Eligibility Criteria

  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
Is the participant undergoing elective CABG surgery?
Description

CABG surgery

Data type

boolean

Alias
UMLS CUI [1,1]
C0206058
UMLS CUI [1,2]
C0010055
Did the participant have therapy with aspirin until at least 2 days before surgery?
Description

Aspirin therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0004057
UMLS CUI [1,2]
C3810854
UMLS CUI [1,3]
C4255413
Does the participant give written informed consent?
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
Is the participant missing written consent?
Description

Missing written consent

Data type

boolean

Alias
UMLS CUI [1,1]
C1705492
UMLS CUI [1,2]
C0009797
Does the participant have no therapy with aspirin or therapy stopped more than 2 days before surgery?
Description

Aspirin therapy insufficient

Data type

boolean

Alias
UMLS CUI [1,1]
C1705492
UMLS CUI [1,2]
C4303556
UMLS CUI [2,1]
C4303556
UMLS CUI [2,2]
C0419823
UMLS CUI [2,3]
C0445204
UMLS CUI [2,4]
C4018905
therapy with clopidogrel more than 3 days before surgery
Description

Clopidogrel treatment

Data type

boolean

Alias
UMLS CUI [1,1]
C0070166
UMLS CUI [1,2]
C3810854
UMLS CUI [1,3]
C4255413
Does the participant have emergency surgery?
Description

Emergency surgery

Data type

boolean

Alias
UMLS CUI [1]
C4264510
Does the surgery including more than CABG?
Description

More than CABG

Data type

boolean

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C0439093
UMLS CUI [1,3]
C0010055
Does the participant have inborn or acquired platelet disorders?
Description

Platelet disorders

Data type

boolean

Alias
UMLS CUI [1,1]
C1744681
UMLS CUI [1,2]
C0005818
UMLS CUI [2]
C0398636
Does the participant have therapy with selective serotonin reuptake inhibitors (SSRI)?
Description

SSRI therapy

Data type

boolean

Alias
UMLS CUI [1]
C0360105
Does the participant have severe hepatopathy (spontaneous quick <70%)?
Description

Severe Hepatopathy

Data type

boolean

Alias
UMLS CUI [1,1]
C0023895
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0086890
Does the participant have severe kidney disease (creatinine clearance < 30 ml/min)?
Description

Severe kidney disease

Data type

boolean

Alias
UMLS CUI [1,1]
C0205082
UMLS CUI [1,2]
C0022658

Similar models

Eligibility Criteria

  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
CABG surgery
Item
Is the participant undergoing elective CABG surgery?
boolean
C0206058 (UMLS CUI [1,1])
C0010055 (UMLS CUI [1,2])
Aspirin therapy
Item
Did the participant have therapy with aspirin until at least 2 days before surgery?
boolean
C0004057 (UMLS CUI [1,1])
C3810854 (UMLS CUI [1,2])
C4255413 (UMLS CUI [1,3])
Informed Consent
Item
Does the participant give written informed consent?
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Missing written consent
Item
Is the participant missing written consent?
boolean
C1705492 (UMLS CUI [1,1])
C0009797 (UMLS CUI [1,2])
Aspirin therapy insufficient
Item
Does the participant have no therapy with aspirin or therapy stopped more than 2 days before surgery?
boolean
C1705492 (UMLS CUI [1,1])
C4303556 (UMLS CUI [1,2])
C4303556 (UMLS CUI [2,1])
C0419823 (UMLS CUI [2,2])
C0445204 (UMLS CUI [2,3])
C4018905 (UMLS CUI [2,4])
Clopidogrel treatment
Item
therapy with clopidogrel more than 3 days before surgery
boolean
C0070166 (UMLS CUI [1,1])
C3810854 (UMLS CUI [1,2])
C4255413 (UMLS CUI [1,3])
Emergency surgery
Item
Does the participant have emergency surgery?
boolean
C4264510 (UMLS CUI [1])
More than CABG
Item
Does the surgery including more than CABG?
boolean
C0543467 (UMLS CUI [1,1])
C0439093 (UMLS CUI [1,2])
C0010055 (UMLS CUI [1,3])
Platelet disorders
Item
Does the participant have inborn or acquired platelet disorders?
boolean
C1744681 (UMLS CUI [1,1])
C0005818 (UMLS CUI [1,2])
C0398636 (UMLS CUI [2])
SSRI therapy
Item
Does the participant have therapy with selective serotonin reuptake inhibitors (SSRI)?
boolean
C0360105 (UMLS CUI [1])
Severe Hepatopathy
Item
Does the participant have severe hepatopathy (spontaneous quick <70%)?
boolean
C0023895 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0086890 (UMLS CUI [2])
Severe kidney disease
Item
Does the participant have severe kidney disease (creatinine clearance < 30 ml/min)?
boolean
C0205082 (UMLS CUI [1,1])
C0022658 (UMLS CUI [1,2])