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Endovascular Treatment in Patients with Persistent Internal Carotid Artery Occlusion after Intravenous Tissue Plasminogen Activator: A Clinical Effectiveness Study

机译:静脉内组织纤溶酶原激活物持续存在颈内动脉闭塞的患者的血管内治疗:临床疗效研究

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Background: There has been no large-scale trial comparing endovascular treatment (add-on EVT) after intravenous tissue plasminogen activator (IV tPA) and IV tPA alone in acute ischemic stroke (AIS) caused by internal carotid artery occlusion (ICAO). We aimed at investigating the effectiveness and safety of add-on EVT after IV tPA in AIS patients with ICAO. Methods: Between March 2010 and March 2013, 3,689 consecutive ischemic stroke patients who were hospitalized within 4.5 h of onset were identified using a prospective stroke registry at 11 centers in Korea. Among them, patients with persistent ICAO after receiving IV tPA and whose 3-month modified Rankin Scale (mRS) was available were finally enrolled. A propensity score analysis with inverse-probability of treatment weighting was used to eliminate baseline imbalances between those receiving add-on EVT and IV tPA alone. Results: Among 264 patients enrolled in this study (mean age 71.4; male 56.4%; median National Institute of Health Stroke Scale score 15), 117 (44.3%) received add-on EVT. The add-on EVT group had a higher frequency of favorable outcome on the mRS <= 2 (35.0 vs. 18.4%; adjusted OR (aOR) 2.79; 95% CI 1.66-4.67) and lower mortality (17.9 vs. 35.4%; aOR 0.24; 95% CI 0.13-0.42) at 3 months, when compared to the IV tPA-alone group. Add-on EVT did not significantly increase the risk of symptomatic hemorrhage (5.1 vs. 4.1%; aOR 1.01; 95% CI 0.37-2.70). The rate of successful recanalization (thrombolysis in cerebral infarction grade >= 2b) in the add-on EVT group was 69.2%. Conclusions: Compared to an IV tPA alone, add-on EVT can improve clinical outcomes in patients with symptomatic ICAO within 4.5 h of onset without a significant increase of symptomatic hemorrhage. (C) 2016 S. Karger AG, Basel
机译:背景:尚无大规模试验比较静脉内组织纤溶酶原激活物(IV tPA)和单独的IV tPA在颈内动脉闭塞(ICAO)引起的急性缺血性卒中(AIS)中的血管内治疗(附加EVT)。我们旨在研究IV tPA后IVA后加用EVT对ICAO AIS患者的有效性和安全性。方法:从2010年3月至2013年3月,在韩国11个中心使用前瞻性卒中登记系统对3,689例在发病4.5 h内住院的连续缺血性卒中患者进行了鉴定。其中,最终接受了接受静脉内tPA治疗后持续存在ICAO并可获得3个月改良Rankin量表(mRS)的患者。使用倾向评分分析和治疗权重的反概率来消除仅接受附加EVT和IV tPA者之间的基线失衡。结果:参加本研究的264例患者(平均年龄71.4;男性56.4%;美国国立卫生研究院卒中量表评分中位数15),其中117例(44.3%)接受了附加EVT。附加的EVT组在mRS <= 2时有较高的有利结果发生率(35.0 vs. 18.4%; OR(aOR)2.79; 95%CI 1.66-4.67)和较低的死亡率(17.9 vs. 35.4%;与单独使用IV tPA的组相比,在3个月时的aOR为0.24; 95%CI为0.13-0.42)。附加的EVT并没有显着增加症状性出血的风险(5.1比4.1%; aOR 1.01; 95%CI 0.37-2.70)。附加EVT组成功再通的成功率(脑梗死级别≥2b的溶栓)为69.2%。结论:与单独使用IV tPA相比,附加的EVT可以改善症状性ICAO患者在发病后4.5小时内的临床结局,而不会明显增加症状性出血。 (C)2016 S.Karger AG,巴塞尔

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