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Published on: January 17, 2011
The interrupter technique to assess airway responsiveness in children with cystic fibrosis
Philip L Davies1, Iolo J Doull, Frances Child
1Department of Respiratory Paediatrics, Central Manchester and Manchester Children's University Hospitals NHS Trust, Manchester, UK. daviep@doctors.net.uk
Insights
The interrupter technique (Rint) is not a suitable alternative to forced expiratory volume in 1 second (FEV1) for assessing airway responsiveness in children with cystic fibrosis, as they measure different aspects of lung function.
Area of Science:
- Pediatric Pulmonology
- Respiratory Physiology
Background:
- Airway hyperresponsiveness is a key feature in cystic fibrosis (CF).
- Accurate measurement of airway responsiveness is crucial for CF management.
- The interrupter technique (Rint) is a potential tool for assessing lung function.
Purpose of the Study:
- To evaluate the validity of the interrupter technique (Rint) for measuring airway responsiveness in children with cystic fibrosis.
- To compare Rint measurements with standard spirometry (FEV1) in this population.
Main Methods:
- Fifty children (aged 6-16 years) with cystic fibrosis participated.
- Airway responsiveness was assessed using Rint and forced expiratory maneuvers (FEV1) before and after bronchodilator administration.
- Correlation between Rint and FEV1 was analyzed.
Main Results:
- A moderate correlation was found between inverse Rint and FEV1 in the overall population.
- No relationship was observed between changes in Rint and FEV1 after bronchodilator.
- Different subsets of children were identified as bronchodilator responsive by each method.
Conclusions:
- Rint and FEV1 reflect distinct aspects of lung function in children with CF.
- Rint is not an appropriate substitute for FEV1 in assessing individual airway responsiveness in this population.
- Clinical decisions regarding airway responsiveness in CF should rely on established FEV1 measures.
Abstract:
The aim of this study was to assess the validity of the interrupter technique (Rint) in measuring airway responsiveness in children with cystic fibrosis. Fifty children (aged 6-16 years) with cystic fibrosis performed six Rint measurements followed by three acceptable forced expiratory maneuvers. Each child then inhaled 5 mg of nebulized salbutamol by facemask. After 20 min the Rint and forced expiratory measurements were repeated. In the population as a whole a moderate but significant correlation between inverse Rint and FEV1 values was observed, both before and after inhaled bronchodilator (r=0.71 and 0.72, respectively, P < 0.001). However, when changes in Rint and FEV1 readings following inhaled bronchodilator were examined, no relationship was seen. Indeed, the two methods identified completely different subsets of children as being bronchodilator responsive. These results indicate that although a relationship exists between Rint and FEV1 in the whole population, this is not the case in individual children. Rint and FEV1 reflect different aspects of lung function. It is not appropriate to use Rint as a simple alternative for FEV1 in children with cystic fibrosis when assessing airway responsiveness.
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