%0 Journal Article %9 ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES %A Ameen, S. M. %A Rolain, J. M. %A Le Poullain, M. N. %A Roux, V. %A Raoult, Didier %A Drancourt, M. %T Serum concentration of co-trimoxazole during a high-dosage regimen %D 2014 %L PAR00011502 %G ENG %J Journal of Antimicrobial Chemotherapy %@ 0305-7453 %K sulfamethoxazole ; trimethoprim ; MRSA %M ISI:000331827200027 %N 3 %P 757-760 %R 10.1093/jac/dkt400 %U https://www.documentation.ird.fr/hor/PAR00011502 %V 69 %W Horizon (IRD) %X Objectives: Sulfamethoxazole and trimethoprim have been used for decades, yet high dosages are rarely reported. We aimed to measure blood concentrations of both molecules in this situation. Methods: Between 2002 and 2010, 22 patients received two tablets of co-trimoxazole three times a day, equivalent to a daily dosage of 2400 mg of sulfamethoxazole and 480 mg of trimethoprim. The trimethoprim and sulfamethoxazole concentrations were determined 3 h after administration using ion-paired HPLC. Results: In the presence of a negative control, which yielded no peaks at the retention times for trimethoprim and sulfamethoxazole, the mean +/- SD value for sulfamethoxazole concentration was 161.01 +/- 69.154 mg/L and the mean +/- SD value for trimethoprim was 5.788 +/- 2.74 mg/L. Conclusions: These concentrations are largely above the trimethoprim and sulfamethoxazole MIC distributions as well as the trimethoprim resistance clinical breakpoint (4 mg/L) reported by EUCAST in 2012 for most bacterial pathogens, including Gram-positive species such as Staphylococcus aureus. Our results support proposing a high-dosage regimen of co-trimoxazole as a suitable alternative for methicillin-resistant S. aureus infections. %$ 050