ID

40184

Description

https://www.hl7.org/fhir/resourcelist.html (accessed at 26.01.2020) This form contains an incomplete implementation of the FHIR Resource Research Subject (1). After preliminary review, it contains the data elements that request clinical information.

Lien

https://www.hl7.org/fhir/resourcelist.html

Mots-clés

Versions (3)
  1. 24/02/2020 24/02/2020 -
  2. 05/03/2020 05/03/2020 -
  3. 18/03/2020 18/03/2020 -
Détendeur de droits

HL7 FHIR

Téléchargé le

18 mars 2020

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 4.0
Modèle Commentaires :

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FHIR v4.0.1

Anglais

Resource Research Subject (1)

1 Formulaires  
ResearchSubject
Description

ResearchSubject

Alias
UMLS CUI-1
C0080105
ResearchSubject.status
Description

The current state of the subject. This element is labeled as a modifier because it is a status element that contains status entered-in-error which means that the resource should not be treated as valid.

Type de données

text

Alias
UMLS CUI [1,1]
C0080105
UMLS CUI [1,2]
C0449438
ResearchSubject.period
Description

The dates the subject began and ended their participation in the study.

Type de données

durationDatetime

Alias
UMLS CUI [1,1]
C0080105
UMLS CUI [1,2]
C0808070
UMLS CUI [1,3]
C0679823
UMLS CUI [2,1]
C0080105
UMLS CUI [2,2]
C0679823
UMLS CUI [2,3]
C0806020
UMLS CUI [3,1]
C0080105
UMLS CUI [3,2]
C0679823
UMLS CUI [3,3]
C0449238
ResearchSubject.study
Description

Reference to the study the subject is participating in.

Type de données

text

Alias
UMLS CUI [1,1]
C0080105
UMLS CUI [1,2]
C1706462
UMLS CUI [1,3]
C0008972
UMLS CUI [1,4]
C0679823
ResearchSubject.assignedArm
Description

The name of the arm in the study the subject is expected to follow as part of this study.

Type de données

text

Alias
UMLS CUI [1,1]
C0080105
UMLS CUI [1,2]
C1522541
UMLS CUI [1,3]
C0027365
UMLS CUI [1,4]
C1516050
ResearchSubject.actualArm
Description

The name of the arm in the study the subject actually followed as part of this study.

Type de données

text

Alias
UMLS CUI [1,1]
C0080105
UMLS CUI [1,2]
C1522541
UMLS CUI [1,3]
C3900116
ResearchSubject.consent
Description

A record of the patient's informed agreement to participate in the study.

Type de données

text

Alias
UMLS CUI [1,1]
C0080105
UMLS CUI [1,2]
C0021430
UMLS CUI [1,3]
C2355580
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Similar models

Resource Research Subject (1)

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
ResearchSubject
C0080105 (UMLS CUI-1)
ResearchSubject.status
Item
ResearchSubject.status
text
C0080105 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
ResearchSubject.period
Item
ResearchSubject.period
durationDatetime
C0080105 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
C0679823 (UMLS CUI [1,3])
C0080105 (UMLS CUI [2,1])
C0679823 (UMLS CUI [2,2])
C0806020 (UMLS CUI [2,3])
C0080105 (UMLS CUI [3,1])
C0679823 (UMLS CUI [3,2])
C0449238 (UMLS CUI [3,3])
ResearchSubject.study
Item
ResearchSubject.study
text
C0080105 (UMLS CUI [1,1])
C1706462 (UMLS CUI [1,2])
C0008972 (UMLS CUI [1,3])
C0679823 (UMLS CUI [1,4])
ResearchSubject.assignedArm
Item
ResearchSubject.assignedArm
text
C0080105 (UMLS CUI [1,1])
C1522541 (UMLS CUI [1,2])
C0027365 (UMLS CUI [1,3])
C1516050 (UMLS CUI [1,4])
ResearchSubject.actualArm
Item
ResearchSubject.actualArm
text
C0080105 (UMLS CUI [1,1])
C1522541 (UMLS CUI [1,2])
C3900116 (UMLS CUI [1,3])
ResearchSubject.consent
Item
ResearchSubject.consent
text
C0080105 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C2355580 (UMLS CUI [1,3])
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