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首页> 外文期刊>EuroIntervention: journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology >Transcatheter valve-in-valve implantation with the Edwards Sapien in patients with bioprosthetic heart valve failure: The Milan experience
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Transcatheter valve-in-valve implantation with the Edwards Sapien in patients with bioprosthetic heart valve failure: The Milan experience

机译:爱德华兹·萨皮恩(Edwards Sapien)经导管置入瓣膜植入术治疗生物人工心脏瓣膜衰竭的患者:米兰经验

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Aims: Reoperation for bioprosthetic heart valve failure is associated with significant morbidity and mortality, particularly in high-risk patients. Transcatheter valve-in-valve (VIV) implantation may offer a less invasive alternative. The aim of this study was to report our initial experience with transcatheter VIV implantation to treat degenerated tissue valves. Methods and results: VIV implantation with the Edwards SAPIEN transcatheter heart valve (THV; Edwards Lifesciences Inc, Irvine, CA, USA) was performed in 18 high-risk patients (STS 8.2±5.2%; logistic EuroSCORE 37.4±20.8%) with symptomatic bioprosthetic failure (17 aortic, one mitral). Valve Academic Research Consortium (VARC) definitions were applied for endpoint adjudication. Transfemoral access was the preferred vascular approach (16 patients, with the mitral VIV delivered anterogradely through the femoral vein; one transaxillary and one transapical). The majority (83%) of procedures were performed under local anaesthesia and sedation. Device success was achieved in all but one patient who had a final transaortic gradient ≥20mmHg. Acute kidney injury occurred in three patients (Stage 3 in 1), life-threatening or major bleeding in four patients, while major vascular complications occurred in one patient. Permanent pacemaker implantation was required in two patients. There were no deaths or neurological events at 30-day follow-up. At a median follow-up of 11 months (interquartile range 6-16), the mortality rate was 5.6% and all patients were in NYHA class II or lower. Conclusions: Transcatheter implantation of the Edwards THV within a degenerated aortic bioprosthesis, performed predominantly via the transfemoral route, is feasible and associated with good periprocedural and clinical outcomes in high-risk surgical patients.
机译:目的:因人工心脏瓣膜衰竭而再次手术会导致较高的发病率和死亡率,特别是在高危患者中。经导管瓣膜内(VIV)植入可能提供侵入性较小的替代方法。这项研究的目的是报告我们在经导管VIV植入治疗变性组织瓣膜方面的初步经验。方法和结果:对有症状的18例高危患者(STS 8.2±5.2%;后勤EuroSCORE 37.4±20.8%)行爱德华兹SAPIEN经导管心脏瓣膜(THV;爱德华兹生命科学公司,欧文,CA,美国)进行VIV植入生物修复失败(主动脉17个,二尖瓣1个)。 Valve学术研究协会(VARC)的定义适用于终点裁决。经股动脉入路是首选的血管介入治疗方法(16例患者,二尖瓣VIV通过股静脉顺行递送;一根经腋窝和一根经心尖)。大多数手术(83%)是在局部麻醉和镇静下进行的。除一名最终主动脉梯度≥20mmHg的患者外,所有患者均获得了设备成功。急性肾损伤发生在3例患者中(第3阶段,共1阶段),危及生命或严重出血的有4例,而重大血管并发症发生在1例患者中。两名患者需要永久性起搏器植入。在30天的随访中没有死亡或神经系统事件。中位随访11个月(四分位间距为6-16),死亡率为5.6%,所有患者均为NYHA II级或更低。结论:主要通过经股动脉途径在变性的主动脉生物假体中经导管植入Edwards THV是可行的,并且在高风险手术患者中具有良好的围手术期和临床效果。

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