Determination of Dabigatran in Human Plasma Samples

被引:65
作者
Harenberg, Job [1 ]
Giese, Christina [1 ]
Marx, Svetlana [1 ]
Kraemer, Roland [2 ]
机构
[1] Heidelberg Univ, Fac Med, Dept Clin Pharmacol, D-68169 Mannheim, Germany
[2] Heidelberg Univ, Inst Inorgan Chem, Heidelberg, Germany
关键词
dabigatran; Hemoclot assay; chromogenic assay; prothrombin-induced clotting time assay; Ecarin clotting time; prothrombin time; activated partial thromboplastin time; INDUCED CLOTTING TIME; ATRIAL-FIBRILLATION; INHIBITORS; WARFARIN; PHENPROCOUMON; ARGATROBAN; MELAGATRAN; ETEXILATE; LEPIRUDIN;
D O I
10.1055/s-0031-1300947
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The oral direct thrombin inhibitor dabigatran effectively prevents arterial and venous thromboembolism using fixed doses without the need for adjustment according to laboratory results. Dabigatran is eliminated from the circulation by similar to 80% through the kidneys. However, the in vitro anticoagulant effect of dabigatran may be necessary to determine in special patient populations such as in the elderly, for renal impairment, before operations, bleeding or thrombotic episodes, and to monitor self-compliance. Several clotting and thrombin-specific chromogenic substrate assays are available to analyze the biological activity of dabigatran. All of them are prolonged in the presence of dabigatran. This article reports the effects of dabigatran on clinical routine assays and the potential usefulness for determination in special risk groups of patients when overdose or lack of compliance are suspected.
引用
收藏
页码:16 / 22
页数:7
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