Key result
Perioperative hyperoxia blunts surfactant protein-A increases vs normoxia and is linked to higher postoperative TNF-α.
Why the study?
Perioperative oxygen therapy is routine during general anesthesia, but its early biological consequences remain incompletely understood.
Does perioperative hyperoxia influence early biomarker responses in adults undergoing elective laparoscopic lower abdominal surgery?
RCT
Does perioperative hyperoxia influence early biomarker responses in adults undergoing elective laparoscopic lower abdominal surgery?
Perioperative hyperoxia during laparoscopic surgery alters early pulmonary epithelial and inflammatory biomarker trajectories compared to normoxia, though clinical implications remain unclear.
Answers are grounded in this paper and cite their sources.
Perioperative hyperoxia may blunt early biomarker rises; extends mechanistic data but leaves clinical outcome effects open.
Although perioperative oxygen therapy is a routine component of general anesthesia, its early biological consequences remain incompletely understood. This prospective randomized study evaluated whether perioperative oxygen concentration influences early biomarker responses in adults undergoing elective laparoscopic lower abdominal surgery. Patients received either normoxia (FiO2 0.35) or hyperoxia (FiO2 0.80) under standardized anesthesia. Clear physiological separation between groups was confirmed by arterial blood gas analysis. The primary biomarker finding was that circulating surfactant protein-A (SP-A) increased significantly in the normoxia group, whereas no comparable increase was observed under hyperoxia. Syndecan-1 and sialic acid showed descriptively similar directional patterns; however, these secondary biomarker findings were interpreted as exploratory and were not robust after Holm correction. By contrast, tumor necrosis factor-alpha (TNF-α) levels were higher postoperatively in the hyperoxia group, while ischemia-modified albumin (IMA) and total protein did not differ significantly between groups. These findings suggest that perioperative hyperoxia was associated with different early circulating biomarker trajectories across pulmonary epithelial and glycocalyx-related domains, without establishing pulmonary or endothelial protection. Further studies are needed to determine whether these early mechanistic findings translate into clinically meaningful outcomes.
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Guliyeva et al. (2026) conducted an RCT in Elective laparoscopic lower abdominal surgery. Perioperative hyperoxia vs. Normoxia (FiO2 0.35) was evaluated on Circulating surfactant protein-A (SP-A) trajectory. Perioperative hyperoxia blunted the significant increase in circulating surfactant protein-A seen with normoxia and was associated with higher postoperative TNF-α levels.
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