medigraphic.com
SPANISH

Revista Latinoamericana de Infectología Pediátrica

ISSN 2683-1678 (Print)
Órgano Oficial de la Sociedad
Latinoamericana de lnfectología Pediátrica.
Órgano de la Asociación Mexicana de
Infectología Pediátrica, A.C.
Órgano difusor de la Sociedad Española
de lnfectología
  • Contents
  • View Archive
  • Information
    • General Information        
    • Directory
  • Publish
    • Instructions for authors        
  • medigraphic.com
    • Home
    • Journals index            
    • Register / Login
  • Mi perfil

2026, Number 1

<< Back Next >>

Rev Latin Infect Pediatr 2026; 39 (1)

Trends in antimicrobial resistance in bloodstream infections due to ESKAPE pathogens in children: a multicenter controlled study from Mexico

Castillo BJI, Rosales-González SP, Larragoity GEA, Abud GM, Ortiz PLF, Romero FR, Pacheco RDO, Chávez RM, Cantú GSP, Baquera AM, Cisneros CM, Vera DJA, Lugo ODL, Mascareñas SAH, Casilla VNG, Sánchez RHM, Rangel SOA, Peña LCD, Almanza CJL
Full text How to cite this article 10.35366/123453

DOI

DOI: 10.35366/123453
URL: https://dx.doi.org/10.35366/123453

Language: Spanish
References: 28
Page: 17-26
PDF size: 797.81 Kb.


Key words:

antimicrobial resistance, ESKAPE pathogens, pediatrics.

ABSTRACT

Introduction: bloodstream infections are among the most common life-threatening infections in hospitalized children. The ESKAPE pathogens are a group of bacteria with the ability to evade the bactericidal activity of antimicrobials. These pathogens possess multiple resistance mechanisms which have been associated with high mortality rates and increased hospitalization costs. Objective: analyze trends in antimicrobial resistance in bloodstream infections caused by ESKAPE pathogens in children. Material and methods: a multicentric study conducted in nine Mexican hospitals from 2020 to 2024 included all positive blood cultures from children ≤ 18 years old with ESKAPE microorganisms after 72 hours of hospitalization, excluding polymicrobial infections and duplicates. Antimicrobial susceptibility was tested using the MicroSCAN Walkaway system, with Minimum Inhibitory Concentrations (MICs) interpreted according to updated Clinical and Laboratory Standards Institute (CLSI) criteria. A Pearson χ2 Test (p ≤ 0.05) assessed annual differences in proportions of Pseudomonas aeruginosa difficult-to-treat (DTR), Staphylococcus aureus methicillin resistance (MRSA), carbapenem-resistant Acinetobacter baumannii, Vancomycin-resistance Enterococcus faecium (VRE), ceftriaxone resistant Klebsiella pneumoniae and E. coli. Results: we identified 4053 cases of bacteremia. Vancomycin-resistant E. faecium accounted for 41.1%, Staphylococcus aureus methicillin resistance comprises 30.9%. Pooled carbapenem-resistance in A. baumannii and P. aeruginosa was 28.8% and 23% respectively. High ceftriaxone resistance was observed in K. pneumoniae (61.9%), E. coli (56.3%), and E. cloacae (28.4%). No significant differences were found. Conclusions: high antimicrobial resistance was documented in all ESKAPE pathogens, with increasing trends throughout the years. Further studies are needed to fully elucidate the problem and track resistance patterns, highlighting the urgent need for action.


REFERENCES

  1. Larru B, Gong W, Vendetti N, Sullivan KV, Localio R, Zaoutis TE et al. Bloodstream infections in hospitalized children: epidemiology and antimicrobial susceptibilities. Pediatr Infect Dis J. 2016; 35 (5): 507-510. doi: 10.1097/INF.0000000000001057.

  2. Christaki E, Marcou M, Tofarides A. Antimicrobial resistance in bacteria: mechanisms, evolution, and persistence. J Mol Evol. 2020; 88 (1): 26-40. doi: 10.1007/s00239-019-09914-3.

  3. Holmes AH, Moore LS, Sundsfjord A, Steinbakk M, Regmi S, Karkey A et al. Understanding the mechanisms and drivers of antimicrobial resistance. Lancet. 2016; 387 (10014): 176-187. doi: 10.1016/S0140-6736(15)00473-0.

  4. Garza-González E, Morfín-Otero R, Mendoza-Olazarán S, Bocanegra-Ibarias P, Flores-Treviño S, Rodríguez-Noriega E et al. A snapshot of antimicrobial resistance in Mexico. Results from 47 centers from 20 states during a six-month period. PLoS One. 2019; 14 (3): e0209865. doi: 10.1371/journal.pone.0209865.

  5. Dharmapalan D, Shet A, Yewale V, Sharland M. High reported rates of antimicrobial resistance in indian neonatal and pediatric blood stream infections. J Pediatr Infect Dis Soc. 2017; 6 (3): e62-e68. doi: 10.1093/jpids/piw092.

  6. Wattal C, Goel N. Pediatric blood cultures and antibiotic resistance: an overview. Indian J Pediatr. 2020; 87 (2): 125-131. doi: 10.1007/s12098-019-03123-y.

  7. Cantón R, Novais A, Valverde A, Machado E, Peixe L, Baquero F et al. Prevalence and spread of extended-spectrum beta-lactamase-producing Enterobacteriaceae in Europe. Clin Microbiol Infect. 2008; 14 Suppl 1: 144-153. doi: 10.1111/j.1469-0691.2007.01850.x.

  8. Antimicrobial resistance surveillance in Europe 2023 - 2021 data. European Centre for Disease Prevention and Control. 2023. Disponible en: https://www.ecdc.europa.eu/en/publications-data/antimicrobial-resistance-surveillance-europe-2023-2021-data

  9. Benko R, Gajdács M, Matuz M, Bodó G, Lázár A, Hajdú E et al. Prevalence and antibiotic resistance of ESKAPE pathogens isolated in the emergency department of a tertiary care teaching hospital in Hungary: a 5-year retrospective survey. Antibiotics (Basel). 2020; 9 (9): 624. doi: 10.3390/antibiotics9090624.

  10. Wesevich A, Sutton G, Ruffin F, Park LP, Fouts DE, Fowler VG Jr et al. Newly named Klebsiella aerogenes (formerly Enterobacter aerogenes) is associated with poor clinical outcomes relative to other Enterobacter species in patients with bloodstream infection. J Clin Microbiol. 2020; 58 (9): e00582-20. doi: 10.1128/JCM.00582-20.

  11. Zhang Y, Wang Q, Yin Y, Chen H, Jin L, Gu B et al. Epidemiology of carbapenem-resistant Enterobacteriaceae infections: report from the China CRE network. Antimicrob Agents Chemother. 2018; 62: e01882-17. doi: 10.1128/aac.01882-17.

  12. Girlich D, Ouzani S, Emeraud C, Gauthier L, Bonnin RA, Le Sache N et al. Uncovering the novel Enterobacter cloacae complex species responsible for septic shock deaths in newborns: a cohort study. Lancet Microbe. 2021; 2 (10): e536-e544. doi: 10.1016/S2666-5247(21)00098-7.

  13. Vostal AC, Grance M, Chukwuma U, Morales C, Lanteri C, Telu K et al. Epidemiology of patients with ESKAPE pathogen bloodstream infection in the US Military Health System. Open Forum Infect Dis. 2020; 7 (Suppl 1): S492. doi: 10.1093/ofid/ofaa439.

  14. Shariati A, Dadashi M, Moghadam MT, van Belkum A, Yaslianifard S, Darban-Sarokhalil D. Global prevalence and distribution of vancomycin resistant, vancomycin intermediate and heterogeneously vancomycin intermediate Staphylococcus aureus clinical isolates: a systematic review and meta-analysis. Sci Rep. 2020; 10 (1): 12689. doi: 10.1038/s41598-020-69058-z.

  15. Haas K, Meyer-Buehn M, von Both U, Hübner J, Schober T. Decrease in vancomycin MICs and prevalence of hGISA in MRSA and MSSA isolates from a German pediatric tertiary care center. Infection. 2023; 51 (3): 583-588. doi: 10.1007/s15010-023-02036-5.

  16. Wang G, Hindler JF, Ward KW, Bruckner DA. Increased vancomycin MICs for Staphylococcus aureus clinical isolates from a university hospital during a 5-year period. J Clin Microbiol. 2006; 44 (11): 3883-3886. doi: 10.1128/JCM.01388-06.

  17. Tamma PD, Robinson GL, Gerber JS, Newland JG, DeLisle CM, Zaoutis TE et al. Pediatric antimicrobial susceptibility trends across the United States. Infect Control Hosp Epidemiol. 2013; 34 (12): 1244-1251. doi: 10.1086/673974.

  18. Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2012; 18 (3): 268-281. doi: 10.1111/j.1469-0691.2011.03570.x.

  19. Cosentino F, Viale P, Giannella M. MDR/XDR/PDR or DTR? Which definition best fits the resistance profile of Pseudomonas aeruginosa? Curr Opin Infect Dis. 2023; 36 (6): 564-571. doi: 10.1097/QCO.0000000000000966.

  20. Kadri SS, Adjemian J, Lai YL, Spaulding AB, Ricotta E, Prevots DR et al. Difficult-to-treat resistance in gram-negative bacteremia at 173 US hospitals: retrospective cohort analysis of prevalence, predictors, and outcome of resistance to all first-line agents. Clin Infect Dis. 2018; 67 (12): 1803-1814. doi: 10.1093/cid/ciy378.

  21. Huh K, Chung DR, Ha YE, Ko JH, Kim SH, Kim MJ et al. Impact of difficult-to-treat resistance in gram-negative bacteremia on mortality: retrospective analysis of nationwide surveillance data. Clin Infect Dis. 2020; 71 (9): e487-e496. doi: 10.1093/cid/ciaa084.

  22. Yang Q, Kamat S, Mohamed N, Valdez RR, Lin S, Su M et al. Antimicrobial susceptibility among gram-negative isolates in pediatric patients in Latin America, Africa-Middle East, and Asia from 2016-2020 compared to 2011-2015: results from the ATLAS surveillance study. J Pediatr Infect Dis Soc. 2023; 12 (8): 459-470. doi: 10.1093/jpids/piad055.

  23. Antimicrobial resistance in the EU/EEA (EARS-Net) - Annual epidemiological report for 2022. European Centre for Disease Prevention and Control. 2023. Disponible en: https://www.ecdc.europa.eu/en/publications-data/surveillance-antimicrobial-resistance-europe-2022

  24. Konca C, Capan H, Geyik M. Susceptibility patterns of multidrug-resistant Acinetobacter baumannii. Indian J Pediatr. 2021; 88 (2): 120-126. doi: 10.1007/s12098-020-03346-4.

  25. Logan LK, Gandra S, Trett A, Weinstein RA, Laxminarayan R. Acinetobacter baumannii resistance trends in children in the United States, 1999-2012. J Pediatr Infect Dis Soc. 2019; 8 (2): 136-142. doi: 10.1093/jpids/piy018.

  26. Cerezales M, Ocampo-Sosa AA, Álvarez-Montes L, Díaz-Ríos C, Bustamante Z, Santos J et al. High prevalence of extensively drug-resistant Acinetobacter baumannii at a children hospital in Bolivia. Pediatr Infect Dis J. 2018; 37 (11): 1118-1123. doi: 10.1097/INF.0000000000001962.

  27. Morfín-Otero R, Alcántar-Curiel MD, Rocha MJ, Alpuche-Aranda CM, Santos-Preciado JI, Gayosso-Vázquez C et al. Acinetobacter baumannii infections in a tertiary care hospital in Mexico over the past 13 years. Chemotherapy. 2013; 59 (1): 57-65. doi: 10.1159/000351098.

  28. Castillo-Bejarano JI, Llaca-Díaz J, E la O-Cavazos ME, Sánchez-Alanís H, Mascareñas-de Los Santos AH, Espinosa-Villaseñor F et al. Carbapenem-resistant Acinetobacter baumannii infection in children from a third-level hospital in Mexico: clinical characteristics and molecular epidemiology. J Pediatric Infect Dis Soc. 2023; 12 (7): 431-435. doi: 10.1093/jpids/piad046.




Table 1
Table 2
Table 3
Table 4
Table 5
Table 6
Table 7
CC BY-NC-ND

2020     |     www.medigraphic.com

Mi perfil

C?MO CITAR (Vancouver)

Rev Latin Infect Pediatr. 2026;39