Authors
- Zorislav Šušak — Zadar General Hospital, Zadar, Croatia — ORCID: 0000-0003-2977-6833
- Ante Anić — Zadar General Hospital, Zadar, Croatia — ORCID: 0000-0002-6864-3999
- Branimir Bukša — Zadar General Hospital, Zadar, Croatia — ORCID: 0000-0001-5206-512X
Keywords
atrial appendage, occluder device, transesophageal echocardiography, atrial fibrillation, stroke
DOI
https://doi.org/10.15836/ccar2017.131Full Text
Percutaneous left atrial appendage closure for stroke prevention in patients with atrial fibrillation has distinctively advanced in recent years (1). The current recommendations by the European Society of Cardiology include patients with high stroke risk and contraindications to long-term oral anticoagulation (2). Preprocedural transesophageal echocardiography remains the reference technique to exclude the presence of left atrial appendage thrombi prior to left atrial appendage closure and to assess left atrial appendage anatomy and accurate measurements regarding challenging anatomies and device sizing (3). Procedural transesophageal guidance is generally recommended with any current CE mark device in addition to fluoroscopy. Transseptal puncture is well positioned with transesophageal bicaval and short axis views. Device sizing depends on the widest landing zone on fluoroscopy or transesophageal echocardiography which is by standard recommendation upsized by 2-5 mm. Device is adequately positioned at landing zone and deployment is controlled by transesophageal echocardiography and fluoroscopy. Prior to device release, evaluation of proper deployment is done by transesophageal echocardiography. Finally, after deployment additional assessment of possible residual flow is performed. Procedural transesophageal guidance is widely available imaging method which is contributing to procedural success and safety. We would like with our patients series to depict key procedural steps.
Literature
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