Associations of interstitial lung disease subtype and CT pattern with lung function and survival

Even in the presence of a UIP CT pattern, there may still be differences in lung function over time and survival, particularly for CTD-ILD.

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Publication Details

Journal
Thorax
Published
2025-06-08
DOI
https://doi.org/10.1136/thorax-2024-222149
Citations
4
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
6.07

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article

Associations of interstitial lung disease subtype and CT pattern with lung function and survival

John S. Kim, Josyf C. Mychaleckyj, Imre Noth, Susan Murray et al.
4 citations
Thorax
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
6.07
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Associations of interstitial lung disease subtype and CT pattern with lung function and survival

John S. Kim, Josyf C. Mychaleckyj, Imre Noth, Susan Murray, Justin M. Oldham, Kevin R. Flaherty, Janelle Vu Pugashetti, David A. Lynch, Andrea Oh, Ani Manichaikul, Anna J. Podolanczuk, Cathie Spino, Yong Huang, Traci N. Adams, Felix Chua, Chad A. Newton, Philip L. Molyneaux, Ayodeji Adegunsoye, Shwu‐Fan Ma, Stephen S. Rich, Stephen M. Humphries, Joseph A. Lasky, Joyce Lee, Fernando J. Martínez, Ganesh Raghu
article en
4 citations

Abstract

Even in the presence of a UIP CT pattern, there may still be differences in lung function over time and survival, particularly for CTD-ILD.

ThoraxVol. 80(12)
Tulane University (US), UMass Memorial Health Care (US), University of California, Los Angeles (US), Guy's and St Thomas' NHS Foundation Trust (GB), University of Washington (US), Cornell University (US), University of Michigan (US), Royal Brompton & Harefield NHS Foundation Trust (GB), National Jewish Health (US), University of Chicago (US), Royal Brompton Hospital (GB), UMass Memorial Medical Center (US), University of Virginia (US), The University of Texas Southwestern Medical Center (US), University of Colorado Denver (US)
National Heart, Lung, and Blood Institute
Good health and well-being
Openalex Percentile: Top 4%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
6.07
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