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出 处:《陕西医学杂志》2012年第5期535-537,564,共4页Shaanxi Medical Journal
摘 要:目的:探讨布地奈德混悬液吸入治疗慢性阻塞性肺疾病急性加重期(AECOPD)的临床疗效与安全性。方法:将165例慢性阻塞性肺疾病(COPD)急性加重期患者随机分为大剂量激素吸入组(A组,42例)、一般剂量激素吸入组(B组,40例)、甲强龙组(C组,42例)和对照组(D组,41例)。四组均接受常规治疗,A组在此基础上雾化吸入布地奈德混悬溶液2mg/次,每日2次;B组吸入布地奈德混悬溶液1mg/次,每日2次;疗程均7d。C组予甲强龙40mg/日静点,好转后改为甲泼尼龙片8mg/d口服,共7d。分别于治疗前和治疗第3、7天测定肺功能、血气分析、呼吸困难评分以及记录不良反应。结果:治疗后第3天,A组及C组各参数与D组比较有显著性差异(P<0.05)。治疗后第7天,A、B、C三组与D组比较均有显著性差异(P<0.05)。而A组与B组组间比较无显著性差异(P>0.05)。吸入激素的局部不良反应主要有咽部不适、声音嘶哑等,均明显低于C组(P<0.05)。结论:大剂量吸入布地奈德混悬液治疗AECOPD疗效较为确切。Objective :To study the clinical effects of nebulized budesonide in the treatment of acute exacerbation of chronic obstructive pulmonary disease(AECOPD).Methods :165 patients with AECOPD were randomly divided into 4 groups : Group A was given conventional treatment and inhaled budesonide,each time 2mg,twice a day.Group B was given conventional treatment and inhaled budesonide,each time 1mg,twice a day.Group C was given conventional treatment and was injected methylpredisolone.Group D was given conventional treatment only.The 4 groups were observed before and after 3 day and the end of treatment.The difference in dyspnea scores,lung function and blood gas analysis were compared.Results :After treatment,compared with Group D,the differences in dyspnea scores,lung function and blood gas analysis of Group A,B and C were statistically significant(P0.05).There was not statistically significant(P0.05) among Group A,B and C after end of treatment.After 3 days'treatment,the differences in corresponding indicators of Group A and C were statistically significant(P0.05),compared with Group D.The adverse reactions in Group A and B were lower than those in Group C.Conclusion :The research shows that nebulized budsonide of large dosage is safe and effective.
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