Abstract:
ObjectiveTo explore the curative effect of budesonide inhalation combined with montelukast sodium and levocetirizine on the treatment of children with cough variant asthma.
MethodsA total of 80 children aged 6-12 diagnosed with cough variant asthma were selected as the research objects, and randomly divided into the observation group and the control group, with 40 cases in each group.The control group received budesonide inhalation aerosol inhalation therapy and corresponding supportive treatment, while the observation group received oral montelukast sodium and levocetirizine on the basis of the control group.The clinical efficacy was evaluated by measuring the levels of inflammatory factors and other pulmonary function indicators before and after treatment, and recording the total effective rate and the occurrence of adverse reactions.
ResultsThe total effective rate of the observation group was 100.00%, which was higher than 72.50% of the control group (P < 0.01).Before treatment, there was no significant difference in the levels of inflammatory factors and lung function indexes between the two groups (P>0.05).After treatment, the levels of IgE, IL-4 and IL-13 in the observation group and the control group were significantly lower than those before treatment (P < 0.01), and the reduction range in the observation group was greater than that in the control group (P < 0.01).After treatment, the indexes of lung function in the observation group and the control group were significantly higher than those before treatment (P < 0.01), and the increase in the observation group was greater than that in the control group (P < 0.01).The rate of adverse reactions in the observation group occurred was also lower than that of the control group, and the difference was statistically significant (P < 0.05).
ConclusionsBudesonide inhalation combined with montelukast sodium and levocetirizine in the treatment of children with cough variant asthma can significantly improve the effective rate and lung function, reduce the levels of inflammatory factors and the incidence of adverse reactions, which is worth promoting in clinical appilcation.