Jartti Tuomas, Lehtinen Pasi, Vanto Timo, Vuorinen Tytti, Hartiala Jaakko, Hiekkanen Heikki, Malmberg Pekka, Mäkelä Mika, Ruuskanen Olli
Department of Pediatrics, Turku University Hospital, Turku, Finland.
Pediatr Allergy Immunol. 2007 Jun;18(4):326-34. doi: 10.1111/j.1399-3038.2007.00512.x.
Data on the efficacy of corticosteroids on respiratory picornavirus-induced wheezing are limited. To determine whether prednisolone is effective in rhinovirus- or enterovirus-induced recurrent wheezing, we conducted a controlled trial comparing oral prednisolone (2 mg/kg/day in three divided doses for 3 days) with placebo in hospitalized wheezing children and studied post hoc virus-specific efficacy in early wheezing (<3 episodes, reported elsewhere) and in recurrent wheezing (>or=3 episodes). Virus-negative children where excluded. Our primary endpoint was the time until children were ready for discharge. Secondary endpoints included oxygen saturation and exhaled nitric oxide during hospitalization, duration of symptoms, blood eosinophil count, and impulse oscillometry 2 wk after discharge, and occurrence of relapses during the following 2 months. Virus-specific effects were analyzed with interaction analysis in a multivariate regression model. During the study period, 661 patients were hospitalized, 293 randomized, and 59 were accepted in this analysis (mean age 2.6 yr, s.d. 1.3). Prednisolone did not significantly decrease the time until ready for discharge in all patients (prednisolone vs. placebo, medians, 18 vs. 24 h, p = 0.11). However, prednisolone decreased the time until ready for discharge in children with picornavirus infection (respectively, 12 vs. 24 h, p = 0.0022) and more specifically, in children with enterovirus infection (6 vs. 35 h, p = 0.0007). In the secondary endpoints, prednisolone decreased the duration of cough and dyspnea in rhinovirus-affected children (p = 0.033 for both). Prospectively designed clinical trial is needed to test the hypothesis that prednisolone reduces symptoms in picornavirus-affected wheezing children.
关于皮质类固醇对呼吸道微小核糖核酸病毒诱发喘息疗效的数据有限。为了确定泼尼松龙对鼻病毒或肠道病毒诱发的反复喘息是否有效,我们进行了一项对照试验,将口服泼尼松龙(2毫克/千克/天,分三次服用,共3天)与安慰剂用于住院喘息儿童,并事后研究了其对早期喘息(<3次发作,其他地方有报道)和反复喘息(≥3次发作)的病毒特异性疗效。排除病毒检测阴性的儿童。我们的主要终点是儿童准备出院的时间。次要终点包括住院期间的血氧饱和度和呼出一氧化氮、症状持续时间、血液嗜酸性粒细胞计数、出院后2周的脉冲振荡法测量结果以及接下来2个月内复发的情况。在多变量回归模型中通过交互分析来分析病毒特异性效应。在研究期间,661名患者住院,293名被随机分组,本分析纳入59名(平均年龄2.6岁,标准差1.3)。泼尼松龙并没有显著缩短所有患者准备出院的时间(泼尼松龙组与安慰剂组,中位数分别为18小时和24小时,p = 0.11)。然而,泼尼松龙缩短了微小核糖核酸病毒感染儿童准备出院的时间(分别为12小时和24小时,p = 0.0022),更具体地说,缩短了肠道病毒感染儿童准备出院的时间(6小时和35小时,p = 0.0007)。在次要终点方面,泼尼松龙缩短了鼻病毒感染儿童咳嗽和呼吸困难的持续时间(两者p值均为0.033)。需要进行前瞻性设计的临床试验来检验泼尼松龙可减轻微小核糖核酸病毒感染的喘息儿童症状这一假设。