High-resolution computed tomography findings in young infants with cystic fibrosis detected by newborn screening
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/163704 |
Resumo: | OBJECTIVE: High-resolution computed tomography (HRCT) allows the early detection of pathological changes in the lung structure, and reproducible scoring systems can be used to quantify chest computed tomography (CT) findings in patients with cystic fibrosis (CF). The aim of the study was to describe early HRCT findings according to a validated scoring system in infants with CF diagnosed by newborn screening (NBS). METHODS: This cross-sectional study included infants with CF diagnosed by NBS who were born between January 2013 and January 2017 and who underwent HRCT scanning within the first year after diagnosis when they were clinically stable. The CT scans were evaluated using the modified Bhalla score. RESULTS: Thirty-two subjects underwent HRCT scanning. The mean total-modified Bhalla score was 3.6±2.1, and 93.8% of the scans were abnormal. Pseudomonas aeruginosa airway colonization was associated with increased modified Bhalla score values. Bronchial wall thickening was the most common feature (90.6%), followed by bronchial collapse/consolidation (59.4%), mosaic attenuation/perfusion (50%), bronchiectasis (37.5%) and mucus plugging (15.6%). Bronchial wall thickening was diffuse in most of the patients. CONCLUSION: A substantial proportion of infants diagnosed with CF after detection by NBS already showed evidence of lung disease. P. aeruginosa colonization was associated with increased Bhalla scores, highlighting the importance of this CF pathogen in early structural lung disease. The presence of bronchial wall thickening at such a young age may reflect the presence of airway inflammatory processes. The detection and quantification of structural abnormalities with the modified Bhalla score may aid in the identification of lung disease before it is clinically apparent. |
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Clinics |
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High-resolution computed tomography findings in young infants with cystic fibrosis detected by newborn screeningLung DiseasesCystic FibrosisNeonatal ScreeningTomographyMicrobiologyOBJECTIVE: High-resolution computed tomography (HRCT) allows the early detection of pathological changes in the lung structure, and reproducible scoring systems can be used to quantify chest computed tomography (CT) findings in patients with cystic fibrosis (CF). The aim of the study was to describe early HRCT findings according to a validated scoring system in infants with CF diagnosed by newborn screening (NBS). METHODS: This cross-sectional study included infants with CF diagnosed by NBS who were born between January 2013 and January 2017 and who underwent HRCT scanning within the first year after diagnosis when they were clinically stable. The CT scans were evaluated using the modified Bhalla score. RESULTS: Thirty-two subjects underwent HRCT scanning. The mean total-modified Bhalla score was 3.6±2.1, and 93.8% of the scans were abnormal. Pseudomonas aeruginosa airway colonization was associated with increased modified Bhalla score values. Bronchial wall thickening was the most common feature (90.6%), followed by bronchial collapse/consolidation (59.4%), mosaic attenuation/perfusion (50%), bronchiectasis (37.5%) and mucus plugging (15.6%). Bronchial wall thickening was diffuse in most of the patients. CONCLUSION: A substantial proportion of infants diagnosed with CF after detection by NBS already showed evidence of lung disease. P. aeruginosa colonization was associated with increased Bhalla scores, highlighting the importance of this CF pathogen in early structural lung disease. The presence of bronchial wall thickening at such a young age may reflect the presence of airway inflammatory processes. The detection and quantification of structural abnormalities with the modified Bhalla score may aid in the identification of lung disease before it is clinically apparent.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2019-10-31info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/xmlhttps://www.revistas.usp.br/clinics/article/view/16370410.6061/clinics/2019/e1399Clinics; Vol. 74 (2019); e1399Clinics; v. 74 (2019); e1399Clinics; Vol. 74 (2019); e13991980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/163704/157270https://www.revistas.usp.br/clinics/article/view/163704/157271Copyright (c) 2019 Clinicsinfo:eu-repo/semantics/openAccessCohen, Renata Wrobel FolescuFolescu, Tânia WrobelBoechat, Marcia Cristina BastosFonseca, Vania MatosMarques, Elizabeth AndradeLeão, Robson Souza2019-10-31T13:00:45Zoai:revistas.usp.br:article/163704Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2019-10-31T13:00:45Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
High-resolution computed tomography findings in young infants with cystic fibrosis detected by newborn screening |
title |
High-resolution computed tomography findings in young infants with cystic fibrosis detected by newborn screening |
spellingShingle |
High-resolution computed tomography findings in young infants with cystic fibrosis detected by newborn screening Cohen, Renata Wrobel Folescu Lung Diseases Cystic Fibrosis Neonatal Screening Tomography Microbiology |
title_short |
High-resolution computed tomography findings in young infants with cystic fibrosis detected by newborn screening |
title_full |
High-resolution computed tomography findings in young infants with cystic fibrosis detected by newborn screening |
title_fullStr |
High-resolution computed tomography findings in young infants with cystic fibrosis detected by newborn screening |
title_full_unstemmed |
High-resolution computed tomography findings in young infants with cystic fibrosis detected by newborn screening |
title_sort |
High-resolution computed tomography findings in young infants with cystic fibrosis detected by newborn screening |
author |
Cohen, Renata Wrobel Folescu |
author_facet |
Cohen, Renata Wrobel Folescu Folescu, Tânia Wrobel Boechat, Marcia Cristina Bastos Fonseca, Vania Matos Marques, Elizabeth Andrade Leão, Robson Souza |
author_role |
author |
author2 |
Folescu, Tânia Wrobel Boechat, Marcia Cristina Bastos Fonseca, Vania Matos Marques, Elizabeth Andrade Leão, Robson Souza |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Cohen, Renata Wrobel Folescu Folescu, Tânia Wrobel Boechat, Marcia Cristina Bastos Fonseca, Vania Matos Marques, Elizabeth Andrade Leão, Robson Souza |
dc.subject.por.fl_str_mv |
Lung Diseases Cystic Fibrosis Neonatal Screening Tomography Microbiology |
topic |
Lung Diseases Cystic Fibrosis Neonatal Screening Tomography Microbiology |
description |
OBJECTIVE: High-resolution computed tomography (HRCT) allows the early detection of pathological changes in the lung structure, and reproducible scoring systems can be used to quantify chest computed tomography (CT) findings in patients with cystic fibrosis (CF). The aim of the study was to describe early HRCT findings according to a validated scoring system in infants with CF diagnosed by newborn screening (NBS). METHODS: This cross-sectional study included infants with CF diagnosed by NBS who were born between January 2013 and January 2017 and who underwent HRCT scanning within the first year after diagnosis when they were clinically stable. The CT scans were evaluated using the modified Bhalla score. RESULTS: Thirty-two subjects underwent HRCT scanning. The mean total-modified Bhalla score was 3.6±2.1, and 93.8% of the scans were abnormal. Pseudomonas aeruginosa airway colonization was associated with increased modified Bhalla score values. Bronchial wall thickening was the most common feature (90.6%), followed by bronchial collapse/consolidation (59.4%), mosaic attenuation/perfusion (50%), bronchiectasis (37.5%) and mucus plugging (15.6%). Bronchial wall thickening was diffuse in most of the patients. CONCLUSION: A substantial proportion of infants diagnosed with CF after detection by NBS already showed evidence of lung disease. P. aeruginosa colonization was associated with increased Bhalla scores, highlighting the importance of this CF pathogen in early structural lung disease. The presence of bronchial wall thickening at such a young age may reflect the presence of airway inflammatory processes. The detection and quantification of structural abnormalities with the modified Bhalla score may aid in the identification of lung disease before it is clinically apparent. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-10-31 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/163704 10.6061/clinics/2019/e1399 |
url |
https://www.revistas.usp.br/clinics/article/view/163704 |
identifier_str_mv |
10.6061/clinics/2019/e1399 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/163704/157270 https://www.revistas.usp.br/clinics/article/view/163704/157271 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2019 Clinics info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2019 Clinics |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf application/xml |
dc.publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
dc.source.none.fl_str_mv |
Clinics; Vol. 74 (2019); e1399 Clinics; v. 74 (2019); e1399 Clinics; Vol. 74 (2019); e1399 1980-5322 1807-5932 reponame:Clinics instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Clinics |
collection |
Clinics |
repository.name.fl_str_mv |
Clinics - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||clinics@hc.fm.usp.br |
_version_ |
1800222764638928896 |