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Ceftaroline activity tested against contemporary Latin American bacterial pathogens (2011)

A total of 2484 target bacterial pathogens were collected (one per patient episode) from patients in 16 Latin American medical centers located in seven nations during 2011. Isolate identity was confirmed at a coordinating laboratory and susceptibility testing was performed for ceftaroline and compar...

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Autores principales: Flamm, Robert K., Sader, Helio S., Jones, Ronald N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427512/
https://www.ncbi.nlm.nih.gov/pubmed/24513484
http://dx.doi.org/10.1016/j.bjid.2013.11.005
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author Flamm, Robert K.
Sader, Helio S.
Jones, Ronald N.
author_facet Flamm, Robert K.
Sader, Helio S.
Jones, Ronald N.
author_sort Flamm, Robert K.
collection PubMed
description A total of 2484 target bacterial pathogens were collected (one per patient episode) from patients in 16 Latin American medical centers located in seven nations during 2011. Isolate identity was confirmed at a coordinating laboratory and susceptibility testing was performed for ceftaroline and comparator agents according to reference broth microdilution methods. A total of 30.0% of isolates were from respiratory tract, 29.4% from skin and skin structure, 21.4% from blood stream, 7.9% from urinary tract and 11.3% from other sites. Ceftaroline was active against Staphylococcus aureus (42.8% MRSA) with 83.6% of the isolates at ≤1 mg/L and all isolates at ≤2 mg/L (MIC(5090), 0.25/2 mg/L). National MRSA rates ranged from a low of 28.8% in Colombia to a high of 68.1% in Chile. All Streptococcus pyogenes and Streptococcus agalactiae were susceptible to ceftaroline (MIC(50/90) values were at ≤0.015/≤0.015 mg/L for both). All Streptococcus pneumoniae were susceptible to ceftaroline, linezolid, tigecycline and vancomycin. Susceptibility to ceftriaxone was at 88.4% (CLSI non-meningitis interpretive criteria) and 73.9% (CLSI meningitis interpretive criteria) for all S. pneumoniae. Ceftriaxone susceptibility was only at 33.3% (CLSI non-meningitis interpretive criteria) and 0.0% (CLSI meningitis interpretive criteria) for penicillin-intermediate (penicillin MIC, 4 mg/L) strains. All Haemophilus influenzae (29.4% β-lactamase-positive) isolates were susceptible to ceftaroline, amoxicillin–clavulanate, ceftriaxone, and levofloxacin. For the Latin American region, the ESBL-phenotype rate was 37.6% for Escherichia coli and 53.3% for Klebsiella pneumoniae. Ceftaroline was not active against ESBL-phenotype strains but was active against >90.0% of the non-ESBL-phenotype. The spectrum of activity of ceftaroline against pathogens from Latin America indicates that it merits further study for its potential use in the Latin American region.
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spelling pubmed-94275122022-09-01 Ceftaroline activity tested against contemporary Latin American bacterial pathogens (2011) Flamm, Robert K. Sader, Helio S. Jones, Ronald N. Braz J Infect Dis Original Article A total of 2484 target bacterial pathogens were collected (one per patient episode) from patients in 16 Latin American medical centers located in seven nations during 2011. Isolate identity was confirmed at a coordinating laboratory and susceptibility testing was performed for ceftaroline and comparator agents according to reference broth microdilution methods. A total of 30.0% of isolates were from respiratory tract, 29.4% from skin and skin structure, 21.4% from blood stream, 7.9% from urinary tract and 11.3% from other sites. Ceftaroline was active against Staphylococcus aureus (42.8% MRSA) with 83.6% of the isolates at ≤1 mg/L and all isolates at ≤2 mg/L (MIC(5090), 0.25/2 mg/L). National MRSA rates ranged from a low of 28.8% in Colombia to a high of 68.1% in Chile. All Streptococcus pyogenes and Streptococcus agalactiae were susceptible to ceftaroline (MIC(50/90) values were at ≤0.015/≤0.015 mg/L for both). All Streptococcus pneumoniae were susceptible to ceftaroline, linezolid, tigecycline and vancomycin. Susceptibility to ceftriaxone was at 88.4% (CLSI non-meningitis interpretive criteria) and 73.9% (CLSI meningitis interpretive criteria) for all S. pneumoniae. Ceftriaxone susceptibility was only at 33.3% (CLSI non-meningitis interpretive criteria) and 0.0% (CLSI meningitis interpretive criteria) for penicillin-intermediate (penicillin MIC, 4 mg/L) strains. All Haemophilus influenzae (29.4% β-lactamase-positive) isolates were susceptible to ceftaroline, amoxicillin–clavulanate, ceftriaxone, and levofloxacin. For the Latin American region, the ESBL-phenotype rate was 37.6% for Escherichia coli and 53.3% for Klebsiella pneumoniae. Ceftaroline was not active against ESBL-phenotype strains but was active against >90.0% of the non-ESBL-phenotype. The spectrum of activity of ceftaroline against pathogens from Latin America indicates that it merits further study for its potential use in the Latin American region. Elsevier 2014-02-07 /pmc/articles/PMC9427512/ /pubmed/24513484 http://dx.doi.org/10.1016/j.bjid.2013.11.005 Text en ©. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Flamm, Robert K.
Sader, Helio S.
Jones, Ronald N.
Ceftaroline activity tested against contemporary Latin American bacterial pathogens (2011)
title Ceftaroline activity tested against contemporary Latin American bacterial pathogens (2011)
title_full Ceftaroline activity tested against contemporary Latin American bacterial pathogens (2011)
title_fullStr Ceftaroline activity tested against contemporary Latin American bacterial pathogens (2011)
title_full_unstemmed Ceftaroline activity tested against contemporary Latin American bacterial pathogens (2011)
title_short Ceftaroline activity tested against contemporary Latin American bacterial pathogens (2011)
title_sort ceftaroline activity tested against contemporary latin american bacterial pathogens (2011)
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427512/
https://www.ncbi.nlm.nih.gov/pubmed/24513484
http://dx.doi.org/10.1016/j.bjid.2013.11.005
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