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Demographic and clinical profile of idiopathic pulmonary fibrosis patients in Spain: the SEPAR National Registry
BACKGROUND: Little is known on the characteristics of patients diagnosed with idiopathic pulmonary fibrosis (IPF) in Spain. We aimed to characterize the demographic and clinical profile of IPF patients included in the IPF National Registry of the Spanish Respiratory Society (SEPAR). METHODS: This is...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580511/ https://www.ncbi.nlm.nih.gov/pubmed/31208406 http://dx.doi.org/10.1186/s12931-019-1084-0 |
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author | Fernández-Fabrellas, Estrella Molina-Molina, María Soriano, Joan B. Portal, José Antonio Rodríguez Ancochea, Julio Valenzuela, Claudia Xaubet, Antoni |
author_facet | Fernández-Fabrellas, Estrella Molina-Molina, María Soriano, Joan B. Portal, José Antonio Rodríguez Ancochea, Julio Valenzuela, Claudia Xaubet, Antoni |
author_sort | Fernández-Fabrellas, Estrella |
collection | PubMed |
description | BACKGROUND: Little is known on the characteristics of patients diagnosed with idiopathic pulmonary fibrosis (IPF) in Spain. We aimed to characterize the demographic and clinical profile of IPF patients included in the IPF National Registry of the Spanish Respiratory Society (SEPAR). METHODS: This is a prospective, observational, multicentre and nationwide study that involved 608 IPF patients included in the SEPAR IPF Registry up to June 27th, 2017, and who received any treatment for their disease. IPF patients were predominantly males, ex-smokers, and aged in their 70s, similar to other registries. RESULTS: Upon inclusion, mean ± SD predicted forced vital capacity was 77.6% ± 19.4, diffusing capacity for carbon monoxide was 48.5% ± 17.7, and the 6-min walk distance was 423.5 m ± 110.4. The diagnosis was mainly established on results from the high-resolution computed tomography in the proper clinical context (55.0% of patients), while 21.2% of patients required invasive procedures (surgical lung biopsy) for definitive diagnosis. Anti-fibrotic treatment was prescribed in 69.4% of cases, 51.5% pirfenidone and 17.9% nintedanib, overall with a good safety profile. CONCLUSIONS: The SEPAR IPF Registry should help to further characterize current characteristics and future trends of IPF patients in Spain and compare/pool them with other registries and cohorts. |
format | Online Article Text |
id | pubmed-6580511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65805112019-06-24 Demographic and clinical profile of idiopathic pulmonary fibrosis patients in Spain: the SEPAR National Registry Fernández-Fabrellas, Estrella Molina-Molina, María Soriano, Joan B. Portal, José Antonio Rodríguez Ancochea, Julio Valenzuela, Claudia Xaubet, Antoni Respir Res Research BACKGROUND: Little is known on the characteristics of patients diagnosed with idiopathic pulmonary fibrosis (IPF) in Spain. We aimed to characterize the demographic and clinical profile of IPF patients included in the IPF National Registry of the Spanish Respiratory Society (SEPAR). METHODS: This is a prospective, observational, multicentre and nationwide study that involved 608 IPF patients included in the SEPAR IPF Registry up to June 27th, 2017, and who received any treatment for their disease. IPF patients were predominantly males, ex-smokers, and aged in their 70s, similar to other registries. RESULTS: Upon inclusion, mean ± SD predicted forced vital capacity was 77.6% ± 19.4, diffusing capacity for carbon monoxide was 48.5% ± 17.7, and the 6-min walk distance was 423.5 m ± 110.4. The diagnosis was mainly established on results from the high-resolution computed tomography in the proper clinical context (55.0% of patients), while 21.2% of patients required invasive procedures (surgical lung biopsy) for definitive diagnosis. Anti-fibrotic treatment was prescribed in 69.4% of cases, 51.5% pirfenidone and 17.9% nintedanib, overall with a good safety profile. CONCLUSIONS: The SEPAR IPF Registry should help to further characterize current characteristics and future trends of IPF patients in Spain and compare/pool them with other registries and cohorts. BioMed Central 2019-06-17 2019 /pmc/articles/PMC6580511/ /pubmed/31208406 http://dx.doi.org/10.1186/s12931-019-1084-0 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Fernández-Fabrellas, Estrella Molina-Molina, María Soriano, Joan B. Portal, José Antonio Rodríguez Ancochea, Julio Valenzuela, Claudia Xaubet, Antoni Demographic and clinical profile of idiopathic pulmonary fibrosis patients in Spain: the SEPAR National Registry |
title | Demographic and clinical profile of idiopathic pulmonary fibrosis patients in Spain: the SEPAR National Registry |
title_full | Demographic and clinical profile of idiopathic pulmonary fibrosis patients in Spain: the SEPAR National Registry |
title_fullStr | Demographic and clinical profile of idiopathic pulmonary fibrosis patients in Spain: the SEPAR National Registry |
title_full_unstemmed | Demographic and clinical profile of idiopathic pulmonary fibrosis patients in Spain: the SEPAR National Registry |
title_short | Demographic and clinical profile of idiopathic pulmonary fibrosis patients in Spain: the SEPAR National Registry |
title_sort | demographic and clinical profile of idiopathic pulmonary fibrosis patients in spain: the separ national registry |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580511/ https://www.ncbi.nlm.nih.gov/pubmed/31208406 http://dx.doi.org/10.1186/s12931-019-1084-0 |
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