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Published on: May 8, 2017
[Microbial population of lower respiratory tract in children from different age groups with cystic fibrosis]
Insights
Chronic lower respiratory tract infections are common in children with cystic fibrosis, with infections increasing with age. Understanding these microbial patterns is key to preventing future complications.
Area of Science:
- Medical Microbiology
- Pediatric Pulmonology
- Infectious Diseases
Background:
- Cystic fibrosis (CF) is a genetic disorder affecting multiple organs, particularly the lungs.
- Chronic respiratory infections are a major cause of morbidity and mortality in CF patients.
- Understanding the dynamic microflora of the lower respiratory tract is crucial for managing CF.
Purpose of the Study:
- To investigate the variability of lower respiratory tract microflora in children with cystic fibrosis (CF).
- To identify potential sources of infectious complications in pediatric CF patients.
- To analyze the progression of microbial colonization with age in CF patients.
Main Methods:
- Analysis of 141 medical histories of CF patients across different age groups and regions.
- Prospective follow-up of 84 pediatric CF patients in Moscow and surrounding regions.
- Utilized microbiological, molecular biological, and statistical methods for microorganism identification and characterization.
Main Results:
- Chronic Pseudomonas, staphylococcal, or mixed infections were present in 25% of 1-4 year olds and 80% of 18-year-olds.
- Microorganism associations (3-5 microbes) were found in 60% of hospitalized patients.
- Beyond Pseudomonas aeruginosa and Staphylococcus aureus, Gram-negative nonfermentative bacteria like Burkholderia cepacia were frequently identified.
Conclusions:
- Chronic mixed infections are a hallmark of cystic fibrosis respiratory disease.
- Identifying mechanisms of lung infection in CF is essential for developing evidence-based prevention strategies.
- Targeted interventions can mitigate infectious complications in pediatric CF patients.
Aim:
To study microflora of lower respiratory tract of children from different age groups with cystic fibrosis during follow-up for determination of its variability and possible sources of infectious complications.
Materials And Methods:
One hundred forty-one medical histories of patients from different age groups with cystic fibrosis living in various regions of Russian Federation were analyzed. Eighty-four children with cystic fibrosis living in Moscow and Moscow region treated as outpatients and inpatients were prospectively followed. For identification and characterization of microorganisms, microbiological, molecular biological, and statistical methods were used.
Results:
It was demonstrated that chronic pseudomonas, staphylococcal or mixed infection was already diagnosed in 25% of children aged 1-4 years, and identified in 80% of patients to the age of 18 years. In two-thirds of cases association of microorganisms was identified, and in hospitalized patients these associations were comprised by 3-5 microorganisms in 60% of cases. Aside from main agents in associations (Pseudomonas aeruginosa and Staphylococcus aureus), representatives of Gram-negative nonfermentative microorganisms (Burkholderia cepacia, Stenotrophomonas maltophilia, Acinetobacter baumanii) were often identified that possibly determined by tropism of these species to lung tissue.
Conclusion:
Chronic mixed infection is characteristic for patients with cystic fibrosis. Identification of possible mechanisms of lung infection in patients with cystic fibrosis will allow to develop evidence-based system of prevention of infectious complications in these patients.
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