Cargando…
Hemophilia A in Brazil – epidemiology and treatment developments
Hemophilia A is an inherited disorder characterized by deficiency of coagulation factor VIII, which predisposes patients to bleeding events. Treatment is based on replacement of the deficient factor, in a therapeutic or prophylactic manner. Brazil is the country with the third largest population of...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4183441/ https://www.ncbi.nlm.nih.gov/pubmed/25288890 http://dx.doi.org/10.2147/JBM.S68234 |
_version_ | 1782337689878528000 |
---|---|
author | Ferreira, Adriana Aparecida Leite, Isabel Cristina Gonçalves Bustamante-Teixeira, Maria Teresa Guerra, Maximiliano Ribeiro |
author_facet | Ferreira, Adriana Aparecida Leite, Isabel Cristina Gonçalves Bustamante-Teixeira, Maria Teresa Guerra, Maximiliano Ribeiro |
author_sort | Ferreira, Adriana Aparecida |
collection | PubMed |
description | Hemophilia A is an inherited disorder characterized by deficiency of coagulation factor VIII, which predisposes patients to bleeding events. Treatment is based on replacement of the deficient factor, in a therapeutic or prophylactic manner. Brazil is the country with the third largest population of people with hemophilia, for which the public health system provides free comprehensive care. Maintaining an updated registry of patients, documenting the prevalence of complications, and assessing the effectiveness of resource use are indispensable elements in the design of a well-coordinated national program. According to sociodemographic, clinical, and laboratory data collected by the computerized Brazilian system on coagulopathies, in June 2013, there were 9,122 registered patients with hemophilia A in Brazil, of which 36.1% had a severe form of the disease. Clotting factor inhibitors were present in 7.5%, but 25.7% of records did not provide this type of data. Around 70% of the patients belonged to the economically active population, being between 15 and 59 years old. Infection by the human immunodeficiency virus was present in 23.4% of the patients tested and infection by hepatitis C virus antibodies in 59.3%. Infection by the hepatitis B virus and human T-lymphotropic virus was also reported. The high percentage of incomplete records regarding serological data shows the fragility of the information system to date. There was also no information available on the prevalence of permanent or disabling joint damage. Although few hemophiliacs receive adequate care in developing countries, and despite Brazil exhibiting great social inequalities, the Ministry of Health has made significant advances in the treatment of hemophilia A. The gradual increase in importation of factor VIII concentrate enabled the implementation of primary and secondary modalities of prophylaxis, in addition to the induction of immune tolerance. There are also plans to set up a factory in the country, to ensure Brazilian self-sufficiency in the production of blood products. |
format | Online Article Text |
id | pubmed-4183441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41834412014-10-06 Hemophilia A in Brazil – epidemiology and treatment developments Ferreira, Adriana Aparecida Leite, Isabel Cristina Gonçalves Bustamante-Teixeira, Maria Teresa Guerra, Maximiliano Ribeiro J Blood Med Review Hemophilia A is an inherited disorder characterized by deficiency of coagulation factor VIII, which predisposes patients to bleeding events. Treatment is based on replacement of the deficient factor, in a therapeutic or prophylactic manner. Brazil is the country with the third largest population of people with hemophilia, for which the public health system provides free comprehensive care. Maintaining an updated registry of patients, documenting the prevalence of complications, and assessing the effectiveness of resource use are indispensable elements in the design of a well-coordinated national program. According to sociodemographic, clinical, and laboratory data collected by the computerized Brazilian system on coagulopathies, in June 2013, there were 9,122 registered patients with hemophilia A in Brazil, of which 36.1% had a severe form of the disease. Clotting factor inhibitors were present in 7.5%, but 25.7% of records did not provide this type of data. Around 70% of the patients belonged to the economically active population, being between 15 and 59 years old. Infection by the human immunodeficiency virus was present in 23.4% of the patients tested and infection by hepatitis C virus antibodies in 59.3%. Infection by the hepatitis B virus and human T-lymphotropic virus was also reported. The high percentage of incomplete records regarding serological data shows the fragility of the information system to date. There was also no information available on the prevalence of permanent or disabling joint damage. Although few hemophiliacs receive adequate care in developing countries, and despite Brazil exhibiting great social inequalities, the Ministry of Health has made significant advances in the treatment of hemophilia A. The gradual increase in importation of factor VIII concentrate enabled the implementation of primary and secondary modalities of prophylaxis, in addition to the induction of immune tolerance. There are also plans to set up a factory in the country, to ensure Brazilian self-sufficiency in the production of blood products. Dove Medical Press 2014-09-23 /pmc/articles/PMC4183441/ /pubmed/25288890 http://dx.doi.org/10.2147/JBM.S68234 Text en © 2014 Ferreira et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Ferreira, Adriana Aparecida Leite, Isabel Cristina Gonçalves Bustamante-Teixeira, Maria Teresa Guerra, Maximiliano Ribeiro Hemophilia A in Brazil – epidemiology and treatment developments |
title | Hemophilia A in Brazil – epidemiology and treatment developments |
title_full | Hemophilia A in Brazil – epidemiology and treatment developments |
title_fullStr | Hemophilia A in Brazil – epidemiology and treatment developments |
title_full_unstemmed | Hemophilia A in Brazil – epidemiology and treatment developments |
title_short | Hemophilia A in Brazil – epidemiology and treatment developments |
title_sort | hemophilia a in brazil – epidemiology and treatment developments |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4183441/ https://www.ncbi.nlm.nih.gov/pubmed/25288890 http://dx.doi.org/10.2147/JBM.S68234 |
work_keys_str_mv | AT ferreiraadrianaaparecida hemophiliaainbrazilepidemiologyandtreatmentdevelopments AT leiteisabelcristinagoncalves hemophiliaainbrazilepidemiologyandtreatmentdevelopments AT bustamanteteixeiramariateresa hemophiliaainbrazilepidemiologyandtreatmentdevelopments AT guerramaximilianoribeiro hemophiliaainbrazilepidemiologyandtreatmentdevelopments |