Literature DB >> 29889317

The socioeconomic burden of patients affected by hemophilia with inhibitors.

Lucia S D'Angiolella1, Paolo A Cortesi1, Angiola Rocino2, Antonio Coppola3, Hamisa J Hassan4, Adele Giampaolo4, Luigi P Solimeno5, Alessandra Lafranconi1, Mariangela Micale1, Sveva Mangano1, Giacomo Crotti1, Federica Pagliarin1, Giancarlo Cesana1, Lorenzo G Mantovani1.   

Abstract

Hemophilia is associated with a high financial burden on individuals, healthcare systems, and society. The development of inhibitors significantly increases the socioeconomic burden of the diseases. This study aimed to review and describe the burden of hemophilia with inhibitors, providing a reference scenario to assess the impact of new products in the real word. Two systematic literature reviews were performed to collect data on (i) health economics and (ii) health-related quality of life evidences in hemophilic patients with inhibitors. The costs associated with patients with hemophilia and inhibitors are more than 3 times greater than the costs incurred in those without inhibitors, with an annual cost per patient that can be higher than €1 000 000. The costs of bypassing agents account for the large majority of the total healthcare direct costs for hemophilia treatment. The quality of life is more compromised in patients with hemophilia and inhibitors compared to those without inhibitors, in particular the physical domains, whereas mental domains were comparable to that of the general population. The development of an inhibitor has a high impact on costs and quality of life. New treatments have the potential to change positively the management and socioeconomic burden of hemophilia with inhibitors.
© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  cost; hemophilia; inhibitors; quality of life

Mesh:

Substances:

Year:  2018        PMID: 29889317     DOI: 10.1111/ejh.13108

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


  13 in total

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Authors:  Luciana W Zuccherato; Silvana M Elói-Santos; Letícia L Jardim; Ricardo M Camelo; Daniel G Chaves; Renan P Souza; Edward J Hollox; Suely M Rezende
Journal:  Haematologica       Date:  2019-03-14       Impact factor: 9.941

3.  A multicenter, open-label phase 3 study of emicizumab prophylaxis in children with hemophilia A with inhibitors.

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Journal:  Blood       Date:  2019-12-12       Impact factor: 22.113

4.  New data from the Italian National Register of Congenital Coagulopathies, 2016 Annual Survey.

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Journal:  Blood Transfus       Date:  2019-02-13       Impact factor: 3.443

Review 5.  Factor-mimetic and rebalancing therapies in hemophilia A and B: the end of factor concentrates?

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6.  TCPro: an In Silico Risk Assessment Tool for Biotherapeutic Protein Immunogenicity.

Authors:  Osman N Yogurtcu; Zuben E Sauna; Joseph R McGill; Million A Tegenge; Hong Yang
Journal:  AAPS J       Date:  2019-08-02       Impact factor: 4.009

7.  Mechanistic Insights into Factor VIII Immune Tolerance Induction via Prenatal Cell Therapy in Hemophilia A.

Authors:  Martin Rodriguez; Christopher D Porada; Graҫa Almeida-Porada
Journal:  Curr Stem Cell Rep       Date:  2019-11-20

8.  Editorial: Tolerating Factor VIII: Novel Strategies to Prevent and Reverse Neutralizing Anti-FVIII Antibodies.

Authors:  Sébastien Lacroix-Desmazes; Kathleen P Pratt
Journal:  Front Immunol       Date:  2021-01-25       Impact factor: 7.561

9.  Emicizumab prophylaxis in a Korean child with severe hemophilia A and high titer inhibitor: a case report.

Authors:  Ji Hyun Ahn; Nani Jung; Ye Jee Shim; Heung Sik Kim
Journal:  Blood Res       Date:  2021-03-31

10.  Predictors of the outcome of immune tolerance induction in patients with haemophilia A and inhibitors: The Brazilian Immune Tolerance (BrazIT) Study protocol.

Authors:  Ricardo Mesquita Camelo; Daniel Gonçalves Chaves; Luciana Werneck Zuccherato; Suely Meireles Rezende
Journal:  PLoS One       Date:  2021-08-26       Impact factor: 3.240

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