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Hemodynamic Analysis of Pulmonary Arterial Hypertension Associated with Congenital Heart Disease: A Numerical Study of Patient-Specific Models

机译:与先天性心脏病相关的肺动脉高压的血流动力学分析:特定患者模型的数值研究

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Pulmonary arterial hypertension (PAH)is a complication of congenital heart disease (CHD). In clinic, Right heart catheterization (RHC)can obtain the pressure of pulmonary arteries and transthoracic echocardiography (TTE)can acquire the velocity of pulmonary blood flow. However, neither RHC nor TTE can provide quantitative hemodynamics. Here, we use computational fluid dynamics (CFD)to study the hemodynamics of pulmonary arterial of patients with PAH associated with CHD. Compared with the normal pulmonary blood flow, the local hemodynamics, especially wall shear stress (WSS), energy loss (EL)and streamlines, displayed obvious differences in the patients with PAH-CHD. Lower WSS, higher EL and rotating flow were generated in the pulmonary artery with PAH-CHD. These results may have a close association with endothelial dysfunction and accelerate the progression of PH.
机译:肺动脉高压(PAH)是先天性心脏病(CHD)的并发症。在临床中,右心导管(RHC)可以获取肺动脉的压力,而经胸超声心动图(TTE)可以获取肺血流的速度。但是,无论是RHC还是TTE都无法提供定量的血流动力学。在这里,我们使用计算流体动力学(CFD)研究患有冠心病相关的PAH患者的肺动脉血流动力学。与正常肺血流相比,PAH-CHD患者的局部血流动力学,尤其是壁切应力(WSS),能量损失(EL)和流线型表现出明显差异。 PAH-CHD在肺动脉中产生较低的WSS,较高的EL和旋转流量。这些结果可能与内皮功能障碍密切相关,并加速PH的发展。

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