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

Abstract

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 e.ects 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 inESRDsubjects, and to compare these results to aFXa activity, the current goldstandard 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 kg1 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. © 2006 International Society on Thrombosis and Haemostasis.