首页> 外文会议>ASME bioengineering conference >DEVELOPMENT AND OPTIMIZATION OF A NOVEL POLYMERIC PROSTHETIC HEART VALVE USING THE DEVICE THROMBOGENICITY EMULATION (DTE) METHODOLGY
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DEVELOPMENT AND OPTIMIZATION OF A NOVEL POLYMERIC PROSTHETIC HEART VALVE USING THE DEVICE THROMBOGENICITY EMULATION (DTE) METHODOLGY

机译:使用器件血栓形成仿真(DTE)法解电术新型聚合物假体心脏瓣膜的开发和优化

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Calcific aortic valve disease (CAVD) is the most common and life threatening form of valvular heart disease, characterized by stenosis and regurgitation, which is currently treated at the symptomatic end-stages via open-heart surgical replacement of the diseased valve with typically either a xenograft tissue valve or mechanical heart valve. These options offer the clinician a choice between structural valve deterioration and anticoagulant therapy respectively, effectively replacing one disease with another [1]. Polymeric heart valves (PHV) offer the promise of reducing or eliminating these complications [2] and may be efficacious for patients who cannot tolerate cardiothoracic surgery by using instead transcatheter valve implantation (TAVI) [3], where there is evidence that tissue valves are damaged during implantation [4], and in pulsatile circulatory support devices such as the SynCardia Total Artificial Heart. But development of PHVs has been slow due to the lack of sufficiently durable and biocompatible formulations.
机译:钙化性主动脉瓣疾病(CAVD)是心脏瓣膜病的最常见的和危及生命的形式,其特征在于通过狭窄和反流,这是目前在症状最终阶段通过开放式心脏外科置换病变瓣膜的处理典型地是异种移植物组织阀或机械心脏瓣膜。这些选项分别提供结构阀恶化和抗凝血剂治疗的临床医生选择,与另一个[1]有效地取代一种疾病。高分子心脏瓣膜(PHV)提供了减少或消除这些并发症的承诺[2],并且可以有效的对谁也不能使用,而不是经导管瓣膜植入术(TAVI)耐受心胸外科的患者[3],其中有证据表明,组织阀植入[4],期间和在脉动循环支持设备,如SynCardia全人工心脏损伤。但是PHVs的发展一直缓慢,由于缺乏足够的耐用性和生物相容性配方。

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