AbstractIn patients with cystic fibrosis (CF) lung damage secondary to chronic infection is the main cause of death. Treatment of lung disease to reduce the impact of infection, inflammation and subsequent lung injury is therefore of major importance. Here we discuss the present status of antibiotic therapy for the major pathogens in CF airways, including prophylaxis against infection, eradication of early infection, suppression of chronic infection, and the treatment of infective exacerbations. We outline measures to optimize maintenance treatment for infection in the light of novel antibiotic drug formulations. We discuss new developments in culture-independent microbiological diagnostic techniques and the use of tools for monitoring the ...
Background: People with cystic fibrosis are susceptible to pulmonary infection with Pseudomonas aeru...
AbstractInflammation plays a major role in the pathophysiology of lung disease in CF. This response ...
Acute pulmonary exacerbations (APE) are well‐described complications of cystic fibrosis (CF) and are...
AbstractIn patients with cystic fibrosis (CF) lung damage secondary to chronic infection is the main...
AbstractCystic fibrosis (CF) patients suffer typically from bacterial infections of their airways. W...
AbstractChronic infection of the respiratory tract is a hallmark of cystic fibrosis (CF). Antibiotic...
SummaryChronic airway infection and inflammation are key events in the clinical course of cystic fib...
Much of the improvement in the survival of individuals with cystic fibrosis (CF) is due to advanceme...
AbstractIn patients with cystic fibrosis (CF), early intervention and prevention of lung disease is ...
Chronic infection of the respiratory tract is a hallmark of cystic fibrosis (CF). Antibiotic treatme...
Clinical presentation of the chronic, heritable condition cystic fibrosis (CF) is complex, with a di...
Cystic fibrosis (CF) is the most common lethal hereditary disorder with autosomal recessive heredity...
Cystic fibrosis (CF) is the most common lethal hereditary disorder with autosomal recessive heredity...
AbstractCystic fibrosis (CF) is a life-shortening disease with significant morbidity. Despite overal...
The ultimate aim of any antimicrobial treatment is a better infection outcome for the patient. Here,...
Background: People with cystic fibrosis are susceptible to pulmonary infection with Pseudomonas aeru...
AbstractInflammation plays a major role in the pathophysiology of lung disease in CF. This response ...
Acute pulmonary exacerbations (APE) are well‐described complications of cystic fibrosis (CF) and are...
AbstractIn patients with cystic fibrosis (CF) lung damage secondary to chronic infection is the main...
AbstractCystic fibrosis (CF) patients suffer typically from bacterial infections of their airways. W...
AbstractChronic infection of the respiratory tract is a hallmark of cystic fibrosis (CF). Antibiotic...
SummaryChronic airway infection and inflammation are key events in the clinical course of cystic fib...
Much of the improvement in the survival of individuals with cystic fibrosis (CF) is due to advanceme...
AbstractIn patients with cystic fibrosis (CF), early intervention and prevention of lung disease is ...
Chronic infection of the respiratory tract is a hallmark of cystic fibrosis (CF). Antibiotic treatme...
Clinical presentation of the chronic, heritable condition cystic fibrosis (CF) is complex, with a di...
Cystic fibrosis (CF) is the most common lethal hereditary disorder with autosomal recessive heredity...
Cystic fibrosis (CF) is the most common lethal hereditary disorder with autosomal recessive heredity...
AbstractCystic fibrosis (CF) is a life-shortening disease with significant morbidity. Despite overal...
The ultimate aim of any antimicrobial treatment is a better infection outcome for the patient. Here,...
Background: People with cystic fibrosis are susceptible to pulmonary infection with Pseudomonas aeru...
AbstractInflammation plays a major role in the pathophysiology of lung disease in CF. This response ...
Acute pulmonary exacerbations (APE) are well‐described complications of cystic fibrosis (CF) and are...