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不同剂量布地奈德对哮喘急性发作患儿的疗效

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目的 探讨不同剂量布地奈德对哮喘急性发作患儿的疗效及嗜酸性粒细胞(EOS)水平的影响.方法 选取2021年3月至2023年6月大同市第一人民医院收治的急性哮喘患儿103例,按随机数表法分为低剂量组(51例)和高剂量组(52例).两组均采用布地奈德联合孟鲁司特钠治疗,仅布地奈德剂量不同(低剂量组每次0.5 mg,高剂量组每次1.0 mg).观察两组患儿的疗效及不良反应发生情况.结果 两组治疗总有效率比较差异无统计学意义(90.19%vs 96.15%,χ2=1.442,P>0.05).治疗后,两组的第1秒用力呼气量(FEV1)、呼吸峰流速(PEF)、用力肺活量(FVC)均较治疗前升高(P<0.05),高剂量组的FEV1、PEF、FVC[分别为(1.87±0.31)L、(3.10±0.38)L·s-1、(3.04±0.69)L]高于低剂量组[分别为(1.46±0.28)L、(2.67±0.34)L·s-1、(2.57±0.62)L](t=7.039、6.048、3.634,均P<0.05).治疗后,两组EOS水平均下降,且高剂量组EOS[(0.27±0.09)×109·L-1]低于低剂量组[(0.19±0.08)×109·L-1](t=4.770,P<0.05).两组不良反应发生率比较差异无统计学意义(7.84%vs 9.61%,χ2=0.101,P>0.05).结论 0.5 mg与1.0 mg剂量的布地奈德治疗哮喘急性发作患儿均具有良好的有效性与安全性,1.0 mg剂量的布地奈德应用效果更佳.
Efficacy of budesonide at different dosages in treatment of acute asthma exacerbation in children
Objective To investigate the clinical efficacy of budesonide at different dosages in the treatment of acute asthma exacerbation in children and its effect on changes in eosinophil(EOS)levels.Methods One hundred and three children with acute asthma exacerbation admitted to Datong First People's Hospital from March 2021 to June 2023 were selected as the research subjects and grouped using the random number table method.All children were subjected to the therapy of budesonide combined with montelu-kast sodium.However,budesonide was given at a dosage of 0.5 mg each time in the low-dosage group(n=51)and 1.0 mg each time in the high-dosage group(n=52).Then the clinical efficacy and adverse reactions were observed in both groups.Results No statistical difference was found in clinical efficacy rate between the two groups(90.19%vs 96.15%,χ2=1.442,P>0.05).An increase in Forced Ex-piratory Volume in First Second(FEV1),peak expiratory flow(PEF),and forced vital capacity(FVC)and a reduction in EOS were found in all patients after treatment,and the high-dosage group showed a larger FEV1((1.87±0.31)L vs(1.46±0.28)L),FVC((3.04±0.69)L vs(2.57±0.62)L)and PEF((3.10±0.38)L·s-1 vs(2.67±0.34)L·s-1),and lower EOS((0.27±0.09)×109·L-1 vs(0.19±0.08)×109·L-1)as com-pared with the low-dosage group,demonstrating statistical difference(t=7.039,6.048,3.634,4.770,all P<0.05).There was no significant difference in the adverse reaction rate between the two groups(7.84%vs 9.61%,χ2=0.101,P>0.05).Conclusion Both 0.5 mg and 1.0 mg of budesonide has good efficacy and safety profile in the treatment of acute asthma exacerbation in children.Budesonide admin-stered at a dosage of 1.0 mg each time can exert better effect.

AsthmaAcute exacerbationChildBudesonideMontelukast sodiumEosinophil

陈占芳、王向平、张泽佳

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大同市第一人民医院儿科,大同 037000

哮喘 急性发作期 儿童 布地奈德 孟鲁司特钠 嗜酸性粒细胞

山西省卫生计生委科研计划项目

201602014

2024

中国药物应用与监测
中国人民解放军总医院

中国药物应用与监测

CSTPCD
影响因子:1.983
ISSN:1672-8157
年,卷(期):2024.21(5)