Table 1.
Clinical trial | Patients in flecainide arm | AF duration | Formulation | Reversion rate |
Capucci et al[38] | 22 patients | ≤ 7 d | Single oral dose (300 mg) | 8 h → 91% |
24 h → 95% | ||||
Donovan et al[39] | 51 patients | ≤ 3 d | iv (2 mg/kg-max 150 mg) | 1 h → 57% |
6 h → 67% | ||||
Donovan et al[40] | 34 patients | ≤ 3 d | iv (2 mg/kg-max 150 mg) | 2 h → 59% |
8 h → 68% | ||||
Boriani et al[41] | 69 patients | < 8 d | Single oral dose (300 mg) | 1 h → 13% |
3 h → 57% | ||||
8 h → 75% | ||||
Martínez-Marcos et al[42] | 50 patients | ≤ 2 d | iv (2 mg/kg followed by 1 mg/kg at 8 h if not SR) | 1 h → 58% |
8 h → 82% | ||||
12 h → 90% | ||||
Romano et al[43] | 138 patients | ≤ 3 d | Intravenous | 1 h → 73% |
3 h → 80% | ||||
6 h → 86% | ||||
24 h → 90% |
AF: Atrial fibrillation; SR: Sinus rhythm.