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Myocardial Infarction and Functional Outcome Assessment in Pigs
Published on: April 25, 2014
Long-term prognostic significance of ventricular late potentials after a first acute myocardial infarction
M Zimmermann1, A Sentici, R Adamec
1Cardiology Center, University Hospital, Geneva, Switzerland.
Insights
Ventricular late potentials (VLP) predict dangerous arrhythmias after a first heart attack. Identifying VLPs can help assess long-term risk in patients, with an open artery potentially reducing this risk.
Area of Science:
- Cardiology
- Electrophysiology
- Clinical Research
Background:
- Ventricular late potentials (VLP) are known predictors of arrhythmic events post-myocardial infarction.
- Previous studies had limitations including short follow-up, small sample sizes, and potential biases.
- Assessing long-term prognostic value in a large, unselected cohort is crucial.
Purpose of the Study:
- To evaluate the long-term predictive capability of VLP for arrhythmic events.
- To analyze VLP in a large group of unselected patients after their first acute myocardial infarction.
- To investigate factors influencing VLP development and their association with adverse outcomes.
Main Methods:
- Time-domain signal averaging performed on 458 patients within 7-13 days of a first acute myocardial infarction.
- Median follow-up of 70 months to track sudden cardiac death and sustained ventricular tachycardia.
- Univariate and multivariate analyses to identify predictors of VLP and arrhythmic events.
Main Results:
- VLP were present in 20% of patients.
- Low left ventricular ejection fraction (<40%) and occluded infarct-related artery predicted VLP development.
- VLP presence, older age, and occluded infarct-related artery were significant predictors of serious arrhythmic events.
- Patients with VLP had a 4.6-fold increased risk of arrhythmic events, persisting for at least 7 years.
Conclusions:
- Ventricular late potentials are powerful, long-term predictors of serious arrhythmic events after a first myocardial infarction.
- The prognostic value of VLP persists for at least 7 years, though it may diminish over time.
- An open infarct-related artery appears to be associated with reduced arrhythmic risk.
Abstract:
Ventricular late potentials (VLP) have been shown to be independent predictors of arrhythmic events after myocardial infarction. However, many studies have had one or more limitations: limited follow-up period, small study group, possible selection bias, inadequate statistical analysis, or inclusion of patients with previous infarction. The purpose of this study was to assess the long-term prognostic value of VLP in a large group of unselected patients after a first acute myocardial infarction. Time-domain signal averaging was performed in 458 patients (380 male, 78 female, mean age 59 +/- 11 years) a mean of 10 days (range 7 to 13 days) after a first acute myocardial infarction. The overall prevalence of VLP was 20% (90 of 458 patients). By univariate analysis a left ventricular ejection fraction <40% (p = 0.002) and the presence of an occluded infarct-related artery (p = 0.006) were the only statistically significant predictors for the development of VLP. During a median follow-up of 70 months, 21 (5%) patients died suddenly, and 11 (2%) patients had documented sustained ventricular tachycardia. The presence of VLP (p < 0.0001), older age (p = 0.02), and an occluded infarct-related artery (p = 0.045) were the only variables significantly associated with the occurrence of serious arrhythmic events during follow-up. The probability of having no arrhythmic events was 99% at 1 year and 96% at 5 years in the absence of VLP and 87% at 1 year and 80% at 5 years in the presence of VLP (4.6-fold increase in arrhythmic risk; 95% confidence interval: 2.3 to 9.1). VLPs are powerful predictors of serious arrhythmic events in patients after a first acute myocardial infarction, and their prognostic value, although waning with time, persists for at least 7 years. This study also provides further evidence that an open infarct-related artery may reduce the arrhythmic risk after myocardial infarction.
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