Department of Orthopaedics, Sahlgrenska University Hospital, Gothenburg, Sweden.
J Thromb Haemost. 2010 Apr;8(4):714-21. doi: 10.1111/j.1538-7836.2010.03748.x. Epub 2010 Jan 17.
Anticoagulant prophylaxis substantially reduces the risk of venous thromboembolism (VTE) after major orthopedic surgery. The direct factor Xa inhibitor YM150 is currently under investigation for the prevention of VTE, stroke and ischemic vascular events in patients after orthopedic surgery, with atrial fibrillation and with acute coronary syndrome, respectively.
To investigate the efficacy and safety of YM150 for the prevention of VTE following elective total hip arthroplasty.
PATIENTS/METHODS: Patients were randomized to postoperative, once-daily, oral YM150 (5, 10, 30, 60 or 120 mg) (double-blind) or preoperative subcutaneous (open label) enoxaparin (40 mg) for 5 weeks. The primary efficacy endpoint comprised VTE diagnosed by mandatory bilateral venography or verified symptomatic deep vein thrombosis (DVT) plus all deaths up to 9 days after surgery. The primary safety outcome was major bleeding up to 9 days after surgery.
Primary efficacy endpoint: of 1017 patients randomized, 960 patients were evaluable for safety and 729 patients for efficacy. A dose-related decrease in VTE incidence from YM150 5 to 60 mg (P = 0.0005) and from 5 to 120 mg (P = 0.0002) was found. The VTE incidence was 27.4%, 31.7%, 19.3%, 13.3% and 14.5% for 5, 10, 30, 60 and 120 mg YM150, respectively, and 18.9% for enoxaparin. Primary safety endpoint: there was one major bleed with YM150 (60 mg) and one with enoxaparin.
The oral direct FXa inhibitor YM150 demonstrated a significant dose response regarding efficacy. Doses from 30 to 120 mg had comparable efficacy to enoxaparin, without compromising safety regarding major bleeding events.
抗凝预防治疗可显著降低骨科大手术后静脉血栓栓塞症(VTE)的风险。直接因子 Xa 抑制剂 YM150 目前正在研究用于预防骨科手术后、伴心房颤动和伴急性冠脉综合征的患者发生 VTE、卒中和缺血性血管事件。
研究 YM150 预防择期全髋关节置换术后 VTE 的疗效和安全性。
患者/方法:患者随机分为术后每日一次口服 YM150(5、10、30、60 或 120mg)(双盲)或术前皮下(开放标签)依诺肝素(40mg)5 周。主要疗效终点包括通过强制性双侧静脉造影或经证实的有症状深静脉血栓形成(DVT)加术后 9 天内所有死亡来诊断的 VTE。主要安全性结果为术后 9 天内的大出血。
主要疗效终点:在 1017 名随机患者中,960 名患者可进行安全性评估,729 名患者可进行疗效评估。发现 YM150 5 至 60mg(P=0.0005)和 5 至 120mg(P=0.0002)剂量相关的 VTE 发生率降低。YM150 5、10、30、60 和 120mg 的 VTE 发生率分别为 27.4%、31.7%、19.3%、13.3%和 14.5%,依诺肝素为 18.9%。主要安全性终点:YM150(60mg)有 1 例大出血,依诺肝素有 1 例大出血。
口服直接因子 Xa 抑制剂 YM150 在疗效方面具有显著的剂量反应。30 至 120mg 剂量与依诺肝素疗效相当,不增加大出血事件的安全性风险。