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首页> 外文期刊>The Lancet >Medical management with or without interventional therapy for unruptured brain arteriovenous malformations (ARUBA): A multicentre, non-blinded, randomised trial
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Medical management with or without interventional therapy for unruptured brain arteriovenous malformations (ARUBA): A multicentre, non-blinded, randomised trial

机译:有无动静脉畸形(ARUBA)的有无介入治疗的药物管理:一项多中心,无盲,随机试验

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摘要

Background: The clinical benefit of preventive eradication of unruptured brain arteriovenous malformations remains uncertain. A Randomised trial of Unruptured Brain Arteriovenous malformations (ARUBA) aims to compare the risk of death and symptomatic stroke in patients with an unruptured brain arteriovenous malformation who are allocated to either medical management alone or medical management with interventional therapy. Methods: Adult patients (≥18 years) with an unruptured brain arteriovenous malformation were enrolled into this trial at 39 clinical sites in nine countries. Patients were randomised (by web-based system, in a 1:1 ratio, with random permuted block design [block size 2, 4, or 6], stratified by clinical site) to medical management with interventional therapy (ie, neurosurgery, embolisation, or stereotactic radiotherapy, alone or in combination) or medical management alone (ie, pharmacological therapy for neurological symptoms as needed). Patients, clinicians, and investigators are aware of treatment assignment. The primary outcome is time to the composite endpoint of death or symptomatic stroke; the primary analysis is by intention to treat. This trial is registered with ClinicalTrials.gov, number NCT00389181. Findings: Randomisation was started on April 4, 2007, and was stopped on April 15, 2013, when a data and safety monitoring board appointed by the National Institute of Neurological Disorders and Stroke of the National Institutes of Health recommended halting randomisation because of superiority of the medical management group (log-rank Z statistic of 4.10, exceeding the prespecified stopping boundary value of 2.87). At this point, outcome data were available for 223 patients (mean follow-up 33.3 months [SD 19.7]), 114 assigned to interventional therapy and 109 to medical management. The primary endpoint had been reached by 11 (10.1%) patients in the medical management group compared with 35 (30.7%) in the interventional therapy group. The risk of death or stroke was significantly lower in the medical management group than in the interventional therapy group (hazard ratio 0.27, 95% CI 0.14-0.54). No harms were identified, other than a higher number of strokes (45 vs 12, p<0.0001) and neurological deficits unrelated to stroke (14 vs 1, p=0.0008) in patients allocated to interventional therapy compared with medical management. Interpretation: The ARUBA trial showed that medical management alone is superior to medical management with interventional therapy for the prevention of death or stroke in patients with unruptured brain arteriovenous malformations followed up for 33 months. The trial is continuing its observational phase to establish whether the disparities will persist over an additional 5 years of follow-up.
机译:背景:预防性根除未破裂的脑动静脉畸形的临床益处仍然不确定。一项未破裂的脑动静脉畸形的随机试验(ARUBA)旨在比较未破裂的脑动静脉畸形患者的死亡和有症状的中风的风险,这些患者被分配到单独的医疗管理或介入治疗的医疗管理中。方法:在九个国家的39个临床地点,将未动过脑动静脉畸形的成年患者(≥18岁)纳入该试验。患者被随机分配(通过基于网络的系统,以1:1的比例,采用随机排列的区组设计[区大小2、4或6],按临床部位分层),进行介入治疗(即神经外科,栓塞术)的医学治疗,或单独或组合使用立体定向放疗)或单独进行药物治疗(即根据需要对神经系统症状进行药物治疗)。患者,临床医生和研究人员都知道治疗分配。主要结果是到达死亡或症状性中风复合终点的时间。主要分析是按意向治疗。该试验已在ClinicalTrials.gov上注册,编号为NCT00389181。调查结果:随机分组于2007年4月4日开始,并于2013年4月15日停止,当时美国国立卫生研究院神经疾病和中风研究所任命的数据和安全监测委员会建议停止随机分组,原因是随机分组的优势医疗管理组(对数秩Z统计量为4.10,超过了预先指定的停止边界值2.87)。此时,可获得223例患者的结果数据(平均随访33.3个月[SD 19.7]),其中114例为介入治疗,109例为药物治疗。药物治疗组中有11名患者(10.1%)达到了主要终点,而介入治疗组中只有35名(30.7%)。药物治疗组的死亡或中风风险显着低于介入治疗组(危险比0.27,95%CI 0.14-0.54)。与医疗管理相比,除介入治疗的患者发生中风的次数较多(45 vs 12,p <0.0001)和与中风无关的神经功能缺损(14 vs 1,p = 0.0008)外,未发现任何危害。解释:ARUBA试验显示,对于随访了33个月的未破裂脑动静脉畸形的患者,单独的药物治疗优于采用介入治疗的药物治疗,以预防死亡或中风。该试验正在继续其观察阶段,以确定这种差异是否还会持续5年以上。

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