Fluid Dynamic and in Vitro Blood Study to Understand Catheter-Related Thrombosis.

IF 1.6 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Hannah Palahnuk, Boyang Su, Thaddeus Harbaugh, Cleo Gesenberg, Shouhao Zhou, Elias Rizk, Jonathan Bernstein, S Will Hazard, Keefe B Manning
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引用次数: 0

Abstract

Purpose: Central venous catheters (CVCs) provide a direct route to the venous circulation but are prone to catheter-related thrombosis (CRT). A known CRT risk factor is a high catheter-to-vein ratio (CVR), or a large catheter diameter with respect to the indwelling vein size. In this study, the CVR's effect on CVC hemodynamics and its impact on CRT is investigated with in vitro and in silico experiments.

Methods: An in vitro flow loop is used to characterize the hemodynamics around CVCs using particle image velocimetry. In addition, CRT is investigated using an in vitro flow loop with human blood and clinical catheters. The wall shear rate of flow around the CVC is computed numerically. CVRs of 0.20, 0.33, and 0.49 and Reynolds numbers of 200, 800, and 1300 are evaluated. No flow is used through CVC lumens to model chronic indwelling catheters.

Results: Results show CVR ≥ 0.33 promotes platelet-rich clot growth at the device tip and at an increased rate compared to lower CVR cases. A high wall shear rate gradient on the CVC tip and an extended wake distal to the tip exists for higher CVR cases, promoting the aggregation of platelets and subsequent stagnation for clot formation. Further, the combination of the CVR and Reynolds number are crucial to CRT potential, not the CVR alone. Specifically, thrombosis risk is increased with low (stasis driven) and/or high (platelet activation driven) flow conditions, with the CVR and CVC's geometry playing an additional role in promoting fluid mechanic driven thrombus development. A high CVR (≥ 0.33) and high flow condition (≥ 1300) results in the highest risk for clot growth at the tip of the device; other locations of the device are at risk for thrombus development in lower flow conditions, regardless of the CVR. The importance of the device geometry and flow in promoting thrombus and fibrin sheath formation is also shown for the device investigated.

Conclusions: This work demonstrates that the CVR, flow, and device geometry affect CRT. For clinical cases with CVR ≥ 0.33 and/or Re ≥ 1300, the device tip may be monitored more consistently for clot formation. Thrombosis risks remain on the entire catheter, regardless of the flow condition, for a CVR = 0.49. Device placement should be chosen carefully with respect to the combination of the Reynolds number and CVR. Further study is needed on the effect of catheterization to confirm these findings.

流体动力学和体外血液研究了解导管相关血栓形成。
目的:中心静脉导管(CVCs)提供静脉循环的直接途径,但容易产生导管相关血栓(CRT)。一个已知的CRT危险因素是高导管与静脉比(CVR),或相对于留置静脉的大导管直径。本研究通过体外和计算机实验研究了CVR对CVC血流动力学的影响及其对CRT的影响。方法:采用颗粒图像测速法建立体外血流环,对cvc周围血流动力学进行表征。此外,CRT研究使用体外循环与人血和临床导管。用数值方法计算了绕流CVC的壁面剪切速率。cvr分别为0.20、0.33、0.49,雷诺数分别为200、800、1300。无血流通过CVC管腔来模拟慢性留置导管。结果:结果显示CVR≥0.33的患者与CVR较低的患者相比,可促进设备尖端富血小板血栓的生长。CVC尖端的高壁剪切速率梯度和尖端远端延伸的尾迹在高CVR病例中存在,促进血小板聚集和随后的凝块形成停滞。此外,CVR和雷诺数的结合对CRT电位至关重要,而不仅仅是CVR。具体来说,低(瘀滞驱动)和/或高(血小板激活驱动)的血流条件会增加血栓形成的风险,CVR和CVC的几何形状在促进流体力学驱动的血栓形成中起着额外的作用。高CVR(≥0.33)和高流量条件(≥1300)导致设备尖端血栓生长的风险最高;无论CVR如何,设备的其他位置在低流量条件下都有血栓形成的风险。该装置的几何形状和流量在促进血栓和纤维蛋白鞘形成方面的重要性也显示在该装置的研究中。结论:这项工作表明CVR、血流和设备几何形状影响CRT。对于CVR≥0.33和/或Re≥1300的临床病例,可以更一致地监测设备尖端是否形成血栓。在CVR = 0.49时,无论血流状况如何,整个导管仍存在血栓形成风险。应结合雷诺数和CVR仔细选择装置放置位置。需要进一步研究导尿的效果来证实这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cardiovascular Engineering and Technology
Cardiovascular Engineering and Technology Engineering-Biomedical Engineering
CiteScore
4.00
自引率
0.00%
发文量
51
期刊介绍: Cardiovascular Engineering and Technology is a journal publishing the spectrum of basic to translational research in all aspects of cardiovascular physiology and medical treatment. It is the forum for academic and industrial investigators to disseminate research that utilizes engineering principles and methods to advance fundamental knowledge and technological solutions related to the cardiovascular system. Manuscripts spanning from subcellular to systems level topics are invited, including but not limited to implantable medical devices, hemodynamics and tissue biomechanics, functional imaging, surgical devices, electrophysiology, tissue engineering and regenerative medicine, diagnostic instruments, transport and delivery of biologics, and sensors. In addition to manuscripts describing the original publication of research, manuscripts reviewing developments in these topics or their state-of-art are also invited.
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