Literature DB >> 18085428

Cost-of-illness study of severe haemophilia A and B in five French haemophilia treatment centres.

Virginie Nerich1, Edgar Tissot, Albert Faradji, Karine Demesmay, Marie Anne Bertrand, Jean-Louis Lorenzini, Marie-Elisabeth Briquel, Patricia Pouzol, Marie-Christine Woronoff-Lemsi.   

Abstract

OBJECTIVE: The aim of this study was to assess the consumption of anti-haemophilic drugs by adults and children with severe haemophilia A or B (residual activity of FVIII or FIX < or =2%) and to quantify the average direct medical costs.
METHOD: A retrospective multicentre cost-of-illness study from the perspective of French national health insurance system. The costs include only the use of clotting factors. MAIN OUTCOME MEASURE: Consumption was expressed in UI/kg/year and costs in euros/kg/year.
RESULTS: From January 1, 2001 to December 31, 2002, data from 81 adults and 30 children with severe haemophilia A (n = 92) or B (n = 19) and included in the "SNH" were collected and analysed. A coagulation factor inhibitor was present in 10 patients (9%). Four of them were high responders. Mean age and body weight were respectively 28 +/- 17 years and 58 +/- 24 kg. Except for one adult patient, all (99%) had outpatient treatment, 44 patients (40%) were hospitalized and treated by recombinant or/and plasma-derived FVIII or FIX or/and rFVIIa. Overall median annual consumption of anti-haemophilic drugs per patient was estimated at 1,333 UI/kg, with a median cost-of-illness of 1,156 euros/kg. Patients with severe haemophilia B consumed more than patients with severe haemophilia A, though not significantly (P = 0.096), with a median of 2,167 vs. 1,100 UI/kg/year and a median cost of 1,760 vs. 917 euros/kg/year (P = 0.13). Children consumed respectively more than adults (P = 0.008), with a median of 3,204 vs. 1,106 UI/kg/year and a median cost of 2,614 vs. 913 euros/kg/year (P = 0.012). The median cost for patients with an inhibitor was 3,291 euros/kg/year, approximately threefold higher than that of patients without an inhibitor (926 euros/kg/year) (P = 0.022).
CONCLUSION: It suggests a higher consumption and cost of anti-haemophilic drugs among children when compared to adults. Haemophilia B patients did not consume significantly more than haemophilia A patients, whereas the consumption and cost for patients with or without inhibitors differed significantly.

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Year:  2007        PMID: 18085428     DOI: 10.1007/s11096-007-9181-4

Source DB:  PubMed          Journal:  Pharm World Sci        ISSN: 0928-1231


  15 in total

1.  Factor VIII inhibitor treatment. Economics of inhibitor treatment in Canada.

Authors:  G E Rivard; S Vick
Journal:  Semin Hematol       Date:  1994-04       Impact factor: 3.851

2.  The natural history of factor VIII inhibitors in patients with hemophilia A.

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Review 3.  Inhibitor treatment: state of the art.

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Authors:  T Calvez; M Biou; D Costagliola; A M Jullien; Y Laurian; F Rossi; C Rothschild; P Sié
Journal:  Haemophilia       Date:  2001-01       Impact factor: 4.287

5.  The impact of inhibitors on the cost of clotting factor replacement therapy in Haemophilia A in Canada.

Authors:  H Chang; G D Sher; V S Blanchette; J M Teitel
Journal:  Haemophilia       Date:  1999-07       Impact factor: 4.287

6.  Treatment patterns and cost-of-illness of severe haemophilia in patients with inhibitors in Germany.

Authors:  G Auerswald; M von Depka Prondzinski; B Ehlken; W Kreuz; K Kurnik; H Lenk; I Scharrer; W Schramm; R Zimmermann
Journal:  Haemophilia       Date:  2004-09       Impact factor: 4.287

7.  Incidence of development of factor VIII and factor IX inhibitors in haemophiliacs.

Authors:  S Ehrenforth; W Kreuz; I Scharrer; R Linde; M Funk; T Güngör; B Krackhardt; B Kornhuber
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8.  The economic impact of factor VIII inhibitors in patients with haemophilia.

Authors:  R L Bohn; L M Aledort; K G Putnam; B M Ewenstein; H Mogun; J Avorn
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9.  Prevalence of inhibitors in a population of 3435 hemophilia patients in France. French Hemophilia Study Group.

Authors:  Y Sultan
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10.  Cost related to replacement therapy during hospitalization in haemophiliacs with or without inhibitors: experience of six French haemophilia centres.

Authors:  P Gautier; M J D'Alche-Gautier; B Coatmelec; A Marques-Verdier; M A Bertrand; J Dieval; A M Berthier
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8.  Preclinical evaluation of a next-generation, subcutaneously administered, coagulation factor IX variant, dalcinonacog alfa.

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