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解析β-内酰胺类药物在面对肠杆菌科细菌中金属β-内酰胺酶介导的耐药性时的疗效:肉汤中超生理水平的锌是罪魁祸首。

Deciphering the Efficacy of β-Lactams in the Face of Metallo-β-Lactamase-Derived Resistance in Enterobacterales: Supraphysiologic Zinc in the Broth Is the Culprit.

作者信息

Abdelraouf Kamilia, Gill Christian M, Gethers Matthew, Tiseo Giusy, Barnini Simona, Falcone Marco, Menichetti Francesco, Nicolau David P

机构信息

Center for Anti-Infective Research & Development, Hartford Hospital, Hartford, Connecticut, USA.

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera Universitaria Pisana, University of Pisa, Pisa, Italy.

出版信息

Open Forum Infect Dis. 2024 Apr 23;11(5):ofae228. doi: 10.1093/ofid/ofae228. eCollection 2024 May.

Abstract

BACKGROUND

discordance in β-lactams' activities against metallo-ß-lactamase (MBL)-producing Enterobacterales has been described. We aimed to assess whether this discordance is attributed to the supra-physiologic zinc concentration in testing media.

METHODS

A clinical and microbiological observational study of patients with bloodstream infections due to New Delhi metallo-ß-lactamase-producing was performed. Outcomes of patients treated empirically with non-MBL-active β-lactam therapy (carbapenems and ceftazidime/avibactam) and MBL-active β-lactam therapy (ceftazidime/avibactam + aztreonam) were documented. The patients' isolates were used to induce septicemia in mice, and survival upon meropenem treatment was recorded. Meropenem minimum inhibitory concentrations (MICs) were determined in standard media and in the presence of physiological zinc concentrations.

RESULTS

Twenty-nine patients receiving empiric non-MBL-active β-lactams (median duration, 4 days) were compared with 29 receiving MBL-active β-lactams. The 14-day mortality rates were 21% and 14%, respectively. In the murine septicemia model, meropenem treatment resulted in protection from mortality ( < .0001). Meropenem MICs in the physiologic zinc concentration broth were 1- to >16-fold lower vs MICs in zinc-unadjusted broth (≥64 mg/L).

CONCLUSIONS

Our data provide foundational support to establish pharmacokinetic/pharmacodynamic relationships using MICs derived in physiologic zinc concentration, which may better predict β-lactam therapy outcome.

摘要

背景

已有研究描述了β-内酰胺类药物对产金属β-内酰胺酶(MBL)的肠杆菌科细菌活性的不一致性。我们旨在评估这种不一致性是否归因于检测培养基中超生理浓度的锌。

方法

对因产新德里金属β-内酰胺酶导致血流感染的患者进行了一项临床和微生物学观察性研究。记录了接受非MBL活性β-内酰胺类药物治疗(碳青霉烯类和头孢他啶/阿维巴坦)和MBL活性β-内酰胺类药物治疗(头孢他啶/阿维巴坦+氨曲南)的患者的治疗结果。将患者的分离株用于诱导小鼠败血症,并记录美罗培南治疗后的生存率。在标准培养基和生理锌浓度存在的情况下测定美罗培南的最低抑菌浓度(MIC)。

结果

将29例接受经验性非MBL活性β-内酰胺类药物治疗(中位疗程4天)的患者与29例接受MBL活性β-内酰胺类药物治疗的患者进行比较。14天死亡率分别为21%和14%。在小鼠败血症模型中,美罗培南治疗可降低死亡率(P<0.0001)。与未调整锌浓度的肉汤(≥64mg/L)相比,生理锌浓度肉汤中美罗培南的MIC低1至>16倍。

结论

我们的数据为使用生理锌浓度下得出的MIC建立药代动力学/药效学关系提供了基础支持,这可能更好地预测β-内酰胺类药物的治疗结果。

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