Literature DB >> 26674816

Beyond stopping the bleed: short-term episodic prophylaxis with recombinant activated factor FVII in haemophilia patients with inhibitors.

Silva Zupančić Šalek1, Günter Auerswald2, Gary Benson3, Gerry Dolan4, Anne Duffy5, Cedric Hermans6, Victor Jiménez-Yuste7, Rolf Ljung8, Massimo Morfini9, Elena Santagostino10, Thierry Lambert11.   

Abstract

Preventing haemarthroses and arthropathy is a major challenge in patients with haemophilia and inhibitors, as treatment options are limited. One potential strategy is short-term episodic prophylaxis, which extends bypassing agent therapy beyond the resolution of bleeding to include the post-bleed inflammatory phase. At the 13th Zürich Haemophilia Forum, an expert panel reviewed the rationale behind this strategy, explored its current use with recombinant activated factor VII (rFVIIa) and considered treatment monitoring and optimisation. Two protocols are currently used for short-term episodic prophylaxis, both of which stipulate on-demand rFVIIa until resolution of bleeding, followed by daily dosing for ≥3 days to prevent re-bleeds. Short-term episodic prophylaxis should be individualised to optimise outcomes, perhaps through early treatment initiation or by combining rFVIIa with other treatments (e.g. factor VIII, tranexamic acid). Encouraging treatment compliance can also improve outcomes. Additionally, there is a need to develop objective clinical outcome measures, biomarkers and imaging protocols that can monitor treatment outcomes and joint disease in patients with inhibitors. A proactive approach incorporating a systematic package of care is needed. Currently, short-term episodic prophylaxis with rFVIIa may be an alternative treatment option to on-demand treatment for patients with inhibitors.

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Year:  2015        PMID: 26674816      PMCID: PMC5269432          DOI: 10.2450/2015.0127-15

Source DB:  PubMed          Journal:  Blood Transfus        ISSN: 1723-2007            Impact factor:   3.443


  38 in total

1.  Combination of FVIII and by-passing agent potentiates in vitro thrombin production in haemophilia A inhibitor plasma.

Authors:  Jenny Klintman; Jan Astermark; Erik Berntorp
Journal:  Br J Haematol       Date:  2010-10-01       Impact factor: 6.998

Review 2.  Understanding haemophilic arthropathy: an exploration of current open issues.

Authors:  Nathalie W D Jansen; Goris Roosendaal; Floris P J G Lafeber
Journal:  Br J Haematol       Date:  2008-10-02       Impact factor: 6.998

3.  The value of early treatment in patients with haemophilia and inhibitors.

Authors:  K Kavakli; A Yesilipek; B Antmen; S Aksu; C Balkan; D Yilmaz; A Kupesiz; I Sasmaz; P Lindgren; J Mesterton
Journal:  Haemophilia       Date:  2010-01-18       Impact factor: 4.287

4.  Sequential therapy with activated prothrombin complex concentrates and recombinant FVIIa in patients with severe haemophilia and inhibitors: update of our previous experience.

Authors:  J Schneiderman; E Rubin; D J Nugent; G Young
Journal:  Haemophilia       Date:  2007-05       Impact factor: 4.287

Review 5.  Paediatric haemophilia with inhibitors: existing management options, treatment gaps and unmet needs.

Authors:  E Santagostino; M Morfini; G K-H Auerswald; G M Benson; S Z Salek; T Lambert; P Salaj; V Jimenez-Yuste; R C R Ljung
Journal:  Haemophilia       Date:  2009-09       Impact factor: 4.287

6.  A new approach to treatment of bleeding episodes in young hemophilia patients: a single bolus megadose of recombinant activated factor VII (NovoSeven).

Authors:  G Kenet; A Lubetsky; J Luboshitz; U Martinowitz
Journal:  J Thromb Haemost       Date:  2003-03       Impact factor: 5.824

7.  Concomitant infusion of low doses of rFVIIa and FEIBA in haemophilia patients with inhibitors.

Authors:  U Martinowitz; T Livnat; A Zivelin; G Kenet
Journal:  Haemophilia       Date:  2009-04-07       Impact factor: 4.287

Review 8.  The burden of bleeding in haemophilia: is one bleed too many?

Authors:  A Gringeri; B Ewenstein; A Reininger
Journal:  Haemophilia       Date:  2014-01-29       Impact factor: 4.287

9.  Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia.

Authors:  Marilyn J Manco-Johnson; Thomas C Abshire; Amy D Shapiro; Brenda Riske; Michele R Hacker; Ray Kilcoyne; J David Ingram; Michael L Manco-Johnson; Sharon Funk; Linda Jacobson; Leonard A Valentino; W Keith Hoots; George R Buchanan; Donna DiMichele; Michael Recht; Deborah Brown; Cindy Leissinger; Shirley Bleak; Alan Cohen; Prasad Mathew; Alison Matsunaga; Desiree Medeiros; Diane Nugent; Gregory A Thomas; Alexis A Thompson; Kevin McRedmond; J Michael Soucie; Harlan Austin; Bruce L Evatt
Journal:  N Engl J Med       Date:  2007-08-09       Impact factor: 91.245

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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  3 in total

Review 1.  Intracranial haemorrhage in children and adults with haemophilia A and B: a literature review of the last 20 years.

Authors:  Ezio Zanon; Samantha Pasca
Journal:  Blood Transfus       Date:  2018-02-04       Impact factor: 3.443

2.  Emicizumab for the treatment of haemophilia A: a narrative review.

Authors:  Massimo Franchini; Giuseppe Marano; Ilaria Pati; Fabio Candura; Samantha Profili; Eva Veropalumbo; Francesca Masiello; Liviana Catalano; Vanessa Piccinini; Stefania Vaglio; Simonetta Pupella; Giancarlo M Liumbruno
Journal:  Blood Transfus       Date:  2019-05       Impact factor: 3.443

Review 3.  Factors affecting the quality, safety and marketing approval of clotting factor concentrates for haemophilia.

Authors:  Albert Farrugia; Giancarlo M Liumbruno; Fabio Candura; Samantha Profili; Josephine Cassar
Journal:  Blood Transfus       Date:  2018-09-03       Impact factor: 3.443

  3 in total

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