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The Journal of Thoracic and Cardiovascular Surgery, Vol 100, 715-723, Copyright © 1990 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
JS Kabas, JA Spratt, JW Davis, JS Rankin and DD Glower
Dopamine frequently is used to improve cardiac performance after acute
myocardial ischemia. Inotropic agents, however, increase myocardial oxygen
demand and could potentially delay recovery from ischemic injury. To
evaluate this problem, we studied eight chronically instrumented dogs in
the conscious state and performed two 15-minute coronary occlusions 48
hours apart. After one of the occlusions, either dopamine (15
micrograms/kg/min) or saline placebo was administered intravenously from
1.0 to 1.5 hours of reperfusion. The alternative infusion was given during
the second study. Preload recruitable work area, the area beneath the
stroke work versus end-diastolic length relationship, was used to assess
intrinsic myocardial performance. Ischemia decreased preload recruitable
work area to 13% of control after both occlusions. After reperfusion, a
30-minute dopamine infusion acutely increased myocardial function nearly
threefold as compared with placebo. Myocardial performance after dopamine
administration, however, was significantly depressed compared with placebo
throughout the remaining 24 hours of reperfusion (p less than 0.01). These
data indicate that dopamine may impair functional recovery after ischemic
myocardial injury and suggest that inotropic interventions should be used
in this setting only when absolutely indicated.
ARTICLES
The effects of dopamine on myocardial functional recovery after reversible ischemic injury
Department of Surgery, Duke University Medical Center, Durham, N.C. 27710.
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