Emanuela Locati Heilbron.
Cattedra di Cardiologia e Fisiopatologia Cardiovascolare, Dipartimento di Medicina Clinica, Patologia e Farmacologia, Universita degli Studi di Perugia, Ospedale Silvestrini, Perugia, Italy
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Sudden cardiac death (SCD) due to life-threatening arrhythmias is a
leading cause of cardiovascular mortality in the European Countries. Effective diagnostic methods to identify
patients at high risk for SCD are still missing. Nowadays, patients at risk of SCD are generally evaluated by
intracardiac electrical stimulation, an expensive and invasive method. The challenge is to develop new broadly
used noninvasive and low-cost methods that will allow the identification of high-risk patients before they
experience a major arrhythmic event.
Recent improvements in digital Holter technology have increased the accuracy of software-based analysis
systems. Also, better signal quality and greater capability of arrhythmia interpretation have increased potential
uses for ambulatory electrocardiography1.
Lately, several new noninvasive markers associated with increased propensity to life-threatening cardiac
arrhythmias have been derived from noninvasive 24-hour Holter monitoring. The most promising noninvasive
index of elevated risk for SCD is low heart rate variability, measured by time- and frequency-domain analysis,
powerful independent risk factors for cardiac mortality and sudden death in several different cardiac
conditions2,3.
More recently, research in risk stratification has been focused on the increased duration and dispersion of
ventricular repolarization, assessed on the surface ECG by the so-called “QT interval”4,5.
Very recent studies are focusing on temporal heterogeneity of ventricular repolarization (defined as “T wave
alternans”, TWA), which is now considered as a new promising index of elevated risk for SCD. However, so far
TWA analysis is restricted to short-term ECG recorded during exercise stress test or atrial pacing, and it has not
been implemented on routine long-term ECG Holter monitoring technique yet.
The positive predictive value of each noninvasive index alone is generally too low to be sufficient to take
decisions about clinical prognosis and therapeutic management. So far, those indexes have never been
combined in a comprehensive noninvasive electrocardiographic (ECG) test, to fully characterize the electrical
substrate that may lead to SCD.
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