Department of Diagnostic and Interventional Neuroradiology, INSERM U 947, University of Lorraine and University Hospital of Nancy, Nancy, France.
Department of Neurology, University of Lorraine and University Hospital of Nancy, Nancy, France.
Lancet Neurol. 2016 Oct;15(11):1138-47. doi: 10.1016/S1474-4422(16)30177-6. Epub 2016 Aug 23.
Intravenous thrombolysis with alteplase alone cannot reperfuse most large-artery strokes. We aimed to determine whether mechanical thrombectomy in addition to intravenous thrombolysis improves clinical outcome in patients with acute ischaemic stroke.
THRACE is a randomised controlled trial done in 26 centres in France. Patients aged 18-80 years with acute ischaemic stroke and proximal cerebral artery occlusion were randomly assigned to receive either intravenous thrombolysis alone (IVT group) or intravenous thrombolysis plus mechanical thrombectomy (IVTMT group). Intravenous thrombolysis (alteplase 0·9 mg/kg [maximum 90 mg], with an initial bolus of 10% of the total dose followed by infusion of the remaining dose over 60 min) had to be started within 4 h and thrombectomy within 5 h of symptom onset. Occlusions had to be confirmed by CT or magnetic resonance angiography. Randomisation was done centrally with a computer-generated sequential minimisation method and was stratified by centre. The primary outcome was the proportion of patients achieving functional independence at 3 months, defined by a score of 0-2 on the modified Rankin scale, assessed in the modified intention-to-treat population (ie, patients lost to follow-up and those with missing data were excluded). Safety outcomes were analysed in the per-protocol population (ie, all patients who did not follow the protocol of their randomisation group precisely were excluded from the analysis). THRACE is registered with ClinicalTrials.gov, NCT01062698.
Between June 1, 2010, and Feb 22, 2015, 414 patients were randomly assigned to the IVT group (n=208) or the IVTMT group (n=204). Four patients (two in each group) lost to follow-up and six (four in the IVT group and two in the IVTMT group) with missing data were excluded. 85 (42%) of 202 patients in the IVT group and 106 (53%) of 200 patients in the IVTMT group achieved functional independence at 3 months (odds ratio 1·55, 95% CI 1·05-2·30; p=0·028). The two groups had no significant differences in mortality at 3 months (24 [12%] deaths of 202 patients vs 27 [13%] of 206; p=0·70) or symptomatic intracranial haemorrhage at 24 h (four [2%] of 185 vs three [2%] of 192; p=0·71). Common adverse events related to thrombectomy were vasospasm (33 [23%] patients) and embolisation in a new territory (nine [6%]).
Mechanical thrombectomy combined with standard intravenous thrombolysis improves functional independence in patients with acute cerebral ischaemia, with no evidence of increased mortality. Bridging therapy should be considered for patients with large-vessel occlusions of the anterior circulation.
French Ministry for Health.
单独使用阿替普酶静脉溶栓治疗不能使大多数大动脉闭塞性卒中再通。我们旨在确定急性缺血性卒中患者接受机械取栓术联合静脉溶栓治疗是否能改善临床结局。
THRACE 是一项在法国 26 家中心进行的随机对照试验。纳入年龄 18-80 岁、急性缺血性卒中且大脑前动脉近端闭塞的患者,随机分为静脉溶栓组(IVT 组)或静脉溶栓联合机械取栓组(IVTMT 组)。静脉溶栓(阿替普酶 0.9mg/kg[最大 90mg],总剂量的 10%作为初始推注剂量,剩余剂量在 60min 内输注)必须在症状发作后 4h 内开始,取栓必须在症状发作后 5h 内进行。闭塞必须通过 CT 或磁共振血管造影确认。采用中央计算机生成的序贯最小化方法进行随机分组,按中心分层。主要结局是改良后的 Rankin 量表评分 0-2 分的功能性独立患者比例,采用改良意向治疗人群进行评估(即失访和缺失数据的患者被排除)。安全性结局在方案人群中进行分析(即未严格遵循随机分组方案的所有患者均被排除在分析之外)。THRACE 在 ClinicalTrials.gov 上注册,编号为 NCT01062698。
2010 年 6 月 1 日至 2015 年 2 月 22 日,414 例患者被随机分为 IVT 组(n=208)或 IVTMT 组(n=204)。4 例(每组各 2 例)失访,6 例(IVT 组 4 例,IVTMT 组 2 例)缺失数据被排除。202 例 IVT 组患者中有 85 例(42%)和 200 例 IVTMT 组患者中有 106 例(53%)在 3 个月时达到功能独立性(比值比 1.55,95%CI 1.05-2.30;p=0.028)。两组 3 个月时死亡率(202 例患者中 24 例[12%]死亡 vs 206 例患者中 27 例[13%];p=0.70)或 24 小时内症状性颅内出血(185 例患者中 4 例[2%] vs 192 例患者中 3 例[2%];p=0.71)无显著差异。与取栓术相关的常见不良事件有血管痉挛(33 例[23%])和新部位栓塞(9 例[6%])。
机械取栓术联合标准静脉溶栓治疗可改善急性脑缺血患者的功能独立性,且无死亡增加的证据。对于前循环大血管闭塞的患者,应考虑桥接治疗。
法国卫生部。