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The Journal of Thoracic and Cardiovascular Surgery, Vol 99, 345-353, Copyright © 1990 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
GS Aldea, RE Austin Jr, AE Flynn, DL Coggins, W Husseini and JI Hoffman
The prevention of intraoperative myocardial damage with cardioplegic
solution depends in large measure on the completeness of its delivery. We
created a model to study the regional flow distribution of cardioplegic
solutions in nondiseased, diastolically arrested, maximally vasodilated
canine hearts. Global and regional myocardial flows were measured at
different perfusion pressures in hearts perfused either with blood
cardioplegic solution (n = 8) or oxygenated crystalloid cardioplegic
solution (n = 2). As coronary perfusion decreased, flow in all layers fell
significantly (p less than 0.001). This fall was most dramatic in the
subendocardium (p less than 0.05). With both types of cardioplegic
solutions, the relationship between pressure and flow was nonlinear: At low
coronary perfusion pressures, a given change in pressure resulted in a
smaller change in flow than at higher perfusion pressures. In addition, we
found that in all dogs and at all pressures there was profound variability
in the delivery of cardioplegic solution to different small regions of the
left ventricular free wall. At a perfusion pressure of 40 mm Hg, the
extremes of regional flow differed on average by 203%. This heterogeneity
increased significantly with decreasing perfusion pressures. At the lowest
perfusion pressure measured (20 mm Hg), the extremes of regional flow
differed on average by 365%. These findings emphasize the importance of
coronary pressure on the delivery of cardioplegic solution. At low
perfusion pressures, not only is mean flow reduced, but a greater number of
regions receive limited amounts of cardioplegic solution. These
observations may explain the patchy nature of subendocardial damage seen
with inadequate myocardial protection.
ARTICLES
Heterogeneous delivery of cardioplegic solution in the absence of coronary artery disease
Cardiovascular Research Institute, University of California, San Francisco 94143.
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