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评价间歇性变应性哮喘或变应性鼻炎患儿应用甘露醇干粉激发试验的支气管高反应性。

Evaluation of bronchial hyperreactivity with mannitol dry powder challenge test in a paediatric population with intermittent allergic asthma or allergic rhinitis.

出版信息

Int J Immunopathol Pharmacol. 2011 Oct-Dec;24(4):1069-74. doi: 10.1177/039463201102400424.

Abstract

We evaluated the bronchial hyperreactivity (BHR) with a new bronchial challenge test, mannitol dry powder, in a paediatric population with intermittent allergic asthma or allergic rhinitis who did not respond to an exercise challenge test. We selected 50 children, aged 9-16 years, with intermittent allergic bronchial asthma (Group 1) or allergic rhinitis without clinical manifestation of asthma for at least 12 months (Group 2). All patients performed the following tests in three different days (≥ 48 hours apart): Day 1: exhaled nitric oxide (FeNO) determination followed by baseline spirometry and reversibility to inhaled beta2-agonists; Day 2: exercise challenge test followed by FeNO determination; Day 3: mannitol challenge test followed by FeNO determination. Forty children completed the study. Eighteen subjects of Group 1 (90 percent) and 5 subjects of Group 2 (25 percent) resulted positive to the mannitol test. Positive mannitol challenge subjects showed no statistically significant differences compared to negative subjects as regard baseline spirometry, reversibility to salbutamol and response to the exercise challenge test, but they had significantly higher FeNO values. In conclusion, the mannitol challenge test can be a diagnostic tool more useful than the exercise challenge test to identify BHR in a paediatric population with intermittent allergic asthma or allergic rhinitis because it is better reproducible, quick and easy to perform and well tolerated.

摘要

我们评估了支气管高反应性(BHR)与新的支气管挑战试验,甘露醇干粉,在儿科人群与间歇性过敏性哮喘或过敏性鼻炎谁没有反应运动挑战试验。我们选择了 50 名儿童,年龄 9-16 岁,与间歇性过敏性支气管哮喘(第 1 组)或过敏性鼻炎没有哮喘的临床表现至少 12 个月(第 2 组)。所有患者在三个不同的日子里进行了以下测试(相隔至少 48 小时):第 1 天:呼出的一氧化氮(FeNO)测定,随后进行基础肺功能检查和吸入β2-激动剂的可逆性;第 2 天:运动挑战试验,随后进行 FeNO 测定;第 3 天:甘露醇挑战试验,随后进行 FeNO 测定。40 名儿童完成了研究。第 1 组的 18 名受试者(90%)和第 2 组的 5 名受试者(25%)对甘露醇试验呈阳性。阳性甘露醇挑战组与阴性组相比,基础肺功能、沙丁胺醇的可逆性和运动挑战试验的反应无统计学差异,但 FeNO 值明显较高。总之,甘露醇挑战试验可以是一种比运动挑战试验更有用的诊断工具,以确定在儿科人群与间歇性过敏性哮喘或过敏性鼻炎因为它是更好的重现性,快速和易于执行和良好的耐受性。

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