Minimum inhibitory concentrations of antibacterial drugs for Staphylococcus epidermidis strains isolated from the contents of the tracheobronchial tree of newborn children
https://doi.org/10.69964/BMCC-2024-1-3-91-98
Abstract
Introduction. Over the past decades, outstanding progress has been made in caring for extremely premature infants and newborns with severe pathologies. Management of this vulnerable category of patients is associated with the continued risk of developing infectious pathology. In the structure of nosological forms, neonatal sepsis caused by coagulase-negative staphylococci occupies one of the leading positions. There is an increase in the number of antibiotic-resistant strains, including among Staphylococcus epidermidis, a typical representative of the normal microbiocenosis of human skin, so colonization of a premature newborn child who is at the stationary stage of nursing with it is a typical process.
Objective. To study changes in the minimum inhibitory concentration of antibacterial drugs for Staphylococcus epidermidis strains isolated from the contents of the tracheobronchial tree of newborn children at the nursing stage in a hospital setting.
Material and methods. To assess the statistical significance of the results obtained, the Chisquare test with Yates correction and the Mann-Whitney U test were used. Research results. All strains tested were resistant to cefoxitin. This, in turn, determines resistance to protected penicillins, amoxicillin clavulanate, ampicillin, sulbactam, and cephalosporins of I-IV generations. 44.4% and 87.5% of Staphylococcus epidermidis strains resistant to gentamicin were registered in 2022 and 87.5% in 2024.When comparing the MIC to gentamicin of Staphylococcus epidermidis isolated from TBD, a significant increase in indicators was established in 2024 compared to 2022 (Mann-Whitney U test is 7.5; p<0.05). The proportion of clindamycin-resistant Staphylococcus epidermidis strains is 44.4% in 2022 and 12.5% in 2024 (p = 0.179). > < 0.05). The proportion of clindamycin-resistant Staphylococcus epidermidis strains is 44.4% in 2022 and 12.5% in 2024 (p = 0.179).
Conclusion. Thus, the analysis of antibiotic resistance of staphylococci isolated during bacteriological examination of the contents of the tracheobronchial tree demonstrates an increase in the MIC of Staphylococcus epidermidis to gentamicin.The high therapeutic potential of vancomycin, a deep reserve antibiotic for the treatment of congenital and hospital-acquired pneumonia in premature newborns, remains high.
About the Authors
Guzel N. ChistyakovaRussian Federation
Guzel N. Chistyakova — MD, Prof., Head of the Department of Immunology, Clinical Microbiology, Pathomorphology and Cytodiagnostics
st. Repina, 1, Ekaterinburg, 620028, Russia
Alexander V. Ustyuzhanin
Russian Federation
Alexandr V. Ustyuzhanin — Candidate of Medical Sciences, Leading Researcher of the Scientific Department of Immunology, Microbiology, Pathomorphology and Cytodiagnostics
st. Repina, 1, Ekaterinburg, 620028, Russia
Ekaterina S. Ivanova
Russian Federation
Ivanova Ekaterina Sergeevna — resident doctor, neonatologist
st. Repina, 1, Ekaterinburg, 620028, Russia
Irina I. Remizova
Russian Federation
Irina I. Remizova — Senior Researcher of the Department of Immunology, Microbiology, Pathomorphology and Cytodiagnostics
st. Repina, 1, Ekaterinburg, 620028
References
1. Gorbacheva AA, Butranova OI. Microbial landscape in the neonatal care intensive unit. Good Clinical Practice. 2024;(3):93-95. (In Russ). https://doi.org/10.37489/2588-0519-2024-3-93-95
2. Dorum B.A., Elmas Bozdemir Ş., Kral B.Z., Erdoğan A., Çakır S.Ç.. Bacteriological Profile and Antibiotic Susceptibility of Neonatal Sepsis Cases in the Neonatal Intensive Care Unit of a Tertiary Hospital in Türkiye. Children (Basel). 2024 Sep 30;11(10):1208. https://doi:10.3390/children11101208
3. Tang X.J., Sun B., Ding X., Li H., Feng X. Changing trends in the bacteriological profiles and antibiotic susceptibility in neonatal sepsis at a tertiary children’s hospital of China. Transl Pediatr. 2020 Dec;9(6):734-742. https://doi.org/10.21037/tp-20-115.
4. Fang P., Gao K., Yang J., Li T., Gong W., Sun Q., Wang Y. Prevalence of Multidrug-Resistant Pathogens Causing Neonatal Early and Late Onset Sepsis, a Retrospective Study from the Tertiary Referral Children’s Hospital. Infect Drug Resist. 2023 Jun 29;16:4213-4225. https://doi:10.2147/IDR.S416020
5. Verizhnikova EV, Evdokimova MA, Glinskaya TO, Kosheleva ON, Nosova OM. Protocol for empirical antibiotic therapy in newborns. Local microbiological monitoring of the perinatal center. Farmakologiya & Farmakoterapiya. 2022. №4. 64-68 (In Russ). https://doi.org/10.46393/27132129_2022_4_64
6. Shalina RI, Spiridonov DS, Plehanova ER, Breusenko LE, Borisov YaS. Premature birth. The role of infection. Vrach. 2021. №1. (In Russ). https://doi.org/10.29296/25877305-2021-01-13
7. Ivanov DO, Panchenko AS, Fedorova LA, Balashova EN, Bem EV, Zelenin NM, Myznikova IV, Levadneva MI, Nabieva AS, Pavlova SE, Romanova LA, Chumakova GN, Yakovleva EE, Belousova TV, Izvekova IYa, Ovsyannikov DYu. Diagnosis and treatment of infection specific to the perinatal period (Draft clinical guidelines for discussion by neonatologists and pediatricians) Pediatr. 2024. T. 15, No 3. S. 5-25. (In Russ). DOI: https://doi.org/10.17816/PED1535-25
8. Mariani M., Parodi A., Minghetti D., Ramenghi L.A., Palmero C., Ugolotti E., Medici C., Saffioti C., Castagnola E. Early and Late Onset Neonatal Sepsis: Epidemiology and Effectiveness of Empirical Antibacterial Therapy in a III Level Neonatal Intensive Care Unit. Antibiotics (Basel). 2022 Feb 21;11(2):284. https://doi.org/10.3390/antibiotics11020284
9. Størdal E.H., Solevåg A.L., Bjørnholt J.V., Rønnestad A., Stensvold H.J. Sepsis treatment options identified by 10-year study of microbial isolates and antibiotic susceptibility in a level-four neonatal intensive care unit. Acta Paediatr. 2022 Mar;111(3):519-526. https://doi.org/10.1111/apa.16189
10. Gostev VV, Sopova YuV, Kalinogorskaya OS, Velizhanina ME, Lazareva IV, Starkova PS, Sidorenko SV. Effect of shock concentrations of vancomycin on the formation of heteroresistance in Staphylococcus aureus. Antibiotiki i himioterapiya. - 2020 - T. 65, № 9-10. - S. 3-7. (In Russ) https://doi.org/10.37489/0235-2990-2020-65-9-10-3-7
11. Huncikova Z., Stensvold H.J., Øymar K.A.A., Vatne A., Lang A.M., Støen R., Brigtsen A.K., Moster D., Eriksen B.H., Selberg T., Rønnestad A., Klingenberg C. Variation in antibiotic consumption in very preterm infants-a 10 year population-based study. J Antimicrob Chemother. 2024 Jan 3;79(1):143-150. https://doi.org/10.1093/jac/dkad358
12. Smith C.A., Bhattacharya M., Toth M., Stewart N.K., Vakulenko S.B. Aminoglycoside resistance profile and structural architecture of the aminoglycoside acetyltransferase AAC(6’)-Im. Microb Cell. 2017 Nov 9;4(12):402- 410. https://doi.org/10.15698/mic2017.12.602
13. Tolkachev BE, Petrov VI, Zayachnikova TE. Therapeutic drug monitoring of vancomycin in newborns: problems and prospects. Lechebnoe delo. - 2021. - № 2. - S. 17- 24. https://doi.org/10.24412/2071-5315-2021-12327
14. Dashtbani-Roozbehani A., Brown M.H. Efflux Pump Mediated Antimicrobial Resistance by Staphylococci in Health-Related Environments: Challenges and the Quest for Inhibition. Antibiotics (Basel). 2021 Dec 7;10(12):1502. https://doi.org/10.3390/antibiotics10121502.
Review
For citations:
Chistyakova G.N., Ustyuzhanin A.V., Ivanova E.S., Remizova I.I. Minimum inhibitory concentrations of antibacterial drugs for Staphylococcus epidermidis strains isolated from the contents of the tracheobronchial tree of newborn children. Bulletin of maternal and child care. 2024;1(3):91-98. (In Russ.) https://doi.org/10.69964/BMCC-2024-1-3-91-98