The Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia 30332, USA.
Ann Thorac Surg. 2013 Mar;95(3):825-30. doi: 10.1016/j.athoracsur.2012.11.039. Epub 2013 Jan 29.
This study was undertaken to evaluate an in vitro mitral valve (MV) simulator's ability to mimic the systolic leaflet coaptation, regurgitation, and leaflet mechanics of a healthy ovine model and an ovine model with chronic ischemic mitral regurgitation (IMR).
Mitral valve size and geometry of both healthy ovine animals and those with chronic IMR were used to recreate systolic MV function in vitro. A2-P2 coaptation length, coaptation depth, tenting area, anterior leaflet strain, and MR were compared between the animal groups and valves simulated in the bench-top model.
For the control conditions, no differences were observed between the healthy animals and simulator in coaptation length (p = 0.681), coaptation depth (p = 0.559), tenting area (p = 0.199), and anterior leaflet strain in the radial (p = 0.230) and circumferential (p = 0.364) directions. For the chronic IMR conditions, no differences were observed between the models in coaptation length (p = 0.596), coaptation depth (p = 0.621), tenting area (p = 0.879), and anterior leaflet strain in the radial (p = 0.151) and circumferential (p = 0.586) directions. MR was similar between IMR models, with an asymmetrical jet originating from the tethered A3-P3 leaflets.
This study is the first to demonstrate the effectiveness of an in vitro simulator to emulate the systolic valvular function and mechanics of a healthy ovine model and one with chronic IMR. The in vitro IMR model provides the capability to recreate intermediary and exacerbated levels of annular and subvalvular distortion for which IMR repairs can be simulated. This system provides a realistic and controllable test platform for the development and evaluation of current and future IMR repairs.
本研究旨在评估体外二尖瓣(MV)模拟器模拟健康绵羊模型和慢性缺血性二尖瓣反流(IMR)绵羊模型收缩期瓣叶贴合、反流和瓣叶力学的能力。
使用健康绵羊动物和慢性 IMR 动物的 MV 大小和几何形状,在体外重建收缩期 MV 功能。比较了动物组和在台式模型中模拟的瓣膜之间的 A2-P2 贴合长度、贴合深度、篷布面积、前瓣应变和 MR。
在对照条件下,健康动物与模拟器在贴合长度(p = 0.681)、贴合深度(p = 0.559)、篷布面积(p = 0.199)和前瓣在径向(p = 0.230)和周向(p = 0.364)方向的应变方面没有差异。在慢性 IMR 条件下,模型之间在贴合长度(p = 0.596)、贴合深度(p = 0.621)、篷布面积(p = 0.879)和前瓣在径向(p = 0.151)和周向(p = 0.586)方向的应变方面没有差异。IMR 模型的 MR 相似,起源于束缚的 A3-P3 瓣叶的不对称射流。
本研究首次证明了体外模拟器在模拟健康绵羊模型和慢性 IMR 模型的收缩期瓣膜功能和力学方面的有效性。体外 IMR 模型为模拟中间和加重的环形和瓣下变形提供了能力,可用于模拟 IMR 修复。该系统为当前和未来的 IMR 修复的开发和评估提供了一个现实可控的测试平台。