Circulation, Vol 70, 681-694, Copyright © 1984 by American Heart Association
TM Bashore, RA Stine, PB Shaffer, CA Bush, CV Leier and SF Schaal
This study was designed to investigate the potential role of radionuclide
angiographic phase imaging in defining ventricular pacing sites. Twenty
patients were paced from multiple right ventricular and left ventricular
sites. Ten patients had both normal wall motion and normal
electrocardiograms (ECGs), while 10 patients had segmental wall motion
abnormalities and/or bundle branch block. Both continuous pacing and
premature ventricular stimuli were performed. Multiple (two to three) views
of each pacing site were obtained by radionuclide angiography and the
ventricular site was determined by subsequent phase imaging. Simultaneous
12-lead ECGs were also obtained. The phase- imaging technique accurately
localized all 35 right ventricular and 21 of 25 (84%) left ventricular
sites to a specific segment. Statistically, this localization ability was
independent of baseline wall motion or conduction system disease. In
addition, sites as close as 1.5 cm were identified. The 12-lead ECG
distinguished left ventricular from right ventricular pacing sites in all
patients. Segmental localization by ECG in the right ventricle was accurate
in 24 of 35 (69%) and in the left ventricle in 17 of 25 (68%). Thus,
radionuclide angiographic phase imaging provides excellent descriptive
information regarding the focus of ventricular pacing ectopy and can define
both sites of continuous pacing and intermittent premature ventricular
stimulation. These findings provide a basis for further assessment of the
role of phase imaging in the evaluation of patients with spontaneous
ventricular ectopy.
ARTICLES
The noninvasive localization of ventricular pacing sites by radionuclide phase imaging
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