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 each...
Accurate testing of muscle function is essential in individuals with cystic fibrosis (CF). A literat...
Chest physiotherapy (CPT) is used to improve the lung function and blood gas tensions in individuals...
ABSTRACT Positive Expiratory Pressure (PEP) improves lung function, however, PEP-induced changes are...
Objectives: Maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) could be useful...
BACKGROUND: Respiratory muscle function in patients with cystic fibrosis (CF) has been studied by me...
International audienceTo analyze breathing pattern and mechanical ventilatory constraints during inc...
Exercise testing and training are cornerstones in regular CF care. However, no consensus exists in l...
Measuring aerobic fitness (V˙O2max) via a maximal cardiopulmonary exercise test is an important clin...
Background: Measurements of maximal voluntary inspiratory (Pimax) and expiratory (Pemax) pressures a...
AbstractBackgroundThe reproducibility of cardiopulmonary exercise testing (CPET) has not been establ...
Objectives: Exercise testing in patients with cystic fibrosis (CF) has become an important tool in a...
BACKGROUND: Cystic Fibrosis (CF) is commonly characterised by thick respiratory mucous. From diagnos...
Functional exercise capacity assessment is recommended in children with cystic fibrosis (CF). The si...
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 ...
Accurate testing of muscle function is essential in individuals with cystic fibrosis (CF). A literat...
Chest physiotherapy (CPT) is used to improve the lung function and blood gas tensions in individuals...
ABSTRACT Positive Expiratory Pressure (PEP) improves lung function, however, PEP-induced changes are...
Objectives: Maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) could be useful...
BACKGROUND: Respiratory muscle function in patients with cystic fibrosis (CF) has been studied by me...
International audienceTo analyze breathing pattern and mechanical ventilatory constraints during inc...
Exercise testing and training are cornerstones in regular CF care. However, no consensus exists in l...
Measuring aerobic fitness (V˙O2max) via a maximal cardiopulmonary exercise test is an important clin...
Background: Measurements of maximal voluntary inspiratory (Pimax) and expiratory (Pemax) pressures a...
AbstractBackgroundThe reproducibility of cardiopulmonary exercise testing (CPET) has not been establ...
Objectives: Exercise testing in patients with cystic fibrosis (CF) has become an important tool in a...
BACKGROUND: Cystic Fibrosis (CF) is commonly characterised by thick respiratory mucous. From diagnos...
Functional exercise capacity assessment is recommended in children with cystic fibrosis (CF). The si...
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 ...
Accurate testing of muscle function is essential in individuals with cystic fibrosis (CF). A literat...
Chest physiotherapy (CPT) is used to improve the lung function and blood gas tensions in individuals...
ABSTRACT Positive Expiratory Pressure (PEP) improves lung function, however, PEP-induced changes are...