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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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Detalles Bibliográficos
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
Descripción
Sumario: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.