Peng Weicheng, Ma Haiyang, Xiang Xinli, Zhao Rui, Lv Meng, Xu Sheng, Jiang Yuhua, Hu Zhiqiang, Guan Feng
Department of Neurosurgery, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.
Department of Pharmacy, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.
Front Neurol. 2025 Mar 25;16:1507339. doi: 10.3389/fneur.2025.1507339. eCollection 2025.
Intracranial stenting with the Neuroform Atlas Stent is an emerging option for patients with symptomatic intracranial atherosclerotic stenosis (sICAS) who do not respond to intensive medical treatment. However, the efficacy, safety, and risk factors associated with postoperative stroke recurrence remain controversial.
A total of 326 consecutive patients with sICAS treated with intracranial stenting using the Neuroform Atlas Stent were retrospectively analyzed to evaluate the efficacy and safety of the procedure. Patients were randomly assigned to a training set and a validation set in a 7:3 ratio. Significant variables in the univariate logistic analyses were included in the final multivariate logistic regression analyses in the training set. Subsequently, we developed a predictive nomogram for sICAS treated with a Neuroform Atlas Stent to predict the likelihood of stroke recurrence at 6 months.
The overall mean stenosis rate of the target artery was 88.85% ± 6.53% before the stenting (T0), 47.58% ± 9.94% at the end of the procedure (T1), and 40.21% ± 7.77% at the 6-month follow-up (T2). The stenosis rate was statistically significant between T0 and T1 ( < 0.01) and between T0 and T2 ( < 0.01). At 6 months postoperatively, 36 patients had a stroke recurrence linked to the target artery. Diabetes, acute ischemic stroke (AIS), plaque burden on vessel wall MRI, enhancement ratio on vessel wall MRI, and stenosis (T1) were independent predictors of stroke recurrence. A predictive nomogram was developed, showing strong predictive capability with the area under the curve of 0.933 for the training set and 0.949 for the validation set.
Intracranial stenting with the Neuroform Atlas Stent is a potentially safe and effective treatment for sICAS. Risk factors for recurrent stroke post-procedure include diabetes, current smoker, current drinker, AIS, plaque burden, enhancement ratio, and stenosis (T1).
对于症状性颅内动脉粥样硬化狭窄(sICAS)且强化药物治疗无效的患者,使用Neuroform Atlas支架进行颅内支架置入术是一种新兴的选择。然而,与术后卒中复发相关的疗效、安全性和危险因素仍存在争议。
回顾性分析326例连续接受Neuroform Atlas支架颅内支架置入术治疗的sICAS患者,以评估该手术的疗效和安全性。患者按7:3的比例随机分为训练集和验证集。单因素逻辑分析中的显著变量纳入训练集的最终多因素逻辑回归分析。随后,我们开发了一种用于接受Neuroform Atlas支架治疗的sICAS的预测列线图,以预测6个月时卒中复发的可能性。
支架置入术前(T0)靶血管的总体平均狭窄率为88.85%±6.53%,手术结束时(T1)为47.58%±9.94%,6个月随访时(T2)为40.21%±7.77%。T0与T1之间(<0.01)以及T0与T2之间(<0.01)的狭窄率具有统计学意义。术后6个月,36例患者发生与靶血管相关的卒中复发。糖尿病、急性缺血性卒中(AIS)、血管壁MRI上的斑块负荷、血管壁MRI上的强化率和狭窄(T1)是卒中复发的独立预测因素。开发了一种预测列线图,训练集曲线下面积为0.933,验证集为0.949,显示出强大的预测能力。
使用Neuroform Atlas支架进行颅内支架置入术是治疗sICAS的一种潜在安全有效的方法。术后卒中复发的危险因素包括糖尿病、当前吸烟者、当前饮酒者、AIS、斑块负荷、强化率和狭窄(T1)。