Translating Idiopathic pulmonary fibrosis guidelines into clinical practice

Detalhes bibliográficos
Autor(a) principal: Robalo-Cordeiro, C.
Data de Publicação: 2021
Outros Autores: Morais, A.
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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spelling 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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