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Investigative radiology · Jul 2013
Highly accelerated T1-weighted abdominal imaging using 2-dimensional controlled aliasing in parallel imaging results in higher acceleration: a comparison with generalized autocalibrating partially parallel acquisitions parallel imaging.
- Philipp Riffel, Ulrike I Attenberger, Stephan Kannengiesser, Marcel D Nickel, Carolyn Arndt, Mathias Meyer, Stefan O Schoenberg, and Henrik J Michaely.
- Department of Clinical Radiology and Nuclear Medicine, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany. Philipp.Riffel@umm.de
- Invest Radiol. 2013 Jul 1; 48 (7): 554-61.
PurposeThe purpose of this study was to evaluate the feasibility and technical quality of an abdominal 3-dimensional interpolated breath-hold (volumetric interpolated breath-hold examination [VIBE]) magnetic resonance examination using the new parallel acquisition technique, controlled aliasing in parallel imaging results in higher acceleration (CAIPIRINHA).Materials And MethodsIn this institutional review board-approved study, 15 volunteers underwent an abdominal magnetic resonance imaging examination including axial unenhanced 3-dimensional VIBE sequences with the conventional parallel acquisition technique, generalized autocalibrating partially parallel acquisitions parallel imaging (GRAPPA), with an acceleration factor (R) of 2, 3, 4, and 2 × 2 in comparison with a CAIPIRINHA-VIBE sequence with an acceleration factor of 2 × 2. Images were evaluated regarding the overall image quality, liver edge sharpness, and parallel imaging artifacts. Signal-to-noise ratio was evaluated using 2 different methods. In a second study population, 17 patients were examined with our new routine protocol for abdominal imaging that now comprises VIBE sequences with CAIPIRINHA with R = 2 × 2.ResultsIn the volunteer population, the overall image quality of CAIPIRINHA with R = 2 × 2 was significantly higher compared with GRAPPA with R = 3, 4, and 2 × 2 (P < 0.05). There were significantly less parallel imaging artifacts with CAIPIRINHA with R = 2 × 2 (P < 0.05). Acquisition time varied between 21.1 (GRAPPA with R = 2, 320 matrix) and 6.9 seconds (CAIPIRINHA with R = 2 × 2, 256 matrix). Signal-to-noise ratio performance of CAIPIRINHA with R = 2 × 2 was superior to GRAPPA with R = 3, 4, and 2 × 2. In the patient population, VIBE sequences with CAIPIRINHA with R = 2 × 2 showed consistently good image quality, minimal motion artifacts, and minimal parallel imaging artifacts.ConclusionsThe CAIPRINHA-VIBE with an acceleration factor of R = 2 × 2 is feasible in a clinical setting and is characterized by fast and robust imaging with an image quality comparable with a 2-fold acceleration with GRAPPA.
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