Translating Idiopathic pulmonary fibrosis guidelines into clinical practice
Autor(a) principal: | |
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Data de Publicação: | 2021 |
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/10316/100790 https://doi.org/10.1016/j.pulmoe.2020.05.017 |
Resumo: | Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive fibrotic interstitial lung disease of unknown cause, which predominantly manifests in older males. IPF diagnosis is a complex, multi-step process and delay in diagnosis cause a negative impact on patient survival. Additionally, a multidisciplinary team of pulmonologists, radiologists and pathologists is necessary for an accurate IPF diagnosis. The present study aims to assess how diagnosis and treatment of IPF are followed in Portugal, as well as the knowledge and implementation of therapeutic guidelines adopted by the Portuguese Society of Pulmonology. |
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Translating Idiopathic pulmonary fibrosis guidelines into clinical practiceAwarenessConsensusDiagnosisGuidelinesIdiopathic pulmonary fibrosisAdultAwarenessBiopsyConsensusCross-Sectional StudiesFemaleFollow-Up StudiesGuideline AdherenceHumansIdiopathic Pulmonary FibrosisInterdisciplinary CommunicationLungMaleMiddle AgedPathologistsPortugalPractice Guidelines as TopicPulmonologistsRadiologistsIdiopathic pulmonary fibrosis (IPF) is a chronic, progressive fibrotic interstitial lung disease of unknown cause, which predominantly manifests in older males. IPF diagnosis is a complex, multi-step process and delay in diagnosis cause a negative impact on patient survival. Additionally, a multidisciplinary team of pulmonologists, radiologists and pathologists is necessary for an accurate IPF diagnosis. The present study aims to assess how diagnosis and treatment of IPF are followed in Portugal, as well as the knowledge and implementation of therapeutic guidelines adopted by the Portuguese Society of Pulmonology.2021info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/100790http://hdl.handle.net/10316/100790https://doi.org/10.1016/j.pulmoe.2020.05.017eng25310437Robalo-Cordeiro, C.Morais, A.info: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:RCAAP2022-07-11T20:31:59Zoai:estudogeral.uc.pt:10316/100790Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:18:06.238677Repositório 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 |
Translating Idiopathic pulmonary fibrosis guidelines into clinical practice |
title |
Translating Idiopathic pulmonary fibrosis guidelines into clinical practice |
spellingShingle |
Translating Idiopathic pulmonary fibrosis guidelines into clinical practice Robalo-Cordeiro, C. Awareness Consensus Diagnosis Guidelines Idiopathic pulmonary fibrosis Adult Awareness Biopsy Consensus Cross-Sectional Studies Female Follow-Up Studies Guideline Adherence Humans Idiopathic Pulmonary Fibrosis Interdisciplinary Communication Lung Male Middle Aged Pathologists Portugal Practice Guidelines as Topic Pulmonologists Radiologists |
title_short |
Translating Idiopathic pulmonary fibrosis guidelines into clinical practice |
title_full |
Translating Idiopathic pulmonary fibrosis guidelines into clinical practice |
title_fullStr |
Translating Idiopathic pulmonary fibrosis guidelines into clinical practice |
title_full_unstemmed |
Translating Idiopathic pulmonary fibrosis guidelines into clinical practice |
title_sort |
Translating Idiopathic pulmonary fibrosis guidelines into clinical practice |
author |
Robalo-Cordeiro, C. |
author_facet |
Robalo-Cordeiro, C. Morais, A. |
author_role |
author |
author2 |
Morais, A. |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Robalo-Cordeiro, C. Morais, A. |
dc.subject.por.fl_str_mv |
Awareness Consensus Diagnosis Guidelines Idiopathic pulmonary fibrosis Adult Awareness Biopsy Consensus Cross-Sectional Studies Female Follow-Up Studies Guideline Adherence Humans Idiopathic Pulmonary Fibrosis Interdisciplinary Communication Lung Male Middle Aged Pathologists Portugal Practice Guidelines as Topic Pulmonologists Radiologists |
topic |
Awareness Consensus Diagnosis Guidelines Idiopathic pulmonary fibrosis Adult Awareness Biopsy Consensus Cross-Sectional Studies Female Follow-Up Studies Guideline Adherence Humans Idiopathic Pulmonary Fibrosis Interdisciplinary Communication Lung Male Middle Aged Pathologists Portugal Practice Guidelines as Topic Pulmonologists Radiologists |
description |
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive fibrotic interstitial lung disease of unknown cause, which predominantly manifests in older males. IPF diagnosis is a complex, multi-step process and delay in diagnosis cause a negative impact on patient survival. Additionally, a multidisciplinary team of pulmonologists, radiologists and pathologists is necessary for an accurate IPF diagnosis. The present study aims to assess how diagnosis and treatment of IPF are followed in Portugal, as well as the knowledge and implementation of therapeutic guidelines adopted by the Portuguese Society of Pulmonology. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021 |
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/10316/100790 http://hdl.handle.net/10316/100790 https://doi.org/10.1016/j.pulmoe.2020.05.017 |
url |
http://hdl.handle.net/10316/100790 https://doi.org/10.1016/j.pulmoe.2020.05.017 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
25310437 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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 |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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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1799134076267921408 |