Venous Thromboembolism Therapy with Edoxaban in Daily Care Patients: Results from the DRESDEN NOAC REGISTRY.
Research article published in TH open : companion journal to thrombosis and haemostasis (2025)
Abstract
Direct oral anticoagulants such as edoxaban are standard of care in current treatment of venous thromboembolism (VTE). However, phase III trial data need confirmation in real-world settings. We extracted data from the prospective, noninterventional multiple-indication DRESDEN NOAC REGISTRY to evaluate outcome rates during VTE treatment with edoxaban. Patients were included in this analysis, if they had acute VTE and if patient enrolment and edoxaban initiation occurred within 30 days after VTE diagnosis. Patient characteristics, treatment persistence, and clinical outcomes were centrally adjudicated using standard definitions. Until December 31, 2023, 323 acute VTE patients (median age 67 years, 56.7% male) were enrolled and initiated edoxaban within 7.8 ± 4.9 days (mean) for isolated deep vein thrombosis (DVT) (57.6%) or pulmonary embolism (PE) ± DVT (42.4%). Mean duration of follow-up was 3.9 ± 1.9 years with a mean duration of edoxaban exposure of 1.5 ± 1.7 years. During ongoing edoxaban therapy, 3/323 patients (0.9%) experienced recurrent VTE (0.6/100 patient-years); 141/323 (43.7%) patients reported clinically relevant International Society on Thrombosis and Haemostasis (ISTH) nonmajor bleeding and 16 reported ISTH major bleeding (5.0%; 3.2/100 patient-years). Death was observed in 53 patients (4.1/100 patient-years). At 6 months, 78.2% were still taking edoxaban, 2% were electively switched to dose-reduced secondary prophylaxis with apixaban 2.5 mg twice a day or rivaroxaban 10 mg once daily. The remaining patients had a scheduled end of VTE treatment (11.4%) or were switched to nonedoxaban therapeutic anticoagulation (6.2%). Our results indicate effectiveness of edoxaban in acute VTE treatment with excellent persistence in the treatment and low rates of unplanned discontinuation. Bleeding was frequently observed, but rates of major bleeding were low and comparable to phase III data.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Zusammenfassung
Direct oral anticoagulants such as edoxaban are standard of care in current treatment of venous thromboembolism (VTE). However, phase III trial data need confirmation in real-world settings.
Warum dies für die Hirudotherapie relevant ist
Diese prospektive, nicht-interventionelle Registeranalyse evaluierte Edoxaban zur Behandlung der akuten venösen Thromboembolie bei 323 Patienten aus dem DRESDEN NOAC REGISTRY und berichtete eine rezidivierende VTE-Rate von 0,6 pro 100 Patientenjahre, eine Rate schwerer Blutungen von 3,2 pro 100 Patientenjahre sowie eine hohe Therapiepersistenz nach 6 Monaten (78,2 %). Die Studie weist keine direkte Relevanz für die Hirudotherapie oder das Blutegelsekretom auf, da Edoxaban ein direkter oraler Faktor-Xa-Inhibitor ist, der nicht mit Hirudin oder einer anderen aus Blutegeln gewonnenen Substanz verwandt ist. Caveat: Es handelt sich um eine realweltliche Beobachtungs-Registeranalyse eines einzelnen oralen Antikoagulans; es besteht keine Beteiligung von Blutegeln, Hirudin, Bivalirudin oder aus Blutegeln stammenden Substanzen, und es gibt keine sinnvolle Verbindung zur Praxis der Hirudotherapie.
Zitation
Venous Thromboembolism Therapy with Edoxaban in Daily Care Patients: Results from the DRESDEN NOAC REGISTRY.
Tittl et al. · TH open : companion journal to thrombosis and haemostasis, 2025
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