Alpha-1 Antitrypsin Deficiency: Principles of Care

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Joana F
Data de Publicação: 2020
Outros Autores: Mineiro, Alexandra, Reis, António, Ventura, David G, Fernandez-Llimos, Fernando, Costa, Filipa, Gomes, Joana, Silva, José Manuel, Lopes, Paulo, Cordeiro, Carlos Robalo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.16/2471
Resumo: Alpha-1 antitrypsin deficiency is an autosomal co-dominant inherited disorder that results in decreased circulating levels of alpha-1 antitrypsin (also known as alpha-1 proteinase inhibitor) and predisposes affected individuals to early onset lung and liver disease. There is currently no cure for alpha-1 antitrypsin deficiency. However, appropriate treatment and a high standard of clinical care can prevent patients from being seriously affected and having to undergo major medical interventions, such as organ transplantation. Beyond managing the symptoms associated with alpha-1 antitrypsin deficiency, alpha-1 proteinase inhibitor therapy is the only treatment for the condition's underlying cause. Early diagnosis is important to ensure efficient therapeutic strategies and to minimize further deterioration of lung function. alpha-1 antitrypsin deficiency is under diagnosed globally, partly because the disease has no unique presenting symptoms. This document was prepared by a Portuguese multidisciplinary group and it aims to set out comprehensive principles of care for Alpha-1 antitrypsin deficiency. These include the importance of registries, the need for clinical research, the need for consistent recommendations (regarding diagnosis, treatment and monitoring), the role of reference centres, the requirement for sustained access to treatment, diagnostic and support services, and the role of patient organizations.
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spelling Alpha-1 Antitrypsin Deficiency: Principles of CareDeficiência de Alfa-1 Antitripsina: Princípios do TratamentoHealth Care QualityAccess, and EvaluationProfessional PracticeStandard of Carealpha 1-Antitrypsin Deficiency/therapyAlpha-1 antitrypsin deficiency is an autosomal co-dominant inherited disorder that results in decreased circulating levels of alpha-1 antitrypsin (also known as alpha-1 proteinase inhibitor) and predisposes affected individuals to early onset lung and liver disease. There is currently no cure for alpha-1 antitrypsin deficiency. However, appropriate treatment and a high standard of clinical care can prevent patients from being seriously affected and having to undergo major medical interventions, such as organ transplantation. Beyond managing the symptoms associated with alpha-1 antitrypsin deficiency, alpha-1 proteinase inhibitor therapy is the only treatment for the condition's underlying cause. Early diagnosis is important to ensure efficient therapeutic strategies and to minimize further deterioration of lung function. alpha-1 antitrypsin deficiency is under diagnosed globally, partly because the disease has no unique presenting symptoms. This document was prepared by a Portuguese multidisciplinary group and it aims to set out comprehensive principles of care for Alpha-1 antitrypsin deficiency. These include the importance of registries, the need for clinical research, the need for consistent recommendations (regarding diagnosis, treatment and monitoring), the role of reference centres, the requirement for sustained access to treatment, diagnostic and support services, and the role of patient organizations.Centro Editor Livreiro da Ordem dos MédicosRepositório Científico do Centro Hospitalar Universitário de Santo AntónioRodrigues, Joana FMineiro, AlexandraReis, AntónioVentura, David GFernandez-Llimos, FernandoCosta, FilipaGomes, JoanaSilva, José ManuelLopes, PauloCordeiro, Carlos Robalo2021-06-11T11:25:48Z2020-06-012020-06-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.16/2471engRodrigues JF, Mineiro A, Reis A, Ventura DG, Fernandez-Llimos F, Costa F, Gomes J, Silva JM, Lopes P, Cordeiro CR. Alpha-1 Antitrypsin Deficiency: Principles of Care. Acta Med Port. 2020 Jun 1;33(6):433-439. doi: 10.20344/amp.12950. Epub 2020 May 31. PMID: 32504520.1646-075810.20344/amp.12950info: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:RCAAP2023-10-20T11:00:49Zoai:repositorio.chporto.pt:10400.16/2471Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:38:39.377603Repositório 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 Alpha-1 Antitrypsin Deficiency: Principles of Care
Deficiência de Alfa-1 Antitripsina: Princípios do Tratamento
title Alpha-1 Antitrypsin Deficiency: Principles of Care
spellingShingle Alpha-1 Antitrypsin Deficiency: Principles of Care
Rodrigues, Joana F
Health Care Quality
Access, and Evaluation
Professional Practice
Standard of Care
alpha 1-Antitrypsin Deficiency/therapy
title_short Alpha-1 Antitrypsin Deficiency: Principles of Care
title_full Alpha-1 Antitrypsin Deficiency: Principles of Care
title_fullStr Alpha-1 Antitrypsin Deficiency: Principles of Care
title_full_unstemmed Alpha-1 Antitrypsin Deficiency: Principles of Care
title_sort Alpha-1 Antitrypsin Deficiency: Principles of Care
author Rodrigues, Joana F
author_facet Rodrigues, Joana F
Mineiro, Alexandra
Reis, António
Ventura, David G
Fernandez-Llimos, Fernando
Costa, Filipa
Gomes, Joana
Silva, José Manuel
Lopes, Paulo
Cordeiro, Carlos Robalo
author_role author
author2 Mineiro, Alexandra
Reis, António
Ventura, David G
Fernandez-Llimos, Fernando
Costa, Filipa
Gomes, Joana
Silva, José Manuel
Lopes, Paulo
Cordeiro, Carlos Robalo
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Centro Hospitalar Universitário de Santo António
dc.contributor.author.fl_str_mv Rodrigues, Joana F
Mineiro, Alexandra
Reis, António
Ventura, David G
Fernandez-Llimos, Fernando
Costa, Filipa
Gomes, Joana
Silva, José Manuel
Lopes, Paulo
Cordeiro, Carlos Robalo
dc.subject.por.fl_str_mv Health Care Quality
Access, and Evaluation
Professional Practice
Standard of Care
alpha 1-Antitrypsin Deficiency/therapy
topic Health Care Quality
Access, and Evaluation
Professional Practice
Standard of Care
alpha 1-Antitrypsin Deficiency/therapy
description Alpha-1 antitrypsin deficiency is an autosomal co-dominant inherited disorder that results in decreased circulating levels of alpha-1 antitrypsin (also known as alpha-1 proteinase inhibitor) and predisposes affected individuals to early onset lung and liver disease. There is currently no cure for alpha-1 antitrypsin deficiency. However, appropriate treatment and a high standard of clinical care can prevent patients from being seriously affected and having to undergo major medical interventions, such as organ transplantation. Beyond managing the symptoms associated with alpha-1 antitrypsin deficiency, alpha-1 proteinase inhibitor therapy is the only treatment for the condition's underlying cause. Early diagnosis is important to ensure efficient therapeutic strategies and to minimize further deterioration of lung function. alpha-1 antitrypsin deficiency is under diagnosed globally, partly because the disease has no unique presenting symptoms. This document was prepared by a Portuguese multidisciplinary group and it aims to set out comprehensive principles of care for Alpha-1 antitrypsin deficiency. These include the importance of registries, the need for clinical research, the need for consistent recommendations (regarding diagnosis, treatment and monitoring), the role of reference centres, the requirement for sustained access to treatment, diagnostic and support services, and the role of patient organizations.
publishDate 2020
dc.date.none.fl_str_mv 2020-06-01
2020-06-01T00:00:00Z
2021-06-11T11:25:48Z
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/10400.16/2471
url http://hdl.handle.net/10400.16/2471
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Rodrigues JF, Mineiro A, Reis A, Ventura DG, Fernandez-Llimos F, Costa F, Gomes J, Silva JM, Lopes P, Cordeiro CR. Alpha-1 Antitrypsin Deficiency: Principles of Care. Acta Med Port. 2020 Jun 1;33(6):433-439. doi: 10.20344/amp.12950. Epub 2020 May 31. PMID: 32504520.
1646-0758
10.20344/amp.12950
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 Centro Editor Livreiro da Ordem dos Médicos
publisher.none.fl_str_mv Centro Editor Livreiro da Ordem dos Médicos
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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