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LEFT ATRIAL APPENDAGE CLOSURE IN PATIENTS WITH MECHANICAL MITRAL VALVE PROSTHESIS: A MULTICENTER ITALIAN PILOT STUDY

医学 心房颤动 内科学 心脏病学 冲程(发动机) 血栓形成 维生素K拮抗剂 心力衰竭 临床终点 不利影响 外科 华法林 随机对照试验 机械工程 工程类
作者
Alberto Preda,Davide Margonato,Carlo Gaspardone,Vincenzo Rizza,Ciro Vella,Lorenzo Rampa,Alessandra Marzi,Fabrizio Guarracini,Paolo Della Bella,Eustachio Agricola,Achille Gaspardone,Matteo Montorfano,Patrizio Mazzone
出处
期刊:Canadian Journal of Cardiology [Elsevier]
被引量:1
标识
DOI:10.1016/j.cjca.2024.01.039
摘要

Introduction In patients with atrial fibrillation (AF) on vitamin K antagonist (VKA) therapy and therapeutical INR range the incidence of cardiac thromboembolism is not negligible and the subgroup carrying a mechanical prosthetic mitral valve (PMV) has the highest risk. We aimed to assess the long-term effects of left atrial appendage closure (LAAC) in AF patients carriers of mechanical PMV who experienced a failure of VKA therapy. Methods In this retrospective, multicenter study, patients underwent LAAC because of thrombotic events including TIA/stroke, systemic embolism and evidence of left atrial appendage thrombosis/sludge despite VKA therapy were enrolled. Patients with mechanical PMV were included and compared with those affected by non valvular AF. The primary endpoint was the composite of all-cause death, major cardiovascular events and major bleedings at follow-up. Feasibility and safety of LAAC was also assessed. Results 55 patients (42% females; mean age 70 ± 9 years) including 12 carriers of mechanical PMV were enrolled. The most frequent indication to LAAC (71%) was LAA thrombosis or sludge. Procedural success was achieved in 96% of overall cases and in 100% of patients with PMV. In 35 patients a cerebral protection device was used. During a median follow-up of 6.1 ± 4.3 years, 4 patients with PMV and 20 patients without PMV reported adverse events (HR 0.73 [95% CI 0.25 – 2.16, p=0.564]). Conclusion LAAC seems to be a valuable alternative in AF carriers of mechanical PMV with failure of VKA therapy. This off-label, real-world clinical practice indication deserve validation in further studies.
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