ID

14887

Beschrijving

NINDS Common Data Elements (Cardiac End Points; Friedreich´s Ataxia) Used from the National Institute of Neurological Disorders and Stroke Common Data Elements (https://www.commondataelements.ninds.nih.gov/) References: Grinnon ST, Miller K, Marler JR, Lu Y, Stout A, Odenkirchen J, Kunitz S. National Institute of Neurological Disorders and Stroke Common Data Element Project - approach and methods. Clin Trials. 2012;9(3):322-9.

Link

https://www.commondataelements.ninds.nih.gov/

Trefwoorden

Versies (1)
  1. 04-05-16 04-05-16 -
Geüploaded op

4 mei 2016

DOI

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Licentie

Creative Commons BY-NC 3.0
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NINDS CDE Cardiac End Points Friedreich´s Ataxia

Engels

Cardiac End Points

1 Formulieren  
  1. StudyEvent: ODM
    1. Cardiac End Points
Cardiac End Points
Beschrijving

Cardiac End Points

Study ID
Beschrijving

Study ID

Datatype

text

Alias
UMLS CUI [1]
C2826693
Study site name
Beschrijving

Study site

Datatype

text

Alias
UMLS CUI [1]
C2825164
Subject ID
Beschrijving

Subject ID

Datatype

text

Alias
UMLS CUI [1]
C2348585
Classify the subject using the ACC/AHA Stage of Heart Failure
Beschrijving

ACC/AHA Stage of Heart Failure

Datatype

integer

Alias
UMLS CUI [1,1]
C0002458
UMLS CUI [1,2]
C0018801
Indicate the number of hospitalizations the participant had in the past year
Beschrijving

Number of hospitalizations

Datatype

integer

Alias
UMLS CUI [1,1]
C0750480
UMLS CUI [1,2]
C0019993
Indicate the start date of participants hospitalization
Beschrijving

Start date hospitalization

Datatype

date

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0808070
Indicate cause for hospitalization
Beschrijving

Reason for hospitalization

Datatype

integer

Alias
UMLS CUI [1]
C1830395
Reason for hospitalization:please specify if other reason than cardiovascular
Beschrijving

Reason for hospitalization

Datatype

text

Alias
UMLS CUI [1]
C1830395
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Similar models

Cardiac End Points

1 Formulieren
  1. StudyEvent: ODM
    1. Cardiac End Points
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Cardiac End Points
Study ID
Item
Study ID
text
C2826693 (UMLS CUI [1])
Study site
Item
Study site name
text
C2825164 (UMLS CUI [1])
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Item
Classify the subject using the ACC/AHA Stage of Heart Failure
integer
C0002458 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
ACC/AHA Stage of Heart Failure
Code List
Classify the subject using the ACC/AHA Stage of Heart Failure
CL Item
(A) Patients at high risk of developing HF because of the presence of conditions that are strongly associated with the development of HF; such patients have no identified structural or functional abnormalities of the pericardium, myocardium, or cardiac valves and have never shown signs or symptoms of HF (1)
CL Item
(B) Patients who have developed structural heart disease that is strongly associated with the development of HF but who have never shown signs or symptoms of HF (2)
CL Item
(C) Patients who have current or prior symptoms of HF associated with underlying structural heart disease (3)
CL Item
(D) Patients with advanced structural heart disease and marked symptoms of HF at rest despite maximal medical therapy and who require specialized interventions (4)
Number of hospitalizations
Item
Indicate the number of hospitalizations the participant had in the past year
integer
C0750480 (UMLS CUI [1,1])
C0019993 (UMLS CUI [1,2])
Start date hospitalization
Item
Indicate the start date of participants hospitalization
date
C0019993 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Item
Indicate cause for hospitalization
integer
C1830395 (UMLS CUI [1])
Reason for hospitalization
Code List
Indicate cause for hospitalization
CL Item
Cardiovascular  (1)
CL Item
Other, specify (2)
Reason for hospitalization
Item
Reason for hospitalization:please specify if other reason than cardiovascular
text
C1830395 (UMLS CUI [1])
Terug naar het begin van de pagina 

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