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Suprasternal TranscatheterAortic Valve Replacement in Patients With Marginal Femoral Access

机译:Suprasternal Transcatheteraortic瓣膜置换边缘股骨通道患者

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Objective: Recently, the PARTNER 2 A trial reported results of transcatheter aortic valve replacement versus surgical aortic valve replacement in 2032 intermediate-risk patients at 2 years. Two hundred thirty-six patients (24%) required an access route other than transfemoral. Compared with transfemoral and surgical aortic valve replacement, nontrans- femoral transcatheter aortic valve replacement was associated with a numerically higher rate of death and disabling stroke at 30 days. This underscores the need for a better alternative surgical approach for patients with marginal femoral access. We reviewed our multicenter experience with minimally invasive suprasternal transcatheter aortic valve replacement.Methods: Consecutive patients with symptomatic severe aortic stenosis at high or intermediate risk for surgical aortic valve replacement underwent suprasternal transcatheter aortic valve replacement. A commercially available transcatheter heart valve was deployed under fluoroscopic guidance through the innominate artery or ascending aorta. Using a 3-cm skin incision just above the sternal notch, the Aegis Transit System (Aegis Surgical Ltd, Galway, Ireland) provided illuminated access to the mediastinum without bone disruption. Through a purse-string suture placed in the innominate artery or ascending aorta, transcatheter aortic valve replacement proceeded similarly to the direct aortic approach.Results: Thirty patients at six medical centers successfully underwent suprasternal transcatheter aortic valve replacement. Implanted valves included 2 CoreValve and 12 Evolut-R (Medtronic, Inc, Minneapolis, MN USA), as well as 10 SAPIEN 3 and 6 SAPIEN XT (Edwards Lifesciences, Corp, Irvine, CA USA) with sizes ranging from 23 to 31 mm. Median procedure time was 90 minutes and median hospital stay was 4 days. Postoperatively, new permanent pacemaker (n = 3) was the most common Vascular Academic Research Consortium 2 complication. Conclusions: These data demonstrate the early clinical feasibility of suprasternal transcatheter aortic valve replacement. Key advantages of this approach include direct access to the innominate artery and ascending aorta, precise sheath control, and confident arterial closure. Additional experience is warranted to confirm these favorable results.
机译:目的:近日,合作伙伴2审判报告报告的经截觉管主动脉瓣膜置换的结果与2年来2032例中间风险患者的外科主动脉瓣膜置换。二百三十六名患者(24%)需要除变酵母以外的接入路线。与经群和外科主动脉瓣膜置换相比,非触发因子转膜管主动脉瓣膜置换与数值较高的死亡率和30天禁用中风有关。这强调了对边际股权患者进行更好的替代外科手术方法。我们审查了多中心体验,具有微创的Suprasternal经截管主动脉瓣更换。方法:手术主动脉瓣膜置换的高或中间风险的连续患者对症状严重主动脉狭窄的患者进行了高血压性主动脉瓣膜主动脉瓣膜置换术。在荧光透视引导下,通过无名的动脉或升压展开市售的经截管心瓣。在胸骨凹口上方的3厘米皮肤切口,Aegis Transit System(Aegis Surgical Ltd,Galway,爱尔兰)提供了对纵隔的照明通道而没有骨干。通过置于无名动脉或上升主动脉的钱包缝合缝合线,经沟管主动脉瓣更换与直接主动脉接近类似。结果:六名医疗中心的30名患者成功完成了Suprasternal经膜转带主动脉瓣膜置换术。植入阀包括2个CoreValve和12 Evolut-R(Medtronic,Inc,Minneapolis,Mn USA),以及10个Sapien 3和6 Sapien XT(Edwards Lifesciences,Corp,Irvine,CA USA),尺寸为23至31毫米。中位数程序时间为90分钟,中位医院住宿时间为4天。术后,新的永久起搏器(n = 3)是最常见的血管学术研究联盟2个复杂性。结论:这些数据表明了Suprasternal经膜转闭管主动脉瓣膜置换的早期临床可行性。这种方法的主要优点包括直接进入无名的动脉和升序主动脉,精确的鞘控制和自信的动脉闭合。额外的经验是有必要确认这些有利的结果。

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