CT findings associated with survival in chronic hypersensitivity pneumonitis

Objectives To identify CT findings in chronic hypersensitivity pneumonitis (cHP) associated with survival. Material and methods Two thoracic radiologists assessed CT scans for specific imaging findings and patterns in 132 subjects with cHP. Survival analyses were performed. Results The majority of s...

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Published inEuropean radiology Vol. 27; no. 12; pp. 5127 - 5135
Main Authors Chung, Jonathan H., Montner, Steven M., Adegunsoye, Ayodeji, Oldham, Justin M., Husain, Aliya N., Vij, Rekha, Noth, Imre, Strek, Mary E.
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer Berlin Heidelberg 01.12.2017
Springer Nature B.V
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ISSN0938-7994
1432-1084
1432-1084
DOI10.1007/s00330-017-4936-3

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Abstract Objectives To identify CT findings in chronic hypersensitivity pneumonitis (cHP) associated with survival. Material and methods Two thoracic radiologists assessed CT scans for specific imaging findings and patterns in 132 subjects with cHP. Survival analyses were performed. Results The majority of subjects had an inconsistent with usual interstitial pneumonitis pattern on CT (55.3%,73/132). Hypersensitivity pneumonitis (HP) diagnosis on CT was less common in those with fibrosis (66.1%, 74/112) than those without fibrosis (85%,17/20). Smoking was associated with a lower prevalence of HP on CT (p=0.04). CT features of pulmonary fibrosis, especially traction bronchiectasis (HR 8.34, 95% CI 1.98–35.21) and increased pulmonary artery (PA)/aorta ratio (HR 2.49, 95% CI 1.27–4.89) were associated with worse survival, while ground-glass opacity (HR 0.31, 95% CI 0.12–0.79) was associated with improved survival. Survival association with imaging was less pronounced after adjustment for gender, age and physiology score. Conclusions A substantial proportion of cHP cases have a non-HP-like appearance. Ground-glass opacity, pulmonary fibrosis features and elevated PA/aorta ratio on CT likely reflect varying degrees of disease severity in cHP and may inform future clinical prediction models. Key Points • A substantial proportion of subjects with chronic HP have a UIP-like pattern. • A UIP pattern in HP may be potentiated by smoking. • A diagnosis of HP should not be excluded based solely on CT appearance. • CT fibrosis and increased PA/aorta ratio signal worse survival.
AbstractList Objectives To identify CT findings in chronic hypersensitivity pneumonitis (cHP) associated with survival. Material and methods Two thoracic radiologists assessed CT scans for specific imaging findings and patterns in 132 subjects with cHP. Survival analyses were performed. Results The majority of subjects had an inconsistent with usual interstitial pneumonitis pattern on CT (55.3%,73/132). Hypersensitivity pneumonitis (HP) diagnosis on CT was less common in those with fibrosis (66.1%, 74/112) than those without fibrosis (85%,17/20). Smoking was associated with a lower prevalence of HP on CT (p=0.04). CT features of pulmonary fibrosis, especially traction bronchiectasis (HR 8.34, 95% CI 1.98–35.21) and increased pulmonary artery (PA)/aorta ratio (HR 2.49, 95% CI 1.27–4.89) were associated with worse survival, while ground-glass opacity (HR 0.31, 95% CI 0.12–0.79) was associated with improved survival. Survival association with imaging was less pronounced after adjustment for gender, age and physiology score. Conclusions A substantial proportion of cHP cases have a non-HP-like appearance. Ground-glass opacity, pulmonary fibrosis features and elevated PA/aorta ratio on CT likely reflect varying degrees of disease severity in cHP and may inform future clinical prediction models. Key Points • A substantial proportion of subjects with chronic HP have a UIP-like pattern. • A UIP pattern in HP may be potentiated by smoking. • A diagnosis of HP should not be excluded based solely on CT appearance. • CT fibrosis and increased PA/aorta ratio signal worse survival.
Objectives To identify CT findings in chronic hypersensitivity pneumonitis (cHP) associated with survival. Material and methods Two thoracic radiologists assessed CT scans for specific imaging findings and patterns in 132 subjects with cHP. Survival analyses were performed. Results The majority of subjects had an inconsistent with usual interstitial pneumonitis pattern on CT (55.3%,73/132). Hypersensitivity pneumonitis (HP) diagnosis on CT was less common in those with fibrosis (66.1%, 74/112) than those without fibrosis (85%,17/20). Smoking was associated with a lower prevalence of HP on CT (p=0.04). CT features of pulmonary fibrosis, especially traction bronchiectasis (HR 8.34, 95% CI 1.98–35.21) and increased pulmonary artery (PA)/aorta ratio (HR 2.49, 95% CI 1.27–4.89) were associated with worse survival, while ground-glass opacity (HR 0.31, 95% CI 0.12–0.79) was associated with improved survival. Survival association with imaging was less pronounced after adjustment for gender, age and physiology score. Conclusions A substantial proportion of cHP cases have a non-HP-like appearance. Ground-glass opacity, pulmonary fibrosis features and elevated PA/aorta ratio on CT likely reflect varying degrees of disease severity in cHP and may inform future clinical prediction models. Key Points • A substantial proportion of subjects with chronic HP have a UIP-like pattern. • A UIP pattern in HP may be potentiated by smoking. • A diagnosis of HP should not be excluded based solely on CT appearance. • CT fibrosis and increased PA/aorta ratio signal worse survival.
To identify CT findings in chronic hypersensitivity pneumonitis (cHP) associated with survival.OBJECTIVESTo identify CT findings in chronic hypersensitivity pneumonitis (cHP) associated with survival.Two thoracic radiologists assessed CT scans for specific imaging findings and patterns in 132 subjects with cHP. Survival analyses were performed.MATERIAL AND METHODSTwo thoracic radiologists assessed CT scans for specific imaging findings and patterns in 132 subjects with cHP. Survival analyses were performed.The majority of subjects had an inconsistent with usual interstitial pneumonitis pattern on CT (55.3%,73/132). Hypersensitivity pneumonitis (HP) diagnosis on CT was less common in those with fibrosis (66.1%, 74/112) than those without fibrosis (85%,17/20). Smoking was associated with a lower prevalence of HP on CT (p=0.04). CT features of pulmonary fibrosis, especially traction bronchiectasis (HR 8.34, 95% CI 1.98-35.21) and increased pulmonary artery (PA)/aorta ratio (HR 2.49, 95% CI 1.27-4.89) were associated with worse survival, while ground-glass opacity (HR 0.31, 95% CI 0.12-0.79) was associated with improved survival. Survival association with imaging was less pronounced after adjustment for gender, age and physiology score.RESULTSThe majority of subjects had an inconsistent with usual interstitial pneumonitis pattern on CT (55.3%,73/132). Hypersensitivity pneumonitis (HP) diagnosis on CT was less common in those with fibrosis (66.1%, 74/112) than those without fibrosis (85%,17/20). Smoking was associated with a lower prevalence of HP on CT (p=0.04). CT features of pulmonary fibrosis, especially traction bronchiectasis (HR 8.34, 95% CI 1.98-35.21) and increased pulmonary artery (PA)/aorta ratio (HR 2.49, 95% CI 1.27-4.89) were associated with worse survival, while ground-glass opacity (HR 0.31, 95% CI 0.12-0.79) was associated with improved survival. Survival association with imaging was less pronounced after adjustment for gender, age and physiology score.A substantial proportion of cHP cases have a non-HP-like appearance. Ground-glass opacity, pulmonary fibrosis features and elevated PA/aorta ratio on CT likely reflect varying degrees of disease severity in cHP and may inform future clinical prediction models.CONCLUSIONSA substantial proportion of cHP cases have a non-HP-like appearance. Ground-glass opacity, pulmonary fibrosis features and elevated PA/aorta ratio on CT likely reflect varying degrees of disease severity in cHP and may inform future clinical prediction models.• A substantial proportion of subjects with chronic HP have a UIP-like pattern. • A UIP pattern in HP may be potentiated by smoking. • A diagnosis of HP should not be excluded based solely on CT appearance. • CT fibrosis and increased PA/aorta ratio signal worse survival.KEY POINTS• A substantial proportion of subjects with chronic HP have a UIP-like pattern. • A UIP pattern in HP may be potentiated by smoking. • A diagnosis of HP should not be excluded based solely on CT appearance. • CT fibrosis and increased PA/aorta ratio signal worse survival.
To identify CT findings in chronic hypersensitivity pneumonitis (cHP) associated with survival. Two thoracic radiologists assessed CT scans for specific imaging findings and patterns in 132 subjects with cHP. Survival analyses were performed. The majority of subjects had an inconsistent with usual interstitial pneumonitis pattern on CT (55.3%,73/132). Hypersensitivity pneumonitis (HP) diagnosis on CT was less common in those with fibrosis (66.1%, 74/112) than those without fibrosis (85%,17/20). Smoking was associated with a lower prevalence of HP on CT (p=0.04). CT features of pulmonary fibrosis, especially traction bronchiectasis (HR 8.34, 95% CI 1.98-35.21) and increased pulmonary artery (PA)/aorta ratio (HR 2.49, 95% CI 1.27-4.89) were associated with worse survival, while ground-glass opacity (HR 0.31, 95% CI 0.12-0.79) was associated with improved survival. Survival association with imaging was less pronounced after adjustment for gender, age and physiology score. A substantial proportion of cHP cases have a non-HP-like appearance. Ground-glass opacity, pulmonary fibrosis features and elevated PA/aorta ratio on CT likely reflect varying degrees of disease severity in cHP and may inform future clinical prediction models. • A substantial proportion of subjects with chronic HP have a UIP-like pattern. • A UIP pattern in HP may be potentiated by smoking. • A diagnosis of HP should not be excluded based solely on CT appearance. • CT fibrosis and increased PA/aorta ratio signal worse survival.
Author Noth, Imre
Chung, Jonathan H.
Oldham, Justin M.
Montner, Steven M.
Vij, Rekha
Adegunsoye, Ayodeji
Husain, Aliya N.
Strek, Mary E.
Author_xml – sequence: 1
  givenname: Jonathan H.
  surname: Chung
  fullname: Chung, Jonathan H.
  email: jonherochung@uchicago.edu
  organization: Department of Radiology, The University of Chicago Medical Center
– sequence: 2
  givenname: Steven M.
  surname: Montner
  fullname: Montner, Steven M.
  organization: Department of Radiology, The University of Chicago Medical Center
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  givenname: Ayodeji
  surname: Adegunsoye
  fullname: Adegunsoye, Ayodeji
  organization: Section of Pulmonary/Critical Care; Department of Medicine, The University of Chicago Medical Center
– sequence: 4
  givenname: Justin M.
  surname: Oldham
  fullname: Oldham, Justin M.
  organization: Section of Pulmonary/Critical Care; Department of Medicine, The University of California at Davis
– sequence: 5
  givenname: Aliya N.
  surname: Husain
  fullname: Husain, Aliya N.
  organization: Department of Pathology, The University of Chicago Medical Center
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  fullname: Vij, Rekha
  organization: Section of Pulmonary/Critical Care; Department of Medicine, The University of Chicago Medical Center
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  surname: Noth
  fullname: Noth, Imre
  organization: Section of Pulmonary/Critical Care; Department of Medicine, The University of Chicago Medical Center
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  givenname: Mary E.
  surname: Strek
  fullname: Strek, Mary E.
  organization: Section of Pulmonary/Critical Care; Department of Medicine, The University of Chicago Medical Center
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28687910$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright European Society of Radiology 2017
European Radiology is a copyright of Springer, (2017). All Rights Reserved.
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Thu Apr 03 07:00:35 EDT 2025
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Fri Feb 21 02:33:06 EST 2025
IsPeerReviewed true
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Issue 12
Keywords CT
Chronic hypersensitivity pneumonitis
Survival
Pulmonary hypertension
Usual interstitial pneumonitis
Language English
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Snippet Objectives To identify CT findings in chronic hypersensitivity pneumonitis (cHP) associated with survival. Material and methods Two thoracic radiologists...
To identify CT findings in chronic hypersensitivity pneumonitis (cHP) associated with survival. Two thoracic radiologists assessed CT scans for specific...
Objectives To identify CT findings in chronic hypersensitivity pneumonitis (cHP) associated with survival. Material and methods Two thoracic radiologists...
To identify CT findings in chronic hypersensitivity pneumonitis (cHP) associated with survival.OBJECTIVESTo identify CT findings in chronic hypersensitivity...
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pubmed
crossref
springer
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 5127
SubjectTerms Adult
Aged
Alveolitis
Alveolitis, Extrinsic Allergic - diagnostic imaging
Alveolitis, Extrinsic Allergic - pathology
Aorta
Bronchiectasis
Chest
Chronic Disease
Computed tomography
Coronary vessels
Diagnosis
Diagnostic Radiology
Female
Fibrosis
Fibrosis - pathology
Humans
Hypersensitivity
Hypertension, Pulmonary - diagnostic imaging
Hypertension, Pulmonary - pathology
Idiopathic Pulmonary Fibrosis - pathology
Imaging
Internal Medicine
Interventional Radiology
Lung diseases
Male
Medicine
Medicine & Public Health
Middle Aged
Neuroradiology
Opacity
Pneumonitis
Prediction models
Prevalence
Pulmonary arteries
Pulmonary artery
Pulmonary Artery - diagnostic imaging
Pulmonary fibrosis
Radiology
Smoking
Survival
Survival Analysis
Thorax
Tomography, X-Ray Computed - methods
Ultrasound
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Title CT findings associated with survival in chronic hypersensitivity pneumonitis
URI https://link.springer.com/article/10.1007/s00330-017-4936-3
https://www.ncbi.nlm.nih.gov/pubmed/28687910
https://www.proquest.com/docview/1961028249
https://www.proquest.com/docview/1917365148
Volume 27
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