Maintenance Therapy with Activated Prothrombin Complex Concentrate (aPCC) for Hemophilia Patients with High Levels of Responding Inhibitors

Background: Eleven percent of severe hemophilia A patients and 5% of severe hemophilia B patients may develop inhibitors. We have conducted aPCC-based maintenance therapy for hemophilia patients with high levels of responding inhibitors and we analyzed the efficacy, safety, the factor consumption and the expense of this treatment, as compared to on-demand therapy. Methods: Eleven hemophilia patients with high levels of responding inhibitors were eligible for the study. We tried to evaluate the longitudinal bleeding episodes, the inhibitor titers, the X-ray findings, the adverse events and the factor consumption between on-demand therapy and maintenance therapy. The bypassing agent in this study was aPCC having a longer half-life. The dosage was 30 ∼50 U/kg, 3 times a week. Results: The mean follow-up period was 6.8 months for on-demand therapy and 10.6 months for main- tenance therapy. The mean dosage of aPCC was 45.2 U/kg. The episodes of hemarthrosis decreased by 61.4% (P=0.003) and other significant bleedings decreased by 45.2% (P=0.109). The inhibitor titers de- creased in 7 patients and these increased in 4 patients, but anamnesis took place in only 1 patient. Radiologically, 2 patients improved, 1 patient got worse and 7 patients were stable. Neither adverse signs nor symptoms were noticed. The mean factor consumption changed from 55.8×103 U for aPCC and 48.6

[1]  L. Valentino The benefits of prophylactic treatment with APCC in patients with haemophilia and high‐titre inhibitors: a retrospective case series , 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

[2]  V. Jiménez‐Yuste,et al.  Experiences in the prevention of arthropathy in haemophila patients with inhibitors , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

[3]  J. Blatny,et al.  Prophylactic treatment of haemophilia patients with inhibitors: clinical experience with recombinant factor VIIa in European Haemophilia Centres , 2007, Haemophilia : the official journal of the World Federation of Hemophilia.

[4]  B. Konkle,et al.  Randomized, prospective clinical trial of recombinant factor VIIa for secondary prophylaxis in hemophilia patients with inhibitors , 2007, Journal of thrombosis and haemostasis : JTH.

[5]  L. Valentino,et al.  Prophylactic treatment with activated prothrombin complex concentrate (FEIBA®) reduces the frequency of bleeding episodes in paediatric patients with haemophilia A and inhibitors , 2007, Haemophilia : the official journal of the World Federation of Hemophilia.

[6]  C. Négrier,et al.  A retrospective postlicensure survey of FEIBA efficacy and safety , 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

[7]  B. Siegmund,et al.  Prophylactic treatment with FEIBA of a haemophilia A patient with inhibitor: what are the costs, what are the benefits? , 2005, Haemophilia : the official journal of the World Federation of Hemophilia.

[8]  B. Ewenstein,et al.  FEIBA® safety profile in multiple modes of clinical and home‐therapy application , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

[9]  P. Giangrande,et al.  Pharmacokinetics of activated recombinant coagulation factor VII (NovoSeven®) in children vs. adults with haemophilia A , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

[10]  E. Rodríguez‐Merchán,et al.  The haemophilic joints: new perspectives , 2004 .

[11]  J. Astermark,et al.  Monitoring the bioavailability of FEIBA with a thrombin generation assay , 2003, Journal of thrombosis and haemostasis : JTH.

[12]  A. Mäkipernaa,et al.  Long‐term FEIBA prophylaxis does not prevent progression of existing joint disease , 2003, Haemophilia : the official journal of the World Federation of Hemophilia.

[13]  Dong Chan Kim,et al.  The Effects of Measurement Time and Blood Temperature on Thromboelastographic Parameters , 2002 .

[14]  Leissinger Use of prothrombin complex concentrates and activated prothrombin complex concentrates as prophylactic therapy in haemophilia patients with inhibitors , 1999, Haemophilia : the official journal of the World Federation of Hemophilia.

[15]  C. Rothschild,et al.  Multicenter Retrospective Study on the Utilization of FEIBA in France in Patients with Factor VIII and Factor IX Inhibitors , 1997, Thrombosis and Haemostasis.

[16]  M. Morfini,et al.  The Design and Analysis of Half-Life and Recovery Studies for Factor VIII and Factor IX , 1991, Thrombosis and Haemostasis.

[17]  H. Riess,et al.  Coagulation changes and the influence of the early perfusate in the course of orthotopic liver transplantation (OLT) when aprotinin is used intra‐operatively , 1991, Blood Coagulation and Fibrinolysis.

[18]  T. Barrowcliffe,et al.  Factor VIII inhibitor bypassing activity: a suggested mechanism of action. , 1981, Thrombosis research.

[19]  M. Hilgartner,et al.  Hemophilic arthropathy. Current concepts of pathogenesis and management. , 1977, The Journal of bone and joint surgery. American volume.