Literature DB >> 12195474

Loss of FEV1 in cystic fibrosis: correlation with HRCT features.

Anastasia Oikonomou1, John Manavis, Paraskevi Karagianni, John Tsanakas, Athol U Wells, David M Hansell, Frederica Papadopoulou, Stavros C Efremidis.   

Abstract

The purpose of this study was to determine which high-resolution computed tomography (HRCT) features in patients with cystic fibrosis are most strongly associated with functional impairment as expressed by forced expiratory volume in one second (FEV1). Forty-seven patients with cystic fibrosis underwent chest HRCT and had pulmonary function tests. The HRCT examinations were evaluated for 11 features scored using a modification of Bhalla system and FEV1 was recorded as percentage of the predicted value. Univariate and multivariate correlations between HRCT scores and FEV1 were performed. The most common HRCT feature was bronchiectasis (98%) followed by atelectasis-consolidation (81%), bronchial wall thickening (77%), tree-in-bud sign (74%), mucous plugging (72%) and mosaic perfusion pattern (47%). On univariate analysis the following features correlated strongly with FEV1: bronchial wall thickening ( p<0.0000001), tree-in-bud sign ( p<0.0000001), mucous plugging ( p<0.0000001), atelectasis-consolidation (p<0.0000001), thickening of interlobular septa ( p<0.0002), severity ( p<0.0002) and extent of bronchiectasis ( p<0.0002). On multivariate analysis bronchial wall thickening and atelectasis-consolidation were the strongest independent determinants of the FEV1. We found a regression equation between FEV1 and the two HRCT features: FEV1=constant variable+a multiplied by bronchial wall thickening+b multiplied by atelectasis-consolidation (a and b=regression coefficients, R(2)=0.48). The major morphological determinants of functional abnormality in cystic fibrosis, as expressed by the loss of FEV1, are bronchial wall thickening and atelectasis-consolidation.

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Year:  2002        PMID: 12195474     DOI: 10.1007/s00330-002-1340-3

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


  11 in total

1.  High resolution computed tomography of the chest in cystic fibrosis (CF): is simplification of scoring systems feasible?

Authors:  Anastasia Oikonomou; John Tsanakas; Elpis Hatziagorou; Fotios Kirvassilis; Stavros Efremidis; Panos Prassopoulos
Journal:  Eur Radiol       Date:  2007-11-27       Impact factor: 5.315

2.  Hyperpolarized 3helium magnetic resonance ventilation imaging of the lung in cystic fibrosis: comparison with high resolution CT and spirometry.

Authors:  Colm J McMahon; Jonathan D Dodd; Catherine Hill; Neil Woodhouse; Jim M Wild; Stan Fichele; Charles G Gallagher; Stephen J Skehan; Edwin J R van Beek; James B Masterson
Journal:  Eur Radiol       Date:  2006-07-27       Impact factor: 5.315

3.  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

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

Authors:  Carlos Carpio; Gustavo Albi; José Carlos Rayón-Aledo; Rodolfo Álvarez-Sala; Rosa Girón; Concepción Prados; Paloma Caballero
Journal:  Eur Radiol       Date:  2015-05-01       Impact factor: 5.315

Review 5.  Cystic fibrosis lung disease: genetic influences, microbial interactions, and radiological assessment.

Authors:  Samuel M Moskowitz; Ronald L Gibson; Eric L Effmann
Journal:  Pediatr Radiol       Date:  2005-05-03

Review 6.  [Thoracic findings in pediatric patients with cystic fibrosis].

Authors:  R Wunsch; C Wunsch
Journal:  Radiologe       Date:  2003-12       Impact factor: 0.635

7.  Partitioning core and satellite taxa from within cystic fibrosis lung bacterial communities.

Authors:  Christopher J van der Gast; Alan W Walker; Franziska A Stressmann; Geraint B Rogers; Paul Scott; Thomas W Daniels; Mary P Carroll; Julian Parkhill; Kenneth D Bruce
Journal:  ISME J       Date:  2010-12-09       Impact factor: 10.302

8.  Determinants of mortality for adults with cystic fibrosis admitted in Intensive Care Unit: a multicenter study.

Authors:  Joëlle Texereau; Dany Jamal; Gérald Choukroun; Pierre-Régis Burgel; Jean-Luc Diehl; Antoine Rabbat; Philippe Loirat; Antoine Parrot; Alexandre Duguet; Joël Coste; Daniel Dusser; Dominique Hubert; Jean-Paul Mira
Journal:  Respir Res       Date:  2006-01-26

9.  Radiography, tomosynthesis, CT and MRI in the evaluation of pulmonary cystic fibrosis: an untangling review of the multitude of scoring systems.

Authors:  Kristina Vult von Steyern; Isabella M Björkman-Burtscher; Mats Geijer
Journal:  Insights Imaging       Date:  2013-09-25

Review 10.  The lower respiratory airway wall in children in health and disease.

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