Suppr超能文献

头孢地尔在成功治疗耐碳青霉烯鲍曼不动杆菌脑膜炎中的血药浓度和脑脊液浓度。

Plasma and cerebrospinal fluid concentrations of cefiderocol during successful treatment of carbapenem-resistant Acinetobacter baumannii meningitis.

机构信息

Department of Pharmacy Practice, Binghamton University School of Pharmacy and Pharmaceutical Sciences, Binghamton, NY, USA.

Division of Infectious Diseases, Department of Medicine, State University of New York Upstate Medical University, Syracuse, NY, USA.

出版信息

J Antimicrob Chemother. 2022 Sep 30;77(10):2737-2741. doi: 10.1093/jac/dkac248.

Abstract

BACKGROUND

To date, no real-world data are available to describe cefiderocol use in carbapenem-resistant Acinetobacter baumannii (CRAB) meningitis. Furthermore, cefiderocol pharmacokinetic (PK) data to support CNS penetration in human subjects are limited. These gaps pose a significant concern for clinicians who are faced with treating such infections when considering cefiderocol use.

OBJECTIVES

To describe cefiderocol CSF and plasma PK and pharmacodynamic (PD) data from two different dosing regimens [2 g IV q6h (regimen 1) and 2 g IV q8h (regimen 2)] during treatment of CRAB meningitis.

PATIENTS AND METHODS

A 61-year-old woman with CRAB meningitis was treated with cefiderocol and intraventricular gentamicin. Steady-state plasma and CSF cefiderocol concentrations were evaluated on Day 19 (regimen 1) and Day 24 (regimen 2) during the cefiderocol treatment course.

RESULTS

CSF AUC was 146.49 and 118.28 mg·h/L, as determined by the linear-log trapezoidal method for regimens 1 and 2, respectively. Penetration into CSF estimated as the AUCCSF/AUCfree plasma ratio was 68% and 60% for regimens 1 and 2, respectively. Estimated free plasma and CSF concentrations exceeded the MIC of the isolate for 100% of the dosing interval. Microbiological and clinical cure were achieved, and no cefiderocol-associated adverse effects were observed.

CONCLUSIONS

Cefiderocol, when given as 2 g q8h and 2 g q6h, attained CSF concentrations that exceeded the organism-specific MIC and the CLSI susceptible breakpoint (≤4 mg/L) for 100% of the dosing interval.

摘要

背景

迄今为止,尚无真实世界的数据可用于描述头孢他啶-阿维巴坦在耐碳青霉烯类鲍曼不动杆菌(CRAB)脑膜炎中的应用。此外,支持人体中枢神经系统渗透的头孢他啶药代动力学(PK)数据有限。对于面临此类感染的临床医生来说,这些空白对考虑使用头孢他啶时存在重大担忧。

目的

描述两种不同给药方案[2 g 静脉注射 q6h(方案 1)和 2 g 静脉注射 q8h(方案 2)]下头孢他啶治疗 CRAB 脑膜炎时的脑脊液(CSF)和血浆 PK 及药效学(PD)数据。

患者和方法

一名 61 岁女性患有 CRAB 脑膜炎,接受头孢他啶和脑室内庆大霉素治疗。在头孢他啶治疗过程中,于第 19 天(方案 1)和第 24 天(方案 2)评估稳态时的血浆和 CSF 头孢他啶浓度。

结果

通过线性对数梯形法,方案 1 和 2 的 CSF AUC 分别为 146.49 和 118.28 mg·h/L。以 CSF AUC 与游离血浆 AUC 的比值估计,方案 1 和 2 的 CSF 渗透分别为 68%和 60%。估计的游离血浆和 CSF 浓度在 100%的给药间隔内超过了分离株的 MIC。达到了微生物学和临床治愈,未观察到与头孢他啶相关的不良反应。

结论

头孢他啶以 2 g q8h 和 2 g q6h 给药时,在 100%的给药间隔内,CSF 浓度超过了特定于病原体的 MIC 和 CLSI 敏感折点(≤4 mg/L)。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验