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The Journal of Thoracic and Cardiovascular Surgery, Vol 105, 513-519, Copyright © 1993 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
G Matheis, DB Tixier, GD Buckberg, K Ihnken, K Morita, MP Sherman and HH Young
This study tests the hypothesis that reoxygenation injury is produced when
cardiopulmonary bypass is initiated in immature hypoxemic piglets and that
it causes cardiopulmonary dysfunction that can be avoided by intravenous
metabolic treatment before and during cardiopulmonary bypass. Of 18
immature Yorkshire-Duroc piglets (aged < 3 weeks), six were
anesthetized, instrumented, and observed for 5 hours (control animals).
Twelve piglets underwent up to 2 hours of hypoxemia (arterial oxygen
tension = 20 to 30 mm Hg) before initiation of reoxygenation on
cardiopulmonary bypass. Six received an intravenous metabolic infusion
solution (mercaptopropionyl glycine, catalase, aspartate, glutamate,
glucose/insulin), which was started before and continued during
cardiopulmonary bypass. Hypoxia produced an initial hyperdynamic response
(39% increase in cardiac index; p < 0.05) followed by progressive
hemodynamic deterioration, necessitating premature initiation of bypass in
8 of 12 hypoxemic piglets (67%). Reoxygenation- induced injury (assessed 30
minutes after cardiopulmonary bypass) was characterized by 39% reduction of
stroke work index (p < 0.05), increased myocardial lipid peroxidation
(79% increase of conjugated dienes; p < 0.05), 254% increase in
pulmonary vascular resistance index (p < 0.05), 22% decrease in static
lung compliance (p < 0.05), and 50% decrease in arterial/alveolar oxygen
tension ratio (p < 0.05). These reoxygenation changes were avoided by
intravenous metabolic treatment. We conclude that the reoxygenation of
immature hypoxemic piglets by initiating cardiopulmonary bypass results in
cardiopulmonary dysfunction that may increase vulnerability to subsequent
ischemia (i.e., aortic crossclamping). The cardiopulmonary reoxygenation
changes are preventable by intravenous metabolic treatment before and
during cardiopulmonary bypass needed for cardiac repair.
ARTICLES
Cardiopulmonary dysfunction produced by reoxygenation of immature hypoxemic animals supported by cardiopulmonary bypass. Prevention by intravenous metabolic pretreatment
Division of Cardiothoracic Surgery, University of California, Los Angeles School of Medicine.
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