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High immunoglobulin E level is associated with increased readmission in children with bronchopneumonia

BACKGROUND: Increased immunoglobulin E (IgE) is associated with lower respiratory tract infections. The study aimed to evaluate the association between IgE and the rate of bronchopneumonia-related readmission within 12 months in children. METHODS: A total of 1099 children aged over 1 year with bronc...

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Autores principales: You, Cun, Ran, Guo, Wu, Xiao, Wang, Yu, Tian, Hua, Fan, Jiabao, Yao, Zezhong, Wang, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783659/
https://www.ncbi.nlm.nih.gov/pubmed/31588854
http://dx.doi.org/10.1177/1753466619879832
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author You, Cun
Ran, Guo
Wu, Xiao
Wang, Yu
Tian, Hua
Fan, Jiabao
Yao, Zezhong
Wang, Fei
author_facet You, Cun
Ran, Guo
Wu, Xiao
Wang, Yu
Tian, Hua
Fan, Jiabao
Yao, Zezhong
Wang, Fei
author_sort You, Cun
collection PubMed
description BACKGROUND: Increased immunoglobulin E (IgE) is associated with lower respiratory tract infections. The study aimed to evaluate the association between IgE and the rate of bronchopneumonia-related readmission within 12 months in children. METHODS: A total of 1099 children aged over 1 year with bronchopneumonia, from 1 January 2015 to 31 December 2016, were enrolled. Unplanned readmissions within 12 months after discharge were observed. Multivariate regression analysis was used to identify independent risk factors for rehospitalization. RESULTS: The rate of rehospitalization was 11.4% (125/1099). Compared to the nonreadmission children, IgE levels, the proportion of children with asthma and hospitalization duration were significantly higher in the readmission children (p < 0.05). Compared to the children with normal IgE (≤ 165 IU/ml) levels, the risk of rehospitalization was significantly higher in children with abnormal IgE [odds ratio (OR) 1.781, 95% confidence interval (CI) 1.209–2.624, p = 0.004]. Children with IgE level more than three times the upper limit had even higher risks of readmission (OR 2.037, 95%CI 1.172–3.540, p = 0.012). Meanwhile, the risk of readmission in children with abnormal IgE combined with or without bronchial asthma was significantly higher (OR 2.548 and 1.918, 95% CI 1.490–4.358 and 1.218–3.020, p = 0.001 and 0.005, respectively). CONCLUSIONS: Children aged over 1 year with bronchopneumonia who had higher IgE levels are at increased risk for rehospitalization within the first 12 months of the index hospitalization and IgE level may be used as a predictor of rehospitalization in children with bronchopneumonia.
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spelling pubmed-67836592019-10-21 High immunoglobulin E level is associated with increased readmission in children with bronchopneumonia You, Cun Ran, Guo Wu, Xiao Wang, Yu Tian, Hua Fan, Jiabao Yao, Zezhong Wang, Fei Ther Adv Respir Dis Original Research BACKGROUND: Increased immunoglobulin E (IgE) is associated with lower respiratory tract infections. The study aimed to evaluate the association between IgE and the rate of bronchopneumonia-related readmission within 12 months in children. METHODS: A total of 1099 children aged over 1 year with bronchopneumonia, from 1 January 2015 to 31 December 2016, were enrolled. Unplanned readmissions within 12 months after discharge were observed. Multivariate regression analysis was used to identify independent risk factors for rehospitalization. RESULTS: The rate of rehospitalization was 11.4% (125/1099). Compared to the nonreadmission children, IgE levels, the proportion of children with asthma and hospitalization duration were significantly higher in the readmission children (p < 0.05). Compared to the children with normal IgE (≤ 165 IU/ml) levels, the risk of rehospitalization was significantly higher in children with abnormal IgE [odds ratio (OR) 1.781, 95% confidence interval (CI) 1.209–2.624, p = 0.004]. Children with IgE level more than three times the upper limit had even higher risks of readmission (OR 2.037, 95%CI 1.172–3.540, p = 0.012). Meanwhile, the risk of readmission in children with abnormal IgE combined with or without bronchial asthma was significantly higher (OR 2.548 and 1.918, 95% CI 1.490–4.358 and 1.218–3.020, p = 0.001 and 0.005, respectively). CONCLUSIONS: Children aged over 1 year with bronchopneumonia who had higher IgE levels are at increased risk for rehospitalization within the first 12 months of the index hospitalization and IgE level may be used as a predictor of rehospitalization in children with bronchopneumonia. SAGE Publications 2019-10-06 /pmc/articles/PMC6783659/ /pubmed/31588854 http://dx.doi.org/10.1177/1753466619879832 Text en © The Author(s), 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
You, Cun
Ran, Guo
Wu, Xiao
Wang, Yu
Tian, Hua
Fan, Jiabao
Yao, Zezhong
Wang, Fei
High immunoglobulin E level is associated with increased readmission in children with bronchopneumonia
title High immunoglobulin E level is associated with increased readmission in children with bronchopneumonia
title_full High immunoglobulin E level is associated with increased readmission in children with bronchopneumonia
title_fullStr High immunoglobulin E level is associated with increased readmission in children with bronchopneumonia
title_full_unstemmed High immunoglobulin E level is associated with increased readmission in children with bronchopneumonia
title_short High immunoglobulin E level is associated with increased readmission in children with bronchopneumonia
title_sort high immunoglobulin e level is associated with increased readmission in children with bronchopneumonia
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783659/
https://www.ncbi.nlm.nih.gov/pubmed/31588854
http://dx.doi.org/10.1177/1753466619879832
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