Rapid B1+ mapping using a preconditioning RF pulse with TurboFLASH readout

In MRI, the transmit radiofrequency field (B 1+) inhomogeneity can lead to signal intensity variations and quantitative measurement errors. By independently mapping the local B 1+ variation, the radiofrequency‐related signal variations can be corrected for. In this study, we present a new fast B 1+...

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Veröffentlicht in:Magnetic resonance in medicine 2010-08, Vol.64 (2), p.439-446
Hauptverfasser: Chung, Sohae, Kim, Daniel, Breton, Elodie, Axel, Leon
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Sprache:eng
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Zusammenfassung:In MRI, the transmit radiofrequency field (B 1+) inhomogeneity can lead to signal intensity variations and quantitative measurement errors. By independently mapping the local B 1+ variation, the radiofrequency‐related signal variations can be corrected for. In this study, we present a new fast B 1+ mapping method using a slice‐selective preconditioning radiofrequency pulse. Immediately after applying a slice‐selective preconditioning pulse, a turbo fast low‐angle‐shot imaging sequence with centric k‐space reordering is performed to capture the residual longitudinal magnetization left behind by the slice‐selective preconditioning pulse due to B 1+ variation. Compared to the reference double‐angle method, this method is considerably faster. Specifically, the total scan time for the double‐angle method is equal to the product of 2 (number of images), the number of phase‐encoding lines, and approximately 5T1, whereas the slice‐selective preconditioning method takes approximately 5T1. This method was validated in vitro and in vivo with a 3‐T whole‐body MRI system. The combined brain and pelvis B 1+ measurements showed excellent agreement and strong correlation with those by the double‐angle method (mean difference = 0.025; upper and lower 95% limits of agreement were −0.07 and 0.12; R = 0.93; P < 0.001). This fast B 1+ mapping method can be used for a variety of applications, including body imaging where fast imaging is desirable. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.
ISSN:0740-3194
1522-2594
1522-2594
DOI:10.1002/mrm.22423