Neurology, Stroke Unit, CHRU de Nancy, Nancy, Lorraine, France.
Neuroradiology, CHRU de Nancy, Nancy, Lorraine, France.
BMJ Open. 2021 Mar 15;11(3):e040522. doi: 10.1136/bmjopen-2020-040522.
Mechanical thrombectomy (MT) increases functional independence in patients with acute ischaemic stroke with anterior circulation large vessel occlusion (LVO), and the probability to achieve functional independence decreases by 20% for each 1-hour delay to reperfusion. Therefore, we aim to investigate whether direct angiosuite transfer (DAT) is superior to standard imaging/emergency department-based management in achieving 90-day functional independence in patients presenting with an acute severe neurological deficit likely due to LVO and requiring emergent treatment with MT.
DIRECT ANGIO (Effect of DIRECT transfer to ANGIOsuite on functional outcome in patient with severe acute stroke treated with thrombectomy: the randomised DIRECT ANGIO Trial) trial is an investigator-initiated, multicentre, prospective, randomised, open-label, blinded endpoint (PROBE) study. Eligibility requires a patient ≤75 years, pre-stroke modified Rankin Scale (mRS) 0-2, presenting an acute severe neurological deficit and admitted within 5 hours of symptoms onset in an endovascular-capable centre. A total of 208 patients are randomly allocated in a 1:1 ratio to DAT or standard management. The primary outcome is the rate of patients achieving a functional independence, assessed as mRS 0-2 at 90 days. Secondary endpoints include patients presenting confirmed LVO, patients eligible to intravenous thrombolysis alone, patients with intracerebral haemorrhage and stroke-mimics, intrahospital time metrics, early neurological improvement (reduction in National Institutes of Health Stroke Scale by ≥8 points or reaching 0-1 at 24 hours) and mRS overall distribution at 90 days and 12 months. Safety outcomes are death and intracerebral haemorrhage transformation. Medico-economics analyses include health-related quality of life and cost utility assessment.
The DIRECT ANGIO trial was approved by the ethics committee of Ile de France 1. Study began in April 2020. Results will be published in an international peer-reviewed medical journal.
NCT03969511.
机械取栓(MT)可提高急性缺血性脑卒中伴前循环大血管闭塞(LVO)患者的功能独立性,每延迟 1 小时再灌注,实现功能独立性的概率就会降低 20%。因此,我们旨在研究直接血管内治疗(DAT)是否优于标准影像学/急诊管理,以提高因 LVO 导致急性严重神经功能缺损且需要进行 MT 紧急治疗的患者在 90 天内实现功能独立性的概率。
DIRECT ANGIO(直接转至 ANGIOsuite 对接受血栓切除术治疗的严重急性卒中患者功能结局的影响:随机 DIRECT ANGIO 试验)试验是一项由研究者发起的、多中心、前瞻性、随机、开放性标签、终点设盲(PROBE)研究。入选标准要求患者年龄≤75 岁,发病前改良Rankin 量表(mRS)评分为 0-2,在血管内治疗中心发病 5 小时内出现急性严重神经功能缺损。共 208 例患者以 1:1 的比例随机分配至 DAT 组或标准治疗组。主要结局是 90 天时达到功能独立性的患者比例,定义为 mRS 评分为 0-2。次要结局包括确诊 LVO 的患者、仅适合静脉溶栓的患者、有颅内出血和卒中样发作的患者、院内时间指标、早期神经功能改善(24 小时内 NIHSS 评分降低≥8 分或降至 0-1 分)和 90 天及 12 个月时的 mRS 总体分布。安全性结局为死亡和颅内出血转化。卫生经济学分析包括健康相关生活质量和成本效用评估。
DIRECT ANGIO 试验已获得法兰西岛 1 区伦理委员会的批准。研究于 2020 年 4 月开始。研究结果将在国际同行评议的医学期刊上发表。
NCT03969511。