BRAIN-TISSUE ACID-BASE RESPONSE TO HYPERCAPNIA IN NEUROSURGICAL PATIENTS

These studies were conducted in neurosurgical patients to determine brain tissue nonbicarbonate buffering of pH changes during hypercapnia. Following a craniotomy, a sensor which continuously measures oxygen pressure, carbon dioxide pressure, pH and temperature was inserted into cortex tissue of nine subjects. Bicarbonate concentration was calculated from the Henderson-Hasselbach equation. Following baseline measures, PaCO2 was increased 10 mmHg for 10 min. Tissue pCO(2) increased 9 mmHg (p < 0.05) without a change in tissue pO(2). In six patients, tissue bicarbonate concentration increased from 18 to 20 meq L(-1) (p<0.05) indicating a 40-50% attenuation of the increase in hydrogen ion (H+) by nonbicarbonate buffering mechanisms. Three patients showed no increase in tissue bicarbonate during hypercapnia; 2 had baseline tissue pH less than 6.5 and one displayed signs of tissue hypoxia during the CO2 challenge. In all patients, increases in tissue H+ during hypercapnia were related to baseline tissue bicarbonate concentration. Marked increases in H+ were seen when baseline bicarbonate decreased below 10 meq L(-1). These results suggest that when tissue bicarbonate is depleted, the risk of H+ induced injury during hypercapnia is increased.