Thrombin generation for monitoring hemostatic therapy in hemophilia A: A narrative review

Patients with severe hemophilia A (HA) have an increased risk of spontaneous and trauma‐related bleeding because of a congenital absence of factor VIII (FVIII). Most severe HA patients use prophylactic FVIII concentrate, the effect of which can be monitored with FVIII activity level measurement. How...

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Detalles Bibliográficos
Autores principales: Verhagen, Marieke J. A., Valke, Lars L. F. G., Schols, Saskia E. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Review Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305107/
https://www.ncbi.nlm.nih.gov/pubmed/35034413
http://dx.doi.org/10.1111/jth.15640

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305107/
https://www.ncbi.nlm.nih.gov/pubmed/35034413
http://dx.doi.org/10.1111/jth.15640

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