Literature DB >> 31935128

The cost of hemophilia treatment: the importance of minimizing it without detriment to its quality.

E Carlos Rodriguez-Merchan1.   

Abstract

Introduction: Hemophilia is a very expensive disease. Ameliorations in the management of hemophilia cause increased patient survival, more complex disease management, and augmented treatment costs. A literature search related to the cost of hemophilia was analyzed.Areas covered: Clotting factor concentrates, which are the keystone of management, are costly. In fact, the yearly expenditure in the USA is 250,000 USD per adult patient. Indirect expenses also play a part in the economic load, and include lost productive capacity, uncompensated caretaker tariffs, and hemophilia-related physical handicap. Factor concentrates are responsible for more than 90% of the direct health-care expenditures of hemophilia. In an evaluation of the cost of management with high-dose prophylaxis in previously untreated patients from childbirth to puberty, including immune tolerance induction (ITI), the average annual treatment cost (Euros per kilogram) was 4391 EUR (approximately 4865 USD), and the average ITI cost was 383,448 EUR (approximately 424,860 USD). The expected ITI recovery period in the aforementioned evaluation was 1.8 years. To reduce costs, strategies such as disease management programs and drug pricing programs have also been implemented.Expert opinion: Knowing the current cost of hemophilia is essential to ensure that patients are treated as efficiently as possible.

Entities:  

Keywords:  Hemophilia; assistance programs; cost of care; disease management programs; drug pricing programs; extended half-life products; inhibitors

Mesh:

Substances:

Year:  2020        PMID: 31935128     DOI: 10.1080/17474086.2020.1716726

Source DB:  PubMed          Journal:  Expert Rev Hematol        ISSN: 1747-4094            Impact factor:   2.929


  3 in total

1.  Hidden blood loss of total knee arthroplasty in hemophilia arthritis: an analysis of influencing factors.

Authors:  Shao Ning Shen; Dong Xiao Wu; Shuai Jie Lv; Pei Jian Tong
Journal:  BMC Musculoskelet Disord       Date:  2022-06-17       Impact factor: 2.562

2.  Bleeding outcomes and factor utilization after switching to an extended half-life product for prophylaxis in haemophilia A in Austria.

Authors:  Cihan Ay; Clemens Feistritzer; Joachim Rettl; Gerhard Schuster; Anna Vavrovsky; Leonard Perschy; Ingrid Pabinger
Journal:  Sci Rep       Date:  2021-06-21       Impact factor: 4.379

3.  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
  3 in total

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