Literature DB >> 26451746

Targeting factor replacement therapy in severe hemophilia: which level is important?

Kathelijn Fischer1, Erik Berntorp2.   

Abstract

The original aim of prophylactic replacement therapy was to convert the bleeding pattern of severe hemophilia to that of moderate hemophilia through regular infusions of clotting factor concentrates. However, targeting prophylaxis on minimum trough levels does not prevent all bleeding. At the group level, there is a clear association of factor levels with bleeding and outcome. But bleeding phenotype in individual patients shows large variation, independent of trough levels maintained. The association of peak levels with bleeding on prophylaxis is not established. Experience with surgery suggests that certain peak levels need to be achieved during other hemostatic challenges, such as playing sports. Individualization of prophylaxis should include timing of infusion according to special activities. The clinical relevance of factor levels is even more urgent since the recent introduction of long-acting clotting factor concentrates with their different pharmacokinetic profiles and the prospect of gene therapy resulting in constant factor levels. It should be considered that the success of any prophylactic regimen is also dependent on other factors, such as the age at initiation of prophylaxis, adherence, lifestyle, cartilage susceptibility, and the other components of the clotting system. Factor levels are thus an important but quite small piece in the total picture of treating hemophilia and we currently cannot identify a specific trough or peak level to use for monitoring. At the same time, knowledge of a patients' level during the infusion intervals may help to individualize and adjust treatment according to the clinical symptoms. Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

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Year:  2015        PMID: 26451746     DOI: 10.1055/s-0035-1552562

Source DB:  PubMed          Journal:  Semin Thromb Hemost        ISSN: 0094-6176            Impact factor:   4.180


  6 in total

1.  Emerging treatments for hemophilia: patients and their treaters spoilt for choice, but laboratories face a difficult path?

Authors:  Emmanuel J Favaloro; Giuseppe Lippi
Journal:  Ann Transl Med       Date:  2017-03

Review 2.  New therapies for hemophilia.

Authors:  Steven W Pipe
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2016-12-02

Review 3.  Novel blood coagulation molecules: Skeletal muscle myosin and cardiac myosin.

Authors:  Hiroshi Deguchi; Shravan Morla; John H Griffin
Journal:  J Thromb Haemost       Date:  2020-10-25       Impact factor: 5.824

Review 4.  Pharmacokinetic-based prediction of real-life dosing of extended half-life clotting factor concentrates on hemophilia.

Authors:  Massimo Morfini; Stefano Gherardini
Journal:  Ther Adv Hematol       Date:  2018-06-05

5.  Impact of pharmacokinetics to reduce bleeding in a cohort of patients with severe hemophilia A in a personalized comprehensive management program.

Authors:  Samuel Sarmiento Doncel; Gina Alejandra Diaz Mosquera; Javier Mauricio Cortes; Nelson Ramirez Plazas; Francisco Javier Meza; Carol Agudelo Rico
Journal:  Hematol Rep       Date:  2021-11-26

6.  Relationship between factor VIII activity, bleeds and individual characteristics in severe hemophilia A patients.

Authors:  João A Abrantes; Alexander Solms; Dirk Garmann; Elisabet I Nielsen; Siv Jönsson; Mats O Karlsson
Journal:  Haematologica       Date:  2019-08-01       Impact factor: 9.941

  6 in total

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