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Bioactive versus bare platinum coils in the treatment of intracranial aneurysms: the MAPS (Matrix and Platinum Science) trial

机译:生物活性与裸铂线圈治疗颅内动脉瘤:maps(matrix和platinum science)试验

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摘要

BACKGROUND AND PURPOSE: The ability of polymer-modified coils to promote stable aneurysm occlusion after endovascular treatment is not well-documented. Angiographic aneurysm recurrence is widely used as a surrogate for treatment failure, but studies documenting the correlation of angiographic recurrence with clinical failure are limited. This trial compares the effectiveness of Matrix(2) polyglycolic/polylactic acid biopolymer-modified coils with bare metal coils and correlates the angiographic findings with clinical failure (ie, target aneurysm recurrence), a composite end point that includes any incident of posttreatment aneurysm rupture, retreatment, or unexplained death.MATERIALS AND METHODS: This was a multicenter randomized noninferiority trial with blinded end point adjudication. We enrolled 626 patients, divided between Matrix(2) and bare metal coil groups. The primary outcome was target aneurysm recurrence at 12 +/- 3 months.RESULTS: At 455 days, at least 1 target aneurysm recurrence event had occurred in 14.6% of patients treated with bare metal coils and 13.3% of Matrix(2) (P = .76, log-rank test) patients; 92.8% of target aneurysm recurrence events were re-interventions for aneurysms that had not bled after treatment, and 5.8% of target aneurysm recurrence events resulted from hemorrhage or rehemorrhage, with or without retreatment. Symptomatic re-intervention occurred in only 4 (0.6%) patients. At 455 days, 95.8% of patients with unruptured aneurysms and 90.4% of those with ruptured aneurysms were independent (mRS ≤ 2). Target aneurysm recurrence was associated with incomplete initial angiographic aneurysm obliteration, presentation with rupture, and a larger aneurysmal dome and neck size.CONCLUSIONS: Tested Matrix(2) coils were not inferior to bare metal coils. Endovascular coiling of intracranial aneurysms was safe, and the rate of technical success was high. Target aneurysm recurrence is a promising clinical outcome measure that correlates well with established angiographic measurements.
机译:背景和目的:血管内治疗后,聚合物修饰的线圈促进稳定的动脉瘤闭塞的能力尚未得到充分证明。血管造影动脉瘤复发被广泛用作治疗失败的替代指标,但是记录血管造影复发与临床失败相关性的研究有限。该试验比较了Matrix(2)聚乙醇酸/聚乳酸生物聚合物修饰的线圈与裸金属线圈的有效性,并将血管造影结果与临床失败(即目标动脉瘤复发)相关联,该终点是包括任何治疗后动脉瘤破裂事件的复合终点。 ,再治疗或无法解释的死亡。材料与方法:这是一项多中心随机非劣效性试验,采用盲法终点裁决。我们招募了626例患者,分为Matrix(2)组和裸金属线圈组。主要结果是在12 +/- 3个月时目标动脉瘤复发。结果:在455天时,裸金属线圈治疗的患者中14.6%发生了至少1例目标动脉瘤复发,而Matrix(2)发生了13.3%(P = 0.76,对数秩检验)患者; 92.8%的目标动脉瘤复发事件是对治疗后未出血的动脉瘤进行的再干预,而5.38%的目标动脉瘤复发事件是由出血或再出血导致的,无论是否进行再治疗。有症状的再次干预仅发生在4名(0.6%)患者中。在455天时,动脉瘤未破裂的患者中有95.8%是独立的,动脉瘤破裂的患者中有90.4%是独立的(mRS≤2)。目标动脉瘤复发与不完全的初始血管造影动脉瘤闭塞,破裂表现以及较大的动脉瘤圆顶和颈部大小有关。结论:经测试的Matrix(2)线圈不劣于裸金属线圈。颅内动脉瘤的血管内盘绕是安全的,技术成功率很高。目标动脉瘤复发是一种有前途的临床结果指标,与已建立的血管造影指标密切相关。

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