Atrial Fibrillation Diagnosis and Initial Treatment
Atrial fibrillation is a supraventricular tachyarrhythmia characterized by chaotic, disorganized electrical activation and inefficient atrial contraction
Atrial fibrillation is the most common sustained cardiac arrhythmia, with a worldwide prevalence of more than 37 million (0.5% of the global population)(1)
Incidence and prevalence have risen steadily over the past 20 years, and they are projected to continue to rise(1)
Etiology
Atrial fibrillation episodes are initiated by premature atrial complexes
Typically originate in the pulmonary veins (called pulmonary vein triggers)
May also come from the other structures (called non–pulmonary vein triggers2), including: • Right atrium • Superior vena cava • Posterior wall of left atrium • Vein of Marshall • Left atrial appendage
Risk Factors
Risk factors for atrial fibrillation
Cardiac factors
Hypertension
Coronary artery disease
Heart failure
Hypertrophic cardiomyopathy
Extracardiac factors
Obesity
Metabolic syndrome
Sleep apnea
Diabetes mellitus
Excessive alcohol consumption
Hyperthyroidism
Genetic factors
Sometimes familial
Patterns of autosomal dominant inheritance have been described in some families3
Numerous genetic mutations have been linked to atrial fibrillation, including:
Ion channel mutations (sodium and potassium channels)
Non–ion channel mutations (eg, lamin, connexin, ryanodine receptor, cardiac transcription factors)3 European ancestry is a risk factor4
Advancing age
Approach to Diagnosis
Presence is suggested by findings on physical examination and confirmed by ECG
Staging or Classification
Classified according to predominant duration of episodes
Paroxysmal (terminating spontaneously or by intervention in less than 7 days)
Persistent (more than 7 days, often requiring direct-current cardioversion)
Long-standing persistent (continuous atrial fibrillation for 1 year or longer)
Permanent (accepted as long-term by the patient and physician, with no plans to pursue rhythm control)
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