Key result
RISE-APOCALYPSE-VT score accurately predicts VT or VF in acute MI with an AUC of 0.83.
Why the study?
The study was conducted to develop and validate a predictive model for ventricular tachycardia and/or fibrillation in patients admitted to a coronary care unit with acute myocardial infarction.
Can the RISE-APOCALYPSE-VT risk score accurately predict the occurrence of ventricular tachycardia or fibrillation in patients admitted to a CCU with acute myocardial infarction?
Cohort (n=15,163)
Can the RISE-APOCALYPSE-VT risk score accurately predict the occurrence of ventricular tachycardia or fibrillation in patients admitted to a CCU with acute myocardial infarction?
Effect estimate: AUC 0.83 (95% CI 0.80-0.85)
The RISE-APOCALYPSE-VT risk score provides a highly accurate, validated tool for predicting VT/VF in patients with acute myocardial infarction admitted to the CCU.
Background The objective of this study was to develop and validate a predictive model for the occurrence of ventricular tachycardia (VT) and/or fibrillation (VF) in patients admitted to a coronary care unit (CCU) with acute myocardial infarction (AMI). Methods We included 15,163 patients with AMI from 2005–2024. Patients were classified as STEMI or NSTEMI, with VT/VF confirmed by ECG/telemetry. The dataset was randomly split into a derivation (70%) and validation cohort (30%). Statistical analysis included logistic regression with penalized B-splines to address non-linearity and a Classification and Regression Tree algorithm for optimal cut-offs. Backward stepwise elimination was used for multivariate modeling, with collinearity assessed via VIF and correlation matrices. Missing data were handled using SPSS surrogate splits. Model validation included 1000 bootstrap, AUC-ROC, Hosmer-Lemeshow, and Brier score. Results 10,651 derivation and 4,512 validation cohort patients, VT/VF incidence was 7.2% and 6.6%, respectively. VT/VF patients were older, had more STEMI, dyspnea, syncope, heart failure, lower BP, and higher HR (p<0.001). They required more mechanical ventilation, vasopressors; also, a higher presentation with CSWG-SCAI score higher in the VT/VF patients in both cohorts (P<0.001).And higher mortality (44.8% vs. 5.2%, P<0.001). (Table 1) A multivariable logistic regression model identified independent VT/VF predictors after VIF correction and variable selection, leading to the RISE-APOCALYPSE-VT score: Risk factors: STEMI (OR 1.32), Killip-Kimball> II (OR 1.36), neurological alterations (OR 2.33), PVC (OR 2.72) mechanical ventilation (OR 3.04), transitory pacemaker (OR 2.22) and SCAI stage > B (OR>1.75) Protective factors: T-wave inversion (OR 0.77) and AV block (OR 0.57) Stratified risk factors: Heart rate, LVEF, eGFR by CKD-EPI, K+, Mg++ and lactate levels. These findings were used to develop a VT/VF risk score. (Figure 1) The ROC curves showed an AUC of 0.82 (95% CI: 0.81–0.84) in the derivation cohort plus HL P=0.137 and Brier score 0.06; and 0.83 (95% CI: 0.80–0.85) in the validation cohort plus HL P=0.459 and a Brier score 0.05, indicating high predictive accuracy. The precision-recall curves confirmed stable performance. Calibration plots showed that the observed and predicted probabilities aligned well, with progressive increases in VT/VF risk as total score increased. (Figure 1) Conclusion The RISE-APOCALYPSE-VT risk score provides a novel tool for predicting VT/VF in AMI, integrating clinical, hemodynamic, electrocardiographic, and biochemical markers with advanced statistical modeling. Its strong discrimination, calibration, and machine learning-based cut-offs enhance early risk stratification, potentially guiding interventions at CCU.Table 1.Demographical characteristics Fig2.Score card, ROC & Calibration
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Ortega-Hernandez et al. (2025) conducted a cohort in Acute myocardial infarction (AMI) (n=15,163). RISE-APOCALYPSE-VT risk score was evaluated on Occurrence of ventricular tachycardia (VT) and/or fibrillation (VF) (AUC 0.83, 95% CI 0.80-0.85). The RISE-APOCALYPSE-VT risk score accurately predicted ventricular tachycardia or fibrillation in patients with acute myocardial infarction, achieving an AUC of 0.83 (95% CI 0.80-0.85) upon validation.
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