Kotaniemi-Syrjänen Anne, Reijonen Tiina M, Korhonen Kaj, Korppi Matti
Kuopio University Hospital, Department of Paediatrics, Kuopio, Finland.
Pediatr Int. 2005 Dec;47(6):627-34. doi: 10.1111/j.1442-200x.2005.02147.x.
In order to affect the natural course of childhood wheezing and asthma, anti-inflammatory therapy is often prescribed for young wheezing children, but there is lack of long-term follow-up data.
Eighty-two of the original 100 children, hospitalized for wheezing under the age of 2 years in 1992-1993, were re-examined at school age in 1999. The children had participated in an open, randomized, parallel-group trial including a 4-month intervention with inhaled sodium cromoglycate (SCG) or budesonide (BUD). The baseline data, including data on atopy, eosinophilia and viral etiology, were prospectively collected on admission.
At early school age (median 7.2 years), asthma was present in 33 (40%) children. There was less asthma in the original SCG (21%) than in the control group (54%) (OR 0.23; 95% CI 0.07-0.77). The figure was 46% in the BUD group. When the analyses were performed separately for atopic and non-atopic infants, the difference was significant only among atopics. The lowered risk for asthma in the SCG group remained significant in the multivariate logistic regression analysis when adjusted for age, sex and atopy, and further when adjusted for earlier episodes of wheezing and respiratory syncytial virus identification. However, after adjustment for blood eosinophilia, the significance was lost, albeit the risk for asthma remained low (OR 0.21; 95% CI 0.04-1.12). A sensitivity analysis, which was done by including the six drop-outs of the SCG group as unfavorable and the 12 drop-outs of other groups as favorable outcomes in the model, did not change the direction of the result (OR 0.70; 95% CI 0.26-1.89).
An early SCG intervention in infants hospitalized for wheezing was associated with a lowered risk for early school-age asthma, especially in infants with evidence of atopy.
为了影响儿童喘息和哮喘的自然病程,通常会对喘息的幼儿进行抗炎治疗,但缺乏长期随访数据。
1992 - 1993年因喘息住院的100名2岁以下儿童中,有82名在1999年学龄期接受了复查。这些儿童参与了一项开放、随机、平行组试验,包括为期4个月的吸入色甘酸钠(SCG)或布地奈德(BUD)干预。入院时前瞻性收集了包括特应性、嗜酸性粒细胞增多和病毒病因的数据等基线数据。
在学龄早期(中位年龄7.2岁),33名(40%)儿童患有哮喘。原SCG组的哮喘患病率(21%)低于对照组(54%)(比值比0.23;95%置信区间0.07 - 0.77)。BUD组的这一数字为46%。当对特应性和非特应性婴儿分别进行分析时,差异仅在特应性婴儿中显著。在多因素逻辑回归分析中,调整年龄、性别和特应性后,SCG组哮喘风险降低仍具有显著性,进一步调整早期喘息发作和呼吸道合胞病毒检测结果后依然如此。然而,调整血液嗜酸性粒细胞增多情况后,显著性消失,尽管哮喘风险仍然较低(比值比0.21;95%置信区间0.04 - 1.12)。一项敏感性分析,通过将SCG组中的6名退出者作为不利结果纳入模型,将其他组的12名退出者作为有利结果纳入模型,并没有改变结果的方向(比值比0.70;95%置信区间0.26 - 1.89)。
对因喘息住院的婴儿进行早期SCG干预与学龄早期哮喘风险降低相关,尤其是在有特应性证据的婴儿中。