ID

4108

Descripción

HIS form from Soarian. Urologie Erlangen" with friendly permission of the urology Erlangen (Prof. Wullich) and the medical informatics department Erlangen (PD Dr. Bürkle)

Palabras clave

Versiones (1)
  1. 7/8/13 7/8/13 -
Subido en

7 de agosto de 2013

DOI

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Licencia

Creative Commons BY-NC 3.0 Legacy
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HIS radiotherapy form prostate cancer

Alemán Inglés

HIS

1 formularios  
  1. StudyEvent: HIS
    1. HIS
Admininstrative Daten
Descripción

Admininstrative Daten

Patient surname
Descripción

Name

Tipo de datos

string

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

Vorname

Tipo de datos

string

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

Titel

Tipo de datos

string

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

früherer Name

Tipo de datos

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
Descripción

Geburtsdatum

Tipo de datos

date

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

Alter

Tipo de datos

integer

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

Nationalität

Tipo de datos

string

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

Adresse

Tipo de datos

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
Descripción

PLZ

Tipo de datos

integer

Alias
UMLS CUI-1
C0421454
SNOMED CT-1
184102003
City of residence
Descripción

Stadt

Tipo de datos

string

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

Fallnummer

Tipo de datos

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
Descripción

Tumordiagnose

Cancer Diagnosis
Descripción

Tumordiagnose (ICD-10)

Tipo de datos

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
Descripción

Diagnose-Datum

Tipo de datos

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
Descripción

Therapeutic radiology procedure

Guideline Adherence
Descripción

Wird die Therapie nach Leitlinien durchgeführt

Tipo de datos

boolean

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

falls nein

Tipo de datos

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
Descripción

Tumortherapie allgemein

Intent
Descripción

Intention

Tipo de datos

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
Descripción

Bestrahlung

Organ target(s)
Descripción

Zielgebiet

Tipo de datos

integer

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

Technik

Tipo de datos

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
Descripción

Strahlenart

Tipo de datos

integer

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

Begonnen am

Tipo de datos

date

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

Ende am

Tipo de datos

date

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

Gesamtdosis

Tipo de datos

string

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

Therapiebeurteilung

Termination of Radiotherapy
Descripción

Beendigung der Strahlentherapie

Tipo de datos

integer

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

Allgemeiner Leistungszustand (nach ECOG)

Tipo de datos

integer

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

Common Terminology Criteria for Adverse Events

Adverse event
Descripción

Nebenwirkungen

Tipo de datos

boolean

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

Niere/Blase

Tipo de datos

integer

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

Gastrointestinaltrakt

Tipo de datos

integer

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

Fieber

Tipo de datos

integer

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

Infektion

Tipo de datos

integer

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

Laborwerte

Tipo de datos

integer

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

Sonstige

Tipo de datos

integer

Alias
Code-1
Adverse event
UMLS CUI-1
C0877248
MedDRA-1
10060933
LOINC-1
MTHU014542
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Similar models

HIS

1 formularios
  1. StudyEvent: HIS
    1. HIS
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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)
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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