Elsevier

American Heart Journal

Volume 134, Issue 6, December 1997, Pages 1019-1028
American Heart Journal

Long-term prognostic significance of ventricular late potentials after a first acute myocardial infarction,☆☆,,★★

https://doi.org/10.1016/S0002-8703(97)70021-8Get rights and content

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. (Am Heart J 1997;134:1019-28.)

Section snippets

Patient population

The study population consisted of 597 unselected patients who were admitted to the Coronary Care Unit of our institution with an acute myocardial infarction and who survived the first 10 days of admission. Patients with a history of myocardial infarction (n = 59), patients who underwent bypass surgery before day 10 (n = 8), patients with bundle branch block (n = 38) or permanent pacemakers (n = 4), and patients who were not in sinus rhythm at the time of signal averaging (atrial fibrillation, n

Prevalence of ventricular late potentials

The overall prevalence of ventricular late potentials was 20% (90 of 458 patients). The characteristics of patients with and of patients without late potentials are listed in Table II. Univariate analysis demonstrated that a low left ventricular ejection fraction and an occluded infarct-related artery were the only statistically significant predictors for the development of late potentials (Table II). The prevalence of ventricular late potentials was significantly higher in patients with a left

Discussion

This study shows that the presence of ventricular late potentials is a strong predictor of serious arrhythmic events after myocardial infarction and that the prognostic value of an abnormal signal-averaged electrocardiogram, although decreasing over time, persists for at least 7 years. The presence of late potentials represents a 4.6-fold increase in the risk of having serious arrhythmic events after myocardial infarction and appears to be a stronger predictor of arrhythmic events than a low

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      Citation Excerpt :

      The results of combining studies are shown in Figure 1and Tables 1 and 2. The incidences of MAE in the patient populations reported (references 18–61; column 2 in Table 1) are the prior probabilitiesfor MAE—that is, the probability of a MAE prior to a test. The individual values of prior probability varied widely (range 3.3% to 34.1%).

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    From the aCardiology Center, bCentre d'Informatique Hospitalière, University Hospital.

    ☆☆

    Supported in part by grant 3.805-0.86 from the Swiss National Foundation for Scientific Reasearch, Bern, Switzerland.

    Reprint requests: M. Zimmermann, MD, Cardiology Center, University Hospital, 24 rue Micheli-du-Crest, CH-1211 Geneva 14, Switzerland.

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