Relationship between QT dispersion and the incidence of early ventricular arrhythmias in patients with acute myocardial infarction

https://doi.org/10.1016/S0167-5273(97)00226-XGet rights and content

Abstract

There is controversy about the influence of QT dispersion on the incidence of early ventricular arrhythmias in patients with acute myocardial infarction (AMI). The QT and QTc dispersion (QTd, QTcd) between two groups of patients with AMI were compared: 39 patients with early sustained ventricular tachycardia or ventricular fibrillation (VT/VF) and 40 patients without such arrhythmias. QTd and QTcd were calculated from the admission and predischarge ECG, expressed as the difference between the maximum and minimum QT and QTc interval in 12 leads. The coefficient of variability was also calculated (VQT, VQTc). Groups did not differ significantly in age, incidence of previous infarction, Killip class, electrolyte status, infarct location, expected and final ECG infarct size, enzymatic infarct size, thrombolytic treatment and reperfusion rate, i.e., in variables that could influence the VT/VF occurrence. On admission, patients with VT/VF had significantly greater QTd (77±23 vs 53±27 ms, P<0.001) and QTcd (90±29 vs 62±28 ms, P<0.001); VQT and VQTc were also significantly higher. Although similar differences existed on predischarge ECG, they were smaller. The results indicate that QT dispersion varies during the illness, and that measurements of QT dispersion could be helpful in predicting serious ventricular arrhythmias.

Introduction

Acute myocardial infarction (AMI) is the leading cause of death in developed countries [1]. Of all deaths due to AMI, more than 60% occur within the first few hours as a consequence of ventricular tachycardia and/or fibrillation (VT/VF) [2]. Therefore, it is of great clinical interest to procure simple and noninvasive measurements of myocardial electrical instability which could predict such fatal events.

It is well known that the prolonged QT interval in patients with AMI reflects abnormal ventricular repolarization and is associated with higher risk of life-threatening arrhythmias 3, 4. More recently, the dispersion of QT interval, defined as the interlead variability of QT interval in surface ECG, was found to be the measure of regional differences in ventricular repolarization important in the pathogenesis of ventricular arrhythmias 5, 6, 7, 8.

Although several studies reported that the measurement of QT dispersion is of value in the prediction of serious ventricular arrhythmias in patients with AMI 9, 10, 11, 12, some authors reached negative conclusions 13, 14. Because of this controversy [15], we tried to determine the relationship between the QT dispersion and the incidence of early ventricular arrhythmias in patients with AMI.

Section snippets

Methods

All patients with AMI admitted to our coronary care unit during 1996 were considered for inclusion in the study. Patients with atrial fibrillation or flutter, ventricular hypertrophy, preexcitation, intraventricular conduction abnormalities, permanent ventricular pacing, those treated with Class I or III antiarrhythmics and patients who died during hospitalization, were excluded. According to the VT/VF occurrence, two groups of patients were formed: 39 patients with early sustained VT or VF

Results

During 1996, 424 patients with AMI were admitted and treated in our coronary care unit. Among them, 48 patients suffered from early malignant ventricular arrhythmias (11.3%). There were 38 patients with sustained VT (9%), and ten patients with VF (2.3%). In four patients with VT, arrhythmia termination was achieved by intravenous lidocaine (10.5% success rate); others were successfully treated with DC cardioversion. Nine patients with early VT/VF were excluded from the study: two with extensive

Discussion

The QT interval does not exactly reflect the ventricular depolarization and repolarization time, because in all portions of the ventricles repolarization is not finished at the time when the end of the QT interval is recorded. These slight physiological differences in regional ventricular recovery time cannot be registered in the surface ECG and are not of clinical relevance. In patients with AMI, regional ischemia, combined with increased sympathetic activity, causes enlarged spacial and

References (30)

  • Kupersmith J. Long QT syndrome. In: Singer I, Kupersmith J, editors. Clinical manual of electrophysiology. Baltimore,...
  • C.P. Day et al.

    QT dispersion: an indication of arrhythmia risk in patients with long QT intervals

    Br Heart J

    (1990)
  • M. Pye et al.

    QT interval dispersion: a non-invasive marker of susceptibility to arrhythmia in patients with sustained ventricular arrhythmias?

    Br Heart J

    (1993)
  • P.D. Higham et al.

    QT dispersion

    Br Heart J

    (1994)
  • M. Zabel et al.

    QT dispersion in the 12-lead surface ECG reflects inhomogeneity in the terminal part of ventricular repolarization (abstract)

    PACE

    (1995)
  • Cited by (27)

    • Does the Magnitude of the Electrocardiogram QT Interval Dispersion Predict Stroke Outcome?

      2019, Journal of Stroke and Cerebrovascular Diseases
      Citation Excerpt :

      QT interval dispersion (QTd), defined as the difference between the maximal and minimal leads on a 12-lead electrocardiogram (ECG), is an expression of cardiac repolarization abnormalities. In a variety of clinical settings, including acute stroke, multiple studies have suggested that an increase in QTd places patients at increased risk to develop ventricular arrhythmias and adverse clinical outcomes.1-4 We sought to determine if admission QTd predicts short-term clinical outcome in patients with acute ischemic stroke (AIS) as well as to investigate if an AIS in the insular cortex region has a greater effect on QTd than strokes in other areas of the brain, as insular cortical involvement has been associated with increased sympathetic nervous system activity including arrhythmias.5

    • Long-term high-intensity interval training associated with lifestyle modifications improves QT dispersion parameters in metabolic syndrome patients

      2013, Annals of Physical and Rehabilitation Medicine
      Citation Excerpt :

      La dispersion du QT (QTd) se définit comme la différence entre l’intervalle le plus long et le plus court du segment QT sur un électrocardiogramme (ECG) à 12 dérivations. La mesure du QTd est une méthode non invasive pour évaluer l’instabilité électrique du myocarde [39] et est un facteur prédictif d’épisodes d’arythmie ventriculaire [8]. Une augmentation du QTd semble refléter une augmentation du tonus sympathique et une baisse du tonus parasympathique [35].

    • Cardiovasular changes after placement of a classic endotracheal tube, double-lumen tube, and Laryngeal Mask Airway

      2011, Journal of Clinical Anesthesia
      Citation Excerpt :

      Atrial fibrillation is characterized by disorganized atrial electrical activity, leading to loss of effective contraction [22]. QTd is a noninvasive method showing myocardial electrical instability [23] and higher sympathetic and lower parasympathetic input to the heart [24]. The QT interval is affected by catecholamines, HR, and autonomic tone [25].

    • The Electrocardiogram as a Prognostic Tool for Predicting Major Cardiac Events

      2007, Progress in Cardiovascular Diseases
      Citation Excerpt :

      QTd was shown to be increased in several cardiac diseases, including AMI, cardiomyopathy, and long QT syndrome, but there is a large overlap of values with normal reference subjects.34 There have been several studies suggesting a prognostic role for QTd in patients with CAD or CHF, and, in some studies, QTd was also found to be higher among patients who suffered from life-threatening ventricular arrhythmias (VAs), compared with those who did not.35-38 Other studies, however, failed to find any significant association between QTd and prognosis in patients with AMI, with or without signs of CHF,39-44 and similar discordant results have been reported in patients with inducibility of ventricular tachyarrhythmias.45-49

    View all citing articles on Scopus
    View full text