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Background: Major adverse cardiovascular and cerebrovascular events (MACCEs) after non-cardiac surgery can lead to substantial morbidity, mortality, and healthcare costs. Therefore, accurate and rapid risk prediction is crucial for targeted perioperative management. This study aimed to develop and validate a minimally burdensome multimodal deep learning model integrating demographic data, the International Classification of Diseases (ICD)-10 procedure codes, and raw preoperative 12-lead electrocardiogram (ECG) waveforms to predict 30-day MACCEs and to compare its performance with the established risk indices.
Materials And Methods: This retrospective cohort study at a single tertiary academic center included adult patients who underwent non-cardiac surgery under regional or general anesthesia from 2006 to 2020. Preoperative 12-lead ECGs were acquired within 3 months before surgery. A transformer-based deep neural network processed raw ECG signals, while a gradient boosting machine (GBM) combined ECG-derived latent features with basic demographic variables (age, sex) and simplified ICD-10 procedure codes. The primary outcome was 30-day MACCEs (cardiac arrest, acute myocardial infarction, congestive heart failure, new arrhythmia, angina, stroke, or cardiovascular/cerebrovascular death). Model performance was assessed using the area under the receiver operating characteristic curve (AUROC), precision-recall curves, sensitivity, specificity, F1 scores, and calibration metrics.
Results: Among the 165,577 cases, 54.5% were female, the median age was 56 years, and 0.6% developed 30-day MACCEs. The multimodal GBM model demonstrated a significantly higher AUROC of 0.902 (95% confidence interval [CI], 0.898-0.906) than the baseline GBM (0.842 [0.838-0.847]). It also outperformed the Revised Cardiac Risk Index (0.813 [0.782-0.843]) and the American Society of Anesthesiologists class (0.759 [0.726-0.792]).
Conclusion: A multimodal deep learning model combining raw ECG waveforms with minimal clinical data yielded superior 30-day MACCE risk prediction compared to that of the conventional indices. This approach could facilitate broad clinical adoption by minimizing data collection requirements while enhancing perioperative risk stratification.
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http://dx.doi.org/10.1097/JS9.0000000000003143 | DOI Listing |
J Immunother Cancer
September 2025
CAS Key Laboratory of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing, China
Neoadjuvant immunochemotherapy (nICT) has demonstrated significant potential in improving pathological response rates and survival outcomes for patients with locally advanced esophageal squamous cell carcinoma (ESCC). However, substantial interindividual variability in therapeutic outcomes highlights the urgent need for more precise predictive tools to guide clinical decision-making. Traditional biomarkers remain limited in both predictive performance and clinical feasibility.
View Article and Find Full Text PDFEur J Radiol
September 2025
Department of Radiology, Affiliated Hospital of Hebei University, Baoding 071000, China. Electronic address:
Purpose: The present study aimed to develop a noninvasive predictive framework that integrates clinical data, conventional radiomics, habitat imaging, and deep learning for the preoperative stratification of MGMT gene promoter methylation in glioma.
Materials And Methods: This retrospective study included 410 patients from the University of California, San Francisco, USA, and 102 patients from our hospital. Seven models were constructed using preoperative contrast-enhanced T1-weighted MRI with gadobenate dimeglumine as the contrast agent.
J Cataract Refract Surg
July 2025
Department of Ophthalmology, West China Hospital of Sichuan University, Chengdu City, Sichuan Province, China.
Purpose: To develop and validate a multimodal deep-learning model for predicting postoperative vault height and selecting implantable collamer lens (ICL) sizes using Anterior Segment Optical Coherence Tomography (AS-OCT) and Ultrasound Biomicroscope (UBM) images combined with clinical features.
Setting: West China Hospital of Sichuan University, China.
Design: Deep-learning study.
Mol Omics
September 2025
Laboratory of Structural Bioinformatics and Computational Biology, Federal University of Rio Grande do Sul, Av. Bento Gonçalves, 9500, Porto Alegre 91501-970, RS, Brazil.
The integration of multimodal single-cell omics data is a state-of-art strategy for deciphering cellular heterogeneity and gene regulatory mechanisms. Recent advances in single-cell technologies have enabled the comprehensive characterization of cellular states and their interactions. However, integrating these high-dimensional and heterogeneous datasets poses significant computational challenges, including batch effects, sparsity, and modality alignment.
View Article and Find Full Text PDFIEEE Trans Comput Biol Bioinform
September 2025
Accurately identifying associations between human genes (proteins) and clinical phenotypes is critical for advancing drug development and precision medicine. While the human phenotype ontology (HPO) standardizes clinical phenotypes, current computational approaches for predicting human protein-phenotype associations suffer from two limitations: (1) underutilization of multimodal protein-related information and (2) lack of state-of-the-art deep learning representations tailored to diverse data modalities, such as text and sequence. To overcome these limitations, we introduce MultiFusion2HPO, a novel multimodal model that integrates diverse features and advanced learning methods from multiple data sources to enhance the prediction of human protein-HPO associations.
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