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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:具有或没有介入脑动脉畸形(Aruba)的医疗管理(Aruba):多期,非蒙蔽,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:预防性消除未破裂的脑动静脉畸形的临床效益仍然不确定。随机试验的悬垂脑动脉畸形(Aruba)旨在比较患者患者死亡和症状性脑卒中的风险,患有单独的医疗管理或介入治疗的医学管理。方法:成年患者(≥18岁)在九个国家的39个临床部位注册了脑动脉畸形畸形。患者被随机(通过基于Web的系统,在1:1的比例中,随机置换块设计[嵌段大小2,4或6],通过临床部位分层)与介入治疗的医学管理(即神​​经外科,栓塞,栓塞或单独或组合的立体定向放疗,单独或组合)或医学管理(即根据需要的神经系统症状的药理治疗)。患者,临床医生和调查人员了解治疗任务。主要结果是时间到死亡或对症中风的复合终点;主要分析是为了治疗。此试验在ClinCoIlicTrials.gov注册,NCT00389181号码。调查结果:2007年4月4日开始随机,2013年4月15日停止,当时由国家神经系统疾病研究所和国家卫生研究院的中风所指定的数据和安全监测委员会建议随机化,因为优势医学管理组(日志排名Z统计为4.10,超过预先限定的停止边值2.87)。此时,可获得223名患者的结果数据(平均随访33.3个月[SD 19.7]),分配给介入治疗和109例医疗管理。在医学管理组中11名(10.1%)患者达到了主要终点,而介入治疗组中的35例(30.7%)。医学管理组死亡或中风的风险显着低于介入治疗组(危害比率0.27,95%CI 0.14-0.54)。除了与医学管理分配给介入治疗的患者中,除了较高数量的中风(45 vs12,P <0.0001)和与中风(14 vs1,p = 0.0008)无关的神经学缺陷,没有危害危害。解释:阿鲁巴试验表明,单独的医疗管理优于医学管理,介入治疗用于预防脑动脉畸形畸形的患者中的死亡或中风,随后33个月。该试验正在继续其观察阶段,以确定差距是否持续在另外5年的随访中。

著录项

  • 来源
    《The Lancet》 |2014年第9917期|共8页
  • 作者单位

    Neurological Institute Columbia University Medical Center New York NY United States;

    International Center for Health Outcomes and Innovation Research Department of Health Evidence and;

    Neurological Institute Columbia University Medical Center New York NY United States Department;

    International Center for Health Outcomes and Innovation Research Department of Health Evidence and;

    Unité de Recherche Clinique France APHPH?pital Lariboisière Univ Paris Diderot-Sorbonne Paris;

    International Center for Health Outcomes and Innovation Research Department of Health Evidence and;

    Division of Clinical Neurosciences Centre for Clinical Brain Sciences University of Edinburgh;

    Unité de Recherche Clinique France;

    Department of Anesthesia and Perioperative Care University of California San Francisco CA;

    Department of Neuroradiology United States;

    Department of Neurology CHRU Lille Université Lille Nord de France Lille France;

    Department of Neurology and Neurosurgery Hospital de Clinicas de Porto Alegre PortoAlegre Brazil;

    Charité-Universit?tsmedizin Berlin Berlin Germany Department of Neurology Klinikum Frankfurt;

    Department of Neuroradiology University Hospital Dresden Dresden Germany;

    Department of Neuroradiology and Endovascular Therapy Jean Minjoz Hospital University of Franche;

    Department of Neuroradiology Universit?tsklinikum Frankfurt Frankfurt am Main Germany;

    Department of Neurology and Neurosurgery Brain Center Rudolf Magnus University Medical Center;

    Department of Neurology Royal Hallamshire Hospital Sheffield United Kingdom;

    Department of Neurology North Shore Long Island Jewish Medical Center New Hyde Park NY United;

    Department of Diagnostic and Interventional Neuroimaging CHU Pellegrin Bordeaux France;

    International Center for Health Outcomes and Innovation Research Department of Health Evidence and;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医药、卫生;
  • 关键词

    Ethics; Law; Paternity test;

    机译:道德;法律;父亲试验;

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