首页> 美国卫生研究院文献>European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-thoracic Surgery >Transcatheter aortic valve implantation using the ACURATE TA™ system: 1-year outcomes and comparison of 500 patients from the SAVI registries
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Transcatheter aortic valve implantation using the ACURATE TA™ system: 1-year outcomes and comparison of 500 patients from the SAVI registries

机译:使用ACURATE TA™系统的经导管主动脉瓣植入术:1年结果并比较SAVI登记处的500名患者

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摘要

>OBJECTIVES: The ACURATE TATM system is a self-expanding transcatheter heart valve system designed for transapical access which has been proven to be safe and effective in the controlled setting of clinical trials. The SAVI-1 and SAVI-2 registries aimed to assess whether these promising outcomes can be translated into all-comers clinical routine. >METHODS: From November 2011 to 2012 (SAVI-1), and November 2013 to 2014 (SAVI-2), a total of 500 patients were enrolled in the prospective, all-comers, multicentre, multinational SAVI registries. Patients were treated according to the standard of care at their respective hospitals. We report and compare 30-day and 1-year clinical outcomes between SAVI-1 and -2. >RESULTS: Patients were 80.8 ± 6.1 years old, the mean logistic EuroSCORE-I was 23.4 ± 14.3%. Valves were deployed under rapid pacing in 71.3% of the procedures in SAVI-1, and in 3.6% in SAVI-2. There was no relevant difference in clinical and echocardiographic outcomes between SAVI-1 and SAVI-2. Overall mortality at 30 days and 1 year was 6.8% and 19.9%, the stroke rate was 2.2% and 3.7%, respectively; 10.2% of patients had received a permanent pacemaker, and no transcatheter valve-related complications after discharge were observed. Paravalvular leakage ≥2+ was reported in 1.9% of the patients at the early follow-up, and in 2.6% at the 1-year follow-up. >CONCLUSIONS: The SAVI-registries have confirmed that transapical implantation using the ACURATE TATM device is safe and effective in an all-comers setting with low complication rates and stable performance outcomes at short-term and 1 year; outcomes were similar between SAVI-1 and -2. >ClinicalTrials.gov:
机译:>目标:ACURATE TA TM 系统是一种专为经心尖通路设计的自扩张式经导管心脏瓣膜系统,已被证明在临床试验的可控环境中是安全有效的。 SAVI-1和SAVI-2注册表旨在评估这些有希望的结果是否可以转化为所有患者的临床常规检查。 >方法:从2011年11月至2012年(SAVI-1)和2013年11月至2014年11月(SAVI-2),共有500名患者入选了前瞻性,全科,多中心,跨国SAVI注册表。按照各自医院的护理标准对患者进行了治疗。我们报告并比较SAVI-1和-2之间30天和1年的临床结果。 >结果:患者年龄为80.8±6.1岁,平均Logistic EuroSCORE-I为23.4±14.3%。在SAVI-1中,以71.3%的程序快速部署阀门,在SAVI-2中以3.6%的速度部署阀门。 SAVI-1和SAVI-2在临床和超声心动图结果方面无相关差异。 30天和1年的总死亡率分别为6.8%和19.9%,中风发生率分别为2.2%和3.7%; 10.2%的患者已接受永久性起搏器,出院后未观察到经导管瓣膜相关的并发症。在早期随访中,有1.9%的患者发生瓣周漏≥2+ and,而在1年随访中,有2.6%的患者发生了瓣周漏。 >结论:SAVI登记处证实,在所有患者中,并发症发生率低且手术结果稳定的条件下,使用ACURATE TA TM 装置进行经心尖植入是安全有效的。短期和一年; SAVI-1和-2的转归相似。 > ClinicalTrials.gov:

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