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Published on: August 19, 2020
Perioperative Normoxia vs Hyperoxia in Neonates With Cyanotic Heart Disease Undergoing Cardiac Surgery: A Randomized
Nathaniel Sznycer-Taub1, Yun-Wen Peng1, Sunkyung Yu1
1Division of Pediatric Cardiology, Department of Pediatrics, University of Michigan, Ann Arbor, Michigan.
Background:
Exposure to supraphysiologic levels of oxygen has been associated with end-organ damage and worse outcomes across multiple populations related to oxidative stress and inflammation. There is limited evidence to guide practice in children undergoing surgery with cardiopulmonary bypass, including neonates with cyanotic congenital heart disease, who are particularly vulnerable to oxidative stress due to immature and depleted antioxidant defenses.
Methods:
We conducted a randomized trial of perioperative normoxia (goal PaO2 60-100 mm Hg during cardiopulmonary bypass and for the first 24 hours) vs hyperoxia (goal PaO2 200-300 mm Hg during cardiopulmonary bypass) exclusively in cyanotic neonates to examine feasibility, systemic oxidative stress response, and safety. The primary outcome was a serum measure of oxidative stress: thiobarbituric acid reactive substances. Additional biomarkers and clinical outcomes were collected.
Results:
Twenty-nine neonates (median age, 5 days) were enrolled. Mean PaO2 in the normoxia arm (n = 15) during cardiopulmonary bypass was 106 ± 27 mm Hg (vs hyperoxia 256 ± 29 mm Hg, P < .0001). Mean postoperative thiobarbituric acid reactive substances expressed as fold-change from baseline was lower in the normoxia arm at 2 hours (1.21 ± 0.26 vs 1.93 ± 0.63), 6 hours (1.09 ± 0.25 vs 1.77 ± 0.7), and 24 hours (0.96 ± 0.16 vs 1.41 ± 0.29); all P < .01. Other biomarkers of oxidative stress were significantly lower in the normoxia arm (all time points P < .01). Safety outcomes including in-hospital mortality and morbidities were similar between arms.
Conclusions:
Controlled normoxia during cardiopulmonary bypass in cyanotic neonates is feasible, safe, and associated with significant improvement in measures of oxidative stress. These data are critical in informing larger-scale studies of end-organ injury and clinical outcomes.
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