Skip to main content
Top
Published in: PharmacoEconomics 10/2003

01-07-2003 | Original Research Article

Determinants of Drug Costs in Hospitalised Patients with Haemophilia

Impact of Recombinant Activated Factor VII

Authors: Jean Philippe Galanaud, Dr Nathalie Pelletier-Fleury, Hélène Logerot-Lebrun, Thierry Lambert

Published in: PharmacoEconomics | Issue 10/2003

Login to get access

Abstract

Objective: To analyse the determinants of anti-haemophilic drug costs in hospitalised patients with haemophilia and to estimate the impact of recombinant activated factor VII (rFVIIa) therapy on this expenditure.
Perspective: The perspective of the study was from the viewpoint of the hospital.
Design and setting: A prospective study was carried out. All patients with haemophilia who were hospitalised in 1999 in Bicêtre public hospital, Paris, France were included in the cohort.
Main outcome measures and results: For each of the 96 patients (154 hospital stays), we estimated the costs of anti-haemophilic drugs (coagulation concentrates) used. Costs were then stratified by different variables (severity of the disease, presence of a circulating inhibitor to coagulation factors, etc.) and a multivariate model was developed to determine the relationship between these variables and total anti-haemophilic drug costs, while controlling for potential confounders. Our study revealed: (i) the independent role of the five following variables in contributing to high anti-haemophilic drug expenditure: presence of a circulating inhibitor to coagulation factors, odds ratio (OR) = 16.9 (95% CI: 4.3–66); severity of the disease (factor VIII or factor IX≤0.01 IU/mL), OR = 3.7 (95% CI: 1.6–8.6); length of hospital stay >4 days, OR = 8 (95% CI: 2.2–29.4); age >18 years old, OR = 6.2 (95% CI: 1.6–24.5); and surgical reasons for hospitalisation (whether surgery was haemophilia related [OR = 35.7 (95% CI: 7.3–175)] or not [OR = 5.4 (95% CI: 1.3–22.5)]); (ii) the large share that rFVIIa represented in this expenditure on medicines: rFVIIa was used in 20.1% of hospital stays and accounted for 56.2% of the total anti-haemophilic drug costs, which were estimated at €4 384 732 (2000 values).
Conclusions: Our data underline the heavy cost of the treatment of haemophilic patients with an inhibitor to coagulation factors. But, to the question of whether the high expenditure linked to rFVIIa utilisation will be balanced out by later benefits, it is not yet possible to reply with any certainty; further cost-benefit evaluation should be carried out.
Footnotes
1
Use of tradenames is for product identification only and does not imply endorsement.
 
Literature
1.
go back to reference Tuddenham EGD, Cooper DN. The molecular genetics of haemostasis and its inherited disorders. Oxford monographs in medical genetics n°25. Oxford, England: Oxford University Press, 1994 Tuddenham EGD, Cooper DN. The molecular genetics of haemostasis and its inherited disorders. Oxford monographs in medical genetics n°25. Oxford, England: Oxford University Press, 1994
2.
go back to reference Mannucci PM, Tuddenham EGD. The haemophilias — from royal genes to gene therapy. N Engl J Med 2001; 344 (23): 1773–9PubMedCrossRef Mannucci PM, Tuddenham EGD. The haemophilias — from royal genes to gene therapy. N Engl J Med 2001; 344 (23): 1773–9PubMedCrossRef
3.
go back to reference Rosendaal FR, Varekamp I, Smith C, et al. Mortality and causes of death in Dutch hemophiliacs, 1973–1986. Br J Haematol 1989; 71: 71–6PubMedCrossRef Rosendaal FR, Varekamp I, Smith C, et al. Mortality and causes of death in Dutch hemophiliacs, 1973–1986. Br J Haematol 1989; 71: 71–6PubMedCrossRef
4.
go back to reference Bohn RL, Avorn J, Glynn RJ, et al. Prophylactic use of factor VIII: an economic evaluation. Thromb Haemost 1998; 79 (5): 932–7PubMed Bohn RL, Avorn J, Glynn RJ, et al. Prophylactic use of factor VIII: an economic evaluation. Thromb Haemost 1998; 79 (5): 932–7PubMed
5.
go back to reference Lee C, Sabin C, Miners A. High cost, low volume care: the case of haemophilia. BMJ 1997; 315: 962–3PubMedCrossRef Lee C, Sabin C, Miners A. High cost, low volume care: the case of haemophilia. BMJ 1997; 315: 962–3PubMedCrossRef
6.
go back to reference Scharrer I, Bray GL, Neutzling O. Incidence of inhibitors in haemophilia A patients — a review of recent studies of recombinant and plasma-derived factor VIII concentrates. Haemophilia 1999; 5: 145–54PubMedCrossRef Scharrer I, Bray GL, Neutzling O. Incidence of inhibitors in haemophilia A patients — a review of recent studies of recombinant and plasma-derived factor VIII concentrates. Haemophilia 1999; 5: 145–54PubMedCrossRef
8.
go back to reference Ross-Degna D, Soumerai SB, Avorn J, et al. Haemophilia home treatment: economic analysis and implications for health policy. Int J Technol Assess Health Care 1995; 11: 327–44CrossRef Ross-Degna D, Soumerai SB, Avorn J, et al. Haemophilia home treatment: economic analysis and implications for health policy. Int J Technol Assess Health Care 1995; 11: 327–44CrossRef
9.
go back to reference Meeting report: economic aspects of haemophilia care in the United States. Haemophilia 1999; 5 (4): 282–5 Meeting report: economic aspects of haemophilia care in the United States. Haemophilia 1999; 5 (4): 282–5
10.
go back to reference Szucs TD, Offner A, Kroner B, et al. Resource utilisation in haemophiliacs treated in Europe: results from the European Study on Socioeconomic Aspects of Haemophilia Care. The European Socioeconomic Study Group. Haemophilia 1998; 4 (4): 498–501PubMedCrossRef Szucs TD, Offner A, Kroner B, et al. Resource utilisation in haemophiliacs treated in Europe: results from the European Study on Socioeconomic Aspects of Haemophilia Care. The European Socioeconomic Study Group. Haemophilia 1998; 4 (4): 498–501PubMedCrossRef
13.
go back to reference SAS/Stat. User’s guide: release 8.1 edition. Cary (NC): SAS Institute, 2001 SAS/Stat. User’s guide: release 8.1 edition. Cary (NC): SAS Institute, 2001
14.
go back to reference Sultan Y. Prevalence of inhibitors in a population of 3435 haemophilia patients in France. French Haemophilia Study Group. Thromb Haemost 1992; 67 (6): 600–2PubMed Sultan Y. Prevalence of inhibitors in a population of 3435 haemophilia patients in France. French Haemophilia Study Group. Thromb Haemost 1992; 67 (6): 600–2PubMed
15.
go back to reference Mannucci PM. Haemophilia treatment protocols around the world: towards a consensus. Haemophilia 1998; 4: 421–30PubMedCrossRef Mannucci PM. Haemophilia treatment protocols around the world: towards a consensus. Haemophilia 1998; 4: 421–30PubMedCrossRef
16.
go back to reference Haemophilia of Georgia. Protocols for the treatment of haemophilia and von Willebrand disease. Haemophilia 2000; 6 (1 Suppl.): 84–93 Haemophilia of Georgia. Protocols for the treatment of haemophilia and von Willebrand disease. Haemophilia 2000; 6 (1 Suppl.): 84–93
17.
go back to reference Miller DG, Stamatoyannopoulos G. Gene therapy for hemophilia. N Engl J Med 2001; 344 (23): 1782–3PubMedCrossRef Miller DG, Stamatoyannopoulos G. Gene therapy for hemophilia. N Engl J Med 2001; 344 (23): 1782–3PubMedCrossRef
18.
go back to reference Lipton RA. The economics of factor VIII inhibitor treatment. Semin Hematol 1994; 31 (2 Suppl. 4): 37–8PubMed Lipton RA. The economics of factor VIII inhibitor treatment. Semin Hematol 1994; 31 (2 Suppl. 4): 37–8PubMed
19.
go back to reference Rivard GE, Vick S. Factor VIII inhibitor treatment: economics of inhibitor treatment in Canada. Semin Hematol 1994; 31 (2 Suppl. 4): 41–3PubMed Rivard GE, Vick S. Factor VIII inhibitor treatment: economics of inhibitor treatment in Canada. Semin Hematol 1994; 31 (2 Suppl. 4): 41–3PubMed
20.
go back to reference Suczs TD, Offner A, Schramm W. Socioeconomic impact of haemophilia care: results of a pilot study. Haemophilia 1996; 2: 211–7CrossRef Suczs TD, Offner A, Schramm W. Socioeconomic impact of haemophilia care: results of a pilot study. Haemophilia 1996; 2: 211–7CrossRef
21.
go back to reference Goudemand J. Pharmaco-economic aspects of inhibitor treatment. Eur J Haematol 1998; 61 (63 Suppl.): 24–7 Goudemand J. Pharmaco-economic aspects of inhibitor treatment. Eur J Haematol 1998; 61 (63 Suppl.): 24–7
22.
go back to reference Wasserman J, Ullman M, Begley C, et al. The impact of changing health care reimbursement methodologies on persons with hemophilia [abstract 191]. Haemophilia 1998; 4: 203 Wasserman J, Ullman M, Begley C, et al. The impact of changing health care reimbursement methodologies on persons with hemophilia [abstract 191]. Haemophilia 1998; 4: 203
23.
go back to reference Chang H, Sher GD, Blanchette VS, et al. The impact of inhibitors on the cost of clotting factor replacement therapy in Haemophilia A in Canada. Haemophilia 1999; 5 (4): 247–52PubMedCrossRef Chang H, Sher GD, Blanchette VS, et al. The impact of inhibitors on the cost of clotting factor replacement therapy in Haemophilia A in Canada. Haemophilia 1999; 5 (4): 247–52PubMedCrossRef
24.
go back to reference Montague O, Chaix C, Harf A, et al. Costs for acute myocardial infarction in a tertiary care centre and nationwide in France. Pharmacoeconomics 2000; 17 (6): 603–9CrossRef Montague O, Chaix C, Harf A, et al. Costs for acute myocardial infarction in a tertiary care centre and nationwide in France. Pharmacoeconomics 2000; 17 (6): 603–9CrossRef
25.
26.
go back to reference Stewart AJ, Hanley JP, Ludlam CA. Safety, efficacy and cost-effectiveness of home therapy with recombinant activated factor VII in a patient with severe haemophilia A and an anti factor VIII inhibitor. Blood Coagul Fibrinolysis 1998; 9 (1 Suppl.): 93–5 Stewart AJ, Hanley JP, Ludlam CA. Safety, efficacy and cost-effectiveness of home therapy with recombinant activated factor VII in a patient with severe haemophilia A and an anti factor VIII inhibitor. Blood Coagul Fibrinolysis 1998; 9 (1 Suppl.): 93–5
27.
go back to reference Ingerslev J, Thykjaer H, Kudsk Jensen O, et al. Home treatment with recombinant activated factor VII: results from one centre. Blood Coagul Fibrinolysis 1998; 9 (1 Suppl.): 107–10 Ingerslev J, Thykjaer H, Kudsk Jensen O, et al. Home treatment with recombinant activated factor VII: results from one centre. Blood Coagul Fibrinolysis 1998; 9 (1 Suppl.): 107–10
28.
go back to reference Ekert H, Brewin T, Boey W, et al. Cost-utility analysis of recombinant factor VIIa (Novoseven®) in six children with long-standing inhibitors to factor VII or IX. Haemophilia 2001; 7 (3): 279–85PubMedCrossRef Ekert H, Brewin T, Boey W, et al. Cost-utility analysis of recombinant factor VIIa (Novoseven®) in six children with long-standing inhibitors to factor VII or IX. Haemophilia 2001; 7 (3): 279–85PubMedCrossRef
Metadata
Title
Determinants of Drug Costs in Hospitalised Patients with Haemophilia
Impact of Recombinant Activated Factor VII
Authors
Jean Philippe Galanaud
Dr Nathalie Pelletier-Fleury
Hélène Logerot-Lebrun
Thierry Lambert
Publication date
01-07-2003
Publisher
Springer International Publishing
Published in
PharmacoEconomics / Issue 10/2003
Print ISSN: 1170-7690
Electronic ISSN: 1179-2027
DOI
https://doi.org/10.2165/00019053-200321100-00002

Other articles of this Issue 10/2003

PharmacoEconomics 10/2003 Go to the issue

Original Research Article

Lower Respiratory Tract Infections