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Boston Scientific Obtains CE Mark for ACURATE Prime Aortic Valve System

Boston Scientific Obtains CE Mark for ACURATE Prime Aortic Valve System

波士頓科學獲得ACURATE Prime主動脈瓣系統的CE標誌。
PR Newswire ·  08/27 06:57

MARLBOROUGH, Mass., Aug. 27, 2024 /PRNewswire/ -- Boston Scientific Corporation (NYSE: BSX) today announced it has obtained CE mark for the ACURATE Prime Aortic Valve System, the newest transcatheter aortic valve replacement (TAVR) technology in the company's structural heart portfolio. The ACURATE Prime valve system is designed with several features to build upon the clinical performance of the ACURATE neo2 platform including an additional valve size, which expands the treatment range to patients with a larger anatomy.

波士頓科學公司(紐交所:BSX)今日宣佈,其最新轉導主動脈瓣系統ACURATE Prime獲得CE標誌,這是該公司結構性心臟產品組合中最新的經導管主動脈瓣置換(TAVR)技術。ACURATE Prime主動脈瓣系統採用了多項功能,以便在ACURATE neo2平台的臨床性能的基礎上進一步提高,包括一個額外的瓣膜尺寸,將治療範圍擴大到有較大解剖結構的患者。

Video: ACURATE Prime Aortic Valve System
視頻:ACURATE Prime經導管主動脈瓣系統
ACURATE Prime Aortic Valve System
ACURATE Prime經導管主動脈瓣系統

The new ACURATE Prime valve system is indicated to restore function and normal blood flow through a narrowed aortic valve in low, intermediate and high-risk patients with severe aortic stenosis. With a self-expanding, supra-annular design, this device has an enhanced frame that equalizes force across the valve for a stable fit against the native, diseased valve. It also offers physicians a redesigned deployment mechanism for highly accurate valve positioning to help ensure positive patient outcomes.

ACURATE Prime瓣系統適用於低、中和高風險重症主動脈狹窄患者,以恢復狹窄的主動脈瓣的功能和正常血液流動。該裝置採用了自擴張的象限上方設計,具有增強的框架,可使閥門穩固貼合在原有的病變閥門上,並均衡施加力量。它還提供醫生重新設計的部署機制,以實現高精確的閥位,確保患者的陽性結果。

"The introduction of the ACURATE Prime technology offers physicians a TAVR option designed for streamlined procedural preparation, improved performance in complex cases and simplified delivery for quick and controlled deployment," said Janar Sathananthan, M.D., chief medical officer, Interventional Cardiology Therapies, Boston Scientific. "Further, our clinical experience with the valve to date has shown the ability for precise positioning of the device in a broader population of patients, allowing more clinicians to consider this technology for treatment in challenging or larger heart structures."

波士頓科學介入心臟病學治療的首席醫學官Janar Sathananthan萬.D.表示:「ACURATE Prime技術的推出爲醫生提供了一種經導管主動脈瓣置換選項,旨在簡化手術準備流程,提高複雜病例的性能,並簡化交付,以快速而精確的部署。」我們對該瓣膜迄今的臨床經驗顯示,能夠在更廣泛的患者群體中精確定位設備,使更多臨床醫生考慮在具有挑戰性或更大的心臟結構的患者中使用這項技術。

The ACURATE Prime valve system will now be available for the treatment of aortic annulus diameters between 20.5 and 29 mm. It will also carry through many of the design features and clinical outcomes demonstrated in global studies with the ACURATE neo2 platform, including low pacemaker and paravalvular leak rates,1,2 strong hemodynamic performance,1 as well as unrestricted coronary access for future procedures.

ACURATE Prime瓣系統現在可以用於治療20.5至2900萬之間的主動脈環直徑。它還延續了全球研究中ACURATE neo2平台所展示的許多設計特點和臨床結果,包括低起搏器和瓣周漏率、強大的血流動力學性能,以及未來操作的不受限制的冠狀動脈通道。

"We are thrilled to offer physicians a new valve with meaningful improvements for the treatment of an increasing number of patients with aortic valve disease," said Lance Bates, senior vice president and president, Interventional Cardiology Therapies, Boston Scientific. "Built on the ACURATE valve platform, which has been implanted in nearly 80,000 patients globally to date, the ACURATE Prime valve system is engineered to improve long-term cardiac function and provide access for future treatment needs, thereby supporting the lifetime management of these patients."

「我們很高興能爲越來越多患有主動脈瓣病的患者提供具有實質性改進的新型瓣膜。」波士頓科學公司介入心臟治療業務高級副總裁兼總裁蘭斯·貝茨表示:「ACURATE瓣膜平台已在全球範圍內植入近8萬名患者身上,ACURATE Prime瓣膜系統的工程設計可以改善長期心臟功能,爲未來的治療需求提供入路,從而支持這些患者的終身管理。」

The company will initiate the launch of the ACURATE Prime valve system in Europe in the coming weeks. For more information on the system, visit .

該公司將在未來幾周內在歐洲推出ACURATE Prime瓣膜系統。有關該系統的更多信息,請訪問 。

*In Europe, the ACURATE neo2 Aortic Valve System and the ACURATE Prime Aortic Valve System are CE-marked. In the USA, the ACURATE neo2 Aortic Valve System and the ACURATE Prime Aortic Valve System are investigational devices and are restricted under federal law to investigational use only. Not available for sale.

*在歐洲,ACURATE neo2主動脈瓣系統和ACURATE Prime主動脈瓣系統已經獲得CE標誌。在美國,ACURATE neo2主動脈瓣系統和ACURATE Prime主動脈瓣系統是研究性設備,僅限於進行研究性使用,不能出售。

About Boston Scientific
Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of health care. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at and connect on LinkedIn and X, formerly Twitter.

關於波士頓科學
波士頓科學通過創新醫療技術改善世界各地患者的健康,改變他們的生活。作爲全球醫療技術領先企業,我們致力於爲患者提供一系列高性能解決方案,滿足未滿足的患者需求,並降低醫療保健成本。我們的設備和療法產品組合幫助醫生診斷和治療複雜的心血管、呼吸、消化、腫瘤、神經和泌尿系統疾病和病症。了解更多,請訪問網址 ,並在LinkedIn和X(以前的Twitter)上進行交流。

Cautionary Statement Regarding Forward-Looking Statements

關於前瞻性聲明的警示聲明

This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Forward-looking statements may be identified by words like "anticipate," "expect," "project," "believe," "plan," "estimate," "intend" and similar words. These forward-looking statements are based on our beliefs, assumptions and estimates using information available to us at the time and are not intended to be guarantees of future events or performance. These forward-looking statements include, among other things, statements regarding our business plans and product performance and impact, and new and anticipated product approvals and launches. If our underlying assumptions turn out to be incorrect, or if certain risks or uncertainties materialize, actual results could vary materially from the expectations and projections expressed or implied by our forward-looking statements. These factors, in some cases, have affected and in the future (together with other factors) could affect our ability to implement our business strategy and may cause actual results to differ materially from those contemplated by the statements expressed in this press release. As a result, readers are cautioned not to place undue reliance on any of our forward-looking statements.

本新聞稿包含根據1933年證券法第27A條和1934年證券交易法第21E條的前瞻性陳述。前瞻性陳述可能被識別出來,例如「預計」、「期望」、「計劃」、「相信」、「估計」、「打算」等類似的字眼。這些前瞻性陳述基於我們在時候可得到的信仰、假設和估計,並且不打算作爲未來事件或業績的保證。這些前瞻性陳述包括但不限於關於我們的業務計劃、產品業績和影響、新產品的批准和發佈等的聲明。如果我們的基本假設被證明是不正確的,或者如果某些風險或不確定性出現,實際結果可能會與我們的前瞻性陳述表達的期望和預測有很大的差異。在某些情況下,這些因素已經影響了並且將來(與其他因素一起)可能會影響我們實施業務策略的能力,並導致實際結果與本新聞稿所表達的聲明所預期的結果出現差異。因此,讀者被警告不要過分依賴我們的任何前瞻性陳述。

Factors that may cause such differences include, among other things: future economic, competitive, reimbursement and regulatory conditions; manufacturing, distribution and supply chain disruptions and cost increases; variations in outcomes of ongoing and future clinical trials and market studies; new product introductions; demographic trends; intellectual property; litigation; financial market conditions; and future business decisions made by us and our competitors. All of these factors are difficult or impossible to predict accurately and many of them are beyond our control. For a further list and description of these and other important risks and uncertainties that may affect our future operations, see Part I, Item 1A – Risk Factors in our most recent Annual Report on Form 10-K filed with the Securities and Exchange Commission, which we may update in Part II, Item 1A – Risk Factors in Quarterly Reports on Form 10-Q we have filed or will file hereafter. We disclaim any intention or obligation to publicly update or revise any forward-looking statements to reflect any change in our expectations or in events, conditions or circumstances on which those expectations may be based, or that may affect the likelihood that actual results will differ from those contained in the forward-looking statements, except as required by law. This cautionary statement is applicable to all forward-looking statements contained in this document.

可能導致這些差異的因素包括但不限於:未來經濟、競爭、報銷和監管條件;製造、分銷和供應鏈中斷和成本增加;正在進行和將來進行的臨床試驗和市場研究結果的變化;新產品推出;人口統計趨勢;知識產權;訴訟;金融市場條件;以及我們和競爭對手未來的業務決策。所有這些因素都難以準確預測,而且其中許多因素超出我們的控制範圍。有關可能影響我們未來運營的其他重要風險和不確定性的進一步清單和描述,請參閱我們最近提交給證券交易委員會的年度報告Form 10-k的第I部分,第1A條 - 風險因素,我們可能在此之後更新的季度報告Form 10-Q的第II部分,第1A條 - 風險因素。我們不承擔公開更新或修訂任何前瞻性聲明以反映我們對期望的任何變化或在可能影響實際結果可能與前瞻性聲明中所含結果不同的事件、條件或情況上的期望,除非法律要求。此警告聲明適用於本文件中包含的所有前瞻性聲明。

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1 Rück A, Kim WK, Abdel-Wahab M, et al. The Early neo2 Registry: Transcatheter Aortic Valve Implantation with ACURATE neo2 in a European Population. J Am Heart Assoc. 2023 Aug;12(15):e029464.
2 Kim WK, Tamburino C, Möllmann H, et al. Clinical outcomes of the ACURATE neo2 transcatheter heart valve: a prospective, multicenter, observational, post-market surveillance study. EuroIntervention. 2023 May 12;19(1):83-92.

1. Ruück A, Kim Wk, Abdel-Wahab m等人。《早期neo2註冊表:使用ACURATE neo2進行經導管主動脈瓣植入術在歐洲人群中的結果》。《美國心臟協會志》2023年8月;12(15):e029464。
2.Kim Wk, Tamburino C, Möllmann H等人。《ACURATE neo2經導管心臟瓣成像學臨床結果:一項前瞻性、多中心、觀察性、市場後期監測研究》。《EuroIntervention》2023年5月12日;19(1):83-92。

SOURCE Boston Scientific Corporation

資訊來源:波士頓科學

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