Klinik und Poliklinik für Neurologie, Kopf- und Neurozentrum, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Hospices Civils de Lyon, Service de Biostatistique, Lyon, France.
JAMA Neurol. 2019 Jun 1;76(6):641-649. doi: 10.1001/jamaneurol.2019.0351.
The rationale for intravenous thrombolysis in patients with lacunar infarcts is debated, since it is hypothesized that the microvascular occlusion underlying lacunar infarcts might not be susceptible to pharmacological reperfusion treatment.
To study the efficacy and safety of intravenous thrombolysis among patients with lacunar infarcts.
DESIGN, SETTING, AND PARTICIPANTS: This exploratory secondary post hoc analysis of the WAKE-UP trial included patients who were screened and enrolled between September 2012 and June 2017 (with final follow-up in September 2017). The WAKE-UP trial was a multicenter, double-blind, placebo-controlled randomized clinical trial to study the efficacy and safety of intravenous thrombolysis with alteplase in patients with an acute stroke of unknown onset time, guided by magnetic resonance imaging. All 503 patients randomized in the WAKE-UP trial were reviewed for lacunar infarcts. Diagnosis of lacunar infarcts was based on magnetic resonance imaging and made by consensus of 2 independent investigators blinded to clinical information.
The primary efficacy variable was favorable outcome defined by a score of 0 to 1 on the modified Rankin Scale at 90 days after stroke, adjusted for age and severity of symptoms.
Of the 503 patients randomized in the WAKE-UP trial, 108 patients (including 74 men [68.5%]) had imaging-defined lacunar infarcts, whereas 395 patients (including 251 men [63.5%]) had nonlacunar infarcts. Patients with lacunar infarcts were younger than patients with nonlacunar infarcts (mean age [SD], 63 [12] years vs 66 [12] years; P = .003). Of patients with lacunar infarcts, 55 (50.9%) were assigned to treatment with alteplase and 53 (49.1%) to receive placebo. Treatment with alteplase was associated with higher odds of favorable outcome, with no heterogeneity of treatment outcome between lacunar and nonlacunar stroke subtypes. In patients with lacunar strokes, a favorable outcome was observed in 31 of 53 patients (59%) in the alteplase group compared with 24 of 52 patients (46%) in the placebo group (adjusted odds ratio [aOR], 1.67 [95% CI, 0.77-3.64]). There was 1 death and 1 symptomatic intracranial hemorrhage according to Safe Implementation of Thrombolysis in Stroke-Monitoring Study criteria in the alteplase group, while no death and no symptomatic intracranial hemorrhage occurred in the placebo group. The distribution of the modified Rankin Scale scores 90 days after stroke also showed a nonsignificant shift toward better outcomes in patients with lacunar infarcts treated with alteplase, with an adjusted common odds ratio of 1.94 (95% CI, 0.95-3.93).
While the WAKE-UP trial was not powered to demonstrate the efficacy of treatment in subgroups of patients, the results indicate that the association of intravenous alteplase with functional outcome does not differ in patients with imaging-defined lacunar infarcts compared with those experiencing other stroke subtypes.
在腔隙性梗死患者中进行静脉溶栓的理由存在争议,因为据推测,腔隙性梗死所涉及的微血管闭塞可能对药物再灌注治疗不敏感。
研究腔隙性梗死患者静脉溶栓的疗效和安全性。
设计、地点和参与者:本研究对 WAKE-UP 试验进行了探索性二次事后分析,共纳入 2012 年 9 月至 2017 年 6 月期间接受筛选和入组的患者(最终随访时间为 2017 年 9 月)。WAKE-UP 试验是一项多中心、双盲、安慰剂对照的随机临床试验,旨在研究急性发病时间未知的卒中患者静脉溶栓的疗效和安全性,通过磁共振成像指导。所有 503 例随机分配至 WAKE-UP 试验的患者均接受了腔隙性梗死的评估。腔隙性梗死的诊断基于磁共振成像,并由 2 名独立于临床信息的研究者进行共识诊断。
主要疗效变量为改良 Rankin 量表评分(0 到 1 分),定义为卒中后 90 天的良好结局,调整年龄和症状严重程度。
在 WAKE-UP 试验的 503 例随机患者中,108 例(包括 74 例男性[68.5%])存在影像学定义的腔隙性梗死,而 395 例(包括 251 例男性[63.5%])存在非腔隙性梗死。腔隙性梗死患者比非腔隙性梗死患者更年轻(平均年龄[标准差],63[12]岁 vs 66[12]岁;P = .003)。在腔隙性梗死患者中,55 例(50.9%)被分配接受阿替普酶治疗,53 例(49.1%)接受安慰剂治疗。与安慰剂相比,阿替普酶治疗与更好的结局相关,腔隙性和非腔隙性卒中亚型之间的治疗结局无异质性。在腔隙性卒中患者中,阿替普酶组 53 例患者中有 31 例(59%)结局良好,而安慰剂组 52 例患者中有 24 例(46%)结局良好(调整优势比[aOR],1.67[95%CI,0.77-3.64])。阿替普酶组发生 1 例死亡和 1 例症状性颅内出血(根据 Safe Implementation of Thrombolysis in Stroke-Monitoring Study 标准),而安慰剂组未发生死亡和症状性颅内出血。卒中后 90 天改良 Rankin 量表评分的分布也表明,接受阿替普酶治疗的腔隙性梗死患者的结局有向更好方向转变的趋势,调整后的共同优势比为 1.94(95%CI,0.95-3.93)。
尽管 WAKE-UP 试验没有足够的效能来证明治疗在患者亚组中的疗效,但结果表明,与其他卒中亚型患者相比,静脉注射阿替普酶与功能结局的相关性在影像学定义的腔隙性梗死患者中并无差异。