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Shuping Ge

Publications and source records attributed to Shuping Ge.

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The First Human-Based In Vitro Flow Loop and Quantification for Fetal Aortic Hemodynamics

Coarctation of the aorta (CoA) is a common congenital defect that remains difficult to diagnose prenatally due to subtle and evolving anatomical features. In the fetus, the ductus arteriosus creates a dual-inflow configuration that generates complex three-dimensional flow patterns not captured by standard imaging. Improved characterization of fetal hemodynamics may enhance diagnostic accuracy beyond anatomy-based assessment. This study presents the first human-based in vitro flow loop of the fetal aorta, constructed from anatomies reconstructed using medical imaging data. Models representing normal and coarctation conditions were fabricated and integrated into a physiological flow loop. Velocity fields were measured using planar and stereoscopic particle image velocimetry (PIV) to resolve near-wall and three-dimensional flow structures, enabling quantitative assessment of velocity gradients and wall shear stress (WSS) under normal and coarctation configurations. The in vitro flow loop closely reproduced target fetal flow segmentation, with segmental flow-rate errors generally below 6%. High-resolution planar and stereoscopic PIV revealed dual jets from the ascending aorta and the ductus arteriosus and predominantly planar flow in the normal aorta, but strong jet acceleration, separation, and reattachment in the coarcted geometry. Coarctation produced markedly elevated and spatially heterogeneous WSS, and 2-component PIV underestimated WSS by up to ~29% compared with 3-component measurements, especially in high-shear regions. These findings show that accurate three-component velocity measurements are critical for reliable WSS estimation and suggest that detailed hemodynamic metrics, such as WSS, may serve as potential biomarkers to enhance fetal CoA diagnosis beyond anatomy alone.

physics.med-ph

A Personalized Fluid-structure Interaction Modeling Paradigm for Aorta in Human Fetuses

Fluid-structure interaction (FSI) modeling, a technique widely used to enhance imaging modalities for adult and pediatric heart diseases, has been underutilized in the context of fetal circulation because of limited data on flow conditions and material properties. Recognizing the significant impact of congenital heart diseases on the fetal aorta, our research aims to address this gap by developing and validating a personalized FSI model for the fetal aorta. Our approach involved reconstructing the anatomy and flow of the fetal aorta using fetal echocardiography and ultrasound. We developed an innovative iterative method that includes: (i) an automated process for incorporating Windkessel models at outflow boundaries when clinical data is limited because of the resolution constraints of fetal imaging, (ii) an inverse approach to estimate bulk material properties, and (iii) an FSI model for high-fidelity hemodynamic evaluation. This method is efficient, typically converging in fewer than three iterations. We analyzed four normal fetal aortas with gestational ages ranging from 23.5 to 35.5 weeks to validate our workflow. We compared results with in vivo velocity waveforms across a cardiac cycle at the aortic isthmus. Strong correlations (R>0.95) were observed. Furthermore, our findings suggest that the stiffness of the fetal aorta increases until 30 weeks of gestation and then decreases. This study marks a first-of-its-kind effort in developing a rigorously validated, personalized flow model for fetal circulation, offering novel insights into fetal aortic development and growth.

physics.med-ph