Thromb Haemost 2010; 103(04): 815-825
DOI: 10.1160/TH09-03-0176
New Technologies, Diagnostic Tools and Drugs
Schattauer GmbH

Assessment of laboratory assays to measure rivaroxaban – an oral, direct factor Xa inhibitor

Meyer Michel Samama
1   Hôtel-Dieu University Hospital, Paris, France
2   Biomnis Laboratory, Ivry-sur-Seine, France
,
Jean-Luc Martinoli
3   Stago, Asnières, France
,
Léna LeFlem
2   Biomnis Laboratory, Ivry-sur-Seine, France
,
Céline Guinet
2   Biomnis Laboratory, Ivry-sur-Seine, France
,
Geneviève Plu-Bureau
1   Hôtel-Dieu University Hospital, Paris, France
,
François Depasse
2   Biomnis Laboratory, Ivry-sur-Seine, France
,
Elisabeth Perzborn
4   Bayer Schering Pharma AG, Wuppertal, Germany
› Author Affiliations
Further Information

Publication History

Received: 19 March 2009

Accepted after major revision: 22 February 2009

Publication Date:
22 November 2017 (online)

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Summary

Although there is no need for routine coagulation monitoring with rivaroxaban – an oral, direct factor Xa inhibitor – a haemostasis assay might be valuable to measure its pharmacodynamic effects. This study aimed to find assays, among those commercially available, to measure rivaroxaban pharmacodynamics. Several global conventional clotting tests, as well as clotting or chromogenic assays to measure anti-factor Xa activity, were studied. A thrombin generation test using calibrated automated thrombogram was also done. Tests were performed with the indirect factor Xa inhibitor fondaparinux for comparison. A concentration-dependent prolongation of prothrombin time (PT), dilute PT, and activated partial thromboplastin time was observed with rivaroxaban. The results varied depending on the reagents. This variability cannot be standardised with the international normalised ratio system commonly used for vitamin K antagonists. Using a standard calibration curve, PT test results can be expressed in plasma concentrations of rivaroxaban rather than PT seconds or ratio. Standard methods for HepTest and two-step prothrombinase-induced clotting time (PiCT) resulted in a paradoxical response, with low concentrations of rivaroxaban reducing clotting times. This was not observed with shorter incubation times, or when antithrombin-deficient (immunodepleted) plasma was used. The chromogenic tests found a dose-dependent relationship between anti-factor Xa activity and rivaroxaban concentration. Modified specific factor Xa chromogenic assays are being further investigated. One-step PiCT and HepTest with shortened incubation times, as well as the widely available PT assay (using a rivaroxaban calibrator) could be useful to monitor the pharmacodynamic effects of rivaroxaban accurately. Finally, all clotting and chromogenic assays showed a concentration-dependent effect induced by rivaroxaban.