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阿替普酶治疗急性单个小皮质下梗死的疗效与安全性

Efficacy and Safety of Alteplase on Treatment of Acute Single Small Subcortical Infarction.

作者信息

Marcelinus Kilanga, Liu Hongbing, Zhang Ke, Zong Ce, Yang Hongxun, Song Bo, Gao Yuan, Xu Yuming

机构信息

Department of Neurology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, China.

National Health Council Key Laboratory of Prevention and Treatment of Cerebrovascular Disease.

出版信息

Curr Neurovasc Res. 2022;19(3):255-266. doi: 10.2174/1567202619666220829111211.

Abstract

BACKGROUND

Single Small Subcortical Infarction (SSSI) is an isolated small infarction in the territory of perforating artery with a maximum diameter of 20 mm in axial Diffusion-Weighted Imaging (DWI). About 20 to 30% of SSSI patients were reported to have Early Neurological Deterioration (END) in the acute phase, which brought adverse effects on long-term outcomes. The effect of the alteplase on the outcome of SSSI, especially END and long-term outcomes, was ambiguous.

OBJECTIVE

The study aims to find out the efficacy and safety of intravenous recombinant tissue Plasminogen Activator (rt-PA) on long-term and short- outcomes of patients with SSSI as compared to patients who received standard medical care.

METHODS

The patients were retrospectively screened from a stroke registry of the neurology department of 1st Affiliated Hospital of Zhengzhou University from January 2013 to December 2020. Based on treatment modality, patients were dichotomized into alteplase and standard medical care groups. To minimize confounding factors in subgroups, a propensity score matching analysis was done. The primary outcome was the favorable functional outcome 3 months after stroke onset, defined by attaining a score of ≤2 points on the modified Rankin scale (mRS), secondary outcome was the prevention of occurrence of END, defined as an increase of ≥2 points in the total score or ≥1point on motor subunit in the National Institutes of Health Stroke Scale (NIHSS) score within 72 hours after admission, safety features were symptomatic intracranial hemorrhage (sICH) or death. Multivariate analysis was employed to find the efficacy and safety of alteplase in the treatment of SSSI.

RESULTS

A total of 717 patients with anterior circulation SSSI were selected, and 132 were included in the final analysis. Forty-five patients were treated with alteplase within 4.5 hours and 87 with standard medical care, and 44 pairs were successfully matched by propensity score. Pre-match data showed that the alteplase thrombolysis group showed a higher proportion of favorable outcomes at 3-month follow-up [OR=0.315, 95%CI:0.106, 0.931, P = 0.037] but did not reduce the incidence of END compared with the non-thrombolytic group [OR = 1.033, 95%CI:0.417,2.554, P = 0.943]. Post-match data showed that the alteplase group also showed a higher proportion of favorable outcomes at 3-month follow-up [OR = 0.247, 95%CI: 0.074, 0.830, P = 0.024]; however, it did not reduce the incidence of END compared with the non-thrombolytic group [OR = 1.241, 95%CI: 0.433,3.554, P = 0.688]. There was one case of asymptomatic ICH in alteplase treated patients.

CONCLUSION

Patients with SSSI in the anterior circulation are more likely to achieve 3 months favorable outcomes than those who were treated with standard medical care; however, treatment with alteplase may not prevent the occurrence of END.

摘要

背景

单个小皮质下梗死(SSSI)是指穿支动脉供血区域内的孤立性小梗死灶,在轴位弥散加权成像(DWI)上最大直径为20mm。据报道,约20%至30%的SSSI患者在急性期会出现早期神经功能恶化(END),这对长期预后产生不利影响。阿替普酶对SSSI患者预后的影响,尤其是对END和长期预后的影响尚不明确。

目的

本研究旨在探讨静脉注射重组组织型纤溶酶原激活剂(rt-PA)与接受标准药物治疗的患者相比,对SSSI患者短期和长期预后的疗效及安全性。

方法

回顾性筛选2013年1月至2020年12月郑州大学第一附属医院神经内科卒中登记处的患者。根据治疗方式,将患者分为阿替普酶组和标准药物治疗组。为尽量减少亚组中的混杂因素,进行了倾向评分匹配分析。主要结局是卒中发作3个月后功能预后良好,定义为改良Rankin量表(mRS)评分≤2分;次要结局是预防END的发生,定义为入院后72小时内美国国立卫生研究院卒中量表(NIHSS)总分增加≥2分或运动亚组增加≥1分;安全性指标是症状性颅内出血(sICH)或死亡。采用多变量分析来确定阿替普酶治疗SSSI的疗效和安全性。

结果

共筛选出717例前循环SSSI患者,132例纳入最终分析。45例患者在4.5小时内接受阿替普酶治疗,87例接受标准药物治疗,44对通过倾向评分成功匹配。匹配前数据显示,阿替普酶溶栓组在3个月随访时预后良好的比例更高[比值比(OR)=0.315,95%置信区间(CI):0.106,0.931,P = 0.037],但与非溶栓组相比,并未降低END的发生率[OR = 1.033,95%CI:0.417,2.554,P = 0.943]。匹配后数据显示,阿替普酶组在3个月随访时预后良好的比例也更高[OR = 0.247,95%CI:0.074,0.830,P = 0.024];然而,与非溶栓组相比,并未降低END的发生率[OR = 1.241,95%CI:0.433,3.554,P = 0.688]。阿替普酶治疗的患者中有1例无症状颅内出血。

结论

前循环SSSI患者比接受标准药物治疗的患者更有可能在3个月时获得良好预后;然而,阿替普酶治疗可能无法预防END的发生。

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