From the Department of Neurology, Beth Israel Deaconess Medical Center, and Harvard Medical School, Boston, MA.
Circ Res. 2017 Feb 3;120(3):541-558. doi: 10.1161/CIRCRESAHA.116.309278.
The treatment of acute ischemic stroke has undergone dramatic changes recently subsequent to the demonstrated efficacy of intra-arterial (IA) device-based therapy in multiple trials. The selection of patients for both intravenous and IA therapy is based on timely imaging with either computed tomography or magnetic resonance imaging, and if IA therapy is considered noninvasive, angiography with one of these modalities is necessary to document a large-vessel occlusion amenable for intervention. More advanced computed tomography and magnetic resonance imaging studies are available that can be used to identify a small ischemic core and ischemic penumbra, and this information will contribute increasingly in treatment decisions as the therapeutic time window is lengthened. Intravenous thrombolysis with tissue-type plasminogen activator remains the mainstay of acute stroke therapy within the initial 4.5 hours after stroke onset, despite the lack of Food and Drug Administration approval in the 3- to 4.5-hour time window. In patients with proximal, large-vessel occlusions, IA device-based treatment should be initiated in patients with small/moderate-sized ischemic cores who can be treated within 6 hours of stroke onset. The organization and implementation of regional stroke care systems will be needed to treat as many eligible patients as expeditiously as possible. Novel treatment paradigms can be envisioned combining neuroprotection with IA device treatment to potentially increase the number of patients who can be treated despite long transport times and to ameliorate the consequences of reperfusion injury. Acute stroke treatment has entered a golden age, and many additional advances can be anticipated.
最近,由于多项试验证明了动脉内(IA)设备治疗的有效性,急性缺血性脑卒中的治疗发生了重大变化。静脉内和 IA 治疗的患者选择均基于计算机断层扫描或磁共振成像的及时成像,如果考虑 IA 治疗为非侵入性,则需要使用这些方式之一进行血管造影,以证明存在适合介入的大血管闭塞。目前还可以使用更先进的计算机断层扫描和磁共振成像研究来识别小的缺血核心和缺血半影,随着治疗时间窗的延长,这些信息将越来越有助于治疗决策。尽管在 3 至 4.5 小时的时间窗内未获得美国食品和药物管理局的批准,但组织型纤溶酶原激活物的静脉内溶栓仍然是卒中发作后最初 4.5 小时内急性卒中治疗的主要方法。对于近端大血管闭塞的患者,如果可以在卒中发作后 6 小时内治疗小/中等大小的缺血核心患者,则应开始进行基于 IA 设备的治疗。需要组织和实施区域性卒中护理系统,以便尽快治疗尽可能多的合格患者。可以设想将神经保护与 IA 设备治疗相结合的新治疗模式,以增加可以治疗的患者数量,尽管转运时间较长,但可以减轻再灌注损伤的后果。急性脑卒中治疗已经进入了一个黄金时代,可以预期会有更多的进展。