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dc.contributor.authorConklin, John
dc.contributor.authorTabari, Azadeh
dc.contributor.authorLongo, Maria G. F.
dc.contributor.authorCobos, Camilo J.
dc.contributor.authorSetsompop, Kawin
dc.contributor.authorCauley, Stephen F.
dc.contributor.authorKirsch, John E.
dc.contributor.authorHuang, Susie Y.
dc.contributor.authorRapalino, Otto
dc.contributor.authorGee, Michael S.
dc.contributor.authorCaruso, Paul J.
dc.date.accessioned2022-05-16T16:11:01Z
dc.date.available2022-05-16T16:11:01Z
dc.date.issued2022-02-04
dc.identifier.urihttps://hdl.handle.net/1721.1/142540
dc.description.abstractAbstract Background Susceptibility-weighted imaging (SWI) is highly sensitive for intracranial hemorrhagic and mineralized lesions but is associated with long scan times. Wave controlled aliasing in parallel imaging (Wave-CAIPI) enables greater acceleration factors and might facilitate broader application of SWI, especially in motion-prone populations. Objective To compare highly accelerated Wave-CAIPI SWI to standard SWI in the non-sedated pediatric outpatient setting, with respect to the following variables: estimated scan time, image noise, artifacts, visualization of normal anatomy and visualization of pathology. Materials and methods Twenty-eight children (11 girls, 17 boys; mean age ± standard deviation [SD] = 128.3±62 months) underwent 3-tesla (T) brain MRI, including standard three-dimensional (3-D) SWI sequence followed by a highly accelerated Wave-CAIPI SWI sequence for each subject. We rated all studies using a predefined 5-point scale and used the Wilcoxon signed rank test to assess the difference for each variable between sequences. Results Wave-CAIPI SWI provided a 78% and 67% reduction in estimated scan time using the 32- and 20-channel coils, respectively, corresponding to estimated scan time reductions of 3.5 min and 3 min, respectively. All 28 children were imaged without anesthesia. Inter-reader agreement ranged from fair to substantial (k=0.67 for evaluation of pathology, 0.55 for anatomical contrast, 0.3 for central noise, and 0.71 for artifacts). Image noise was rated higher in the central brain with wave SWI (P<0.01), but not in the peripheral brain. There was no significant difference in the visualization of normal anatomical structures and visualization of pathology between the standard and wave SWI sequences (P=0.77 and P=0.79, respectively). Conclusion Highly accelerated Wave-CAIPI SWI of the brain can provide similar image quality to standard SWI, with estimated scan time reduction of 3–3.5 min depending on the radiofrequency coil used, with fewer motion artifacts, at a cost of mild but perceptibly increased noise in the central brain.en_US
dc.publisherSpringer Berlin Heidelbergen_US
dc.relation.isversionofhttps://doi.org/10.1007/s00247-021-05273-8en_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.titleEvaluation of highly accelerated wave controlled aliasing in parallel imaging (Wave-CAIPI) susceptibility-weighted imaging in the non-sedated pediatric setting: a pilot studyen_US
dc.typeArticleen_US
dc.identifier.citationConklin, John, Tabari, Azadeh, Longo, Maria G. F., Cobos, Camilo J., Setsompop, Kawin et al. 2022. "Evaluation of highly accelerated wave controlled aliasing in parallel imaging (Wave-CAIPI) susceptibility-weighted imaging in the non-sedated pediatric setting: a pilot study."
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technology
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.updated2022-05-15T04:21:43Z
dc.language.rfc3066en
dc.rights.holderThe Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature
dspace.embargo.termsY
dspace.date.submission2022-05-15T04:21:43Z
mit.licensePUBLISHER_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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