Similar adverse outcome rates with high or low oxygen saturation targets in an area with low background mortality
Nina Willgerodt1, Christoph Bührer2, Rainer Rossi3
1Division of Neonatology, University Hospital for Children, Leipzig, Germany.
Insights
Lower oxygen saturation targets in extremely preterm infants did not increase safety risks. This retrospective study found no significant differences in mortality or retinopathy of prematurity between high and low oxygen saturation groups.
Area of Science:
- Neonatal Intensive Care
- Pediatric Medicine
- Clinical Research
Background:
- Randomized trials suggest lower mortality with high oxygen saturation targets in very preterm infants.
- High oxygen saturation is linked to increased retinopathy of prematurity and bronchopulmonary dysplasia.
- Benefit-to-harm ratio of oxygen saturation targets may vary with local mortality risk.
Purpose of the Study:
- To quantify risk-benefit ratios of different oxygen saturation (SpO2) target ranges.
- To evaluate SpO2 targets in 10 tertiary newborn intensive care units (NICUs) in East Germany.
Main Methods:
- Retrospective multicenter study of 1,399 infants (2008-2012).
- Infants born between 24 0/7 and 27 6/7 weeks gestational age, birthweight <1,250g.
- Grouped by high (HOSG, >90%) vs. low (LOSG, <90%) SpO2 target ranges and unit compliance.
Main Results:
- Five NICUs were HOSG, five were LOSG; nine met their targets.
- Necrotizing enterocolitis and severe intraventricular hemorrhage were more frequent in HOSG.
- No significant differences in mortality or retinopathy of prematurity rates between groups.
Conclusions:
- Lower SpO2 target range was not associated with increased safety risks in this population.
- Study limitations include retrospective design and variations in site practices, precluding definitive causal links.
Background:
Randomized controlled trials have indicated reduced mortality rates in very preterm infants assigned to high compared to low oxygen saturation (SpO2) target levels, accompanied by higher rates of retinopathy of prematurity and bronchopulmonary dysplasia. However, the benefit-to-harm ratio may depend on the local background mortality risk. We therefore aimed to quantify the risk-benefit ratios of different SpO2 target ranges in 10 tertiary newborn intensive care units (NICUs) in East Germany.
Methods:
In a retrospective multicenter study, 1,399 infants born between 2008 and 2012 at a gestational age between 24 0/7 and 27 6/7 weeks and with a birthweight below 1,250 g were grouped according to the hospital's target SpO2 range [high oxygen saturation group (HOSG) above 90%], low oxygen saturation group (LOSG) below 90%] and the compliance of units with their target SpO2 range. The association between neonatal morbidities, neurodevelopmental outcomes, selected treatment strategies, and target SpO2 ranges was calculated using chi-squared and Mann Whitney U tests.
Results:
Nine of the ten participating NICUs met their SpO2 target ranges. Five units were considered as HOSG, and five units were considered as LOSG. Necrotizing enterocolitis and intraventricular hemorrhage grade ≥ 2 occurred significantly more frequently in the HOSG than in the LOSG (8.4% vs. 5.1%, p = 0.02; and 26.6% vs. 17.7%, p < 0.001). No significant differences in the mortality rate and the rate of retinopathy of prematurity were found.
Conclusion:
In our patient population, a lower SpO2 target range was not associated with increased safety risks in extremely preterm infants. We cannot be sure that our outcome differences are associated with differences in oxygen saturations due to the retrospective study design and the differences in site practices.
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