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舒利迭与普米克吸入治疗中重度哮喘疗效观察 被引量:1

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摘要 目的:评价吸入舒利迭治疗中重度哮喘的疗效。方法:选取中重度哮喘患者43例,随机分为两组,治疗组26例,观察组17例。均在初诊及治疗第1、3、6个月详细记录哮喘每周发作次数、每天吸入短效β2激动剂的次数及呼气峰流数(PEFR)。结果:初治时两组患者的发病次数、吸入短效β2激动剂及PEFR无明显差异(P>0.5);治疗后1、3、6个月时舒利迭组发病次数、吸入短效β2激动剂次数明显少于普米克组,PEFR明显增加,有明显差异(P<0.01)。结论:吸入舒利迭治疗中重度哮喘安全可靠。
作者 原雪晴 高峰
出处 《中国社区医师(医学专业)》 2008年第4期21-21,共1页
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