Amerikanische Gesellschaft für Hirudotherapie

Sonorheometry parameters during dabigatran reversal with idarucizumab for major bleeding

Research article published in The Journal of pharmacology and experimental therapeutics (2025)

Zuletzt aktualisiert: June 18, 2026Geprüft von: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Observational studyKlinische StudienSpeichel-PharmakologieTeissandier D et al. · The Journal of pharmacology and experimental therapeutics, 2025

Abstract

Bleeding during oral anticoagulant therapy is currently codified by expert guidelines. Monitoring coagulation during bleeding events remains challenging. This study aimed to assess viscoelastic hemostatic assays (VHAs) using the Quantra analyzer (HemoSonics) in dabigatran-treated patients with International Society on Thrombosis and Haemostasis major bleeding. We conducted a prospective, multicenter study at 2 university hospitals from January 2021 to December 2023. VHA were evaluated using whole blood sample collected upon emergency admission and 30 minutes after reversal therapy. Six dabigatran-treated patients with major bleeding were included in this study and received idarucizumab: 4 patients with an intracranial bleeding and 2 with gastrointestinal major bleeding. Prior to reversal therapy, clot time (CT) and clot time with heparinase coagulation time (CTH) were prolonged beyond normal range for all patients but clot stiffness (CS) was notably low, indicating a hypocoagulable state. After idarucizumab administration, both CT (median [interquartile range], 179.5 s [169.3-238.5 s] vs 126 s [96-135.5 s]; P = .002) and CTH (181.5 s [166.3-224.3 s] vs 118.5 s [99.5-121.3 s], P = .002) significantly decreased, whereas CS increased significantly (median [interquartile range], 18 hPa [12.3-24.3 hPa] vs 26.6 hPa [25.5-33.8 hPa]; P = .03), all values falling within the normal range. Median anti-IIa activity at emergency arrivals decreased under 30 ng/mL 30 minutes, 6 hours, and 24 hours after idarucizumab administration (P = .0008). No complications were reported during follow-up. After idarucizumab administration, VHA demonstrated significant reductions in CT and CTH, with a corresponding increase in CS within normal ranges. These findings suggest that VHA using the Quantra analyzer may be a valuable tool in assessing the presence of dabigatran and the efficacy of idarucizumab reversal in patients with major bleeding. SIGNIFICANCE STATEMENT: This study highlights viscoelastic hemostatic assays using the Quantra analyzer to monitor reversal therapy in dabigatran-treated patients with major bleeding. It demonstrates the efficacy of idarucizumab in restoring coagulation parameters, offering insights into clinical management.

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

Publication typeJournal ArticleMulticenter Study
Indexed MeSH termsDabigatranHumansAntibodies, Monoclonal, HumanizedMaleFemaleAgedProspective StudiesAntithrombinsMiddle AgedBlood CoagulationHemorrhageAged, 80 and over

Zusammenfassung

Bleeding during oral anticoagulant therapy is currently codified by expert guidelines.

Warum dies für die Hirudotherapie relevant ist

This prospective, multicenter study assessed viscoelastic hemostatic assays (Quantra analyzer) in six dabigatran-treated patients with major bleeding (four intracranial, two gastrointestinal) who received idarucizumab, finding significant normalization of clot time, clot time with heparinase, and clot stiffness after reversal therapy, with no complications during follow-up. The abstract makes no mention of leeches, hirudotherapy, hirudin, or any leech-derived compounds, so no connection to ASH's domain can be established. The study is clinical in nature with a very small sample of six patients, focused entirely on pharmaceutical anticoagulant reversal monitoring, with no defensible relevance to hirudotherapy or the leech secretome.

Zitation

Sonorheometry parameters during dabigatran reversal with idarucizumab for major bleeding

Teissandier D et al. · The Journal of pharmacology and experimental therapeutics, 2025

Verwandter klinischer Kontext

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