共 33 条
Diffusion-weighted imaging in the prostate: an apparent diffusion coefficient comparison of half-Fourier acquisition single-shot turbo spin-echo and echo planar imaging
被引:19
作者:
Babourina-Brooks, Ben
[1
]
Cowin, Gary J.
[1
]
Wang, Deming
[1
]
机构:
[1] Univ Queensland, Ctr Adv Imaging, Brisbane, Qld, Australia
关键词:
Prostate;
Diffusion;
ADC;
b value;
DWI;
EPI;
HASTE;
CANCER;
MRI;
VALUES;
CARCINOMA;
DIAGNOSIS;
BIOPSY;
TISSUE;
TIME;
MEN;
D O I:
10.1016/j.mri.2011.09.024
中图分类号:
R8 [特种医学];
R445 [影像诊断学];
学科分类号:
1002 ;
100207 ;
1009 ;
摘要:
Prostate cancer detection using diffusion-weighted imaging is highly affected by the accuracy of the apparent diffusion coefficient (ADC) values in an image. Echo planar imaging (EPI) is a fast sequence commonly used for diffusion imaging but has inherent magnetic susceptibility and chemical shift artefacts associated. A diffusion sequence that is less affected by these artefacts is therefore advantageous. The half-Fourier acquisition single-shot turbo spin-echo (HASTE) sequence was chosen. The diffusion sequences were compared in image quality, repeatability of the ADC value and the effect on the ADC value with varied h values. Eight volunteers underwent three scans of each sequence, on a 1.5-T Siemens system, using b values of 0, 150, 300, 450, 600, 750, 900 and 1000 s/mm(2). ADC maps were created to address the reproducibility of the ADC value when using two b values compared to eight b values. The ADC value using all h values with the HASTE sequence gave the best performance in all tested categories. Both sequences gave significantly different ADC mean values for two b values compared to when using eight b values (P<.05) suggesting larger error is present when using two h values. HASTE was shown to be an improvement over EPI in terms of repeatability, signal variation within a region of interest and standard deviation over the volunteer set. The improved accuracy of the ADC value in the HASTE sequence makes it potentially a more sensitive tumor detection technique. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:189 / 194
页数:6
相关论文