首页> 外文会议>ASME summer bioengineering conference;SBC2012 >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:装置血栓性模拟(DTE)方法开发和优化新型聚合物人工心脏瓣膜

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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:钙化主动脉瓣膜病(CAVD)是瓣膜性心脏病的最常见且危及生命的形式,其特征是狭窄和反流,目前在有症状的末期通过对心脏瓣膜进行心脏直视手术更换来治疗,通常是通过异种移植组织瓣膜或机械心脏瓣膜。这些选择为临床医生分别提供了结构性瓣膜恶化和抗凝治疗之间的选择,从而有效地将一种疾病替换为另一种疾病[1]。聚合体心脏瓣膜(PHV)有望减少或消除这些并发症[2],对于不能忍受心胸外科手术的患者,通过使用经导管瓣膜植入术(TAVI)[3]可能是有效的,其中有证据表明组织瓣膜是在植入期间[4]以及脉动循环支持设备(例如SynCardia全人工心脏)中受损。但是由于缺乏足够的持久性和生物相容性制剂,PHV的发展一直很缓慢。

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