Li Xia, Chen Yan, Dong Zhong, Zhang Fangfang, Chen Ping, Zhang Peilan
Clinical College of Neurology, Neurosurgery and Neurorehabilitation, Tianjin Medical University, Tianjin, China.
Department of Neurology, Tianjin Huanhu Hospital, Tianjin, China.
Front Neurol. 2025 Mar 5;16:1482078. doi: 10.3389/fneur.2025.1482078. eCollection 2025.
The objective of this study was to evaluate the safety and efficacy of dual antiplatelet pretreatment combined with low-dose rtPA therapy in patients with acute mild ischemic stroke, guided by multimodal MRI.
In this study, 383 patients with acute mild ischemic stroke (NIHSS ≤ 5) who had symptom onset within 4.5 hours of MRI screening were selected. Patients in the dual antiplatelet pretreatment plus low-dose rtPA group (164 cases) received dual antiplatelet therapy combined with low-dose (0.6 mg/kg) rtPA intravenous thrombolysis. Patients in the standard-dose group (112 cases) received conventional-dose (0.9 mg/kg) rtPA intravenous thrombolysis. Additionally, patients in the dual antiplatelet group who did not receive intravenous thrombolysis (107 cases) underwent 21 days of oral dual antiplatelet treatment.
There was no significant difference in the baseline NIHSS scores among the three groups before treatment ( > 0.05). The proportion of early neurological improvement within 24 hours and within 7 days was significantly higher in the DAPT plus low-dose group compared to both the standard-dose group and the DAPT group, with statistical significance ( < 0.05). After 90 days of follow-up, the proportion of good functional outcomes in the DAPT plus low-dose group was significantly higher than in both the standard-dose group and the DAPT group ( < 0.05), but there was no significant difference between the standard-dose group and the DAPT group. Safety studies indicated that, under MRI guidance, the DAPT plus low-dose group and the standard-dose group had lower incidences of intracranial hemorrhage transformation and symptomatic intracranial hemorrhage, with no statistical difference among the three groups ( > 0.05). Mortality rates were also similar across the three groups ( > 0.05), with only one patient passing away in the standard-dose group.
After dual antiplatelet pretreatment combined with low-dose rtPA intravenous thrombolysis for acute mild stroke under multimodal MRI guidance, the proportion of patients with good functional outcomes within 90 days was higher compared to the DAPT group and the standard-dose group, with statistical significance. There was no significant increase in the risk of cerebral hemorrhage compared to the standard-dose group and the DAPT group.
本研究的目的是在多模态磁共振成像(MRI)的引导下,评估双重抗血小板预处理联合低剂量重组组织型纤溶酶原激活剂(rtPA)治疗急性轻度缺血性卒中患者的安全性和有效性。
在本研究中,选取了383例在MRI筛查后4.5小时内出现症状的急性轻度缺血性卒中患者(美国国立卫生研究院卒中量表[NIHSS]评分≤5分)。双重抗血小板预处理加低剂量rtPA组(164例)患者接受双重抗血小板治疗联合低剂量(0.6mg/kg)rtPA静脉溶栓。标准剂量组(112例)患者接受常规剂量(0.9mg/kg)rtPA静脉溶栓。此外,未接受静脉溶栓的双重抗血小板组(107例)患者接受21天的口服双重抗血小板治疗。
三组治疗前基线NIHSS评分无显著差异(P>0.05)。双重抗血小板预处理加低剂量组在24小时内和7天内早期神经功能改善的比例显著高于标准剂量组和双重抗血小板组,差异有统计学意义(P<0.05)。随访90天后,双重抗血小板预处理加低剂量组良好功能结局的比例显著高于标准剂量组和双重抗血小板组(P<0.05),但标准剂量组和双重抗血小板组之间无显著差异。安全性研究表明,在MRI引导下,双重抗血小板预处理加低剂量组和标准剂量组颅内出血转化和症状性颅内出血的发生率较低,三组之间无统计学差异(P>0.05)。三组的死亡率也相似(P>0.05),标准剂量组仅有1例患者死亡。
在多模态MRI引导下,对急性轻度卒中患者进行双重抗血小板预处理联合低剂量rtPA静脉溶栓后,90天内良好功能结局患者的比例高于双重抗血小板组和标准剂量组,差异有统计学意义。与标准剂量组和双重抗血小板组相比,脑出血风险无显著增加。