Everyday practice of cardioversion safety on apixaban: The French AMPER-AF cardioversion study - 06/01/20
Résumé |
Purpose |
To evaluate thromboembolic complications in patients taking apixaban and undergoing a cardioversion procedure in everyday clinical practice.
Methods |
It is a multicenter, observational, prospective study of patients with non-valvular atrial fibrillation (AF) undergoing cardioversion (electric or medical). Eligible patients had been taking apixaban (2.5 or 5mg twice daily) for ≥3 weeks before the procedure, and were followed for 30 days afterwards.
Results |
A total of 278 patients (68 [61,76] years, 71% male, mean CHA2DS2-VASc score 2, mean HAS BLED score 2) were enrolled at 25 academic/non-academic centres in France; 248 patients (89%) were receiving apixaban 10mg/day and 29 (11%) 5mg/day. The most prevalent concomitant disorders were hypertension (50% of patients) and diabetes (15%). The mean creatinine clearance (Cockroft−Gault) was 81±34mL/min. The majority of patients had an electric cardioversion (264, 95%)and 14 patients (5%) received amiodarone only. Cardioversion was a planned procedure in the most of cases (97%). Sixty-seven patients (24%) had a transeophageal echocardiogram before procedure. There were no reported thromboembolic events.
Conclusion |
These observational data of patients on apixaban undergoing cardiversion in everyday practice show no thromboembolic events on a follow-up of 30 days.
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Vol 12 - N° 1
P. 117 - janvier 2020 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.