Alpha-1 Antitrypsin Deficiency: Principles of Care
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , |
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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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) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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