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The small for gestational age infant: accelerated or delayed pulmonary maturation? Increased or decreased survival?

J E Tyson1, K Kennedy, S Broyles

  • 1Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas 75235-9063, USA.

Pediatrics
|April 1, 1995
PubMed

Insights

Small for gestational age (SGA) neonates do not have accelerated pulmonary maturation and a lower risk of respiratory distress syndrome (RDS). Instead, SGA infants face increased risks for RDS, respiratory failure, and death compared to appropriate for gestational age (AGA) infants.

Area of Science:

  • Neonatal Medicine
  • Perinatal Research
  • Pediatric Pulmonology

Background:

  • Small for gestational age (SGA) neonates are often presumed to have accelerated pulmonary maturation, leading to a reduced risk of respiratory distress syndrome (RDS).
  • This widely held belief has not been rigorously investigated, necessitating a direct comparison between SGA and appropriate for gestational age (AGA) neonates.

Purpose of the Study:

  • To compare the risk of RDS, respiratory failure, and mortality in SGA infants versus AGA infants of the same gestational age.
  • To critically evaluate the concept of accelerated lung maturation in SGA neonates.

Main Methods:

  • Retrospective analysis of neonates born to an indigent population at a large county hospital.
  • Multivariate analyses were conducted, controlling for gestational age (GA), race, sex, and congenital anomalies.
  • Separate analyses utilized different gestational age estimates and intrauterine growth grids to define SGA status.

Main Results:

  • SGA infants did not demonstrate better outcomes than AGA infants across any analysis.
  • SGA infants exhibited a significantly increased risk of RDS in some analyses and a markedly higher risk of respiratory failure and death in most analyses.
  • The increased risk associated with being SGA was comparable to that of being male or of White race.

Conclusions:

  • The prevailing concept that intrauterine growth restriction accelerates lung maturation and improves neonatal outcomes is not supported by this study.
  • The findings challenge the established understanding of lung development in SGA infants and call for a critical re-evaluation of this widely accepted notion.
Abstract

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