首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Inhaled budesonide for the treatment of acute wheezing and dyspnea in children up to 24 months old receiving intravenous hydrocortisone.
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Inhaled budesonide for the treatment of acute wheezing and dyspnea in children up to 24 months old receiving intravenous hydrocortisone.

机译:吸入布地奈德治疗接受静脉注射氢化可的松治疗的24个月以下儿童的急性喘息和呼吸困难。

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BACKGROUND: Inhaled corticosteroids are highly effective in the treatment of asthma at all ages, and their use in younger children is increasing. There are no data currently available on the treatment of infants with acute wheeze and dyspnea with nebulized budesonide. OBJECTIVE: Our purpose was to assess the clinical effect of nebulized budesonide in infants with acute wheeze and dyspnea. METHODS: A prospective study was performed comparing the addition of nebulized budesonide 0.25 mg every 6 hours (group A, n = 32) and nebulized ipratropium bromide 0.1 mg every 6 hours (group B, n = 39) with the normal treatment regimen with intravenous fluid, hydrocortisone, and nebulized fenoterol. A clinical score was made at admission and every 12 hours. The score included wheezing and costal retraction (0-6) and respiratory rate (counts per minute). RESULTS: Seventy-one infants aged 3 to 24 months were studied (42 boys). A statistically significant reduction was seen in clinical score and respiratory rate in both groups 12 hours after admission. The children who received budesonide improved significantly faster than the children who received ipratropium bromide, and the hospitalization period was significantly lower in the budesonide group (66.4 hours) compared with the ipratropium bromide group (93 hours) (P <.01). Three patients from the budesonide group and 2 from the ipratropium bromide group were readmitted within the first 4 weeks. CONCLUSION: Treatment of infants with acute wheeze with nebulized budesonide is associated with faster clinical improvement and reduction in hospital stay period.
机译:背景:吸入皮质类固醇在所有年龄段的哮喘中都非常有效,并且在年幼儿童中的使用正在增加。目前尚无有关雾化布地奈德治疗急性喘息和呼吸困难的婴儿的数据。目的:我们的目的是评估布地奈德雾化剂对婴儿的急性喘息和呼吸困难的临床效果。方法:进行一项前瞻性研究,比较每6小时加入雾化布地奈德0.25 mg(A组,n = 32)和每6小时加入雾化异丙托溴铵0.1 mg(B组,n = 39)与常规静脉内治疗方案液体,氢化可的松和雾化非诺特罗。入院时和每12小时进行一次临床评分。分数包括喘息和肋缩(0-6)和呼吸频率(每分钟计数)。结果:研究了71名3至24个月大的婴儿(42名男孩)。入院12小时后两组的临床评分和呼吸频率均有统计学意义的降低。接受布地奈德治疗的患儿比接受异丙托溴铵治疗的患儿改善显着快,与使用异丙托溴铵治疗组(93小时)相比,布地奈德治疗组(66.4小时)的住院时间明显缩短(P <.01)。在布地奈德组的三名患者和异丙托溴铵组的两名患者在头4周内重新入院。结论:布地奈德雾化治疗婴儿急性喘息与临床改善更快,住院时间减少有关。

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