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Published on: February 14, 2011
Oral anti-pseudomonal antibiotics for cystic fibrosis
T Remmington1, N Jahnke, C Harkensee
1University of Liverpool, Institute of Child Health, Alder Hey Children's Hospital, Eaton Road, Liverpool, UK, L12 2AP. traceyr@liverpool.ac.uk
Background:
Pseudomonas aeruginosa is the most common bacterial pathogen causing infection in the lungs of people with CF and appropriate antibiotic therapy is vital. Antibiotics for exacerbations are usually given intravenously, and for long-term treatment, via a nebuliser. Oral anti-pseudomonal antibiotics with the same efficacy and safety as intravenous or nebulised antibiotics would benefit the quality of life of people with CF due to ease of treatment and avoidance of hospitalisation.
Objectives:
To determine the benefit or harm of oral anti-pseudomonal antibiotic therapy for people with CF, colonised with Pseudomonas aeruginosa, in the: (1) treatment of an exacerbation of respiratory tract infection; and (2) long-term treatment in chronic infection.
Search Strategy:
We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group Trials Register comprising references identified from comprehensive electronic database searches and handsearches of relevant journals and abstract books of conference proceedings. We contacted pharmaceutical companies for information on relevant trials and checked reference lists of identified trials. Most recent search: March 2007.
Selection Criteria:
Randomised or quasi-randomised controlled trials comparing any dose of oral anti-pseudomonal antibiotics, with other combinations of inhaled, oral or intravenous antibiotics, or with placebo or usual treatment for exacerbations and long-term treatment.
Data Collection And Analysis:
Two authors independently selected the trials, extracted data and assessed quality. We contacted trialists to obtain missing information.
Main Results:
We included four trials examining exacerbations (197 participants) and two trials examining long-term therapy (85 participants). We regarded the most important outcomes as quality of life and lung function. In our analysis, we were unable to identify any statistically significant difference between oral anti-pseudomonal antibiotics and other treatments for these outcome measures for either exacerbations or long-term treatment. One of the included trials reported significantly better lung function when treating an exacerbation with ciprofloxacin when compared with intravenous treatment; however, our analysis did not confirm this finding. We found no evidence of difference between oral anti-pseudomonal antibiotics and other treatments regarding adverse events or development of antibiotic resistance, but trials were not adequately powered to detect this.
Authors' Conclusions:
We found no conclusive evidence that an oral anti-pseudomonal antibiotic regimen is more or less effective than an alternative treatment for either exacerbations or long-term treatment of chronic infection with P. aeruginosa. Until results of adequately-powered future trials are available, treatment needs to be selected on a pragmatic basis, based upon known effectiveness against local strains and upon individual preference.
Insights
Oral antibiotics for Pseudomonas aeruginosa infections in cystic fibrosis (CF) show no clear benefit over other treatments for exacerbations or long-term care. Further research is needed to determine optimal therapeutic strategies for CF patients.
Area of Science:
- Medical research
- Clinical trials
- Pharmacology
Background:
- Pseudomonas aeruginosa is a common lung pathogen in cystic fibrosis (CF).
- Current treatments for P. aeruginosa infections in CF involve intravenous or nebulised antibiotics.
- Oral antibiotics could improve quality of life for CF patients if effective and safe.
Purpose of the Study:
- To evaluate the efficacy and safety of oral anti-pseudomonal antibiotics for CF patients with P. aeruginosa.
- To assess oral antibiotics in treating respiratory exacerbations and chronic infections in CF.
Main Methods:
- Systematic review of randomized or quasi-randomized controlled trials.
- Searched Cochrane Cystic Fibrosis and Genetic Disorders Group Trials Register and contacted pharmaceutical companies.
- Two authors independently selected trials, extracted data, and assessed quality.
Main Results:
- Four trials on exacerbations (197 participants) and two on long-term therapy (85 participants) were included.
- No statistically significant differences in quality of life or lung function were found between oral antibiotics and other treatments.
- No significant differences in adverse events or antibiotic resistance were detected, though trials were underpowered.
Conclusions:
- Current evidence does not conclusively support or refute the effectiveness of oral anti-pseudomonal antibiotics for P. aeruginosa in CF.
- Treatment decisions should be individualized based on local resistance patterns and patient preference pending further research.
- Adequately powered future trials are necessary to establish definitive treatment guidelines.
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