神经血管急症:影像诊断与神经介入治疗

W. T. Rahman, J. Griauzde, Suzanne T. Chong
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引用次数: 0

摘要

急性缺血性中风急性缺血性中风占急性神经血管紧急情况的大多数,每年约有795000例新发或复发性中风。据估计,有660万20岁以上的美国人中风。在美国,每40秒就会发生一次中风,而与中风相关的死亡则每4分钟发生一次。中风的一线影像学检查是头部CT平扫,以排除脑肿块或颅内出血,并识别缺血的早期迹象。这些缺血性中风的早期CT征象包括豆状核和岛叶皮层的低衰减、灰白色分化丧失、脑沟消失和代表动脉内血栓的致密血管(图1)。CT或MR血管造影术可以识别动脉闭塞。可以进行CT灌注,以区分有缺血风险的梗死和存活的脑组织,这可能受益于早期干预。在MRI上,早期超急性缺血(定义为动脉闭塞后0至6小时内发生)显示扩散受限。流体衰减反转恢复(FLAIR)信号在这一时期可以是可变的。晚期超急性卒中发生在动脉闭塞后6至24小时内,也会限制扩散;然而,通常在16小时后出现高FLAIR信号和T1低强度。症状出现后24小时至1周出现的急性卒中将表现为扩散受限、FLAIR高信号、低T1信号和高T2信号。随着中风从急性发展到慢性,限制性扩散的强度减弱,动脉增强可以在任何时间点发生。中风治疗的主要方法是静脉注射重组组织型纤溶酶原激活剂(tPA),应在血管内治疗前和症状出现后4.5小时内给予,以改善疗效。任何中风治疗前应进行未强化CT检查,以排除急性颅内出血或脑肿瘤的禁忌症。如果患者符合特定标准,则有资格使用支架回收装置接受血管内治疗(表1)。艾伯塔省卒中项目早期CT评分(ASPECTS)可能影响tPA治疗的资格,tPA治疗量化了大脑中动脉(MCA)的缺血性变化
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Neurovascular Emergencies: Imaging Diagnosis and Neurointerventional Therapy
Acute Ischemic Stroke Acute ischemic stroke accounts for the majority of acute neurovascular emergencies, with approximately 795,000 cases of new or recurrent stroke occurring annually. An estimated 6.6 million Americans over the age of 20 have had a stroke. In the United States, a stroke occurs every 40 seconds while a stroke-related death occurs every 4 minutes. The first-line imaging examination for stroke is unenhanced head CT to exclude a brain mass or intracranial hemorrhage and to identify early signs of ischemia. These early signs of ischemic stroke on CT include hypoattenuation of the lentiform nuclei and insular cortex, loss of graywhite differentiation, sulcal effacement, and dense vessels representing intra-arterial thrombus (Figure 1). CT or MR angiography can identify arterial occlusion. CT perfusion may be performed to differentiate infarcted from viable brain tissue at risk of ischemia that may benefit from early intervention. On MRI, early hyperacute ischemia, defined as occurring within 0 to 6 hours of arterial occlusion, demonstrates restricted diffusion. Fluid-attenuated inversion recovery (FLAIR) signal can be variable in this period. Late hyperacute stroke, occurring within 6 to 24 hours of arterial occlusion, also will restrict diffusion; however, there is usually high FLAIR signal and T1 hypointensity after 16 hours. Acute stroke presenting from 24 hours to 1 week after symptom onset will demonstrate restricted diffusion, FLAIR hyperintensity, low T1 signal, and high T2 signal. The intensity of restricted diffusion diminishes as the stroke evolves from acute to chronic, and arterial enhancement can occur at any time point. The mainstay of stroke therapy is IV recombinant tissuetype plasminogen activator (tPA), which should be administered before endovascular treatment and within 4.5 hours of symptom onset to improve outcome. Unenhanced CT should be performed before any stroke treatment to exclude the contraindications of acute intracranial hemorrhage or brain tumor. Patients are eligible to receive endovascular therapy with a stent retriever device if they meet specific criteria (Table 1). The Alberta Stroke Program Early CT Score (ASPECTS) may affect eligibility for tPA therapy, which quantifies ischemic changes in the middle cerebral artery (MCA)
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