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利伐沙班(拜瑞妥):疗效与安全性

[Rivaroxaban (Xarelto): efficacy and safety].

作者信息

Rosencher N, Arnaout L, Chabbouh T, Bellamy L

机构信息

Service d'Anesthésie-Réanimation, Hôpital Cochin, 27, rue du Faubourg Saint-Jacques, 75014 Paris, France.

出版信息

Ann Fr Anesth Reanim. 2008 Dec;27 Suppl 3:S22-7. doi: 10.1016/S0750-7658(08)75143-8.

Abstract

The oral direct Xa inhibitor rivaroxaban (Xarelto) shows great promise for prevention of venous thromboembolic events after major elective orthopedic surgery. Its consistent and predictable pharmacokinetics and pharmacodynamics across a wide range of patient populations allow administration with fixed dosing and with no coagulation monitoring. In 4 orthopaedic surgery clinical trials (12,700 patients), 10mg postoperative (6-10 hours after the end of surgery) dose, once daily, of oral rivaroxaban, achieved superior efficacy and similar safety to enoxaparin, whatever the dose of enoxaparin. Indeed, 40 mg once a day in Europe and 30 mg bid in US of enoxaparin were compared to the same dose of 10mg once daily of rivaroxaban. Furthermore, there is no difference according to liver enzymes elevation and cardio-vascular adverse events. Although the risk of spinal haematoma after neuraxial anaesthesia is rare, it is increased by concomitant use of anticoagulants. In orthopedic surgery trials with rivaroxaban to date, complications such as spinal haematoma have not been reported. The pharmacokinetic profile of rivaroxaban suggests that concurrent use with neuraxial anaesthesia should require no further precautions than currently necessary with low-molecular-weight heparin.

摘要

口服直接Xa因子抑制剂利伐沙班(拜瑞妥)在预防大型择期骨科手术后静脉血栓栓塞事件方面显示出巨大潜力。其在广泛患者群体中具有一致且可预测的药代动力学和药效学特性,允许采用固定剂量给药且无需凝血监测。在4项骨科手术临床试验(12700例患者)中,术后(手术结束后6 - 10小时)口服利伐沙班10mg,每日1次,无论依诺肝素剂量如何,其疗效均优于依诺肝素,安全性相似。实际上,将欧洲每日1次40mg的依诺肝素和美国每日2次30mg的依诺肝素与每日1次相同剂量10mg的利伐沙班进行了比较。此外,在肝酶升高和心血管不良事件方面没有差异。虽然神经轴索麻醉后发生脊髓血肿的风险罕见,但联合使用抗凝剂会增加该风险。在迄今为止使用利伐沙班的骨科手术试验中,尚未报告脊髓血肿等并发症。利伐沙班的药代动力学特征表明,与神经轴索麻醉同时使用时,所需的预防措施不应比目前使用低分子量肝素时更多。

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