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Analysis of the Efficacy of Eradication Therapy Regimens for the First Isolation of Pseudomonas aeruginosa

https://doi.org/10.66825/2949-4664-apps-4-2-37-45

Abstract

Microbial inflammation caused by P. aeruginosa is associated with low lung function, inadequate nutritional status, severe disease course, the presence of respiratory complications and early mortality. The window of opportunity for eradication is the early detection of colonization of P. aeruginosa in the respiratory tract. The highest chance of completely eradicating P. aeruginosa exists if treatment is started in the first month after its detection.

Objective. To evaluate the strategies of inhaled antibiotic therapy in children with cystic fibrosis when P. aeruginosa is initially detected in the sputum.

Materials. The study included pediatric patients with CF who were observed in the Department of Cystic Fibrosis of the Moscow Regional Research Institute of Childhood of the Ministry of Health of the Moscow Region. The number of patients with the first isolation of P. aeruginosa among patients in the Moscow Region during the 4-year follow-up period was 37 children (19 males / 18 females). The median age of the children was 4.87 (3.33; 9.9) years. 89% of the patients had a ‘’severe genotype’’. The median age of diagnosis was Me (Q1; Q3) 0.2 (0.1; 0.2) years. All children underwent microbiological monitoring on a regular basis, once a quarter, before inclusion in the study.

Results. Patients on inhaled tobramycin or colistimethate sodium in combination with ciprofloxacin had a 100% positive result in both cases, with all children achieving eradication during follow-up for 2 years or more. A high percentage of eradication was achieved in patients receiving inhaled tobramycin therapy, with 93.3% achieving persistent eradication. Lower rates were observed in patients receiving only sodium colistimethate inhalation therapy, with 75% achieving eradication, and in patients alternating between inhaled tobramycin and sodium colistimethate, with 66.6% achieving eradication. However, a statistical analysis of the results of the effectiveness of the antibacterial therapy schemes did not show any advantage of any of the schemes (p = 0.94). Patients with primary P. aeruginosa isolation showed better external respiratory function results one year after eradication therapy compared to patients with chronic P. aeruginosa – Me (Q1; Q3) FEV1 (p1-2 = 0.004), FVC (p1-2 = 0.039). Children who underwent eradication therapy had a statistical difference in terms of nutritional status according to the BMI percentile – Me (Q1; Q3) per BMI kg/m2 compared to the group with chronic P. aeruginosa (p1-2 = 0.016).

Conclusion. Early eradication therapy at the first P. aeruginosa isolation helps to prevent chronic infection, avoid lung function decline, structural damage to the lungs, and delay chronic colonization. Early start of eradication therapy depends on constant regular microbiological monitoring, which requires a modern organization of dynamic monitoring of patients with cystic fibrosis.

About the Authors

N. D. Odinaeva
Research Clinical Institute of Childhood of the Moscow Region
Russian Federation

Nuriniso D. Odinaeva, Doct. Sci. (Med.), Professor, Director

Bldg. 1, 24a Kominterna str., Mytishchi, 141009


Competing Interests:

All authors declare no conflicts of interest..



E. I. Kondratyeva
Research Clinical Institute of Childhood of the Moscow Region; Research Centre for Medical Genetic
Russian Federation

Elena I. Kondratyeva, Doct. Sci. (Med.), Head of Scientific Advisory Department of Cystic Fibrosis, Research Centre for Medical Genetics. Head of the Department of Genetics of Diseases of the Respiratory System of the Institute of Higher and Additional Professional Education of the Research Centre for Medical Genetics, Moscow. Deputy Director for Scientific Work of the Research Clinical Institute of Childhood of the Moscow Region

Bldg. 1, 24a Kominterna str., Mytishchi, 141009

Moskvorechye str., Moscow, 115522


Competing Interests:

All authors declare no conflicts of interest..



V. V. Shadrina
Research Clinical Institute of Childhood of the Moscow Region; Research Centre for Medical Genetic
Russian Federation

Vera V. Shadrina, Cand. Sci. (Med.), Head of the Department of Hereditary and Metabolic Diseases, Research Clinical Institute of Childhood of the Moscow Region; Leading Researcher, Cystic Fibrosis Clinical Department, Research Centre for Medical Genetics

Bldg. 1, 24a Kominterna str., Mytishchi, 141009

Moskvorechye str., Moscow, 115522


Competing Interests:

All authors declare no conflicts of interest..



V. N. Kovalev
Research Clinical Institute of Childhood of the Moscow Region
Russian Federation

Viktor N. Kovalev, Head of the Cystic Fibrosis Department

Bldg. 1, 24a Kominterna str., Mytishchi, 141009


Competing Interests:

All authors declare no conflicts of interest..



I. R. Fatkhullina
Research Clinical Institute of Childhood of the Moscow Region; Research Centre for Medical Genetic
Russian Federation

Irina R. Fatkhullina, Head of the Department of Cystic Fibrosis, pediatrician, researcher at the Department of Genetic and Metabolic Diseases of the, researcher at the Scientific and Clinical Department of Cystic Fibrosis of the Research Centre for Medical Genetics

phone: +7(498)699-53-20

Bldg. 1, 24a Kominterna str., Mytishchi, 141009

Moskvorechye str., Moscow, 115522


Competing Interests:

All authors declare no conflicts of interest..



E. K. Zhekaite
Research Clinical Institute of Childhood of the Moscow Region; Research Centre for Medical Genetic
Russian Federation

Elena K. Zhekaite, Cand. Sci. (Med.), Leading Researcher, Department of Cystic Fibrosis, Federal State Budgetary Scientific Institution “Research Centre for Medical Genetics”, Ministry of Science and Higher Education of the Russian Federation; Pediatrician, Department of Cystic Fibrosis, Research Clinical Institute of Childhood of the Moscow Region

Bldg. 1, 24a Kominterna str., Mytishchi, 141009

Moskvorechye str., Moscow, 115522


Competing Interests:

All authors declare no conflicts of interest..



T. V. Tronza
Central Research Institute of Epidemiology of Rospotrebnadzor
Russian Federation

Tatyana V. Tronza. Head of Laboratory Research, Clinical Microbiology Laboratory

3a Novogireevskaya str., Moscow, 111123


Competing Interests:

All authors declare no conflicts of interest..



A. Yu. Voronkova
Research Clinical Institute of Childhood of the Moscow Region; Research Centre for Medical Genetic
Russian Federation

Anna Yu. Voronkova, Cand. Sci. (Med.), Leading Researcher of the Research and Clinical Cystic Fibrosis Department

Bldg. 1, 24a Kominterna str., Mytishchi, 141009

Moskvorechye str., Moscow, 115522


Competing Interests:

All authors declare no conflicts of interest..



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For citations:


Odinaeva N.D., Kondratyeva E.I., Shadrina V.V., Kovalev V.N., Fatkhullina I.R., Zhekaite E.K., Tronza T.V., Voronkova A.Yu. Analysis of the Efficacy of Eradication Therapy Regimens for the First Isolation of Pseudomonas aeruginosa. Archives of Pediatrics and Pediatric Surgery. 2026;4(2):37-45. (In Russ.) https://doi.org/10.66825/2949-4664-apps-4-2-37-45

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