Literature DB >> 15357777

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

G Auerswald1, M von Depka Prondzinski, B Ehlken, W Kreuz, K Kurnik, H Lenk, I Scharrer, W Schramm, R Zimmermann.   

Abstract

To evaluate current treatment patterns and resource utilization as well as related cost in the management of severe haemophilia patients with inhibitors in Germany, a cost-of-illness study was conducted. Generally, data were generated by structured literature search. Missing data were collected by expert interviews. All data were validated by a panel of German experts in haemophilia care. In Germany, immune tolerance therapy (ITT) is first-line therapy in inhibitor management for children in the initial year after inhibitor development, particularly for high responders (HR). In adult HR patients ITT is applied but to a remarkably lower extent than in children. To treat bleeding episodes, factor VIII (FVIII) is first-line therapy in low responders (LR). For paediatric HR patients, bleeds are mainly treated with recombinant FVIIa (rFVIIa). In adult HR patients, activated prothrombin complex concentrate (aPCC) and rFVIIa are more equally distributed as treatment options. Treatment costs were calculated for paediatric patients (15 kg) and adult patients (75 kg) from third party payers' perspective. Cost for ITT ranges from Euro 70,290 (2 months; LR) to Euro 3 812,400 (24 months; with aPCC; HR) in a paediatric patient. For an adult patient ITT cost ranges from Euro 287,500 (6 months; LR) to Euro 17,253,000 (36 months; HR). For on average 12.5 acute bleeds, average annual treatment costs amount to Euro 77,000 for a child and Euro 354,000 for an adult. Assessing the results it has been taken into consideration that ITT can last longer and annual number of bleeds can be extremely higher than on average 12.5 episodes. This indicates more health care resource consumption in some patients.

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Year:  2004        PMID: 15357777     DOI: 10.1111/j.1365-2516.2004.00950.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  6 in total

1.  The social burden and quality of life of patients with haemophilia in Italy.

Authors:  Yllka Kodra; Marianna Cavazza; Arrigo Schieppati; Marta De Santis; Patrizio Armeni; Romano Arcieri; Gabriele Calizzani; Giovanni Fattore; Lamberto Manzoli; Lorenzo Mantovani; Domenica Taruscio
Journal:  Blood Transfus       Date:  2014-04       Impact factor: 3.443

2.  Healthcare expenditures for males with haemophilia and employer-sponsored insurance in the United States, 2008.

Authors:  S Guh; S D Grosse; S McAlister; C M Kessler; J M Soucie
Journal:  Haemophilia       Date:  2011-12-12       Impact factor: 4.287

3.  Social/economic costs and quality of life in patients with haemophilia in Europe.

Authors:  Marianna Cavazza; Yllka Kodra; Patrizio Armeni; Marta De Santis; Julio López-Bastida; Renata Linertová; Juan Oliva-Moreno; Pedro Serrano-Aguilar; Manuel Posada-de-la-Paz; Domenica Taruscio; Arrigo Schieppati; Georgi Iskrov; László Gulácsi; Johann Matthias Graf von der Schulenburg; Panos Kanavos; Karine Chevreul; Ulf Persson; Giovanni Fattore
Journal:  Eur J Health Econ       Date:  2016-04-05

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

Authors:  Virginie Nerich; Edgar Tissot; Albert Faradji; Karine Demesmay; Marie Anne Bertrand; Jean-Louis Lorenzini; Marie-Elisabeth Briquel; Patricia Pouzol; Marie-Christine Woronoff-Lemsi
Journal:  Pharm World Sci       Date:  2007-12-18

5.  Economic analysis of not running tenders for recombinant Factor VIII procurement: a simplified analysis to estimate an otherwise unknown pharmacoeconomic index.

Authors:  Dario Maratea; Valeria Fadda; Sabrina Trippoli; Andrea Messori
Journal:  Eur J Hosp Pharm       Date:  2015-12-23

6.  Haemophilia A: health and economic burden of a rare disease in Portugal.

Authors:  Andreia Café; Manuela Carvalho; Miguel Crato; Miguel Faria; Paula Kjollerstrom; Cristina Oliveira; Patrícia R Pinto; Ramón Salvado; Alexandra Aires Dos Santos; Catarina Silva
Journal:  Orphanet J Rare Dis       Date:  2019-09-04       Impact factor: 4.123

  6 in total

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