TY - JOUR
T1 - Standardized Clinical Terms and Definitions for Interstitial Lung Disease: A Consensus Statement from the Fleischner Society
AU - Ryerson, Christopher J
AU - Bankier, Alexander
AU - Beasley, Mary Beth
AU - Brown, Kevin
AU - Colby, Thomas
AU - Cottin, Vincent
AU - Desai, Sujal
AU - Galvin, Jeffrey
AU - Haramati, Linda B.
AU - Hariri, Lida P
AU - Inoue, Yoshikazu
AU - Johkoh, Takeshi
AU - Lee, Ho Yun
AU - Leung, Ann
AU - Lynch, David
AU - Muller, Nestor
AU - Nicholson, Andrew
AU - Raoof, Suhail
AU - Revel, Marie-Pierre
AU - Remy-Jardin, Martine
AU - Richeldi, Luca
AU - Ryu, Jay H
AU - Schiebler, Mark
AU - Sholl, Lynette
AU - Sverzellati, Nicola
AU - Travis, William
AU - Walsh, Simon L. F.
AU - Wells, Athol U.
AU - White, Charles S.
AU - Johannson, Kerri
PY - 2025
Y1 - 2025
N2 - Background: Despite advances in diagnosis and management, the interstitial lung disease (ILD) lexicon is plagued by ambiguous and inconsistent terminology that complicates communication and impedes knowledge generation. The objective of this Fleischner Society Consensus Statement was to produce standardized terminology for ILD multidisciplinary diagnoses and major phenotypes. Methods: Interviews with 10 experts were used to identify ILD clinical diagnoses and major phenotypes. The preferred term for each entity and potential alternatives were identified, alongside rationale for the preferred term. Entities with >1 potential term were the subject of an online modified Delphi survey posed to the 29 committee members, aiming to achieve consensus. Committee members rated their agreement with the initially preferred term (strongly agree, agree, neutral/unsure, disagree, strongly disagree; scored from 5 to 1, respectively), with the option to provide additional comments. Median score 4 and interquartile range 1 was considered consensus agreement. Terms not reaching agreement were discussed by video conference, followed by an additional survey that incorporated feedback. Results: From the 60 initial terms, there were 2 root terms that required upfront consensus prior to survey initiation (ILD and interstitial pneumonia) and another 8 terms that had no alternative suggested by the committee or in the literature. Agreement was met by 47/50 terms (94%) in round 1 of the survey. The 3 terms (6%) not reaching agreement met agreement in round 2. Conclusions: This document provides standardized recommended terms for ILD multidisciplinary diagnoses and major phenotypes that will facilitate communication among clinicians, researchers, patients, and other stakeholders.
AB - Background: Despite advances in diagnosis and management, the interstitial lung disease (ILD) lexicon is plagued by ambiguous and inconsistent terminology that complicates communication and impedes knowledge generation. The objective of this Fleischner Society Consensus Statement was to produce standardized terminology for ILD multidisciplinary diagnoses and major phenotypes. Methods: Interviews with 10 experts were used to identify ILD clinical diagnoses and major phenotypes. The preferred term for each entity and potential alternatives were identified, alongside rationale for the preferred term. Entities with >1 potential term were the subject of an online modified Delphi survey posed to the 29 committee members, aiming to achieve consensus. Committee members rated their agreement with the initially preferred term (strongly agree, agree, neutral/unsure, disagree, strongly disagree; scored from 5 to 1, respectively), with the option to provide additional comments. Median score 4 and interquartile range 1 was considered consensus agreement. Terms not reaching agreement were discussed by video conference, followed by an additional survey that incorporated feedback. Results: From the 60 initial terms, there were 2 root terms that required upfront consensus prior to survey initiation (ILD and interstitial pneumonia) and another 8 terms that had no alternative suggested by the committee or in the literature. Agreement was met by 47/50 terms (94%) in round 1 of the survey. The 3 terms (6%) not reaching agreement met agreement in round 2. Conclusions: This document provides standardized recommended terms for ILD multidisciplinary diagnoses and major phenotypes that will facilitate communication among clinicians, researchers, patients, and other stakeholders.
KW - classification
KW - interstitial lung disease
KW - interstitial pneumonia
KW - pulmonary fibrosis
KW - terminology
KW - classification
KW - interstitial lung disease
KW - interstitial pneumonia
KW - pulmonary fibrosis
KW - terminology
UR - https://publicatt.unicatt.it/handle/10807/320259
U2 - 10.1164/rccm.202505-1142so
DO - 10.1164/rccm.202505-1142so
M3 - Article
SN - 1073-449X
VL - 2025
SP - 1
EP - 6
JO - American Journal of Respiratory and Critical Care Medicine
JF - American Journal of Respiratory and Critical Care Medicine
IS - 2025
ER -