Flecainide for Paroxysmal Atrial Fibrillation
Flecainide is an effective first-line antiarrhythmic medication for paroxysmal atrial fibrillation in patients without structural heart disease, with both therapeutic dosing and "pill-in-pocket" approaches being viable options for symptom control and prevention of recurrences. 1, 2
Patient Selection Criteria
Flecainide is appropriate for:
- Patients with paroxysmal AF without structural heart disease 1
- Patients with symptomatic episodes requiring rhythm control 2
- "Lone AF" patients (no significant cardiac disease) 2
Contraindications (absolute):
- Recent myocardial infarction 1
- Structural heart disease 2
- Heart failure with reduced ejection fraction (HFrEF) 2
- Coronary artery disease 2
- Severe left ventricular hypertrophy 2
- Chronic atrial fibrillation (NOT recommended) 1
- Brugada syndrome 2
Administration Approaches
Standard Therapeutic Dosing
- Initial dose: 200-300 mg/day (divided doses) 2
- Maintenance dose: Can be adjusted to 200-300 mg/day based on response 3
- Monitor for QRS widening (should not exceed 150% of baseline) 2
"Pill-in-Pocket" Approach
This strategy allows patients to self-administer a single oral dose shortly after onset of symptomatic AF:
Initial conversion trial must be performed in-hospital to ensure safety 2
Only for selected patients with:
Important safety measure: A beta-blocker or non-dihydropyridine calcium channel blocker should be given at least 30 minutes before flecainide administration to prevent rapid AV conduction if atrial flutter develops 2
Efficacy and Outcomes
- Conversion efficacy: Up to 82% for recent-onset AF (duration <24 hours) 4
- Maintenance efficacy: Moderately effective for preventing recurrences, comparable to other antiarrhythmics except amiodarone (which has superior efficacy but more side effects) 5
- Combined therapy with metoprolol has shown superior outcomes compared to flecainide alone in persistent AF (66.7% vs. 46.8% freedom from recurrence at 1 year) 6
Safety Considerations and Monitoring
Proarrhythmic Risk
- Risk of ventricular proarrhythmia is low in patients without structural heart disease 5
- Female gender is a risk factor for proarrhythmic toxicity 2
- 1:1 AV conduction with atrial flutter can occur, leading to paradoxical increase in ventricular rate 1
- Cardiogenic shock has been reported in rare cases even with therapeutic doses 7
Required Monitoring
- Initial ECG to assess QRS duration and QT interval
- Exercise testing may help detect use-dependent conduction slowing 2
- Follow-up ECG to ensure QRS widening does not exceed 150% of baseline 2
Practical Algorithm for Flecainide Use in Paroxysmal AF
Assessment phase:
- Confirm paroxysmal AF diagnosis
- Rule out structural heart disease with echocardiogram
- Ensure normal QRS duration and QT interval
- Check for contraindications
Initiation phase:
- Start with 50-100 mg twice daily
- Consider in-hospital monitoring for first dose in high-risk patients
- Add beta-blocker or non-dihydropyridine calcium channel blocker
Titration phase:
- Increase to 100-150 mg twice daily if needed and tolerated
- Maximum daily dose: 300 mg (400 mg in selected cases) 3
For "pill-in-pocket" approach:
Monitoring phase:
- ECG at baseline and with dose changes
- Monitor for symptoms of proarrhythmia (syncope, palpitations)
- Assess efficacy by symptom reduction and ECG documentation
Comparative Efficacy
Flecainide has been shown to be:
- More effective than placebo for maintaining sinus rhythm 2
- More effective than verapamil for acute conversion (82% vs. 6%) 4
- Less effective than amiodarone for long-term maintenance of sinus rhythm 2, 5
- Comparable to propafenone in efficacy 2
In conclusion, flecainide is an important option in the management of paroxysmal atrial fibrillation, particularly for patients without structural heart disease who require rhythm control. Its efficacy in both acute conversion and maintenance therapy, combined with its relatively favorable side effect profile in appropriate patients, makes it a valuable tool in AF management.