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14935

Beskrivning

The MEDUSA project (medical education for sepsis source control and antibiotics) is a scientific study of the integrated research and treatment center "Center for Sepsis Control and Care" (CSCC) of the University Hospital Jena, Thuringia, Germany. Its aim is to investigate whether a multimodal and interdisciplinary training concept for the early recognition and standardized treatment of patients with sepsis improves time to administration of first antibiotic and survival of patients. Original forms obtained from: http://www.medusa.uniklinikum-jena.de/Datenerfassung.html

Länk

http://www.medusa.uniklinikum-jena.de/Datenerfassung.html

Nyckelord

Versioner (1)
  1. 09/05/2016 09/05/2016 -
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9 mai 2016

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Creative Commons BY-NC 3.0
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    Case Report Form Day 5 MEDUSA project

    Engelsk

    Diagnosis of blood culture report form

    1 Formulär  
    Header module
    Beskrivning

    Header module

    Study Subject ID
    Beskrivning

    Study Identifier

    Datatyp

    integer

    Alias
    UMLS CUI [1]
    C2826693
    document creator
    Beskrivning

    document creator

    Datatyp

    integer

    Alias
    UMLS CUI [1]
    C1707531
    Day 5 - general aspects of treatment
    Beskrivning

    Day 5 - general aspects of treatment

    Was the diagnosis of sepsis confirmed?
    Beskrivning

    Was the diagnosis of sepsis confirmed?

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0243026
    UMLS CUI [1,2]
    C0011900
    Other causes for organ dysfunction
    Beskrivning

    Other causes for organ dysfunction

    Datatyp

    integer

    Alias
    UMLS CUI [1]
    C0349410
    How was the diagnosis carried out?
    Beskrivning

    How was the diagnosis carried out?

    Datatyp

    integer

    Alias
    UMLS CUI [1]
    C0011900
    Lactate at day 2
    Beskrivning

    Lactate at day 2

    Datatyp

    integer

    Måttenheter
    • mmol/l
    Alias
    UMLS CUI [1]
    C0376261
    mmol/l
    Procalcitonin at day 3
    Beskrivning

    Procalcitonin at day 3

    Datatyp

    integer

    Måttenheter
    • ng/ml
    Alias
    UMLS CUI [1]
    C0072027
    ng/ml
    Procalcitonin at day 4
    Beskrivning

    Procalcitonin at day 4

    Datatyp

    integer

    Måttenheter
    • ng/ml
    Alias
    UMLS CUI [1]
    C0072027
    ng/ml
    Procalcitonin at day 5
    Beskrivning

    Procalcitonin at day 5

    Datatyp

    integer

    Måttenheter
    • ng/ml
    Alias
    UMLS CUI [1]
    C0072027
    ng/ml
    Blood culture results
    Beskrivning

    Blood culture results

    Result of blood culture
    Beskrivning

    Result of blood culture

    Datatyp

    integer

    Alias
    UMLS CUI [1]
    C0200949
    Identification of pathogenic agent
    Beskrivning

    only if blood culture is positive

    Datatyp

    integer

    Alias
    UMLS CUI [1]
    C1740302
    Blood culture result from primary source of infection
    Beskrivning

    Blood culture result from primary source of infection

    Blood culture result from primary source of infection
    Beskrivning

    Blood culture result from primary source of infection

    Datatyp

    integer

    Alias
    UMLS CUI [1,1]
    C0449426
    UMLS CUI [1,2]
    C2981519
    Identification of pathogenic agent from primary source of infection
    Beskrivning

    Identification of pathogenic agent from primary source of infection

    Datatyp

    integer

    Alias
    UMLS CUI [1,1]
    C1740302
    UMLS CUI [1,2]
    C0449426
    Is the pathogen sensitive to antibiotics?
    Beskrivning

    Is the pathogen sensitive to antibiotics?

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0860788
    Therapy alterations within first five days of treatment
    Beskrivning

    Therapy alterations within first five days of treatment

    Was the treatment changed within the first five days?
    Beskrivning

    Therapy change

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C3665894
    Typ of therapy change: Enhancement
    Beskrivning

    Typ of therapy change: Enhancement

    Datatyp

    integer

    Alias
    UMLS CUI [1]
    C3267098
    Therapy change: de-escalation
    Beskrivning

    Typ of therapy change: de-escalation

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C3651014
    Clinical outcome
    Beskrivning

    Clinical outcome

    Dialysis-dependent within first 14 days of treatment?
    Beskrivning

    dialysis-dependent

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0524376
    Day 28
    Beskrivning

    Day 28

    Status at day 28
    Beskrivning

    Status at day 28

    Datatyp

    integer

    Alias
    UMLS CUI [1]
    C0023913
    Discharge from intensive care unit
    Beskrivning

    Discharge from intensive care unit

    Reason for discharge from intensive care unit
    Beskrivning

    Reason for discharge from intensive care unit

    Datatyp

    integer

    Alias
    UMLS CUI [1]
    C4034196
    Hospital discharge
    Beskrivning

    Hospital discharge

    Hospital discharge
    Beskrivning

    Discharge

    Datatyp

    integer

    Alias
    UMLS CUI [1]
    C0586514
    Tillbaka till toppen

    Similar models

    Diagnosis of blood culture report form

    1 Formulär
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    Header module
    Study Identifier
    Item
    Study Subject ID
    integer
    C2826693 (UMLS CUI [1])
    document creator
    Item
    document creator
    integer
    C1707531 (UMLS CUI [1])
    Item Group
    Day 5 - general aspects of treatment
    Was the diagnosis of sepsis confirmed?
    Item
    Was the diagnosis of sepsis confirmed?
    boolean
    C0243026 (UMLS CUI [1,1])
    C0011900 (UMLS CUI [1,2])
    Item
    Other causes for organ dysfunction
    integer
    C0349410 (UMLS CUI [1])
    Other causes for organ dysfunction
    Code List
    Other causes for organ dysfunction
    CL Item
    not applicable, becuase organ dysfunction caused by sepsis (1)
    CL Item
    cardiogenic shock  (2)
    C0036980 (UMLS CUI-1)
    CL Item
    hemorrhagic shock (3)
    C0036982 (UMLS CUI-1)
    CL Item
    hypovolaemia (4)
    C0546884 (UMLS CUI-1)
    CL Item
    other cause (5)
    CL Item
    unknown (6)
    C0439673 (UMLS CUI-1)
    Item
    How was the diagnosis carried out?
    integer
    C0011900 (UMLS CUI [1])
    How was the diagnosis carried out?
    Code List
    How was the diagnosis carried out?
    CL Item
    microbiology procedure (1)
    C0085672 (UMLS CUI-1)
    CL Item
    clinical criteria (2)
    C3845710 (UMLS CUI-1)
    CL Item
    suspected infection (3)
    C3476266 (UMLS CUI-1)
    Lactate at day 2
    Item
    Lactate at day 2
    integer
    C0376261 (UMLS CUI [1])
    Procalcitonin at day 3
    Item
    Procalcitonin at day 3
    integer
    C0072027 (UMLS CUI [1])
    Procalcitonin at day 4
    Item
    Procalcitonin at day 4
    integer
    C0072027 (UMLS CUI [1])
    Procalcitonin at day 5
    Item
    Procalcitonin at day 5
    integer
    C0072027 (UMLS CUI [1])
    Item Group
    Blood culture results
    Item
    Result of blood culture
    integer
    C0200949 (UMLS CUI [1])
    Result of blood culture
    Code List
    Result of blood culture
    CL Item
    positive (pathogen) (1)
    C0159125 (UMLS CUI-1)
    CL Item
    positive (bacterial contamination) (2)
    C0159125 (UMLS CUI-1)
    C2349974 (UMLS CUI-2)
    CL Item
    negative (3)
    C0855652 (UMLS CUI-1)
    CL Item
    No blood culture (4)
    C0200949 (UMLS CUI-1)
    CL Item
    unknown (5)
    C0439673 (UMLS CUI-1)
    Item
    Identification of pathogenic agent
    integer
    C1740302 (UMLS CUI [1])
    Identification of pathogenic agent
    Code List
    Identification of pathogenic agent
    CL Item
    sensitive to treatment? (1)
    C0332324 (UMLS CUI-1)
    Item Group
    Blood culture result from primary source of infection
    Item
    Blood culture result from primary source of infection
    integer
    C0449426 (UMLS CUI [1,1])
    C2981519 (UMLS CUI [1,2])
    Blood culture result from primary source of infection
    Code List
    Blood culture result from primary source of infection
    CL Item
    positive (pathogen) (1)
    C0159125 (UMLS CUI-1)
    CL Item
    positive (bacterial contamination, human microbiome) (2)
    C1956109 (UMLS CUI-1)
    C0159125 (UMLS CUI-2)
    CL Item
    negative (3)
    C0205160 (UMLS CUI-1)
    C0200949 (UMLS CUI-2)
    CL Item
    no blood culture (4)
    C0200949 (UMLS CUI-1)
    CL Item
    unknown (5)
    C0439673 (UMLS CUI-1)
    Item
    Identification of pathogenic agent from primary source of infection
    integer
    C1740302 (UMLS CUI [1,1])
    C0449426 (UMLS CUI [1,2])
    Identification of pathogenic agent from primary source of infection
    Code List
    Identification of pathogenic agent from primary source of infection
    CL Item
    Pathogen (1)
    C0450254 (UMLS CUI-1)
    CL Item
    unknown (2)
    C0439673 (UMLS CUI-1)
    Is the pathogen sensitive to antibiotics?
    Item
    Is the pathogen sensitive to antibiotics?
    boolean
    C0860788 (UMLS CUI [1])
    Item Group
    Therapy alterations within first five days of treatment
    Therapy change
    Item
    Was the treatment changed within the first five days?
    boolean
    C3665894 (UMLS CUI [1])
    Item
    Typ of therapy change: Enhancement
    integer
    C3267098 (UMLS CUI [1])
    Typ of therapy change: Enhancement
    Code List
    Typ of therapy change: Enhancement
    CL Item
    date of therapy enhancement (1)
    C3267098 (UMLS CUI-1)
    C0011008 (UMLS CUI-2)
    CL Item
    clinical deterioration (2)
    C0563273 (UMLS CUI-1)
    CL Item
    calculated enhancement without clinical deterioration (3)
    C3267098 (UMLS CUI-1)
    C0868945 (UMLS CUI-2)
    CL Item
    resistance oriented enhancement (4)
    C0013203 (UMLS CUI-1)
    Item
    Therapy change: de-escalation
    text
    C3651014 (UMLS CUI [1])
    Typ of therapy change: de-escalation
    Code List
    Therapy change: de-escalation
    CL Item
    date of de-escalation (date of de-escalation)
    C3651014 (UMLS CUI-1)
    C0011008 (UMLS CUI-2)
    CL Item
    de-escalation in accordance with resistance (de-escalation in accordance with resitence)
    C3651014 (UMLS CUI-1)
    C0013203 (UMLS CUI-2)
    Item Group
    Clinical outcome
    dialysis-dependent
    Item
    Dialysis-dependent within first 14 days of treatment?
    boolean
    C0524376 (UMLS CUI [1])
    Item Group
    Day 28
    Item
    Status at day 28
    integer
    C0023913 (UMLS CUI [1])
    Status at day 28
    Code List
    Status at day 28
    CL Item
    Deceased (1)
    C0011065 (UMLS CUI-1)
    CL Item
    Survived (2)
    C0038952 (UMLS CUI-1)
    Item Group
    Discharge from intensive care unit
    Item
    Reason for discharge from intensive care unit
    integer
    C4034196 (UMLS CUI [1])
    Reason for discharge from intensive care unit
    Code List
    Reason for discharge from intensive care unit
    CL Item
    Date of discharge (1)
    C2361123 (UMLS CUI-1)
    CL Item
    Survived (2)
    C0038952 (UMLS CUI-1)
    CL Item
    Deceased (3)
    C0011065 (UMLS CUI-1)
    Item Group
    Hospital discharge
    Item
    Hospital discharge
    integer
    C0586514 (UMLS CUI [1])
    Discharge
    Code List
    Hospital discharge
    CL Item
    Date (1)
    C2361123 (UMLS CUI-1)
    CL Item
    Survived (2)
    C0038952 (UMLS CUI-1)
    CL Item
    Deceased (3)
    C0011065 (UMLS CUI-1)
    Tillbaka till toppen 

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