Fondaparinux as a treatment option for heparin-induced thrombocytopenia

被引:30
作者
Papadopoulos, Stella
Flynn, Jeremy D.
Lewis, Daniel A.
机构
[1] Univ Kentucky, Albert B Chandler Med Ctr, Dept Pharm, Lexington, KY 40536 USA
[2] Boston Med Ctr, Dept Pharm, Boston, MA USA
来源
PHARMACOTHERAPY | 2007年 / 27卷 / 06期
关键词
heparin-induced thrombocytopenia; HIT; fondaparinux; pentasaccharides; anticoagulation therapy; unfractionated heparin; low-molecular-weight heparin;
D O I
10.1592/phco.27.6.921
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Heparin-induced thrombocytopenia (HIT) is an immune-mediated complication that can occur after exposure to heparin products. Because patients with HIT are at increased risk for thrombosis, anticoagulation is warranted. The direct thrombin inhibitors lepirudin and argatroban are approved by the United States Food and Drug Administration (FDA) for this indication. Bivalirudin, another direct thrombin inhibitor, is approved for use in patients with HIT who must undergo percutaneous coronary intervention. The synthetic pentasaccharide fondaparinux lacks FDA approval for treating patients with HIT; however, a few published reports describe its use. Furthermore, various small-scale, in vitro studies have demonstrated a lack of cross-reactivity between fondaparinux and HIT antibodies. Large, in vivo comparison trials must be performed before fondaparinux can become a standard treatment option in the setting of HIT.
引用
收藏
页码:921 / 926
页数:6
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