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      Padrão de sensibilidade de 117 amostras clínicas de Staphylococcus aureus isoladas em 12 hospitais Translated title: In vitro antimicrobial susceptibility of 117 clinical isolates of Staphylococcus aureus from 12 hospitals

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          Abstract

          OBJETIVO. Avaliar o padrão de sensibilidade in vitro de amostras clínicas de Staphylococcus aureus sensíveis (OSSA) e resistentes à oxacilina (ORSA) a outros antimicrobianos que podem ser utilizados no tratamento de infecções estafilocócicas. MATERIAL E MÉTODO. Foram analisadas 117 amostras clínicas de S. aureus isoladas em vários hospitais de São Paulo. Também foram incluídas amostras isoladas em Campinas, SP, e João Pessoa, PB. A avaliação da sensibilidade in vitro aos antimicrobianos foi realizada pela técnica de microdiluição em caldo, utilizando os procedimentos preconizados pelo National Committee for Clinical Laboratory Standards (NCCLS). Foi avaliada a concentração inibitória mínima (MIC) para 24 antimicrobianos da classe dos beta-lactâmicos, fluoroquinolonas, aminoglicosídeos, glicopeptídeos, macrolídeos, lincosaminas e estreptograminas. Foram avaliadas tanto drogas disponíveis comercialmente quanto as que ainda se encontram em fase de pesquisa. A resistência cruzada entre dez fluoroquinolonas foi avaliada em 24 amostras. RESULTADOS. Os glicopeptídeos, o RP-59500 e a mupirocina foram os antimicrobianos que apresentaram maior atividade in vitro contra amostras de ORSA (100% sensibilidade). Oitenta e sete por cento das amostras de OSSA foram sensíveis à ciprofloxacina (MIC50 0,25mig/mL), enquanto que, para os ORSA, a sensibilidade foi de apenas 38% (MIC50 >4mig/mL). A resistência cruzada para as fluoroquinolonas foi observada mesmo para drogas não disponíveis comercialmente. As fluoroquinolonas que permaneceram ativas contra amostras resistentes à ciprofloxacina (clinafloxacina e WIN-57.273) apresentaram MICs 8 a 64 vezes mais elevados que as amostras sensíveis à ciprofloxacina, sugerindo que, quando lançadas na prática clínica, esses MICs possam se elevar ainda mais, inviabilizando o uso clínico desses compostos. CONCLUSÃO. Os resultados do presente estudo mostraram uma alta taxa de resistência a antimicrobianos das amostras de S. aureus nos hospitais do Brasil, restando poucas opções para o tratamento de infecções causadas por ORSA.

          Translated abstract

          OBJECTIVE. To evaluate the antimicrobial susceptibility pattern of oxacillin susceptible (OSSA) and resistant Staphylococcus aureus (ORSA) isolates to other antimicrobial agents that can be used for the treatment of staphylococcal infections. MATERIAL AND METHOD. We evaluated 117 clinical S. aureus isolates from several São Paulo hospitals. Clinical isolates from Campinas, SP and from João Pessoa, PB, were also included. The in vitro susceptibility testing was performed by broth microdilution as described by the National Committee for Clinical Laboratory Standards (NCCLS). The minimum inhibitory concentration (MIC) was evaluated for 24 antimicrobial agents, including beta-lactams, fluoroquinolones, aminoglycosides, glycopeptides, macrolides, lincosamides and streptogramins. Both commercially available and experimental drugs were included in the study. Cross-resistance among fluoroquinolones was evaluated by susceptibility testing 24 isolates to 10 fluoroquinolones. RESULTS. The antimicrobial agents that showed the highest in vitro activity were the glycopeptides, the streptogramin RP-59.500, and the mupirocin (100% susceptibility). Eighty-seven percent of the OSSA and only 38% of the ORSA isolates were susceptible to ciprofloxacin (MIC50 0.25mug/mL and > 4mug/mL, respectively). Cross-resistance among fluoroquinolones were noted even for the experimental drugs. Two fluoroquinolones remained active against ciprofloxacin-resistant isolates, clinafloxacin and WIN-57.273. However, the ciprofloxacin-resistant isolates had MICs eight-to 64-fold higher than the ciprofloxacin-susceptible isolates, suggesting that the MICs may continue to increase when these fluoroquinolones become commercially available. CONCLUSION. Our results showed a high rate of antimicrobial resistance among S. aureus from the Brazilian hospitals. Very few drugs can still be used for the treatment of staphylococcal infections.

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          Most cited references16

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          Emergence of vancomycin resistance in coagulase-negative staphylococci.

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            Methicillin-resistant staphylococci.

            Strains of staphylococci resistant to methicillin were identified immediately after introduction of this drug. Methicillin-resistant strains have unusual properties, the most notable of which is extreme variability in expression of the resistance trait. The conditions associated with this heterogeneous expression of resistance are described. Methicillin resistance is associated with production of a unique penicillin-binding protein (PBP), 2a, which is bound and inactivated only at high concentrations of beta-lactam antibiotics. PBP2a appears to be encoded by the mec determinant, which also is unique to methicillin-resistant strains. The relationships between PBP2a and expression of resistance and implications for the mechanism of resistance are discussed. The heterogeneous expression of methicillin resistance by staphylococci poses problems in the detection of resistant strains. Experience with several susceptibility test methods is reviewed and guidelines for performance of these tests are given. Treatment of infections caused by methicillin-resistant staphylococci is discussed. Vancomycin is the treatment of choice. Alternatives have been few because methicillin-resistant strains often are resistant to multiple antibiotics in addition to beta-lactam antibiotics. New agents which are active against methicillin-resistant staphylococci are becoming available, and their potential role in treatment is discussed.
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              Comparative in vitro activities of new 14-, 15-, and 16-membered macrolides.

              The in vitro activities of several 14-, 15- and 16-membered macrolides were compared with that of erythromycin. In general, 14-membered macrolides such as erythromycin, clarithromycin, and flurithromycin were more active against streptococci and Bordetella pertussis than was the 15-membered macrolide azithromycin, which was more active than 16-membered macrolides such as miocamycin and rokitamycin. Clarithromycin was the most active compound against Streptococcus pyogenes, pneumococci, Listeria monocytogenes, and Corynebacterium species. Legionella pneumophila was most susceptible to miocamycin, clarithromycin, and rokitamycin. Branhamella catarrhalis, Neisseria gonorrhoeae, and Haemophilus influenzae were most susceptible to azithromycin. Azithromycin and dirithromycin were the most active compounds against Campylobacter jejuni. MICs of 16-membered macrolides for strains expressing inducible-type resistance to erythromycin were less than or equal to 1 microgram/ml, whereas none of the compounds had activity against strains expressing constitutive-type resistance. The MICs of roxithromycin, miocamycin, rokitamycin, and josamycin increased in the presence of human serum, whereas MICs of the other compounds either were unchanged or decreased.
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                Author and article information

                Journal
                ramb
                Revista da Associação Médica Brasileira
                Rev. Assoc. Med. Bras.
                Associação Médica Brasileira (São Paulo, SP, Brazil )
                0104-4230
                1806-9282
                September 1997
                : 43
                : 3
                : 199-204
                Affiliations
                [01] São Paulo SP orgnameUniversidade Federal de São Paulo orgdiv1Escola Paulista de Medicina orgdiv2Laboratório Especial de Microbiologia Clínica
                Article
                S0104-42301997000300006 S0104-4230(97)04300306
                090c26df-609f-4532-b2ac-169a1829de1f

                This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

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                Figures: 0, Tables: 0, Equations: 0, References: 16, Pages: 6
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                SciELO Brazil

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                Glicopeptídeos,Resistência a antimicrobianos,Atividade antimicrobiana in vitro,Staphylococcus aureus,Glycopeptides,Fluoroquinolones,Antimicrobial resistance,In vitro antimicrobial activity,Quinolonas

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