本文選題：布地奈德混懸液 + 霧化吸入��； 參考：《中華醫(yī)院感染學雜志》2014年12期

【摘要】：目的探討布地奈德混懸液霧化吸入治療急性感染性喉炎患兒的臨床效果,以期為臨床治療提供科學依據(jù)。方法選取2010-2013年兒科住院治療的159例急性感染性喉炎患兒為研究對象,依據(jù)治療方案分為觀察組、對照組及常規(guī)組,每組各53例,觀察組采取常規(guī)治療加布地奈德混懸液霧化吸入;對照組采取常規(guī)治療加地塞米松霧化吸入;常規(guī)組實行常規(guī)治療,比較3組患兒的治療起效時間、治療效果以及治療依從率,評價布地奈德混懸液霧化吸入治療急性感染性喉炎的臨床價值,數(shù)據(jù)采用SPSS15.0軟件進行統(tǒng)計分析。結(jié)果經(jīng)過系統(tǒng)治療,所有患兒的癥狀均有所好轉(zhuǎn),其中觀察組患兒的起效時間明顯最短,與對照組、常規(guī)組比較差異有統(tǒng)計學意義(P0.05);8h治療總有效率觀察組為56.60%、對照組為18.87%、常規(guī)組為15.09%,24h治療總有效率觀察組為100.00%、對照組為96.23%、常規(guī)組為62.26%,組間數(shù)據(jù)比較,差異有統(tǒng)計學意義(P0.05);治療依從率觀察組為81.13%、對照組為83.02%、常規(guī)組為100.00%,3組數(shù)據(jù)比較差異有統(tǒng)計學意義(P0.05)。結(jié)論布地奈德混懸液霧化吸入治療急性感染性喉炎見效快、療效好,但對患兒的治療依從性有一定影響,臨床推廣過程應加以注意。
[Abstract]:Objective to investigate the clinical effect of budesonide suspension aerosol inhalation in children with acute infectious laryngitis. Methods 159 children with acute infectious laryngitis who were hospitalized in pediatrics from 2010 to 2013 were divided into three groups: observation group, control group and routine group, 53 cases in each group. The observation group received routine treatment plus budesonide suspension atomization inhalation, the control group received routine therapy plus dexamethasone atomization inhalation, and the routine treatment group was given routine treatment. To evaluate the clinical value of budesonide suspension aerosol inhalation in the treatment of acute infectious laryngitis, the data were analyzed by SPSS15.0 software. Results after systematic treatment, the symptoms of all the children were improved, among which the observation group had the shortest effective time and the control group. The total effective rate of the routine group was 56.60, that of the control group was 18.87, that of the routine group was 15.09 and that of the control group was 100.00,96.23cm, and that of the routine group was 62.260.The total effective rate was 56.60 in the observation group, 18.87 in the control group, 100.00in the control group, 96.23in the control group, and 62.26 in the routine group. The therapeutic compliance rate was 81.13 in the observation group, 83.022 in the control group, and 100.00,0.05 in the routine group. Conclusion budesonide suspension aerosol inhalation is effective and effective in the treatment of acute infectious laryngitis, but it has a certain effect on the treatment compliance of children.
【作者單位】： 湖北省建始縣人民醫(yī)院兒科;
【基金】：建始縣衛(wèi)生局醫(yī)藥專科科研基金項目(TW-201013-036)
【分類號】：R767.11

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【共引文獻】

相關(guān)期刊論文 前10條

1 翟磊;;布地奈德霧化吸入治療小兒肺炎臨床分析[J];臨床醫(yī)學;2014年11期

2 王笑芳;;布地奈德混懸液霧化吸入治療耳鼻喉科急性炎癥療效觀察[J];中國醫(yī)藥科學;2015年04期

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本文編號：1814646