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Published on: November 4, 2010
Long-term asthma treatment guided by airway hyperresponsiveness in children: a randomised controlled trial
M Nuijsink1, W C J Hop, P J Sterk
1Department of Paediatric Respiratory Medicine, Juliana Children's Hospital, The Hague, The Netherlands.
Insights
Airway hyperresponsiveness (AHR) guided asthma treatment did not increase symptom-free days in children. However, this strategy improved lung function (FEV1) in allergic asthmatic children, particularly those with low symptoms but high AHR.
Area of Science:
- Pediatric Pulmonology
- Allergy and Immunology
- Clinical Trial Research
Background:
- Childhood asthma management plans often yield suboptimal asthma control.
- Current strategies may not fully address underlying airway hyperresponsiveness (AHR).
Purpose of the Study:
- To determine if a treatment strategy guided by AHR improves symptom control and lung function in children with asthma.
- To compare AHR-guided treatment with a standard symptom-driven approach.
Main Methods:
- A 2-year, multicenter, randomized trial involving 210 children (6-16 years) with moderate atopic asthma.
- Medication was adjusted using algorithms based on either symptom scores alone (reference) or AHR and symptom scores (AHR strategy).
- Outcomes included symptom-free days, forced expiratory volume in one second (FEV1), and methacholine challenge results.
Main Results:
- No significant difference in symptom-free days was observed between the AHR-guided and symptom-driven strategies.
- The AHR strategy resulted in higher pre-bronchodilator FEV1 (2.3% predicted).
- This improvement was primarily seen in hyperresponsive children with low symptom scores, where FEV1 was 6% higher in the AHR group.
Conclusions:
- AHR-guided asthma management in children does not enhance symptom control compared to symptom-driven approaches.
- This strategy may offer benefits for lung function (FEV1) in allergic asthmatic children, especially those with low symptom burden but significant AHR.
Abstract:
Management plans for childhood asthma show limited success in optimising asthma control. The aim of the present study was to assess whether a treatment strategy guided by airway hyperresponsiveness (AHR) increased the number of symptom-free days and improved lung function in asthmatic children, compared with a symptom-driven reference strategy. In a multicentre, double-blind, parallel-group, randomised, 2-yr intervention trial, 210 children (aged 6-16 yrs) with moderate atopic asthma, selected on the basis of symptom scores and/or the presence of AHR, were studied. At 3-monthly visits, symptom scores, forced expiratory volume in one second (FEV(1)) and methacholine challenge results were obtained, and medication (five levels of fluticasone with or without salmeterol) adjusted according to algorithms based on symptom score (reference strategy, n = 104) or AHR and symptom score (AHR strategy, n = 102). After 2 yrs, no difference was found in the percentage of symptom-free days between treatment strategies. Pre-bronchodilator FEV(1) was higher in the AHR strategy (2.3% predicted). This was entirely explained by a gradual worsening of FEV(1) in a subgroup of 91 hyperresponsive children enrolled with low symptom scores (final difference between study arms was 6%). Asthma treatment guided by airway hyperresponsiveness showed no benefits in terms of number of symptom-free days, but produced a better outcome in terms of pre-bronchodilator forced expiratory volume in one second in allergic asthmatic children, especially those characterised by low symptom scores despite airway hyperresponsiveness.
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