Pey Vincent, Stephan Marion, Gros Pierre, Dray Cédric, Bounes Fanny, Marcheix Bertrand, Minville Vincent, Galinier Anne, Labaste François
RESTORE Research Center, University Toulouse 3-Paul Sabatier, INSERM, CNRS, EFS, ENVT, Toulouse, France.
Department of Anaesthesiology and Critical Care, University Hospital of Toulouse, University Toulouse 3-Paul Sabatier.
PLoS One. 2025 May 27;20(5):e0324437. doi: 10.1371/journal.pone.0324437. eCollection 2025.
Imbalance in the redox equilibrium is common in any type of aggression. Cardiopulmonary bypass (CPB) initiation induces metabolic perturbations, and reliable biological monitoring tools for this condition are currently limited (e.g., lactate/pyruvate ratio). The measurement of arterial whole blood redox potential (Eredox) provides a systemic assessment of the redox state and may serve as a valuable marker for detecting metabolic perturbations during CPB. In this prospective exploratory study involving patients undergoing cardiac surgery, we investigated variations in Eredox and lactate/pyruvate ratio during CPB initiation.
Using a prospective exploratory study design, we assessed the changes in Eredox and relevant variables during the initiation of CPB in 16 cardiac surgery patients.
Upon initiation of CPB we observed a significant decrease in arterial whole blood redox potential (101.90 mV + /- 11.52 vs. 41.80 mV + /- 10,26; p < 0.0001). Concomitantly, the lactate/pyruvate ratio significantly increased (12.81 + /- 0.90 vs 67.1 + /- 7.94; p < 0.0001) while the acetoacetate/β-hydroxybutyrate ratio significantly decreased (1.11 + /- 0.19 vs. 0.54 + /- 0.05 at 0 min; p = 0.0055). The circulatory failure indicated by changes in the lactate/pyruvate ratio and ketone bodies at the initiation of CPB correlated with a significant reduction in Eredox.
Arterial Eredox is a novel variable that holds promise in the detection and monitoring of metabolic aggression during CPB. Its assessment during CPB initiation could provide valuable insights into the patient's circulatory status, as the Eredox appears to be more sensitive than lactate for monitoring circulatory insufficiency.
氧化还原平衡失衡在任何类型的侵袭中都很常见。体外循环(CPB)启动会引发代谢紊乱,而目前用于这种情况的可靠生物监测工具有限(例如乳酸/丙酮酸比值)。动脉全血氧化还原电位(Eredox)的测量可提供对氧化还原状态的系统评估,并可能作为检测CPB期间代谢紊乱的有价值标志物。在这项涉及心脏手术患者的前瞻性探索性研究中,我们调查了CPB启动期间Eredox和乳酸/丙酮酸比值的变化。
采用前瞻性探索性研究设计,我们评估了16例心脏手术患者CPB启动期间Eredox和相关变量的变化。
CPB启动后,我们观察到动脉全血氧化还原电位显著降低(101.90 mV ± 11.52 vs. 41.80 mV ± 10.26;p < 0.0001)。同时,乳酸/丙酮酸比值显著升高(12.81 ± 0.90 vs 67.1 ± 7.94;p < 0.0001),而乙酰乙酸/β-羟基丁酸比值显著降低(0分钟时为1.11 ± 0.19 vs. 0.54 ± 0.05;p = 0.0055)。CPB启动时乳酸/丙酮酸比值和酮体变化所表明的循环衰竭与Eredox的显著降低相关。
动脉Eredox是一个新的变量,在CPB期间代谢侵袭的检测和监测方面具有前景。在CPB启动期间对其进行评估可为患者的循环状态提供有价值的见解,因为Eredox在监测循环功能不全方面似乎比乳酸更敏感。