Left atrial appendage exclusion using a stapler with thoracoscopic ablation of atrial fibrillation

A. Revishvili, M. Kadirova, E. Strebkova, E. S. Malishenko, M. Novikov, E. V. Yalova, K. A. Babadjanova, K. E. Bandurko, G. Karmazanovsky
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引用次数: 1

Abstract

Highlights. Stroke prevention in patients with atrial fibrillation is extremely important and difficult. Lifelong anticoagulant therapy is not always an effective way of preventing thrombosis in the left atrial appendage in this group of patients. In this regard, one of the most urgent problems of modern surgical arrhythmology and cardiac surgery is the search for new open and minimally invasive surgical methods of excluding the left atrial appendage from the blood flow.Aim. To investigate the safety and efficacy of using the left atrial appendage stapler for video-guided thoracoscopic ablation (TSA) of non-valvular atrial fibrillation (AF).Methods. The retrospective, single-center study included 100 patients with non-valvular AF who underwent video-guided thoracoscopic ablation of AF with single-stage left atrial appendage exclusion using an Endo GIA stapler (Medtronic, Minneapolis, Minnesota, USA).Results. The mean age of the patients was 56,2±8,8 years, the majority of the patients (73 patients, 73%) were male. Patients with persistent 50 (50%) AF and longstanding AF 50 (50%) were included in the study. The duration of atrial fibrillation was 4 (1,7–7) years. The median CHA2DS2-VASc and HAS-BLED scores were 2 (1–1,5) and 1 (0-1), respectively. The mean anticoagulation therapy-to-ablation time was 4,2±1,9 years. Thirty-eight (38%) patients were prescribed warfarin preoperatively. The completeness of left atrial appendage (LAA) exclusion was confirmed by intraoperative transesophageal echocardiography. The average length of the staple lines was 48 (35–75). A single left atrial appendage exclusion was performed using a 60 mm staples. In 12 (12%) patients, stapler exclusions were performed using two 45 mm staples due to insufficient staple length. None of the patients had ruptures, punctures along the staple lines or rupture of the surrounding epicardial tissue. Anticoagulant therapy was discontinued 6 months after TSA in 70 (70%) patients with sustained sinus rhythm observed on 24-h Holter Monitoring, satisfactory CHA2DS2-VASc scores and after confirmation of absence of left atrial thrombus by transesophageal echocardiography and contrast-enhanced MSCT. No strokes were reported within 1,2±0,7 years after discontinuing anticoagulation therapy.Conclusion. Exclusion of LAA using a stapler for TSA is a highly effective and safe technique for patients with non-valvular atrial fibrillation compared to alternative methods of excluding the LAA from the systemic blood flow.
胸腔镜下心房颤动消融术联合吻合器排除左心房附件
高光。房颤患者脑卒中的预防是极其重要和困难的。终生抗凝治疗并不总是预防左心耳血栓形成的有效方法。在这方面,现代外科心律失常学和心脏外科最紧迫的问题之一是寻找新的开放和微创的手术方法,使左心耳与血流隔绝。探讨左心耳吻合器在视频引导下胸腔镜消融(TSA)治疗非瓣膜性心房颤动(AF)的安全性和有效性。这项回顾性、单中心研究纳入了100例非瓣膜性房颤患者,这些患者使用Endo GIA吻合器(Medtronic, Minneapolis, Minnesota, USA)接受了视频引导的房颤胸腔镜消融并单期左房附件排除。患者平均年龄56,2±8.8岁,男性居多(73例,73%)。持续性50型房颤(50%)和长期50型房颤(50%)患者被纳入研究。房颤持续时间为4(1,7 - 7)年。CHA2DS2-VASc和HAS-BLED评分中位数分别为2(1 - 1,5)和1(0-1)。抗凝治疗至消融的平均时间为4.2±1.9年。38例(38%)患者术前使用华法林。术中经食管超声心动图证实左心耳排除的完全性。短绒线平均长度为48(35-75)。单左心房附件排除使用60毫米订书钉。在12例(12%)患者中,由于订书机长度不足,使用两个45毫米订书机进行订书机排除。没有患者有破裂,沿着钉线穿刺或周围心外膜组织破裂。经24小时动态心电图监测、CHA2DS2-VASc评分满意、经食管超声心动图和增强MSCT确认左房无血栓的70例(70%)患者,在TSA后6个月停止抗凝治疗。停止抗凝治疗后1、2±0.7年内无卒中报告。与从全身血流中排除LAA的其他方法相比,使用吻合器排除LAA对于非瓣膜性心房颤动患者是一种非常有效和安全的技术。
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