ID

39948

Beschreibung

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

Link

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

Stichworte

Versionen (3)
  1. 24.02.20 24.02.20 -
  2. 05.03.20 05.03.20 -
  3. 18.03.20 18.03.20 -
Rechteinhaber

HL7 FHIR

Hochgeladen am

5. März 2020

DOI

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Creative Commons BY-NC 4.0
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FHIR v4.0.1

Englisch

Resource ResearchSubject (1)

1 Formulare  
ResearchSubject
Beschreibung

ResearchSubject

Alias
UMLS CUI-1
C0080105
ResearchSubject.status
Beschreibung

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.

Datentyp

text

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

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

Datentyp

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
Beschreibung

Reference to the study the subject is participating in.

Datentyp

text

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

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

Datentyp

text

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

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

Datentyp

text

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

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

Datentyp

text

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

Resource ResearchSubject (1)

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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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