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Comparison of Combined Nebulization of Salbutamol-Ipratropium Bromide with Salbutamol Alone in Children with Mild and Moderate Acute Asthma

机译:单纯沙丁胺醇 - 普罗吡啶溴铵与轻度和中度急性哮喘儿童盐豆蛋白单独的比较

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摘要

ntroduction: The β2 agonists are potent bronchodilators but their repeated and high doses are related to adrenergic side effects. While ipratropium bromide, an anticholinergic bronchodilator has less adverse effects.Objective: To compare the efficacy of combined nebulization of salbutamol-ipratropium bromide with salbutamol alone in children with mild and moderate acute asthma.Materials and Methods: This randomised control trial was done on 80 children aged 5 to 12 years who presented with mild to moderate acute asthma in the emergency department of Children Hospital of Pakistan Institute of Medical Sciences (PIMS) from July 2014 to June 2016 and randomized into 2 groups. In the experimental group each child received 2 nebulizations of combined salbutamol (5mg) and ipratropium Bromide (0.25mg) at presentation and 20 minutes later. Similarly, each child of the control group received 2 nebulizations of 5mg Salbutamol and 2 ml of Normal saline. Asthma clinical score (ACS) was assessed at baseline and then after every 20 minutes up to one hour after the presentation.Results: In the experimental group, the mean + SD ACS at presentation and 60 minutes were 3.50±1.8 and 3.45±1.7 respectively with mean + SD change in ACS of 0.05 ± 0.1. In the control group, the mean + SD ACS at presentation and 60 minutes were 3.70 ± 1.2 and 3.60 ± 1.9, respectively with mean + SD change in ACS of 0.1 ± 0.7. This difference in mean + SD change in ACS between 2 groups was not statistically significant (P=0.6560).Conclusion: There is no statistically significant benefit of adding ipratropium bromide with salbutamol nebulization as compared to salbutamol alone for the management of children with mild to moderate asthma attacks.
机译:ntroduction:β2激动剂是有效的支气管扩张剂,但它们的重复和高剂量与肾上腺素能副作用有关。虽然溴化钡溴化物,但抗胆碱能支气管扩张剂具有较小的不良反应。目的:比较Salbutamol-Ipratiropium Bromide与单独在温和和中度急性哮喘的儿童中单独乳酪蛋白酶雾化的疗效。材料和方法:该随机对照试验于2014年7月至2016年6月介绍了5至12岁以上的50至12岁儿童,患有轻度至中度急性哮喘,从2016年7月至2016年6月和随机分组分为2组。在实验组中,每个儿童在呈现中接受了2个杂交的Salbutamol(5mg)和β-溴化钠(0.25mg)和20分钟后。类似地,对照组的每个孩子接受2个雾化5mg Salbutamol和2ml的生理盐水。在基线评估哮喘临床评分(ACS),然后在介绍后每20分钟达1小时后评估。结果:在实验组中,分别为3.50±1.8和3.45±1.7的平均值+ SD AC分别,AC的平均+ SD变化为0.05±0.1。在对照组中,介绍的平均值+ SD ACS和60分钟分别为3.70±1.2和3.60±1.9,AC的平均+ SD变化为0.1±0.7。 2组之间ACS的平均值+ SD变化的这种差异在统计学上没有统计学意义(P = 0.6560)。结论:与单独的Salbutamol相比,与Salbutamol Noxization一起用于管理轻度至中度哮喘发作的儿童,没有统计学显着的益处。

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