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TARGET®颅内动脉瘤栓塞术前瞻性多中心注册研究:围手术期及长期安全性和有效性结果的最终分析

TARGET® Intracranial Aneurysm Coiling Prospective Multicenter Registry: Final Analysis of Peri-Procedural and Long-Term Safety and Efficacy Results.

作者信息

Zaidat Osama O, Castonguay Alicia C, Rai Ansaar T, Badruddin Aamir, Mack William J, Alshekhlee Amer K, Shah Qaisar A, Hussain Syed I, Kabbani Mouhammed R, Bulsara Ketan R, Taqi Asif M, Janardhan Vallabh, Patterson Mary S, Nordhaus Brittany L, Elijovich Lucas, Puri Ajit S

机构信息

Neuroscience Institute, Bon Secours Mercy Health St. Vincent Hospital, Toledo, OH, United States.

Department of Neurology, University of Toledo, Toledo, OH, United States.

出版信息

Front Neurol. 2019 Jul 9;10:737. doi: 10.3389/fneur.2019.00737. eCollection 2019.

Abstract

To describe the final results of the TARGET Registry, a multicenter, real-world study of patients with intracranial aneurysms treated with new generation TARGET Coils. The TARGET Registry is a prospective, single-arm study with independent medical event monitoring and core-lab adjudication. Patients with intracranial aneurysms were embolized with either TARGET-360° or helical coils in 12 US centers. The primary outcome was aneurysm packing density (PD), which was assessed immediately post-procedure. The secondary outcomes were immediate and long-term aneurysm occlusion rate using the Raymond Scale, and independent functional outcome using the modified Rankin Scale (mRS). A secondary analysis investigated the influence of the use of 100% 360-complex coils on clinical and angiographic outcomes. 148 patients with 157 aneurysms met the inclusion and exclusion criteria. 58 (39.2%) patients with ruptured and 90 (61.8%) with unruptured aneurysms were treated using TARGET 360°, helical Coils, or both. Median age was 58.3 (IQR 48.1-67.4), 73% female, and 71.6% were Caucasian. Median follow-up time was 5.9 (IQR 4.0-6.9) months. The majority were treated with TARGET 360-coils (63.7%), followed by mixed and helical coils only. Peri-procedural morbidity and mortality was seen in 2.7% of patients. A good outcome at discharge (mRS 0-2) was seen in 89.9% of the full cohort, and in 84.5 and 93.3% in the ruptured and unruptured patients, respectively. The median packing density was 28.8% (IQR 20.3-41.1). Long-term complete and near complete occlusion rate was seen in 90.4% of aneurysms and complete obliteration was seen in 66.2% of the aneurysms. No significant difference in clinical and angiographic outcomes were noted between the pure 360-complex coiling vs. mixed 360-complex/Helical coiling strategies. In a multivariate analysis, predictors for long-term aneurysm occlusion were aneurysm location, immediate occlusion grade, and aneurysm size. The long-term independent functional outcome was achieved in 128/135 (94.8%) patients and all-cause mortality was seen in 3/148 (2%) patients. In the multicenter TARGET Registry, two-thirds of aneurysms achieved long-term complete occlusion and 91.0% achieved complete or near complete occlusion with excellent independent functional outcome. www.ClinicalTrials.gov, identifier: NCT01748903.

摘要

为描述TARGET注册研究的最终结果,这是一项针对使用新一代TARGET线圈治疗的颅内动脉瘤患者的多中心、真实世界研究。TARGET注册研究是一项前瞻性、单臂研究,有独立的医学事件监测和核心实验室判定。美国12个中心的颅内动脉瘤患者使用TARGET - 360°或螺旋线圈进行栓塞。主要结局是动脉瘤填充密度(PD),在术后立即进行评估。次要结局是使用雷蒙德量表评估的即刻和长期动脉瘤闭塞率,以及使用改良Rankin量表(mRS)评估的独立功能结局。一项次要分析研究了使用100% 360复合线圈对临床和血管造影结局的影响。148例患有157个动脉瘤的患者符合纳入和排除标准。58例(39.2%)破裂动脉瘤患者和90例(61.8%)未破裂动脉瘤患者使用TARGET 360°、螺旋线圈或两者联合进行治疗。中位年龄为58.3岁(四分位间距48.1 - 67.4),73%为女性,71.6%为白种人。中位随访时间为5.9个月(四分位间距4.0 - 6.9)。大多数患者使用TARGET 360线圈治疗(63.7%),其次是混合线圈和仅使用螺旋线圈。2.7%的患者出现围手术期发病率和死亡率。整个队列中89.9%的患者出院时预后良好(mRS 0 - 2),破裂和未破裂患者中分别为84.5%和93.3%。中位填充密度为28.8%(四分位间距20.3 - 41.1)。90.4%的动脉瘤出现长期完全和接近完全闭塞率,66.2%的动脉瘤出现完全闭塞。单纯360复合线圈与混合360复合/螺旋线圈策略在临床和血管造影结局方面未发现显著差异。在多变量分析中,长期动脉瘤闭塞的预测因素是动脉瘤位置、即刻闭塞分级和动脉瘤大小。128/135例(94.8%)患者实现了长期独立功能结局,3/148例(2%)患者出现全因死亡。在多中心TARGET注册研究中,三分之二的动脉瘤实现了长期完全闭塞,91.0%实现了完全或接近完全闭塞,且独立功能结局良好。ClinicalTrials.gov网站,标识符:NCT01748903。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35b6/6629893/63f400db6f6b/fneur-10-00737-g0001.jpg

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