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Effects of 100% oxygen during deferred cord clamping on oxidative stress markers: a sub-study of a randomized
Anup C Katheria1, Satyan Lakshminrusimha2, Ana Morales3
1Neonatal Research Institute, Sharp Mary Birch Hospital for Women & Newborns, San Diego, CA, USA. anup.katheria@sharp.com.
Insights
This study found no significant difference in oxidative stress markers between premature infants receiving 100% or 30% oxygen during deferred cord clamping (DCC). Further research is needed to clarify redox effects in neonatal resuscitation.
Area of Science:
- Neonatal physiology and oxidative stress research.
- Biomarker analysis in premature infants.
Background:
- Premature infants are vulnerable to oxidative stress.
- Deferred cord clamping (DCC) is a common practice in neonatal care.
- Oxygen administration during DCC may influence oxidative changes.
Purpose of the Study:
- To evaluate oxidative changes in premature infants receiving 100% oxygen versus 30% oxygen during DCC.
- To compare reduced-to-oxidized glutathione (GSH/GSSG) ratios between oxygen groups.
Main Methods:
- Premature infants (220/7-286/7 weeks) received DCC with either 30% or 100% oxygen.
- Blood samples were collected from umbilical segments and postnatal lines.
- GSH/GSSG ratios were analyzed using liquid chromatography-tandem mass spectrometry.
Main Results:
- No statistically significant differences in GSH/GSSG ratios were observed between the 100% and 30% oxygen groups in arterial cord blood, venous cord blood, or postnatal samples.
- Gestational age was similar between groups (median 264/7 weeks).
Conclusions:
- Brief oxygen administration (30% vs. 100%) during DCC did not show significant differences in GSH/GSSG ratios.
- Redox effects remain unclear due to high variability and limited statistical power.
- Further studies are required to understand oxidative damage during neonatal resuscitation and DCC.
Background:
We sought to evaluate oxidative changes in premature infants receiving 100% oxygen compared with 30% during deferred cord clamping (DCC).
Methods:
Premature infants born at 220/7 to 286/7 weeks received DCC in conjunction with either 30% (LO Group) or 100% (HI Group) oxygen. Blood was extracted from a preserved umbilical segment and a postnatal sample was collected from umbilical vascular lines within two hours of birth. Reduced-to-oxidized glutathione (GSH/GSSG) ratios were analyzed using liquid chromatography coupled to tandem mass spectrometry.
Results:
Sixty-eight infants had data available for analysis. The median (IQR) gestational age of infants was 264/7 (246/7, 282/7) weeks in both groups. Among infants receiving 100% versus 30% oxygen, median (IQR) GSH/GSSG ratio were not statistically different in arterial cord blood [7.5 (0.6, 290) vs 37 (1.1, 265), p = 0.52] or venous cord blood [8.4 (2,50) vs 76 (5, 210), p = 0.12] or postnatal samples [14 (2, 290) vs 8 (2, 280), p = 0.98)].
Conclusion:
Briefly providing 30% vs. 100% oxygen for 90 seconds during DCC showed no significant difference in GSH/GSSG ratios, but redox effects remain unclear given variability, sample size and limited power. Further studies are needed to ascertain potential oxidative damage during neonatal resuscitation and deferred cord clamping. THIS TRIAL IS REGISTERED ON CLINICALTRIALS.
Gov Id:
NCT04413097 IMPACT: The effect of oxygen administration during deferred cord clamping on redox status is unclear due to large variability in GSH and GSSG values and small sample size. These data provide some insights about umbilical arterial and venous oxygen levels and the effect of placenta on GSH/GSSG in preterm infants. Further basic and clinical studies are needed to better ascertain the potential for oxidative damage during neonatal resuscitation and deferred cord clamping.
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