Related Experiment Video
Updated: Jul 20, 2026

Robotic Ablation of Atrial Fibrillation
Published on: May 29, 2015
[TEE-guided cardioversion in patients with atrial fibrillation without previous anticoagulation]
P Halbfass1, A Plewan, K Dennig
1Städtisches Klinikum München-Bogenhausen I. Medizinische Abteilung, Englschalkinger Str. 77, 81925 München, Germany.
Transesophageal echocardiography (TEE)-guided cardioversion (CV) is safe and effective for patients with nonvalvular atrial fibrillation (AF) over 48 hours. This method successfully restored normal heart rhythm without causing periprocedural embolism.
Area of Science:
- Cardiology
- Medical Imaging
Background:
- Nonvalvular atrial fibrillation (AF) exceeding 48 hours duration often requires cardioversion (CV).
- Insufficient anticoagulation poses a risk of thromboembolic complications during CV.
Purpose of the Study:
- To evaluate the safety and efficacy of transesophageal echocardiography (TEE)-guided cardioversion (CV) in patients with nonvalvular atrial fibrillation (AF) of more than 48 hours duration and insufficient anticoagulation.
- To assess the incidence of periprocedural embolism and atrial thrombi detection.
Main Methods:
- 332 patients with nonvalvular AF (>48 hours) and insufficient anticoagulation were included.
- Transesophageal echocardiography (TEE) was used to exclude left atrial thrombi before cardioversion (CV).
- CV was performed within 24 hours if no thrombi were detected; otherwise, after at least four weeks of anticoagulation.
Main Results:
- In 9.9% of patients, TEE revealed left atrial or appendage thrombi, or thrombi could not be excluded.
- 383 TEEs were performed without complications.
- No thromboembolic complications were observed during periprocedural monitoring or within four weeks after 305 CV procedures.
Conclusions:
- TEE-guided CV is a safe and effective strategy for patients with nonvalvular AF persisting for over 48 hours and without prior adequate anticoagulation.
- This approach minimizes the risk of periprocedural embolism in this patient cohort.
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