Qureshi A I, Ali Z, Suri M F, Kim S H, Shatla A A, Ringer A J, Lopes D K, Guterman L R, Hopkins L N
Department of Neurosurgery, School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, USA.
Neurosurgery. 2001 Jul;49(1):41-8; discussion 48-50. doi: 10.1097/00006123-200107000-00006.
We prospectively evaluated the safety and recanalization efficacy of intra-arterially administered reteplase, a third-generation recombinant tissue plasminogen activator, for treating ischemic stroke in patients considered poor candidates for intravenously administered alteplase therapy.
Patients were considered poor candidates for intravenously administered therapy because of severity of neurological deficits, interval from onset of symptoms to presentation of 3 hours or more, or recent major surgery. We administered a maximum total dose of 8 U of reteplase intra-arterially in 1-U increments via superselective catheterization. Adjunctive angioplasty of the occluded artery was performed in seven patients. Angiographic evidence of perfusion and thrombus was graded by use of modified Thrombolysis in Myocardial Infarction (TIMI) criteria. Neurological examinations were performed before and 24 hours and 7 to 10 days after treatment.
Sixteen consecutive patients were treated (mean age, 64.1 +/- 16.4 yr; seven were men). Initial National Institutes of Health Stroke Scale scores ranged from 10 to 26. Time from onset of symptoms to treatment ranged from 2 to 9 hours. Occlusion sites were the cervical internal carotid artery (n = 4), intracranial internal carotid artery (n = 4), middle cerebral artery (n = 6), and vertebrobasilar artery (n = 2). Complete or near-complete perfusion (TIMI Grade 3 or 4) was achieved in the arteries in 14 patients (88%), with partial recanalization (TIMI Grade 2) or minimal response (TIMI Grade 1) in the arteries in one patient each. Neurological improvement (defined as decrease of four or more points in National Institutes of Health Stroke Scale score) was observed in 7 (44%) of the 16 patients at 24 hours. Symptomatic intracerebral hemorrhage occurred in one patient; three other patients experienced intracerebral hemorrhages that did not result in neurological worsening. The overall mortality during hospitalization was 56%, related to massive ischemic stroke (n = 7), withdrawal of care at the family's request after the development of aspiration pneumonia and renal failure (n = 1), and a combination of intracerebral hemorrhage and massive ischemic stroke (n = 1).
In this study, intra-arterially administered reteplase in doses up to 8 U with or without angioplasty resulted in a high rate of recanalization. This strategy should be considered in treating patients considered poor candidates for intravenous thrombolysis.
我们前瞻性评估了动脉内给予第三代重组组织型纤溶酶原激活剂瑞替普酶治疗静脉注射阿替普酶治疗效果不佳的缺血性脑卒中患者的安全性和再通疗效。
由于神经功能缺损严重、症状发作至就诊间隔3小时或更长时间或近期接受过大手术,这些患者被认为不适合静脉注射治疗。我们通过超选择性导管插入术以1U递增的方式动脉内给予瑞替普酶,最大总剂量为8U。7例患者对闭塞动脉进行了辅助血管成形术。使用改良的心肌梗死溶栓(TIMI)标准对灌注和血栓的血管造影证据进行分级。在治疗前、治疗后24小时以及7至10天进行神经学检查。
连续治疗16例患者(平均年龄64.1±16.4岁;7例为男性)。初始美国国立卫生研究院卒中量表评分范围为10至26分。症状发作至治疗的时间范围为2至9小时。闭塞部位为颈内动脉(n = 4)、颅内段颈内动脉(n = 4)、大脑中动脉(n = 6)和椎基底动脉(n = 2)。14例患者(88%)的动脉实现了完全或近乎完全灌注(TIMI 3级或4级),1例患者动脉部分再通(TIMI 2级),1例患者动脉反应极小(TIMI 1级)。16例患者中有7例(44%)在24小时时神经功能改善(定义为美国国立卫生研究院卒中量表评分降低4分或更多)。1例患者发生症状性脑出血;另外3例患者发生脑出血,但未导致神经功能恶化。住院期间的总死亡率为56%,原因包括大面积缺血性脑卒中(n = 7)、在发生吸入性肺炎和肾衰竭后家属要求停止治疗(n = 1)以及脑出血和大面积缺血性脑卒中合并(n = 1)。
在本研究中,动脉内给予剂量高达8U的瑞替普酶,无论是否进行血管成形术,再通率都很高。对于被认为不适合静脉溶栓的患者,应考虑采用这种策略进行治疗。