Evaluation of the Prothrombin Time for Measuring Rivaroxaban Plasma Concentrations Using Calibrators and Controls

Author:

Samama Meyer Michel12,Contant Genevieve3,Spiro Theodore E.4,Perzborn Elisabeth5,Flem Lena Le2,Guinet Céline2,Gourmelin Yves3,Martinoli Jean Luc3

Affiliation:

1. Hôtel-Dieu University Hospital, Paris, France

2. Biomnis Laboratories R&D, Ivry-sur-Seine, France

3. Diagnostica Stago SA, Gennevilliers, France

4. Bayer HealthCare Pharmaceuticals Inc, Montville, NJ, USA

5. Bayer HealthCare AG, Wuppertal, Germany

Abstract

This study evaluated the prothrombin time (PT) assay for the measurement of plasma concentrations of rivaroxaban using calibrators and controls. The intra- and interlaboratory precision of the measurement was investigated in a field trial involving 21 laboratories. Each laboratory was provided with rivaroxaban calibrators and control plasma samples containing different concentrations of rivaroxaban, and PT reagents. The evaluation was carried out over 2 consecutive weeks using centrally provided and local PT reagents. A calibration curve was produced each day (for inter-run precision), and day-to-day precision was evaluated by testing 3 control plasma samples. A large interlaboratory variation (in seconds) was observed with local PT reagents. The results were less variable when expressed as rivaroxaban concentrations (ng/mL) or when central PT reagent was used (STA Neoplastine CI Plus). The widely available PT assay, in conjunction with rivaroxaban calibrators, may be useful for the measurement of peak plasma levels of rivaroxaban.

Publisher

SAGE Publications

Subject

Hematology,General Medicine

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