• Lauren S Mott, Judy Park, Catherine L Gangell, Nicholas H de Klerk, Peter D Sly, Conor P Murray, Stephen M Stick, and Australian Respiratory Early Surveillance Team for Cystic Fibrosis Study Group.
• Telethon Institute for Child Health Research and Center for Child Health Research, The University of Western Australia, Perth, Australia. lmott@ichr.uwa.edu.au
• J. Pediatr. 2013 Jul 1;163(1):243-8.e1-3.

ObjectiveTo examine the distribution of early structural lung changes in clinically stable infants and young children with cystic fibrosis using chest computed tomography (CT).Study DesignThis cross-sectional study included 62 children aged 1-6 years with volume-controlled volumetric chest CT scans performed under general anesthesia as part of an early surveillance program. Each lobe was scored for presence and extent of bronchiectasis, mucus plugging, and air trapping using a semiquantitative score. The topographic distribution of structural abnormalities was evaluated by comparing the presence and extent of abnormalities in different lung regions and examining relationships between components.ResultsAlthough bronchiectasis was most common in the right upper lobe, overall changes in lung structure were not more common or more extensive in the upper lobes. Rather, bronchiectasis was more common in the right lung (right lung 0.95, left lung 0.68, P = .003), and mucus plugging (upper 0.41, middle 0.41, lower 0.72, P = .028) and air trapping (upper 0.79, middle 0.48, lower 0.96, P < .001) were more common in the lower lobes. The extents of bronchiectasis (P < .001) and air trapping (P = .011) were greater in the right lung. Scans with bronchiectasis were also more likely to have coexisting mucus plugging (P = .008) and air trapping (P < .001).ConclusionEarly structural lung disease is heterogeneously distributed in the lung. Quantitative scoring tools for studies using chest CT as an end point, and mechanistic studies that seek to better understand the pathogenesis of early cystic fibrosis lung disease, should take account of this differential topographic expression of disease early in life.Copyright © 2013 Mosby, Inc. All rights reserved.

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