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1.
J Antimicrob Chemother ; 75(6): 1623-1630, 2020 06 01.
Artigo em Inglês | MEDLINE | ID: mdl-32097475

RESUMO

BACKGROUND: Preoperative decolonization is recommended in Staphylococcus aureus nasal carriers scheduled for cardiac surgery. We aimed to evaluate the effectiveness of and compliance with mupirocin use in nasal S. aureus carriers in a real-life setting. METHODS: Prospective study including consecutive patients scheduled for cardiac surgery screened for S. aureus nasal carriage at preoperative consultation. Carriers were prescribed mupirocin nasal ointment, chlorhexidine shower and mouthwash. Effectiveness of decolonization was evaluated with a postoperative nasal sample. Compliance was evaluated objectively by determination of nasal mupirocin concentration using UPLC-MS/MS and self-reported by questionnaire. RESULTS: Over 10 months, 361 patients were included, 286 had preoperative screening, 75 (26.2%) were S. aureus nasal carriers and 19 of them (25.3%) failed to be effectively decolonized. No resistance to mupirocin was documented. Preoperative and postoperative strains were identical in all cases. Declared good compliance was associated with decolonization success (OR = 24; 95% CI 4-143, P < 0.0001). Mupirocin detection was significantly associated with the level of compliance. Mupirocin was detected in 52.2% (24/46) of patients effectively decolonized and in 12.5% (2/16) of patients with decolonization failure (P < 0.01). In 2/19 patients, failure of decolonization was not associated with a compliance issue. Postoperative carriage was associated with an increased risk of S. aureus infection (OR = 9.8; 95% CI 1.8-53, P < 0.01). CONCLUSIONS: In real life, decolonization is not always effective, hence there is a persisting risk of S. aureus endogenous infection. Mupirocin concentration measurement may help to understand compliance issues and failures in decolonization.


Assuntos
Mupirocina , Infecções Estafilocócicas , Administração Intranasal , Antibacterianos/uso terapêutico , Portador Sadio/tratamento farmacológico , Clorexidina/uso terapêutico , Cromatografia Líquida de Alta Pressão , Cromatografia Líquida , Humanos , Mupirocina/uso terapêutico , Pomadas/uso terapêutico , Estudos Prospectivos , Infecções Estafilocócicas/tratamento farmacológico , Staphylococcus aureus , Infecção da Ferida Cirúrgica/tratamento farmacológico , Espectrometria de Massas em Tandem
2.
Antimicrob Agents Chemother ; 58(2): 1231-4, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24295978

RESUMO

The emergence of carbapenemase-producing bacteria poses a new challenge in the management of antibiotic therapies for patients. This report describes a new method using ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) for rapid detection of carbapenemase activity in enterobacteria, Pseudomonas aeruginosa, and Acinetobacter baumannii. In a panel of 78 isolates, including 41 carbapenemase-producing strains, the ULPC-MS/MS assay showed 100% agreement with molecular characterization, whereas six carbapenemase-producing isolates were not detected by the modified Hodge test.


Assuntos
Acinetobacter baumannii/isolamento & purificação , Antibacterianos/metabolismo , Proteínas de Bactérias/metabolismo , Infecções por Bactérias Gram-Negativas/microbiologia , Pseudomonas aeruginosa/isolamento & purificação , beta-Lactamases/metabolismo , beta-Lactamas/metabolismo , Acinetobacter baumannii/efeitos dos fármacos , Acinetobacter baumannii/enzimologia , Acinetobacter baumannii/genética , Antibacterianos/farmacologia , Proteínas de Bactérias/classificação , Proteínas de Bactérias/genética , Cromatografia Líquida de Alta Pressão/métodos , Ensaios Enzimáticos , Expressão Gênica , Infecções por Bactérias Gram-Negativas/tratamento farmacológico , Humanos , Testes de Sensibilidade Microbiana , Plasmídeos , Pseudomonas aeruginosa/efeitos dos fármacos , Pseudomonas aeruginosa/enzimologia , Pseudomonas aeruginosa/genética , Espectrometria de Massas em Tandem , Resistência beta-Lactâmica/genética , beta-Lactamases/classificação , beta-Lactamases/genética , beta-Lactamas/farmacologia
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