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Evaluation of Vancomycin in Combination with Piperacillin-Tazobactam or Oxacillin against Clinical Methicillin-Resistant Staphylococcus aureus Isolates and Vancomycin-Intermediate S. aureus Isolates In Vitro

机译:万古霉素联合哌拉西林-他唑巴坦或奥沙西林对耐甲氧西林金黄色葡萄球菌分离株和万古霉素中间金黄色葡萄球菌分离株的评价

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摘要

Vancomycin with piperacillin-tazobactam is used as empirical therapy for critically ill patients. Studies of this combination against methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-intermediate S. aureus (VISA) are limited, but β-lactams in combination with vancomycin have shown synergistic activity against MRSA and VISA. The goal of this study was to evaluate whether piperacillin-tazobactam and vancomycin were synergistic against MRSA and VISA in vitro. Bloodstream MRSA (n = 20) and VISA (n = 4) strains were selected. In vitro antimicrobial activities of piperacillin-tazobactam and oxacillin were evaluated by disk diffusion, and MICs were determined by Etest using Muller-Hinton agar with and without vancomycin at one-half the MIC. Time-kill studies evaluated 14 MRSA and all 4 VISA isolates using piperacillin-tazobactam at 300/35 mg/liter or oxacillin at 40 mg/liter alone and with vancomycin at one-half the MIC. Mean zones of inhibition for piperacillin-tazobactam and oxacillin increased with vancomycin against MRSA and VISA (P < 0.001 for all), and the MIC90 decreased with vancomycin against MRSA and VISA to values meeting susceptibility criteria for S. aureus (P < 0.001 for both antibiotics against MRSA). In MRSA time-kill studies, the mean 24-h reductions in inoculum for piperacillin-tazobactam, piperacillin-tazobactam with vancomycin, and oxacillin with vancomycin were 3.53, 3.69, and 2.62 log10 CFU/ml, respectively. The mean 24-h reductions in VISA inoculum for piperacillin-tazobactam, piperacillin-tazobactam with vancomycin, and oxacillin with vancomycin were 2.85, 2.93, and 3.45 log10 CFU/ml, respectively. Vancomycin with piperacillin-tazobactam or oxacillin demonstrated synergistic activity against MRSA and VISA. The clinical implications of these combinations against MRSA and VISA should be investigated.
机译:万古霉素与哌拉西林-他唑巴坦被用作重症患者的经验疗法。对耐甲氧西林金黄色葡萄球菌(MRSA)和万古霉素中间金黄色葡萄球菌(VISA)的这种组合的研究有限,但β-内酰胺类与万古霉素的组合已显示出对MRSA和VISA的协同活性。这项研究的目的是评估哌拉西林-他唑巴坦和万古霉素在体外对MRSA和VISA是否具有协同作用。选择血流MRSA(n = 20)和VISA(n = 4)菌株。通过圆盘扩散法评估哌拉西林-他唑巴坦和奥沙西林的体外抗菌活性,并通过Etest使用Muller-Hinton琼脂(含和不含万古霉素)将MIC的一半确定MIC。时间杀灭研究使用单独的300/35 mg /升哌拉西林-他唑巴坦或40 mg /升的奥沙西林和MIC一半的万古霉素评估了14种MRSA和所有4种VISA分离株。万古霉素对MRSA和VISA的哌拉西林-他唑巴坦和奥沙西林的平均抑制范围增加(所有P均<0.001),万古霉素对MRSA和VISA的MIC90降低至满足金黄色葡萄球菌敏感性标准的值(两者P均<0.001)抗MRSA的抗生素)。在MRSA时间杀灭研究中,哌拉西林-他唑巴坦,哌拉西林-他唑巴坦与万古霉素和奥沙西林与万古霉素的平均接种量分别降低了3.53、3.69和2.62 log10 CFU / ml。哌拉西林-他唑巴坦,哌拉西林-他唑巴坦与万古霉素和奥沙西林与万古霉素的VISA接种物平均减少24小时分别为2.85、2.93和3.45 log10 CFU / ml。万古霉素与哌拉西林-他唑巴坦或奥沙西林显示出对MRSA和VISA的协同活性。应研究这些组合抗MRSA和VISA的临床意义。

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