Successful treatment with recombinant factor VIIa of therapy-resistant severe bleeding in a patient with acquired von Willebrand disease

P. W. Friederich, P. C. Wever, E. Briët, C. J. Doorenbos, M. [=Marcel M.] Levi

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Abstract

We describe an elderly man who presented with life-threatening hematuria and gastrointestinal bleeding caused by acquired von Willebrand disease associated with monoclonal gammopathy of undetermined significance (MGUS). Standard therapy with desmopressin, von Willebrand factor-containing factor VIII concentrate, tranexamic acid, and immunoglobulin failed to achieve adequate hemostasis. However, treatment with recombinant activated factor VII (rFVIIa) arrested the bleeding completely. Since acquired von Willebrand disease can lead to life-threatening hemorrhage, clinicians should consider rFVIIa as an effective treatment option if standard therapy fails
Original languageEnglish
Pages (from-to)292-294
JournalAmerican Journal of Hematology
Volume66
Issue number4
DOIs
Publication statusPublished - 2001

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