Paediatric Respiratory Reviews
Volume 9, Issue 3 , Pages 168-175, September 2008

Role of high-resolution computed tomography in the detection of early cystic fibrosis lung disease

  • Barry Linnane

      Affiliations

    • Department of Respiratory Medicine, Royal Children's Hospital, Melbourne, Australia
    • Infection, Immunity and Environment Theme, Murdoch Children's Research Institute, Melbourne, Australia
    • Corresponding Author InformationCorresponding author. Department of Respiratory Medicine, Royal Children's Hospital, Flemington Road, Parkville, Melbourne, VIC 3054, Australia.
  • ,
  • Phil Robinson

      Affiliations

    • Department of Respiratory Medicine, Royal Children's Hospital, Melbourne, Australia
    • Infection, Immunity and Environment Theme, Murdoch Children's Research Institute, Melbourne, Australia
  • ,
  • Sarath Ranganathan

      Affiliations

    • Department of Respiratory Medicine, Royal Children's Hospital, Melbourne, Australia
    • Department of Paediatrics, University of Melbourne, Melbourne, Australia
    • Infection, Immunity and Environment Theme, Murdoch Children's Research Institute, Melbourne, Australia
  • ,
  • Stephen Stick

      Affiliations

    • Department of Respiratory Medicine, Princess Margaret Hospital for Children, Perth, Australia
    • Department of Paediatrics, University of Western Australia, Perth, Australia
    • Division of Clinical Sciences, Telethon Institute for Child Health Research, Perth, Australia
  • ,
  • Conor Murray

      Affiliations

    • Department of Diagnostic Imaging, Princess Margaret Hospital for Children, Perth, Australia

Summary 

High-resolution computed tomography (HRCT) has been demonstrated to be sensitive at detecting early lung disease in cystic fibrosis (CF), often before it is apparent clinically. There is emerging evidence that structural changes in the lung occur earlier in life than previously appreciated. Despite this, the role of HRCT in young children with CF has yet to be defined, principally because the repeated exposure of children to X-ray doses several multiples that of a standard chest X-ray raises the concern of the long-term risks of ionizing radiation. With the challenges of acquiring HRCT images in young children in mind, we review scanning protocols and settings specific to young children, and review the best available evidence that describes early structural lung disease in young children with CF. The role of CT scoring and quantitative measures of CF lung disease are reviewed. The challenge for the future is to develop techniques that provide clinically useful information at the lowest possible radiation risk.

Keywords: cystic fibrosis, child, preschool, infant, computed tomography, X-ray, radiation

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PII: S1526-0542(08)00035-3

doi:10.1016/j.prrv.2008.05.009

Paediatric Respiratory Reviews
Volume 9, Issue 3 , Pages 168-175, September 2008