In this thesis, studies on the treatment of CF patients with antibiotic containing aerosols are described. After an overview of the history of cystic fibrosis related to inhalation therapy in chapter 1, chapter 2 deals with the first European consensus on inhaled medication and inhalation devices in CF. This document describes the current knowledge on treatment with inhaled drugs (among which are antimicrobial agents). Next to the drugs currently in use and new drug therapies in development, the fundamentals of inhalation in CF treatment and practical aspects of inhalation of drugs (e.g. compatibility of mixtures and cleaning) are described. This comprehensive review incorporates the fact that several new drugs, drug formulations and new in...
Much of the improvement in the survival of individuals with cystic fibrosis (CF) is due to advanceme...
The aim of this study was to investigate the pulmonary administration of antibiotics as dry powder t...
The primary clinical characteristics of cystic fibrosis (CF) are malnutrition caused by malabsorptio...
In cystic fibrosis inhalation of drugs for the treatment of CF related lung disease has been proven ...
AbstractIn cystic fibrosis inhalation of drugs for the treatment of CF related lung disease has been...
ABSTRACT: Aerosol administration of antipseudomonal antibiotics is commonly used in cystic fibrosis...
Aerosol administration of antipseudomonal antibiotics is commonly used in cystic fibrosis. However, ...
Key points There have been significant advances in both inhalation medicines and delivery devices wi...
This PhD thesis aimed at developing synergistic combinations of antibiotics in the form of dry powde...
SummaryChronic airway infection and inflammation are key events in the clinical course of cystic fib...
Inhalation of antipseudomonal antibiotics is a cornerstone in treating cystic fibrosis patients. It ...
Bronchiectasis is a pathological diagnosis describing dilatation of the airways and is characterized...
Cystic Fibrosis (CF) is the most frequent lethal inherited disease in the white population. In CF pa...
Introduction: Nebulisation therapy plays a key role in the treatment of cystic fibrosis (CF). Its ef...
The aim of this study was to investigate the pulmonary administration of antibiotics as dry powder t...
Much of the improvement in the survival of individuals with cystic fibrosis (CF) is due to advanceme...
The aim of this study was to investigate the pulmonary administration of antibiotics as dry powder t...
The primary clinical characteristics of cystic fibrosis (CF) are malnutrition caused by malabsorptio...
In cystic fibrosis inhalation of drugs for the treatment of CF related lung disease has been proven ...
AbstractIn cystic fibrosis inhalation of drugs for the treatment of CF related lung disease has been...
ABSTRACT: Aerosol administration of antipseudomonal antibiotics is commonly used in cystic fibrosis...
Aerosol administration of antipseudomonal antibiotics is commonly used in cystic fibrosis. However, ...
Key points There have been significant advances in both inhalation medicines and delivery devices wi...
This PhD thesis aimed at developing synergistic combinations of antibiotics in the form of dry powde...
SummaryChronic airway infection and inflammation are key events in the clinical course of cystic fib...
Inhalation of antipseudomonal antibiotics is a cornerstone in treating cystic fibrosis patients. It ...
Bronchiectasis is a pathological diagnosis describing dilatation of the airways and is characterized...
Cystic Fibrosis (CF) is the most frequent lethal inherited disease in the white population. In CF pa...
Introduction: Nebulisation therapy plays a key role in the treatment of cystic fibrosis (CF). Its ef...
The aim of this study was to investigate the pulmonary administration of antibiotics as dry powder t...
Much of the improvement in the survival of individuals with cystic fibrosis (CF) is due to advanceme...
The aim of this study was to investigate the pulmonary administration of antibiotics as dry powder t...
The primary clinical characteristics of cystic fibrosis (CF) are malnutrition caused by malabsorptio...