AI Article Synopsis

  • The study aimed to analyze how different grades of histological chorioamnionitis (HCA) are related to gestational age in both term and preterm pregnancies.
  • It involved 392 women with spontaneous labor, classifying placentas into three HCA grades based on histological findings, and included microbiological cultures from placental and fetal membranes.
  • Results indicated that certain HCA grades were more common at specific gestational ages, with a notable increase in positive bacterial cultures associated with the most severe form, HCA3, highlighting different underlying causes and immune responses based on gestational age.

Article Abstract

Objective: The aim of this study was to investigate the rate of the different histological chorioamnionitis (HCA) grade in relation to the gestational age in term and preterm delivery.

Methods: Three hundred and ninety-two women with singleton pregnancy with spontaneous onset of labor either prematurely or at term, with histologic diagnosis of HCA, were enrolled. Placentas were classified as: deciduitis and/or histologic chorioamnionitis within the membranes (HCA1); amnionitis or inflammation of the chorionic plate without funisitis (HCA2); and histologic chorioamnionitis with funisitis (HCA3). Microbiological culture was performed on both placental and fetal membrane samples.

Results: HCA1 was more frequent in women delivering at term than in preterm (p < 0.001). HCA2 was more represented in women delivering between 32 and 36 weeks (p < 0.001) and HCA3 occurred more frequently in those delivering within 32 weeks (p < 0.001). The positive bacterial culture was higher (p = 0.008) in presence of HCA3 in comparison with HCA1 and HCA2.

Conclusions: This study showed a significantly different distribution of HCA grades in relation to gestational age at delivery. HCA may represent the expression of different subtending etiologies and may also reflect specific immune competence of gestational tissues at different gestational ages, strengthening as pregnancy advances.

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Source
http://dx.doi.org/10.3109/14767058.2013.846313DOI Listing

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