Department of Neurosurgery, The Jikei University School of Medicine, Tokyo , Japan.
Department of Neuroendovascular Therapy and Neurosurgery, Juntendo University Faculty of Medicine, Tokyo , Japan.
Oper Neurosurg (Hagerstown). 2024 Feb 1;26(2):180-187. doi: 10.1227/ons.0000000000000928. Epub 2023 Oct 11.
Planning/guidance software became important tools for physicians' presurgical optimal decision-making. However, there are no intracranial stent products with specifically associated simulation software. We report the "premarket" clinical trial of a new braided stent with a customized simulation software.
A stent system with 3 mesh density types (16, 24, and 32 wire mesh) was designed based on computational flow dynamics technology, and a simulation software (virtual stent planner [VSP]) was developed for the optimal stent deployment planning. Stents were selected after simulation on preoperative 3D-processed angioimages, and accuracy of the VSP was evaluated.
Thirty-three unruptured intracranial aneurysms were successfully treated with VSP guidance. Twenty aneurysms (61%) were anterior circulation aneurysms, and 13 (39%) were posterior circulation aneurysms. The average aneurysm size was 7.1 mm, and the mean follow-up period was 19.2 months (11-39.0). There was no major recurrence or retreatment during follow-up, 2 morbidity cases, and no mortality. VSP planning presented slightly smaller stent dimensions compared with postdeployment: 24.2 vs 25.5 mm average, error -1.3 mm, and difference rate-5.46%.
Based on this result, the new stents and software guidance system were approved by the Ministry of Health and Welfare as a combined medical device. VSP provided precise deployment with minimal error compared with actual stent and can contribute to better stent deployment even for less experienced physicians.
规划/指导软件已成为医生术前进行最佳决策的重要工具。然而,目前尚无与特定模拟软件相关联的颅内支架产品。我们报告一种新型编织支架及其配套模拟软件的“上市前”临床试验结果。
根据计算流体动力学技术设计了具有 3 种网孔密度类型(16、24 和 32 个金属丝网格)的支架系统,并开发了一种模拟软件(虚拟支架规划器[VSP])用于进行最佳支架放置规划。在术前 3D 处理血管造影图像上进行模拟后选择支架,并评估 VSP 的准确性。
33 例未破裂颅内动脉瘤成功接受 VSP 引导治疗。20 例(61%)为前循环动脉瘤,13 例(39%)为后循环动脉瘤。平均动脉瘤大小为 7.1mm,平均随访时间为 19.2 个月(11-39.0)。随访期间无重大复发或再治疗,2 例发生并发症,无死亡。VSP 规划的支架尺寸略小于实际放置后的尺寸:平均 24.2 毫米 vs 25.5 毫米,误差 1.3 毫米,差异率为-5.46%。
基于这一结果,新支架和软件引导系统获得了韩国保健福祉部的批准,作为一种组合医疗器械。与实际支架相比,VSP 提供了更精确的放置,误差最小,即使对于经验较少的医生,也有助于更好地放置支架。