Yupeng Zhu1, Di Hu1, Yanqiu Lv1, Yang Wen1, Huiying Kang1, Xiaomin Duan1, Jiazheng Wang2, Queenie Chan2, and Yun Peng1
1Department of Radiology, Beijing Children’s Hospital, Capital Medical University, National Center for Children's Health, Beijing, China, 2Philips Healthcare, Beijing, China
Synopsis
The
use of three dimensional (3D) volumetric acquisition in clinical settings has
been limited due to long scan time. However, 3D volumetric acquisition could
provide higher spatial resolution and decrease partial volume effects. The
introduction of compressed sensing in combination of the parallel imaging
technique SENSE allows shortening of scan time and provide
comparable overall image quality when compared with standard sequences. The purpose
of the study is to determine the feasibility of 3D PDWI accelerated with compressed
SENSE(CS) for evaluating the pediatric joint image quality and
compared with 2D PDWI.
Introduction
The
use of three dimensional (3D) volumetric acquisition in clinical settings has
been limited due to long scan time. However, 3D volumetric acquisition could
provide higher spatial resolution and decrease partial volume effects. The
introduction of compressed sensing in combination of the parallel imaging
technique SENSE1-3 allows shortening of scan time and provide
comparable overall image quality when compared with standard sequences. The purpose
of the study is to determine the feasibility of 3D PDWI accelerated with compressed
SENSE1-3 (CS) for evaluating the pediatric joint image quality and
compared with 2D PDWI.Materials and Methods
Twenty
pediatric patients (age, 1 to 10 years old) for joint examinations were
performed on a 3.0T MR scanner (Ingenia CX, Philips Healthcare, the Netherlands)
using knee and hip coils. The protocol consisted of 2D sagittal proton density weighted image (2D-PDWI) and 3D PDWI accelerated with CS
(3D-PDWI-CS). Signal-to-noise ratio (SNR) and contrast-to-noise ratio (CNR,
between bone and muscle) of 3D-PDWI-CS were compared with those of 2D-PDWI. Image
quality of two sequences was analyzed by two readers independently, who were blinded
to any clinical information (5 years of experience in MR imaging and 10 years
of experience in MR imaging). Subsequently, a final interpretation was made in
consensus. A third experienced radiologist (15 years of experience in MR
imaging) involved in case of disagreements. Image quality of both sequences for
each patient was rated according to a 5-point Likert scale (score of 1,
nondiagnostic; score of 2, poor; score of 3, moderate; score of 4, good; and
score of 5, excellent). The main evaluation indexes include the following: 1) patients
with normal joint: articular cartilage and bone cortex, bone trabecula,
muscle texture and boundary, fine details of anatomic structures, noise and
artifacts, and overall image quality. 2) patients with abnormal joint: lesion
location, contrast of lesions, muscle injury boundary and contrast between lesions
and surrounding tissue.4 Image quality was measured by the quantitative
and qualitative methods described above. The paired t-test or a Wilcoxon rank
analyses were performed between 2D-PDWI and 3D-PDWI-CS. Interobserver agreement
for the qualitative evaluation of image quality was calculated using weighted
kappa analysis, and weighted kappa analysis for ordinal variables including the
five-point visual scoring systems. P values< 0.05 were considered
significant.3Results
The
bone SNR (26.45±13.65 vs. 26.87±11.86;
P>0.05) and muscle SNR (34.79±17.94
vs. 34.65±10.28; P>0.05) showed no statistical significant
different between 2D-PDWI and 3D-PDWI-CS. The joint CNR
between bone and muscle (8.97±7.83 vs. 10.42±6.51;
P>0.05) showed no statistical significant between 2D-PDWI and 3D-PDWI-CS.
Compared with 2D-PDWI, more imaging anatomical details were clearly shown at 3D-PDWI-CS
at the double scan time. At the double scan time, articular
cartilage and bone cortex, bone trabecula and muscle texture and boundary were
clearly shown on the sagittal images at 3D-PDWI-CS. The more details
of lesion location, contrast of lesions, muscle injury boundary and contrast
between lesions and surrounding tissue were shown at 3D-PDWI-CS. Although the
contrast of the original image was better, the image contrast of reformatted
image from 3D-PDWI-CS was poorer than that of 2D-PDWI, especially on the display
of lesions. The two observers showed moderate and good interobserver agreement
on the five-point visual scoring system for 2D-PDWI and 3D-PDWI-CS respectively
(weighted kappa, 0.508 and 0.681 respectively. p<0.05).Conclusions
3D-PDWI-CS outperforms conventional 2D-PDWI sequence
in pediatric joint MR imaging as scan times doubling changed while image
quality is maintained or even improved. Although the scan time of a single
sequence is longer, the overall inspection time is shorter. 3D-PDWI-CS is a
reliable alternative for clinical use in pediatric joint MR imaging. Although reformatted
image contrast is poor, 3D-PDWI-CS can provide higher resolution with less
partial volume effect, multi-directional image reformat, and further image
analysis.Acknowledgements
No acknowledgement found.References
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