Using finite element analysis to obtain the pressure gradient between the left renal vein and the inferior vena cava: a new method for the diagnosis and follow-up of patients with nutcracker syndrome

利用有限元分析法获取左肾静脉与下腔静脉之间的压力梯度:一种诊断和随访胡桃夹综合征患者的新方法

阅读:2

Abstract

BACKGROUND: Nutcracker syndrome (NCS) diagnosis remains challenging due to the lack of non-invasive, reliable methods. Current techniques, including Doppler ultrasound and computed tomography angiography (CTA), lack hemodynamic data, with invasive measurement of the left renal vein-inferior vena cava (LRV-IVC) pressure gradient (true pressure gradient, TPG) being the gold standard. This study aimed to validate a novel non-invasive approach using finite element analysis (FEA) to simulate the LRV-IVC pressure gradient (SPG) to assist in diagnosing and monitoring NCS. METHODS: This retrospective study included 46 patients (35 NCS, 11 controls) who underwent CTA and invasive TPG measurement. Patient-specific 3D left renal vein (LRV) models were reconstructed from CTA data using MIMICS and 3-matic software. Hemodynamic simulations were performed via ANSYS (an engineering simulation software) to calculate SPG. Diagnostic performance of SPG and imaging parameters (e.g., beak sign, LRV diameter ratio) was evaluated using receiver operating characteristic (ROC) analysis. RESULTS: SPG showed no significant difference from TPG (5.6±3.9 vs. 5.5±1.9 mmHg, P>0.05) in NCS patients. Postoperative SPG and TPG decreased comparably (P<0.05). SPG achieved an area under the curve (AUC) of 0.808 [95% confidence interval (CI): 0.69-0.92] with 81.8% sensitivity and 80.0% specificity at a cutoff of 3.3 mmHg, outperforming traditional imaging markers. The aortomesenteric angle, LRV diameter ratio, and beak sign also demonstrated diagnostic utility. CONCLUSIONS: FEA-derived SPG correlates closely with invasive TPG, offering a reliable, non-invasive alternative for NCS diagnosis and postoperative monitoring. This approach enhances objectivity, reduces reliance on operator-dependent techniques, and may facilitate early intervention. Further refinement of FEA models and multicenter validation are warranted.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。