Abstract

Predicting infarct size and location is important for decision-making and prognosis in patients with acute stroke. To determine whether a deep learning model can predict final infarct lesions using magnetic resonance images (MRIs) acquired at initial presentation (baseline) and to compare the model with current clinical prediction methods. In this multicenter prognostic study, a specific type of neural network for image segmentation (U-net) was trained, validated, and tested using patients from the Imaging Collaterals in Acute Stroke (iCAS) study from April 14, 2014, to April 15, 2018, and the Diffusion Weighted Imaging Evaluation for Understanding Stroke Evolution Study-2 (DEFUSE-2) study from July 14, 2008, to September 17, 2011 (reported in October 2012). Patients underwent baseline perfusion-weighted and diffusion-weighted imaging and MRI at 3 to 7 days after baseline. Patients were grouped into unknown, minimal, partial, and major reperfusion status based on 24-hour imaging results. Baseline images acquired at presentation were inputs, and the final true infarct lesion at 3 to 7 days was considered the ground truth for the model. The model calculated the probability of infarction for every voxel, which can be thresholded to produce a prediction. Data were analyzed from July 1, 2018, to March 7, 2019. Area under the curve, Dice score coefficient (DSC) (a metric from 0-1 indicating the extent of overlap between the prediction and the ground truth; a DSC of ≥0.5 represents significant overlap), and volume error. Current clinical methods were compared with model performance in subgroups of patients with minimal or major reperfusion. Among the 182 patients included in the model (97 women [53.3%]; mean [SD] age, 65 [16] years), the deep learning model achieved a median area under the curve of 0.92 (interquartile range [IQR], 0.87-0.96), DSC of 0.53 (IQR, 0.31-0.68), and volume error of 9 (IQR, -14 to 29) mL. In subgroups with minimal (DSC, 0.58 [IQR, 0.31-0.67] vs 0.55 [IQR, 0.40-0.65]; P = .37) or major (DSC, 0.48 [IQR, 0.29-0.65] vs 0.45 [IQR, 0.15-0.54]; P = .002) reperfusion for which comparison with existing clinical methods was possible, the deep learning model had comparable or better performance. The deep learning model appears to have successfully predicted infarct lesions from baseline imaging without reperfusion information and achieved comparable performance to existing clinical methods. Predicting the subacute infarct lesion may help clinicians prepare for decompression treatment and aid in patient selection for neuroprotective clinical trials.

Highlights

  • Stroke is a leading cause of mortality and disability worldwide, with a global lifetime risk of approximately 25%.1 Reperfusion therapies, such as intravenous tissue plasminogen activator and thrombectomy, are the only effective treatments to reverse the ischemic changes

  • Among the 182 patients included in the model (97 women [53.3%]; mean [SD] age, 65 [16] years), the deep learning model achieved a median area under the curve of 0.92, Dice score coefficient (DSC) of 0.53 (IQR, 0.31-0.68), and volume error of 9 (IQR, −14 to 29) mL

  • Predicting the subacute infarct lesion may help clinicians prepare for decompression treatment and aid in patient selection for neuroprotective clinical trials

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Summary

Introduction

Stroke is a leading cause of mortality and disability worldwide, with a global lifetime risk of approximately 25%.1 Reperfusion therapies, such as intravenous tissue plasminogen activator and thrombectomy, are the only effective treatments to reverse the ischemic changes. Stroke is a leading cause of mortality and disability worldwide, with a global lifetime risk of approximately 25%.1 Reperfusion therapies, such as intravenous tissue plasminogen activator and thrombectomy, are the only effective treatments to reverse the ischemic changes. Patient selection for endovascular therapy is commonly performed using the diffusion-perfusion mismatch paradigm on the imaging acquired at initial presentation (baseline imaging) This process defines 2 classes of tissue: the ischemic core, which is presumed to be irreversibly damaged, visualized on diffusion-weighted imaging (DWI) and quantified using the apparent diffusion coefficient (ADC); and the penumbra, which is the region at risk of infarction in the absence of rapid reperfusion, visualized on perfusion-weighted imaging (PWI) and quantified using the perfusion parameter time to maximum of the residue function (Tmax). Advances have been made to automate the segmentations produced by these software programs, they often still require human interpretation and manual editing to remove nonphysiological signals, such as periventricular and contralateral lesions

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