Suwanwela Nijasri C, Phanthumchinda Kammant, Likitjaroen Yuttachai
Neurological Unit, Department of Medicine, Faculty of Medicine, Chulalongkorn University, Rama IV Road, Bangkok 10330, Thailand.
Clin Neurol Neurosurg. 2006 Sep;108(6):549-52. doi: 10.1016/j.clineuro.2005.09.008. Epub 2005 Nov 9.
Intravenous thrombolytic therapy has been widely recommended as a standard treatment for acute ischemic stroke in most clinical practice guidelines. However, the experience in Asia is still limited. We report the first prospective case series of thrombolytic therapy in a developing Asian country.
Consecutive patients with acute ischemic stroke who presented within 3 h of onset were screened under stroke fast track program. Those who were eligible were treated with intravenous recombinant tissue plasminogen activator (rt-PA). General and neurological examinations together with the National Institute of Health stroke scale (NHISS) and modified Rankin scale (MRS) were recorded prior to and after the treatment at 1 h, 24 h, on discharge and at 3 months. Hemorrhagic brain lesion and death within 3 months were also recorded.
Thirty-four patients or 2.1% of patients with acute stroke received intravenous thrombolysis. The mean pretreatment NIHSS was 18.8 and the majority of patients had stroke in the middle cerebral artery territory. The mean door-to-needle time was 72.6 min (ranged 20-150 min). Major neurological improvement, defined as improving of the NIHSS >8 points or NIHSS of 0 points at 24 h, was observed in 17 patients (50%). Intracerebral hemorrhage was detected in four cases (11.8%), two of them were symptomatic (5.9%) and one was fatal.
Intravenous thrombolysis can be given in patients with acute stroke in our population. Our cases were more severe than other studies. However, half of them experienced major neurological improvement. The risk of hemorrhagic brain lesion is not much higher than previously reported.
在大多数临床实践指南中,静脉溶栓疗法已被广泛推荐为急性缺血性卒中的标准治疗方法。然而,亚洲的经验仍然有限。我们报告了在一个亚洲发展中国家进行的首例溶栓治疗前瞻性病例系列。
在卒中快速通道计划下,对发病3小时内就诊的急性缺血性卒中连续患者进行筛查。符合条件的患者接受静脉注射重组组织型纤溶酶原激活剂(rt-PA)治疗。在治疗前以及治疗后1小时、24小时、出院时和3个月时,记录患者的一般情况和神经学检查结果,同时记录美国国立卫生研究院卒中量表(NHISS)和改良Rankin量表(MRS)评分。还记录3个月内的脑内出血性病变和死亡情况。
34例急性卒中患者(占急性卒中患者的2.1%)接受了静脉溶栓治疗。治疗前NIHSS平均评分为18.8分,大多数患者的卒中发生在大脑中动脉区域。平均门到针时间为72.6分钟(范围为20 - 150分钟)。17例患者(50%)出现主要神经功能改善,定义为24小时时NIHSS评分提高>8分或NIHSS评分为0分。4例(11.8%)检测到颅内出血,其中2例有症状(5.9%),1例死亡。
在我们的人群中,急性卒中患者可以接受静脉溶栓治疗。我们的病例比其他研究中的病例病情更严重。然而,其中一半患者出现了主要神经功能改善。脑内出血性病变的风险并不比先前报道的高很多。