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 in | European radiology Vol. 27; no. 12; pp. 5127 - 5135 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.12.2017
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 0938-7994 1432-1084 1432-1084 |
DOI | 10.1007/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. |
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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. |
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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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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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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 |
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