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Long Term Chronic Pseudomonas aeruginosa Airway Infection in Mice
Published on: March 17, 2014
Clinical outcomes after initial pseudomonas acquisition in cystic fibrosis
Edith T Zemanick1, Julia Emerson, Valeria Thompson
1Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado.
Insights
Newly acquired Pseudomonas aeruginosa (Pa) in cystic fibrosis (CF) patients did not impact lung function or growth. However, Pa acquisition increased pulmonary exacerbations and respiratory symptoms, suggesting a marker of disease severity.
Area of Science:
- Pediatric Pulmonology
- Infectious Diseases
- Cystic Fibrosis Research
Background:
- Pseudomonas aeruginosa (Pa) is a critical pathogen in cystic fibrosis (CF) affecting lung health.
- Early eradication therapy is standard, but outcomes after initial Pa isolation require ongoing evaluation.
- Understanding the impact of Pa acquisition is crucial for managing CF progression.
Purpose of the Study:
- To assess clinical outcomes following initial Pseudomonas aeruginosa isolation in a U.S. pediatric CF cohort.
- To evaluate the effect of Pa acquisition on lung function, growth, and exacerbations.
- To determine associations between Pa acquisition and other respiratory pathogen co-infections.
Main Methods:
- Analysis of data from the Early Pseudomonas Infection Control (EPIC) Observational Study.
- Inclusion of pediatric CF patients with no prior Pa isolation.
- Utilized population-averaged regression models (generalized estimating equations) to analyze outcomes.
Main Results:
- No significant effect of Pa acquisition on lung function (FEV1 % predicted) or growth parameters.
- Increased pulmonary exacerbation rate (IRR 1.40) and odds of crackles/wheeze (OR 1.23) post-Pa acquisition.
- Increased odds of MRSA and S. maltophilia isolation, with decreased odds of H. influenzae.
Conclusions:
- Initial Pseudomonas aeruginosa acquisition in CF patients was not linked to lung function or nutritional decline.
- Pa acquisition correlated with a higher rate of pulmonary exacerbations and respiratory symptoms.
- These findings suggest Pa acquisition may indicate more severe disease or contribute to exacerbations.
Objectives:
To evaluate clinical outcomes associated with initial isolation of Pseudomonas aeruginosa (Pa) in a large U.S. cystic fibrosis (CF) cohort in the current era of widespread early Pa eradication therapy.
Methods:
Participants were children with CF enrolled in the Early Pseudomonas Infection Control (EPIC) Observational Study who had no isolation of Pa from respiratory cultures prior to enrollment. Population-averaged regression models using generalized estimating equation methods were used to estimate the effect of Pa acquisition on endpoints including lung function, growth, pulmonary exacerbation rate, respiratory signs and symptoms, and respiratory cultures.
Results:
Eight hundred thirty-eight subjects were observed for a mean 4.6 (SD 1.2) years during which 431 (51%) acquired Pa. There was no statistically significant effect of Pa acquisition on the slopes of FEV1 % predicted or growth parameters. Pulmonary exacerbation rate was statistically significantly greater after Pa acquisition (incident rate ratio 1.40, 95% CI 1.07, 1.84) as were odds of crackles or wheeze on physical exam (OR 1.23, 95% CI 1.00, 1.52). Odds of isolation of MRSA (OR 1.86, 95% CI 1.38, 2.49) and S. maltophilia (OR 2.11, 95% CI 1.49, 2.98) increased after Pa acquisition, while the odds of H. influenzae (OR 0.54, 95% CI 0.46, 0.64) decreased.
Conclusions:
In this large U.S. cohort, we did not detect an association between acquisition of Pa and deterioration in lung function or nutrition. Pa acquisition was associated with significantly increased pulmonary exacerbation rate and odds of crackles or wheeze. Pa infection may be the cause of these outcomes or a marker of more severe disease.
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