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Licensed Unlicensed Requires Authentication Published by De Gruyter August 5, 2014

Is there a stepwise increase in neonatal morbidities according to histological stage (or grade) of acute chorioamnionitis and funisitis?: effect of gestational age at delivery

  • Yeri Lee , Hyun-Joo Kim , Suk-Joo Choi , Soo-young Oh EMAIL logo , Jung-Sun Kim EMAIL logo , Cheong-Rae Roh and Jong-Hwa Kim

Abstract

Aims: To test if there is a stepwise difference in neonatal outcomes according to the stage (or grade) of histological inflammatory response in the chorioamniotic membranes and umbilical cords of preterm premature rupture of membranes (PPROM).

Method: This retrospective study included singleton pregnancies diagnosed as PPROM and delivered prior to 34 weeks of gestation (n=339). Acute histological chorioamnionitis and funisitis were subdivided into stages (or grade) as defined by Redline et al. Neonatal composite morbidities and mortality were also monitored. Univariate and multivariate analyses were conducted.

Results: Increasing stage (or grade) of acute histological chorioamnionitis and funisitis was significantly associated with an earlier gestational age at membrane rupture and delivery. Among neonatal outcomes, respiratory distress syndrome (RDS), bronchopulmonary dysplasia (BPD), intraventricular hemorrhage, retinopathy of prematurity, and composite morbidity showed incremental incidence according to increased stage (or grade) of acute chorioamnionitis, while periventricular leukomalacia and necrotizing enterocolitis did not. Only RDS, BPD, and composite morbidity showed similar incremental incidences associated with severity of funisitis stage. However, the incremental trends of each neonatal outcome were found to be nonsignificant by multivariate analysis adjusting confounding variables including gestational age at delivery.

Conclusion: Higher incidences of neonatal morbidity according to increased stage (or grade) of either acute histological chorioamnionitis or funisitis were due to an earlier gestational age at delivery.


Corresponding authors: Soo-young Oh, MD, PhD, Department of Obstetrics and Gynecology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Ilwon-dong, Gangnam-gu, Seoul 135-710, South Korea, Tel.: +82-2-3410-3517, Fax: +82-2-3410-0630, e-mail: and Jung-Sun Kim, MD, PhD, Department of Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Ilwon-dong, Gangnam-gu, Seoul 135-710, South Korea, Tel.: +82-2-3410-2767, Fax: +82-2-3410-0025, e-mail:

Funding statement: Funding: This study was supported by a grant of the Korean Health Technology R&D Project, Ministry of Health & Welfare, Republic of Korea (South Korea) [HI12C0024(A120035)].

Acknowledgments

The authors thank Sook-Young Woo, MS (Samsung Biomedical Research Institute, Biostatistic Team, Seoul, South Korea) for technical support of the statistical analysis of this study.

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Supplemental Material

The online version of this article (DOI: 10.1515/jpm-2014-0035) offers supplementary material, available to authorized users.


The authors stated that there are no conflicts of interest regarding the publication of this article.

Received: 2014-2-3
Accepted: 2014-7-7
Published Online: 2014-8-5
Published in Print: 2015-3-1

©2015 by De Gruyter

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