Jing Hang, Yi-Jia Guo, -Bai-Li Song, Ya-Peng Lin, Yu-Qiao Zhang, Cong Geng, -Li Hao Jun, -Jun Zou Jian, Jie Yang
Pharmazie. 2020 Jan 2;75(1):23-26. doi: 10.1691/ph.2020.9826.
Early administration of antiplatelet agents in acute ischemic stroke patients (AIS) receiving intravenous thrombolysis (IVT) is a potential therapeutic strategy, however, safety and efficacy are not well established. We hypothesize that antiplatelet pretreatment (AP) before IVT have a similarly role as initiation of AP within the first 24 hours following IVT. We aimed to explore the effect of AP on platelet aggregation and clinical outcomes in thrombolysis-treated AIS patients. We enrolled AIS patients treated with IVT at the Neurology Department of the Nanjing First Hospital from January 2016 to June 2018. Prior use of antiplatelet agent was recorded. Light transmittance aggregometry was used to estimate the maximum platelet aggregation (MPA). Linear regression model was performed to investigate the factors associated with MPA. Multivariate logistic regression was used to analyse the association between AP and clinical outcomes. A total of 59 patients were included; 23 (38.9 %) were taking antiplatelet agent before stroke. Prior AP (β = -20.209, SE mean=6.574; P=0.004) was significantly lower the arachidonic acid-induced MPA at the time point of 3h after thrombolysis. AP did not increase of the risk for sICH (OR=3.41, 95%CI 0.16-7.20, p=0.436) or mortality (OR=3.55, 95%CI 0.39-8.52, p=0.260). There were no associations between AP and improved clinical outcomes (all P>0.05). In thrombolysis-treated AIS patients, AP was associated with lower MPA after thrombolysis. AP is safe in these patients, however, further studies are required to confirm the efficacy.
在接受静脉溶栓治疗(IVT)的急性缺血性卒中(AIS)患者中早期使用抗血小板药物是一种潜在的治疗策略,然而,其安全性和有效性尚未得到充分证实。我们假设在IVT之前进行抗血小板预处理(AP)与在IVT后的最初24小时内开始使用AP具有相似的作用。我们旨在探讨AP对接受溶栓治疗的AIS患者血小板聚集和临床结局的影响。我们纳入了2016年1月至2018年6月在南京医科大学第一附属医院神经内科接受IVT治疗的AIS患者。记录先前使用抗血小板药物的情况。采用透光率聚集法估计最大血小板聚集率(MPA)。采用线性回归模型研究与MPA相关的因素。采用多因素logistic回归分析AP与临床结局之间的关联。共纳入59例患者;23例(38.9%)在卒中前服用抗血小板药物。溶栓后3小时,先前的AP(β=-20.209,标准误均值=6.574;P=0.004)显著降低花生四烯酸诱导的MPA。AP并未增加症状性脑出血(sICH)风险(OR=3.41,95%CI 0.16-7.20,p=0.436)或死亡率(OR=3.55,95%CI 0.39-8.52,p=0.260)。AP与改善的临床结局之间无关联(所有P>0.05)。在接受溶栓治疗的AIS患者中,AP与溶栓后较低的MPA相关。AP在这些患者中是安全的,然而,需要进一步研究来证实其疗效。