Rose Warren E, Leonard Steven N, Rossi Kerri L, Kaatz Glenn W, Rybak Michael J
Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Detroit, Michigan 48201, USA.
Antimicrob Agents Chemother. 2009 Feb;53(2):805-7. doi: 10.1128/AAC.01009-08. Epub 2008 Nov 17.
The activity of vancomycin against heterogeneous vancomycin-intermediate Staphylococcus aureus (hVISA) and non-hVISA isolates, using an in vitro pharmacodynamic model, was reduced in the presence of a high inoculum amount (10(8) CFU/ml). A high bacterial load of >10(5) CFU/ml persisted for all strains with doses up to 5 g every 12 h against high inoculum amounts. No change in the vancomycin MIC was detected in any isolate at a moderate inoculum amount (10(6) CFU/ml), and bactericidal activity occurred only against the non-hVISA isolate (time to 99% kill, 7.5 h; P = 0.001).
在体外药效学模型中,当接种量较高(10⁸ CFU/ml)时,万古霉素对异质性万古霉素中介金黄色葡萄球菌(hVISA)和非hVISA菌株的活性降低。对于所有菌株,每12小时给予高达5 g的剂量,针对高接种量,细菌载量>10⁵ CFU/ml持续存在。在中等接种量(10⁶ CFU/ml)下,未检测到任何分离株的万古霉素最低抑菌浓度(MIC)有变化,并且杀菌活性仅针对非hVISA分离株(达到99%杀灭的时间,7.5小时;P = 0.001)。