Pavcnik Dusan, Uchida Barry, Kaufman John, Hinds Monica, Keller Frederick S, Rösch Josef
Dotter Interventional Institute, Department of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon 97239-3098, USA.
Vasc Med. 2008 Feb;13(1):75-84. doi: 10.1177/1358863X07083474.
Lower extremity chronic deep venous insufficiency (CDVI) is common and remains a major health problem worldwide. Selected patients benefited from direct deep vein valve surgical repair or valve transplantation. A major limitation of this approach is that most of the patients are not candidates for these procedures due to obstructions or residual thrombus throughout the vein. The past 15 years have witnessed experimental efforts at catheter-based management of CDVI. This review describes the initial designs and experimental evolution of a mechanical and bioprosthetic venous valve that can be implanted by using a transcatheter technique. These valves consisted of single, double, or triple cusp leaflets made of synthetic or biological materials attached to a carrier or frame. All described devices for percutaneous transcatheter valve placement rely on some form of a vascular stent for valve attachment.
下肢慢性静脉功能不全(CDVI)很常见,仍是全球主要的健康问题。部分患者受益于直接深静脉瓣膜手术修复或瓣膜移植。这种方法的一个主要局限性在于,由于整个静脉存在梗阻或残余血栓,大多数患者不适合这些手术。在过去15年里,人们一直在尝试通过导管技术治疗CDVI。这篇综述描述了一种可通过经导管技术植入的机械和生物人工静脉瓣膜的初始设计及实验进展。这些瓣膜由附着在载体或框架上的单尖瓣、双尖瓣或三尖瓣小叶组成,小叶由合成材料或生物材料制成。所有描述的经皮经导管瓣膜置入装置都依靠某种形式的血管支架来固定瓣膜。