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股动脉入路受限患者的胸骨上窝经导管主动脉瓣置换术

Suprasternal Transcatheter Aortic Valve Replacement in Patients With Marginal Femoral Access.

作者信息

Kiser Andy C, Caranasos Thomas G, Peterson Mark D, Holzhey David M, Kiefer Philipp, Nifong L Wiley, Borger Michael A

出版信息

Innovations (Phila). 2018 Jan/Feb;13(1):1-4. doi: 10.1097/IMI.0000000000000462.

Abstract

OBJECTIVE

Recently, the PARTNER 2A 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, nontransfemoral 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.

摘要

目的

近期,“PARTNER 2A试验”报告了2032例中度风险患者接受经导管主动脉瓣置换术与外科主动脉瓣置换术2年的结果。236例患者(24%)需要经股动脉以外的入路途径。与经股动脉和外科主动脉瓣置换术相比,非经股动脉经导管主动脉瓣置换术在30天时的死亡和致残性卒中发生率在数值上更高。这凸显了为股动脉入路条件欠佳的患者寻求更好的替代手术方法的必要性。我们回顾了我们在微创胸骨上窝经导管主动脉瓣置换术方面的多中心经验。

方法

对有症状的重度主动脉瓣狭窄且外科主动脉瓣置换术风险高或中度的连续患者进行胸骨上窝经导管主动脉瓣置换术。在透视引导下,通过无名动脉或升主动脉植入市售经导管心脏瓣膜。在胸骨切迹上方做一个3厘米的皮肤切口,使用Aegis Transit系统(Aegis Surgical Ltd,爱尔兰戈尔韦)在不破坏骨骼的情况下提供照亮的纵隔入路。通过在无名动脉或升主动脉放置荷包缝线,经导管主动脉瓣置换术的操作与直接主动脉入路相似。

结果

六个医学中心的30例患者成功接受了胸骨上窝经导管主动脉瓣置换术。植入的瓣膜包括2个CoreValve和12个Evolut - R(美敦力公司,美国明尼阿波利斯),以及10个SAPIEN 3和6个SAPIEN XT(爱德华生命科学公司,美国加利福尼亚州欧文),尺寸范围为23至31毫米。手术中位时间为90分钟,住院中位时间为4天。术后,新的永久性起搏器(n = 3)是最常见的血管学术研究联盟2级并发症。

结论

这些数据证明了胸骨上窝经导管主动脉瓣置换术的早期临床可行性。该方法的主要优点包括直接进入无名动脉和升主动脉、精确的鞘管控制以及可靠的动脉闭合。需要更多经验来证实这些良好结果。

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