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Ann Thorac Surg 1994;58:1123-1130
© 1994 The Society of Thoracic Surgeons
Department of Cardiothoracic Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin, USA
Accepted for publication March 8, 1994.
* Address reprint requests to Dr Baker, Department of Cardiothoracic Surgery. Medical College of Wisconsin, 8701 Watertown Plank Rd, Milwaukee, WI 53226.
* Address reprint requests to Dr Baker, Department of Cardiothoracic Surgery. Medical College of Wisconsin, 8701 Watertown Plank Rd, Milwaukee, WI 53226.
Because many infants who require cardiac operation have cyanotic heart disease, we determined whether the existing calcium content of St. Thomas' II solution (1.2 mmol/L) is optimal to protect the immature rabbit heart hypoxemic from birth during subsequent ischemia. Modified hypothermic St Thomas' II solutions (calcium content, 0 to 2.4 mmol/L) were compared with hypothermic Krebs bicarbonate buffer in protecting chronically hypoxemic (PaO2 = 34 ± 11 mmHg, SaO2 = 63% ± 3%) versus normoxemic (PaO2 = 76 ± 11 mmHg, SaO2 = 92% ± 3%) immature hearts (7 to 12 days old) during ischemia. Hearts (n = 6 per group) underwent aerobic working perfusion with Krebs bicarbonate buffer and cardiac function was measured. The hearts were then arrested with a 3 minute infusion of either cold (14 °C) Krebs buffer (1.8 mmol calcium/L) as hypothermia alone or modified St. Thomas' II solution before 6 hours of hypothermic (14 °C) global ischemia. Hearts were reperfused and postischemic enzyme leakage and recovery of function were measured. A bell-shaped dose-response profile was observed for recovery of postischemic aortic flow but not for postischemic creatine kinase leakage, with improved protection occurring at lower calcium concentrations. Optimal myocardial protection occurred at a calcium content of 0.4 mmol/L, which was significantly better than with hypothermia alone or standard St. Thomas' II solution. We conclude that the existing calcium concentration of St Thomas' II solution is responsible, in part, for its inadequate protection of immature myocardium hypoxemic from birth during ischemia.
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