Effectiveness of vancomycin plus cloxacillin compared with vancomycin, cloxacillin and daptomycin single therapies in the treatment of methicillin-resistant and methicillin-susceptible Staphylococcus aureus in a rabbit model of experimental endocarditis

Ximena Castañeda, Cristina García-De-La-Mària, Oriol Gasch, Juan M. Pericàs, Dolors Soy, Maria Alejandra Cañas-Pacheco, Carlos Falces, Javier García-González, Marta Hernández-Meneses, Bàrbara Vidal, Manel Almela, Eduard Quintana, José M. Tolosana, David Fuster, Jaume Llopis, Anders Dahl, Asuncion Moreno, Francesc Marco, Jose M. Miró, Jose M. MiróMarta Hernández-Meneses, Juan Ambrosioni, Anders Dahl, Adrian Téllez, Juan M. Pericàs, Asuncion Moreno, Cristina García De La Mària, Maria Alexandra Cañas, Javier García-González, Manel Almela, Climent Casals, Francisco Javier Morales, Francesc Marco, Jordi Vila, Eduard Quintana, Elena Sandoval, Juan C. Paré, Carlos Falces, Daniel Pereda, Ramon Cartañá, Salvador Ninot, Manel Azqueta, Marta Sitges, Barbara Vidal, Rut Andrea, José L. Pomar, Manuel Castella, José M. Tolosana, José Ortiz, Guillermina Fita, Irene Rovira, Andrés Perissinotti, David Fuster, Jose Ramírez, Dolors Soy, Pedro Castro, Jaume Llopis

9 Citationer (Scopus)

Abstract

Objectives: To investigate if the addition of cloxacillin to vancomycin enhances the activity of both monotherapies for treating MSSA and MRSA experimental endocarditis (EE) in rabbits. Methods: Vancomycin plus cloxacillin was compared with the respective monotherapies and daptomycin. In vitro time-kill studies were performed using standard (105 cfu) and high (108 cfu) inocula of five MRSA, one glycopeptide-intermediate (GISA) and five MSSA strains. One MSSA (MSSA-678) and one MRSA (MRSA-277) strain were selected to be used in the in vivo model. A human-like pharmacokinetics model was applied and the equivalents of cloxacillin 2 g/4 h IV and daptomycin 6 mg/kg/day IV were administered. To optimize vancomycin activity, dosage was adjusted to achieve an AUC/MIC ≥400. Results: Daptomycin sterilized significantly more vegetations than cloxacillin (13/13, 100% versus 9/15, 60%; P=0.02) and showed a trend of better activity than vancomycin (10/14, 71%; P=0.09) and vancomycin plus cloxacillin (10/14, 71%; P=0.09) against MSSA-678. Addition of cloxacillin to vancomycin (13/15, 87%) was significantly more effective than vancomycin (8/16, 50%; P=0.05) and showed similar activity to daptomycin (13/18, 72%; P=0.6) against MRSA-277. In all treatment arms, the bacterial isolates recovered from vegetations were re-tested and showed the same daptomycin susceptibility as the original strains. Conclusions: Vancomycin plus cloxacillin proved synergistic and bactericidal activity against MRSA. Daptomycin was the most efficacious option against MSSA and similar to vancomycin plus cloxacillin against MRSA. In settings with high MRSA prevalence, vancomycin plus cloxacillin might be a good alternative for empirical therapy of S. aureus IE.

OriginalsprogEngelsk
TidsskriftJournal of Antimicrobial Chemotherapy
Vol/bind76
Udgave nummer6
Sider (fra-til)1539-1546
Antal sider8
ISSN0305-7453
DOI
StatusUdgivet - 1 jun. 2021

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