Our objective was to compare the efficacy, safety, and microbiology of once-daily intravenous (IV) tobramycin with conventional 8-hourly tobramycin/ceftazidime IV therapy for acute Pseudomonas aeruginosa (PA) pulmonary exacerbations in cystic fibrosis (CF). CF patients with PA-induced pulmonary exacerbations were allocated to receive either once-daily tobramycin (Mono) or conventional therapy with tobramycin/ceftazidime given 8-hourly (Conv). The two longitudinal groups received therapy in a double-blind, randomized manner over a period of 2 years. Tobramycin doses were adjusted to achieve a daily area under the time-concentration curve of 100 mg x hr/L in both groups. Results were assessed for both short-term changes (efficacy and safety a...
Background: Although anti-pseudomonal antibiotics are routinely used in the treatment of acute respi...
AbstractEarly studies of the use of antibiotics in patients with cystic fibrosis suggested that they...
Acute pulmonary exacerbations (APE) are well‐described complications of cystic fibrosis (CF) and are...
This randomized, multicentre, open-label, two-period crossover study showed that inhaling tobramycin...
AbstractBackgroundOnce daily dosing of aminoglycosides is widely used but is limited by the inconven...
Objectives: Previous studies have examined renal safety of once daily intravenous tobramycin in indi...
Intravenous (IV) anti‐pseudomonal aminoglycosides (i.e., amikacin and tobramycin) have been shown to...
BACKGROUND: Cystic fibrosis (CF) is characterized by chronic bacterial broncho-pulmonary infection. ...
Introduction: CF pulmonary guidelines recommend alternate therapy (one month on, one month off) with...
AbstractBackgroundCystic fibrosis (CF) is characterized by chronic bacterial broncho-pulmonary infec...
Summary. Intravenous (IV) anti-pseudomonal aminoglycosides (i.e., amikacin and tobramycin) have been...
It is estimated that about 60-70% of Cystic Fibrosis patients develop Pseudomonas aeruginosa chronic...
Background: People with cystic fibrosis, who are chronically colonised with the organism Pseudomonas...
Background/Aims: In cystic fibrosis (CF), chronic microbial lung infections are difficult to treat...
Acute pulmonary exacerbations (APE) are well‐described complications of cystic fibrosis (CF) and are...
Background: Although anti-pseudomonal antibiotics are routinely used in the treatment of acute respi...
AbstractEarly studies of the use of antibiotics in patients with cystic fibrosis suggested that they...
Acute pulmonary exacerbations (APE) are well‐described complications of cystic fibrosis (CF) and are...
This randomized, multicentre, open-label, two-period crossover study showed that inhaling tobramycin...
AbstractBackgroundOnce daily dosing of aminoglycosides is widely used but is limited by the inconven...
Objectives: Previous studies have examined renal safety of once daily intravenous tobramycin in indi...
Intravenous (IV) anti‐pseudomonal aminoglycosides (i.e., amikacin and tobramycin) have been shown to...
BACKGROUND: Cystic fibrosis (CF) is characterized by chronic bacterial broncho-pulmonary infection. ...
Introduction: CF pulmonary guidelines recommend alternate therapy (one month on, one month off) with...
AbstractBackgroundCystic fibrosis (CF) is characterized by chronic bacterial broncho-pulmonary infec...
Summary. Intravenous (IV) anti-pseudomonal aminoglycosides (i.e., amikacin and tobramycin) have been...
It is estimated that about 60-70% of Cystic Fibrosis patients develop Pseudomonas aeruginosa chronic...
Background: People with cystic fibrosis, who are chronically colonised with the organism Pseudomonas...
Background/Aims: In cystic fibrosis (CF), chronic microbial lung infections are difficult to treat...
Acute pulmonary exacerbations (APE) are well‐described complications of cystic fibrosis (CF) and are...
Background: Although anti-pseudomonal antibiotics are routinely used in the treatment of acute respi...
AbstractEarly studies of the use of antibiotics in patients with cystic fibrosis suggested that they...
Acute pulmonary exacerbations (APE) are well‐described complications of cystic fibrosis (CF) and are...