Bauersachs R M
Medizinische Klinik IV, Max-Ratschow-Klinik für Angiologie, Klinikum Darmstadt.
Internist (Berl). 2004 Dec;45(12):1345-55. doi: 10.1007/s00108-004-1302-8.
Current antithrombotic therapy of deep vein thrombosis (DVT) consists of an initial course of heparin, followed by the secondary prevention with oral anticoagulation (OAC). Low molecular weight heparin has several advantages over unfractionated heparin, however, renal insufficiency has to be observed to avoid accumulation. The synthetic pentasaccharide Fondaparinux is a factor Xa inhibitor, that will shortly be available for the initial treatment of DVT. Oral anticoagulation with vitamin K antagonists (VKA) is highly effective, the standard target INR is 2.0-3.0. For a first episode of DVT the duration of OAC usually is six months, but has to be adjusted according to the estimated risk for recurrence. Because of the narrow therapeutic window of VKA, low molecular weight heparins are increasingly being used for secondary prevention in patients with an increased risk for bleeding, mostly in 1/2-therapeutic dose. At present, several new antithrombotic agents are being studied and may become available shortly for DVT treatment.
目前深静脉血栓形成(DVT)的抗栓治疗包括初始阶段使用肝素,随后采用口服抗凝药(OAC)进行二级预防。低分子量肝素相对于普通肝素具有若干优势,然而,必须留意肾功能不全情况以避免蓄积。合成五糖磺达肝癸钠是一种Xa因子抑制剂,不久将可用于DVT的初始治疗。使用维生素K拮抗剂(VKA)进行口服抗凝非常有效,标准的目标国际标准化比值(INR)为2.0 - 3.0。对于首次发生的DVT,OAC的疗程通常为6个月,但必须根据复发的估计风险进行调整。由于VKA的治疗窗较窄,低分子量肝素越来越多地用于出血风险增加的患者的二级预防,大多采用半治疗剂量。目前,几种新型抗栓药物正在研究中,可能很快可用于DVT治疗。