Four separate categories of chronic Pseudomonas aeruginosa (Pa) infection in children with cystic fibrosis (CF) have been previously defined, based on airway cultures taken over the previous year. The aim of the present study was to evaluate this definition in the current authors' paediatric and adult CF clinic using clinical, immunological and lung function parameters. During follow-up, out of 193 patients, 55 (34%) CF patients had never been infected with Pa, 27 (17%) were free of Pa, 29 (18%) were intermittently infected and 51 (31%) were chronically infected. Disease severity markers, such as lung function, were significantly worse in the chronic group, especially in the paediatric population. Differences in adult patients were smaller ...
Evidence-based techniques have been increasingly used in the creation of clinical guidelines and the...
BACKGROUND: Data from the Belgian Cystic Fibrosis Registry consistently show that in one of the seve...
BACKGROUND: Data from the Belgian Cystic Fibrosis Registry consistently show that in one of the seve...
Pseudomonas aeruginosa status influences cystic fibrosis (CF) clinical management but no 'gold stand...
AbstractBackground: Patients were defined each successive month as either ‘chronic’ when more than 5...
Cystic fibrosis (CF) is the most frequent life threatening autosomal recessive disease in white subj...
Pseudomonas aeruginosa status influences cystic fibrosis (CF) clinical management but no 'gold stand...
The purpose of the study was to determine the frequency rate of Pseudomonas aeruginosa infection amo...
AbstractBackground: Patients were defined each successive month as either ‘chronic’ when more than 5...
The purpose of the study was to determine the frequency rate of Pseudomonas aeruginosa infection amo...
AbstractChronic pulmonary infection with P. aeruginosa develops in most patients with cystic fibrosi...
Background Pseudomonas aeruginosa (PA) infection is associated with an increased morbidity and adver...
Pseudomonas aeruginosa lung infection is an important cause of morbidity and mortality in cystic ®br...
AbstractBackgroundData from the Belgian Cystic Fibrosis Registry consistently show that in one of th...
Abstract Background and Objective: Cystic fibrosis (CF) is an autosomal recessive genetic disease a...
Evidence-based techniques have been increasingly used in the creation of clinical guidelines and the...
BACKGROUND: Data from the Belgian Cystic Fibrosis Registry consistently show that in one of the seve...
BACKGROUND: Data from the Belgian Cystic Fibrosis Registry consistently show that in one of the seve...
Pseudomonas aeruginosa status influences cystic fibrosis (CF) clinical management but no 'gold stand...
AbstractBackground: Patients were defined each successive month as either ‘chronic’ when more than 5...
Cystic fibrosis (CF) is the most frequent life threatening autosomal recessive disease in white subj...
Pseudomonas aeruginosa status influences cystic fibrosis (CF) clinical management but no 'gold stand...
The purpose of the study was to determine the frequency rate of Pseudomonas aeruginosa infection amo...
AbstractBackground: Patients were defined each successive month as either ‘chronic’ when more than 5...
The purpose of the study was to determine the frequency rate of Pseudomonas aeruginosa infection amo...
AbstractChronic pulmonary infection with P. aeruginosa develops in most patients with cystic fibrosi...
Background Pseudomonas aeruginosa (PA) infection is associated with an increased morbidity and adver...
Pseudomonas aeruginosa lung infection is an important cause of morbidity and mortality in cystic ®br...
AbstractBackgroundData from the Belgian Cystic Fibrosis Registry consistently show that in one of th...
Abstract Background and Objective: Cystic fibrosis (CF) is an autosomal recessive genetic disease a...
Evidence-based techniques have been increasingly used in the creation of clinical guidelines and the...
BACKGROUND: Data from the Belgian Cystic Fibrosis Registry consistently show that in one of the seve...
BACKGROUND: Data from the Belgian Cystic Fibrosis Registry consistently show that in one of the seve...