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作 者:黄娟[1] 张军[1] 舒俊华[1] 陈颖[1] 陈霞[1] 龙珍[1] 周小勤[1] 戚红[1]
出 处:《武汉大学学报(医学版)》2015年第6期948-951,共4页Medical Journal of Wuhan University
基 金:湖北省自然科学基金资助项目(编号:2013CFB048)
摘 要:目的:观察抗胆碱能药物-噻托溴铵在哮喘控制不良患儿中的疗效。方法:2013年1月至2014年1月我院哮喘门诊诊断中度持续性哮喘患儿,按2008年修订《儿童支气管哮喘诊断与防治指南》进行临床评估,予丙酸氟替卡松气雾剂(辅舒酮,125μg/次,2次/d)治疗3个月仍评估为哮喘未控制者60例。随机分为A组:辅舒酮125μg/次,早晚各2喷;B组:辅舒酮125μg/次,2次/d+福莫特罗粉吸入剂(奥克斯都保)4.5μg 1次/d;C组:辅舒酮125μg/次,2次/d+噻托溴铵粉吸入剂(思力华,18μg 1次/d),观察4周。结果:A组患儿治疗前后肺功能无显著改善,差异无统计学意义;B组及C组治疗后FEV1和PEF占预计值百分比均较治疗前有显著改善(P<0.001)。哮喘控制不良患儿夜间临床症状评分显著高于日间临床症状评分(P<0.001);无论是日间还是夜间临床症状评分3组患儿治疗后均较治疗前有显著改善(P<0.001);C组夜间临床症状评分较B组改善更显著(P<0.05)。结论:对于低剂量糖皮质激素吸入哮喘控制不良的中度持续性患儿,每日加用一次长效受体阻滞剂-噻托溴铵与联合长效β2受体激动剂疗效相当,不良反应罕见,可成为哮喘治疗效果不佳患儿的另一种可选择方案。Objective:To observe the efficacy of inhaled tiotropium in children with asthma,uncontrolled with standard combination therapy.Methods:60uncontrolled patients which inhaled fluticasone(125μg,bid)for 3months from January 2013 to January 2014 in our hospital.They were randomly divided into Group A:Flixotide 250μg,bid;Group B:flixotide(125μg,bid)+ formoterol(4.5μg,qd);Group C:Flixotide(125μg,bid)+tiotropium(18μg,qd)and were followed up for four weeks.Results:There was no significant improvement in the lung function of Group A before and after treatment.But the FEV1%and PEF% of group B and group C had significantly improved,P〈0.001.Uncontrolled asthma in children with the nocturnal symptoms score was significantly higher than daytime clinical symptom score in uncontrolled asthma,P〈0.001;after treatment there had a significant improvements in either the daytime or nighttimeclinical symptom scores than pre-treatment of the three groups,P〈0.001;the nighttime clinical symptom scores of group C had significantly improved than that in group B,P 0.05.Conclusion:Low-dose inhaled corticosteroids plus tiotropium has an equal effect with plus longactingβ2-agonist to the uncontrolled asthma in children and has no considerable adverse reaction,which may become a new treatment in poorly controlled asthma in children.
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