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Updated: Aug 17, 2026

Visualization of Pseudomonas aeruginosa within the Sputum of Cystic Fibrosis Patients
Published on: July 16, 2020
Eradication of early Pseudomonas aeruginosa infection
N Høiby1, B Frederiksen, T Pressler
1Department of Clinical Microbiology 9301, Rigshospitalet, University of Copenhagen, Juliane Maries Vej 22, 2100 Copenhagen, Denmark. hoiby@inet.uni2.dk
Abstract:
Chronic pulmonary infection with Pseudomonas aeruginosa is responsible for most of the morbidity and mortality in cystic fibrosis (CF). Once established as a biofilm, chronic P. aeruginosa infection caused by the mucoid phenotype cannot be eradicated. However, a period of intermittent colonization with P. aeruginosa precedes the establishment of the chronic infection. This window of opportunity can be utilized to eradicate P. aeruginosa from the respiratory tract of CF patients by means of oral ciprofloxacin in combination with nebulized colistin for 3 weeks or, even better, for 3 months or by means of inhaled tobramycin as monotherapy for 4 weeks or longer. This early, aggressive eradication therapy has now been used for 15 years without giving rise to resistance to the antibiotics and without serious side effects. The therapeutic results have been very successful and have completely changed the epidemiology in the Danish Cystic Fibrosis Center and a few other centers which have used this strategy for several years. The chronic P. aeruginosa lung infection is not seen in CF infants and children anymore due to the aggressive therapy, and no other bacteria have replaced P. aeruginosa in these young patients. The aggressive therapy has been shown to very cost-effective, and a European Consensus report recommends this approach.
Insights
Early, aggressive eradication therapy for Pseudomonas aeruginosa in cystic fibrosis (CF) prevents chronic lung infection. This successful strategy, using antibiotics like ciprofloxacin, colistin, or tobramycin, is safe, cost-effective, and recommended.
Area of Science:
- Pulmonology
- Infectious Diseases
- Cystic Fibrosis Research
Background:
- Chronic Pseudomonas aeruginosa infection, often as a biofilm, causes significant morbidity and mortality in cystic fibrosis (CF).
- A critical window exists for eradicating P. aeruginosa before it establishes chronic infection in CF patients.
Purpose of the Study:
- To evaluate the efficacy and impact of early, aggressive eradication therapy for P. aeruginosa in CF patients.
- To assess the long-term outcomes, safety, and cost-effectiveness of this therapeutic strategy.
Main Methods:
- Treatment regimens included oral ciprofloxacin with nebulized colistin (3 weeks to 3 months) or inhaled tobramycin monotherapy (≥4 weeks).
- Therapy was administered during the intermittent colonization phase of P. aeruginosa infection.
- Data collected over 15 years from CF centers employing this strategy.
Main Results:
- Chronic P. aeruginosa lung infections are no longer observed in infants and children at centers using this aggressive therapy.
- The strategy has demonstrated high success rates without inducing antibiotic resistance or significant side effects.
- Epidemiology of P. aeruginosa in CF has been significantly altered, with no replacement by other pathogens.
Conclusions:
- Early, aggressive eradication therapy is a highly effective, safe, and cost-effective approach to prevent chronic P. aeruginosa infection in CF.
- This strategy has transformed CF patient outcomes and is recommended by European consensus.
- Continued implementation of this approach is crucial for managing P. aeruginosa in cystic fibrosis.
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