Haemophilia A: A Review of Clinical Manifestations, Treatment, Mutations, and the Development of Inhibitors

Author:

Sarmiento Doncel Samuel12ORCID,Díaz Mosquera Gina Alejandra1,Cortes Javier Mauricio1,Agudelo Rico Carol1,Meza Cadavid Francisco Javier13,Peláez Ronald Guillermo2ORCID

Affiliation:

1. Integral Solutions SD SAS, Integral Solutions Research, Bogota 110121, Colombia

2. Life Sciences and Health Research Group, Graduates School, CES University, Medellin 050021, Colombia

3. Hospital Universitario San Jorge, Pereira 660002, Colombia

Abstract

The purpose of this narrative review was to provide an overview that allows readers to improve their understanding of hemophilia A, which is considered a genetic disease with a high impact on the quality of life of people who suffer from it is considered one of the diseases with the highest cost for health systems (In Colombia it is part of the five diseases with the greatest economic impact). After this exhaustive review, we can see that the treatment of hemophilia is on the way to precision medicine, which involves genetic variables specific to each race and ethnicity, pharmacokinetics (PK), as well as environmental factors and lifestyle. Knowing the impact of each of these variables and their relationship with the efficacy of treatment (prophylaxis: regular infusion of the missing clotting factor VIII in order to prevent spontaneous bleeding) will allow for individualizing the medical behavior in a cost-effective way. For this is required to build more strong scientific evidence with statistical power that allows us to infer.

Publisher

MDPI AG

Subject

Hematology

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