Eggers C C J, Bocksrucker C, Seyfang L
Department of Neurology, Hospital Barmherzige Brüder, Linz, Austria.
Department for Clinical Neuroscience and Preventive Medicine, Danube University Krems, Krems, Austria.
Eur J Neurol. 2017 Jun;24(6):780-787. doi: 10.1111/ene.13288. Epub 2017 Apr 27.
Intravenous thrombolysis (ivT) with recombinant tissue plasminogen activator is established in acute ischaemic stroke. Little is known, however, about its efficacy in different stroke subtypes.
A retrospective analysis of 128 733 patients from the Austrian Stroke Unit Registry was performed. Patients were classified as lacunar (LacS) or non-lacunar ischaemic stroke (nonLacS) by use of the clinical syndrome and technical findings. Outcome parameters were the short term improvement in the stroke unit [the difference of the National Institutes of Health Stroke Scale (NIHSS) score at admission and at discharge] and the modified Rankin Scale (mRS) score at 3 months. Patients were assigned to four groups according to thrombolysis and stroke subtype. To control for confounding, patients were matched for variables identified with impact outcome and for variables of general interest (NIHSS at admission, mRS before stroke and general risk factors).
There were four matched groups of 401 cases each. In LacS median short term improvement was 3 [interquartile range (IQR) 2-5] NIHSS points in the thrombolysed patients and 2 (IQR 1-4) in the non-thrombolysed patients (P < 0.001). In the nonLacS groups median short term improvement was 3 (IQR 1-5) in the thrombolysed and 2 (IQR 0-4) in the non-thrombolysed patients (P < 0.001). At 3-month follow-up, ivT was significantly associated with a better functional outcome in LacS (P < 0.001) and nonLacS patients (P < 0.001). Taking magnetic resonance imaging as a requirement for stroke subtyping led to similar results.
Patients with both lacunar and non-lacunar stroke benefitted from ivT. The degree of improvement was similar in both groups.
重组组织型纤溶酶原激活剂静脉溶栓(ivT)已被确立用于急性缺血性卒中。然而,对于其在不同卒中亚型中的疗效知之甚少。
对来自奥地利卒中单元登记处的128733例患者进行回顾性分析。根据临床综合征和技术检查结果,将患者分为腔隙性卒中(LacS)或非腔隙性缺血性卒中(nonLacS)。结局参数为卒中单元内的短期改善情况[入院时和出院时美国国立卫生研究院卒中量表(NIHSS)评分的差值]以及3个月时的改良Rankin量表(mRS)评分。根据溶栓治疗和卒中亚型将患者分为四组。为控制混杂因素,对影响结局的变量以及一般感兴趣的变量(入院时的NIHSS、卒中前的mRS和一般危险因素)进行患者匹配。
有四组匹配组,每组401例。在腔隙性卒中组中,溶栓患者的NIHSS短期改善中位数为3分[四分位间距(IQR)2 - 5],未溶栓患者为2分(IQR 1 - 4)(P < 0.001)。在非腔隙性缺血性卒中组中,溶栓患者的NIHSS短期改善中位数为3分(IQR 1 - 5),未溶栓患者为2分(IQR 0 - 4)(P < 0.001)。在3个月随访时,静脉溶栓与腔隙性卒中患者(P < 0.001)和非腔隙性缺血性卒中患者(P < 0.001)更好的功能结局显著相关。将磁共振成像作为卒中亚型分类的要求也得出了类似结果。
腔隙性卒中和非腔隙性卒中患者均从静脉溶栓中获益。两组的改善程度相似。