Sotalol BID Dosing
The typical dosing of Sotalol is 40-80 mg twice daily (BID) for initiation, with a maintenance dose of up to 160 mg twice daily, requiring careful QT interval monitoring during titration. 1
Initial Dosing
- Starting dose: 40-80 mg every 12 hours (BID) 1
- For patients with normal renal function (creatinine clearance >60 mL/min): 80 mg BID 2
- For patients with moderate renal impairment (creatinine clearance 40-60 mL/min): 80 mg once daily 2
- Contraindicated in patients with severe renal impairment (creatinine clearance <40 mL/min) 2
Titration and Maintenance Dosing
- Maximum maintenance dose: 160 mg BID 1, 2
- Dose increases should be made gradually (every 3 days) with continuous ECG monitoring 2
- During initiation and titration, QT interval should be monitored 2-4 hours after each dose 1
- If QT interval prolongs to ≥500 ms, the dose must be reduced or the drug discontinued 1
Monitoring Requirements
- Initial therapy requires continuous ECG monitoring for a minimum of 3 days 2
- QT interval should be measured 2-4 hours after each dose during initiation and titration 1
- Patients should not be discharged within 12 hours of conversion to normal sinus rhythm 2
- Baseline QT interval must be ≤450 msec to start therapy 2
Important Precautions
- QT prolongation risk: The primary safety concern with sotalol is QT prolongation and risk of torsades de pointes 1, 3
- Renal function: Dose must be adjusted based on creatinine clearance 2
- Contraindications: Avoid in patients with:
Clinical Pearls
- Sotalol has both Class III antiarrhythmic and beta-blocking properties 3
- More effective than conventional beta-blockers for controlling arrhythmias due to its additional Class III properties 3
- Patients with low body mass index or impaired renal function are at higher risk for QT prolongation 3
- Hypokalemia should be corrected before initiation of therapy 2
- Unlike some other antiarrhythmics (e.g., amiodarone), sotalol has no significant pharmacokinetic drug-drug interactions 4
Sotalol is not metabolized and is entirely renally excreted, making renal function assessment critical before initiating therapy 4. While higher starting doses (120-160 mg BID) have been studied, they showed marginally increased risk of cardiac and non-cardiac side effects without shortening hospitalization or improving efficacy 5.