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Objective: To develop and validate a robust risk prediction model for stroke and systemic embolism (SSE) in adult patients with congenital heart disease (ACHD), using artificial intelligence.
Patients And Methods: Deidentified insurance claims from the Optum Labs Data Warehouse, including enrollment records and medical and pharmacy claims for commercial and Medicare Advantage enrollees, were used to identify 49,276 patients with ACHD, followed between January 1, 2009, and December 31, 2014. The group was randomly divided into development (70%) and validation (30%) cohorts. The development cohort was used to train 2 machine learning (ML) algorithms, regularized Cox regression (RegCox), and extreme gradient boosting (XGBoost) to predict SSE at 1, 2, and 5 years. The Shapley additive explanations (SHAP) model was used to identify the variables particularly driving the SSE risk.
Results: Within this large and diverse cohort of patients with ACHD (mean age, 59 ± 19 years; 25,390 (51.5%) female, 35,766 [77.6%]) white), 1756 (3.6%) patients experienced SSE during follow-up. In the Validation cohort, CHADS-VASC had an area under the receiver operating characteristics curve (AUC) of 0.66 for predicting SSE at 1-,2, and 5-years. RegCox had the best predictive performance, with AUCs of 0.82,.81, and.80 at 1-, 2, and 5-years. XGBoost had AUCs of 0.81, 0.80, and 0.79 respectively. Atrial septal defect (ASD) emerged as an important predictor for SSE uncovered by the unbiased ML algorithms. A new clinical risk score, the CHADS-VASC-ASD score, provides improved SSE prediction in ACHD. Yet, the ML models still outperformed this.
Conclusion: ML models significantly outperformed the clinical risk scores in patients with ACHD.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11975817 | PMC |
http://dx.doi.org/10.1016/j.mcpdig.2023.12.002 | DOI Listing |
World J Pediatr Congenit Heart Surg
September 2025
Congenital Heart Center, Departments of Surgery and Pediatrics, University of Florida, Gainesville, FL, USA.
The purpose of this study is to identify 35-year trends in adult congenital heart disease (ACHD) heart transplant volume, transplant centers, patient characteristics, and longitudinal survival up to ten years. We performed a retrospective review of ACHD patients (≥18 years) who underwent heart transplantation (N = 2,297 transplants) between January 1, 1988, and December 31, 2022, using the United Network for Organ Sharing Database. Trends in transplant volume, transplant centers, patient characteristics, and longitudinal survival were analyzed.
View Article and Find Full Text PDFRev Cardiovasc Med
August 2025
Department of Cardiology, University Hospitals of Leicester NHS Trust, Glenfield Hospital, LE3 9QP Leicester, UK.
Adult congenital heart disease (ACHD) constitutes a heterogeneous and expanding patient cohort with distinctive diagnostic and management challenges. Conventional detection methods are ineffective at reflecting lesion heterogeneity and the variability in risk profiles. Artificial intelligence (AI), including machine learning (ML) and deep learning (DL) models, has revolutionized the potential for improving diagnosis, risk stratification, and personalized care across the ACHD spectrum.
View Article and Find Full Text PDFCureus
August 2025
Physiology, Alkindy College of Medicine, Baghdad University, Baghdad, IRQ.
Cor triatriatum is a rare congenital heart defect that divides the right or left atrium into three chambers. Although the diagnosis is typically made within the first years of birth, it can occasionally be made later in adulthood and is frequently associated with other cardiac defects but may be present in isolation. Clinical manifestations range from lung congestion, exhaustion, coughing, and dyspnea to the onset of heart failure.
View Article and Find Full Text PDFObjective: Our objective was to build classifiers for multiple phenotypes that categorize a cohort of adults with congenital heart disease (ACHD), that can be used to populate variables in a biobank.
Materials And Methods: A dataset of 1492 ACHD patients, with expert-created labels for eight phenotypes, was created and used to train classifiers with three different architectures. A larger unlabeled dataset containing 15869 patients was used to pre-train the classifiers, and a 20% subset of the unlabeled dataset was used to validate the classifier predictions.
Cureus
July 2025
Cardiovascular Surgery, Kitasato University School of Medicine, Sagamihara, JPN.
Ebstein's anomaly (EA) is a rare congenital defect of the tricuspid valve (TV), typically characterized by downward displacement of the septal and posterior leaflets into the right ventricle, resulting in tricuspid regurgitation (TR), right heart enlargement, and heart failure. While surgical outcomes for EA have improved significantly in pediatric and young adult populations, data on surgical intervention in elderly patients remain limited. Elderly patients often present with comorbidities and diminished physiological reserve, which complicate both surgical decision-making and perioperative management.
View Article and Find Full Text PDF