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DOI 10.1038/pr.2017.300

Медицинская библиотека · Pediatric research · 2017

Late preterm prelabor rupture of fetal membranes: fetal inflammatory response and neonatal outcome.

Musilova Ivana, Andrys Ctirad, Drahosova Marcela, Zednikova Barbora, Hornychova Helena, Pliskova Lenka, Zemlickova Helena, Jacobsson Bo, Kacerovsky Marian

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BackgroundTo characterize the influence of microbial invasion of the amniotic cavity (MIAC) and/or intra-amniotic inflammation (IAI) on the intensity of the fetal inflammatory response and the association between the presence of the fetal inflammatory response syndrome (FIRS) and short-term neonatal morbidity in the preterm prelabor rupture of membranes (PPROM) between the gestational ages of 34 and 37 weeks.MethodsOne hundred and fifty-nine women were included in the study. The umbilical cord blood interleukin (IL)-6 concentrations were determined using enzyme-linked immunosorbent assay kits. FIRS was defined based on the umbilical cord blood IL-6 concentration and the presence of funisitis and/or chorionic plate vasculitis.ResultsWomen with both MIAC and IAI had the highest median umbilical cord blood IL-6 concentrations and highest rates of FIRS. Women with FIRS had the higher rates of early-onset sepsis and intraventricular hemorrhage grades I and II when FIRS was characterized based on the umbilical cord blood IL-6 concentrations and the histopathological findings.ConclusionThe presence of both MIAC and IAI was associated with a higher fetal inflammatory response and a higher rate of FIRS. Different aspects of short-term neonatal morbidity were related to FIRS when defined by umbilical cord blood IL-6 concentrations and the histopathology of the placenta.

Для цитирования: Musilova Ivana, Andrys Ctirad, Drahosova Marcela, Zednikova Barbora, Hornychova Helena, Pliskova Lenka, Zemlickova Helena, Jacobsson Bo, Kacerovsky Marian. Late preterm prelabor rupture of fetal membranes: fetal inflammatory response and neonatal outcome.. Pediatric research. 2017. DOI: 10.1038/pr.2017.300.

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