Department of Endovascular Neurosurgery, Toranomon Hospital, Tokyo, Japan.
J Vasc Surg. 2010 Jan;51(1):51-6. doi: 10.1016/j.jvs.2009.08.040. Epub 2009 Oct 30.
Although carotid artery stenting (CAS) has been proposed as an alternative to carotid endarterectomy in cerebral revascularization, restenosis remains an unsolved issue. Cilostazol is a unique antiplatelet drug that has vasodilatory effects and inhibits smooth muscle cell proliferation. We investigated whether cilostazol reduces restenosis after CAS.
A database of 113 consecutive CAS procedures between April 2002 and December 2007 was assessed retrospectively. All patients received aspirin (100 mg/d) and another antiplatelet drug such as cilostazol (200 mg/d), ticlopidine (200 mg/d), or clopidogrel (75 mg/d) at least 3 days before CAS. Two antiplatelet drugs were continued for 2 to 3 months after CAS and reduced to one thereafter. Patients were evaluated at 3 and 6 months and at 6-month intervals thereafter with duplex ultrasound (DUS) imaging. Angiography was used for confirmation when stenosis was suspected as >50% with DUS imaging.
We were able to monitor 97 patients for a 12-month period. The overall combined rate of stroke, myocardial infarction, and death was 3.1% at 30 days and 4.1% at 1 year. In-stent recurrent stenosis was documented in 11 patients (11%); in 10 patients (9.7%), this occurred <or=12 months of CAS. In-stent restenosis was significantly reduced in the cilostazol (+) group (0% vs 15.7% [11 of 70], P = .03). Patient characteristics were similar between the cilostazol (+) and cilostazol (-) groups.
Although this study was retrospective and nonrandomized, the results suggest that cilostazol administration improves long-term patency after CAS due to its inhibitory effect on smooth muscle cell growth.
虽然颈动脉支架置入术(CAS)已被提议作为脑血运重建中颈动脉内膜切除术的替代方法,但再狭窄仍然是一个未解决的问题。西洛他唑是一种独特的抗血小板药物,具有血管扩张作用并抑制平滑肌细胞增殖。我们研究了西洛他唑是否可以降低 CAS 后的再狭窄率。
回顾性评估了 2002 年 4 月至 2007 年 12 月期间连续进行的 113 例 CAS 手术的数据库。所有患者在 CAS 前至少 3 天接受阿司匹林(100 mg/d)和另一种抗血小板药物,如西洛他唑(200 mg/d)、噻氯匹定(200 mg/d)或氯吡格雷(75 mg/d)。CAS 后继续使用两种抗血小板药物 2-3 个月,然后减少至一种。患者在 3 个月和 6 个月以及此后每 6 个月进行一次双功能超声(DUS)成像检查。当 DUS 成像怀疑狭窄 >50%时,使用血管造影进行确认。
我们能够对 97 例患者进行 12 个月的监测。30 天时总的卒中和心肌梗死合并死亡率为 3.1%,1 年时为 4.1%。11 例(11%)患者发现支架内再狭窄;10 例(9.7%)患者在 CAS 后 <或=12 个月时发生再狭窄。西洛他唑(+)组的支架内再狭窄率明显降低(0% vs 15.7%[70 例中的 11 例],P =.03)。西洛他唑(+)组和西洛他唑(-)组的患者特征相似。
尽管本研究为回顾性和非随机的,但结果表明,西洛他唑的给药通过抑制平滑肌细胞生长,改善了 CAS 后的长期通畅率。