Watanasomsiri Apassorn, Phipatanakul Wanda
Department of Pediatrics, Thammasat Chalerm Prakiat Hospital, Thammasat University Medical School, Pathumthani, Thailand.
Ann Allergy Asthma Immunol. 2006 May;96(5):701-6. doi: 10.1016/S1081-1206(10)61068-X.
Despite multiple doses of beta2-agonists in the treatment of acute asthma exacerbation, significant residual airways obstruction often remains.
To determine whether the addition of inhaled ipratropium bromide to salbutamol provides improvement in lung function and clinical asthma symptoms in young children with acute asthma exacerbation.
This study was a prospective, double-blind randomized control trial of children aged 3 to 15 years who presented with an acute asthma exacerbation at the emergency department or outpatient clinic of Thammasat University Hospital, Pathumthani, Thailand, between September 2001 and February 2003. Subjects were randomized to receive 3 doses of nebulized salbutamol mixed with isotonic sodium chloride solution (control) or ipratropium bromide (treatment) every 20 minutes. Additional doses of salbutamol were given every 30 minutes as needed. Asthma outcome measures were evaluated 40, 70, 100, and 120 minutes after baseline. Primary outcomes were the differences in percent change in asthma clinical score and percent change in peak expiratory flow rate (PEFR) from baseline. Secondary outcomes included change in percent predicted PEFR.
Of 74 children randomized and enrolled in the trial, 71 had complete data for analysis. Thirty-three children were in the control group and 38 were in the treatment group. Both the percent change in PEFR and the change in percent predicted PEFR at any time were higher in the treatment group, but these findings were not statistically significantly different. The number of subjects with at least a 100% percent predicted PEFR at any time point was greater in the treatment group.
Although this study did not demonstrate a significant advantage in clinical score and PEFR, the trend toward additional effect of ipratropium bromide was consistent with previous studies.
尽管在治疗急性哮喘发作时使用了多剂β2激动剂,但往往仍存在明显的残余气道阻塞。
确定在沙丁胺醇中加用吸入性异丙托溴铵是否能改善急性哮喘发作幼儿的肺功能和临床哮喘症状。
本研究是一项前瞻性、双盲随机对照试验,研究对象为2001年9月至2003年2月在泰国巴吞他尼府法政大学医院急诊科或门诊就诊的3至15岁急性哮喘发作儿童。受试者被随机分为两组,每20分钟接受3剂雾化沙丁胺醇与等渗氯化钠溶液混合液(对照组)或异丙托溴铵(治疗组)。根据需要每30分钟额外给予沙丁胺醇。在基线后40、70、100和120分钟评估哮喘结局指标。主要结局是哮喘临床评分的变化百分比和呼气峰值流速(PEFR)较基线的变化百分比的差异。次要结局包括预计PEFR变化百分比。
74名随机分组并纳入试验的儿童中,71名有完整数据用于分析。33名儿童在对照组,38名在治疗组。治疗组在任何时间的PEFR变化百分比和预计PEFR变化百分比均较高,但这些结果在统计学上无显著差异。治疗组在任何时间点至少有100%预计PEFR的受试者数量更多。
尽管本研究未显示在临床评分和PEFR方面有显著优势,但异丙托溴铵额外作用的趋势与先前研究一致。