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Published on: June 4, 2020
Advancing Point-of-Care Analysis: The Future of Thromboelastographic DOAC-Detection: A Systematic Review
Gerrit U Herpertz1, Johannes Altmann1, Sven Poli2,3
1Department of Anaesthesiology, Intensive Care Medicine, Emergency Medicine and Pain Medicine, Carl von Ossietzky Universität Oldenburg, Klinikum Oldenburg, Oldenburg, Germany.
Modified viscoelastic testing (VET) assays show promise for rapidly detecting direct oral anticoagulants (DOACs) in emergencies. Ecarin tests reliably detect dabigatran, while other modified VET assays show potential for factor Xa inhibitors.
Area of Science:
- Clinical Chemistry and Hematology
- Pharmacology and Toxicology
- Point-of-Care Diagnostics
Background:
- Direct oral anticoagulants (DOACs) are increasingly used, necessitating rapid activity assessment in emergencies.
- Conventional viscoelastic testing (VET) lacks sensitivity for DOAC detection.
- Novel VET assays with specific activators are being developed for DOAC monitoring.
Purpose of the Study:
- To systematically review recent advances in VET-based DOAC detection.
- To evaluate the diagnostic performance of novel assay strategies.
- To assess the correlation between VET assay results and plasma DOAC concentrations.
Main Methods:
- Systematic literature search of PubMed and Google Scholar (January 2019-June 2025).
- Inclusion of 12 studies meeting PRISMA 2020 recommendations.
- Analysis of modified VET assays, including ecarin-based, Russell's Viper Venom, factor Xa-based, and low-tissue-factor activation methods.
Main Results:
- Ecarin-based assays showed 100% sensitivity and specificity for dabigatran.
- Modified assays for factor Xa inhibitors demonstrated variable but good correlation with drug levels (r=0.571-0.969).
- Sensitivities for factor Xa inhibitors ranged from 83% (apixaban) to 100% (rivaroxaban, edoxaban), with specificities of 62-100%.
Conclusions:
- Modified VET assays offer potential as rapid point-of-care tools for DOAC detection in emergency settings.
- Ecarin-based tests are reliable for dabigatran; Russell's Viper Venom and low-tissue-factor assays show promise for factor Xa inhibitors.
- Further clinical validation and standardization are essential for routine implementation.
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