Patient-specific 3D in vitro modeling and fluid dynamic analysis of primary pulmonary vein stenosis

被引:0
|
作者
Devlin, Christian [1 ,2 ]
Tomov, Martin L. [1 ,2 ]
Chen, Huang [1 ,2 ]
Nama, Sindhu [1 ,2 ]
Ali, Siraj [1 ,2 ]
Neelakantan, Sunder [3 ]
Avazmohammadi, Reza [3 ,4 ,5 ]
Dasi, Lakshmi Prasad [1 ,2 ]
Bauser-Heaton, Holly D. [1 ,2 ,6 ,7 ,8 ]
Serpooshan, Vahid [1 ,2 ,6 ,7 ]
机构
[1] Emory Univ, Wallace H Coulter Dept Biomed Engn, Sch Med, Atlanta, GA 30307 USA
[2] Georgia Inst Technol, Atlanta, GA 30332 USA
[3] Texas A&M Univ, Dept Biomed Engn, College Stn, TX USA
[4] Texas A&M Univ, J Mike Walker Dept Mech Engn 66, College Stn, TX USA
[5] Texas A&M Univ, Sch Engn Med, Houston, TX USA
[6] Emory Univ, Dept Pediat, Sch Med, Atlanta, GA 30307 USA
[7] Childrens Healthcare Atlanta, Atlanta, GA 30322 USA
[8] Childrens Healthcare Atlanta, Sibley Heart Ctr, Atlanta, GA USA
来源
基金
美国国家卫生研究院;
关键词
3D printing; pulmonary vein stenosis (PVS); flow hemodynamics; particle image velocimetry; computational fluid dynamics; stenting; cardiac intervention; CARDIAC TISSUES;
D O I
10.3389/fcvm.2024.1432784
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Primary pulmonary vein stenosis (PVS) is a rare congenital heart disease that proves to be a clinical challenge due to the rapidly progressive disease course and high rates of treatment complications. PVS intervention is frequently faced with in-stent restenosis and persistent disease progression despite initial venous recanalization with balloon angioplasty or stenting. Alterations in wall shear stress (WSS) have been previously associated with neointimal hyperplasia and venous stenosis underlying PVS progression. Thus, the development of patient-specific three-dimensional (3D) in vitro models is needed to further investigate the biomechanical outcomes of endovascular and surgical interventions. Methods : In this study, deidentified computed tomography images from three patients were segmented to generate perfusable phantom models of pulmonary veins before and after catheterization. These 3D reconstructions were 3D printed using a clear resin ink and used in a benchtop experimental setup. Computational fluid dynamic (CFD) analysis was performed on models in silico utilizing Doppler echocardiography data to represent the in vivo flow conditions at the inlets. Particle image velocimetry was conducted using the benchtop perfusion setup to analyze WSS and velocity profiles and the results were compared with those predicted by the CFD model. Results: Our findings indicated areas of undesirable alterations in WSS before and after catheterization, in comparison with the published baseline levels in the healthy in vivo tissues that may lead to regional disease progression. Discussion: The established patient-specific 3D in vitro models and the developed in vitro-in silico platform demonstrate great promise to refine interventional approaches and mitigate complications in treating patients with primary PVS.
引用
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页数:11
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