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Impact of being large-for-gestational-age on neonatal mortality and morbidities in extremely premature infants

BACKGROUND: Small for gestational age (SGA) infants have an increased risk for neonatal mortality and morbidities. However, few studies have examined the risk of large for gestational age (LGA) on these factors. We compared the risk of mortality and morbidities in LGA premature infants with those of...

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Autores principales: Ozawa, Junichi, Tanaka, Kosuke, Kabe, Kazuhiko, Namba, Fumihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838861/
https://www.ncbi.nlm.nih.gov/pubmed/33504968
http://dx.doi.org/10.1038/s41390-021-01375-z
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author Ozawa, Junichi
Tanaka, Kosuke
Kabe, Kazuhiko
Namba, Fumihiko
author_facet Ozawa, Junichi
Tanaka, Kosuke
Kabe, Kazuhiko
Namba, Fumihiko
author_sort Ozawa, Junichi
collection PubMed
description BACKGROUND: Small for gestational age (SGA) infants have an increased risk for neonatal mortality and morbidities. However, few studies have examined the risk of large for gestational age (LGA) on these factors. We compared the risk of mortality and morbidities in LGA premature infants with those of appropriate for gestational age (AGA) infants. METHODS: Premature infants who were born between 2003 and 2012 at <26 weeks of gestational age were included. Relative risks of mortality and morbidities were evaluated between LGA and AGA infants. RESULTS: From 6898 extremely premature infants, 357 (5.2%), 5530 (80.2%), and 1011 (14.7%) were LGA, AGA, and SGA, respectively. A total of 5887 infants (5530 AGA and 357 LGA) were examined after excluding infants with congenital anomalies, unknown sex, and deficient data. The risk of mortality in LGA and AGA infants did not differ (relative risk (95% confidence interval) 1.04 (0.83–1.32)). Compared to AGA infants, LGA infants did not increase the risk of morbidities, including intraventricular hemorrhage, cystic periventricular leukomalacia, treated retinopathy of prematurity, necrotizing enterocolitis, and bronchopulmonary dysplasia. CONCLUSIONS: This study demonstrates that being born LGA does not correlate with an increased risk of mortality and morbidities in extremely premature infants. IMPACT: It is currently unknown if being large for gestational age is a risk for neonatal morbidity. A total of 6898 preterm infants born <26 weeks gestational age were included in the study. It was found that being large for gestational age was not related to increased risk of mortality and morbidities.
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spelling pubmed-78388612021-01-28 Impact of being large-for-gestational-age on neonatal mortality and morbidities in extremely premature infants Ozawa, Junichi Tanaka, Kosuke Kabe, Kazuhiko Namba, Fumihiko Pediatr Res Population Study Article BACKGROUND: Small for gestational age (SGA) infants have an increased risk for neonatal mortality and morbidities. However, few studies have examined the risk of large for gestational age (LGA) on these factors. We compared the risk of mortality and morbidities in LGA premature infants with those of appropriate for gestational age (AGA) infants. METHODS: Premature infants who were born between 2003 and 2012 at <26 weeks of gestational age were included. Relative risks of mortality and morbidities were evaluated between LGA and AGA infants. RESULTS: From 6898 extremely premature infants, 357 (5.2%), 5530 (80.2%), and 1011 (14.7%) were LGA, AGA, and SGA, respectively. A total of 5887 infants (5530 AGA and 357 LGA) were examined after excluding infants with congenital anomalies, unknown sex, and deficient data. The risk of mortality in LGA and AGA infants did not differ (relative risk (95% confidence interval) 1.04 (0.83–1.32)). Compared to AGA infants, LGA infants did not increase the risk of morbidities, including intraventricular hemorrhage, cystic periventricular leukomalacia, treated retinopathy of prematurity, necrotizing enterocolitis, and bronchopulmonary dysplasia. CONCLUSIONS: This study demonstrates that being born LGA does not correlate with an increased risk of mortality and morbidities in extremely premature infants. IMPACT: It is currently unknown if being large for gestational age is a risk for neonatal morbidity. A total of 6898 preterm infants born <26 weeks gestational age were included in the study. It was found that being large for gestational age was not related to increased risk of mortality and morbidities. Nature Publishing Group US 2021-01-27 2021 /pmc/articles/PMC7838861/ /pubmed/33504968 http://dx.doi.org/10.1038/s41390-021-01375-z Text en © The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Population Study Article
Ozawa, Junichi
Tanaka, Kosuke
Kabe, Kazuhiko
Namba, Fumihiko
Impact of being large-for-gestational-age on neonatal mortality and morbidities in extremely premature infants
title Impact of being large-for-gestational-age on neonatal mortality and morbidities in extremely premature infants
title_full Impact of being large-for-gestational-age on neonatal mortality and morbidities in extremely premature infants
title_fullStr Impact of being large-for-gestational-age on neonatal mortality and morbidities in extremely premature infants
title_full_unstemmed Impact of being large-for-gestational-age on neonatal mortality and morbidities in extremely premature infants
title_short Impact of being large-for-gestational-age on neonatal mortality and morbidities in extremely premature infants
title_sort impact of being large-for-gestational-age on neonatal mortality and morbidities in extremely premature infants
topic Population Study Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838861/
https://www.ncbi.nlm.nih.gov/pubmed/33504968
http://dx.doi.org/10.1038/s41390-021-01375-z
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