López-Callejas Orlando, Ortiz-Giraldo Andres F, Vera Daniela D, Ramirez-Rojas Diego A, Villamizar-Barahona Ana B, Ferreira-Prada Carlos A, Galvis Melquizidel, Vargas-Pérez Oliverio, Serrano-Gómez Sergio, Reyes-Gonzalez Adriana, Mantilla Daniel
Department of Interventional Radiology, Fundación Oftalmológica de Santander-Clínica Ardila Lülle, Floridablanca, Colombia.
Department of Radiology, Clínica Medicadiz, Ibagué, Colombia.
Neurointervention. 2023 Mar;18(1):23-29. doi: 10.5469/neuroint.2022.00458. Epub 2023 Feb 22.
Internal carotid artery (ICA) aneurysm treatment with a flow diverter (FD) has shown an adequate efficacy and safety profile, presenting high complete occlusion or near occlusion rates with low complications during follow-up. The purpose of this study was to evaluate the efficacy and safety of FD treatment in non-ruptured internal carotid aneurysms.
This is a retrospective, single-center, observational study evaluating patients diagnosed with unruptured ICA aneurysms treated with an FD between January 1, 2014, and January 1, 2020. We analyzed an anonymized database. The primary effectiveness endpoint was complete occlusion (O'Kelly-Marotta D, OKM-D) of the target aneurysm through 1-year follow-up. The safety endpoint was the evaluation of modified Rankin Scale (mRS) 90 days after treatment, considering a favorable outcome an mRS 0-2.
A total of 106 patients were treated with an FD, 91.5% were women; the mean follow- up was 427.2±144.8 days. Technical success was achieved in 105 cases (99.1%). All patients included had 1-year follow-up digital subtraction angiography control; 78 patients (73.6%) completed the primary efficacy endpoint by achieving total occlusion (OKM-D). Giant aneurysms had a higher risk of not achieving complete occlusion (risk ratio, 3.07; 95% confidence interval, 1.70 - 5.54]). The safety endpoint of mRS 0-2 at 90 days was accomplished in 103 patients (97.2%).
Treatment of unruptured ICA aneurysms with an FD showed high 1-year total occlusion results, with very low morbidity and mortality complications.
采用血流导向装置(FD)治疗颈内动脉(ICA)动脉瘤已显示出足够的疗效和安全性,随访期间呈现出高完全闭塞或接近闭塞率以及低并发症发生率。本研究的目的是评估FD治疗非破裂性颈内动脉动脉瘤的疗效和安全性。
这是一项回顾性、单中心观察性研究,评估2014年1月1日至2020年1月1日期间诊断为未破裂ICA动脉瘤并接受FD治疗的患者。我们分析了一个匿名数据库。主要有效性终点是通过1年随访实现目标动脉瘤的完全闭塞(奥凯利 - 马罗塔D级,OKM - D)。安全性终点是治疗后90天改良Rankin量表(mRS)的评估,将mRS 0 - 2视为良好结局。
共有106例患者接受了FD治疗,91.5%为女性;平均随访时间为427.2±144.8天。105例(99.1%)实现了技术成功。所有纳入患者均进行了1年随访的数字减影血管造影对照;78例患者(73.6%)通过实现完全闭塞(OKM - D)完成了主要有效性终点。巨大动脉瘤未实现完全闭塞的风险更高(风险比,3.07;95%置信区间,1.70 - 5.54)。103例患者(97.2%)在90天时达到了mRS 0 - 2的安全性终点。
采用FD治疗未破裂ICA动脉瘤显示出1年高完全闭塞结果,发病率和死亡率并发症极低。