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Toxicity of hydroxyurea in the treatment of sickle cell anemia

Bibliographic Details
Main Author: Marçal, Pedro Henrique Ferreira
Publication Date: 2022
Other Authors: Paula, Claudia Costa da Silva, Silva, Carlos Alberto, Trindade, Zeina Calek Graize, Lima, Marlucy Rodrigues, Peçanha, Michel, Menezes, Claudine de, Brandão, Marileny Boechat Frauches, Silva, Leonardo Oliveira Leão e, Rodrigues, Suely Maria
Format: Article
Language: por
Source: Research, Society and Development
Download full: https://rsdjournal.org/index.php/rsd/article/view/26264
Summary: Sickle cell anemia is a hereditary disease, characterized by the alteration of red blood cells, making them look like a sickle, hence the name sickle cell. In Brazil, it affects about 8% of the black population, but due to the intense miscegenation historically occurred in the country, it can also be observed in white or brown people. The work was developed with the general objective of analyzing the characteristics of sickle cell anemia and the toxicity presented by hydroxyueria in its treatment. The work was elaborated through a bibliographic review in books and articles selected through searches in databases and books websites, the period of the researched material covers the works published between the years 2010 and 2019. Hydroxyurea is now one of the drugs most used in the treatment of sickle cell anemia for being able to increase the production of another type of hemoglobin, known as fetal hemoglobin (more present during the uterine life). High levels of fetal hemoglobin decrease the polymerization of defective red cells and reduce the risk of vaso-occlusion. Like any chemotherapy drug, however, hydroxyurea has adverse effects. Hydroxyurea represents the first drug option for patients experiencing moderate to severe clinical conditions. However, it is important to highlight the incidence of clinical improvement in all patients who use this drug.
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spelling Toxicity of hydroxyurea in the treatment of sickle cell anemiaToxicidad de la hidroxiurea en el tratamiento de la anemia de células falciformesToxidade da hidroxiueria no tratamento da anemia falciformeHidroxiureaAnemia de células falciformesHemoglobina fetal.HydroxyureaSickle cell anemiaFetal hemoglobin.HidroxiuréiaAnemia falciformeHemoglobina fetal.Sickle cell anemia is a hereditary disease, characterized by the alteration of red blood cells, making them look like a sickle, hence the name sickle cell. In Brazil, it affects about 8% of the black population, but due to the intense miscegenation historically occurred in the country, it can also be observed in white or brown people. The work was developed with the general objective of analyzing the characteristics of sickle cell anemia and the toxicity presented by hydroxyueria in its treatment. The work was elaborated through a bibliographic review in books and articles selected through searches in databases and books websites, the period of the researched material covers the works published between the years 2010 and 2019. Hydroxyurea is now one of the drugs most used in the treatment of sickle cell anemia for being able to increase the production of another type of hemoglobin, known as fetal hemoglobin (more present during the uterine life). High levels of fetal hemoglobin decrease the polymerization of defective red cells and reduce the risk of vaso-occlusion. Like any chemotherapy drug, however, hydroxyurea has adverse effects. Hydroxyurea represents the first drug option for patients experiencing moderate to severe clinical conditions. However, it is important to highlight the incidence of clinical improvement in all patients who use this drug.La anemia de células falciformes es una enfermedad hereditaria, caracterizada por la alteración de los glóbulos rojos, haciéndolos parecer una hoz, de ahí el nombre de células falciformes. En Brasil afecta alrededor del 8% de la población negra, pero debido al intenso mestizaje ocurrido históricamente en el país, también se puede observar en personas blancas o pardas. El trabajo se desarrolló con el objetivo general de analizar las características de la anemia falciforme y la toxicidad que presenta la hidroxiueria en su tratamiento. El trabajo fue elaborado a través de una revisión bibliográfica en libros y artículos seleccionados a través de búsquedas en bases de datos y sitios web de libros, el período del material investigado abarca los trabajos publicados entre los años 2010 y 2019. La hidroxiurea es ahora uno de los fármacos más utilizados en el tratamiento de anemia falciforme por poder aumentar la producción de otro tipo de hemoglobina, conocida como hemoglobina fetal (más presente durante la vida uterina). Los altos niveles de hemoglobina fetal disminuyen la polimerización de glóbulos rojos defectuosos y reducen el riesgo de vaso-oclusión. Sin embargo, como cualquier medicamento de quimioterapia, la hidroxiurea tiene efectos adversos. La hidroxiurea representa la primera opción de fármaco para pacientes que experimentan condiciones clínicas de moderadas a graves. Sin embargo, es importante destacar la incidencia de mejoría clínica en todos los pacientes que utilizan este fármaco.Anemia falciforme é uma doença hereditária, caracterizada pela alteração dos glóbulos vermelhos do sangue, tornando-os parecidos com uma foice, daí o nome falciforme. No Brasil, cerca 8% da população negra é afetada, mas devido à intensa história de miscigenação ocorrida no país, observa-se também em pessoas de outras raças. O trabalho foi desenvolvido com o objetivo geral de analisar as características da anemia falciforme e a toxidade apresentada pela hidroxiueria em seu tratamento. O trabalho foi elaborado através de uma revisão bibliográfica em livros e artigos selecionados por meio de buscas em sites de bancos de dados e livros, o período do material pesquisado abrange os trabalhos publicados entre os anos de 2010 e 2019. A hidroxiureia é hoje uma das drogas mais usadas no tratamento da anemia falciforme por ser capaz de aumentar a produção de um outro tipo de hemoglobina, conhecida como hemoglobina fetal (mais presente no período de vida uterina). Altos níveis de hemoglobina fetal diminuem a polimerização das hemácias defeituosas e reduzem o risco de vaso-oclusão. Como qualquer quimioterápico, porém, a hidroxiureia apresenta efeitos adversos. A hidroxiuréia representa a primeira opção medicamentosa para pacientes que vivenciam quadros clínicos considerados de moderados a graves. Todavia, é importante destacar a incidência de melhora clínica em todos os pacientes que fazem uso desse medicamento.Research, Society and Development2022-03-25info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/2626410.33448/rsd-v11i4.26264Research, Society and Development; Vol. 11 No. 4; e51211426264Research, Society and Development; Vol. 11 Núm. 4; e51211426264Research, Society and Development; v. 11 n. 4; e512114262642525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/26264/24145Copyright (c) 2022 Pedro Henrique Ferreira Marçal; Claudia Costa da Silva Paula; Carlos Alberto Silva; Zeina Calek Graize Trindade; Marlucy Rodrigues Lima; Michel Peçanha; Claudine de Menezes; Marileny Boechat Frauches Brandão; Leonardo Oliveira Leão e Silva; Suely Maria Rodrigues; Pedro Henrique Ferreira Marçalhttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessMarçal, Pedro Henrique Ferreira Paula, Claudia Costa da Silva Silva, Carlos Alberto Trindade, Zeina Calek Graize Lima, Marlucy Rodrigues Peçanha, MichelMenezes, Claudine de Brandão, Marileny Boechat Frauches Silva, Leonardo Oliveira Leão e Rodrigues, Suely Maria Marçal, Pedro Henrique Ferreira 2022-03-27T17:17:09Zoai:ojs.pkp.sfu.ca:article/26264Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:44:20.999867Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Toxicity of hydroxyurea in the treatment of sickle cell anemia
Toxicidad de la hidroxiurea en el tratamiento de la anemia de células falciformes
Toxidade da hidroxiueria no tratamento da anemia falciforme
title Toxicity of hydroxyurea in the treatment of sickle cell anemia
spellingShingle Toxicity of hydroxyurea in the treatment of sickle cell anemia
Marçal, Pedro Henrique Ferreira
Hidroxiurea
Anemia de células falciformes
Hemoglobina fetal.
Hydroxyurea
Sickle cell anemia
Fetal hemoglobin.
Hidroxiuréia
Anemia falciforme
Hemoglobina fetal.
title_short Toxicity of hydroxyurea in the treatment of sickle cell anemia
title_full Toxicity of hydroxyurea in the treatment of sickle cell anemia
title_fullStr Toxicity of hydroxyurea in the treatment of sickle cell anemia
title_full_unstemmed Toxicity of hydroxyurea in the treatment of sickle cell anemia
title_sort Toxicity of hydroxyurea in the treatment of sickle cell anemia
author Marçal, Pedro Henrique Ferreira
author_facet Marçal, Pedro Henrique Ferreira
Paula, Claudia Costa da Silva
Silva, Carlos Alberto
Trindade, Zeina Calek Graize
Lima, Marlucy Rodrigues
Peçanha, Michel
Menezes, Claudine de
Brandão, Marileny Boechat Frauches
Silva, Leonardo Oliveira Leão e
Rodrigues, Suely Maria
author_role author
author2 Paula, Claudia Costa da Silva
Silva, Carlos Alberto
Trindade, Zeina Calek Graize
Lima, Marlucy Rodrigues
Peçanha, Michel
Menezes, Claudine de
Brandão, Marileny Boechat Frauches
Silva, Leonardo Oliveira Leão e
Rodrigues, Suely Maria
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Marçal, Pedro Henrique Ferreira
Paula, Claudia Costa da Silva
Silva, Carlos Alberto
Trindade, Zeina Calek Graize
Lima, Marlucy Rodrigues
Peçanha, Michel
Menezes, Claudine de
Brandão, Marileny Boechat Frauches
Silva, Leonardo Oliveira Leão e
Rodrigues, Suely Maria
Marçal, Pedro Henrique Ferreira
dc.subject.por.fl_str_mv Hidroxiurea
Anemia de células falciformes
Hemoglobina fetal.
Hydroxyurea
Sickle cell anemia
Fetal hemoglobin.
Hidroxiuréia
Anemia falciforme
Hemoglobina fetal.
topic Hidroxiurea
Anemia de células falciformes
Hemoglobina fetal.
Hydroxyurea
Sickle cell anemia
Fetal hemoglobin.
Hidroxiuréia
Anemia falciforme
Hemoglobina fetal.
description Sickle cell anemia is a hereditary disease, characterized by the alteration of red blood cells, making them look like a sickle, hence the name sickle cell. In Brazil, it affects about 8% of the black population, but due to the intense miscegenation historically occurred in the country, it can also be observed in white or brown people. The work was developed with the general objective of analyzing the characteristics of sickle cell anemia and the toxicity presented by hydroxyueria in its treatment. The work was elaborated through a bibliographic review in books and articles selected through searches in databases and books websites, the period of the researched material covers the works published between the years 2010 and 2019. Hydroxyurea is now one of the drugs most used in the treatment of sickle cell anemia for being able to increase the production of another type of hemoglobin, known as fetal hemoglobin (more present during the uterine life). High levels of fetal hemoglobin decrease the polymerization of defective red cells and reduce the risk of vaso-occlusion. Like any chemotherapy drug, however, hydroxyurea has adverse effects. Hydroxyurea represents the first drug option for patients experiencing moderate to severe clinical conditions. However, it is important to highlight the incidence of clinical improvement in all patients who use this drug.
publishDate 2022
dc.date.none.fl_str_mv 2022-03-25
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/26264
10.33448/rsd-v11i4.26264
url https://rsdjournal.org/index.php/rsd/article/view/26264
identifier_str_mv 10.33448/rsd-v11i4.26264
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/26264/24145
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Research, Society and Development
publisher.none.fl_str_mv Research, Society and Development
dc.source.none.fl_str_mv Research, Society and Development; Vol. 11 No. 4; e51211426264
Research, Society and Development; Vol. 11 Núm. 4; e51211426264
Research, Society and Development; v. 11 n. 4; e51211426264
2525-3409
reponame:Research, Society and Development
instname:Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
instname_str Universidade Federal de Itajubá (UNIFEI)
instacron_str UNIFEI
institution UNIFEI
reponame_str Research, Society and Development
collection Research, Society and Development
repository.name.fl_str_mv Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)
repository.mail.fl_str_mv rsd.articles@gmail.com
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