患者特异性,左心发育不全综合征三尖瓣模拟和规划的动态模型

N. Boone, Hannah H. Nam, John Moore, Patrick Carnahan, Olivia K. Ginty, Christian Herz, A. Lasso, M. Jolley, E. Chen, T. Peters
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引用次数: 3

摘要

患者特定心脏瓣膜病理的物理复制品可能提高临床医生为复杂瓣膜病患者计划最佳治疗的能力。我们之前的工作已经证明了在动态环境中复制成人二尖瓣(MV)患者病理的能力[13]。婴儿先天性心脏缺陷可能是最具挑战性的瓣膜疾病形式,考虑到病理的范围,这些瓣膜与成人解剖结构的相对大小,以及先天性心脏病的罕见性。患者特定的瓣膜模型对于儿科心脏病专家和外科医生来说尤其有价值,可以作为计划和实施干预措施的一种手段。我们目前的目标是评估将我们的工作流程应用于左心发育不全综合征(HLHS)病例中更具挑战性的三尖瓣(TV)病例的能力。我们探索了将我们之前的工作流程调整为术前计划和模拟训练创建动态硅胶MV模型的可行性,以开发用于物理心脏模拟器的3D超声心动图衍生的患者特定电视模型。这些模型旨在表征TV,并探索特定解剖特征与三尖瓣反流(TR)严重程度之间的关系。模拟可能与术前计划修复特别复杂和独特的解剖病理呈现在儿童HLHS。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patient-specific, dynamic models of hypoplastic left heart syndrome tricuspid valves for simulation and planning
Physical replicas of patient specific heart valve pathologies may improve clinicians’ ability to plan the optimal treatment for patients with complex valvular heart disease. Our previous work has demonstrated the ability to replicate patient pathology of the adult mitral valve (MV) in a dynamic environment [13]. Infant congenital heart defects present possibly the most challenging form of valvular disease, given the range of pathologies, the relative size of these valves compared to adult anatomy, and the rarity of congenital heart disease. Patient specific valve models could be particularly valuable for pediatric cardiologists and surgeons, as a means to both plan for and practice interventions. Our current goal is to assess our ability to apply our workflow to the more challenging case of the tricuspid valve (TV) presented in cases of hypoplastic left heart syndrome (HLHS). We explore the feasibility of adapting our previous workflow for creating dynamic silicone MV models for pre-surgical planning and simulation training, to developing 3D echocardiogram derived, patient specific TV models for use in a physical heart simulator. These models are intended for characterization of the TV, and exploration of the relationship between specific anatomical features and tricuspid regurgitation (TR) severity. The simulations may be relevant to pre-surgical planning of repair of the particularly complex and unique anatomical pathologies presented in children with HLHS.
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