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Development and validation of a nomogram for predicting severe respiratory syncytial virus-associated bronchiolitis

BACKGROUND: Respiratory syncytial virus (RSV) is the most common cause of bronchiolitis and is related to the severity of the disease. This study aimed to develop and validate a nomogram for predicting severe bronchiolitis in infants and young children with RSV infection. METHODS: A total of 325 chi...

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Autores principales: Yan, Jisi, Zhao, LiHua, Zhang, Tongqiang, Wei, Yupeng, Guo, Detong, Guo, Wei, Zheng, Jun, Xu, Yongsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114343/
https://www.ncbi.nlm.nih.gov/pubmed/37072700
http://dx.doi.org/10.1186/s12879-023-08179-y
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author Yan, Jisi
Zhao, LiHua
Zhang, Tongqiang
Wei, Yupeng
Guo, Detong
Guo, Wei
Zheng, Jun
Xu, Yongsheng
author_facet Yan, Jisi
Zhao, LiHua
Zhang, Tongqiang
Wei, Yupeng
Guo, Detong
Guo, Wei
Zheng, Jun
Xu, Yongsheng
author_sort Yan, Jisi
collection PubMed
description BACKGROUND: Respiratory syncytial virus (RSV) is the most common cause of bronchiolitis and is related to the severity of the disease. This study aimed to develop and validate a nomogram for predicting severe bronchiolitis in infants and young children with RSV infection. METHODS: A total of 325 children with RSV-associated bronchiolitis were enrolled, including 125 severe cases and 200 mild cases. A prediction model was built on 227 cases and validated on 98 cases, which were divided by random sampling in R software. Relevant clinical, laboratory and imaging data were collected. Multivariate logistic regression models were used to determine optimal predictors and to construct nomograms. The performance of the nomogram was evaluated by the area under the characteristic curve (AUC), calibration ability and decision curve analysis (DCA). RESULTS: There were 137 (60.4%) mild and 90 (39.6%) severe RSV-associated bronchiolitis cases in the training group (n = 227) and 63 (64.3%) mild and 35 (35.7%) severe cases in the validation group (n = 98). Multivariate logistic regression analysis identified 5 variables as significant predictive factors to construct the nomogram for predicting severe RSV-associated bronchiolitis, including preterm birth (OR = 3.80; 95% CI, 1.39–10.39; P = 0.009), weight at admission (OR = 0.76; 95% CI, 0.63–0.91; P = 0.003), breathing rate (OR = 1.11; 95% CI, 1.05–1.18; P = 0.001), lymphocyte percentage (OR = 0.97; 95% CI, 0.95–0.99; P = 0.001) and outpatient use of glucocorticoids (OR = 2.27; 95% CI, 1.05–4.9; P = 0.038). The AUC value of the nomogram was 0.784 (95% CI, 0.722–0.846) in the training set and 0.832 (95% CI, 0.741–0.923) in the validation set, which showed a good fit. The calibration plot and Hosmer‒Lemeshow test indicated that the predicted probability had good consistency with the actual probability both in the training group (P = 0.817) and validation group (P = 0.290). The DCA curve shows that the nomogram has good clinical value. CONCLUSION: A nomogram for predicting severe RSV-associated bronchiolitis in the early clinical stage was established and validated, which can help physicians identify severe RSV-associated bronchiolitis and then choose reasonable treatment.
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spelling pubmed-101143432023-04-20 Development and validation of a nomogram for predicting severe respiratory syncytial virus-associated bronchiolitis Yan, Jisi Zhao, LiHua Zhang, Tongqiang Wei, Yupeng Guo, Detong Guo, Wei Zheng, Jun Xu, Yongsheng BMC Infect Dis Research BACKGROUND: Respiratory syncytial virus (RSV) is the most common cause of bronchiolitis and is related to the severity of the disease. This study aimed to develop and validate a nomogram for predicting severe bronchiolitis in infants and young children with RSV infection. METHODS: A total of 325 children with RSV-associated bronchiolitis were enrolled, including 125 severe cases and 200 mild cases. A prediction model was built on 227 cases and validated on 98 cases, which were divided by random sampling in R software. Relevant clinical, laboratory and imaging data were collected. Multivariate logistic regression models were used to determine optimal predictors and to construct nomograms. The performance of the nomogram was evaluated by the area under the characteristic curve (AUC), calibration ability and decision curve analysis (DCA). RESULTS: There were 137 (60.4%) mild and 90 (39.6%) severe RSV-associated bronchiolitis cases in the training group (n = 227) and 63 (64.3%) mild and 35 (35.7%) severe cases in the validation group (n = 98). Multivariate logistic regression analysis identified 5 variables as significant predictive factors to construct the nomogram for predicting severe RSV-associated bronchiolitis, including preterm birth (OR = 3.80; 95% CI, 1.39–10.39; P = 0.009), weight at admission (OR = 0.76; 95% CI, 0.63–0.91; P = 0.003), breathing rate (OR = 1.11; 95% CI, 1.05–1.18; P = 0.001), lymphocyte percentage (OR = 0.97; 95% CI, 0.95–0.99; P = 0.001) and outpatient use of glucocorticoids (OR = 2.27; 95% CI, 1.05–4.9; P = 0.038). The AUC value of the nomogram was 0.784 (95% CI, 0.722–0.846) in the training set and 0.832 (95% CI, 0.741–0.923) in the validation set, which showed a good fit. The calibration plot and Hosmer‒Lemeshow test indicated that the predicted probability had good consistency with the actual probability both in the training group (P = 0.817) and validation group (P = 0.290). The DCA curve shows that the nomogram has good clinical value. CONCLUSION: A nomogram for predicting severe RSV-associated bronchiolitis in the early clinical stage was established and validated, which can help physicians identify severe RSV-associated bronchiolitis and then choose reasonable treatment. BioMed Central 2023-04-18 /pmc/articles/PMC10114343/ /pubmed/37072700 http://dx.doi.org/10.1186/s12879-023-08179-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yan, Jisi
Zhao, LiHua
Zhang, Tongqiang
Wei, Yupeng
Guo, Detong
Guo, Wei
Zheng, Jun
Xu, Yongsheng
Development and validation of a nomogram for predicting severe respiratory syncytial virus-associated bronchiolitis
title Development and validation of a nomogram for predicting severe respiratory syncytial virus-associated bronchiolitis
title_full Development and validation of a nomogram for predicting severe respiratory syncytial virus-associated bronchiolitis
title_fullStr Development and validation of a nomogram for predicting severe respiratory syncytial virus-associated bronchiolitis
title_full_unstemmed Development and validation of a nomogram for predicting severe respiratory syncytial virus-associated bronchiolitis
title_short Development and validation of a nomogram for predicting severe respiratory syncytial virus-associated bronchiolitis
title_sort development and validation of a nomogram for predicting severe respiratory syncytial virus-associated bronchiolitis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114343/
https://www.ncbi.nlm.nih.gov/pubmed/37072700
http://dx.doi.org/10.1186/s12879-023-08179-y
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