ID

40184

Descripción

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.

Link

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

Palabras clave

  1. 24/2/20 24/2/20 -
  2. 5/3/20 5/3/20 -
  3. 18/3/20 18/3/20 -
Titular de derechos de autor

HL7 FHIR

Subido en

18 de marzo de 2020

DOI

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Licencia

Creative Commons BY-NC 4.0

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FHIR v4.0.1

Resource Research Subject (1)

ResearchSubject
Descripción

ResearchSubject

Alias
UMLS CUI-1
C0080105
ResearchSubject.status
Descripción

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.

Tipo de datos

text

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

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

Tipo de datos

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
Descripción

Reference to the study the subject is participating in.

Tipo de datos

text

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

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

Tipo de datos

text

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

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

Tipo de datos

text

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

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

Tipo de datos

text

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

Similar models

Resource Research Subject (1)

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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