Literature DB >> 19149850

Prophylaxis in 10 patients with severe haemophilia A and inhibitor: different approaches for different clinical situations.

V Jiménez-Yuste1, M T Alvarez, M Martín-Salces, M Quintana, C Rodriguez-Merchan, C Lopez-Cabarcos, F Velasco, F Hernández-Navarro.   

Abstract

The effect of bypassing agents is not as predictable as replacement therapy with the deficient factor in inhibitor patients. Consequently, these patients have more levels of arthropathy than patients without inhibitors. Prophylaxis for inhibitor patients has gained attention over the last decade and some papers have reported that bypassing agents could work in the prevention of arthropathy. However, there is a lack data to support any specific agent or regimen or even to recommend their use in different clinical conditions. We report ten patients with haemophilia A and inhibitors treated prophylacticaly with bypassing agents (5 with FEIBA and 5 with NovoSeven). The variable conditioning the choice of one agent or the other was the intention to initiate of immune tolerance induction therapy (ITI) in the future. In 8/10 patients (4 in FEIBA group and 4 in rFVIIa group) there was a decrease of bleeding episodes while 9/10 maintained or increased their joint range of motion (ROM). In the rFVIIa prophylaxis group, prophylaxis can be considered primary since all of them had had less than one joint bleed before prophylaxis. Economic analysis showed that prophylaxis is an expensive treatment. In our experience both agents seem to be safe and effective in reducing the number of bleeds in patients with inhibitors. The anamnestic response provoked by FEIBA could be an issue while awaiting a decline in titres before ITI can be initiated and so rFVIIa may be the best option for prophylaxis in patients with inhibitors who have not yet begun ITI.

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Year:  2009        PMID: 19149850     DOI: 10.1111/j.1365-2516.2008.01915.x

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


  12 in total

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Authors:  Keith Gomez; Robert Klamroth; Johnny Mahlangu; Maria E Mancuso; María E Mingot; Margareth Castro Ozelo
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Review 2.  Clinical use and the Italian demand for activated prothrombin complex and activated recombinant factor VII concentrates.

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Journal:  Blood Transfus       Date:  2013-09       Impact factor: 3.443

3.  Thromboembolic event rate in patients exposed to anti-inhibitor coagulant complex: a meta-analysis of 40-year published data.

Authors:  Matteo Rota; Paolo A Cortesi; Roberto Crea; Alessandro Gringeri; Lorenzo G Mantovani
Journal:  Blood Adv       Date:  2017-12-12

4.  Redistribution and hemostatic action of recombinant activated factor VII associated with platelets.

Authors:  Irene Lopez-Vilchez; Ulla Hedner; Carmen Altisent; Maribel Diaz-Ricart; Gines Escolar; Ana M Galan
Journal:  Am J Pathol       Date:  2011-06       Impact factor: 4.307

5.  Animal models of FVIIa gene expression: their role in the future development of haemophilia treatment.

Authors:  A Obergfell; T Nichols; M Ezban
Journal:  Haemophilia       Date:  2010-03       Impact factor: 4.287

6.  Recombinant factor VIII in the management of hemophilia A: current use and future promise.

Authors:  Jerry S Powell
Journal:  Ther Clin Risk Manag       Date:  2009-05-20       Impact factor: 2.423

Review 7.  Optimal use of recombinant factor VIIa in the control of bleeding episodes in hemophilic patients.

Authors:  John Puetz
Journal:  Drug Des Devel Ther       Date:  2010-07-21       Impact factor: 4.162

8.  Critical appraisal of the role of recombinant activated factor VII in the treatment of hemophilia patients with inhibitors.

Authors:  Ampaiwan Chuansumrit; Pantep Angchaisuksiri; Nongnuch Sirachainan
Journal:  J Blood Med       Date:  2010-03-30

9.  Revisiting hemophilia management in acute medicine.

Authors:  Sandeep Sahu; Indu Lata; Surendra Singh; Mukesh Kumar
Journal:  J Emerg Trauma Shock       Date:  2011-04

10.  Barriers and perceived limitations to early treatment of hemophilia.

Authors:  Kapil Saxena
Journal:  J Blood Med       Date:  2013-05-16
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