A chest radiograph scoring system in adult cystic fibrosis: correlation with pulmonary function

Clin Radiol. 1991 May;43(5):308-10. doi: 10.1016/s0009-9260(05)80535-5.

Abstract

The Birmingham scoring system for chest radiographs was assessed in 40 adult cystic fibrosis patients, with particular reference to correlation with pulmonary function values. Forty 'initial' and forty 'follow-up' chest radiographs were scored. The mean initial age of the group was 17.5 +/- 5.0 years, and the mean age at follow-up was 23.3 +/- 5.3 years. The cross-sectional radiographic score correlated significantly with the values of three commonly measured, pulmonary function parameters (r = 0.65, 0.67, 0.58, P less than 0.0001). There was a significant correlation (r = 0.64, P less than 0.0001), between the change in radiographic score, and the change in percent predicted forced vital capacity (FVC%). There was a less significant correlation (r = 0.45, P less than 0.006) between the change in radiographic score and the change in per cent predicted forced expiratory volume in one second (FEV1%). We conclude that the Birmingham radiographic scoring system is suitable for quantitative radiological evaluation in adult cystic fibrosis.

MeSH terms

  • Adolescent
  • Adult
  • Cystic Fibrosis / diagnostic imaging*
  • Cystic Fibrosis / physiopathology
  • Forced Expiratory Volume / physiology
  • Humans
  • Lung / physiopathology*
  • Peak Expiratory Flow Rate / physiology
  • Prognosis
  • Radiography, Thoracic*
  • Time Factors
  • Vital Capacity / physiology