Role of Intrauterine Infectious and Inflammatory Complications in the Development of Necrotizing Enterocolitis in a

Jana Leskova, Marian Kacerovsky1, Julie Ledvinova2,3,4

  • 1Department of Pediatric Surgery and Traumatology, University Hospital Hradec Kralove, Charles University, Faculty of Medicine in Hradec Kralove, Hradec Kralove, Czechia.

PubMed
Abstract

Insights

Microbial invasion of the amniotic cavity (MIAC) and acute histological chorioamnionitis (HCA) do not increase the risk of necrotizing enterocolitis (NEC) in infants born after preterm prelabor rupture of membranes (PPROM). This finding suggests these infections are not predictive of NEC development.

Area of Science:

  • Perinatal Medicine
  • Neonatalogy
  • Infectious Disease

Background:

  • Preterm prelabor rupture of membranes (PPROM) is a significant risk factor for adverse neonatal outcomes.
  • Microbial invasion of the amniotic cavity (MIAC) and acute histological chorioamnionitis (HCA) are common complications of PPROM.
  • Necrotizing enterocolitis (NEC) is a serious gastrointestinal condition affecting preterm infants.

Purpose of the Study:

  • To investigate the association between MIAC and/or HCA in pregnancies with PPROM and the subsequent development of NEC in neonates.
  • To determine if specific subtypes of MIAC or HCA influence NEC risk.

Main Methods:

  • Retrospective study of 295 singleton pregnancies with PPROM (24-31 weeks gestation).
  • Transabdominal amniocentesis for MIAC detection (cultivated and non-cultivated methods).
  • Histopathological placental examination for HCA; NEC defined by modified Bell's criteria (stage IIa).

Main Results:

  • NEC developed in 3% of newborns.
  • No significant differences in MIAC rates between NEC and non-NEC groups (p=0.33).
  • No significant differences in HCA rates (with or without fetal inflammatory response, or with amnion inflammation) between NEC and non-NEC groups (p=1.00, p=0.52, p=0.20 respectively).

Conclusions:

  • Neither MIAC nor HCA is associated with an increased risk of NEC in neonates born from pregnancies complicated by PPROM.
  • These findings suggest that intra-amniotic infection markers may not be reliable predictors for NEC development in this specific preterm population.

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