ID
42476
Beskrivning
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).
Länk
Nyckelord
Versioner (3)
- 2021-07-02 2021-07-02 - Sarah Riepenhausen
- 2021-07-15 2021-07-15 - Sarah Riepenhausen
- 2021-07-16 2021-07-16 - Sarah Riepenhausen
Rättsinnehavare
LEOSS
Uppladdad den
16 juli 2021
DOI
10.21961/mdm:42476
Licens
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
Beskrivning
Hemoglobin A1c (HbA1c ) in blood
Alias
- UMLS CUI-1
- C0474680
Beskrivning
C-peptide in blood
Alias
- UMLS CUI-1
- C0006558
- UMLS CUI-2
- C0005768
Beskrivning
Indicate values determined at admission day.
Datatyp
integer
Måttenheter
- pmol/l
Alias
- UMLS CUI [1,1]
- C0006558
- UMLS CUI [1,2]
- C0005768
- UMLS CUI [1,3]
- C1302393
Beskrivning
Indicate values determined in blood at next morning after admission, sober.
Datatyp
integer
Måttenheter
- 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
Beskrivning
Glucose in blood
Alias
- UMLS CUI-1
- C0392201
Beskrivning
Indicate values determined at admission day.
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1302393
- UMLS CUI [1,2]
- C0392201
Beskrivning
Indicate values determined at next morning after admission, fasting glucose.
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0428568
- UMLS CUI [1,2]
- C0332170
- UMLS CUI [1,3]
- C0687676
- UMLS CUI [1,4]
- C1302393
Beskrivning
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
Beskrivning
Indicate values determined at admission day. C-peptide in (pmol/l); Glucose in (mg/dl).
Datatyp
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
Beskrivning
Indicate values determined at next morning after admission, sober. C-peptide in (pmol/l); Glucose in (mg/dl).
Datatyp
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
Beskrivning
Insulin level in blood
Alias
- UMLS CUI-1
- C0021641
- UMLS CUI-2
- C0005768
Beskrivning
Indicate values determined at admission day.
Datatyp
integer
Måttenheter
- mU/l
Alias
- UMLS CUI [1,1]
- C0021641
- UMLS CUI [1,2]
- C0005768
- UMLS CUI [1,3]
- C1302393
Beskrivning
Indicate values determined at next morning after admission, sober.
Datatyp
integer
Måttenheter
- 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
Beskrivning
Cortisol level in blood
Alias
- UMLS CUI-1
- C0201968
- UMLS CUI-2
- C0005768
Beskrivning
Indicate values determined at admission day.
Datatyp
integer
Måttenheter
- µg/dl
Alias
- UMLS CUI [1,1]
- C0201968
- UMLS CUI [1,2]
- C0005768
- UMLS CUI [1,3]
- C1302393
Beskrivning
Indicate values determined at next morning after admission, sober.
Datatyp
integer
Måttenheter
- 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
Beskrivning
Has insulin treatment been used before SARS-CoV-2 detection?
Alias
- UMLS CUI-1
- C0745343
- UMLS CUI-2
- C0332152
- UMLS CUI-3
- C1442488
Beskrivning
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
Beskrivning
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
Beskrivning
Indicate treatment before diagnosis of SARS-CoV-2.
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0038766
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C1442488
Beskrivning
Indicate treatment before diagnosis of SARS-CoV-2.
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0025598
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C1442488
Beskrivning
Indicate treatment before diagnosis of SARS-CoV-2.
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C3273809
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C1442488
Beskrivning
Indicate treatment before diagnosis of SARS-CoV-2.
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C1827106
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C1442488
Beskrivning
Indicate treatment before diagnosis of SARS-CoV-2.
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C3273807
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C1442488
Beskrivning
Indicate treatment before diagnosis of SARS-CoV-2.
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0359086
- UMLS CUI [1,3]
- C0332152
- UMLS CUI [1,4]
- C1442488
Beskrivning
Indicate other oral antidiabetic treatment before Baseline
Datatyp
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
Beskrivning
Indicate treatment before diagnosis of SARS-CoV-2.
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0549184
- UMLS CUI [1,2]
- C0359086
- UMLS CUI [1,3]
- C0332152
- UMLS CUI [1,4]
- C1442488
Beskrivning
Oral antidiabetic treatment before Baseline, unknown
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0359086
- UMLS CUI [1,2]
- C0439673
- UMLS CUI [1,3]
- C0332152
- UMLS CUI [1,4]
- C1442488
Beskrivning
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])