2017, Number 3
Carbapenemase-producing Klebsiella in pediatrics: literature review
Language: Spanish
References: 11
Page: 107-115
PDF size: 284.55 Kb.
ABSTRACT
The widespread use of carbapenemics for the treatment of Klebsiella spp. infections has resulted in the appearance of carbapenemase-producing strains, which has resulted in increased mortality due to enterobacterial infection. The carbapenemase resistance pattern ranges from 24 to 70%, depending on the revised series. Carbapenemase-producing bacteria often have plasmidic genes that confer resistance to sulfonamides and aminoglycosides, as well as a high level of resistance to quinolones mediated by alteration at the binding site, which makes them multidrug-resistant bacteria, making it difficult to treat. The problem of antibiotic resistance to carbapenems is worrying, considering that we do not have a large therapeutic arsenal, which is why it has been necessary to reuse antibiotics that had previously been out of the market such as colistin, use pharmacodynamic properties of the carbapenems and to use them in high doses and extended infusions and to use therapies combined with tigecycline, fosfomycin, quinolones or aminoglycosides; thus exposing patients to great toxicity. Most reports of carbapenemase-producing entorobacteria are from adult infections. In this work, antibiotic resistance of enterobacterial infections in children, is described.REFERENCES
Esparza G, Ariza B, Bedoya AM, Bustos I, Castañeda-Ramírez CR, De la Cadena E et al. Estrategias para la implementación y reporte de los puntos de corte CLSI vigentes y pruebas fenotípicas confirmatorias para BLEE y carbapenemasas en bacilos Gram negativos en laboratorios clínicos de Colombia. Infectio. 2013; 17 (2): 80-89.
Rodríguez-Baño J, Cisneros JM, Cobos-Trigueros N, Fresco G, Navarro-San Francisco C, Gudiol C et al. Diagnosis and antimicrobial treatment of invasive infections due to multidrug-resistant Enterobacteriaceae. Guidelines of the Spanish Society of Infectious Diseases and Clinical Microbiology. Enferm Infecc Microbiol Clin. 2015; 33 (5): 337.e1-337.e21.