The clinical meaning of the UIP pattern in fibrotic hypersensitivity pneumonitis on cryobiopsy: A multicentre retrospective study

Fibrotic hypersensitivity pneumonitis (f-HP) is an interstitial lung disease in which various antigens in susceptible individuals may play a pathogenetic role. This study evaluates the role of transbronchial lung cryobiopsy (TBLC) and bronchoalveolar lavage (BAL) in identifying a UIP-like pattern and its association with fibrosis progression. We conducted a multicentre retrospective cohort study of patients diagnosed with f-HP who underwent BAL and TBLC between 2011 and 2023. A UIP-like pattern was defined by the presence of (A) patchy fibrosis and fibroblastic foci or (B) honeycombing ± (A). We investigated BAL's role in predicting UIP-like patterns within a clinical-radiological-serological framework, examining disease progression in these patients using spirometry and mortality data. A total of 195 patients were enrolled, 59 (30%) of whom exhibited a UIP-like pattern. These patients showed greater lung function decline, lower BAL lymphocytosis (14.4% vs. 37.4%, <i>p</i> < 0.001), higher nintedanib prescription (35% vs. 14%, <i>p</i> < 0.001), and higher 10-year mortality (HR 2.8, 95% CI 1.3-5.8, <i>p</i> = 0.004). f-HP patients with a UIP-like pattern exhibit worse clinical outcomes and higher mortality. In cases of low BAL lymphocytosis with a high pre-test clinical suspicion of f-HP, lung biopsy may not be necessary as it increases the likelihood of identifying a UIP-like pattern.

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Journal
Pulmonology
Published
2024-11-12
DOI
https://doi.org/10.1080/25310429.2024.2425503
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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article
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article

The clinical meaning of the UIP pattern in fibrotic hypersensitivity pneumonitis on cryobiopsy: A multicentre retrospective study

Claudia Ravaglia, Elisabeth Bendstrup, Venerino Poletti, Sara Piciucchi et al.
Pulmonology
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

The clinical meaning of the UIP pattern in fibrotic hypersensitivity pneumonitis on cryobiopsy: A multicentre retrospective study

Claudia Ravaglia, Elisabeth Bendstrup, Venerino Poletti, Sara Piciucchi, Alessandra Dubini, Simone Petrarulo, Paolo Spagnolo, Line Bille Madsen, Elisabetta Fabbri, S. White, Frederik Lex
article en

Abstract

Fibrotic hypersensitivity pneumonitis (f-HP) is an interstitial lung disease in which various antigens in susceptible individuals may play a pathogenetic role. This study evaluates the role of transbronchial lung cryobiopsy (TBLC) and bronchoalveolar lavage (BAL) in identifying a UIP-like pattern and its association with fibrosis progression. We conducted a multicentre retrospective cohort study of patients diagnosed with f-HP who underwent BAL and TBLC between 2011 and 2023. A UIP-like pattern was defined by the presence of (A) patchy fibrosis and fibroblastic foci or (B) honeycombing ± (A). We investigated BAL's role in predicting UIP-like patterns within a clinical-radiological-serological framework, examining disease progression in these patients using spirometry and mortality data. A total of 195 patients were enrolled, 59 (30%) of whom exhibited a UIP-like pattern. These patients showed greater lung function decline, lower BAL lymphocytosis (14.4% vs. 37.4%, <i>p</i> < 0.001), higher nintedanib prescription (35% vs. 14%, <i>p</i> < 0.001), and higher 10-year mortality (HR 2.8, 95% CI 1.3-5.8, <i>p</i> = 0.004). f-HP patients with a UIP-like pattern exhibit worse clinical outcomes and higher mortality. In cases of low BAL lymphocytosis with a high pre-test clinical suspicion of f-HP, lung biopsy may not be necessary as it increases the likelihood of identifying a UIP-like pattern.

PulmonologyVol. 31(1)
University of Padua (IT), Aarhus University (DK), Aarhus University Hospital (DK), GNA University (IN), Azienda Unità Sanitaria Locale Della Romagna (IT), Ospedale G.B. Morgagni - L.Pierantoni (IT), University of Bologna (IT)
Openalex Percentile: Top 55%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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