Beneficial short-term effect of autogenic drainage on peripheral resistance in childhood cystic fibrosis disease
- PMID: 35729620
- PMCID: PMC9210656
- DOI: 10.1186/s12890-022-02039-2
Beneficial short-term effect of autogenic drainage on peripheral resistance in childhood cystic fibrosis disease
Abstract
Background: Airway clearance techniques are supposed to be a necessary adjunct for the enhancement of impaired peripheral clearance in cystic fibrosis (CF). The objective was to assess the effect of one physiotherapy session (autogenic drainage: AD) on mucus clearance (sputum wet weight) and impulse oscillometry system (IOS) indices, including those obtained from extended Resistance-Inertance-Compliance (eRIC) modelling, considering the degree of bronchial congestion.
Methods: Thirty children with CF (median age: 12.7 years) in a stable condition prospectively underwent IOS measurements at baseline and after AD. They were divided in two groups: with (visual analog scale of bronchial congestion by the physiotherapist ≥ 5/10) and without (scale < 5/10) bronchial congestion. Paired-comparison of the effects of AD on airway resistance measurements was done with Wilcoxon test.
Results: The congestion scale correlated with the wet weight of sputum production during the session (Pearson test: p < 0.0001, R = 0.66). Ten children had bronchial congestion and 20 were without congestion. In the whole group, R5-20 Hz significantly decreased after AD (P = 0.049), which was related to a decrease in the children with congestion (P = 0.025), whereas it was not significantly modified in the children without congestion (P = 0.327). The eRIC model allowed the calculation of the peripheral resistance of the respiratory system, which also decreased in the children with congestion (P = 0.037), however, not modified in the children without congestion (P = 0.390).
Conclusion: One session of autogenic drainage has the ability to decrease peripheral resistance obtained from IOS measurements, more specifically in children with CF with moderate to severe bronchial congestion.
Trial registration: ClinicalTrials.gov Identifier: NCT04094441.
Keywords: Chest physiotherapy; Childhood; Cystic fibrosis; Impulse oscillometry; Lung model.
© 2022. The Author(s).
Conflict of interest statement
The authors declare that they have no competing interests.
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