Thrombin generation time is a novel parameter for monitoring enoxaparin therapy in patients with end-stage renal disease

被引:16
作者
Brophy, DF
Martin, EJ
Gehr, TWB
Best, AM
Paul, K
Carr, ME
机构
[1] Virginia Commonwealth Univ, Med Coll Virginia, Sch Pharm, Richmond, VA 23298 USA
[2] Virginia Commonwealth Univ, Med Coll Virginia, Dept Pharm Practice, Richmond, VA 23298 USA
[3] Virginia Commonwealth Univ, Med Coll Virginia, Dept Internal Med, Richmond, VA 23298 USA
[4] Virginia Commonwealth Univ, Med Coll Virginia, Dept Biostat, Richmond, VA 23298 USA
[5] Virginia Commonwealth Univ, Med Coll Virginia, Coagulat Special Studies Lab, Richmond, VA 23298 USA
[6] Hemodyne Inc, Richmond, VA USA
关键词
antifactor Xa activity; enoxaparin; thrombin generation time;
D O I
10.1111/j.1538-7836.2006.01731.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Patients with end-stage renal disease (ESRD) who receive enoxaparin are at increased risk for adverse bleeding episodes. This phenomenon appears to occur despite judicious monitoring of antifactor Xa (aFXa) activity. Better monitoring parameters are needed to quantify the anticoagulant effects of enoxaparin in the ESRD population. Objectives: The objective of this study was to determine the utility of using thrombin generation time (TGT), platelet contractile force (PCF) and clot elastic modulus (CEM) to monitor the degree of anticoagulation in ESRD subjects, and to compare these results to aFXa activity, the current gold-standard monitoring parameter. Methods: Eight healthy volunteers without renal dysfunction and eight ESRD subjects were enrolled into this study. Subjects received a single dose of enoxaparin 1 mg kg(-1) subcutaneously, and blood samples were obtained for the determination of aFXa activity, TGT, PCF and CEM at baseline, 4, 8, and 12 h postdose. Results: Baseline, 4, 8, and 12-h aFXa activity concentrations were not different between groups. However, the corresponding TGT at 8 and 12 h was significantly prolonged in the ESRD group (P = 0.04, and P = 0.008, respectively). The 4-h peak TGT trended toward significance (P = 0.06). There were no differences in PCF or CEM across time. Conclusions: These data suggest that the parameter aFXa activity is a poor predictor of the anticoagulant effect of enoxaparin in patients with ESRD. Thrombin generation time appears to be more sensitive to the antithrombotic effects of enoxaparin in this population. Further large-scale trials are needed to corroborate these data.
引用
收藏
页码:372 / 376
页数:5
相关论文
共 36 条
[1]   Impact of procoagulant concentration on rate, peak and total thrombin generation in a model system [J].
Allen, GA ;
Wolberg, AS ;
Oliver, JA ;
Hoffman, M ;
Roberts, HR ;
Monroe, DM .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (03) :402-413
[2]   Influence of patient characteristics and renal function on factor Xa inhibition pharmacokinetics and pharmacodynamics after enoxaparin administration in non-ST-segment elevation acute coronary syndromes [J].
Becker, RC ;
Spencer, FA ;
Gibson, M ;
Rush, JE ;
Sanderink, G ;
Murphy, SA ;
Ball, SP ;
Antman, EM .
AMERICAN HEART JOURNAL, 2002, 143 (05) :753-759
[3]   Is laboratory monitoring of low-molecular-weight heparin therapy necessary? No [J].
Bounameaux, H ;
De Moerloose, P .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (04) :551-554
[4]  
BRIEGER D, 1994, THROMB HAEMOSTASIS, V72, P275
[5]   Antifactor Xa activity correlates to thrombin generation time, platelet contractile force and clot elastic modulus following ex vivo enoxaparin exposure in patients with and without renal dysfunction [J].
Brophy, DF ;
Martin, EJ ;
Best, AM ;
Gehr, TWB ;
Carr, ME .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (08) :1299-1304
[6]   Enhanced anticoagulant activity of enoxaparin in patients with ESRD as measured by thrombin generation time [J].
Brophy, DF ;
Martin, EJ ;
Gehr, TWB ;
Carr, ME .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2004, 44 (02) :270-277
[7]   The pharmacokinetics of subcutaneous enoxaparin in end-stage renal disease [J].
Brophy, DF ;
Wazny, LD ;
Gehr, TWB ;
Comstock, TJ ;
Venitz, J .
PHARMACOTHERAPY, 2001, 21 (02) :169-174
[8]   A hypothesis-generating study to evaluate platelet activity in diabetics with chronic kidney disease [J].
Brophy D.F. ;
Martin R.J. ;
Gehr T.W.B. ;
Carr Jr. M.E. .
Thrombosis Journal, 3 (1)
[9]   Thrombin functions during tissue factor-induced blood coagulation [J].
Brummel, KE ;
Paradis, SG ;
Butenas, S ;
Mann, KG .
BLOOD, 2002, 100 (01) :148-152
[10]   Normal thrombin generation [J].
Butenas, S ;
van't Veer, C ;
Mann, KG .
BLOOD, 1999, 94 (07) :2169-2178