| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5600511 | Chest | 2017 | 24 Pages |
Abstract
No clinically significant differences in pulmonary function to distinguish between patients with AI-ILD, IPAF, CTD-ILD, and Lone-IPF were observed after 1 year. Longer periods of follow-up are needed to understand the outcomes of these patients. It is not yet clear whether AI-ILD is a distinct phenotype or a variant of the newly proposed entity IPAF.
Keywords
CTDDLCOIPFPFTNSIPCTD-ILDUIPIPAFILDConnective tissue diseaseInterstitial lung diseaseconnective tissue disease-associated interstitial lung diseasePulmonary function testDiffusion capacityidiopathic pulmonary fibrosisinterstitial pneumonia with autoimmune featuresUsual interstitial pneumoniaInterstitial pneumoniaNonspecific interstitial pneumonia
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Authors
Bridget F. MD, Charles F. PhD, Megan A. MD, Lawrence A. MD, Jennifer RN, Carolyn A. RN, Caroline M. MPH, Ganesh MD,