Abstract

Objectives: We investigated the alterations of acid-base characteristics of the blood cardioplegia (BCP) solution during aortic cross-clamping in hearts arrested with BCP and during in vitro-simulated ischemia. Methods: Following aortic cross-clamping, the hearts of 40 patients undergoing cardiac surgery were intermittently infused with an 18°C BCP solution and finally with a 34°C BCP solution prior to aortic cross-clamp release. We measured the pH, partial CO<sub>2</sub> pressure (pCO<sub>2</sub>), [HCO<sub>3</sub><sup>–</sup>], and [Cl<sup>–</sup>] of the coronary sinus effluent in the final BCP solution. The BCP solution was assessed under in vitro gassing at 34°C with 95% N<sub>2</sub> + 5% CO<sub>2</sub> (n = 6), 50% N<sub>2</sub> + 50% CO<sub>2</sub> (n = 3), or 100% CO<sub>2</sub> (n = 6). Results: The coronary sinus effluent, compared with the preinfusion BCP solution, exhibited a significantly lower pH and a greater pCO<sub>2</sub> with no change in the [HCO<sub>3</sub><sup>–</sup>] level. In vitro, the 95% N<sub>2</sub> + 5% CO<sub>2</sub> gassing (simulated hypoxia) group exhibited a slight increase in [HCO<sub>3</sub><sup>–</sup>] with no change in pCO<sub>2</sub> or pH whereas the 50% N<sub>2</sub> + 50% CO<sub>2</sub> gassing and the 100% CO<sub>2</sub> gassing (simulated hypoxia and hypercapnia) groups exhibited a significant increase in [HCO<sub>3</sub><sup>–</sup>] under high pCO<sub>2</sub>-induced acidification. Conclusions: Under anoxia and CO<sub>2</sub> retention during aortic cross-clamping, the BCP solution can be a bicarbonate donor to the myocardium.

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