ID

20978

Description

Hospital Routine Documentation Subform at the University Hospital Cologne Original Form name: DE Datenerfassung RIS

Mots-clés

  1. 01/04/2017 01/04/2017 -
Téléchargé le

1 avril 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Data entry RIS, University Hospital Cologne

Data entry RIS, University Hospital Cologne

Datenerfassung RIS
Description

Datenerfassung RIS

Alias
UMLS CUI-1
C0034601
UMLS CUI-2
C0748230
Diagnosing provider
Description

Diagnosing provider

Type de données

text

Alias
UMLS CUI [1,1]
C3260207
UMLS CUI [1,2]
C2607850
Person performing diagnosing
Description

Person performing diagnosing

Type de données

text

Alias
UMLS CUI [1]
C3260206
Pregnancy
Description

Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
Gonadal shielding
Description

Gonadal shielding

Type de données

boolean

Alias
UMLS CUI [1]
C0183268
Dose area product
Description

Dose area product

Type de données

float

Unités de mesure
  • mGy x cm²
Alias
UMLS CUI [1]
C1999052
UMLS CUI [2,1]
C1533134
UMLS CUI [2,2]
C0205146
UMLS CUI [2,3]
C1704444
mGy x cm²
Dose length product
Description

Dose length product

Type de données

float

Unités de mesure
  • mGy x cm
Alias
UMLS CUI [1]
C1999052
UMLS CUI [2]
C3539930
mGy x cm
Computed Tomography Dose Index Volume
Description

Computed Tomography Dose Index Volume

Type de données

float

Unités de mesure
  • mGy
Alias
UMLS CUI [1]
C3640003
mGy
Computed Tomography Dose Index (weighted)
Description

Computed Tomography Dose Index (weighted)

Type de données

float

Unités de mesure
  • mGy
Alias
UMLS CUI [1]
C3640003
mGy
Average Glandular Dose
Description

Average Glandular Dose

Type de données

float

Unités de mesure
  • mGy
Alias
UMLS CUI [1]
C1999052
UMLS CUI [2]
C0225353
mGy
Informed consent
Description

Informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Informed consent provider
Description

Informed consent provider

Type de données

text

Unités de mesure
  • Name
Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C3476341
Name
Informed consent date
Description

Informed consent date

Type de données

date

Unités de mesure
  • dd.mm.yyyy
Alias
UMLS CUI [1]
C2985782
dd.mm.yyyy
Informed consent given
Description

Informed consent given

Type de données

integer

Alias
UMLS CUI [1]
C0021430
Medication administered
Description

Medication administered

Type de données

text

Alias
UMLS CUI [1]
C0806914
Contrast media volume
Description

Contrast media volume

Type de données

integer

Unités de mesure
  • ml
Alias
UMLS CUI [1,1]
C0009924
UMLS CUI [1,2]
C0449971
ml
Complications, Adverse Reactions
Description

Complications, Adverse Reactions

Type de données

text

Alias
UMLS CUI [1]
C0009566
UMLS CUI [2]
C0559546
Severity complication/adverse reaction
Description

Severity complication/adverse reaction

Type de données

text

Alias
UMLS CUI [1,1]
C0392364
UMLS CUI [1,2]
C0559546
Note
Description

Note

Type de données

text

Alias
UMLS CUI [1]
C1317574
Patient rejected, reason for rejection
Description

Patient rejected, reason for rejection

Type de données

text

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1548437
UMLS CUI [1,3]
C0566251
Patient rejected, person rejecting patient
Description

Patient rejected, person rejecting patient

Type de données

text

Unités de mesure
  • Name
Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1548437
UMLS CUI [1,3]
C3476341
Name
Laboratory results
Description

Laboratory results

Type de données

text

Alias
UMLS CUI [1]
C1254595
Type of examination
Description

Type of examination

Type de données

text

Alias
UMLS CUI [1,1]
C0748230
UMLS CUI [1,2]
C0332307
Date and time of examination
Description

Date and time of examination

Type de données

datetime

Alias
UMLS CUI [1,1]
C1264639
UMLS CUI [1,2]
C0748230
Finding radiological exam
Description

Finding radiological exam

Type de données

text

Alias
UMLS CUI [1,1]
C0243095
UMLS CUI [1,2]
C0748230
Evaluation of examination
Description

Evaluation of examination

Type de données

text

Alias
UMLS CUI [1,1]
C0220825
UMLS CUI [1,2]
C0748230
Amount of incomplete examinations
Description

Amount of incomplete examinations

Type de données

float

Alias
UMLS CUI [1,1]
C0205257
UMLS CUI [1,2]
C0748230
UMLS CUI [1,3]
C0750480
Signature
Description

Signature

Type de données

text

Alias
UMLS CUI [1]
C1519316

Similar models

Data entry RIS, University Hospital Cologne

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Datenerfassung RIS
C0034601 (UMLS CUI-1)
C0748230 (UMLS CUI-2)
Diagnosing provider
Item
text
C3260207 (UMLS CUI [1,1])
C2607850 (UMLS CUI [1,2])
Person performing diagnosing
Item
text
C3260206 (UMLS CUI [1])
Pregnancy
Item
boolean
C0032961 (UMLS CUI [1])
Gonadal shielding
Item
boolean
C0183268 (UMLS CUI [1])
Dose area product
Item
float
C1999052 (UMLS CUI [1])
C1533134 (UMLS CUI [2,1])
C0205146 (UMLS CUI [2,2])
C1704444 (UMLS CUI [2,3])
Dose length product
Item
float
C1999052 (UMLS CUI [1])
C3539930 (UMLS CUI [2])
Computed Tomography Dose Index Volume
Item
float
C3640003 (UMLS CUI [1])
Computed Tomography Dose Index (weighted)
Item
float
C3640003 (UMLS CUI [1])
Average Glandular Dose
Item
float
C1999052 (UMLS CUI [1])
C0225353 (UMLS CUI [2])
Informed consent
Item
boolean
C0021430 (UMLS CUI [1])
Informed consent provider
Item
text
C0021430 (UMLS CUI [1,1])
C3476341 (UMLS CUI [1,2])
Informed consent date
Item
date
C2985782 (UMLS CUI [1])
Item
integer
C0021430 (UMLS CUI [1])
Code List
Informed consent given
CL Item
 (1)
CL Item
 (2)
Medication administered
Item
text
C0806914 (UMLS CUI [1])
Contrast media volume
Item
integer
C0009924 (UMLS CUI [1,1])
C0449971 (UMLS CUI [1,2])
Complications, Adverse Reactions
Item
text
C0009566 (UMLS CUI [1])
C0559546 (UMLS CUI [2])
Severity complication/adverse reaction
Item
text
C0392364 (UMLS CUI [1,1])
C0559546 (UMLS CUI [1,2])
Note
Item
text
C1317574 (UMLS CUI [1])
Patient rejected, reason for rejection
Item
text
C0030705 (UMLS CUI [1,1])
C1548437 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
Patient rejected, person rejecting patient
Item
text
C0030705 (UMLS CUI [1,1])
C1548437 (UMLS CUI [1,2])
C3476341 (UMLS CUI [1,3])
Laboratory results
Item
text
C1254595 (UMLS CUI [1])
Type of examination
Item
text
C0748230 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Date and time of examination
Item
datetime
C1264639 (UMLS CUI [1,1])
C0748230 (UMLS CUI [1,2])
Finding radiological exam
Item
text
C0243095 (UMLS CUI [1,1])
C0748230 (UMLS CUI [1,2])
Evaluation of examination
Item
text
C0220825 (UMLS CUI [1,1])
C0748230 (UMLS CUI [1,2])
Amount of incomplete examinations
Item
float
C0205257 (UMLS CUI [1,1])
C0748230 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,3])
Signature
Item
text
C1519316 (UMLS CUI [1])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

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