Table 2.
| Parameter | Digoxin | Flecainide | Sotalol | Amiodarone |
|---|---|---|---|---|
| Indication | Paroxymal SVT, short VA SVT, nonhydropic fetuses | SVT with NIHF, refractory SVT, SVT with heart failure unresponsive to soltalol and digoxin | AF, SVT | SVT resistant to digoxin, AF |
| Dose | Loading: 1.5–2 mg over 24–48 h; Maintenance: 0.375–1 mg/day |
Loading: 200–300 mg divided b.i.d., or t.i.d.; Maintenance: 450 mg/day if no response |
Loading: 160–320 mg divided b.i.d.; Maintenance: increased to 480 mg/day |
Loading: 1600–2400 mg/day 2–4 times per day; Maintenance: 200–400 mg/day b.i.d. |
| Route | p.o., or i.v. | p.o. | p.o. | p.o., or i.v. |
| Fetal/maternal serum level (%) | 40–90 | 10–50 | ||
| Advantage | Safe and effective | Not accumulate in fetus, not cause intrauterine growth retardation | Little or no negative inotropic effect | |
| Adverse effect |
Digoxin monotherapy showed a lower effective rate than combined; Hydropic fetuses refractory to digoxin |
Intrauterine death | Negative inotropic effect, intrauterine death | Arrhythmogenic effect, fetal thyroid functional impairement, maternal thrombocytopenia and skin rash |
AF atrial flutter, NIHF nonimmune hydrops fetalis, SVT supraventricular tachycardia, VA ventrioatrial conduction