SummarySwedish Cystic Fibrosis (CF) care follows international guidelines in general. The only difference in our CF care package since 25 years is the physiotherapy regimen. Airway clearance therapy has since the early 1980s, from the day of diagnosis, been based upon daily physical exercise in conjunction with techniques for transporting and evacuating mucus. Postural Drainage±percussion and vibration has not been used in any age. The aim of this study was to evaluate our CF care package.Lung function data from the start of the study and with a 3-year interval were collected in the entire Swedish CF population ≥7 years old. Data were analysed for the age groups 7–17 and ≥18 years of age. Change of lung function over the study period was ca...
Objectives: To describe the current use of airway clearance techniques among people with cystic fibr...
Characterizing seasonal trend in lung function in individuals with chronic lung disease may lead to ...
Objective: To determine the pattern of lung function in stable cystic fibrosis (CF) patients and to ...
SummarySwedish Cystic Fibrosis (CF) care follows international guidelines in general. The only diffe...
Cystic Fibrosis (CF) is a severe hereditary disorder leading to progressive deterioration of lung fu...
A key measure of lung function in people with Cystic Fibrosis (CF) is Forced Expiratory Volume in th...
Background: Rate of change in lung function is used as a measure of disease progression and a predic...
Assessing the results of modern cystic fibrosis (CF)-care and estimating the future population and i...
AbstractAssessing the results of modern cystic fibrosis (CF)-care and estimating the future populati...
Muscular strength, lung function and exercise capacity are internationally reported to be markedly i...
AbstractBackgroundWe examined the year-to-year change in FEV1 for individuals and the overall cystic...
Improvements in the quality and implementation of medical care for individuals with cystic fibrosis ...
Summary. The severity of lung disease in cystic fibrosis (CF) may be related to the type of mutation...
Objective: To assess the impact of lifetime continuous care within the John Hunter Hospital cystic f...
Introduction: Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the CF t...
Objectives: To describe the current use of airway clearance techniques among people with cystic fibr...
Characterizing seasonal trend in lung function in individuals with chronic lung disease may lead to ...
Objective: To determine the pattern of lung function in stable cystic fibrosis (CF) patients and to ...
SummarySwedish Cystic Fibrosis (CF) care follows international guidelines in general. The only diffe...
Cystic Fibrosis (CF) is a severe hereditary disorder leading to progressive deterioration of lung fu...
A key measure of lung function in people with Cystic Fibrosis (CF) is Forced Expiratory Volume in th...
Background: Rate of change in lung function is used as a measure of disease progression and a predic...
Assessing the results of modern cystic fibrosis (CF)-care and estimating the future population and i...
AbstractAssessing the results of modern cystic fibrosis (CF)-care and estimating the future populati...
Muscular strength, lung function and exercise capacity are internationally reported to be markedly i...
AbstractBackgroundWe examined the year-to-year change in FEV1 for individuals and the overall cystic...
Improvements in the quality and implementation of medical care for individuals with cystic fibrosis ...
Summary. The severity of lung disease in cystic fibrosis (CF) may be related to the type of mutation...
Objective: To assess the impact of lifetime continuous care within the John Hunter Hospital cystic f...
Introduction: Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the CF t...
Objectives: To describe the current use of airway clearance techniques among people with cystic fibr...
Characterizing seasonal trend in lung function in individuals with chronic lung disease may lead to ...
Objective: To determine the pattern of lung function in stable cystic fibrosis (CF) patients and to ...