AI post-intervention operational and functional outcomes prediction in ischemic stroke patients using MRIs
- PMID: 40814085
- PMCID: PMC12355742
- DOI: 10.1186/s12880-025-01864-1
AI post-intervention operational and functional outcomes prediction in ischemic stroke patients using MRIs
Abstract
Background: Despite the potential clinical utility for acute ischemic stroke patients, predicting short-term operational outcomes like length of stay (LOS) and long-term functional outcomes such as the 90-day Modified Rankin Scale (mRS) remain a challenge, with limited current clinical guidance on expected patient trajectories. Machine learning approaches have increasingly aimed to bridge this gap, often utilizing admission-based clinical features; yet, the integration of imaging biomarkers remains underexplored, especially regarding whole 2.5D image fusion using advanced deep learning techniques.
Methods: This study introduces a novel method leveraging autoencoders to integrate 2.5D diffusion weighted imaging (DWI) with clinical features for refined outcome prediction.
Results: Results on a comprehensive dataset of AIS patients demonstrate that our autoencoder-based method has comparable performance to traditional convolutional neural networks image fusion methods and clinical data alone (LOS > 8 days: AUC 0.817, AUPRC 0.573, F1-Score 0.552; 90-day mRS > 2: AUC 0.754, AUPRC 0.685, F1-Score 0.626).
Conclusion: This novel integration of imaging and clinical data for post-intervention stroke prognosis has numerous computational and operational advantages over traditional image fusion methods. While further validation of the presented models is necessary before adoption, this approach aims to enhance personalized patient management and operational decision-making in healthcare settings.
Clinical trial number: Not applicable.
Keywords: Acute ischemic stroke; Artificial intelligence; Autoencoder; Deep learning; Length of stay; MRI; Modified rankin scale; Resnet.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: This study was approved by the Institutional Review Board at University of Michigan (protocol number: HUM00234328), ensuring ethical conduct in accordance with all relevant guidelines for research involving human subjects including the Helsinki Declaration. Written informed consent from patients in this published dataset was waived by the Johns Hopkins Internal Review Board (IRB00228775) since this study involved no more than minimal risk to the involved subjects. Consent for publication: Not applicable. Competing interests: The authors are applying for a patent on the methodologies and applications discussed in this manuscript.
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