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Hydrocortisone to Improve Survival without Bronchopulmonary Dysplasia

  • Eunice Kennedy Shriver NICHD Neonatal Research Network
  • University of New Mexico
  • Case Western Reserve University
  • RTI International
  • Wayne State University
  • Central Michigan University
  • University of Rochester
  • Duke University
  • Stanford University
  • University of North Carolina at Chapel Hill
  • University of Utah
  • University of Texas Health Science Center at Houston
  • Brown University
  • Indiana University Bloomington
  • University of Cincinnati
  • Emory University
  • University of Alabama at Birmingham
  • Children's Mercy Hospitals and Clinics
  • University of Pennsylvania
  • University of Texas Southwestern Medical Center
  • University of California at Los Angeles
  • Ohio State University
  • University of Iowa
  • University of South Dakota

Research output: Contribution to journalArticlepeer-review

103 Scopus citations

Abstract

Background: Bronchopulmonary dysplasia is a prevalent complication after extremely preterm birth. Inflammation with mechanical ventilation may contribute to its development. Whether hydrocortisone treatment after the second postnatal week can improve survival without bronchopulmonary dysplasia and without adverse neurodevelopmental effects is unknown. Methods: We conducted a trial involving infants who had a gestational age of less than 30 weeks and who had been intubated for at least 7 days at 14 to 28 days. Infants were randomly assigned to receive either hydrocortisone (4 mg per kilogram of body weight per day tapered over a period of 10 days) or placebo. Mandatory extubation thresholds were specified. The primary efficacy outcome was survival without moderate or severe bronchopulmonary dysplasia at 36 weeks of postmenstrual age, and the primary safety outcome was survival without moderate or severe neurodevelopmental impairment at 22 to 26 months of corrected age. Results: We enrolled 800 infants (mean [±SD] birth weight, 715±167 g; mean gestational age, 24.9±1.5 weeks). Survival without moderate or severe bronchopulmonary dysplasia at 36 weeks occurred in 66 of 398 infants (16.6%) in the hydrocortisone group and in 53 of 402 (13.2%) in the placebo group (adjusted rate ratio, 1.27; 95% confidence interval [CI], 0.93 to 1.74). Two-year outcomes were known for 91.0% of the infants. Survival without moderate or severe neurodevelopmental impairment occurred in 132 of 358 infants (36.9%) in the hydrocortisone group and in 134 of 359 (37.3%) in the placebo group (adjusted rate ratio, 0.98; 95% CI, 0.81 to 1.18). Hypertension that was treated with medication occurred more frequently with hydrocortisone than with placebo (4.3% vs. 1.0%). Other adverse events were similar in the two groups. Conclusions: In this trial involving preterm infants, hydrocortisone treatment starting on postnatal day 14 to 28 did not result in substantially higher survival without moderate or severe bronchopulmonary dysplasia than placebo. Survival without moderate or severe neurodevelopmental impairment did not differ substantially between the two groups.

Original languageEnglish
Pages (from-to)1121-1131
Number of pages11
JournalNew England Journal of Medicine
Volume386
Issue number12
DOIs
StatePublished - Mar 24 2022

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