Robertson Colin F, Price David, Henry Richard, Mellis Craig, Glasgow Nicholas, Fitzgerald Dominic, Lee Amanda J, Turner Jane, Sant Melissa
Department of Respiratory Medicine, Royal Children's Hospital, Parkville, Victoria, Australia.
Am J Respir Crit Care Med. 2007 Feb 15;175(4):323-9. doi: 10.1164/rccm.200510-1546OC. Epub 2006 Nov 16.
In children, intermittent asthma is the most common pattern and is responsible for the majority of exacerbations. Montelukast has a rapid onset of action and may be effective if used intermittently.
To determine whether a short course of montelukast in children with intermittent asthma would modify the severity of an asthma episode.
Children, aged 2-14 years with intermittent asthma participated in this multicenter, randomized, double-blind, placebo-controlled clinical trial over a 12-month period. Treatment with montelukast or placebo was initiated by parents at the onset of each upper respiratory tract infection or asthma symptoms and continued for a minimum of 7 days or until symptoms had resolved for 48 hours.
A total of 220 children were randomized, 107 to montelukast and 113 to placebo. There were 681 treated episodes (345 montelukast, 336 placebo) provided by 202 patients. The montelukast group had 163 unscheduled health care resource utilizations for asthma compared with 228 in the placebo group (odds ratio, 0.65; 95% confidence interval, 0.47-0.89). There was a nonsignificant reduction in specialist attendances and hospitalizations, duration of episode, and beta-agonist and prednisolone use. Symptoms were reduced by 14% and nights awakened by 8.6% (p = 0.043), and days off from school or childcare by 37% and parent time off from work by 33% (p < 0.0001 for both).
A short course of montelukast, introduced at the first signs of an asthma episode, results in a modest reduction in acute health care resource utilization, symptoms, time off from school, and parental time off from work in children with intermittent asthma.
在儿童中,间歇性哮喘是最常见的类型,也是大多数病情加重的原因。孟鲁司特起效迅速,间歇性使用可能有效。
确定短期使用孟鲁司特对间歇性哮喘儿童哮喘发作严重程度的影响。
2至14岁的间歇性哮喘儿童参与了这项为期12个月的多中心、随机、双盲、安慰剂对照临床试验。在每次上呼吸道感染或哮喘症状发作时,家长开始给孩子使用孟鲁司特或安慰剂治疗,持续至少7天或直至症状缓解48小时。
共220名儿童被随机分组,107名接受孟鲁司特治疗,113名接受安慰剂治疗。202名患者共提供了681次治疗发作(345次孟鲁司特治疗,336次安慰剂治疗)。孟鲁司特组因哮喘进行的非计划医疗资源使用有163次,而安慰剂组为228次(比值比,0.65;95%置信区间,0.47 - 0.89)。专科就诊和住院次数、发作持续时间、β受体激动剂和泼尼松龙的使用有非显著减少。症状减轻了14%,夜间惊醒次数减少了8.6%(p = 0.043),缺课或缺托育天数减少了37%,家长误工天数减少了33%(两者p均<0.0001)。
在哮喘发作的最初迹象出现时开始短期使用孟鲁司特,可适度减少间歇性哮喘儿童的急性医疗资源使用、症状、缺课时间和家长误工时间。