Why the study?
Does the application of two consecutive ventricular premature stimuli (S1S2) increase dispersion of repolarization and induce ventricular arrhythmias in a dog model?
Does the application of two consecutive ventricular premature stimuli (S1S2) increase dispersion of repolarization and induce ventricular arrhythmias in a dog model?
Two consecutive ventricular premature stimuli significantly increase the dispersion of repolarization compared to a single stimulus, though this alone did not induce ventricular arrhythmias in the control dog model.
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S1S2 markedly increases repolarization dispersion beyond single stimuli in dogs without inducing arrhythmias; leaves open its arrhythmogenic role in humans.
Kuo et al. (1985) studied this question.
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