The George Institute for Global Health at Peking University Health Science Center, Beijing, China.
Department of Neurology, 85 Hospital of People's Liberation Army, Shanghai, China.
Stroke Vasc Neurol. 2017 May 22;2(2):53-58. doi: 10.1136/svn-2017-000085. eCollection 2017 Jun.
The characteristics of patients with acute ischaemic stroke (AIS) and their management vary across regions, which may influence outcomes. We examined for differential patterns of outcome between China and non-China participants of the ENhanced Control of Hypertension And Thrombolysis strokE stuDy (ENCHANTED), which tested different alteplase doses in AIS.
ENCHANTED was an international, multicentre, open, blinded-endpoint trial of the effects of low-dose (0.6 mg/kg) versus standard-dose (0.9 mg/kg) intravenous alteplase on 90-day disability outcomes and symptomatic intracerebral haemorrhage (sICH) in 3310 patients with AIS.
Participants (n=1419, 48%) in China were younger, and more often male, hypertensive and with prior stroke and coronary artery disease, but less likely to have atrial fibrillation and use antihypertensive, antithrombotic and lipid-lowering agents, compared with non-China patients with AIS. Although China participants had more AIS due to large artery occlusion, were treated later and had differing ancillary management, there was no significant difference in 90-day modified Rankin scale scores 2-6 (55.6% vs 47.8%; OR, adjusted for baseline and management factors 0.87 (95% CI 0.71 to 1.07; p=0.20)) and risk of sICH (Safe Implementation of Thrombolysis in Stroke-Monitoring Study criteria: 1.4% vs 1.8%; p=0.12) compared with non-China participants. There was no heterogeneity in the treatment effects of low-dose versus standard-dose alteplase between China and non-China participants.
Patients with AIS recruited to the ENCHANTED trial in China had similar outcomes in response to thrombolysis treatment despite significantly differing demographic, clinical and management factors to patients with AIS in other regions.
急性缺血性脑卒中(AIS)患者的特点及其治疗方式在不同地区存在差异,这可能会影响治疗结果。我们研究了中国和非中国的 ENhanced Control of Hypertension And Thrombolysis strokE stuDy(ENCHANTED)试验参与者之间结果的差异模式,该试验旨在测试 AIS 中不同剂量的阿替普酶。
ENCHANTED 是一项国际性、多中心、开放性、盲终点试验,旨在评估低剂量(0.6mg/kg)与标准剂量(0.9mg/kg)静脉内阿替普酶对 3310 例 AIS 患者 90 天残疾结局和症状性颅内出血(sICH)的影响。
与非中国 AIS 患者相比,中国患者(n=1419,48%)年龄更小,男性更多,高血压更多,既往有卒中和冠心病,但心房颤动更少,使用降压药、抗血栓药和降脂药的可能性更小。尽管中国患者 AIS 中大动脉闭塞的比例更高,治疗时间更晚,辅助治疗管理方式也有所不同,但 90 天改良 Rankin 量表评分 2-6 分(55.6%比 47.8%;OR,根据基线和管理因素调整后为 0.87(95%CI 0.71 至 1.07;p=0.20))和 sICH 风险(Safe Implementation of Thrombolysis in Stroke-Monitoring Study 标准:1.4%比 1.8%;p=0.12)与非中国患者相比无显著差异。在中国和非中国患者中,低剂量与标准剂量阿替普酶治疗效果无显著差异。
尽管中国的 ENCHANTED 试验中招募的 AIS 患者在人口统计学、临床和管理因素方面与其他地区的 AIS 患者存在显著差异,但他们对溶栓治疗的反应相似。