Risk stratification for sudden death in congenital heart disease: bridging evidence, uncertainty, and individual decision-making

SCD risk prediction in CHD is evolving toward a multimodal, individualized approach that emphasizes probabilistic reasoning, shared decision-making, and epistemic humility. Although new models and technologies offer incremental gains, they do not eliminate the uncertainty inherent in predicting rare events. The application of population-based tools to individual patients must be interpreted cautiously, recognizing that SCD represents a final common pathway for diverse pathophysiological processes, and that decisions about ICD implantation entail complex trade-offs.