Allergic bronchopulmonary aspergillosis in patients with Cystic Fibrosis

Detalhes bibliográficos
Autor(a) principal: Santos Júnior, Reinaldo José dos
Data de Publicação: 2021
Outros Autores: Silva, Natália Millena, Souza, Pâmella Grasielle Vital Dias de
Tipo de documento: Artigo
Idioma: por
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/17227
Resumo: Cystic fibrosis (CF) is a genetic disease of autosomal recessive profile and is characterized by dysfunction of the CFTR gene, which will affect some organs such as the lungs, pancreas, liver, intestines, and testes, with the lungs being the most characteristic. Such changes are capable of causing consistent obstructions due to the viscous mucus produced. Infections are a recurrent factor in carriers of this disease due to the presence of secretion, becoming an ideal environment for the propagation of microorganisms, such as fungi and bacteria, which can colonize the airways of patients and bring about an aggravation, worsening the patient's clinical picture. This is the case of the fungus Aspergillus fumigattus, the cause of allergic bronchopulmonary aspergillosis (ABPA), which can lead to relevant complications, especially in lung function. Analyzing the factors that make CF patients more likely to contract ABPA and how this can worsen their clinical condition, searching for materials from the PUBMED and SCIELO platforms, using the recommendations of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA), the results obtained in this study show that the presence of ABPA in cystic fibrosis patients brings increased microbial colonization, lung deterioration, poorer nutritional status, and greater respiratory obstruction by mucus that causes a greater increase in hospitalization.
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spelling Allergic bronchopulmonary aspergillosis in patients with Cystic FibrosisAspergilosis broncopulmonar alérgica em pacientes com Fibrosis Quística Aspergilose broncopulmonar alérgica em pacientes com Fibrose CísticaFibrosis quísticaAspergillus fumigatusAspergilosis broncopulmonar alérgica.Cystic fibrosisAspergillus fumigatusAllergic bronchopulmonary aspergillosis.Fibrose císticaAspergillus fumigatusAspergilose broncopulmonar alérgica.Cystic fibrosis (CF) is a genetic disease of autosomal recessive profile and is characterized by dysfunction of the CFTR gene, which will affect some organs such as the lungs, pancreas, liver, intestines, and testes, with the lungs being the most characteristic. Such changes are capable of causing consistent obstructions due to the viscous mucus produced. Infections are a recurrent factor in carriers of this disease due to the presence of secretion, becoming an ideal environment for the propagation of microorganisms, such as fungi and bacteria, which can colonize the airways of patients and bring about an aggravation, worsening the patient's clinical picture. This is the case of the fungus Aspergillus fumigattus, the cause of allergic bronchopulmonary aspergillosis (ABPA), which can lead to relevant complications, especially in lung function. Analyzing the factors that make CF patients more likely to contract ABPA and how this can worsen their clinical condition, searching for materials from the PUBMED and SCIELO platforms, using the recommendations of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA), the results obtained in this study show that the presence of ABPA in cystic fibrosis patients brings increased microbial colonization, lung deterioration, poorer nutritional status, and greater respiratory obstruction by mucus that causes a greater increase in hospitalization.La fibrosis quística (FQ) es una enfermedad genética de perfil autosómico recesivo y se caracteriza por la disfunción del gen CFTR, que afectará a algunos órganos como los pulmones, el páncreas, el hígado, el intestino y los testículos, siendo los pulmones los más característicos. Estas alteraciones son capaces de provocar obstrucciones consistentes debido al moco viscoso producido. Las infecciones son un factor recurrente en los portadores de esta enfermedad debido a la presencia de secreciones, convirtiéndose en un ambiente ideal para la propagación de microorganismos como hongos y bacterias, que pueden colonizar las vías respiratorias de los pacientes y traer un agravamiento, empeorando el cuadro clínico del paciente. Es el caso del hongo Aspergillus fumigattus, causante de la aspergilosis broncopulmonar alérgica (ABPA), que puede dar lugar a complicaciones relevantes, especialmente en la función pulmonar. Analizando los factores que hacen que los pacientes con FQ sean más propensos a contraer ABPA y cómo esto puede empeorar su condición clínica, con una búsqueda de materiales de las plataformas PUBMED y SCIELO, utilizando las recomendaciones de los Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA), los resultados obtenidos en este estudio muestran que la presencia de ABPA en los pacientes con fibrosis quística conlleva un aumento de la colonización microbiana, deterioro pulmonar, peor estado nutricional y mayor obstrucción respiratoria por mucosidad, lo que provoca un mayor aumento de la hospitalización.A fibrose cística (FC) é uma doença genética de perfil autossômico recessivo e é caracterizada pela disfunção do gene CFTR, o que irá afetar alguns órgãos como pulmão, pâncreas, fígado, intestino e testículos, sendo os pulmões o mais acometido. Tais alterações são capazes de provocar obstruções consistentes devido ao muco viscoso produzido. As infecções são um fator recorrente nos portadores dessa doença devido a presença da secreção, tornando-se um ambiente ideal para propagação de micro-organismos, como fungos e bactérias, que podem colonizar as vias aéreas dos pacientes e provocar agravos, piorando o quadro clínico do paciente. Como é o caso do fungo Aspergillus fumigattus, causador da aspergilose broncopulmonar alérgica (ABPA), que pode acarretar relevantes complicações principalmente nas funções pulmonares. Analisando os fatores que faz com que os pacientes com FC tenha maior facilidade em contrair a ABPA e como isso pode agravar seu quadro clínico,  com busca de materiais a partir das plataformas PUBMED e SCIELO, utilizando as recomendações do Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA), os resultados obtidos nesse estudo mostram que a presença de ABPA nos fibrocísticos favorecem um aumento nas colonizações microbianas, deterioração pulmonar, pior estado nutricional além de maior obstrução respiratória por muco, contribuindo pelo aumento nos índices de hospitalização.Research, Society and Development2021-06-18info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/1722710.33448/rsd-v10i7.17227Research, Society and Development; Vol. 10 No. 7; e47610717227Research, Society and Development; Vol. 10 Núm. 7; e47610717227Research, Society and Development; v. 10 n. 7; e476107172272525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/17227/14695Copyright (c) 2021 Reinaldo José dos Santos Júnior; Natália Millena Silva; Pâmella Grasielle Vital Dias de Souzahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessSantos Júnior, Reinaldo José dosSilva, Natália MillenaSouza, Pâmella Grasielle Vital Dias de 2021-07-18T21:07:03Zoai:ojs.pkp.sfu.ca:article/17227Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:37:36.743054Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Allergic bronchopulmonary aspergillosis in patients with Cystic Fibrosis
Aspergilosis broncopulmonar alérgica em pacientes com Fibrosis Quística
Aspergilose broncopulmonar alérgica em pacientes com Fibrose Cística
title Allergic bronchopulmonary aspergillosis in patients with Cystic Fibrosis
spellingShingle Allergic bronchopulmonary aspergillosis in patients with Cystic Fibrosis
Santos Júnior, Reinaldo José dos
Fibrosis quística
Aspergillus fumigatus
Aspergilosis broncopulmonar alérgica.
Cystic fibrosis
Aspergillus fumigatus
Allergic bronchopulmonary aspergillosis.
Fibrose cística
Aspergillus fumigatus
Aspergilose broncopulmonar alérgica.
title_short Allergic bronchopulmonary aspergillosis in patients with Cystic Fibrosis
title_full Allergic bronchopulmonary aspergillosis in patients with Cystic Fibrosis
title_fullStr Allergic bronchopulmonary aspergillosis in patients with Cystic Fibrosis
title_full_unstemmed Allergic bronchopulmonary aspergillosis in patients with Cystic Fibrosis
title_sort Allergic bronchopulmonary aspergillosis in patients with Cystic Fibrosis
author Santos Júnior, Reinaldo José dos
author_facet Santos Júnior, Reinaldo José dos
Silva, Natália Millena
Souza, Pâmella Grasielle Vital Dias de
author_role author
author2 Silva, Natália Millena
Souza, Pâmella Grasielle Vital Dias de
author2_role author
author
dc.contributor.author.fl_str_mv Santos Júnior, Reinaldo José dos
Silva, Natália Millena
Souza, Pâmella Grasielle Vital Dias de
dc.subject.por.fl_str_mv Fibrosis quística
Aspergillus fumigatus
Aspergilosis broncopulmonar alérgica.
Cystic fibrosis
Aspergillus fumigatus
Allergic bronchopulmonary aspergillosis.
Fibrose cística
Aspergillus fumigatus
Aspergilose broncopulmonar alérgica.
topic Fibrosis quística
Aspergillus fumigatus
Aspergilosis broncopulmonar alérgica.
Cystic fibrosis
Aspergillus fumigatus
Allergic bronchopulmonary aspergillosis.
Fibrose cística
Aspergillus fumigatus
Aspergilose broncopulmonar alérgica.
description Cystic fibrosis (CF) is a genetic disease of autosomal recessive profile and is characterized by dysfunction of the CFTR gene, which will affect some organs such as the lungs, pancreas, liver, intestines, and testes, with the lungs being the most characteristic. Such changes are capable of causing consistent obstructions due to the viscous mucus produced. Infections are a recurrent factor in carriers of this disease due to the presence of secretion, becoming an ideal environment for the propagation of microorganisms, such as fungi and bacteria, which can colonize the airways of patients and bring about an aggravation, worsening the patient's clinical picture. This is the case of the fungus Aspergillus fumigattus, the cause of allergic bronchopulmonary aspergillosis (ABPA), which can lead to relevant complications, especially in lung function. Analyzing the factors that make CF patients more likely to contract ABPA and how this can worsen their clinical condition, searching for materials from the PUBMED and SCIELO platforms, using the recommendations of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA), the results obtained in this study show that the presence of ABPA in cystic fibrosis patients brings increased microbial colonization, lung deterioration, poorer nutritional status, and greater respiratory obstruction by mucus that causes a greater increase in hospitalization.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-18
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/17227
10.33448/rsd-v10i7.17227
url https://rsdjournal.org/index.php/rsd/article/view/17227
identifier_str_mv 10.33448/rsd-v10i7.17227
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/17227/14695
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; e47610717227
Research, Society and Development; Vol. 10 Núm. 7; e47610717227
Research, Society and Development; v. 10 n. 7; e47610717227
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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