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In addition to the more commonly investigated techniques for risk
stratification of SCD, several other risk indices have been reported. For instance, QT dispersion detected by
magnetocardiograph36 or by precordial mapping
techniques37 was reported to be a sensitive marker of the
susceptibility to malignant VT. However, the prohibitive cost of a magnetocardiography laboratory and the
technical demands of precordial mapping techniques are obvious deterrents to their wide application in a
clinical setting. Beat-to-beat repolarization lability was found in one study to be a better identifier of SCD than
other indicators of abnormal repolarization, including spatial QT dispersion and
TWA38. Low variability of cycle
lengths of non-sustained VT was also suggested as an independent predictor of mortality after AMI39. Increased
heart rate, assessed from a 24-hour Holter recording, or even from a standard ECG tracing, was found to be a
strong predictor of mortality after AMI23,40. On the other hand, “non electrophysiologic” indices may also be
associated with increased risk for SCD, for instance, LV mass and hypertrophy41.
The practical value of many of the risk stratifiers of SCD remains largely unanswered. Although risk stratification
for SCD may be improved by using several variables in combination, one problem that has been alluded to is
that dichotomous limits derived from univariate analysis may be different when used in the multivariate
setting42.
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