Literature DB >> 27343002

Objective airway artery dimensions compared to CT scoring methods assessing structural cystic fibrosis lung disease.

Wieying Kuo1, Eleni-Rosalina Andrinopoulou2, Adria Perez-Rovira3, Hadiye Ozturk4, Marleen de Bruijne5, Harm A W M Tiddens6.   

Abstract

Background: CF-CT and PRAGMA-CF are commonly used scoring methods to quantify the severity of bronchiectasis (BE) and airway wall thickening (AWT) on chest CTs of children with cystic fibrosis (CF). We aimed to validate CF-CT and PRAGMA-CF sub-scores for BE and AWT against quantitative airway–artery (AA) dimensions.
Methods: This is a retrospective study with 23 spirometer guided inspiratory chest CTs (11 CF, 12 controls; age range 6 to 16 years old) included. AA-, and AWTA-ratios of all visible AA pairs were computed by dividing diameters of the outer airway and wall (outer-inner airway) by the accompanying artery diameter, respectively. BE, AWT and total airway disease (TAD) were scored using CF-CT (% max score) and PRAGMA-CF (% extent). Correlations were computed using Spearman rank. Akaike information criterion (AIC) from the mixed-effects models were used to investigate whether CF-CT or PRAGMA-CF was a better predictor for AA-, and AWTA-ratios (lower AIC equals a better fitted model).
Results: 4861 AA pairs were measured in total. Correlations between CF-CT and PRAGMA-CF: BE (r = 0.93, P < 0.001); AWT (r = 0.62, P < 0.001); TAD (r = 0.88, P < 0.001). PRAGMA-CF TAD sub-score had lowest AIC in the mixed-model predicting AA-ratio. CF-CT AWT and PRAGMA-CF TAD sub-score had equal low AIC in the mixed-model predicting AWTA-ratio.
Conclusion: PRAGMA-CF TAD sub-score was more precise predicting BE. CF-CT AWT and PRAGMA-CF TAD sub-scores predicted AWT equally well. CF-CT and PRAGMA-CF were both sensitive methods to score BE and AWT in children with CF lung disease, with PRAGMA-CT TAD sub-score being most accurate in predicting AA dimensions.

Entities:  

Keywords:  Bronchiectasis; Chest CT; Cystic fibrosis; Pediatrics; Scoring

Mesh:

Year:  2016        PMID: 27343002     DOI: 10.1016/j.jcf.2016.05.015

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  5 in total

1.  Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification.

Authors:  Wieying Kuo; Marleen de Bruijne; Jens Petersen; Kazem Nasserinejad; Hadiye Ozturk; Yong Chen; Adria Perez-Rovira; Harm A W M Tiddens
Journal:  Eur Radiol       Date:  2017-05-18       Impact factor: 5.315

2.  Validation of automated lobe segmentation on paired inspiratory-expiratory chest CT in 8-14 year-old children with cystic fibrosis.

Authors:  Philip Konietzke; Oliver Weinheimer; Mark O Wielpütz; Dasha Savage; Tiglath Ziyeh; Christin Tu; Beverly Newman; Craig J Galbán; Marcus A Mall; Hans-Ulrich Kauczor; Terry E Robinson
Journal:  PLoS One       Date:  2018-04-09       Impact factor: 3.240

3.  Assessment of early lung disease in young children with CF: A comparison between pressure-controlled and free-breathing chest computed tomography.

Authors:  Merel C J Oudraad; Wieying Kuo; Tim Rosenow; Eleni-Rosalina Andrinopoulou; Stephen M Stick; Harm A W M Tiddens
Journal:  Pediatr Pulmonol       Date:  2020-03-02

4.  Airway disease on chest computed tomography of preschool children with cystic fibrosis is associated with school-age bronchiectasis.

Authors:  Nynke R Bouma; Hettie M Janssens; Eleni-Rosalina Andrinopoulou; Harm A W M Tiddens
Journal:  Pediatr Pulmonol       Date:  2019-09-09

Review 5.  The lower respiratory airway wall in children in health and disease.

Authors:  Michael Fayon; Fabien Beaufils
Journal:  ERJ Open Res       Date:  2021-07-26
  5 in total

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