Bergsrud Elizabeth A, Gandhi Pritesh J
UMass Memorial Medical Center, 55 Lake Avenue North Worcester, MA 01655, USA.
J Thromb Thrombolysis. 2003 Dec;16(3):175-88. doi: 10.1023/B:THRO.0000024056.84909.b0.
Ximelagatran, an oral direct thrombin inhibitor, has been investigated for the prevention and treatment of venous thromboembolism as well as for anticoagulation in atrial fibrillation. Unique properties of ximelagatran are that it is a prodrug, it does not require routine laboratory monitoring and it has minimal drug interactions. The dose of ximelagatran needs to be modified in patients with renal failure; however, dosing guidelines in this specific patient population have not been established. Preliminary and emerging data suggest that ximelagatran is superior or at least as effective as low molecular weight heparins and warfarin in the setting of venous thromboembolism prevention and treatment. Ximelagatran has comparable bleeding rates to low molecular weight heparins and warfarin; however, it is associated with transient elevations in hepatic transaminases.
希美加群是一种口服直接凝血酶抑制剂,已被研究用于预防和治疗静脉血栓栓塞以及心房颤动的抗凝治疗。希美加群的独特特性在于它是一种前体药物,不需要常规实验室监测,且药物相互作用极小。肾功能衰竭患者需要调整希美加群的剂量;然而,尚未建立针对这一特定患者群体的给药指南。初步和新出现的数据表明,在预防和治疗静脉血栓栓塞方面,希美加群优于或至少与低分子量肝素和华法林同样有效。希美加群的出血率与低分子量肝素和华法林相当;然而,它与肝转氨酶的短暂升高有关。