

RC (No not recovered symptoms / sequelae)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0549184
UMLS CUI [1,4]
C0243088
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0549184
UMLS CUI [2,4]
C1709277
UMLS CUI [2,5]
C1457887
Unknown
Descripción

RC (Unknown not recovered symptoms / sequelae)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0439673
UMLS CUI [1,4]
C0243088
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0439673
UMLS CUI [2,4]
C1709277
UMLS CUI [2,5]
C1457887
Recovery phase: Vital signs
Descripción

Recovery phase: Vital signs

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C0518766
Systolic BP in RC
Descripción

Indicate worst value. Worst means farthest from normal range.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Diastolic BP in RC
Descripción

Indicate worst value. Worst means farthest from normal range.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0428883
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Pulse in RC
Descripción

Indicate worst value. Worst means farthest from normal range.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0232117
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
SO2 in RC
Descripción

Indicate worst value. Worst means farthest from normal range.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0523807
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
paO2 in RC
Descripción

Indicate worst value. Worst means farthest from normal range.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0202155
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
paCO2 in RC
Descripción

Indicate worst value. Worst means farthest from normal range.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1822070
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Temperature in RC
Descripción

Indicate worst value. Worst means farthest from normal range.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0039476
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Respiratory rate / minute in RC
Descripción

Indicate worst value. Worst means farthest from normal range.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0231832
UMLS CUI [1,4]
C1522166
UMLS CUI [1,5]
C2004454
UMLS CUI [1,6]
C0205390
Glasgow Coma scale (GCS) in RC
Descripción

Indicate worst value. Worst means farthest from normal range.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0017594
UMLS CUI [1,2]
C1522166
UMLS CUI [1,3]
C2004454
UMLS CUI [1,4]
C0205390
Recovery phase: Lung ultrasound
Descripción

Recovery phase: Lung ultrasound

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C0203463
B lines (multifocal, discrete or confluent)
Descripción

Indicate worst results from all ultrasounds during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0203463
UMLS CUI [1,4]
C1522166
UMLS CUI [1,5]
C3846158
Confluent B lines
Descripción

Indicate worst results from all ultrasounds during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0203463
UMLS CUI [1,4]
C1522166
UMLS CUI [1,5]
C3846158
UMLS CUI [1,6]
C0205200
Consolidation (non translobar and translobar)
Descripción

Indicate worst results from all ultrasounds during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0203463
UMLS CUI [1,4]
C1522166
UMLS CUI [1,5]
C0521530
Multilobar distribution of abnormalities
Descripción

Indicate worst results from all ultrasounds during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0203463
UMLS CUI [1,4]
C1522166
UMLS CUI [1,5]
C0439064
UMLS CUI [1,6]
C1522010
UMLS CUI [1,7]
C1704711
UMLS CUI [1,8]
C1704258
Small (centomeric) lesions
Descripción

Indicate worst results from all ultrasounds during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0203463
UMLS CUI [1,4]
C1522166
UMLS CUI [1,5]
C0700321
UMLS CUI [1,6]
C0221198
Thickened pleural line
Descripción

Indicate worst results from all ultrasounds during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0203463
UMLS CUI [1,4]
C1522166
UMLS CUI [1,5]
C0264545
Other lung ultrasound results
Descripción

RC (Other lung ultrasound results)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0203463
UMLS CUI [1,4]
C0205394
UMLS CUI [1,5]
C1274040
Indicate other lung ultrasound results
Descripción

RC (indicate other lung ultrasound results)

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0203463
UMLS CUI [1,4]
C0205394
UMLS CUI [1,5]
C1274040
UMLS CUI [1,6]
C1521902
Not done
Descripción

RC (lung ultrasound, not done)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0203463
UMLS CUI [1,4]
C1272696
Unknown
Descripción

RC (lung ultrasound, unknown)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0203463
UMLS CUI [1,4]
C0439673
Recovery phase: Chest CT results
Descripción

Recovery phase: Chest CT results

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C1522166
UMLS CUI-4
C0202823
UMLS CUI-5
C1274040
Air trapping
Descripción

Most recent results from all CTs during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C1522166
UMLS CUI [1,4]
C0231819
UMLS CUI [1,5]
C0202823
Areas of consolidation
Descripción

Most recent results from all CTs during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C1522166
UMLS CUI [1,4]
C0521530
UMLS CUI [1,5]
C0202823
Bronchiolitis
Descripción

Most recent results from all CTs during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C1522166
UMLS CUI [1,4]
C0006271
UMLS CUI [1,5]
C0202823
Crazy paving pattern
Descripción

Most recent results from all CTs during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C1522166
UMLS CUI [1,4]
C4476749
Ground glass opacities
Descripción

Most recent results from all CTs during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C1522166
UMLS CUI [1,4]
C3827002
UMLS CUI [1,5]
C0202823
Interlobular septal thickening
Descripción

Most recent results from all CTs during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C1522166
UMLS CUI [1,4]
C4280727
Nodulary lesions
Descripción

Most recent results from all CTs during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C1522166
UMLS CUI [1,4]
C1518345
UMLS CUI [1,5]
C0202823
Pleural effusion
Descripción

Most recent results from all CTs during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C1522166
UMLS CUI [1,4]
C0032227
UMLS CUI [1,5]
C0202823
Chest x-ray results
Descripción

RC (Chest x-ray)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0039985
Indicate chest x-ray results
Descripción

RC (indicate chest x-ray result)

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0039985
UMLS CUI [1,4]
C1274040
Other relevant chest CT results
Descripción

Most recent results from all CTs during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C1274040
UMLS CUI [1,5]
C2347946
UMLS CUI [1,6]
C0202823
Indicate other relevant chest CT results
Descripción

RC (indicate other relevant CT results)

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C1274040
UMLS CUI [1,5]
C2347946
UMLS CUI [1,6]
C1521902
UMLS CUI [1,7]
C0202823
Normal CT
Descripción

Most recent results from all CTs during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0205307
UMLS CUI [1,4]
C0202823
Not done
Descripción

Most recent results from all CTs during this phase of disease.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C1272696
UMLS CUI [1,4]
C0202823
Recovery phase: Co/Superinfections
Descripción

Recovery phase: Co/Superinfections

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C0038826
UMLS CUI-4
C0275524
Proven bacterial infection
Descripción

RC (Proven bacterial infection)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0004623
UMLS CUI [1,4]
C0456369
Indicate site and respective pathogen of proven bacterial infection
Descripción

Please fill in the site and respective pathogen if available.

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0004623
UMLS CUI [1,4]
C0456369
UMLS CUI [1,5]
C1521902
Probable or suspected bacterial infection
Descripción

RC (Probable or suspected bacterial infection)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0004623
UMLS CUI [1,4]
C0332147
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0004623
UMLS CUI [2,4]
C0332148
Indicate site and respective pathogen of probable or suspected bacterial infection
Descripción

Please fill in the site and respective pathogen if available.

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0004623
UMLS CUI [1,4]
C0332147
UMLS CUI [1,5]
C1521902
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0004623
UMLS CUI [2,4]
C0332148
UMLS CUI [2,5]
C1521902
Proven fungal infection
Descripción

RC (Proven fungal infection)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0026946
UMLS CUI [1,4]
C0456369
Indicate site and respective pathogen of proven fungal infection
Descripción

Please fill in the site and respective pathogen if available.

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0026946
UMLS CUI [1,4]
C0456369
UMLS CUI [1,5]
C1521902
Probable or suspected fungal infection
Descripción

RC (Probable or suspected fungal infection)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0026946
UMLS CUI [1,4]
C0332147
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0026946
UMLS CUI [2,4]
C0332148
Indicate site and respective pathogen of probable or suspected fungal infection
Descripción

Please fill in the site and respective pathogen if available.

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0026946
UMLS CUI [1,4]
C0332147
UMLS CUI [1,5]
C1521902
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0026946
UMLS CUI [2,4]
C0332148
UMLS CUI [2,5]
C1521902
None
Descripción

RC (No Co/Superinfection)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0549184
UMLS CUI [1,4]
C0038826
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0549184
UMLS CUI [2,4]
C0275524
Unknown
Descripción

RC (Unknown Co/superinfection)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0439673
UMLS CUI [1,4]
C0038826
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0439673
UMLS CUI [2,4]
C0275524
Recovery phase: Antibacterial treatment: Betalactams
Descripción

Recovery phase: Antibacterial treatment: Betalactams

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C0279516
UMLS CUI-4
C0282215
Penicillins/ aminopenicilins
Descripción

Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0030842
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0304324
Cephalosporins I-III
Descripción

Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0304317
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0304319
UMLS CUI [3,1]
C2004454
UMLS CUI [3,2]
C0205390
UMLS CUI [3,3]
C0304320
Carbapenems (meropenem, imipenem, ertapenem, doripenem)
Descripción

Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0006968
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0066005
UMLS CUI [3,1]
C2004454
UMLS CUI [3,2]
C0205390
UMLS CUI [3,3]
C0020933
UMLS CUI [4,1]
C2004454
UMLS CUI [4,2]
C0205390
UMLS CUI [4,3]
C1120106
UMLS CUI [5,1]
C2004454
UMLS CUI [5,2]
C0205390
UMLS CUI [5,3]
C0389169
Piperacillin/tazobactam
Descripción

Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0250480
New betalactams for multi-resistent bacteria (ceftazidime/avibactam, ceftolozane/tazobactam, cefiderocol)
Descripción

Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0205314
UMLS CUI [1,4]
C0282215
UMLS CUI [1,5]
C3826980
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C3656596
UMLS CUI [3,1]
C2004454
UMLS CUI [3,2]
C0205390
UMLS CUI [3,3]
C3656593
UMLS CUI [4,1]
C2004454
UMLS CUI [4,2]
C0205390
UMLS CUI [4,3]
C4548369
Recovery phase: Antibacterial treatment: Macrolides
Descripción

Recovery phase: Antibacterial treatment: Macrolides

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C0279516
UMLS CUI-4
C0003240
Azithromycin
Descripción

Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0052796
Other macrolide (erythromycin, clarithromycin, roxithromycin)
Descripción

Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0003240
UMLS CUI [1,4]
C0205394
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0014806
UMLS CUI [3,1]
C2004454
UMLS CUI [3,2]
C0205390
UMLS CUI [3,3]
C0055856
UMLS CUI [4,1]
C2004454
UMLS CUI [4,2]
C0205390
UMLS CUI [4,3]
C0035891
Recovery phase: Antibacterial treatment: Other antibacterial treatment
Descripción

Recovery phase: Antibacterial treatment: Other antibacterial treatment

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C0279516
UMLS CUI-4
C0205394
Glycopeptides (vancomycin, teicoplanin)
Descripción

Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0017953
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0042313
UMLS CUI [3,1]
C2004454
UMLS CUI [3,2]
C0205390
UMLS CUI [3,3]
C0145106
Other gram-positive active drugs for multiresistant bacteria (e.g. linezolid, daptomycin)
Descripción

Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C0018154
UMLS CUI [1,5]
C3826980
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0663241
UMLS CUI [3,1]
C2004454
UMLS CUI [3,2]
C0205390
UMLS CUI [3,3]
C0057144
Fluorochinolones (ciprofloxacin, moxifloxacin, levofloxacin)
Descripción

Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0034428
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0008809
UMLS CUI [3,1]
C2004454
UMLS CUI [3,2]
C0205390
UMLS CUI [3,3]
C0536495
UMLS CUI [4,1]
C2004454
UMLS CUI [4,2]
C0205390
UMLS CUI [4,3]
C0282386
Other antibacterial treatment
Descripción

Please indicate all antibacterials administered at least once for antibacterial treatment during this phase. Please note that antibacterial prophylaxis should not be mentioned here.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0279516
UMLS CUI [1,4]
C0205394
Indicate other antibacterial treatment
Descripción

CR (Indicate other antibacterial treatment)

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0279516
UMLS CUI [1,4]
C0205394
UMLS CUI [1,5]
C1521902
Recovery phase: Severity of multiple sclerosis after COVID-19 infection
Descripción

Recovery phase: Severity of multiple sclerosis after COVID-19 infection

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C0026769
UMLS CUI-4
C0439793
UMLS CUI-5
C0687676
UMLS CUI-6
C5203670
Severity of multiple sclerosis after COVID-19 infection
Descripción

RC (MS severity after COVID-19 infection)

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0026769
UMLS CUI [1,4]
C0439793
UMLS CUI [1,5]
C0687676
UMLS CUI [1,6]
C5203670
Recovery phase: Pulmonary function test (Spirometry)
Descripción

Recovery phase: Pulmonary function test (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)
Descripción

RC (pulmonary function test, spirometry), percent predicted FEV1

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0024119
UMLS CUI [2,1]
C2004454
UMLS CUI [2,2]
C0205390
UMLS CUI [2,3]
C0037981
UMLS CUI [3]
C0730561
Recovery phase: Deterioration of the prior chronic pulmonary disease
Descripción

Recovery phase: Deterioration of the prior chronic pulmonary disease

Alias
UMLS CUI-1
C2004454
UMLS CUI-2
C0205390
UMLS CUI-3
C0746102
UMLS CUI-4
C2347662
UMLS CUI-5
C0868945
Change in medication because of deterioration of prior chronic pulmonary disease
Descripción

RC (Change in medication due to prior chronic pulmonary disease deterioration)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C2169461
UMLS CUI [1,4]
C0746102
UMLS CUI [1,5]
C2347662
UMLS CUI [1,6]
C0868945
Continuous use of oxygen therapy because of deterioration of prior chronic pulmonary disease
Descripción

RC (Continuous use of oxygen therapy due to prior chronic pulmonary disease deterioration)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0184633
UMLS CUI [1,4]
C0549178
UMLS CUI [1,5]
C0746102
UMLS CUI [1,6]
C2347662
UMLS CUI [1,7]
C0868945
Other deterioration of prior chronic pulmonary disease
Descripción

RC (Other deterioration of prior chronic pulmonary disease)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C0746102
UMLS CUI [1,5]
C2347662
UMLS CUI [1,6]
C0868945
Indicate other deterioration of prior chronic pulmonary disease
Descripción

RC (Indicate other deterioration of prior chronic pulmonary disease)

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C0746102
UMLS CUI [1,5]
C2347662
UMLS CUI [1,6]
C0868945
UMLS CUI [1,7]
C1521902
No deterioration of prior chronic pulmonary disease
Descripción

RC (No deterioration of prior chronic pulmonary disease)

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0549184
UMLS CUI [1,4]
C0746102
UMLS CUI [1,5]
C2347662
UMLS CUI [1,6]
C0868945
Unknown
Descripción

RC (Unknown deterioration of prior chronic pulmonary disease )

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2004454
UMLS CUI [1,2]
C0205390
UMLS CUI [1,3]
C0439673
UMLS CUI [1,4]
C0746102
UMLS CUI [1,5]
C2347662
UMLS CUI [1,6]
C0868945
Recovery phase: Is data entry for this section finished?
Descripción

Recovery phase: Is data entry for this section finished?

Alias
UMLS CUI-1
C4684556
UMLS CUI-2
C1828479
UMLS CUI-3
C0205197
Recovery phase: Is data entry for this section finished?
Descripción

RC_Completed

Tipo de datos

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
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Recovery phase: Respiratory findings
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0035237 (UMLS CUI-3)
C0243095 (UMLS CUI-4)
RC (Cough)
Item
Cough
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0010200 (UMLS CUI [1,3])
RC (Shortness of breath)
Item
Shortness of breath
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0013404 (UMLS CUI [1,3])
RC (Need for oxygen supplementation)
Item
Need for oxygen supplementation
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0686904 (UMLS CUI [1,3])
C0919655 (UMLS CUI [1,4])
Item Group
Recovery phase: Cardiovascular findings
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0007226 (UMLS CUI-3)
C0243095 (UMLS CUI-4)
RC (Congestive heart failure)
Item
Congestive heart failure
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0018802 (UMLS CUI [1,3])
RC (Arrhythmia)
Item
Arrhythmia
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0003811 (UMLS CUI [1,3])
Item Group
Recovery phase: Neurological findings
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0235031 (UMLS CUI-3)
C0243095 (UMLS CUI-4)
RC (Headache)
Item
Headache
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0018681 (UMLS CUI [1,3])
RC (Neurologic deficits)
Item
Neurologic deficits
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0521654 (UMLS CUI [1,3])
RC (Severe cognitive impairment)
Item
Severe cognitive impairment
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C3554639 (UMLS CUI [1,3])
Item Group
Recovery phase: Further findings
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0243095 (UMLS CUI-3)
C0205394 (UMLS CUI-4)
RC (Muscle aches)
Item
Muscle aches
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0231528 (UMLS CUI [1,3])
RC (Mild fatigue)
Item
Mild fatigue
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0015672 (UMLS CUI [1,3])
C2945599 (UMLS CUI [1,4])
RC (Severe fatigue)
Item
Severe fatigue
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0015672 (UMLS CUI [1,3])
C0205082 (UMLS CUI [1,4])
RC (Kidney failure)
Item
Kidney failure
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0035078 (UMLS CUI [1,3])
RC (Other not recovered symptoms / sequelae)
Item
Other not recovered symptoms / sequelae
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0243088 (UMLS CUI [1,4])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0205394 (UMLS CUI [2,3])
C1709277 (UMLS CUI [2,4])
C1457887 (UMLS CUI [2,5])
CR (indicate other not recovered symptoms / sequelae)
Item
Indicate other not recovered symptoms / sequelae
text
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0243088 (UMLS CUI [1,4])
C1521902 (UMLS CUI [1,5])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0205394 (UMLS CUI [2,3])
C1709277 (UMLS CUI [2,4])
C1457887 (UMLS CUI [2,5])
C1521902 (UMLS CUI [2,6])
RC (No not recovered symptoms / sequelae)
Item
None
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0549184 (UMLS CUI [1,3])
C0243088 (UMLS CUI [1,4])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0549184 (UMLS CUI [2,3])
C1709277 (UMLS CUI [2,4])
C1457887 (UMLS CUI [2,5])
RC (Unknown not recovered symptoms / sequelae)
Item
Unknown
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,3])
C0243088 (UMLS CUI [1,4])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0439673 (UMLS CUI [2,3])
C1709277 (UMLS CUI [2,4])
C1457887 (UMLS CUI [2,5])
Item Group
Recovery phase: Vital signs
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0518766 (UMLS CUI-3)
Item
Systolic BP in RC
integer
C0871470 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
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
Diastolic BP in RC
integer
C0428883 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
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
Pulse in RC
integer
C0232117 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
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 in RC
integer
C0523807 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
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 in RC
integer
C0202155 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
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 in RC
integer
C1822070 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
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 in RC
integer
C0039476 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
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 in RC
integer
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0231832 (UMLS CUI [1,3])
C1522166 (UMLS CUI [1,4])
C2004454 (UMLS CUI [1,5])
C0205390 (UMLS CUI [1,6])
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 (GCS) in RC
integer
C0017594 (UMLS CUI [1,1])
C1522166 (UMLS CUI [1,2])
C2004454 (UMLS CUI [1,3])
C0205390 (UMLS CUI [1,4])
Code List
Glasgow Coma scale (GCS) in RC
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
Recovery phase: Lung ultrasound
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0203463 (UMLS CUI-3)
RC (worst lung ultrasound, B lines)
Item
B lines (multifocal, discrete or confluent)
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0203463 (UMLS CUI [1,3])
C1522166 (UMLS CUI [1,4])
C3846158 (UMLS CUI [1,5])
RC (worst lung ultrasound, confluent B lines)
Item
Confluent B lines
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0203463 (UMLS CUI [1,3])
C1522166 (UMLS CUI [1,4])
C3846158 (UMLS CUI [1,5])
C0205200 (UMLS CUI [1,6])
RC (worst lung ultrasound, consolidation)
Item
Consolidation (non translobar and translobar)
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0203463 (UMLS CUI [1,3])
C1522166 (UMLS CUI [1,4])
C0521530 (UMLS CUI [1,5])
RC (worst lung ultrasound, multilobar distribution of abnormalities)
Item
Multilobar distribution of abnormalities
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0203463 (UMLS CUI [1,3])
C1522166 (UMLS CUI [1,4])
C0439064 (UMLS CUI [1,5])
C1522010 (UMLS CUI [1,6])
C1704711 (UMLS CUI [1,7])
C1704258 (UMLS CUI [1,8])
RC (worst lung ultrasound, Small lesions)
Item
Small (centomeric) lesions
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0203463 (UMLS CUI [1,3])
C1522166 (UMLS CUI [1,4])
C0700321 (UMLS CUI [1,5])
C0221198 (UMLS CUI [1,6])
RC (worst lung ultrasound, Thickened pleural line)
Item
Thickened pleural line
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0203463 (UMLS CUI [1,3])
C1522166 (UMLS CUI [1,4])
C0264545 (UMLS CUI [1,5])
RC (Other lung ultrasound results)
Item
Other lung ultrasound results
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0203463 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C1274040 (UMLS CUI [1,5])
RC (indicate other lung ultrasound results)
Item
Indicate other lung ultrasound results
text
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0203463 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C1274040 (UMLS CUI [1,5])
C1521902 (UMLS CUI [1,6])
RC (lung ultrasound, not done)
Item
Not done
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0203463 (UMLS CUI [1,3])
C1272696 (UMLS CUI [1,4])
RC (lung ultrasound, unknown)
Item
Unknown
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0203463 (UMLS CUI [1,3])
C0439673 (UMLS CUI [1,4])
Item Group
Recovery phase: Chest CT results
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C1522166 (UMLS CUI-3)
C0202823 (UMLS CUI-4)
C1274040 (UMLS CUI-5)
RC (worst chest CT, air trapping)
Item
Air trapping
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1522166 (UMLS CUI [1,3])
C0231819 (UMLS CUI [1,4])
C0202823 (UMLS CUI [1,5])
RC (worst chest CT, Areas of consolidation)
Item
Areas of consolidation
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1522166 (UMLS CUI [1,3])
C0521530 (UMLS CUI [1,4])
C0202823 (UMLS CUI [1,5])
RC (worst chest CT, Bronchiolitis)
Item
Bronchiolitis
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1522166 (UMLS CUI [1,3])
C0006271 (UMLS CUI [1,4])
C0202823 (UMLS CUI [1,5])
RC (worst chest CT, Crazy paving pattern)
Item
Crazy paving pattern
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1522166 (UMLS CUI [1,3])
C4476749 (UMLS CUI [1,4])
RC (worst chest CT, Ground glass opacities)
Item
Ground glass opacities
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1522166 (UMLS CUI [1,3])
C3827002 (UMLS CUI [1,4])
C0202823 (UMLS CUI [1,5])
RC (worst chest CT, Interlobular septal thickening)
Item
Interlobular septal thickening
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1522166 (UMLS CUI [1,3])
C4280727 (UMLS CUI [1,4])
RC (worst chest CT, nodulary lesions)
Item
Nodulary lesions
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1522166 (UMLS CUI [1,3])
C1518345 (UMLS CUI [1,4])
C0202823 (UMLS CUI [1,5])
RC (worst chest CT, Pleural effusion)
Item
Pleural effusion
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1522166 (UMLS CUI [1,3])
C0032227 (UMLS CUI [1,4])
C0202823 (UMLS CUI [1,5])
RC (Chest x-ray)
Item
Chest x-ray results
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0039985 (UMLS CUI [1,3])
RC (indicate chest x-ray result)
Item
Indicate chest x-ray results
text
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0039985 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
RC (Other relevant CT results)
Item
Other relevant chest CT results
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
C2347946 (UMLS CUI [1,5])
C0202823 (UMLS CUI [1,6])
RC (indicate other relevant CT results)
Item
Indicate other relevant chest CT results
text
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
C2347946 (UMLS CUI [1,5])
C1521902 (UMLS CUI [1,6])
C0202823 (UMLS CUI [1,7])
RC (Normal CT)
Item
Normal CT
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0205307 (UMLS CUI [1,3])
C0202823 (UMLS CUI [1,4])
RC (chest CT not done)
Item
Not done
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,3])
C0202823 (UMLS CUI [1,4])
Item Group
Recovery phase: Co/Superinfections
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0038826 (UMLS CUI-3)
C0275524 (UMLS CUI-4)
RC (Proven bacterial infection)
Item
Proven bacterial infection
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0004623 (UMLS CUI [1,3])
C0456369 (UMLS CUI [1,4])
RC (indicate proven bacterial infection)
Item
Indicate site and respective pathogen of proven bacterial infection
text
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0004623 (UMLS CUI [1,3])
C0456369 (UMLS CUI [1,4])
C1521902 (UMLS CUI [1,5])
RC (Probable or suspected bacterial infection)
Item
Probable or suspected bacterial infection
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0004623 (UMLS CUI [1,3])
C0332147 (UMLS CUI [1,4])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0004623 (UMLS CUI [2,3])
C0332148 (UMLS CUI [2,4])
RC (indicate probable or suspected bacterial infection)
Item
Indicate site and respective pathogen of probable or suspected bacterial infection
text
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0004623 (UMLS CUI [1,3])
C0332147 (UMLS CUI [1,4])
C1521902 (UMLS CUI [1,5])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0004623 (UMLS CUI [2,3])
C0332148 (UMLS CUI [2,4])
C1521902 (UMLS CUI [2,5])
RC (Proven fungal infection)
Item
Proven fungal infection
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0026946 (UMLS CUI [1,3])
C0456369 (UMLS CUI [1,4])
RC (indicate proven fungal infection)
Item
Indicate site and respective pathogen of proven fungal infection
text
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0026946 (UMLS CUI [1,3])
C0456369 (UMLS CUI [1,4])
C1521902 (UMLS CUI [1,5])
RC (Probable or suspected fungal infection)
Item
Probable or suspected fungal infection
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0026946 (UMLS CUI [1,3])
C0332147 (UMLS CUI [1,4])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0026946 (UMLS CUI [2,3])
C0332148 (UMLS CUI [2,4])
RC (indicate probable or suspected fungal infection)
Item
Indicate site and respective pathogen of probable or suspected fungal infection
text
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0026946 (UMLS CUI [1,3])
C0332147 (UMLS CUI [1,4])
C1521902 (UMLS CUI [1,5])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0026946 (UMLS CUI [2,3])
C0332148 (UMLS CUI [2,4])
C1521902 (UMLS CUI [2,5])
RC (No Co/Superinfection)
Item
None
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0549184 (UMLS CUI [1,3])
C0038826 (UMLS CUI [1,4])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0549184 (UMLS CUI [2,3])
C0275524 (UMLS CUI [2,4])
RC (Unknown Co/superinfection)
Item
Unknown
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,3])
C0038826 (UMLS CUI [1,4])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0439673 (UMLS CUI [2,3])
C0275524 (UMLS CUI [2,4])
Item Group
Recovery phase: Antibacterial treatment: Betalactams
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0279516 (UMLS CUI-3)
C0282215 (UMLS CUI-4)
Item
Penicillins/ aminopenicilins
integer
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0030842 (UMLS CUI [1,3])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0304324 (UMLS CUI [2,3])
Code List
Penicillins/ aminopenicilins
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Cephalosporins I-III
integer
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0304317 (UMLS CUI [1,3])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0304319 (UMLS CUI [2,3])
C2004454 (UMLS CUI [3,1])
C0205390 (UMLS CUI [3,2])
C0304320 (UMLS CUI [3,3])
Code List
Cephalosporins I-III
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Carbapenems (meropenem, imipenem, ertapenem, doripenem)
integer
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0006968 (UMLS CUI [1,3])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0066005 (UMLS CUI [2,3])
C2004454 (UMLS CUI [3,1])
C0205390 (UMLS CUI [3,2])
C0020933 (UMLS CUI [3,3])
C2004454 (UMLS CUI [4,1])
C0205390 (UMLS CUI [4,2])
C1120106 (UMLS CUI [4,3])
C2004454 (UMLS CUI [5,1])
C0205390 (UMLS CUI [5,2])
C0389169 (UMLS CUI [5,3])
Code List
Carbapenems (meropenem, imipenem, ertapenem, doripenem)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Piperacillin/tazobactam
integer
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0250480 (UMLS CUI [1,3])
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
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0205314 (UMLS CUI [1,3])
C0282215 (UMLS CUI [1,4])
C3826980 (UMLS CUI [1,5])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C3656596 (UMLS CUI [2,3])
C2004454 (UMLS CUI [3,1])
C0205390 (UMLS CUI [3,2])
C3656593 (UMLS CUI [3,3])
C2004454 (UMLS CUI [4,1])
C0205390 (UMLS CUI [4,2])
C4548369 (UMLS CUI [4,3])
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
Recovery phase: Antibacterial treatment: Macrolides
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0279516 (UMLS CUI-3)
C0003240 (UMLS CUI-4)
Item
Azithromycin
integer
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0052796 (UMLS CUI [1,3])
Code List
Azithromycin
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other macrolide (erythromycin, clarithromycin, roxithromycin)
integer
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0003240 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0014806 (UMLS CUI [2,3])
C2004454 (UMLS CUI [3,1])
C0205390 (UMLS CUI [3,2])
C0055856 (UMLS CUI [3,3])
C2004454 (UMLS CUI [4,1])
C0205390 (UMLS CUI [4,2])
C0035891 (UMLS CUI [4,3])
Code List
Other macrolide (erythromycin, clarithromycin, roxithromycin)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Recovery phase: Antibacterial treatment: Other antibacterial treatment
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0279516 (UMLS CUI-3)
C0205394 (UMLS CUI-4)
Item
Glycopeptides (vancomycin, teicoplanin)
integer
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0017953 (UMLS CUI [1,3])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0042313 (UMLS CUI [2,3])
C2004454 (UMLS CUI [3,1])
C0205390 (UMLS CUI [3,2])
C0145106 (UMLS CUI [3,3])
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
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0018154 (UMLS CUI [1,4])
C3826980 (UMLS CUI [1,5])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0663241 (UMLS CUI [2,3])
C2004454 (UMLS CUI [3,1])
C0205390 (UMLS CUI [3,2])
C0057144 (UMLS CUI [3,3])
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
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0034428 (UMLS CUI [1,3])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0008809 (UMLS CUI [2,3])
C2004454 (UMLS CUI [3,1])
C0205390 (UMLS CUI [3,2])
C0536495 (UMLS CUI [3,3])
C2004454 (UMLS CUI [4,1])
C0205390 (UMLS CUI [4,2])
C0282386 (UMLS CUI [4,3])
Code List
Fluorochinolones (ciprofloxacin, moxifloxacin, levofloxacin)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Other antibacterial treatment
integer
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0279516 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
Code List
Other antibacterial treatment
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item
Indicate other antibacterial treatment
text
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0279516 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C1521902 (UMLS CUI [1,5])
Code List
Indicate other antibacterial treatment
CL Item
Yes (1)
CL Item
No (2)
CL Item
Unknown (3)
Item Group
Recovery phase: Severity of multiple sclerosis after COVID-19 infection
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0026769 (UMLS CUI-3)
C0439793 (UMLS CUI-4)
C0687676 (UMLS CUI-5)
C5203670 (UMLS CUI-6)
Item
Severity of multiple sclerosis after COVID-19 infection
integer
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0026769 (UMLS CUI [1,3])
C0439793 (UMLS CUI [1,4])
C0687676 (UMLS CUI [1,5])
C5203670 (UMLS CUI [1,6])
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
Recovery phase: Pulmonary function test (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])
C2004454 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0037981 (UMLS CUI [2,3])
C0730561 (UMLS CUI [3])
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
Recovery phase: Deterioration of the prior chronic pulmonary disease
C2004454 (UMLS CUI-1)
C0205390 (UMLS CUI-2)
C0746102 (UMLS CUI-3)
C2347662 (UMLS CUI-4)
C0868945 (UMLS CUI-5)
RC (Change in medication due to prior chronic pulmonary disease deterioration)
Item
Change in medication because of deterioration of prior chronic pulmonary disease
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C2169461 (UMLS CUI [1,3])
C0746102 (UMLS CUI [1,4])
C2347662 (UMLS CUI [1,5])
C0868945 (UMLS CUI [1,6])
RC (Continuous use of oxygen therapy due to prior chronic pulmonary disease deterioration)
Item
Continuous use of oxygen therapy because of deterioration of prior chronic pulmonary disease
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0184633 (UMLS CUI [1,3])
C0549178 (UMLS CUI [1,4])
C0746102 (UMLS CUI [1,5])
C2347662 (UMLS CUI [1,6])
C0868945 (UMLS CUI [1,7])
RC (Other deterioration of prior chronic pulmonary disease)
Item
Other deterioration of prior chronic pulmonary disease
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0746102 (UMLS CUI [1,4])
C2347662 (UMLS CUI [1,5])
C0868945 (UMLS CUI [1,6])
RC (Indicate other deterioration of prior chronic pulmonary disease)
Item
Indicate other deterioration of prior chronic pulmonary disease
text
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0746102 (UMLS CUI [1,4])
C2347662 (UMLS CUI [1,5])
C0868945 (UMLS CUI [1,6])
C1521902 (UMLS CUI [1,7])
RC (No deterioration of prior chronic pulmonary disease)
Item
No deterioration of prior chronic pulmonary disease
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0549184 (UMLS CUI [1,3])
C0746102 (UMLS CUI [1,4])
C2347662 (UMLS CUI [1,5])
C0868945 (UMLS CUI [1,6])
RC (Unknown deterioration of prior chronic pulmonary disease )
Item
Unknown
boolean
C2004454 (UMLS CUI [1,1])
C0205390 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,3])
C0746102 (UMLS CUI [1,4])
C2347662 (UMLS CUI [1,5])
C0868945 (UMLS CUI [1,6])
Item Group
Recovery phase: Is data entry for this section finished?
C4684556 (UMLS CUI-1)
C1828479 (UMLS CUI-2)
C0205197 (UMLS CUI-3)
Item
Recovery phase: 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
Recovery phase: Is data entry for this section finished?
CL Item
Yes (1)
CL Item
No (2)

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