Circulation, Vol 62, 1172-1179, Copyright © 1980 by American Heart Association
M Sami, H Kraemer, DC Harrison, N Houston, C Shimasaki and RF DeBusk
To develop standards for distinguishing antiarrhythmic drug effect from
spontaneous variability of premature ventricular complexes (PVCs), 21 males
(mean age 56 +/- 8 years) with chronic ischemic heart disease and PVCs
underwent symptom-limited treadmill exercise testing and 24-hour ambulatory
monitoring before and after 2 weeks of placebo medication. Linear
regression analysis was used to describe the relationship between baseline
and placebo PVC frequency for various indexes of ventricular ectopic
activity and to establish 95% and 99% one-tailed confidence intervals for
this relationship within the group of 21 patients. The lower limit of
baseline PVC frequency for which the procedure could distinguish a placebo
from a true drug response, termed the "sensitivity threshold," was an
average frequency of 2.2 PVCs/hour for ambulatory electrocardiographic
monitoring and 1.2 PVCs/min for treadmill exercise testing. All patients
exceeded the sensitivity threshold on baseline ambulatory ECGs, but only
38% of patients did so on baseline treadmill exercise tests. To establish
antiarrhythmic efficacy with 95% confidence, the minimal percent reduction
of PVCs between baseline and placebo visits was 68% for treadmill exercise
testing and 65% for ambulatory electrocardiography. Although these
standards were developed in patients with chronic ischemic heart disease,
the model can be used to establish antiarrhythmic drug efficacy in any
patient group.
ARTICLES
A new method for evaluating antiarrhythmic drug efficacy
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