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Persistent wheezing in infants with an atopic tendency respondsto inhaled fluticasone

机译:患有特应性倾向的婴儿持续气喘反应吸入氟替卡松

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摘要

BACKGROUND—The role of inhaled corticosteroids for the treatment of wheeze in infancy remains unclear.
AIM—To investigate the effect of inhaled fluticasone on symptoms in a group of wheezy infants who had a high risk of progressing to childhood asthma.
METHODS—A total of 52 infants, under 1 year of age, with a history of wheeze or cough and a history (personal or first degree relative) of atopy were prescribed either 150 µg fluticasone twice daily (group F) or placebo (group P), via metered dose inhaler, for 12 weeks following a two week run in period. Symptoms were scored in a parent held diary and the mean daily symptom score (MDS) and symptom free days (SFD) calculated for each two week period.
RESULTS—Thirty seven infants completed the study. Both MDS and SFD improved significantly between the run in and final two week period in group F, but not group P, with a mean difference in change (95% CI) between groups of 1.12 (0.05 to 2.18) for MDS and median difference of 3.0 (0.002 to 8.0) for SFD.
CONCLUSION—Improvement of clinical symptoms in response to fluticasone can be shown in this high risk group of infants. In the absence of effective alternatives inhaled corticosteroids should be considered in this patient group.

机译:背景—吸入性糖皮质激素在婴儿期喘息治疗中的作用尚不清楚。
目的—研究吸入氟替卡松对一组具有发展为儿童哮喘高风险的喘息婴儿的症状的影响。方法-总计52例1岁以下,有喘息或咳嗽病史和特应性史(个人或一级亲戚)的婴儿,每天两次150μg氟替卡松(F组)或安慰剂处方(P组),在经过两周的定期服用后,通过定量吸入器治疗12周。在父母的日记中对症状进行评分,并计算每两周的每日平均症状评分(MDS)和无症状天数(SFD)。
结果-三十七名婴儿完成了研究。 F组的跑步和最后两周之间,MDS和SFD均显着改善,但P组没有,MDS组之间的平均变化差异(95%CI)为1.12(0.05至2.18),而MDS的中位数差异为SFD为3.0(0.002至8.0)。
结论—在这一高危婴儿组中,对氟替卡松的反应可改善临床症状。在缺乏有效替代品的情况下,该患者组应考虑吸入糖皮质激素。

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