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Published on: November 4, 2010
Phenotype-specific treatment of difficult asthma in children
1Department of Paediatric Respiratory Medicine, Royal Brompton Hospital, Sydney Street, London SW3 6NP, UK.
Insights
Children with difficult asthma require personalized treatment. Identifying steroid-resistant inflammation, airflow limitation, and airway reactivity guides tailored therapies for better asthma management.
Area of Science:
- Pediatric Pulmonology
- Immunology
- Pharmacology
Background:
- Asthma treatment in children often involves inhaled corticosteroids and long-acting beta-2 agonists.
- A subset of children exhibit persistent, difficult-to-treat asthma despite standard therapies.
- Current guidelines may offer generalized advice, potentially leading to suboptimal management for complex cases.
Purpose of the Study:
- To propose a rational, individualized treatment approach for children with difficult-to-treat asthma.
- To differentiate between various underlying causes of persistent asthma symptoms.
- To guide therapeutic decisions based on specific inflammatory profiles and physiological limitations.
Main Methods:
- Utilizing non-invasive and invasive (bronchoscopic) techniques to assess asthma phenotypes.
- Documenting the inflammatory response to systemic steroids, such as depot triamcinolone.
- Characterizing steroid-resistant inflammation, persistent airflow limitation, and bronchial hyper-reactivity.
Main Results:
- Identified distinct reasons for persistent difficult asthma, including eosinophilic and non-eosinophilic inflammation, airway reactivity without inflammation, and airflow limitation.
- Proposed a diagnostic protocol to categorize these distinct phenotypes.
- Suggested targeted therapies based on the identified asthma phenotype.
Conclusions:
- A personalized treatment strategy is crucial for children with difficult asthma.
- Differentiating between steroid-resistant inflammation, airflow limitation, and hyper-reactivity enables tailored interventions.
- Further multi-center studies are needed to validate this individualized approach for improved asthma outcomes.
Abstract:
Most children with asthma can be treated successfully with low-to-moderate doses of inhaled corticosteroid and long-acting beta-2 agonist. Those that fail to respond are a heterogeneous group. We propose that the nature and type of any steroid-resistant inflammation, the extent of any persistent airflow limitation and the extent of bronchial hyper-reactivity should be determined separately to allow a rational treatment approach to these children, rather than the haphazard advice of many current guidelines. Reasons for persistent difficult asthma include persistent eosinophilic inflammation, non-eosinophilic inflammation, airway reactivity without residual inflammation and persistent airflow limitation. We propose a protocol that uses non-invasive and invasive (bronchoscopic) methods to document the response to systemic steroids (depot triamcinolone). The aim of the protocol is to determine an individualised treatment plan; for example, cyclosporin for persistent eosinophilic inflammation, azithromycin for persistent neutrophilic inflammation and continuous subcutaneous terbutaline if there is airway reactivity without residual inflammation. Multi-centre studies are required to test the utility of this approach.
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