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Frequency of pharmacological target attainment with flucloxacillin and cefazolin in invasive methicillin-susceptible Staphylococcus aureus infection: a prospective cohort study in hospitalized patients.
Campbell, Patrick O; Chin, Paul K L; Dalton, Simon C; Metcalf, Sarah C L; Douglas, Nicholas M; Chambers, Stephen T.
Afiliación
  • Campbell PO; Department of Infectious Diseases, Christchurch Hospital, Canterbury District Health Board, Christchurch, New Zealand. Electronic address: Patrick.campbell@cdhb.health.nz.
  • Chin PKL; Department of Clinical Pharmacology, Christchurch Hospital, Christchurch, New Zealand.
  • Dalton SC; Department of Infectious Diseases, Christchurch Hospital, Canterbury District Health Board, Christchurch, New Zealand.
  • Metcalf SCL; Department of Infectious Diseases, Christchurch Hospital, Canterbury District Health Board, Christchurch, New Zealand.
  • Douglas NM; Department of Infectious Diseases, Christchurch Hospital, Canterbury District Health Board, Christchurch, New Zealand; Department of Medicine, University of Otago, Christchurch, New Zealand; Division of Global and Tropical Health, Menzies School of Health Research, Charles Darwin University, Darwin,
  • Chambers ST; Department of Pathology, University of Otago, Christchurch, New Zealand.
Int J Antimicrob Agents ; 61(1): 106695, 2023 Jan.
Article en En | MEDLINE | ID: mdl-36464153
BACKGROUND: The proportion of patients with invasive methicillin-susceptible Staphylococcus aureus (MSSA) infection who achieve target concentrations of flucloxacillin or cefazolin with standard dosing regimens is uncertain. This study measured drug concentrations in a prospective cohort of patients with invasive S. aureus infections to determine the frequency of target concentration attainment, and risk factors for failure to achieve target concentrations. PATIENTS AND METHODS: Unbound flucloxacillin and cefazolin plasma concentrations were measured at the midpoint between intravenous doses. Adequate and optimal targets were defined as an unbound plasma concentration of ≥1 and ≥2 times the minimum inhibitory concentration (MIC) (flucloxacillin 0.5 mg/L, cefazolin 2 mg/L), respectively (50%fT≥1MIC, 50%fT≥2MIC). RESULTS: There were 50 patients in each of the flucloxacillin and cefazolin groups. Eighty-five (85%) patients met the target of 50%fT≥2MIC and 95 (95%) patients met the target of 50%fT≥1MIC. The median unbound flucloxacillin concentration was 2.6 mg/L [interquartile range (IQR) 1.0-8.1]. The median unbound cefazolin concentration was 15.4 mg/L (IQR 8.8-28.2). A higher proportion of patients in the flucloxacillin group failed to achieve the optimal target compared with the cefazolin group [13 (26%) vs 2 (4%); P=0.002]. Younger age and higher creatinine clearance were associated with lower plasma concentrations. CONCLUSIONS: Standard dosing of flucloxacillin and cefazolin in the treatment of invasive MSSA infections may not achieve target plasma concentrations for a subgroup of patients. Measuring drug concentrations identifies this subgroup and facilitates dose individualization.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones Estafilocócicas / Cefazolina Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Int J Antimicrob Agents Año: 2023 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones Estafilocócicas / Cefazolina Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Int J Antimicrob Agents Año: 2023 Tipo del documento: Article Pais de publicación: Países Bajos