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高血栓栓塞风险患者的可选下腔静脉滤器:有待解答的问题

Optional vena cava filters for patients with high thromboembolic risk: questions to be answered.

作者信息

Sing Ronald F, Rogers Frederick B, Novitsky Yuri W, Heniford B Todd

机构信息

Carolinas Laparoscopic and Advanced Surgery Program, Carolinas Medical Center, Charlotte, NC 28203, USA.

出版信息

Surg Innov. 2005 Sep;12(3):195-202. doi: 10.1177/155335060501200303.

Abstract

The use of vena cava filters has increased rapidly over the past few years to more than 140,000 filters inserted worldwide in 2003. Continued improvements in filter design have increased the safety of intravascular caval filtration. Although there are many factors attributed to this increase, the most significant contributing factor has been the development of optional vena cava filters. That is, filters that can be left as a permanent device or can be removed endovascularly at a later date. Three filters are approved for removal in the United States, the Günther Tulip, the OptEase, and the Recovery. Recent reports have demonstrated the safety and feasibility of these devices in appropriate patients, but a number of questions have arisen regarding their use.

摘要

在过去几年中,腔静脉滤器的使用迅速增加,2003年全球植入的滤器超过14万个。滤器设计的不断改进提高了血管内腔静脉滤过的安全性。尽管导致这种增加的因素很多,但最重要的因素是可选腔静脉滤器的发展。也就是说,滤器既可以作为永久性装置留置,也可以在以后通过血管内方式取出。在美国,有三种滤器被批准可取出,即Günther Tulip滤器、OptEase滤器和Recovery滤器。最近的报告已经证明了这些装置在合适患者中的安全性和可行性,但关于它们的使用也出现了一些问题。

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