Persistent atrial fibrillation Duration | Pharmacological cardioversion Patient need for | Electric Countershock Patient need for
Item
patients with persistent (more than 7 days, or less than 7 days needing pharmacologic or electric cardioversion)
boolean
C2585653 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C1963873 (UMLS CUI [2,1])
C0686904 (UMLS CUI [2,2])
C0013778 (UMLS CUI [3,1])
C0686904 (UMLS CUI [3,2])
Atrial Fibrillation
Item
presence of atrial fibrillation at the beginning of the procedure
boolean
C0004238 (UMLS CUI [1])
Hypothyroidism | Hyperthyroidism
Item
hypo or hyperthyroidism
boolean
C0020676 (UMLS CUI [1])
C0020550 (UMLS CUI [2])
Longstanding persistent atrial fibrillation | Atrial Fibrillation Duration Unspecified
Item
persistent long-lasting or non-defined duration atrial fibrillation
boolean
C3873617 (UMLS CUI [1])
C0004238 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
C0205370 (UMLS CUI [2,3])
Hypertrophic Cardiomyopathy
Item
hypertrophic myocardiopathy
boolean
C0007194 (UMLS CUI [1])
Implantable defibrillator | pacemaker implant
Item
implantable defibrillation or pacemaker implanted
boolean
C0162589 (UMLS CUI [1])
C0848753 (UMLS CUI [2])
Disease of mitral valve Moderate | Disease of mitral valve Severe | Mitral valve prosthesis
Item
moderate or severe mitral valve disease or mitral prosthetic valve
boolean
C0026265 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C0026265 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0182494 (UMLS CUI [3])
Cardiac ejection fraction
Item
ejection fraction less than 30%
boolean
C0232174 (UMLS CUI [1])
Left atrium Diameter Antero-posterior
Item
left atrial anteroposterior diameter more than 50 mm.
boolean
C0225860 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
C0442212 (UMLS CUI [1,3])
ablation for atrial fibrillation
Item
previous atrial fibrillation ablation
boolean
C2702800 (UMLS CUI [1])
Medical contraindication Anticoagulation Therapy
Item
contraindication to anticoagulation
boolean
C1301624 (UMLS CUI [1,1])
C0003281 (UMLS CUI [1,2])
Thrombus of left atrium
Item
left atrium thrombus
boolean
C3532827 (UMLS CUI [1])
Communicable Disease | Sepsis
Item
current infective disease or sepsis
boolean
C0009450 (UMLS CUI [1])
C0243026 (UMLS CUI [2])
Pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
Angina, Unstable
Item
current unstable angor
boolean
C0002965 (UMLS CUI [1])
Myocardial Infarction
Item
acute myocardial infarction in last 3 months
boolean
C0027051 (UMLS CUI [1])
Atrial Fibrillation Secondary to Ionic Disturbance | Atrial Fibrillation Secondary to Thyroid Disease | Atrial Fibrillation Secondary to Disease Reversible | Atrial Fibrillation Secondary to Disease | Exception Cardiovascular Diseases
Item
atrial fibrillation secondary to ionic disturbance, thyroids disease or secondary to any other reversible or non cardiovascular disease
boolean
C0004238 (UMLS CUI [1,1])
C0175668 (UMLS CUI [1,2])
C0598358 (UMLS CUI [1,3])
C2699787 (UMLS CUI [1,4])
C0004238 (UMLS CUI [2,1])
C0175668 (UMLS CUI [2,2])
C0040128 (UMLS CUI [2,3])
C0004238 (UMLS CUI [3,1])
C0175668 (UMLS CUI [3,2])
C0012634 (UMLS CUI [3,3])
C0205343 (UMLS CUI [3,4])
C0004238 (UMLS CUI [4,1])
C0175668 (UMLS CUI [4,2])
C0012634 (UMLS CUI [4,3])
C1705847 (UMLS CUI [5,1])
C0007222 (UMLS CUI [5,2])
Reduced life expectancy
Item
reduced expectancy of life (less than 12 months)
boolean
C1858274 (UMLS CUI [1])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
patient participating in another clinical study that investigates a drug or device
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
Unstable status Psychologic | Informed Consent Refused
Item
psychologically unstable patient or denies to give informed consent
boolean
C0443343 (UMLS CUI [1,1])
C0205486 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
Medical contraindication Ablation | Medical contraindication Anti-Arrhythmia Agents
Item
any cause that contraindicate ablation procedure or antiarrhythmic drug
boolean
C1301624 (UMLS CUI [1,1])
C0547070 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0003195 (UMLS CUI [2,2])