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Estimating the individual singleton preterm birth risk: nomogram establishment and independent validation
BACKGROUND: To establish and independently validate nomograms for predicting singleton preterm birth (PTB) risk based on a large sample size comprising data from two independent datasets. METHODS: This cohort study used data from 50 states and the District of Columbia in the National Vital Statistic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10416119/ https://www.ncbi.nlm.nih.gov/pubmed/37575903 http://dx.doi.org/10.21037/tp-22-611 |
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author | Gao, Ting Wang, Tianwei Tang, Wan Xu, Pu Qian, Tianyang Qiu, Han Wang, Laishuan |
author_facet | Gao, Ting Wang, Tianwei Tang, Wan Xu, Pu Qian, Tianyang Qiu, Han Wang, Laishuan |
author_sort | Gao, Ting |
collection | PubMed |
description | BACKGROUND: To establish and independently validate nomograms for predicting singleton preterm birth (PTB) risk based on a large sample size comprising data from two independent datasets. METHODS: This cohort study used data from 50 states and the District of Columbia in the National Vital Statistics System (NVSS) database between January 2016 and December 2020. Multivariate logistic regression analysis was used to confirm the independent risk factors for PTB. Statistically significant variables were incorporated into the logistic regression models to establish PTB prediction nomograms. The models were developed using the United States (US)-derived data and were independently validated using data from US Territories. RESULTS: A total of 16,294,529 mother-newborn pairs from the US were included in the training set, and 54,708 mother-newborn pairs from the US Territories were included in the validation set. In all, 4 nomograms were built: 1 to predict PTB probability, and another 3 to predict moderately and late PTB probability, very PTB probability, and extremely PTB probability, respectively. Hypertensive eclampsia and infertility treatment were found to be the top 2 contributors to PTB. CONCLUSIONS: We developed and validated nomograms to predict the individualized probability of PTB, which could be useful to physicians for improved early identification of PTB and in making individualized clinical decisions. |
format | Online Article Text |
id | pubmed-10416119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-104161192023-08-12 Estimating the individual singleton preterm birth risk: nomogram establishment and independent validation Gao, Ting Wang, Tianwei Tang, Wan Xu, Pu Qian, Tianyang Qiu, Han Wang, Laishuan Transl Pediatr Original Article BACKGROUND: To establish and independently validate nomograms for predicting singleton preterm birth (PTB) risk based on a large sample size comprising data from two independent datasets. METHODS: This cohort study used data from 50 states and the District of Columbia in the National Vital Statistics System (NVSS) database between January 2016 and December 2020. Multivariate logistic regression analysis was used to confirm the independent risk factors for PTB. Statistically significant variables were incorporated into the logistic regression models to establish PTB prediction nomograms. The models were developed using the United States (US)-derived data and were independently validated using data from US Territories. RESULTS: A total of 16,294,529 mother-newborn pairs from the US were included in the training set, and 54,708 mother-newborn pairs from the US Territories were included in the validation set. In all, 4 nomograms were built: 1 to predict PTB probability, and another 3 to predict moderately and late PTB probability, very PTB probability, and extremely PTB probability, respectively. Hypertensive eclampsia and infertility treatment were found to be the top 2 contributors to PTB. CONCLUSIONS: We developed and validated nomograms to predict the individualized probability of PTB, which could be useful to physicians for improved early identification of PTB and in making individualized clinical decisions. AME Publishing Company 2023-06-29 2023-07-31 /pmc/articles/PMC10416119/ /pubmed/37575903 http://dx.doi.org/10.21037/tp-22-611 Text en 2023 Translational Pediatrics. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Gao, Ting Wang, Tianwei Tang, Wan Xu, Pu Qian, Tianyang Qiu, Han Wang, Laishuan Estimating the individual singleton preterm birth risk: nomogram establishment and independent validation |
title | Estimating the individual singleton preterm birth risk: nomogram establishment and independent validation |
title_full | Estimating the individual singleton preterm birth risk: nomogram establishment and independent validation |
title_fullStr | Estimating the individual singleton preterm birth risk: nomogram establishment and independent validation |
title_full_unstemmed | Estimating the individual singleton preterm birth risk: nomogram establishment and independent validation |
title_short | Estimating the individual singleton preterm birth risk: nomogram establishment and independent validation |
title_sort | estimating the individual singleton preterm birth risk: nomogram establishment and independent validation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10416119/ https://www.ncbi.nlm.nih.gov/pubmed/37575903 http://dx.doi.org/10.21037/tp-22-611 |
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