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Published on: September 9, 2012
Influence of DOAC Stop on coagulation assays in samples from patients on rivaroxaban or apixaban
Sean Platton1, Christina Hunt2
1The Royal London Hospital Haemophilia Centre, Barts Health NHS Trust, The Royal London Hospital, London, UK.
Insights
DOAC Stop effectively removes direct oral anticoagulant (DOAC) interference in clotting tests for rivaroxaban and apixaban. This aids in accurate laboratory screening for coagulopathy and lupus anticoagulants in treated patients.
Area of Science:
- Hematology
- Clinical Chemistry
- Pharmacology
Background:
- Direct oral anticoagulants (DOACs) are widely used but interfere with laboratory coagulation assays.
- Accurate interpretation of hemostasis tests in patients on DOACs is challenging due to variable drug interference.
- DOAC Stop is a novel agent designed to adsorb DOACs from plasma samples.
Purpose of the Study:
- To evaluate the efficacy of DOAC Stop in removing the interference of rivaroxaban and apixaban on various hemostasis assays.
- To assess if DOAC Stop enables more accurate interpretation of coagulation tests in patients treated with these DOACs.
Main Methods:
- Plasma samples from patients on rivaroxaban, apixaban, or no anticoagulant were analyzed.
- Standard coagulation tests including PT, APTT, anti-Xa assay, factor VIII assays, and DRVVT were performed.
- Tests were conducted before and after sample treatment with DOAC Stop.
Main Results:
- DOAC Stop significantly reversed the effects of rivaroxaban and apixaban on PT, APTT, anti-Xa activity, factor VIII, and DRVVT assays.
- The reagent reduced false positive lupus anticoagulant interpretations in patients on rivaroxaban.
- No impact on results was observed in non-anticoagulated patient samples.
Conclusions:
- DOAC Stop shows promise for laboratory screening of coagulopathy and lupus anticoagulants in patients on rivaroxaban or apixaban.
- Careful interpretation is advised as complete reversal of anti-Xa effects was not universally achieved.
Introduction:
Direct oral anticoagulants (DOACs) require no laboratory monitoring, but they interfere with almost all clotting tests to a varying degree, depending on the DOAC, assay principles and reagents used. DOAC Stop (Haematex Research, Sydney, Australia) has recently been shown to adsorb DOACs from spiked and patient plasmas. The aim of our work was to investigate the DOAC Stop effect on a range of haemostasis assays on plasmas collected from patients on rivaroxaban or apixaban, to see whether it removes the effect of these drugs to enable more accurate interpretation of coagulation assays.
Methods:
Samples from patients anticoagulated with either rivaroxaban, apixaban or no anticoagulant were tested for prothrombin time (PT), activated partial thromboplastin time (APTT), DOAC-specific anti-Xa assay, factor VIII (one-stage and chromogenic assay) and DRVVT (low and high phospholipid) before and after sample treatment with DOAC-Stop.
Results:
DOAC Stop significantly removed the effects of rivaroxaban and apixaban on PT, APTT, anti-Xa activity, factor VIII (one-stage and chromogenic assays), and DRVVT (low and high phospholipid reagents), and reduced the number of false positive of lupus anticoagulant interpretations in patients on rivaroxaban. There was no effect on the results from patients that were not anticoagulated.
Conclusion:
This small study suggests that it is likely that DOAC Stop can be used in laboratories to screen for coagulopathy or lupus anticoagulants in samples containing rivaroxaban or apixaban. Care should be taken in the interpretation of results since complete reversal of the anti-Xa effect did not occur in every sample.
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