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急性缺血性脑卒中患者接受 0.6mg/kg 重组组织型纤溶酶原激活剂静脉溶栓后短期大剂量双联抗血小板治疗的疗效和安全性。

Efficacy and safety of short-term high dosage dual antiplatelet therapy after 0.6 mg/kg rt-PA intravenous thrombolysis for acute ischemic stroke.

机构信息

Department of Neurology, Characteristic Medical Centre of People's Armed Police Force, Tianjin, P.R. China.

Tianjin Medical University, Tianjin, P.R. China.

出版信息

Medicine (Baltimore). 2023 Sep 8;102(36):e35099. doi: 10.1097/MD.0000000000035099.

Abstract

OBJECTIVE

To evaluate the efficacy and safety of short-term high-dose of dual antiplatelet therapy after 0.6 mg/kg rt-PA intravenous thrombolysis for acute ischemic stroke (AIS).

METHODS

All 208 patients with AIS were randomized into group 1 (103 cases, after 0.6 mg/kg rt-PA, 300 mg of oral aspirin(ASP) q.d. and 225 mg of oral clopidogrel (CLO) q.d. for for 5 days, then 100 mg of oral ASP q.d. for the next 85 days and 75 mg of oral CLO q.d. for the next 16 days) and group 2 (105 cases, after 0.9 mg/kg rt-PA, 100 mg of oral ASP q.d. for 90 days and 75 mg of oral CLO q.d. for 21 days).The efficacy index was the mRS score, NIHSS score and recurrence risk of stroke, while the safety index was the incidence of bleeding events and mortality. All parameters were evaluated at 30 and 90 days after thrombolysis. Patients whose characteristics may provide the best treatment benefit were further analyzed using the logistic regression model in group 1.

RESULTS

The proportion of mRS scores between 0 and 1 in group 1 was higher than that in group 2 at both 30 days (44.7% vs 32.4%, P < .05) and 90 days (50.5% vs 35.2%, P < .05). Compared to group 2, the proportion of NIHSS scores less than 4 was significantly higher in group 1 at both 30 days (37.9% vs 25.7%, P < .05) and 90 days (46.6% vs 30.5%, P < .05). At 90 days, Group 1 had a lower stroke recurrence risk than Group 2 (3.9% vs 10.5%, P < .05). The incidence of SICH was significantly different between the 2 groups at both 30 days (2.9% vs 9.5%, P < .05) and 90 days (2.9% vs 10.5%, P < .05). However, other bleeding events and mortality rates were not significantly different between the 2 groups. The lower the baseline NIHSS score and the shorter the OTT, the more favorable the outcomes obtained at 90 days.

CONCLUSIONS

Compared to standard doses, short term high-dose dual antiplatelet therapy after 0.6 mg/kg rt-PA intravenous thrombolysis may be a good choice for AIS patients.

摘要

目的

评估急性缺血性脑卒中(AIS)患者接受 0.6mg/kg 重组组织型纤溶酶原激活剂(rt-PA)静脉溶栓后短期高剂量双联抗血小板治疗的疗效和安全性。

方法

将 208 例 AIS 患者随机分为 1 组(103 例)和 2 组(105 例)。1 组患者在接受 0.6mg/kg rt-PA 治疗后,分别给予 300mg 阿司匹林(ASP)口服,每天 1 次,225mg 氯吡格雷(CLO)口服,每天 1 次,连续 5 天,随后改为每天 100mg ASP 口服 85 天,每天 75mg CLO 口服 16 天;2 组患者在接受 0.9mg/kg rt-PA 治疗后,给予每天 100mg ASP 口服 90 天,每天 75mg CLO 口服 21 天。疗效指标为改良 Rankin 量表(mRS)评分、美国国立卫生研究院卒中量表(NIHSS)评分和卒中复发风险,安全性指标为出血事件和死亡率。所有参数在溶栓后 30 天和 90 天进行评估。在 1 组中,进一步使用逻辑回归模型分析了可能提供最佳治疗效果的患者特征。

结果

1 组患者在溶栓后 30 天(44.7%比 32.4%,P<0.05)和 90 天(50.5%比 35.2%,P<0.05)mRS 评分 0~1 分的比例均高于 2 组;1 组患者在溶栓后 30 天(37.9%比 25.7%,P<0.05)和 90 天(46.6%比 30.5%,P<0.05)NIHSS 评分<4 分的比例均显著高于 2 组。90 天时,1 组卒中复发风险低于 2 组(3.9%比 10.5%,P<0.05)。两组在溶栓后 30 天(2.9%比 9.5%,P<0.05)和 90 天(2.9%比 10.5%,P<0.05)的 SICH 发生率均有显著差异,但两组其他出血事件和死亡率无显著差异。基线 NIHSS 评分越低,OTI 越短,90 天时的预后越好。

结论

与标准剂量相比,0.6mg/kg rt-PA 静脉溶栓后短期高剂量双联抗血小板治疗可能是 AIS 患者的一种较好选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4272/10489488/69ba30cb77c0/medi-102-e35099-g001.jpg

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