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Deep Learning HASTE for Upper Abdominal MRI: Improved Image Quality, Speed, and Energy Efficiency in a Prospective
Jennifer Gotta1, Ahmed Ait Bachir1, Leon D Gruenewald1
1Department of Radiology, Goethe University Hospital Frankfurt, Frankfurt am Main, Germany.
None:
This prospective study aimed to perform a qualitative and quantitative comparison of deep learning (DL) and conventional T2-weighted Half-Fourier Acquisition Single-shot Turbo spin Echo (HASTE) sequences for 3T MRI acquisition of the upper abdomen. From January 2024 to April 2024, 166 patients (60 ± 14 years) scheduled for MRI of the upper abdomen were prospectively enrolled. Each patient underwent two MRI examinations: one using a conventional T2-weighted HASTE sequence, followed by a fast T2-weighted HASTE sequence reconstructed with DL. Image quality, anatomical structure visualization, and diagnostic performance were independently assessed by three readers using a 5-point Likert scale. Quantitative analysis included measurements of signal-to-noise ratio (SNR) and contrast-to-noise ratio (CNR) for both sequences. Additionally, radiomic features were extracted and analyzed for significant variations. Interreader agreement was evaluated using Fleiss' Kappa. The DL HASTE sequence showed significantly superior overall image quality (p < 0.001), fewer artifacts (p < 0.001), and improved delineation of anatomical structures (p < 0.01) compared to the conventional T2-weighted HASTE sequence. DL sequences exhibited better SNR (p < 0.001), whereas CNR values did not show a difference between the two acquisition types. Radiomics feature analysis unveiled significant differences in contrast and gray-level characteristics (p ≤ 0.001). DL HASTE demonstrated a significant time reduction of 62.5% together with significant energy cost savings of 0.34 kW per scan compared to the conventional sequence acquisition. The DL HASTE sequence enhanced image quality and diagnostic confidence while minimizing artifacts, time, and energy costs, enabling a more accurate detection of pathologies than the conventional T2-weighted product solution with potential clinical impact.
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