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Slow fetal growth between first and early second trimester ultrasound scans and risk of small for gestational age (SGA) birth
OBJECTIVES: To investigate the association between fetal growth between first and early second trimester ultrasound scan and the risk of severe small for gestational age (SGA) birth. METHODS: This cohort study included 69 550 singleton pregnancies with first trimester dating and an early second trim...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608242/ https://www.ncbi.nlm.nih.gov/pubmed/28934257 http://dx.doi.org/10.1371/journal.pone.0184853 |
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author | Simic, Marija Stephansson, Olof Petersson, Gunnar Cnattingius, Sven Wikström, Anna-Karin |
author_facet | Simic, Marija Stephansson, Olof Petersson, Gunnar Cnattingius, Sven Wikström, Anna-Karin |
author_sort | Simic, Marija |
collection | PubMed |
description | OBJECTIVES: To investigate the association between fetal growth between first and early second trimester ultrasound scan and the risk of severe small for gestational age (SGA) birth. METHODS: This cohort study included 69 550 singleton pregnancies with first trimester dating and an early second trimester growth scan in Stockholm and Gotland Counties, Sweden between 2008 and 2014. Exposure was difference in biparietal diameter growth between observed and expected at the second trimester scan, calculated by z-scores. Risk of birth of a severe SGA infant (birth weight for gestational age by fetal sex less than the 3(rd) centile) was calculated using multivariable logistic regression analysis and presented as adjusted odds ratio (aOR). RESULTS: Parietal growth less than 2.5 percentile between first and second trimester ultrasound examination was associated with elevated risk of being born severe SGA. (aOR 1.67; 95% Confidence Interval 1.28–2.18). The risks of preterm severe SGA (birth before 37 weeks) and term severe SGA (birth 37 weeks or later) were at similar levels, and risk of severe SGA were also elevated in the absence of preeclampsia, hypertensive diseases or gestational diabetes. CONCLUSIONS: Fetuses with slow growth of biparietal diameter at ultrasound examination in early second trimester exhibit increased risk of being born SGA independent of gestational age at birth and presence of maternal hypertensive diseases or diabetes mellitus. |
format | Online Article Text |
id | pubmed-5608242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56082422017-10-09 Slow fetal growth between first and early second trimester ultrasound scans and risk of small for gestational age (SGA) birth Simic, Marija Stephansson, Olof Petersson, Gunnar Cnattingius, Sven Wikström, Anna-Karin PLoS One Research Article OBJECTIVES: To investigate the association between fetal growth between first and early second trimester ultrasound scan and the risk of severe small for gestational age (SGA) birth. METHODS: This cohort study included 69 550 singleton pregnancies with first trimester dating and an early second trimester growth scan in Stockholm and Gotland Counties, Sweden between 2008 and 2014. Exposure was difference in biparietal diameter growth between observed and expected at the second trimester scan, calculated by z-scores. Risk of birth of a severe SGA infant (birth weight for gestational age by fetal sex less than the 3(rd) centile) was calculated using multivariable logistic regression analysis and presented as adjusted odds ratio (aOR). RESULTS: Parietal growth less than 2.5 percentile between first and second trimester ultrasound examination was associated with elevated risk of being born severe SGA. (aOR 1.67; 95% Confidence Interval 1.28–2.18). The risks of preterm severe SGA (birth before 37 weeks) and term severe SGA (birth 37 weeks or later) were at similar levels, and risk of severe SGA were also elevated in the absence of preeclampsia, hypertensive diseases or gestational diabetes. CONCLUSIONS: Fetuses with slow growth of biparietal diameter at ultrasound examination in early second trimester exhibit increased risk of being born SGA independent of gestational age at birth and presence of maternal hypertensive diseases or diabetes mellitus. Public Library of Science 2017-09-21 /pmc/articles/PMC5608242/ /pubmed/28934257 http://dx.doi.org/10.1371/journal.pone.0184853 Text en © 2017 Simic et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Simic, Marija Stephansson, Olof Petersson, Gunnar Cnattingius, Sven Wikström, Anna-Karin Slow fetal growth between first and early second trimester ultrasound scans and risk of small for gestational age (SGA) birth |
title | Slow fetal growth between first and early second trimester ultrasound scans and risk of small for gestational age (SGA) birth |
title_full | Slow fetal growth between first and early second trimester ultrasound scans and risk of small for gestational age (SGA) birth |
title_fullStr | Slow fetal growth between first and early second trimester ultrasound scans and risk of small for gestational age (SGA) birth |
title_full_unstemmed | Slow fetal growth between first and early second trimester ultrasound scans and risk of small for gestational age (SGA) birth |
title_short | Slow fetal growth between first and early second trimester ultrasound scans and risk of small for gestational age (SGA) birth |
title_sort | slow fetal growth between first and early second trimester ultrasound scans and risk of small for gestational age (sga) birth |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608242/ https://www.ncbi.nlm.nih.gov/pubmed/28934257 http://dx.doi.org/10.1371/journal.pone.0184853 |
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