Lee C S, Aluri S, Chandran K B
Department of Chemical Engineering, Pennsylvania State University, College Station, USA.
J Heart Valve Dis. 1996 Jan;5(1):104-13.
Several in vitro studies have reported on cavitation bubble visualization with mechanical heart valves and the cavitation intensity has been correlated with the design of the valve, the load on the valve occluder, the velocity of the occluder tip, and the negative pressure transients in the vicinity of the occluder. These studies demonstrated the presence of cavitation for certain types of valves under simulated normal physiological loading conditions. However, extrapolation of these results to cavitation initiation in vivo has been questioned due to limitations of the in vitro studies in simulating the in vivo tissue compliance. The present study was intended to analyze the effect of valve holder flexibility (simulating compliance of the suture ring and the surrounding tissue in vivo) on cavitation dynamics.
Cavitation bubbles were visualized on three types of mechanical heart valves (Medtronic Hall, Edwards-Duromedics, and CarboMedics) in our in vitro set up, and pressure transients were measured close to the occluder at valve closure. Two different flexible valve holders made of Teflon (elastic modulus, E = 400 MPa) and low density polyethylene (E = 180 MPa) were employed and the results were compared with those with a rigid Plexiglas holder (E = 2930 MPa) of the same geometry (3'' by 3'' wide and 1/8'' thick).
Significant reductions were noted in the intensity of cavitation bubbles appearing along the clearance region of the Medtronic Hall and CarboMedics valves, with increasing valve holder flexibility. However, no attenuation was observed for the bubbles appearing around the seating lip or stop of the Edwards-Duromedics and Medtronic Hall valves that are believed to be caused by the fluid squeezing effect.
The results of the study suggest that timing of the mechanism to initiate cavitation is a critical factor in cavitation attenuation with flexible valve holders. If cavitation is initiated before the flexible valve holder responds to the impact at valve closure (such as due to squeeze film effect), cavitation intensity remains unchanged. Based on the results of the study, we propose that tissue compliance in vivo may not attenuate cavitation initiation for certain types of mechanical heart valves depending on the cavitation initiation mechanism.
多项体外研究报道了机械心脏瓣膜的空化气泡可视化情况,且空化强度与瓣膜设计、瓣膜封堵器上的负荷、封堵器尖端速度以及封堵器附近的负压瞬变相关。这些研究表明,在模拟正常生理负荷条件下,某些类型的瓣膜存在空化现象。然而,由于体外研究在模拟体内组织顺应性方面存在局限性,这些结果能否外推至体内空化起始情况受到了质疑。本研究旨在分析瓣膜固定器柔韧性(模拟体内缝线环和周围组织的顺应性)对空化动力学的影响。
在我们的体外实验装置中,对三种类型的机械心脏瓣膜(美敦力霍尔瓣膜、爱德华兹 - 杜罗美迪克瓣膜和卡波美迪克瓣膜)上的空化气泡进行可视化观察,并在瓣膜关闭时测量封堵器附近的压力瞬变。使用了两种由聚四氟乙烯(弹性模量,E = 400 MPa)和低密度聚乙烯(E = 180 MPa)制成的不同柔性瓣膜固定器,并将结果与相同几何形状(3英寸×3英寸宽,1/8英寸厚)的刚性有机玻璃固定器(E = 2930 MPa)的结果进行比较。
随着瓣膜固定器柔韧性增加,在美敦力霍尔瓣膜和卡波美迪克瓣膜的间隙区域出现的空化气泡强度显著降低。然而,对于爱德华兹 - 杜罗美迪克瓣膜和美敦力霍尔瓣膜座唇或止动处周围出现的气泡,未观察到衰减,这些气泡被认为是由流体挤压效应引起的。
研究结果表明,空化起始机制的时机是柔性瓣膜固定器使空化衰减的关键因素。如果空化在柔性瓣膜固定器对瓣膜关闭时的冲击做出响应之前就已起始(例如由于挤压膜效应),空化强度将保持不变。基于该研究结果,我们提出,体内组织顺应性可能不会根据空化起始机制减弱某些类型机械心脏瓣膜的空化起始。