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The Journal of Thoracic and Cardiovascular Surgery, Vol 84, 609-618, Copyright © 1982 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
PF McDonagh and H Laks
The effect of cold blood cardioplegia in preventing microvascular injury
owing to myocardial ischemia and reperfusion was studied. Two groups of
eight dogs each were placed on cardiopulmonary bypass with separate
coronary perfusion at 80 mm Hg. Microcirculatory function was assessed by
measuring the extraction and permeability surface area product (PS) for
inulin and albumin. These changes were correlated with the transport and
extraction of oxygen, coronary blood flow, and morphologic studies of the
microvasculature. In Group I, ischemic hearts were kept normothermic for 45
minutes. In Group II, 250 ml of cold (4 degrees C) blood cardioplegic
solution (potassium chloride 30 mEq/L) was infused and the infusion
repeated at 15 and 30 minutes. Reperfusion resulted in marked reactive
hyperemia for Group I (p less than 0.05) but no hyperemic response in Group
II. In Group I, but not II, ischemia-reperfusion caused a significant
decrease in PS inulin (0.47 +/- 0.10 ml/min/gm) compared to the preischemic
value (1.04 +/- 0.23) (p less than 0.05). There was a threefold decrease in
the PS inulin/PS albumin ratio with reperfusion in Group I, indicating
increased vascular permeability to albumin. There was also a significant
decrease in myocardial oxygen consumption (from 5.1 +/- 0.7 to 3.4 +/- 0.5
ml/min/100 gm, p less than 0.05) for Group I. These did not decrease for
Group II. Histologic studies showed diffused areas of no reflow in the
unprotected hearts. The wet/dry weight ratio for Group I (4.97 +/- 0.09)
was significantly greater than for Group II (4.49 +/- 0.07) (p less than
0.001). The results indicate that in the unprotected heart,
ischemia-reperfusion caused microcirculatory injury resulting in increased
permeability to albumin, edema, a reduction in surface area, and areas of
no reflow. In contrast, in the hearts protected with cold blood
cardioplegia, no evidence of microcirculatory injury occurred.
ARTICLES
Use of cold blood cardioplegia to protect against coronary microcirculatory injury due to ischemia and reperfusion
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