Literature DB >> 30993845

Regional variation and cost implications of prescribed extended half-life factor concentrates among U.S. Haemophilia Treatment Centres for patients with moderate and severe haemophilia.

Stacy E Croteau1, Dunlei Cheng2, Alice J Cohen3, Chris E Holmes4, Lynn M Malec5, Michael Silvey6, Courtney D Thornburg7, Allison P Wheeler8, Peter A Kouides9, Leslie J Raffini10, Ellis J Neufeld11.   

Abstract

BACKGROUND: Extended half-life (EHL) factor VIII (FVIII) and IX (FIX) products are intended to decrease the burden of prophylaxis for patients with haemophilia A or B. Whether these newer concentrates have led to meaningful clinical practice change remains vague. AIM: To characterize the longitudinal use of standard (SHL) and EHL factor concentrates at haemophilia treatment centres (HTCs), using the ATHNdataset, a US database of 138 ATHN-affiliated HTCs.
METHODS: Factor concentrate use among moderate and severe haemophilia A and B patients without inhibitors was analysed at three time points over 18 months.
RESULTS: Use of EHL concentrates rose from 10% of patients to 22% during this study. EHL FVIII prophylaxis is prescribed to the minority of patients, 28%; EHL FIX now predominates for prophylaxis, 52%. Rates of prescribed EHL products varied significantly by age group and HTC region. Median prescribed prophylaxis for SHL compared to EHL products was FVIII 6240 and 5200 and FIX 6968 and FIX 3900 IU/kg/y, respectively. On-demand EHL use has grown but has minimal contribution to overall usage (2%).
CONCLUSION: Haemophilia treatment centre region and patient age impact the rate of adoption of EHL products; however, EHL prescribing continues to rise nationally, particularly for EHL FIX. Careful attention to annual cost of prophylaxis is imperative as the decrease in median EHL prophylaxis consumption is not offset by the higher unit cost of these products. It is unclear how further growth in use of EHLs will be impacted by emerging non-factor replacement and gene therapies.
© 2019 John Wiley & Sons Ltd.

Entities:  

Keywords:  EHL; haemophilia A; haemophilia B; pharmacokinetics; prophylaxis; utilization

Year:  2019        PMID: 30993845     DOI: 10.1111/hae.13758

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


  5 in total

1.  Optimising prophylaxis outcomes and costs in haemophilia patients switching to recombinant FVIII-Fc: a single-centre real-world experience.

Authors:  Annarita Tagliaferri; Annalisa Matichecchia; Gianna F Rivolta; Federica Riccardi; Gabriele Quintavalle; Anna Benegiamo; Rossana Rossi; Antonio Coppola
Journal:  Blood Transfus       Date:  2019-11-04       Impact factor: 3.443

2.  Resource utilization and treatment costs of patients with severe hemophilia A: Real-world data from the ATHNdataset.

Authors:  Michael Recht; Chunla He; Er Chen; Dunlei Cheng; Paul Solari; David Hinds
Journal:  EJHaem       Date:  2022-03-27

3.  Optimizing language for effective communication of gene therapy concepts with hemophilia patients: a qualitative study.

Authors:  Daniel P Hart; Brian R Branchford; Sarah Hendry; Robert Ledniczky; Robert F Sidonio; Claude Négrier; Michelle Kim; Michelle Rice; Matthew Minshall; Claire Arcé; Steve Prince; Maria Kelleher; Sharon Lee
Journal:  Orphanet J Rare Dis       Date:  2021-04-28       Impact factor: 4.123

4.  Trends in the Use of Conventional and New Pharmaceuticals for Hemophilia Treatments Among Medicaid Enrollees, 2005-2020.

Authors:  Inmaculada Hernandez; Deanna Rowe; Walid F Gellad; Chester B Good
Journal:  JAMA Netw Open       Date:  2021-06-01

5.  Recombinant Factor VIII Fc Fusion Protein (rFVIIIFc) in Real Life: One-Year Clinical and Economic Outcomes.

Authors:  Romain Giraud; Nicolas Delmotte; Sophie Gensollen; Martine Roche; Céline Falaise; Hervé Chambost; Manon Roche
Journal:  Drugs Real World Outcomes       Date:  2021-06-25
  5 in total

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