Development and validation of a clinical, CT, genomic classifier and BAL scoring system for diagnosing idiopathic pulmonary fibrosis

The clinical-HRCT-BAL-GC IPF score may accurately estimate the post-test probability of IPF in patients with a non-definite HRCT UIP pattern.

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Publication Details

Journal
European Respiratory Journal
Published
2025-01-16
DOI
https://doi.org/10.1183/13993003.01077-2024
Citations
3
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
4.56
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article

Development and validation of a clinical, CT, genomic classifier and BAL scoring system for diagnosing idiopathic pulmonary fibrosis

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3 citations
European Respiratory Journal
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
4.56
article

Development and validation of a clinical, CT, genomic classifier and BAL scoring system for diagnosing idiopathic pulmonary fibrosis

Michelle Li Wei Kam, Sachin Chaudhary, Jeffrey J. Swigris, Joshua J. Solomon, Michael P. Mohning, Tilman Koelsch, Joseph B. Pryor, Matthew Koslow, E. Tjong, Tristan J. Huie, Evans R. Fernández Pérez
article en
3 citations

Abstract

The clinical-HRCT-BAL-GC IPF score may accurately estimate the post-test probability of IPF in patients with a non-definite HRCT UIP pattern.

European Respiratory JournalVol. 65(3)
University of Colorado Hospital (US), University of Arizona (US), Singapore General Hospital (SG), National Jewish Health (US), University of Colorado Denver (US)
Good health and well-being
Openalex Percentile: Top 7%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
4.56
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