Eligibility Coronary Artery Disease NCT01623193

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients (male and female) undergoing isolated coronary artery bypass grafting,
Descrição

ID.1

Tipo de dados

boolean

isolated aortic or mitral repair or replacement, and
Descrição

ID.2

Tipo de dados

boolean

combined aortic or mitral valve repair or replacement and
Descrição

ID.3

Tipo de dados

boolean

coronary bypass grafting
Descrição

ID.4

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
reoperation,
Descrição

ID.5

Tipo de dados

boolean

endocarditis,
Descrição

ID.6

Tipo de dados

boolean

dialysis dependant renal failure,
Descrição

ID.7

Tipo de dados

boolean

pre-operative ecmo or lvad support,
Descrição

ID.8

Tipo de dados

boolean

contraindication to blood transfusion (ie. jehovah's witness), and
Descrição

ID.9

Tipo de dados

boolean

use of irreversible anti-platelet (other than asa) and anticoagulant agents within 48h (ie. plavix, dabigitran, gpiib/iiia inhibitors, argatroban).
Descrição

ID.10

Tipo de dados

boolean

Similar models

Eligibility Coronary Artery Disease NCT01623193

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients (male and female) undergoing isolated coronary artery bypass grafting,
boolean
ID.2
Item
isolated aortic or mitral repair or replacement, and
boolean
ID.3
Item
combined aortic or mitral valve repair or replacement and
boolean
ID.4
Item
coronary bypass grafting
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
reoperation,
boolean
ID.6
Item
endocarditis,
boolean
ID.7
Item
dialysis dependant renal failure,
boolean
ID.8
Item
pre-operative ecmo or lvad support,
boolean
ID.9
Item
contraindication to blood transfusion (ie. jehovah's witness), and
boolean
ID.10
Item
use of irreversible anti-platelet (other than asa) and anticoagulant agents within 48h (ie. plavix, dabigitran, gpiib/iiia inhibitors, argatroban).
boolean