Cardiology Clinical Academic Group, St. George's, University of London and St. George's Hospital, St. George's University Hospitals NHS Foundation Trust, London, UK.
Department of Cardiology, Harefield Hospital, Royal Brompton and Harefield NHS Foundation Trust, London, UK.
Catheter Cardiovasc Interv. 2020 Jun 1;95(7):1340-1346. doi: 10.1002/ccd.28512. Epub 2019 Nov 11.
The United Kingdom and Ireland Implanters' registry is a multicenter registry which reports on real-world experience with new transcatheter heart valves.
The Evolut PRO (Medtronic, Minneapolis, MN) transcatheter aortic valve is a self-expanding transcatheter aortic valve with an outer pericardial wrap, designed to minimize paravalvular regurgitation.
Between July 2017 and December 2018, clinical, procedural, and 30-day outcome data were prospectively collected from all patients receiving the Evolut PRO valve across nine participating centers in the United Kingdom and Ireland. The primary efficacy outcome was the Valve Academic Research Consortium-2 (VARC-2)-defined endpoint of device success. The primary safety outcome was the VARC-2-defined composite endpoint of early safety at 30 days.
A total of 317 patients underwent implantation. Mean age was 81.8 ± 6.4 years and Society of Thoracic Surgeons Predicted Risk of Mortality Score 5.5 ± 1.8%. Iliofemoral access was used in 99.1% of patients. Device success was 91.2%. Mean gradient was 7.6 ± 4.7 mmHg and effective orifice area 1.9 ± 0.7 cm . The incidence of moderate paravalvular regurgitation was 1.7% and there was no severe paravalvular regurgitation. A new permanent pacemaker was implanted in 17.8% of patients without a pacemaker at baseline. Early safety was demonstrated in 92.7%. At 30 days, all-cause mortality was 0.6%, stroke 3.8%, and major vascular complication 2.8%.
Real-world experience of the Evolut PRO transcatheter aortic valve demonstrated favorable procedural success, safety, valve function, and incidence of new permanent pacemaker implantation.
英国和爱尔兰植入者登记处是一个多中心登记处,报告了新经导管心脏瓣膜的真实世界经验。
Evolut PRO(美敦力,明尼苏达州明尼阿波利斯)经导管主动脉瓣是一种自扩张经导管主动脉瓣,带有外心包包裹,旨在最大限度地减少瓣周漏。
2017 年 7 月至 2018 年 12 月,在英国和爱尔兰的 9 个参与中心,前瞻性地收集了所有接受 Evolut PRO 瓣膜治疗的患者的临床、手术和 30 天结局数据。主要疗效终点是 Valve Academic Research Consortium-2(VARC-2)定义的器械成功终点。主要安全性终点是 30 天早期安全性的 VARC-2 定义的复合终点。
共 317 例患者接受了植入术。平均年龄为 81.8±6.4 岁,胸外科医生协会预测死亡率评分 5.5±1.8%。股髂入路在 99.1%的患者中使用。器械成功率为 91.2%。平均梯度为 7.6±4.7mmHg,有效瓣口面积为 1.9±0.7cm²。中度瓣周漏的发生率为 1.7%,无严重瓣周漏。基线时无起搏器的患者中有 17.8%植入了新的永久性起搏器。早期安全性为 92.7%。30 天时,总死亡率为 0.6%,卒中 3.8%,大血管并发症 2.8%。
Evolut PRO 经导管主动脉瓣的真实世界经验显示了良好的手术成功率、安全性、瓣膜功能和新的永久性起搏器植入率。