Related Experiment Video
Updated: Jan 26, 2026

Phage Therapy Application to Counteract Pseudomonas aeruginosa Infection in Cystic Fibrosis Zebrafish Embryos
Published on: May 12, 2020
Oscillating Positive Expiratory Pressure Therapy May Be Performed Poorly by Children With Cystic Fibrosis
Kevin J O'Sullivan1,2, Louise Collins3, Deirdre McGrath2,3
1Design Factors Research Group, School of Design, University of Limerick, Limerick, Ireland.
Insights
Pediatric cystic fibrosis patients often use oscillating positive expiratory pressure (OPEP) therapy incorrectly. This study found that even with training, most patients did not achieve target pressures, compromising airway clearance effectiveness.
Area of Science:
- Pulmonary Medicine
- Pediatric Respiratory Care
- Medical Device Performance
Background:
- Oscillating positive expiratory pressure (OPEP) devices assist secretion removal and reduce gas trapping in hypersecretory lung diseases like cystic fibrosis.
- OPEP therapy involves exhaling against a resistor, creating positive airway pressure with fluctuations to enhance mucus clearance.
- Effective OPEP use requires achieving specific intrapulmonary pressure targets (10-20 cm H2O) with adequate expiratory flow.
Purpose of the Study:
- To evaluate the adherence to target therapeutic pressures during oscillating positive expiratory pressure therapy in pediatric cystic fibrosis patients.
- To assess the performance and technique variability of OPEP device use in a pediatric cystic fibrosis cohort.
Main Methods:
- Twenty-one pediatric cystic fibrosis patients with prior OPEP training were recruited.
- Performance was measured using an in-line flow and pressure sensor during participants' routine expirations.
- Standardized training and instruction were provided by a specialist physiotherapist prior to evaluation.
Main Results:
- No participants achieved the target therapeutic pressure ranges during OPEP use.
- The mean generated pressure was 16.2 ± 6.8 cm H2O, with a mean flow of 31.3 ± 8.9 L/min.
- The average expiration length was 2.5 ± 1.4 seconds, indicating potential technique limitations.
Conclusions:
- Significant variability in OPEP technique was observed among pediatric cystic fibrosis patients, despite standardized instruction.
- Poor patient technique compromised the effectiveness of airway clearance, potentially limiting the therapeutic benefits of OPEP.
- Further interventions may be needed to improve OPEP technique and optimize airway clearance in this population.
Background:
Oscillating positive expiratory pressure devices aid removal of excess secretions and reduce gas trapping in patients with hypersecretory pulmonary diseases, for example, cystic fibrosis. Oscillating positive expiratory pressure works when the patient exhales actively against a fixed resistor, which generates mean intrapulmonary pressures of 10-20 cm H2O with rapid fluctuations of at least 1 cm H2O from the mean. In this study, we evaluated the performance of oscillating positive expiratory pressure therapy by pediatric subjects with cystic fibrosis to determine adherence to target therapeutic pressures.
Methods:
Twenty-one pediatric subjects were recruited. Each had a history of using an oscillating positive expiratory pressure device twice daily and had received standardized training and instructions from the same specialist physiotherapist. Performance was evaluated by using a flow and pressure sensor placed in-line between the participant's mouth and the device. The participants performed expirations as per their normal routine.
Results:
None of the participants achieved target therapeutic pressure ranges during expiration. The mean ± SD pressure generated was 16.2 ± 6.8 cm H2O, whereas mean ± SD flow was 31.3 ± 8.9 L/min. The mean ± SD expiration length was 2.5 ± 1.4 s.
Conclusions:
Despite standardized instruction, the results demonstrated considerable variation among the participants and overall poor technique during use. Outcomes of this study indicated that airway clearance effects of oscillating positive expiratory pressure were compromised due to poor technique.
More Related Videos
05:56Implementation of Non-invasive Point of Care Transient Elastography for Evaluation of Liver Disease in Pediatric Populations with Cystic Fibrosis
Published on: August 29, 2025
03:53Growing a Cystic Fibrosis-Relevant Polymicrobial Biofilm to Probe Community Phenotypes
Published on: April 19, 2024
Related Concept Videos
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
Cystic Fibrosis: Management
Sinus disease and chronic...
Oscillations about an Equilibrium Position
Oscillations In An LC Circuit
Forced Oscillations
Damped Oscillations
Although friction and other non-conservative...