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Early vs. late enoxaparin for the prevention of venous thromboembolism in patients with ICH: A double blind placebo controlled multicenter study

医学 脑出血 血肿 安慰剂 随机化 低分子肝素 静脉血栓栓塞 华法林 麻醉 随机对照试验 间歇气动压缩 压力袜 外科 肝素 内科学 血栓形成 替代医学 病理 蛛网膜下腔出血 心房颤动
作者
Cheng Qian,Juha Huhtakangas,Seppo Juvela,Michaela K. Bode,Turgut Tatlisumak,M. Savolainen,Heikki Numminen,Jyrki Ollikainen,Liisa Luostarinen,Laura Kupila,Sami Tetri
出处
期刊:Clinical Neurology and Neurosurgery [Elsevier BV]
卷期号:202: 106534-106534 被引量:23
标识
DOI:10.1016/j.clineuro.2021.106534
摘要

BACKROUND: Venous thromboembolism (VTE) after primary intracerebral hemorrhage (ICH) worsens patient prognosis. Administering low-molecular weight heparins (LMWH) to prevent VTE early (24 h) may increase the risk of hematoma enlargement, whereas administering late (72 h) after onset may decrease its effect on VTE prevention. The authors investigated when it is safe and effective to start LMWH in ICH patients. METHODS: In the setting of double blinded, placebo controlled randomization, patients >18 years of age with paretic lower extremity, and admitted to the emergency room within 12 h of the onset of ICH, were randomized into two groups. Patients in the enoxaparin group received 20 mg twice a day 24 h (early) after the onset of ICH and in the placebo group 72 h (late) after onset respectively. Both groups immediately received intermittent pneumatic compression stockings at the ER. Patients were prospectively and routinely screened for VTE and hemorrhagic complications 1 day after entering the study and again before discharge. RESULTS: 139 patients were included for randomization in this study. Only 3 patients developed VTE, 2 in the early enoxaparin group and one in the late enoxaparin group. No patients developed PE. Thromboembolic events (p = 0.901), risk of hematoma enlargement (p = 0.927) and overall outcome (P = 0.904) did not differ significantly between the groups. CONCLUSION: Administering 40 mg/d LMWH for prevention of VTE to a spontaneous ICH patient is safe regardless of whether it is started 24 h (early) or 72 h (late) after the hemorrhage. Risk of hemorrhage enlargement is not associated with early LMWH treatment. Administering LMWH late did not increase VTEs.
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