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经导管治疗原发性主动脉瓣反流:使用经股动脉ACURATE瓣膜的国际注册研究结果

Transcatheter treatment of native aortic valve regurgitation: Results from an international registry using the transfemoral ACURATE valve.

作者信息

Purita Paola Angela Maria, Tahoces Luisa Salido, Fraccaro Chiara, Nai Fovino Luca, Kim Won-Keun, Espada-Guerreiro Cláudio, De Backer Ole, Seiffert Morritz, Nombela-Franco Luis, Gomez Raul Moreno, Mangieri Antonio, Franzone Anna, Bedogni Francesco, Castriota Fausto, Attisano Tiziana, Søndergaard Lars, Antolin Rosana Hernandez, Tarantini Giuseppe

机构信息

Division of Cardiology Ospedale dell'Angelo, Mestre, Italy.

University Hospital Ramon y Cajal, Madrid, Spain.

出版信息

Int J Cardiol Heart Vasc. 2020 Feb 12;27:100480. doi: 10.1016/j.ijcha.2020.100480. eCollection 2020 Apr.

Abstract

BACKGROUND

Transcatheter aortic valve replacement (TAVR) has been validated for the treatment of severe symptomatic aortic stenosis in patients at high and intermediate surgical risk. Recently, TAVR has been proposed as an alternative to medical therapy in inoperable patients with severe native aortic valve regurgitation (NAVR). This multicenter international registry sought to evaluate safety and efficacy of TAVR with the self-expandable ACURATE valve in a cohort of patients with NAVR.

METHODS

A total of 24 patients with severe NAVR treated by TAVR between September 2016 and October 2018 in 13 European centers were included. Clinical, procedural and follow up data were inserted in a dedicated database. Outcomes were codified according to Valve Academic Research Consortium-2 criteria.

RESULTS

Mean age was 79.4 years, 58.4% were female. Mean EuroSCORE II and STS score were 5% and 3.9%, respectively. Device success was 87.5%. Moderate paravalvular leak (PVL) was found in two (8.3%) of patients, both with a perimeter oversizing index <10%. Implantation of a second device was necessary in three cases (12.5%), one for severe PVL and two for device displacement. New pacemaker implantation rate was 21.1%. At 30 days, stroke and all-cause mortality rates were 0% and 4.1%, respectively.

CONCLUSIONS

This multicenter study suggests good feasibility and early safety of transfemoral TAVR with the self-expandable ACURATE device in patients with severe NAVR refused for surgery. Rates of moderate PVL, new pacemaker implantation and need for a second valve were higher than those reported for TAVR in aortic stenosis.

摘要

背景

经导管主动脉瓣置换术(TAVR)已被证实可用于治疗手术风险高和中等的严重症状性主动脉瓣狭窄患者。最近,TAVR被提议作为无法手术的严重原发性主动脉瓣反流(NAVR)患者药物治疗的替代方案。这项多中心国际注册研究旨在评估使用自膨胀式ACURATE瓣膜进行TAVR在一组NAVR患者中的安全性和有效性。

方法

纳入了2016年9月至2018年10月期间在13个欧洲中心接受TAVR治疗的24例严重NAVR患者。临床、手术和随访数据被录入一个专用数据库。结局根据瓣膜学术研究联盟-2标准进行编码。

结果

平均年龄为79.4岁,58.4%为女性。平均欧洲心脏手术风险评估系统II(EuroSCORE II)和胸外科医师协会(STS)评分分别为5%和3.9%。器械成功率为87.5%。两名(8.3%)患者发现有中度瓣周漏(PVL),两者外周扩大指数均<10%。3例(12.5%)患者需要植入第二个器械,1例因严重PVL,2例因器械移位。新起搏器植入率为21.1%。在30天时,卒中率和全因死亡率分别为0%和4.1%。

结论

这项多中心研究表明,对于拒绝手术的严重NAVR患者,经股动脉TAVR使用自膨胀式ACURATE器械具有良好的可行性和早期安全性。中度PVL、新起搏器植入率和第二个瓣膜的需求率高于主动脉瓣狭窄患者TAVR报告的比率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9483/7016455/a0a7d8451deb/gr1.jpg

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