Yi Xingyang, Lin Jing, Wang Chun, Zhang Biao, Chi Wanzhang
Department of Neurology, People's Hospital of Deyang City, Deyang 618000, Sichuan, China.
Department of Neurology, 3(rd) Affiliated Hospital of Wenzhou Medical College, Wenzhou 325200, Zhejiang, China.
J Stroke Cerebrovasc Dis. 2014 Jul;23(6):1537-44. doi: 10.1016/j.jstrokecerebrovasdis.2013.12.036. Epub 2014 Mar 19.
We evaluated the efficacy of low-molecular-weight heparin (LMWH) relative to aspirin in preventing early neurologic deterioration (END), venous thromboembolism (VTE), and outcomes at 6 months.
Patients were randomly assigned to receive either subcutaneous enoxaparin 4000 anti-factor Xa IU/0.4 mL twice daily or oral aspirin 200 mg daily for 10 days. After day 10, all subjects received aspirin 100 mg once daily for 6 months. We assessed whether LMWH was superior to aspirin in preventing END and VTE within the first 10 days after index stroke and evaluated 6-month outcomes.
Of the total 1368 patients, 7.89% suffered from END, and 2.85% suffered from deep-vein thrombosis during the first 10 days, with a significance difference between the LMWH group and aspirin group (3.95%, 1.46% versus 11.82%, 4.23%, respectively). At 6 months, there was a significant difference in the frequency of good outcomes among patients over the median age of 70 years (LMWH 63.8% versus aspirin 44.6%). The benefit of LMWH was also significant in patients with symptomatic stenosis of the posterior circulation and basilar artery (75.2% and 82% for LMWH versus 40.5% and 48% for aspirin, respectively).
For patients with acute ischemic stroke, treatment with LMWH within 48 hours of stroke until 10 days later may reduce END and deep-vein thrombosis during the first 10 days. LMWH appears to have advantages over aspirin in certain subgroups, such as elderly patients and patients with posterior circulation and basilar artery stenosis.
我们评估了低分子量肝素(LMWH)相对于阿司匹林在预防早期神经功能恶化(END)、静脉血栓栓塞(VTE)及6个月时的预后方面的疗效。
患者被随机分配接受皮下注射依诺肝素4000抗Xa因子国际单位/0.4毫升,每日两次,或口服阿司匹林200毫克,每日一次,持续10天。在第10天后,所有受试者接受阿司匹林100毫克,每日一次,持续6个月。我们评估了在首次卒中后的前10天内,LMWH在预防END和VTE方面是否优于阿司匹林,并评估了6个月时的预后。
在总共1368例患者中,7.89%的患者在最初10天内发生了END,2.85%的患者发生了深静脉血栓形成,LMWH组和阿司匹林组之间存在显著差异(分别为3.95%、1.46%和11.82%、4.23%)。在6个月时,年龄中位数超过70岁的患者中,良好预后的频率存在显著差异(LMWH组为63.8%,阿司匹林组为44.6%)。LMWH在伴有后循环和基底动脉症状性狭窄的患者中获益也很显著(LMWH组分别为75.2%和82%,阿司匹林组分别为40.5%和48%)。
对于急性缺血性卒中患者,在卒中后48小时内至10天后使用LMWH治疗,可能会减少最初10天内的END和深静脉血栓形成。在某些亚组中,如老年患者以及伴有后循环和基底动脉狭窄的患者,LMWH似乎比阿司匹林更具优势。