Oxygen Saturation Targets in Preterm Infants and Outcomes at 18-24 Months: A Systematic Review

Pediatrics. 2017 Jan;139(1):e20161609. doi: 10.1542/peds.2016-1609. Epub 2016 Dec 5.

Abstract

Context: The optimal oxygen saturation target for extremely preterm infants remains unclear.

Objective: To systematically review evidence evaluating the effect of lower (85%-89%) versus higher (91%-95%) pulse oxygen saturation (Spo2) target on mortality and neurodevelopmental impairment (NDI) at 18 to 24 months.

Data sources: Electronic databases and all published randomized trials evaluating lower versus higher Spo2 target in preterm infants.

Study selection: A total of 2896 relevant citations were identified; 5 trials were included in the final analysis.

Data extraction: Data from 5 trials were analyzed for quality of evidence and risk of bias.

Limitations: Limitations include heterogeneity in age at enrollment and comorbidities between trials and change in oximeter algorithm midway through 3 trials.

Results: There was no difference in the incidence of primary outcome (death/NDI at 18-24 months) in the 2 groups; risk ratio,1.05, 95% confidence interval 0.98-1.12, P = .18. Mortality before 18 to 24 months was higher in the lower-target group (risk ratio,1.16, 95% confidence interval 1.03-1.31, P = .02). Rates of NDI and severe visual loss did not differ between the 2 groups. Proportion of time infants spent outside the target range while on supplemental oxygen ranged from 8.2% to 27.4% <85% and 8.1% to 22.4% >95% with significant overlap between the 2 groups.

Conclusions: There was no difference in primary outcome between the 2 Spo2 target groups. The collective data suggest that risks associated with restricting the upper Spo2 target limit to 89% outweigh the benefits. The quality of evidence was moderate. We speculate that a wider target range (lower alarm limit, 89% and upper, 96%) may increase time spent within range, but the safety profile of this approach remains to be determined.

Publication types

  • Comparative Study
  • Review
  • Systematic Review

MeSH terms

  • Child, Preschool
  • Dose-Response Relationship, Drug
  • Humans
  • Infant
  • Infant, Extremely Premature / blood*
  • Infant, Newborn
  • Neurodevelopmental Disorders / blood
  • Neurodevelopmental Disorders / mortality
  • Outcome Assessment, Health Care*
  • Oximetry
  • Oxygen / blood*
  • Randomized Controlled Trials as Topic
  • Risk Assessment
  • Survival Rate

Substances

  • Oxygen