Cardiovascular Biology and Biomechanics Laboratory, Cardiovascular Division, University of Nebraska Medical Center, Omaha, NE, USA.
California Medical Innovation Institute, San Diego, CA, USA.
Sci Rep. 2021 Aug 13;11(1):16486. doi: 10.1038/s41598-021-95026-2.
Patient-specific and lesion-specific computational simulation of bifurcation stenting is an attractive approach to achieve individualized pre-procedural planning that could improve outcomes. The objectives of this work were to describe and validate a novel platform for fully computational patient-specific coronary bifurcation stenting. Our computational stent simulation platform was trained using n = 4 patient-specific bench bifurcation models (n = 17 simulations), and n = 5 clinical bifurcation cases (training group, n = 23 simulations). The platform was blindly tested in n = 5 clinical bifurcation cases (testing group, n = 29 simulations). A variety of stent platforms and stent techniques with 1- or 2-stents was used. Post-stenting imaging with micro-computed tomography (μCT) for bench group and optical coherence tomography (OCT) for clinical groups were used as reference for the training and testing of computational coronary bifurcation stenting. There was a very high agreement for mean lumen diameter (MLD) between stent simulations and post-stenting μCT in bench cases yielding an overall bias of 0.03 (- 0.28 to 0.34) mm. Similarly, there was a high agreement for MLD between stent simulation and OCT in clinical training group [bias 0.08 (- 0.24 to 0.41) mm], and clinical testing group [bias 0.08 (- 0.29 to 0.46) mm]. Quantitatively and qualitatively stent size and shape in computational stenting was in high agreement with clinical cases, yielding an overall bias of < 0.15 mm. Patient-specific computational stenting of coronary bifurcations is a feasible and accurate approach. Future clinical studies are warranted to investigate the ability of computational stenting simulations to guide decision-making in the cardiac catheterization laboratory and improve clinical outcomes.
针对分叉病变的个体化和病变特异性计算模拟是实现个体化术前规划的一种有吸引力的方法,可改善治疗效果。本研究旨在描述和验证一种全新的全计算个体化冠状动脉分叉病变支架置入术模拟平台。我们的计算支架模拟平台使用 n=4 例个体化的分叉模型(n=17 次模拟)和 n=5 例临床分叉病例(训练组,n=23 次模拟)进行训练。该平台在 n=5 例临床分叉病例(测试组,n=29 次模拟)中进行了盲测。平台中使用了各种支架平台和支架技术,包括单支架和双支架。对于支架模拟平台的训练和测试,使用 bench 模型的 micro-computed tomography(μCT)和临床病例的 optical coherence tomography(OCT)进行了 post-stenting 成像。在 bench 模型中,支架模拟与 post-stenting μCT 测量的平均管腔直径(MLD)之间具有非常高的一致性,总体偏差为 0.03(-0.28 至 0.34)mm。同样,在临床训练组[支架模拟与 OCT 测量的 MLD 之间的偏差为 0.08(-0.24 至 0.41)mm]和临床测试组[支架模拟与 OCT 测量的 MLD 之间的偏差为 0.08(-0.29 至 0.46)mm]中,支架模拟与 post-stenting OCT 测量的 MLD 之间也具有高度一致性。在计算支架中,支架的大小和形状与临床病例具有高度一致性,总体偏差<0.15mm。针对冠状动脉分叉病变的个体化计算支架置入术是一种可行且准确的方法。未来需要开展临床研究,以评估计算支架模拟在指导心导管实验室决策和改善临床结果方面的能力。