Department of Neurology, General Hospital of Northern Theater Command, Shenyang, P.R. China.
Brain Behav. 2022 Jul;12(7):e2664. doi: 10.1002/brb3.2664. Epub 2022 Jun 8.
Previous studies suggest the benefit of dual antiplatelet therapy (DAPT) for acute ischemic stroke with large artery atherosclerosis (LAA) etiology, but there is no study about the effect of DAPT plus anticoagulant in this population.
A prospective single arm trial was performed to determine the effect of DAPT combined with argatroban on acute mild to moderate ischemic stroke patients with LAA, which was compared with historical populations. The main outcome was the proportion of early neurological deterioration (END). The secondary outcomes included scores of 0 to 1 and 0 to 2 on the modified Rankin Scale (mRS) at 90 days, and changes in National Institutes of Health Stroke Scale (NIHSS) from baseline to day 7 after admission. The safety outcomes included intracranial hemorrhage at 7 days, organ hemorrhage, and all-cause mortality at 90 days.
A total of 120 patients with argatroban plus DAPT were prospectively enrolled and 529 patients with only DAPT were retrospectively collected. There was no significant difference in baseline characteristics between groups. Compared with control group, combined treatment group had lower proportion of END (4.2% vs. 10.0%, adjusted p = .046), more reduction in NIHSS score from the baseline to day 7 after admission (1.06 ± 2.03 vs. 0.39 ± 1.97, adjusted p = .003), and higher proportion of mRS (0-2) at 90 days (87.5% vs. 79.2%, adjusted p = .048). No intracranial hemorrhage was found between groups.
This is the first report that short-term argatroban combined with DAPT seems to be safe and may effectively prevent END and improve neurological prognosis for acute mild to moderate ischemic stroke patients with LAA; however, interpretation of the conclusion required caution due to nonrandomized controlled trial with medium sample size.
先前的研究表明,对于大动脉粥样硬化(LAA)病因引起的急性缺血性脑卒中患者,双联抗血小板治疗(DAPT)有益,但针对该人群中 DAPT 联合抗凝的效果尚无研究。
一项前瞻性单臂试验旨在确定 DAPT 联合阿加曲班治疗 LAA 所致急性轻中度缺血性脑卒中患者的效果,并与历史人群进行比较。主要结局为早期神经功能恶化(END)的比例。次要结局包括 90 天时改良Rankin 量表(mRS)评分 0-1 和 0-2 的比例,以及入院后第 7 天的国立卫生研究院卒中量表(NIHSS)评分变化。安全性结局包括 7 天内颅内出血、器官出血和 90 天内全因死亡率。
共前瞻性纳入 120 例接受阿加曲班联合 DAPT 的患者,回顾性收集 529 例仅接受 DAPT 的患者。两组间基线特征无显著差异。与对照组相比,联合治疗组 END 比例较低(4.2% vs. 10.0%,调整后 p =.046),入院后第 7 天 NIHSS 评分降低更明显(1.06 ± 2.03 vs. 0.39 ± 1.97,调整后 p =.003),90 天时 mRS(0-2)评分比例更高(87.5% vs. 79.2%,调整后 p =.048)。两组间均未发生颅内出血。
这是首个报告表明,短期阿加曲班联合 DAPT 似乎安全,可有效预防 END,并改善 LAA 所致急性轻中度缺血性脑卒中患者的神经预后;但由于该试验为非随机对照、样本量中等,解释结论时需谨慎。