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Antibiotic Efficacy Testing in an Ex vivo Model of Pseudomonas aeruginosa and Staphylococcus aureus Biofilms in the Cystic Fibrosis Lung
Published on: January 22, 2021
The association between Staphylococcus aureus and subsequent bronchiectasis in children with cystic fibrosis
Daan Caudri1, Lidija Turkovic2, Jolyn Ng2
1Telethon Kids Institute, Perth, Australia; Dept. of Respiratory Medicine, Princess Margaret Hospital, Perth, Australia; Dept. of Pediatrics/Respiratory Medicine, Erasmus MC, Rotterdam, The Netherlands.
Insights
Early Staphylococcus aureus (S. aureus) infection in children with cystic fibrosis (CF) is linked to lung damage. This finding highlights the importance of monitoring S. aureus in young CF patients for better lung health outcomes.
Area of Science:
- Pediatric Pulmonology
- Infectious Diseases
- Genetics
Background:
- Staphylococcus aureus (S. aureus) colonization is a concern in cystic fibrosis (CF) patients.
- The impact of early S. aureus acquisition on CF lung disease progression requires further investigation.
Purpose of the Study:
- To investigate the association between de novo S. aureus acquisition before school age and lung structure and function in children with CF.
Main Methods:
- The AREST CF cohort study followed children with CF from diagnosis.
- Annual bronchoscopies, chest CT scans, and 3-monthly spirometry were performed.
- Statistical models adjusted for baseline disease severity markers.
Main Results:
- S. aureus acquisition at age 3 was associated with increased bronchiectasis at ages 5-6.
- This association persisted after adjusting for confounders.
- S. aureus at age 3 correlated with reduced FEF25-75, but not FEV1-%-predicted, at ages 5-7.
Conclusions:
- Early S. aureus acquisition at age 3 is linked to later bronchiectasis and impaired lung function (FEF25-75) in children with CF.
- These findings underscore the clinical significance of early S. aureus detection and management in pediatric CF care.
Background:
Staphylococcus aureus (S. aureus) may be related to more rapid progression of cystic fibrosis (CF) lung disease.
Methods:
In the AREST CF cohort study, children diagnosed with CF undergo annual bronchoscopies with bronchoalveolar lavage and ultra-low-dose, chest computed tomography (CT) up to 6-years-old. Spirometry was assessed 3-monthly from the age of 4years. Associations between de novo S. aureus acquisition before school age and CT and lung function at ages 5-7years were investigated. Models were adjusted for multiple markers of disease severity at baseline.
Results:
De novo S. aureus acquisition at 3-years-old (n/N=12/122) was associated with increased bronchiectasis score at age 5-6years. This association decreased but remained significant after adjustment for confounders. S. aureus at 3 was associated with significantly reduced FEF25-75 at age 5-7years, but not with FEV1-%-predicted.
Conclusion:
De novo S. aureus acquisition at age 3 is associated with later bronchiectasis and FEF25-75 in children with CF.
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