Therapeutics of coagulopathies in patients attended at the blood center of a northeastern region of Brazil

Detalhes bibliográficos
Autor(a) principal: Teles, Weber de Santana
Data de Publicação: 2021
Outros Autores: Silva, Max Cruz da, Torres, Ruth Cristini, Azevedo, Marcel Vinícius Cunha, Andrade, Ana Fátima Souza Melo de, Calasans, Taíssa Alice Soledade, Debbo, Alejandra, Barros, Ângela Maria Melo Sá, Santos Junior, Paulo Celso Curvelo, Silva, Rute Nascimento da
Tipo de documento: Artigo
Idioma: por
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/17813
Resumo: Hemophilia is a congenital and genetic hemorrhagic disease that is characterized by a deficiency of a plasma protein responsible for clotting, and affects more males due to an alteration in the X chromosome. Data were analyzed at the blood center of a region in northeastern Brazil. The objective of this study was to evaluate the epidemiological profile and treatment of coagulopathies in patients treated at the Blood Center during the years 2018 and 2019. In total, 242 patient records were analyzed, and tabulated in absolute frequency using epidemiological variables, type of hemophilia, and use of coagulation factors. The results showed that of the 242 patients with coagulopathies, 154 (63.6%) were male and 87 (36.4%), of these, 113 (47%) had hemophilia A, with a higher prevalence between 16 and 30 (43 %) years old. Hemophilia B 18 (8%) patients, aged between 36 and 50 (33%) years. Regarding the location, the urban region had the highest prevalence for patients with hemophilia type A. Of the 141 patients who received coagulation factor, 76 used recombinant Factor VIII, 66 used Urgent Home Dose (DDU) . The number of International Units (UI) dispensed with the highest proportion occurred in August 2018 and June 2019. It is concluded that the need to implement monitoring of patients who make use of coagulation factors, as well as the implementation of investments the federal government in order for the treatment to be continued.
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spelling Therapeutics of coagulopathies in patients attended at the blood center of a northeastern region of BrazilTerapéutica de las coagulopatías en pacientes atendidos en el centro de sangre de una región nororiental de BrasilTerapêutica das coagulopatias em pacientes atendidos no hemocentro de uma região do nordeste brasileiroHemofiliaDiagnósticoConductas terapéuticas.HemophiliaDiagnosisTherapeutic conducts.HemofiliaDiagnósticoCondutas terapêuticas. Hemophilia is a congenital and genetic hemorrhagic disease that is characterized by a deficiency of a plasma protein responsible for clotting, and affects more males due to an alteration in the X chromosome. Data were analyzed at the blood center of a region in northeastern Brazil. The objective of this study was to evaluate the epidemiological profile and treatment of coagulopathies in patients treated at the Blood Center during the years 2018 and 2019. In total, 242 patient records were analyzed, and tabulated in absolute frequency using epidemiological variables, type of hemophilia, and use of coagulation factors. The results showed that of the 242 patients with coagulopathies, 154 (63.6%) were male and 87 (36.4%), of these, 113 (47%) had hemophilia A, with a higher prevalence between 16 and 30 (43 %) years old. Hemophilia B 18 (8%) patients, aged between 36 and 50 (33%) years. Regarding the location, the urban region had the highest prevalence for patients with hemophilia type A. Of the 141 patients who received coagulation factor, 76 used recombinant Factor VIII, 66 used Urgent Home Dose (DDU) . The number of International Units (UI) dispensed with the highest proportion occurred in August 2018 and June 2019. It is concluded that the need to implement monitoring of patients who make use of coagulation factors, as well as the implementation of investments the federal government in order for the treatment to be continued.La hemofilia es una enfermedad hemorrágica congénita y genética que se caracteriza por la deficiencia de una proteína plasmática responsable de la coagulación, y afecta a más hombres debido a una alteración en el cromosoma X. Los datos fueron analizados en el centro de sangre de una región del noreste de Brasil. El objetivo de este estudio fue evaluar el perfil epidemiológico y tratamiento de las coagulopatías en pacientes atendidos en el Centro de Sangre durante los años 2018 y 2019. En total, se analizaron 242 historias clínicas y se tabularon en frecuencia absoluta utilizando variables epidemiológicas, tipo de hemofilia. y uso de factores de coagulación. Los resultados mostraron que de los 242 pacientes con coagulopatías, 154 (63,6%) eran del sexo masculino y 87 (36,4%), de estos 113 (47%) tenían hemofilia A, con una mayor prevalencia entre los 16 y 30 (43%) años. viejo. Pacientes con hemofilia B 18 (8%), con edades comprendidas entre 36 y 50 (33%) años. En cuanto a la ubicación, la región urbana tuvo la mayor prevalencia de pacientes con hemofilia tipo A. De los 141 pacientes que recibieron factor de coagulación, 76 usaron Factor VIII recombinante, 66 usaron Urgent Home Dose (DDU). El número de Unidades Internacionales (UI) prescindidas de mayor proporción ocurrió en agosto de 2018 y junio de 2019. Se concluye que la necesidad de implementar el monitoreo de los pacientes que hacen uso de factores de coagulación, así como la implementación de inversiones del gobierno federal en Orden de continuación del tratamiento.A hemofilia é uma doença hemorrágica congênita e genética que se configura pela deficiência de uma proteína plasmática responsável pela coagulação, e acomete mais indivíduos do sexo masculino devido a uma alteração no cromossomo X. Os dados foram analisados no hemocentro de uma região do nordeste brasileiro. O objetivo do trabalho foi avaliar o perfil epidemiológico e tratamento das coagulopatias em pacientes atendidos no Hemocentro, durante os anos de 2018 e 2019. No total foram analisados 242 prontuários de pacientes, e tabulados em frequência absoluta utilizando variáveis epidemiológicas, tipo de hemofilia, e uso dos fatores de coagulação. Os resultados mostraram que dos 242 pacientes portadores de coagulopatias, 154 (63,6%) eram sexo masculino e 87(36,4%), destes, 113 (47%) apresentaram hemofilia A, com maior prevalência entre 16 à 30 (43%) anos.  A hemofilia B 18 (8%) pacientes, com faixa etária entre 36 a 50 (33%) anos. Em relação a localização a região urbana apresentou a maior prevalência para os portadores de hemofilia do tipo A.  Dos 141pacientes que receberam fator de coagulação, 76 fizeram o uso de o Fator VIII recombinante, 66 fizeram o uso da Dose Domiciliar de Urgência (D.D.u). A quantidade de Unidades Internacionais (UI) dispensadas com maior proporção ocorreu no mês de agosto de 2018 e junho de 2019.  Conclui-se que a necessidade de implementação de acompanhamento aos pacientes que fazem uso dos fatores de coagulação, assim como a implementação de investimentos do governo federal afim de que o tratamento tenha continuidade.Research, Society and Development2021-07-23info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/1781310.33448/rsd-v10i9.17813Research, Society and Development; Vol. 10 No. 9; e15510917813Research, Society and Development; Vol. 10 Núm. 9; e15510917813Research, Society and Development; v. 10 n. 9; e155109178132525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/17813/16006Copyright (c) 2021 Weber de Santana Teles; Max Cruz da Silva; Ruth Cristini Torres; Marcel Vinícius Cunha Azevedo; Ana Fátima Souza Melo de Andrade; Taíssa Alice Soledade Calasans; Alejandra Debbo; Ângela Maria Melo Sá Barros; Paulo Celso Curvelo Santos Junior; Rute Nascimento da Silvahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessTeles, Weber de Santana Silva, Max Cruz da Torres, Ruth Cristini Azevedo, Marcel Vinícius Cunha Andrade, Ana Fátima Souza Melo de Calasans, Taíssa Alice Soledade Debbo, AlejandraBarros, Ângela Maria Melo Sá Santos Junior, Paulo Celso Curvelo Silva, Rute Nascimento da 2021-09-12T14:28:06Zoai:ojs.pkp.sfu.ca:article/17813Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:38:05.182385Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Therapeutics of coagulopathies in patients attended at the blood center of a northeastern region of Brazil
Terapéutica de las coagulopatías en pacientes atendidos en el centro de sangre de una región nororiental de Brasil
Terapêutica das coagulopatias em pacientes atendidos no hemocentro de uma região do nordeste brasileiro
title Therapeutics of coagulopathies in patients attended at the blood center of a northeastern region of Brazil
spellingShingle Therapeutics of coagulopathies in patients attended at the blood center of a northeastern region of Brazil
Teles, Weber de Santana
Hemofilia
Diagnóstico
Conductas terapéuticas.
Hemophilia
Diagnosis
Therapeutic conducts.
Hemofilia
Diagnóstico
Condutas terapêuticas.
title_short Therapeutics of coagulopathies in patients attended at the blood center of a northeastern region of Brazil
title_full Therapeutics of coagulopathies in patients attended at the blood center of a northeastern region of Brazil
title_fullStr Therapeutics of coagulopathies in patients attended at the blood center of a northeastern region of Brazil
title_full_unstemmed Therapeutics of coagulopathies in patients attended at the blood center of a northeastern region of Brazil
title_sort Therapeutics of coagulopathies in patients attended at the blood center of a northeastern region of Brazil
author Teles, Weber de Santana
author_facet Teles, Weber de Santana
Silva, Max Cruz da
Torres, Ruth Cristini
Azevedo, Marcel Vinícius Cunha
Andrade, Ana Fátima Souza Melo de
Calasans, Taíssa Alice Soledade
Debbo, Alejandra
Barros, Ângela Maria Melo Sá
Santos Junior, Paulo Celso Curvelo
Silva, Rute Nascimento da
author_role author
author2 Silva, Max Cruz da
Torres, Ruth Cristini
Azevedo, Marcel Vinícius Cunha
Andrade, Ana Fátima Souza Melo de
Calasans, Taíssa Alice Soledade
Debbo, Alejandra
Barros, Ângela Maria Melo Sá
Santos Junior, Paulo Celso Curvelo
Silva, Rute Nascimento da
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Teles, Weber de Santana
Silva, Max Cruz da
Torres, Ruth Cristini
Azevedo, Marcel Vinícius Cunha
Andrade, Ana Fátima Souza Melo de
Calasans, Taíssa Alice Soledade
Debbo, Alejandra
Barros, Ângela Maria Melo Sá
Santos Junior, Paulo Celso Curvelo
Silva, Rute Nascimento da
dc.subject.por.fl_str_mv Hemofilia
Diagnóstico
Conductas terapéuticas.
Hemophilia
Diagnosis
Therapeutic conducts.
Hemofilia
Diagnóstico
Condutas terapêuticas.
topic Hemofilia
Diagnóstico
Conductas terapéuticas.
Hemophilia
Diagnosis
Therapeutic conducts.
Hemofilia
Diagnóstico
Condutas terapêuticas.
description Hemophilia is a congenital and genetic hemorrhagic disease that is characterized by a deficiency of a plasma protein responsible for clotting, and affects more males due to an alteration in the X chromosome. Data were analyzed at the blood center of a region in northeastern Brazil. The objective of this study was to evaluate the epidemiological profile and treatment of coagulopathies in patients treated at the Blood Center during the years 2018 and 2019. In total, 242 patient records were analyzed, and tabulated in absolute frequency using epidemiological variables, type of hemophilia, and use of coagulation factors. The results showed that of the 242 patients with coagulopathies, 154 (63.6%) were male and 87 (36.4%), of these, 113 (47%) had hemophilia A, with a higher prevalence between 16 and 30 (43 %) years old. Hemophilia B 18 (8%) patients, aged between 36 and 50 (33%) years. Regarding the location, the urban region had the highest prevalence for patients with hemophilia type A. Of the 141 patients who received coagulation factor, 76 used recombinant Factor VIII, 66 used Urgent Home Dose (DDU) . The number of International Units (UI) dispensed with the highest proportion occurred in August 2018 and June 2019. It is concluded that the need to implement monitoring of patients who make use of coagulation factors, as well as the implementation of investments the federal government in order for the treatment to be continued.
publishDate 2021
dc.date.none.fl_str_mv 2021-07-23
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/17813
10.33448/rsd-v10i9.17813
url https://rsdjournal.org/index.php/rsd/article/view/17813
identifier_str_mv 10.33448/rsd-v10i9.17813
dc.language.iso.fl_str_mv por
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dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/17813/16006
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. 10 No. 9; e15510917813
Research, Society and Development; Vol. 10 Núm. 9; e15510917813
Research, Society and Development; v. 10 n. 9; e15510917813
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)
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