Innovation
Coughing is an important defense and airway clearance mechanism for the removal of thick and viscous secretions in cystic fibrosis (CF). The main aim of this study was to investigate the effect of expiratory muscle training (EMT) on peak cough flow (PCF) and, secondly, on respiratory muscle functions, functional exercise capacity and quality of life (QoL) in CF.
Evaluation System
Both groups were trained with the EMT protocol, which involved twice a day, at least 5 days a week, for 6 weeks. The training intensity in the training group was 30% of the maximum expiratory pressure (MEP). In the control group, the lowest pressure (5 cmH2O) was maintained. The primary endpoint was PCF. The secondary endpoints were MEP, maximum inspiratory pressure (MIP), spirometric measurements, six-minute walk distance (6MWD) and QoL (Cystic Fibrosis Questionnaire - Revised). Changes in PCF (p = 0.041) and MEP (p = 0.003) were higher in the training group than in the simulated group. In addition, treatment weight (p = 0.008), digestive symptoms (p = 0.019) and vitality (p = 0.042) in QoL improved more in the training group. MIP (p = 0.028) and 6MWD (p = 0.035) changed significantly only in the training group. Spirometry measurements did not change (p > 0.05).
Assessment
Expiratory muscle training can improve peak cough flow, maximum expiratory pressure, treatment weight, digestive symptoms and Quality of Life vitality domains in cystic fibrosis patients.
References
Emirza, C., Aslan, G. K., Kilinc, A. A., & Cokugras, H. (2021). Effect of expiratory muscle training on peak cough flow in children and adolescents with cystic fibrosis: A randomized controlled trial. Pediatric Pulmonology, 56(5), 939-947.
doi.org/10.1002/ppul.25259" target="_blank">doi.org/10.1002/ppul.25259" target="_blank">doi.org/10.1002/ppul.25259