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Syndrome of Combined Pulmonary Fibrosis and Emphysema: An official research statement from American Thoracic Society (ATS), European Respiratory Society (ERS), Japanese Respiratory Society (JRS), and Asociación Latinoamericana de Tórax (ALAT)

BACKGROUND: The presence of emphysema is relatively common in patients with fibrotic interstitial lung disease. This has been designated combined pulmonary fibrosis and emphysema (CPFE). The lack of consensus over definitions and diagnostic criteria has limited CPFE research. GOALS: The objectives o...

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Autores principales: Cottin, Vincent, Selman, Moises, Inoue, Yoshikazu, Wong, Alyson W., Corte, Tamera J., Flaherty, Kevin R., Han, MeiLan K., Jacob, Joseph, Johannson, Kerri A., Kitaichi, Masanori, Lee, Joyce S., Agusti, Alvar, Antoniou, Katerina M., Bianchi, Pauline, Caro, Fabian, Florenzano, Matias, Galvin, Liam, Iwasawa, Tae, Martinez, Fernando J., Morgan, Rebecca L., Myers, Jeffrey L., Nicholson, Andrew G., Occhipinti, Mariaelena, Poletti, Venerino, Salisbury, Margaret L., Sin, Don D., Sverzellati, Nicola, Tonia, Thomy, Valenzuela, Claudia, Ryerson, Christopher J., Wells, Athol U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7615200/
https://www.ncbi.nlm.nih.gov/pubmed/35969190
http://dx.doi.org/10.1164/rccm.202206-1041ST
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author Cottin, Vincent
Selman, Moises
Inoue, Yoshikazu
Wong, Alyson W.
Corte, Tamera J.
Flaherty, Kevin R.
Han, MeiLan K.
Jacob, Joseph
Johannson, Kerri A.
Kitaichi, Masanori
Lee, Joyce S.
Agusti, Alvar
Antoniou, Katerina M.
Bianchi, Pauline
Caro, Fabian
Florenzano, Matias
Galvin, Liam
Iwasawa, Tae
Martinez, Fernando J.
Morgan, Rebecca L.
Myers, Jeffrey L.
Nicholson, Andrew G.
Occhipinti, Mariaelena
Poletti, Venerino
Salisbury, Margaret L.
Sin, Don D.
Sverzellati, Nicola
Tonia, Thomy
Valenzuela, Claudia
Ryerson, Christopher J.
Wells, Athol U.
author_facet Cottin, Vincent
Selman, Moises
Inoue, Yoshikazu
Wong, Alyson W.
Corte, Tamera J.
Flaherty, Kevin R.
Han, MeiLan K.
Jacob, Joseph
Johannson, Kerri A.
Kitaichi, Masanori
Lee, Joyce S.
Agusti, Alvar
Antoniou, Katerina M.
Bianchi, Pauline
Caro, Fabian
Florenzano, Matias
Galvin, Liam
Iwasawa, Tae
Martinez, Fernando J.
Morgan, Rebecca L.
Myers, Jeffrey L.
Nicholson, Andrew G.
Occhipinti, Mariaelena
Poletti, Venerino
Salisbury, Margaret L.
Sin, Don D.
Sverzellati, Nicola
Tonia, Thomy
Valenzuela, Claudia
Ryerson, Christopher J.
Wells, Athol U.
author_sort Cottin, Vincent
collection PubMed
description BACKGROUND: The presence of emphysema is relatively common in patients with fibrotic interstitial lung disease. This has been designated combined pulmonary fibrosis and emphysema (CPFE). The lack of consensus over definitions and diagnostic criteria has limited CPFE research. GOALS: The objectives of this taskforce were to review the terminology, definition, characteristics, pathophysiology, and research priorities of CPFE, and to explore whether CPFE is a syndrome. METHODS: This research statement was developed by a committee including 19 pulmonologists, 5 radiologists, 3 pathologists, 2 methodologists, and 2 patient representatives. The final document was supported by a focused systematic review that identified and summarized all recent publications related to CPFE. RESULTS: This taskforce identified that patients with CPFE are predominantly male, with history of smoking, severe dyspnea, relatively preserved airflow rates and lung volumes on spirometry, severely impaired diffusion capacity for carbon monoxide, exertional hypoxemia, frequent pulmonary hypertension, and a dismal prognosis. The committee proposes to identify CPFE as a syndrome given the clustering of pulmonary fibrosis and emphysema, shared pathogenetic pathways, unique considerations related to disease progression, increased risk of complications (pulmonary hypertension, lung cancer, mortality), and implications for clinical trial design. There are varying features of interstitial lung disease and emphysema in CPFE. The committee offers a research definition and classification criteria, and proposes that studies on CPFE include a comprehensive description of radiologic and, when available, pathological patterns including some recently described patterns such as smoking-related interstitial fibrosis. CONCLUSIONS: This statement delineates the syndrome of CPFE and highlights research priorities.
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spelling pubmed-76152002023-10-13 Syndrome of Combined Pulmonary Fibrosis and Emphysema: An official research statement from American Thoracic Society (ATS), European Respiratory Society (ERS), Japanese Respiratory Society (JRS), and Asociación Latinoamericana de Tórax (ALAT) Cottin, Vincent Selman, Moises Inoue, Yoshikazu Wong, Alyson W. Corte, Tamera J. Flaherty, Kevin R. Han, MeiLan K. Jacob, Joseph Johannson, Kerri A. Kitaichi, Masanori Lee, Joyce S. Agusti, Alvar Antoniou, Katerina M. Bianchi, Pauline Caro, Fabian Florenzano, Matias Galvin, Liam Iwasawa, Tae Martinez, Fernando J. Morgan, Rebecca L. Myers, Jeffrey L. Nicholson, Andrew G. Occhipinti, Mariaelena Poletti, Venerino Salisbury, Margaret L. Sin, Don D. Sverzellati, Nicola Tonia, Thomy Valenzuela, Claudia Ryerson, Christopher J. Wells, Athol U. Am J Respir Crit Care Med Article BACKGROUND: The presence of emphysema is relatively common in patients with fibrotic interstitial lung disease. This has been designated combined pulmonary fibrosis and emphysema (CPFE). The lack of consensus over definitions and diagnostic criteria has limited CPFE research. GOALS: The objectives of this taskforce were to review the terminology, definition, characteristics, pathophysiology, and research priorities of CPFE, and to explore whether CPFE is a syndrome. METHODS: This research statement was developed by a committee including 19 pulmonologists, 5 radiologists, 3 pathologists, 2 methodologists, and 2 patient representatives. The final document was supported by a focused systematic review that identified and summarized all recent publications related to CPFE. RESULTS: This taskforce identified that patients with CPFE are predominantly male, with history of smoking, severe dyspnea, relatively preserved airflow rates and lung volumes on spirometry, severely impaired diffusion capacity for carbon monoxide, exertional hypoxemia, frequent pulmonary hypertension, and a dismal prognosis. The committee proposes to identify CPFE as a syndrome given the clustering of pulmonary fibrosis and emphysema, shared pathogenetic pathways, unique considerations related to disease progression, increased risk of complications (pulmonary hypertension, lung cancer, mortality), and implications for clinical trial design. There are varying features of interstitial lung disease and emphysema in CPFE. The committee offers a research definition and classification criteria, and proposes that studies on CPFE include a comprehensive description of radiologic and, when available, pathological patterns including some recently described patterns such as smoking-related interstitial fibrosis. CONCLUSIONS: This statement delineates the syndrome of CPFE and highlights research priorities. 2022-08-15 /pmc/articles/PMC7615200/ /pubmed/35969190 http://dx.doi.org/10.1164/rccm.202206-1041ST Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a BY 4.0 (https://creativecommons.org/licenses/by/4.0/) International license.
spellingShingle Article
Cottin, Vincent
Selman, Moises
Inoue, Yoshikazu
Wong, Alyson W.
Corte, Tamera J.
Flaherty, Kevin R.
Han, MeiLan K.
Jacob, Joseph
Johannson, Kerri A.
Kitaichi, Masanori
Lee, Joyce S.
Agusti, Alvar
Antoniou, Katerina M.
Bianchi, Pauline
Caro, Fabian
Florenzano, Matias
Galvin, Liam
Iwasawa, Tae
Martinez, Fernando J.
Morgan, Rebecca L.
Myers, Jeffrey L.
Nicholson, Andrew G.
Occhipinti, Mariaelena
Poletti, Venerino
Salisbury, Margaret L.
Sin, Don D.
Sverzellati, Nicola
Tonia, Thomy
Valenzuela, Claudia
Ryerson, Christopher J.
Wells, Athol U.
Syndrome of Combined Pulmonary Fibrosis and Emphysema: An official research statement from American Thoracic Society (ATS), European Respiratory Society (ERS), Japanese Respiratory Society (JRS), and Asociación Latinoamericana de Tórax (ALAT)
title Syndrome of Combined Pulmonary Fibrosis and Emphysema: An official research statement from American Thoracic Society (ATS), European Respiratory Society (ERS), Japanese Respiratory Society (JRS), and Asociación Latinoamericana de Tórax (ALAT)
title_full Syndrome of Combined Pulmonary Fibrosis and Emphysema: An official research statement from American Thoracic Society (ATS), European Respiratory Society (ERS), Japanese Respiratory Society (JRS), and Asociación Latinoamericana de Tórax (ALAT)
title_fullStr Syndrome of Combined Pulmonary Fibrosis and Emphysema: An official research statement from American Thoracic Society (ATS), European Respiratory Society (ERS), Japanese Respiratory Society (JRS), and Asociación Latinoamericana de Tórax (ALAT)
title_full_unstemmed Syndrome of Combined Pulmonary Fibrosis and Emphysema: An official research statement from American Thoracic Society (ATS), European Respiratory Society (ERS), Japanese Respiratory Society (JRS), and Asociación Latinoamericana de Tórax (ALAT)
title_short Syndrome of Combined Pulmonary Fibrosis and Emphysema: An official research statement from American Thoracic Society (ATS), European Respiratory Society (ERS), Japanese Respiratory Society (JRS), and Asociación Latinoamericana de Tórax (ALAT)
title_sort syndrome of combined pulmonary fibrosis and emphysema: an official research statement from american thoracic society (ats), european respiratory society (ers), japanese respiratory society (jrs), and asociación latinoamericana de tórax (alat)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7615200/
https://www.ncbi.nlm.nih.gov/pubmed/35969190
http://dx.doi.org/10.1164/rccm.202206-1041ST
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