Percutaneous Left Atrial Appendage Transcatheter Occlusion to Prevent Stroke in High-Risk Patients With Atrial Fibrillation

Author:

Sievert Horst1,Lesh Michael D.1,Trepels Thomas1,Omran Heyder1,Bartorelli Antonio1,Della Bella Paola1,Nakai Toshiko1,Reisman Mark1,DiMario Carlo1,Block Peter1,Kramer Paul1,Fleschenberg Dirk1,Krumsdorf Ulrike1,Scherer Detlef1

Affiliation:

1. From the Cardiovascular Center Bethanien (H.S., T.T., D.F., U.K., D.S.), Frankfurt; Germany; University of California (M.D.L., T.N.), San Francisco; Appriva Medical (M.D., T.N.), Sunnyvale, Calif; the Department of Cardiology (H.O.), University Hospital Bonn, Bonn, Germany; Centro Cardiologico Monzino Istituto di Ricerca e Cura a Carattere Scientifico (A.B., P.D.B.), Milano, Italy; Swedish Medical Center (M.R.), Seattle, Wash; Hospital S Raffaele (C.D.), Milano, Italy; Emory University Hospital (P.B...

Abstract

Background Thromboembolism due to atrial fibrillation (AF) is a frequent cause of stroke. More than 90% of thrombi in AF form in the left atrial appendage (LAA). Obliteration of the appendage may prevent embolic complications. Methods and Results We evaluated the feasibility and safety of implanting a novel device for percutaneous left atrial appendage transcatheter occlusion (PLAATO). LAA occlusion using the PLAATO system was attempted in 15 patients with chronic AF at high risk for stroke, who are poor candidates for long-term warfarin therapy. The implant consists of a self-expanding nitinol cage covered with a polymeric membrane (ePTFE). The LAA was successfully occluded in 15/15 patients (100%). Angiography and transesophageal echocardiography (TEE) during the procedure showed that the device was well-seated in all patients and that there was no evidence of perforation, device embolization, or interference with surrounding structures. In 1 patient, the first procedure was complicated by a hemopericardium, which occurred during LAA access. A second attempt 30 days later was successful with no untoward sequela. No other complications occurred. At 1-month follow-up, chest fluoroscopy and TEE revealed continued stable implant position with smooth atrial-facing surface and no evidence of thrombus. Conclusions Thus, transcatheter closure of the LAA is feasible in humans. This novel implant technology may be appropriate for patients with AF who are not suitable candidates for anticoagulation therapy. Further trials are needed to show the long-term safety and its efficacy in reducing stroke.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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