Background: Computed tomography (CT) of the lungs is the gold standard for assessing the extent of structural changes in the lungs. Spirometry-controlled chest CT (SCCCT) has improved the usefulness of CT by standardising inspiratory and expiratory lung volumes during imaging. This was a single-centre cross-sectional study in children with cystic fibrosis (CF). Using SCCCT we wished to investigate the association between the quantity and extent of structural lung changes and pulmonary function outcomes, and prevalence of known CF lung pathogens. Methods: CT images were analysed by CF-CT scoring (expressed as % of maximum score) to quantify different aspects of structural lung changes including bronchiectasis, airway wall thickening, mucus p...
Background: To reduce the mortality and morbidity rates of cystic fibrosis (CF) patients, and to hav...
BACKGROUND: Accelerated lung function decline in individuals with cystic fibrosis (CF) starts in ado...
Running title: CT worsens faster than lung function in children and adults with CF What this paper a...
AbstractBackgroundThe quality of chest Computed Tomography (CT) images in children is dependent upon...
Background/Aims Morphological changes due to lung disease in patients with cystic fibrosis (CF) were...
AbstractBackgroundChildren with cystic fibrosis (CF) are often Pseudomonas aeruginosa (PsA) free and...
Rationale: The lung clearance index is a measure of ventilation distribution derived from the multip...
Background: Computed tomography (CT) is used to monitor progression of structural lung disease (SLD)...
textabstractBackground: A study was undertaken to compare the ability of computed tomographic (CT) s...
Introduction: Mosaic attenuation on expiratory chest computed tomography (CT) is common in early lif...
In school-aged children with cystic fibrosis (CF) structural lung damage assessed using chest CT is ...
Background: Chest computerized tomography (CT) scores are associated with the frequency of future pu...
textabstractPurpose: To determine if fluorine 18 fluorodeoxyglucose (FDG) positron emission tomograp...
Objective: to correlate the findings of high resolution computed tomography of the chest based on t...
BACKGROUND: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
Background: To reduce the mortality and morbidity rates of cystic fibrosis (CF) patients, and to hav...
BACKGROUND: Accelerated lung function decline in individuals with cystic fibrosis (CF) starts in ado...
Running title: CT worsens faster than lung function in children and adults with CF What this paper a...
AbstractBackgroundThe quality of chest Computed Tomography (CT) images in children is dependent upon...
Background/Aims Morphological changes due to lung disease in patients with cystic fibrosis (CF) were...
AbstractBackgroundChildren with cystic fibrosis (CF) are often Pseudomonas aeruginosa (PsA) free and...
Rationale: The lung clearance index is a measure of ventilation distribution derived from the multip...
Background: Computed tomography (CT) is used to monitor progression of structural lung disease (SLD)...
textabstractBackground: A study was undertaken to compare the ability of computed tomographic (CT) s...
Introduction: Mosaic attenuation on expiratory chest computed tomography (CT) is common in early lif...
In school-aged children with cystic fibrosis (CF) structural lung damage assessed using chest CT is ...
Background: Chest computerized tomography (CT) scores are associated with the frequency of future pu...
textabstractPurpose: To determine if fluorine 18 fluorodeoxyglucose (FDG) positron emission tomograp...
Objective: to correlate the findings of high resolution computed tomography of the chest based on t...
BACKGROUND: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
Background: To reduce the mortality and morbidity rates of cystic fibrosis (CF) patients, and to hav...
BACKGROUND: Accelerated lung function decline in individuals with cystic fibrosis (CF) starts in ado...
Running title: CT worsens faster than lung function in children and adults with CF What this paper a...