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Pulmonary MRI of neonates in the intensive care unit using 3D ultrashort echo time and a small footprint MRI system
Author(s) -
Hahn Andrew D.,
Higano Nara S.,
Walkup Laura L.,
Thomen Robert P.,
Cao Xuefeng,
Merhar Stephanie L.,
Tkach Jean A.,
Woods Jason C.,
Fain Sean B.
Publication year - 2017
Publication title -
journal of magnetic resonance imaging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.563
H-Index - 160
eISSN - 1522-2586
pISSN - 1053-1807
DOI - 10.1002/jmri.25394
Subject(s) - medicine , neonatal intensive care unit , bronchopulmonary dysplasia , magnetic resonance imaging , radiology , lung , breathing , gestational age , pediatrics , anesthesia , pregnancy , biology , genetics
Purpose To determine the feasibility of pulmonary magnetic resonance imaging (MRI) of neonatal lung structures enabled by combining two novel technologies: first, a 3D radial ultrashort echo time (UTE) pulse sequence capable of high spatial resolution full‐chest imaging in nonsedated quiet‐breathing neonates; and second, a unique, small‐footprint 1.5T MRI scanner design adapted for neonatal imaging and installed within the neonatal intensive care unit (NICU). Materials and Methods Ten patients underwent MRI within the NICU, in accordance with an approved Institutional Review Board protocol. Five had clinical diagnoses of bronchopulmonary dysplasia (BPD), and five had putatively normal lung function. Pulmonary imaging was performed at 1.5T using 3D radial UTE and standard 3D fast gradient recalled echo (FGRE). Diagnostic quality, presence of motion artifacts, and apparent severity of lung pathology were evaluated by two radiologists. Quantitative metrics were additionally used to evaluate lung parenchymal signal. Results UTE images showed significantly higher signal in lung parenchyma ( P < 0.0001) and fewer apparent motion artifacts compared to FGRE ( P = 0.046). Pulmonary pathology was more severe in patients diagnosed with BPD relative to controls ( P = 0.001). Infants diagnosed with BPD also had significantly higher signal in lung parenchyma, measured using UTE, relative to controls ( P = 0.002). Conclusion These results demonstrate the technical feasibility of pulmonary MRI in free‐breathing, nonsedated infants in the NICU at high, isotropic resolutions approaching that achievable with computed tomography (CT). There is potential for pulmonary MRI to play a role in improving how clinicians understand and manage care of neonatal and pediatric pulmonary diseases. J. Magn. Reson. Imaging 2016. Level of Evidence: 2 J. Magn. Reson. Imaging 2017;45:463–471.