Abstract 8: Hypoperfusion Lesion And Target Mismatch Prediction In Acute Ischemic Stroke From Baseline Mr Diffusion Imaging Using A 3d Convolutional Neural Network

Abstract

Purpose: Perfusion imaging assesses target mismatch but requires contrast and processing software. Clinical/diffusion mismatch can miss cases that have target mismatch and could benefit from thrombectomy. We explored whether a neural network can predict hypoperfusion and identify target mismatch from diffusion-weighted imaging (DWI) and clinical information alone. Methods: Acute ischemic stroke cases with baseline MR perfusion and DWI were included from two multi-center trials and one registry for model development and a separate randomized trial for external validation. MR perfusion images were processed by RAPID, which segments Tmax lesion (Tmax≥6s) and the ischemic core lesion (apparent diffusion coefficient [ADC]≤ 620). A 3D U-Net was trained using baseline DWI, ADC, NIH stroke scale, and side of stroke as input, and the union of Tmax and ischemic core segmentation as the ground truth. 5-fold cross-validation was performed for model development cohort. Model performance was evaluated by Dice score coefficient (DSC) and volume difference. Sensitivity and specificity of model target mismatch and clinical/diffusion mismatch criteria from the DAWN were compared, using the DEFUSE 3 target mismatch as reference. Results: 413 patients were included for model development and 46 for external validation. In model development and external validation cohort, the model achieved median DSC of 0.61 (IQR 0.45, 0.71) and 0.62 (IQR 0.53, 0.72); and volume difference of 3 ml (IQR -37, 41) and 7 ml (IQR -24, 32), respectively. Compared to the clinical/diffusion mismatch approach, the model identified target mismatch with a sensitivity of 89.5% vs 49.3%, a specificity of 77.5% vs 89.2% in the model development cohort, and a sensitivity of 95.6% vs 41.3% in external validation cohort. Conclusion: A 3D U-Net can predict hypoperfusion lesions from baseline DWI and clinical information, with more sensitive classification of target mismatch than clinical/diffusion mismatch.