The late preterm infant and the control of breathing, sleep, and brainstem development: a review

Robert A Darnall1, Ronald L Ariagno, Hannah C Kinney

  • 1Department of Physiology, Dartmouth-Hitchcock Medical Center, Lebanon, NH 03756, USA. robert.a.darnall@hitchcock.org

Clinics in Perinatology
|December 7, 2006
PubMed

Insights

Late preterm infants (33-38 weeks gestation) show immature brainstem development, impacting breathing and feeding coordination. Further research is crucial for understanding and managing these infants.

Area of Science:

  • Neonatal neuroscience
  • Developmental pediatrics
  • Respiratory physiology

Background:

  • Late preterm infants (33-38 weeks gestation) exhibit less mature brainstem development compared to full-term infants.
  • Significant, nonlinear developmental changes occur in the brainstem during late gestation.
  • This immaturity affects upper airway control, lung volume regulation, laryngeal reflexes, breathing's chemical control, and sleep patterns.

Purpose of the Study:

  • To investigate the neurodevelopmental aspects of late preterm infants.
  • To address the paucity of clinical, physiological, neuroanatomic, and neurochemical data in this population.
  • To improve the understanding and management strategies for late preterm infants.

Main Methods:

  • The study focuses on analyzing existing data and highlighting research gaps.
  • It emphasizes the need for clinical, physiological, neuroanatomic, and neurochemical investigations.
  • Research will concentrate on brainstem maturation during the high-risk late preterm period.

Main Results:

  • Ten percent of late preterm infants experience significant apnea of prematurity.
  • These infants often present with delayed coordination of feeding and breathing.
  • Brainstem immaturity is linked to impaired control of vital functions.

Conclusions:

  • Late preterm infants require focused research to understand their unique developmental trajectory.
  • Enhanced knowledge of brainstem maturation is essential for targeted clinical interventions.
  • Developing specific management plans will improve outcomes for these vulnerable infants.

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