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P097: Antimicrobial usage in the treatment of patients with bloodstream infection
© Paula et al; licensee BioMed Central Ltd. 2013
Published: 20 June 2013
Although indiscriminate use of broad-spectrum antibiotics is related to the occurrence of bacterial resistance, there is an abusive use of such drugs.
To determine the antimicrobial usage in the treatment of patients with bloodstream infection (BSI) caused by methicillin-resistant and susceptible Staphylococcus aureus (MRSA and MSSA, respectively).
Retrospective cohort study performed in an Intensive Care Unit of a large hospital in Belo Horizonte. The population is comprised of patients diagnosed with Staphylococcus aureus BSI from 2007 to 2011. Data were obtained through patients’ medical records and Hospital Infection Control Committee. Therapy were categorized in: empirical treatment (before the culture test result) or directed (according to the BSI causing agent). Descriptive and univariate analysis were performed (using chi-square test or a Fisher's exact test). The hospital’s Ethics Committee approved the project.
62 patients were included, 31 in each group (MRSA and MSSA). The most common antibiotics prescribed for empirical treatment were vancomycin (69.4%), polymyxin B (46.8%), ertapenem (29.0%), meropenem (24.2%) and cefepime (3.2%). There was no significant difference between the groups analyzed and the class of antimicrobials empirically prescribed (p>0.05). For directed treatment, the antibiotics prescribed were vancomycin (45.2%) and methicillin (40.3%). On one hand, MRSA group used significantly more vancomycin (p=0,000). On the other hand, MSSA patients used more methicillin after the culture result (p=0,000).
A large use of broad-spectrum antibiotics in empirical treatments was observed, given the hospital’s microbiological profile and the need to initiate appropriate treatment during the first 24 hours. However, the treatment targeting favored a rational use of antibiotics, reducing the action spectrum after culture results.
Disclosure of interest
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.