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Fetal Growth and Risk of Stillbirth: A Population-Based Case–Control Study

BACKGROUND: Stillbirth is strongly related to impaired fetal growth. However, the relationship between fetal growth and stillbirth is difficult to determine because of uncertainty in the timing of death and confounding characteristics affecting normal fetal growth. METHODS AND FINDINGS: We conducted...

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Autores principales: Bukowski, Radek, Hansen, Nellie I., Willinger, Marian, Reddy, Uma M., Parker, Corette B., Pinar, Halit, Silver, Robert M., Dudley, Donald J., Stoll, Barbara J., Saade, George R., Koch, Matthew A., Rowland Hogue, Carol J., Varner, Michael W., Conway, Deborah L., Coustan, Donald, Goldenberg, Robert L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995658/
https://www.ncbi.nlm.nih.gov/pubmed/24755550
http://dx.doi.org/10.1371/journal.pmed.1001633
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author Bukowski, Radek
Hansen, Nellie I.
Willinger, Marian
Reddy, Uma M.
Parker, Corette B.
Pinar, Halit
Silver, Robert M.
Dudley, Donald J.
Stoll, Barbara J.
Saade, George R.
Koch, Matthew A.
Rowland Hogue, Carol J.
Varner, Michael W.
Conway, Deborah L.
Coustan, Donald
Goldenberg, Robert L.
author_facet Bukowski, Radek
Hansen, Nellie I.
Willinger, Marian
Reddy, Uma M.
Parker, Corette B.
Pinar, Halit
Silver, Robert M.
Dudley, Donald J.
Stoll, Barbara J.
Saade, George R.
Koch, Matthew A.
Rowland Hogue, Carol J.
Varner, Michael W.
Conway, Deborah L.
Coustan, Donald
Goldenberg, Robert L.
author_sort Bukowski, Radek
collection PubMed
description BACKGROUND: Stillbirth is strongly related to impaired fetal growth. However, the relationship between fetal growth and stillbirth is difficult to determine because of uncertainty in the timing of death and confounding characteristics affecting normal fetal growth. METHODS AND FINDINGS: We conducted a population-based case–control study of all stillbirths and a representative sample of live births in 59 hospitals in five geographic areas in the US. Fetal growth abnormalities were categorized as small for gestational age (SGA) (<10th percentile) or large for gestational age (LGA) (>90th percentile) at death (stillbirth) or delivery (live birth) using population, ultrasound, and individualized norms. Gestational age at death was determined using an algorithm that considered the time-of-death interval, postmortem examination, and reliability of the gestational age estimate. Data were weighted to account for the sampling design and differential participation rates in various subgroups. Among 527 singleton stillbirths and 1,821 singleton live births studied, stillbirth was associated with SGA based on population, ultrasound, and individualized norms (odds ratio [OR] [95% CI]: 3.0 [2.2 to 4.0]; 4.7 [3.7 to 5.9]; 4.6 [3.6 to 5.9], respectively). LGA was also associated with increased risk of stillbirth using ultrasound and individualized norms (OR [95% CI]: 3.5 [2.4 to 5.0]; 2.3 [1.7 to 3.1], respectively), but not population norms (OR [95% CI]: 0.6 [0.4 to 1.0]). The associations were stronger with more severe SGA and LGA (<5th and >95th percentile). Analyses adjusted for stillbirth risk factors, subset analyses excluding potential confounders, and analyses in preterm and term pregnancies showed similar patterns of association. In this study 70% of cases and 63% of controls agreed to participate. Analysis weights accounted for differences between consenting and non-consenting women. Some of the characteristics used for individualized fetal growth estimates were missing and were replaced with reference values. However, a sensitivity analysis using individualized norms based on the subset of stillbirths and live births with non-missing variables showed similar findings. CONCLUSIONS: Stillbirth is associated with both growth restriction and excessive fetal growth. These findings suggest that, contrary to current practices and recommendations, stillbirth prevention strategies should focus on both severe SGA and severe LGA pregnancies. Please see later in the article for the Editors' Summary
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spelling pubmed-39956582014-04-25 Fetal Growth and Risk of Stillbirth: A Population-Based Case–Control Study Bukowski, Radek Hansen, Nellie I. Willinger, Marian Reddy, Uma M. Parker, Corette B. Pinar, Halit Silver, Robert M. Dudley, Donald J. Stoll, Barbara J. Saade, George R. Koch, Matthew A. Rowland Hogue, Carol J. Varner, Michael W. Conway, Deborah L. Coustan, Donald Goldenberg, Robert L. PLoS Med Research Article BACKGROUND: Stillbirth is strongly related to impaired fetal growth. However, the relationship between fetal growth and stillbirth is difficult to determine because of uncertainty in the timing of death and confounding characteristics affecting normal fetal growth. METHODS AND FINDINGS: We conducted a population-based case–control study of all stillbirths and a representative sample of live births in 59 hospitals in five geographic areas in the US. Fetal growth abnormalities were categorized as small for gestational age (SGA) (<10th percentile) or large for gestational age (LGA) (>90th percentile) at death (stillbirth) or delivery (live birth) using population, ultrasound, and individualized norms. Gestational age at death was determined using an algorithm that considered the time-of-death interval, postmortem examination, and reliability of the gestational age estimate. Data were weighted to account for the sampling design and differential participation rates in various subgroups. Among 527 singleton stillbirths and 1,821 singleton live births studied, stillbirth was associated with SGA based on population, ultrasound, and individualized norms (odds ratio [OR] [95% CI]: 3.0 [2.2 to 4.0]; 4.7 [3.7 to 5.9]; 4.6 [3.6 to 5.9], respectively). LGA was also associated with increased risk of stillbirth using ultrasound and individualized norms (OR [95% CI]: 3.5 [2.4 to 5.0]; 2.3 [1.7 to 3.1], respectively), but not population norms (OR [95% CI]: 0.6 [0.4 to 1.0]). The associations were stronger with more severe SGA and LGA (<5th and >95th percentile). Analyses adjusted for stillbirth risk factors, subset analyses excluding potential confounders, and analyses in preterm and term pregnancies showed similar patterns of association. In this study 70% of cases and 63% of controls agreed to participate. Analysis weights accounted for differences between consenting and non-consenting women. Some of the characteristics used for individualized fetal growth estimates were missing and were replaced with reference values. However, a sensitivity analysis using individualized norms based on the subset of stillbirths and live births with non-missing variables showed similar findings. CONCLUSIONS: Stillbirth is associated with both growth restriction and excessive fetal growth. These findings suggest that, contrary to current practices and recommendations, stillbirth prevention strategies should focus on both severe SGA and severe LGA pregnancies. Please see later in the article for the Editors' Summary Public Library of Science 2014-04-22 /pmc/articles/PMC3995658/ /pubmed/24755550 http://dx.doi.org/10.1371/journal.pmed.1001633 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Bukowski, Radek
Hansen, Nellie I.
Willinger, Marian
Reddy, Uma M.
Parker, Corette B.
Pinar, Halit
Silver, Robert M.
Dudley, Donald J.
Stoll, Barbara J.
Saade, George R.
Koch, Matthew A.
Rowland Hogue, Carol J.
Varner, Michael W.
Conway, Deborah L.
Coustan, Donald
Goldenberg, Robert L.
Fetal Growth and Risk of Stillbirth: A Population-Based Case–Control Study
title Fetal Growth and Risk of Stillbirth: A Population-Based Case–Control Study
title_full Fetal Growth and Risk of Stillbirth: A Population-Based Case–Control Study
title_fullStr Fetal Growth and Risk of Stillbirth: A Population-Based Case–Control Study
title_full_unstemmed Fetal Growth and Risk of Stillbirth: A Population-Based Case–Control Study
title_short Fetal Growth and Risk of Stillbirth: A Population-Based Case–Control Study
title_sort fetal growth and risk of stillbirth: a population-based case–control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995658/
https://www.ncbi.nlm.nih.gov/pubmed/24755550
http://dx.doi.org/10.1371/journal.pmed.1001633
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