Prelabor rupture of membranes between 34 and 37 weeks: the intraamniotic inflammatory response and neonatal outcomes

Marian Kacerovsky1, Ivana Musilova2, Ctirad Andrys3

  • 1Biomedical Research Center, University Hospital in Hradec Kralove, Hradec Kralove, Czech Republic; Department of Obstetrics and Gynecology, Charles University in Prague, Faculty of Medicine in Hradec Kralove, Hradec Kralove, Czech Republic.

Abstract

Insights

Microbial invasion of the amniotic cavity (MIAC) and acute histologic chorioamnionitis (HCA) significantly increase intraamniotic inflammation and early-onset sepsis in preterm prelabor rupture of membranes (PPROM) between 34-37 weeks.

Area of Science:

  • Obstetrics and Gynecology
  • Maternal-Fetal Medicine
  • Neonatology

Background:

  • Preterm prelabor rupture of membranes (PPROM) between 34-37 weeks is a significant obstetric complication.
  • Microbial invasion of the amniotic cavity (MIAC) and acute histologic chorioamnionitis (HCA) are potential contributors to adverse pregnancy outcomes.
  • The interplay between MIAC, HCA, and neonatal morbidity requires further elucidation.

Purpose of the Study:

  • To investigate the impact of MIAC and HCA on the intraamniotic inflammatory response.
  • To assess the association between MIAC, HCA, and neonatal morbidity in PPROM pregnancies (34-37 weeks).

Main Methods:

  • Amniocentesis was performed on 99 women with PPROM (34-37 weeks) to determine MIAC and interleukin-6 (IL-6) levels.
  • Placental evaluation for HCA was conducted post-delivery.
  • Neonatal outcomes, including early-onset sepsis, were recorded.

Main Results:

  • Women with both MIAC and HCA exhibited the highest IL-6 concentrations, indicating a heightened inflammatory response.
  • The combined presence of MIAC and HCA was associated with the highest incidence of early-onset sepsis in newborns.
  • Individual presence of MIAC or HCA also correlated with increased inflammation and sepsis risk compared to neither.

Conclusions:

  • Both MIAC and HCA significantly influence the intensity of the intraamniotic inflammatory response in PPROM (34-37 weeks).
  • The presence of MIAC and HCA increases the risk of neonatal early-onset sepsis.
  • Clinical management of PPROM should consider the intensity of the intraamniotic inflammatory response, informed by MIAC and HCA status.

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