Department of Radiology, Division of Neurointerventional Radiology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Neurosurgery. 2011 Aug;69(2):369-75. doi: 10.1227/NEU.0b013e31821bc49c.
The Neuroform Stent has facilitated the endovascular treatment of wide-necked cerebral aneurysms. It is unknown which factors pose risks of thromboembolic events after stent placement.
This series is the largest single-center study reporting on the incidence of and factors influencing thromboembolic complications after Neuroform stent placement.
A total of 235 patients were treated with 274 Neuroform stents. The thromboembolic event rate was determined by imaging or clinical evidence of cerebrovascular accident within 90 days of stent placement; for patients with incomplete follow-up through chart review, telephone interviews were conducted. Analyses were performed to investigate patient factors that may be associated with stroke.
Most aneurysms were unruptured; 30 patients (12.8%) presented with acute subarachnoid hemorrhage. Twelve patients of the 224 with follow-up (5.4%, 95% confidence interval: 2.4%-8.3%) demonstrated imaging or clinical evidence of a new thromboembolic event within 90 days of stent placement. There was a 3.1% thromboembolic rate for unruptured aneurysms and a 20% rate in patients with subarachnoid bleed. Hemorrhage was significantly associated with having a thromboembolic event (P = .002). There was a trend toward an increased thromboembolic event rate for patients with hypertension (P = .07). Larger stent caliber was significantly associated with a decreased thromboembolic event rate (P = .032).
Our results suggest that the thromboembolic event rate associated with Neuroform stent use is low in unruptured aneurysms. In ruptured aneurysms, the complication rate is high, possibly partly related to restricted use of antiplatelet therapy. Stent size and hypertension may be associated with the risk of stroke, but additional studies are needed to confirm their significance.
Neuroform 支架促进了宽颈颅内动脉瘤的血管内治疗。目前尚不清楚支架置入后哪些因素会增加血栓栓塞事件的风险。
本系列研究是最大的单中心研究,报告了 Neuroform 支架置入后血栓栓塞并发症的发生率和影响因素。
共 235 例患者使用 274 枚 Neuroform 支架进行治疗。通过支架置入后 90 天内的影像学或脑血管意外的临床证据确定血栓栓塞事件的发生率;对于通过病历回顾随访不完整的患者,进行电话访谈。分析了可能与卒中相关的患者因素。
大多数动脉瘤为未破裂;30 例(12.8%)患者表现为急性蛛网膜下腔出血。224 例有随访的患者中,12 例(5.4%,95%置信区间:2.4%-8.3%)在支架置入后 90 天内出现新的血栓栓塞事件的影像学或临床证据。未破裂动脉瘤的血栓栓塞发生率为 3.1%,蛛网膜下腔出血患者的发生率为 20%。出血与发生血栓栓塞事件显著相关(P =.002)。高血压患者的血栓栓塞事件发生率呈上升趋势(P =.07)。支架口径较大与血栓栓塞事件发生率降低显著相关(P =.032)。
我们的结果表明,Neuroform 支架使用与未破裂动脉瘤相关的血栓栓塞事件发生率较低。在破裂的动脉瘤中,并发症发生率较高,可能部分与抗血小板治疗受限有关。支架大小和高血压可能与卒中风险相关,但需要进一步研究来确认其意义。