Circulation, Vol 82, 879-896, Copyright © 1990 by American Heart Association
A SippensGroenewegen, H Spekhorst, NM van Hemel, JH Kingma, RN Hauer, MJ Janse and AJ Dunning
The value of simultaneous 62-lead electrocardiographic recordings in
localizing the site of origin of ectopic ventricular activation in a
structurally normal heart was assessed by examining body surface QRS
integral maps in 12 patients during left and right ventricular (LV and RV)
pacing at 182 distinct endocardial sites. A data base of 38 characteristic
mean integral maps was composed after visually selecting subgroups with
nearly identical total QRS integral morphology and numerically evaluating
intrasubgroup pattern uniformity and intersubgroup pattern variability.
Corresponding endocardial pacing site locations were computed by a biplane
cineradiographic method and outlined as segments on a standardized LV and
RV polar projection. LV pacing resulted in 25 markedly different mean total
QRS integral patterns, showing higher electrocardiographic sensitivity for
anteroseptal (18 patterns) compared with posterolateral regions (seven
patterns). RV pacing demonstrated 13 mean total QRS integral patterns,
exhibiting less intersubgroup variation and comparatively low
electrocardiographic sensitivity for the basal anterior and outflow
regions. Comparison of LV with RV pacing revealed that QRS configurations
produced at LV apical and LV midseptal sites closely resembled QRS
configurations generated at RV apical, RV septal, and RV anterior sites,
respectively. Total QRS time integral amplitudes showed considerable
intrasubgroup variation but permitted global differentiation of spatially
similar QRS patterns obtained during pacing at LV and RV sites. This study
demonstrates that the QRS pattern of the total body surface
electrocardiogram allows discrimination among 38 different LV and RV
segments of ectopic endocardial impulse formation in patients with normal
cardiac anatomy.
ARTICLES
Body surface mapping of ectopic left and right ventricular activation. QRS spectrum in patients without structural heart disease
Department of Clinical and Experimental Cardiology, University of Amsterdam, The Netherlands.
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