This single-center randomized trial compared two intraoperative arterial oxygen tension (PaO2) target strategies in adults undergoing elective isolated coronary artery bypass graft surgery. Sixty-four participants were assigned 1:1 to a higher target (PaO2 200 mmHg or greater) or a lower target (PaO2 80 to less than 200 mmHg). The study evaluated perioperative changes in thiol-disulfide homeostasis and ischemia-modified albumin.
Hyperoxemia is frequently used during cardiac surgery to reduce the risk of hypoxemia, but excessive oxygen exposure may increase oxidative stress and ischemia-reperfusion injury. In this prospective, randomized, parallel-group study, inspired oxygen concentration was adjusted intraoperatively to achieve the assigned PaO2 target. Allocation was generated by computer and concealed with sealed envelopes. The clinical team was aware of group assignment because oxygen administration had to be titrated, whereas laboratory personnel were blinded. Biomarker samples were collected before anesthesia induction, 30 minutes after aortic cross-clamp removal, at the end of surgery, and 6 hours postoperatively. Sixty-four participants were randomized (32 per group), and 59 participants were included in the final analysis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Enrollment
64
The fraction of inspired oxygen was actively titrated during anesthesia and cardiopulmonary bypass to achieve an arterial oxygen tension (PaO2) of 200 mmHg or greater. The assigned strategy was maintained intraoperatively, subject to predefined cerebral oxygen saturation safety management.
The fraction of inspired oxygen was actively titrated during anesthesia and cardiopulmonary bypass to achieve an arterial oxygen tension (PaO2) from 80 to less than 200 mmHg. The assigned strategy was maintained intraoperatively, subject to predefined cerebral oxygen saturation safety management.
University of Health Sciences Bursa Yüksek İhtisas Training and Research Hospital
Bursa, Bursa, Turkey (Türkiye)
Native Thiol Concentration
Serum native thiol concentration measured by the automated spectrophotometric thiol-disulfide homeostasis method and reported in micromoles per liter (micromol/L).
Time frame: Before anesthesia induction; 30 minutes after aortic cross-clamp removal; at the end of surgery; and 6 hours postoperatively
Total Thiol Concentration
Serum total thiol concentration measured by the automated spectrophotometric thiol-disulfide homeostasis method and reported in micromoles per liter (micromol/L).
Time frame: Before anesthesia induction; 30 minutes after aortic cross-clamp removal; at the end of surgery; and 6 hours postoperatively
Disulfide Concentration
Serum disulfide concentration calculated as one half of the difference between total thiol and native thiol concentrations and reported in micromoles per liter (micromol/L).
Time frame: Before anesthesia induction; 30 minutes after aortic cross-clamp removal; at the end of surgery; and 6 hours postoperatively
Disulfide-to-Native Thiol Ratio
The ratio of serum disulfide concentration to native thiol concentration, calculated and reported as a percentage.
Time frame: Before anesthesia induction; 30 minutes after aortic cross-clamp removal; at the end of surgery; and 6 hours postoperatively
Disulfide-to-Total Thiol Ratio
The ratio of serum disulfide concentration to total thiol concentration, calculated and reported as a percentage.
Time frame: Before anesthesia induction; 30 minutes after aortic cross-clamp removal; at the end of surgery; and 6 hours postoperatively
Native Thiol-to-Total Thiol Ratio
The ratio of serum native thiol concentration to total thiol concentration, calculated and reported as a percentage.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Time frame: Before anesthesia induction; 30 minutes after aortic cross-clamp removal; at the end of surgery; and 6 hours postoperatively
Ischemia-Modified Albumin Level
Serum ischemia-modified albumin measured using the albumin cobalt-binding assay and reported in absorbance units (ABSU).
Time frame: Before anesthesia induction; 30 minutes after aortic cross-clamp removal; at the end of surgery; and 6 hours postoperatively