Keris V, Rudnicka S, Vorona V, Enina G, Tilgale B, Fricbergs J
Department of Neurosurgery, Medical Academy of Latvia, Clinical Hospital Gailezers, Riga.
AJNR Am J Neuroradiol. 2001 Feb;22(2):352-8.
The intravenous use of recombinant tissue-type plasminogen activator (rTPA) in acute ischemic stroke has been investigated in three large trials. Limited series have reflected outcome after local intraarterial thrombolysis (LIT) in the cerebral territory. The purpose of this study was to evaluate the safety and efficacy of combined intraarterial/intravenous thrombolysis using rTPA (actilyse) for acute ischemic stroke.
Forty-five patients with acute onset of severe hemispheric stroke and without signs of major cerebral infarction on early CT scans were randomized by order of admission. Twelve patients were treated with 50 mg actilyse (maximal dose, 0.7 mg/kg); three had occlusion of the internal carotid artery and nine had occlusion of the middle cerebral artery. Thrombolysis was started by LIT and continued intravenously within 6 hours of stroke onset. Outcome, assessed after 1 and 12 months according to the modified Rankin scale (MRS), was considered good (MRS score, 0-3) for patients who were functionally independent and poor (MRS score, 4-5) for those who were dependent or had died.
In the thrombolysis group, outcome was good in eight patients at 1 month and in 10 patients at 12 months; in the control group, outcome was good in seven (21%) and 11 (33%) patients, respectively. Of the eight patients with a good outcome after thrombolysis, four had complete and one had partial recanalization. In the control group, the rate of intracerebral hemorrhage was 6%. Mortality at 1 month in the thrombolysis and control groups was 17% and 48%, respectively.
Combined intraarterial/intravenous thrombolysis with low-dose rTPA may be a safe and effective treatment for acute ischemic stroke within 6 hours in carefully selected patients.
三项大型试验对重组组织型纤溶酶原激活剂(rTPA)在急性缺血性卒中的静脉应用进行了研究。有限的系列研究反映了脑区局部动脉内溶栓(LIT)后的结局。本研究的目的是评估使用rTPA(阿替普酶)进行动脉内/静脉联合溶栓治疗急性缺血性卒中的安全性和有效性。
45例急性重度半球性卒中起病且早期CT扫描无大面积脑梗死征象的患者按入院顺序随机分组。12例患者接受50mg阿替普酶治疗(最大剂量0.7mg/kg);其中3例为颈内动脉闭塞,9例为大脑中动脉闭塞。溶栓从动脉内溶栓开始,并在卒中发作6小时内持续静脉溶栓。根据改良Rankin量表(MRS)在1个月和12个月后评估结局,功能独立的患者结局为良好(MRS评分0 - 3),依赖或死亡的患者结局为不良(MRS评分4 - 5)。
溶栓组1个月时8例患者结局良好,12个月时10例患者结局良好;对照组分别有7例(21%)和11例(33%)患者结局良好。溶栓后结局良好的8例患者中,4例实现完全再通,1例实现部分再通。对照组颅内出血发生率为6%。溶栓组和对照组1个月时的死亡率分别为17%和48%。
对于精心挑选的患者,低剂量rTPA动脉内/静脉联合溶栓可能是急性缺血性卒中6小时内安全有效的治疗方法。