Department of Neurology, General Hospital of Northern Theater Command, Shenyang, People's Republic of China.
Clin Appl Thromb Hemost. 2020 Jan-Dec;26:1076029620904131. doi: 10.1177/1076029620904131.
There is a lack of studies on anticoagulant plus antiplatelet therapy for acute ischemic stroke. The present study made a pilot effort to investigate the efficacy and safety of argatroban plus dual antiplatelet therapy (DAPT) in patients with acute posterior circulation ischemic stroke (PCIS). We retrospectively collected patients diagnosed with acute PCIS according to inclusion/exclusion criteria. According to treatment drugs, patients were divided into an argatroban plus DAPT group and a DAPT group. The primary efficacy end point was the proportion of early neurological deterioration (END). The primary safety outcome was symptomatic intracranial hemorrhage. All outcomes were compared between the 2 groups before and after propensity score matching (PSM). A total of 502 patients were enrolled in the study, including 35 patients with argatroban plus DAPT and 467 patients with DAPT. There was a higher National Institutes of Health Stroke Scale (NIHSS) score in the argatroban plus DAPT group than the DAPT group before PSM (3 vs 2, = .017). Compared with the DAPT group, the argatroban plus DAPT group had no END (before PSM: 0% vs 6.2%, = .250; after PSM: 0% vs 5.9%, = .298). Argatroban plus DAPT yielded a significant decrease in the NIHSS score from baseline to 7 days after hospitalization, compared with that of the DAPT group before PSM ( = .032), but not after PSM ( = .369). No symptomatic intracranial hemorrhage was found in any patient. A short-term combination of argatroban with DAPT appears safe in acute minor PCIS.
针对急性缺血性脑卒中的抗凝联合抗血小板治疗研究较少。本研究初步探讨了阿加曲班联合双联抗血小板治疗(DAPT)治疗急性后循环缺血性脑卒中(PCIS)的疗效和安全性。我们回顾性收集了符合纳入排除标准的急性 PCIS 患者。根据治疗药物将患者分为阿加曲班联合 DAPT 组和 DAPT 组。主要疗效终点为早期神经功能恶化(END)的比例。主要安全性结局为症状性颅内出血。所有结局均在倾向评分匹配(PSM)前后进行两组间比较。共纳入 502 例患者,其中阿加曲班联合 DAPT 组 35 例,DAPT 组 467 例。PSM 前,阿加曲班联合 DAPT 组的国立卫生研究院卒中量表(NIHSS)评分高于 DAPT 组(3 分比 2 分, =.017)。与 DAPT 组相比,阿加曲班联合 DAPT 组无 END(PSM 前:0%比 6.2%, =.250;PSM 后:0%比 5.9%, =.298)。与 DAPT 组相比,阿加曲班联合 DAPT 组 NIHSS 评分从入院时到第 7 天明显下降,PSM 前差异有统计学意义( =.032),但 PSM 后差异无统计学意义( =.369)。任何患者均未发生症状性颅内出血。急性小面积 PCIS 患者短期联合应用阿加曲班和 DAPT 似乎是安全的。