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Updated: Jun 23, 2026

The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
Conversion of atrial fibrillation to sinus rhythm and rate control by digoxin in comparison to placebo
L Jordaens1, J Trouerbach, P Calle
1Department of Cardiology, University Hospital, Ghent, Belgium.
Insights
High-dose intravenous digoxin showed no significant advantage over placebo for converting recent-onset atrial fibrillation to sinus rhythm. Digoxin provided only weak rate control in this patient group.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Atrial fibrillation is a common arrhythmia requiring effective treatment for rhythm and rate control.
- Intravenous digoxin is used for rate control and sometimes for rhythm conversion in atrial fibrillation.
Purpose of the Study:
- To evaluate the efficacy of high-dose intravenous digoxin for conversion to sinus rhythm and for rate control in patients with recent-onset atrial fibrillation.
- To compare digoxin's effectiveness against placebo in a randomized, double-blind study.
Main Methods:
- A randomized, double-blind study involving 40 patients with recent-onset atrial fibrillation (< 1 week).
- Patients received either intravenous digoxin (1.25 mg) or intravenous saline (placebo).
- Outcomes included conversion to sinus rhythm within 12 hours, time to conversion, and early/stable rate control.
Main Results:
- Conversion rates were similar between digoxin (9/19) and placebo (8/20) groups (not significant).
- Digoxin showed a trend towards shorter conversion time but provided only weak rate control, with persistent slowing in only 3/10 non-converters.
- Adverse events included bradyarrhythmias in two patients; QTc interval was shortened post-conversion.
Conclusions:
- Intravenous digoxin does not offer significant advantages over placebo for converting recent-onset atrial fibrillation to sinus rhythm.
- Digoxin provides weak rate control in this clinical setting.
- Further research may be needed to clarify digoxin's role in specific atrial fibrillation scenarios.
Aims:
A randomized, double-blind study with a high dose of digoxin administered intravenously for conversion of atrial fibrillation (not due to haemodynamic alternations) to sinus rhythm, and for rate control in converters and non-converters was set up. Outcome measures were conversion within 12 h; time to conversion; early rate control; and stable slowing within 12 h.
Methods:
We studied 40 patients with recent onset (< 1 week) atrial fibrillation; controls received saline intravenously, the other patients digoxin 1.25 mg.
Results:
One patient converted before digoxin administration. Conversion occurred in 9/19 patients on digoxin and in 8/20 on placebo (ns). The mean time to conversion tended to be shorter only for digoxin. Two late conversions on placebo were observed within 24 h. Heart rate during atrial fibrillation decreased after 30 min for converters and non-converters (P < 0.05). For all patients on digoxin, heart rate after 30 min was lower compared to baseline (P < 0.002) and to placebo (P < 0.02). Persistent, stable slowing occurred only in 3/10 non-converters on digoxin (P < 0.05), and two patients developed bradyarrhythmias. QTc was shortened immediately after conversion in all patients. Converters had baseline characteristics similar to those of non-converters.
Conclusions:
Intravenous digoxin offers no substantial advantages over placebo in recent onset atrial fibrillation with respect to conversion, and provides weak rate control.
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