Sarah Svenningsen1,2, Miranda Kirby1,2, Hassaan Ahmed1,2, Nigel Paterson3, Grace Parraga1,4
1Imaging Research Laboratories, Robarts Research Institute, London, Ontario, Canada; 2Department of Medical Biophysics, The University of Western Ontario, London, Ontario, Canada; 3Division of Respirology, Department of Medicine, the University of Western Ontario, London, Ontario, Canada; 4Graduate Program in Biomedical Engineering, The University of Western Ontario, London, Ontario, Canada
With the recent rapid development of a wider array of cystic fibrosis (CF) treatment options there is an urgent requirement for precise, practical and sensitive clinical endpoint measures that can be used to determine treatment response and CF disease progression over time. With the generation of a semi-automated method for the determination of pulmonary ventilation in CF, the short-term (7 2 days) precision and specificity of hyperpolarized 3He MRI measurements was evaluated. We were able to conclude that the semi-automated method provides superior precision for the detection of significant changes in pulmonary function over short periods of time.