Literature DB >> 18624696

Clinical efficacy in bleeding and surgery in von Willebrand patients treated with Fanhdi a highly purified, doubly inactivated FVIII/VWF concentrate.

F Hernandez-Navarro1, M Quintana, V Jimenez-Yuste, M T Alvarez, R Fernandez-Morata.   

Abstract

Therapy with factor VIII/von Willebrand factor (FVIII/VWF) concentrate is the mainstay therapy in patients with von Willebrand disease (VWD) unresponsive to desmopressin. There are several commercially available FVIII/VWF concentrates that have been tested in VWD patients. We retrospectively analized the clinical efficacy in bleeding episodes and surgery of a highly purified FVIII/VWF complex with two inactivation steps (Fanhdi) in VWD patients. Sixty patients were included in the study. Treatment schedule consisted of one or more doses (standard dose 40 IU/kg body weight of FVIII) of Fanhdi. One hundred and fifty bleeding episodes were treated. These were: 28 serious bleedings; 92 moderate and 30 mild. An excellent clinical efficacy in almost 95% of cases was observed. Fanhdi was administered during 66 surgical procedures (38 major and 28 minor) with an overall efficacy of 98%. Fanhdi a highly purified, doubly virus-inactivated FVIII/VWF concentrate, with a high content of active VWF and an excellent record of clinical safety, is a valid choice in treating VWD.

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Year:  2008        PMID: 18624696     DOI: 10.1111/j.1365-2516.2008.01784.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  4 in total

Review 1.  Current challenges in the diagnosis and management of patients with inherited von Willebrand's disease in Italy: an Expert Meeting Report on the diagnosis and surgical and secondary long-term prophylaxis.

Authors:  Piercarla Schinco; Giancarlo Castaman; Antonio Coppola; Dorina Cultrera; Cosimo Ettorre; Anna C Giuffrida; Emanuela Marchesini; Renato Marino; Marta Milan; Claudio Molinari; Simona M Siboni; Ezio Zanon; Augusto B Federici
Journal:  Blood Transfus       Date:  2017-05-26       Impact factor: 3.443

2.  A phase III study comparing secondary long-term prophylaxis versus on-demand treatment with vWF/FVIII concentrates in severe inherited von Willebrand disease.

Authors:  Flora Peyvandi; Giancarlo Castaman; Paolo Gresele; Raimondo De Cristofaro; Piercarla Schinco; Antonella Bertomoro; Massino Morfini; Gabriella Gamba; Giovanni Barillari; Víctor Jiménez-Yuste; Cristoph Königs; Alfonso Iorio; Augusto B Federici
Journal:  Blood Transfus       Date:  2019-02-04       Impact factor: 3.443

Review 3.  Tranexamic acid for treatment and prophylaxis of bleeding and hyperfibrinolysis.

Authors:  Ingrid Pabinger; Dietmar Fries; Herbert Schöchl; Werner Streif; Wolfgang Toller
Journal:  Wien Klin Wochenschr       Date:  2017-04-21       Impact factor: 1.704

4.  Clinical Efficacy and Safety of Fanhdi®, a Plasma-Derived VWF/Factor VIII Concentrate, in von Willebrand Disease in Spain: A Retrospective Study.

Authors:  Víctor Jiménez-Yuste; María Teresa Alvarez-Román; Ángeles Palomo Bravo; Bernardo J Galmes; Maria Del Mar Nieto Hernández; Olga Benítez Hidalgo; Cristina Marzo Alonso; Noelia Florencia Pérez González; Julia Coll; Ramiro Núñez; Marina Carrasco; Faustino García Candel; Jose Ramon Gonzalez-Porras; Carmen Hernández García; Maria José Varó Castro; Roser Mir
Journal:  Clin Appl Thromb Hemost       Date:  2022 Jan-Dec       Impact factor: 2.389

  4 in total

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