The combined exposure to intra-amniotic inflammation and neonatal respiratory distress syndrome increases the risk of intraventricular hemorrhage in preterm neonates

Author:

Oh Kyung Joon12,Park Jee Yoon1,Lee JoonHo3,Hong Joon-Seok12,Romero Roberto4567,Yoon Bo Hyun1

Affiliation:

1. Department of Obstetrics and Gynecology , Seoul National University College of Medicine , Seoul , Korea

2. Department of Obstetrics and Gynecology , Seoul National University Bundang Hospital , Seongnam-si , Korea

3. Department of Obstetrics and Gynecology , Yonsei University College of Medicine , Seoul , Korea

4. Perinatology Research Branch, NICHD/NIH/DHHS , Bethesda, MD, USA , and Detroit, MI , USA

5. Department of Obstetrics and Gynecology , University of Michigan , Ann Arbor, MI , USA

6. Department of Epidemiology and Biostatistics , Michigan State University , East Lansing, MI , USA

7. Center for Molecular Medicine and Genetics , Wayne State University , Detroit, MI , USA

Abstract

Abstract Objective: To evaluate the impact of combined exposure to intra-amniotic inflammation and neonatal respiratory distress syndrome (RDS) on the development of intraventricular hemorrhage (IVH) in preterm neonates. Methods: This retrospective cohort study includes 207 consecutive preterm births (24.0–33.0 weeks of gestation). Intra-amniotic inflammation was defined as an amniotic fluid matrix metalloproteinase-8 concentration >23 ng/mL. According to McMenamin’s classification, IVH was defined as grade II or higher when detected by neurosonography within the first weeks of life. Results: (1) IVH was diagnosed in 6.8% (14/207) of neonates in the study population; (2) IVH was frequent among newborns exposed to intra-amniotic inflammation when followed by postnatal RDS [33% (6/18)]. The frequency of IVH was 7% (8/115) among neonates exposed to either of these conditions – intra-amniotic inflammation or RDS – and 0% (0/64) among those who were not exposed to these conditions; and (3) Neonates exposed to intra-amniotic inflammation and postnatal RDS had a significantly higher risk of IVH than those with only intra-amniotic inflammation [odds ratio (OR) 4.6, 95% confidence interval (CI) 1.1–19.3] and those with RDS alone (OR 5.6, 95% CI 1.0–30.9), after adjusting for gestational age. Conclusion: The combined exposure to intra-amniotic inflammation and postnatal RDS markedly increased the risk of IVH in preterm neonates.

Publisher

Walter de Gruyter GmbH

Subject

Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health

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