Rationale: Asthma treatment might improve when inhaled steroids are titrated on airway inflammation. Fractional exhaled nitric oxide (FE NO0.05), a marker of eosinophilic airway inflammation, can be measured at home. Objectives: We assessed daily FENO0.05 telemonitoring in the management of childhood asthma. Methods: Children with atopic asthma (n = 151) were randomly assigned to two groups: FE NO0.05 plus symptom monitoring, or monitoring of symptoms only. All patients scored asthma symptoms in an electronic diary over 30 weeks; 77 received a portable nitric oxide (NO) analyzer. Data were transmitted daily to the coordinating centers. Patients were phoned every 3 weeks and their steroid dose was adapted according to FENO0.05 and symptoms, or according to symptoms. Children were seen at 3, 12, 21, and 30 weeks for examination and lung function testing. The primary end point was the proportion of symptom-free days in the last 12 study weeks. Measurements and Main Results: Telemonitoring was feasible with reliable FENO0.05 data for 86% of days, and valid diary entries for 79% of days. Both groups showed an increase in symptom-free days, improvement of FEV1 and quality of life, and a reduction in steroid dose. None of the changes from baseline differed between groups. The difference in symptom-free days over the last 12 weekswas0.3% (P = 0.95; 95% confidence interval, -10 to 11%). There was a trend for fewer exacerbations in the FE NO0.05 group. Conclusions: Thirty weeks of daily FENO0.05 and symptom telemonitoring was associated with improved asthma control and a lower steroid dose. We found no added value of daily FENO0.05 monitoring compared with daily symptom monitoring only.

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doi.org/10.1164/rccm.200807-1010OC, hdl.handle.net/1765/15055
American Journal of Respiratory and Critical Care Medicine
Erasmus MC: University Medical Center Rotterdam

de Jongste, J.C, Carraro, S, Hop, W.C.J, & Baraldi, E. (2009). Daily telemonitoring of exhaled nitric oxide and symptoms in the treatment of childhood asthma. American Journal of Respiratory and Critical Care Medicine, 179(2), 93–97. doi:10.1164/rccm.200807-1010OC