Prospective motion correction for R2* and susceptibility mapping using spherical navigators
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作者:
Hewlett, Miriam
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Univ Western Ontario, Robarts Res Inst, London, ON, Canada
Univ Western Ontario, Dept Med Biophys, London, ON, CanadaUniv Western Ontario, Robarts Res Inst, London, ON, Canada
Hewlett, Miriam
[1
,2
]
Oran, Omer
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Siemens Healthcare Ltd, Oakville, ON, CanadaUniv Western Ontario, Robarts Res Inst, London, ON, Canada
Oran, Omer
[3
]
Liu, Junmin
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机构:
Univ Western Ontario, Robarts Res Inst, London, ON, CanadaUniv Western Ontario, Robarts Res Inst, London, ON, Canada
Liu, Junmin
[1
]
Drangova, Maria
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机构:
Univ Western Ontario, Robarts Res Inst, London, ON, Canada
Univ Western Ontario, Dept Med Biophys, London, ON, CanadaUniv Western Ontario, Robarts Res Inst, London, ON, Canada
Drangova, Maria
[1
,2
]
机构:
[1] Univ Western Ontario, Robarts Res Inst, London, ON, Canada
[2] Univ Western Ontario, Dept Med Biophys, London, ON, Canada
Purpose: To perform prospective motion correction (PMC) for improved R-2* and susceptibility mapping using a purely navigator-based approach. Methods: Spherical navigators (SNAVs) were combined with an additional FID readout for simultaneous measurement of motion and zeroth-order field shifts. The resulting FIDSNAVs were interleaved for PMC of a multi-echo gradient echo sequence with retrospective B-0 correction. Experiments were performed on a 3T scanner with a 32-channel head coil. Performance was assessed in five volunteers with motion prompts derived from real unintentional motion trajectories. Results: At short TEs, PMC alone was sufficient to achieve good image quality; at longer TEs, retrospective B-0 correction was often just as important for artifact reduction as motion correction. Both PMC and retrospective B-0 correction reduced error in R-2* and susceptibility maps for all participants. Residual artifacts were observed in the most severe motion case. Conclusion: Combining SNAVs with an additional FID readout enables simultaneous motion and field correction with no additional hardware requirements, improving the fidelity of quantitative mapping in the presence of motion.
机构:
Med Univ Graz, Dept Neurol, A-8036 Graz, AustriaMed Univ Graz, Dept Neurol, A-8036 Graz, Austria
Enzinger, Christian
Rocca, Maria A.
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Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Div Neurosci, Neuroimaging Res Unit,Inst Expt Neurol, Milan, ItalyMed Univ Graz, Dept Neurol, A-8036 Graz, Austria
机构:
Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Div Neurosci, Neuroimaging Res Unit,Inst Expt Neurol, Milan, ItalyMed Univ Graz, Dept Neurol, A-8036 Graz, Austria
机构:
Cornell Univ, Weill Med Coll, Dept Radiol, New York, NY 10021 USACornell Univ, Weill Med Coll, Dept Radiol, New York, NY 10021 USA
Hectors, Stefanie J.
Koehne de Gonzalez, Anne K.
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Columbia Univ, Dept Pathol, Med Ctr, New York, NY 10032 USACornell Univ, Weill Med Coll, Dept Radiol, New York, NY 10021 USA
Koehne de Gonzalez, Anne K.
Spincemaille, Pascal
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Cornell Univ, Weill Med Coll, Dept Radiol, New York, NY 10021 USACornell Univ, Weill Med Coll, Dept Radiol, New York, NY 10021 USA
Spincemaille, Pascal
Prince, Martin R.
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Cornell Univ, Weill Med Coll, Dept Radiol, New York, NY 10021 USACornell Univ, Weill Med Coll, Dept Radiol, New York, NY 10021 USA
Prince, Martin R.
Brittenham, Gary M.
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Columbia Univ, Dept Pediat, New York, NY 10032 USACornell Univ, Weill Med Coll, Dept Radiol, New York, NY 10021 USA
Brittenham, Gary M.
Wang, Yi
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Cornell Univ, Weill Med Coll, Dept Radiol, New York, NY 10021 USA
Cornell Univ, Meinig Sch Biomed Engn, Ithaca, NY 14853 USACornell Univ, Weill Med Coll, Dept Radiol, New York, NY 10021 USA