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沙美特罗替卡松联合孟鲁司特对咳嗽变异性哮喘患儿肺功能及血清炎性因子的影响 被引量:10

Effects of salmeterol xinafoate and fluticasone propionate powder in combination with montelukast on pulmonary function and serum inflammatory cytokines in children with cough variant asthma
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摘要 目的 探讨沙美特罗替卡松联合孟鲁司特对儿童咳嗽变异性哮喘(CVA)的疗效,及对肺功能、血清炎性因子的影响.方法 选取CVA患儿200例,采用随机数字表法将其分为观察组与对照组,各100例.对照组给予沙美特罗替卡松吸入,观察组在对照组基础上加用孟鲁司特钠咀嚼片,疗程为3个月.比较两组临床疗效、治疗前后肺功能指标和血清炎性因子的变化情况.结果 观察组总有效率(88.3%)明显高于对照组(70.3%)(χ2=9.146,P〈0.05).观察组咳嗽缓解时间(5.45±1.32)d、消失时间(8.63±1.96)d,均显著短于对照组的(7.33±2.46)d、(12.61±1.84)d(t=6.505、14.229,均P〈0.05).治疗前,两组第1秒用力呼气量(FEV1)、FEV1占用力肺活量的百分比(FEV1/FVC)、最大呼气峰流速占预计值百分比(PEF%)、免疫球蛋白E(IgE)、肿瘤坏死因子α(TNF-α)及白介素-17(IL-17)差异均无统计学意义(P〉0.05);治疗后,观察组和对照组FEV1、FEV1/FVC、PEF均较同组治疗前明显升高[观察组:(2.11±0.34)L、(73.71±11.44)%、(86.34±7.85)%,t=18.149、7.664、19.196,均P〈0.05;对照组:(1.82±0.35)L、(69.36±10.79)%、(81.66±8.03)%,t=9.312、5.418、13.627,均P〈0.05],IgE、TNF-α、IL-17较同组治疗前明显降低[观察组:(141.3±38.2)ng/L、(624.7±213.2)ng/L、(6.1±2.1)ng/L,t=15.200、13.708、15.881,均P〈0.05;对照组:(191.5±41.9)ng/L、(835.5±326.3)ng/L、(9.4±2.7)ng/L,t=6.784、6.206、8.550,P〈0.05],且两组治疗后的差异均有统计学意义(t=5.717、2.659、4.008、8.521、4.842、9.296,均P〈0.05).结论 沙美特罗替卡松联合孟鲁斯特钠治疗儿童咳嗽变异性哮喘具有良好的临床疗效,有助于改善患儿肺功能,降低炎性因子水平. Objective To investigate the therapeutic effects of salmeterol xinafoate and fluticasone propio-nate powder(seretide) in combination with montelukast on children with cough variant asthma (CVA),and its effect on pulmonary function and serum inflammatory cytokines .Methods 200 patients with CVA were enrolled ,and they were randomly divided into two groups according to the random number table ,100 cases in each group .The control group was treated with seretide ,while the observation group was treated with seretide and montelukast sodium ,both two groups were treated for 3 months.The clinical efficacy,pulmonary function and serum inflammatory cytokines were compared between the two groups .Results The total effective rate of the observation group ( 88.3%) was significantly higher than that of the control group (70.3%;χ2 =9.146,P〈0.05).The duration of remission and disappearance of cough symptoms in the observation group were (5.45 ±1.32) d,(8.63 ±1.96) d,respectively, which were significantly shorter than those in the control group [(7.33 ±2.46) d,(12.61 ±1.84) d;t =6.505, 14.229,all P〈0.05].There were no statistically significant differences in FEV 1,FEV1/FVC,PEF,IgE,TNF-αand IL-17 between the two groups before treatment (all P〉0.05).After treatment,the levels of FEV1,FEV1/FVC, PEF were all significantly higher than those before treatment [(2.11 ±0.34) L,(73.71 ±11.44)%,(86.34 ± 7.85)%,t=18.149,7.664,19.196,all P〈0.05;(1.82 ±0.35)L,(69.36 ±10.79)%,(81.66 ±8.03)%,t=9.312,5.418,13.627,all P 〈0.05],and IgE,TNF -α,IL -17 levels were significantly decreased [(141.3 ± 38.2)ng/L,(624.7 ±213.2) ng/L,(6.1 ±2.1) ng/L,t =15.200,13.708,15.881,all P 〈0.05;(191.5 ±41.9) ng/L,(835.5 ±326.3)ng/L,(9.4 ±2.7) ng/L,t=6.784,6.206,8.550,all P〈0.05].The differences between the two groups were statistically significant(t=5.717,2.659,4.008,8.521,4.842,9.296,all P〈0.05). Conclusion Salmeterol xinafoate and fluticasone propionate powder in combination with montelukast sodium has excellent clinical effect in the treatment of children with CVA ,which can improve the pulmonary function and reduce inflammatory cytokines .
出处 《中国基层医药》 CAS 2018年第2期182-185,共4页 Chinese Journal of Primary Medicine and Pharmacy
关键词 沙美特罗替卡松 孟鲁司特 哮喘 咳嗽 儿童 呼吸功能试验 炎症趋化因子类 Salmeterol xinafoate and fluticasone propionate powder Montelukast Asthma Cough Child Respiratory function tests Chemokines
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  • 1赖克方.咳嗽严重度界定与咳嗽激发试验[J].中国实用内科杂志,2006,26(1):15-17. 被引量:95
  • 2袁壮.要重视儿童慢性咳嗽的诊断和治疗[J].国际儿科学杂志,2006,33(1):1-2. 被引量:52
  • 3彭珉娟,戴缨,张彤.沙美特罗替卡松干粉剂吸入治疗儿童咳嗽变异型哮喘疗效评价[J].中国呼吸与危重监护杂志,2006,5(2):122-124. 被引量:8
  • 4于化鹏 刘兰平.咳嗽变异性哮喘与神经源性气道炎症的关系[J].中华结核和呼吸杂志,2000,23(4):211-211.
  • 5中华医学会呼吸病学分会哮喘学组.咳嗽的诊断与治疗指南(草案).中华结核和呼吸杂志,2009,32(6):355-358.
  • 6Global Strategy for Asthma Management and Prevention, Global Initiative for Asthma (GINA) 2007. [ R/OL ]. [ 2008 - 03 - 27 ].
  • 7Park JJ.Li Z,Yang XO,et al. A distinct lineage of CD4+T cellsregulates tissue inflammation by producing interleukin 17[J]. NatImmunol.2005 .6(11) : 1133-1141.
  • 8Harrington LE, Hatton RD, Mangan PR, et al. Interleukin 17-producting CD4+ effector T cells develop via a lineage distinctfrom the T helper type 1 and 2 lineages[J]. Nat Immunol,2005,6(11):1123-1132.
  • 9van Hamburg J P, Asmawidjaja PS,Davelaar N,et al. Thl7 cells,but not Thl cells. from patients with early rheumatoid arthritisare potent inducers of matrix metalloproteinases and proinflamma-tory cytokines upon synovial fibroblast interaction, including auto-crine interleukin-17A production[J]. Arthritis Rheum, 2011,63(1):73-83.
  • 10Kreindler JL.Bertrand CA,Lee RJ, et al. Interleukin-17A inducesbicarbonate secretion in normal human bronchial epithelial cells[J]. Am J Physiol Lung Cell Mol Physiol,2009,296(2) ;257-266.

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