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Published on: May 4, 2021
Exhaled nitric oxide in the management of childhood asthma: a prospective 6-months study
Maria Fritsch1, Sabine Uxa, Friedrich Horak
1Department of General Paediatrics, University Children's Hospital, Vienna, Austria.
Insights
Fractional exhaled nitric oxide (FeNO) monitoring in children with asthma improved small airway function but did not significantly alter clinical outcomes like exacerbations or symptoms. FeNO levels correlated with asthma control markers.
Area of Science:
- Pediatric Pulmonology
- Allergy and Immunology
- Respiratory Medicine
Background:
- Fractional exhaled nitric oxide (FeNO) is an established biomarker for eosinophilic airway inflammation in asthma.
- Elevated FeNO levels are indicative of underlying inflammation, guiding asthma management strategies.
Purpose of the Study:
- To investigate if incorporating repeated FeNO measurements into asthma monitoring improves clinical outcomes in children.
- To assess the impact of FeNO-guided therapy on asthma control parameters.
Main Methods:
- A prospective, randomized, single-blind study involving 47 children with mild to moderate asthma.
- Two groups were compared: a FeNO group (therapy guided by FeNO, symptoms, lung function, and beta-agonist use) and a control group (therapy guided by symptoms, lung function, and beta-agonist use only).
- Measurements included respiratory symptoms, beta-agonist use, FEV(1)% predicted, MEF(50)% predicted, and FeNO levels over five visits in 6 weeks intervals.
Main Results:
- The FeNO group received higher doses of inhaled corticosteroids (ICS) and demonstrated significantly improved MEF(50)% predicted, indicating better small airway function.
- No significant differences were observed in the frequency of respiratory symptoms, beta-agonist use, or exacerbations between the groups.
- A FeNO cut-off of 22.9 ppb showed 80% sensitivity and 60% specificity for predicting exacerbations. FeNO correlated significantly with ICS dose, beta-agonist use, asthma symptoms, and bronchial hyperresponsiveness.
Conclusions:
- FeNO is closely related to key asthma control indicators, including ICS dosage and symptom severity.
- While FeNO-guided therapy improved small airway function in children with asthma, it did not lead to significant improvements in overall clinical asthma control markers.
Abstract:
Fractional exhaled nitric oxide (FeNO) is elevated in asthma and reflects eosinophilic airway inflammation. The aim of this prospective, randomized, single-blind study was to examine whether the inclusion of repeated FeNO measurements into asthma monitoring leads to an improvement in asthma outcome. Forty-seven children with mild to moderate asthma were allocated to a FeNO group (n = 22) and to a control group (n = 25). In the FeNO group therapy was based on symptoms, beta-agonist use, lung function, and FeNO whereas in the control group therapy was based on symptoms, beta-agonist use and lung function only. Patients performed five visits in 6 weeks intervals. Frequency of respiratory symptoms, beta-agonist use, FEV(1)% predicted and the frequency of exacerbations were similar between groups. Patients in the FeNO group received higher doses of inhaled corticosteroids (ICS) (control group: median (interquartile range): 241 microg (26-607 microg); FeNo group: 316 microg (200-500 microg) and had significantly higher MEF(50)% predicted (control group: median (interquartile range): 68.5% (55.8-83.1%); FeNO group: 83.2% (62.9%-98.3%). At a cut-off point of 22.9 ppb FeNO the best predictive value for exacerbations with a sensitivity of 80% and specificity of 60% was found. Significant relationships were observed between FeNO and dose of ICS (beta = -8.77; P < 0.002), beta-agonist use 2 weeks prior to a visit (beta = 0.11; P < 0.05), asthma symptoms (beta = 0.02; P < 0.0001), and bronchial hyperresponsiveness (beta = 0.04; P = 0.02). In conclusion, FeNO was related to important markers of asthma control. A therapy regimen aimed at lowering FeNO in children with asthma improved parameters of small airway function, but was not able to improve clinical markers of asthma control.
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