BACKGROUND: Repeated measurements of spirometry and fractional exhaled nitric oxide (FENO) are recommended as part of the management of childhood asthma, but the evidence base for such recommendations is small. We tested the hypothesis that reducing spirometric indices or increasing FENO will predict poor future asthma outcomes. METHODS: A one-stage individual patient data meta-analysis used data from seven randomized controlled trials in which FENO was used to guide asthma treatment; spirometric indices were also measured. Change in %FEV1 and % change in FENO between baseline and 3 months were related to having poor asthma control and to having an asthma exacerbation between 3 and 6 months after baseline. RESULTS: Data were available from 1,112 children (mean age, 12.6 years; mean %FEV1, 94%). A 10% reduction in %FEV1 between baseline and 3 months was associated with 28% increased odds for asthma exacerbation (95% CI, 3-58) and with 21% increased odds for having poor asthma control (95% CI, 0-45) 6 months after baseline. A 50% increase in FENO between baseline and 3 months was associated with 11% increase in oddsfor poor asthma control 6 months after baseline (95% CI, 0-16). Baseline FENO and %FEV1 were not related to asthma outcomes at 3 months. CONCLUSIONS: Repeated measurements of %FEV1 that are typically within the “normal” range add to clinical risk assessment of future asthma outcomes in children. The role of repeated FENO measurements is less certain because large changes were associated with small changes in outcome risk.

Additional Metadata
Keywords asthma, child, monitoring, nitric oxide, spirometry
Persistent URL dx.doi.org/10.1016/j.chest.2018.10.009, hdl.handle.net/1765/115238
Journal Chest: the cardiopulmonary and critical care journal
Citation
Fielding, S., Pijnenburg, M.W.H, de Jongste, J.C, Pike, K.C, Roberts, G, Petsky, H., … Turner, S.D. (2019). Change in FEV1 and FENO Measurements as Predictors of Future Asthma Outcomes in Children. Chest: the cardiopulmonary and critical care journal, 155(2), 331–341. doi:10.1016/j.chest.2018.10.009