Eriksson Bengt I, Dahl Ola E
Department of Orthopaedic Surgery, Sahlgrenska University Hospital/Ostra, SE-416 85 Göteborg, Sweden.
Drugs. 2004;64(6):577-95. doi: 10.2165/00003495-200464060-00002.
Patients undergoing total hip or total knee replacement are at high risk of venous thromboembolism (VTE), and are therefore considered to be populations well suited for the evaluation and dose optimisation of new anticoagulants. Deep vein thrombosis may lead to life-threatening pulmonary embolism, disabling morbidity in the form of the post-thrombotic syndrome, and risk of recurrent thrombotic events. There is increasing evidence that anticoagulant treatment for the prevention of VTE should be extended from 1 to at least 4 weeks after surgery. Anticoagulation with vitamin K antagonists (such as warfarin), low molecular weight heparin or unfractionated heparin effectively lowers the risk of VTE, but these anticoagulants have limitations such as the need for coagulation monitoring and subsequent dose adjustment (vitamin K antagonists), difficulty of continuing prophylaxis out of hospital because of the requirement for parenteral administration, and risk of heparin-induced thrombocytopenia. The development of new anticoagulants has been pursued with the aim of finding more effective, safer and/or more convenient therapies. Thrombin is a central regulator in the coagulation and inflammation process and several direct thrombin inhibitors (DTIs) with distinct pharmacological profiles, as well as pharmacological differences from the conventional anticoagulants, are currently in clinical use for certain indications or are under development. Clinical experience with parenterally administered DTIs has accumulated since the mid 1990s, although only desirudin (a recombinant hirudin) is currently approved for use in patients undergoing orthopaedic surgery. Two oral DTIs, ximelagatran and dabigatran etexilate, are in clinical development. Dabigatran etexilate has recently been evaluated in phase II clinical trials in patients undergoing total hip replacement. Several large phase III trials have now demonstrated the efficacy and safety of ximelagatran in the prevention of VTE following total hip or knee replacement. Ximelagatran can be used with an oral fixed dose without the need for coagulation monitoring or dose adjustment. Hence, it offers significant potential to facilitate the management of anticoagulation in or out of hospital.
接受全髋关节或全膝关节置换术的患者发生静脉血栓栓塞(VTE)的风险很高,因此被认为是非常适合评估新型抗凝剂并进行剂量优化的人群。深静脉血栓形成可能导致危及生命的肺栓塞、以血栓形成后综合征形式出现的致残性疾病以及复发性血栓事件的风险。越来越多的证据表明,预防VTE的抗凝治疗应从术后1周延长至至少4周。使用维生素K拮抗剂(如华法林)、低分子肝素或普通肝素进行抗凝可有效降低VTE风险,但这些抗凝剂存在局限性,如需要进行凝血监测及随后的剂量调整(维生素K拮抗剂)、因需要胃肠外给药而难以在院外继续进行预防以及肝素诱导的血小板减少症风险。人们一直在研发新型抗凝剂,目的是找到更有效、更安全和/或更方便的治疗方法。凝血酶是凝血和炎症过程中的核心调节因子,目前有几种具有不同药理学特征且与传统抗凝剂存在药理学差异的直接凝血酶抑制剂(DTIs)已在临床上用于某些适应症或正处于研发阶段。自20世纪90年代中期以来,胃肠外给药DTIs的临床经验不断积累,尽管目前仅地西卢定(一种重组水蛭素)被批准用于接受骨科手术的患者。两种口服DTIs,希美加群和达比加群酯正在进行临床研发。达比加群酯最近在接受全髋关节置换术的患者中进行了II期临床试验评估。现在,几项大型III期试验已证明希美加群在预防全髋关节或全膝关节置换术后VTE方面的有效性和安全性。希美加群可以采用口服固定剂量使用,无需进行凝血监测或剂量调整。因此,它在促进院内外抗凝管理方面具有巨大潜力。