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Clinical effect analysis of medication regimens on the treatment of cough variant asthma in children

Published on Jun. 28, 2024Total Views: 86 times Total Downloads: 32 times Download Mobile

Author: LOU Nannan 1 GUO Jing 1 MA Xiang 1, 2 GAI Zhongtao 1, 2

Affiliation: 1. Department of Respiratory Disease, Children’s Hospital Affiliated to Shandong University, Jinan 250000, China 2. Jinan Key Laboratory of Pediatric Respiratory Diseases, Jinan Children’s Hospital, Jinan 250000, China

Keywords: Child Asthma Cough variant asthma;ICS+LABA ICS+LTRA

DOI: 10.12173/j.issn.1004-5511.202403150

Reference: Lou NN, Guo J, Ma X, Gai ZT. Clinical effect analysis of medication regimens on the treatment of cough variant asthma in children[J]. Journal of Mathematical Medicine, 2024, 37(6): 418-424. DOI: 10.12173/j.issn.1004-5511.202403150[Article in Chinese]

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Abstract

Objective  To explore the clinical efficacy and the best course of treatment of cough variant asthma (CVA) in children.

Methods  The clinical data of children with CVA who were treated in Children 's Hospital Affiliated to Shandong University from October 2019 to June 2022 were retrospectively analyzed. According to different treatment regimens, they were divided into two groups: inhaled corticosteroids combined with long-acting β2 receptor agonist (ICS+LABA) or ICS combined with leukotriene receptor antagonist (ICS+LTRA). The disease control and cough symptom recurrence rate were compared between the two groups.

Results  A total of 187 patients were included, with 50 in ICS+LABA group and 137 in ICS+LTRA group. There was no significant difference in CVA control rate (92.0% vs. 89.8%) and cough recurrence rate (4.0% vs. 11.7%) between the two regimens (P>0.05). Compared with ICS+LABA, ICS+LTRA regimen had the most significant effect at the 16th week of treatment.

Conclusion  The efficacy of ICS+LABA and ICS+LTRA in the treatment of CVA in children is equivalent. It can be selected according to the age of the children and the wishes of the patients. In order to achieve better clinical control,  a minimum of 16 weeks of medication is recommended.

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References

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