Falciform Anemia: Conception of the family caregiver about the disease and its treatment in a City in Maranhão

Detalhes bibliográficos
Autor(a) principal: Barroso, Helen Lucy Maria Rocha
Data de Publicação: 2021
Outros Autores: Sipaúba, Alana Jéssyca Costa, Andrade, Thátila Larissa da Cruz, Maciel, Josielen Barroso Leal, Silva, Klécia de Sousa Marques da, Fonseca, Suélly Mayara Rodrigues da, Batista, Gardênia Monteiro
Tipo de documento: Artigo
Idioma: por
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/16450
Resumo: Introduction: Sickle cell anemia - AF is a genetic alteration, since hemoglobin mutation occurs, designated as hemoglobin S or HbS. Objective: to know the conception of the family caregiver of the PA patient about the disease and its treatment in the city of Colinas. Methodology: This is a descriptive study with a qualitative approach, carried out in the municipality of Colinas - MA, from May to June 2019. Where semi-structured questionnaires were used as a data collection instrument. Results and Discussion: Eight (8) responsible for sickle cell anemia patients were interviewed, of the eight (8), six (6) is the mother of the carrier, one (1) is the grandmother and one (1) is the great-grandmother of the child , age 25 to 64 years. When asked about ethnicity, 75% considered themselves brown, 12.5% ​​black and 12.5% ​​white; on family income 12.5% ​​declared to receive two minimum wages, 62.5% live on one minimum wage and 25% live on less than one minimum wage; when asking about education, 50% have not completed elementary school, 25% have incomplete high school and 25% have completed high school; on the number of children 37.5% have three (3) children, 37.5% have two (2) children and 25% only one (1) child. Conclusion: In this study, it was analyzed that the municipality does not provide all the centers that integrate the treatment of sickle cell disease.
id UNIFEI_626ce83daed75aa31e0016d4ccd68490
oai_identifier_str oai:ojs.pkp.sfu.ca:article/16450
network_acronym_str UNIFEI
network_name_str Research, Society and Development
repository_id_str
spelling Falciform Anemia: Conception of the family caregiver about the disease and its treatment in a City in MaranhãoAnemia Falciforme: Concepción del cuidador familiar de la enfermedad y su tratamiento en un Municipio de MaranhãoAnemia Falciforme: Concepção do cuidador familiar sobre a doença e seu tratamento em um Município do MaranhãoSickle Cell AnemiaMedical GeneticsFamily caregiver.Anemia FalciformeGenética MédicaCuidador familiar.Anemia de células falciformesGenética MédicaCuidador familiar.Introduction: Sickle cell anemia - AF is a genetic alteration, since hemoglobin mutation occurs, designated as hemoglobin S or HbS. Objective: to know the conception of the family caregiver of the PA patient about the disease and its treatment in the city of Colinas. Methodology: This is a descriptive study with a qualitative approach, carried out in the municipality of Colinas - MA, from May to June 2019. Where semi-structured questionnaires were used as a data collection instrument. Results and Discussion: Eight (8) responsible for sickle cell anemia patients were interviewed, of the eight (8), six (6) is the mother of the carrier, one (1) is the grandmother and one (1) is the great-grandmother of the child , age 25 to 64 years. When asked about ethnicity, 75% considered themselves brown, 12.5% ​​black and 12.5% ​​white; on family income 12.5% ​​declared to receive two minimum wages, 62.5% live on one minimum wage and 25% live on less than one minimum wage; when asking about education, 50% have not completed elementary school, 25% have incomplete high school and 25% have completed high school; on the number of children 37.5% have three (3) children, 37.5% have two (2) children and 25% only one (1) child. Conclusion: In this study, it was analyzed that the municipality does not provide all the centers that integrate the treatment of sickle cell disease.Indroducción: La anemia de células falciformes - AF es una alteración genética, ya que se produce una mutación de la hemoglobina, denominada hemoglobina S o HbS. Objetivo: conocer la concepción del cuidador familiar del paciente AP sobre la enfermedad y su tratamiento en la ciudad de Colinas. Metodología: Se trata de un estudio descriptivo con enfoque cualitativo, realizado en la ciudad de Colinas - MA, de mayo a junio de 2019. Donde se utilizaron cuestionarios semiestructurados como instrumento de recolección de datos. Resultados y Discusión: Se entrevistaron ocho (8) pacientes responsables de anemia falciforme, de los ocho (8), seis (6) es la madre del portador, uno (1) es la abuela y uno (1) es el tatarabuelo. -abuela del niño, de 25 a 64 años. Cuando se les preguntó sobre la etnia, el 75% se consideró moreno, el 12,5% negro y el 12,5% blanco; de los ingresos familiares, el 12,5% declaró recibir dos salarios mínimos, el 62,5% vive con un salario mínimo y el 25% vive con menos de un salario mínimo; al preguntar sobre educación, el 50% no completó la educación primaria, el 25% tiene educación secundaria incompleta y el 25% la educación secundaria completa; sobre el número de hijos el 37,5% tiene tres (3) hijos, el 37,5% tiene dos (2) hijos y el 25% solo un (1) hijo. Conclusión: En el presente estudio se analizó que el municipio no cuenta con todos los centros que integran el tratamiento de la anemia falciforme.Introdução: A anemia falciforme - AF é uma alteração genética, pois acontece a mutação da hemoglobina, designada como hemoglobina S ou HbS. Objetivo: conhecer a concepção do cuidador familiar do portador da AF, sobre a doença e seu tratamento no município de Colinas. Metodologia: Trata-se de um estudo na forma descritiva com abordagem qualitativa, realizado no município de Colinas - MA, no período de maio a junho de 2019. Onde utilizou-se como instrumento de coleta de dados, questionários semiestruturados. Resultados e Discussão: Foram entrevistadas oito (8) responsáveis pelos portadores de anemia falciforme, dos oito (8), seis (6) é a mãe do portador, um (1) é a avó e um (1) é a bisavó da criança, idade de 25 a 64 anos. Ao questionar sobre a etnia 75% se consideraram pardos, 12,5% negros e 12,5% brancos; sobre a renda familiar 12,5% declararam receber dois salários mínimos, 62,5% vivem com um salário mínimo e 25% vivem com menos de um salário mínimo; ao indagar sobre a escolaridade 50% não concluíram o ensino fundamental, 25% têm ensino médio incompleto e 25% concluíram ensino médio; sobre a quantidade de filhos 37,5% tem três (3) filhos, 37,5% possuem dois (2) filhos e 25% apenas um (1) filho. Conclusão: No presente estudo foi analisado que o município não fornece todos os núcleos que integra o tratamento da siclemia.Research, Society and Development2021-06-20info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/1645010.33448/rsd-v10i7.16450Research, Society and Development; Vol. 10 No. 7; e24010716450Research, Society and Development; Vol. 10 Núm. 7; e24010716450Research, Society and Development; v. 10 n. 7; e240107164502525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/16450/14744Copyright (c) 2021 Helen Lucy Maria Rocha Barroso; Alana Jéssyca Costa Sipaúba; Thátila Larissa da Cruz Andrade; Josielen Barroso Leal Maciel; Klécia de Sousa Marques da Silva; Suélly Mayara Rodrigues da Fonseca; Gardênia Monteiro Batistahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessBarroso, Helen Lucy Maria Rocha Sipaúba, Alana Jéssyca Costa Andrade, Thátila Larissa da Cruz Maciel, Josielen Barroso Leal Silva, Klécia de Sousa Marques da Fonseca, Suélly Mayara Rodrigues da Batista, Gardênia Monteiro 2021-07-18T21:07:03Zoai:ojs.pkp.sfu.ca:article/16450Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:36:59.957472Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Falciform Anemia: Conception of the family caregiver about the disease and its treatment in a City in Maranhão
Anemia Falciforme: Concepción del cuidador familiar de la enfermedad y su tratamiento en un Municipio de Maranhão
Anemia Falciforme: Concepção do cuidador familiar sobre a doença e seu tratamento em um Município do Maranhão
title Falciform Anemia: Conception of the family caregiver about the disease and its treatment in a City in Maranhão
spellingShingle Falciform Anemia: Conception of the family caregiver about the disease and its treatment in a City in Maranhão
Barroso, Helen Lucy Maria Rocha
Sickle Cell Anemia
Medical Genetics
Family caregiver.
Anemia Falciforme
Genética Médica
Cuidador familiar.
Anemia de células falciformes
Genética Médica
Cuidador familiar.
title_short Falciform Anemia: Conception of the family caregiver about the disease and its treatment in a City in Maranhão
title_full Falciform Anemia: Conception of the family caregiver about the disease and its treatment in a City in Maranhão
title_fullStr Falciform Anemia: Conception of the family caregiver about the disease and its treatment in a City in Maranhão
title_full_unstemmed Falciform Anemia: Conception of the family caregiver about the disease and its treatment in a City in Maranhão
title_sort Falciform Anemia: Conception of the family caregiver about the disease and its treatment in a City in Maranhão
author Barroso, Helen Lucy Maria Rocha
author_facet Barroso, Helen Lucy Maria Rocha
Sipaúba, Alana Jéssyca Costa
Andrade, Thátila Larissa da Cruz
Maciel, Josielen Barroso Leal
Silva, Klécia de Sousa Marques da
Fonseca, Suélly Mayara Rodrigues da
Batista, Gardênia Monteiro
author_role author
author2 Sipaúba, Alana Jéssyca Costa
Andrade, Thátila Larissa da Cruz
Maciel, Josielen Barroso Leal
Silva, Klécia de Sousa Marques da
Fonseca, Suélly Mayara Rodrigues da
Batista, Gardênia Monteiro
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Barroso, Helen Lucy Maria Rocha
Sipaúba, Alana Jéssyca Costa
Andrade, Thátila Larissa da Cruz
Maciel, Josielen Barroso Leal
Silva, Klécia de Sousa Marques da
Fonseca, Suélly Mayara Rodrigues da
Batista, Gardênia Monteiro
dc.subject.por.fl_str_mv Sickle Cell Anemia
Medical Genetics
Family caregiver.
Anemia Falciforme
Genética Médica
Cuidador familiar.
Anemia de células falciformes
Genética Médica
Cuidador familiar.
topic Sickle Cell Anemia
Medical Genetics
Family caregiver.
Anemia Falciforme
Genética Médica
Cuidador familiar.
Anemia de células falciformes
Genética Médica
Cuidador familiar.
description Introduction: Sickle cell anemia - AF is a genetic alteration, since hemoglobin mutation occurs, designated as hemoglobin S or HbS. Objective: to know the conception of the family caregiver of the PA patient about the disease and its treatment in the city of Colinas. Methodology: This is a descriptive study with a qualitative approach, carried out in the municipality of Colinas - MA, from May to June 2019. Where semi-structured questionnaires were used as a data collection instrument. Results and Discussion: Eight (8) responsible for sickle cell anemia patients were interviewed, of the eight (8), six (6) is the mother of the carrier, one (1) is the grandmother and one (1) is the great-grandmother of the child , age 25 to 64 years. When asked about ethnicity, 75% considered themselves brown, 12.5% ​​black and 12.5% ​​white; on family income 12.5% ​​declared to receive two minimum wages, 62.5% live on one minimum wage and 25% live on less than one minimum wage; when asking about education, 50% have not completed elementary school, 25% have incomplete high school and 25% have completed high school; on the number of children 37.5% have three (3) children, 37.5% have two (2) children and 25% only one (1) child. Conclusion: In this study, it was analyzed that the municipality does not provide all the centers that integrate the treatment of sickle cell disease.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-20
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/16450
10.33448/rsd-v10i7.16450
url https://rsdjournal.org/index.php/rsd/article/view/16450
identifier_str_mv 10.33448/rsd-v10i7.16450
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/16450/14744
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. 7; e24010716450
Research, Society and Development; Vol. 10 Núm. 7; e24010716450
Research, Society and Development; v. 10 n. 7; e24010716450
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
_version_ 1797052679807041536