Secondary prophylaxis treatment versus on‐demand treatment for patients with severe haemophilia A: comparisons of cost and outcomes in Taiwan

Summary.  This study compared secondary prophylaxis treatment with on‐demand treatment for severe haemophilia A in Taiwan. Fifty patients from one medical centre were evaluated over a 5‐year period. Differences in annual bleed rates and factor VIII (FVIII) utilization were assessed between patients receiving secondary prophylaxis and patients receiving FVIII concentrates on‐demand. Results were then used as inputs in a pharmacoeconomic model to predict outcomes of future haemophilia therapy strategies in Taiwan. The median annual number of total bleeding episodes was significantly lower in the 13 (26%) patients who received secondary prophylaxis than in the 37 patients who received FVIII on‐demand (7.76 vs. 31.91, P < 0.0001). The between‐group difference in median annual factor VIII utilization was statistically significant (1824.41 IU kg−1 for the prophylaxis group and 1324.81 IU kg−1 for the on‐demand group, P < 0.01). It was estimated that approximately $2 million (USD) per year would be added to the cost of treatment by having all severe haemophilia A patients in Taiwan receive secondary prophylaxis instead of on‐demand therapy while 12 566 bleeding will be prevented. It is recommended that National Health Insurance officials utilize these data to evaluate the benefits of enhanced treatment strategies and before making substantial policy changes to haemophilia care in Taiwan.

[1]  J. Mahlangu,et al.  Guidelines for the management of hemophilia , 2013, Haemophilia : the official journal of the World Federation of Hemophilia.

[2]  C. Sabin,et al.  Cost-Utility Analysis of Primary Prophylaxis versus Treatment On-Demand for Individuals with Severe Haemophilia , 2012, PharmacoEconomics.

[3]  L. Valentino,et al.  Factor VIII prophylaxis for adult patients with severe haemophilia A: results of a US survey of attitudes and practices , 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

[4]  Y. Suzuki,et al.  Assessment of haemophilia treatment practice pattern in Japan , 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

[5]  M. Franchini,et al.  Prophylaxis in people with haemophilia , 2009, Thrombosis and Haemostasis.

[6]  R. Madhok,et al.  Challenges and controversies in haemophilia care in adulthood , 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

[7]  A. Tagliaferri,et al.  Secondary prophylaxis in adolescent and adult haemophiliacs. , 2008, Blood transfusion = Trasfusione del sangue.

[8]  P. Mannucci,et al.  Effects of secondary prophylaxis started in adolescent and adult haemophiliacs , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

[9]  P. Q. Chen,et al.  Total knee arthroplasty for severe haemophilic arthropathy: long‐term experience in Taiwan , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

[10]  J. Astermark,et al.  European principles of haemophilia care , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

[11]  L. Valentino,et al.  Optimizing outcomes for patients with severe haemophilia A , 2007, Haemophilia : the official journal of the World Federation of Hemophilia.

[12]  R. Ljung Prevention of bleeding in haemophilia: trends, overcoming barriers and future treatment options , 2007 .

[13]  C. Hermans,et al.  Should prophylaxis be used in adolescent and adult patients with severe haemophilia? An European survey of practice and outcome data , 2007, Haemophilia : the official journal of the World Federation of Hemophilia.

[14]  Alan R. Cohen,et al.  Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia. , 2007, The New England journal of medicine.

[15]  M. Carcao,et al.  Prophylaxis in the haemophilia population‐optimizing therapy , 2007, Haemophilia : the official journal of the World Federation of Hemophilia.

[16]  D. Nugent,et al.  Evidence for the benefits of prophylaxis in the management of hemophilia A , 2006, Thrombosis and Haemostasis.

[17]  S. Donadel-Claeyssens Current co‐ordinated activities of the PEDNET (European Paediatric Network for Haemophilia Management) , 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

[18]  J. Maahs,et al.  Practice patterns in haemophilia A therapy – global progress towards optimal care , 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

[19]  K. Fischer,et al.  Can long‐term prophylaxis for severe haemophilia be stopped in adulthood? Results from Denmark and the Netherlands , 2005, British journal of haematology.

[20]  U. Siebert,et al.  Cost effectiveness of haemophilia treatment: a cross-national assessment , 2005, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

[21]  L. Valentino Secondary prophylaxis therapy: what are the benefits, limitations and unknowns? , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

[22]  B. Lindgren,et al.  On‐demand vs. prophylactic treatment for severe haemophilia in Norway and Sweden: differences in treatment characteristics and outcome , 2003, Haemophilia : the official journal of the World Federation of Hemophilia.

[23]  I. Warrier,et al.  The overall effectiveness of prophylaxis in severe haemophilia , 2003, Haemophilia : the official journal of the World Federation of Hemophilia.

[24]  J. Astermark,et al.  Consensus perspectives on prophylactic therapy for haemophilia: summary statement , 2003, Haemophilia : the official journal of the World Federation of Hemophilia.

[25]  A. Gringeri Prospective controlled studies on prophylaxis: an Italian approach , 2003, Haemophilia : the official journal of the World Federation of Hemophilia.

[26]  Hsing-Yi Chang,et al.  Prevalence of dyslipidemia and mean blood lipid values in Taiwan: results from the Nutrition and Health Survey in Taiwan (NAHSIT, 1993-1996). , 2002, The Chinese journal of physiology.

[27]  D. Grobbee,et al.  Prophylactic versus on‐demand treatment strategies for severe haemophilia: a comparison of costs and long‐term outcome , 2002, Haemophilia : the official journal of the World Federation of Hemophilia.

[28]  J. Horsman,et al.  Health status and health‐related quality of life associated with hemophilia , 2002, American journal of hematology.

[29]  F. Beek,et al.  Long‐term outcome of individualized prophylactic treatment of children with severe haemophilia , 2001, British journal of haematology.

[30]  D. Brettler,et al.  Home‐based factor infusion therapy and hospitalization for bleeding complications among males with haemophilia , 2001, Haemophilia : the official journal of the World Federation of Hemophilia.

[31]  C. Sabin,et al.  Primary prophylaxis for individuals with severe haemophilia: how many hospital visits could treatment prevent? , 2000, Journal of internal medicine.

[32]  Lauri Tabur,et al.  MINISTRY OF INTERIOR , 2000 .

[33]  P. Giangrande,et al.  Resource utilisation in haemophiliacs treated in Europe: Results from the European Study on Socioeconomic Aspects of Haemophilia Care , 1998, Haemophilia : the official journal of the World Federation of Hemophilia.

[34]  J. Avorn,et al.  Prophylactic Use of Factor VIII: an Economic Evaluation , 1998, Thrombosis and Haemostasis.

[35]  Sabin,et al.  The changing patterns of factor VIII (FVIII) and factor IX (FIX) clotting factor usage in a comprehensive care centre between 1980 and 1994 , 1998, Haemophilia : the official journal of the World Federation of Hemophilia.

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

[37]  L. Radwin Practice patterns. , 1997, Image--the journal of nursing scholarship.

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

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

[40]  P. Mannucci,et al.  Modern treatment of haemophilia. , 1995, Bulletin of the World Health Organization.

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

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

[43]  R. Wenzel,et al.  Challenges and Controversies , 1989, Infection Control &#x0026; Hospital Epidemiology.

[44]  M. Painter,et al.  Patterns of bleeding in adolescents with severe haemophilia A. , 1979, British medical journal.

[45]  D. Ramsay,et al.  A five-year study of a haemophilia reference centre. , 1975, Journal of clinical pathology.

[46]  Eric F. Gardner,et al.  Summary Statement , 1946 .