Qureshi A I, Kirmani J F, Harris-Lane P, Divani A A, Ahmed S, Ebrihimi A, Al Kawi A, Janjua N
Clinical Trials Division, Zeenat Qureshi Stroke Research Center, Department of Neurology and Neurosciences, New Jersey Medical School, University of Medicine and Dentistry of New Jersey, Newark, NJ, USA.
AJNR Am J Neuroradiol. 2006 May;27(5):1140-5.
To report the feasibility, safety, and 1-month results of performing stent placement for vertebral origin stenosis with the use of a distal protection device. Distal protection devices have been shown to reduce the number of cerebral emboli and subsequent ischemic events when used as adjuncts to percutaneous carotid intervention; however, one case of the use of a distal protection device for vertebral artery has been reported in the literature.
We retrospectively determined rates of technical success and 1-month stroke or death associated with stent placement by using distal protection (Filter EX; Boston Scientific, Natick, Mass) in patients with symptomatic vertebral artery origin stenosis. Technical success was defined as successful deployment of distal protection device and stent at target lesion followed by successful retrieval of the device and a final residual stenosis of less than 30%. Other outcomes ascertained included any stroke, death, and semiquantitative assessment of particulate material retained by the filter device.
The mean age of the 12 treated patients was 68 years (range, 52-88 years) and the group included 9 men and 3 women. The mean percentage of vertebral artery origin stenosis was 71 +/- 6%. Femoral and radial approaches were used in 9 and 3 cases, respectively. Technical success was achieved in 11 of the 12 patients in whom distal protection device placement was attempted. Postprocedure residual stenosis was 5 +/- 4%. Eight devices held macroscopically visible embolic debris (large and small amounts in 3 and 5 devices, respectively). No stroke or death was observed in the 1-month follow-up.
The present study demonstrates the feasibility of performing stent placement for vertebral artery origin stenosis by using a distal protection device. Further studies are required to determine the effectiveness of this approach for vertebral artery origin atherosclerosis.
报告使用远端保护装置对椎动脉起始部狭窄进行支架置入术的可行性、安全性及1个月的结果。远端保护装置在作为经皮颈动脉介入治疗的辅助手段时,已被证明可减少脑栓塞数量及后续缺血性事件;然而,文献中仅报道过1例使用远端保护装置治疗椎动脉的病例。
我们回顾性分析了有症状的椎动脉起始部狭窄患者使用远端保护装置(Filter EX;波士顿科学公司,马萨诸塞州纳蒂克)进行支架置入术的技术成功率以及1个月内发生卒中或死亡的情况。技术成功定义为在目标病变处成功部署远端保护装置和支架,随后成功取出装置,最终残余狭窄小于30%。确定的其他结果包括任何卒中、死亡以及对滤器装置截留的颗粒物质进行半定量评估。
12例接受治疗的患者平均年龄为68岁(范围52 - 88岁),其中男性9例,女性3例。椎动脉起始部狭窄的平均百分比为71±6%。分别有9例和3例采用股动脉和桡动脉入路。在尝试放置远端保护装置的12例患者中,11例取得技术成功。术后残余狭窄为5±4%。8个装置截留了肉眼可见的栓塞碎片(分别有3个和5个装置截留了大量和少量碎片)。在1个月的随访中未观察到卒中或死亡。
本研究证明了使用远端保护装置对椎动脉起始部狭窄进行支架置入术的可行性。需要进一步研究来确定这种方法对椎动脉起始部动脉粥样硬化的有效性。