Fairman Ronald, Gray William A, Scicli Andrea P, Wilburn Olivia, Verta Patrick, Atkinson Richard, Yadav Jay S, Wholey Mark, Hopkins L Nelson, Raabe Rod, Barnwell Stanley, Green Richard
Division of Vascular Surgery and Endovascular Therapy, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Ann Surg. 2007 Oct;246(4):551-6; discussion 556-8. doi: 10.1097/SLA.0b013e3181567a39.
Although previous reports of carotid stenting with embolic protection (CAS) have focused on clinical outcomes of death, stroke and myocardial infarction, there are few data available characterizing the strokes that occur during CAS, thus limiting understanding of potential mechanisms. This report examines the timing, location, severity, and type of strokes occurring with CAS in the Carotid ACCULINK/ACCUNET Post Approval Trial to Uncover Unanticipated or Rare Events (CAPTURE) study.
The CAPTURE is a prospective, multicenter registry conducted to assess outcomes of CAS in the postapproval setting after device approval. A neurologist examined the patients before the procedure, at 24 hours and 30 days post-procedure. The primary end point was a composite of death, any stroke, or myocardial infarction within 30 days post-procedure. Strokes and all neurologic events suspected to be strokes were adjudicated by an independent Clinical Events Adjudication Committee using prespecified definitions. Source documents of all patients with strokes in this cohort were reviewed.
The 30-day results were available for 3500 patients. The 30-day primary end point event rate of death, stroke, and myocardial infarction was 6.3% (95% confidence interval: 5.5%-7.1%), and the rate of major stroke and death was 2.9% (95% confidence interval: 2.4 to 3.5). 4.8% of patients experienced a stroke (3.9% ipsilateral and 0.9% nonipsilateral, 2% major). A majority of stroke symptoms (57.7%) were noted post-procedure and pre-discharge, whereas 22.3% were noted during the procedure and 20% postdischarge. A similar timing distribution regardless of preprocedural symptomatic status was found.Overall, 41% (69 of 170) of all strokes were major. The incidence of major strokes was statistically significantly greater among symptomatic compared with asymptomatic patients, 4.6% (22 of 482) and 1.6% (47 of 3018), respectively. There were more minor than major strokes in asymptomatic patients (63% vs. 37%; P=0.10), whereas stroke severity was equally distributed in symptomatic patients. Among the ipsilateral strokes, almost half (44%) were major, whereas only one-quarter (26%) of the nonipsilateral strokes were major.Overall, 23% of the major strokes were hemorrhagic and 94% of these strokes were noted on the ipsilateral side. There was a tendency toward more major hemorrhagic strokes in symptomatic than in asymptomatic patients (36% vs. 17%; P=0.07). Fifty-four percent of the strokes post-procedure and pre-discharge were major, whereas 27% of the strokes postdischarge were major. Furthermore, 65% of hemorrhagic strokes were noted post-procedure and pre-discharge, 30% postdischarge.
Strokes related to CAS seem to become clinically apparent after the procedure but before discharge in the majority of events. Nevertheless, a significant minority of stroke symptoms follows discharge from the hospital, typically after 24 hours. Timing of stroke after CAS seems to be similar to timing of stroke after carotid endarterectomy. Moreover, nearly 1 in 5 strokes occur in a nonipsilateral distribution, with the exception of intraprocedural events, which were all ipsilateral to the stent being implanted. Hemorrhagic stroke seemed to be more prevalent in the strokes occurring in the post-procedure period. These descriptors of stroke severity, location, and timing may provide insight in to the mechanistic causes of adverse neurologic outcomes in CAS.
尽管先前有关带栓子保护装置的颈动脉支架置入术(CAS)的报告主要关注死亡、卒中及心肌梗死的临床结局,但关于CAS期间发生的卒中的特征性数据很少,这限制了对潜在机制的理解。本报告在颈动脉ACCULINK/ACCUNET批准后试验以发现意外或罕见事件(CAPTURE)研究中,对CAS相关卒中的发生时间、部位、严重程度及类型进行了研究。
CAPTURE是一项前瞻性、多中心注册研究,旨在评估器械批准后在批准后环境中CAS的结局。在手术前、术后24小时及30天,由一名神经科医生对患者进行检查。主要终点为术后30天内死亡、任何卒中或心肌梗死的复合终点。卒中及所有疑似卒中的神经事件由独立的临床事件判定委员会根据预先设定的定义进行判定。对该队列中所有卒中患者的原始文件进行了审查。
3500例患者的30天结果可用。术后30天死亡、卒中和心肌梗死的主要终点事件发生率为6.3%(95%置信区间:5.5%-7.1%),主要卒中和死亡发生率为2.9%(95%置信区间:2.4%-3.5%)。4.8%的患者发生了卒中(同侧3.9%,对侧0.9%,严重卒中2%)。大多数卒中症状(57.7%)在术后且出院前被发现,而22.3%在术中被发现,20%在出院后被发现。无论术前症状状态如何,均发现了类似的时间分布。总体而言,所有卒中中有41%(170例中的69例)为严重卒中。有症状患者的严重卒中发生率在统计学上显著高于无症状患者,分别为4.