ArticleRadiologia brasileira
Quantitative computed tomography analysis of the airways in patients with cystic fibrosis using automated software: correlation with spirometry in the evaluation of severity.
Article in Radiologia brasileira. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Article
- Computed tomography in cystic fibrosis lung disease: a focus on radiation exposure.Pediatric radiology · 2021Review
- Chest computed tomography in bronchiolitis obliterans after bone marrow transplantation.Radiologia brasileiraArticle
- Radiologist agreement on the quantification of bronchiectasis by high-resolution computed tomography.Radiologia brasileiraArticle
- Artificial intelligence, machine learning, computer-aided diagnosis, and radiomics: advances in imaging towards to precision medicine.Radiologia brasileiraReview
- Idiopathic interstitial pneumonias: review of the latest American Thoracic Society/European Respiratory Society classification.Radiologia brasileiraArticle
- Article
Corrections and comments
- Erratum issued
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveTo perform a quantitative analysis of the airways using automated software, in computed tomography images of patients with cystic fibrosis, correlating the results with spirometric findings. MATERIALS AND
methodsThirty-four patients with cystic fibrosis were studied-20 males and 14 females; mean age 18 ± 9 years-divided into two groups according to the spirometry findings: group I (
resultsOn average, 52 bronchi per patient were studied. The number of bronchi analyzed was higher in group II. The correlation with spirometry findings, especially between the relative wall thickness of third to eighth bronchial generation and predicted FEV1, was better in group I.
conclusionQuantitative analysis of the airways by computed tomography can be useful for assessing disease severity in cystic fibrosis patients. In patients with severe airflow obstruction, the number of bronchi studied by the method is higher, indicating more bronchiectasis. In patients without severe obstruction, the relative bronchial wall thickness showed a good correlation with the predicted FEV1.
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