In diffusion imaging, bulk and physiological motion together with strong diffusion encoding gradient introduces extra image phase or data corruption in the diffusion-weighted images. Corrupted data identification/rejection procedure has not been integrated in the recently proposed k-space based multi-shot diffusion reconstruction pipelines. In this work, two corrupted data rejection strategies were proposed, compared and evaluated. Results show that using corrupted data identification and rejection after the CK-GRAPPA reconstruction is potentially a robust choice for multi-shot diffusion imaging reconstruction.
Theory
In this work, diffusion weighted interleaved EPI acquisition with CK-GRAPPA (GRAPPA with a compact kernel2) reconstruction (Fig. 1A and Fig. 2A) is used for demonstration. For the original CK-GRAPPA implementation (Fig. 2A), each shot is recovered to a fully-sampled k-space using CK-GRAPPA interpolation from multi-shot and multi-channel data. When the data corruption occurs, the identification/rejection can be done before (method 1) or after (method 2) the k-space interpolation, and the corresponding pipeline is shown in Fig. 2B and Fig. 2C. When the corrupted data are excluded before the k-space reconstruction, the acquired data are no longer uniformly interleaved in k-space. In this work, we used flexible kernel GRAPPA reconstruction (FK-GRAPPA, Fig. 1B) for reconstruction under this circumstance. By skipping the corrupted k-space lines, the kernel shapes and weights will be flexible when the different shots are excluded.Results and Discussion
Fig. 3 shows the reconstruction from two typical slices and Table. 1 shows the RMSE of different methods. For CK-GRAPPA without corrupted data rejection, the error maps show large deviation (the brainstem, the cerebellum and the corpus callosum in Fig. 3, yellow arrowheads) from the reference. The error area corresponds with the corrupted shot at the right column. For the GRAPPA with data rejection, the erroneous deviation is reduced, but the RMSE is still large in some case. For the proposed two methods, the RMSEs are both smaller than both CK-GRAPPA without corrupted data rejection and GRAPPA with data rejection (P<0.01, paired t-test). Between the two methods, the proposed method 2 (data rejection after the k-space based reconstruction) shows smaller (P=0.032) RMSE than the proposed method 1 (data rejection before the k-space based reconstruction).
In this simulation, the data from single-shot acquisition were used to generate multi-shot data, in order to keep the gold standard reference and simulate the real pulsatile motion. The results show that the corrupted data identification and rejection is an indispensable procedure. Using corrupted data identification and rejection after the CK-GRAPPA reconstruction provides the result with minimum error compared with the reference. Future work should be focused on testing the algorithm on different b values, different organs (cervical spine, liver, heart, etc.) and different multi-shot acquisition settings.
Conclusion
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