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HIS radiotherapy form prostate cancer

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  1. 2013-05-15 2013-05-15 -
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15 maj 2013

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    HIS radiotherapy form prostate cancer

    Tysk Engelsk

    HIS

    1 Formulär  
    1. StudyEvent: HIS
      1. HIS
    Admininstrative Daten
    Beskrivning

    Admininstrative Daten

    Patient surname
    Beskrivning

    Name

    Datatyp

    string

    Alias
    UMLS CUI-1
    C0421448
    SNOMED CT-1
    184096005
    Patient forename
    Beskrivning

    Vorname

    Datatyp

    string

    Alias
    UMLS CUI-1
    C0421447
    SNOMED CT-1
    184095009
    Patient title
    Beskrivning

    Titel

    Datatyp

    string

    Alias
    Code-1
    Patient title (observable entity)
    UMLS CUI-1
    C0421450
    SNOMED CT-1
    184098006
    former Patient name
    Beskrivning

    früherer Name

    Datatyp

    string

    Alias
    Code-1
    Previous
    UMLS CUI-1
    C0205156
    SNOMED CT-1
    9130008
    Code-2
    Patient name (observable entity)
    UMLS CUI-2
    C1299487
    SNOMED CT-2
    371484003
    Patient date of birth
    Beskrivning

    Geburtsdatum

    Datatyp

    date

    Alias
    UMLS CUI-1
    C0421451
    SNOMED CT-1
    184099003
    patient age
    Beskrivning

    Alter

    Datatyp

    integer

    Alias
    Code-1
    patient age
    UMLS CUI-1
    CL386174
    Ethnicity / related nationality data
    Beskrivning

    Nationalität

    Datatyp

    string

    Alias
    UMLS CUI-1
    C0438960
    SNOMED CT-1
    186034007
    Code-2
    Patients
    UMLS CUI-2
    C0030705
    SNOMED CT-2
    116154003
    Street Address
    Beskrivning

    Adresse

    Datatyp

    string

    Alias
    UMLS CUI-1
    C1301826
    SNOMED CT-1
    398099009
    Code-2
    Patient address
    UMLS CUI-2
    C0421449
    SNOMED CT-2
    184097001
    Patient postal code
    Beskrivning

    PLZ

    Datatyp

    integer

    Alias
    UMLS CUI-1
    C0421454
    SNOMED CT-1
    184102003
    Code-2
    Patient address
    UMLS CUI-2
    C0421449
    SNOMED CT-2
    184097001
    City of residence
    Beskrivning

    Stadt

    Datatyp

    string

    Alias
    UMLS CUI-1
    C2316883
    SNOMED CT-1
    433178008
    Code-2
    Patient address
    UMLS CUI-2
    C0421449
    SNOMED CT-2
    184097001
    Case Identifier
    Beskrivning

    Fallnummer

    Datatyp

    integer

    Alias
    Code-1
    Case - situation (qualifier value)
    UMLS CUI-1
    C0868928
    SNOMED CT-1
    398241000
    Code-2
    Identifier
    UMLS CUI-2
    C0600091
    SNOMED CT-2
    118522005
    Tumordiagnose
    Beskrivning

    Tumordiagnose

    Cancer Diagnosis
    Beskrivning

    Tumordiagnose (ICD-10)

    Datatyp

    string

    Alias
    Code-1
    Tumor finding (finding)
    UMLS CUI-1
    C1274082
    SNOMED CT-1
    395557000
    Code-2
    Diagnosis ICD code
    UMLS CUI-2
    C2598420
    Date of diagnosis
    Beskrivning

    Diagnose-Datum

    Datatyp

    date

    Alias
    UMLS CUI-1
    C2316983
    SNOMED CT-1
    432213005
    Code-2
    Tumor finding (finding)
    UMLS CUI-2
    C1274082
    SNOMED CT-2
    395557000
    Therapeutic radiology procedure
    Beskrivning

    Therapeutic radiology procedure

    Guideline Adherence
    Beskrivning

    Wird die Therapie nach Leitlinien durchgeführt

    Datatyp

    boolean

    Alias
    Item-Info
    must_have
    UMLS CUI-1
    C0525059
    Reason for Guidelines Adherence
    Beskrivning

    falls nein

    Datatyp

    string

    Alias
    Code-1
    Indication of (contextual qualifier)
    UMLS CUI-1
    C0392360
    SNOMED CT-1
    410666004
    LOINC-1
    MTHU008862
    Code-2
    Guideline Adherence
    UMLS CUI-2
    C0525059
    Tumortherapie allgemein
    Beskrivning

    Tumortherapie allgemein

    Intent
    Beskrivning

    Intention

    Datatyp

    integer

    Alias
    UMLS CUI-1
    C1283828
    SNOMED CT-1
    367565008
    Code-2
    Therapeutic radiology procedure
    UMLS CUI-2
    C1522449
    SNOMED CT-2
    108290001
    MedDRA-2
    10037794
    Bestrahlung
    Beskrivning

    Bestrahlung

    Organ target(s)
    Beskrivning

    Zielgebiet

    Datatyp

    integer

    Alias
    Item-Info
    must_have
    UMLS CUI-1
    C0807185
    Radiotherapy Technique
    Beskrivning

    Technik

    Datatyp

    integer

    Alias
    Item-Info
    must_have
    Code-1
    Technique
    UMLS CUI-1
    C0449851
    SNOMED CT-1
    246501002
    Code-2
    Therapeutic radiology procedure
    UMLS CUI-2
    C1522449
    SNOMED CT-2
    108290001
    MedDRA-2
    10037770
    Radiation
    Beskrivning

    Strahlenart

    Datatyp

    integer

    Alias
    Code-Info
    for_compare
    UMLS CUI-1
    C0851346
    SNOMED CT-1
    82107009
    LOINC-1
    MTHU026213
    Start Radiotherapy
    Beskrivning

    Begonnen am

    Datatyp

    date

    Alias
    Code-1
    Radiotherapy started (situation)
    UMLS CUI-1
    C0436382
    SNOMED CT-1
    168531007
    End Radiotherapy
    Beskrivning

    Ende am

    Datatyp

    date

    Alias
    Code-1
    Radiotherapy completed (situation)
    UMLS CUI-1
    C0436385
    SNOMED CT-1
    168534004
    total amount of radiation
    Beskrivning

    Gesamtdosis

    Datatyp

    string

    Alias
    Code-1
    Radiotherapy Dosage
    UMLS CUI-1
    C0034620
    Therapiebeurteilung
    Beskrivning

    Therapiebeurteilung

    Termination of Radiotherapy
    Beskrivning

    Beendigung der Strahlentherapie

    Datatyp

    integer

    Alias
    Item-Info
    must_have
    Code-1
    Radiotherapy stopped (situation)
    UMLS CUI-1
    C0436384
    SNOMED CT-1
    168533005
    ECOG performance status grade
    Beskrivning

    Allgemeiner Leistungszustand (nach ECOG)

    Datatyp

    integer

    Alias
    UMLS CUI-1
    C1632812
    Common Terminology Criteria for Adverse Events
    Beskrivning

    Common Terminology Criteria for Adverse Events

    Adverse event
    Beskrivning

    Nebenwirkungen

    Datatyp

    boolean

    Alias
    Code-Info
    for_compare
    UMLS CUI-1
    C0877248
    MedDRA-1
    10060933
    LOINC-1
    MTHU014542
    Genitourinary system
    Beskrivning

    Niere/Blase

    Datatyp

    integer

    Alias
    Code-1
    Renal or Genitourinary Other Adverse Event
    UMLS CUI-1
    C1558061
    CTCAE-1
    MTHU117419
    Gastrointestinal system
    Beskrivning

    Gastrointestinaltrakt

    Datatyp

    integer

    Alias
    Code-1
    Adverse Event Associated with the Gastrointestinal System
    UMLS CUI-1
    C1559265
    CTCAE-1
    MTHU112146
    Fever
    Beskrivning

    Fieber

    Datatyp

    integer

    Alias
    Code-1
    Fever Without Neutropenia Adverse Event
    UMLS CUI-1
    C1556366
    CTCAE-1
    MTHU116933
    Infection
    Beskrivning

    Infektion

    Datatyp

    integer

    Alias
    Code-1
    Adverse Event Associated with Infection
    UMLS CUI-1
    C1556682
    CTCAE-1
    MTHU112135
    Laboratory Values
    Beskrivning

    Laborwerte

    Datatyp

    integer

    Alias
    Code-1
    Other Metabolic and Laboratory Adverse Event
    UMLS CUI-1
    C1559945
    CTCAE-1
    MTHU117254
    other adverse event
    Beskrivning

    Sonstige

    Datatyp

    integer

    Alias
    Code-1
    Adverse event
    UMLS CUI-1
    C0877248
    MedDRA-1
    10060933
    LOINC-1
    MTHU014542
    Tillbaka till toppen

    Similar models

    HIS

    1 Formulär
    1. StudyEvent: HIS
      1. HIS
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    Admininstrative Daten
    Name
    Item
    Patient surname
    string
    C0421448 (UMLS CUI-1)
    184096005 (SNOMED CT-1)
    Vorname
    Item
    Patient forename
    string
    C0421447 (UMLS CUI-1)
    184095009 (SNOMED CT-1)
    Titel
    Item
    Patient title
    string
    Patient title (observable entity) (Code-1)
    C0421450 (UMLS CUI-1)
    184098006 (SNOMED CT-1)
    früherer Name
    Item
    former Patient name
    string
    Previous (Code-1)
    C0205156 (UMLS CUI-1)
    9130008 (SNOMED CT-1)
    Patient name (observable entity) (Code-2)
    C1299487 (UMLS CUI-2)
    371484003 (SNOMED CT-2)
    Geburtsdatum
    Item
    Patient date of birth
    date
    C0421451 (UMLS CUI-1)
    184099003 (SNOMED CT-1)
    Alter
    Item
    patient age
    integer
    patient age (Code-1)
    CL386174 (UMLS CUI-1)
    Nationalität
    Item
    Ethnicity / related nationality data
    string
    C0438960 (UMLS CUI-1)
    186034007 (SNOMED CT-1)
    Patients (Code-2)
    C0030705 (UMLS CUI-2)
    116154003 (SNOMED CT-2)
    Adresse
    Item
    Street Address
    string
    C1301826 (UMLS CUI-1)
    398099009 (SNOMED CT-1)
    Patient address (Code-2)
    C0421449 (UMLS CUI-2)
    184097001 (SNOMED CT-2)
    PLZ
    Item
    Patient postal code
    integer
    C0421454 (UMLS CUI-1)
    184102003 (SNOMED CT-1)
    Patient address (Code-2)
    C0421449 (UMLS CUI-2)
    184097001 (SNOMED CT-2)
    Stadt
    Item
    City of residence
    string
    C2316883 (UMLS CUI-1)
    433178008 (SNOMED CT-1)
    Patient address (Code-2)
    C0421449 (UMLS CUI-2)
    184097001 (SNOMED CT-2)
    Fallnummer
    Item
    Case Identifier
    integer
    Case - situation (qualifier value) (Code-1)
    C0868928 (UMLS CUI-1)
    398241000 (SNOMED CT-1)
    Identifier (Code-2)
    C0600091 (UMLS CUI-2)
    118522005 (SNOMED CT-2)
    Item Group
    Tumordiagnose
    Tumordiagnose (ICD-10)
    Item
    Cancer Diagnosis
    string
    Tumor finding (finding) (Code-1)
    C1274082 (UMLS CUI-1)
    395557000 (SNOMED CT-1)
    Diagnosis ICD code (Code-2)
    C2598420 (UMLS CUI-2)
    Diagnose-Datum
    Item
    Date of diagnosis
    date
    C2316983 (UMLS CUI-1)
    432213005 (SNOMED CT-1)
    Tumor finding (finding) (Code-2)
    C1274082 (UMLS CUI-2)
    395557000 (SNOMED CT-2)
    Item Group
    Therapeutic radiology procedure
    Wird die Therapie nach Leitlinien durchgeführt
    Item
    Guideline Adherence
    boolean
    must_have (Item-Info)
    C0525059 (UMLS CUI-1)
    falls nein
    Item
    Reason for Guidelines Adherence
    string
    Indication of (contextual qualifier) (Code-1)
    C0392360 (UMLS CUI-1)
    410666004 (SNOMED CT-1)
    MTHU008862 (LOINC-1)
    Guideline Adherence (Code-2)
    C0525059 (UMLS CUI-2)
    Item Group
    Tumortherapie allgemein
    Item
    Intent
    integer
    C1283828 (UMLS CUI-1)
    367565008 (SNOMED CT-1)
    Therapeutic radiology procedure (Code-2)
    C1522449 (UMLS CUI-2)
    108290001 (SNOMED CT-2)
    10037794 (MedDRA-2)
    Intention
    Code List
    Intent
    CL Item
    Curative - procedure intent  (kurativ)
    Curative - procedure intent (qualifier value) (Code-1)
    C1276305 (UMLS CUI-1)
    373808002 (SNOMED CT-1)
    CL Item
    Palliative - procedure intent (palliativ)
    Palliative - procedure intent (qualifier value) (Code-1)
    C1285530 (UMLS CUI-1)
    363676003 (SNOMED CT-1)
    CL Item
    Adjuvant - intent (adjuvant)
    Adjuvant - intent (qualifier value) (Code-1)
    C1298675 (UMLS CUI-1)
    373846009 (SNOMED CT-1)
    CL Item
    Neo-adjuvant - intent  (neoadjuvant)
    Neo-adjuvant - intent (qualifier value) (Code-1)
    C1298676 (UMLS CUI-1)
    373847000 (SNOMED CT-1)
    Item Group
    Bestrahlung
    Item
    Organ target(s)
    integer
    must_have (Item-Info)
    C0807185 (UMLS CUI-1)
    Zielgebiet
    Code List
    Organ target(s)
    CL Item
    Prostate  (Prostata)
    Prostate (Code-1)
    C0033572 (UMLS CUI-1)
    41216001 (SNOMED CT-1)
    MTHU004957 (LOINC-1)
    CL Item
    not_useful_for_research (Prostata + LK kleines Becken)
    CL Item
    not_useful_for_research (Prostata + pelvine paraaortale LK im Bauchraum)
    CL Item
    not_useful_for_research (Prostataloge)
    CL Item
    not_useful_for_research (Prostataloge + LK kleines Becken)
    CL Item
    not_useful_for_research (Prostataloge + pelvine paraaortale LK im Bauchraum)
    CL Item
    not_useful_for_research (sonstiges)
    CL Item
    Sonstiges (Other)
    C0205394 (UMLS CUI-1)
    74964007 (SNOMED CT-1)
    Item
    Radiotherapy Technique
    integer
    must_have (Item-Info)
    Technique (Code-1)
    C0449851 (UMLS CUI-1)
    246501002 (SNOMED CT-1)
    Therapeutic radiology procedure (Code-2)
    C1522449 (UMLS CUI-2)
    108290001 (SNOMED CT-2)
    10037770 (MedDRA-2)
    Technik
    Code List
    Radiotherapy Technique
    CL Item
    Teleradiotherapy procedure (percutane Strahlentherapie)
    Teleradiotherapy procedure (procedure) (Code-1)
    C0419095 (UMLS CUI-1)
    33195004 (SNOMED CT-1)
    CL Item
    PDR temporary Brachytherapy (PDR temporäre Brachytherapie)
    Brachytherapy (Code-1)
    C0006098 (UMLS CUI-1)
    399315003 (SNOMED CT-1)
    10061018 (MedDRA-1)
    Temporary (Code-2)
    C0205374 (UMLS CUI-2)
    14803004 (SNOMED CT-2)
    pulsed-dose rate brachytherapy (Code-3)
    CL413609 (UMLS CUI-3)
    CL Item
    HDR temporary Brachytherapy (HDR temporäre Brachytherapie)
    Brachytherapy (Code-1)
    C0006098 (UMLS CUI-1)
    399315003 (SNOMED CT-1)
    10061018 (MedDRA-1)
    Temporary (Code-2)
    C0205374 (UMLS CUI-2)
    14803004 (SNOMED CT-2)
    High-Dose Rate Brachytherapy (Code-3)
    C0454270 (UMLS CUI-3)
    228867005 (SNOMED CT-3)
    CL Item
    Brachytherapy (Brachytherapie)
    Brachytherapy (Code-1)
    C0006098 (UMLS CUI-1)
    399315003 (SNOMED CT-1)
    10061018 (MedDRA-1)
    Item
    Radiation
    integer
    for_compare (Code-Info)
    C0851346 (UMLS CUI-1)
    82107009 (SNOMED CT-1)
    MTHU026213 (LOINC-1)
    Strahlenart
    Code List
    Radiation
    CL Item
    Iridium 192 (IR-Iridium-192)
    ^192^Iridium (substance) (Code-1)
    C0303472 (UMLS CUI-1)
    48341001 (SNOMED CT-1)
    CL Item
    Iodine-125  (J1-Jod-125)
    Iodine-125 (Code-1)
    C0796396 (UMLS CUI-1)
    68630002 (SNOMED CT-1)
    CL Item
    Palladium Pd-103  (Palladium Pd-103 )
    Palladium Pd-103 (Code-1)
    C0303566 (UMLS CUI-1)
    9351000 (SNOMED CT-1)
    Begonnen am
    Item
    Start Radiotherapy
    date
    Radiotherapy started (situation) (Code-1)
    C0436382 (UMLS CUI-1)
    168531007 (SNOMED CT-1)
    Ende am
    Item
    End Radiotherapy
    date
    Radiotherapy completed (situation) (Code-1)
    C0436385 (UMLS CUI-1)
    168534004 (SNOMED CT-1)
    Gesamtdosis
    Item
    total amount of radiation
    string
    Radiotherapy Dosage (Code-1)
    C0034620 (UMLS CUI-1)
    Item Group
    Therapiebeurteilung
    Item
    Termination of Radiotherapy
    integer
    must_have (Item-Info)
    Radiotherapy stopped (situation) (Code-1)
    C0436384 (UMLS CUI-1)
    168533005 (SNOMED CT-1)
    Beendigung der Strahlentherapie
    Code List
    Termination of Radiotherapy
    CL Item
    regular End of Therapy (reguläres Ende)
    Regular (Code-1)
    C0449581 (UMLS CUI-1)
    17854005 (SNOMED CT-1)
    End (Code-2)
    C1272693 (UMLS CUI-2)
    385656004 (SNOMED CT-2)
    CL Item
    Discontinue because of adverse effects (Abbruch wegen Nebenwirkungen)
    Adverse effects (Code-1)
    C0879626 (UMLS CUI-1)
    281647001 (SNOMED CT-1)
    10067484 (MedDRA-1)
    Discontinue (Code-2)
    C1444662 (UMLS CUI-2)
    410546004 (SNOMED CT-2)
    Indication of (contextual qualifier) (Code-3)
    C0392360 (UMLS CUI-3)
    230165009 (SNOMED CT-3)
    MTHU008319 (LOINC-3)
    CL Item
    Refusal of Treatment (Patient verweigert die Therapie)
    C0040809 (UMLS CUI-1)
    105480006 (SNOMED CT-1)
    10056407 (MedDRA-1)
    Item
    ECOG performance status grade
    integer
    C1632812 (UMLS CUI-1)
    Allgemeiner Leistungszustand (nach ECOG)
    Code List
    ECOG performance status grade
    CL Item
    0 (0)
    Eastern Cooperative Oncology Group performance status - grade 0 (finding) (Code-1)
    C1828078 (UMLS CUI-1)
    25389002 (SNOMED CT-1)
    CL Item
    1 (1)
    Eastern Cooperative Oncology Group performance status - grade 1 (finding) (Code-1)
    C1827388 (UMLS CUI-1)
    422512005 (SNOMED CT-1)
    CL Item
    2 (2)
    Eastern Cooperative Oncology Group performance status - grade 2 (finding) (Code-1)
    C1828242 (UMLS CUI-1)
    422894000 (SNOMED CT-1)
    CL Item
    3 (3)
    Eastern Cooperative Oncology Group performance status - grade 3 (finding) (Code-1)
    C1827126 (UMLS CUI-1)
    423053003 (SNOMED CT-1)
    CL Item
    4 (4)
    Eastern Cooperative Oncology Group performance status - grade 4 (finding) (Code-1)
    C1827528 (UMLS CUI-1)
    423237006 (SNOMED CT-1)
    Item Group
    Common Terminology Criteria for Adverse Events
    Nebenwirkungen
    Item
    Adverse event
    boolean
    for_compare (Code-Info)
    C0877248 (UMLS CUI-1)
    10060933 (MedDRA-1)
    MTHU014542 (LOINC-1)
    Item
    Genitourinary system
    integer
    Renal or Genitourinary Other Adverse Event (Code-1)
    C1558061 (UMLS CUI-1)
    MTHU117419 (CTCAE-1)
    Niere/Blase
    Code List
    Genitourinary system
    CL Item
    no adverse event (0 = keine Nebenwirkungen)
    Absent Adverse Event (Code-1)
    C2699517 (UMLS CUI-1)
    CL Item
    mild adverse event (1 = geringe/leichte Nebenwirkungen)
    Mild Adverse Event (Code-1)
    C1513302 (UMLS CUI-1)
    CL Item
    moderate adverse event (2 = mäßige / deutliche Nebenwirkungen)
    Moderate Adverse Event (Code-1)
    C1513374 (UMLS CUI-1)
    CL Item
    strong adverse event (3 = starke / ausgeprägte Nebenwirkungen)
    Severe Adverse Event (Code-1)
    C1519275 (UMLS CUI-1)
    CL Item
    Life Threatening adverse event (4 = lebensbedrohliche Nebenwirkungen)
    Life Threatening Adverse Event (Code-1)
    C1517874 (UMLS CUI-1)
    CL Item
    unknown adverse event (X = Grad der Nebenwirkungen unbekannt)
    Unknown (Code-1)
    C0439673 (UMLS CUI-1)
    261665006 (SNOMED CT-1)
    Item
    Gastrointestinal system
    integer
    Adverse Event Associated with the Gastrointestinal System (Code-1)
    C1559265 (UMLS CUI-1)
    MTHU112146 (CTCAE-1)
    Gastrointestinaltrakt
    Code List
    Gastrointestinal system
    CL Item
    no adverse event (0 = keine Nebenwirkungen)
    Absent Adverse Event (Code-1)
    C2699517 (UMLS CUI-1)
    CL Item
    mild adverse event (1 = geringe/leichte Nebenwirkungen)
    Mild Adverse Event (Code-1)
    C1513302 (UMLS CUI-1)
    CL Item
    moderate adverse event (2 = mäßige / deutliche Nebenwirkungen)
    Moderate Adverse Event (Code-1)
    C1513374 (UMLS CUI-1)
    CL Item
    strong adverse event (3 = starke / ausgeprägte Nebenwirkungen)
    Severe Adverse Event (Code-1)
    C1519275 (UMLS CUI-1)
    CL Item
    Life Threatening adverse event (4 = lebensbedrohliche Nebenwirkungen)
    Life Threatening Adverse Event (Code-1)
    C1517874 (UMLS CUI-1)
    CL Item
    unknown adverse event (X = Grad der Nebenwirkungen unbekannt)
    Unknown (Code-1)
    C0439673 (UMLS CUI-1)
    261665006 (SNOMED CT-1)
    Item
    Fever
    integer
    Fever Without Neutropenia Adverse Event (Code-1)
    C1556366 (UMLS CUI-1)
    MTHU116933 (CTCAE-1)
    Fieber
    Code List
    Fever
    CL Item
    no adverse event (0 = keine)
    Absent Adverse Event (Code-1)
    C2699517 (UMLS CUI-1)
    CL Item
    mild adverse event (1 = gering/leicht)
    Mild Adverse Event (Code-1)
    C1513302 (UMLS CUI-1)
    CL Item
    moderate adverse event (2 = mäßig/deutlich)
    Moderate Adverse Event (Code-1)
    C1513374 (UMLS CUI-1)
    CL Item
    strong adverse event (3 = stark/ausgeprägt)
    Severe Adverse Event (Code-1)
    C1519275 (UMLS CUI-1)
    CL Item
    Life Threatening adverse event (4 = lebensbedrohlich)
    Life Threatening Adverse Event (Code-1)
    C1517874 (UMLS CUI-1)
    CL Item
    unknown adverse event (X = Nebenwirkungen unbekannt)
    Unknown (Code-1)
    C0439673 (UMLS CUI-1)
    261665006 (SNOMED CT-1)
    CL Item
    only in connection with Infection (only in connection with Infection)
    Item
    Infection
    integer
    Adverse Event Associated with Infection (Code-1)
    C1556682 (UMLS CUI-1)
    MTHU112135 (CTCAE-1)
    Infektion
    Code List
    Infection
    CL Item
    no adverse event (0 = keine)
    Absent Adverse Event (Code-1)
    C2699517 (UMLS CUI-1)
    CL Item
    mild adverse event (1 = gering/leicht)
    Mild Adverse Event (Code-1)
    C1513302 (UMLS CUI-1)
    CL Item
    moderate adverse event (2 = mäßig/deutlich)
    Moderate Adverse Event (Code-1)
    C1513374 (UMLS CUI-1)
    CL Item
    strong adverse event (3 = stark/ausgeprägt)
    Severe Adverse Event (Code-1)
    C1519275 (UMLS CUI-1)
    CL Item
    Life Threatening adverse event (4 = lebensbedrohlich)
    Life Threatening Adverse Event (Code-1)
    C1517874 (UMLS CUI-1)
    CL Item
    unknown adverse event (X = Nebenwirkungen unbekannt)
    Unknown (Code-1)
    C0439673 (UMLS CUI-1)
    261665006 (SNOMED CT-1)
    CL Item
    only in connection with fever (only in connection with fever)
    Item
    Laboratory Values
    integer
    Other Metabolic and Laboratory Adverse Event (Code-1)
    C1559945 (UMLS CUI-1)
    MTHU117254 (CTCAE-1)
    Laborwerte
    Code List
    Laboratory Values
    CL Item
    no adverse event (0 = keine Nebenwirkungen)
    Absent Adverse Event (Code-1)
    C2699517 (UMLS CUI-1)
    CL Item
    mild adverse event (1 = geringe/leichte Nebenwirkungen)
    Mild Adverse Event (Code-1)
    C1513302 (UMLS CUI-1)
    CL Item
    moderate adverse event (2 = mäßige / deutliche Nebenwirkungen)
    Moderate Adverse Event (Code-1)
    C1513374 (UMLS CUI-1)
    CL Item
    strong adverse event (3 = starke / ausgeprägte Nebenwirkungen)
    Severe Adverse Event (Code-1)
    C1519275 (UMLS CUI-1)
    CL Item
    Life Threatening adverse event (4 = lebensbedrohliche Nebenwirkungen)
    Life Threatening Adverse Event (Code-1)
    C1517874 (UMLS CUI-1)
    CL Item
    unknown adverse event (X = Grad der Nebenwirkungen unbekannt)
    Unknown (Code-1)
    C0439673 (UMLS CUI-1)
    261665006 (SNOMED CT-1)
    Item
    other adverse event
    integer
    Adverse event (Code-1)
    C0877248 (UMLS CUI-1)
    10060933 (MedDRA-1)
    MTHU014542 (LOINC-1)
    Sonstige
    Code List
    other adverse event
    CL Item
    no adverse event (0 = keine Nebenwirkungen)
    Absent Adverse Event (Code-1)
    C2699517 (UMLS CUI-1)
    CL Item
    mild adverse event (1 = geringe/leichte Nebenwirkungen)
    Mild Adverse Event (Code-1)
    C1513302 (UMLS CUI-1)
    CL Item
    moderate adverse event (2 = mäßige / deutliche Nebenwirkungen)
    Moderate Adverse Event (Code-1)
    C1513374 (UMLS CUI-1)
    CL Item
    strong adverse event (3 = starke / ausgeprägte Nebenwirkungen)
    Severe Adverse Event (Code-1)
    C1519275 (UMLS CUI-1)
    CL Item
    Life Threatening adverse event (4 = lebensbedrohliche Nebenwirkungen)
    Life Threatening Adverse Event (Code-1)
    C1517874 (UMLS CUI-1)
    CL Item
    unknown adverse event (X = Grad der Nebenwirkungen unbekannt)
    Unknown (Code-1)
    C0439673 (UMLS CUI-1)
    261665006 (SNOMED CT-1)
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