Chiara Manini1, Markus Hüllebrand1,2, Marius Pullig3, Titus Kühne1,4, Sarah Nordmeyer5, Lina Jarmatz5, Andreas Harloff6, Jeanette Schulz-Menger4,5, and Anja Hennemuth1,2,4,7
1Institute of Computer-assisted Cardiovascular Medicine, Charité – Universitätsmedizin Berlin, Berlin, Germany, 2Fraunhofer MEVIS, Bremen, Germany, 3IBM Germany, Berlin, Germany, 4DZHK (German Center for Cardiovascular Research), Partner site Berlin, Germany, 5Charité – Universitätsmedizin Berlin, Berlin, Germany, 6University Hospital Freiburg, Freiburg, Germany, 7University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Synopsis
Keywords: Flow, Velocity & Flow, Aorta segmentation
Standardized 4D PCMRI postprocessing
protocols could enable comparable bloodflow quantification. We propose an
automatic segmentation of aortic cross section over time with a residual trained
data from different imaging sequences, scanner types, pathologies and position
of cross section planes. Dice score, Hausdorff metric as well as flow and velocity
curves for the segmented areas show good performance both in the validation and
test sets.
Introduction
4D PCMRI enables comprehensive assessment
of aortic bloodflow, and medical societies suggest standardized postprocessing protocols
to enable comparative quantitative analysis. Data acquired with different protocols,
scanners and sequences can differ regarding intensity ranges and velocity encoding.
Existing approaches for 3D and 4D segmentation of 4D PCMRI data achieve good
results for specific imaging sequences and scanner manufacturers [1-3].
The authors propose a multi-site ML model for
automatic segmentation of aorta cross sections over time and evaluate the results
in terms of accuracy of segmentation masks and the effect of segmentation differences
on derived clinical parameters such as throughflow.Methods
We considered 4D-flow MRI data from 205
subjects; 130 without known aortic pathology (Siemens Trio Tim 3T) [4], 59 with
aortic stenosis (Philips Achieva 1.5T) [5], and 8 healthy volunteers (Siemens
Prisma Fit 3T, Philips Ingenia 3T) [6].
Per dataset 11-12 planes (Figure 1) were placed perpendicular
to the aortic centerline obtaining a total number of 2316 cross sections, and lumen
boundaries were annotated by medical experts (21 to 57 frames/cardiac cycle
depending on the heart rate).
A residual
Unet [7] was trained to generate 3D aortic cross sectional segmentations (x,y,t)
on preprocessed (phase unwrapping, offset correction) 4D flow MRI data. 2D+t
planes of magnitude and velocities fields were prepared for processing as follows:
- Z-score
normalization
- Spatiotemporal
resampling to obtain a final in-plane resolution of 1.54 mm2 and 64
timesteps
- Padding/cropping
to an in-plane dimension of 64x64
- Concatenation
of magnitude and velocity fields as channels.
A composite
loss function (cross entropy and Dice) was used during training. A sigmoid
function generates probabilities per voxel, which are thresholded with 0.5.
The model
was implemented in Python 3.7.6 using monai 0.8.1. Training and testing were
performed on an AMD EPYC 7302 16-Core Processor with a Nvidia A40 GPU.
Dice score
(DS) and Hausdorff Distance (HD) were computed with monai 0.8.1.
On the test
set we computed flow I(t) and velocity v(t) curve as:
$$v(t) =
\frac{1}{\mid A(t)\mid} \int_{A(t)}^{}\parallel v(x,y,t)\parallel dA$$
$$I(t) = \int_{A(t)}^{} <v(x,y,t),n>dA$$
With:
- ||v|| the magnitude of the velocity vector
- v(x,y,t) the
velocity vector in the point (x,y) at time t
- |A(t)| the area of the segmentation on timeframe t
- n normal
vector of the cross-sectional plane
- And <a,b> denotes the scalar product between the vectors
a and b
Results
The data were randomly divided into 88% for
training, 10% for validation and 2% for testing (see Figure 1). DS and HD were:
- Validation set: DS = 0.89±0.04, HD = 2.99±1.89
- Test set: DS = 0.89±0.12,
HD = 3.95±2.17.
Flow and velocity curves were computed for exemplary
cross sections, results are shown in Figure 3, Figure 4 and Figure 5 (best case,
exemplary and worst one respectively).
In general, the model tends to underestimate
the vessel area, but the effect on the flow and velocity curves is minimal (Figure
2 and Figure 3). For the case with lower DS the opposite trend for the segmentation
contours is observed (Figure 4). The model segmentation results in a higher throughflow.
The manual segmentation might have missed low flow regions.
Discussion
The 3D Unet trained on the multi-scanner,
multi-sequence dataset showed good performance for the different manufacturers,
pathologies, and cross section positions for all age groups (21-81). The automatic
segmentation provided flow and velocity curves comparable with expert
analyses. The inspection of cases with lower DS indicates that the model might perform
better than the expert in low contrast regions (Figure 4).Conclusion
With a multicenter, multiscanner,
multisequence dataset it might be possible to provide automatized segmentation
methods, which enable comparable measurements on 4D flow datasets acquired in
different scenarios.Acknowledgements
Funding from the German Research Foundation (GRK2260, BIOQIC).
Funding by the German Research Foundation (DFG) as part of SFB-1470, B06.
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