ID
42476
Descrição
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/. Please note that only cases with known outcome are collected! Baseline / diagnosis is defined as the day the sample of the first positive SARS-CoV-2 result was taken. Criteria of the Uncomplicated Phase: Asymptomatic OR Symptoms of upper respiratory tract infection and/or Nausea, emesis, diarrhea and/or Fever Remember: The Uncomplicated Phase ends, if a previously febrile patient has no fever anymore and has completed 14 days of follow-up without entering Complicated or Critical Phase; then move to Recovery Phase. Also, as soon as one of the criteria of the Complicated or Critical Phase are fulfilled, Uncomplicated Phase ends; move over to there. If the patient has died, the phase ends with the death of the patient. If the patient has died, do not report terminal values, e.g. those recorded after switching off life-support or heart rate "0" after death of the patient. Criteria of the Complicated Phase: * Need for oxygen supplementation (In patients with prior oxygen home therapy, clinically meaningful increase in need for oxygenation.) * paO2 at room air < 70 mmHg * SO2 at room air < 90 % * GOT or GPT > 5x ULN * New cardiac arrhythmia * New pericardial effusion >1cm * New heart failure with pulmonary edema, congestive hepatopathy or peripheral edema Remember: The Complicated Phase ends, if none of the criteria for the Complicated Phase is fulfilled anymore AND the patient is free of fever; then move to Recovery Phase. Also, as soon as one of the criteria of the Critical Phase are fulfilled, Complicated Phase ends; move over to Critical Phase. If the patient has died, the phase ends with the death of the patient. If the patient has died, do not report terminal values, e.g. those recorded after switching off life-support or heart rate "0" after death of the patient. Criteria of the Critical Phase: * Need for catecholamines * Life-threatening cardiac arrhythmia * Mechanical ventilation (invasive or non-invasive) * Liver failure with Quick< 50% * qSOFA >= 2 * Renal failure in need of dialysis Remember: The Critical Phase ends as soon as none of the criteria for the Critical Phase is fulfilled anymore AND the patient is free of fever. If the patient has died, it ends with the death of the patient. If the patient has died, do not report terminal values, i.e. those recorded after turning off life-support or heart rate "0" after death of the patient. 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 If a text field can't be filled out, note 'ND' (for not determined).
Link
Palavras-chave
Versões (3)
- 02/07/2021 02/07/2021 - Sarah Riepenhausen
- 15/07/2021 15/07/2021 - Sarah Riepenhausen
- 16/07/2021 16/07/2021 - Sarah Riepenhausen
Titular dos direitos
LEOSS
Transferido a
16 de julho de 2021
DOI
10.21961/mdm:42476
Licença
Creative Commons BY 4.0
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LEOSS: Lean European Open Survey on SARS-CoV-2 Infected Patients
Diabetes mellitus sub-cohort
- StudyEvent: Baseline
- StudyEvent: Comorbidities and Pre-medication
- StudyEvent: Phases
- StudyEvent: Therapeutics
- StudyEvent: Diagnostics
Descrição
Hemoglobin A1c (HbA1c ) in blood
Alias
- UMLS CUI-1
- C0474680
Descrição
C-peptide in blood
Alias
- UMLS CUI-1
- C0006558
- UMLS CUI-2
- C0005768
Descrição
Indicate values determined at admission day.
Tipo de dados
integer
Unidades de medida
- pmol/l
Alias
- UMLS CUI [1,1]
- C0006558
- UMLS CUI [1,2]
- C0005768
- UMLS CUI [1,3]
- C1302393
Descrição
Indicate values determined in blood at next morning after admission, sober.
Tipo de dados
integer
Unidades de medida
- pmol/l
Alias
- UMLS CUI [1,1]
- C2208720
- UMLS CUI [1,2]
- C0005768
- UMLS CUI [1,3]
- C0332170
- UMLS CUI [1,4]
- C0687676
- UMLS CUI [1,5]
- C1302393
Descrição
Glucose in blood
Alias
- UMLS CUI-1
- C0392201
Descrição
Indicate values determined at admission day.
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C1302393
- UMLS CUI [1,2]
- C0392201
Descrição
Indicate values determined at next morning after admission, fasting glucose.
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0428568
- UMLS CUI [1,2]
- C0332170
- UMLS CUI [1,3]
- C0687676
- UMLS CUI [1,4]
- C1302393
Descrição
C-peptide-to-Glucose Ratio (CGR) in blood
Alias
- UMLS CUI-1
- C0006558
- UMLS CUI-2
- C0017725
- UMLS CUI-3
- C0456603
- UMLS CUI-4
- C0005768
Descrição
Indicate values determined at admission day. C-peptide in (pmol/l); Glucose in (mg/dl).
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0006558
- UMLS CUI [1,2]
- C0017725
- UMLS CUI [1,3]
- C0456603
- UMLS CUI [1,4]
- C0005768
- UMLS CUI [1,5]
- C1302393
Descrição
Indicate values determined at next morning after admission, sober. C-peptide in (pmol/l); Glucose in (mg/dl).
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0006558
- UMLS CUI [1,2]
- C0017725
- UMLS CUI [1,3]
- C0456603
- UMLS CUI [1,4]
- C0005768
- UMLS CUI [1,5]
- C0332170
- UMLS CUI [1,6]
- C0687676
- UMLS CUI [1,7]
- C1302393
- UMLS CUI [1,8]
- C0015663
Descrição
Insulin level in blood
Alias
- UMLS CUI-1
- C0021641
- UMLS CUI-2
- C0005768
Descrição
Indicate values determined at admission day.
Tipo de dados
integer
Unidades de medida
- mU/l
Alias
- UMLS CUI [1,1]
- C0021641
- UMLS CUI [1,2]
- C0005768
- UMLS CUI [1,3]
- C1302393
Descrição
Indicate values determined at next morning after admission, sober.
Tipo de dados
integer
Unidades de medida
- mU/l
Alias
- UMLS CUI [1,1]
- C0021641
- UMLS CUI [1,2]
- C0005768
- UMLS CUI [1,3]
- C0332170
- UMLS CUI [1,4]
- C0687676
- UMLS CUI [1,5]
- C1302393
- UMLS CUI [1,6]
- C0015663
Descrição
Cortisol level in blood
Alias
- UMLS CUI-1
- C0201968
- UMLS CUI-2
- C0005768
Descrição
Indicate values determined at admission day.
Tipo de dados
integer
Unidades de medida
- µg/dl
Alias
- UMLS CUI [1,1]
- C0201968
- UMLS CUI [1,2]
- C0005768
- UMLS CUI [1,3]
- C1302393
Descrição
Indicate values determined at next morning after admission, sober.
Tipo de dados
integer
Unidades de medida
- µg/dl
Alias
- UMLS CUI [1,1]
- C0201968
- UMLS CUI [1,2]
- C0005768
- UMLS CUI [1,3]
- C0332170
- UMLS CUI [1,4]
- C0687676
- UMLS CUI [1,5]
- C1302393
- UMLS CUI [1,6]
- C0015663
Descrição
Has insulin treatment been used before SARS-CoV-2 detection?
Alias
- UMLS CUI-1
- C0745343
- UMLS CUI-2
- C0332152
- UMLS CUI-3
- C1442488
Descrição
Has the insulin scheme been changed at the time of SARS-CoV-2 detection (+/- 48 h)?
Alias
- UMLS CUI-1
- C0745343
- UMLS CUI-2
- C4319952
- UMLS CUI-3
- C1442488
Descrição
Which oral antidiabetic treatment has been used before SARS-CoV-2 detection?
Alias
- UMLS CUI-1
- C0359086
- UMLS CUI-2
- C0332152
- UMLS CUI-3
- C1442488
Descrição
Indicate treatment before diagnosis of SARS-CoV-2.
Tipo de dados
boolean
Alias
- UMLS CUI [1,1]
- C0038766
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C1442488
Descrição
Indicate treatment before diagnosis of SARS-CoV-2.
Tipo de dados
boolean
Alias
- UMLS CUI [1,1]
- C0025598
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C1442488
Descrição
Indicate treatment before diagnosis of SARS-CoV-2.
Tipo de dados
boolean
Alias
- UMLS CUI [1,1]
- C3273809
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C1442488
Descrição
Indicate treatment before diagnosis of SARS-CoV-2.
Tipo de dados
boolean
Alias
- UMLS CUI [1,1]
- C1827106
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C1442488
Descrição
Indicate treatment before diagnosis of SARS-CoV-2.
Tipo de dados
boolean
Alias
- UMLS CUI [1,1]
- C3273807
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C1442488
Descrição
Indicate treatment before diagnosis of SARS-CoV-2.
Tipo de dados
boolean
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0359086
- UMLS CUI [1,3]
- C0332152
- UMLS CUI [1,4]
- C1442488
Descrição
Indicate other oral antidiabetic treatment before Baseline
Tipo de dados
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0359086
- UMLS CUI [1,3]
- C1521902
- UMLS CUI [1,4]
- C0332152
- UMLS CUI [1,5]
- C1442488
Descrição
Indicate treatment before diagnosis of SARS-CoV-2.
Tipo de dados
boolean
Alias
- UMLS CUI [1,1]
- C0549184
- UMLS CUI [1,2]
- C0359086
- UMLS CUI [1,3]
- C0332152
- UMLS CUI [1,4]
- C1442488
Descrição
Oral antidiabetic treatment before Baseline, unknown
Tipo de dados
boolean
Alias
- UMLS CUI [1,1]
- C0359086
- UMLS CUI [1,2]
- C0439673
- UMLS CUI [1,3]
- C0332152
- UMLS CUI [1,4]
- C1442488
Descrição
Is data entry for this section finished?
Alias
- UMLS CUI-1
- C4684556
- UMLS CUI-2
- C1828479
- UMLS CUI-3
- C0205197
Similar models
Diabetes mellitus sub-cohort
- StudyEvent: Baseline
- StudyEvent: Comorbidities and Pre-medication
- StudyEvent: Phases
- StudyEvent: Therapeutics
- StudyEvent: Diagnostics
C1522508 (UMLS CUI-2)
C0441731 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
C0449238 (UMLS CUI [1,2])
C0005768 (UMLS CUI [1,2])
C1302393 (UMLS CUI [1,3])
C0005768 (UMLS CUI [1,2])
C0332170 (UMLS CUI [1,3])
C0687676 (UMLS CUI [1,4])
C1302393 (UMLS CUI [1,5])
C0392201 (UMLS CUI [1,2])
C0332170 (UMLS CUI [1,2])
C0687676 (UMLS CUI [1,3])
C1302393 (UMLS CUI [1,4])
C0017725 (UMLS CUI-2)
C0456603 (UMLS CUI-3)
C0005768 (UMLS CUI-4)
C0017725 (UMLS CUI [1,2])
C0456603 (UMLS CUI [1,3])
C0005768 (UMLS CUI [1,4])
C1302393 (UMLS CUI [1,5])
C0017725 (UMLS CUI [1,2])
C0456603 (UMLS CUI [1,3])
C0005768 (UMLS CUI [1,4])
C0332170 (UMLS CUI [1,5])
C0687676 (UMLS CUI [1,6])
C1302393 (UMLS CUI [1,7])
C0015663 (UMLS CUI [1,8])
C0005768 (UMLS CUI-2)
C0005768 (UMLS CUI [1,2])
C1302393 (UMLS CUI [1,3])
C0005768 (UMLS CUI [1,2])
C0332170 (UMLS CUI [1,3])
C0687676 (UMLS CUI [1,4])
C1302393 (UMLS CUI [1,5])
C0015663 (UMLS CUI [1,6])
C0005768 (UMLS CUI-2)
C0005768 (UMLS CUI [1,2])
C1302393 (UMLS CUI [1,3])
C0005768 (UMLS CUI [1,2])
C0332170 (UMLS CUI [1,3])
C0687676 (UMLS CUI [1,4])
C1302393 (UMLS CUI [1,5])
C0015663 (UMLS CUI [1,6])
C0332152 (UMLS CUI-2)
C1442488 (UMLS CUI-3)
C0332152 (UMLS CUI [1,2])
C1442488 (UMLS CUI [1,3])
C4319952 (UMLS CUI-2)
C1442488 (UMLS CUI-3)
C4319952 (UMLS CUI [1,2])
C1442488 (UMLS CUI [1,3])
C0332152 (UMLS CUI-2)
C1442488 (UMLS CUI-3)
C0332152 (UMLS CUI [1,2])
C1442488 (UMLS CUI [1,3])
C0332152 (UMLS CUI [1,2])
C1442488 (UMLS CUI [1,3])
C0332152 (UMLS CUI [1,2])
C1442488 (UMLS CUI [1,3])
C0332152 (UMLS CUI [1,2])
C1442488 (UMLS CUI [1,3])
C0332152 (UMLS CUI [1,2])
C1442488 (UMLS CUI [1,3])
C0359086 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C1442488 (UMLS CUI [1,4])
C0359086 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
C0332152 (UMLS CUI [1,4])
C1442488 (UMLS CUI [1,5])
C0359086 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C1442488 (UMLS CUI [1,4])
C0439673 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C1442488 (UMLS CUI [1,4])
C1828479 (UMLS CUI-2)
C0205197 (UMLS CUI-3)
C1828479 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])