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42268

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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 Apheresis therapy details. If a text field can't be filled out, note 'ND' (for not determined).

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https://leoss.net

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Versionen (2)
  1. 30.10.20 30.10.20 -
  2. 26.04.21 26.04.21 -
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LEOSS

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26. April 2021

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    LEOSS: Lean European Open Survey on SARS-CoV-2 Infected Patients

    Englisch

    Apheresis therapy details

    1 Formulare  
    Type of apheresis therapy that was performed
    Beschreibung

    Type of apheresis therapy that was performed

    Alias
    UMLS CUI-1
    C0005791
    UMLS CUI-2
    C0332307
    Therapeutic plasma exchange
    Beschreibung

    Therapeutic plasma exchange

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0032113
    CytoSorb® therapy
    Beschreibung

    CytoSorb® therapy

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C3521106
    UMLS CUI [1,2]
    C0079189
    Double Filtration Plasmapheresis (DFPP)
    Beschreibung

    Double Filtration Plasmapheresis (DFPP)

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C5200809
    Other type of apheresis therapy
    Beschreibung

    Other type of apheresis

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0205394
    UMLS CUI [1,2]
    C0005791
    UMLS CUI [1,3]
    C0332307
    Indicate other type of apheresis therapy
    Beschreibung

    Indicate other type of apharesis

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C0205394
    UMLS CUI [1,2]
    C0005791
    UMLS CUI [1,3]
    C0332307
    UMLS CUI [1,4]
    C1521902
    Treatment initiated in disease phase
    Beschreibung

    Treatment initiated in disease phase

    Alias
    UMLS CUI-1
    C0005791
    UMLS CUI-2
    C0457338
    UMLS CUI-3
    C1704686
    Phase when apheresis therapy has started
    Beschreibung

    Indicate in which disease phase the apheresis therapy was started.

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0005791
    UMLS CUI [1,2]
    C0457338
    UMLS CUI [1,3]
    C1704686
    Treatment details
    Beschreibung

    Treatment details

    Alias
    UMLS CUI-1
    C0005791
    UMLS CUI-2
    C0087111
    UMLS CUI-3
    C1522508
    Quantity of the average plasma volume per treatment
    Beschreibung

    Indicate quantity of the average plasma volume per treatment (apheresis therapy).

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0032127
    UMLS CUI [1,2]
    C1510992
    UMLS CUI [1,3]
    C1265611
    UMLS CUI [1,4]
    C0005791
    Overall number of treatments
    Beschreibung

    Please indicate the number of treatment sessions during the observational period

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C0005791
    UMLS CUI [1,2]
    C0750480
    Duration of treatment
    Beschreibung

    Please indicate the number of days when apheresis has been applied

    Datentyp

    text

    Maßeinheiten
    • day
    Alias
    UMLS CUI [1,1]
    C0005791
    UMLS CUI [1,2]
    C0449238
    UMLS CUI [1,3]
    C0439810
    day
    Perceived therapeutic effect
    Beschreibung

    Indicate if the treating physician experience a therapeutic effect.

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C1710470
    UMLS CUI [1,2]
    C1527144
    UMLS CUI [1,3]
    C0005791
    UMLS CUI [1,4]
    C0022423
    Is data entry for this section finished?
    Beschreibung

    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?
    Beschreibung

    Is data entry for this section finished?

    Datentyp

    boolean

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

    Ähnliche Modelle

    Apheresis therapy details

    1 Formulare
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    Type of apheresis therapy that was performed
    C0005791 (UMLS CUI-1)
    C0332307 (UMLS CUI-2)
    Therapeutic plasma exchange
    Item
    Therapeutic plasma exchange
    boolean
    C0032113 (UMLS CUI [1])
    CytoSorb® therapy
    Item
    CytoSorb® therapy
    boolean
    C3521106 (UMLS CUI [1,1])
    C0079189 (UMLS CUI [1,2])
    Double Filtration Plasmapheresis (DFPP)
    Item
    Double Filtration Plasmapheresis (DFPP)
    boolean
    C5200809 (UMLS CUI [1])
    Other type of apheresis
    Item
    Other type of apheresis therapy
    boolean
    C0205394 (UMLS CUI [1,1])
    C0005791 (UMLS CUI [1,2])
    C0332307 (UMLS CUI [1,3])
    Indicate other type of apharesis
    Item
    Indicate other type of apheresis therapy
    text
    C0205394 (UMLS CUI [1,1])
    C0005791 (UMLS CUI [1,2])
    C0332307 (UMLS CUI [1,3])
    C1521902 (UMLS CUI [1,4])
    Item Group
    Treatment initiated in disease phase
    C0005791 (UMLS CUI-1)
    C0457338 (UMLS CUI-2)
    C1704686 (UMLS CUI-3)
    Item
    Phase when apheresis therapy has started
    integer
    C0005791 (UMLS CUI [1,1])
    C0457338 (UMLS CUI [1,2])
    C1704686 (UMLS CUI [1,3])
    AP_start
    Code List
    Phase when apheresis therapy has started
    CL Item
    Uncomplicated phase (1)
    CL Item
    Complicated phase (2)
    CL Item
    Critical Phase (3)
    CL Item
    Recovery Phase (4)
    CL Item
    Unknown (5)
    Item Group
    Treatment details
    C0005791 (UMLS CUI-1)
    C0087111 (UMLS CUI-2)
    C1522508 (UMLS CUI-3)
    Item
    Quantity of the average plasma volume per treatment
    integer
    C0032127 (UMLS CUI [1,1])
    C1510992 (UMLS CUI [1,2])
    C1265611 (UMLS CUI [1,3])
    C0005791 (UMLS CUI [1,4])
    AP_quantity
    Code List
    Quantity of the average plasma volume per treatment
    CL Item
    30 - 44 ml/kg (1)
    CL Item
    45 - 60 ml/kg (2)
    CL Item
    > 60 ml/kg (3)
    CL Item
    Not done (4)
    CL Item
    Unknown (5)
    Treatments count
    Item
    Overall number of treatments
    text
    C0005791 (UMLS CUI [1,1])
    C0750480 (UMLS CUI [1,2])
    Duration of treatment
    Item
    Duration of treatment
    text
    C0005791 (UMLS CUI [1,1])
    C0449238 (UMLS CUI [1,2])
    C0439810 (UMLS CUI [1,3])
    Item
    Perceived therapeutic effect
    integer
    C1710470 (UMLS CUI [1,1])
    C1527144 (UMLS CUI [1,2])
    C0005791 (UMLS CUI [1,3])
    C0022423 (UMLS CUI [1,4])
    AP_effect
    Code List
    Perceived therapeutic effect
    CL Item
    Yes (1)
    CL Item
    No (2)
    CL Item
    Unknown (3)
    Item Group
    Is data entry for this section finished?
    C4684556 (UMLS CUI-1)
    C1828479 (UMLS CUI-2)
    C0205197 (UMLS CUI-3)
    Is data entry for this section finished?
    Item
    Is data entry for this section finished?
    boolean
    C4684556 (UMLS CUI [1,1])
    C1828479 (UMLS CUI [1,2])
    C0205197 (UMLS CUI [1,3])
    Zum Seitenanfang zurückkehren 

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