The use of near-infrared cerebral oximetry in awake carotid endarterectomy

Study Objective: To determine the utility of cerebral oximetry for monitoring the adequacy of cerebral bloodflow (CBF) during carotid cross-clamp. Design: Prospective study. Setting: University hospital. Patients: 16 consecutive ASA physical status III (or higher) patients for awake carotid endarterectomy (CEA). Interventions: Regional cerebral oxygen saturation (SaO(2)) was monitored continuously during CEA, which was performed by the same surgeon, and with standard regional anesthetic, sedation, monitoring and operative techniques. Data were recorded and analyzed using repeated measures analysis of variance (ANOVA). Measurements and Main Results: 14 hemodynamically stable patients demonstrated significant decreases in cerebral SaO(2) from baseline: 69 + 1.8% to 64 + 1.2% at carotid cross-clamp (p < 0.001). After 5, 10, and 15-minute cross-clamp time, cerebral SaO(2) was 63 + 1.4%, 64 + 1.5%, and 63 + 1.4%, respectively (p < 0.001, vs. baseline). On cross-clamp removal cerebral SaO(2) rose significantly: 67 + 1.6% (p < 0.02 vs. 5, 10, and 15 min). Two hypotensive patients (mean arterial pressures of 40 and 43 mmHg) developed signs and symptoms of global cerebral ischemia, with a concomitant decrease in cerebral oximetry (40% and 48%, respectively). These changes resolved with correction of hypotension. Conclusion: Cerebral SaO(2) decreased significantly on carotid cross-clamp in patients undergoing awake CEA. Hemodynamically stable patients demonstrated no evidence of regional brain failure when SaO(2) decreased to 63% (mean decrease of 7.2%). Two hemodynamically unstable patients had evidence of global brain failure when SaO(2) was less than 48% (mean decrease of 36%). Our findings suggest that cerebral oximetry reflects CBF, and it may be an effective noninvasive method of monitoring regional cerebral oxygenation changes during CEA. Significant reductions in regional SaO(2) may be tolerated without evidence of brain failure. Further studies are needed to define an SaO, threshold that reflects regional brain failure. (C) 1998 by Elsevier Science Inc.