کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5666866 | 1591748 | 2016 | 6 صفحه PDF | دانلود رایگان |

- Ertapenem displayed inferior pharmacodynamics compared with the other carbapenems.
- A large inoculum effect at 108âCFU/mL was observed for all carbapenem combinations.
- Carbapenem MICs were poorly predictive of killing in combination with polymyxin B.
- Doripenem, meropenem and imipenem displayed similar pharmacodynamics.
The objective of this study was to determine the comparative pharmacodynamics of four different carbapenems in combination with polymyxin B (PMB) against carbapenem-resistant Acinetobacter baumannii isolates using time-kill experiments at two different inocula. Two A. baumannii strains (03-149-1 and N16870) with carbapenem minimum inhibitory concentrations (MICs) ranging from 8 to 64âmg/L were investigated in 48-h time-kill experiments using starting inocula of 106âCFU/mL and 108âCFU/mL. Concentration arrays of ertapenem, doripenem, meropenem and imipenem at 0.25Ã, 0.5Ã, 1Ã, 1.5à and 2à published maximum serum concentration (Cmax) values (Cmax concentrations of 12, 21, 48 and 60âmg/L, respectively) were investigated in the presence of 1.5âmg/L PMB. Use of carbapenems without PMB resulted in drastic re-growth. All carbapenem combinations were able to achieve a â¥3 log10 CFU/mL reduction by 4âh against both strains at 106âCFU/mL, whereas maximum reductions against strain 03-149-1 at 108âCFU/mL were 1.0, 3.2, 2.2 and 3.3 log10 CFU/mL for ertapenem, doripenem, meropenem and imipenem, respectively. None of the combinations were capable of reducing 108âCFU/mL of N16870 by â¥2 log10 CFU/mL. Ertapenem combinations consistently displayed the least activity, whereas doripenem, meropenem and imipenem combinations had similar activities that were poorly predicted by carbapenem MICs. As doripenem, meropenem, or imipenem displayed similar pharmacodyanmics in combination, the decision of which carbapenem to use in combination with PMB may be based on toxicodynamic profiles if drastic discordance in MICs is not present.
Journal: International Journal of Antimicrobial Agents - Volume 48, Issue 6, December 2016, Pages 719-724