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首页> 外文期刊>Case Reports & Clinical Practice Review >“Mind the Gap”: An 85-Year-Old Man with Severe Tricuspid Valve Regurgitation Who Underwent Percutaneous Edge-to-Edge Valve Leaflet Plication Using the New and Advanced MitraClip XTR System
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“Mind the Gap”: An 85-Year-Old Man with Severe Tricuspid Valve Regurgitation Who Underwent Percutaneous Edge-to-Edge Valve Leaflet Plication Using the New and Advanced MitraClip XTR System

机译:“思想差距”:一个85岁的男子,具有严重的三尖瓣反流,使用新的和先进的MITRACLIP XTR系统进行经皮到边缘阀门传单。

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Severe tricuspid valve regurgitation (TR) is associated with high cardiovascular mortality. Safe and feasible interventional approaches to treat severe TR are of clinical relevance. The MitraClip is a device that has been approved by the US Food and Drug Administration (FDA) for the repair of mitral valve lesions. Percutaneous femoral venous access with fluoroscopic and echocardiographic guidance is used to deliver a cobalt-chromium clip to secure the mitral valve leaflets. We report on an 85-year-old man with tricuspid valve regurgitation who underwent percutaneous edge-to-edge tricuspid valve leaflet plication with the new, advanced MitraClip XTR System. CASE REPORT: An 85-year-old man with severe TR due to annulus dilation of the right ventricle and short septal leaflet presented repeatedly at our hospital with severe right heart failure symptoms. Transesophageal echocardiography revealed severe TR with a large coaptation gap size of 10.6 mm. Percutaneous edge-to-edge valve repair with the new-generation MitraClip System XTR with wider clip arms could overcome the large coaptation gap. We achieved a strong reduction of TR after deploying 2 MitraClips XTR. The patient recovered quickly and has not been admitted to hospital due to heart failure symptoms since the intervention for more than 6 months. CONCLUSIONS: Previous studies have shown the safety and effectiveness of the MitraClip device and supported FDA approval for tricuspid valve repair. This report of a patient with complex tricuspid regurgitation demonstrated the feasible use of the new MitraClip XTR System, which improved edge-to-edge tricuspid valve repair due to its increased span and improved grip.
机译:严重的三尖瓣反流(TR)与高心血管死亡率相关。治疗严重TR的安全和可行的介入方法具有临床相关性。 MitroAclip是美国食品和药物管理局(FDA)批准的装置,用于修复二尖瓣病变。用荧光镜和超声心动图引导经皮股静脉静脉接触用于递送钴铬夹以固定二尖瓣小叶。我们报告了一名85岁男性,具有三尖瓣反流的阀门反流,经历了经过经皮到边缘三尖瓣传单,具有新的先进的MITRACLIP XTR系统。案例报告:由于右心室的右心室和短隔行传单的环扩张,一个85岁男性,具有严重的右心力衰竭症状,右心室扩张和短的间隔传单。经细胞眼镜超声心动图显示出严重的TR,施胶差间隙尺寸为10.6毫米。具有较宽夹子臂的新一代Mitraclip系统XTR的经皮边缘到边缘阀门修复可以克服大的拟涂差距。我们在部署2 Mitraclips XTR后,我们实现了强大的TR。患者迅速恢复,并且由于心力衰竭症状,由于干预超过6个月,尚未入院。结论:以前的研究表明,Mitraclip器件的安全性和有效性,并支持FDA对三尖瓣修复的批准。具有复杂三尖瓣反流的患者的报告证明了新的MitraClip XTR系统的可行性,该XTR系统改善了边缘到边缘的三尖瓣修复,这是由于其跨度的增加和改进的抓地力。

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