A single‐breath‐hold protocol for hyperpolarized 129Xe ventilation and gas exchange imaging

Author:

Niedbalski Peter J.123ORCID,Willmering Matthew M.4,Thomen Robert P.5,Mugler John P.6,Choi Jiwoong12,Hall Chase1,Castro Mario1

Affiliation:

1. Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Internal Medicine University of Kansas Medical Center Kansas City KS USA

2. Department of Bioengineering University of Kansas Lawrence KS USA

3. Hoglund Biomedical Imaging Center University of Kansas Medical Center Kansas City KS USA

4. Center for Pulmonary Imaging Research Cincinnati Children's Hospital Medical Center Cincinnati OH USA

5. Departments of Radiology and Bioengineering University of Missouri School of Medicine Columbia MO USA

6. Department of Radiology & Medical Imaging University of Virginia School of Medicine Charlottesville VA USA

Abstract

Hyperpolarized 129Xe MRI (Xe‐MRI) is increasingly used to image the structure and function of the lungs. Because 129Xe imaging can provide multiple contrasts (ventilation, alveolar airspace size, and gas exchange), imaging often occurs over several breath‐holds, which increases the time, expense, and patient burden of scans. We propose an imaging sequence that can be used to acquire Xe‐MRI gas exchange and high‐quality ventilation images within a single, approximately 10 s, breath‐hold. This method uses a radial one‐point Dixon approach to sample dissolved 129Xe signal, which is interleaved with a 3D spiral (“FLORET”) encoding pattern for gaseous 129Xe. Thus, ventilation images are obtained at higher nominal spatial resolution (4.2 × 4.2 × 4.2 mm3) compared with gas‐exchange images (6.25 × 6.25 × 6.25 mm3), both competitive with current standards within the Xe‐MRI field. Moreover, the short 10 s Xe‐MRI acquisition time allows for 1H “anatomic” images used for thoracic cavity masking to be acquired within the same breath‐hold for a total scan time of about 14 s. Images were acquired using this single‐breath method in 11 volunteers (N = 4 healthy, N = 7 post‐acute COVID). For 11 of these participants, a separate breath‐hold was used to acquire a “dedicated” ventilation scan and five had an additional “dedicated” gas exchange scan. The images acquired using the single‐breath protocol were compared with those from dedicated scans using Bland–Altman analysis, intraclass correlation (ICC), structural similarity, peak signal‐to‐noise ratio, Dice coefficients, and average distance. Imaging markers from the single‐breath protocol showed high correlation with dedicated scans (ventilation defect percent, ICC = 0.77, p = 0.01; membrane/gas, ICC = 0.97, p = 0.001; red blood cell/gas, ICC = 0.99, p < 0.001). Images showed good qualitative and quantitative regional agreement. This single‐breath protocol enables the collection of essential Xe‐MRI information within one breath‐hold, simplifying scanning sessions and reducing costs associated with Xe‐MRI.

Funder

American Heart Association

Scleroderma Foundation

Publisher

Wiley

Subject

Spectroscopy,Radiology, Nuclear Medicine and imaging,Molecular Medicine

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