Work

Survival According to Radiomic and Visual Usual Interstitial Pneumonia Classification in Fibrotic Interstitial Lung Disease

Year: 2026

Type: article

Abstract: The use of chest CT scan has largely replaced invasive surgical lung biopsies to diagnose interstitial lung disease (ILD).1 Early and systematic identification of a usual interstitial pneumonia (UIP) pattern on chest CT scan has prognostic implications on lung function decline and survival depending on disease subtype.2 However, even among thoracic radiologists, interobserver agreement when classifying CT scan patterns is poor-to-moderate.3 Thus, a reliable and reproducible method of identifying a UIP pattern is needed.

Source: CHEST Journal

DOI: 10.1016/j.chest.2026.08.002

Authors: Jennifer M. Wang, Janelle V. Pugashetti, James Thompson, Edward Kang, Ella A. Kazerooni, Kevin R. Flaherty, Elizabeth A. Belloli, Jamie S. Sheth, David N. O’Dwyer, MeiLan K. Han, Charles R. Hatt, Justin M. Oldham, Jonathan H. Chung

Institutions: University of Michigan, Michigan Medicine, University of Chicago

Language: English

Topic: Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis

Subfield: Pulmonary and Respiratory Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: hybrid

Estimated APC paid: $4,160

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute

Awards: G2655142861, Prognostic Biomarker Development in Progressive Fibrosing Interstitial Lung Disease, Defining Pathways in COPD Patient Oriented Research, A Multi-Dimensional Signature to Predict Treatment Failure in Patients with Connective Tissue Disease-Associated Interstitial Lung Disease, Proteomic Profiling of Idiopathic Pulmonary Fibrosis Progression Trajectory, Defining Combined Pulmonary Fibrosis and Emphysema (CPFE) using Quantitative CT Imaging

OpenAlex ID: W7202298726

FWCI:

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