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The influence of inhaled corticosteroid discontinuation in children with well-controlled asthma
Asthma is a chronic inflammatory disease that requires adherence to both preventative and therapeutic interventions in disease management. Children with asthma are likely to discontinue inhaled corticosteroids (ICS), especially when symptoms are under control. We aimed to investigate the impact of I...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5585489/ https://www.ncbi.nlm.nih.gov/pubmed/28858095 http://dx.doi.org/10.1097/MD.0000000000007848 |
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author | Zheng, Shengkun Yu, Qiying Zeng, Xiangyan Sun, Wangming Sun, Yan Li, Mengrong |
author_facet | Zheng, Shengkun Yu, Qiying Zeng, Xiangyan Sun, Wangming Sun, Yan Li, Mengrong |
author_sort | Zheng, Shengkun |
collection | PubMed |
description | Asthma is a chronic inflammatory disease that requires adherence to both preventative and therapeutic interventions in disease management. Children with asthma are likely to discontinue inhaled corticosteroids (ICS), especially when symptoms are under control. We aimed to investigate the impact of ICS adherence in children whose symptoms were under control. The study is cohort study; 35 children with controlled asthma that had undergone 3 years of follow-up were included. Serum eosinophil count, serum total IgE (tIgE), and lung function (FEV1, FEV1/FVC, PEF, FEF20–75%, and PC20) were evaluated at the beginning and end of the follow-up. At baseline, patients in both the adherent and nonadherent groups were similar. After 3 years, the nonadherent group who had discontinued ICS had a decrease in FEV1 (P < .05), FEV1/FVC (P < .05), PEF (P < .05), and FEF20–75% (P < .05). The nonadherent group had no significant improvement in PC20 compared with their values at the beginning of the follow-up, whereas the adherent group had improvement in PC20. Furthermore, there was an increase in serum eosinophil (P < .001) and tIgE (P < .05) in the nonadherent compared with the adherent group. Despite good asthma control, airway hyperresponsiveness (AHR) was detected in a large proportion of children with asthma. ICS discontinuation affected lung function, serum eosinophil count, tIgE, and AHR. Adequate adherence is important in asthma management. The benefits of ICS and the influence of drug discontinuation despite good asthma control may encourage better adherence from patients. |
format | Online Article Text |
id | pubmed-5585489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-55854892017-09-11 The influence of inhaled corticosteroid discontinuation in children with well-controlled asthma Zheng, Shengkun Yu, Qiying Zeng, Xiangyan Sun, Wangming Sun, Yan Li, Mengrong Medicine (Baltimore) 6200 Asthma is a chronic inflammatory disease that requires adherence to both preventative and therapeutic interventions in disease management. Children with asthma are likely to discontinue inhaled corticosteroids (ICS), especially when symptoms are under control. We aimed to investigate the impact of ICS adherence in children whose symptoms were under control. The study is cohort study; 35 children with controlled asthma that had undergone 3 years of follow-up were included. Serum eosinophil count, serum total IgE (tIgE), and lung function (FEV1, FEV1/FVC, PEF, FEF20–75%, and PC20) were evaluated at the beginning and end of the follow-up. At baseline, patients in both the adherent and nonadherent groups were similar. After 3 years, the nonadherent group who had discontinued ICS had a decrease in FEV1 (P < .05), FEV1/FVC (P < .05), PEF (P < .05), and FEF20–75% (P < .05). The nonadherent group had no significant improvement in PC20 compared with their values at the beginning of the follow-up, whereas the adherent group had improvement in PC20. Furthermore, there was an increase in serum eosinophil (P < .001) and tIgE (P < .05) in the nonadherent compared with the adherent group. Despite good asthma control, airway hyperresponsiveness (AHR) was detected in a large proportion of children with asthma. ICS discontinuation affected lung function, serum eosinophil count, tIgE, and AHR. Adequate adherence is important in asthma management. The benefits of ICS and the influence of drug discontinuation despite good asthma control may encourage better adherence from patients. Wolters Kluwer Health 2017-09-01 /pmc/articles/PMC5585489/ /pubmed/28858095 http://dx.doi.org/10.1097/MD.0000000000007848 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 6200 Zheng, Shengkun Yu, Qiying Zeng, Xiangyan Sun, Wangming Sun, Yan Li, Mengrong The influence of inhaled corticosteroid discontinuation in children with well-controlled asthma |
title | The influence of inhaled corticosteroid discontinuation in children with well-controlled asthma |
title_full | The influence of inhaled corticosteroid discontinuation in children with well-controlled asthma |
title_fullStr | The influence of inhaled corticosteroid discontinuation in children with well-controlled asthma |
title_full_unstemmed | The influence of inhaled corticosteroid discontinuation in children with well-controlled asthma |
title_short | The influence of inhaled corticosteroid discontinuation in children with well-controlled asthma |
title_sort | influence of inhaled corticosteroid discontinuation in children with well-controlled asthma |
topic | 6200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5585489/ https://www.ncbi.nlm.nih.gov/pubmed/28858095 http://dx.doi.org/10.1097/MD.0000000000007848 |
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