Circulation, Vol 68, 400-405, Copyright © 1983 by American Heart Association
CD Swerdlow, RA Winkle and JW Mason
We analyzed 255 long-term trials of antiarrhythmic therapy, each of which
had been evaluated at electrophysiologic study, to identify the maximum
number of induced ventricular complexes consistent with the long-term
efficacy of antiarrhythmic therapy. All patients had spontaneous and
inducible sustained ventricular tachycardia or ventricular fibrillation.
The incidence of therapeutic efficacy at 1 month and throughout follow-up
was similar for trials in which zero, one, two, three, four, five, six to
10, and 11 to 15 complexes were induced, but significantly lower (p less
than .001) for trials in which 16 or more complexes were induced. The
cumulative incidence of efficacy at 1 year was 75 +/- 5% for 0 to 5 induced
complexes, 72 +/- 11% for six to 10 complexes, 83 +/- 15% for 11 to 15
complexes, 42 +/- 10% for 16 complexes to 15 sec, and 48 +/- 6% for
sustained ventricular tachycardia. At 1 year, the incidence of "sudden
death-free" survival was higher for patients in trials that prevented
initiation of sustained ventricular tachycardia than for those in trials
that permitted initiation of sustained ventricular tachycardia (91 +/- 3%
vs 75 +/- 6%; p = .01). The duration of the arrhythmia induced at therapy
assessment was in the range of 11 to 20 complexes for only 4% of trials.
Antiarrhythmic therapy is likely to be effective if as many as 15 complexes
are induced at therapy assessment. The best cutoff, between 11 and 20
complexes, is difficult to identify because of the small fraction of trials
in this range. Patients in whom initiation of sustained ventricular
tachycardia is not prevented are at high risk for arrhythmia recurrence and
sudden death.
ARTICLES
Prognostic significance of the number of induced ventricular complexes during assessment of therapy for ventricular tachyarrhythmias
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