Department of Neurology, University of California San Francisco, San Francisco, CA 94143-0114, USA.
Stroke. 2012 Feb;43(2):412-6. doi: 10.1161/STROKEAHA.111.634147. Epub 2011 Dec 8.
Unruptured cerebral aneurysms are currently considered a contraindication to intravenous tissue-type plasminogen activator for acute ischemic stroke. This is due to a theoretical increase in the risk of hemorrhage from aneurysm rupture, although it is unknown whether this risk is a significant one. We sought to determine the safety of intravenous tissue-type plasminogen activator administration in a cohort of patients with pre-existing aneurysms.
We reviewed the medical records of patients treated for acute ischemic stroke with intravenous tissue-type plasminogen activator during an 11-year period at 2 academic medical centers. We identified a subset of patients with unruptured cerebral aneurysms present on prethrombolysis vascular imaging. Our outcomes of interest were any intracranial hemorrhage, symptomatic intracranial hemorrhage, and subarachnoid hemorrhage. Fisher exact test was used to compare the rates of hemorrhage among patients with and without aneurysms.
We identified 236 eligible patients, of whom 22 had unruptured cerebral aneurysms. The rate of intracranial hemorrhage among patients with aneurysms (14%; 95% CI, 3%-35%) did not significantly differ from the rate among patients without aneurysms (19%; 95% CI, 14%-25%). None of the patients with aneurysms developed symptomatic intracranial hemorrhage (0%; 95% CI, 0%-15%) compared with 10 of 214 patients without aneurysms (5%; 95% CI, 2%-8%). Similar proportions of patients developed subarachnoid hemorrhage (5%; 95% CI, 0%-23% versus 6%; 95% CI, 3%-10%).
Our findings suggest that intravenous tissue-type plasminogen activator for acute ischemic stroke is safe to administer in patients with pre-existing cerebral aneurysms because the risk of aneurysm rupture and symptomatic intracranial hemorrhage is low.
目前,未破裂的脑动脉瘤被认为是急性缺血性脑卒中静脉组织型纤溶酶原激活物治疗的禁忌证。这是由于理论上动脉瘤破裂导致出血的风险增加,尽管尚不清楚这种风险是否显著。我们旨在确定在存在预先存在的动脉瘤的患者队列中使用静脉内组织型纤溶酶原激活物的安全性。
我们回顾了在 2 个学术医疗中心的 11 年期间接受急性缺血性脑卒中静脉内组织型纤溶酶原激活物治疗的患者的病历。我们确定了一组在溶栓前血管成像上存在未破裂脑动脉瘤的患者亚组。我们感兴趣的结局是任何颅内出血、症状性颅内出血和蛛网膜下腔出血。Fisher 确切检验用于比较有和无动脉瘤患者的出血率。
我们确定了 236 名符合条件的患者,其中 22 名患者有未破裂的脑动脉瘤。有动脉瘤的患者颅内出血率(14%;95%CI,3%-35%)与无动脉瘤的患者无显著差异(19%;95%CI,14%-25%)。有动脉瘤的患者无一例发生症状性颅内出血(0%;95%CI,0%-15%),而 214 名无动脉瘤的患者中有 10 例(5%;95%CI,2%-8%)。蛛网膜下腔出血的患者比例相似(5%;95%CI,0%-23%与 6%;95%CI,3%-10%)。
我们的发现表明,急性缺血性脑卒中静脉组织型纤溶酶原激活物对存在预先存在的脑动脉瘤的患者是安全的,因为动脉瘤破裂和症状性颅内出血的风险较低。