Literature DB >> 19016901

Differential response to bypassing agents complicates treatment in patients with haemophilia and inhibitors.

E Berntorp1.   

Abstract

The bypassing agents factor eight inhibitor bypassing activity (FEIBA) anti-inhibitor coagulant complex and recombinant activated factor VII (rFVIIa) have been established as safe and effective therapies for treating bleeding episodes in haemophilia patients with inhibitors. However, the efficacy of each bypassing agent can vary, and neither agent is universally effective. The reasons for such variability have yet to be confirmed, but may involve patient-specific factors and the mechanisms of action (MOAs) and pharmacokinetic profiles of these two agents. This issue underscores the necessity of both products in the comprehensive care of patients with haemophilia and inhibitors. The objective of this review is to discuss the evidence of a differential haemostatic response to bypassing agents and the potential roles of MOA and patient-specific factors in contributing to the differences in response.

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Year:  2008        PMID: 19016901     DOI: 10.1111/j.1365-2516.2008.01931.x

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


  18 in total

1.  Tissue factor pathway inhibitor in activated prothrombin complex concentrates (aPCC) moderates the effectiveness of therapy in some severe hemophilia A patients with inhibitor.

Authors:  Kenichi Ogiwara; Keiji Nogami; Tomoko Matsumoto; Midori Shima
Journal:  Int J Hematol       Date:  2014-04-01       Impact factor: 2.490

Review 2.  Rendering factor Xa zymogen-like as a therapeutic strategy to treat bleeding.

Authors:  Nabil K Thalji; Rodney M Camire
Journal:  Curr Opin Hematol       Date:  2017-09       Impact factor: 3.284

3.  Zymogen-like factor Xa variants restore thrombin generation and effectively bypass the intrinsic pathway in vitro.

Authors:  Matthew W Bunce; Raffaella Toso; Rodney M Camire
Journal:  Blood       Date:  2010-09-23       Impact factor: 22.113

4.  Intravascular inhibition of factor VIIa and the analogue NN1731 by antithrombin.

Authors:  Lars C Petersen; Ditte M Karpf; Henrik Agersø; Mette B Hermit; Hermann Pelzer; Egon Persson; Timothy C Nichols; Mirella Ezban
Journal:  Br J Haematol       Date:  2010-11-18       Impact factor: 6.998

Review 5.  The role of recombinant activated factor VII in the haematological management of elective orthopaedic surgery in haemophilia A patients with inhibitors.

Authors:  Giancarlo Castaman
Journal:  Blood Transfus       Date:  2017-05-16       Impact factor: 3.443

Review 6.  Acquired hemophilia: a rare but life-threatening potential cause of bleeding in the intensive care unit.

Authors:  Aryeh Shander; Christopher E Walsh; Caroline Cromwell
Journal:  Intensive Care Med       Date:  2011-05-31       Impact factor: 41.787

7.  Attempts to treat patients with hemophilia, the "royal disease".

Authors:  Rojin Park
Journal:  Blood Res       Date:  2013-12

8.  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 9.  Thrombin generation and whole blood viscoelastic assays in the management of hemophilia: current state of art and future perspectives.

Authors:  Guy Young; Benny Sørensen; Yesim Dargaud; Claude Negrier; Kathleen Brummel-Ziedins; Nigel S Key
Journal:  Blood       Date:  2013-01-14       Impact factor: 22.113

10.  The effect of emicizumab and bypassing agents in patients with hemophilia - An in vitro study.

Authors:  Nina Haagenrud Schultz; Heidi Glosli; Stine Bjørnsen; Pål Andre Holme
Journal:  Res Pract Thromb Haemost       Date:  2021-06-27
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