ID

44280

Description

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

Link

https://aktin.org/

Keywords

Versions (4)
  1. 5/14/18 5/14/18 - Sarah Riepenhausen
  2. 5/14/18 5/14/18 - Sarah Riepenhausen
  3. 5/14/18 5/14/18 - Sarah Riepenhausen
  4. 9/20/21 9/20/21 -
Copyright Holder

AKTIN Projekt

Uploaded on

September 20, 2021

DOI

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License

Creative Commons BY-NC 3.0
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AKTIN: Basismodul des Notaufnahmeprotokolls

German English

Emergency Anamnesis, Ailments, basic patient data and allergies

5 forms  
Emergency Anamnesis
Description

Emergency Anamnesis

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

Emergency Anamnesis of the patient

Data type

text

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

Date and Time of first contact with emergency room physician

Data type

datetime

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

Medication Anamnesis

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

Name of Active Ingredient

Data type

text

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

Code of Active Ingredient

Data type

text

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

Active ingredient concentration/content

Data type

text

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

Dosage Form of active ingredient

Data type

text

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

Pharmaceutical preparation name

Data type

text

Alias
UMLS CUI [1]
C2360065
Pharmaceutical Prearation code
Description

Pharmaceutical Prearation code

Data type

text

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

Pharmaceutical Preparation content

Data type

text

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

Dosage Form of Pharmaceutical Preparation

Data type

text

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

Dose and Dose unit

Data type

text

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

Dose rate (continuous administration)

Data type

text

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

(Start) Date and time of Administration

Data type

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
Description

Stop date and time of administration of pharmaceutical preparation

Data type

datetime

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

Dosage Form of Administration

Data type

text

Alias
UMLS CUI [1]
C0013058
Route of Administration
Description

Route of Administration

Data type

text

Alias
UMLS CUI [1]
C0013153
Indication
Description

Indication

Data type

text

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

Prehospital emergency Medication

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

Name of Active Ingredient

Data type

text

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

Code of Active Ingredient

Data type

text

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

Active ingredient concentration/content

Data type

text

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

Dosage Form of active ingredient

Data type

text

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

Pharmaceutical preparation name

Data type

text

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

Pharmaceutical Prearation code

Data type

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
Description

Pharmaceutical Preparation content

Data type

text

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

Dosage Form of Pharmaceutical Preparation

Data type

text

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

Dose and Dose unit

Data type

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)
Description

Dose rate (continuous administration)

Data type

text

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

(Start) Date and time of Administration

Data type

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
Description

Stop date and time of administration of pharmaceutical preparation

Data type

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
Description

Dosage Form of Administration

Data type

text

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

Route of Administration

Data type

text

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

Indication

Data type

text

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

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
Description

Medical condition leading to emergency room contact

Data type

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
Description

Medical condition leading to Emergency Room Contact - CEDIS

Data type

text

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

Duration of Symptoms

Data type

float

Measurement units
  • h
Alias
UMLS CUI [1]
C0436359
h
Patient Basic Clinical Data
Description

Patient Basic Clinical Data

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

Pregnancy Status

Data type

integer

Alias
UMLS CUI [1]
C0032961
Tetanus vaccination status
Description

Tetanus vaccination status

Data type

integer

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

(Modified) Rankin Scale Score

Data type

integer

Alias
UMLS CUI [1]
C2984908
Multiple Drug Resistence
Description

Multiple Drug Resistence

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

Type of multidrug-resistent pathogen

Data type

text

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

multidrug-resistent pathogen status

Data type

text

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

Allergies

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

Allergy / Intolerance

Data type

boolean

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

Hypersensitivity to antibiotics

Data type

boolean

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

Allergy to Contrast agents

Data type

boolean

Alias
UMLS CUI [1]
C0570562
Other allergy
Description

Other allergy

Data type

boolean

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

Description of Allergy

Data type

text

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0678257
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Similar models

Emergency Anamnesis, Ailments, basic patient data and allergies

5 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
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