Objectives: Maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) could be useful clinical parameters in monitoring many conditions including cystic fibrosis (CF). However, current protocols for undertaking the measurements lack standardization including the number of repeated attempts to achieve best values. We aimed to (a) determine the optimum number of attempts to achieve best MIP/MEP values, and (b) evaluate if the number of attempts is consistent across two different test days. Methods: We analyzed data of a previous randomized controlled trial involving the effect of singing on respiratory muscle strength in 35 children with CF. On two different days (T1, T2) children performed MIP/MEP with at least ten attempts ea...
Chest physiotherapy (CPT) is used to improve the lung function and blood gas tensions in individuals...
Although pulmonary function testing plays a key role in the diagnosis and management of chronic pulm...
the respiratory muscles ’ ability to generate force is important for recognizing respiratory muscle ...
Objectives Maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) could be useful ...
International audienceTo analyze breathing pattern and mechanical ventilatory constraints during inc...
BACKGROUND: Respiratory muscle function in patients with cystic fibrosis (CF) has been studied by me...
Background: Measurements of maximal voluntary inspiratory (Pimax) and expiratory (Pemax) pressures a...
Exercise testing and training are cornerstones in regular CF care. However, no consensus exists in l...
BACKGROUND: Cystic Fibrosis (CF) is commonly characterised by thick respiratory mucous. From diagnos...
Objectives: Exercise testing in patients with cystic fibrosis (CF) has become an important tool in a...
Measuring aerobic fitness (V˙O2max) via a maximal cardiopulmonary exercise test is an important clin...
BACKGROUND: Functional exercise capacity assessment is recommended in children with cystic fibrosis ...
AbstractBackgroundThe reproducibility of cardiopulmonary exercise testing (CPET) has not been establ...
Introduction: Coughing is the body’s defense mechanism to clear the airways from the foreign bodies ...
Introduction: Decreased respiratory muscle strength in patients with cystic fibrosis (CF) may cause ...
Chest physiotherapy (CPT) is used to improve the lung function and blood gas tensions in individuals...
Although pulmonary function testing plays a key role in the diagnosis and management of chronic pulm...
the respiratory muscles ’ ability to generate force is important for recognizing respiratory muscle ...
Objectives Maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) could be useful ...
International audienceTo analyze breathing pattern and mechanical ventilatory constraints during inc...
BACKGROUND: Respiratory muscle function in patients with cystic fibrosis (CF) has been studied by me...
Background: Measurements of maximal voluntary inspiratory (Pimax) and expiratory (Pemax) pressures a...
Exercise testing and training are cornerstones in regular CF care. However, no consensus exists in l...
BACKGROUND: Cystic Fibrosis (CF) is commonly characterised by thick respiratory mucous. From diagnos...
Objectives: Exercise testing in patients with cystic fibrosis (CF) has become an important tool in a...
Measuring aerobic fitness (V˙O2max) via a maximal cardiopulmonary exercise test is an important clin...
BACKGROUND: Functional exercise capacity assessment is recommended in children with cystic fibrosis ...
AbstractBackgroundThe reproducibility of cardiopulmonary exercise testing (CPET) has not been establ...
Introduction: Coughing is the body’s defense mechanism to clear the airways from the foreign bodies ...
Introduction: Decreased respiratory muscle strength in patients with cystic fibrosis (CF) may cause ...
Chest physiotherapy (CPT) is used to improve the lung function and blood gas tensions in individuals...
Although pulmonary function testing plays a key role in the diagnosis and management of chronic pulm...
the respiratory muscles ’ ability to generate force is important for recognizing respiratory muscle ...