Agnelli Giancarlo, Sonaglia Francesco, Becattini Cecilia
Stroke Unit & Division of Internal and Cardiovascular Medicine, Department of Internal Medicine, University of Perugia, Italy.
Curr Pharm Des. 2005;11(30):3885-91. doi: 10.2174/138161205774580615.
Unfractionated heparin, low-molecular-weight heparins and vitamin K antagonists are established antithrombotic agents, but all have a number of limitations. Unfractionated heparin requires parenteral administration, has a short half-life and variable dose-response relationship. Low molecular weight heparins are more effective than low-fixed-dose unfractionated heparin in the prevention of postoperative venous thromboembolism in high-risk surgical patients but they still require subcutaneous administration. Vitamin K antagonists have a narrow therapeutic window and require a careful laboratory monitoring to minimize the risk of bleeding or thrombosis. Direct thrombin inhibitors are selective inhibitors of this key enzyme. Direct thrombin inhibitors inactivate thrombin without requiring any plasma cofactor, inhibit both free and fibrin-bound thrombin, and do not appreciably bind to plasma proteins. Ximelagatran, the first oral direct thrombin inhibitor, is rapidly absorbed and converted to its active form melagatran, which can itself be administered subcutaneously. Ximelagatran has been evaluated in the prevention of venous thromboembolism after major orthopaedic surgery, in the treatment of venous thromboembolism, in the prevention of stroke in patients with atrial fibrillation and in the prevention of recurrence after acute coronary syndromes. In the European studies in major orthopaedic surgery ximelagatran was administered orally after one or two days of melagatran, given subcutaneously. This review will report on the mechanism of action and clinical pharmacology of direct antithrombin agents and on the results of the clinical trials performed with direct thrombin inhibitors in the prevention of venous thromboembolism after major orthopaedic surgery. Taken together, these results indicate that direct thrombin inhibitors, ximelagatran in particular, have the potential to be a valid alternative to low molecular weight heparins and oral anticoagulants in the prevention of venous thromboembolism after major orthopaedic surgery.
普通肝素、低分子量肝素和维生素K拮抗剂是已确立的抗血栓药物,但它们都有一些局限性。普通肝素需要胃肠外给药,半衰期短且剂量-反应关系可变。低分子量肝素在预防高危手术患者术后静脉血栓栓塞方面比低固定剂量普通肝素更有效,但仍需要皮下给药。维生素K拮抗剂的治疗窗较窄,需要仔细的实验室监测以将出血或血栓形成风险降至最低。直接凝血酶抑制剂是这种关键酶的选择性抑制剂。直接凝血酶抑制剂无需任何血浆辅因子即可使凝血酶失活,抑制游离和纤维蛋白结合的凝血酶,且与血浆蛋白的结合不明显。首个口服直接凝血酶抑制剂希美加群吸收迅速并转化为其活性形式美拉加群,后者本身也可皮下给药。希美加群已在大型骨科手术后静脉血栓栓塞的预防、静脉血栓栓塞的治疗、房颤患者中风的预防以及急性冠状动脉综合征后复发的预防中进行了评估。在欧洲针对大型骨科手术的研究中,在皮下给予美拉加群一或两天后口服希美加群。本综述将报告直接抗凝血酶药物的作用机制和临床药理学,以及直接凝血酶抑制剂在预防大型骨科手术后静脉血栓栓塞方面进行的临床试验结果。综合来看,这些结果表明,直接凝血酶抑制剂,尤其是希美加群,在预防大型骨科手术后静脉血栓栓塞方面有可能成为低分子量肝素和口服抗凝剂的有效替代药物。