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Safety and Efficacy Analyses of Angioplasty and Stenting for Severe Intracranial Arterial Stenosis: A Single-Center Retrospective Study in China

机译:严重颅内动脉狭窄的血管成形术和支架置入术的安全性和有效性分析:在中国的单中心回顾性研究

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BACKGROUND The value of percutaneous transluminal angioplasty and stenting (PTAS) in the context of aggressive medical treatment for severe intracranial artery stenosis (ICAS) is under debate. This study compared the effects of PTAS and aggressive medical treatment in patients with severe ICAS and transient ischemic attack or stroke. MATERIAL AND METHODS A retrospective cohort study was performed. Patients with severe ICAS were assigned to a PTAS group or aggressive medical treatment group, according to the angiographic features of the stenotic lesions. The primary outcome was defined as stroke or death within 30 days or cerebral ischemia occurring ipsilaterally to the qualifying artery beyond 30 days. RESULTS We included 220 patients: 48 in the PTAS group and 172 in the medical group. The median follow-up was 32 months. PTAS was not associated with an increased incidence of the primary outcomes (10/42 [i]vs.[/i] 39/172, p=0.96) or increased risks of the secondary outcomes of stroke, cardiovascular events, major bleeding, or mortality. The results of log-rank tests did not support a significant difference in event-free survival as a primary outcome between the 2 groups (chi-square=0.07, p=0.79). Moreover, although not significantly greater, the mean survival of patients in the PTAS group appeared to be better than that among patients in the medical group, as indicated by the curve for cumulative survival. CONCLUSIONS A suitable PTAS procedure is safe for patients with severe ICAS, and no significant differences in incidence of recurrent stroke or death were found between PTAS and aggressive medication treatment.
机译:背景技术在积极治疗严重颅内动脉狭窄(ICAS)的背景下,经皮腔内血管成形术和支架置入术(PTAS)的价值正在争论中。这项研究比较了PTAS和积极药物治疗对严重ICAS和短暂性脑缺血发作或中风的影响。材料与方法进行了一项回顾性队列研究。根据狭窄病变的血管造影特征,将患有严重ICAS的患者分为PTAS组或积极药物治疗组。主要结局定义为30天内发生中风或死亡,或30天内在合格动脉同侧发生脑缺血。结果我们纳入了220例患者:PTAS组48例,医学组172例。中位随访时间为32个月。 PTAS与主要结局发生率增加(10/42 [i] vs。[/ i] 39/172,p = 0.96)或中风,心血管事件,大出血或死亡。对数秩检验的结果不支持两组之间无事件生存作为主要结局的显着差异(卡方= 0.07,p = 0.79)。而且,尽管累积存活率曲线显示,尽管没有明显增加,但PTAS组患者的平均存活率似乎比医学组患者更好。结论适当的PTAS程序对重症ICAS患者是安全的,并且在PTAS和积极药物治疗之间未发现复发性中风或死亡的发生率有显着差异。

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