Hu Yaozhi, Zheng Haifei, Chen Xiaohui, Gao Zongen
Department of Neurology, Shengli Oilfield Central Hospital, Dongying, Shandong 257000, P.R. China.
Department of International Special Needs Medicine, Shengli Oilfield Central Hospital, Dongying, Shandong 257000, P.R. China.
Med Int (Lond). 2022 Mar 1;2(2):8. doi: 10.3892/mi.2022.33. eCollection 2022 Mar-Apr.
At present, recombinant tissue-type plasminogen activator (rt-PA) thrombolytic therapy is widely used in patients with acute ischemic stroke within 4.5 h following stroke onset. However, the efficacy of intravenous alteplase thrombolytic therapy for posterior circulation stroke (PCS) has been rarely described. The present study aimed to predict the outcome of patients with PCS following rt-PA thrombolytic therapy in a more efficient manner. Data were collected from patients who had suffered from posterior circulation ischemic stroke, who had been treated with rt-PA over a period of 4 years (2016-2020), and had been treated at a stroke center. All patients were treated with alteplase at a standard dose of 0.9 mg/kg. According to the onset to needle time (ONT), these patients were divided into the 0-3 and 3-4.5 h groups, and the National Institutes of Health Stroke Scale (NIHSS) score was compared before thrombolysis and at 24 h after thrombolysis. Subsequently, the patients with acute PCS whose ONT was ≤3 h were divided into the NIHSS score >3 points and NIHSS score ≤3 points groups, and the NIHSS score improvement rate was compared 24 h later. A total of 989 patients were included in the study; there were 783 patients with acute anterior circulation stroke (ACS) and 203 patients with acute PCS (of note, 2 patients had negative results from brain magnetic resonance imaging); 63 patients were treated with urokinase (UK) thrombolysis and 140 patients were treated with alteplase intravenous thrombolysis. The 140 patients that received alteplase thrombolytic therapy were divided into two groups, namely the ≤3 h group and 3-4.5 h group, which, on the basis of the ONT, no significant differences were found between the two the groups according to the NIHSS score before thrombolysis (P>0.05). The NHISS scores in the ≤3 h group were significantly lower than those in the 3-4.5 h group following thrombolysis therapy, and the differences between the two groups were statistically significant (P<0.05); the patients with acute PCS treated with rt-PA in the ≤3 h group were divided into the NIHSS score ≤3 points group and the NIHSS score >3 points group. In this ≤3 h group, the average NIHSS score improvement rate following rt-PA thrombolysis was 0.535 (53.5%) in the NIHSS score ≤3 points group and that in the NIHSS score >3 points group was 0.336 (33.6%); the difference between the two groups was statistically significant (P<0.05). The patients treated with intravenous alteplase thrombolysis within 3 h following stroke onset benefited more than those treated with thrombolysis therapy within 3 to 4.5 h after stroke onset. On the whole, the present study demonstrates that the patients with mild stroke (NIHSS score ≤3 points) who were treated at an earlier stage (received alteplase thrombolysis therapy within 3 h after stroke onset) benefited to a greater extent from the therapy.
目前,重组组织型纤溶酶原激活剂(rt-PA)溶栓治疗广泛应用于卒中发作后4.5小时内的急性缺血性卒中患者。然而,静脉注射阿替普酶溶栓治疗后循环卒中(PCS)的疗效鲜有描述。本研究旨在更有效地预测rt-PA溶栓治疗后PCS患者的预后。收集了4年间(2016 - 2020年)在卒中中心接受rt-PA治疗的后循环缺血性卒中患者的数据。所有患者均接受标准剂量0.9mg/kg的阿替普酶治疗。根据从发病到穿刺时间(ONT),将这些患者分为0 - 3小时组和3 - 4.5小时组,并比较溶栓前和溶栓后24小时的美国国立卫生研究院卒中量表(NIHSS)评分。随后,将ONT≤3小时的急性PCS患者分为NIHSS评分>3分和NIHSS评分≤3分两组,并比较24小时后的NIHSS评分改善率。本研究共纳入989例患者;其中急性前循环卒中(ACS)患者783例,急性PCS患者203例(值得注意的是,2例患者脑磁共振成像结果为阴性);63例患者接受尿激酶(UK)溶栓治疗,140例患者接受阿替普酶静脉溶栓治疗。接受阿替普酶溶栓治疗的140例患者分为两组,即≤3小时组和3 - 4.5小时组,基于ONT,两组溶栓前NIHSS评分差异无统计学意义(P>0.05)。溶栓治疗后,≤3小时组的NHISS评分显著低于3 - 4.5小时组,两组差异有统计学意义(P<0.05);将≤3小时组接受rt-PA治疗的急性PCS患者分为NIHSS评分≤3分和NIHSS评分>3分两组。在该≤3小时组中,rt-PA溶栓后NIHSS评分≤3分的组平均NIHSS评分改善率为0.535(53.5%),NIHSS评分>3分的组为0.336(33.6%);两组差异有统计学意义(P<0.05)。卒中发作后3小时内接受静脉阿替普酶溶栓治疗的患者比卒中发作后3至4.5小时接受溶栓治疗的患者获益更多。总体而言,本研究表明,早期(卒中发作后3小时内接受阿替普酶溶栓治疗)治疗的轻度卒中(NIHSS评分≤3分)患者从该治疗中获益更大。