Abstract

BackgroundGuidance for periprocedural anticoagulant management is mainly based on limited data from Phase III or observational studies and expert opinion.HypothesisEMIT‐AF/VTE was designed to document the risks of bleeding and thromboembolic events in more than 1000 patients on edoxaban undergoing diagnostic and therapeutic procedures in clinical practice.MethodsRoutine care in a multinational multicenter, prospective observational study. Participants were adult patients with atrial fibrillation and/or venous thromboembolism treated with edoxaban for stroke prevention or for secondary prevention in venous thromboembolic disease, undergoing a wide range of diagnostic and therapeutic procedures. Edoxaban therapy was interrupted periprocedurally at the treating physician's discretion. Patients were evaluated from 5 days pre‐ until 30 days postprocedure. Primary outcome was the incidence of International Society on Thrombosis and Haemostasis defined major bleeding; secondary outcomes included incidence of clinically relevant non‐major bleeding, acute coronary syndrome, and acute thromboembolic events.ResultsOutcomes and management are reported for the first procedures in 1155 unselected patients. Five cases of major bleeding (0.4%) and eight of clinically relevant non‐major bleeding (0.7%) were documented, five (38%) of which occurred outside the period of likely edoxaban effect (last edoxaban dose ≥3 days prior to bleeding). Five (0.4%) deaths from any cause, seven acute thromboembolic events (0.6%) including two cardiac deaths (0.2%) in six patients, and one acute coronary event (0.1%) occurred.ConclusionsThe periprocedural bleeding and acute thromboembolic event risks for patients treated with edoxaban were low. This can help inform both clinical routine and guidelines for the periprocedural management of edoxaban.

Highlights

  • Guidance for periprocedural anticoagulant management is mainly basedHypothesis: EMIT-atrial fibrillation (AF)/venous thromboembolism (VTE) was designed to document the risks of bleeding and Hematology Department, Alicante University, Hospitals University Vinalopó Salut and Torrevieja Salut, Alicante, Spain thromboembolic events in more than 1000 patients on edoxaban undergoing diagnostic and therapeutic procedures in clinical practice.William Harvey Research Institute, BartsHealth NHS Trust, Charterhouse Square, London, UK

  • Hypothesis: EMIT-AF/VTE was designed to document the risks of bleeding and Hematology Department, Alicante University, Hospitals University Vinalopó Salut and Torrevieja Salut, Alicante, Spain thromboembolic events in more than 1000 patients on edoxaban undergoing diagnostic and therapeutic procedures in clinical practice

  • Participants were adult patients with atrial fibrillation and/or venous thromboembolism treated with edoxaban for stroke prevention or for secondary prevention in venous thromboembolic disease, undergoing a wide range of diagnostic and therapeutic procedures

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Summary

Background

Hypothesis: EMIT-AF/VTE was designed to document the risks of bleeding and Hematology Department, Alicante University, Hospitals University Vinalopó Salut and Torrevieja Salut, Alicante, Spain thromboembolic events in more than 1000 patients on edoxaban undergoing diagnostic and therapeutic procedures in clinical practice

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