Sociedad Americana de Hirudoterapia

Uninterrupted edoxaban vs. vitamin K antagonists for ablation of atrial fibrillation: the ELIMINATE-AF trial

Randomized controlled trial published in European heart journal (2019)

Última actualización: 18 de junio de 2026Revisado por: ASH Editorial Board
Artículo de investigación — revisión de evidenciaReferencia del artículo
Evidence: Randomized controlled trialEnsayos clínicosHohnloser SH et al. · European heart journal, 2019

Abstract

AIMS: Edoxaban is a direct factor Xa inhibitor approved for stroke prevention in atrial fibrillation (AF). Uninterrupted edoxaban therapy in patients undergoing AF ablation has not been tested. METHODS AND RESULTS: The ELIMINATE-AF trial, a multinational, multicentre, randomized, open-label, parallel-group study, was conducted to assess the safety and efficacy of once-daily edoxaban 60 mg (30 mg in patients indicated for dose reduction) vs. vitamin K antagonists (VKAs) in AF patients undergoing catheter ablation. Patients were randomized 2:1 to edoxaban vs. VKA. The primary endpoint (per-protocol population) was time to first occurrence of all-cause death, stroke, or International Society of Thrombosis and Haemostasis-defined major bleeding during the period from the end of the ablation procedure to end of treatment (90 days). Overall, 632 patients were enrolled, 614 randomized, and 553 received study drug and underwent ablation; 177 subjects underwent brain magnetic resonance imaging to assess silent cerebral infarcts. The primary endpoint (only major bleeds occurred) was observed in 0.3% (1 patient) on edoxaban and 2.0% (2 patients) on VKA [hazard ratio (95% confidence interval): 0.16 (0.02-1.73)]. In the ablation population (modified intent-to-treat population including patients with ablation), the primary endpoint was observed in 2.7% of edoxaban (N = 10) and 1.7% of VKA patients (N = 3) between start of ablation and end of treatment. There were one ischaemic and one haemorrhagic stroke, both in patients on edoxaban. Cerebral microemboli were detected in 13.8% (16) patients who received edoxaban and 9.6% (5) patients in the VKA group (nominal P = 0.62). CONCLUSION: Uninterrupted edoxaban therapy represents an alternative to uninterrupted VKA treatment in patients undergoing AF ablation.

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

Publication typeJournal ArticleMulticenter StudyRandomized Controlled TrialResearch Support, Non-U.S. Gov't
Indexed MeSH termsAgedAtrial FibrillationCatheter AblationCerebral HemorrhageFactor Xa InhibitorsFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedPostoperative HemorrhagePyridines

Resumen

Edoxaban is a direct factor Xa inhibitor approved for stroke prevention in atrial fibrillation (AF).

Por qué esto importa para la hirudoterapia

El ensayo ELIMINATE-AF fue un estudio multinacional aleatorizado que comparó edoxabán ininterrumpido, un inhibidor directo del factor Xa, con antagonistas de la vitamina K en pacientes sometidos a ablación por catéter de fibrilación auricular. El estudio concluyó que el edoxabán representa una alternativa segura a los antagonistas de la vitamina K. Aunque la investigación trata sobre anticoagulación —un proceso fisiológico fuertemente dirigido por las secreciones de las sanguijuelas— no involucra sanguijuelas ni terapéuticas derivadas de sanguijuelas. Su relevancia para la American Society of Hirudotherapy se limita al contexto clínico más amplio del manejo de la anticoagulación sistémica.

Citación

Uninterrupted edoxaban vs. vitamin K antagonists for ablation of atrial fibrillation: the ELIMINATE-AF trial

Hohnloser SH et al. · European heart journal, 2019

Contexto clínico relacionado

Añadido a la biblioteca ASH: May 27, 2026 · Última actualización del sitio: 18 de junio de 2026

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