AbstractThe value of adjusting the diffusing capacity for the lung volume has been demonstrated in a large number of patients with other lung diseases but has not been validated in patients with cystic fibrosis (CF). Pulmonary function test results on a cohort of 52 adult CF patients were analyzed to determine whether the diffusing capacity of carbon monoxide by single breath method (DL COSB), when adjusted for alveolar volume (VA%), correlated with the severity of pulmonary dysfunction. The DL COSB remained within the reference range except in those with severe lung impairment (61.88±15.48%). DL COSB has a significant (P<0.05) positive correlation (0.70, 0.67, 0.48, 0.69, and 0.31, respectively) with measures of airflow limitation (FVC%, F...
We investigated the extent of convective ventilation heterogeneity contributing to the observed lung...
BACKGROUND: Cystic fibrosis (CF) is a disease marked by airway inflammation and airflow obstruction,...
A key measure of lung function in people with Cystic Fibrosis (CF) is Forced Expiratory Volume in th...
AbstractThe value of adjusting the diffusing capacity for the lung volume has been demonstrated in a...
We evaluated the intra-session and inter-session variability of the diffusing capacity of nitric oxi...
Background Due to large-scale destruction, changes in membrane diffusion (Dm) may occur in cystic f...
Although a fall in arterial oxygen saturation (SaO2) during exercise has been reported in patients w...
AbstractBackgroundExercise has been shown to be beneficial for patients with cystic fibrosis (CF), b...
RATIONALE: Despite being a hallmark and an independent prognostic factor in several cardiopulmonary ...
BACKGROUND: Recent studies described a progressive decline in lung volumes in adult bron-chiectasis....
We studied distribution of ventilation in patients with cystic fibrosis (CF) who had not had an exac...
Lung function has been studied in 41 patients with cystic fibrosis, aged 5 to 21, with a complete ba...
BACKGROUND: Cystic fibrosis (CF) is a hereditary condition in which lung disease affects all patien...
SummaryIntroductionCystic fibrosis (CF) is the most common life-limiting, recessively inherited dise...
Clinical research in cystic fibrosis (CF) requires study endpoints that are sensitive to airways dis...
We investigated the extent of convective ventilation heterogeneity contributing to the observed lung...
BACKGROUND: Cystic fibrosis (CF) is a disease marked by airway inflammation and airflow obstruction,...
A key measure of lung function in people with Cystic Fibrosis (CF) is Forced Expiratory Volume in th...
AbstractThe value of adjusting the diffusing capacity for the lung volume has been demonstrated in a...
We evaluated the intra-session and inter-session variability of the diffusing capacity of nitric oxi...
Background Due to large-scale destruction, changes in membrane diffusion (Dm) may occur in cystic f...
Although a fall in arterial oxygen saturation (SaO2) during exercise has been reported in patients w...
AbstractBackgroundExercise has been shown to be beneficial for patients with cystic fibrosis (CF), b...
RATIONALE: Despite being a hallmark and an independent prognostic factor in several cardiopulmonary ...
BACKGROUND: Recent studies described a progressive decline in lung volumes in adult bron-chiectasis....
We studied distribution of ventilation in patients with cystic fibrosis (CF) who had not had an exac...
Lung function has been studied in 41 patients with cystic fibrosis, aged 5 to 21, with a complete ba...
BACKGROUND: Cystic fibrosis (CF) is a hereditary condition in which lung disease affects all patien...
SummaryIntroductionCystic fibrosis (CF) is the most common life-limiting, recessively inherited dise...
Clinical research in cystic fibrosis (CF) requires study endpoints that are sensitive to airways dis...
We investigated the extent of convective ventilation heterogeneity contributing to the observed lung...
BACKGROUND: Cystic fibrosis (CF) is a disease marked by airway inflammation and airflow obstruction,...
A key measure of lung function in people with Cystic Fibrosis (CF) is Forced Expiratory Volume in th...