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首页> 外文期刊>Journal of Biomechanics >Quantification of thrombus formation in malapposed coronary stents deployed in vitro through imaging analysis
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Quantification of thrombus formation in malapposed coronary stents deployed in vitro through imaging analysis

机译:通过成像分析在体外部署的血栓形成血栓形成的定量

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摘要

Stent thrombosis is a major complication of coronary stent and scaffold intervention. While often unanticipated and lethal, its incidence is low making mechanistic examination difficult through clinical investigation alone. Thus, throughout the technological advancement of these devices, experimental models have been indispensable in furthering our understanding of device safety and efficacy. As we refine model systems to gain deeper insight into adverse events, it is equally important that we continue to refine our measurement methods. We used digital signal processing in an established flow loop model to investigate local flow effects due to geometric stent features and ultimately its relationship to thrombus formation. A new metric of clot distribution on each microCT slice termed normalized clot ratio was defined to quantify this distribution. Three under expanded coronary bare-metal stents were run in a flow loop model to induce clotting. Samples were then scanned in a MicroCT machine and digital signal processing methods applied to analyze geometric stent conformation and spatial clot formation. Results indicated that geometric stent features play a significant role in clotting patterns, specifically at a frequency of 0.6225 Hz corresponding to a geometric distance of 1.606 mm. The magnitude-squared coherence between geometric features and clot distribution was greater than 0.4 in all samples. In stents with poor wall apposition, ranging from 0.27 mm to 0.64 mm maximum malapposition (model of real-world heterogeneity), clots were found to have formed in between stent struts rather than directly adjacent to struts. This early work shows how the combination of tools in the areas of image processing and signal analysis can advance the resolution at which we are able to define thrombotic mechanisms in in vitro models, and ultimately, gain further insight into clinical performance. (C) 2018 Elsevier Ltd. All rights reserved.
机译:支架血栓形成是冠状动脉支架和支架介入的主要复杂性。虽然经常意想不到的和致命,其发病率低通过单独的临床调查难以进行机械检查。因此,在整个技术的技术进步方面,实验模型在进一步推动我们对设备安全性和功效的理解方面是必不可少的。当我们改进模型系统以获得更深入的洞察不良事件时,我们同样重要的是,我们继续改进我们的测量方法。我们在建立的流回路模型中使用数字信号处理来研究由于几何支架特征引起的局部流动效应,并最终与血栓形成的关系。定义了每个MicroCT片上称为归一化凝块比的凝块分布的新度量,以量化该分布。在膨胀冠状动脉晶体支架下进行三个在流量回路模型中以诱导凝血。然后在MicroCT机器和数字信号处理方法中扫描样品,用于分析几何支架构象和空间凝块形成。结果表明,几何支架特征在凝血模式中发挥着重要作用,特别是0.6225Hz的频率对应于1.606mm的几何距离。在所有样品中,几何特征和凝块分布之间的大小平方相干性大于0.4。在壁挂差的支架中,范围为0.27毫米至0.64毫米的最大malapposition(现实世界异质性的模型),发现凝块形成在支架支柱之间而不是直接邻近支柱。这项早期工作表明了图像处理和信号分析领域的工具组合如何推进我们能够在体外模型中定义血栓性机制的分辨率,并最终进一步了解临床表现。 (c)2018年elestvier有限公司保留所有权利。

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