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Abstract #0063

Acceleration of Ventilation-Weighted Free-Breathing Functional 1H MRI in Pediatric Cystic Fibrosis Lung Disease

Samal Munidasa1,2,3, Brandon Zanette3, Marie-Pier Dumas4, Wallace Wee4, Sharon Braganza3, Daniel Li3, Jason Woods1, Felix Ratjen4, and Giles Santyr3
1Pulmonary Medicine, Cincinnati Children's Hospital, Cincinnati, OH, United States, 2Medical Biophysics, University of Toronto, Toronto, ON, Canada, 3Translational Medicine, The Hospital for Sick Children, Toronto, ON, Canada, 4Division of Respiratory Medicine, The Hospital for Sick Children, Toronto, ON, Canada

Synopsis

Keywords: Lung, Lung, hyperpolarized 129-Xenon, functional lung MRI

Motivation: Free-breathing pulmonary MRI acquisitions can be lengthy (i.e. 1-minute per slice) which can prove challenging for imaging pediatric lung diseases.

Goal(s): The purpose of this work is to determine if reducing the free-breathing MRI scan time will produce stable ventilation defect measures that agree with hyperpolarized 129Xenon-MRI (Xe-MRI).

Approach: Free-breathing MRI data acquired in cystic fibrosis patients were retrospectively truncated to compare measured Xe-MRI ventilation defects at shorter acquisition times.

Results: Free-breathing MRI ventilation defects showed minimal variability and similar correlation strength to Xe-MRI following approximately 40% reductions in scan time.

Impact: Free-breathing MRI can evaluate pulmonary ventilation in pediatric cystic fibrosis lung disease in agreement with 129Xenon-MRI but is lengthy. Accelerated free-breathing MRI allows for decreased scan durations, without compromising ventilation maps. This can potentially improve clinical translation, especially in pediatrics.

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Keywords