Rapid assessment of direct oral anticoagulants in acute stroke—An educational systematic review

Author:

Mbroh Joshua12ORCID,Birschmann Ingvild3,Ebner Matthias456,Kremer Hovinga Johanna A.7,Lindhoff-Last Edelgard8,Purrucker Jan9,Schäfer Simon T.10,Tünnerhoff Johannes12,Wang Yi12,Poli Sven12ORCID

Affiliation:

1. Department of Neurology & Stroke, University of Tübingen, Tübingen, Germany

2. Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany

3. Institute for Laboratory and Transfusion Medicine, Heart and Diabetes Center, Ruhr University, Bad Oeynhausen, Germany

4. Deutsches Herzzentrum der Charité, Department of Cardiology, Angiology and Intensive Care Medicine, Berlin, Germany

5. Charité - Universitätsmedizin Berlin, Corporate member of Freie Universität Berlin and Humboldt Universität zu Berlin, Berlin, Germany

6. German Center for Cardiovascular Research (DZHK), Partner site Berlin, Berlin, Germany

7. Department of Hematology and Central Hematology Laboratory, Bern University Hospital, University of Bern, Bern, Switzerland

8. Vascular Center, Coagulation Center and Coagulation Research Center, CardioAngiology Center (CCB) Bethanienhospital, Frankfurt, Germany

9. Department of Neurology, Heidelberg University Hospital, Heidelberg, Germany

10. Department of Anesthesia, Intensive Care Medicine, Emergency Medicine and Pain Therapy, University Hospital, Carl-von-Ossietzky University Oldenburg, Klinikum Oldenburg AöR, Oldenburg, Germany

Abstract

Purpose: To provide an overview on commercially available point-of-care tests (POCT) for rapid assessment of direct oral anticoagulant (DOAC) activity, their diagnostic accuracy in identifying blood samples containing clinically relevant DOAC concentrations, and guidance on selecting the appropriate POCT system/assay for decision-making in emergencies. Methods: Systematic review with PubMed and Cochrane library search for published studies until September 6, 2024. Papers were included if in English, original research using blood samples from DOAC patients and POCT was implemented. Two reviewers assessed studies for eligibility and quality. Data from studies were aggregated and diagnostic accuracy at DOAC plasma thresholds of 30/50/100 ng/ml was recalculated. Findings: 16 studies involving four commercially available POCT systems/assays were identified. Eleven studies evaluated blood-based POCT and five used urine for indirect estimation of DOAC plasma levels. Discussion: DOAC Dipsticks do not require knowledge about the taken DOAC, but measure urine and, due to low specificity, require blood testing in case of positive results. Hemochron Signature Elite (HSE) and CoaguChek use global coagulation assays and provide high sensitivity for edoxaban and rivaroxaban, HSE additionally for dabigatran. Due to insufficient correlation, both POCT are not recommended for apixaban, CoaguChek also not for dabigatran. The thromboelastometric ClotPro performs well for all DOAC, does not require knowledge about the DOAC, but was taken off the market recently. Conclusion: Studies have shown feasibility of POCT in identifying blood samples containing clinically relevant DOAC plasma concentrations. Each POCT device has its own unique limitations. Knowledge about the POCT assays, time since last intake and type of DOAC enhances confidence in making appropriate therapeutic decisions. We propose an algorithm that could help guiding physicians in selecting an appropriate POCT system/assay in DOAC-related emergencies.

Publisher

SAGE Publications

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