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Tolerability of High Doses of Daptomycin in the Treatment of Prosthetic Vascular Graft Infection: A Retrospective Study.
Legout, Laurence; D'Elia, Piervito; Sarraz-Bournet, Beatrice; Ettahar, Nicolas; Haulon, Stephan; Leroy, Olivier; Senneville, Eric.
Afiliação
  • Legout L; Infectious Diseases Department, Dron Hospital, Tourcoing, France. laurence.legout@free.fr.
  • D'Elia P; Department of Vascular Surgery, Dron Hospital of Tourcoing, Tourcoing, France.
  • Sarraz-Bournet B; Department of Vascular Surgery, University Hospital of Lille, Lille, France.
  • Ettahar N; Department of Vascular Surgery, Dron Hospital of Tourcoing, Tourcoing, France.
  • Haulon S; Infectious Diseases Department, Dron Hospital, Tourcoing, France.
  • Leroy O; Department of Vascular Surgery, University Hospital of Lille, Lille, France.
  • Senneville E; Intensive Care and Infectious Diseases Unit, Dron Hospital of Tourcoing, Tourcoing, France.
Infect Dis Ther ; 3(2): 215-23, 2014 Dec.
Article em En | MEDLINE | ID: mdl-25186318
INTRODUCTION: In treatment of prosthetic vascular graft infection (PVGI), appropriate antimicrobial treatment is crucial for controlling the septic process and preventing re-infection of the new graft. Glycopeptides are the mainstay of treatment for device-related infections by methicillin-resistant Staphylococcus aureus strains, but with some limitations, especially concerning vancomycin-intermediate and glycopeptide-intermediate S. aureus. We report our experience using a high dose of daptomycin (DAP) for treatment of PVGI. METHODS: We reviewed medical reports of 26 patients treated with high doses of DAP (>8 mg/kg) and beta-lactams/aminosides for PVGI, defined as positive bacterial culture of intraoperative specimens or blood samples and/or clinical, biological, and radiological signs of infection. Clinical success was defined by resolution of all clinical signs at the end of follow-up, without the need for additional antibiotic therapy, and/or negative culture in case of new surgery. RESULTS: Cultures of intraoperative samples were positive in 21 patients (80.8%). Blood and intraoperative cultures were concomitantly positive in 10 patients. The main microorganism identified in microbiological samples was S. aureus (n = 18). Surgery was performed in 23 patients (88.4%). The mean duration of the DAP regimen was 12.3 ± 11.9 days. DAP was discontinued in 26 patients [need to switch to microbiological results (n = 19), bacterial pneumonia (n = 2), and increased creatine phosphokinase levels (n = 4)]. One patient had myalgia, while 9 received concomitant statins. CONCLUSION: High-dose DAP therapy shows a satisfactory toxicity profile even in severely ill patients with multiple comorbidities, and may favorably compete with vancomycin, especially concerning the risk of induced nephrotoxicity.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2014 Tipo de documento: Article