Aberrant Hematopoiesis and Morbidity in Extremely Preterm Infants With Intrauterine Growth Restriction

Nora J Reibel1, Christof Dame1, Christoph Bührer1

  • 1Department of Neonatology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Frontiers in Pediatrics
|December 6, 2021
PubMed

Insights

Infants born with intrauterine growth restriction (IUGR) and extremely low gestational age (ELGANs) experience significant hematological disturbances and higher rates of infection and severe pulmonary complications, including death.

Area of Science:

  • Neonatology
  • Pediatric Hematology
  • Perinatology

Background:

  • Intrauterine growth restriction (IUGR) presents unique challenges for extremely low gestational age newborns (ELGANs).
  • Understanding the impact of IUGR on neonatal hematopoiesis and associated morbidities is critical for improving outcomes.
  • Hematological profiles and clinical outcomes in IUGR-ELGANs require further investigation.

Purpose of the Study:

  • To assess the disturbed hematopoiesis in IUGR-ELGANs.
  • To evaluate the major morbidities and mortality associated with IUGR in ELGANs.
  • To compare hematological profiles and clinical outcomes between IUGR-ELGANs and non-IUGR ELGANs.

Main Methods:

  • A single-center retrospective case-control study.
  • Comparison of 49 IUGR-ELGANs (gestational age <28 weeks, birth weight ≤ 3rd percentile) with 98 matched non-IUGR ELGANs (birth weight >10th percentile).
  • Analysis of perinatal hematological profiles, blood product transfusions, antibiotic use, morbidities, and mortality.

Main Results:

  • IUGR-ELGANs exhibited elevated nucleated red blood cells and reduced neutrophil and platelet counts.
  • IUGR-ELGANs required more transfusions (red blood cells, platelets, plasma) and intensive antibiotic treatment.
  • Significantly higher rates of early-onset infections, severe bronchopulmonary dysplasia or death, and overall mortality were observed in IUGR-ELGANs.

Conclusions:

  • IUGR-ELGANs demonstrate significant hematological abnormalities and a heightened risk of early-life infections.
  • Severe pulmonary morbidity, including bronchopulmonary dysplasia and mortality, is markedly increased in IUGR-ELGANs.
  • The high incidence of transfusions in IUGR-ELGANs necessitates further research and clinical scrutiny.

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