1 From the Division of Nuclear Medicine, Department of Radiology, and the Division of Cardiology, Department of Medicine, The Johns Hopkins Medical Institutions, Baltimore, Maryland 21205.
The ability of ionic potassium-43 (43K) to reflect alterations in regional myocardial perfusion was determined by comparing the distribution of this tracer to that of labeled microspheres and flowmeter measurements under several conditions of coronary blood flow. When flow was normal, the regional distribution of ionic 43K and labeled microspheres were similar. In ischemia induced by partial occlusion and pacing, both 43K and microspheres showed the same decrease in activity (0.7 of control). When a coronary artery was completely occluded, both tracers were decreased to 0.3 of control. In other experiments, resting coronary blood flow was decreased by 25%, 50% and 75% as determined by flowmeter measurements. When this was done, regional distribution of ionic 43K and microspheres both decreased in parallel but to a lesser degree than flowmeter data suggesting a contribution from collateral vessels. The endocardial/epicardial activity in the ischemic region also decreased proportionally. However, under conditions of increased flow during myocardial reactive hyperemia, 43K activity (1.02 of control) did not increase to the same degree as microsphere activity (1.5 of control).
Submitted on April 5, 1974
© 1974 American Heart Association, Inc.
Comparison of Regional Myocardial Perfusion Determined by Ionic Potassium-43 to That Determined by Microspheres
Key Words: Radioisotope Hyperemia Infarction Ischemia Coronary blood flow
Accepted on July 22, 1974
This article has been cited by other articles:
![]() |
P. A. Kaufmann and P. G. Camici Myocardial Blood Flow Measurement by PET: Technical Aspects and Clinical Applications J. Nucl. Med., January 1, 2005; 46(1): 75 - 88. [Full Text] [PDF] |
||||
![]() |
P. Chareonthaitawee, P. A Kaufmann, O. Rimoldi, and P. G Camici Heterogeneity of resting and hyperemic myocardial blood flow in healthy humans Cardiovasc Res, April 1, 2001; 50(1): 151 - 161. [Abstract] [Full Text] [PDF] |
||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1974 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |