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P reincubation in the P rothrombinase‐induced C lotting T ime test ( P i CT ) is necessary for in vitro evaluation of fondaparinux and to be avoided for the reversible, direct factor X a inhibitor, rivaroxaban
Author(s) -
Kluft C.,
Meijer P.,
Kret R.,
Burggraaf J.
Publication year - 2013
Publication title -
international journal of laboratory hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.705
H-Index - 55
eISSN - 1751-553X
pISSN - 1751-5521
DOI - 10.1111/ijlh.12027
Subject(s) - rivaroxaban , fondaparinux , chemistry , context (archaeology) , prothrombinase , in vitro , thrombin , biochemistry , immunology , biology , medicine , platelet , warfarin , paleontology , thrombosis , venous thromboembolism , atrial fibrillation
Summary Introduction There is no clear consensus about tests in vitro that are suitable for evaluating various factor X a inhibitors. The availability of reversible and irreversible inhibitors further complicates the application of available assays. Methods We evaluated the suitability of the prothrombinase‐induced clotting test ( P i CT ) for fondaparinux and rivaroxaban, as representatives for irreversible and reversible inhibition of factor X a, with specific attention to preincubation times prior to re‐calcification, in the context of automate program limitations. Results We demonstrate that the P i CT assay requires a preincubation step to allow inhibitory activity by fondaparinux. Without this step, inhibition in the test is minimal and lacking sufficient dynamic range. In contrast, to measure the reversible inhibition by rivaroxaban, we found any preincubation introduced an artifact in inhibition as exemplified by a biphasic pattern and only the test without a preincubation phase gave informative results. Conclusion It is concluded that P i CT in its format with two steps is suitable for fondaparinux evaluation, while its format without preincubation (the one‐addition format) is suitable for reversible inhibitors such as rivaroxaban. Unfortunately, both types of inhibitors cannot be compared in vitro in a single assay format.