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The etiology of neonatal pneumonia, complicated by bronchopulmonary dysplasia
M V Kushnareva1, E S Keshishyan1, E D Balashova2
1Academician Yu. E. Veltishchev Research Clinical Institute of Pediatrics, N.I. Pirogov Russian National Research Medical University, Ministry of Health of the Russian Federation, Moscow; Russian Federation.
Insights
Bronchopulmonary dysplasia (BPD) is more common in preterm infants with ventilator-associated pneumonia (VAP). Timely antibiotic treatment of VAP may reduce BPD incidence.
Area of Science:
- Neonatal Medicine
- Pediatric Pulmonology
- Infectious Diseases
Background:
- Bronchopulmonary dysplasia (BPD) affects 7-50% of preterm infants with ventilator-associated pneumonia (VAP).
- Understanding the etiological factors of VAP-complicated BPD is crucial for prevention and treatment.
Purpose of the Study:
- To investigate the etiological structure of neonatal pneumonia in preterm infants complicated by BPD.
- To determine the antibiotic sensitivity of identified pathogens.
Main Methods:
- Retrospective chart review of 194 preterm infants diagnosed with VAP.
- Microbiological analysis of respiratory tract washings using standard qualitative and quantitative methods.
Main Results:
- Specific pathogens (E. coli, Enterococcus spp., P. aeruginosa, S. maltophilia, Mycoplasma, S. aureus, C. krusei) were 4-13 times more frequent in preterm infants with BPD.
- Prolonged VAP with pathogen shifts increased BPD development 7-11 times; polymicrobial infections increased it 5-7 times.
- Early massive respiratory pathogen colonization (1-3 days) was an unfavorable prognostic factor for VAP complicated by BPD.
Conclusions:
- Timely and adequate antibacterial therapy for VAP may reduce the incidence of BPD in preterm infants.
- Identifying specific pathogens and their antibiotic sensitivities is key to effective VAP management and BPD prevention.
Background:
The frequency of bronchopulmonary dysplasia (BPD) in preterm infants with a "ventilator-associated" pneumonia (VAP) ranges between 7 to 50%.
Objective:
To investigate the features of the etiological structure of neonatal pneumonia complicated by BPD, and to determine the sensitivity of pathogens to antibiotics.
Methods:
A retrospective chart review of 194 preterm infants with VAP, birth weight from 780 to 2820 g and gestational age from 27 to 37 weeks was conducted. A microbiological study of washings from the respiratory tract was conducted by standard qualitative and quantitative methods.
Results:
Respiratory tract infections caused by E. coli (with hemolytic properties), Enterococcus spp. (with hemolytic properties), Pseudomonas aeruginosa, Stenotrophomonas maltophilia, various types of mycoplasmas, Staphylococcus aureus, and Candida krusei were found 4- 13 times more frequent in preterm infants with BPD than in preterm infants without BPD and more mature infants with or without this complication. BPD developed 7- 11 times more frequent in preterm infants with prolonged VAP and change in pathogens than in preterm infants with VAP without change of agent. BPD developed 5- 7 times more frequent in preterm infants with the association of pathogens than in preterm infants with a monoinfection. Massive colonization of respiratory tract pathogens by 1- 3 days of life (lg4 colony forming units in 1 ml and above) was an unfavorable prognostic factor for the development of VAP, complicated by BPD.
Conclusion:
The reduction in the frequency of BPD is might be possible with timeous and adequate antibacterial therapy of VAP.
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