Portuguese consensus document for the management of alpha-1-antitrypsin deficiency

Detalhes bibliográficos
Autor(a) principal: Lopes, A.P.
Data de Publicação: 2018
Outros Autores: Mineiro, M.A., Costa, F., Gomes, J., Santos, C., Antunes, C., Maia, D., Melo, R., Canotilho, M., Magalhães, E., Vicente, I., Valente, C., Gonçalves, B.G., Conde, B., Guimarães, C., Sousa, C., Amado, J., Brandão, M.E., Sucena, M., Oliveira, M.J., Seixas, S., Teixeira, V., Telo, L.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.26/33996
Resumo: Alpha-1-antitrypsin deficiency (AATD) is a genetic autosomal codominant disorder caused by mutations in SERPINA1 gene. It is one of the most prevalent genetic disorders, although it remains underdiagnosed. Whereas at international level there are several areas of consensus on this disorder, in Portugal, inter-hospital heterogeneity in clinical practice and resources available have been adding difficulties in reaching a diagnosis and in making therapeutic decisions in this group of patients. This raised a need to draft a document expressing a national consensus for AATD. To this end, a group of experts in this field was created within the Portuguese Pulmonology Society - Study group on AATD, in order to elaborate the current manuscript. The authors reviewed the existing literature and provide here general guidance and extensive recommendations for the diagnosis and management of AATD that can be adopted by Portuguese clinicians from different areas of Medicine. This article is part of a supplement entitled "Portuguese consensus document for the management of alpha-1-antitrypsin deficiency" which is sponsored by Sociedade Portuguesa de Pneumologia.
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spelling Portuguese consensus document for the management of alpha-1-antitrypsin deficiencyAlgorithmsHumansLung DiseasesPatient SelectionPortugalPractice Guidelines as Topicalpha 1-Antitrypsin DeficiencyMadeira IslandAlpha-1-antitrypsin deficiency (AATD) is a genetic autosomal codominant disorder caused by mutations in SERPINA1 gene. It is one of the most prevalent genetic disorders, although it remains underdiagnosed. Whereas at international level there are several areas of consensus on this disorder, in Portugal, inter-hospital heterogeneity in clinical practice and resources available have been adding difficulties in reaching a diagnosis and in making therapeutic decisions in this group of patients. This raised a need to draft a document expressing a national consensus for AATD. To this end, a group of experts in this field was created within the Portuguese Pulmonology Society - Study group on AATD, in order to elaborate the current manuscript. The authors reviewed the existing literature and provide here general guidance and extensive recommendations for the diagnosis and management of AATD that can be adopted by Portuguese clinicians from different areas of Medicine. This article is part of a supplement entitled "Portuguese consensus document for the management of alpha-1-antitrypsin deficiency" which is sponsored by Sociedade Portuguesa de Pneumologia.Official Journal of the Portuguese Society of PulmonologyRepositório ComumLopes, A.P.Mineiro, M.A.Costa, F.Gomes, J.Santos, C.Antunes, C.Maia, D.Melo, R.Canotilho, M.Magalhães, E.Vicente, I.Valente, C.Gonçalves, B.G.Conde, B.Guimarães, C.Sousa, C.Amado, J.Brandão, M.E.Sucena, M.Oliveira, M.J.Seixas, S.Teixeira, V.Telo, L.2020-11-08T23:14:36Z20182018-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.26/33996engPulmonol. 2018, 24(S1):1-22531-043710.1016/j.pulmoe.2018.09.004info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-10T02:17:04Zoai:comum.rcaap.pt:10400.26/33996Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T22:34:29.293268Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Portuguese consensus document for the management of alpha-1-antitrypsin deficiency
title Portuguese consensus document for the management of alpha-1-antitrypsin deficiency
spellingShingle Portuguese consensus document for the management of alpha-1-antitrypsin deficiency
Lopes, A.P.
Algorithms
Humans
Lung Diseases
Patient Selection
Portugal
Practice Guidelines as Topic
alpha 1-Antitrypsin Deficiency
Madeira Island
title_short Portuguese consensus document for the management of alpha-1-antitrypsin deficiency
title_full Portuguese consensus document for the management of alpha-1-antitrypsin deficiency
title_fullStr Portuguese consensus document for the management of alpha-1-antitrypsin deficiency
title_full_unstemmed Portuguese consensus document for the management of alpha-1-antitrypsin deficiency
title_sort Portuguese consensus document for the management of alpha-1-antitrypsin deficiency
author Lopes, A.P.
author_facet Lopes, A.P.
Mineiro, M.A.
Costa, F.
Gomes, J.
Santos, C.
Antunes, C.
Maia, D.
Melo, R.
Canotilho, M.
Magalhães, E.
Vicente, I.
Valente, C.
Gonçalves, B.G.
Conde, B.
Guimarães, C.
Sousa, C.
Amado, J.
Brandão, M.E.
Sucena, M.
Oliveira, M.J.
Seixas, S.
Teixeira, V.
Telo, L.
author_role author
author2 Mineiro, M.A.
Costa, F.
Gomes, J.
Santos, C.
Antunes, C.
Maia, D.
Melo, R.
Canotilho, M.
Magalhães, E.
Vicente, I.
Valente, C.
Gonçalves, B.G.
Conde, B.
Guimarães, C.
Sousa, C.
Amado, J.
Brandão, M.E.
Sucena, M.
Oliveira, M.J.
Seixas, S.
Teixeira, V.
Telo, L.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Comum
dc.contributor.author.fl_str_mv Lopes, A.P.
Mineiro, M.A.
Costa, F.
Gomes, J.
Santos, C.
Antunes, C.
Maia, D.
Melo, R.
Canotilho, M.
Magalhães, E.
Vicente, I.
Valente, C.
Gonçalves, B.G.
Conde, B.
Guimarães, C.
Sousa, C.
Amado, J.
Brandão, M.E.
Sucena, M.
Oliveira, M.J.
Seixas, S.
Teixeira, V.
Telo, L.
dc.subject.por.fl_str_mv Algorithms
Humans
Lung Diseases
Patient Selection
Portugal
Practice Guidelines as Topic
alpha 1-Antitrypsin Deficiency
Madeira Island
topic Algorithms
Humans
Lung Diseases
Patient Selection
Portugal
Practice Guidelines as Topic
alpha 1-Antitrypsin Deficiency
Madeira Island
description Alpha-1-antitrypsin deficiency (AATD) is a genetic autosomal codominant disorder caused by mutations in SERPINA1 gene. It is one of the most prevalent genetic disorders, although it remains underdiagnosed. Whereas at international level there are several areas of consensus on this disorder, in Portugal, inter-hospital heterogeneity in clinical practice and resources available have been adding difficulties in reaching a diagnosis and in making therapeutic decisions in this group of patients. This raised a need to draft a document expressing a national consensus for AATD. To this end, a group of experts in this field was created within the Portuguese Pulmonology Society - Study group on AATD, in order to elaborate the current manuscript. The authors reviewed the existing literature and provide here general guidance and extensive recommendations for the diagnosis and management of AATD that can be adopted by Portuguese clinicians from different areas of Medicine. This article is part of a supplement entitled "Portuguese consensus document for the management of alpha-1-antitrypsin deficiency" which is sponsored by Sociedade Portuguesa de Pneumologia.
publishDate 2018
dc.date.none.fl_str_mv 2018
2018-01-01T00:00:00Z
2020-11-08T23:14:36Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.26/33996
url http://hdl.handle.net/10400.26/33996
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Pulmonol. 2018, 24(S1):1-2
2531-0437
10.1016/j.pulmoe.2018.09.004
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Official Journal of the Portuguese Society of Pulmonology
publisher.none.fl_str_mv Official Journal of the Portuguese Society of Pulmonology
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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