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轻度至中度哮喘患儿呼出一氧化氮与疾病活动度指标之间的关系。

Relations between exhaled nitric oxide and measures of disease activity among children with mild-to-moderate asthma.

作者信息

Covar Ronina A, Szefler Stanley J, Martin Richard J, Sundstrom D A, Silkoff Philip E, Murphy James, Young David A, Spahn Joseph D

机构信息

Ira J. and Jacqueline Neimark Laboratory of Clinical Pharmacology and the Division of Allergy-Clinical Immunology, Department of Pediatrics, Denver, Colorado, USA.

出版信息

J Pediatr. 2003 May;142(5):469-75. doi: 10.1067/mpd.2003.187.

Abstract

OBJECTIVE

Exhaled nitric oxide (FE(NO)) was evaluated in children with asthma after 4 to 6 years of treatment with budesonide, nedocromil, or albuterol as needed.

STUDY DESIGN

FE(NO), spirometry, total eosinophil count, and serum eosinophil cationic protein levels were obtained from 118 children at the Denver site of the Childhood Asthma Management Program upon completion of treatment and after a 2- to 4-month washout.

RESULTS

Budesonide-treated patients had significantly lower median (1st, 3rd quartile) FE(NO) (21.5 [13.2, 84.4] vs 62.5 [26.2, 115.0] ppb, P <.01) and eosinophil cationic protein levels (17.4 [10.1, 24.3] vs 24.0 [15.4, 33.9] mg/dL, P =.05) compared with placebo, whereas no differences were noted between nedocromil and placebo groups. After washout, FE(NO) levels were similar between the three treatments. FE(NO) levels significantly correlated with degree of bronchial hyperresponsiveness, bronchodilator reversibility, allergen skin prick tests, serum IgE, and total eosinophil count. FE(NO) levels were also higher in patients with nocturnal symptoms and in patients requiring beta-agonist use at least once weekly.

CONCLUSIONS

Budesonide therapy was more effective than nedocromil in reducing FE(NO). Unfortunately, the effects of long-term budesonide were not sustained after its discontinuation. FE(NO) may be a complementary tool to current practice guidelines in assessing asthma control and medication response.

摘要

目的

对按需使用布地奈德、奈多罗米或沙丁胺醇治疗4至6年的哮喘儿童进行呼出一氧化氮(FE(NO))评估。

研究设计

在儿童哮喘管理项目丹佛站点,118名儿童完成治疗并经过2至4个月洗脱期后,获取其FE(NO)、肺功能、嗜酸性粒细胞总数及血清嗜酸性粒细胞阳离子蛋白水平。

结果

与安慰剂相比,布地奈德治疗的患者FE(NO)中位数(第1、第3四分位数)显著更低(21.5 [13.2, 84.4] 对62.5 [26.2, 115.0] ppb,P <.01),嗜酸性粒细胞阳离子蛋白水平也更低(17.4 [10.1, 24.3] 对24.0 [15.4, 33.9] mg/dL,P =.05),而奈多罗米组与安慰剂组之间未观察到差异。洗脱期后,三种治疗的FE(NO)水平相似。FE(NO)水平与支气管高反应性程度、支气管扩张剂可逆性、变应原皮肤点刺试验、血清IgE及嗜酸性粒细胞总数显著相关。夜间有症状的患者以及每周至少使用一次β受体激动剂的患者FE(NO)水平也更高。

结论

布地奈德治疗在降低FE(NO)方面比奈多罗米更有效。遗憾的是,停用布地奈德后其长期效果未持续。FE(NO)可能是评估哮喘控制和药物反应的现行实践指南的补充工具。

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