机械主动脉瓣的流体-结构相互作用模拟:探索其在整个产品生命周期中作用的叙述性综述。

IF 2.7 Q3 ENGINEERING, BIOMEDICAL
Frontiers in medical technology Pub Date : 2024-07-01 eCollection Date: 2024-01-01 DOI:10.3389/fmedt.2024.1399729
Mariachiara Arminio, Dario Carbonaro, Umberto Morbiducci, Diego Gallo, Claudio Chiastra
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引用次数: 0

摘要

在过去几年中,计算机建模和模拟已成为支持心血管设备整个产品生命周期的有效工具,特别是在设备临床前评估和上市后评估方面。计算建模与心脏瓣膜假体的关系尤为密切,因为心脏瓣膜假体需要对其流体力学性能、溶血风险以及与机械性血液损伤相关的血栓栓塞并发症进行广泛评估。这些生物力学方面的评估通常采用流固耦合(FSI)方法,该方法可对瓣膜流体动力学进行评估,并考虑瓣叶运动。在此背景下,本综述重点介绍通过 FSI 方法对双叶机械主动脉瓣进行计算建模的情况,旨在促进和指导模拟在设备整个产品生命周期中的应用。本文回顾了心脏瓣膜假体的 FSI 仿真技术现状,重点介绍了文献中采用的各种建模策略。此外,还讨论了在双叶主动脉瓣的整个产品生命周期中整合 FSI 模拟的问题,特别强调了模拟在补充和可能取代国际标准建议的实验测试方面的作用。还根据最近发布的指南讨论了模拟可信度评估,从而为在监管申请中更广泛地纳入硅学证据铺平了道路。本综述强调了 FSI 模拟可以成功地融入双叶主动脉瓣机械瓣膜的整个产品生命周期,强调了评估植入式设备性能的可靠硅学模型可以(至少)部分取代临床前体外实验,并支持上市后的生物力学评估,从而减少设备开发所需的时间和成本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fluid-structure interaction simulation of mechanical aortic valves: a narrative review exploring its role in total product life cycle.

Over the last years computer modelling and simulation has emerged as an effective tool to support the total product life cycle of cardiovascular devices, particularly in the device preclinical evaluation and post-market assessment. Computational modelling is particularly relevant for heart valve prostheses, which require an extensive assessment of their hydrodynamic performance and of risks of hemolysis and thromboembolic complications associated with mechanically-induced blood damage. These biomechanical aspects are typically evaluated through a fluid-structure interaction (FSI) approach, which enables valve fluid dynamics evaluation accounting for leaflets movement. In this context, the present narrative review focuses on the computational modelling of bileaflet mechanical aortic valves through FSI approach, aiming to foster and guide the use of simulations in device total product life cycle. The state of the art of FSI simulation of heart valve prostheses is reviewed to highlight the variety of modelling strategies adopted in the literature. Furthermore, the integration of FSI simulations in the total product life cycle of bileaflet aortic valves is discussed, with particular emphasis on the role of simulations in complementing and potentially replacing the experimental tests suggested by international standards. Simulations credibility assessment is also discussed in the light of recently published guidelines, thus paving the way for a broader inclusion of in silico evidence in regulatory submissions. The present narrative review highlights that FSI simulations can be successfully framed within the total product life cycle of bileaflet mechanical aortic valves, emphasizing that credible in silico models evaluating the performance of implantable devices can (at least) partially replace preclinical in vitro experimentation and support post-market biomechanical evaluation, leading to a reduction in both time and cost required for device development.

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来源期刊
CiteScore
3.70
自引率
0.00%
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审稿时长
13 weeks
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