The pharmacokinetics of enoxaparin do not correlate with its pharmacodynamic effect in patients receiving dialysis therapies

被引:27
作者
Brophy, Donald F.
Carr, Marcus E., Jr.
Martin, Erika J.
Venitz, Jurgen
Gehr, Todd W. B.
机构
[1] Virginia Commonwealth Univ, Med Coll Virginia, Dept Pharm, Richmond, VA 23298 USA
[2] Virginia Commonwealth Univ, Med Coll Virginia, Coagulat Special Studies Lab, Richmond, VA 23298 USA
[3] Hemodyne Inc, Richmond, VA USA
关键词
thrombin generation time; antifactor Xa activity; enoxaparin; low-molecular weight heparin; dialysis;
D O I
10.1177/0091270006289975
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The pharmacokinetics and pharmacodynamics of enoxaparin were studied in healthy volunteers and hemodialysis and peritoneal dialysis subjects. Antifactor Xa activity estimated the pharmacokinetics, whereas thrombin generation time (TGT) estimated the pharmacodynamics. Enoxaparin 1 mg/kg was given subcutaneously to all subjects. Antifactor Xa A(max) and AUC(0-12) were similar between groups, but the TGT(max) was significantly greater in the dialysis groups (P =.001). The thrombin generation time remained significantly more prolonged throughout the 12-hour study period, and there was a trend toward greater TGT AUEC(0-12) for both dialysis groups (P =.07). Patients receiving hemodialysis had greater sensitivity to enoxaparin compared to the other groups. These results suggest that in dialysis patients, there may be accumulation of active heparin metabolites that are undetected by the antifactor Xa assay. Therefore, these subjects exhibit greater thrombin generation time prolongation despite similar antifactor Xa exposure. Further large-scale studies are needed to corroborate the results of this exploratory pilot study.
引用
收藏
页码:887 / 894
页数:8
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