American Society of Hirudotherapy

Direct thrombin inhibitors and factor xa inhibitors can influence the diluted prothrombin time used as the initial screen for lupus anticoagulant

Research article published in Archives of pathology & laboratory medicine (2013)

Last Updated: June 18, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Research reportDrug DevelopmentOlah et al. · Archives of pathology & laboratory medicine, 2013

Abstract

CONTEXT: Lupus anticoagulant (LA) is a heterogeneous group of antiphospholipid antibodies. Among others, diluted prothrombin time (dPT) is a sensitive screening test for LA; however, the interpretation of LA tests is difficult in patients treated with anticoagulants. The effect of different types of anticoagulants on the result of LA tests, particularly on dPT, has not been studied extensively. OBJECTIVE: To determine whether the direct thrombin inhibitors lepirudin and argatroban and the predominantly factor Xa inhibitors enoxaparin, danaparoid, and fondaparinux could interfere with LA screening based on dPT. DESIGN: Each drug was added to normal and LA-positive plasmas in clinically relevant concentrations. Each sample was tested for dPT. Samples with factor Xa inhibitors were investigated before and after addition of heparinase. Mixing and confirmatory tests for LA were not performed. RESULTS: In the presence of lepirudin or argatroban, dPT increased notably and the dPT ratio exceeded the cutoff value even at subtherapeutic concentrations resulting in false positivity. With increasing factor Xa inhibitor concentrations, a linear increase of dPT ratios and false-positive results were also demonstrated. Although heparinase could almost completely neutralize the anti-Xa effect of all investigated factor Xa inhibitors, dPT ratio returned to the basal level only in case of enoxaparin. CONCLUSIONS: Here we provide evidence that both the direct thrombin and indirect factor Xa inhibitors influence dPT assay for LA, causing false positivity. This should be considered when interpreting LA results during anticoagulant therapy. However, dPT seems to be a reliable test for LA screening under enoxaparin therapy after neutralization by heparinase.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal ArticleResearch Support, Non-U.S. Gov't
Indexed MeSH termsAnticoagulantsAntithrombinsArginineChondroitin SulfatesDermatan SulfateEnoxaparinFactor Xa InhibitorsFalse Positive ReactionsFondaparinuxHeparan SulfateHirudinsHumans

Summary

Peer-reviewed pharmacology and drug-development research relevant to antithrombotic agents and leech-derived compounds. Indexed in PubMed and verified against the NCBI record.

Why This Matters for Hirudotherapy

In this in vitro plasma-spiking study, the direct thrombin inhibitors lepirudin (a recombinant hirudin) and argatroban, plus the factor Xa inhibitors enoxaparin, danaparoid, and fondaparinux, were added to normal and lupus-anticoagulant-positive plasma to test their effect on the diluted prothrombin time (dPT) screen; the thrombin inhibitors raised the dPT ratio into false-positive range even at subtherapeutic levels, and Xa inhibitors caused a concentration-dependent false positivity that heparinase reversed completely only for enoxaparin. The hirudotherapy relevance lies in lepirudin, a hirudin analogue derived from the medicinal-leech secretome, demonstrating that hirudin-class direct thrombin inhibitors can confound a common coagulation assay. Being a controlled laboratory study without mixing/confirmatory LA testing, it informs interpretation of lab tests rather than any patient outcome, and it does not evaluate leech therapy clinically.

Citation

Direct thrombin inhibitors and factor xa inhibitors can influence the diluted prothrombin time used as the initial screen for lupus anticoagulant.

Olah et al. · Archives of pathology & laboratory medicine, 2013

Added to ASH library: May 28, 2026 · Site last updated: June 18, 2026

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