Paroxysmal atrial fibrillation Symptomatic
Item
history of symptomatic paroxysmal atrial fibrillation defined as:
boolean
C0235480 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
Atrial Fibrillation Duration Ending Spontaneous
Item
self terminating af lasting no more than 7 days
boolean
C0004238 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C2746065 (UMLS CUI [1,3])
C0205359 (UMLS CUI [1,4])
Atrial Fibrillation Event | Conversion Spontaneous Sinus rhythm
Item
af events demostrating spontaneous conversion back to sinus rhythm
boolean
C0004238 (UMLS CUI [1,1])
C0441471 (UMLS CUI [1,2])
C0439836 (UMLS CUI [2,1])
C0205359 (UMLS CUI [2,2])
C0232201 (UMLS CUI [2,3])
Event Quantity | Atrial Fibrillation Postoperative Electrocardiography | Cardiac event recording | Electrocardiographic recording from artificial pacemaker | Rhythm strip monitoring
Item
documentation of one or more events with paf tracings by ecg, event recordings, pacemaker strips or monitor rhythm strips within the past year
boolean
C0441471 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0004238 (UMLS CUI [2,1])
C0032790 (UMLS CUI [2,2])
C1623258 (UMLS CUI [2,3])
C1273297 (UMLS CUI [3])
C0199561 (UMLS CUI [4])
C0204917 (UMLS CUI [5])
Atrial Fibrillation Symptoms | Palpitations | Fatigue | Dyspnea on exertion | Effort intolerant
Item
af symptoms defined as the manisfestation of any of the following: palpitations, fatigue, exertional dyspnea, effort intolerance
boolean
C0004238 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0030252 (UMLS CUI [2])
C0015672 (UMLS CUI [3])
C0231807 (UMLS CUI [4])
C0015264 (UMLS CUI [5,1])
C0231200 (UMLS CUI [5,2])
Age
Item
age between 18 and 70
boolean
C0001779 (UMLS CUI [1])
Participation Evaluation | Participation Follow-up Evaluation
Item
willingness, ability and commitment to participate in baseline and follow-up evaluations for the full length of the study
boolean
C0679823 (UMLS CUI [1,1])
C1261322 (UMLS CUI [1,2])
C0679823 (UMLS CUI [2,1])
C1522577 (UMLS CUI [2,2])
C1261322 (UMLS CUI [2,3])
Structural disorder of heart
Item
structural heart disease of clinical significance
boolean
C1290384 (UMLS CUI [1])
Ablation operation for arrhythmia | Exception Atrial Fibrillation
Item
prior ablation for arrhythmias other than af within the past three months
boolean
C0397403 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0004238 (UMLS CUI [2,2])
Ablation Atrial Fibrillation Left sided
Item
prior left sided af ablation
boolean
C0547070 (UMLS CUI [1,1])
C0004238 (UMLS CUI [1,2])
C0443246 (UMLS CUI [1,3])
Study Subject Participation Status | Cardiac Arrhythmia
Item
enrollment in any other ongoing arrhythmia study protocol
boolean
C2348568 (UMLS CUI [1])
C0003811 (UMLS CUI [2])
Ventricular Tachycardia Treated Interferes with Clinical Trial | Disease Management Interferes with Clinical Trial
Item
any ventricular tachyarrhythmias currently being treated where the arrhythmia or the management may interfere with this study
boolean
C0042514 (UMLS CUI [1,1])
C1522326 (UMLS CUI [1,2])
C0521102 (UMLS CUI [1,3])
C0008976 (UMLS CUI [1,4])
C0376636 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
Communicable Disease | Sepsis
Item
active infection or sepsis
boolean
C0009450 (UMLS CUI [1])
C0243026 (UMLS CUI [2])
Cerebrovascular Disorders | Cerebrovascular accident | Transient Ischemic Attack
Item
any history of cerebral vascular disease including stroke or tias
boolean
C0007820 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0007787 (UMLS CUI [3])
Pregnancy | Breast Feeding
Item
pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Contrast media allergy | Therapeutic procedure Unsuccessful
Item
untreatable allergy to contrast media
boolean
C0570562 (UMLS CUI [1])
C0087111 (UMLS CUI [2,1])
C1272705 (UMLS CUI [2,2])
Atrial Fibrillation Secondary to Electrolyte imbalance | Atrial Fibrillation Secondary to Thyroid Diseases | Atrial Fibrillation Secondary to Causes Reversible | Atrial Fibrillation Secondary to Causes
Item
any diagnosis of atrial fibrillation secondary to electrolyte imbalance, thyroid disease, or any other reversible or non-cardiovascular causes
boolean
C0004238 (UMLS CUI [1,1])
C0175668 (UMLS CUI [1,2])
C0342579 (UMLS CUI [1,3])
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])
C0015127 (UMLS CUI [3,3])
C0205343 (UMLS CUI [3,4])
C0004238 (UMLS CUI [4,1])
C0175668 (UMLS CUI [4,2])
C0015127 (UMLS CUI [4,3])
Abnormality of coagulation | Bleeding tendency | Abnormal thrombosis
Item
history of blood clotting (bleeding or thrombotic) abnormalities
boolean
C1846821 (UMLS CUI [1])
C1458140 (UMLS CUI [2])
C4025731 (UMLS CUI [3])
Heparin allergy | Warfarin allergy
Item
known sensitivities to heparin or warfarin
boolean
C0571776 (UMLS CUI [1])
C0571785 (UMLS CUI [2])
Severe chronic obstructive pulmonary disease Pulmonary Function Test/Forced Expiratory Volume 1
Item
severe copd (identified by an fev1 < 1)
boolean
C0730607 (UMLS CUI [1,1])
C0849974 (UMLS CUI [1,2])
Comorbidity Severe Study Subject Participation Status Unfavorable | General health poor Study Subject Participation Status Unfavorable | Disease Process | Mental state | Substance Use Disorders | Life expectancy shortened
Item
severe co morbidity or poor general physical/mental health that, in the opinion of the investigator, will not allow the patient to be a good study candidate (i.e. other disease processes, mental capacity, substance abuse, shortened life expectance, etc.)
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
C3640815 (UMLS CUI [1,4])
C1277248 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C3640815 (UMLS CUI [2,3])
C0012634 (UMLS CUI [3,1])
C1522240 (UMLS CUI [3,2])
C0278060 (UMLS CUI [4])
C0038586 (UMLS CUI [5])
C1504437 (UMLS CUI [6])