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Placental histopathology in late preterm infants: clinical implications

BACKGROUND: The etiopathogenesis of late preterm (LPT) birth is undetermined. Placental histopathology, which reflects an adverse intrauterine environment and is reportedly associated with preterm labor and neonatal morbidities, has not been studied in LPT infants. PURPOSE: We investigated placental...

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Autores principales: Ericksen, Kristina, Fogel, Joshua, Verma, Rita P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Pediatric Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029669/
https://www.ncbi.nlm.nih.gov/pubmed/31431602
http://dx.doi.org/10.3345/kjp.2019.00038
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author Ericksen, Kristina
Fogel, Joshua
Verma, Rita P.
author_facet Ericksen, Kristina
Fogel, Joshua
Verma, Rita P.
author_sort Ericksen, Kristina
collection PubMed
description BACKGROUND: The etiopathogenesis of late preterm (LPT) birth is undetermined. Placental histopathology, which reflects an adverse intrauterine environment and is reportedly associated with preterm labor and neonatal morbidities, has not been studied in LPT infants. PURPOSE: We investigated placental pathological lesion as markers of an adverse intrauterine environment during LPT labor. METHODS: This retrospective case-control study compared placental histopathological and clinical variables between LPT and term neonates. Placental variables included chorioamnionitis, funisitis, hemorrhage, abruption, infarction, calcification, and syncytial knots. Maternal variables included age, substance abuse, pregnancyassociated diabetes mellitus and hypertension, duration of rupture of membrane, antibiotic use, and magnesium sulfate, whereas, those of neonates included gestational age, birth weight, race, sex, and Apgar scores. Standard statistical proedures were applied to analyze the data. RESULTS: Chorioamnionitis (50% vs. 17.8%, P<0.001) and funisitis (20% vs. 4.4%, P=0.002) were more common in term infants. Placental infarction rate was insignificantly higher in LPT infants (25.6% vs. 14.3%, P=0.08). The mothers in the LPT group were older (30.4 years vs. 28.1 years, P=0.05; odds ratio [OR], 1.06; 95% confidence interval [CI], 0.998–1.12, P=0.056) and more often suffered from hypertension (28.9 vs. 12.9 %, P=0.02), and received magnesium sulfate (48.9 vs. 20%, P< 0.001; OR, 2.86; 95% CI, 1.12–7.29, P<0.05). Duration of rupture of membrane was higher in term infants (13.6 hours vs. 9.1 hours, P<0.001). Chorioamnionitis (OR, 0.33; 95% CI, 0.13–0.79; P<0.05) was associated with a lower risk of LPT delivery. CONCLUSION: Placental infection is not a risk factor for LPT births. There is a nonsignificant predominance of vascular anomalies in LPT placentas. Higher maternal age, magnesium sulfate therapy, and maternal hypertension are clinical risk factors for LPT labor.
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spelling pubmed-70296692020-02-24 Placental histopathology in late preterm infants: clinical implications Ericksen, Kristina Fogel, Joshua Verma, Rita P. Clin Exp Pediatr Original Article BACKGROUND: The etiopathogenesis of late preterm (LPT) birth is undetermined. Placental histopathology, which reflects an adverse intrauterine environment and is reportedly associated with preterm labor and neonatal morbidities, has not been studied in LPT infants. PURPOSE: We investigated placental pathological lesion as markers of an adverse intrauterine environment during LPT labor. METHODS: This retrospective case-control study compared placental histopathological and clinical variables between LPT and term neonates. Placental variables included chorioamnionitis, funisitis, hemorrhage, abruption, infarction, calcification, and syncytial knots. Maternal variables included age, substance abuse, pregnancyassociated diabetes mellitus and hypertension, duration of rupture of membrane, antibiotic use, and magnesium sulfate, whereas, those of neonates included gestational age, birth weight, race, sex, and Apgar scores. Standard statistical proedures were applied to analyze the data. RESULTS: Chorioamnionitis (50% vs. 17.8%, P<0.001) and funisitis (20% vs. 4.4%, P=0.002) were more common in term infants. Placental infarction rate was insignificantly higher in LPT infants (25.6% vs. 14.3%, P=0.08). The mothers in the LPT group were older (30.4 years vs. 28.1 years, P=0.05; odds ratio [OR], 1.06; 95% confidence interval [CI], 0.998–1.12, P=0.056) and more often suffered from hypertension (28.9 vs. 12.9 %, P=0.02), and received magnesium sulfate (48.9 vs. 20%, P< 0.001; OR, 2.86; 95% CI, 1.12–7.29, P<0.05). Duration of rupture of membrane was higher in term infants (13.6 hours vs. 9.1 hours, P<0.001). Chorioamnionitis (OR, 0.33; 95% CI, 0.13–0.79; P<0.05) was associated with a lower risk of LPT delivery. CONCLUSION: Placental infection is not a risk factor for LPT births. There is a nonsignificant predominance of vascular anomalies in LPT placentas. Higher maternal age, magnesium sulfate therapy, and maternal hypertension are clinical risk factors for LPT labor. Korean Pediatric Society 2020-02-06 /pmc/articles/PMC7029669/ /pubmed/31431602 http://dx.doi.org/10.3345/kjp.2019.00038 Text en Copyright © 2020 by The Korean Pediatric Society This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ericksen, Kristina
Fogel, Joshua
Verma, Rita P.
Placental histopathology in late preterm infants: clinical implications
title Placental histopathology in late preterm infants: clinical implications
title_full Placental histopathology in late preterm infants: clinical implications
title_fullStr Placental histopathology in late preterm infants: clinical implications
title_full_unstemmed Placental histopathology in late preterm infants: clinical implications
title_short Placental histopathology in late preterm infants: clinical implications
title_sort placental histopathology in late preterm infants: clinical implications
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029669/
https://www.ncbi.nlm.nih.gov/pubmed/31431602
http://dx.doi.org/10.3345/kjp.2019.00038
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