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Updated: Dec 7, 2025

Development of a Polymicrobial Colony Biofilm Model to Test Antimicrobials in Cystic Fibrosis
Published on: September 20, 2024
Prophylactic anti-staphylococcal antibiotics for cystic fibrosis
Margaret Rosenfeld1,2, Oli Rayner3, Alan R Smyth4
1Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington, USA.
Insights
Continuous prophylactic antibiotics may reduce Staphylococcus aureus in children with cystic fibrosis but have uncertain clinical benefits. Long-term effects and the emergence of Pseudomonas aeruginosa require further investigation.
Area of Science:
- Pediatric Pulmonology
- Infectious Diseases
- Pharmacology
Background:
- Staphylococcus aureus is a common cause of pulmonary infections in young children with cystic fibrosis (CF).
- Prophylactic antibiotics are used to prevent S. aureus infection and lung damage in CF patients.
- Long-term antibiotic use may lead to adverse effects and infection with Pseudomonas aeruginosa.
Purpose of the Study:
- To assess the efficacy of continuous oral antibiotic prophylaxis in preventing Staphylococcus aureus acquisition in children with CF.
- To evaluate the impact of prophylaxis on clinical status, lung function, survival, adverse effects, and the emergence of other pathogens, including Pseudomonas aeruginosa.
Main Methods:
- Systematic review and meta-analysis of randomized controlled trials (RCTs) comparing continuous oral prophylactic antibiotics with no prophylaxis in individuals with CF.
- Searched multiple databases and trial registries up to September 2020.
- Assessed study eligibility, methodological quality (GRADE criteria), and extracted data on primary outcomes like lung function (FEV1) and S. aureus isolates.
Main Results:
- Four RCTs with 401 participants were included; evidence quality was low.
- Prophylaxis likely makes little difference to lung function (FEV1) after six years.
- Antibiotic prophylaxis may reduce Staphylococcus aureus isolates at two years but has uncertain clinical importance.
- No significant difference in Pseudomonas aeruginosa isolates at two years, with a trend towards higher rates after four to six years.
Conclusions:
- Anti-staphylococcal antibiotic prophylaxis may reduce Staphylococcus aureus isolates in young children with CF.
- The clinical significance of reduced S. aureus isolates is uncertain.
- Further research is needed to clarify the trend of Pseudomonas aeruginosa emergence and the influence of antibiotic choice and duration.
Background:
Staphylococcus aureus causes pulmonary infection in young children with cystic fibrosis. Prophylactic antibiotics are prescribed hoping to prevent such infection and lung damage. Antibiotics have adverse effects and long-term use might lead to infection with Pseudomonas aeruginosa. This is an update of a previously published review.
Objectives:
To assess continuous oral antibiotic prophylaxis to prevent the acquisition of Staphylococcus aureus versus no prophylaxis in people with cystic fibrosis, we tested the following hypotheses to investigate whether prophylaxis: 1. improves clinical status, lung function and survival; 2. leads to fewer isolates of Staphylococcus aureus; 3. causes adverse effects (e.g. diarrhoea, skin rash, candidiasis); 4. leads to fewer isolates of other common pathogens from respiratory secretions; 5. leads to the emergence of antibiotic resistance and colonisation of the respiratory tract with Pseudomonas aeruginosa.
Search Methods:
We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group Trials Register, comprising references identified from comprehensive electronic database searches, handsearches of relevant journals and abstract books of conference proceedings. Companies manufacturing anti-staphylococcal antibiotics were contacted. Most recent search of the Group's Register: 27 February 2020. Online trials registries were also searched. Most recent search of online trials registries: 15 September 2020.
Selection Criteria:
Randomised trials of continuous oral prophylactic antibiotics (given for at least one year) compared to intermittent antibiotics given 'as required', in people with cystic fibrosis of any disease severity.
Data Collection And Analysis:
The authors assessed studies for eligibility and methodological quality and extracted data. The quality of the evidence was assessed using the GRADE criteria. The review's primary outcomes of interest were lung function by spirometry (forced expiratory volume in one second (FEV1)) and the number of people with one or more isolates of Staphylococcus aureus (sensitive strains).
Main Results:
We included four studies, with a total of 401 randomised participants aged zero to seven years on enrolment; one study is ongoing. The two older included studies generally had a higher risk of bias across all domains, but in particular due to a lack of blinding and incomplete outcome data, than the two more recent studies. We only regarded the most recent study as being generally free of bias, although even here we were not certain of the effect of the per protocol analysis on the study results. Evidence quality was judged to be low for all outcomes assessed after being downgraded based on GRADE assessments. Downgrading decisions were due to limitations in study design (all outcomes), for imprecision and for inconsistency . Prophylactic anti-staphylococcal antibiotics probably make little or no difference to lung function measured as FEV1 % predicted after six years (mean difference (MD) -2.30, 95% confidence interval (CI) -13.59 to 8.99, one study, n = 119, low-quality evidence); but may reduce the number of children having one or more isolates of Staphylococcus aureus at two years (odds ratio (OR) 0.21, 95% CI 0.13 to 0.35, three studies, n = 315, low-quality evidence). At the same time point, there may be little or no effect on nutrition as reported using weight z score (MD 0.06, 95% CI -0.33 to 0.45, two studies, n = 140, low-quality evidence), additional courses of antibiotics (OR 0.18, 95% CI 0.01 to 3.60, one study, n = 119, low-quality evidence) or adverse effects (low-quality evidence). There was no difference in the number of isolates of Pseudomonas aeruginosa between groups at two years (OR 0.74, 95% CI 0.45 to 1.23, three studies, n = 312, low-quality evidence), though there was a trend towards a lower cumulative isolation rate of Pseudomonas aeruginosa in the prophylaxis group at two and three years and towards a higher rate from four to six years. As the studies reviewed lasted six years or less, conclusions cannot be drawn about the long-term effects of prophylaxis.
Authors' Conclusions:
Anti-staphylococcal antibiotic prophylaxis may lead to fewer children having isolates of Staphylococcus aureus, when commenced early in infancy and continued up to six years of age. The clinical importance of this finding is uncertain. Further research may establish whether the trend towards more children with CF with Pseudomonas aeruginosa, after four to six years of prophylaxis, is a chance finding and whether choice of antibiotic or duration of treatment might influence this.
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