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在滤器保护下对颈总动脉分叉处进行血管成形术和支架置入术:对53例患者的前瞻性研究。

Angioplasty and stenting of the cervical carotid bifurcation under filter protection: a prospective study in a series of 53 patients.

作者信息

Bonaldi G, Aiazzi L, Baruzzi F, Biroli F, Facchinetti A, Fachinetti P, Lunghi A, Terraneo F

机构信息

Neuroradiology Department, Ospedali Riuniti, Largo Barozzi 1, 24128 Bergamo, Italy.

出版信息

J Neuroradiol. 2005 Mar;32(2):109-17. doi: 10.1016/s0150-9861(05)83125-6.

Abstract

The aim of this study is to assess safety, reliability, ease of use and usefulness of filter protection devices during angioplasty and stenting of stenotic lesions of the cervical carotid bifurcation. Over a period of 42 months, 53 patients harboring a cervical carotid bifurcation stenotic lesion were treated, by angioplasty and/or stenting using filter protection devices of different kinds. The stenosis was atherosclerotic in 48 cases, post-surgical in four and post-radiation in one case. In all cases, the treatment was successful, with good restoration of the luminal diameter. There were three major strokes (5.6%) and one minor stroke (1.9%). Two of these (one major, one minor) occurred a few hours after the stenting procedure and both seemed by all evidence due to a hemorrhagic hyperperfusion syndrome. One hemiparesis and dysphasia occurred two days after the procedure, secondary to subacute thrombosis with occlusion of the stent. One patient complained of three episodes of decrease in visual acuity of the eye ipsilateral to the stenting in the two weeks following treatment. In conclusion, in our experience, use of the devices adds only few minutes to the procedure time; direct lesions of the arterial wall, such as dissections or intraluminal thrombi, related to the use of filters were never observed, and spasm of the distal I.C.A. also proved rapidly regressive. The content of all filters, if any, was histologically examined, but plaque material was found only in one case, probably owing to our primary stenting technique without use of pre-dilation. The major technical drawback is in-filter coagulation, which occurred in 16 cases, occluding the membrane of the filter and thus slowing or blocking intracranial flow. Such an event can be counteracted by a more aggressive anti-coagulation protocol, which could, however, be responsible for the two complications with hemorrhagic brain infarction. Furthermore, we observed two other major neurological events, which bring the incidence of neurological complications in this series as high as 7.5%. Therefore, it is our opinion that safety of filters is not yet proven, and consequently great care must be taken in their use.

摘要

本研究的目的是评估在颈总动脉分叉处狭窄病变的血管成形术和支架置入术中滤器保护装置的安全性、可靠性、易用性和实用性。在42个月的时间里,对53例患有颈总动脉分叉处狭窄病变的患者进行了治疗,采用了不同类型的滤器保护装置进行血管成形术和/或支架置入术。其中48例狭窄为动脉粥样硬化性,4例为术后狭窄,1例为放疗后狭窄。所有病例治疗均成功,管腔直径恢复良好。发生了3例严重卒中(5.6%)和1例轻度卒中(1.9%)。其中2例(1例严重,1例轻度)在支架置入术后数小时发生,所有证据显示均因出血性高灌注综合征所致。1例偏瘫和言语困难在术后两天发生,继发于亚急性血栓形成并导致支架闭塞。1例患者在治疗后的两周内主诉支架同侧眼视力下降3次。总之,根据我们的经验,使用这些装置只会使手术时间增加几分钟;从未观察到与滤器使用相关的动脉壁直接损伤,如夹层或腔内血栓形成,并且颈内动脉远端的痉挛也迅速消退。对所有滤器的内容物(如有)进行了组织学检查,但仅在1例中发现斑块物质,可能是由于我们采用的是未使用预扩张的初次支架置入技术。主要的技术缺点是滤器内凝血,发生了16例,阻塞了滤器膜,从而减慢或阻断了颅内血流。这种情况可以通过更积极的抗凝方案来抵消,然而,这可能是导致两例出血性脑梗死并发症的原因。此外,我们还观察到另外两例严重的神经事件,这使得本系列中神经并发症的发生率高达7.5%。因此,我们认为滤器的安全性尚未得到证实,因此在使用时必须格外小心。

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