Lihua Chen1, Ailian Liu2, Jiazheng Wang3, Yishi Wang3, Yaxin Niu2, and Qingwei Song2
1The First Affiliated Hospital of Dalian Medical University, DaLian, China, 2The First Affiliated Hospital of Dalian Medical University, Dalian, China, 3Philips Healthcare, Beijing, China
Synopsis
The
quantitative flow measurements at 4D - flow MRI in the portal system and flow
change in response to a meal challenge. Significant increased blood flow velocity
and volume were observed in PV and SMV and significantly decreased blood flow
was observed in SV after a meal.
Introduction
Emerging
time-resolved, 4D-flow MRI sequences for assessing blood flow to the liver
provides simultaneous and spatially coregistered anatomical and hemodynamic
information of all vessels within the imaging volume[1-2].Meal challenges are standard
clinical procedures applied in imaging modalities such as ultrasound and MRI to
induce physiological hyperemia [3]. The purpose of this study was tomonitor the
flow changes in the portal system through a meal challenge in healthy
volunteers with 4D flow MRI to investigate the feasibility of non-invasively
quantifying the hemodynamic changes in pathological conditions.Purpose
This study monitors the flow changes in the portal system through a meal
challenge in healthy volunteers with 4D flow MRI to investigate the feasibility
of non-invasively quantifying the hemodynamics changes in pathological conditions.Methods
Ten
healthy subjects were prospectively enrolled for MRI examination at 3.0 T (Ingenia
CX, Philips Healthcare, the Netherlands) with a 16-channel abdominal array coil.
The
MR protocol included a 2D quantitative flow sequence (axial, TR/TE = 4.4/2.7
ms, FOV = 200×200 mm2, resolution = 1.5×1.5×8 mm3,
PC direction = RL, PC velocity = 200 cm/s, scan time = 13 s) to measure the
flow velocity in the portal vein as a reference for velocity encodings (VENC)
and a 4Dflow sequence with compressed sensing (CS) acceleration (axial, TR/TE =
5.0/3.2 ms, FOV = 300×350 mm2,
resolution = 2.5×2.5×2.5 mm3,
PC direction = RL-AP-FH, CS =8, scan time = 370 s) for hemodynamic quantification.
VENC was set to 30 cm/s for the 4D flow sequence to slightly surpass the
measured velocity and avoid phase wrapping. The acquired images were processed
in CVI42 (Canada Circle Cardiovascular Imaging)by a single
radiologist to obtain a 3D angiogram (Figure 1). The measurement planes were put
at the middle of the portal vein (PV), superior mesenteric vein (SMV), and splenic
vein (SV) trunk. Flow velocity (cm/s)and volume (ml/cardiac cycle) measurements
were performed blinded to subject status (fasting/meal).The intra-class
correlation coefficients (ICC) was used to check the consistency of the data
measured by the two observers. The flow velocity and volume for each vessel
were compared before and after the meal using paired t test.Results
The
consistency of the data obtained by the two observers were good (Table 1), ICC
value > 0. 75. After meal, significant increased blood flow velocity and
volume were observed in PV and SMV and significantly decreased blood flow was
observed in SV (P<0.05) (Table
2).Discussion and Conclusions
We have non-invasively measured the increase of flow velocity and volume
in both PV and SMV and a decrease in SV after the meal uptake in all the
healthy volunteers using 4D-flow MRI, indicating this technique a sensitive
tool for the quantification of portal system flow changes [3]. A
varying range of complicated abdominal and whole-body conditions may involve
changes in portal system flow, such as hepatic encephalopathy and hypersplenism,
for which 4D-flow MRI can help to provide both diagnosis and therapy monitoring
information.Acknowledgements
No acknowledgement found.References
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