Circulation, Vol 78, 1135-1143, Copyright © 1988 by American Heart Association
M Shenasa, R Cardinal, T Kus, P Savard, M Fromer and P Page
Our purpose was to investigate the efficacy, safety, and
electrophysiological mechanism of ultrarapid subthreshold electrical
stimulation in terminating sustained ventricular tachycardia (VT) in
humans. Fifteen patients with inducible sustained hemodynamically stable VT
and whose VT cycle length ranged between 295 and 440 msec (337 +/- 60 msec)
were included in this study. The stimulation threshold and ventricular
myocardial effective refractory period were determined during VT, and the
values ranged between 0.4 and 1.2 mA (mean, 0.7 +/- 0.3 mA) and between 185
and 245 msec (mean, 225 +/- 20 msec), respectively. Trains of ultrarapid
subthreshold stimulation were delivered with cycle lengths of 100 to 10
msec in decremental steps of 10 msec. A 5-second pause was allowed between
each step (decrement). A 2-msec pulse width was used in all patients, and a
4-msec pulse width was also tested in eight patients. Any apparent captured
beat was disregarded. In eight (53%) patients, ultrarapid subthreshold
stimulation terminated VT, and in the remaining seven (47%) patients, it
did not. The lowest subthreshold stimulation that effectively terminated VT
was 0.05 mA. In 10 patients, the site of early activity during VT was
determined by endocardial catheter mapping, and subthreshold stimulation
more effectively terminated VT in eight patients when it was applied close
to the site of early activity. In seven patients who underwent
mapping-guided arrhythmia surgery, subthreshold stimulation was applied
close to the site of early activity and successfully terminated VT. In no
patient did subthreshold stimulation produce acceleration of VT or induce
ventricular fibrillation.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Termination of sustained ventricular tachycardia by ultrarapid subthreshold stimulation in humans
Clinical Electrophysiology Laboratory, Sacre-Coeur Hospital, Montreal, Quebec, Canada.
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