Literature DB >> 25929944

Changes in structural lung disease in cystic fibrosis children over 4 years as evaluated by high-resolution computed tomography.

Carlos Carpio1, Gustavo Albi2, José Carlos Rayón-Aledo3, Rodolfo Álvarez-Sala4, Rosa Girón5, Concepción Prados4, Paloma Caballero3.   

Abstract

OBJECTIVES: To compare the worsening of structural lung disease on high-resolution computed tomography (HRCT) with changes in spirometry results in cystic fibrosis (CF) patients, and analyse factors associated with the worsening of structural lung disease over time.
METHODS: A total of 31 CF subjects (mean age 11.03 ± 3.67 years old) were prospectively evaluated by two HRCT and spirometry tests performed 4 years apart. HRCT abnormalities were scored using the Bhalla scoring system. Comparisons between changes on HRCT and spirometry were made for all patients, and also for groups categorized by age, sex, genotypic alterations and lung obstruction.
RESULTS: The mean HRCT Bhalla scoring, forced expiratory volume in 1 s (FEV1 %pred.) and forced vital capacity (FVC %pred.) were 7.92 ± 3.59, 87.76 ± 20.52 and 96.54 ± 15.12, respectively. There was a significant deterioration in the Bhalla score (p < 0.01) and in certain categories: severity of bronchiectasis, peribronchial thickening, mucous plugging and bronchial divisions. Females had a more pronounced worsening of the Bhalla score than males (p = 0.048). No change over time was found in FEV1 and FVC. Only sex was associated with a deterioration in HRCT.
CONCLUSIONS: HRCT Bhalla scoring changes statistically significantly over 4 years, but spirometry results do not. Worsening on HRCT is more evident in females. KEY POINTS: • HRCT Bhalla scoring changes significantly over 4 years, spirometry results do not. • Females experience faster respiratory deterioration than males. • Spirometry results are not associated with deterioration in HRCT.

Entities:  

Keywords:  Bronchiectasis; Computed tomography; Cystic fibrosis; Spirometry; Thoracic radiography; X-ray

Mesh:

Year:  2015        PMID: 25929944     DOI: 10.1007/s00330-015-3782-4

Source DB:  PubMed          Journal:  Eur Radiol        ISSN: 0938-7994            Impact factor:   5.315


  33 in total

1.  High resolution CT in children with cystic fibrosis: correlation with pulmonary functions and radiographic scores.

Authors:  F B Demirkazik; O M Ariyürek; U Ozçelik; A Göçmen; H K Hassanabad; N Kiper
Journal:  Eur J Radiol       Date:  2001-01       Impact factor: 3.528

2.  An automated approach to quantitative air trapping measurements in mild cystic fibrosis.

Authors:  Michael L Goris; Hongyun J Zhu; Francis Blankenberg; Frandics Chan; Terry E Robinson
Journal:  Chest       Date:  2003-05       Impact factor: 9.410

3.  Bronchial measurement with three-dimensional quantitative thin-section CT in patients with cystic fibrosis.

Authors:  Michel Montaudon; Patrick Berger; Agathe Cangini-Sacher; Gabriel de Dietrich; José Manuel Tunon-de-Lara; Roger Marthan; François Laurent
Journal:  Radiology       Date:  2006-12-19       Impact factor: 11.105

4.  Progression of early structural lung disease in young children with cystic fibrosis assessed using CT.

Authors:  Lauren S Mott; Judy Park; Conor P Murray; Catherine L Gangell; Nicholas H de Klerk; Philip J Robinson; Colin F Robertson; Sarath C Ranganathan; Peter D Sly; Stephen M Stick
Journal:  Thorax       Date:  2011-12-26       Impact factor: 9.139

5.  Spirometric response to a bronchodilator. Reference values for healthy children and adolescents.

Authors:  P Casan; J Roca; J Sanchis
Journal:  Bull Eur Physiopathol Respir       Date:  1983 Nov-Dec

6.  Evaluation of scoring system of the chest radiograph in cystic fibrosis: a collaborative study.

Authors:  D Brasfield; G Hicks; S Soong; J Peters; R Tiller
Journal:  AJR Am J Roentgenol       Date:  1980-06       Impact factor: 3.959

7.  Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis.

Authors:  M Corey; L Edwards; H Levison; M Knowles
Journal:  J Pediatr       Date:  1997-12       Impact factor: 4.406

8.  Pulmonary abnormalities on high-resolution CT demonstrate more rapid decline than FEV1 in adults with cystic fibrosis.

Authors:  Eoin P Judge; Jonathan D Dodd; James B Masterson; Charles G Gallagher
Journal:  Chest       Date:  2006-11       Impact factor: 9.410

9.  Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening.

Authors:  Peter D Sly; Siobhain Brennan; Catherine Gangell; Nicholas de Klerk; Conor Murray; Lauren Mott; Stephen M Stick; Philip J Robinson; Colin F Robertson; Sarath C Ranganathan
Journal:  Am J Respir Crit Care Med       Date:  2009-04-16       Impact factor: 21.405

10.  Risk factors for bronchiectasis in children with cystic fibrosis.

Authors:  Peter D Sly; Catherine L Gangell; Linping Chen; Robert S Ware; Sarath Ranganathan; Lauren S Mott; Conor P Murray; Stephen M Stick
Journal:  N Engl J Med       Date:  2013-05-23       Impact factor: 91.245

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  2 in total

1.  A semiquantitative MRI-Score can predict loss of lung function in patients with cystic fibrosis: Preliminary results.

Authors:  Juergen F Schaefer; Andreas Hector; Katharina Schmidt; Matthias Teufel; Sabrina Fleischer; Ute Graepler-Mainka; Joachim Riethmueller; Sergios Gatidis; Susanne Schaefer; Konstantin Nikolaou; Dominik Hartl; Ilias Tsiflikas
Journal:  Eur Radiol       Date:  2017-06-29       Impact factor: 5.315

2.  High-resolution computed tomography findings in young infants with cystic fibrosis detected by newborn screening.

Authors:  Renata Wrobel Folescu Cohen; Tânia Wrobel Folescu; Marcia Cristina Bastos Boechat; Vania Matos Fonseca; Elizabeth Andrade Marques; Robson Souza Leão
Journal:  Clinics (Sao Paulo)       Date:  2019-10-21       Impact factor: 2.365

  2 in total

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