Time-related changes in steroid use and bronchopulmonary dysplasia in preterm infants

Bradley A Yoder1, Megan Harrison, Reese H Clark

  • 1aDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah 84158-1289, USA. bradley.yoder@hsc.utah.edu

Pediatrics
|July 22, 2009
PubMed

Insights

Decreased use of dexamethasone (DEX) in premature infants was linked to higher rates of bronchopulmonary dysplasia (BPD). Hydrocortisone (HC) use increased as DEX use declined, highlighting a shift in steroid management for neonates.

Area of Science:

  • Neonatal Medicine
  • Pediatric Pulmonology
  • Pharmacology

Background:

  • Bronchopulmonary dysplasia (BPD) remains a significant concern in extremely preterm infants.
  • Steroid use, including dexamethasone (DEX) and hydrocortisone (HC), has been explored for managing BPD.
  • Trends in steroid use and their impact on BPD incidence require ongoing evaluation.

Purpose of the Study:

  • To analyze temporal trends in the use of dexamethasone (DEX) and hydrocortisone (HC) in premature infants.
  • To investigate the association between changing steroid use patterns and the incidence of bronchopulmonary dysplasia (BPD) at 36 weeks' postmenstrual age.

Main Methods:

  • Analysis of a large cohort (N=77520) of neonates born between 23 to 32 weeks' gestation (1997-2006).
  • Comparison of DEX and HC usage, and BPD rates (defined by oxygen use at 36 weeks' postmenstrual age) across different years and gestational ages.
  • Statistical analysis using Mantel-Haenszel chi-squared tests to assess trends.

Main Results:

  • Dexamethasone (DEX) use significantly decreased from 25.0% in 1998 to 6.8% in 2006, while hydrocortisone (HC) use increased.
  • The median age for initiating DEX therapy increased by over two weeks during the study period.
  • Overall BPD rates rose from 19% to 25% between 1997 and 2006, with a notable increase in severe BPD and a significant association between decreased DEX use and increased BPD rates in infants between 23 and 28 weeks' gestation.

Conclusions:

  • Significant shifts in steroid preferences (away from DEX, towards HC) occurred in neonatal care over a decade.
  • Reduced dexamethasone (DEX) administration correlated with increased incidence of bronchopulmonary dysplasia (BPD), including severe cases, in very preterm infants.
  • Further high-quality randomized trials are necessary to guide optimal steroid therapy and long-term outcomes for high-risk infants.
Abstract

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