Division of Hematology/Oncology, University of Pennsylvania School of Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Curr Opin Hematol. 2010 Sep;17(5):424-31. doi: 10.1097/MOH.0b013e32833c07a7.
Heparin-induced thrombocytopenia (HIT) is a significant cause of morbidity and mortality in hospitalized patients, due to life and limb-threatening thrombosis. Prompt recognition, laboratory testing, and alternate anticoagulation are essential. At present, HIT remains an underdiagnosed and undertreated condition. This review will discuss the relative merits of the approved treatment options, as well as address additional anticoagulants that show promise for the future.
Argatroban and lepirudin are well studied and approved drugs for treatment of HIT. Both of these drugs are equal in efficacy, and differences in pharmacokinetic profiles allow the choice of drug to be tailored to the clinical scenario. Bivalirudin and fondaparinux have been used to treat HIT in small case series. New oral anticoagulants, such as factor IIa and factor Xa inhibitors, may provide a novel treatment approach in HIT.
First-line therapies for HIT are argatroban or lepirudin. Patient-specific factors determine which drug should be used, and taking advantage of their differences allows effective anticoagulation with minimal risk of bleeding. Bivalirudin and fondaparinux require further study before they can be recommended. Once proven well tolerated and effective for treating thrombosis, these new oral anticoagulants should next be studied for treating HIT.
肝素诱导的血小板减少症(HIT)是住院患者发病率和死亡率的重要原因,因为它会导致危及生命和肢体的血栓形成。及时识别、实验室检测和替代抗凝是至关重要的。目前,HIT 仍然是一种诊断不足和治疗不足的疾病。这篇综述将讨论已批准的治疗方案的相对优势,并探讨未来有前途的其他抗凝剂。
阿加曲班和来匹卢定是研究充分且已批准用于治疗 HIT 的药物。这两种药物在疗效上是等效的,药代动力学特征的差异使得可以根据临床情况选择药物。比伐卢定和磺达肝癸钠已在小病例系列中用于治疗 HIT。新型口服抗凝剂,如因子 IIa 和因子 Xa 抑制剂,可能为 HIT 提供一种新的治疗方法。
HIT 的一线治疗药物是阿加曲班或来匹卢定。患者的具体情况决定了应使用哪种药物,利用它们的差异可以在最小出血风险下进行有效的抗凝治疗。比伐卢定和磺达肝癸钠需要进一步研究才能推荐使用。一旦这些新型口服抗凝剂被证明耐受良好且对治疗血栓形成有效,就应该进一步研究它们治疗 HIT 的效果。