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      Improved assessment of aortic hemodynamics by k-t accelerated dual- venc 4D flow MRI in pediatric patients

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      1 , , 2 , 1 , 1 , 3 , 1 , 4 , 1 , 3 , 2
      Journal of Cardiovascular Magnetic Resonance
      BioMed Central
      19th Annual SCMR Scientific Sessions
      27-30 January 2016

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          Abstract

          Background Bicuspid aortic valve (BAV) is often associated with aortic stenosis, resulting in high velocity blood flow in the ascending aorta, with slow flow areas in the dilated aorta or adjacent vessels. Similarly, Marfan syndrome patients develop aortic root dilatation and regurgitation with both high and low velocity blood flow. 4D flow MRI is typically acquired with a velocity encoding (venc) gradient adjusted to the estimated peak velocity. As the velocity noise is directly related to the velocity sensitivity (σv~venc), a high venc can substantially limit the assessment of low flow velocities (v < < venc). We therefore developed a fully integrated low- and high-venc PC-MRI in a single measurement (dual-venc) to avoid aliasing and improve velocity-to-noise ratio (VNR). Methods In addition to standard clinical contrast enhanced cardiac MRI, k-t GRAPPA accelerated dual-venc 4D flow MRI was acquired with full volumetric coverage of the ascending (AAo) and descending (DAo) aorta in 4 Marfan syndrome patients (age = 16.3 ± 1.9 yrs, 1 female, low-venc = 81 cm/s, high-venc = 200 cm/s) and 1 BAV patient (age = 20 yrs, male, low-venc = 125 cm/s, high-venc = 350 cm/s) on a 1.5T Siemens MAGNETOM Aera MRI scanner with the following imaging parameters: R = 5, TE/TR = 2.93 ± 0.08/5.46 ± 0.08ms, voxel size = 1.9 × 1.9 × 2.0 mm3. Background correction was performed separately of the low- and high-venc phase images. High-venc data were used for complete anti-aliasing of the low-venc data while maintaining the favorable VNR of the low-venc data. A pseudo-complex MRA was derived from the 4D flow data and used to segment the angiogram using commercial software (MIMICS, Materialize). Velocity noise was estimated in static tissue using region of interest analysis. Velocity maximum intensity projection maps (MIPs) were calculated and used to determine peak velocities in the overall aorta and in the three sub-segments AAo, Arch and DAo. In addition, blood flow was visualized using streamlines within the segmented vessels during peak systole. Results Velocity noise was significantly improved in the dual-venc 4D flow data by 230% ± 20% compared to the high-venc velocity scan for the four Marfan patients, which corresponded with the high-venc/low-venc ratio of 2.5. In the BAV patient, velocity noise was improved by 276% in the dual-venc compared to the high-venc scan (high-venc/low-venc ratio=2.4). Peak velocity showed significant correlation between high- and dual-venc results in the AAo (R2 = 0.85, p = 0.04) and Arch (R2 = 0.95, p = 0.006) using velocity MIP analysis. Streamline comparison showed substantially improved qualitative visualization of aortic blood flow patterns and more coherent streamlines especially in slow flow areas and no aliasing artifacts in areas that were aliased in the low-venc images. Conclusions This feasibility study demonstrates the potential of k-t accelerated dual-venc 4D flow MRI to improve the assessment of aortic hemodynamics with large dynamic range while maintaining the scan time of standard 4D flow MRI. Figure 1

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          Author and article information

          Conference
          J Cardiovasc Magn Reson
          J Cardiovasc Magn Reson
          Journal of Cardiovascular Magnetic Resonance
          BioMed Central (London )
          1097-6647
          1532-429X
          27 January 2016
          27 January 2016
          2016
          : 18
          Issue : Suppl 1 Issue sponsor : Publication of this supplement was funded by the Society for Cardiovascular Magnetic Resonance.
          : O96
          Affiliations
          [1 ]grid.465264.7Dept. of Radiology, Northwestern University, Feinberg Medical School, Chicago, IL USA
          [2 ]grid.413808.60000000403882248Pediatric Radiology, Lurie Children's Hospital of Chicago, Chicago, IL USA
          [3 ]grid.16753.360000000122993507McCormick School of Engineering, Northwestern University, Evanston, IL USA
          [4 ]grid.413808.60000000403882248Pediatrics-Cardiology, Lurie Children's Hospital of Chicago, Chicago, IL USA
          Article
          4884
          10.1186/1532-429X-18-S1-O96
          5032482
          5be97bb5-74a3-4ce4-931f-91cf3df897dd
          © Schnell et al. 2016

          This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

          19th Annual SCMR Scientific Sessions
          Los Angeles, CA, USA
          27-30 January 2016
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          © The Author(s) 2016

          Cardiovascular Medicine
          Cardiovascular Medicine

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