Same‐Day Repeatability and 28‐Day Reproducibility of Xenon MRI Ventilation in Children With Cystic Fibrosis in a Multi‐Site Trial

Author:

Walkup Laura L.123ORCID,Roach David J.1,Plummer Joseph W.13ORCID,Willmering Matthew M.12,Zanette Brandon4,Santyr Giles45ORCID,Fain Sean B.678ORCID,Rock Michael J.9,Mata Jaime10,Froh Deborah11,Stanojevic Sanja12,Cleveland Zackary I.123,Ratjen Felix413,Woods Jason C.12

Affiliation:

1. Division of Pulmonary Medicine Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA

2. Department of Pediatrics University of Cincinnati Cincinnati Ohio USA

3. Department of Biomedical Engineering University of Cincinnati Cincinnati Ohio USA

4. Program in Translational Medicine The Hospital for Sick Children Toronto Ontario Canada

5. Department of Medical Biophysics University of Toronto Toronto Ontario Canada

6. Department of Radiology, Carver College of Medicine University of Iowa Iowa City Iowa USA

7. Department of Medicine University of Wisconsin‐Madison Madison Wisconsin USA

8. Department of Medical Physics University of Wisconsin‐Madison Madison Wisconsin USA

9. Department of Pediatrics University of Wisconsin School of Medicine and Public Health Madison Wisconsin USA

10. Department of Radiology and Medical Imaging University of Virginia Charlottesville Virginia USA

11. Department of Pediatrics University of Virginia Charlottesville Virginia USA

12. Department of Community Health and Epidemiology Dalhousie University Halifax Nova Scotia Canada

13. Department of Pediatrics University of Toronto Toronto Ontario Canada

Abstract

BackgroundMRI with xenon‐129 gas (Xe MRI) can assess airflow obstruction and heterogeneity in lung diseases. Specifically, Xe MRI may represent a sensitive modality for future therapeutic trials of cystic fibrosis (CF) therapies. The reproducibility of Xe MRI has not yet been assessed in the context of a multi‐site study.PurposeTo determine the same‐day repeatability and 28‐day reproducibility of Xe MRI in children with CF.Study TypeFour‐center prospective, longitudinal.PopulationThirty‐eight children (18 females, 47%), median interquartile range (IQR) age 12 (9–14) years old, with mild CF (forced expiratory volume in 1 second (FEV1) ≥85% predicted).Field Strength/Sequence3‐T, two‐dimensional (2D) gradient‐echo (GRE) sequence.AssessmentXe MRI, FEV1, and nitrogen multiple‐breath wash‐out for lung‐clearance index (LCI2.5) were performed. To assess same‐day reproducibility, Xe MRI was performed twice within the first visit, and procedures were repeated at 28 days. Xe hypoventilation was quantified using ventilation‐defect percentage (VDP) and reader‐defect volume (RDV). For VDP, hypoventilated voxels from segmented images were identified using a threshold of <60% mean whole‐lung signal and expressed as a percentage of the lung volume. For RDV, hypoventilation was identified by two trained readers and expressed as a percentage.Statistical TestsInter‐site comparisons were conducted using Kruskal–Wallis nonparametric tests with Dunn's multiple‐comparisons tests. Differences for individuals were assessed using Wilcoxon matched‐pairs tests. Bland–Altman tests were used to evaluate same‐day repeatability, 28‐day reproducibility, and inter‐reader agreement. A P‐value ≤0.05 was considered significant.ResultsMedian FEV1 %‐predicted was 96.8% (86%–106%), and median LCI2.5 was 6.6 (6.3–7.4). Xe MRI had high same‐day reproducibility (mean VDP difference 0.12%, 95% limits of agreement [−3.2, 3.4]; mean RDV difference 0.42% [−2.5, 3.3]). At 28 days, 26/31 participants (84%) fell within the same‐day 95% limits of agreement.Data ConclusionXe MRI may offer excellent same‐day and short‐term reproducibility.Evidence Level2Technical EfficacyStage 2

Funder

Cystic Fibrosis Foundation

Publisher

Wiley

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