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Predicting the Risk of Adverse Events in Pregnant Women With Congenital Heart Disease
BACKGROUND: Women with congenital heart disease are considered at high risk for adverse events. Therefore, we aim to establish 2 prediction models for mothers and their offspring, which can predict the risk of adverse events occurred in pregnant women with congenital heart disease. METHODS AND RESUL...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660735/ https://www.ncbi.nlm.nih.gov/pubmed/32662348 http://dx.doi.org/10.1161/JAHA.120.016371 |
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author | Chu, Ran Chen, Wei Song, Guangmin Yao, Shu Xie, Lin Song, Li Zhang, Yue Chen, Lijun Zhang, Xiangli Ma, Yuyan Luo, Xia Liu, Yuan Sun, Ping Zhang, Shuquan Fang, Yan Dong, Taotao Zhang, Qing Peng, Jin Zhang, Lu Wei, Yuan Zhang, Wenxia Su, Xuantao Qiao, Xu Song, Kun Yang, Xingsheng Kong, Beihua |
author_facet | Chu, Ran Chen, Wei Song, Guangmin Yao, Shu Xie, Lin Song, Li Zhang, Yue Chen, Lijun Zhang, Xiangli Ma, Yuyan Luo, Xia Liu, Yuan Sun, Ping Zhang, Shuquan Fang, Yan Dong, Taotao Zhang, Qing Peng, Jin Zhang, Lu Wei, Yuan Zhang, Wenxia Su, Xuantao Qiao, Xu Song, Kun Yang, Xingsheng Kong, Beihua |
author_sort | Chu, Ran |
collection | PubMed |
description | BACKGROUND: Women with congenital heart disease are considered at high risk for adverse events. Therefore, we aim to establish 2 prediction models for mothers and their offspring, which can predict the risk of adverse events occurred in pregnant women with congenital heart disease. METHODS AND RESULTS: A total of 318 pregnant women with congenital heart disease were included; 213 women were divided into the development cohort, and 105 women were divided into the validation cohort. Least absolute shrinkage and selection operator was used for predictor selection. After validation, multivariate logistic regression analysis was used to develop the model. Machine learning algorithms (support vector machine, random forest, AdaBoost, decision tree, k‐nearest neighbor, naïve Bayes, and multilayer perceptron) were used to further verify the predictive ability of the model. Forty‐one (12.9%) women experienced adverse maternal events, and 93 (29.2%) neonates experienced adverse neonatal events. Seven high‐risk factors were discovered in the maternal model, including New York Heart Association class, Eisenmenger syndrome, pulmonary hypertension, left ventricular ejection fraction, sinus tachycardia, arterial blood oxygen saturation, and pregnancy duration. The machine learning–based algorithms showed that the maternal model had an accuracy of 0.76 to 0.86 (area under the receiver operating characteristic curve=0.74–0.87) in the development cohort, and 0.72 to 0.86 (area under the receiver operating characteristic curve=0.68–0.80) in the validation cohort. Three high‐risk factors were discovered in the neonatal model, including Eisenmenger syndrome, preeclampsia, and arterial blood oxygen saturation. The machine learning–based algorithms showed that the neonatal model had an accuracy of 0.75 to 0.80 (area under the receiver operating characteristic curve=0.71–0.77) in the development cohort, and 0.72 to 0.79 (area under the receiver operating characteristic curve=0.69–0.76) in the validation cohort. CONCLUSIONS: Two prenatal risk assessment models for both adverse maternal and neonatal events were established, which might assist clinicians in tailoring precise management and therapy in pregnant women with congenital heart disease. |
format | Online Article Text |
id | pubmed-7660735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76607352020-11-17 Predicting the Risk of Adverse Events in Pregnant Women With Congenital Heart Disease Chu, Ran Chen, Wei Song, Guangmin Yao, Shu Xie, Lin Song, Li Zhang, Yue Chen, Lijun Zhang, Xiangli Ma, Yuyan Luo, Xia Liu, Yuan Sun, Ping Zhang, Shuquan Fang, Yan Dong, Taotao Zhang, Qing Peng, Jin Zhang, Lu Wei, Yuan Zhang, Wenxia Su, Xuantao Qiao, Xu Song, Kun Yang, Xingsheng Kong, Beihua J Am Heart Assoc Original Research BACKGROUND: Women with congenital heart disease are considered at high risk for adverse events. Therefore, we aim to establish 2 prediction models for mothers and their offspring, which can predict the risk of adverse events occurred in pregnant women with congenital heart disease. METHODS AND RESULTS: A total of 318 pregnant women with congenital heart disease were included; 213 women were divided into the development cohort, and 105 women were divided into the validation cohort. Least absolute shrinkage and selection operator was used for predictor selection. After validation, multivariate logistic regression analysis was used to develop the model. Machine learning algorithms (support vector machine, random forest, AdaBoost, decision tree, k‐nearest neighbor, naïve Bayes, and multilayer perceptron) were used to further verify the predictive ability of the model. Forty‐one (12.9%) women experienced adverse maternal events, and 93 (29.2%) neonates experienced adverse neonatal events. Seven high‐risk factors were discovered in the maternal model, including New York Heart Association class, Eisenmenger syndrome, pulmonary hypertension, left ventricular ejection fraction, sinus tachycardia, arterial blood oxygen saturation, and pregnancy duration. The machine learning–based algorithms showed that the maternal model had an accuracy of 0.76 to 0.86 (area under the receiver operating characteristic curve=0.74–0.87) in the development cohort, and 0.72 to 0.86 (area under the receiver operating characteristic curve=0.68–0.80) in the validation cohort. Three high‐risk factors were discovered in the neonatal model, including Eisenmenger syndrome, preeclampsia, and arterial blood oxygen saturation. The machine learning–based algorithms showed that the neonatal model had an accuracy of 0.75 to 0.80 (area under the receiver operating characteristic curve=0.71–0.77) in the development cohort, and 0.72 to 0.79 (area under the receiver operating characteristic curve=0.69–0.76) in the validation cohort. CONCLUSIONS: Two prenatal risk assessment models for both adverse maternal and neonatal events were established, which might assist clinicians in tailoring precise management and therapy in pregnant women with congenital heart disease. John Wiley and Sons Inc. 2020-07-14 /pmc/articles/PMC7660735/ /pubmed/32662348 http://dx.doi.org/10.1161/JAHA.120.016371 Text en © 2020 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Chu, Ran Chen, Wei Song, Guangmin Yao, Shu Xie, Lin Song, Li Zhang, Yue Chen, Lijun Zhang, Xiangli Ma, Yuyan Luo, Xia Liu, Yuan Sun, Ping Zhang, Shuquan Fang, Yan Dong, Taotao Zhang, Qing Peng, Jin Zhang, Lu Wei, Yuan Zhang, Wenxia Su, Xuantao Qiao, Xu Song, Kun Yang, Xingsheng Kong, Beihua Predicting the Risk of Adverse Events in Pregnant Women With Congenital Heart Disease |
title | Predicting the Risk of Adverse Events in Pregnant Women With Congenital Heart Disease |
title_full | Predicting the Risk of Adverse Events in Pregnant Women With Congenital Heart Disease |
title_fullStr | Predicting the Risk of Adverse Events in Pregnant Women With Congenital Heart Disease |
title_full_unstemmed | Predicting the Risk of Adverse Events in Pregnant Women With Congenital Heart Disease |
title_short | Predicting the Risk of Adverse Events in Pregnant Women With Congenital Heart Disease |
title_sort | predicting the risk of adverse events in pregnant women with congenital heart disease |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660735/ https://www.ncbi.nlm.nih.gov/pubmed/32662348 http://dx.doi.org/10.1161/JAHA.120.016371 |
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