Greenfield L J, Cho K J, Tauscher J R
Department of Surgery, University of Michigan Hospital, Ann Arbor 48109.
J Vasc Surg. 1990 Sep;12(3):345-53.
The titanium Greenfield filter was developed to facilitate operative and percutaneous insertion by a carrier (12F) smaller than that required for the standard stainless steel filter (24F). In preliminary clinical studies however, it proved to have an unacceptable rate of distal slippage and caval wall penetration. Therefore four modifications in hook design and base diameter have been tested in 20 sheep by implantation above and below the renal veins. In comparison to control titanium Greenfield filters (n = 8), neither changes in hook angle with smaller diameter base (type I, n = 4), elimination of limb flare (type II, n = 4), or 80 degree hook angle (type IV, n = 10) prevented migration and entry into venous tributaries or penetration. Penetration scores on the basis of autopsy findings did not correlate with antemortem predictions based on cavograms and showed 1.5 +/- 2.0/filter for controls, 1.0 +/- 1.15/filter for type I, 1.75 +/- 0.96/filter for type II and 1.67 +/- 1.37/filter for type IV. It was necessary to change the configuration of the hook completely to a recurved hook design providing a base pad for the 80 degree hook (type VI, n = 6) to limit migration and penetration with a score of 0.33 +/- 0.82/filter. Effects of experimental embolism were studied in six sheep (two acute, four chronic) and showed effective trapping by both type IV and type VI filters with no evidence of filter migration or damage to the caval wall. Persistent thrombus appeared to be caused by the remnants of oxidized cellulose used to induce thrombi, but there was no evidence of propagation proximal to the filter.(ABSTRACT TRUNCATED AT 250 WORDS)
钛制格林菲尔德滤器的设计目的是通过比标准不锈钢滤器(24F)所需尺寸更小的载体(12F)来便于手术植入和经皮插入。然而,在初步临床研究中,它被证明远端移位和腔静脉壁穿透率不可接受。因此,在20只绵羊的肾静脉上方和下方植入了四种钩设计和基部直径的改良型滤器进行测试。与对照钛制格林菲尔德滤器(n = 8)相比,基部直径较小的钩角度改变(I型,n = 4)、消除肢体扩张(II型,n = 4)或80度钩角度(IV型,n = 10)均未能防止滤器迁移并进入静脉分支或穿透。基于尸检结果的穿透评分与基于腔静脉造影的生前预测不相关,对照滤器为1.5 +/- 2.0/滤器,I型为1.0 +/- 1.15/滤器,II型为1.75 +/- 0.96/滤器,IV型为1.67 +/- 1.37/滤器。有必要将钩的结构完全改为带有80度钩基部垫的弯形钩设计(VI型,n = 6),以将迁移和穿透限制在0.33 +/- 0.82/滤器的评分。在六只绵羊(两只急性,四只慢性)中研究了实验性栓塞的效果,结果显示IV型和VI型滤器均能有效捕获栓子,且无滤器迁移或腔静脉壁损伤的迹象。持续性血栓似乎是由用于诱导血栓形成的氧化纤维素残余物引起的,但没有证据表明血栓在滤器近端扩展。(摘要截断于250字)