Automated CT Analysis of Major Forms of Interstitial Lung Disease.
connective tissue disease
high-resolution computed tomography
hypersensitivity pneumonitis
idiopathic pulmonary fibrosis
interstitial pneumonia with autoimmune features
Journal
Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588
Informations de publication
Date de publication:
23 Nov 2020
23 Nov 2020
Historique:
received:
22
10
2020
revised:
13
11
2020
accepted:
19
11
2020
entrez:
26
11
2020
pubmed:
27
11
2020
medline:
27
11
2020
Statut:
epublish
Résumé
This study aimed to determine diagnostic and prognostic differences in major forms of interstitial lung disease using quantitative CT imaging. A retrospective study of 225 subjects with a multidisciplinary diagnosis of idiopathic pulmonary fibrosis (IPF), interstitial pneumonia with autoimmune features (IPAF), connective tissue disease (CTD), or chronic hypersensitivity pneumonitis (cHP) was conducted. Non-contrast CT scans were analyzed using the Computer Aided Lung Informatics for Pathology Evaluation and Rating (CALIPER) program. Resulting data were analyzed statistically using ANOVA and Student's
Identifiants
pubmed: 33238466
pii: jcm9113776
doi: 10.3390/jcm9113776
pmc: PMC7700631
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : NHLBI NIH HHS
ID : K23 HL138190
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL130796
Pays : United States
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