Management of Atrial Fibrillation
For most patients with atrial fibrillation, initiate rate control with beta-blockers or non-dihydropyridine calcium channel blockers (diltiazem/verapamil) combined with anticoagulation based on stroke risk—this approach is equally effective as rhythm control for reducing mortality and cardiovascular events while causing fewer adverse effects. 1
Initial Assessment
Upon diagnosis of atrial fibrillation, immediately assess three critical domains:
- Hemodynamic stability: Check for hypotension, ongoing chest pain, altered mental status, acute heart failure, or shock—any of these mandate immediate electrical cardioversion without delay 1
- Left ventricular function: Obtain transthoracic echocardiogram to determine LVEF, as this dictates medication selection 1
- Stroke risk: Calculate CHA₂DS₂-VASc score immediately (1 point each for: CHF, hypertension, age 65-74, diabetes, vascular disease, female sex; 2 points each for: age ≥75, prior stroke/TIA/thromboembolism) 1, 2
Anticoagulation Strategy (Initiate Immediately)
Start oral anticoagulation for all patients with CHA₂DS₂-VASc score ≥2 in men or ≥3 in women. 1
- Preferred agents: Direct oral anticoagulants (DOACs)—apixaban, rivaroxaban, edoxaban, or dabigatran—are superior to warfarin due to lower intracranial hemorrhage risk 1
- DOAC dosing example: Apixaban 5 mg twice daily (reduce to 2.5 mg twice daily if patient meets ≥2 of: age ≥80 years, weight ≤60 kg, creatinine ≥1.5 mg/dL) 2
- Warfarin alternative: Only use if mechanical heart valve or moderate-to-severe mitral stenosis present; target INR 2.0-3.0 with weekly monitoring during initiation, then monthly when stable 1
- Continue anticoagulation indefinitely based on stroke risk regardless of whether sinus rhythm is restored—most strokes occur after anticoagulation is stopped or when subtherapeutic 1
Rate Control Strategy (Primary Approach for Most Patients)
For Preserved Ejection Fraction (LVEF >40%)
First-line options (choose based on comorbidities): 1
- Beta-blockers: Metoprolol 25-200 mg twice daily OR metoprolol succinate 50-400 mg daily 3
- Diltiazem: 60-120 mg three times daily OR 120-360 mg extended-release daily 1, 3
- Verapamil: 40-120 mg three times daily OR 120-480 mg extended-release daily 1, 3
Acute setting (IV administration for rapid control):
- Metoprolol 2.5-5 mg IV over 2 minutes (may repeat up to 3 doses) 3
- Diltiazem 0.25 mg/kg IV over 2 minutes, then 5-15 mg/hour infusion 3
- Esmolol 500 μg/kg bolus, then 50-300 μg/kg/min infusion (ultra-short acting, ideal for unstable patients) 1, 3
For Reduced Ejection Fraction (LVEF ≤40%)
Use only beta-blockers and/or digoxin—calcium channel blockers are contraindicated due to negative inotropic effects. 1
- Beta-blockers: Metoprolol, carvedilol, or bisoprolol (start low, titrate carefully) 1, 3
- Digoxin: 0.0625-0.25 mg daily (particularly useful when combined with beta-blockers or in sedentary elderly patients) 1, 3
- Acute setting: IV digoxin 0.25-0.5 mg over several minutes OR IV amiodarone if hemodynamically unstable 1
Rate Control Targets
- Initial target: Lenient control with resting heart rate <110 bpm 1
- Stricter control: Target <80 bpm only if symptoms persist despite lenient control 1
- The RACE II trial demonstrated lenient rate control was non-inferior to strict control for clinical outcomes 1
Combination Therapy
If single agent fails to control rate or symptoms, add a second agent: 1
- Combine digoxin with beta-blocker (for any LVEF) 1
- Combine digoxin with diltiazem/verapamil (only if LVEF >40%) 1
- Monitor closely for bradycardia when using combination therapy 1
Special Clinical Scenarios
Heart Failure with Recent Hospitalization
- Consider AV node ablation combined with cardiac resynchronization therapy for severely symptomatic patients with permanent AF and ≥1 heart failure hospitalization 1
COPD or Active Bronchospasm
- Use diltiazem or verapamil as first-line (avoid beta-blockers during active bronchospasm) 1
- Beta-1 selective blockers (bisoprolol) in small doses may be considered as alternative 1
- Never use non-selective beta-blockers, sotalol, or propafenone 1
Wolff-Parkinson-White Syndrome with Pre-excitation
- Avoid all AV nodal blockers (beta-blockers, calcium channel blockers, digoxin, adenosine, amiodarone)—they can accelerate ventricular rate and precipitate ventricular fibrillation 1
- If hemodynamically unstable: immediate DC cardioversion 1
- If stable: IV procainamide or ibutilide 1
- Definitive treatment: catheter ablation of accessory pathway 1
Rhythm Control Considerations
Consider rhythm control strategy for: 1
- Symptomatic patients despite adequate rate control
- Young patients with new-onset AF
- Suspected tachycardia-induced cardiomyopathy (newly detected heart failure with rapid ventricular response)
- Hemodynamically unstable patients
Cardioversion Protocol
For AF duration >48 hours or unknown duration: 1
- Provide 3 weeks of therapeutic anticoagulation before cardioversion
- Continue anticoagulation for minimum 4 weeks after cardioversion
- Continue long-term anticoagulation based on CHA₂DS₂-VASc score regardless of rhythm
For AF duration <48 hours: 1
- May proceed with cardioversion after initiating anticoagulation
- Alternative: perform transesophageal echocardiogram to exclude thrombus
Antiarrhythmic Drug Selection (If Rhythm Control Pursued)
Selection is strictly based on cardiac structure and LVEF: 1
- No structural heart disease: Flecainide, propafenone, or sotalol 1
- Coronary artery disease with LVEF >35%: Sotalol (requires hospitalization with continuous ECG monitoring for minimum 3 days) 1
- Heart failure or LVEF ≤35%: Amiodarone only (all other antiarrhythmics carry proarrhythmic risk) 1
When Rate Control Fails
If intensive pharmacological rate and rhythm control fail or are not tolerated: 1
- Consider AV node ablation with pacemaker implantation 1
- For patients with heart failure: AV node ablation combined with cardiac resynchronization therapy 1
- Before proceeding with AV node ablation, consider catheter ablation of AF as it preserves AV conduction 4
Common Pitfalls to Avoid
- Never use digoxin as sole agent for paroxysmal AF—it is ineffective during high sympathetic states and does not control exercise heart rate 1
- Never use calcium channel blockers in patients with LVEF ≤40% or decompensated heart failure—they worsen outcomes 1, 3
- Never discontinue anticoagulation after successful cardioversion if stroke risk factors persist—rhythm status does not eliminate stroke risk 1
- Never delay cardioversion for anticoagulation in truly hemodynamically unstable patients 1
- Never combine beta-blockers with diltiazem/verapamil without specialist guidance and ambulatory ECG monitoring for bradycardia 1
Ongoing Management
- Reassess therapy periodically and evaluate for new modifiable risk factors (hypertension, heart failure, diabetes, obesity, sleep apnea, alcohol intake) 1
- Monitor renal function at least annually when using DOACs, more frequently if clinically indicated 2
- For warfarin: monitor INR weekly during initiation, then monthly when stable 1
- Continue anticoagulation according to stroke risk regardless of rhythm status 1