Hôtel-Dieu University Hospital, Paris, France.
Clin Appl Thromb Hemost. 2012 Mar-Apr;18(2):150-8. doi: 10.1177/1076029611426282. Epub 2012 Mar 2.
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.
本研究评估了使用校准品和质控品的凝血酶原时间(PT)检测法来测量利伐沙班的血浆浓度。在一项涉及 21 家实验室的现场试验中,研究了该测量方法的实验室内和实验室间精密度。每个实验室都提供了利伐沙班校准品和含有不同浓度利伐沙班的质控血浆样本以及 PT 试剂。使用中央提供的和本地的 PT 试剂在连续两周内进行评估。每天生成一条校准曲线(用于评估批内精密度),并通过测试 3 个质控血浆样本来评估日间精密度。使用本地 PT 试剂时,观察到较大的实验室间变异性(以秒为单位)。当以利伐沙班浓度(ng/mL)表示或使用中央 PT 试剂(STA Neoplastine CI Plus)时,结果的变异性较小。广泛可用的 PT 检测法与利伐沙班校准品结合使用,可能有助于测量利伐沙班的血浆峰浓度。