Literature DB >> 11554944

Rationale for the use of high dose rFVIIa in a high-titre inhibitor patient with haemophilia B during major orthopaedic procedures.

H A Cooper1, C P Jones, E Campion, H R Roberts, U Hedner.   

Abstract

Inhibitor development is a serious complication in patients with haemophilia A and B. Historically, a lack of optimal therapies and factor products for treating inhibitor patients resulted in many patients developing chronic haemophilic arthropathies and flexion contractures of the involved joints. The introduction of immune-tolerance protocols to eradicate high-titre inhibitors has greatly diminished the incidence of these types of complications but as in the case reported here, immune tolerance is not always successful. Various elective surgical procedures were often delayed or not even considered in patients with inhibitor because of the variability in achieving adequate haemostasis and the thrombotic risks involved with the use of activated prothrombin-complex concentrates (APCCs) over extended periods of time. The development of recombinant factor VIIa (rFVIIa; NovoSeven) and its demonstrated safety and efficacy in treating inhibitor patients has opened new possibilities for addressing severe arthropathy with flexion contracture. This case report demonstrates that the use of rFVIIa in such a situation must include dosing flexibility that is both patient-specific and related to the potential for bleeding; the ability to maintain clinical haemostasis with a prophylactic dose of rFVIIa given as little as once daily; and the capacity for higher doses of rFVIIa, particularly in children because their kinetic profiles differ from adults.

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Year:  2001        PMID: 11554944     DOI: 10.1046/j.1365-2516.2001.00553.x

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


  8 in total

1.  Pseudoprolongation of the prothrombin time during treatment with recombinant factor VIIa for bleeding in a patient with a spontaneous factor VIII inhibitor.

Authors:  Marcus E Carr; Jan G Kuhn; Erika J Martin; Ann R Tidwell; Maura K Hagan
Journal:  Int J Hematol       Date:  2003-04       Impact factor: 2.490

Review 2.  Recombinant factor VIIa: a review on its clinical use.

Authors:  Massimo Franchini
Journal:  Int J Hematol       Date:  2006-02       Impact factor: 2.490

3.  Recombinant factor VIIa analog NN1731 (V158D/E296V/M298Q-FVIIa) enhances fibrin formation, structure and stability in lipidated hemophilic plasma.

Authors:  Laura D Gray; Michael A Hussey; Brittany M Larson; Kellie R Machlus; Robert A Campbell; Gary Koch; Mirella Ezban; Ulla Hedner; Alisa S Wolberg
Journal:  Thromb Res       Date:  2011-05-10       Impact factor: 3.944

Review 4.  Advances in bypassing agent therapy for hemophilia patients with inhibitors to close care gaps and improve outcomes.

Authors:  Amy D Shapiro; Ulla Hedner
Journal:  Ther Adv Drug Saf       Date:  2011-10

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

Review 6.  Evidence supporting the use of recombinant activated factor VII in congenital bleeding disorders.

Authors:  Pär I Johansson; Sisse R Ostrowski
Journal:  Drug Des Devel Ther       Date:  2010-07-21       Impact factor: 4.162

7.  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

Review 8.  Recombinant activated clotting factor VII (rFVIIa) in the treatment of surgical and spontaneous bleeding episodes in hemophilic patients.

Authors:  Heng Joo Ng; Lai Heng Lee
Journal:  Vasc Health Risk Manag       Date:  2006
  8 in total

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