ID

44280

Beskrivning

AKTIN: Verbesserung der Versorgungsforschung in der Akutmedizin in Deutschland durch den Aufbau eines Nationalen Notaufnahmeregisters (Establishment of a German Registry for Emergency Room Care) This study is the Basic module of the Emergency Room protocol used for the AKTIN project (Version v2015.2-b from 2018-03-23). https://aktin.org/ ODM derived from http://art-decor.org/decor/services/RetrieveTransaction?language=de-DE&version=2018-03-23T20%3A16%3A38&hidecolumns=45ghi&id=2.16.840.1.113883.2.6.60.3.1.3&effectiveDate=2015-11-01T00%3A00%3A00&format=html

Länk

https://aktin.org/

Nyckelord

Versioner (4)
  1. 2018-05-14 2018-05-14 - Sarah Riepenhausen
  2. 2018-05-14 2018-05-14 - Sarah Riepenhausen
  3. 2018-05-14 2018-05-14 - Sarah Riepenhausen
  4. 2021-09-20 2021-09-20 -
Rättsinnehavare

AKTIN Projekt

Uppladdad den

20 september 2021

DOI

För en begäran logga in.

Licens

Creative Commons BY-NC 3.0
Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Tillbaka till modellkommentarer
Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

AKTIN: Basismodul des Notaufnahmeprotokolls

Tysk Engelsk

Emergency Anamnesis, Ailments, basic patient data and allergies

5 Formulär  
Emergency Anamnesis
Beskrivning

Emergency Anamnesis

Alias
UMLS CUI-1
C0013956
UMLS CUI-2
C0199182
Emergency Anamnesis of the patient
Beskrivning

Emergency Anamnesis of the patient

Datatyp

text

Alias
UMLS CUI [1,1]
C0199182
UMLS CUI [1,2]
C0013956
Date and Time of first contact with emergency room physician
Beskrivning

Date and Time of first contact with emergency room physician

Datatyp

datetime

Alias
UMLS CUI [1,1]
C1264639
UMLS CUI [1,2]
C0332158
UMLS CUI [1,3]
C0031831
Medication Anamnesis
Beskrivning

Medication Anamnesis

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C0199182
Name of Active Ingredient
Beskrivning

Name of Active Ingredient

Datatyp

text

Alias
UMLS CUI [1]
C1372955
Code of Active Ingredient
Beskrivning

Code of Active Ingredient

Datatyp

text

Alias
UMLS CUI [1]
C3242405
Active ingredient concentration/content
Beskrivning

Active ingredient concentration/content

Datatyp

text

Alias
UMLS CUI [1,1]
C1372955
UMLS CUI [1,2]
C0456205
Dosage Form of active ingredient
Beskrivning

Dosage Form of active ingredient

Datatyp

text

Alias
UMLS CUI [1,1]
C1372955
UMLS CUI [1,2]
C0013058
Pharmaceutical preparation name
Beskrivning

Pharmaceutical preparation name

Datatyp

text

Alias
UMLS CUI [1]
C2360065
Pharmaceutical Prearation code
Beskrivning

Pharmaceutical Prearation code

Datatyp

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0805701
UMLS CUI [1,3]
C0600091
Pharmaceutical Preparation content
Beskrivning

Pharmaceutical Preparation content

Datatyp

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0456205
Dosage Form of Pharmaceutical Preparation
Beskrivning

Dosage Form of Pharmaceutical Preparation

Datatyp

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0013058
Dose and Dose unit
Beskrivning

Dose and Dose unit

Datatyp

text

Alias
UMLS CUI [1]
C0869039
UMLS CUI [2]
C3174092
Dose rate (continuous administration)
Beskrivning

Dose rate (continuous administration)

Datatyp

text

Alias
UMLS CUI [1,1]
C0684252
UMLS CUI [1,2]
C0549178
(Start) Date and time of Administration
Beskrivning

(Start) Date and time of Administration

Datatyp

datetime

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C1301880
UMLS CUI [1,3]
C0013227
Stop date and time of administration of pharmaceutical preparation
Beskrivning

Stop date and time of administration of pharmaceutical preparation

Datatyp

datetime

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C1522314
UMLS CUI [1,3]
C0013227
Dosage Form of Administration
Beskrivning

Dosage Form of Administration

Datatyp

text

Alias
UMLS CUI [1]
C0013058
Route of Administration
Beskrivning

Route of Administration

Datatyp

text

Alias
UMLS CUI [1]
C0013153
Indication
Beskrivning

Indication

Datatyp

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0013227
Prehospital emergency Medication
Beskrivning

Prehospital emergency Medication

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C0033021
Name of Active Ingredient
Beskrivning

Name of Active Ingredient

Datatyp

text

Alias
UMLS CUI [1,1]
C1372955
UMLS CUI [1,2]
C0033021
Code of Active Ingredient
Beskrivning

Code of Active Ingredient

Datatyp

text

Alias
UMLS CUI [1,1]
C3242405
UMLS CUI [1,2]
C0033021
Active ingredient concentration/content
Beskrivning

Active ingredient concentration/content

Datatyp

text

Alias
UMLS CUI [1,1]
C1372955
UMLS CUI [1,2]
C0456205
UMLS CUI [1,3]
C0033021
Dosage Form of active ingredient
Beskrivning

Dosage Form of active ingredient

Datatyp

text

Alias
UMLS CUI [1,1]
C1372955
UMLS CUI [1,2]
C0013058
UMLS CUI [1,3]
C0033021
Pharmaceutical preparation name
Beskrivning

Pharmaceutical preparation name

Datatyp

text

Alias
UMLS CUI [1,1]
C2360065
UMLS CUI [1,2]
C0033021
Pharmaceutical Prearation code
Beskrivning

Pharmaceutical Prearation code

Datatyp

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0805701
UMLS CUI [1,3]
C0600091
UMLS CUI [1,4]
C0033021
Pharmaceutical Preparation content
Beskrivning

Pharmaceutical Preparation content

Datatyp

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0456205
UMLS CUI [1,3]
C0033021
Dosage Form of Pharmaceutical Preparation
Beskrivning

Dosage Form of Pharmaceutical Preparation

Datatyp

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0013058
UMLS CUI [1,3]
C0033021
Dose and Dose unit
Beskrivning

Dose and Dose unit

Datatyp

text

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0033021
UMLS CUI [2,1]
C3174092
UMLS CUI [2,2]
C0033021
Dose rate (continuous administration)
Beskrivning

Dose rate (continuous administration)

Datatyp

text

Alias
UMLS CUI [1,1]
C0684252
UMLS CUI [1,2]
C0549178
UMLS CUI [1,3]
C0033021
(Start) Date and time of Administration
Beskrivning

(Start) Date and time of Administration

Datatyp

datetime

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C1301880
UMLS CUI [1,3]
C0013227
UMLS CUI [1,4]
C0033021
Stop date and time of administration of pharmaceutical preparation
Beskrivning

Stop date and time of administration of pharmaceutical preparation

Datatyp

datetime

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C1522314
UMLS CUI [1,3]
C0013227
UMLS CUI [1,4]
C0033021
Dosage Form of Administration
Beskrivning

Dosage Form of Administration

Datatyp

text

Alias
UMLS CUI [1,1]
C0013058
UMLS CUI [1,2]
C0033021
Route of Administration
Beskrivning

Route of Administration

Datatyp

text

Alias
UMLS CUI [1,1]
C0013153
UMLS CUI [1,2]
C0033021
Indication
Beskrivning

Indication

Datatyp

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0033021
Medical condition leading to Emergency Room contact
Beskrivning

Medical condition leading to Emergency Room contact

Alias
UMLS CUI-1
C0583237
UMLS CUI-2
C0205476
UMLS CUI-3
C0348080
Medical condition leading to emergency room contact
Beskrivning

Medical condition leading to emergency room contact

Datatyp

text

Alias
UMLS CUI [1,1]
C0583237
UMLS CUI [1,2]
C0205476
UMLS CUI [1,3]
C0348080
Medical condition leading to Emergency Room Contact - CEDIS
Beskrivning

Medical condition leading to Emergency Room Contact - CEDIS

Datatyp

text

Alias
UMLS CUI [1,1]
C0583237
UMLS CUI [1,2]
C0205476
UMLS CUI [1,3]
C0348080
Duration of Symptoms
Beskrivning

Duration of Symptoms

Datatyp

float

Måttenheter
  • h
Alias
UMLS CUI [1]
C0436359
h
Patient Basic Clinical Data
Beskrivning

Patient Basic Clinical Data

Alias
UMLS CUI-1
C1516606
UMLS CUI-2
C2707520
UMLS CUI-3
C0178499
Pregnancy Status
Beskrivning

Pregnancy Status

Datatyp

integer

Alias
UMLS CUI [1]
C0032961
Tetanus vaccination status
Beskrivning

Tetanus vaccination status

Datatyp

integer

Alias
UMLS CUI [1,1]
C0199807
UMLS CUI [1,2]
C1443394
(Modified) Rankin Scale Score
Beskrivning

(Modified) Rankin Scale Score

Datatyp

integer

Alias
UMLS CUI [1]
C2984908
Multiple Drug Resistence
Beskrivning

Multiple Drug Resistence

Alias
UMLS CUI-1
C0242640
Type of multidrug-resistent pathogen
Beskrivning

Type of multidrug-resistent pathogen

Datatyp

text

Alias
UMLS CUI [1]
C1444089
multidrug-resistent pathogen status
Beskrivning

multidrug-resistent pathogen status

Datatyp

text

Alias
UMLS CUI [1,1]
C0450254
UMLS CUI [1,2]
C0242640
UMLS CUI [1,3]
C0449438
Allergies
Beskrivning

Allergies

Alias
UMLS CUI-1
C0020517
UMLS CUI-2
C0262926
Allergy / Intolerance
Beskrivning

Allergy / Intolerance

Datatyp

boolean

Alias
UMLS CUI [1]
C0020517
UMLS CUI [2]
C1744706
Hypersensitivity to antibiotics
Beskrivning

Hypersensitivity to antibiotics

Datatyp

boolean

Alias
UMLS CUI [1]
C0455591
Allergy to Contrast agents
Beskrivning

Allergy to Contrast agents

Datatyp

boolean

Alias
UMLS CUI [1]
C0570562
Other allergy
Beskrivning

Other allergy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0205394
Description of Allergy
Beskrivning

Description of Allergy

Datatyp

text

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0678257
Tillbaka till toppen

Similar models

Emergency Anamnesis, Ailments, basic patient data and allergies

5 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C0013956 (UMLS CUI-1)
C0199182 (UMLS CUI-2)
Emergency Anamnesis of the patient
Item
text
C0199182 (UMLS CUI [1,1])
C0013956 (UMLS CUI [1,2])
Date and Time of first contact with emergency room physician
Item
datetime
C1264639 (UMLS CUI [1,1])
C0332158 (UMLS CUI [1,2])
C0031831 (UMLS CUI [1,3])
Item Group
C0013227 (UMLS CUI-1)
C0199182 (UMLS CUI-2)
Name of Active Ingredient
Item
text
C1372955 (UMLS CUI [1])
Code of Active Ingredient
Item
text
C3242405 (UMLS CUI [1])
Active ingredient concentration/content
Item
text
C1372955 (UMLS CUI [1,1])
C0456205 (UMLS CUI [1,2])
Dosage Form of active ingredient
Item
text
C1372955 (UMLS CUI [1,1])
C0013058 (UMLS CUI [1,2])
Pharmaceutical preparation name
Item
text
C2360065 (UMLS CUI [1])
Pharmaceutical Prearation code
Item
text
C0013227 (UMLS CUI [1,1])
C0805701 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
Pharmaceutical Preparation content
Item
text
C0013227 (UMLS CUI [1,1])
C0456205 (UMLS CUI [1,2])
Dosage Form of Pharmaceutical Preparation
Item
text
C0013227 (UMLS CUI [1,1])
C0013058 (UMLS CUI [1,2])
Dose and Dose unit
Item
text
C0869039 (UMLS CUI [1])
C3174092 (UMLS CUI [2])
Dose rate (continuous administration)
Item
text
C0684252 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])
(Start) Date and time of Administration
Item
datetime
C0808070 (UMLS CUI [1,1])
C1301880 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
Stop date and time of administration of pharmaceutical preparation
Item
datetime
C0806020 (UMLS CUI [1,1])
C1522314 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
Dosage Form of Administration
Item
text
C0013058 (UMLS CUI [1])
Route of Administration
Item
text
C0013153 (UMLS CUI [1])
Indication
Item
text
C3146298 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Item Group
C0013227 (UMLS CUI-1)
C0033021 (UMLS CUI-2)
Name of Active Ingredient
Item
text
C1372955 (UMLS CUI [1,1])
C0033021 (UMLS CUI [1,2])
Code of Active Ingredient
Item
text
C3242405 (UMLS CUI [1,1])
C0033021 (UMLS CUI [1,2])
Active ingredient concentration/content
Item
text
C1372955 (UMLS CUI [1,1])
C0456205 (UMLS CUI [1,2])
C0033021 (UMLS CUI [1,3])
Dosage Form of active ingredient
Item
text
C1372955 (UMLS CUI [1,1])
C0013058 (UMLS CUI [1,2])
C0033021 (UMLS CUI [1,3])
Pharmaceutical preparation name
Item
text
C2360065 (UMLS CUI [1,1])
C0033021 (UMLS CUI [1,2])
Pharmaceutical Prearation code
Item
text
C0013227 (UMLS CUI [1,1])
C0805701 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C0033021 (UMLS CUI [1,4])
Pharmaceutical Preparation content
Item
text
C0013227 (UMLS CUI [1,1])
C0456205 (UMLS CUI [1,2])
C0033021 (UMLS CUI [1,3])
Dosage Form of Pharmaceutical Preparation
Item
text
C0013227 (UMLS CUI [1,1])
C0013058 (UMLS CUI [1,2])
C0033021 (UMLS CUI [1,3])
Dose and Dose unit
Item
text
C0869039 (UMLS CUI [1,1])
C0033021 (UMLS CUI [1,2])
C3174092 (UMLS CUI [2,1])
C0033021 (UMLS CUI [2,2])
Dose rate (continuous administration)
Item
text
C0684252 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])
C0033021 (UMLS CUI [1,3])
(Start) Date and time of Administration
Item
datetime
C0808070 (UMLS CUI [1,1])
C1301880 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C0033021 (UMLS CUI [1,4])
Stop date and time of administration of pharmaceutical preparation
Item
datetime
C0806020 (UMLS CUI [1,1])
C1522314 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C0033021 (UMLS CUI [1,4])
Dosage Form of Administration
Item
text
C0013058 (UMLS CUI [1,1])
C0033021 (UMLS CUI [1,2])
Route of Administration
Item
text
C0013153 (UMLS CUI [1,1])
C0033021 (UMLS CUI [1,2])
Indication
Item
text
C3146298 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0033021 (UMLS CUI [1,3])
Item Group
C0583237 (UMLS CUI-1)
C0205476 (UMLS CUI-2)
C0348080 (UMLS CUI-3)
Medical condition leading to emergency room contact
Item
text
C0583237 (UMLS CUI [1,1])
C0205476 (UMLS CUI [1,2])
C0348080 (UMLS CUI [1,3])
Medical condition leading to Emergency Room Contact - CEDIS
Item
text
C0583237 (UMLS CUI [1,1])
C0205476 (UMLS CUI [1,2])
C0348080 (UMLS CUI [1,3])
Duration of Symptoms
Item
float
C0436359 (UMLS CUI [1])
Item Group
C1516606 (UMLS CUI-1)
C2707520 (UMLS CUI-2)
C0178499 (UMLS CUI-3)
Item
integer
C0032961 (UMLS CUI [1])
Pregnancy Status
Code List
Pregnancy Status
CL Item
 (1)
C0549206 (UMLS CUI-1)
(Comment:de)
CL Item
 (2)
C0232973 (UMLS CUI-1)
(Comment:de)
CL Item
 (0)
C0686905 (UMLS CUI-1)
C0552579 (UMLS CUI-2)
C1272460 (UMLS CUI-4)
(Comment:de)
Item
integer
C0199807 (UMLS CUI [1,1])
C1443394 (UMLS CUI [1,2])
Tetanus vaccination status
Code List
Tetanus vaccination status
CL Item
 (1)
C0199807 (UMLS CUI-1)
(Comment:de)
CL Item
 (2)
C0199807 (UMLS CUI-1)
C1298908 (UMLS CUI-2)
(Comment:de)
CL Item
 (0)
C0199807 (UMLS CUI-1)
C0439673 (UMLS CUI-2)
(Comment:de)
Item
integer
C2984908 (UMLS CUI [1])
(Modified) Rankin Scale Score
Code List
(Modified) Rankin Scale Score
CL Item
 (0)
C2984908 (UMLS CUI-1)
C0919414 (UMLS CUI-2)
(Comment:de)
CL Item
 (1)
C2984908 (UMLS CUI-1)
C0205447 (UMLS CUI-2)
(Comment:de)
CL Item
 (2)
C2984908 (UMLS CUI-1)
C0205448 (UMLS CUI-2)
(Comment:de)
CL Item
 (3)
C2984908 (UMLS CUI-1)
C0205449 (UMLS CUI-2)
(Comment:de)
CL Item
 (4)
C2984908 (UMLS CUI-1)
C0205450 (UMLS CUI-2)
(Comment:de)
CL Item
 (5)
C2984908 (UMLS CUI-1)
C0205451 (UMLS CUI-2)
(Comment:de)
CL Item
 (6)
C2984908 (UMLS CUI-1)
C0205452 (UMLS CUI-2)
(Comment:de)
Item Group
C0242640 (UMLS CUI-1)
Item
text
C1444089 (UMLS CUI [1])
Type of multiresistent pathogen
Code List
Type of multidrug-resistent pathogen
CL Item
 (MRSA)
C1265292 (UMLS CUI-1)
(Comment:de)
CL Item
 (3-MRGN)
C4076168 (UMLS CUI-1)
C0018150 (UMLS CUI-2)
C0205449 (UMLS CUI-3)
(Comment:de)
CL Item
 (4-MRGN)
C4076168 (UMLS CUI-1)
C0018150 (UMLS CUI-2)
C0205450 (UMLS CUI-3)
(Comment:de)
CL Item
 (VRE)
C1265175 (UMLS CUI-1)
(Comment:de)
CL Item
 (andere)
C1444089 (UMLS CUI-1)
C0205394 (UMLS CUI-2)
(Comment:de)
Item
text
C0450254 (UMLS CUI [1,1])
C0242640 (UMLS CUI [1,2])
C0449438 (UMLS CUI [1,3])
multidrug-resistent pathogen status
Code List
multidrug-resistent pathogen status
CL Item
 (Ja)
C1444089 (UMLS CUI-1)
C1298907 (UMLS CUI-2)
(Comment:de)
CL Item
 (Verdacht)
C1444089 (UMLS CUI-1)
C0750491 (UMLS CUI-2)
(Comment:de)
CL Item
 (Nein)
C1444089 (UMLS CUI-1)
C1513916 (UMLS CUI-2)
(Comment:de)
Item Group
C0020517 (UMLS CUI-1)
C0262926 (UMLS CUI-2)
Allergy / Intolerance
Item
boolean
C0020517 (UMLS CUI [1])
C1744706 (UMLS CUI [2])
Hypersensitivity to antibiotics
Item
boolean
C0455591 (UMLS CUI [1])
Allergy to Contrast agents
Item
boolean
C0570562 (UMLS CUI [1])
Other allergy
Item
boolean
C0020517 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Description of Allergy
Item
text
C0020517 (UMLS CUI [1,1])
C0678257 (UMLS CUI [1,2])
Tillbaka till toppen 

Kontakt

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Hjälp

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial