From the Department of Neurosurgery, (J.-m.L., Y.Z., P.-f.Y., B.H., Y.X., Q.L., R.Z., Y.F., K.Z., Q.H.), Shanghai Changhai Hospital, Shanghai, China
From the Department of Neurosurgery, (J.-m.L., Y.Z., P.-f.Y., B.H., Y.X., Q.L., R.Z., Y.F., K.Z., Q.H.), Shanghai Changhai Hospital, Shanghai, China.
AJNR Am J Neuroradiol. 2018 May;39(5):807-816. doi: 10.3174/ajnr.A5619. Epub 2018 Mar 29.
Although flow diverters have been reported with favorable clinical and angiographic outcomes in various literatures, randomized trials determining their true effectiveness and safety are still in lack. The Parent Artery Reconstruction for Large or Giant Cerebral Aneurysms Using the Tubridge Flow Diverter (PARAT) trial was designed to evaluate the safety and efficacy of the Tubridge flow diverter in the treatment of large or giant aneurysms in comparison with Enterprise stent-assisted coiling.
This prospective, multicenter, randomized trial was conducted at 12 hospitals throughout China. Enrolled adults with unruptured large/giant intracranial aneurysms were randomly assigned (1:1) to receive either Enterprise stent-assisted coiling or Tubridge flow diverter implantation. The primary end point was complete occlusion at 6-month follow-up, while secondary end points included technical success, mortality, target vessel-related stroke, aneurysm bleeding, in-stent stenosis, parent artery occlusion, and the frequency of all adverse events.
Among 185 enrolled subjects, 41 withdrew before procedure initiation. Overall, 82 subjects underwent Tubridge implantation, and 62 subjects were primarily treated with stent-assisted coiling. The results of 6-month follow-up imaging included complete occlusion rates of 75.34% versus 24.53% for the Tubridge and stent-assisted coiling groups, respectively, with a calculated common odds ratio of 9.4 (95% confidence interval, 4.14-21.38; < .001). There was a higher, nonsignificant frequency of complications for Tubridge subjects. Multivariate analysis showed a decreased stroke rate at the primary investigational site, with a marginal value ( = .051).
This trial showed an obviously higher rate of large and giant aneurysm obliteration with the Tubridge FD over Enterprise stent-assisted coiling. However, this higher obliteration rate came at the cost of a nonsignificantly higher rate of complications. Investigational site comparisons suggested that a learning curve for flow-diverter implantation should be recognized and factored into trial designs.
尽管在各种文献中已有报道称血流导向装置具有良好的临床和血管造影结果,但仍缺乏确定其真正有效性和安全性的随机试验。Parent Artery Reconstruction for Large or Giant Cerebral Aneurysms Using the Tubridge Flow Diverter (PARAT) 试验旨在评估 Tubridge 血流导向装置在治疗大型或巨大型动脉瘤中的安全性和有效性,并与 Enterprise 支架辅助弹簧圈治疗进行比较。
这是一项在中国 12 家医院进行的前瞻性、多中心、随机试验。纳入的未破裂的大型/巨大颅内动脉瘤成年患者被随机分配(1:1)接受 Enterprise 支架辅助弹簧圈或 Tubridge 血流导向装置植入治疗。主要终点为 6 个月随访时完全闭塞,次要终点包括技术成功率、死亡率、靶血管相关卒中、动脉瘤出血、支架内狭窄、载瘤动脉闭塞以及所有不良事件的发生频率。
在 185 名入组患者中,有 41 名在开始治疗前退出。共有 82 名患者接受了 Tubridge 植入,62 名患者主要接受了支架辅助弹簧圈治疗。6 个月随访的影像学结果显示,Tubridge 组和支架辅助弹簧圈组的完全闭塞率分别为 75.34%和 24.53%,Tubridge 组的共同优势比为 9.4(95%置信区间:4.14-21.38;<0.001)。Tubridge 组的并发症发生率更高,但无统计学意义。多变量分析显示,主要研究部位的卒中发生率降低,具有边缘显著性(=0.051)。
该试验显示,与 Enterprise 支架辅助弹簧圈相比,Tubridge FD 治疗大型和巨大型动脉瘤的闭塞率明显更高。然而,这种更高的闭塞率是以并发症发生率略有增加为代价的。对研究部位的比较表明,应认识到血流导向装置植入的学习曲线,并将其纳入试验设计中。