ID
42476
Beschrijving
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
Trefwoorden
Versies (3)
- 02-07-21 02-07-21 - Sarah Riepenhausen
- 15-07-21 15-07-21 - Sarah Riepenhausen
- 16-07-21 16-07-21 - Sarah Riepenhausen
Houder van rechten
LEOSS
Geüploaded op
16 juli 2021
DOI
10.21961/mdm:42476
Licentie
Creative Commons BY 4.0
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LEOSS: Lean European Open Survey on SARS-CoV-2 Infected Patients
Ethics and palliative care details
- StudyEvent: Baseline
- StudyEvent: Comorbidities and Pre-medication
- StudyEvent: Phases
- StudyEvent: Therapeutics
- StudyEvent: Diagnostics
Beschrijving
Ethics consultation
Alias
- UMLS CUI-1
- C0600380
Beschrijving
Did the patient decline specific life-prolonging measures in case of life threatening diseases?
Alias
- UMLS CUI-1
- C0030705
- UMLS CUI-2
- C1705116
- UMLS CUI-3
- C3897860
- UMLS CUI-4
- C0012634
- UMLS CUI-5
- C2826244
Beschrijving
Please indicate if any known statement either personal, an advance directive or via a patient representative was available.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0184666
- UMLS CUI [1,2]
- C1705116
- UMLS CUI [2,1]
- C0332300
- UMLS CUI [2,2]
- C0583239
Beschrijving
Please indicate if any known statement either personal, an advance directive or via a patient representative was available.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0583239
- UMLS CUI [1,2]
- C1705116
Beschrijving
Please indicate if any known statement either personal, an advance directive or via a patient representative was available.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0021925
- UMLS CUI [1,2]
- C1705116
Beschrijving
Please indicate if any known statement either personal, an advance directive or via a patient representative was available.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0035273
- UMLS CUI [1,2]
- C1705116
Beschrijving
In which specialist palliative care setting was the patient cared for?
Alias
- UMLS CUI-1
- C1273400
- UMLS CUI-2
- C4034203
Beschrijving
Specialist palliative home care
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C0204977
Beschrijving
Note: This question is critical for the further course of the questionnaire.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C0009818
Beschrijving
Note: This question is critical for the further course of the questionnaire.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C0019988
Beschrijving
Note: This question is critical for the further course of the questionnaire.
Datatype
boolean
Alias
- UMLS CUI [1]
- C1551311
Beschrijving
Note: This question is critical for the further course of the questionnaire.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C1273400
- UMLS CUI [1,3]
- C4034203
Beschrijving
Note: This question is critical for the further course of the questionnaire.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1298908
- UMLS CUI [1,2]
- C1273400
- UMLS CUI [1,3]
- C4034203
Beschrijving
Note: This question is critical for the further course of the questionnaire.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0439673
- UMLS CUI [1,2]
- C1273400
- UMLS CUI [1,3]
- C4034203
Beschrijving
Which type of specialist palliative care did the patient receive?
Alias
- UMLS CUI-1
- C1273400
- UMLS CUI-2
- C0332307
Beschrijving
Specialist palliative care: Symptom control
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C1274136
Beschrijving
Specialist palliative care: Psychological support
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C0205486
- UMLS CUI [1,3]
- C1521721
Beschrijving
Specialist palliative care: Social support
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C0037438
Beschrijving
Specialist palliative care: Spiritual support
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C0150355
Beschrijving
Specialist palliative care: Support of relatives
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C0150232
Beschrijving
Which type of specialist palliative care professionals were involved?
Alias
- UMLS CUI-1
- C1273400
- UMLS CUI-2
- C1704312
- UMLS CUI-3
- C0205428
Beschrijving
Palliative physician
Datatype
integer
Alias
- UMLS CUI [1]
- C0586875
Beschrijving
Palliative care nurse
Datatype
integer
Alias
- UMLS CUI [1]
- C3714595
Beschrijving
Psychologist
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C0033908
Beschrijving
Specialist palliative care: Chaplain/pastoral worker
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C0558269
- UMLS CUI [2,1]
- C1273400
- UMLS CUI [2,2]
- C0030643
Beschrijving
Specialist palliative care: Physiotherapist
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C2362565
Beschrijving
Specialist palliative care: Music therapist
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C0586937
Beschrijving
Specialist palliative care: Art therapist
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C0586935
Beschrijving
Specialist palliative care: Social worker
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1273400
- UMLS CUI [1,2]
- C0037444
Beschrijving
Specialist palliative care: Hospice volunteers
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0019989
- UMLS CUI [1,2]
- C0085555
Beschrijving
Other specialist palliative care professionals involved
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C1273400
- UMLS CUI [1,3]
- C1704312
- UMLS CUI [1,4]
- C0205428
Beschrijving
Which drugs were prescribed for symptom control (e.g. breathlessness, pain, death rattle)?
Alias
- UMLS CUI-1
- C3166216
- UMLS CUI-2
- C1274136
- UMLS CUI-3
- C0013404
- UMLS CUI-4
- C0030193
- UMLS CUI-5
- C0547002
Beschrijving
Please indicate only the use in palliative intention for symptom control, not as part of analgosedation in the context of intubation.
Datatype
integer
Alias
- UMLS CUI [1]
- C0242402
- UMLS CUI [2]
- C0026549
- UMLS CUI [3]
- C0012306
- UMLS CUI [4]
- C0030049
Beschrijving
Please indicate only the use in palliative intention for symptom control, not as part of analgosedation in the context of intubation.
Datatype
integer
Alias
- UMLS CUI [1]
- C0005064
- UMLS CUI [2]
- C0024002
- UMLS CUI [3]
- C0026056
Beschrijving
Please indicate only the use in palliative intention for symptom control, not as part of analgosedation in the context of intubation.
Datatype
integer
Alias
- UMLS CUI [1]
- C0040615
- UMLS CUI [2]
- C0018546
- UMLS CUI [3]
- C0025678
Beschrijving
Please indicate only the use in palliative intention for symptom control, not as part of analgosedation in the context of intubation.
Datatype
integer
Alias
- UMLS CUI [1]
- C0242896
- UMLS CUI [2]
- C0006519
- UMLS CUI [3]
- C3814772
Beschrijving
Please indicate only the use in palliative intention for symptom control, not as part of analgosedation in the context of intubation.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C3166216
- UMLS CUI [1,3]
- C1274136
Beschrijving
Please indicate only the use in palliative intention for symptom control, not as part of analgosedation in the context of intubation.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C3166216
- UMLS CUI [1,3]
- C1274136
- UMLS CUI [1,4]
- C1521902
Beschrijving
Is data entry for this section finished?
Alias
- UMLS CUI-1
- C4684556
- UMLS CUI-2
- C1828479
- UMLS CUI-3
- C0205197
Similar models
Ethics and palliative care details
- StudyEvent: Baseline
- StudyEvent: Comorbidities and Pre-medication
- StudyEvent: Phases
- StudyEvent: Therapeutics
- StudyEvent: Diagnostics
C0392747 (UMLS CUI-2)
C3897860 (UMLS CUI-3)
C0030231 (UMLS CUI-4)
C5203670 (UMLS CUI [1,2])
C2347662 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,4])
C0023671 (UMLS CUI [1,5])
C0001314 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
C0023671 (UMLS CUI [1,4])
C0205394 (UMLS CUI [1,5])
C0332268 (UMLS CUI [1,2])
C0018741 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
C0750491 (UMLS CUI [2,3])
C0566251 (UMLS CUI [1,2])
C0392747 (UMLS CUI [1,3])
C3897860 (UMLS CUI [1,4])
C0030231 (UMLS CUI [1,5])
C0566251 (UMLS CUI [1,2])
C0392747 (UMLS CUI [1,3])
C3897860 (UMLS CUI [1,4])
C0030231 (UMLS CUI [1,5])
C0566251 (UMLS CUI [1,2])
C0392747 (UMLS CUI [1,3])
C3897860 (UMLS CUI [1,4])
C0030231 (UMLS CUI [1,5])
C1705116 (UMLS CUI-2)
C3897860 (UMLS CUI-3)
C0012634 (UMLS CUI-4)
C2826244 (UMLS CUI-5)
C1705116 (UMLS CUI [1,2])
C0332300 (UMLS CUI [2,1])
C0583239 (UMLS CUI [2,2])
C1705116 (UMLS CUI [1,2])
C1705116 (UMLS CUI [1,2])
C4034203 (UMLS CUI-2)
C0204977 (UMLS CUI [1,2])
C0009818 (UMLS CUI [1,2])
C0019988 (UMLS CUI [1,2])
C1273400 (UMLS CUI [1,2])
C4034203 (UMLS CUI [1,3])
C1273400 (UMLS CUI [1,2])
C4034203 (UMLS CUI [1,3])
C1273400 (UMLS CUI [1,2])
C4034203 (UMLS CUI [1,3])
C0332307 (UMLS CUI-2)
C1274136 (UMLS CUI [1,2])
C0205486 (UMLS CUI [1,2])
C1521721 (UMLS CUI [1,3])
C0037438 (UMLS CUI [1,2])
C0150355 (UMLS CUI [1,2])
C0150232 (UMLS CUI [1,2])
C1704312 (UMLS CUI-2)
C0205428 (UMLS CUI-3)
C0558269 (UMLS CUI [1,2])
C1273400 (UMLS CUI [2,1])
C0030643 (UMLS CUI [2,2])
C2362565 (UMLS CUI [1,2])
C0586937 (UMLS CUI [1,2])
C0586935 (UMLS CUI [1,2])
C0037444 (UMLS CUI [1,2])
C0085555 (UMLS CUI [1,2])
C1273400 (UMLS CUI [1,2])
C1704312 (UMLS CUI [1,3])
C0205428 (UMLS CUI [1,4])
C1274136 (UMLS CUI-2)
C0013404 (UMLS CUI-3)
C0030193 (UMLS CUI-4)
C0547002 (UMLS CUI-5)
C0026549 (UMLS CUI [2])
C0012306 (UMLS CUI [3])
C0030049 (UMLS CUI [4])
C0024002 (UMLS CUI [2])
C0026056 (UMLS CUI [3])
C0018546 (UMLS CUI [2])
C0025678 (UMLS CUI [3])
C0006519 (UMLS CUI [2])
C3814772 (UMLS CUI [3])
C3166216 (UMLS CUI [1,2])
C1274136 (UMLS CUI [1,3])
C3166216 (UMLS CUI [1,2])
C1274136 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C1828479 (UMLS CUI-2)
C0205197 (UMLS CUI-3)
C1828479 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])