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美敦力 ·  11/27 13:00

Two data releases at London Valves 2024 build on Evolut's legacy of valve design and performance:

2024 年伦敦阀门展上发布的两份数据建立在 Evolut 的阀门设计和性能传统基础上:

Optimize PRO study demonstrates improved procedure efficiencies and valve performance

Optimize PRO 研究表明手术效率和阀门性能得到改善

Pooled analysis shows improvement in PVL with Evolut PRO TAVR system through 3 years

汇总分析显示,使用 Evolut PRO TAVR 系统的 PVL 在 3 年内有所改善

Medtronic plc, a global leader in healthcare technology, today announced new data for the Evolut Transcatheter Aortic Valve Replacement System (TAVR) at PCR London Valves 2024. This new clinical evidence brings further insights to global implanters treating patients with symptomatic severe aortic stenosis (SASS). New findings from the Optimize PRO clinical study demonstrated favorable procedural and clinical outcomes following use of an optimized care pathway and the cusp overlap technique (COT) to deploy Evolut valves. Additionally, a pooled analysis of Evolut PRO patients was shared showing improvement in rates of paravalvular leak (PVL) in TAVR patients, over time following hospital discharge.

医疗保健技术领域的全球领导者美敦力集团今天在2024年伦敦聚合酶链反应会议上公布了Evolut经导管主动脉瓣置换系统(TAVR)的新数据。这些新的临床证据为治疗有症状的严重主动脉瓣狭窄(SASS)患者的全球植入者提供了进一步的见解。Optimize PRO临床研究的新发现表明,在使用优化的护理途径和尖点重叠技术(COT)部署Evolut瓣膜后,程序和临床效果良好。此外,还分享了对Evolut PRO患者的汇总分析,结果显示,随着时间的推移,TAVR患者的肺泡旁渗漏(PVL)率在出院后有所改善。

Optimize PRO Study: Global Standardized TAVR Technique Delivers Favorable Procedural and Clinical Outcomes

优化 PRO 研究:全球标准化 TAVR 技术提供良好的手术和临床结果

Full 30-day findings from the Optimize PRO global study show utilization of the cusp overlap technique with the Evolut PRO and PRO+ devices led to favorable procedural and clinical outcomes. Findings of the multi-center, post-market, prospective study conducted in 50 centers globally demonstrated low rates of new 30-day permanent pacemaker implantation (6.4% with cusp overlap technique compliance) and no moderate or severe aortic regurgitation at discharge.

Optimize PRO全球研究为期30天的完整发现表明,将尖点重叠技术与Evolut PRO和PRO+设备一起使用可带来良好的手术和临床结果。这项在全球50个中心进行的多中心、上市后的前瞻性研究表明,新的30天永久起搏器植入率很低(牙尖重叠技术合规性为6.4%),出院时没有中度或重度主动脉反流。

The Optimize PRO clinical study evaluated valve performance and procedural outcomes associated with an "optimized" pre- and post-procedural TAVR care pathway, utilizing the cusp overlap technique to deploy the Evolut valves. The cusp overlap technique is designed to help implanters assess and achieve the optimal implant depth to reduce interaction with the conduction system. At 30 days, the primary endpoint of all-cause mortality or all stroke was 5.1%, all-cause mortality 0.8%, disabling stroke 1.7%, and cardiovascular rehospitalization was 5.7%.

Optimize PRO临床研究利用尖点重叠技术部署Evolut瓣膜,评估了与 “优化” 术前和术后TAVR护理途径相关的瓣膜性能和手术结果。牙尖重叠技术旨在帮助植入者评估和实现最佳植入深度,以减少与传导系统的相互作用。在30天时,全因死亡率或所有中风的主要终点为5.1%,全因死亡率为0.8%,致残性中风为1.7%,心血管再住院率为5.7%。

"We are encouraged by this data as it demonstrates significant positive outcomes when leveraging the cusp overlap technique with the Evolut valve," said Steven J. Yakubov, MD, MSCAI, FACC, OhioHealth Riverside Methodist Hospital and co-principal investigator. "The new results support a standardized protocol that will help support early hospital discharge and lower rates of complications for our patients, improving their quality of life."

俄亥俄健康河滨卫理公会医院FACC医学博士、联合首席研究员史蒂芬·雅库博夫说:“这些数据表明,在利用尖点重叠技术与Evolut瓣膜合作时,我们对这些数据感到鼓舞。”“新结果支持标准化方案,这将有助于支持患者尽早出院和降低并发症发生率,改善他们的生活质量。”

Improvement in Paravalvular Leak Over Time with Evolut PRO Transcatheter Aortic Valve

使用 Evolut PRO 经导管主动脉瓣随着时间的推移改善瓣膜旁渗漏

This paired analysis assessed improvement in PVL over time post-TAVR with the Evolut PRO valve in patients with SSAS. The study analyzed core lab echocardiographic data from 620 patients treated with Evolut PRO from the prospective Evolut Low Risk Trial, FORWARD PRO Study, and Evolut PRO US Study. The analysis demonstrated improvements in severity of PVL - a leak that occurs when blood flows backward between the heart's natural tissue and a replacement valve - after 30 days post-hospital discharge to 3-year follow-up.

该配对分析评估了SSAS患者在使用Evolut PRO瓣膜进行TAVR后一段时间内PVL的改善。该研究分析了来自前瞻性Evolut低风险试验、FORWARD PRO研究和Evolut PRO美国研究的620名接受Evolut PRO治疗的患者的核心实验室超声心动图数据。分析表明,PVL(一种血液在心脏自然组织和替代瓣膜之间向后流动时发生的泄漏)的严重程度有所改善,PVL(一种血液在心脏自然组织和替代瓣膜之间向后流动时发生的泄漏)在出院30天后进行为期3年的随访。

From the paired analysis of patients with available data at all follow-up visits, the PVL severity for 30 days post-hospital discharge was 60.8% none/trace, 36.0% mild, 2.9% moderate, and 0.3% severe. At 3-year follow-up, the PVL severity was 79.8% none/trace, 19.6% mild, 0.6% moderate and 0.0% severe. The occurrence of worsened PVL from discharge/30 days to 3-year follow-up was uncommon.

根据对患者的配对分析以及所有随访就诊的可用数据,出院后30天的PVL严重程度为60.8%无/痕量,36.0%为轻度,2.9%为中度,0.3%为重度。在3年随访中,PVL的严重程度为79.8%为无/痕迹,19.6%为轻度,0.6%为中度,0.0%为重度。从出院/30天到3年随访期间PVL恶化的情况并不常见。

"This analysis expands upon previous studies and found a majority of patients classified with mild or greater PVL improved in their PVL severity at 3 years," said Nicolas Van Mieghem, MD, PhD, Thoraxcenter, Erasmus University Medical Center in Rotterdam, The Netherlands, and lead investigator "This study will help inform physicians on the treatment of this complication post-TAVR."

荷兰鹿特丹伊拉斯姆斯大学医学中心胸科中心医学博士、首席研究员尼古拉斯·范·米格姆说:“这项分析扩展了先前的研究,发现大多数被归类为轻度或更高PVL的患者的PVL严重程度在3年后有所改善。” 这项研究将帮助医生了解TAVR后这种并发症的治疗方法。”

"With the Evolut TAVR system, we are committed to improving outcomes for patients while maintaining exceptional safety and efficiency" said Nina Goodheart, senior vice president and president of the Structural Heart & Aortic business, which is part of the Cardiovascular Portfolio at Medtronic. "The data presented at London Valves 2024 further establishes Medtronic and Evolut as leaders in the supporting and sharing the robust clinical evidence physicians need to make the best decisions for their patients when choosing and performing TAVR."

美敦力心血管产品组合中的结构心脏和主动脉业务高级副总裁兼总裁妮娜·古德哈特说:“借助Evolut TAVR系统,我们致力于改善患者的预后,同时保持卓越的安全性和效率。”“2024年伦敦Valves上公布的数据进一步确立了美敦力和Evolut在支持和分享医生在选择和实施TAVR时为患者做出最佳决策所需的有力临床证据方面的领导者。”

About Medtronic

关于美敦力

Bold thinking. Bolder actions. We are Medtronic. Medtronic plc, headquartered in Galway, Ireland, is the leading global healthcare technology company that boldly attacks the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people across 150 countries. Our technologies and therapies treat 70 health conditions and include cardiac devices, surgical robotics, insulin pumps, surgical tools, patient monitoring systems, and more. Powered by our diverse knowledge, insatiable curiosity, and desire to help all those who need it, we deliver innovative technologies that transform the lives of two people every second, every hour, every day. Expect more from us as we empower insight-driven care, experiences that put people first, and better outcomes for our world. In everything we do, we are engineering the extraordinary. For more information on Medtronic, visit , and follow Medtronic on LinkedIn.

大胆思考。更大胆的行动。我们是美敦力。总部位于爱尔兰戈尔韦的美敦力公司是全球领先的医疗保健技术公司,通过寻找和寻找解决方案,大胆地应对人类面临的最具挑战性的健康问题。我们的使命——减轻痛苦、恢复健康和延长寿命——团结了一支由来自150个国家的95,000多名充满激情的人组成的全球团队。我们的技术和疗法可治疗 70 种健康状况,包括心脏设备、手术机器人、胰岛素泵、手术工具、患者监护系统等。在我们多样的知识、永不满足的好奇心以及帮助所有有需要的人的愿望的推动下,我们提供创新技术,每秒、每小时、每天都在改变两个人的生活。随着我们赋予以洞察为导向的医疗服务、以人为本的体验以及为我们的世界带来更好的成果,我们对我们的期望更高。在我们所做的每件事中,我们都在设计非凡的事物。有关美敦力的更多信息,请访问并在LinkedIn上关注美敦力。

Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic's periodic reports on file with the Securities and Exchange Commission. Actual results may differ materially from anticipated results.

任何前瞻性陈述都受风险和不确定性的影响,例如美敦力向美国证券交易委员会提交的定期报告中描述的风险和不确定性。实际结果可能与预期结果存在重大差异。

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