Klinik für Neuroradiologie, Neurozentrum, Klinikum Stuttgart, Kriegsbergstr. 60, 70174 Stuttgart, Germany.
Clin Neuroradiol. 2012 Sep;22(3):227-33. doi: 10.1007/s00062-011-0125-y. Epub 2012 Jan 18.
Procedural safety and high rates of in-stent recurrent stenotic lesions (ISR) remain a concern in the endovascular treatment of intracranial atherosclerotic disease (ICAD). In the present study technical feasibility, safety and efficacy of the paclitaxel eluting balloon-expandable coronary stent Coroflex(®) Please was assessed in the treatment of ICAD.
A total of 95 patients (79 male; median age 68 years) with 106 intracranial atherosclerotic stenotic lesions underwent endovascular treatment using Coroflex(®) Please stents (B. Braun, Melsungen, Germany). Location and degree of target stenoses before and after treatment and at follow-up and adverse clinical sequelae of treatment were registered. Post-procedural medication included 100 mg acetylsalicylic acid (ASA) and 75 mg clopidogrel for 1 year. Angiographic follow-up was scheduled for 6, 12, 26 and 52 weeks after the treatment.
The lesion locations were as follows: internal carotid artery (ICA) petrous (n = 44, 42%), ICA cavernous (n = 43, 41%), ICA paraclinoid (n = 4, 4%), intradural vertebral artery (VA; n = 11, 10%) and basilar artery (BA; n = 4, 4%). Of the lesions seven could not be treated due to difficult anatomy and stent stiffness (7% technical failure rate). The combined post-interventional neurological morbidity and mortality rate, including stroke, intracerebral hemorrhage (ICH), subarachnoid hemorrhage (SAH) and carotid cavernous fistula (CCF) was n = 4 (3.7%) within and n = 1 (0.9%) at and beyond 30 days, respectively. Angiographic and clinical follow-up examinations were carried out for 78 (78%) of the lesions (mean 16.1 months, maximum 48 months). Asymptomatic recurrent stenosis was seen in 3 out of 78 (3.8%) lesions and there was 1 case of late stent thrombosis (0.9%).
Treatment of ICAD using drug-eluting coronary stents is safe and effective but technical failure due to stent stiffness remains a problem. Application of the more flexible, newest generation thin-strut stents, however, shows promising results.
在颅内动脉粥样硬化性疾病(ICAD)的血管内治疗中,手术安全性和支架内再狭窄率(ISR)仍然令人担忧。在本研究中,评估了紫杉醇洗脱球囊扩张冠状动脉支架 Coroflex ® Please 在治疗 ICAD 中的技术可行性、安全性和疗效。
95 例(79 例男性;中位年龄 68 岁)共 106 例颅内动脉粥样硬化性狭窄病变患者采用 Coroflex ® Please 支架(B. Braun,Melsungen,德国)进行血管内治疗。记录治疗前后和随访时靶狭窄的位置和程度以及治疗的不良临床后果。术后用药包括 100mg 阿司匹林(ASA)和 75mg 氯吡格雷,持续 1 年。治疗后 6、12、26 和 52 周进行血管造影随访。
病变部位如下:颈内动脉(ICA)岩骨段(n=44,42%)、ICA 海绵窦段(n=43,41%)、ICA 床突旁段(n=4,4%)、颅内椎动脉(VA;n=11,10%)和基底动脉(BA;n=4,4%)。由于解剖结构困难和支架僵硬,有 7 处病变无法治疗(技术失败率 7%)。包括卒中、颅内出血(ICH)、蛛网膜下腔出血(SAH)和颈动脉海绵窦瘘(CCF)在内的围手术期神经发病率和死亡率分别为 n=4(3.7%)和 n=1(0.9%),分别发生在 30 天内和 30 天外。对 78 个(78%)病变进行了血管造影和临床随访检查(平均随访时间为 16.1 个月,最长随访时间为 48 个月)。无症状性再狭窄发生在 3 个病变中(3.8%),1 个支架内血栓形成(0.9%)。
颅内动脉粥样硬化性疾病采用药物洗脱冠状动脉支架治疗是安全有效的,但由于支架僵硬,技术失败仍然是一个问题。然而,应用更灵活、最新一代的薄壁支架显示出有前景的结果。