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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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.
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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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