Gur Alexander Y, Shopin Ludmila, Bornstein Natan M
Stroke Unit, Department of Neurology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Isr Med Assoc J. 2009 Dec;11(12):714-6, 718.
Intravenous tissue plasminogen activator has been approved treatment for acute (< or = 3 hours) ischemic stroke in Israel since late 2004. The Israeli experience with IV tPA is still limited. Several factors may influence the response to IV thrombolysis, including time-to-treatment parameters and tandem internal carotid artery/middle cerebral artery stenosis/occlusion.
To compare our experience with IV tPA treatment of patients with acute ischemic stroke to the findings of the SITS-MOST (Safe Implementation of Thrombolysis in Stroke-MOnitoring STudy, international data) and of the Sheba Medical Center (national data) and to compare the early outcome among patients with ischemic stroke in the MCA with and without severe ICA stenosis.
We obtained demographic data, timing details, stroke severity, hemorrhagic complications, mortality, and early outcome from the records of IV tPA-treated acute ischemic stroke patients.
Fifty-eight patients (median age 69 years, 26 females) with acute ischemic stroke were treated by IV tPA at the Tel Aviv Sourasky Medical Center in 2006-2007. Median time between stroke onset and IV tPA administration was 148 minutes for the Sourasky center, 150 minutes for the Sheba center, and 140 minutes for SITS-MOST. The Sourasky mortality rate was 10.5%. Of the 31 patients who suffered MCA stroke, 8 had severe ipsilateral ICA stenosis. These 8 had significantly lower neurological improvement than the 23 without ipsilateral ICA stenosis (1/8 versus 15/23, P < 0.001).
Our data demonstrate fairly similar parameters of IV tPA treatment compared to other centers and suggest that patients with severe ICA stenosis might be less likely to benefit from IV tPA.
自2004年末起,静脉注射组织型纤溶酶原激活剂在以色列已被批准用于治疗急性(小于或等于3小时)缺血性中风。以色列在静脉注射组织型纤溶酶原激活剂方面的经验仍然有限。几个因素可能会影响对静脉溶栓的反应,包括治疗时间参数以及串联性颈内动脉/大脑中动脉狭窄/闭塞。
将我们使用静脉注射组织型纤溶酶原激活剂治疗急性缺血性中风患者的经验与SITS-MOST(中风溶栓安全实施监测研究,国际数据)以及舍巴医疗中心(国家数据)的研究结果进行比较,并比较大脑中动脉缺血性中风患者中伴有和不伴有严重颈内动脉狭窄患者的早期预后。
我们从接受静脉注射组织型纤溶酶原激活剂治疗的急性缺血性中风患者的记录中获取了人口统计学数据、时间细节、中风严重程度、出血并发症、死亡率以及早期预后情况。
2006 - 2007年,特拉维夫索拉斯基医疗中心有58例急性缺血性中风患者接受了静脉注射组织型纤溶酶原激活剂治疗(中位年龄69岁,26名女性)。索拉斯基中心中风发作至静脉注射组织型纤溶酶原激活剂给药的中位时间为148分钟,舍巴中心为150分钟,SITS-MOST为140分钟。索拉斯基中心的死亡率为10.5%。在31例大脑中动脉中风患者中,8例有同侧严重颈内动脉狭窄。这8例患者的神经功能改善明显低于23例无同侧颈内动脉狭窄的患者(1/8对15/23,P < 0.001)。
我们的数据表明,与其他中心相比,静脉注射组织型纤溶酶原激活剂治疗的参数相当相似,并提示严重颈内动脉狭窄患者可能不太可能从静脉注射组织型纤溶酶原激活剂中获益。