4.7 Article

Daptomycin Plus Fosfomycin Versus Daptomycin Alone for Methicillin-resistant Staphylococcus aureus Bacteremia and Endocarditis: A Randomized Clinical Trial

Journal

CLINICAL INFECTIOUS DISEASES
Volume 72, Issue 9, Pages 1517-1525

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciaa1081

Keywords

MRSA; bacteremia; daptomycin; fosfomycin; clinical trial

Funding

  1. Spanish Ministry of Science, Innovation and Universities [PI12/01907]
  2. Spanish Network for Research in Infectious Diseases [RD16/0016/0005]
  3. Instituto de Salud Carlos III (ISCIII)
  4. Spanish Ministry of Economy, Industry and Competitiveness
  5. European Development Regional Fund A way to achieve Europe, Operational Programme Intelligent Growth 2014-2020
  6. Spanish Clinical Research Network (SCReN)
  7. Plan Nacional de I+D and ISCIII, Subdireccion General de Evaluacion y Fomento de la Investigacion [PT13/0002/0007]
  8. Grupo de Estudio de la Infeccion Relacionada con la Asistencia Sanitaria
  9. Institut d'Investigacions Biomediques Agust Pi i Sunyer, Barcelona, Spain

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The study found that daptomycin plus fosfomycin provided a slightly higher treatment success rate for MRSA bacteremia and endocarditis compared to daptomycin alone, but this difference was not statistically significant. The antibiotic combination was associated with lower rates of microbiological failure and complicated bacteremia, but was also more frequently linked to adverse events.
Background. We aimed to determine whether daptomycin plus fosfomycin provides higher treatment success than daptomycin alone for methicillin-resistant Staphylococcus aureus (MRSA) bacteremia and endocarditis. Methods. A randomized (1:1) phase 3 superiority, open-label, and parallel group clinical trial of adult inpatients with MRSA bacteremia was conducted at 18 Spanish hospitals. Patients were randomly assigned to receive either 10 mg/kg of daptomycin intravenously daily plus 2 g of fosfomycin intravenously every 6 hours, or 10 mg/kg of daptomycin intravenously daily. Primary endpoint was treatment success 6 weeks after the end of therapy. Results. Of 167 patients randomized, 155 completed the trial and were assessed for the primary endpoint. Treatment success at 6 weeks after the end of therapy was achieved in 40 of 74 patients who received daptomycin plus fosfomycin and in 34 of 81 patients who were given daptomycin alone (54.1% vs 42.0%; relative risk, 1.29 [95% confidence interval, .93-1.8]; P = .135). At 6 weeks, daptomycin plus fosfomycin was associated with lower microbiologic failure (0 vs 9 patients; P = .003) and lower complicated bacteremia (16.2% vs 32.1%; P = .022). Adverse events leading to treatment discontinuation occurred in 13 of 74 patients (17.6%) receiving daptomycin plus fosfomycin, and in 4 of 81 patients (4.9%) receiving daptomycin alone (P = .018). Conclusions. Daptomycin plus fosfomycin provided 12% higher rate of treatment success than daptomycin alone, but this difference did not reach statistical significance. This antibiotic combination prevented microbiological failure and complicated bacteremia, but it was more often associated with adverse events.

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