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Exhaled nitric oxide predicts asthma relapse in children with clinical asthma remission

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Pijnenburg, M W·2005·Thorax

Abstract

BACKGROUND: Nitric oxide in exhaled air (FE(NO)) is a marker of eosinophilic airway inflammation. A study was undertaken to determine whether FE(NO) predicts asthma relapse in asymptomatic asthmatic children in whom inhaled corticosteroids are discontinued. METHODS: Forty children (21 boys) of mean age 12.2 years on a median dose of 400 mug budesonide or equivalent (range 100-400) were included. FE(NO) was measured before and 2, 4, 12, and 24 weeks after withdrawal of steroids. A relapse was defined as more than one exacerbation per month, or need for beta agonist treatment on 4 days per week for at least 2 weeks, or diurnal peak flow variability of >20%. FE(NO) measurements were performed online with an expiratory flow of 50 ml/s. RESULTS: Nine patients relapsed. Two and 4 weeks after withdrawal of steroids geometric mean FE(NO) in children who were about to relapse was higher than in those who did not relapse: 35.3 ppb v 15.7 ppb at 2 weeks (ratio 2.3; 95% CI 1.2 to 4.1; p = 0.01) and 40.8 ppb v 15.9 ppb at 4 weeks (ratio 2.6; 95% CI 1.3 to 5.1). An FE(NO) value of 49 ppb at 4 weeks after discontinuation of steroids had the best combination of sensitivity (71%) and specificity (93%) for asthma relapse. CONCLUSION: FE(NO) 2 and 4 weeks after discontinuation of steroids in asymptomatic asthmatic children may be an objective predictor of asthma relapse.

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Metadata

Authors
Pijnenburg, M. W.
Venue
Thorax
Publisher
BMJ
Published
2005-03-01
Volume
60
Issue
3
Pages
215-218
ISSN
0040-6376 (ISSN-L)
OpenAlex
W2034276359
Cited by
294
References
0
FWCI
18.98
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Exhaled nitric oxide predicts asthma relapse in children with clinical asthma remission. https://app.cochat.ai/papers/10.1136/thx.2004.023374
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Pijnenburg, M. W. (2005). Exhaled nitric oxide predicts asthma relapse in children with clinical asthma remission. Thorax. https://doi.org/10.1136/thx.2004.023374

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