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Stillbirth risk prediction using machine learning for a large cohort of births from Western Australia, 1980–2015

Quantification of stillbirth risk has potential to support clinical decision-making. Studies that have attempted to quantify stillbirth risk have been hampered by small event rates, a limited range of predictors that typically exclude obstetric history, lack of validation, and restriction to a singl...

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Autores principales: Malacova, Eva, Tippaya, Sawitchaya, Bailey, Helen D., Chai, Kevin, Farrant, Brad M., Gebremedhin, Amanuel T., Leonard, Helen, Marinovich, Michael L., Nassar, Natasha, Phatak, Aloke, Raynes-Greenow, Camille, Regan, Annette K., Shand, Antonia W., Shepherd, Carrington C. J., Srinivasjois, Ravisha, Tessema, Gizachew A., Pereira, Gavin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093523/
https://www.ncbi.nlm.nih.gov/pubmed/32210300
http://dx.doi.org/10.1038/s41598-020-62210-9
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author Malacova, Eva
Tippaya, Sawitchaya
Bailey, Helen D.
Chai, Kevin
Farrant, Brad M.
Gebremedhin, Amanuel T.
Leonard, Helen
Marinovich, Michael L.
Nassar, Natasha
Phatak, Aloke
Raynes-Greenow, Camille
Regan, Annette K.
Shand, Antonia W.
Shepherd, Carrington C. J.
Srinivasjois, Ravisha
Tessema, Gizachew A.
Pereira, Gavin
author_facet Malacova, Eva
Tippaya, Sawitchaya
Bailey, Helen D.
Chai, Kevin
Farrant, Brad M.
Gebremedhin, Amanuel T.
Leonard, Helen
Marinovich, Michael L.
Nassar, Natasha
Phatak, Aloke
Raynes-Greenow, Camille
Regan, Annette K.
Shand, Antonia W.
Shepherd, Carrington C. J.
Srinivasjois, Ravisha
Tessema, Gizachew A.
Pereira, Gavin
author_sort Malacova, Eva
collection PubMed
description Quantification of stillbirth risk has potential to support clinical decision-making. Studies that have attempted to quantify stillbirth risk have been hampered by small event rates, a limited range of predictors that typically exclude obstetric history, lack of validation, and restriction to a single classifier (logistic regression). Consequently, predictive performance remains low, and risk quantification has not been adopted into antenatal practice. The study population consisted of all births to women in Western Australia from 1980 to 2015, excluding terminations. After all exclusions there were 947,025 livebirths and 5,788 stillbirths. Predictive models for stillbirth were developed using multiple machine learning classifiers: regularised logistic regression, decision trees based on classification and regression trees, random forest, extreme gradient boosting (XGBoost), and a multilayer perceptron neural network. We applied 10-fold cross-validation using independent data not used to develop the models. Predictors included maternal socio-demographic characteristics, chronic medical conditions, obstetric complications and family history in both the current and previous pregnancy. In this cohort, 66% of stillbirths were observed for multiparous women. The best performing classifier (XGBoost) predicted 45% (95% CI: 43%, 46%) of stillbirths for all women and 45% (95% CI: 43%, 47%) of stillbirths after the inclusion of previous pregnancy history. Almost half of stillbirths could be potentially identified antenatally based on a combination of current pregnancy complications, congenital anomalies, maternal characteristics, and medical history. Greatest sensitivity is achieved with addition of current pregnancy complications. Ensemble classifiers offered marginal improvement for prediction compared to logistic regression.
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spelling pubmed-70935232020-03-27 Stillbirth risk prediction using machine learning for a large cohort of births from Western Australia, 1980–2015 Malacova, Eva Tippaya, Sawitchaya Bailey, Helen D. Chai, Kevin Farrant, Brad M. Gebremedhin, Amanuel T. Leonard, Helen Marinovich, Michael L. Nassar, Natasha Phatak, Aloke Raynes-Greenow, Camille Regan, Annette K. Shand, Antonia W. Shepherd, Carrington C. J. Srinivasjois, Ravisha Tessema, Gizachew A. Pereira, Gavin Sci Rep Article Quantification of stillbirth risk has potential to support clinical decision-making. Studies that have attempted to quantify stillbirth risk have been hampered by small event rates, a limited range of predictors that typically exclude obstetric history, lack of validation, and restriction to a single classifier (logistic regression). Consequently, predictive performance remains low, and risk quantification has not been adopted into antenatal practice. The study population consisted of all births to women in Western Australia from 1980 to 2015, excluding terminations. After all exclusions there were 947,025 livebirths and 5,788 stillbirths. Predictive models for stillbirth were developed using multiple machine learning classifiers: regularised logistic regression, decision trees based on classification and regression trees, random forest, extreme gradient boosting (XGBoost), and a multilayer perceptron neural network. We applied 10-fold cross-validation using independent data not used to develop the models. Predictors included maternal socio-demographic characteristics, chronic medical conditions, obstetric complications and family history in both the current and previous pregnancy. In this cohort, 66% of stillbirths were observed for multiparous women. The best performing classifier (XGBoost) predicted 45% (95% CI: 43%, 46%) of stillbirths for all women and 45% (95% CI: 43%, 47%) of stillbirths after the inclusion of previous pregnancy history. Almost half of stillbirths could be potentially identified antenatally based on a combination of current pregnancy complications, congenital anomalies, maternal characteristics, and medical history. Greatest sensitivity is achieved with addition of current pregnancy complications. Ensemble classifiers offered marginal improvement for prediction compared to logistic regression. Nature Publishing Group UK 2020-03-24 /pmc/articles/PMC7093523/ /pubmed/32210300 http://dx.doi.org/10.1038/s41598-020-62210-9 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Malacova, Eva
Tippaya, Sawitchaya
Bailey, Helen D.
Chai, Kevin
Farrant, Brad M.
Gebremedhin, Amanuel T.
Leonard, Helen
Marinovich, Michael L.
Nassar, Natasha
Phatak, Aloke
Raynes-Greenow, Camille
Regan, Annette K.
Shand, Antonia W.
Shepherd, Carrington C. J.
Srinivasjois, Ravisha
Tessema, Gizachew A.
Pereira, Gavin
Stillbirth risk prediction using machine learning for a large cohort of births from Western Australia, 1980–2015
title Stillbirth risk prediction using machine learning for a large cohort of births from Western Australia, 1980–2015
title_full Stillbirth risk prediction using machine learning for a large cohort of births from Western Australia, 1980–2015
title_fullStr Stillbirth risk prediction using machine learning for a large cohort of births from Western Australia, 1980–2015
title_full_unstemmed Stillbirth risk prediction using machine learning for a large cohort of births from Western Australia, 1980–2015
title_short Stillbirth risk prediction using machine learning for a large cohort of births from Western Australia, 1980–2015
title_sort stillbirth risk prediction using machine learning for a large cohort of births from western australia, 1980–2015
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093523/
https://www.ncbi.nlm.nih.gov/pubmed/32210300
http://dx.doi.org/10.1038/s41598-020-62210-9
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