Why the study?
Anticoagulants complicate coagulation assay interpretation, and no universal methodology across different anticoagulant classes is available to eliminate these interferences.
Does ciraparantag or DOAC-Stop remove DOAC- or heparin-associated interferences in routine coagulation testing in vitro?
Does ciraparantag or DOAC-Stop remove DOAC- or heparin-associated interferences in routine coagulation testing in vitro?
Ciraparantag is ineffective as an in vitro universal anticoagulant chelator for coagulation testing, but activated charcoal-based adsorbents like DOAC-Stop can mitigate interferences from DOACs and ciraparantag.
Answers are grounded in this paper and cite their sources.
Should not be used to neutralize anticoagulants before coagulation testing; leaves open a true universal in-vitro chelator.
Anticoagulants can complicate the interpretation of routine and specialised coagulation assays. Several methodologies have been developed to minimise or eliminate anticoagulant-associated interferences; however, no ‘universal methodology’ that encompasses different anticoagulant classes is currently available. Ciraparantag is a promising reversal agent that can bind both direct oral anticoagulants (DOACs) and heparin-like anticoagulants. As such, we aimed to investigate whether ciraparantag could be employed as a ‘universal’ anticoagulant chelator in vitro. Human plasma was spiked with ascending concentrations of ciraparantag, with or without DOACs or heparin, and assayed for routine coagulation parameters. Ciraparantag had minimal effects on coagulation testing when added to human plasma at concentrations similar to pharmacokinetic maxima; however, ciraparantag did not remove DOAC- or heparin-associated activities in vitro, which was likely due to the preferential chelation of anionic substances in the coagulation reagents. In contrast, DOAC-Stop™, a commercial activated charcoal-based adsorbent, efficiently removed both DOAC- and ciraparantag-associated interferences. In conclusion, although ciraparantag is not effective as a ‘universal’ anticoagulant chelator in vitro, we report that activated charcoal-based adsorbents may be clinically useful in situations where laboratory investigations are complicated by the presence of DOACs and/or ciraparantag.
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Harte et al. (2024) studied this question.
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