Use of antithrombotic therapy in patients with hemophilia: a selected synopsis of the European Hematology Association - International Society on Thrombosis and Haemostasis - European Association for Hemophilia and Allied Disorders - European Stroke Organization Clinical Practice Guidance document
- PMID: 39571935
- DOI: 10.1016/j.jtha.2024.10.033
Use of antithrombotic therapy in patients with hemophilia: a selected synopsis of the European Hematology Association - International Society on Thrombosis and Haemostasis - European Association for Hemophilia and Allied Disorders - European Stroke Organization Clinical Practice Guidance document
Abstract
Here, we summarize the European Hematology Association - International Society on Thrombosis and Haemostasis - European Association for Hemophilia and Allied Disorders - European Stroke Organization Clinical Practice Guidance document recommendations on antithrombotic therapy for cardiovascular indications among patients with hemophilia. This summary includes a discussion on primary and secondary prevention of venous and arterial thrombosis. The guidance document considers distinct and controversial challenges presented by various clinical scenarios in this aging patient population and provides thoughtful recommendations to assist the hemophilia care provider in clinical decision-making.
Keywords: antithrombotic therapy; cardiovascular disease; clinical guidelines; hemophilia; venous thromboembolism.
Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of competing interests M.E.: consultancy fees from Novo Nordisk, BioMarin, CSL Behring, Genentech/Roche, Sanofi, Takeda, Pfizer, Bayer, Hemobiologics/LFB, Kedrion, and UniQure. Participated in clinical trials sponsored by Novo Nordisk, UniQure, Takeda, Bayer, Genentech/Roche, CSL Behring, and Sanofi. R.L.: consultancy fees from Alexion, AstraZeneca, Bayer, BioMarin, CSL Behring, Novo Nordisk, Pfizer, Roche, Sanofi, SOBI, and Takeda. T.O.: consulting fees from Bayer, Sobi, and Novo Nordisk. M.S.: unrestricted research funding from Octapharma, Pfizer, and Amgen (to the institution); honoraria from advisory boards from Amgen, Novartis, Octapharma, Pfizer, and Amgen. C.B.: none. M.S.: unrestricted research funding from Octapharma, Pfizer, and Amgen (to the institution); honoraria from advisory boards from Amgen, Novartis, Octapharma, Pfizer, and Amgen.
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