Virus-induced asthma exacerbations in children: efficiency and tolerability of the «Esberitox» medication
DOI:
https://doi.org/10.15574/PP.2020.81.64Keywords:
bronchial asthma, viral infection, children, «Esberitox»Abstract
Purpose — to assess the effectiveness and tolerability of «Esberitox» in children with asthma and acute respiratory viral infections.Patients and methods. 34 children aged 6–14 years with asthma of varying severity and acute respiratory viral infection were examined, which were divided into two groups by simple randomization. Children of the main group (n=20) received treatment in accordance with GINA (2019) and additionally «Esberitox» at an age dosage for 10 days. The children of the comparison group (n=14) were given symptomatic treatment (antipyretic, nasal and local antiseptic drugs) and basic therapy. The criteria for the effectiveness of the treatment were: regression of the symptoms of catarrh of the upper respiratory tract, dynamics of local immunity (immunoglobulins and saliva lysozyme, expression of CD56+ cells in a smear from the nasal mucosa and tonsils, number of macrophages in induced sputum), number of children with exacerbation of asthma.
Results. The use of «Esberitox» in the complex treatment of the examined children contributed to: regression of the symptoms of catarrh of the upper respiratory tract by 3–5 days compared with the persistence of symptoms in children of the comparison group); increase in the number of expressing CD 56+ cells in the nasal mucosa and tonsils, sIgA and lysozyme in saliva, macrophages in induced sputum; reducing the risk of exacerbation of bronchial asthma (no exacerbations in 65.0% of children in the main group and 35.7% of the comparison group). When prescribing «Esberitox» no adverse reactions.
Conclusions. The clinical efficacy and high safety profile of «Esberitox» in children with asthma and acute respiratory infections allows it to be recommended for the treatment and prevention of virus-induced exacerbations of bronchial obstructive diseases in children.
The research was carried out in accordance with the principles of the Helsinki Declaration. The study protocol was approved by the Local Ethics Committee of this Institute. The informed consent of the patient was obtained for conducting the studies.
No conflict of interest were declared by the authors.
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