Placental histology predicted adverse outcomes in extremely premature neonates in Norway—population‐based study. (6th December 2021)

• Record Type: Journal Article
• Authors: Budal, Elisabeth B.; Ebbing, Cathrine; Kessler, Jørg; Bains, Sukhjeet; Haugen, Olav H.; Aukland, Stein M.; Eide, Geir Egil; Halvorsen, Thomas; Bentsen, Mariann H. L.; Collett, Karin
• Is Part Of: Acta pædiatrica. Volume 111:Number 3(2022)
• Page Start: 546
• Page End: 553
• Publication Date: 2021-12-06
• Subjects: adverse outcomes -- extremely premature birth -- neonates -- pathology -- placenta; Pediatrics -- Periodicals; Pediatrics; 618.92
• DOI: 10.1111/apa.16198
• Languages: English
• ISSNs: 0803-5253

Abstract

Abstract: Aim: We evaluated the role of placental pathology in predicting adverse outcomes for neonates born extremely preterm (EPT) before 28 weeks of gestation. Methods: This was a prospective observational study of 123 extremely preterm singletons born in a hospital in western Norway, and the placentas were classified according to the Amsterdam criteria. The associations between histologic chorioamnionitis (HCA), by the presence or the absence of a foetal inflammatory response (FIR+ or FIR−), maternal vascular malperfusion (MVM) as a whole and adverse neonatal outcomes were evaluated by logistic regression analyses. Adverse outcomes were defined as perinatal death, necrotising enterocolitis (NEC), bronchopulmonary dysplasia (BPD), brain pathology by magnetic resonance imaging at term‐equivalent age, retinopathy of prematurity and early‐onset neonatal sepsis. The results are reported as odds ratios (ORs) with 95% confidence intervals (CIs). Results: HCA was associated with NEC (OR 12.2, 95% CI 1.1 to 137.1). HCA/FIR+ was associated with BPD (OR 14.9, 95% CI 1.8–122.3) and brain pathology (OR 9.8, 95% CI 1.4–71.6), but HCA/FIR− was not. The only neonatal outcome that MVM was associated with was low birthweight. Conclusion: Placental histology provided important information when assessing the risk of adverse neonatal outcomes following EPT birth.