Key result
Higher NORPACS score predicts greater risk of in-hospital malignant ventricular arrhythmias post-PCI in STEMI.
Why the study?
Malignant ventricular arrhythmias remain a major early complication after STEMI, and the NORPACS score—originally developed to predict no-reflow—may help identify patients at high arrhythmic risk.
Does the NORPACS score predict early inhospital malignant ventricular arrhythmias in STEMI patients undergoing primary PCI?
Does the NORPACS score predict early inhospital malignant ventricular arrhythmias in STEMI patients undergoing primary PCI?
The NORPACS score, originally designed to predict no-reflow, is an independent and incremental predictor of early malignant ventricular arrhythmias in STEMI patients following primary PCI.
Answers are grounded in this paper and cite their sources.
May aid post-PCI MVA risk stratification in STEMI; supports no-reflow score extension but leaves prospective validation open.
Background Malignant ventricular arrhythmias (MVA)—sustained ventricular tachycardia or fibrillation—remain a major early complication after ST-segment elevation myocardial infarction (STEMI) despite timely reperfusion. The no-reflow phenomenon is a key substrate for arrhythmogenesis. The no-reflow prediction in acute coronary syndrome (NORPACS) score, originally developed to predict no-reflow, may also help identify patients at high arrhythmic risk. Methods We retrospectively analyzed 1050 consecutive STEMI patients undergoing successful primary percutaneous coronary intervention (PCI) between January 2020 and December 2024. The primary endpoint was inhospital MVA. Univariable and multivariable logistic regression models were constructed incorporating clinical, laboratory, and angiographic variables. The incremental predictive value of the NORPACS score was assessed using receiver operating characteristic analysis, net reclassification improvement (NRI), and integrated discrimination improvement (IDI). Kaplan–Meier and restricted cubic spline analyses evaluated temporal risk patterns. Results MVA occurred in 79 patients (7.5%), all within the first 8-h post-PCI. Patients with MVA more often had diabetes, anterior infarcts, lower LVEF, higher inflammatory markers, and no-reflow. The NORPACS score was significantly higher in the MVA group (7.1 ± 1.3 vs. 6.2 ± 1.7, p < 0.001) and independently predicted events across all multivariable models (adjusted OR range: 1.20–1.44, all p < 0.05). Adding NORPACS to clinical–laboratory models improved discrimination (ΔAUC up to 0.07) and yielded significant IDI (0.022–0.024) and NRI (0.10–0.14). Kaplan–Meier curves confirmed earlier arrhythmia onset with higher scores. Conclusions The NORPACS score is an independent and incremental predictor of early MVA in STEMI patients undergoing PCI. Its integration into clinical–laboratory risk models enhances risk stratification and may guide intensified monitoring in high-risk patients. Prospective multicenter validation is warranted. Graphical Abstract This study evaluated the prognostic utility of the NORPACS score for predicting malignant ventricular arrhythmias (VT/VF) in 1050 patients with STEMI undergoing successful primary PCI. The NORPACS score, incorporating angiographic and clinical parameters such as TIMI flow, vessel diameter, stent length, shock status, and ischemia time, was independently associated with inhospital VT/VF risk. Higher NORPACS scores were linked to a stepwise increase in arrhythmic events, as demonstrated by ROC, spline, and Kaplan–Meier analyses. The score remained a significant predictor across all multivariable models (adjusted OR range: 1.20–1.44, all p < 0.05).
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Kalkan et al. (2026) studied this question. The NORPACS score independently predicted in-hospital malignant ventricular arrhythmias in STEMI patients, with an adjusted OR range of 1.20–1.44 (p < 0.05).
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