Eligibility Heart; Dysfunction Postoperative, Cardiac Surgery NCT01352416

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
indications for cardiac surgery (cabg, valve surgery or cabg and valve surgery, able to provide informed consent.
Descrizione

ID.1

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
documented atrial fibrillation within the previous 3 months
Descrizione

ID.2

Tipo di dati

boolean

ongoing therapy with suppressive antiarrhythmic drugs
Descrizione

ID.3

Tipo di dati

boolean

patient currently on digoxin
Descrizione

ID.4

Tipo di dati

boolean

emergent surgery
Descrizione

ID.5

Tipo di dati

boolean

patient receiving hemodialysis
Descrizione

ID.6

Tipo di dati

boolean

concomitant use of ketoconazole, diltiazem, verapamil
Descrizione

ID.7

Tipo di dati

boolean

known tolerance or hypersensitivity to ranolazine
Descrizione

ID.8

Tipo di dati

boolean

pregnant individuals
Descrizione

ID.9

Tipo di dati

boolean

maze procedure performed during concurrent cardiac surgery
Descrizione

ID.10

Tipo di dati

boolean

Similar models

Eligibility Heart; Dysfunction Postoperative, Cardiac Surgery NCT01352416

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
indications for cardiac surgery (cabg, valve surgery or cabg and valve surgery, able to provide informed consent.
boolean
Item Group
C0680251 (UMLS CUI)
ID.2
Item
documented atrial fibrillation within the previous 3 months
boolean
ID.3
Item
ongoing therapy with suppressive antiarrhythmic drugs
boolean
ID.4
Item
patient currently on digoxin
boolean
ID.5
Item
emergent surgery
boolean
ID.6
Item
patient receiving hemodialysis
boolean
ID.7
Item
concomitant use of ketoconazole, diltiazem, verapamil
boolean
ID.8
Item
known tolerance or hypersensitivity to ranolazine
boolean
ID.9
Item
pregnant individuals
boolean
ID.10
Item
maze procedure performed during concurrent cardiac surgery
boolean