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dc.contributor.authorConklin, John
dc.contributor.authorFigueiro Longo, Maria G.
dc.contributor.authorTabari, Azadeh
dc.contributor.authorLio Goncalves Filho, Augusto
dc.contributor.authorLiu, Wei
dc.contributor.authorSplitthoff, Daniel N.
dc.contributor.authorLo, Wei-Ching
dc.contributor.authorCauley, Stephen F.
dc.contributor.authorSetsompop, Kawin
dc.contributor.authorSchaefer, Pamela W.
dc.contributor.authorKirsch, John E.
dc.contributor.authorRapalino, Otto
dc.contributor.authorHuang, Susie Y.
dc.date.accessioned2022-09-15T12:02:42Z
dc.date.available2022-09-15T12:02:42Z
dc.date.issued2022-08-04
dc.identifier.urihttps://hdl.handle.net/1721.1/145422
dc.description.abstractAbstract Objectives Wave-CAIPI (Controlled Aliasing in Parallel Imaging) enables dramatic reduction in acquisition time of 3D MRI sequences such as 3D susceptibility-weighted imaging (SWI) but has not been clinically evaluated at 1.5 T. We sought to compare highly accelerated Wave-CAIPI SWI (Wave-SWI) with two alternative standard sequences, conventional three-dimensional SWI and two-dimensional T2*-weighted Gradient-Echo (T2*w-GRE), in patients undergoing routine brain MRI at 1.5 T. Methods In this study, 172 patients undergoing 1.5 T brain MRI were scanned with a more commonly used susceptibility sequence (standard SWI or T2*w-GRE) and a highly accelerated Wave-SWI sequence. Two radiologists blinded to the acquisition technique scored each sequence for visualization of pathology, motion and signal dropout artifacts, image noise, visualization of normal anatomy (vessels and basal ganglia mineralization), and overall diagnostic quality. Superiority testing was performed to compare Wave-SWI to T2*w-GRE, and non-inferiority testing with 15% margin was performed to compare Wave-SWI to standard SWI. Results Wave-SWI performed superior in terms of visualization of pathology, signal dropout artifacts, visualization of normal anatomy, and overall image quality when compared to T2*w-GRE (all p < 0.001). Wave-SWI was non-inferior to standard SWI for visualization of normal anatomy and pathology, signal dropout artifacts, and overall image quality (all p < 0.001). Wave-SWI was superior to standard SWI for motion artifact (p < 0.001), while both conventional susceptibility sequences were superior to Wave-SWI for image noise (p < 0.001). Conclusions Wave-SWI can be performed in a 1.5 T clinical setting with robust performance and preservation of diagnostic quality. Key Points • Wave-SWI accelerated the acquisition of 3D high-resolution susceptibility images in 70% of the acquisition time of the conventional T2*GRE. • Wave-SWI performed superior to T2*w-GRE for visualization of pathology, signal dropout artifacts, and overall diagnostic image quality. • Wave-SWI was noninferior to standard SWI for visualization of normal anatomy and pathology, signal dropout artifacts, and overall diagnostic image quality.en_US
dc.publisherSpringer Berlin Heidelbergen_US
dc.relation.isversionofhttps://doi.org/10.1007/s00330-022-08871-8en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceSpringer Berlin Heidelbergen_US
dc.titleClinical validation of Wave-CAIPI susceptibility-weighted imaging for routine brain MRI at 1.5 Ten_US
dc.typeArticleen_US
dc.identifier.citationConklin, J., Figueiro Longo, M.G., Tabari, A. et al. Clinical validation of Wave-CAIPI susceptibility-weighted imaging for routine brain MRI at 1.5 T. Eur Radiol 32, 7128–7135 (2022).en_US
dc.contributor.departmentHarvard-MIT Program in Health Sciences and Technologyen_US
dc.relation.journalEuropean Radiologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-09-15T03:22:15Z
dc.language.rfc3066en
dc.rights.holderThe Author(s), under exclusive licence to European Society of Radiology
dspace.embargo.termsY
dspace.date.submission2022-09-15T03:22:15Z
mit.journal.volume32en_US
mit.licensePUBLISHER_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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