Cystic Fibrosis
Conditions
Brief summary
Cystic Fibrosis (CF) patients perform airway clearance incorporating various breathing strategies, to clear secretions from their lungs. Hand held devices may aid mucus expectoration, and also motivate the patient to manage by themselves. Our aims was to study if resistive expiration through volumetric incentive spirometer (VISex) can improve lung function in the short term in Cystic Fibrosis (CF) patients.
Interventions
40 CF patients performed airway clearance using the VISex, by exhaling against chosen resistance being motivated by visual feedback of raising colored balls. The level of resistance was set to cause longest expiration/volume, until mucus was transported from the peripheral to the central airways, to be expectorated by the subsequent cough.
Sponsors
Study design
Eligibility
Inclusion criteria
* cystic fibrosis patients
Exclusion criteria
* i.v. antibiotic therapy during the experiment day
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| lung function | fifteen minutes after intervention | Forced expiratory maneuvers were measured before and 15 minutes after intervention. |
Countries
Israel