Prednisolone oral solution plus inhaled procaterol for acute asthma in children: a double-blind randomized controlled trial.

Li-Hsin Huang, S. Shyur, D. Wen, Yi-Chi Chang, Yi-Chun Ma, Sheng-Chieh Lin, Wen-Chiu Wu, Jiunn-Yi Wu
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引用次数: 4

Abstract

BACKGROUND To evaluate the efficacy of prednisolone sodium phosphate oral solution plus inhaled procaterol in the treatment of acute asthma in children. METHODS Forty-three patients aged 6 to 12 years with an acute exacerbation of asthma were double-blind randomized into one of two treatment groups in a 1:1 ratio:1) prednisolone oral solution +placebo tablets + procaterol MDI or 2) prednisolone tablets +placebo oral solution + procaterol MDI, all given three times daily for 7 days. Peak expiratory flow rate (PEFR), 24-hour reflective asthma symptom scores, spirometry and pulmonary index score (PIS) were recorded before and after treatment. Net changes in PEFR, symptom score, PIS, Forced Expiratory Volume in the first second (FEV1), FEV1/forced vital capacity (FVC), forced expiratory flow between 25 and 75 percent of the forced vital capacity (FEF(25-75%)) (before and after treatment) and global assessment by the investigator and the subjects or their parents were analyzed. RESULTS The two groups were statistically similar at baseline values of these parameters. After a 7-day course of treatment, the net change of PEFR before and after treatment was significantly improved in both groups, but there was no significant difference in the net change of PEFR between the two groups (57.27+/-31.44 L/min vs. 54.29 +/-30.04 L/min, difference 2.99 +/-30.76 L/min, mean +/-SD, P=0.752). The net change in PIS and total symptom score did not differ between the two groups (P=0.091 and 0.827, respectively). Similarly, the FEV1, FEV1/FVC and FEF25-75% all improved with either treatment, and neither group was significantly superior to the other group (P=0.162, 0.48 and 0.081, respectively). Global assessment by the investigator and the subjects or their parents at the end of study indicated an essentially comparable result. CONCLUSIONS Prednisolone sodium phosphate oral solution plus inhaled procaterol is as efficacious as prednisolone tablets plus inhaled procaterol in the management of acute asthma in children.
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泼尼松龙口服溶液加普洛特罗吸入治疗儿童急性哮喘:一项双盲随机对照试验。
目的:评价泼尼松龙磷酸钠口服溶液联合普洛特罗吸入治疗儿童急性哮喘的疗效。方法43例6 ~ 12岁哮喘急性加重患者,按1:1的比例随机分为2组:1)强的松龙口服液+安慰剂片+ procaterol MDI或2)强的松龙片+安慰剂口服液+ procaterol MDI,每日3次,连用7天。治疗前后记录呼气峰流速(PEFR)、24小时反射性哮喘症状评分、肺活量测定和肺指数评分(PIS)。分析PEFR、症状评分、PIS、第一秒用力呼气量(FEV1)、FEV1/用力肺活量(FVC)、用力呼气流量在用力肺活量(FEF(25-75%))的25%至75%之间(治疗前后)的净变化以及研究者和受试者或其父母的整体评估。结果两组在这些参数的基线值上具有统计学上的相似。治疗7 d后,两组患者治疗前后PEFR净变化均显著改善,但两组患者PEFR净变化无显著差异(57.27+/-31.44 L/min vs. 54.29 +/-30.04 L/min,差异2.99 +/-30.76 L/min,平均+/-SD, P=0.752)。两组患者PIS和总症状评分的净变化量无显著差异(P分别为0.091和0.827)。同样,FEV1、FEV1/FVC和FEF25-75%均改善,且两组均不显著优于另一组(P分别为0.162、0.48和0.081)。研究者和受试者或其父母在研究结束时进行的全面评估表明,结果基本相当。结论泼尼松龙磷酸钠口服液联合吸入普罗卡特罗治疗儿童急性哮喘的疗效与泼尼松龙片联合吸入普罗卡特罗相同。
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