The overall effectiveness of prophylaxis in severe haemophilia

Summary.  The aim of this retrospective review was to assess the overall effectiveness of prophylaxis when compared with on‐demand treatment of haemophilic patients. Twenty‐five children (22 with severe haemophilia A and three with severe haemophilia B) were evaluated. Five haemophilia A patients received primary prophylaxis (instituted before the onset of any joint bleed) while the other 17 haemophilia A and all three haemophilia B patients were on secondary prophylaxis. We compared factor usage, number of bleeding episodes, emergency room (ER) visits and hospitalizations while on prophylaxis to those while on demand therapy. All subjects were male, the median age at time of review was 11.4 years and at start of prophylaxis was 4.5 years. Thirteen of the 25 patients (52%) required indwelling venous catheters for access, seven of these had one or more (one–six) episodes of line sepsis. Haemophilia A patients received an average of 23.8 U kg−1 (20–30 U kg−1) of recombinant factor VIII three times a week while haemophilia B patients received 50 U kg−1 recombinant FIX twice weekly. There was a significant reduction in the mean number of major bleeds on prophylaxis from 15.5 to 1.9 per year and a significant decrease in target joints, ER visits and hospitalizations. Although factor usage per year was higher on prophylaxis, there was an overall reduction in number of bleeds and resultant decrease in hospitalizations and ER visits. By preventing new target joints, prophylaxis can lead to reduction in long‐term morbidity and a better quality of life despite increased central lines and higher factor usage.

[1]  C. Sabin,et al.  Assessing the effectiveness and cost‐effectiveness of prophylaxis against bleeding in patients with severe haemophilia and severe von Willebrand's disease , 1998, Journal of internal medicine.

[2]  I. Warrier,et al.  Use of central venous catheters in children with haemophilia: one haemophilia treatment centre experience , 1997, Haemophilia : the official journal of the World Federation of Hemophilia.

[3]  H. Pettersson,et al.  Haemophilia prophylaxis in young patients–a long‐term follow‐up , 1997, Journal of internal medicine.

[4]  M. Ragni,et al.  Central venous catheter infection in haemophiliacs undergoing prophylaxis or immune tolerance with clotting factor concentrate , 1997, Haemophilia : the official journal of the World Federation of Hemophilia.

[5]  S. Teutsch,et al.  Episodic versus prophylactic infusions for hemophilia A: a cost-effectiveness analysis. , 1996, The Journal of pediatrics.

[6]  K. Khair,et al.  The impact of prophylactic treatment on children with severe haemophilia , 1996, British journal of haematology.

[7]  A. Vora,et al.  Use of central venous catheters in children with severe congenital coagulopathy , 1995, British journal of haematology.

[8]  H. Pettersson,et al.  A longitudinal study of orthopaedic outcomes for severe factor‐VIII‐deficient haemophiliacs , 1994, Journal of internal medicine.

[9]  M. Manco‐Johnson,et al.  Results of secondary prophylaxis in children with severe hemophilia , 1994, American journal of hematology.

[10]  R. Talamini,et al.  Mitoxantrone in combination with etoposide and prednimustine in patients older than 70 years with unfavorable non-Hodgkin's lymphoma: a prospective study in 52 patients. , 1994, Seminars in hematology.

[11]  M. Manco‐Johnson,et al.  A prophylactic program in the United States : experience and issues , 1994 .

[12]  W. Schramm Experience with prophylaxis in Germany. , 1993, Seminars in hematology.

[13]  I. Nilsson Experience with prophylaxis in Sweden. , 1993, Seminars in hematology.

[14]  R. Ljung,et al.  Implantable central venous catheter facilitates prophylactic treatment in children with haemophilia , 1992, Acta paediatrica.

[15]  H. Pettersson,et al.  Twenty‐five years' experience of prophylactic treatment in severe haemophilia A and B , 1992, Journal of internal medicine.

[16]  M. Blombäck,et al.  Prophylaxis with factor concentrates in preventing hemophilic arthropathy. , 1991, The American journal of pediatric hematology/oncology.

[17]  J. Luck,et al.  Surgical management of advanced hemophilic arthropathy. , 1990, Progress in clinical and biological research.

[18]  J. Luck,et al.  Surgical management of advanced hemophilic arthropathy. An overview of 20 years' experience. , 1989, Clinical orthopaedics and related research.

[19]  G. Buchanan,et al.  Intracranial hemorrhage in newborn and young infants with hemophilia. , 1988, The Journal of pediatrics.

[20]  Å. Ahlberg Haemophilia in Sweden. VII. Incidence, treatment and prophylaxis of arthropathy and other musculo-skeletal manifestations of haemophilia A and B. , 1965, Acta orthopaedica Scandinavica. Supplementum.