Authors
- Krešimir Kordić — University Hospital Centre “Sestre milosrdnice”, Zagreb, Croatia — ORCID: 0000-0002-9707-6946
- Nikola Kos — University Hospital Centre “Sestre milosrdnice”, Zagreb, Croatia — ORCID: 0000-0001-8829-2543
- Nikola Pavlović — University Hospital Centre “Sestre milosrdnice”, Zagreb, Croatia — ORCID: 0000-0001-9187-7681
- Vjekoslav Radeljić — University Hospital Centre “Sestre milosrdnice”, Zagreb, Croatia — ORCID: 0000-0003-2471-4035
- Nikola Bulj — University Hospital Centre “Sestre milosrdnice”, Zagreb, Croatia — ORCID: 0000-0002-7859-3374
- Ivan Zeljković — University Hospital Centre “Sestre milosrdnice”, Zagreb, Croatia — ORCID: 0000-0002-4550-4056
- Ines Zadro — General Hospital “Dr. Ivo Pedišić”, Sisak, Croatia — ORCID: 0000-0002-0754-7194
- Karlo Golubić — University Hospital Centre “Sestre milosrdnice”, Zagreb, Croatia — ORCID: 0000-0003-0684-6333
- Diana Delić-Brkljačić — University Hospital Centre “Sestre milosrdnice”, Zagreb, Croatia — ORCID: 0000-0002-7116-2360
- Šime Manola — University Hospital Centre “Sestre milosrdnice”, Zagreb, Croatia — ORCID: 0000-0001-6444-2674
Keywords
atrial fibrillation, cardioversion, left atrial appendage
DOI
https://doi.org/10.15836/ccar2016.423Full Text
**Background:** Direct current (DC) cardioversion is an effective method for converting atrial fibrillation (AF) to sinus rhythm. Current ESC Guidelines (1) suggest that transoesophageal echocardiography (TOE) should be performed to rule out atrial thrombi in patients undergoing DC cardioversion, unless adequate anticoagulation has been documented for 3 weeks or AF is 48 hours admitted to the Emergency department or Department of Cardiology at the University Hospital Centre “Sestre milosrdnice” Zagreb from January 2013 to May 2016 who underwent DC cardioversion were included in the study. Patients with AF lasting <48 hours were excluded from the study. All patients underwent preprocedural TOE to exclude LA thrombus regardless on anticoagulation status. The thromboembolic risk status was calculated for each patient using a CHA2DS2-VASc score. DC cardioversion was performed according to local protocols. **Results:** Total of 139 patients were included (106/139; 76% were male) with median age of 66 years (59-72). The overall prevalence of LA thrombi was 30/139 (21.6%). 49 patients were adequately anticoagulated for at least 3 weeks prior to the peri-procedural TOE (35.2%), whereas 90 patients were inadequately anticoagulated (64.8%). 12 patients with a detected thrombus were adequately anticoagulated with warfarin (N=11) or new oral anticoagulants (N=1) out of totally 49 adequately anticoagulated patients (12/49; 24.5%). 18 patients with a detected thrombus were inadequately anticoagulated (20%) (**Table 1**.) There was no statistical significance between prevalence of LA thrombi between adequately vs. inadequately anticoagulated patients (12 out of 49; 24.5% vs 18 out of 90, 20%, p=0.582) ### Table 1: Number of patients with left atrial thrombus in patients with low thromboembolic risk (CHA2DS2VASc score 0-1) and with high risk (CHA2DS2VASc score 2). | **CHA2DS2-VASc** | **TOTAL PATIENTS** | **TOTAL THROMBI (n)** | | --- | --- | --- | | **0-1** | 45 | 6 | | **2-6** | 94 | 24 | **Conclusion:** The prevalence of LA thrombi is high, even in patients who have been adequately anticoagulated. Further research with larger number of patients is needed to determine whether all patients should undergo TEE before elective DC cardioversion.
Literature
- European Heart Rhythm Association, European Association for Cardio-Thoracic Surgery, Camm AJ, Kirchhof P, Lip GY, Schotten U, Savelieva I, Ernst S, et al. Guidelines for the management of atrial fibrillation: the Task Force for the Management of Atrial Fibrillation of the European Society of Cardiology (ESC). Eur Heart J. 2010;31(19):2369–429. https://doi.org/10.1093/eurheartj/ehq278