Computed Tomography Honeycombing Identifies a Progressive Fibrotic Phenotype with Increased Mortality across Diverse Interstitial Lung Diseases-Reference-Cited by-同舟云学术

Computed Tomography Honeycombing Identifies a Progressive Fibrotic Phenotype with Increased Mortality across Diverse Interstitial Lung Diseases

Published:2019-05 Issue:5 Volume:16 Page:580-588
ISSN:2329-6933
Container-title:Annals of the American Thoracic Society
language:en
Short-container-title:Annals ATS

Author:

Adegunsoye Ayodeji¹^ORCID,Oldham Justin M.²,Bellam Shashi K.³,Montner Steven⁴,Churpek Matthew M.¹⁵,Noth Imre⁶,Vij Rekha¹,Strek Mary E.¹,Chung Jonathan H.⁴

Affiliation:

1. Section of Pulmonary and Critical Care, Department of Medicine

2. Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of California at Davis, Davis, California

3. Division of Pulmonary and Critical Care, Department of Medicine, NorthShore University HealthSystem, Evanston, Illinois; and

4. Department of Radiology, and

5. Department of Public Health Sciences, The University of Chicago, Chicago, Illinois

6. Pulmonary and Critical Care Medicine, University of Virginia, Charlottesville, Virginia

Publisher

American Thoracic Society

Subject

Pulmonary and Respiratory Medicine

Link

https://www.atsjournals.org/doi/pdf/10.1513/AnnalsATS.201807-443OC

Reference38 articles.

1. Idiopathic Pulmonary Fibrosis

2. An Official ATS/ERS/JRS/ALAT Statement: Idiopathic Pulmonary Fibrosis: Evidence-based Guidelines for Diagnosis and Management

3. Possible UIP pattern on high-resolution computed tomography is associated with better survival than definite UIP in IPF patients

4. Clinical Course and Prediction of Survival in Idiopathic Pulmonary Fibrosis

5. Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline

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