Toyota S, Sugiura S, Iwaisako K
Center for Endovascular Neurosurgery, Osaka Neurological Institute, Osaka, Japan.
Interv Neuroradiol. 2011 Mar;17(1):115-22. doi: 10.1177/159101991101700118. Epub 2011 Apr 29.
We investigated the efficacy and safety of combined intravenous (IV) recombinant tissue plasminogen activator (rtPA) and simultaneous endovascular therapy (ET) for hyperacute middle cerebral artery (MCA) M1 occlusion. Between October 2005 and April 2007, in the combined group, 22 patients eligible for IV rtPA, who were diagnosed as having MCA M1 occlusion, were treated with IV rtPA and simultaneous ET was initiated as soon as possible. The other patients were treated with IV rtPA alone (IV group A: n = 11). Between May 2007 and November 2008, all patients eligible for IV rtPA, who were diagnosed as having MCA M1 occlusion, underwent thrombolysis by IV rtPA alone (IV group B: n = 24). The improvement of the National Institutes of Health Stroke Scale score at 24 hours was highest in the combined group (10 ± 4.1). In contrast, it was 5.1 ± 4.7 in the IV group A (P = 0.017) and 5.6 ± 5.6 in IV group B (P = 0.006). In the combined group, successful recanalization was observed in 18 of 22 patients with one symptomatic intracranial hemorrhage. The rate of mRS0-2 at three months was highest in the combined group, 36% in the IV group A and 33% in the IV group B (P = 0.008).Simultaneous treatment with IV rtPA and ET improved the clinical outcome of MCA M1 occlusion without a significant increase of adverse effects in our study.
我们研究了静脉注射重组组织型纤溶酶原激活剂(rtPA)联合同期血管内治疗(ET)用于超急性期大脑中动脉(MCA)M1段闭塞的疗效和安全性。2005年10月至2007年4月期间,在联合治疗组中,22例符合静脉注射rtPA标准、被诊断为MCA M1段闭塞的患者接受了静脉注射rtPA治疗,并尽快启动同期ET。其他患者仅接受静脉注射rtPA治疗(静脉注射A组:n = 11)。2007年5月至2008年11月期间,所有符合静脉注射rtPA标准、被诊断为MCA M1段闭塞的患者均仅接受静脉注射rtPA溶栓治疗(静脉注射B组:n = 24)。联合治疗组在24小时时美国国立卫生研究院卒中量表评分的改善最为显著(10±4.1)。相比之下,静脉注射A组为5.1±4.7(P = 0.017),静脉注射B组为5.6±5.6(P = 0.006)。联合治疗组中,22例患者中有18例实现成功再通,发生1例有症状性颅内出血。联合治疗组在3个月时改良Rankin量表评分为0 - 2分的比例最高,静脉注射A组为36%,静脉注射B组为33%(P = 0.008)。在我们的研究中,静脉注射rtPA与ET联合治疗改善了MCA M1段闭塞的临床结局,且未显著增加不良反应。