Early Hypoxic Respiratory Failure in Extreme Prematurity: Mortality and Neurodevelopmental Outcomes

Praveen Chandrasekharan1, Satyan Lakshminrusimha2, Dhuly Chowdhury3

  • 1Division of Neonatology, Department of Pediatrics, UBMD, University at Buffalo, Buffalo, New York; pkchandr@buffalo.edu.

Pediatrics
|September 18, 2020
PubMed

Insights

Extremely low birth weight infants with early hypoxemic respiratory failure face high mortality and neurodevelopmental impairment. Inhaled nitric oxide did not improve outcomes, with no significant differences observed in African American infants.

Area of Science:

  • Neonatalogy
  • Pediatric Critical Care
  • Respiratory Medicine

Background:

  • Extremely low birth weight (ELBW) infants, particularly those born at or before 26 weeks' gestation, are at high risk for respiratory complications.
  • Early hypoxemic respiratory failure (HRF) is a significant predictor of adverse outcomes in this vulnerable population.
  • Inhaled nitric oxide (iNO) is used to treat pulmonary hypertension, but its efficacy in improving survival and neurodevelopmental outcomes in ELBW infants with early HRF is not fully established.

Purpose of the Study:

  • To evaluate the survival and neurodevelopmental impairment (NDI) rates in ELBW infants experiencing early HRF at 18 to 26 months corrected age.
  • To assess the impact of inhaled nitric oxide (iNO) exposure on outcomes for ELBW infants with early HRF.
  • To specifically examine whether African American infants with early HRF experience different outcomes after iNO exposure compared to other racial groups.

Main Methods:

  • Retrospective cohort study of ELBW infants (≤1000 g, ≤26 weeks' gestation) born between 2007 and 2015.
  • Identification of infants with "early HRF" based on oxygen requirements (≥60% maximal oxygen on day 1 or 3).
  • Propensity score regression modeling was used to analyze outcomes, including mortality and NDI, and the effect of iNO exposure, stratified by race.

Main Results:

  • Of 7639 ELBW infants, 22.7% had early HRF, associated with a 51.3% mortality rate.
  • Among survivors, 41.2% had moderate-to-severe NDI at 18-26 months; iNO-treated infants had a 59.4% mortality rate.
  • While African American infants had similar HRF incidence, they received iNO less frequently. Intact survival among iNO-exposed infants did not differ significantly by race.

Conclusions:

  • Early HRF in preterm infants (≤26 weeks) is linked to substantial mortality and NDI.
  • The use of iNO in this cohort did not demonstrate a benefit in reducing mortality or NDI.
  • Outcomes following iNO exposure were comparable between African American and other racial groups.
Abstract

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