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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 年倫敦閥門展上發佈的兩份數據建立在 Evolut 的閥門設計和性能傳統基礎上:

Optimize PRO study demonstrates improved procedure efficiencies and valve performance

Optimize PRO 研究表明手術效率和閥門性能得到改善

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

彙總分析顯示,使用 Evolut PRO TAVR 系統的 PVL 在 3 年內有所改善

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.

醫療保健技術領域的全球領導者美敦力集團今天在2024年倫敦聚合酶鏈反應會議上公佈了Evolut經導管主動脈瓣置換系統(TAVR)的新數據。這些新的臨床證據爲治療有症狀的嚴重主動脈瓣狹窄(SASS)患者的全球植入者提供了進一步的見解。Optimize PRO臨床研究的新發現表明,在使用優化的護理途徑和尖點重疊技術(COT)部署Evolut瓣膜後,程序和臨床效果良好。此外,還分享了對Evolut PRO患者的彙總分析,結果顯示,隨着時間的推移,TAVR患者的肺泡旁滲漏(PVL)率在出院後有所改善。

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

優化 PRO 研究:全球標準化 TAVR 技術提供良好的手術和臨床結果

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全球研究爲期30天的完整發現表明,將尖點重疊技術與Evolut PRO和PRO+設備一起使用可帶來良好的手術和臨床結果。這項在全球50箇中心進行的多中心、上市後的前瞻性研究表明,新的30天永久起搏器植入率很低(牙尖重疊技術合規性爲6.4%),出院時沒有中度或重度主動脈反流。

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臨床研究利用尖點重疊技術部署Evolut瓣膜,評估了與 「優化」 術前和術後TAVR護理途徑相關的瓣膜性能和手術結果。牙尖重疊技術旨在幫助植入者評估和實現最佳植入深度,以減少與傳導系統的相互作用。在30天時,全因死亡率或所有中風的主要終點爲5.1%,全因死亡率爲0.8%,致殘性中風爲1.7%,心血管再住院率爲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."

俄亥俄健康河濱衛理公會醫院FACC醫學博士、聯合首席研究員史蒂芬·雅庫博夫說:「這些數據表明,在利用尖點重疊技術與Evolut瓣膜合作時,我們對這些數據感到鼓舞。」「新結果支持標準化方案,這將有助於支持患者儘早出院和降低併發症發生率,改善他們的生活質量。」

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

使用 Evolut PRO 經導管主動脈瓣隨着時間的推移改善瓣膜旁滲漏

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.

該配對分析評估了SSAS患者在使用Evolut PRO瓣膜進行TAVR後一段時間內PVL的改善。該研究分析了來自前瞻性Evolut低風險試驗、FORWARD PRO研究和Evolut PRO美國研究的620名接受Evolut PRO治療的患者的核心實驗室超聲心動圖數據。分析表明,PVL(一種血液在心臟自然組織和替代瓣膜之間向後流動時發生的泄漏)的嚴重程度有所改善,PVL(一種血液在心臟自然組織和替代瓣膜之間向後流動時發生的泄漏)在出院30天后進行爲期3年的隨訪。

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.

根據對患者的配對分析以及所有隨訪就診的可用數據,出院後30天的PVL嚴重程度爲60.8%無/痕量,36.0%爲輕度,2.9%爲中度,0.3%爲重度。在3年隨訪中,PVL的嚴重程度爲79.8%爲無/痕跡,19.6%爲輕度,0.6%爲中度,0.0%爲重度。從出院/30天到3年隨訪期間PVL惡化的情況並不常見。

"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."

荷蘭鹿特丹伊拉斯姆斯大學醫學中心胸科中心醫學博士、首席研究員尼古拉斯·範·米格姆說:「這項分析擴展了先前的研究,發現大多數被歸類爲輕度或更高PVL的患者的PVL嚴重程度在3年後有所改善。」 這項研究將幫助醫生了解TAVR後這種併發症的治療方法。”

"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."

美敦力心血管產品組合中的結構心臟和主動脈業務高級副總裁兼總裁妮娜·古德哈特說:「藉助Evolut TAVR系統,我們致力於改善患者的預後,同時保持卓越的安全性和效率。」「2024年倫敦Valves上公佈的數據進一步確立了美敦力和Evolut在支持和分享醫生在選擇和實施TAVR時爲患者做出最佳決策所需的有力臨床證據方面的領導者。」

About Medtronic

關於美敦力

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.

大膽思考。更大膽的行動。我們是美敦力。總部位於愛爾蘭戈爾韋的美敦力公司是全球領先的醫療保健技術公司,通過尋找和尋找解決方案,大膽地應對人類面臨的最具挑戰性的健康問題。我們的使命——減輕痛苦、恢復健康和延長壽命——團結了一支由來自150個國家的95,000多名充滿激情的人組成的全球團隊。我們的技術和療法可治療 70 種健康狀況,包括心臟設備、手術機器人、胰島素泵、手術工具、患者監護系統等。在我們多樣的知識、永不滿足的好奇心以及幫助所有有需要的人的願望的推動下,我們提供創新技術,每秒、每小時、每天都在改變兩個人的生活。隨着我們賦予以洞察爲導向的醫療服務、以人爲本的體驗以及爲我們的世界帶來更好的成果,我們對我們的期望更高。在我們所做的每件事中,我們都在設計非凡的事物。有關美敦力的更多信息,請訪問並在LinkedIn上關注美敦力。

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.

任何前瞻性陳述都受風險和不確定性的影響,例如美敦力向美國證券交易委員會提交的定期報告中描述的風險和不確定性。實際結果可能與預期結果存在重大差異。

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