1. StudyEvent: HIS
    1. HIS
Admininstrative Daten
Descrizione

Admininstrative Daten

Patienten-Nachname
Descrizione

Name

Tipo di dati

string

Alias
UMLS CUI-1
C0421448
SNOMED CT-1
184096005
Patienten-Vorname
Descrizione

Vorname

Tipo di dati

string

Alias
UMLS CUI-1
C0421447
SNOMED CT-1
184095009
Patienten-Titel
Descrizione

Titel

Tipo di dati

string

Alias
Code-1
Patient title (observable entity)
UMLS CUI-1
C0421450
SNOMED CT-1
184098006
früherer Name
Descrizione

früherer Name

Tipo di dati

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
Patienten-Geburtsdatum
Descrizione

Geburtsdatum

Tipo di dati

date

Alias
UMLS CUI-1
C0421451
SNOMED CT-1
184099003
Alter des Patienten
Descrizione

Alter

Tipo di dati

integer

Alias
Code-1
patient age
UMLS CUI-1
CL386174
Nationalität/Staatsangehörigkeit
Descrizione

Nationalität

Tipo di dati

string

Alias
UMLS CUI-1
C0438960
SNOMED CT-1
186034007
Code-2
Patients
UMLS CUI-2
C0030705
SNOMED CT-2
116154003
Straße
Descrizione

Adresse

Tipo di dati

string

Alias
UMLS CUI-1
C1301826
SNOMED CT-1
398099009
Code-2
Patient address
UMLS CUI-2
C0421449
SNOMED CT-2
184097001
Postleitzahl Patient
Descrizione

PLZ

Tipo di dati

integer

Alias
UMLS CUI-1
C0421454
SNOMED CT-1
184102003
Wohnort
Descrizione

Stadt

Tipo di dati

string

Alias
UMLS CUI-1
C2316883
SNOMED CT-1
433178008
Code-2
Patient address
UMLS CUI-2
C0421449
SNOMED CT-2
184097001
Fallnummer
Descrizione

Fallnummer

Tipo di dati

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
Studienbogen
Descrizione

Studienbogen

Name der Studie
Descrizione

Name der Studie

Tipo di dati

string

Alias
Code-1
Trial name
UMLS CUI-1
C1629065
LOINC-1
MTHU019350
Intention der Therapie
Descrizione

Therapieart

Tipo di dati

integer

Alias
Code-1
Intent
UMLS CUI-1
C1283828
SNOMED CT-1
367565008
Code-2
Therapeutic procedure
UMLS CUI-2
C0087111
SNOMED CT-2
277132007
MedDRA-2
10053757
LOINC-2
MTHU008880
Einschlussdatum
Descrizione

Einschluss in die Studie

Tipo di dati

date

Alias
Code-1
Date in time
UMLS CUI-1
C0011008
SNOMED CT-1
410671006
LOINC-1
MTHU021546
Code-2
Inclusion Criteria
UMLS CUI-2
C1512693
Zyklen geplant
Descrizione

geplante Zyklen

Tipo di dati

integer

Alias
Code-1
Plan
UMLS CUI-1
C1301732
SNOMED CT-1
397943006
Code-2
Chemotherapy cycle (procedure)
UMLS CUI-2
C1302181
SNOMED CT-2
399042005
Zyklen durchgeführt
Descrizione

tatsächliche Zyklen

Tipo di dati

integer

Alias
Code-1
Execution
UMLS CUI-1
C1705848
Code-2
Chemotherapy cycle (procedure)
UMLS CUI-2
C1302181
SNOMED CT-2
399042005
letztes Follow-Up
Descrizione

letztes Follow-Up

Tipo di dati

date

Alias
Code-1
Date last contact
UMLS CUI-1
C0805839
LOINC-1
MTHU010432
Vital Status
Descrizione

Status

Tipo di dati

integer

Alias
Code-1
Vital Status
UMLS CUI-1
C1148433
Datum Staging
Descrizione

Staging am

Tipo di dati

date

Alias
Code-1
disease stage
UMLS CUI-1
C0699749
Code-2
Date in time
UMLS CUI-2
C0011008
SNOMED CT-2
410671006
LOINC-2
MTHU021546
Ergebnis Staging
Descrizione

Ergebnis Staging

Tipo di dati

string

Alias
Code-1
disease stage
UMLS CUI-1
C0699749
Code-2
Result
UMLS CUI-2
C1274040
SNOMED CT-2
394617004

Similar models

  1. StudyEvent: HIS
    1. HIS
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Admininstrative Daten
Name
Item
Patienten-Nachname
string
C0421448 (UMLS CUI-1)
184096005 (SNOMED CT-1)
Vorname
Item
Patienten-Vorname
string
C0421447 (UMLS CUI-1)
184095009 (SNOMED CT-1)
Titel
Item
Patienten-Titel
string
Patient title (observable entity) (Code-1)
C0421450 (UMLS CUI-1)
184098006 (SNOMED CT-1)
früherer Name
Item
früherer 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
Patienten-Geburtsdatum
date
C0421451 (UMLS CUI-1)
184099003 (SNOMED CT-1)
Alter
Item
Alter des Patienten
integer
patient age (Code-1)
CL386174 (UMLS CUI-1)
Nationalität
Item
Nationalität/Staatsangehörigkeit
string
C0438960 (UMLS CUI-1)
186034007 (SNOMED CT-1)
Patients (Code-2)
C0030705 (UMLS CUI-2)
116154003 (SNOMED CT-2)
Adresse
Item
Straße
string
C1301826 (UMLS CUI-1)
398099009 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
PLZ
Item
Postleitzahl Patient
integer
C0421454 (UMLS CUI-1)
184102003 (SNOMED CT-1)
Stadt
Item
Wohnort
string
C2316883 (UMLS CUI-1)
433178008 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
Fallnummer
Item
Fallnummer
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
Studienbogen
Name der Studie
Item
Name der Studie
string
Trial name (Code-1)
C1629065 (UMLS CUI-1)
MTHU019350 (LOINC-1)
Item
Intention der Therapie
integer
Intent (Code-1)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Therapeutic procedure (Code-2)
C0087111 (UMLS CUI-2)
277132007 (SNOMED CT-2)
10053757 (MedDRA-2)
MTHU008880 (LOINC-2)
Code List
Intention der Therapie
CL Item
Neoadjuvant (neoadjuvant)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
CL Item
Adjuvant (adjuvant)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
CL Item
Palliativ (palliativ)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
Einschluss in die Studie
Item
Einschlussdatum
date
Date in time (Code-1)
C0011008 (UMLS CUI-1)
410671006 (SNOMED CT-1)
MTHU021546 (LOINC-1)
Inclusion Criteria (Code-2)
C1512693 (UMLS CUI-2)
geplante Zyklen
Item
Zyklen geplant
integer
Plan (Code-1)
C1301732 (UMLS CUI-1)
397943006 (SNOMED CT-1)
Chemotherapy cycle (procedure) (Code-2)
C1302181 (UMLS CUI-2)
399042005 (SNOMED CT-2)
tatsächliche Zyklen
Item
Zyklen durchgeführt
integer
Execution (Code-1)
C1705848 (UMLS CUI-1)
Chemotherapy cycle (procedure) (Code-2)
C1302181 (UMLS CUI-2)
399042005 (SNOMED CT-2)
letztes Follow-Up
Item
letztes Follow-Up
date
Date last contact (Code-1)
C0805839 (UMLS CUI-1)
MTHU010432 (LOINC-1)
Item
Vital Status
integer
Vital Status (Code-1)
C1148433 (UMLS CUI-1)
Code List
Vital Status
CL Item
unbekannt (unknown)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Patient lebt (alive)
Alive (finding) (Code-1)
C2584946 (UMLS CUI-1)
438949009 (SNOMED CT-1)
CL Item
Patient verstorben (dead)
Patient died (finding) (Code-1)
C1306577 (UMLS CUI-1)
397709008 (SNOMED CT-1)
10011906 (MedDRA-1)
Staging am
Item
Datum Staging
date
disease stage (Code-1)
C0699749 (UMLS CUI-1)
Date in time (Code-2)
C0011008 (UMLS CUI-2)
410671006 (SNOMED CT-2)
MTHU021546 (LOINC-2)
Ergebnis Staging
Item
Ergebnis Staging
string
disease stage (Code-1)
C0699749 (UMLS CUI-1)
Result (Code-2)
C1274040 (UMLS CUI-2)
394617004 (SNOMED CT-2)